3BER-S工艺用于再生水深度脱氮同步去除PAEs的可行性

为了考察三维电极生物膜硫自养耦合工艺(3BER-S)对再生水进行深度脱氮同步去除邻苯二甲酸酯(PAEs)的可行性,基于3BER-S反应器内已挂膜活性炭填料静态吸附PAEs能力测定和动态反硝化脱氮同步除PAEs运行结果,分析了3BER-S反应器同步脱氮去除PAEs的工艺特性和作用机制.结果表明,挂膜活性炭填料对邻苯二甲酸二丁酯(DBP)、邻苯二甲酸二(2-乙基)己酯(DEHP)的平均吸附去除率分别为85.84%、97.12%,平衡吸附容量为0.142 6mg·g-1、0.162 mg·g-1,达到吸附饱和的时间分别为120 min、60 min;PAEs对3BER-S反硝化系统脱氮效果影响不明显,加入PAEs前后反应器出水TN的浓度在1~2 mg·L-1之间,TN的平均去除率达到了94%以上;3BER-S反硝化系统对PAEs有较强的去除能力,出水中DBP和DEHP的浓度在0~6μg·L-1范围内、去除率均在96%以上;3BER-S对PAEs的去除是吸附、生物降解和电化学协同作用结果.模拟污水厂二级出水经过3BER-S工艺处理后,DBP和DEHP的浓度满足《城市污水再生利用地下水回灌水质标准》(GB/T 19772-2005)所规定的限值.     

纳米材料对环境中微生物活性的影响研究

研究纳米材料对环境中微生物细胞活性的影响可为纳米材料的生物安全性评价提供一定的理论基础.以大肠杆菌和枯草芽孢杆菌为受试生物,采用电导率仪测定细菌培养液电导率变化,分别研究了纳米TiO2、纳米ZnO、纳米Fe3O4、纳米SiO2、纳米二氧化钛载银、纳米磷酸锆载银、纳米棕色银对细菌细胞膜通透性的影响.结果表明,纳米材料对革兰氏阳性枯草芽孢杆菌细胞活性影响更大;同种纳米材料,粒径越小,对细菌的细胞活性影响越强;对细菌细胞活性影响最大的是纳米棕色银,对细菌细胞活性影响最小的是纳米SiO2和Fe3O4.     

石墨炉原子吸收光谱法测定土壤中痕量铋

建立了微波消解土壤、石墨炉原子吸收法测定土壤中痕量铋的方法。采用磷酸二氢铵作为基体改进剂,热解涂层石墨管,塞曼扣背景。此方法对测定土壤中铋的灵敏度、准确度都有很大的提高。方法的最低检出浓度为0.02μg/g,加标回收率为94.5%~103.8%,能够满足环境监测分析的要求。     

滤膜法测定悬浮物出现负误差原因研究

为了对滤膜法测定水中悬浮物出现负误差的情况进行研究,从滤膜的前处理到滤膜的选择进行了一系列实验,发现主要原因是滤膜在实验的过程中产生失重。对几种微孔滤膜进行了空白实验,得出有机滤膜的空白校正值为0.0000～0.0004g,低于或等于悬浮物的称量误差,此类滤膜用于水中悬浮物的测定,能减少恒重次数,缩短实验时间,提高测定结果的科学性和准确性。     

膜-生物反应器处理高盐废水膜面污染物特性研究

研究MBR在低有机负荷条件下处理高盐废水的膜面污染物特征.结果表明,稳定运行121 d后,MBR对有机物和NH+4-N去除率稳定,出水效果良好;污泥性质发生较大变化,挥发性固体含量(VSS)/固体含量(SS)的下降,污泥体积指数(SVI)下降,表明污泥中无机成分含量增加,絮体更为紧密,沉降性能变好;污泥溶解性微生物产物(SMP)和胞外聚合物(EPS)成分发生较大变化,蛋白质所占比例降低,腐殖酸所占比例增加;扫描电子显微镜-X射线能谱仪(SEM-EDX)结果表明膜面存在无机污染物,其主要组成元素为Na、Al、Mg、Ca、K、Fe、Ti、Cr、W、Si和Cl;凝胶过滤色谱(GFC)分析表明,SMP中的大分子有机物被膜截留并累积是形成膜污染的原因之一;傅立叶红外(FTIR)光谱和三维荧光光谱(EEM)分析表明,膜面有机污染物的主要成分为糖类、蛋白质和腐殖酸;膜污染物组分质量分析说明在处理高盐废水时无机膜污染不可忽略.     

纳米Ag粒子原位杂化PVDF超滤膜的抗污染性能

以AgNO3为前驱体,聚偏氟乙烯(PVDF)为聚合物基体,聚乙烯吡咯烷酮(PVP)为分散剂和成孔剂,N,N-二甲基甲酰胺(DMF)为还原剂和溶剂,利用相转化法制备了纳米Ag粒子原位杂化PVDF超滤膜.采用扫描电镜、透射电镜、原子力显微镜及接触角测定仪对杂化膜的结构和性能进行了表征.结果表明:原位形成的纳米Ag粒子均匀地分散在聚合物基体中,纳米Ag粒子的添加改善了PVDF膜的亲水性能.以腐殖酸和牛血清蛋白作为污染物的代表,考察了Ag/PVDF膜的抗有机污染性能.以大肠杆菌、耐甲氧西林金黄色葡萄球菌及活性污泥作为微生物的代表,考察了杂化膜的抗生物污染性能.结果证实了与纯PVDF膜相比,Ag/PVDF膜通量衰减较慢,可有效抑制微生物的生长,表面受活性污泥污染程度小,具有显著的抗有机污染和抗生物污染性能.     

氨水混合吸收剂脱除CO2实验研究

氨水作为一种很有应用前景的CO2化学吸收剂,存在吸收速率慢的问题.使用湿壁塔实验台,考察了不同种类的添加剂(MEA、PZ、1-MPZ、2-MPZ)对氨水吸收CO2速率的影响.结果表明,4种添加剂均能明显提高氨水吸收CO2的速率,其中PZ具有最好的促进效果.0、0.1、0.3和0.5 mol·mol-1负荷下,3 mol·L-1NH3+0.3 mol·L-1PZ溶液的总传质系数(KG)分别是3 mol·L-1NH3溶液在相应负荷下的3、3.2、3.2和2.9倍.改变反应温度、添加剂量、PZ浓度等条件对基于NH3/PZ混合吸收剂吸收CO2的反应过程进行实验,得到了其在不同条件下的KG,初步探讨CO2吸收的反应机制,并计算出准一级反应速率常数为42.7 m3·(mol·s)-1.     

Gas separation using porous cement membrane

Gas separation is a key issue in various industrial fields. Hydrogen has the potential for application in clean fuel technologies. Therefore, the separation and purification of hydrogen is an important research subject. CO2 capture and storage have important roles in ＂green chemistry＂. As an effective clean technology, gas separation using inorganic membranes has attracted much attention in the last several decades. Membrane processes have many applications in the field of gas separation. Cement is one type of inorganic material, with the advantages of a lower cost and a longer lifespan. An experimental setup has been created and improved to measure twenty different cement membranes. The purpose of this work was to investigate the influence of gas molecule properties on the material transport and to explore the influence of operating conditions and membrane composition on separation efficiency. The influences of the above parameters are determined, the best conditions and membrane type are found, it is shown that cementitious material has the ability to separate gas mixtures, and the gas transport mechanism is studied.     

Effect of ozone on the performance of a hybrid ceramic membrane-biological activated carbon process

Two hybrid processes including ozonation-ceramic membrane-biological activated carbon （BAC） （Process A） and ceramic membrane-BAC （Process B） were compared to treat polluted raw water. The performance of hybrid processes was evaluated with the removal efficiencies of turbidity, ammonia and organic matter. The results indicated that more than 99% of particle count was removed by both hybrid processes and ozonation had no significant effect on its removal. BAC filtration greatly improved the removal of ammonia. Increasing the dissolved oxygen to 30.0 mg/L could lead to a removal of ammonia with concentrations as high as 7.80 mg/L and 8.69 mg/L for Processes A and B, respectively. The average removal efficiencies of total organic carbon and ultraviolet absorbance at 254 nm （UV254, a parameter indicating organic matter with aromatic structure） were 49% and 52% for Process A, 51% and 48% for Process B, respectively. Some organic matter was oxidized by ozone and this resulted in reduced membrane fouling and increased membrane flux by 25%-30%. However, pre-ozonation altered the components of the raw water and affected the microorganisms in the BAC, which may impact the removals of organic matter and nitrite negatively.     

Anoxic gas recirculation system for fouling control in anoxic membrane reactor

Anoxic gas recirculation system was applied to control the membrane fouling in pilot-scale 4-stage anoxic membrane bioreactor(MBR). In the anaerobic-anoxic-anoxic-aerobic flow scheme,hydrophilic polytetrafluoroethylene(PTFE) membrane(0.2 μm, 7.2 m2/module) was submerged in the second anoxic zone. During 8 months operation, the average flux of the membrane was 21.3L/(m2·hr). Chemical cleaning of the membrane was conducted only once with sodium hydroxide and sodium hypochlorite. Dissolved oxygen(DO) concentration in the second anoxic zone was maintained with an average of 0.19 ± 0.05 mg/L. Gas chromatography analysis showed that the headspace gas in the second anoxic reactor was mainly consisted of N2(93.0% ± 2.5%), O2(3.8% ± 0.6%), and CO2(3.0% ± 0.5%), where the saturation DO concentration in liquid phase was 1.57 mg/L. Atmospheric O2 content(20.5% ± 0.8%) was significantly reduced in the anoxic gas. The average pH in the reactor was 7.2 ± 0.4. As a result, the recirculation of the anoxic gas was successfully applied to control the membrane fouling in the anoxic MBR.