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1.
Sci Total Environ ; 583: 142-152, 2017 Apr 01.
Article in English | MEDLINE | ID: mdl-28117153

ABSTRACT

Arsenic contamination mitigation technologies have been adsorption-based, but the most widely-used and traditionally available adsorbents suffered inherent limitations, including cost infeasibility and problems associated with regeneration and disposal of the spent adsorbent. The present technology is based on indigenously developed activated laterite prepared from the naturally and abundantly available material, and can hence easily be scaled up for community usage and large scale implementation. The total arsenic removal capacity is 32.5mg/g, which is the highest among all naturally occurring arsenic adsorbents. A major issue in earlier adsorbents was that during regeneration, the adsorbed arsenic would be released back into the environment (leaching), and would eventually contaminate the groundwater again. But the adsorbent in this filter does not require regeneration during its five-year lifespan and does not leach upon disposal. An attempt is made to test and demonstrate the practical implementation of the technology - its effectiveness and viability in three community (primary schools - one in Malda and two in north 24 Parganas, West Bengal, India) and 20 household filters, catering to over 5000 people in different areas of West Bengal exposed to high arsenic contamination of groundwater (ranging from 0.05 to 0.5mg/l). The work also focuses on the social impact of the real life technological solution on the lives on the affected people in the worst hit arsenic affected communities, perhaps the greatest public health risk emergency of the decade.


Subject(s)
Arsenic/analysis , Water Pollutants, Chemical/analysis , Water Purification/methods , India , Socioeconomic Factors
2.
J Hazard Mater ; 265: 8-19, 2014 Jan 30.
Article in English | MEDLINE | ID: mdl-24333710

ABSTRACT

Mixed matrix membranes (MMMs) were prepared using alumina nanoparticles and cellulose acetate phthalate (CAP) by varying concentration of nanoparticles in the range of 10 to 25wt%. The membranes were characterized by scanning electron micrograph, porosity, permeability, molecular weight cut off, contact angle, surface zeta potential, mechanical strength. Addition of nanoparticles increased the porosity, permeability of the membrane up to 20wt% of alumina. pH at point of zero charge of the membrane was 5.4. Zeta potential of the membrane became more negative up to 20wt% of nanoparticles. Adsorption of phenolic derivatives, catechol, paranitrophenol, phenol, orthochloro phenol, metanitrophenol, by MMMs were investigated. Variation of rejection and permeate flux profiles were studied for different solutes as a function of various operating conditions, namely, solution pH, solute concentration in feed and transmembrane pressure drop. Difference in rejection of phenolic derivatives is consequence of interplay of surface charge and adsorption by alumina. Adsorption isotherm was fitted for different solutes and effects of pH were investigated. Catechol showed the maximum rejection 91% at solution pH 9. Addition of electrolyte reduced the rejection of solutes. Transmembrane pressure drop has insignificant effects on solute rejection. Competitive adsorption reduced the rejection of individual solute.


Subject(s)
Aluminum Oxide/chemistry , Cellulose/analogs & derivatives , Nanoparticles/chemistry , Phenols/chemistry , Water Pollutants, Chemical/chemistry , Adsorption , Cellulose/chemistry , Hydrophobic and Hydrophilic Interactions , Membranes, Artificial , Permeability , Porosity , Water Purification
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