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131.
Modeling VOC-odor exposure risk in livestock buildings 总被引:1,自引:0,他引:1
This paper describes a novel idea of linking models of exposure, internal dosimetry, and health effects. Risk assessment approach that integrates predicted odor caused by volatile organic compounds (VOC-odor) of toluene/xylene concentrations in human tissues leads to predict exposure risks in livestock buildings. First, VOC transport model was developed to calculate airborne toluene/xylene concentrations. Based on a physiologically based pharmacokinetic (PBPK) model, concentrations within five compartments representing lung, liver, fat, slowly perfused tissues, and rapidly perfused tissues could be quantified. By using a pharmacodynamic (PD) Hill model, we can optimally fit data from rat and human experiments to reconstruct dose-response relationships for accounting human health effects from nose poke and eye irritation. Results demonstrated that peak tissue concentration occurring at 5-10h in that fat contains the highest concentration than other tissues at around 4ppm of toluene and 1.8ppm of xylene. The EC(10) values are 114 and 232ppm, whereas expected risks are estimated to be 0.71% and 0.26% of human exposure to toluene and xylene, respectively. Risk analyses indicate that inhalation exposure in livestock buildings poses no significant threat to human health under the present environmental conditions. This method provides a rigorous and effective approach to relate target tissue concentration to human nose poke or eye irritation. We suggest that our probabilistic framework and methods be taken seriously because they produce general conclusions that are more robust and could offer a risk-management framework for discussion of future establishment of limits for respiratory exposure to VOC-odor. 相似文献
132.
Dechlorination of octachlorodibenzo-p-dioxin (OCDD) was carried out in ethanol-water (v/v=1:1) solution of NaOH in the presence of Pd/C catalysts with the use of H(2). The substrate was dechlorinated with Pd/C under mild conditions (atmospheric pressure and <100 degrees C) to give a chlorine-free product, dibenzo-p-dioxin (DD), in high yields. After reaction of 3h at 50 degrees C, 95.9% OCDD was degraded to low dechlorinated congeners and the yield of DD was 77.4%. We have also studied the dechlorination selectivity of chlorine atoms on the different substituted positions and postulated the dechlorination pathway of OCDD. For OCDD, the 2-position has higher reactivity than 1-position, but the difference is very small. From the distribution statistics of the intermediates during the reaction, we postulate that the steric effect plays an important role during the reaction and affect the dechlorination pathway of OCDD. 相似文献
133.
In this study, an aqueous solution of purified, hydrolyzed C.I. Reactive Red 120 (RR 120, Color Index), was selected as a model to investigate the degradation pathways and to obtain additional information on the reaction intermediate formation. The dye was purified to avoid the influence of the impurities on the ozonation process and on the formation of oxidation by-products. To simulate the dye-bath effluents from dyeing processes with azo reactive dyes, a hydrolyzed form of the dye was chosen as a representative compound. High performance liquid chromatography/mass spectrometry and its tandem mass spectrometry was chosen to identify the decomposition pathways and reaction intermediate formation during the ozonation process. In addition total organic carbon and high performance ion chromatography analysis were employed to obtain further information on the reaction processes during ozonation. Purified, hydrolyzed RR 120 was decomposed under the direct nucleophilic attack by ozone resulting in oxidation and cleavage of azo group and aromatic ring, while the triazine group still remained in the solution even after prolonged oxidation time (120 min) due to its high resistance to ozonation. Phenol, 1,2-dihydroxysulfobezene, 1-hydroxysulfonbezene were detected as the degradation intermediates, which were further oxidized by O(3) and *OH to other open-ring products and then eventually led to simple oxalic and formic acid identified by HPIC. 相似文献
134.
The determination of trace amount nitrobenzene in wastewater on a hanging mercury drop electrode was studied. The determination
conditions of pH, supporting electrolyte, accumulation potential, accumulation time, and voltammetric response were optimized.
The sharp peak of the nitrobenzene was appeared at 0.05 V. The peak electric current was proportional to the concentration
of nitrobenzene in the range of 1.47 × 10−5 ∼ 1.0 × 10−3 mol/l with relative standard deviations of 3.99 ∼ 8.94%. The detection limit of the nitrobenzene in water was 5 × 10−6 mol/l. The proposed method offered low limit of determination, easy operation, the use of simple instrumentation, high sensitivity
and good reproducibility. It was applied to the determination of nitrobenzene in wastewater with an average recovery of 94.0%
∼ 105%. The proposed method provided fast, sensitive and sometimes real time detection of nitrobenzene. 相似文献
135.
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137.
以五水硝酸铋为铋源、钼酸钠为钼源、硫脲为硫源,采用简单的一步水热法合成了MoS_2/Bi_2S_3异质结光催化剂,采用XRD,SEM,TEM,BET,UV-Vis DRS技术对其进行了表征。表征结果显示,MoS_2纳米片在Bi_2S_3微棒表面生长,增加了比表面积和活性位点,并形成异质结构,促进了光生载流子的迁移,抑制了电子-空穴对的再复合。实验结果表明:钼酸钠与五水硝酸铋的质量比为1∶2时制备的复合光催化剂性能最好,反应180min时对亚甲基蓝的去除率可达96.4%,明显高于MoS_2和Bi_2S_3,且具有较高的稳定性;该催化剂对罗丹明B、甲基橙和4-硝基苯酚的去除率分别为97.1%、93.1%和90.5%,表明其对污染物具有普适性。 相似文献
138.
用水解酸化池-膜生物反应器处理活性艳红X-3B废水 总被引:1,自引:0,他引:1
采用水解酸化池-膜生物反应器处理含活性艳红X-3B的模拟废水,研究了水力停留时间(HRT)对水解酸化池废水处理效果的影响,考察了水解酸化池-膜生物反应器对废水的处理效果及膜生物反应器中污泥沉降性能对膜污染的影响。实验结果表明:水解酸化池HRT为16h时,废水的可生化性最好,挥发性脂肪酸质量浓度与COD比值为0.5;HRT为17h时,废水脱色率达69%,而COD的去除率受HRT影响较小;膜生物反应器主要起去除废水中COD的作用;水解酸化池-膜生物反应器处理后废水的脱色率和COD去除率分别为83%和97%;膜生物反应器中活性污泥沉降性能的变化直接影响膜污染的速率。 相似文献
139.
气相色谱法直接测定水中微量有机胺 总被引:2,自引:0,他引:2
用配有氢火焰离子化检测器(FID)的气相色谱仪直接测定水中多种微量有机胺。试样经过滤后直接进样,在气相色谱仪上使用CP7448毛细管柱,用外标法测定水中微量甲胺、二甲胺、一乙胺、二乙胺的含量。在所选择的色谱操作条件下,甲胺、二甲胺、一乙胺、二乙胺的质量浓度分别在一定范围内与峰面积呈良好的线性关系。4种组分的回收率分别为96.7%,99.0%,101.2%,99.2%;精密度分别为4.3%,3.7%,5.5%,3.1%;检出限分别为2.0,2.0,1.5,1.5mg/L。该方法操作简便,回收率、精密度高。 相似文献
140.