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Biological removal of antiandrogenic activity in gray wastewater and coking wastewater by membrane reactor process 总被引:1,自引:0,他引:1
A recombinant human androgen receptor yeast assay was applied to investigate the occurrence of antiandrogens as well as the mechanism for their removal during gray wastewater and coking wastewater treatment. The membrane reactor (MBR) system for gray wastewater treatment could remove 88.0% of antiandrogenic activity exerted by weakly polar extracts and 97.3% of that by moderately strong polar extracts, but only 32.5% of that contributed by strong polar extracts. Biodegradation by microorganisms in the MBR contributed to 95.9% of the total removal. After the treatment, the concentration of antiandrogenic activity in the effluent was still 1.05 μg flutamide equivalence (FEQ)/L, 36.2% of which was due to strong polar extracts. In the anaerobic reactor, anoxic reactor, and membrane reactor system for coking wastewater treatment, the antiandrogenic activity of raw coking wastewater was 78.6 mg FEQ/L, and the effluent of the treatment system had only 0.34 mg FEQ/L. The antiandrogenic activity mainly existed in the medium strong polar and strong polar extracts. Biodegradation by microorganisms contributed to at least 89.2% of the total antiandrogenic activity removal in the system. Biodegradation was the main removal mechanism of antiandrogenic activity in both the wastewater treatment systems. 相似文献
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焦化废水是一种典型的含有难降解有机污染物的工业废水,除含有酚类化合物外,还含有多种芳香烃和杂环类有机污染物,成分复杂,水量大,对环境污染严重。因此,焦化废水处理技术越来越受到环保部门的重视。本文摸索了改性粉煤灰处理焦化含酚废水的试验工艺条件,确定了反应条件,反应时间和反应温度。 相似文献
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炼焦过程排放挥发性有机物的排放特征和组成分布研究 总被引:1,自引:0,他引:1
为控制炼焦排放以及为预防城市大气污染提供可靠的污染源数据支持,利用不锈钢采样罐和全自动预浓缩/GC/MS系统,研究了58-Ⅱ型和JN43-80型焦炉在装煤时刻和炼焦过程(包括装煤时刻)中挥发有机物(VOCs)的排放特征及其组成分布,分析了焦化行业排放VOCs的反应活性。研究发现,在装煤时刻和炼焦过程中,58-Ⅱ型焦炉产生的总挥发性有机物(TVOCs)浓度分别为7022μg/m~3和6266μg/m~3;JN43-80型焦炉产生的TVOCs浓度分别为4185μg/m~3和3298μg/m~3。装煤时刻产生的TVOCs浓度明显高于炼焦过程产生的。炼焦过程无组织排放的VOCs包含烯烃、烷烃、芳香烃、卤代烃以及少量的醛和酮,其中乙烯、乙烷、丙烯、苯、甲苯等为主要成分。这些产生的VOCs反应活性各不相同,活性最大的是烯烃类物质,其活性占TVOCs反应活性比重为(86.2±2.1)%;其次是芳香烃类物质,其活性比重为(9.2±3.1)%;反应活性最大的5个物种分别是丙烯、乙烯、1,3-丁二烯、1-丁烯以及苯乙烯。 相似文献
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我厂工业废水处理及闭路循环与生产工艺的改造 总被引:1,自引:0,他引:1
阐述了我厂生产工艺及污水治理的思路.取消黄血盐工序,上PT水处理装置,将改善我厂的生产管理和技术经济指标,具有不可估量的环境效益和社会效益. 相似文献
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Zhao Rongfang Ye Shufeng Xie Yusheng Chen Yunfa 《Journal of Material Cycles and Waste Management》2007,9(1):7-14
A new way to implement the simultaneous reutilization of solid waste, the desulfurization of coke oven gas (COG), and even
the desulfurization of coke by the co-coking of coking coal (CC) and waste plastic (WP) blended with a sorbent is proposed;
the evolution of H2S and the removal efficiency of H2S from COG during the co-coking process were investigated in a lab-scale cylindrical reactor. The experimental results indicated
that for the coking of CC blended with ZnO, Fe2O3, or blast furnace dust (BFD) as a sorbent, the instantaneous concentration of H2S in COG was lower than 500 mg/m3 (which meets the technical specification requirement of the Chinese Cleaner Production Standard–Coking Industry, HJ/T 126-2003)
when the molar ratio between the key component of the sorbent and the volatile S in CC or the CC/WP blend, n
Zn+Fe/n
S, was about 1.2 for ZnO and Fe2O3, but not for BFD under the same conditions, suggesting that ZnO and Fe2O3 are promising sorbents, but that BFD must be treated chemical or thermally before being used as a sorbent because of the
size and complicated nature of the influence of its phase/chemical composition on its desulfurization ability. However, for
the co-coking of CC and WP blended with ZnO as a sorbent, n
Zn+Fe/n
S must increase to 1.4 and 1.7 for 100/2 and 100/5 blends of CC/WP, respectively, to ensure a satisfactory efficiency for H2S removal from COG.
Part of this paper was presented at the International Symposium on EcoTopia Science 2005 (ISET05), Aug 8–9, 2005, Chikusa-ku,
Nagoya, Japan 相似文献
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To clarify the effect of coking dust, sintering dust and fly ash on the activity of activated carbon for various industrial flue gas desulfurization and denitrification, the coupling mechanism of the mixed activated carbon and dust was investigated to provide theoretical reference for the stable operation. The results show that coking dust had 34% desulfurization efficiency and 10% denitrification efficiency; correspondingly, sintering dust and fly ash had no obvious desulfurization and denitrification activities. For the mixture of activated carbon and dust, the coking dust reduced the desulfurization and denitrification efficiencies by blocking the pores of activated carbon, and its inhibiting effect on activated carbon was larger than its own desulfurization and denitrification activity. The sintering dust also reduced the desulfurization efficiency on the activated carbon while enhancing the denitrification efficiency. Fly ash blocked the pores of activated carbon and reduced its reaction activity. The reaction activity of coking dust mainly came from the surface functional groups, similar to that of activated carbon. The reaction activity of sintering dust mainly came from the oxidative property of Fe2O3, which oxidized NO to NO2 and promoted the fast selectively catalytic reduction (SCR) of NO to form N2. Sintering dust was activated by the joint action of activated carbon, and both had a coupling function. Sintering dust enhanced the adsorption and oxidation of NO, and activated carbon further promoted the reduction of NOx by NH3; thus, the denitrification efficiency increased by 5%-7% on the activated carbon. 相似文献