有机颜料废水的混凝预处理研究

利用絮凝剂阳离子聚丙烯酰胺(CPAM)和混凝剂聚合氯化铝(PAC)对有机颜料废水进行混凝处理,考察了单独使用CPAM、PAC及两者联合使用的处理效果,探讨了初始pH值、混凝剂投加量对处理效果的影响.结果表明,CPAM与PAC复配处理该废水时效果较好,水样pH值为7.0;CPAM与PAC的投药量分别为10mg/L和150mg/L时,浊度去除率可达97.56％.     

新型阳离子聚丙烯酰胺的合成及絮凝性能研究

以丙烯腈和二异丁烯为原料,通过里特反应,合成了具有较大空间体积、疏水性好的树枝状功能性单体,并通过质谱、核磁对其结构进行了表征。在复合引发体系的催化下,把功能性单体、丙烯酰胺(AM)和阳离子单体甲基丙烯酰氧乙基三甲基氯化铵(DMC)进行共聚合,合成了不同阳离子度的高性能阳离子聚丙烯酰胺并对其絮凝特性进行了研究。实验结果表明该絮凝剂具有很好的除油、除污效果,有望在污水处理领域得到实际的推广应用。     

热水解污泥厌氧消化过程中肠球菌抗生素抗性基因与毒力基因的转归

城市污泥中含有大量肠球菌,可携带抗生素抗性基因(antibiotic resistance genes,ARGs)和毒力基因(virulence gene,VGs),从而具有潜在的耐药性和致病性,对人类健康存在巨大威胁.为此考察了热水解污泥在中温(40℃)/高温(55℃)厌氧消化过程中肠球菌的耐药表型、基因型及携带VGs的变化规律.结果表明,厌氧进泥中肠球菌对阿奇霉素的耐药率均显著高于螺旋霉素和四环素.高温厌氧对肠球菌的数量及耐药性具有更好地控制及削减效果.高温厌氧消化可能会促进四环素类抗性基因在肠球菌的表达.中温、高温厌氧消化可促进ARGs在肠球菌中发生水平转移,导致其潜在双重甚至多重耐药性增加.中温厌氧消化可降低肠球菌同时具有潜在致病性和耐药性的几率,而高温厌氧消化则会增加此风险.     

Performance of dithiocarbamate-type flocculant in treating simulated polymer flooding produced water

Produced water from polymer flooding is di cult to treat due to its high polymer concentration, high viscosity, and emulsified characteristics. The dithiocarbamate flocculant, DTC (T403), was prepared by the amine-terminated polyoxypropane-ether compound known as Je amine-T403. The product was characterized by IR spectra and elemental analysis. The DTC agent chelating with Fe2+ produced a network polymer matrix, which captured and removed oil droplets e ciently. Oil removal by the flocculent on simulated produced water with 0, 200, 500, 900 mg/L of partially hydrolyzed polyacrylamide (HPAM) was investigated for aspects of e ectiveness of DTC (T403) dosage and concentrations of HPAM and Fe2+ ions in the wastewater. Results showed that HPAM had a negative influence on oil removal e ciency when DTC (T403) dosage was lower than 20 mg/L. However, residual oil concentrations in tested samples with di erent concentrations of HPAM all decreased below 10 mg/L when DTC (T403) dosage reached 30 mg/L. The concentration of Fe2+ in the initial wastewater had a slight e ect on oil removal at the range of 2–12 mg/L. Results showed that Fe3+ could not be used in place of Fe2+ as Fe3+ could not react with DTC under flocculated conditions. The e ects of mineral salts ions were also investigated.