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.     

非溶解态胡敏酸对土壤中硬碳有机质解吸多环芳烃的影响

土壤有机碳是控制土壤中多环芳烃的吸附解吸及其生物有效性的主要因素之一,土壤中硬碳类吸附剂是土壤有机碳中的重要部分,土壤中软碳类物质和硬碳类物质的相互作用对研究土壤中多环芳烃的解吸行为和生物有效性有重要影响。研究将溶解有机质胡敏酸,通过条件的变化使其转变为非溶解态,研究其对土壤碳质吸附剂(胡敏素和黑碳)吸附多环芳烃的解吸行为的影响。研究结果表明:非溶解态胡敏酸会显著降低土壤硬碳类物质中多环芳烃的解吸能力,解吸滞后性增加,作者认为非溶解态胡敏酸的添加会覆盖土壤硬碳类物质的表面吸附位点和填充吸附多环芳烃的孔隙,造成硬碳类有机质中的多环芳烃解吸能力下降,滞后性增强。研究还发现硬碳类有机质的比表面积和孔隙度和解吸能力的变化强度呈正相关关系。     

Long-term nitrogen and phosphorus removal,shifts of functional bacteria and fate of resistance genes in bioretention systems under sulfamethoxazole stress

To understand the long-term performance of bioretention systems under sulfamethoxazole (SMX) stress, an unplanted bioretention system (BRS) and two modified BRSs with coconut-shell activated carbon (CAC) and CAC/zero-valent-iron (Fe0) granules (CAC-BRS and Fe/CAC-BRS) were established. Both CAC-BRS and Fe/CAC-BRS significantly outperformed BRS in removing total nitrogen (TN)(CAC-BRS:82.48%; Fe/CAC-BRS:78.08%; BRS:47.51%), total phosphorous (TP)(CAC-BRS:79.36%; Fe/CAC-BRS:98.26%; BRS:41.99%),and...     

巢湖地区早三叠世碳氧同位素地层对比及其古生态环境意义

二叠纪—三叠纪之交的环境恶化事件不但导致了生物大绝灭,而且造成了自然界正常的碳循环崩溃。为了研究三叠纪早期生物复苏过程中的环境特征、碳氧同位素演化上的地层学意义,对巢湖平顶山西坡剖面下三叠统碳酸盐岩取样分析。研究结果表明,巢湖平顶山西坡剖面早三叠世碳氧同位素地层曲线与已知的平顶山北坡剖面碳氧同位素地层曲线相似。δ13C值在Induan阶、Olenekian阶底部首先表现为大幅度负漂,随后呈上升趋势。δ18O值除了表现出1Ma的周期性波动之外,与δ13C低值区对应处也具负偏趋势。δ13C、δ18O值的演化趋势反映了早三叠世海洋环境恶化、生物复苏十分缓慢。     

微型反应柱在含铬废水处理试验研究中的应用

针对镀铬车间废水,采用活性炭吸附处理法对Cr6 和Cr3 的去除效果进行了系统的试验.通过微型反应柱集成装置对穿透时间、吸附容量及活性炭再生方法进行了研究,动态试验表明该装置能有效地处理含铬废水.     

人工神经元网络对水处理系统建模适应性的研究

针对水处理系统的特点和研究中的难点，引入人工神经元网络的理论和思想，提出了水处理系统的神经网络分析方法．通过建立基于ＢＰ人工神经元网络的臭氧生物活性炭系统的模型，具体地考察了人工神经元网络对水处理系统建模的适应性，使水处理系统的研究迈向智能化和控制化．     

饮用水反硝化脱氮方法研究

为去除饮用水中的硝酸盐氮(NO3ˉ-N)，采用上流式厌氧污泥床(UASB)反应器和固定化微生物进行异养反硝化；自制固定化反硝化菌涂层电极和生物电化学脱氮装置，并用于自养反硝化。试验结果表明。若以甲醇为碳源。当碳氮比(C／N)≥1．o时，室温下经UASB处理4h，NO3ˉ-N去除率为97．7％；若以乙酸为碳源。当C／N≥1．0时，30C下经固定化微生物处理6h，N03ˉ-N去除率为98．6％；在无外加碳源的条件下处理东湖现场水样，30C下经60h后。N03ˉ-N去除率达93．5％。生物电化学脱氮装置可迅速建立自养反硝化菌所需的厌氧环境，水样在室温下经72h处理，脱氮率达96．3％。     

不同前处理方法对活性炭吸附一氧化碳的影响

本文采用颗粒状活性炭（GH-A)作吸附剂，通过不同的前处理方法，以一氧化碳CO与空气的混合物为分离测定对象，用气固色谱法测定被活性炭充分吸附前、后的混合气体中CO的含量，对比评价几种前处理方法。结果表明，对CO的吸附量显著提高的前处理方法分别是研磨筛分至32—38目、酸洗、添加改性剂So而水洗则降低了活性炭吸附CO的能力。