污水处理中影响因素及其最佳操作条件的确定

采用正交试验设计法在厦门杏林污水处理厂进行试验 ,通过极差分析和方差分析确定污泥负荷和污泥龄是活性污泥法去除污水中有机污染物和磷的显著影响因素 ;其最佳操作条件为HRT =5h ,F/M>0 0 5kg (BOD5 ) /kg (MLSS) ;SRT =2 3-4 0d ,可生化比 >4 5,温度 =1 5-33℃。     

SBR处理制药废水影响因素的研究

结合工程实际采用水解酸化-SBR工艺处理制药废水,处理水量为2 000 m3/d。SBR对CODcr的处理率稳定在92.2%～95.8%间,平均为94.23%,对氨氮的去除率在82.7%～97.6%,平均去除率达到90.73%。水解酸化-SBR稳定运行后,系统出水各项指标均达到国家《污水综合排放标准》(8978-1996)二级排放标准。运行结果表明,SBR运行最佳参数为:曝气时间8小时,污泥负荷控制0.23～0.28(kg CODcr/kg MLSS.d),温度26℃～30℃。该工艺用于处理高浓度制药废水效果稳定,耐冲击负荷高。     

热处理对剩余污泥中温厌氧消化的影响

在70℃条件下对处理实际生活污水所产生的剩余污泥进行不同时间(0~100min)的热预处理,再通过批量试验研究了不同预处理时间和不同固体停留时间(SRT)(20d和30d)对剩余污泥中温(35℃)厌氧消化的影响.结果表明,在SRT为20d,预处理时间为100min的条件下,厌氧消化后总化学需氧量(TCOD)的平均去除率最高,达到55.76%;预处理时间为100min,SRT分别为20d和30d的条件下,毛细吸水时间(CST)平均值较对照组分别下降了26%和37%;在SRT为20d,预处理时间为60min条件下,甲烷平均产量最高,达到10.83mL/d;经济分析表明经过70℃预处理后,剩余污泥厌氧消化处理费用可以减少50.9~499.5元/吨干污泥.因此,本试验得出热预处理的最佳SRT为20d,最佳预处理时间为60min.     

高浓度有机废水厌氧膜生物工艺处理的中试研究

高浓度有机废水ADUF工艺处理的中试研究结果表明 ,(1)厌氧池污泥SRT为 5 0d时 ,不仅COD去除率高 ,膜水通量也更稳定 ;(2 ) pH值宜采用在线控制为 7 0 ,温度则应在材质允许范围内尽可能高些 (本实验中为 39℃ ) ;(3)污泥负荷在1 0— 3 5kg/ (kg·d)之间时 ,污泥负荷对ADUF工艺的运行效果没有影响     

“热水解-高温厌氧消化”工艺处理高含固率剩余污泥的中试研究

采取热水解(70℃)-高温厌氧消化工艺处理高固含率(8%~9%)的剩余污泥(中试).该工艺利用SRT为3 d的热水解促进细胞溶解以及高温厌氧消化加快污泥消化速率,有机物去除能力较强,并获得了较好的污泥稳定化效果.当厌氧消化的SRT在20 d以上时,总VSS去除率达到42.22%以上,且VSS去除率与厌氧消化的SRT呈线性正相关,相关系数达到0.915 3.在实际应用中,推荐高温厌氧消化的SRT为25 d.当停留时间接近时,本工艺与运行良好的传统污泥厌氧消化工程(含固率3%~5%)以及采用德国技术的高固消化工程的有机物去除率和甲烷产率相当.     

ABR-MBR反硝化除磷工艺的启动及稳定运行

以低C/N值生活污水为处理对象,重点考察了以厌氧/缺氧(A/A)运行的ABR耦合好氧MBR系统启动过程中脱氮除磷特性及系统长期运行的稳定性.结果表明,控制ABR容积负荷(VLR)为0. 8 kg·(m3·d)-1,污泥回流比为80%,硝化液回流比从150%逐步提升稳定至300%,反硝化除磷功能区污泥停留时间(sludge retention time,SRT)为25 d,MBR溶解氧(DO)为1～2 mg·L~(-1),温度为30℃±2℃,于46 d成功富集了反硝化聚磷菌(denitrifying phosphorus bacteria,DPBs),净释磷量为20. 56 mg·L~(-1),净吸磷量达到27. 74 mg·L~(-1),批次实验表明约84. 8%的聚磷菌(PAOs)能够利用NO-3-N作为电子受体进行反硝化除磷.启动成功后稳定运行50 d,对COD、NH+4-N、TN和PO_4~(3-)-P的平均去除率分别为91. 8%、99. 0%、71. 5%和94. 2%,系统缺氧反硝化除磷去除1 mg·L~(-1)的PO_4~(3-)-P,同步消耗约0. 83 mg·L~(-1)的NO-3-N,满足同步脱氮除磷的要求.     

悬浮态污泥的SRT对复合式A2/O工艺性能的影响

采用厌氧/缺氧/好氧复合工艺(复合式A2/O工艺)及其对照工艺(传统A2/O工艺),进行了悬浮态污泥SRT的变化对系统性能影响的试验研究结果表明,悬浮态污泥浓度与其SRT的关系仍符合劳伦斯-麦卡蒂方程式的导出公式所反映的变化趋势,但其同时和反应器中填料上的生物膜数量呈相反变化趋势在总HRT为12.76 h、COD容积负荷小于1.5kg·m-3·d-1、TKN容积负荷小于0.13kg·m-3·d-1、悬浮态污泥SRT为25～5 d、水温为12～15 ℃时,悬浮态污泥SRT的变化对COD的去除几乎没有影响,出水COD均小于50 mg·L-1;但SRT的变化对氮和磷的去除有较大的影响,当悬浮态污泥SRT大于10 d时,出水NH4+-N和TN浓度分别低于15 mg·L-2和20mg·L-1,随SRT的增大,TP的去除效率下降;附着态生物膜参与硝化过程,能够提高系统总的NH4+-N去除率20%～30%.悬浮态污泥SRT宜控制为10～15 d,这可在一定程度上解决或缓解传统A2/O工艺中硝化和除磷过程对污泥龄要求的矛盾.     

中温两相UBF反应器处理养鸡场离心废水的试验分析

在中温 35℃采用两相 UBF反应器处理养鸡场离心废水 ,结果表明 :进水 CODcr为 190 0 0 mg/ L,系统容积负荷 2 1.5 4kg CODcr/ m3· d,水力停留时间 2 1.17hr,CODcr去除率为 81.98% ,BOD5 去除率为 90 .45 % ,产气率为 0 .44 6 m3/kg CODcr     

不同污泥龄(SRT)对SNEDPR系统脱氮除磷影响

为了解不同污泥龄(SRT)对同步硝化内源反硝化除磷(SNEDPR)系统脱氮除磷性能的影响,采用4组延时厌氧(180min)/低氧(溶解氧0.5~1.0mg·L-1)运行的SBR反应器,以实际城市污水为处理对象,考察不同的SRT(5、10、15、25d)条件下系统的脱氮除磷性能及其污泥性状的变化情况.结果表明,当SRT≥10d时,短SRT有利于提高PAOs的竞争优势;在SRT为15d和10d时,系统除磷性能均较高,尤其是当SRT=10d时,PPAOs,An平均为68.4%,PRA和PUA分别高达31.9mg·L-1和34.3mg·L-1.在SRT为15d和10d时,系统的硝化性能不受SRT变化的影响,且在SRT=15d时,系统具有最高的脱氮性能,TN去除率和SNED率分别平均为89.6%和71.8%.在SRT≥10d时,系统的COD去除性能不受SRT的变化影响,去除率达78%以上;但SRT=5d时,由于系统生物量的流失使得系统的对C、N、P的去除性能均较差,SNED率和PO43--P去除率分别低至5.7%和0.5%.此外,在SRT=15d时,系统污泥沉降性能最好,SV和SVI分别为20%和64m L·g-1,且污泥浓度随着SRT的延长而升高;长SRT(25d)下系统抗冲击负荷能力较强,但污泥的沉降性能变差.     

EGSB反应器处理链霉素有机废水工业性试验研究

本文介绍了在厌氧中温发酵 (35± l℃ )条件下 ,采用膨胀颗粒污泥床 (EGSB)反应器日处理 2 0 0 t链霉素有机废水的工业性试验研究。试验结果表明 :在控制低浓度进料 ,COD在 2 0 0 0～ 70 0 0 mg/L、COD/SO2 - 4=7～ 1 0的条件下 ,有效地降低了毒性物质的抑制作用 ,使反应器成功启动并培养出颗粒污泥 ;当进料 COD在 70 0 0～ 1 30 0 0 mg/L,HRT为 3～ 5h,p H值为 6.8～ 7.2时 ,COD去除率可达75% ,反应器容积负荷最高可达 1 5.8kg COD/(m3.d) ,而 SO2 - 4去除率可有效地控制在 60 %～ 70 % ,实现了 EGSB反应器对链霉素废水中有机物和硫酸盐的有效去除。     

Evaluation of phytoextracting cadmium and lead by sunflower, ricinus, alfalfa and mustard in hydroponic culture

Soil contaminated with heavy metals cadmium(Cd)and lead(Pb)is hard to be remediated.Phytoremediation may be a feasible method to remove toxic metals from soil,but there are few suitable plants which can hyperaccumulate metals.In this study,Cd and Pb accumulation by four plants including sunflower(Helianthus annuus L.),mustard(Brassica juncea L.),alfalfa(Medicago sativa L.), ricinus(Ricinus communis L.)in hydroponic cultures was compared.Results showed that these plants could phytocxtract heavy metals, the ability of accumulation differed with species,concentrations and categories of heavy metals.Values of BCF(bioconcentration factor)and TF(translocation factor)indicated that four species had dissimilar abilities of phytoextraction and transportation of heavy metals.Changes on the biomass of plants,pH and Eh at different treatments revealed that these four plants had distinct responses to Cd and Pb in cultures.Measurements should be taken to improve the phytoremediation of sites contaminated with heavy metals,such as pH and Eh regulations,and so forth.     

Oxidation of As(Ⅲ) by potassium permanganate

The oxidation of As(Ⅲ) with potassium permanganate was studied under conditions including pH, initial As(Ⅲ) concentration and dosage of Mn(Ⅶ). The results have shown that potassium permanganate was an effective agent for oxidizing of As(Ⅲ) in a wide pH range. The pH value of tested water was not a significant factor affecting the oxidation of As(Ⅲ) by Mn(Ⅶ). Although theoretical redox analyses suggest that Mn(Ⅶ) should have better performance in oxidization of As(Ⅲ) within lower pH ranges, the experimental results show that the oxidation efficiencies of As(Ⅲ) under basic and acidic conditions were similar, which may be due to the adsorption of As(Ⅲ) on the Mn(OH)2 and MnO2 resulting from the oxidation of As(Ⅲ).     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

Chlorobenzenes in waterweeds from the Xijiang River （Guangdong section） of the Pearl River

The Xijiang River is the major source of water for about 4.5 millions of urban population and 28.7 millions of rural population. The water quality is very important for the health of the rural population. The concentration and distribution of chlorobenzenes (CBs) in both water and waterweeds collected from 4 stations in the Xijiang River (Gangdong section) of the Pearl River in April and November were determined. The result showed that nearly every congener of CBs was detected. The total contents of CBs (∑CBs) in the river water ranged from 111.1 to 360.0 ng/L in April and from 151.9 to 481.7 ng/L in November, respectively. The pollution level of CBs in the water in April was higher than that in November. The contents of ∑ CBs in waterweeds ranged from 13.53×102 μg/g to 38.27×102μg/g dry weight (dw). There was no significant difference between April and November in waterweeds. The distribution of CBs in roots, caulis, and leaves of Vallisneria spiralis L. showed different patterns. The leaves mainly contained low-molecular-weight CBs(DCBs), whereas the roots accumulated more PCBs and HCBs. The average lgBCFlip (bioconcentration factor) of CBs ranged from 0.64 to 3.57 in the waterweeds. The spatial distribution character of CBs in the Xijiang River was: Fengkai County ＜ Yunan County ＜Yun'an County ＜ Gaoyao County according to the ∑CBs, and the pollution deteriorated from the upstream to the downstream of the Xijiang River. Further analysis demonstrated that the discharge of waste containing CBs may be the main source of CBs pollution in the Xijiang River.     

Degradation of 2,4-dichlorophenol with a novel TiO2/Ti-Fe-graphite felt photoelectrocatalytic oxidation process

Degradation of 2,4-dichlorophenol(2,4-DCP)was studied in a novel three-electrode photoelectrocatalytic(PEC)integrative oxidation process,and the factors influencing the degradation rate,such as applied current,flow speed of O_2,pH,adscititious voltage and initial 2,4-DCP concentration were investigated and optimized.H_2O_2 was produced nearby cathode and Fe~(2 )continuously generated from Fe anode in solution when current and O_2 were applied,so,main reactions,H_2O_2-assisted TiO_2 PEC oxidation and E-Fenton reaction,occurred during degradation of 2,4-DCP in this integrative system.The degradation ratio of 2,4-DCP was 93% in this integrative oxidation process,while it was only 31% in E-Fenton process and 46% in H_2O_2-assisted TiO_2 PEC process.So,it revealed that the degradation of 2,4-DCP was improved greatly by photoelectrical cooperation effect.By the investigation of pH,it showed that this integrative process could work well in a wide pH range from pH 3 to pH 9.     

Effect of copper on the degradation of pesticides cypermethrin and cyhalothrin

The influence of coexisting copper (Cu) ion on the degradation of pesticides pyrethroid cypermethrin and cyhalothrin in soil and photodegradation in water system were studied.Serial concentrations of the pesticides with the addition of copper ion were spiked in the soil and incubated for a regular period of time,the analysis of the extracts from the soil was carried out using gas chromatography (GC).The photodegradation of pyrethroids in water system was conducted under UV irradiation.The effect of Cu~(2 ) on the pesticides degradation was measured with half life (t_(0.5)) of degradation.It was found that a negative correlation between the degradation of the pyrethroid pesticides in soil and Cu addition was observed.But Cu~(2 ) could accelerate photodegradation of the pyrethroids in water.The t_(0.5) for cyhalothrin extended from 6.7 to 6.8 d while for cypermethrin extended from 8.1 to 10.9 d with the presence of copper ion in soil.As for photodegradation,t_(0.5) for cyhalothrin reduced from 173.3 to 115.5 rain and for cypermethrin from 115.5 to 99.0 min.The results suggested that copper influenced the degradation of the pesticides in soil by affecting the activity of microorganisms.However, it had catalyst tendency for photodegradation in water system.The difference for the degradation efficiency of pyrethroid isomers in soil was also observed.Copper could obviously accelerate the degradation of some special isomers.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.