水热法制备BiVO4及其可见光催化降解糖蜜酒精废水

以Bi(NO3)3•5H2O为铋源,NH4VO3为钒源,采用简单的水热法制备了BiVO4 光催化剂,并用X-射线衍射(XRD)、扫描电子显微镜(SEM)、红外光谱(IR)和紫外-可见光漫反射光谱(UV-vis)对产品进行了结构表征。同时,在BiVO4光催化降解糖蜜酒精废水反应中考察了催化剂用量、通氧量、溶液pH值、双氧水用量及光照强度对糖蜜酒精废水脱色率的影响。实验结果表明,水热产品属于单斜晶系BiVO4,其带隙能为2.398 eV,并具有良好的可见光催化活性。当降解经30倍稀释的糖蜜酒精废水,BiVO4添加量为3.0 g•L−1 ,通氧量为120 L•h-1,助氧化剂H2O2添加量为9 %,不改变废水pH值,在400W镝灯离液面11cm照射反应180 min的条件下,糖蜜酒精废水的脱色率为88.60 %,COD去除率为25.84%,而添加5g•L−1的FeSO4•7H2O后其脱色率和COD去除率分别提高到90.90 %和91.26%。单斜晶型BiVO4晶体的可见光催化糖蜜酒精废水过程符合一级动力学反应。     

Evaluation of reusing alum sludge for the coagulation of industrial wastewater containing mixed anionic surfactants

A coagulation-flocculation process is typically employed to treat the industrial wastewater generated by the consumer products industry manufacturing detergents, soaps, and others. The expenditure of chemicals including coagulants and chemicals for pH adjustment is costly for treating this wastewater. The objective of this study was to evaluate the feasibility of reusing the aluminum sulfate (alum) sludge as a coagulant or as a coagulation aid so that the fresh alum dosage can be minimized or the removal e ciency can be enhanced. The experiments were conducted in a jar-test apparatus simulating the coagulation-flocculation process for simultaneous removals of organic matters, anionic surfactants, suspended solids, and turbidity. At the optimum initial pH value of 10 and the fresh alum concentration of 400 mg/L, the total suspended solids (TSS), total chemical oxygen demand (TCOD), total anionic surfactants, and turbidity removal e ciencies were 71.5%, 76.4%, 95.4%, and 98.2%, respectively. The addition of alum sludge as a coagulant alone without any fresh alum addition could significantly remove the turbidity, TCOD, and anionic surfactants. The TSS was left in the supernatants after the settling period, but would subsequently be removed by adding the fresh alum. The TSS, TCOD, and turbidity removal e ciencies were also enhanced when both the alum sludge and the fresh alum were employed. The TCOD removal e ciency over 80% has been accomplished, which has never fulfilled by using the fresh alum alone. It is concluded that the alum sludge could be reused for the treatment of industrial wastewater generated by the consumer products industry.     

湛江特呈岛红树林区底泥TOC的释放研究

以湛江特呈岛红树林区为考察对象,通过底泥TOC向上覆海水释放的模拟对比实验,研究了红树林区底泥中TOC的释放规律和泥水比、温度、pH值三个环境因子对TOC释放的影响,同时对静态和动态体系底泥TOC的释放进行了对比。结果表明,静态下,不同条件释放规律一致,上覆海水TOC的变化呈近似"W"的趋势;泥水比增大会使底泥向上覆海水的TOC释放量增加;温度对底泥TOC释放的影响较为复杂,上覆海水温度较高或较低都有利于底泥TOC的释放;碱性条件有利于沉积物中TOC的释放;海水的运动对沉积物TOC的释放有很好的促进作用。     

免烧粉煤灰陶粒作为BAF填料处理城市污水

以电厂粉煤灰为主要试验原料,辅以外加药剂(水泥、石灰、石膏、水玻璃),经混合、成球、陈化和养护等工序,制得免烧粉煤灰陶粒,并将其作为曝气生物滤池(BAF)工艺的载体填料处理城市污水.待挂膜启动成功后,考察了水力停留时间( HRT)、COD负荷、氨氮负荷对COD和氨氮去除效果的影响.实验结果表明:在温度为18～21℃、气...     

淀山湖沉积物碳-氮垂直分布特征

近年来,经过一系列污染治理措施,淀山湖的营养水平持续下降,但每年仍有不同程度的蓝藻水华暴发,严重影响其作为水源地的安全性。为了进一步探讨淀山湖水质改善策略,本研究对淀山湖沉积物营养状况进行了调查研究,分析了淀山湖沉积物碳、氮分布特征及垂直变化规律,并用沉积物肥力评价了淀山湖沉积物营养程度。结果表明,淀山湖沉积物营养盐存在明显的富集作用,二十多年来沉积物碳、氮含量大幅上升,表层沉积物均属于重污染状态。空间分布上,沉积物营养盐北部高,南部低,北部样点大部分属于重污染状态,南部样点基本属于中污染状态。垂直分布上,受航道回淤与北部围网养殖影响,部分样点营养盐垂直分布规律不显著,其他样点均表现出随深度增加营养盐显著降低的趋势。除出水口D1样点外,淀山湖有机质与TN表现出显著的同源相关性,表明有机质是淀山湖内源负荷的主要来源。     

絮凝-SBR-Fenton氧化处理酶制剂废水的研究

以某酶制品厂的废水为研究对象,确定了絮凝-SBR-Fenton高级氧化的试验方法.结果表明,在絮凝阶段,当聚合氯化铝(PAC)投加量为0.6g/L,搅拌6 min,絮凝70min的条件下,预处理的出水CODCr效果最好,去除率为44.6%;再经过SBR工艺处理,停留时间为14 h时,CODCr去除率达到了89.2%;之后再进行Fenton高级氧化,氧化的最佳条件是:ρ(FeSO4·7H2O)为3 g/L,ρ(H2O2)为0.8g/L,反应时间2 h.最终出水达到了GB 8978-1996<污水综合排放标准>中二级排放标准.     

物化法处理生活垃圾渗滤液新进展

概述了物化法处理垃圾渗滤液的研究现状和最新进展,并展望了物化法处理垃圾渗滤液的研究方向。     

活性炭纤维固定化菌对微囊藻毒素MC-LR的去除研究

研究了藻蓝蛋白提取过程中微囊藻毒素MC-LR的释放分布规律,并用活性炭纤维对一株微囊藻毒素降解菌株进行了固定化,考察了不同活性炭纤维预处理方法、活性炭纤维用量、pH值、温度以及MC-LR浓度对固定化藻毒素降解菌去除MC-LR的影响.结果表明,藻蓝蛋白提取过程中MC-LR主要分布在超滤滤液中,占MC-LR总含量的81.2%.固定化藻毒素降解菌去除MC-LR的效率明显高于非固定化藻毒素降解菌.藻毒素降解菌用(1+9)盐酸预处理后的活性炭纤维固定化,其去除效果最佳.MC-LR去除的最适条件为:活性炭纤维用量为10g/L,温度为35℃,pH值为8.0.固定化藻毒素降解菌对pH值,温度具有一定的耐受性,能够在pH5~pH9、10℃~35℃范围内有效地去除MC-LR.     

Reaction mechanism and metal ion transformation in photocatalytic ozonation of phenol and oxalic acid with Ag+/TiO2

Photocatalytic ozonation of phenol and oxalic acid （OA） was conducted with a Ag^＋/TiO2 catalyst and different pathways were found for the degradation of different compounds. Ag^＋ greatly promoted the photocatalytic degradation of contaminants due to its role as an electron scavenger. It also accelerated the removal rate of OA in ozonation and the simultaneous process for its complex reaction with oxalate. Phenol could be degraded both in direct ozonation and photolysis, but the TOC removal rates were much higher in the simultaneous processes due to the oxidation of hydroxyl radicals resulting from synergetic effects. The sequence of photo-illumination and ozone exposure in the combined process showed quite different effects in phenol degradation and TOC removal. The synergetic effects in different combined processes were found to be highly related to the properties of the target pollutants. The color change of the solution and TEM result confirmed that Ag＋ was easily reduced and deposited on the surface of Tit2 under photo-illumination, and dissolved again into solution in the presence of ozone. This simple cycle of enrichment and distribution of Ag^＋ can greatly benefit the design of advanced oxidation processes, in which the sequences of ozone and photo-illumination can be varied according to the needs for catalyst recycling and the different properties of pollutants.     

制备工艺对La改性湿式氧化催化剂活性和稳定性的影响

采用CWAO(催化湿式空气氧化)法处理甲基橙模拟印染废水,以过量浸渍法制备催化剂,以水样COD Cr去除率和脱色率表征催化剂的活性,以催化剂使用后处理出水中溶出的金属离子质量浓度表征催化剂的稳定性.结果表明,多组分催化剂的金属组分构成为Cu、Fe、La,m(Cu)∶m(Fe)∶m(La)为1∶1∶2,35℃下动态共浸渍8 h,450℃下焙烧3 h,由此制备得到Cu-Fe-La/FSC催化剂.应用该催化剂,以CWAO法处理模拟印染废水,废水COD Cr去除率和脱色率可分别达到79.1%和98.9%,催化剂的活性较高;使用该催化剂处理后的废水中Cu、Fe、La、Al的溶出量(以ρ计)分别为6.1、2.4、2.2、3.2 mg/L,说明金属元素的溶出量较低,催化剂的稳定性较高.