膜电解技术处理含氯及重金属的废酸

采用离子交换膜电解技术处理铜冶炼过程产生的含氯及重金属的废酸。考察了废酸处理工艺、电解温度、电解时间、电流密度和催化剂的添加等条件对处理效果的影响。实验结果表明：采用先沉淀重金属后脱氯的废酸处理工艺,氯离子和铜离子的去除效果均较好;当以钛盐为催化剂时,在电解温度为40 ℃、电解时间为2.0 h、电流密度为825 A/m²的最佳工艺条件下,处理后废酸中的氯离子质量浓度为0.22 g/L,氯离子去除率为98.59%,铜离子质量浓度为0.45 g/L,铜离子去除率为95.08%,其他重金属大部分也得到有效去除。净化后的废酸可回用至铜冶炼的生产过程中。     

化学沉淀组合电催化氧化处理脱硫废液技术研究

真空碳酸钾脱硫工艺碱洗段废液因含有高浓度硫化物、COD等有毒成分而影响焦化废水后续生物处理。以焦化企业实际碱洗段废液为研究对象,选用化学沉淀和电催化氧化的组合方式对其进行预处理。结果表明,室温下当氧化铜的投加量为65 g/L、反应时间60 min时废液中S2-去除率可达93%,且经过高温灼烧可实现Cu O沉淀剂的再生使用。沉淀后出水经电催化氧化处理,在电流10 A、电压4.9 V、电解时间120 min的条件下,出水COD可降至2 400 mg/L,满足常规生化系统进水的要求。     

微波在废树脂中的穿透厚度研究

通过对不同功率微波在不同规格钢桶中对不同含水率的树脂中的穿透厚度的研究可知,微波在树脂中的穿透厚度主要与树脂自身含水率有关,与钢桶的规格尺寸也有一定的关系,而微波功率的影响则可基本忽略不计;对于含水率50％左右的树脂,微波在12L钢桶中的穿透厚度是130 mm;在200L钢桶中的穿透厚度是70mm.该研究成果对微波干燥工艺的具体参数的选取和扩大规模台架装置的设计研究等有重要意义.     

凹凸棒石/γ-Fe_2O_3/碳纳米复合材料的制备及其对苯酚的吸附作用

为获得同时具有有机亲和性和磁分离特性的吸附材料,以凹凸棒石黏土和废活性白土为原材料,通过铁盐水解共沉淀和在氢气气氛下程序升温煅烧的方法,制备廉价的凹凸棒石γ-Fe2O3/碳纳米复合材料.运用磁化率分析,红外吸收光谱,透射电镜,X射线衍射分析和碳含量分析对其进行了表征,并研究了复合材料吸附去除水中苯酚的动力学、吸附试验中pH的影响及同等条件下与其他吸附材料吸附性能的对比.结果表明,复合材料的磁化率值为2 769×10-8m3/kg,用磁分离工序即可把该吸附材料从溶液中快速分离出来;铁的磁性氧化物以γ-Fe2O3的形态负载到凹凸棒石表面,颗粒直径为10～60nm;碳以无定形的形态负载在凹凸棒石晶体表面;复合材料中的ω(碳)为7.4%,材料中出现了有机官能团-CH3和-CH2-.对苯酚的吸附试验表明,复合材料对苯酚的去除率是凹凸棒石原矿的3倍.     

超声辅助生物淋滤废旧Zn-C电池锌锰溶出的研究

以氧化硫硫杆菌(A.thiooxidans)为淋滤菌株对废旧Zn-C电池电极材料中的Zn、Mn进行了生物浸提,比较研究了化学浸提、生物淋滤和不同超声辅助方法生物淋滤体系下的Zn、Mn的溶出效率及溶出动力学.结果表明:不同超声辅助方法中,超声+生物淋滤体系Zn、Mn溶出最优,Zn、Mn的最大溶出率分别为94.2%和65.5%,并提高了溶释速率.此外,对于Mn的溶出,化学淋滤体系符合边界层扩散控制模型,生物淋滤和超声+生物淋滤体系符合收缩核Stoke's regime模型,而Zn的溶出均符合化学反应控制模型.     

化学镀镍废液的处理及再生技术研究进展

介绍了化学镀镍废液的产生和危害,综述了近年来国内外采用化学沉淀法、电解法、氧化还原法、萃取法、离子交换法、电渗析法等对化学镀镍废液进行处理及净化再生的技术研究进展,对各种方法的实用性进行了评价,并指出今后的发展方向。     

UV-catalytic treatment of spent caustic from ethene plant with hydrogen peroxide and ozone oxidation

The performance of UV/H2O2, UV/O3 and UV/H2O2/O3 oxidation systems for treating spent caustic from an ethylene plant was investigated, in UV/H2O2 system, with the increase of H202 dosage, removal efficiencies of COD and the ratio of biochemical oxygen demand(BOD) to chemical oxygen demand(COD) of the effluent were increased and a better performance was obtained than the H2O2 system alone. In UV/H2O2 system, removal efficiency of COD reach 68% under the optimum condition, and BOD/COD ratio was significantly increased from 0.22 to 0.52. In UV/O3 system, with the increase of O3 dosage, removal efficiency of COD and BOD/COD ratio were increased, and a better performance was obtained than the O3 system alone. Under the optimum condition, removal efficiency of COD was 54%, and BOD/COD ratio was significantly increased from 0.22 to 0.48. In UV/H2O2/O3 system, COD removal efficiency was found to be 22.0% higher than UV/O3 system.     

酸性氯化铜蚀刻废液一步沉淀法制备碱式碳酸铜

以酸性氯化铜蚀刻废液为原料,在Na₂CO₃和助剂A存在下,采用一步沉淀法制备碱式碳酸铜。考察了反应pH、n（Na₂CO₃）∶n（助剂A）、反应时间和反应温度对碱式碳酸铜制备效果的影响,并采用XRD、TG 及SEM对产品进行了表征。实验结果表明：在反应pH 7.0、沉淀剂配比n（Na₂CO₃）∶n（助剂A）=1∶2、反应时间1.0 h、反应温度70 ℃的条件下,产品的w（Cu²⁺）达55.62%,w（Cl^-）为0.013%,符合HG/T 4825—2015《工业碱式碳酸铜》的要求;蚀刻废液中Cu²⁺的回收率接近100%。表征结果表明,制得的产品为单一组分CuCO₃·Cu（OH）₂,小颗粒为直径1.8~5.4 μm的不规则球形,团聚后的大颗粒呈姜块状形貌,粒径为48~75 μm。     

利用蚀刻废液生产碱式氯化铜过程中二英类污染物的去除

针对蚀刻废液及其回收后生产的碱式氯化铜产品中二英(PCDD/Fs)和二英类多氯联苯(dl-PCBs)进行了分析研究,并比较了采用去除工艺前后两类污染物含量水平的变化特征.利用高分辨气相色谱/高分辨质谱对样品中PCDD/Fs和dl-PCBs进行分析,结果表明,氯化铜废液中PCDD/Fs和dl-PCBs的平均总浓度分别为264、139 pg·mL-1,而铜氨液中浓度分别为0.09、0.50 pg·mL-1;碱式氯化铜产品中浓度分别为106 pg·g-1(2.79 pg WHO-TEQ2005·g-1)和27.8 pg·g-1(0.69 pg WHO-TEQ2005·g-1);而经过吸附和过滤等去除工艺后,产品中PCDD/Fs和dl-PCBs的TEQ浓度水平分别降低至0.10—0.25 pg WHO-TEQ2005·g-1和0.05—0.72 pg WHO-TEQ2005·g-1,满足欧盟对于矿物源性饲料添加剂中PCDD/Fs和dl-PCBs的限量标准要求.研究表明该工艺能够有效去除利用蚀刻废液生产碱式氯化铜过程中的二英类污染物.     

Combined use of earthworm (Alma millsoni) and bacterium (Bacillus sp.) improved the bioremediation of spent engine oil contaminated soil

This study was carried out to assess the effectiveness of the combined use of earthworm (Alma millsoni) and bacterium (Bacillus sp.) in the bioremediation of spent engine oil (SEO) contaminated soils. A. millisoni were collected from the Botanical Garden of University of Ibadan, Nigeria. The stock culture of hydrocarbonoclastic Bacillus sp. was used for the bioremediation study. A set-up of eight pots containing 1000?g soil sample and 20?g of cow dung were mixed with 100, 75, 50 and 0?mL SEO respectively. Each of the set up was subjected to bioremediation agents; A. millisoni alone, Bacillus sp alone, A. millisoni and Bacillus sp, no treatment (control) in duplicate. Treatment of 100?ml SEO contaminated soil with combined A. millisoni and Bacillus sp resulted in significantly (P? bacterium > vermi-remediating agents. Earthworms exposed to 100?mLSEO-contaminated soil had higher CAT, SOD, and GPx activities compared to the control. Findings indicated that A. millisoni with Bacillus sp. can synergistically improve bioremediation of SEO contaminated soils.