啤酒行业涉氨环境风险特征、评估及防控对策

为了解和掌握啤酒行业涉氨环境风险状况,分析了啤酒行业液氨在运输、贮存和使用过程中的环境风险单元和特征。以典型啤酒厂为例,对其环境风险进行评估,确定环境风险等级,并利用环境风险评价系统(RiskSystem)模型对其在不同风速条件下发生液氨泄漏的环境风险进行了预测分析,进而提出有针对性的环境风险防控对策。研究结果表明:啤酒行业在液氨贮存和运输环节存在较大的环境风险,阀门、法兰、接口等连接部位腐蚀和操作不当是氨泄漏的主要原因。根据典型案例环境风险评估和模拟预测结果,在受体敏感区域环境风险较大,风速对氨泄漏事故的影响范围有较大作用,需要严格预防和加强风险控制。建议国家和地方尽快出台相应的环境风险防范技术规范;涉氨单位应以预防为主,加强环境风险单元和重点环节的隐患排查力度,严格落实风险防控措施和要求。     

南海莺琼盆地沉积环境中厌氧纤维素分解菌的分布与作用

在严格厌氧条件下，研究了驾琼盆地东方１－１－１井垂直剖面不同沉积层地质样品中的厌氧纤维素分解菌．结果表明：厌氧纤维素分解菌在各样品中都存在，但其分布有很大随机性，与样品埋藏深度无相关性，与样品中一些有机物含量，如纤维素、半纤维素也无相关性，厌氧纤维素分解菌数量高的样品，其在生物模拟产甲烷实验中的单位有机质产气量也较高，有显著的相关性．菌体形态主要为杆菌和球菌．     

聚丙烯酰胺类絮凝剂的制备及应用研究

为了研究絮凝效果与絮凝剂分子结构的关系,实验中制备了聚丙烯酰胺（ＰＡＭ）、阳离子化聚丙烯酰胺（ＣＰＡＭ）和部分水解聚丙烯酰胺（ＰＨＰ）,将其分别与ＦｅＣｌ３复配后处理钻井废水。实验探讨了絮凝剂的分子量、ＰＨＰ的水解度及阳离子度对絮凝作用的影响。实验结果表明：ＰＡＭ、ＣＰＡＭ、ＰＨＰ与无机混凝剂复配使用处理钻井废水时,最佳分子量是５００万,处理效果依次为ＰＨＰ＞ＰＡＭ＞ＣＰＡＭ。     

炉渣用于深层过滤的试验研究

将炉渣用作深层过滤的床层过滤,在油田水处理中具有良好的应用前景。通过对炉渣滤料的物性测定,对流体力学性能、过滤性能及反洗性能的研究,获得了有关炉渣滤料的粒径分布、床层孔隙率、密度、吸水率等物性参数,以及清洁滤料床层阻力与速度的关系曲线和流化曲线,过滤条件下床层阻力随时间的变化关系和悬浮物脱除率随时间的变化曲线,炉渣床层的反洗曲线。结果表明：炉渣表面粗糙,有棱角,吸附表面积大,孔隙率大,过滤效果好;炉渣滤料密度小,反洗效果较好,反洗用水量只是过滤水量的５％左右;同时,炉渣作为滤料用于深层过滤,不仅来源广泛,而且属废物利用。     

Detection of polycyclic aromatic hydrocarbons using a high performance-single particle aerosol mass spectrometer

The real-time detection of the mixing states of polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs in ambient particles is of great significance for analyzing the source, aging process, and health effects of PAHs and nitro-PAHs; yet there is still few effective technology to achieve this type of detection. In this study, 11 types of PAH and nitro-PAH standard samples were analyzed using a high performance-single particle aerosol mass spectrometer (HP-SPAMS) in lab studies. The identification principles ‘parent ions’ and ‘mass-to-charge (m/z) = 77’ of each compound were obtained in this study. It was found that different laser energies did not affect the identification of the parent ions. The comparative experiments of ambient atmospheric particles, cooking and biomass burning emitted particles with and without the addition of PAHs were conducted and ruled out the interferences from primary and secondary organics on the identification of PAHs. Besides, the reliability of the characteristic ions extraction method was evaluated through the comparative study of similarity algorithm and deep learning algorithm. In addition, the real PAH-containing particles from vehicle exhaust emissions and ambient particles were also analyzed. This study improves the ability of single particle mass spectrometry technology to detect PAHs and nitro-PAHs, and HP-SPAMS was superior to SPAMS for detecting single particles containing PAHs and nitro-PAHs. This study provides support for subsequent ambient observations to identify the characteristic spectrum of single particles containing PAHs and nitro-PAHs.     

Effect of organic acids on adsorption and desorption of rare earth elements

Effect of citric, malic, tartaric and acetic acids on adsorption of La, Ce, Pr and Nd by and desorption from four typical Chinese soils was studied. Generally, adsorption capacities of rare earth elements (REEs) were significantly correlated with the cation exchange capacity (CEC) of soils. In the presence of acetic acids adsorption of REEs was similar to that in the presence of Ca(NO3)2. However, in the presence of citric, malic and tartaric acids adsorption of REEs by Heilongjiang, Zhejiang and Guangdong soils decreased to varying extents if compared with that in the presence of nitrate and acetic acid. The significance of suppression followed the order of citric acid > malic acid > tartaric acid > acetic acid, which was consistent with the order of stability of complexes of REEs with these organic acids. However, the adsorption increased with increasing equilibrium solution pH. For Jiangxi soil with low soil pH, CEC and organic matter these organic acids exerted an even more serious suppression effect on the adsorption of REEs. Another feature of the relationship between the adsorption of REEs and equilibrium solution pH was that the adsorption of REEs decreased with increase of pH from 2 to 4.5 and then slightly increased with further increase of pH. Desorption of REEs varied with soils and with organic acids as well. REEs were released easily from Heilongjiang, Zhejiang and Guangdong soils in the presence of organic acid. Generally, desorption of REEs decreased with increasing equilibrium solution pH. Effect of organic acids on desorption of REEs from Jiangxi soil was more complicated. In the presence of citric and malic acids no decrement and/or slight increase in desorption of REEs were observed over the equilibrium solution pH from 3 to 6.5. The reasons for this were ascribed to the strong complexing capacity of citric and malic acids and low soil pH, CEC and organic matter of Jiangxi soil.     

Photodegradation of surfactants on the nanosized TiO2 prepared by hydrolysis of the alkoxide titanium

Nanosized TiO(2) was synthesized by hydrolysis of titanium tetraisopropoxide in the nanodroplets of microemulsions. The microemulsion provided by functionalized surfactants derived from the mixture of the commercially available sodium dodecylbenzensulfonate (DBS) and sodium dodecyl sulfate (DS). The resulting TiO(2) nanoparticles were characterized by transmission electron microscopy, X-ray diffraction, and differential thermal analysis. Nanosized TiO(2) of anatase was found to show good photocatalytic properties in the photodegradation of DBS and DS surfactants. The cleavage of the aromatic moiety, the intermediate products and ultimate mineralization to CO(2) were examined in the process of photodegradation. A mechanism is also proposed on the basis of these experimental results.     

含重金属水处理污泥的固化和浸出毒性研究

工业危险固体废物在进行安全填埋前需要进行固化稳定处理。针对电镀厂和皮革厂含重金属的水处理污泥 ,用不同比例的水泥、粉煤灰进行固化稳定处理。考虑酸雨环境 ,浸出实验采用TCLP标准。电镀厂污泥单独固化时 ,其浸出液中铜离子浓度由 78 0mg/L下降到 1 5mg/L ;镍离子浓度由 2 2 4 5mg/L下降到 2 2 2mg/L ,高于危险废物允许进入填埋区 15mg/L的控制限值。电镀厂污泥与皮革厂污泥混合后固化 ,浸出液毒性明显降低。铜离子的浸出浓度降低到1 98mg/L ,镍离子降低到 4 10mg/L ,总铬降低到 0 4 0mg/L ,各项指标均低于国家危险废物允许进入填埋区的控制限值 ,可安全填埋。     

高含固污泥厌氧消化中蛋白质转化规律

采用剩余污泥在含固率(total solid,TS)为12%条件下进行中温(37℃)厌氧消化,通过分析厌氧消化前后污泥蛋白质组分的变化情况,研究了高含固污泥厌氧消化中蛋白质的转化规律,探讨了高含固条件下污泥蛋白质转化效率较低的原因.结果表明,经过45 d的厌氧消化处理,污泥蛋白质的转化率为34.26%.污泥蛋白质转化效率较低的原因主要表现在:(1)高含固条件下污泥的传质较差;同时,污泥蛋白质经水解过程形成大量的氨氮,反应结束后污泥总氨氮(total ammonia nitrogen,TAN)质量浓度达到1 201 mg·L~(-1),导致对厌氧消化过程,尤其对蛋白质的分解表现出一定的抑制作用;(2)三维荧光光谱(three-dimensional fluorescence spectroscopy,3D-EEM)分析表明,部分蛋白质向腐殖质类、富里酸类物质转化,从而更难分解;(3)通过二维电泳(two-dimensional electrophoresis,2-DE)-质谱(mass spectrometry,MS)分析发现,厌氧消化后污泥蛋白质的相对分子质量和等电点(isoelectric point,p I)降低;最终,污泥中残留的大部分蛋白质来源于微生物体内.由于微生物代谢能力随着厌氧消化过程的进行而减弱,难以继续利用这些蛋白质,或消化体系中不具备分解这些蛋白质的酶,从而限制了污泥中蛋白质的分解效率.