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71.
Geochemistry of high arsenic groundwater in Chia-Nan plain, Southwestern Taiwan: possible sources and reactive transport of arsenic 总被引:3,自引:1,他引:2
Major ion, trace element, and stable isotope analyses were performed on groundwater samples collected during November 2005 and 2006 in Chia-Nan plain of southwestern Taiwan to examine As mobilization in aquifers. The high concentrations of As, Fe and Mn in the groundwater is consistent with low Eh values (under moderately reduced state). Moreover, the observed Na/Cl and SO(4)/Cl molar ratios in groundwater demonstrate the influence of seawater intrusion. Seawater intrusion could provide required electron acceptors (i.e., SO(4)) for bacterial sulfate reduction and promote reducing conditions that are favorable for As mobilization. The concurrent increases in the concentrations of Fe and Mn from 2005 to 2006 may be caused by bacterial Fe(III) and Mn(IV) reduction. Geochemical modeling demonstrate that As(III) is the dominant As species and the presence of Fe-bearing carbonates, sulfides, and oxide phases may locally act as potential sinks for As. Mud volcano fluids were also collected and analyzed to assess the possible source of As in the Chia-Nan plain groundwater. The oxygen and hydrogen isotopic signatures indicate that the As-rich mud volcano fluids may have been modified by chemical exchange with (18)O-rich crustal rocks and possibly originated from mixing of deep brines with circulating meteoric water. Thus As in the Chia-Nan plain groundwater may have been evolved from deep crustal fluids or rock sources. The hydrogeochemistry and widespread As enrichment in groundwater of Chia-Nan plain result from multiple processes, e.g., de-watering of deep crustal fluids, seawater intrusion, and biogeochemical cycling of Fe, As, and S in alluvial sediments. 相似文献
72.
Mukherjee-Goswami A Nath B Jana J Sahu SJ Sarkar MJ Jacks G Bhattacharya P Mukherjee A Polya DA Jean JS Chatterjee D 《Journal of contaminant hydrology》2008,99(1-4):22-30
Groundwaters have been collected from deltaic areas of West Bengal (Chakdaha and Baruipur blocks) to record their hydrogeochemical characteristics, and to verify the mechanism of arsenic (As) release. The data reveals that shallow (<70 m) groundwaters in both areas are of Ca-Mg-HCO(3) type; however deeper (>70 m) groundwaters in Baruipur areas are slightly enriched with Na, Cl and SO(4), indicating possible saline water intrusion. The groundwater is anoxic (mean Eh: -124 and -131 mV) with high levels of As (mean: 116 and 293 mug/L), Fe (mean: 4.74 and 3.83 mg/L), PO(4) (mean: 3.73 and 3.21 mg/L) and Mn (mean: 0.37 and 0.49 mg/L), respectively for Chakdaha and Baruipur areas. The observed values of As and bicarbonate (mean: 409 and 499 mg/L) in the shallow aquifer are indicative of redox processes (e.g., oxidation of organic matter) favouring the release of As. Moreover, the presence of DOC in the shallow aquifer suggests that organic matter is young and reactive, and may actively engage in redox driven processes. Our study further confirms that both Fe- and Mn-reduction processes are the dominant mechanisms for As release in these groundwaters. 相似文献
73.
Anirban Biswas Debasree Deb Aloke Ghose Gijs Du Laing Jan De Neve Subhas Chandra Santra Debendra Nath Guha Mazumder 《Environmental science and pollution research international》2014,21(1):609-619
We assessed the association between arsenic intake through water and diet, and arsenic levels in first morning-void urine under variable conditions of water contamination. This was done in a 2-year consecutive study in an endemic population. Exposure of arsenic through water and diet was assessed for participants using arsenic-contaminated water (≥50 μg L?1) in a first year (group I) and for participants using water lower in arsenic (<50 μg L?1) in the next year (group II). Participants with and without arsenical skin lesions were considered in the statistical analysis. Median dose of arsenic intake through drinking water in groups I and II males was 7.44 and 0.85 μg kg body wt.?1 day?1 (p <0.0001). In females, it was 5.3 and 0.63 μg kg body wt.?1 day?1 (p <0.0001) for groups I and II, respectively. Arsenic dose through diet was 3.3 and 2.6 μg kg body wt.?1 day?1 (p?=?0.088) in males and 2.6 and 1.9 μg kg body wt.?1 day?1 (p?=?0.0081) in females. Median arsenic levels in urine of groups I and II males were 124 and 61 μg L?1 (p?=?0.052) and in females 130 and 52 μg L?1 (p?=?0.0001), respectively. When arsenic levels in the water were reduced to below 50 μg L?1 (Indian permissible limit), total arsenic intake and arsenic intake through the water significantly decreased, but arsenic uptake through the diet was found to be not significantly affected. Moreover, it was found that drinking water mainly contributed to variations in urine arsenic concentrations. However, differences between male and female participants also indicate that not only arsenic uptake, but also many physiological factors affect arsenic behavior in the body and its excretion. As total median arsenic exposure still often exceeded 3.0 μg kg body wt.?1 day?1 (the permissible lower limit established by the Joint Expert Committee on Food Additives) after installation of the drinking water filters, it can be concluded that supplying the filtered water only may not be sufficient to minimize arsenic availability for an already endemic population. 相似文献
74.
Evaluation of the individuality of white rot macro fungus for the decolorization of synthetic dye 总被引:1,自引:0,他引:1
Priyanka Pandey Ram Praksh Singh Kailash Nath Singh Paramasivam Manisankar 《Environmental science and pollution research international》2013,20(1):238-249
Introduction
A biosorbent was developed by simple dried Agaricus bisporus (SDAB) and effectively used for the biosorption of cationic dyes, Crystal Violet and Brilliant Green.Materials and methods
For the evaluation of the biosorbent system, all the batch equilibrium parameters like pH, biomass dose, contact time, and temperature were optimized to determine the decolorization efficiency of the biosorbent. The maximum yields of dye removal were achieved at pH 4.0 for Crystal Violet (CV) and pH 5.0 for Brilliant Green (BG), which are closer to their natural pH also.Result and discussion
Equilibrium was established at 60 and 40 min for CV and BG, respectively. Pseudo first-order, pseudo second-order, and intraparticle-diffusion kinetic models were studied at different temperatures. Isotherm models such as Freundlich, Langmuir, and Dubinin–Radushkevich were also studied. Biosorption processes were successfully described by Langmuir isotherm model and the pseudo second-order kinetic model.Conclusions
The biosorption capacity of A. bisporus over CV and BG were found as 21.74 and 12.16 mg gm?1. Thermodynamic parameters indicated that the CV and BG dye adsorption onto A. bisporus is spontaneous and exothermic in the single and ternary systems. Scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy were used for the surface morphology, crystalline structure of biosorbent, and dye–biosorbent interaction, respectively. This analysis of the biosorption data confirmed that these biosorption processes are ecofriendly and economical. Thus, this biomass system may be useful for the removal of contaminating cationic dyes. 相似文献75.
Mamta Goyal Durga Nath Dhar S. K. Singh 《Environmental monitoring and assessment》2010,171(1-4):425-427
The variations of Cl???, F???, and Fe?+?+? in the underground water during pre- and post-monsoon periods for 2003 have been examined, for two places in Unnao district, by argentrometric titration method (Sodic Land Reclamation Project Uttar Pradesh 1998) and atomic absorption spectrometry (Sodic Land Reclamation Project Uttar Pradesh 1998). The concentration of these ions falls outside the limits prescribed by the World Health Organization (WHO 1984). 相似文献
76.
The present research deals with the quantification of health hazard in a fluorosis prone area from east-coast of India. The average health hazard quotients are 2.09, 2.42, 1.79, and 1.69 for infants, children, male, and female adults, respectively. These values are more than the tolerance limit (1) in 92% groundwater samples and 96% of the study area. The children are more vulnerable to fluorosis than infants and adults. Ca2+/ Na+ versus HCO3−/Na+ and Ca2+/Na+ versus Mg2+/Na+ plots suggest silicate weathering as the prime factor while linear relationship of TDS versus NO3− + (Cl−/HCO3−) supports the anthropogenic input of F− to the aquifer system. The study suggests that the F− ions are chiefly derived from fluorite, apatite, biotite, and hornblende present in the granitic basement under alkaline environment. The secondary sources are domestic and industrial sewage as well as return flow from irrigation with ingredients of phosphate fertilizers. The adverse effects of fluorosis can be minimized by mass awareness programmes, alternative source of potable drinking water, defluoridation techniques, dilution of high F− concentration in groundwater, and minimizing the use of phosphate fertilizers. 相似文献
77.
Chandra Nath Shiv G. Kapoor Anil K. Srivastava Jon Iverson 《Journal of Manufacturing Processes》2013,15(4):419-425
The aim of this work is to investigate the effect of metal-working fluid (MWF) concentration on the machining responses including tool life and wear, cutting force, friction coefficient, chip morphology, and surface roughness during the machining of titanium with the use of the ACF spray system. Five different concentrations from 5 to 15% of a water-soluble metalworking fluid (MWF) were applied during turning of a titanium alloy, Ti–6Al–4V. The thermo-physical properties such as viscosity, surface tension and thermal conductivity of these concentrations were also measured. The test results demonstrate that the tool life first extends with the increase in MWF concentration and then drops with further increase. At low concentration (e.g., 5%), a lack of the lubrication effect causes to increase in a higher friction at the tool–chip interface resulting in severe chipping and tool nose/flank wear within a short machining time. On the other hand, at high concentration, the cooling effect is less. This increases cutting temperature and a faster thermal softening/chipping/notching of the tool material and higher friction at the tool–chip–workpiece interaction zones resulting in early tool failure. A good balance between the cooling and the lubrication effects seems to be found at the 10% MWF concentration as it offers the best machining performance. However, machining with flood coolant is observed to perform the best in the range of 5–7%. 相似文献
78.
Shreemoyee Bordoloi Manoranjan Nath Robin K. Dutta 《Process Safety and Environmental Protection》2013,91(5):405-414
The effects of some commonly used pH conditioners, viz., lime, banana ash, the carbonate and the bicarbonate of sodium and potassium and their binary mixture, on simultaneous removal of arsenic and iron ions from water have been studied. KHCO3 has been found to be the most suitable pH conditioner for the purpose. About 80 mg/L KHCO3 can remove both arsenate and iron ions from initial 250 μg/L and 20 mg/L to below their respective guideline values of the WHO for drinking water, retaining the final pH in the acceptable range for drinking. The simultaneous removal of arsenate and iron by the pH-conditioners decreases in the order: Lime > KHCO3 > NaHCO3 > K2CO3 > Na2CO3 > ash. However, lime requires post-treatment correction of highly alkaline pH. The arsenate ion is removed predominantly through goethite or ferrihydrite in the presence of the bicarbonates and through ferric hydroxide in the presence of the more alkaline pH-conditioners. KHCO3 is more advantageous over the more basic substances including NaHCO3, because with it, one not only needs the smallest dose but also can avoid careful adjustment of the dose for regulating the initial and the final pH. The paper clearly demonstrates the potential of KHCO3 to substitute the currently used pH-conditioners, viz., ash, lime and NaHCO3 for simultaneous removal of arsenate and iron ions. 相似文献
79.
80.
The photodegradation of some aromatic sulfur compounds dissolved in n‐hexane and spread as a thin liquid film on water was investigated. Dibenzothiophene and diphenylsulfide were found to be the most reactive towards photooxidation process among the compounds studied. The degraded compounds were investigated by HPLC and GC/MS. 相似文献