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1.
Emission characterization of unintentionally produced persistent organic pollutants from iron ore sintering process in China 总被引:5,自引:0,他引:5
Emission of unintentionally produced persistent organic pollutants (Unintentional POPs), including polychlorinated dibenzo-p-dioxins (PCDDs), polychlorinated dibenzofurans (PCDFs), polychorinated biphenyls (PCBs), hexachlorobenzene (HxCBz) and pentachlorobenzene (PeCBz), were investigated in four typical iron ore sintering plants in China. The emission factors and annual mass releases of the Unintentional POPs were calculated. The results indicated that PCDFs contributed more than 60% to the overall toxic equivalent quantity (TEQ) values, while the contribution of the dl-PCBs is relatively low, and only in the range of 8-9%. The dominant congeners of PCDD/Fs and dl-PCBs contributing most to the total TEQ were 1,2,3,7,8-PeCDD, 2,3,4,7,8-PeCDF and PCB-126. With regard to the TEQ contributions, the most abundant homologues were PeCDFs and HxCDD/Fs, followed by PeCDDs and non-ortho dl-PCB, whereas HpCDD/Fs, OCDD/Fs and mono-ortho dl-PCBs almost made no contributions. Due to the massive use of recycled waste in the feeding materials, the average emission factor of PCDD/Fs and dl-PCBs of the four plants was 3.95 μg WHO-TEQ ton−1. Based on the results, the annual release of PCDD/Fs and dl-PCBs in 2007-2009 were estimated to be 2070 g, 2212 g, and 2307 g WHO-TEQ, respectively. 相似文献
2.
聚丙烯酰胺对聚合物驱含油污水中油珠沉降分离的影响 总被引:37,自引:1,他引:37
研究发现阴离子聚丙烯酰胺(HPAM)对聚合物驱含油污水处理有正反2方面影响.聚合物能增加污水粘度,降低油珠上浮速度,而且聚合物能增加油水界面水膜强度,延缓油珠聚并时间,这是聚合物对油珠沉降分离的不利影响;同时,聚丙烯酰胺具有絮凝性,能将水中油珠连接到一起,有利于油珠聚并.当聚丙烯酰胺相对分子质量为2.72×106,浓度小于800mg/L时,絮凝作用大于粘度作用,有利于油珠的沉降分离.初始油珠粒径小是聚合物驱含油污水难处理的主要原因.横向流除油器可以加速油珠聚并,缩短沉降时间,适合处理聚合物驱含油污水. 相似文献
3.
Fang Shubo Cui Qu Dai Xiaoyan 《Environmental science and pollution research international》2020,27(9):8835-8845
Environmental Science and Pollution Research - This study proposed an in situ soil experimental system to quantify concentration and accumulation rates of polychlorinated biphenyl (PCB) congeners... 相似文献
4.
Xiaoling Yang Jun Huang Kunlun Zhang Gang Yu Shubo Deng Bin Wang 《Environmental science and pollution research international》2014,21(6):4634-4642
Perfluorooctane sulfonate (PFOS), a widely used mist suppressant in hard chrome electroplating industry, has been listed in the Stockholm Convention for global ban. 6:2 Fluorotelomer sulfonate (6:2 FTS) acid and salts have been adopted as alternative products in the market, but no data about their abiotic degradation has been reported. In the present study, the degradability of 6:2 FTS potassium salt (6:2 FTS-K) was evaluated under various advanced oxidation processes, including ultraviolet (UV) irradiation, UV with hydrogen peroxide (H2O2), alkaline ozonation (O3, pH = 11), peroxone (O3/H2O2), and Fenton reagent oxidation (Fe2+/H2O2). UV/H2O2 was found to be the most effective approach, where the degradation of 6:2 FTS-K followed the pseudo-first-order kinetics. The intermediates were mainly shorter chain perfluoroalkyl carboxylic acid (C7 to C2), while sulfate (SO4 2?) and fluoride (F?) were found to be the final products. The high yields of SO4 2? and F? indicate that 6:2 FTS-K can be nearly completely desulfonated and defluorinated under UV/H2O2 condition. The degradation should firstly begin with the substitution of hydrogen atom by hydroxyl radicals, followed by desulfonation, carboxylation, and sequential “flake off” of CF2 unit. Compared with PFOS which is inert in most advanced oxidation processes, 6:2 FTS-K is more degradable as the alternative. 相似文献
5.
Pentachlorobenzene (PeCB) in simulated flue gas was destructed by a commercial V2O5-WO3/TiO2 catalyst in this study. The effects of reaction temperature, oxygen concentration, space velocity and some co-existing pollutants on PeCB conversion were investigated. Furthermore, a possible mechanism for the oxidation of PeCB over the vanadium oxide on the catalysts was proposed. Results show that the increase of gas hourly space velocity (GHSV) and the decrease of operating temperature both resulted in the decrease of PeCB removal over the catalyst, while the effect of the oxygen content in the range of 5-20% (v/v) on PeCB conversion was negligible. PeCB decomposition could be obviously affected by the denitration reactions under the conditions because of the positive effect of NO but negative effect of NH3. The introduction of SO2 caused the catalyst poisoning, probably due to the sulfur-containing species formed and deposited on the catalyst surface. The PeCB molecules were first adsorbed on the catalyst surface, and then oxidized into the non-aromatic acyclic intermediates, low chlorinated aromatics and maleic anhydride. 相似文献
6.
In recent years, increasing attention has been paid to the trace-level contamination of pharmaceuticals in the water environment all over the world. Considering a large number of pharmaceuticals used, it is crucial to establish a priority list of pharmaceuticals that should be monitored and/or treated first. In the present study, we developed a ranking system based on the pharmaceutical consumption, removal performance in the wastewater treatment plants (WWTPs) and potential ecological effects, and applied to the situation of China. 39 pharmaceuticals, which had available consumption data and also been reported previously in the WWTPs of China, were selected as candidate pharmaceuticals. Among them, seventeen pharmaceuticals were considered as priority pharmaceuticals, out of which, erythromycin, diclofenac acid and ibuprofen, had the high priority. Compared with other literatures, we found that some pharmaceuticals given concerns to globally should also be included in the priority list in China; while some pharmaceuticals, not mentioned in other literatures, such as cefalexin, ketoconazole, should be also given prior consideration in China. Among all the therapeutic classes, antibiotics, which were grossly abused in China, contributed the most to the priority pharmaceuticals. However, priority antibiotics accounted for only 32% of candidate antibiotics, while 71% and 100% of the candidate anti-inflammatory and antilipidemic respectively were identified as the priority pharmaceuticals, indicating that antibiotics might be overanxiously considered in the previous studies on their behaviors in the WWTPs of China. 相似文献
7.
药物水环境污染是一个严重的环境问题,引起了人们越来越多的关注。磺胺类药物是一类广泛使用的药物。文章应用水质毒性快速检测仪测定一系列磺胺类药物的发光菌毒性,建立发光菌毒性QSAR模型,从而解决ICE模型的基准物种毒性数据缺失的问题。基于发光菌毒性测试和QSAR、ICE毒性估算方法获得更多毒性数据,初步推导了保护水生生物的磺胺类化合物的水质基准,并为建立更加具有生态统计学意义的物种敏感性分布(SSD)模型提供一定的数据支撑。同时,结合国内外水环境中磺胺类药物的暴露水平,对我国磺胺类药物的风险水平做了初步评估,其中磺胺甲恶唑、磺胺嘧啶和磺胺喹恶林的风险较高。 相似文献
8.
Tong Li Ke Xiao Bo Yang Guilong Peng Fenglei Liu Liyan Tao Siyuan Chen Haoran Wei Gang Yu Shubo Deng 《Frontiers of Environmental Science & Engineering》2019,13(6):91
9.
Zhijian LI Shubo DENG Xueying ZHANG Wei ZHOU Jun HUANG Gang YU 《Frontiers of Environmental Science & Engineering in China》2010,4(4):414-420
Three adsorbents including TiO2, Ti-Ce, and Ti-La hybrid oxides were prepared to remove fluoride from aqueous solution. The Ti-Ce and Ti-La hybrid adsorbents
obtained by the hydrolysis-precipitation method had much higher sorption capacity for fluoride than the TiO2 adsorbent prepared through hydrolysis. Rare earth (Ce and La) oxides and TiO2 exhibited a synergistic effect in the hybrid adsorbents for fluoride sorption. The sorption equilibrium of fluoride on the
three adsorbents was achieved within 4 h, and the pseudo-second-order model described the sorption kinetics well. The sorption
isotherms fitted the Langmuir model well, and the adsorption capacities of fluoride on the Ti-Ce and Ti-La adsorbents were
about 9.6 and 15.1 mg·g−1, respectively, at the equilibrium fluoride concentration of 1.0 mg·L−1, much higher than the 1.7 mg·g−1 on the TiO2. The sorption capacities of fluoride on the three adsorbents decreased significantly when the solution pH increased from
3 to 9.5. The electrostatic interaction played an important role in fluoride removal by the three adsorbents, and Fourier
transform infrared (FTIR) analysis indicated that the hydroxyl groups on the adsorbent surface were involved in fluoride adsorption. 相似文献
10.
Shubo Deng Danmeng Shuai Qiang Yu Jun Huang Gang Yu 《Frontiers of Environmental Science & Engineering in China》2009,3(2):171-177
Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments,
and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques.
Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents
were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane
sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects
and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics, isotherms, and
effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS on the
MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed
to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the
MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS
micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction
between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially
be applied in water and wastewater treatment for selective removal of PFOS. 相似文献