阳离子聚丙烯酰胺絮凝剂的合成

氨甲基聚丙烯酰胺，是一种性能良好的阳离子型高分子有机絮凝剂，对污水具有较强的絮凝，助凝和污凝脱水能力。本文研究了它的合成方法，并对合成条件进行了探讨，用所得产品进行了剖份试验，效果良好。     

水性油墨废水絮凝污泥制备吸附剂及阳离子染料的吸附

以水性油墨废水絮凝污泥为原料、采用一步炭化活化法制备了吸附剂,并将其用于阳离子蓝X-GRRL溶液(300 mg/L)的吸附处理。考察了吸附剂投加量、吸附时间、吸附温度和吸附pH对吸附效果的影响,并对吸附动力学进行了探讨。结果表明:所制得吸附剂的总孔体积为0.5 cm~3/g,平均孔径为7.12 nm;在吸附剂投加量0.6g/L、吸附时间420 min、吸附温度25℃、吸附pH 5.4的条件下,吸附量高达486.21 mg/g,脱色率达97.24%;该吸附剂对于阳离子蓝X-GRRL的吸附过程可用准二级动力学模型和颗粒内扩散效应模型很好地描述。     

废钻井液固液分离处理用化学剂性能评价

为了满足废钻井液固液分离处理要求,通过试验优化出两种无机破胶剂,同时对该处理用化学剂的性能进行了详细的评价。结果表明,所合成阳离子聚合物与无机破胶剂配伍使用可以保证滤出液具有较好的透明性,且具有良好的协同增效作用。用滤出液配制处理液进行反复处理,效果同用清水配制处理液处理相当,可节约处理费用。     

Preparation of activated carbon from cattail and its application for dyes removal

Activated carbon was prepared from cattail by H3PO4 activation. The effects influencing the surface area of the resulting activated carbon followed the sequence of activated temperature activated time impregnation ratio impregnation time. The optimum condition was found at an impregnation ratio of 2.5, an impregnation time of 9 hr, an activated temperature of 500°C, and an activated time of 80 min. The Brunauer-Emmett-Teller surface area and average pore size of the activated carbon were 1279 m2/g and 5.585 nm, respectively. A heterogeneous structure in terms of both size and shape was highly developed and widely distributed on the carbon surface. Some groups containing oxygen and phosphorus were formed, and the carboxyl group was the major oxygen-containing functional group. An isotherm equilibrium study was carried out to investigate the adsorption capacity of the activated carbon. The data fit the Langmuir isotherm equation, with maximum monolayer adsorption capacities of 192.30 mg/g for Neutral Red and 196.08 mg/g for Malachite Green. Dye-exhausted carbon could be regenerated effectively by thermal treatment. The results indicated that cattail-derived activated carbon was a promising adsorbent for the removal of cationic dyes from aqueous solutions.     

活性污泥胞外聚合物提取方法的研究

对两种不同来源的活性污泥中EPS的提取效率进行了研究,采用的提取方法有NaOH法,阳离子交换树脂法（CER法）,加热法和离心法。结果表明,CER法是两种污泥EPS提取中最有效的方法。经过16h的提取,EPS中DNA的含量分别为0．73％和1．61％,这表明EPS的提取没有受到胞内物质的污染。两种污泥EPS的提取量分别为74mg／gVSS和80mg／gVSS,其中多糖和蛋白质是EPS的主要成分。在研究中,CER法最佳提取时间为8h,高搅拌强度和CER投加量都有利于EPS提取量的增加。     

降雨条件下典型岩溶流域地下水中的物质运移

通过对2008年4月下旬降雨期间,重庆青木关地下河系统出口姜家泉泉水的水文过程、浊度、悬浮颗粒物、主要阳离子和TOC浓度的监测,结合悬浮颗粒物的扫描电镜和能谱分析图,来研究岩溶流域地下水中悬浮颗粒物浓度、浊度、主要阳离子和TOC等物质的运移特征.结果表明,在单一岩溶管道较发育的地下河出口,泉水流量、浊度、悬浮颗粒物浓度、主要阳离子和TOC浓度对降雨事件响应迅速;与碳酸盐岩溶解有关的Ca2+、Mg2+和Sr2+等在流量上升的过程中表现为稀释效应;降雨期间,地下河中受雨水侵蚀的土壤输入量增大,引起泉水中浊度和悬浮颗粒物浓度的增大;泉水中Al3+、Fe、Mn、Ba2+和TOC等物质是悬浮颗粒物的伴生物,其浓度随浊度的增大而增大;在研究的2场降雨期间,地下水携带悬浮颗粒物(0.45μm)的总量约为9.7t;在泉水流量的上升和衰减的过程中,水质较差或极差;降雨期间流域内土壤侵蚀和养分的流失,不但严重破坏了脆弱的岩溶生态环境,而且极易造成地下水由土壤侵蚀引起的非点源污染,对当地居民的饮水安全造成严重的威胁.     

微生物絮凝剂作用下厌氧颗粒污泥的形成及特性

以3个同样的UASB(R1、R2、R3)处理COD浓度为5 500~6 500 mg.L-1的废水,在相同的工艺条件下,采用每7 d投加1次方式,R1中每次投加7.5 g CaCl2和400 mL微生物絮凝剂MBF21,R2中每次投加140 mg阳离子PAM,R3作为对照,进行厌氧颗粒污泥培育试验,以考察微生物絮凝剂MBF21对培育厌氧颗粒污泥的促进作用.结果表明,经过67 d的运行,R1、R2、R3中均培育出厌氧颗粒污泥,对应的平均粒径分别为1.18、1.21、0.76 mm,平均粒径增长速率分别为15.37、15.82、9.10μm.d-1,比产甲烷活性SMA(COD-CH4/VSS.t)值分别为0.740、0.657、0.558 g.(g.d)-1,VSS/SS分别为0.667、0.629、0.607,SVI值分别为14.7、13.1、20.4 mL.g-1,湿污泥密度分别为1.061、1.064、1.054 g.cm-3,强度系数ζ分别为92.1、93.5、84.7.电镜扫描发现R1和R2中的颗粒污泥比对照组R3中的颗粒污泥更密实,在形成成熟颗粒污泥过程中,3个反应器均呈现相似规律,即污泥表面由丝状菌占优逐渐向杆菌、球菌占优方向转化.本研究证明了微生物絮凝剂MBF21在促进厌氧污泥颗粒化过程中,在提高颗粒污泥物理性能方面接近阳离子PAM,在提高颗粒污泥生理、生化性能方面优于阳离子PAM.     

Adsorption characteristics of humic acid-immobilized amine modified polyacrylamide/bentonite composite for cationic dyes in aqueous solutions

Humic acid-immobilized amine modified polyacrylamide/bentonite composite (HA-Am-PAA-B) was prepared and used as an adsorbent for the adsorption of cationic dyes (Malachite Green (MG), Methylene Blue (MB) and Crystal Violet (CV)) from aqueous solutions. The polyacrylamide/bentonite composite (PAA-B) was prepared by intercalative polymerization of acrylamide with Nabentonite in the presence of N,N0-methylenebisacrylamide as a crosslinking agent and hexamethylenediammine as propagater. PAA-B was subsequently treated with ethylenediammine to increase its loading capacity for HA. The surface characterizations of the adsorbent were investigated. The adsorbent behaved like a cation exchanger and more than 99.0% removal of dyes was detected at pH range 6.0–8.0. The capacity of HA-Am-PAA-B was found to decrease in the following order: MG > MB > CV. The kinetic and isotherm data were interpreted by pseudo-second order rate equation and Freundlich isotherm model, respectively. Experiments were carried out using binary solute systems to assess the competitive adsorption phenomenon. The experimental isotherm data for each binary solute combination of MG, MB and CV were analyzed using Sheindrof-Rebhun-Sheintuch (SRS) (multicomponent Freundlich type) equation.     

阳离子聚丙烯酰胺（PAM）改善污泥脱水性能的研究

通过对污泥含水率的测定和滤液蛋白质的测定,考察了阳离子聚丙烯酰胺（PAM）对污泥脱水性能的影响。结果表明,PAM能够改善污泥的脱水性能,最佳的投加量为0.96mg/g,污泥的含水率73.38%。通过激光粒度分析研究PAM对污泥的作用机理,发现投加PAM之后,污泥的絮体变大,占体积分数90%的颗粒粒径大于206.170μm,明显的大于原泥。实验表明,PAM是通过＂架桥吸附＂和＂水化作用＂改善污泥的脱水性能。     

Solubilization and degradation of perchloroethylene （PCE） in cationic and nonionic surfactant solutions

Solubilization of perchloroethylene (PCE) in a nonionic (Triton X-100) and a cationic (cetyltrimethylammonium bromide (CTAB)) surfactant solutions and the degradation of surfactant solubilized PCE using fine to nanosize Fe and bi-metallic Fe-Ni particles were investigated. Micelle partition coefficients (Km) and molar solubility ratio (MSR) for PCE in 10 g/L of surfactant solutions have been quantified and the solubility of PCE (100 mg/L in water) in the surfactant solutions increased by about ten fold. Of the two surfactants studied, Triton X-100 solubilized the higher amount of PCE per gram of surfactant. To degrade solubilized PCE, both iron and bimetallic Fe-Ni particles were used in continuously stirred batch reactors. The iron and bi-metallic particles were synthesized using the solution method and the particles were characterized using the SEM, EDS, TEM and XRD. The PCE solubilized up to 500 mg/L in both surfactant solutions were totally degraded at various rates by 200 g/L of bi-metallic Fe-Ni particles in less than 20 hr, which is the highest concentration of PCE degraded in the shortest time compared to data in the literature. The degradations of PCE solubilized in surfactant solutions were represented by nonlinear kinetic relationships which depended on the type of surfactant used for solubilizing the PCE.