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Research on drinking water purification technologies for household use by reducing total dissolved solids (TDS)
Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing
* E-mail: [email protected]
Affiliation Redlands East Valley High School, Redlands, California, United States of America
![tap water purification research paper ORCID logo](https://journals.plos.org/resource/img/orcid_16x16.png)
- Bill B. Wang
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- Published: September 28, 2021
- https://doi.org/10.1371/journal.pone.0257865
- Reader Comments
This study, based in San Bernardino County, Southern California, collected and examined tap water samples within the area to explore the feasibility of adopting non-industrial equipment and methods to reduce water hardness and total dissolved solids(TDS). We investigated how water quality could be improved by utilizing water boiling, activated carbon and sodium bicarbonate additives, as well as electrolysis methods. The results show that heating is effective at lower temperatures rather than long boils, as none of the boiling tests were lower than the original value. Activated carbon is unable to lower TDS, because it is unable to bind to any impurities present in the water. This resulted in an overall TDS increase of 3.5%. However, adding small amounts of sodium bicarbonate(NaHCO 3 ) will further eliminate water hardness by reacting with magnesium ions and improve taste, while increasing the pH. When added to room temperature tap water, there is a continuous increase in TDS of 24.8% at the 30 mg/L mark. The new findings presented in this study showed that electrolysis was the most successful method in eliminating TDS, showing an inverse proportion where an increasing electrical current and duration of electrical lowers more amounts of solids. This method created a maximum decrease in TDS by a maximum of 22.7%, with 3 tests resulting in 15.3–16.6% decreases. Furthermore, when water is heated to a temperature around 50°C (122°F), a decrease in TDS of around 16% was also shown. The reduction of these solids will help lower water hardness and improve the taste of tap water. These results will help direct residents to drink more tap water rather than bottled water with similar taste and health benefits for a cheaper price as well as a reduction on plastic usage.
Citation: Wang BB (2021) Research on drinking water purification technologies for household use by reducing total dissolved solids (TDS). PLoS ONE 16(9): e0257865. https://doi.org/10.1371/journal.pone.0257865
Editor: Mahendra Singh Dhaka, Mohanlal Sukhadia University, INDIA
Received: June 22, 2021; Accepted: September 14, 2021; Published: September 28, 2021
Copyright: © 2021 Bill B. Wang. This is an open access article distributed under the terms of the Creative Commons Attribution License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: The author received no specific funding for this work.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The concentration of total dissolved solids(TDS) present in water is one of the most significant factors in giving water taste and also provides important ions such as calcium, magnesium, potassium, and sodium [ 1 – 3 ]. However, water with high TDS measurements usually indicates contamination by human activities, such as soil and agricultural runoff caused by irrigation, unregulated animal grazing and wildlife impacts, environmentally damaging farming methods such as slash and burn agriculture, and the overuse of nitrate-based fertilizer [ 4 , 5 ], etc. Around tourist areas as well as state parks, these factors will slowly add up over time and influence the water sources nearby [ 5 ]. Water that flows through natural springs and waterways with high concentrations of organic salts within minerals and rocks, or groundwater that originates from wells with high salt concentration will also result in higher particle measurements [ 6 ].
Water sources can be contaminated by substances and ions such as nitrate, lead, arsenic, and copper [ 7 , 8 ] and may cause many health problems related to heavy metal consumption and poisoning. Water reservoirs and treatments plants that do not consider water contamination by motor vehicles, as well as locations that struggle to provide the necessary components required for water treatment will be more prone to indirect contamination [ 9 – 11 ]. Many plants are effective in ensuring the quality and reduction of these contaminants, but often leave out the secondary considerations, The United States Environmental Protection Agency(US EPA)’s secondary regulations recommend that TDS should be below 500 mg/L [ 2 ], which is also supported by the World Health Organization(WHO) recommendation of below 600 mg/L and an absolute maximum of less than 1,000 mg/L [ 3 ]. These substances also form calcium or magnesium scales within water boilers, heaters, and pipes, causing excess buildup and drain problems, and nitrate ions may pose a risk to human health by risking the formation of N -nitroso compounds(NOC) and less public knowledge about such substances [ 12 – 15 ]. Nitrates can pose a non-carcinogenic threat to different communities, but continue to slip past water treatment standards [ 15 ]. Furthermore, most people do not tolerate or prefer water with high hardness or chlorine additives [ 16 ], as the taste changes tremendously and becomes unpreferable. Even so, TDS levels are not accounted for in mandatory water regulations, because the essential removal of harmful toxins and heavy metals is what matters the most in water safety. Some companies indicate risks in certain ions and alkali metals, showing how water hardness is mostly disregarded and is not as well treated as commercial water bottling companies [ 17 , 18 ].
In Southern California, water quality is not as well maintained than the northern counties as most treatment plants in violation of a regulation or standard are located in Central-Southern California [ 19 ], with southern counties having the largest number of people affected [ 20 ]. This study is focused on the Redlands area, which has had no state code violations within the last decade [ 21 ]. A previous study has analyzed TDS concentrations throughout the Santa Ana Basin, and found concentrations ranging from 190–600 ppm as treated wastewater and samples obtained from mountain sites, taking into account the urban runoff and untreated groundwater as reasons for elevated levels of TDS but providing no solution in helping reduce TDS [ 22 ]. Also, samples have not been taken directly through home water supplies, where the consumer is most affected. Other water quality studies in this region have been focused on the elimination of perchlorates in soil and groundwater and distribution of nitrates, but such research on chemicals have ceased for the last decade, demonstrated by safe levels of perchlorates and nitrates in water reports [ 23 , 24 ]. In addition to these studies, despite the improving quality of the local water treatment process, people prefer bottled water instead of tap water because of the taste and hardness of tap water [ 25 ]. Although water quality tests are taken and documented regularly, the taste of the water is not a factor to be accounted for in city water supplies, and neither is the residue left behind after boiling water. The residue can build up over time and cause appliance damage or clogs in drainage pipes.
This study will build upon previous analyses of TDS studies and attempt to raise new solutions to help develop a more efficient method in reducing local TDS levels, as well as compare current measurements to previous analyses to determine the magnitude to which local treatment plants have improved and regulated its treatment processes.
Several methods that lower TDS are reviewed: boiling and heating tap water with and without NaHCO₃, absorption by food-grade activated carbon [ 26 , 27 ], and battery-powered electrolysis [ 28 – 30 ]. By obtaining water samples and determining the difference in TDS before and after the listed experiments, we can determine the effectiveness of lowering TDS. The results of this study will provide options for residents and water treatment plants to find ways to maintain the general taste of the tap water, but also preserve the lifespan of accessories and pipelines. By determining a better way to lower TDS and treat water hardness, water standards can be updated to include TDS levels as a mandatory measurement.
Materials and methods
All experiments utilized tap water sourced from Redlands homes. This water is partially supplied from the Mill Creek (Henry Tate) and Santa Ana (Hinckley) Water Sheds/Treatment Plants, as well as local groundwater pumps. Water sampling and sourcing were done at relatively stable temperatures of 26.9°C (80.42°F) through tap water supplies. The average TDS was measured at 159 ppm, which is slightly lower than the reported 175 ppm by the City of Redlands. Permission is obtained by the author from the San Bernardino Municipal Water Department website to permit the testing procedures and the usage of private water treatment devices for the purpose of lowering water hardness and improving taste and odor. The turbidity was reported as 0.03 Nephelometric Turbidity Units (NTU) post-treatment. Residual nitrate measured at 2.3mg/L in groundwater before treatment and 0.2 mg/L after treatment and perchlorate measured at 0.9 μg/L before treatment, barely staying below the standard of 1 μg/L; it was not detected within post-treatment water. Lead content was not detected at all, while copper was detected at 0.15 mg/L.
For each test, all procedures were done indoors under controlled temperatures, and 20 L of fresh water was retrieved before each test. Water samples were taken before each experimental set and measured for TDS and temperature, and all equipment were cleaned thoroughly with purified water before and after each measurement. TDS consists of inorganic salts and organic material present in solution, and consists mostly of calcium, magnesium, sodium, potassium, carbonate, chloride, nitrate, and sulfate ions. These ions can be drawn out by leaving the water to settle, or binding to added ions and purified by directly separating the water and ions. Equipment include a 50 L container, 1 L beakers for water, a graduated cylinder, a stir rod, a measuring spoon, tweezers, a scale, purified water, and a TDS meter. A standard TDS meter is used, operated by measuring the conductivity of the total amount of ionized solids in the water, and is also cleaned in the same manner as aforementioned equipment. The instrument is also calibrated by 3 pH solutions prior to testing.All results were recorded for and then compiled for graphing and analysis.
Heating/Boiling water for various lengths of time
The heating method was selected because heat is able to break down calcium bicarbonate into calcium carbonate ions that are able to settle to the bottom of the sample. Four flasks of 1 L of tap water were each heated to 40°C, 50°C, 60°C, and 80°C (104–176°F) and observed using a laser thermometer. The heated water was then left to cool and measurements were made using a TDS meter at the 5, 10, 20, 30, and 60-minute marks.
For the boiling experiments, five flasks of 1 L of tap water were heated to boil at 100°C (212°F). Each flask, which was labeled corresponding to its boiling duration, was marked with 2, 4, 6, 10, and 20 minutes. Each flask was boiled for its designated time, left to cool under open air, and measurements were made using a TDS meter at the 5, 10, 20, 30, 60, and 120-minute marks. The reason that the boiling experiment was extended to 120 minutes was to allow the water to cool down to room temperature.
Activated carbon as a water purification additive
This test was performed to see if food-grade, powdered activated carbon had any possibility of binding with and settling out residual particles. Activated carbon was measured using a milligram scale and separated into batches of 1, 2, 4, 5, 10, 30, and 50 mg. Each batch of the activated carbon were added to a separate flask of water and stirred for five minutes, and finally left to settle for another five minutes. TDS measurements were recorded after the water settled.
Baking soda as a water purification additive
To lower scale error and increase experimental accuracy, a concentration of 200 mg/L NaHCO₃ solution was made with purified water and pure NaHCO₃. For each part, an initial TDS measurement was taken before each experiment.
In separate flasks of 1 L tap water, each labeled 1, 2, 4, 5, 10, and 30 mg of NaHCO 3 , a batch was added to each flask appropriately and stirred for 5 minutes to ensure that everything dissolved. Measurements were taken after the water was left to settle for another 5 minutes for any TDS to settle.
Next, 6 flasks of 1 L tap water were labeled, with 5 mg (25 mL solution) of NaHCO₃ added to three flasks and 10 mg (50 mL solution) of NaHCO₃ added to the remaining three. One flask from each concentration of NaHCO₃ was boiled for 2 mins., 4 mins., or 6 mins., and then left to cool. A TDS measurement was taken at the 5, 10, 20, 30, 60, and 120-minute marks after removal from heat.
Electrolysis under low voltages
This test was performed because the ionization of the TDS could be manipulated with electricity to isolate an area of water with lower TDS. For this test, two 10cm long graphite pieces were connected via copper wiring to a group of batteries, with each end of the graphite pieces submerged in a beaker of tap water, ~3 cm apart.
Using groups of 1.5 V double-A batteries, 4 beakers with 40mL of tap water were each treated with either 7.5, 9.0, 10.5, and 12.0 V of current. Electrolysis was observed to be present by the bubbling of the water each test, and measurements were taken at the 3, 5, 7, and 10 minute marks.
Results/Discussion
Heating water to various temperatures until the boiling point.
The goal for this test was to use heat to reduce the amount of dissolved oxygen and carbon dioxide within the water, as shown by this chemical equation: Heat: Ca(HCO 3 ) 2 → CaCO 3 ↓ + H 2 O + CO 2 ↑.
This would decompose ions of calcium bicarbonate down into calcium carbonate and water and carbon dioxide byproducts.
Patterns and trends in decreasing temperatures.
The following trend lines are based on a dataset of changes in temperature obtained from the test results and graphed as Fig 1 .
- PPT PowerPoint slide
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- TIFF original image
https://doi.org/10.1371/journal.pone.0257865.g001
To predict the precise temperature measurements of the tap water at 26.9°C, calculations were made based on Fig 1 . The fitting equations are in the format, y = a.e bx . The values for the fitting coefficients a and b, and correlation coefficient R 2 are listed in Table 1 as column a, b and R 2 . The calculated values and the target temperature are listed in Table 1 .
https://doi.org/10.1371/journal.pone.0257865.t001
Fig 2 was obtained by compiling TDS results with different temperatures and times.
https://doi.org/10.1371/journal.pone.0257865.g002
The fitting equations for Fig 2 are also in the format, y = a.e bx . The fitting coefficients a and b, and correlation coefficient R 2 values are listed in Table 2 . Based on the fitting curves in Fig 2 and the duration to the target temperature in Table 1 , We calculated the TDS at 26.9°C as listed in column calculated TDS in Table 2 based on the values we reported on Fig 2 .
https://doi.org/10.1371/journal.pone.0257865.t002
Based on the heating temperature and the calculated TDS with the same target water temperature, we obtained the following heating temperature vs TDS removal trend line and its corresponding fitting curve in Table 2 .
In Fig 1 , a trend in the rate of cooling is seen, where a higher heating temperature creates a steeper curve. During the first five minutes of cooling, the water cools quicker as the absorbed heat is quickly released into the surrounding environment. By the 10-minute mark, the water begins to cool in a linear rate of change. One detail to note is that the 100°C water cools quicker than the 80°C and eventually cools even faster than the 60°C graph. Table 1 supports this observation as the duration to target temperature begins to decrease from a maximum point of 94.8 mins to 80.95 mins after the 80°C mark.
As shown in Fig 2 , all TDS values decrease as the temperature starts to cool to room temperature, demonstrating a proportional relationship where a lower temperature shows lower TDS. This can partially be explained by the ions settling in the flasks. Visible particles can also be observed during experimentation as small white masses on the bottom, as well as a thin ring that forms where the edge of the water contacts the flask. When the water is heated to 40°C and cooled, a 3.8% decrease in TDS is observed. When 50°C is reached, the TDS drops at its fastest rate from an initial value of 202 ppm to 160 ppm after 60 minutes of settling and cooling. The TDS measurements in these experiements reach a maximum of 204 ppm at the 60°C mark. However, an interesting phenomenon to point out is that the water does not hit a new maximum at 100°C. meaning that TDS reaches a plateau at 60°C. Also, the rate of decrease begins to slow down after 20 minutes, showing that an unknown factor is affecting the rate of decrease. It is also hypothesized that the slight increase in TDS between the 5–20 minute range is caused by a disturbance in the settling of the water, where the temperature starts to decrease at a more gradual and constant rate. The unstable and easy formation of CaCO 3 scaling has also been the subject of a study of antiscaling methods, which also supports the result that temperature is a significant influence for scale formation [ 12 ].
In Table 2 , calculations for TDS and the time it takes for each test to cool were made. Using the data, it is determined that the test with 50°C water decreased the most by 16% from the initial measurement of 159ppm. This means that it is most effective when water is heated between temperatures of 40–60°C when it comes to lowering TDS, with a difference of ~7–16%. When water is heated to temperatures greater than 80°C, the water begins to evaporate, increasing the concentration of the ions, causing the TDS to increase substantially when cooled to room temperature.
Finally, in Fig 3 , a line of best fit of function f(x) = -0.0007x 3 + 0.1641x 2 –10.962x + 369.36 is used with R 2 = 0.9341. Using this function, the local minimum of the graph would be reached at 48.4°C.
https://doi.org/10.1371/journal.pone.0257865.g003
This data shows that heating water at low temperatures (i.e. 40–50°C) may be more beneficial than heating water to higher temperatures. This study segment has not been presented in any section within the United States EPA Report on water management for different residual particles/substances. However, warmer water temperatures are more prone to microorganism growth and algal blooms, requiring more intensive treatment in other areas such as chlorine, ozone, and ultraviolet disinfection.
Using the specific heat capacity equation, we can also determine the amount of energy and voltage needed to heat 1 L of water up to 50°C: Q = mcΔT, where c, the specific heat capacity of water, is 4.186 J/g°C, ΔT, the change in temperature from the experimental maximum to room temperature, is 30°C, and m, the mass of the water, is 1000 g. This means that the amount of energy required will be 125580 J, which is 0.035 kWh or 2.1 kW.
After taking all of the different measurements obtained during TDS testing, and compiling the data onto this plot, Fig 4 is created with a corresponding line of best fit:
https://doi.org/10.1371/journal.pone.0257865.g004
In Fig 4 , it can be observed that the relationship between the temperature of the water and its relative TDS value is a downwards facing parabolic graph. As the temperature increases, the TDS begins to decrease after the steep incline at 50–60°C. The line of best fit is represented by the function f(x) = -0.0142x 2 + 2.258x + 105.84. R 2 = 0.6781. Because the R 2 value is less than expected, factors such as the time spent settling and the reaction rate of the ions should be considered. To determine the specifics within this experiment, deeper research and prolonged studies with more highly accurate analyses must be utilized to solve this problem.
Boiling water for various amounts of time
Trend of boiling duration and rate of cooling..
Using the same methods to create the figures and tables for the previous section, Fig 5 depicts how the duration of time spent boiling water affects how fast the water cools.
https://doi.org/10.1371/journal.pone.0257865.g005
As seen in Fig 5 , within the first 10 minutes of the cooling time, the five different graphs are entwined with each other, with all lines following a similar pattern. However, the graph showing 20 minutes of boiling is much steeper than the other graphs, showing a faster rate of cooling. This data continues to support a previous claim in Fig 2 , as this is most likely represented by a relationship a longer the boil creates a faster cooling curve. This also shows that the first 5 minutes of cooling have the largest deviance compared to any other time frame.
The cooling pattern is hypothesized by possible changes in the orderly structure of the hydrogen bonds in the water molecules, or the decreased heat capacity of water due to the increasing concentration of TDS.
Effect on TDS as boiling duration increases.
In Fig 6 , all lines except for the 20-minute line are clustered in the bottom area of the graph. By excluding the last measurement temporarily due to it being an outlier, we have observed that the difference between the initial and final TDS value of each test decreases.
https://doi.org/10.1371/journal.pone.0257865.g006
Despite following a similar trend of an increase in TDS at the start of the tests and a slow decrease overtime, this experiment had an interesting result, with the final test measuring nearly twice the amount of particles compared to any previous tests at 310 ppm, as shown in Fig 6 . It is confirmed that the long boiling time caused a significant amount of water to evaporate, causing the minerals to be more concentrated, thus resulting in a 300 ppm reading. Fig 6 follows the same trend as Fig 2 , except the TDS reading veers away when the boiling duration reaches 20 minutes. Also, with the long duration of heating, the water has developed an unfavorable taste from intense concentrations of CaCO₃. This also causes a buildup of a thin crust of CaCO₃ and other impurities around the container that is difficult to remove entirely. This finding is in accordance with the introductory statement of hot boiling water causing mineral buildups within pipes and appliances [ 9 ]. A TDS reading of 300ppm is still well below federal secondary standards of TDS, and can still even be compared to bottled water, in which companies may fluctuate and contain 335ppm within their water [ 1 , 2 ].
This experiment continues to stupport that the cooling rate of the water increases as the time spent boiling increases. Based on this test, a prediction can be made in which an increased concentration of dissolved solids lowers the total specific heat capacity of the sample, as the total volume of water decreases. This means that a method can be derived to measure TDS using the heat capacity of a tap water mixture and volume, in addition to current methods of using the electrical conductivity of aqueous ions.
Adding food-grade activated carbon to untreated tap water
Fig 7 presents a line graph with little to no change in TDS, with an initial spike from 157 to 163 ppm. The insoluble carbon remains in the water and shows no benefit.
https://doi.org/10.1371/journal.pone.0257865.g007
The food-grade activated carbon proved no benefit to removing TDS from tap water, and instead added around 5–7 ppm extra, which settled down to around +4 ppm at 120 minutes. The carbon, which is not 100% pure from inorganic compounds and materials present in the carbon, can dissolve into the water, adding to the existing concentration of TDS. Furthermore, household tap water has already been treated in processing facilities using a variety of filters, including carbon, so household charcoal filters are not effective in further reducing dissolved solids [ 18 ].
Adding sodium bicarbonate solution to boiled tap water
As seen in Fig 8 , after adding 1 mg of NaHCO 3 in, the TDS rises to 161 ppm, showing a minuscule increase. When 4 mg was added, the TDS drops down to 158 ppm. Then, when 5 mg was added, a sudden spike to 172 ppm was observed. This means that NaHCO 3 is able to ionize some Ca 2+ and Mg 2+ ions, but also adds Na + back into the water. This also means that adding NaHCO 3 has little to no effect on TDS, with 4mg being the upper limit of effectiveness.
https://doi.org/10.1371/journal.pone.0257865.g008
To examine whether or not the temperature plays a role in the effectiveness in adding NaHCO 3 , a boiling experiment was performed, and the data is graphed in Fig 9 .
https://doi.org/10.1371/journal.pone.0257865.g009
Fig 9 presents the relationship between the amount of common baking soda(NaHCO₃) added, the boiling time involved, and the resulting TDS measurements. After boiling each flask for designated amounts of time, the results showed a downward trend line from a spike but does not reach a TDS value significantly lower than the initial sample. It is apparent that the NaHCO₃ has not lowered the TDS of the boiling water, but instead adds smaller quantities of ions, raising the final value. This additive does not contribute to the lowering of the hardness of the tap water. However, tests boiled with 5 mg/L of baking soda maintained a downward pattern as the water was boiled for an increasing amount of time, compared to the seemingly random graphs of boiling with 10 mg/L.
In some households, however, people often add NaHCO₃ to increase the pH for taste and health benefits. However, as shown in the test results, it is not an effective way of reducing TDS levels in the water [ 10 , 16 ], but instead raises the pH, determined by the concentration added. Even under boiling conditions, the water continues to follow the trend of high growth in TDS, of +25–43 ppm right after boiling and the slow drop in TDS (but maintaining a high concentration) as the particles settle to the bottom.
Utilizing the experimental results, we can summarize that after adding small batches of NaHCO3 and waiting up to 5 minutes will reduce water hardness making it less prone to crystallizing within household appliances such as water brewers. Also, this process raises the pH, which is used more within commercial water companies. However, the cost comes at increasing TDS.
Using electrolysis to treat TDS in tap water
Different voltages were passed through the water to observe the change in TDS overtime, with the data being compiled as Fig 10 .
https://doi.org/10.1371/journal.pone.0257865.g010
The process of electrolysis in this experiment was not to and directly remove the existing TDS, but to separate the water sample into three different areas: the anode, cathode, and an area of clean water between the two nodes [ 19 ]. The anions in the water such as OH - , SO 4 2- , HCO 3 - move to the anode, while the cations such as H + , Ca 2+ 、Mg 2+ 、Na + move to the cathode. The middle area would then be left as an area that is more deprived of such ions, with Fig 10 proving this.
As shown in Fig 10 , electrolysis is effective in lower the TDS within tap water. Despite the lines being extremely tangled and unpredictable, the general trend was a larger decrease with a longer duration of time. At 10 minutes, all lines except 10.5 V are approaching the same value, meaning that the deviation was most likely caused by disturbances to the water during measurement from the low volume of water. With each different voltage test, a decrease of 12.7% for 6.0 V, 14.9% for 9.0 V, 22.7% for 10.5 V. and 19.5% for 12.0 V respectfully were observed. In the treatment of wastewate leachate, a study has shown that with 90 minutes of electrical treatment, 34.58% of TDS content were removed, supporting the effectiveness of electricity and its usage in wastewater treatment [ 29 ].
This experiment concludes that electrolysis is effective in lowering TDS, with the possibility to improve this process by further experimentation, development of a water cleaning system utilizing this cathode-anode setup to process water. This system would be a more specific and limited version of a reverse osmosis system by taking away ions through attraction, rather than a filter.
The Southern Californian tap water supply maintains TDS values below the federal regulations. However, crystalline scale buildup in household appliances is a major issue as it is hard to clean and eliminate. To easily improve the taste and quality of tap water at home as well as eliminating the formation of scales, the following methods were demonstrated as viable:
- By heating water to around 50°C (122°F), TDS and water hardness will decrease the most. Also, the boiling process is effective in killing microorganisms and removing contaminants. This process cannot surpass 10 minutes, as the concentration of the ions in the water is too high, which poses human health risks if consumed. These, along with activated carbon and NaHCO₃ additives, are inefficient methods that have minimal effects for lowering TDS.
- Electrolysis is one of the most effective methods of eliminating TDS. Experiments have proven that increased current and duration of time helps lower TDS. However, this method has yet to be implemented into conventional commercial water filtration systems.
Also, some observations made in these experiments could not be explained, and require further research and experimentation to resolve these problems. The first observation is that TDS and increasing water temperature maintain a parabolic relationship, with a maximum being reached at 80°C, followed by a gradual decrease. The second observation is that when water is boiled for an increased duration of time, the rate of cooling also increases.
This experiment utilized non-professional scientific equipment which are prone to mistakes and less precise. These results may deviate from professionally derived data, and will require further study using more advanced equipment to support these findings.
Acknowledgments
The author thanks Tsinghua University Professor and PLOS ONE editor Dr. Huan Li for assisting in experimental setups as well as data processing and treatment. The author also thanks Redlands East Valley High School’s Dr. Melissa Cartagena for her experimental guidance, and Tsinghua University Professor Dr. Cheng Yang for proofreading the manuscript.
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Research Progress of Tap Water Treatment Process
Yian Wang 1 , Chao Wang 1 , Xinshuai Wang 1 , Hui Qin 1 , Hua Lin 1 , Kong Chhuon 2 and Qi Chen 3
Published under licence by IOP Publishing Ltd IOP Conference Series: Earth and Environmental Science , Volume 546 , R&D and Application of Electrochemical Technology Citation Yian Wang et al 2020 IOP Conf. Ser.: Earth Environ. Sci. 546 052025 DOI 10.1088/1755-1315/546/5/052025
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1 College of Environmental Science and Engineering, Guilin University of Technology, Guilin, Guangxi 541000, China
2 Faculty of Hydrology and Water Resources Engineering, Institute of Technology of Cambodia, Phnom Penh 120000, Cambodia
3 Shandong Haipu Safety and Environmental Protection Science and Technology Research Institute, Qingdao 266000, Shandong, China
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With the rapid decrease of available water resources, to satisfy the needs of human life, it is urgent to treat and purify the water resources of waterworks so that the purified water can satisfy people's needs. This article mainly elaborates on the current research progress of tap water treatment technology and advanced treatment technology. Provide some basis for the application of social enterprises and scientific research workers.
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- Published: 20 March 2008
Science and technology for water purification in the coming decades
- Mark A. Shannon 1 , 4 ,
- Paul W. Bohn 1 , 2 ,
- Menachem Elimelech 1 , 3 ,
- John G. Georgiadis 1 , 4 ,
- Benito J. Mariñas 1 , 5 &
- Anne M. Mayes 1 , 6
Nature volume 452 , pages 301–310 ( 2008 ) Cite this article
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One of the most pervasive problems afflicting people throughout the world is inadequate access to clean water and sanitation. Problems with water are expected to grow worse in the coming decades, with water scarcity occurring globally, even in regions currently considered water-rich. Addressing these problems calls out for a tremendous amount of research to be conducted to identify robust new methods of purifying water at lower cost and with less energy, while at the same time minimizing the use of chemicals and impact on the environment. Here we highlight some of the science and technology being developed to improve the disinfection and decontamination of water, as well as efforts to increase water supplies through the safe re-use of wastewater and efficient desalination of sea and brackish water.
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A critical review of point-of-use drinking water treatment in the United States
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Recent developments in hazardous pollutants removal from wastewater and water reuse within a circular economy
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Electrolysis of low-grade and saline surface water
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Acknowledgements
We acknowledge the US National Science Foundation Science and Technology Center, WaterCAMPWS , Center for Advanced Materials for the Purification of Water with Systems.
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Mark A. Shannon, Paul W. Bohn, Menachem Elimelech, John G. Georgiadis, Benito J. Mariñas & Anne M. Mayes
Department of Chemical and Biomolecular Engineering and Department of Chemistry, University of Notre Dame, Notre Dame, Indiana 46556, USA,
Paul W. Bohn
Department of Environmental and Chemical Engineering, Yale University, New Haven, Connecticut 06520, USA,
Menachem Elimelech
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DOI : https://doi.org/10.1038/nature06599
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Nanofiltration for drinking water treatment: a review
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- Published: 26 November 2021
- Volume 16 , pages 681–698, ( 2022 )
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- Hao Guo 1 na1 ,
- Xianhui Li 2 na1 ,
- Wulin Yang 3 ,
- Zhikan Yao 4 ,
- Ying Mei 5 ,
- Lu Elfa Peng 1 ,
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In recent decades, nanofiltration (NF) is considered as a promising separation technique to produce drinking water from different types of water source. In this paper, we comprehensively reviewed the progress of NF-based drinking water treatment, through summarizing the development of materials/fabrication and applications of NF membranes in various scenarios including surface water treatment, groundwater treatment, water reuse, brackish water treatment, and point of use applications. We not only summarized the removal of target major pollutants (e.g., hardness, pathogen, and natural organic matter), but also paid attention to the removal of micropollutants of major concern (e.g., disinfection byproducts, per- and polyfluoroalkyl substances, and arsenic). We highlighted that, for different applications, fit-for-purpose design is needed to improve the separation capability for target compounds of NF membranes in addition to their removal of salts. Outlook and perspectives on membrane fouling control, chlorine resistance, integrity, and selectivity are also discussed to provide potential insights for future development of high-efficiency NF membranes for stable and reliable drinking water treatment.
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Acknowledgements
This work is supported by Senior Research Fellow Scheme of Research Grant Council (Grant No. SRFS2021-7S04) in Hong Kong and Seed Fund for Translational and Applied Research at The University of Hong Kong, China (Grant No. 104006007).
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Authors and Affiliations
Membrane-based Environmental & Sustainable Technology (MembEST) Group, Department of Civil Engineering, The University of Hong Kong, Hong Kong, China
Hao Guo, Lu Elfa Peng, Zhe Yang & Chuyang Y. Tang
Key Laboratory for City Cluster Environmental Safety and Green Development of the Ministry of Education, Institute of Environmental and Ecological Engineering, Guangdong University of Technology, Guangzhou, 510006, China
College of Environmental Science and Engineering, Peking University, Beijing, 100871, China
College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, 310027, China
Research and Development Center for Watershed Environmental Eco-Engineering, Advanced Institute of Natural Sciences, Beijing Normal University, Zhuhai, 519087, China
School of Civil Engineering, Wuhan University, Wuhan, 430072, China
Senlin Shao
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Guo, H., Li, X., Yang, W. et al. Nanofiltration for drinking water treatment: a review. Front. Chem. Sci. Eng. 16 , 681–698 (2022). https://doi.org/10.1007/s11705-021-2103-5
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Published : 26 November 2021
Issue Date : May 2022
DOI : https://doi.org/10.1007/s11705-021-2103-5
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Recent advancements in water treatment
For immediate release, acs news service weekly presspac: january 19, 2022.
Generating clean, safe water is becoming increasingly difficult. Water sources themselves can be contaminated, but in addition, some purification methods can cause unintended harmful byproducts to form. And not all treatment processes are created equal with regard to their ability to remove impurities or pollutants. Below are some recent papers published in ACS journals that report insights into how well water treatment methods work and the quality of the resulting water. Reporters can request free access to these papers by emailing newsroom@acs.org .
“Drivers of Disinfection Byproduct Cytotoxicity in U.S. Drinking Water: Should Other DBPs Be Considered for Regulation?” Environmental Science & Technology Dec.15, 2021
In this paper, researchers surveyed both conventional and advanced disinfection processes in the U.S., testing the quality of their drinking waters. Treatment plants with advanced removal technologies, such as activated carbon, formed fewer types and lower levels of harmful disinfection byproducts (known as DBPs) in their water. Based on the prevalence and cytotoxicity of haloacetonitriles and iodoacetic acids within some of the treated waters, the researchers recommend that these two groups be considered when forming future water quality regulations.
“Complete System to Generate Clean Water from a Contaminated Water Body by a Handmade Flower-like Light Absorber” ACS Omega Dec. 9, 2021 As a step toward a low-cost water purification technology, researchers crocheted a coated black yarn into a flower-like pattern. When the flower was placed in dirty or salty water, the water wicked up the yarn. Sunlight caused the water to evaporate, leaving the contaminants in the yarn, and a clean vapor condensed and was collected. People in rural locations could easily make this material for desalination or cleaning polluted water, the researchers say.
“Data Analytics Determines Co-occurrence of Odorants in Raw Water and Evaluates Drinking Water Treatment Removal Strategies” Environmental Science & Technology Dec. 2, 2021
Sometimes drinking water smells foul or “off,” even after treatment. In this first-of-its-kind study, researchers identified the major odorants in raw water. They also report that treatment plants using a combination of ozonation and activated carbon remove more of the odor compounds responsible for the stink compared to a conventional process. However, both methods generated some odorants not originally present in the water.
“Self-Powered Water Flow-Triggered Piezocatalytic Generation of Reactive Oxygen Species for Water Purification in Simulated Water Drainage” ACS ES&T Engineering Nov. 23, 2021
Here, researchers harvested energy from the movement of water to break down chemical contaminants. As microscopic sheets of molybdenum disulfide (MoS2) swirled inside a spiral tube filled with dirty water, the MoS2 particles generated electric charges. The charges reacted with water and created reactive oxygen species, which decomposed pollutant compounds, including benzotriazole and antibiotics. The researchers say these self-powered catalysts are a “green” energy resource for water purification.
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Research on drinking water purification technologies for household use by reducing total dissolved solids (TDS)
Bill b. wang.
Redlands East Valley High School, Redlands, California, United States of America
Associated Data
All relevant data are within the manuscript and its Supporting Information files.
This study, based in San Bernardino County, Southern California, collected and examined tap water samples within the area to explore the feasibility of adopting non-industrial equipment and methods to reduce water hardness and total dissolved solids(TDS). We investigated how water quality could be improved by utilizing water boiling, activated carbon and sodium bicarbonate additives, as well as electrolysis methods. The results show that heating is effective at lower temperatures rather than long boils, as none of the boiling tests were lower than the original value. Activated carbon is unable to lower TDS, because it is unable to bind to any impurities present in the water. This resulted in an overall TDS increase of 3.5%. However, adding small amounts of sodium bicarbonate(NaHCO 3 ) will further eliminate water hardness by reacting with magnesium ions and improve taste, while increasing the pH. When added to room temperature tap water, there is a continuous increase in TDS of 24.8% at the 30 mg/L mark. The new findings presented in this study showed that electrolysis was the most successful method in eliminating TDS, showing an inverse proportion where an increasing electrical current and duration of electrical lowers more amounts of solids. This method created a maximum decrease in TDS by a maximum of 22.7%, with 3 tests resulting in 15.3–16.6% decreases. Furthermore, when water is heated to a temperature around 50°C (122°F), a decrease in TDS of around 16% was also shown. The reduction of these solids will help lower water hardness and improve the taste of tap water. These results will help direct residents to drink more tap water rather than bottled water with similar taste and health benefits for a cheaper price as well as a reduction on plastic usage.
Introduction
The concentration of total dissolved solids(TDS) present in water is one of the most significant factors in giving water taste and also provides important ions such as calcium, magnesium, potassium, and sodium [ 1 – 3 ]. However, water with high TDS measurements usually indicates contamination by human activities, such as soil and agricultural runoff caused by irrigation, unregulated animal grazing and wildlife impacts, environmentally damaging farming methods such as slash and burn agriculture, and the overuse of nitrate-based fertilizer [ 4 , 5 ], etc. Around tourist areas as well as state parks, these factors will slowly add up over time and influence the water sources nearby [ 5 ]. Water that flows through natural springs and waterways with high concentrations of organic salts within minerals and rocks, or groundwater that originates from wells with high salt concentration will also result in higher particle measurements [ 6 ].
Water sources can be contaminated by substances and ions such as nitrate, lead, arsenic, and copper [ 7 , 8 ] and may cause many health problems related to heavy metal consumption and poisoning. Water reservoirs and treatments plants that do not consider water contamination by motor vehicles, as well as locations that struggle to provide the necessary components required for water treatment will be more prone to indirect contamination [ 9 – 11 ]. Many plants are effective in ensuring the quality and reduction of these contaminants, but often leave out the secondary considerations, The United States Environmental Protection Agency(US EPA)’s secondary regulations recommend that TDS should be below 500 mg/L [ 2 ], which is also supported by the World Health Organization(WHO) recommendation of below 600 mg/L and an absolute maximum of less than 1,000 mg/L [ 3 ]. These substances also form calcium or magnesium scales within water boilers, heaters, and pipes, causing excess buildup and drain problems, and nitrate ions may pose a risk to human health by risking the formation of N -nitroso compounds(NOC) and less public knowledge about such substances [ 12 – 15 ]. Nitrates can pose a non-carcinogenic threat to different communities, but continue to slip past water treatment standards [ 15 ]. Furthermore, most people do not tolerate or prefer water with high hardness or chlorine additives [ 16 ], as the taste changes tremendously and becomes unpreferable. Even so, TDS levels are not accounted for in mandatory water regulations, because the essential removal of harmful toxins and heavy metals is what matters the most in water safety. Some companies indicate risks in certain ions and alkali metals, showing how water hardness is mostly disregarded and is not as well treated as commercial water bottling companies [ 17 , 18 ].
In Southern California, water quality is not as well maintained than the northern counties as most treatment plants in violation of a regulation or standard are located in Central-Southern California [ 19 ], with southern counties having the largest number of people affected [ 20 ]. This study is focused on the Redlands area, which has had no state code violations within the last decade [ 21 ]. A previous study has analyzed TDS concentrations throughout the Santa Ana Basin, and found concentrations ranging from 190–600 ppm as treated wastewater and samples obtained from mountain sites, taking into account the urban runoff and untreated groundwater as reasons for elevated levels of TDS but providing no solution in helping reduce TDS [ 22 ]. Also, samples have not been taken directly through home water supplies, where the consumer is most affected. Other water quality studies in this region have been focused on the elimination of perchlorates in soil and groundwater and distribution of nitrates, but such research on chemicals have ceased for the last decade, demonstrated by safe levels of perchlorates and nitrates in water reports [ 23 , 24 ]. In addition to these studies, despite the improving quality of the local water treatment process, people prefer bottled water instead of tap water because of the taste and hardness of tap water [ 25 ]. Although water quality tests are taken and documented regularly, the taste of the water is not a factor to be accounted for in city water supplies, and neither is the residue left behind after boiling water. The residue can build up over time and cause appliance damage or clogs in drainage pipes.
This study will build upon previous analyses of TDS studies and attempt to raise new solutions to help develop a more efficient method in reducing local TDS levels, as well as compare current measurements to previous analyses to determine the magnitude to which local treatment plants have improved and regulated its treatment processes.
Several methods that lower TDS are reviewed: boiling and heating tap water with and without NaHCO₃, absorption by food-grade activated carbon [ 26 , 27 ], and battery-powered electrolysis [ 28 – 30 ]. By obtaining water samples and determining the difference in TDS before and after the listed experiments, we can determine the effectiveness of lowering TDS. The results of this study will provide options for residents and water treatment plants to find ways to maintain the general taste of the tap water, but also preserve the lifespan of accessories and pipelines. By determining a better way to lower TDS and treat water hardness, water standards can be updated to include TDS levels as a mandatory measurement.
Materials and methods
All experiments utilized tap water sourced from Redlands homes. This water is partially supplied from the Mill Creek (Henry Tate) and Santa Ana (Hinckley) Water Sheds/Treatment Plants, as well as local groundwater pumps. Water sampling and sourcing were done at relatively stable temperatures of 26.9°C (80.42°F) through tap water supplies. The average TDS was measured at 159 ppm, which is slightly lower than the reported 175 ppm by the City of Redlands. Permission is obtained by the author from the San Bernardino Municipal Water Department website to permit the testing procedures and the usage of private water treatment devices for the purpose of lowering water hardness and improving taste and odor. The turbidity was reported as 0.03 Nephelometric Turbidity Units (NTU) post-treatment. Residual nitrate measured at 2.3mg/L in groundwater before treatment and 0.2 mg/L after treatment and perchlorate measured at 0.9 μg/L before treatment, barely staying below the standard of 1 μg/L; it was not detected within post-treatment water. Lead content was not detected at all, while copper was detected at 0.15 mg/L.
For each test, all procedures were done indoors under controlled temperatures, and 20 L of fresh water was retrieved before each test. Water samples were taken before each experimental set and measured for TDS and temperature, and all equipment were cleaned thoroughly with purified water before and after each measurement. TDS consists of inorganic salts and organic material present in solution, and consists mostly of calcium, magnesium, sodium, potassium, carbonate, chloride, nitrate, and sulfate ions. These ions can be drawn out by leaving the water to settle, or binding to added ions and purified by directly separating the water and ions. Equipment include a 50 L container, 1 L beakers for water, a graduated cylinder, a stir rod, a measuring spoon, tweezers, a scale, purified water, and a TDS meter. A standard TDS meter is used, operated by measuring the conductivity of the total amount of ionized solids in the water, and is also cleaned in the same manner as aforementioned equipment. The instrument is also calibrated by 3 pH solutions prior to testing.All results were recorded for and then compiled for graphing and analysis.
Heating/Boiling water for various lengths of time
The heating method was selected because heat is able to break down calcium bicarbonate into calcium carbonate ions that are able to settle to the bottom of the sample. Four flasks of 1 L of tap water were each heated to 40°C, 50°C, 60°C, and 80°C (104–176°F) and observed using a laser thermometer. The heated water was then left to cool and measurements were made using a TDS meter at the 5, 10, 20, 30, and 60-minute marks.
For the boiling experiments, five flasks of 1 L of tap water were heated to boil at 100°C (212°F). Each flask, which was labeled corresponding to its boiling duration, was marked with 2, 4, 6, 10, and 20 minutes. Each flask was boiled for its designated time, left to cool under open air, and measurements were made using a TDS meter at the 5, 10, 20, 30, 60, and 120-minute marks. The reason that the boiling experiment was extended to 120 minutes was to allow the water to cool down to room temperature.
Activated carbon as a water purification additive
This test was performed to see if food-grade, powdered activated carbon had any possibility of binding with and settling out residual particles. Activated carbon was measured using a milligram scale and separated into batches of 1, 2, 4, 5, 10, 30, and 50 mg. Each batch of the activated carbon were added to a separate flask of water and stirred for five minutes, and finally left to settle for another five minutes. TDS measurements were recorded after the water settled.
Baking soda as a water purification additive
To lower scale error and increase experimental accuracy, a concentration of 200 mg/L NaHCO₃ solution was made with purified water and pure NaHCO₃. For each part, an initial TDS measurement was taken before each experiment.
In separate flasks of 1 L tap water, each labeled 1, 2, 4, 5, 10, and 30 mg of NaHCO 3 , a batch was added to each flask appropriately and stirred for 5 minutes to ensure that everything dissolved. Measurements were taken after the water was left to settle for another 5 minutes for any TDS to settle.
Next, 6 flasks of 1 L tap water were labeled, with 5 mg (25 mL solution) of NaHCO₃ added to three flasks and 10 mg (50 mL solution) of NaHCO₃ added to the remaining three. One flask from each concentration of NaHCO₃ was boiled for 2 mins., 4 mins., or 6 mins., and then left to cool. A TDS measurement was taken at the 5, 10, 20, 30, 60, and 120-minute marks after removal from heat.
Electrolysis under low voltages
This test was performed because the ionization of the TDS could be manipulated with electricity to isolate an area of water with lower TDS. For this test, two 10cm long graphite pieces were connected via copper wiring to a group of batteries, with each end of the graphite pieces submerged in a beaker of tap water, ~3 cm apart.
Using groups of 1.5 V double-A batteries, 4 beakers with 40mL of tap water were each treated with either 7.5, 9.0, 10.5, and 12.0 V of current. Electrolysis was observed to be present by the bubbling of the water each test, and measurements were taken at the 3, 5, 7, and 10 minute marks.
Results/Discussion
Heating water to various temperatures until the boiling point.
The goal for this test was to use heat to reduce the amount of dissolved oxygen and carbon dioxide within the water, as shown by this chemical equation: Heat: Ca(HCO 3 ) 2 → CaCO 3 ↓ + H 2 O + CO 2 ↑.
This would decompose ions of calcium bicarbonate down into calcium carbonate and water and carbon dioxide byproducts.
Patterns and trends in decreasing temperatures
The following trend lines are based on a dataset of changes in temperature obtained from the test results and graphed as Fig 1 .
![Click on image to zoom An external file that holds a picture, illustration, etc.
Object name is pone.0257865.g001.jpg](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478203/bin/pone.0257865.g001.jpg)
To predict the precise temperature measurements of the tap water at 26.9°C, calculations were made based on Fig 1 . The fitting equations are in the format, y = a.e bx . The values for the fitting coefficients a and b, and correlation coefficient R 2 are listed in Table 1 as column a, b and R 2 . The calculated values and the target temperature are listed in Table 1 .
Fig 2 was obtained by compiling TDS results with different temperatures and times.
![Click on image to zoom An external file that holds a picture, illustration, etc.
Object name is pone.0257865.g002.jpg](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478203/bin/pone.0257865.g002.jpg)
The fitting equations for Fig 2 are also in the format, y = a.e bx . The fitting coefficients a and b, and correlation coefficient R 2 values are listed in Table 2 . Based on the fitting curves in Fig 2 and the duration to the target temperature in Table 1 , We calculated the TDS at 26.9°C as listed in column calculated TDS in Table 2 based on the values we reported on Fig 2 .
Based on the heating temperature and the calculated TDS with the same target water temperature, we obtained the following heating temperature vs TDS removal trend line and its corresponding fitting curve in Table 2 .
In Fig 1 , a trend in the rate of cooling is seen, where a higher heating temperature creates a steeper curve. During the first five minutes of cooling, the water cools quicker as the absorbed heat is quickly released into the surrounding environment. By the 10-minute mark, the water begins to cool in a linear rate of change. One detail to note is that the 100°C water cools quicker than the 80°C and eventually cools even faster than the 60°C graph. Table 1 supports this observation as the duration to target temperature begins to decrease from a maximum point of 94.8 mins to 80.95 mins after the 80°C mark.
As shown in Fig 2 , all TDS values decrease as the temperature starts to cool to room temperature, demonstrating a proportional relationship where a lower temperature shows lower TDS. This can partially be explained by the ions settling in the flasks. Visible particles can also be observed during experimentation as small white masses on the bottom, as well as a thin ring that forms where the edge of the water contacts the flask. When the water is heated to 40°C and cooled, a 3.8% decrease in TDS is observed. When 50°C is reached, the TDS drops at its fastest rate from an initial value of 202 ppm to 160 ppm after 60 minutes of settling and cooling. The TDS measurements in these experiements reach a maximum of 204 ppm at the 60°C mark. However, an interesting phenomenon to point out is that the water does not hit a new maximum at 100°C. meaning that TDS reaches a plateau at 60°C. Also, the rate of decrease begins to slow down after 20 minutes, showing that an unknown factor is affecting the rate of decrease. It is also hypothesized that the slight increase in TDS between the 5–20 minute range is caused by a disturbance in the settling of the water, where the temperature starts to decrease at a more gradual and constant rate. The unstable and easy formation of CaCO 3 scaling has also been the subject of a study of antiscaling methods, which also supports the result that temperature is a significant influence for scale formation [ 12 ].
In Table 2 , calculations for TDS and the time it takes for each test to cool were made. Using the data, it is determined that the test with 50°C water decreased the most by 16% from the initial measurement of 159ppm. This means that it is most effective when water is heated between temperatures of 40–60°C when it comes to lowering TDS, with a difference of ~7–16%. When water is heated to temperatures greater than 80°C, the water begins to evaporate, increasing the concentration of the ions, causing the TDS to increase substantially when cooled to room temperature.
Finally, in Fig 3 , a line of best fit of function f(x) = -0.0007x 3 + 0.1641x 2 –10.962x + 369.36 is used with R 2 = 0.9341. Using this function, the local minimum of the graph would be reached at 48.4°C.
![Click on image to zoom An external file that holds a picture, illustration, etc.
Object name is pone.0257865.g003.jpg](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478203/bin/pone.0257865.g003.jpg)
This data shows that heating water at low temperatures (i.e. 40–50°C) may be more beneficial than heating water to higher temperatures. This study segment has not been presented in any section within the United States EPA Report on water management for different residual particles/substances. However, warmer water temperatures are more prone to microorganism growth and algal blooms, requiring more intensive treatment in other areas such as chlorine, ozone, and ultraviolet disinfection.
Using the specific heat capacity equation, we can also determine the amount of energy and voltage needed to heat 1 L of water up to 50°C: Q = mcΔT, where c, the specific heat capacity of water, is 4.186 J/g°C, ΔT, the change in temperature from the experimental maximum to room temperature, is 30°C, and m, the mass of the water, is 1000 g. This means that the amount of energy required will be 125580 J, which is 0.035 kWh or 2.1 kW.
After taking all of the different measurements obtained during TDS testing, and compiling the data onto this plot, Fig 4 is created with a corresponding line of best fit:
![Click on image to zoom An external file that holds a picture, illustration, etc.
Object name is pone.0257865.g004.jpg](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478203/bin/pone.0257865.g004.jpg)
In Fig 4 , it can be observed that the relationship between the temperature of the water and its relative TDS value is a downwards facing parabolic graph. As the temperature increases, the TDS begins to decrease after the steep incline at 50–60°C. The line of best fit is represented by the function f(x) = -0.0142x 2 + 2.258x + 105.84. R 2 = 0.6781. Because the R 2 value is less than expected, factors such as the time spent settling and the reaction rate of the ions should be considered. To determine the specifics within this experiment, deeper research and prolonged studies with more highly accurate analyses must be utilized to solve this problem.
Boiling water for various amounts of time
Trend of boiling duration and rate of cooling.
Using the same methods to create the figures and tables for the previous section, Fig 5 depicts how the duration of time spent boiling water affects how fast the water cools.
![Click on image to zoom An external file that holds a picture, illustration, etc.
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As seen in Fig 5 , within the first 10 minutes of the cooling time, the five different graphs are entwined with each other, with all lines following a similar pattern. However, the graph showing 20 minutes of boiling is much steeper than the other graphs, showing a faster rate of cooling. This data continues to support a previous claim in Fig 2 , as this is most likely represented by a relationship a longer the boil creates a faster cooling curve. This also shows that the first 5 minutes of cooling have the largest deviance compared to any other time frame.
The cooling pattern is hypothesized by possible changes in the orderly structure of the hydrogen bonds in the water molecules, or the decreased heat capacity of water due to the increasing concentration of TDS.
Effect on TDS as boiling duration increases
In Fig 6 , all lines except for the 20-minute line are clustered in the bottom area of the graph. By excluding the last measurement temporarily due to it being an outlier, we have observed that the difference between the initial and final TDS value of each test decreases.
![Click on image to zoom An external file that holds a picture, illustration, etc.
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Despite following a similar trend of an increase in TDS at the start of the tests and a slow decrease overtime, this experiment had an interesting result, with the final test measuring nearly twice the amount of particles compared to any previous tests at 310 ppm, as shown in Fig 6 . It is confirmed that the long boiling time caused a significant amount of water to evaporate, causing the minerals to be more concentrated, thus resulting in a 300 ppm reading. Fig 6 follows the same trend as Fig 2 , except the TDS reading veers away when the boiling duration reaches 20 minutes. Also, with the long duration of heating, the water has developed an unfavorable taste from intense concentrations of CaCO₃. This also causes a buildup of a thin crust of CaCO₃ and other impurities around the container that is difficult to remove entirely. This finding is in accordance with the introductory statement of hot boiling water causing mineral buildups within pipes and appliances [ 9 ]. A TDS reading of 300ppm is still well below federal secondary standards of TDS, and can still even be compared to bottled water, in which companies may fluctuate and contain 335ppm within their water [ 1 , 2 ].
This experiment continues to stupport that the cooling rate of the water increases as the time spent boiling increases. Based on this test, a prediction can be made in which an increased concentration of dissolved solids lowers the total specific heat capacity of the sample, as the total volume of water decreases. This means that a method can be derived to measure TDS using the heat capacity of a tap water mixture and volume, in addition to current methods of using the electrical conductivity of aqueous ions.
Adding food-grade activated carbon to untreated tap water
Fig 7 presents a line graph with little to no change in TDS, with an initial spike from 157 to 163 ppm. The insoluble carbon remains in the water and shows no benefit.
![Click on image to zoom An external file that holds a picture, illustration, etc.
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The food-grade activated carbon proved no benefit to removing TDS from tap water, and instead added around 5–7 ppm extra, which settled down to around +4 ppm at 120 minutes. The carbon, which is not 100% pure from inorganic compounds and materials present in the carbon, can dissolve into the water, adding to the existing concentration of TDS. Furthermore, household tap water has already been treated in processing facilities using a variety of filters, including carbon, so household charcoal filters are not effective in further reducing dissolved solids [ 18 ].
Adding sodium bicarbonate solution to boiled tap water
As seen in Fig 8 , after adding 1 mg of NaHCO 3 in, the TDS rises to 161 ppm, showing a minuscule increase. When 4 mg was added, the TDS drops down to 158 ppm. Then, when 5 mg was added, a sudden spike to 172 ppm was observed. This means that NaHCO 3 is able to ionize some Ca 2+ and Mg 2+ ions, but also adds Na + back into the water. This also means that adding NaHCO 3 has little to no effect on TDS, with 4mg being the upper limit of effectiveness.
![Click on image to zoom An external file that holds a picture, illustration, etc.
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To examine whether or not the temperature plays a role in the effectiveness in adding NaHCO 3 , a boiling experiment was performed, and the data is graphed in Fig 9 .
![Click on image to zoom An external file that holds a picture, illustration, etc.
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Fig 9 presents the relationship between the amount of common baking soda(NaHCO₃) added, the boiling time involved, and the resulting TDS measurements. After boiling each flask for designated amounts of time, the results showed a downward trend line from a spike but does not reach a TDS value significantly lower than the initial sample. It is apparent that the NaHCO₃ has not lowered the TDS of the boiling water, but instead adds smaller quantities of ions, raising the final value. This additive does not contribute to the lowering of the hardness of the tap water. However, tests boiled with 5 mg/L of baking soda maintained a downward pattern as the water was boiled for an increasing amount of time, compared to the seemingly random graphs of boiling with 10 mg/L.
In some households, however, people often add NaHCO₃ to increase the pH for taste and health benefits. However, as shown in the test results, it is not an effective way of reducing TDS levels in the water [ 10 , 16 ], but instead raises the pH, determined by the concentration added. Even under boiling conditions, the water continues to follow the trend of high growth in TDS, of +25–43 ppm right after boiling and the slow drop in TDS (but maintaining a high concentration) as the particles settle to the bottom.
Utilizing the experimental results, we can summarize that after adding small batches of NaHCO3 and waiting up to 5 minutes will reduce water hardness making it less prone to crystallizing within household appliances such as water brewers. Also, this process raises the pH, which is used more within commercial water companies. However, the cost comes at increasing TDS.
Using electrolysis to treat TDS in tap water
Different voltages were passed through the water to observe the change in TDS overtime, with the data being compiled as Fig 10 .
![Click on image to zoom An external file that holds a picture, illustration, etc.
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The process of electrolysis in this experiment was not to and directly remove the existing TDS, but to separate the water sample into three different areas: the anode, cathode, and an area of clean water between the two nodes [ 19 ]. The anions in the water such as OH - , SO 4 2- , HCO 3 - move to the anode, while the cations such as H + , Ca 2+ 、Mg 2+ 、Na + move to the cathode. The middle area would then be left as an area that is more deprived of such ions, with Fig 10 proving this.
As shown in Fig 10 , electrolysis is effective in lower the TDS within tap water. Despite the lines being extremely tangled and unpredictable, the general trend was a larger decrease with a longer duration of time. At 10 minutes, all lines except 10.5 V are approaching the same value, meaning that the deviation was most likely caused by disturbances to the water during measurement from the low volume of water. With each different voltage test, a decrease of 12.7% for 6.0 V, 14.9% for 9.0 V, 22.7% for 10.5 V. and 19.5% for 12.0 V respectfully were observed. In the treatment of wastewate leachate, a study has shown that with 90 minutes of electrical treatment, 34.58% of TDS content were removed, supporting the effectiveness of electricity and its usage in wastewater treatment [ 29 ].
This experiment concludes that electrolysis is effective in lowering TDS, with the possibility to improve this process by further experimentation, development of a water cleaning system utilizing this cathode-anode setup to process water. This system would be a more specific and limited version of a reverse osmosis system by taking away ions through attraction, rather than a filter.
The Southern Californian tap water supply maintains TDS values below the federal regulations. However, crystalline scale buildup in household appliances is a major issue as it is hard to clean and eliminate. To easily improve the taste and quality of tap water at home as well as eliminating the formation of scales, the following methods were demonstrated as viable:
- By heating water to around 50°C (122°F), TDS and water hardness will decrease the most. Also, the boiling process is effective in killing microorganisms and removing contaminants. This process cannot surpass 10 minutes, as the concentration of the ions in the water is too high, which poses human health risks if consumed. These, along with activated carbon and NaHCO₃ additives, are inefficient methods that have minimal effects for lowering TDS.
- Electrolysis is one of the most effective methods of eliminating TDS. Experiments have proven that increased current and duration of time helps lower TDS. However, this method has yet to be implemented into conventional commercial water filtration systems.
Also, some observations made in these experiments could not be explained, and require further research and experimentation to resolve these problems. The first observation is that TDS and increasing water temperature maintain a parabolic relationship, with a maximum being reached at 80°C, followed by a gradual decrease. The second observation is that when water is boiled for an increased duration of time, the rate of cooling also increases.
This experiment utilized non-professional scientific equipment which are prone to mistakes and less precise. These results may deviate from professionally derived data, and will require further study using more advanced equipment to support these findings.
Acknowledgments
The author thanks Tsinghua University Professor and PLOS ONE editor Dr. Huan Li for assisting in experimental setups as well as data processing and treatment. The author also thanks Redlands East Valley High School’s Dr. Melissa Cartagena for her experimental guidance, and Tsinghua University Professor Dr. Cheng Yang for proofreading the manuscript.
Funding Statement
The author received no specific funding for this work.
Data Availability
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Inorganics Treatment: Arsenic and Nitrate Webinar
- June 25, 2024 from 2 to 3:30pm ET
- The webinar recording will be posted to this page within two weeks of the live broadcast.
- Small Drinking Water Systems Webinar Series
About the Webinar
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1. Biological Nitrate Treatment: Innovations and Challenges
This presentation will focus on a biological nitrate treatment pilot study conducted at a water treatment plant. The study used an innovative denitrification system and nitrogen gas sparging to lower dissolved oxygen concentration, and it sometimes achieved complete denitrification. This discussion will also focus on the challenges of matching the acetic acid feed to a variable influent nitrate concentration and addressing clogging by bacterial flocs. The treatment approach showed promise; however, reactor design enhancements are needed to bring this technology to small systems.
Presenter: Asher Keithley, EPA Office of Research and Development. Asher is a general engineer with EPA’s Office of Research and Development, Center for Environmental Solutions and Emergency Response, Water Infrastructure Division. Their research focuses on drinking water treatment of inorganics and contaminants of emerging concern, such as manganese and nitrate. They are particularly interested in biological drinking water treatment processes. Asher is a licensed Professional Engineer in the state of Ohio.
2. Arsenic Refresher
This presentation will provide an overview of arsenic chemistry and treatment considerations. Arsenic accumulation in the distribution system and potential release back to the water will also be discussed, based on retrospective data analysis from EPA’s arsenic demonstration program.
Presenter: Simoni Triantafyllidou, EPA Office of Research and Development. Simoni is an environmental engineer with EPA's Office of Research and Development, Center for Environmental Solutions and Emergency Response, Water Infrastructure Division. Her research and technical support efforts revolve around aquatic chemistry, drinking water quality and treatment, corrosion science, inorganic contaminants, and sustainable drinking water infrastructure such as premise plumbing and distribution systems.
3. An Arsenic Case Study in California: Oasis Mobile Home Park
This presentation will provide an overview of EPA Region 9’s enforcement case with Oasis Mobile Home Park for violation of the Arsenic Rule. Key topics will include environmental justice, enforcement, technical conditions, and community and stakeholder engagement. The unique challenges and successes of trying to bring a small public water system back into compliance will also be discussed.
Presenter: Maria Alberty, EPA Region 9. Maria is an environmental protection specialist with EPA Region 9, Enforcement and Compliance Assurance Division in San Francisco, California. Maria is a credentialed drinking water inspector, and she leads cross-organizational teams to evaluate public water systems and ensure that those systems achieve and maintain public health and environmental compliance under the Safe Drinking Water Act. Prior to enforcement, she was a contracting officer for 18 years at EPA and NASA.
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What are leaking underground storage tanks and how are they being cleaned up?
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For more than a decade, some residents of the tiny Richmond, Rhode Island, neighborhood of Canob Park drank and bathed using tap water that had been tainted by gasoline that leaked from storage tanks buried under service stations a few hundred yards from their homes. They spent years battling oil companies, dealing with the daily misery of boiling most of their water and wondering about lasting damage to themselves and their children.
The Canob Park disaster sparked a national outcry in the 1980s to clean up and regulate the thousands of underground tanks storing petroleum, heating oil and other hazardous chemicals across the United States. It’s a program that continues today, where the tanks are a leading cause of groundwater pollution even after more than a half-million sites have been cleaned up.
EDITOR’S NOTE: This article is a collaboration between The Associated Press and The Uproot Project.
Nearly half of Americans depend on groundwater for their drinking water, according to the Environmental Protection Agency, and it’s not just well water that is threatened. A city’s water supply, while treated and processed to make sure it meets federal standards, may still collect contaminants from gas leaks on its way to the tap. In some cases, this can happen when the water originates from an unregulated well — some cities get their drinking water from a mix of surface and groundwater — or through cracked pipes.
For privately owned wells, which aren’t regulated by the government, the homeowner has the responsibility to treat and filter the water.
HOW LEAKS HAPPEN Environmental experts say even a pinprick-size hole in an underground tank can send 400 gallons of fuel a year into the ground, polluting soil and water. Spills can also destroy habitat and kill wildlife. Roughly 81 million people live within a quarter-mile of an underground storage tank that’s experienced at least one leak, based on the latest EPA data .
Most tanks were made of steel in the mid-1980s and likely to corrode over time. Modern tanks are fiberglass, which is more resistant to corrosion, but all tanks begin to leak sooner or later, said Dr. Kelly Pennell, a professor of environmental engineering and water resources at the University of Kentucky. The cylindrical tanks typically hold tens of thousands of gallons of fuel.
Detecting leaks is not easy, she said.
“If a gasoline station operated for 10 or 15 years, you may not be able to detect those small leaks,” said Dr. Pennell. “You wouldn’t be losing 1,000 gallons a day – you’re losing drips – but over time those matter.”
Leaks can form chemical plumes that move through groundwater and turn into vapor that rises up through cracks in the foundations of homes and businesses. Those fumes can contain cancer-causing chemicals including benzene, an ingredient in gasoline. And they carry a risk of fire and explosion. When contamination was found in Canob Park, the local fire chief sampled drinking water at one of the service stations and said it was “almost ignitable.”
Cleaning up groundwater pollution is costly, said Anne Rabe, environmental policy director at the New York Public Interest Research Group, a non-profit that works on environmental issues, including leaking underground storage tanks.
“You really have to do extensive testing to determine when these underground storage tanks are leaking and take immediate action or every week it spreads and spreads, and that increases the cost of remediation,” Rabe said.
More than 516,000 leaks have been cleaned up since Congress directed EPA to begin regulating underground tanks in 1984, but more than 57,000 known sites still await a full cleanup, the EPA said.
COSTS OF CLEANUP The average cost to clean up a site is $154,000, according to the Association of State and Territorial Solid Waste Management Officials, an organization that acts as a liaison between state and territorial leaking underground storage tank programs and the EPA. But that cost can be much higher or lower depending on how much work is needed.
The owners of tanks are supposed to carry insurance and pay for cleanup, but that doesn’t always happen. A trust fund that gets money from a gas tax helps — it currently holds about $1.5 billion — but the program costs states and the federal government about $1 billion a year beyond the fund.
While leaking underground storage tanks are located in nearly every town in the U.S., those who live closest to these sites tend to be in communities that are lower income with a higher proportion of minorities, according to the EPA.
The EPA requires owners and operators of underground storage tanks to install approved leak detection equipment and to regularly test these systems. But they aren’t foolproof. There are different types of systems, and any one type can miss a leak or its magnitude. Trade associations suggest building a system that uses more than one leak detection method, but that doesn’t always happen, and sometimes the one chosen may not be the best one for a particular tank. And owners may not maintain them properly.
Complying with the regulations, the EPA estimated in 2015, would cost tank owners and operators a total of $160 million a year — or about $715 per facility per year. But it would mean less taxpayer money needed for cleanups, the agency said.
Some of the properties cleaned up since the program began got funding from federal and state brownfields programs, which encourage the cleanup and reuse of contaminated or potentially contaminated sites.
The EPA last year announced a $315 million historic investment in the brownfields program, with most of the money coming from the bipartisan infrastructure deal President Joe Biden signed into law more than two years ago.
The Associated Press’ climate and environmental coverage receives financial support from multiple private foundations. AP is solely responsible for all content. Find AP’s standards for working with philanthropies, a list of supporters and funded coverage areas at AP.org .
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IMAGES
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This study, based in San Bernardino County, Southern California, collected and examined tap water samples within the area to explore the feasibility of adopting non-industrial equipment and methods to reduce water hardness and total dissolved solids(TDS). We investigated how water quality could be improved by utilizing water boiling, activated carbon and sodium bicarbonate additives, as well ...
Abstract. With the rapid decrease of available water resources, to satisfy the needs of human life, it is urgent to treat and purify the water resources of waterworks so that the purified water ...
In 2019, about 6% of public water utilities in the U.S. had a health-based violation. Due to the high risk of exposure to various contaminants in drinking water, point-of-use (POU) drinking water ...
Veysel Dogan. In this research, the chemical and microbiological quality of 20 tap water samples were randomly selected from Bingöl University in Bingöl. The Heterotrophic Plate Counts (HPC ...
Closing the water cycle by either desalination or wastewater purification promises to provide virtually unlimited volumes of freshwater: in principle, it would enable an increase in water ...
the actual situation to achieve the purpose of purifying tap water, thereby contributing to the safe and reliable drinking water that humans can drink. The advanced treatment process is essential for the purification of tap water. The development of new, efficient, sustainable, and diversified treatment processes is a research focus in the future.
With the rapid decrease of available water resources, to satisfy the needs of human life, it is urgent to treat and purify the water resources of waterworks so that the purified water can satisfy people's needs. This article mainly elaborates on the current research progress of tap water treatment technology and advanced treatment technology.
The need for research into water purification is pressing. In an extensive Review Article, Mark Shannon et al. highlight the developing technologies that — it is hoped — can provide our ...
Sedimentation and Filtration. Sedimentation and filtration have been widely employed for drinking water treatment to separate dissolved and particulate fractions from solution, which are the simple, effective, and low-cost approaches to improve overall water quality [46, 47].Sedimentation is a pretreatment technology in water treatment, which can remove one or more substances from a solution ...
Given the increasing degradation of source waters in many regions, the impact of pollutants on biological processes in drinking water treatment is an important research question. 2.5. Disinfection2.5.1. Residual disinfectant. Residual disinfectant is used in many jurisdictions to inhibit microbial regrowth in distribution systems.
Based on the data gathered from all water purification devices set in different regions, the level of fluoride was significantly different before and after using home water purifier (p= 0.001). It was found that home water purifiers nearly eliminated fluoride from tap water. Table 2 represents the results of t-test.
In recent decades, nanofiltration (NF) is considered as a promising separation technique to produce drinking water from different types of water source. In this paper, we comprehensively reviewed the progress of NF-based drinking water treatment, through summarizing the development of materials/fabrication and applications of NF membranes in various scenarios including surface water treatment ...
This review paper focuses on the various types of Filtration techniques. available and whic h tec hnique is most suitable for which t ype of region. W e. will study the t ypes of natural ...
Even these days, research on drinking water treatment is very scattered and even scarce (Bolisetty et al., Citation 2019). This scientometric analysis has the purpose of showing a range of possibilities and routes in the treatment of water for its purification to the scientific community and the interested public, especially to show the trends ...
This chapter contains the findings of the Subcommittee on Adsorption of the National Research Council's Safe Drinking Water Committee, which studied the efficacy of granular activated carbon (GAC) and related adsorbents in the treatment of drinking water. Some attention is given to an examination of the potential health effects related to the use of these adsorbents, but detailed toxicological ...
Dec.15, 2021. In this paper, researchers surveyed both conventional and advanced disinfection processes in the U.S., testing the quality of their drinking waters. Treatment plants with advanced removal technologies, such as activated carbon, formed fewer types and lower levels of harmful disinfection byproducts (known as DBPs) in their water.
Tap water nano/microplastics (NMPs) escaping from centralized water treatment systems are of increasing global concern, because they pose potential health risk to humans via water consumption. Drinking boiled water, an ancient tradition in some Asian countries, is supposedly beneficial for human health, as boiling can remove some chemicals and most biological substances. However, it remains ...
Sustainable nanotechnology has made substantial contributions in providing contaminant-free water to humanity. In this Review, we present the compelling need for providing access to clean water through nanotechnology-enabled solutions and the large disparities in ensuring their implementation. We also discuss the current nanotechnology frontiers in diverse areas of the clean water space with ...
The area of water purification has been one of the most dynamic research fields in recent years with strong public policy implications with over 39,000 papers. Similarly, the areas of nanomaterials and nanoprocesses have been one of the most dynamic research fields in recent years with significant public policy implications with over 1,000,000 ...
Introduction. The concentration of total dissolved solids(TDS) present in water is one of the most significant factors in giving water taste and also provides important ions such as calcium, magnesium, potassium, and sodium [1-3].However, water with high TDS measurements usually indicates contamination by human activities, such as soil and agricultural runoff caused by irrigation ...
In drinking water treatment, filtration plays an important role in the multi-barrier approach employed for the removal of pathogens. The presence of suspended solids and other particulate matter in water increases the resistance of most microbes to disinfection. Therefore, high performance in the removal of particles achieved by granular filtration can increase the disinfection efficiency ...
Agricultural development, extensive industrialization, and rapid growth of the global population have inadvertently been accompanied by environmental pollution. Water pollution is exacerbated by the decreasing ability of traditional treatment methods to comply with tightening environmental standards. This review provides a comprehensive description of the principles and applications of ...
Addressing water scarcity and pollution is imperative in tackling global environmental challenges, prompting the exploration of innovative techniques for effective water and wastewater treatment. Nanotechnology presents promising solutions through the customization of nanoparticles and nanocomposites specifically designed for water purification applications. This review delves into recent ...
Their research focuses on drinking water treatment of inorganics and contaminants of emerging concern, such as manganese and nitrate. They are particularly interested in biological drinking water treatment processes. Asher is a licensed Professional Engineer in the state of Ohio. 2. Arsenic Refresher
Herein, an intelligent collaborative optimal scheduling method is proposed for the water intake pump groups, clean-water reservoirs, and water supply pump groups. A long short-term memory (LSTM) network is applied to predict the flow of the water supply pump group, and a data-driven approach is used to plan the flow of the water intake pump ...
For privately owned wells, which aren't regulated by the government, the homeowner has the responsibility to treat and filter the water. HOW LEAKS HAPPEN Environmental experts say even a ...