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41.
Polycyclic aromatic hydrocarbons are very stable compounds and tend to bioaccumulate in the environment due to their high degree of conjugation and aromaticity. Hydrous pyrolysis is explored as a technique for the treatment of industrial water containing PAH, using anthracene as a model compound. The reactivity of anthracene under a range of temperatures and durations are studied in this paper. Aliquots of 1.0-10.0 mg of anthracene in a range of 1.0-5.0 mL of H2O are subjected to hydrous pyrolysis under varied conditions of temperature, reagents and duration. The conditions include oxidising systems comprising distilled water, hydrogen peroxide and Nafion-SiO2 solid catalyst in water; and reducing systems of formic acid and formic acid/Nafion-SiO2/Pd-C catalysts to assess a range of redox reaction conditions. Oxygen in air played a role in some of the reaction conditions. Pyrolysed products were identified and quantified by the use of Gas Chromatography-Mass Spectrometry (GC-MS). The major products were anthrone, anthraquinone, xanthone from oxidation; and multiple hydro-anthracene derivatives from reductive hydogenation. The nature of reaction conditions influenced the extent of anthracene degradation. The products formed are more reactive (less stable) as compared to anthracene the starting material and will therefore be less persistent in the environment.  相似文献   
42.
Removal of polycyclic aromatic hydrocarbons (PAHs) from different soil fractions of contaminated soil was investigated by using activated persulfate oxidation remediation in our research. The results showed that the light fraction, which accounted for only 10% of the soil, contained 30% of the PAHs at a concentration of 4352?mg/kg. The heavy fraction contained more high-molecular-weight PAHs, and the total PAH concentration was 625?mg/kg. After being oxidized, the removal rate of PAHs was 39% in the light fraction and nearly 90% in the heavy fraction. Among the different fractions of the heavy fraction, humic acid contained the highest concentration of PAHs, and consequently, the highest removal efficiency of PAHs was also in humic acid. Compared with the light fraction, the heavy fraction has more aromatic compounds and those compounds were broken down during the oxidation process, which may be the removal mechanism involved in the oxidation of high-ring PAHs. Similarly, the enhancement of C = C bonds after oxidation can also explain the poor removal of high-ring PAHs in the light fraction. These results imply that different fractions of soil vary in composition and structure, leading to differences in the distribution and oxidation efficiencies of PAHs.  相似文献   
43.
人类致病菌(HPB)在市政污水中广泛存在,对人类健康产生严重威胁.以南京市某污水处理厂为例,采集1年内污水处理厂进水、污泥和生化处理出水样品,利用16S rRNA基因PCR扩增和高通量测序技术解析了 HPB群落组成特征,研究了生化处理过程中水质理化指标与HPB群落组成的相关性.结果表明,进水和生化处理出水中HPB的检出...  相似文献   
44.
Chang MB  Huang HC  Tsai SS  Chi KH  Chang-Chien GP 《Chemosphere》2006,62(11):1761-1773
Distribution of PCDD/F (polychlorinated dibenzo-p-dioxin and polychlorinated dibenzofuran) congeners at two electric arc furnaces (EAFs) in Taiwan is evaluated via intensive stack sampling and analysis. Two kinds of exhaust system in EAFs including stack system and shutter system are selected for measuring dioxin emissions. In addition, dioxin emissions during oxidation and reduction stages at EAF-A were characterized. Results indicate that the PCDD/F concentration of stack gas in EAF-A was 4.39 ng/N m3 while total Toxic Equivalent Quantity (TEQ) concentration was 0.35 ng I-TEQ/N m3. The PCDD/F concentration of stack gas in EAF-B was 2.20 ng/N m3 and the TEQ concentration was 0.14 ng I-TEQ/N m3. 1,2,3,4,6,7,8-HpCDF, OCDD and OCDF are the major contributors of the dioxin concentrations for two EAFs investigated and the percentage of PCDD/F in particulate phase increases as the chlorination level of the PCDD/F congener increases. The results obtained on gas/particulate partitioning of PCDD/Fs in flue gases prior to the APCD in EAFs indicate that more than 90% exists in particulate phase. In EAF-A, the PCDD/F concentration during oxidation stage is slightly higher than that measured during reduction stage, including the sampling points of CO converter outlet, prior to bag filter and stack. Majority of PCDD/Fs emitted from steel-making processes exists in particulate-phase (about 60–70%) at both EAFs investigated.  相似文献   
45.
通过实验模拟烟气,观察SO_2在一种特殊的脉冲电晕放电等离子体环境中的氧化变化过程,研究了烟气温度、SO_2初始浓度等参数对SO_2氧化率、单位能量氧化量的影响规律。  相似文献   
46.
Heterogeneous water phase catalysis as an environmental application: a review   总被引:15,自引:0,他引:15  
Catalytic water phase processes as an environmental application is a relatively novel subject with tremendous potential in the near future. This review of 120 references presents the wide scale of heterogeneous water phase applications studied mainly within past five years. Both oxidation and hydrogenation processes are included as well as TiO2 assisted photocatalysis. According to the references, heterogeneous catalysis is developing rapidly. New bimetallic catalysts and supports with higher surface area have improved catalytic efficiency in both oxidation and hydrogenation processes. It also seems that study on use of some waste materials such as red mud as catalyst is a very progressive field. On the whole, the chemical aspects are pretty well known, but the catalyst durability, and in many cases activity as well, has to be improved.  相似文献   
47.
钛白副产硫酸亚铁的综合利用研究   总被引:3,自引:0,他引:3  
以钛白副产硫酸亚铁、氯化钾和氨水为原料,采用硫酸钾铵法制取硫酸钾。实验结果表明,该工艺生产的产品,其质量达到ZBG-21006-89国家标准,且此工艺流程简单、操作方便、条件易控制,无二次污染。  相似文献   
48.
通过中试试验考察了高锰酸盐复合药剂(PPC)预氧化强化混凝/沉淀/超滤的组合工艺的除藻效能以及PPC预氧化对藻类引起的膜污染的缓解作用,并对其机理进行了探讨.试验结果表明,投加0.6mg·L-1PPC能使预处理阶段对藻类的平均去除率提高约28%.组合工艺处理高藻水时,PPC预氧化通过强化预处理,降低膜表面的污染负荷,对藻源污染物引起可逆和不可逆污染均具有一定的缓解作用.化学清洗试验结果表明,碱洗对超滤膜TMP恢复效果远远强于酸洗,因而有机物是超滤膜处理高藻水时的主要污染物质.  相似文献   
49.
温小鹏  施昌平  谢雄文 《环境科技》2009,22(1):67-70,74
通过介绍厌氧氨氧化技术(ANAMMOX)和亚硝化技术(SHARON)在污水脱氯处理中的原理,着重从工艺特性分析以及控制因数方面介绍SHARON—ANAMMOX联合工艺,并通过与传统工艺的比较,指出SHARON—ANAMMOX联合工艺是可持续性处理工艺。  相似文献   
50.
流动注射法测定水中高锰酸盐指数的研究   总被引:1,自引:0,他引:1  
研究了用流动注射分析技术测定水体中高锰酸盐指数。使用新发明的耐腐蚀恒流泵、低记忆高效混合器、不存留气泡流通池等部件,通过高温高压,缩短消解时间,从而建立了一种可用于无人值守的自动在线快速监测水体中高锰酸盐指数的分析方法。通过实验研究了流动注射法测定水中高锰酸盐指数的优越性。对方法的检出限、精密度和准确度进行了测定,并与GB/T11892—89《水质高锰酸盐指数的测定》进行了比对,取得了满意的结果。  相似文献   
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