scholarly journals Recently Developed Adsorbing Materials for Fluoride Removal from Water and Fluoride Analytical Determination Techniques: A Review

2021 ◽  
Vol 13 (13) ◽  
pp. 7061
Author(s):  
Athanasia K. Tolkou ◽  
Natalia Manousi ◽  
George A. Zachariadis ◽  
Ioannis A. Katsoyiannis ◽  
Eleni A. Deliyanni
Keyword(s):  
Drinking Water ◽  
Activated Carbon ◽  
Public Perception ◽  
Absorption Spectrometry ◽  
Sequential Injection Analysis ◽  
Analytical Determination ◽  
Fluoride Removal ◽  
Drinking Waters ◽  
Fluoride Determination ◽  
Microfluidic Analysis

In recent years, there has been an increase in public perception of the detrimental side-effects of fluoride to human health due to its effects on teeth and bones. Today, there is a plethora of techniques available for the removal of fluoride from drinking water. Among them, adsorption is a very prospective method because of its handy operation, cost efficiency, and high selectivity. Along with efforts to assist fluoride removal from drinking waters, extensive attention has been also paid to the accurate measurement of fluoride in water. Currently, the analytical methods that are used for fluoride determination can be classified into chromatographic methods (e.g., ionic chromatography), electrochemical methods (e.g., voltammetry, potentiometry, and polarography), spectroscopic methods (e.g., molecular absorption spectrometry), microfluidic analysis (e.g., flow injection analysis and sequential injection analysis), titration, and sensors. In this review article, we discuss the available techniques and the ongoing effort for achieving enhanced fluoride removal by applying novel adsorbents such as carbon-based materials (i.e., activated carbon, graphene oxide, and carbon nanotubes) and nanostructured materials, combining metals and their oxides or hydroxides as well as natural materials. Emphasis has been given to the use of lanthanum (La) in the modification of materials, both activated carbon and hybrid materials (i.e., La/Mg/Si-AC, La/MA, LaFeO3 NPs), and in the use of MgO nanostructures, which are found to exhibit an adsorption capacity of up to 29,131 mg g−1. The existing analytical methodologies and the current trends in analytical chemistry for fluoride determination in drinking water are also discussed.

scholarly journals Sustainable Conversion of Agriculture and Food Waste into Activated Carbons Devoted to Fluoride Removal from Drinking Water in Senegal

2015 ◽  
Vol 8 (1) ◽  
pp. 8 ◽  
Author(s):  
Mohamad M. Diémé ◽  
Maxime Hervy ◽  
Saïdou N. Diop ◽  
Claire Gérente ◽  
Audrey Villot ◽  
...  
Keyword(s):  
Drinking Water ◽  
Activated Carbon ◽  
Activated Carbons ◽  
Public Health Problem ◽  
Calcium Content ◽  
Fluoride Removal ◽  
Carbonaceous Materials ◽  
Water Steam ◽  
Surface Areas ◽  
Fluoride Adsorption

<p>The objective of this study was to investigate the production of activated carbons (AC) from cashew shells, and millet stalks and their efficiency in fluoride retention. These agricultural residues are collected from Senegal. It is known that some regions of Sénégal, commonly called the groundnut basin, are affected by a public health problem caused by an excess of fluoride in drinking water used by these populations. The activated carbons were produced by a combined pyrolysis and activation with water steam; no other chemical compounds were added. Then, activated carbonaceous materials obtained from cashew shells and millet stalks were called CS-H<sub>2</sub>O and MS-H<sub>2</sub>O respectively. CS-H<sub>2</sub>O and MS-H<sub>2</sub>O show very good adsorbent features, and present carbon content ranges between 71 % and 86 %. The BET surface areas are 942 m² g<sup>-1</sup> and 1234 m².g<sup>-1</sup> for CS-H<sub>2</sub>O and MS-H<sub>2</sub>O respectively. A third activated carbon produced from food wastes and coagulation-flocculation sludge (FW/CFS-H<sub>2</sub>O) was produced in the same conditions. Carbon and calcium content of FW/CFS-H<sub>2</sub>O are 32.6 and 39.3 % respectively. The kinetics sorption were performed with all these activated carbons, then the pseudo-first equation was used to describe the kinetics sorption. Fluoride adsorption isotherms were performed with synthetic and natural water with the best activated carbon from kinetics sorption, Langmuir and Freundlich models were used to describe the experimental data. The results showed that carbonaceous materials obtained from CS-H<sub>2</sub>O and MS-H<sub>2</sub>O were weakly efficient for fluoride removal. With FW/CFS-H<sub>2</sub>O, the adsorption capacity is 28.48 mg.g<sup>-1 </sup>with r² = 0.99 with synthetic water.</p>

scholarly journals Elementary Iodine-Doped Activated Carbon as an Oxidizing Agent for the Treatment of Arsenic-Enriched Drinking Water

Water ◽  
2019 ◽  
Vol 11 (9) ◽  
pp. 1778 ◽  
Author(s):  
Fabio Spaziani ◽  
Yuli Natori ◽  
Yoshiaki Kinase ◽  
Tomohiko Kawakami ◽  
Katsuyoshi Tatenuma
Keyword(s):  
Drinking Water ◽  
Activated Carbon ◽  
Oxidation Potential ◽  
Column Experiments ◽  
Oxidizing Agent ◽  
Column Tests ◽  
Oxidizing Agents ◽  
Drinking Waters ◽  
Iron Based ◽  
Elementary Iodine

An activated carbon impregnated with elementary iodine (I2), named IodAC, characterized by oxidation capability, was developed and applied to oxidize arsenite, As(III), to arsenate, As(V), in arsenic-rich waters. Batch and column experiments were conducted to test the oxidation ability of the material. Comparisons with the oxidizing agents usually used in arsenic treatment systems were also conducted. In addition, the material has been tested coupled with an iron-based arsenic sorbent, in order to verify its suitability for the dearsenication of drinking waters. IodAC exhibited a high and lasting oxidation potential, since the column tests executed on water spiked with 50 mg/L of arsenic (100% arsenite) showed that 1 cc of IodAC (30 wt% I2) can oxidize about 25 mg of As(III) (0.33 mmol) before showing a dwindling in the oxidation ability. Moreover, an improvement of the arsenic sorption capability of the tested sorbent was also proved. The results confirmed that IodAC is suitable for implementation in water dearsenication plants, in place of the commonly used oxidizing agents, such as sodium hypochlorite or potassium permanganate, and in association with arsenic sorbents. In addition, the well-known antibacterial ability of iodine makes IodAC particularly suitable in areas (such developing countries) where the sanitation of water is a critical topic.

scholarly journals Partial renewal of granular activated carbon biofilters for improved drinking water treatment

2018 ◽  
Vol 4 (4) ◽  
pp. 529-538 ◽  
Author(s):  
Nashita Moona ◽  
Kathleen R. Murphy ◽  
Mia Bondelind ◽  
Olof Bergstedt ◽  
Thomas J. R. Pettersson
Keyword(s):  
Climate Change ◽  
Drinking Water ◽  
Organic Matter ◽  
Activated Carbon ◽  
Water Treatment ◽  
Natural Organic Matter ◽  
Drinking Water Treatment ◽  
Granular Activated Carbon ◽  
Nordic Countries ◽  
Drinking Waters

There is a trend of increasing natural organic matter (NOM) in raw drinking waters of Nordic countries due to climate change.

scholarly journals Determination of beryllium in various types of natural waters by electrothermal atomic absorption spectrometry

2013 ◽  
Vol 14 (1) ◽  
pp. 40-47
Keyword(s):  
Drinking Water ◽  
Natural Waters ◽  
Electrothermal Atomic Absorption Spectrometry ◽  
Absorption Spectrometry ◽  
Mineral Waters ◽  
Waste Waters ◽  
Reliable Determination ◽  
Drinking Waters ◽  
Characteristic Mass

The procedure for the reliable determination of Be in natural waters by ETAAS was elaborated. Various modifiers (EDTA, Ca(NO3)2, Mg(NO3)2, Pd(NO3)2 and the mixture of Pd(NO3)2 and Mg(NO3)2) for the determination of beryllium was examined. The applicability of the selected Mg(NO3)2 as the appropriate and generally used modifier for the determination of Be in the different types of natural waters by ETAAS has been confirmed. The accuracy of the method was verified by analyzing of the certified reference material of drinking water ("Trace Metals in Drinking Water"). The real drinking waters and waste waters with the reference values of Be concentration, spiked tap water, mineral waters and model river water were utilized for the determination of Be. Using Mg(NO3)2 for modification, the detection limit of 0.07 μg L-1, the quantification limit of 0.22 μg L-1 and characteristic mass of 3.7 pg of Be were obtained. The recovery was in the range 95–111% and (%) RSD value was less than 8%.

Resorcinarene Cavitand Polymers for the Remediation of Halomethanes and 1,4-Dioxane

2019 ◽  
Author(s):  
Luke Skala ◽  
Anna Yang ◽  
Max Justin Klemes ◽  
Leilei Xiao ◽  
William Dichtel
Keyword(s):  
Drinking Water ◽  
Activated Carbon ◽  
High Capacity ◽  
The United States ◽  
Water Sources ◽  
Disinfection Byproducts ◽  
Porous Polymer ◽  
Organic Micropollutants ◽  
Executive Summary ◽  
Regulatory Limits

<p>Executive summary: Porous resorcinarene-containing polymers are used to remove halomethane disinfection byproducts and 1,4-dioxane from water.<br></p><p><br></p><p>Disinfection byproducts such as trihalomethanes are some of the most common micropollutants found in drinking water. Trihalomethanes are formed upon chlorination of natural organic matter (NOM) found in many drinking water sources. Municipalities that produce drinking water from surface water sources struggle to remain below regulatory limits for CHCl<sub>3</sub> and other trihalomethanes (80 mg L<sup>–1</sup> in the United States). Inspired by molecular CHCl<sub>3</sub>⊂cavitand host-guest complexes, we designed a porous polymer comprised of resorcinarene receptors. These materials show higher affinity for halomethanes than a specialty activated carbon used for trihalomethane removal. The cavitand polymers show similar removal kinetics as activated carbon and have high capacity (49 mg g<sup>–1</sup> of CHCl<sub>3</sub>). Furthermore, these materials maintain their performance in real drinking water and can be thermally regenerated under mild conditions. Cavitand polymers also outperform activated carbon in their adsorption of 1,4-dioxane, which is difficult to remove and contaminates many public water sources. These materials show promise for removing toxic organic micropollutants and further demonstrate the value of using supramolecular chemistry to design novel absorbents for water purification.<br></p>

ECOLOGICAL AND PHYSIOLOGICAL ASSESSMENT OF CHEMICAL COMPOSITION OF DRINKING TAP WATER IN KHANTY-MANSIYSK AND SALEKHARD

2020 ◽  
pp. 159-167
Author(s):  
V.V. Lapenko ◽  
L.N. Bikbulatova ◽  
E.M. Ternikova
Keyword(s):  
Drinking Water ◽  
Chemical Composition ◽  
Water Samples ◽  
Tap Water ◽  
Iron Concentration ◽  
Absorption Spectrometry ◽  
Northern Region ◽  
Transport Processes ◽  
Magnesium Concentration ◽  
Geochemical Environment

Water is very important for humans, as it is a solvent for metabolic products. Moreover, it is necessary for metabolism, biochemical and transport processes. The elemental status in persons depends on the geochemical environment and consumption of bioelements with food and water. The aim of the paper is to conduct a comprehensive assessment of chemical composition of drinking tap water in Khanty-Mansiysk and Salekhard. Materials and Methods. The chemical composition of 100 samples of drinking tap water was analyzed by atomic absorption spectrometry, spectrophotometry and capillary electrophoresis. All in all, there were 50 samples from Khanty-Mansiysk and 50 samples from Salekhard. The results were compared with Sanitary Rules and Norms 2.1.4.1074-01. Results. Drinking tap water in Salekhard contains a significantly higher concentration of iron, which is much above the maximum allowable concentration, if compared to water samples in Khanty-Mansiysk (p=0.03). In the cities under consideration, the water undergoes high-quality reagent-free treatment. However, the deterioration of the water supply networks in Salekhard is 3 times as high as in Khanty-Mansiysk. Calcium and magnesium concentration in water samples from Khanty-Mansiysk is 5.6 and 3.9 times lower than the MAC; in water samples from Salekhard calcium concentration is 6.3 (p=0.008) and magnesium concentration 4.6 (p<0.001) times lower than the MAC. Conclusion. The consumption of ultra-fresh drinking water leads to low intake of bioelements, which are a part of enzymes contributing to the human antioxidant defense and can result in manifestation of cardiovascular diseases. This is especially true for Salekhard with very soft drinking water and high iron concentration, which excess can exhibit prooxidant properties. Keywords: tap water, bioelements, northern region, antioxidants. Вода является важнейшим соединением для человека: необходима в качестве растворителя продуктов метаболизма и протекания обменных, биохимических и транспортных процессов. Элементный статус организма человека зависит от геохимического окружения и поступления биоэлементов с пищей и водой. Цель. Провести комплексную оценку химического состава водопроводной воды городов Ханты-Мансийск и Салехард. Материалы и методы. Методами атомно-абсорбционной спектрометрии, спектрофотометрии и капиллярного электрофореза проанализирован химический состав 100 проб водопроводной воды: по 50 из Ханты-Мансийска и Салехарда. Результаты сравнивали с СанПиН 2.1.4.1074-01. Результаты. В водопроводной воде Салехарда установлена превышающая ПДК и достоверно более высокая концентрация железа сравнительно с водой Ханты-Мансийска (р=0,03). При условии качественной безреагентной водоподготовки в изучаемых городах это обусловлено изношенностью водопроводных сетей в Салехарде, более чем в 3 раза превышающей этот показатель в Ханты-Мансийске. Концентрация кальция и магния в воде Ханты-Мансийска в 5,6 и 3,9 раза ниже ПДК; в воде Салехарда – в 6,3 (р=0,008) и 4,6 (р<0,001) раза ниже ПДК соответственно. Заключение. Употребление ультрапресной питьевой воды на фоне очень малого поступления с водой биоэлементов, входящих в состав ферментов антиоксидантной защиты организма человека, может привести к манифестации кардиоваскулярных заболеваний. Это особенно актуально для г. Салехарда с очень мягкой питьевой водой с повышенным содержанием железа, избыток которого может проявлять прооксидантные свойства. Ключевые слова: водопроводная вода, биоэлементы, северный регион, антиоксиданты.

Removal of microcystin-LR from drinking water with TiO2-coated activated carbon

2004 ◽  
Vol 4 (5-6) ◽  
pp. 21-28
Author(s):  
S.-C. Kim ◽  
D.-K. Lee
Keyword(s):  
Drinking Water ◽  
Activated Carbon ◽  
Synergistic Effect ◽  
Fluidized Bed ◽  
Continuous Flow ◽  
High Surface ◽  
High Surface Area ◽  
Fluidized Bed Reactor ◽  
Exterior Surface ◽  
Tio2 Particles

TiO2-coated granular activated carbon was employed for the removal of toxic microcystin-LR from water. High surface area of the activated carbon provided sites for the adsorption of microcystin-LR, and the adsorbed microcystin-LR migrated continuously onto the surface of TiO2 particles which located mainly at the exterior surface in the vicinity of the entrances of the macropores of the activated carbon. The migrated microcystin-LR was finally degraded into nontoxic products and CO2 very quickly. These combined roles of the activated carbon and TiO2 showed a synergistic effect on the efficient degradation of toxic microcystin-LR. A continuous flow fluidized bed reactor with the TiO2-coated activated carbon could successfully be employed for the efficient photocatalytic of microcystin-LR.

Determination of Hg(II) in drinking water by atomic absorption spectrometry - Cold vapour method after concentration by column extraction chromatography

1984 ◽  
Vol 49 (5) ◽  
pp. 1134-1139 ◽  
Author(s):  
Zdeněk Šmejkal ◽  
Jitka Tauferová ◽  
Mária Madová ◽  
Zlatica Teplá
Keyword(s):  
Drinking Water ◽  
Atomic Absorption Spectrometry ◽  
Atomic Absorption ◽  
Extraction Chromatography ◽  
Absorption Spectrometry ◽  
Average Yield ◽  
Water Mains ◽  
Cold Vapour ◽  
Column Extraction

The method describes concentration of mercury in samples of drinking water from water mains with Hg concentration above 1.0 . 10-7 g l-1 (5.0 . 10-10mol l-1) by means of extraction chromatography on a column packed with a carrier Synachrom E-5 wetted with saturated solution of bis(diethyldithiocarbamate)copper(II) complex in 1 : 1 mixture 1,2-dichlorobenzene + cyclohexane. After elution with 3.0 mol l-1 HCl the mercury concentration in the eluate is determined by atomic absorption spectrometry - cold vapour method. Average yield of the mercury separation from the model solutions was 95.8%.

Sign in / Sign up

Export Citation Format

Share Document