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Open AccessJournal ArticleDOI

Design and development of low cost, simple, rapid and safe, modified field kits for the visual detection and determination of arsenic in drinking water samples.

TLDR
A field kit which offers rapid, simple and safe method for precise estimation of arsenic at 10ppb in drinking water samples is developed and employs cupric chloride in combination with ferric chloride or Fenton’s reagent for the removal of hydrogen sulphide.
Abstract
Arsenic is naturally found in surface and ground waters and the inorganic forms of arsenic are the most toxic forms. The adverse health effects of arsenic may involve the respiratory, gastrointestinal, cardiovascular, nervous, and haematopoietic systems. Arsenic contamination in drinking water is a global problem widely seen in Bangladesh and West Bengal of the Indian sub continent. As there is a great demand for field test kits due to the anticipated reduction of the US EPA arsenic standard from 50ppb to 10ppb a field kit which offers rapid, simple and safe method for precise estimation of arsenic at 10ppb in drinking water samples is developed. Field methods, based on the mercuric-bromide-stain, consist of three different major parts, which are carried out stepwise. The first part of the procedure is to remove serious interference caused by hydrogen sulphide. In commercially available kits either the sulphide is oxidized to sulphate and the excess oxidizing reagent removed prior to the hydride generation step or, the hydrogen sulphide is filtered out by passing the gas stream through a filter impregnated with lead acetate during the hydride generation step. The present method employs cupric chloride in combination with ferric chloride or Fenton’s reagent for the removal of hydrogen sulphide, which is rapid, simple and more efficient. Other interferences at this step of the analyses are normally not expected for drinking water analysis. In the second step, the generation of the arsine gas involves the classical way of using zinc metal and hydrochloric acid, which produce the ‘nascent’ hydrogen, which is the actual reducing agent. Hydrochloric acid can be replaced by sulfamic acid, which is solid and avoids a major disadvantage of having to handle a corrosive liquid in the field. The arsine gas produces a yellowish spot on the reagent paper. Depending on the arsenic content, either, Yellow – H (HgBr)2 As (10–50ppb), Brown – (HgBr)3 As (50–100ppb) or Black – Hg3 As2 (>100ppb) are formed which can be precisely estimated by visual comparison with standard color chart. The results obtained by field kits agree well with the data obtained through I.C.P.AES methods. The most important characteristic for field measurement is that analytical results can be obtained on the site where the sample is taken with high precision and can be conveniently utilized for monitoring arsenic rapidly in a highly contaminated large geographical area.

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Citations
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Journal ArticleDOI

Arsenic contamination in groundwater in the Southeast Asia region.

TL;DR: An overview of the As crisis in the Southeast Asian region where groundwater is contaminated with naturally occurring As and where contamination has become more widespread in recent years is presented.
Journal ArticleDOI

Screening of arsenic in tubewell water with field test kits: evaluation of the method from public health perspective.

TL;DR: There is an urgent need for Bangladesh to identify the arsenic (As) contaminated tubewells (TWs) in order to assess the health risks and initiate appropriate mitigation measures, and field test kits offer the only practical tool within the time frame and financial resources available for screening and assessment of the As contaminated TWs as well as their monitoring than that of the laboratory measurement.
Journal ArticleDOI

Arsenicosis: Diagnosis and treatment

TL;DR: Diagnosis of arsenicosis relies on both clinical and laboratory criteria, but principally it can be diagnosed on the basis of its cutaneous manifestations, which are essential clues in the diagnosis.
Journal ArticleDOI

Field based speciation of arsenic in UK and Argentinean water samples

TL;DR: A field method is reported for the speciation of arsenic in water samples that is simple, rapid, safe to use beyond laboratory environments, and cost effective and suitable for on-site separation and preservation of arsenic species from water.
Journal ArticleDOI

Magnetic MWCNTs-dendrimer: A potential modifier for electrochemical evaluation of As (III) ions in real water samples

TL;DR: In this article, a magnetic multi-walled carbon nanotubes modified with polyamidoamine (PAMAM) dendrimers (MMWCNTs-D-NH2) was used for detecting As(III) in water matrices.
References
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Journal ArticleDOI

Simultaneous determination of trace concentrations of arsenic, antimony, bismuth, selenium and tellurium in aqueous solution by introduction of the gaseous hydrides into an inductively coupled plasma source for emission spectrometry. Part I. Preliminary studies

TL;DR: In this article, the atomic line emission from the elements in an inductively coupled plasma source after their introduction as the gaseous hydrides was investigated, and mutual interferences between the analytes were found to be negligible under the operating conditions used.
Journal ArticleDOI

Mechanisms of transition metal interferences in hydride generation atomic-absorption spectrometry. Part 2. Influence of the valency state of arsenic on the degree of signal depression caused by copper, iron and nickel

Bernhard Welz, +1 more
- 01 Jan 1984 - 
TL;DR: In this article, a significant influence of the valency state of arsenic was found on the degree of signal depression owing to transition metals in hydride generation AAS, which supports the theory that the interferences are due to a gassolid reaction.
Journal ArticleDOI

Mechanisms of transition metal interferences in hydride generation atomic-absorption spectrometry. Part 3. Releasing effect of iron(III) on nickel interference on arsenic and selenium

Bernhard Welz, +1 more
- 01 Jan 1984 - 
TL;DR: In this article, a preferential reduction of Fe(III) to Fe(II), which inhibits the precipitation of the interfering nickel as the metal, is proposed mechanism of reaction, which can extend the range of interference-free determination for these elements by three orders of magnitude.
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