紫外辐射对小球藻混凝效果作用途径探讨

针对藻类在常规水处理过程中难以被有效去除的现状,采用紫外辐射对藻类混凝过程进行强化处理.结果表明,随着紫外照射时间的增加,混凝后对藻细胞和浊度的去除均呈先上升后下降的趋势,并在照射50 min时达到最大值.PAC(聚合氯化铝)投加量为5 mg·L~(-1)时,照射样的除藻率和去浊率达到最大,分别比空白样高20.1%和18%左右.pH值在6~9范围内,紫外辐射强化混凝效果的变化较小.溶液pH=8、紫外照射50 min,混凝后的除藻率和去浊率分别达到了93.5%和90.6%.此时,藻细胞Zeta电位最大,同时释放出藻黏液,有利于混凝沉降.而当紫外照射超过60 min后,出现细胞膜破裂,胞内有机物渗出,使得溶液中的有机物浓度急剧上升,Zeta电位开始下降,不利于后续混凝的进行.     

覆盖金属氧化物对湖泊沉积物溶解性有机质特征的影响

为揭示不同金属氧化物对湖泊沉积物DOM（溶解性有机质）影响机制,通过室内模拟试验,在沉积物表层分别覆盖Fe、Al、Mn氧化物及湖沙后培养1 a,并利用三维荧光和紫外光谱方法进行表征.结果表明:① 覆盖Al、Fe、Mn氧化物和湖沙主要降低了0~3 cm沉积物的w（DOC）,降幅分别为8.61%、6.27%、22.38%和0.44%. ② 沉积物中DOM的类络氨酸峰（peak B₁）和类色氨酸峰（peak T₂）均产生较大变化.其中三种氧化物均显著降低了上层沉积物中DOM的peak T₂,使底层DOM的peakT₂显著增加. Mn氧化物使DOM的peak B₁降低,Fe和Al氧化物使DOM的peak B₁增加,湖沙则使两类峰均降低. ③ 覆盖金属氧化物改变了沉积物DOM结构特征,其中覆盖Fe氧化物增强了其芳香性,而覆盖Mn氧化物和Al氧化却降低其芳香性,但三者均使DOM腐质化程度及官能团数量增加,并使FI（Fluorescence Index,荧光指数）增大,表明DOM向生物源转化.研究显示,沉积物表层覆盖金属氧化物影响了沉积物中DOM迁移和转化,并促进了其降解,导致其分子量和腐殖化程度增加.      

紫外消毒对城市污水处理厂耐药菌去除的影响研究

通过选取假单胞杆菌、鲍曼不动杆菌以及芽孢杆菌3种耐药菌作为研究对象,研究紫外光变化对这3种耐药菌的去除效果,得出较好的紫外消毒条件,应用到实际的污水处理厂消毒过程中。结果表明,紫外消毒对3种耐药菌都有很好的灭活效果。     

Cu2+强化UV活化过氧乙酸降解水中的双氯芬酸

研究了Cu²⁺强化UV活化过氧乙酸（Cu²⁺/UV/PAA）对水中双氯芬酸（DCF）的降解,考察了pH值、PAA投加量、Cu²⁺投加量、无机阴离子（Cl^-、SO₄^2-、NO₃^-和CO₃^2-）和溶解有机物（DOM）对DCF去除的影响;探讨了DCF在该体系中的降解产物和转化机理.结果表明：UV和Cu²⁺都能活化PAA产生活性自由基促进DCF降解.DCF在Cu²⁺/UV/PAA中的降解遵循准一级动力学,其降解可能归因于直接光解、HO^·氧化和CH₃COO^·、CH₃COOO^·等其它自由基氧化.在pH=3~11范围内,DCF降解的最佳pH=8.5.DCF的降解效率随着PAA投加量的增大而逐渐增高,过量的PAA能与DCF竞争HO^·.Cu²⁺用量的提高也能促进DCF的去除,但是过量的Cu²⁺可生成Cu（OH）₂导致其催化能力下降.由于NO₃^-在UV照射下可以产生HO^·,其对DCF降解有促进作用,且NO₃^-浓度越高,促进作用越明显.不同浓度的Cl^-、SO₄^2-、CO₃^2-和DOM对DCF降解影响较小.在Cu²⁺/UV/PAA降解DCF的过程中,共检测出13种降解产物.根据这些降解产物,提出了DCF可能的转化机理,包括8种不同的反应路径.     

紫外催化过硫酸盐深度处理垃圾焚烧厂渗滤液

为研究垃圾焚烧厂渗滤液生化出水的处理特性,对比了单独紫外(UV)体系、单独过硫酸盐(PS)体系以及紫外/过硫酸盐(UV/PS)体系深度处理垃圾渗滤液效果,发现UV/PS体系对渗滤液中有机污染物的去除效果较另外两体系的效果优异,因此采用UV/PS体系处理典型难降解有机物腐殖酸并考察体系的处理效能.在初始腐殖酸浓度为200...     

紫外辐射下的生物降解及微生物群落的变化

分别采用一体式循环床紫外光/生物膜反应器（PCBBR）和气升式内循环的紫外光/生物膜反应器（ILPBR）,用于苯酚、2,4,6-三氯酚（TCP）和抗生素药物磺胺甲恶唑（SMX）的降解.结果表明,苯酚、TCP和SMX在紫外光解与生物降解的共同作用下,其去除速率分别达到0.65、0.11和0.17 mg.（L.min）–1...     

UV/H2O2光化学氧化降解对氯苯酚废水的反应动力学

研究了UV/H₂O₂体系降解对氯苯酚废水的过程及动力学结果表明,反应降解速率与双氧水加入量、污染物初始浓度及载气种类有关.在双氧水理论投加量一半的情况下,通入氧气或空气,总酚的降解率可达到96%,COD_Cr去除率接近50%.反应体系加入载气,显著影响污染物的去除率.在本实验中,总酚降解为拟一级反应.     

CFD技术在水处理紫外消毒中的应用

介绍了紫外消毒在水处理中应用的现状,阐述了计算流体力学(CFD)的基本原理及其应用背景;论述了CFD技术在紫外消毒模型建立方面的关键因素:水力、辐射和剂量模拟;从消毒效率预测和设备结构优化两个方面对CFD技术在水处理紫外消毒中的应用进行了分析,并对其前景进行了展望,提出了今后的研究重点。     

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.     

Enhanced cyanogen chloride formation after UV/PS and UV/H2O2 pre-oxidation and chlorination in natural river water

Ultraviolet/persulfate (UV/PS) and Ultraviolet/hydrogen peroxide (UV/H₂O₂) have attracted much attention in recent years as advanced oxidation processes for water treatment. However, it is not all clear how these two methods affect the formation of cyanogen chloride (CNCl) in the subsequent water chlorination process. In this study, it was found that both UV/H₂O₂ and UV/PS pre-oxidation promoted the formation of CNCl in six actual water samples collected from urban rivers. Glycine, uric acid, arginine and histidine were investigated as the model compounds to explore the effects of different methods on the production of CNCl. The results showed that compared with chlorination alone, pre-oxidation by UV/H₂O₂ and UV/PS can reduce the production of CNCl for glycine and uric acid by up to 95% during post-chlorination process. However, they can greatly promote the formation of CNCl for arginine and histidine by up to 120-fold. In a more detailed investigation, pre-oxidation of histidine formed highly reactive intermediates to chlorine, leading to increased CNCl formation and chlorine consumption. The results showed that the precursors of CNCl was altered after pre-oxidation, and need to be re-evaluated.