影响土壤电动力学修复技术的主要因素

综述了影响土壤电动修复的几个主要因素，如土壤的pH值、Zeta电位、极化问题、化学性质以及含水率等等，并提出了一些可行性解决措施。如能解决好这几个问题，必将加速土壤电动修复的研究进展。     

PREDICTIVE REAL TIME CONTROL OF SURCHARGED INTERCEPTORS: IMPACT OF SEVERAL CONTROL PARAMETERS1

ABSTRACT: A global predictive real time control strategy minimizing overflow volumes from combined sewers during rainfall was applied to control flows entering the Marigot interceptor (Laval, Canada) for 23 rain events that occurred in this urban area during the summer of 1989. Different surcharge intensities were allowed in the sewer. The duration of the control horizon as well as the location and number of control regulators were varied to assess the impact of these parameters on total overflow volumes and on control safety. Due to the high propagation speed of flow waves in pressurized conduits, it was found that five‐ minute control horizons were sufficient to ensure control performance and safety when important surcharges were permitted in the interceptor and when the controlled regulators were located where pressurized flow occurred. It was also found that it is possible to reduce the number of controlled regulators by placing them at locations intercepting the largest volumes of water during rain periods.     

周期切换电极极性对电动-微生物修复石油污染土壤的影响

以石油作为处理对象,研究周期性切换电极极性对电动-微生物联合修复石油污染土壤的影响。结果表明,2 h/次的电极转换使pH值稳定在6.2~6.4,土壤温度在(29.8±0.4)℃。在修复100 d后,土壤微生物数量达到7.3×107cfu/g,有机碳消耗率比非极性控制组多2 g/kg。石油去除率达到65.5%,比非极性控制组和单一的微生物组高1.2和2.9倍。可见,周期性极性控制可为电动-微生物联合修复提供良好的土壤环境,加速石油污染土壤的修复效率。     

pH对藻类生物膜脱氮除磷的影响研究

在室温(25±2)℃和4 000 lx的连续光照条件下,分别以斜生栅藻、水华鱼腥藻为实验藻种,附着固定于立体弹性载体上形成藻类生物膜,研究不同p H对2种藻类膜生长状况及脱氮除磷能力及方式的影响。结果表明:斜生栅藻和水华鱼腥藻藻类膜生长最适p H均为9;2种藻类膜分别在p H为8和9时EPS产量、磷去除率最大,EPS产量分别为48.50×10-2,48.22×10-2g/m2,磷去除率分别为95.24%和94.71%;p H为10时,2种藻类膜对氨氮有最大去除率,分别为98.96%、97.93%;藻类膜对磷的去除在p H≤7时以同化吸收为主,当p H>7时同化吸收与化学沉淀共同作用;藻类膜对氨氮的去除在p H<8时以同化吸收为主,当p H≥8时同化吸收与化学挥发共同作用。     

羟胺抑制协同pH调控对人工快渗系统短程硝化的影响

针对人工快渗系统(CRI)总氮去除率低的问题,研究了羟胺抑制协同pH调控对人工快渗系统实现由全程硝化向短程硝化转化的可行性,探讨了其对系统内氮素污染物迁移转化和硝化功能菌空间分布及活性的影响.结果表明,0.5 mmol·L~(-1)羟胺连续添加13 d后可实现CRI系统短程硝化的快速启动,氨氮去除率、亚硝氮积累率分别为91.1%、77.9%,经16 d不添加羟胺运行后氨氮去除率、亚硝氮积累率分别降低3.9%、9.8%,此时调控进水pH至8.4,氨氮去除率和亚硝氮积累率均超过90%,CRI系统短程硝化效果显著且稳定性较高.羟胺对硝化菌具有选择性抑制,对AOB和NOB产生明显抑制的浓度分别为0.7、0.5 mmol·L~(-1),羟胺浓度为1.0 mmol·L~(-1)时AOB和NOB活性均被严重抑制且解抑较难;pH调控对短程硝化的影响主要与游离氨(FA)的抑制作用有关,对AOB和NOB产生明显抑制的FA浓度分别为26.5、5.6 mg·L~(-1),NOB比AOB对FA的敏感性更高.     

氧氟沙星和诺氟沙星的水环境光化学转化:pH值及溶解性物质的影响

在模拟日光照射下,考察了氧氟沙星和诺氟沙星在纯水和天然水中的光降解行为,结果表明,氧氟沙星和诺氟沙星的光降解随p H增加(p H=4—10)先增快后减慢,两种抗生素以两性离子形态存在时光解最快.氧氟沙星和诺氟沙星在天然水中的光降解显著慢于其在相似p H条件下(p H=8)纯水中的光降解,天然水中的溶解性物质对两种抗生素的光降解总体表现为抑制作用.以Suwannee河富里酸为例,研究了溶解性有机质(DOM)的影响机制,发现淡水中高浓度的DOM主要通过竞争光吸收抑制氧氟沙星和诺氟沙星的光解,而海水中低浓度的DOM可以通过淬灭活性物种抑制两种抗生素的光解.天然水中的金属阳离子(Ca2+和Fe3+)和NO-3分别通过配位作用和光致生成·OH影响氧氟沙星和诺氟沙星的降解.由此可见,氧氟沙星和诺氟沙星在天然水中的光化学行为依赖于水体p H值和溶解性物质的综合影响.     

pH对氢基质自养微生物还原降解对氯硝基苯的影响

在建立的一种MBfR(氢基质生物膜反应器)中系统考察pH对氢基质自养微生物还原降解p-CNB(对氯硝基苯)的影响,并重点分析pH影响下p-CNB、p-CAN(对氯苯胺)、NO-3-N(硝酸盐)和SO2-4(硫酸盐)的去除效率、通量及当量电子转移通量的变化趋势.结果表明,pH在5.7~8.7之间变化时对硝基还原、还原脱氯、反硝化和硫酸盐还原过程影响显著.氢基质自养微生物生长较适宜的pH范围为6.7~8.2,其中硝基还原、还原脱氯、反硝化和硫酸盐还原的最佳pH分别是7.7、8.2、7.2和7.2.当量电子转移通量分析表明,反硝化和硫酸盐还原对pH变化的敏感性均强于p-CNB还原.为了维持较高水平的p-CNB、NO-3-N和SO2-4同步去除效率,可将pH调控在7.2~8.2之间.适当地调节pH有利于微生物的生长以及控制中空纤维膜表面矿物质沉淀引起的膜污染.     

基于pH调控的城市污泥厌氧发酵产酸小试研究

本研究设计了热碱预处理-半连续流厌氧发酵污泥处理工艺,探究了p H对热碱预处理污泥产酸性能的影响,同时对发酵液作为碳源回用于污水厂强化脱氮除磷进行了质量衡算.在30 L厌氧发酵罐中考察了偏中性(p H=6.5)和碱性(p H=10.0)条件下热碱预处理污泥发酵的挥发性脂肪酸(VFA)产生及分布、蛋白质及碳水化合物的消耗和氮磷释放情况.结果表明,污泥热碱预处理-半连续流厌氧发酵工艺的VFA产量稳定,在p H为6.5和10.0的条件下,发酵罐中平均VFA产率分别为333.29 mg·g-1(以每g VS产生的COD(mg)计,下同)和250.64 mg·g-1,p H为6.5时产酸更稳定,且产量较高,但碱性条件更适合产乙酸.两种p H条件下的SCOD、溶解性蛋白质、溶解性多糖、氮和磷的释放都无较大差异.质量衡算结果表明,以处理量为50000 m3·d-1的城市污水处理厂为例,其产生的污泥经过热碱预处理-半连续流厌氧发酵产酸工艺,产生的VFA能够满足该污水处理厂脱氮除磷提标改造的碳源需求.     

Influences of pH value in deposition-precipitation synthesis process on Pt-doped TiO2 catalysts for photocatalytic oxidation of NO

This work has been undertaken to study the influences of pH value on the characteristics and activity of photocatalyst by deposition-precipitation method during its preparation process. A series of Pt-modified TiO₂ were prepared by deposition-precipitation method at different pH values as well as wet impregnation method, and characterized by XRD, XPS, TEM, UV-Vis and photoluminescence (PL). It was found that the catalysts had the highest photocatalytic activity for NO conversion when pH value was kept at around 7. And the sample prepared by deposition-precipitation method showed higher activity than that by impregnation method. This was mainly due to their high value in highly-dispersed platinum oxides (PtOx) content on the surface of the catalysts. The results from UV-Vis absorption showed that highest absorbance was obtained for Pt/TiO₂ prepared at pH values of around 7. And PL spectra results indicated that the recombination rate of photogenerated electrons and holes of the samples prepared by deposition-precipitation method was lower than that prepared by impregnation method. And in the zeta potential study, the pH values for the isoelectric point of the preparing slurry of 0.05 wt.%Pt/TiO₂ and 0.5 wt.%Pt/TiO₂ were determined to be 6.5-8.5, which further confirmed the enrichment of PtOx dopants for the catalysts repapered when pH value was around 7.     

聚合氯化铝及聚合氯化铝铁处理微污染地表水效果

选用两种无机高分子混凝剂聚合氯化铝(PAC)和聚合氯化铝铁(PAFC),与传统混凝剂Al2(SO4)3处理微污染地表水。以浊度和CODMn去除率为主要指标,考察投药量和pH对混凝效果的影响。通过考察沉淀时间对浊度去除效果的影响,结合实验现象,讨论三种混凝剂生成矾花的大小和沉降性能。结果发现,PAC和PAFC在5mg/L的投药量下可以取得较好的混凝效果,出水符合GB 5749-2006《生活饮用水卫生标准》。三种混凝剂的最佳pH为6,PAFC受pH影响较小,当pH为5～8时可取得较好的CODMn去除效果。PAFC生成的矾花体积较大,沉降性能较好,在实际应用中可缩短沉淀池的水力停留时间。