"生态浮岛+"对黑臭水体的净化效果与机制研究

传统生态浮岛在水质净化处理时存在浮水植物吸收污染物能力有限,深水处理效果不佳等问题。针对上述局限性,尝试将生态浮岛、活性炭纤维组件和曝气组件进行自由组合,形成"生态浮岛+"装置并用于黑臭水体净化处理。经过22d的处理,基于生态浮岛+活性炭纤维+曝气的"生态浮岛+"全组合装置对COD、TN和TP的去除率分别达到83.9%、50.2%和26.4%,而传统生态浮岛对COD、TN、TP的去除率分别为70.5%、39.2%、17.9%,COD、TN、TP的去除率分别提升了13.4、11.0、8.5百分点。"生态浮岛+"利用颗粒物沉降、植物吸收、微生物降解以及活性炭纤维吸附等协同作用净化水质,可以适应不同水质、水深的水体,使用范围更广,适应性更强。     

曝气吹脱法用于牛场沼液污染物的去除

氨吹脱是一种有效的污水脱氮处理技术,其中曝气吹脱法又简单易行。为了探究曝气吹脱法用于牛场沼液污染物去除的最优条件,实验研究了温度、曝气量、初始p H等参数对氨氮去除效果的影响,并探讨了投加Ca(OH)2及曝气吹脱对COD、TP的去除作用。结果显示:温度、曝气量是影响氨氮去除效果的关键因素,30℃、4 000曝气量条件下氨氮去除率最高;由于沼液本身p H会受吹脱影响升高,因此,调节初始p H在8~9.5范围内对氨氮去除效果无显著影响;Ca(OH)_2能去除少量COD及TP,吹脱也能对COD去除有一定影响,投加7.7 g/L Ca(OH)_2吹脱后,沼液COD、TP去除率分别为9.7%、14.8%。最优条件30℃、4 000曝气量下,不加Ca(OH)2吹脱能得到70%以上的的氨氮去除率。一般情况下建议不加Ca(OH)_2进行沼液氨吹脱。     

基于新型有机多孔复合基质的生物系统去除污染水体中的氮磷

针对太湖入湖河道污染水体中的氮磷超标问题,以海绵铁、沸石、砾石和土壤为基质,采用动态吸附+生物法,对氮磷开展基于新型有机多孔复合填料的去除效果研究,结果表明,生物系统中的新型有机多孔复合基质在空间上形成了好氧-缺氧微环境,获得了较好的同步硝化-反硝化效果;通过正交实验确定流量0.00075 L/s,曝气时间24 h,pH值7,曝气量20 L/min为去除氮磷的最优条件;相对一级动力学方程、双常数方程而言,Elovich方程对3种填料的吸附动力学特征拟合最好,决定系数R2在0.81～0.92之间。通过平均去除效果较优分析,好氧条件下,NH3-N平均去除70.6%,TP平均去除81.2%;厌氧条件下,TN平均去除62.4%,COD平均去除42.6%;NH3-N、TP、TN和COD的最低浓度分别为0.75、0.095、1.1和18.3 mg/L,综合考虑主要污染物的去除效果和经济效益,本项新型有机多孔复合填料结合生物系统适宜去除河原平网地区污染水体中的氮磷。     

二级絮凝-活性炭处理实验室无机废水的效果

采用两级絮凝-活性炭吸附法处理实验室无机废水,研究了该方法对重金属、硫化物、挥发酚、苯胺和浊度等的处理效果。结果表明,在絮凝温度、搅拌、曝气及污水pH值调节范围一定的情况下,硫酸亚铁(FeSO4.7H2O)与聚合氯化铝(PAC)结合的二级絮凝方法能有效地降低污水中的重金属和硫化物等污染物。二级絮凝处理中,使用聚合氯化铝(PAC)对一级絮凝中去除效果不好的Cr6+的去除效果显著,去除率达到90%以上;活性炭对苯胺和硫化物的去除效果最佳,去除率都在90%以上。同时,该方法还有效降低了废水的浊度和色度。因此,是一种快速、低成本和工艺简单的处理实验室废水的有效途径。     

臭氧光催化降解地下水中天然有机物的研究

在现场开展了中试规模的臭氧光催化降解天然有机物的研究.研究表明,对大分子天然有机物占很大比例且重碳酸盐含量较高的地下水,臭氧投加量10 mg/L和反应时间10 min条件下,TOC的去除率不到20%,但UV254和三卤甲烷生成潜力(THMFP)去除率分别达到近60%和33.5%.臭氧光催化与活性炭吸附相连,能显著提高UV254的THMFP的去除率,但TOC去除率并不明显高于单独活性炭吸附.臭氧光催化使大分子有机物转化为小分子有机物,后者在活性炭上的吸附性提高且生化性改善,可望在生物活性炭上更有效地去除.     

粉末活性炭对水中农药的吸附性能研究

研究了粉末活性炭对2,4-滴、呋喃丹、甲萘威和莠去津的吸附过程和吸附规律以及投炭量和水质对粉末活性炭吸附性能的影响。结果表明,粉末活性炭能有效去除4种农药;吸附规律符合Freundlich吸附等温线和Langmuir吸附等温线;吸附时间为30 min时,去离子水中的去除率已达到80%以上;随着投炭量的增加,去除率提高,粉末活性炭的吸附容量降低;在不同水质条件下,粉末活性炭的吸附等温线可能不同,因此在应急处理中,首先应该确定该水质下的吸附等温线,然后求出投炭量。     

活性炭海绵动态膜生物反应器处理生活污水的研究

采用序批式活性炭海绵基材动态膜生物反应器处理模拟生活污水。在反应周期为6 h,好氧、厌氧时间比为2∶1,处理水量为18 L的条件下,讨论反应器及动态膜分别对COD、TN、NH3-N、TP的去除效果,并分析反应器中氮的去除机理。结果表明:活性炭海绵基材动态膜生物反应器对COD、TN、NH3-N和TP平均去除率分别为97.99%、84.24%、95.52%和78.94%,动态膜对COD、TN、NH3-N和TP平均去除率为8.96%4、.75%、1.30%和7.54%;好氧结束时,反应器中的氮主要以硝态氮形式存在,浓度稳定在16 mg/L左右,出水中的硝态氮和亚硝态氮平均含量相近,分别为4.10 mg/L和3.69 mg/L;滤饼层对浊度有很好的去除效果,稳定运行时出水浊度可降至2 NTU以下。     

不同吸附剂对三氯乙醛及其前体物的去除

研究了粉末活性炭、硅藻土和膨润土等3种常用吸附剂对三氯乙醛(CH)的去除作用,并以南方某水源原水为研究对象,分析3种吸附剂对于CH前体物(CH1d和CHFP)的去除效果。结果表明,膨润土和粉末活性炭适用于对CH的去除,最大去除率分别为95.93%和86.86%。225 mg·L-1投加量条件下,前15 min膨润土和粉末活性炭对CH吸附效果最快,2种吸附剂对CH去除率分别为63.36%和51.84%;反应2 h后,对CH的吸附已达到饱和,此时膨润土和粉末活性炭对CH去除率分别为89.36%和61.75%。粉末活性炭和硅藻土适用于对CH前体物的去除,最适投加量均为30 mg·L-1,此时对CH1d和CHFP的去除率分别为57.49%和75.21%、28.27%和50.19%。可根据CH的风险程度高低选择硅藻土或粉末活性炭对CH前体物予以去除。     

阶段曝气和植物对人工湿地处理城镇污水厂尾水的影响

采用人工配水模拟城镇污水处理厂尾水水质,利用3套阶段曝气垂直潜流人工湿地(VSFCW)对其进行处理。结果表明:当水力负荷分别为30、90和180 cm·d-1时,3套人工湿地对COD具有较好的去除效果,其去除率都大于66.7%;在处理总磷(TP)和总氮(TN)方面,VSFCW-1(无植物-曝气垂直潜流人工湿地)去除效果远远低于VSFCW-2(芦苇-曝气垂直潜流人工湿地)和VSFCW-3(芦苇-不曝气垂直潜流人工湿地),VSFCW-2(芦苇-曝气垂直潜流人工湿地)和VSFCW-3(芦苇-不曝气垂直潜流人工湿地)对TP和TN的去除率分别在80.0%和75.0%以上且具有较强的抗水力负荷冲击能力。VSFCW-2(芦苇-曝气垂直潜流人工湿地)和VSFCW-3(芦苇-不曝气垂直潜流人工湿地)对COD、TP的去除主要是集中在沿程的前1/4段(0~24 cm),后3/4段(24~115 cm)保证了出水水质的稳定。     

水处理工艺去除藻毒素的效果探讨

探讨了饮用水处理的各工艺过程对藻毒素的去除作用,并根据前期已进行的实验对各工艺的优化组合进行了讨论,认为以气浮代替沉淀,并附之以粉末活性炭吸附预处理可有效地去除藻毒素;对没有条件改造沉淀池的水厂可暂时采用预氯化和粉末活性炭吸附组合的工艺也可达到较好的效果;对生物预处理工艺进行适当的强化,可达到对有机物、藻类、藻毒素等物质的有效去除.     

吸附-氧化法应急处理饮用水源突发苯酚污染的研究

以黄浦江上游水源地突发苯酚污染为背景,重点考察了粉末活性炭（PAC）吸附、高锰酸钾（KMnO4）氧化及两者联用技术的除酚效能。结果表明,活性炭及氧化剂种类的选择是影响处理效果的重要因素,微孔发达、比表面积巨大的竹炭对苯酚的去除效果明显优于煤质炭、椰壳炭和木质炭;KMnO4对苯酚的氧化能力强于次氯酸钠和高铁酸钾。增大PAC和KMnO4的投加量,可有效提高对苯酚的去除率;PAC吸附-KMnO4氧化联用技术可大大提高除酚效能,投加50mg／LPAC,2mg／LKMnO4可将初始浓度为250／μg／L和500／μg／L的含酚原水分别处理至18μg／L和66／μg／L,是应对高浓度苯酚突发污染的有效应急措施。     

Adsorption capacity of powdered activated carbon for 3,5-dichlorophenol in activated sludge

The objectives of this study were to evaluate the performance of powdered activated carbon treatment (PACT) process based on the adsorption capacity of powdered activated carbon (PAC) in activated sludge and the effect of dissolved organic substances in activated sludge on the adsorption capacity of PAC. The DCP adsorption capacity of three PACs originated from different raw materials (coal, soft coal and sawdust) in activated sludge were 29%, 34% and 17% of that of new PAC, respectively. The performance of PACT process for shock loading of 3,5-dichlorophenol (3,5-DCP) was different among PACs in spite of the same adsorption capacity in new PAC. The performance of PACT process for removal of DCP is dependent not on the adsorption capacity of new PAC but on the adsorption capacity of PAC in the aeration tank. Dissolved organic matter (DOM) with molecular weight smaller than 50kDa did not affect the adsorption capacity of PAC for 3,5-DCP in the activated sludge reactor. DOM with molecular weight larger than 50kDa and biofilm developed on the surface of PAC seemed to be responsible for the decreased adsorption capacity of PAC for the DCP.     

粉末活性炭对三烯丙基异氰脲酸酯的吸附性能简

用静态吸附法考察粉末活性炭对水中三烯丙基异氰脲酸酯（CAIC）的吸附行为,采用单因素分析法对活性炭吸附化工废水中TAIC的工艺条件进行研究。实验结果表明,在TAIC模拟废水中,其TAIC初始浓度为800 mg/L,pH为7,在温度为298 K、转速为150 r/min的条件下,当活性炭的投加量达到4.4 g/L,吸附反应时间为50 min时,TAIC的去除效率最高为96.17%;对于实际废水,其TAIC初始浓度为1 500 mg/L,溶液pH为3,在温度为298 K、转速为150 r/min的条件下,当活性炭投加量达到10 g/L,吸附反应时间为2 h时,TAIC的去除效率最高为46.8%。这也是由于实际废水组分复杂,其他有机物存在一定的吸附竞争机制。     

可吸附有机卤化物的深度处理实验研究

可吸附有机卤化物（AOX）是人为污染的重要标志之一,北京高碑店污水处理厂二级出水中约90％的AOX为可吸附有机氧化物（AOCl),研究了自氧氧化,粒状活性炭吸附,粉末活性炭吸附3种深度处理工艺对二级出水中AOX的去除作用,臭氧的氧化反应最多可去除约38％的AOX,粒状活性炭床可运行3200床体积,吸附容量为0.14mgAOX/g GH-16型活性炭,投加木质粉末活性炭200mg/L及25mg/L的聚合氯化铝,能去除24．7％的AOX。     

Removal of carbonyl sulfide using activated carbon adsorption

Wastewater treatment plant odors are caused by compounds such as hydrogen sulfide (H2S), methyl mercaptans, and carbonyl sulfide (COS). One of the most efficient odor control processes is activated carbon adsorption; however, very few studies have been conducted on COS adsorption. COS is not only an odor causing compound but is also listed in the Clean Air Act as a hazardous air pollutant. Objectives of this study were to determine the following: (1) the adsorption capacity of 3 different carbons for COS removal; (2) the impact of relative humidity (RH) on COS adsorption; (3) the extent of competitive adsorption of COS in the presence of H2S; and (4) whether ammonia injection would increase COS adsorption capacity. Vapor phase react (VPR; reactivated), BPL (bituminous coal-based), and Centaur (physically modified to enhance H2S adsorption) carbons manufactured by Calgon Carbon Corp. were tested in three laboratory-scale columns, 6 in. in depth and 1 in. in diameter. Inlet COS concentrations varied from 35 to 49 ppmv (86-120 mg/m3). RHs of 17%, 30%, 50%, and 90% were tested. For competitive adsorption studies, H2S was tested at 60 ppmv, with COS at 30 ppmv. COS, RH, H2S, and ammonia concentrations were measured using an International Sensor Technology Model IQ-350 solid state sensor, Cole-Parmer humidity stick, Interscan Corp. 1000 series portable analyzer, and Drager Accuro ammonia sensor, respectively. It was found that the adsorption capacity of Centaur carbon for COS was higher than the other two carbons, regardless of RH. As humidity increased, the percentage of decrease in adsorption capacity of Centaur carbon, however, was greater than the other two carbons. The carbon adsorption capacity for COS decreased in proportion to the percentage of H2S in the gas stream. More adsorption sites appear to be available to H2S, a smaller molecule. Ammonia, which has been found to increase H2S adsorption capacity, did not increase the capacity for COS.     

聚合氯化铝与粉末活性炭联合强化混凝处理垃圾渗滤液

研究了联合粉末活性炭与聚合氯化铝(PAC)强化混凝对垃圾渗滤液原水的处理效果。结果表明,在原水COD为4 100 mg/L、浊度为147 NTU、UV254为20的条件下,粉末活性炭的加入可以有效增加垃圾渗滤液中有机物的去除率,PAC投加量为0.6 g/L时,投加0.6 g/L粉末活性炭,COD的去除率由21.6%提高到29.1%,UV254去除率由29.8%提高到39.9%,剩余浊度由138 NTU降到133 NTU。该强化混凝过程使原水中溶解性小分子有机物的去除率提高显著,PAC投加量为0.6 g/L时,投加0.6 g/L粉末活性炭,在分子量小于1 kDa的范围内,UV254去除率由2.9%上升为10%。     

Ozonation of aniline promoted by activated carbon

The removal of aniline from aqueous solutions by simultaneous use of ozone and activated carbon was investigated at different solution pH. For comparative purposes, single ozonation and adsorption on activated carbon were carried out in the same experimental set-up. In order to evaluate the role of the activated carbon surface chemistry during ozonation, a commercial activated carbon, Norit GAC 1240 PLUS, was submitted to oxidation in the liquid phase with HNO(3). The texture and surface chemistry of the activated carbon samples were characterized. During ozonation, complete conversion of aniline was achieved after approximately 20 min, regardless of the presence of activated carbon. In all cases, several by-products were formed during ozonation. Nitrobenzene, o- and p-aminophenol were the primary aromatic oxidation by-products identified. In terms of TOC removal, best results were achieved by the simultaneous use of ozone and activated carbon. Though there is a strong contribution of adsorption, a considerable synergetic effect between ozone and activated carbon is observed. In general, activated carbon promotes the reaction of ozonation enhancing the efficiency of this treatment process. The basic activated carbon presented greater activity in this process leading to higher mineralization rates.     

褐煤活性炭吸附处理焦化废水

研究褐煤活性炭吸附处理焦化废水的性能,为褐煤活性炭用于废水处理提供理论依据和技术指导。以河南某气化厂的焦化废水为吸附原水,进行褐煤活性炭对酚吸附性能的静态和动态实验。静态实验表明,褐煤活性炭对酚的吸附性能符合弗兰德里希（Freundlich）吸附方程式。在室温条件下,对于150 mL焦化废水,当活性炭的用量为10 g,吸附反应时间为1 h,酚的去除率可达92%以上。动态实验研究表明,当进水酚浓度为3 800 mg/L,吸附1.5 h,活性炭的吸附容量可达21.38 mg/g。水处理的实验研究表明,利用褐煤制备的活性炭,对焦化废水具有良好的处理效果。     

Biological treatment process of air loaded with an ammonia and hydrogen sulfide mixture

The physico-chemical characteristics of granulated sludge lead us to develop its use as a packing material in air biofiltration. Then, the aim of this study is to investigate the potential of unit systems packed with this support in terms of ammonia and hydrogen sulfide emissions treatment. Two laboratory scale pilot biofilters were used. A volumetric load of 680 g H2S m(-3) empty bed day(-1) and 85 g NH3 m(-3) empty bed day(-1) was applied for eight weeks to a unit called BGSn (column packed with granulated sludge and mainly supplied with hydrogen sulfide); a volumetric load of 170 g H2S m(-3) empty bed day(-1) and 340 g NH3 m(-3) empty bed day(-1) was applied for eight weeks to the other called BGNs (column packed with granulated sludge and mainly supplied with ammonia). Ammonia and hydrogen sulfide elimination occur in the biofilters simultaneously. The hydrogen sulphide and ammonia removal efficiencies reached are very high: 100% and 80% for BGSn; 100% and 80% for BGNs respectively. Hydrogen sulfide is oxidized into sulphate and sulfur. The ammonia oxidation products are nitrite and nitrate. The nitrogen error mass balance is high for BGSn (60%) and BGNs (36%). This result could be explained by the denitrification process which would have occurred in anaerobic zones. High percentages of ammonia or hydrogen sulfide are oxidized on the first half of the column. The oxidation of high amounts of hydrogen sulfide would involve some environmental stress on nitrifying bacterial growth and activity.     

活性炭吸附硫化氢及微波辐照解吸研究

研究了两种活性炭对硫化氢的平衡吸附性能力,并对活性炭床层的穿透性进行了考察;吸附饱和和活性炭在微波辐射的作用下进行解吸。实验表明,解吸效率与微波作用时间及温度有关,在本实验条件下H2S解吸效率达90．1％。