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31.
A review on sources,toxicity and remediation technologies for removing arsenic from drinking water 总被引:2,自引:0,他引:2
Ankita Basu Debabrata Saha Rumpa Saha Tuhin Ghosh Bidyut Saha 《Research on Chemical Intermediates》2014,40(2):447-485
Arsenic is a natural element found in the environment in organic and inorganic forms. The inorganic form is much more toxic and is found in ground water, surface water and many foods. This form is responsible for many adverse health effects like cancer (skin, lung, liver, kidney and bladder mainly), and cardiovascular and neurological effects. The estimated number of people in Bangladesh in 1998 exposed to arsenic concentrations above 0.05 mg/l is 28–35 million, and the number of those exposed to more than 0.01 mg/l is 46–57 million. The estimated number of people in West Bengal, India (the border province to Bangladesh), in 1997 actually using arsenic-rich water is more than 1 million for concentrations above 0.05 mg/l and is 1.3 million for concentrations above 0.01 mg/l. The United States Environmental Protection Agency (USEPA) has estimated that 13 million of the US population are exposed to arsenic in drinking water at 0.01 mg/l. The situation has prevailed for more than 10 years and is more severe now. The USEPA lowered the maximum contaminant level (MCL) for drinking water arsenic from 50 to 10 μg/l in 2001 based on international data analysis and research. This recommendation is now on hold. The level of 10 ppb become standard in the European Union (EU) in 2001. Arsenic may be found in water flowing through arsenic-rich rocks. The source is diverse. These include the earth's crust, introduced into water through the dissociation of minerals and ores, industrial effluents to water, combustion of fossil fuels and seafoods. Arsenic-removal methods are coagulation (ferric sulfate, ferrous sulfate, ferric chloride, aluminum sulfate, copper sulfate, and calcium hydroxide as coagulants), adsorption (activated carbon, activated alumina, activated bauxite) ion exchange, bio-sorption, etc. 相似文献
32.
Dr. Uttam Dutta Sandip Porey Sandeep Pimparkar Astam Mandal Jagrit Grover Adithyaraj Koodan Dr. Debabrata Maiti 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(47):21017-21022
Biaryl compounds are extremely important structural motifs in natural products, biologically active components and pharmaceuticals. Selective synthesis of biaryls by distinguishing the subtle reactivity difference of distal arene C−H bonds are significantly challenging. Herein, we describe para-selective C−H arylation, which is acheived by a unique combination of a meta-directing group and norbornene as a transient mediator. Upon direct meta-C−H palladation, one-bond relay palladation occurs in presence of norbornene and subsequently para-C−H arylation is achieved for sulfonates, phosphonates and phenols bearing 2,6-disubstitution patterns. The protocol is amenable to electron-deficient aryl iodides. Multisubstituted arenes and phenols are obtained by postsynthetic modification of the products. The protocol allows the synthesis of hexa-substituted benzene by sequential selective distal C−H functionalization. 相似文献
33.
Gautam Rajesh Kumar Seth Debabrata 《Journal of Thermal Analysis and Calorimetry》2020,140(6):2633-2640
Journal of Thermal Analysis and Calorimetry - We have reported the thermal conductivities of three deep eutectic solvents (DESs). We have used choline chloride, N,N-diethyl ethanol ammonium... 相似文献
34.
Oxidation of Ru(III)‐Bound Thiocyanate with Peroxomonosulfate: Kinetic and Mechanistic Studies
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The reaction of [RuIII(edta)(SCN)]2? (edta4? = ethylenediaminetetraacetate; SCN? = thiocyanate ion) with the peroxomonosulfate ion (HSO5?) has been studied by using stopped‐flow and rapid scan spectrophotometry as a function of [RuIII(edta)], [HSO5?], and temperature (15–30ºC) at constant pH 6.2 (phosphate buffer). Spectral analyses and kinetic data are suggestive of a pathway in which HSO5? effects the oxidation of the coordinated SCN? by its direct attack at the S‐atom (of SCN?) coordinated to the RuIII(edta). The high negative value of entropy of activation (ΔS≠ = ?90 ± 6 J mol?1 deg?1) is consistent with the values reported for the oxygen atom transfer process involving heterolytic cleavage of the O‐O bond in HSO5?. Formation of SO42?, SO32?, and OCN? was identified as oxidation products in ESI‐MS experiments. A detailed mechanism in agreement with the spectral and kinetic data is presented. 相似文献
35.
Goswami D 《Physical review letters》2002,88(17):177901
Selective control of decoherence is demonstrated for a multilevel system by generalizing the instantaneous phase of any chirped pulse as individual terms of a Taylor series expansion. In the case of a simple two-level system, all odd terms in the series lead to population inversion, while the even terms lead to self-induced transparency. These results also hold for multiphoton transitions that do not have any lower-order photon resonance or any intermediate virtual state dynamics within the laser pulse width. Such results form the basis of a robustly implementable CNOT gate. 相似文献
36.
The ψ′ → ψπ0 decay rate is studied in a chiral symmetry breaking scheme by including effects from π0-η mixing only. The result obtained is in very good agreement with the experiment. 相似文献
37.
Vibrational dephasing of the nitrogen molecule is known to show highly interesting anomalies near its gas-liquid critical point. Here we present theoretical and computational studies of the Raman linewidth of nitrogen along the critical isochore. The linewidth is found to have a lambda-shaped temperature dependence near the critical point. As observed in experimental studies, the calculated line shape becomes Gaussian as the critical temperature (T(c)) is approached. Both the present simulation and a mode coupling theory analysis show that the slow decay of the enhanced density fluctuations near the critical point, probed at the subpicosecond time scales by vibrational frequency modulation, along with an enhanced vibration-rotation coupling, are the main causes of the observed anomalies. 相似文献
38.
We demonstrate coded self-assembly in nanostructures using the code seeded at the component level through computer simulations.
Defects or cavities occur in all natural assembly processes including crystallization and our simulations capture this essential
aspect under surface minimization constraints for self-assembly. Our bottom-up approach to nanostructures would provide a
new dimension towards nanofabrication and better understanding of defects and crystallization process.
相似文献
39.
40.
We introduce a single step memory dependence in the fully chaotic logistic map. This makes it a two dimensional system in general. However, we show that by using composite functions to define two one dimensional maps, it is possible to obtain some analytic results for the bifurcation structure. Numerical results support the calculated bifurcation scheme and, in addition, yield a further insight which allows the calculation of the convergence ratio for a new period adding scenario. 相似文献