Solid phase extraction of methomyl and thiodicarb from environmental water with an activated carbon cartridge and their determination by HPLC

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生物过滤饮用水深度处理:机遇与挑战

源水水质的恶化给传统的饮用水处理工艺带来了挑战.生物过滤是饮用水消毒输配之前管理、维护及增强颗粒滤料表面生物活性以去除有机和无机物的过程.由于具有高效、低成本等优点，生物过滤在饮用水深度处理工艺中逐渐得到广泛的应用.本文综述了生物过滤在饮用水处理过程中对水中溶解性有机质（消毒副产物前体物）的去除、微量污染物的削减、嗅味化合物及氨氮的去除等.此外，针对生物过滤在水深度处理过程中存在的问题，本文详细讨论了含氮消毒副产物前体物的生成、低温下生物过滤效能下降等挑战，并提出了今后需要研究的问题.     

含油废水深度处理后回用于港区除尘系统的设计与运行

介绍了某港区作业区利用处理后的含油废水深度处理后回用于港口煤炭除尘系统工程的设计、运行和管理。该系统设计处理量为400m^3／d。采用了水解酸化预处理 生物接触氧化 生物活性炭的处理工艺流程，处理后的污水主要用于港区煤炭储存场冲洗地面、洒水抑尘等。     

改性烟气脱硫球形活性炭的研究

以糠醛渣和炭粉的混合物为原料,分别掺入一定比例的CuO V2O5,MnO2,制备具有低温催化活性的炭载脱硫催化剂,并对其脱硫效果、孔径、脱硫反应前后Cu,V,Mn离子的存在形式进行了研究。结果表明,CuO V2O5,MnO2的加入使球形炭的比表面积降低,平均孔径增大,但脱硫效果却进一步提高,说明这两种金属活性组分在脱硫过程中确实起到了催化的作用。     

Mechanisms of granular activated carbon anaerobic fluidized-bed process for treating phenols wastewater

ＩｎｔｒｏｄｕｃｔｉｏｎＢｅｆｏｒｅｔｈｅ 1 980ｓｃｏｎｖｅｎｔｉｏｎａｌｔｒｅａｔｍｅｎｔｐｒｏｃｅｓｓｅｓｏｆｐｈｅｎｏｌｓｗａｓｔｅｗａｔｅｒａｒｅｓｏｌｖｅｎｔｅｘｔｒａｃｔｉｏｎ ,ｐｈｙｓｉｃａｌａｄｓｏｒｐｔｉｏｎ ,ｃｈｅｍｉｃａｌｏｘｉｄａｔｉｏｎａｎｄａｅｒｏｂｉｃｂｉｏｌｏｇｉｃａｌｐｒｏｃｅｓｓ.Ａｍｏｎｇｔｈｅｂｉｏｌｏｇｉｃａｌｕｎｉｔｐｒｏｃｅｓｓｅｓａｃｔｉｖａｔｅｄｓｌｕｄｇｅｐｒｏｃｅｓｓｉｓｍａｉｎｏｎｅ.Ａｆｔｅｒｔｈｅ 1 980ｓａｎａｅｒｏｂｉｃｂｉｏｌｏｇｉｃ…     

活性污泥数学模型中进水易降解有机物的测定

ASM系列模型 (ASMs)自推出以来在欧美得到广泛应用。要想利用ASMs对特定污水处理过程进行准确的模拟 ,首先必须得到该过程污水的水质特性参数。介绍了连续式OUR计量法、序批式OUR计量法和絮凝过滤物理化学法等 3种测定ASMs中进水易降解有机物的方法 ,通过分析比较指出了各自的优缺点及适用情况。     

活性污泥法的多变量最优控制Ⅱ.限制有机物(BOD)的排放总量

着重研究了在限制有机物排放总量时，使其运行费用最低的最优周期控制问题．通过增加新的状态变量和用补偿函数法，将本课题的有约束条件问题化为无约束条件问题，并提出了最优步长参数的动态搜索法来修改传统的梯度法，从而较完善地解决了多变量最优周期控制的计算问题．研究中还发现了不同初始条件下最优控制所需要的运行费用也大不相同，进而提出了最优初始状态下最优周期控制的新概念，这对保证出水质量的同时进一步降低污水处理成本来说具有更重要的意义．本文还强调指出：对于尚不具备实现最优控制条件的处理系统，可根据最优控制的研究结果实现具有广泛实用价值的准最优控制．     

加压活性炭生物膜法处理DSD有机废水

采用加压活性炭生物膜法处理以对硝基甲苯磺酸盐为主的难降解的有机废水的研究,是在活性炭生物膜法处理有机废水基础上发展起来的新技术。本实验结果表明,在加压9.8×10~4Pa(1kgt/cm~2)的条件下,COD_(Cr)去除率为62％～70％,比常压活性炭生物膜法高20％～25％;其容积负荷Nv=1.7～2.9kgCOD/m~3·d,比一般活性污泥法高3～6倍。     

活性碳纤维吸附CS2蒸气的热力学研究

通过吸附热力学研究,计算出CS_2蒸气在活性碳纤维(ACF)上的吸附热、吸附功和吸附熵.结果表明,吸附属物理吸附范畴,所用吸附剂样品表面是不均匀的.     

Comparison of UV-based advanced oxidation processes for the removal of different fractions of NOM from drinking water

This study examined the effectiveness for degradation of hydrophobic (HPO), transphilic (TPI) and hydrophilic (HPI) fractions of natural organic matter (NOM) during UV/H₂O₂, UV/TiO₂ and UV/K₂S₂O₈ (UV/PS) advanced oxidation processes (AOPs). The changing characteristics of NOM were evaluated by dissolved organic carbon (DOC), the specific UV absorbance (SUVA), trihalomethanes formation potential (THMFP), organic halogen adsorbable on activated carbon formation potential (AOXFP) and parallel factor analysis of excitation–emission matrices (PARAFAC-EEMs). In the three UV-based AOPs, HPI fraction with low molecular weight and aromaticity was more likely to degradate than HPO and TPI, and the removal efficiency of SUVA for HPO was much higher than TPI and HPI fraction. In terms of the specific THMFP of HPO, TPI and HPI, a reduction was achieved in the UV/H₂O₂ process, and the higest removal rate even reached to 83%. UV/TiO₂ and UV/PS processes can only decrease the specific THMFP of HPI. The specific AOXFP of HPO, TPI and HPI fractions were all able to be degraded by the three UV-based AOPs, and HPO content is more susceptible to decompose than TPI and HPI content. UV/H₂O₂ was found to be the most effective treatment for the removal of THMFP and AOXFP under given conditions. C1 (microbial or marine derived humic-like substances), C2 (terrestrially derived humic-like substances) and C3 (tryptophan-like proteins) fluorescent components of HPO fraction were fairly labile across the UV-based AOPs treatment. C3 of each fraction of NOM was the most resistant to degrade upon the UV-based AOPs. Results from this study may provide the prediction about the consequence of UV-based AOPs for the degradation of different fractions of NOM with varied characteristics.