乙二醇生产废水中特征污染物含量的测定

建立了气相色谱(氢火焰离子化检测器)检测乙二醇生产废水中乙二醇、二乙二醇、三乙二醇含量的新方法。该方法采用HP-FFAP型毛细管色谱柱,优化的色谱条件为:进样口温度230℃,初始柱温50℃,载气流量1.0mL/min,分流比1∶1。在质量浓度为1.0~150.0mg/L范围内,废水中各组分色谱峰面积与浓度呈良好的线性关系,相关系数均在0.9989~0.9996之间;相对标准偏差均小于2.0％;乙二醇、二乙二醇、三乙二醇的最低检出限分别为0.63,0.21,0.25mg/L,加标回收率为97.72％~103.52％。     

铬盐工业污染防治对策与建议

在对全国铬盐工业多家企业调研的基础之上,对铬盐工业的生产现状、主要生产工艺及排污节点、污染物排放特征、污染控制技术等进行了论述,指出了污染防治存在的问题,并提出了对策和建议。     

电镀污泥中铜和镍的回收

采用硫酸酸浸#x02014;铜镍分离#x02014;净化除杂#x02014;沉淀制取硫酸镍的工艺从电镀污泥中回收铜和镍,分别采用硫化钠沉淀法和铁粉置换法研究电镀污泥酸浸液中铜和镍的分离效果。实验结果表明,硫化钠沉淀法对铜和镍的分离效果较好,其最优工艺条件为：硫化钠加入量为理论需求量的1.2倍,硫化钠沉淀温度60℃,硫化钠沉淀时间30min。利用本回收工艺制得的硫酸镍产品中镍的质量分数为18%,镍的回收率达80%以上,铜的回收率达90%以上。     

磁性铁矿石对CO还原SO2的催化活性

采用磁性强弱不同的铁矿石以及制备的Fe3O4作为催化剂,催化CO还原SO2。实验结果表明:在3种催化剂中弱磁性铁矿石对CO还原SO2的催化活性最好;当反应温度为700℃时,在弱磁性铁矿石催化作用下的SO2转化率达84.3%。该方法既可以有效去除炼油厂催化裂化再生装置排放的SO2,同时又利用了低品位的磁性铁矿石,实现了SO2的治理和资源的综合利用。     

铈离子光催化降解茜素绿的性能和机理简

主要研究了简单铈离子（Ce³⁺）在紫外光（UV）的作用下对蒽醌染料茜素绿（AG）的光催化降解效果和反应机理。结果表明,UV/Ce³⁺体系能够有效降解AG,初始反应速率随AG浓度的倒数值和Ce³⁺浓度的增加而线性增加,随初始溶液pH的增加先降低后增加,在酸性条件下有很高的TOC去除率。荧光探针实验表明,反应过程中可以产生·OH自由基。UV/Ce³⁺体系对其他类型染料和对硝基苯酚都有较好的降解效果。     

基于响应面法的污泥快速固化效能综合影响简

针对现有污泥固化技术存在的固化养护时间长、低温条件下固化效能低等问题。研究提出污泥快速（3 d）固化技术,采用响应曲面分析方法,重点考察了石灰、组分A、硅酸盐水泥、粉煤灰和温度等5因素对固化效能的综合影响,研究结果表明,石灰、组分A、硅酸盐水泥、粉煤灰和养护温度等因素对3 d固化体的无侧限抗压强度和含水率的线性效应显著,石灰和组分A、石灰和养护温度对无侧限抗压强度的交互影响显著,石灰和粉煤灰、组分A和养护温度、硅酸盐水泥和粉煤灰对含水率的交互影响显著;得出了5因素对固化体3 d无侧限抗压强度和含水率影响的定量模型,可对污泥快速固化进行优化和预测;并利用XRD和SED对污泥固化块的化学成分和微观结构进行了分析。     

4种高级氧化法处理高浓度正丙醇废水的动力学比较

研究了1%和10%(V/V)模拟正丙醇废水在UV/TiO2体系、UV/H2O2体系、Fe2+/H2O2体系和UV/TiO2/Fe2+/H2O2体系等4种工艺条件下的降解动力学过程,对比了降解动力学特点及工艺参数对动力学常数的影响,优化工艺参数。结果表明,UV/TiO2体系和Fe2+/H2O2体系的降解过程可分为零级反应阶段和一级反应阶段,转折点分别在反应开始后2 h和氧化剂浓度为6.7 g/L,UV/H2O2体系和UV/TiO2/Fe2+/H2O2体系分别符合零级反应和一级反应规律;相同工艺参数条件下,6 h反应后,组合工艺UV/TiO2/Fe2+/H2O2体系在处理效率达85%,比前3个体系分别高52.0%、8.3%和32.0%,与UV/TiO2体系和Fe2+/H2O2体系的处理效率之和持平,其协同效应提高了速率常数,在目标物浓度降低时依然可维持较高降解速率。而目标物浓度提高10倍后,UV能量利用率提高35.5倍,氧化剂用量是Fe2+/H2O2体系的1/7.1。     

Influence of lead acetate on soil microbial biomass and community structure in two different soils with the growth of Chinese cabbage (Brassica chinensis)

A greenhouse pot experiment was conducted to evaluate the impact of different concentrations of lead acetate on soil microbial biomass and community structure during growth of Chinese cabbage (Brassica chinensis) in two different soils. The field soils were used for a small pot, short-term 60-day growth chamber study. The soils were amended with different Pb concentrations, ranging from 0 to 900mgkg(-1) soil. The experimental design was a 2 soilx2 vegetation/non-vegetationx6 treatments (Pb)x3 replicate factorial experiment. At 60 days the study was terminated and soils were analyzed for microbial parameters, namely, microbial biomass, basal respiration and PLFAs. The results indicated that the application of Pb at lower concentrations (100 and 300mgkg(-1)) as lead acetate resulted in a slight increase in soil microbial biomass, whereas Pb concentrations >500mgkg(-1) caused an immediate gradual significant decline in biomass. However, the degree of impact on soil microbial biomass and basal respiration by Pb was related to management (plant vegetation) or the contents of clay and organic matter in soils. The profiles of 21 phospholipid fatty acids (PLFAs) were used to assess whether observed changes in functional microbial parameters were accompanied by changes in the composition of the microbial communities after Pb application at 0, 300 and 900mg Pbkg(-1) soil. The results of principal component analyses (PCA) indicated that there were significant increases in fungi biomarkers of 18:3omega6c, 18:1omega9c and a decrease in cy17:0, which is an indicator of gram-negative bacteria for the high levels of Pb treatments In a word, soil microbial biomass and community structure, therefore, may be sensitive indicators reflecting environmental stress in soil-Pb-plant system. However, further studies will be needed to better understand how these changes in microbial community structure might actually impact soil microbial community function.     

Removal of Pb and MDF from contaminated soils by EDTA- and SDS-enhanced washing

Heavy metal- and organic-contaminated sites are ubiquitous, but few studies have been conducted to address such an issue. EDTA- and SDS-enhanced washing was studied for remediation of Pb- and/or marine diesel fuel (MDF)-contaminated soils. The feasibility of recovery and reuse of EDTA and SDS, as well as the physicochemical interactions among the chemical agents, contaminants and soils were extensively investigated using batch experiments. The optimal washing sequence was then determined. The experimental results showed that EDTA could be recovered and reused for four cycles without significant loss of its chelating capacity, while the extraction capability of SDS was noticeably reduced after each reuse cycle. The free phase of marine diesel fuel (MDF) in soils physically isolated the sorbed Pb on soils and thus reducing its extraction by EDTA. The presence of SDS alone or together with low concentration of EDTA was found to enhance Pb removal probably via electrostatic interaction and dissolution of soil organic matter. However, it hindered Pb extraction by high concentration of EDTA, because of the potential formation of complexes between some strongly-bound Pb and SDS, that are more resistant to desorption. Therefore, EDTA washing followed by SDS achieved the highest Pb removal efficiency. On the other hand, MDF removal by SDS was significantly hindered by coexisting Pb in soils, probably because the formation of Pb-dodecyl sulfate (DS) complex would decrease the effective amount of SDS available for forming micelles in solution and enhance MDF sorption. EDTA alone or together with SDS could enhance MDF removal, but the residual MDF after EDTA-washing became more resistant to SDS removal. Consequently, SDS washing followed by EDTA is considered as the optimal washing sequence for MDF removal.     

Effect of condensed organic matter on solvent extraction and aqueous leaching of polycyclic aromatic hydrocarbons in soils and sediments

The contents of nonhydrolyzable organic matter (NHC) and black carbon (BC) were measured in soils and sediments from the Pearl River Delta, South China. Polycyclic aromatic hydrocarbons (PAHs) were extracted respectively by Soxhlet and an accelerated solvent extraction device (ASE) using different solvents. In addition, sequential aqueous leaching at different temperatures was carried out. The PAH content extracted with the sequential three solvent ASE is two times higher than that using the Soxhlet extraction method. The relationship of the PAH content with the NHC content is very significant. The PAH concentrations measured at various temperature steps fit well to the Van't Hoff equation and the enthalpy was estimated. The investigation indicates that condensed organic matter such as kerogen carbon, aged organic matter, and BC is relevant for the extraction and distribution of native PAHs in the investigated field soils and sediments.