超声协同紫外灭活大肠杆菌实验研究

应用紫外、超声、超声协同紫外对大肠杆菌进行灭活,并从生物学角度对协同机理进行探讨。结果表明:实验条件下,紫外辐照剂量与大肠杆菌灭活率之间具有良好的线性关系,各紫外辐照剂量下的E.coli均发生了光复活现象。超声功率密度对于灭活结果具有显著意义(p0.05),研究中超声灭活大肠杆菌的最大相对功效值对应的工况为7.18W/cm2作用80s。超声的协同作用使紫外线消毒动力学方程K值由0.1增至0.1358,减小了细菌对UV的抗性;与单独紫外作用比较,超声与紫外协同作用的光复活率有所降低。超声与紫外同时作用对细胞形态结构产生严重的破坏,超声作用只能改变细胞的结构,而不能破坏其DNA;利用T4-EndoⅤ对CPDs的特异性识别特性,可发现经各工况处理后,大肠杆菌DNA均被降解,产生大量CPDS,且各工况下ESS含量变化曲线与各工况下大肠杆菌灭活率曲线的相关系数达到0.92。     

气体扩散电极体系的电化学消毒

以自制活性炭/聚四氟乙烯(PTFE)气体扩散电极在无隔膜体系发生H2O2进行电化学消毒的系统研究,探讨了膜电极中PTFE质量分数WPTFE对氧气电还原特性的影响,研究了膜电极中载铂量WPt和造孔剂含量WNH4HCO3、外部操作条件pH值、氧气流速、溶液含盐量和电流密度对杀菌效率的影响.结果表明,WPTFE对H2O2的产率有明显的影响:产H2O2的峰电流先是随着WPTFE的增加而增大,然后减小.当WPTFE=50%时,峰电流最高.杀菌效果随着载铂量的提高而改善,WPt增加到4‰,杀菌效果和WPt=3‰时的杀菌效果基本相当.适量造孔剂的添加有效地改善了杀菌效果.杀菌效率随着pH值的下降迅速提高;该体系pH值适用范围较广:当原水细菌总数为106cfu.ml-1,pH=3—10,以载铂量WPt=3‰的气体扩散电极作为阴极进行电解,30 min后杀菌效率均能达到80%以上.在一定范围内增加氧气流速对H2O2的产生及杀菌效率的变化无太大影响.一方面,高的氧气流速增大了水的电阻,增加了杀菌能耗,提高了气体扩散电极体系杀菌的运行成本;另一方面,高的氧气流速在一定程度上缩短了处理时间,降低了设备投资.含盐量的增加使杀菌能耗减小,因此本电化学杀菌体系更加适合于高含盐量的水.杀菌效率随电流的升高而增加,但电流较大时,杀菌效率增加幅度较小.电流密度控制在6.6 mA.cm-2较为适宜.     

评价饮水DBPs致HepG2细胞损伤的2种试验方法

应用结晶紫染色法细胞毒性试验和胞质分裂阻滞法微核试验(CBMNT)评价饮水消毒副产物(DBPs)的HepG2细胞毒性和遗传毒性,探讨该2种试验方法纳入饮水安全性评价体系的可行性.根据遗传毒性和致癌性选用了5种DBPs,分别对HepG2细胞进行染毒,结果表明,5种DBPs的细胞毒性大小排序为3-氯-4-二氯甲基-5-羟基-2(5氢)-呋喃酮(MX)>二氯乙腈>二溴乙酸>二氯乙酸>三氯乙酸,其细胞毒性潜力(%C?值)分别为89.74,283.81,1217.02,5066.81,9335.38μmol/L,该5种DBPs在一定浓度下均可致HepG2细胞微核率显著增加,表现出明显的遗传毒性,其遗传损伤能力排序与细胞毒性大小相同.可考虑将这两种实验方法纳入到饮水安全性评价体系中.     

Evaluate HAA removal in biologically active carbon filters using the ICR database

The effects of biologically active carbon (BAC) filtration on haloacetic acid (HAA) levels in plant effluents and distribution systems were investigated using the United States Environmental Protection Agency’s Information Collection Rule (ICR) database. The results showed that average HAA5 concentrations in all locations were 20.4 μg·L^-1 and 29.6 μg·L^-1 in ICR plants with granular activated carbon (GAC) and ICR plants without GAC process, respectively. For plants without GAC, the highest HAA levels were observed in the quarters of April to June and July to September. However, for plants with GAC, the highest HAA levels were observed in the quarters of April to June and January to March. This HAA level profile inversely correlated well with water temperature, or biologic activity. For GAC plants, simulated distribution samples matched well with distribution system equivalent samples for Cl₃AA and THMs. For plants with and without GAC, simulated distribution samples overestimated readily biodegradable HAAs in distribution systems. The study indicated that through HAA biodegradation, GAC process plays an important role in lowering HAA levels in finished drinking water.     

二氧化氯处理医院污水的研究

本文采用的二氧化氯消毒剂,经过鉴定,完全符合国家规定的《消毒剂规范》要求。     

不同消毒剂对水中脊髓灰质炎病毒灭活的比较

将脊髓灰质炎病毒（ Ｐｏｌｉｏ Ｖ） 及不同消毒剂投加到模拟水样中,按不同接触时间１ ,３ ,１０ ,３０ ｍｉｎ 取样,空斑定量． 当模拟水有机质含量 Ｃ Ｏ Ｄ 为２０ ｍｇ／ Ｌ,病毒浓度ｎ（ Ｐ Ｆ Ｕ） ≈１ ×１０５ ｍ Ｌ－ １ 时,分别投加氯制剂有效氯ρ（ Ｃｌ）１６ ｍｇ／ Ｌ,接触３０ ｍｉｎ ;ρ（ Ｃｌ Ｏ２） ＝ ８ ．０ ｍｇ／ Ｌ,３０ ｍｉｎ ; Ｃｌ＋ Ｃｌ Ｏ２ 联合消毒剂（５ ．０ ＋ ５ ．０） ｍｇ／ Ｌ,３０ ｍｉｎ ;ρ（ Ｏ３） ＝ １ ．２２ ｍｇ／ Ｌ,１０ ｍｉｎ 时;可使病毒彻底灭活． 它们使 Ｐｏｌｉｏ Ｖ 达到９９ ．９９ ％ 灭活的浓度时间乘积（ ρ×ｔ） 值分别是６６２ ．５ ,１２９ ．５ ,２００ ．０ 和３ ．２ ｍｇ Ｌ－ １ ｍｉｎ ． 消毒效果（ 顺序） 为 Ｏ３ ＞ Ｃｌ Ｏ２ ＞ Ｃｌ＋ Ｃｌ Ｏ２ ＞ Ｃｌ． 联合消毒灭活 Ｐｏｌｉｏ Ｖ 的效果为 Ｃｌ 的３ ．３ 倍,表明将 Ｃｌ 与 Ｃｌ Ｏ２ 联合应用具有协同效应,优于传统的单一加氯消毒方式     

Effects of cucl2 on UV‐mutagenesis and on DNA damage in a restriction fragment of E. Coli gpt∗

CuCl₂ does not cause Trp⁺ reversion in E. coli WP2. However, when the bacteria are exposed to CuCl₂ and UV‐irradiated, a greater than 3‐fold enhancement of mutagenesis (compared to UV alone) is seen at 30 μMCuCl₂, and significant enhancement is seen even at 3 μM. The mechanism for this comutagenic effect was studied using a restriction fragment of the E. coli gpt gene. Whereas UV or CuCl₂ alone caused few strand breaks, UV + CuCl₂ induced breaks at every site. This reaction was blocked by KI, a free radical scavenger. While UV alone induced alkali‐labile sites, UV+ CuCl₂ induced many more such sites and altered the sequence specificity. We suggest that at least some of the comutagenic effect might be due to hydroxyl radical formed via a Fenton reaction.     

臭氧氧化深度处理二级处理出水的研究

以某城市污水处理厂二级处理出水为原水,研究了臭氧氧化深度处理对水中残留有机物以及病原微生物的降解和去除效果.结果表明,臭氧投加量达到6mg/L时,DOC、UV254、色度的去除率分别为15.49%、36.36%、73.61%,环境激素类痕量有机物邻苯二甲酸二丁酯(DBP)和邻苯二甲酸二(2-乙基己基)酯(DEHP)的去除率分别为37.29%和14.6%,三维荧光光谱荧光峰的各区域有机物质平均去除率在80%以上,DBP出水浓度为2.64mg/L,DEHP出水浓度为1.4mg/L,满足《城市污水再生利用地下水回灌水质》(GB/T 19772-2005)的标准.臭氧投加量达到10mg/L时,出水中指示性微生物粪大肠菌群仍接近103CFU/L,5mg/L有效氯消毒后出水粪大肠菌群仍接近10CFU/L,6mg/L臭氧与5mg/L有效氯组合消毒出水的粪大肠菌群下降至3CFU/L,满足《城市污水再生利用景观环境用水水质》(GB/T 18921-2002)的标准.三卤甲烷(THMs)的生成量随着有效氯投加量的增加而增加,臭氧与氯组合消毒过程与氯单独消毒过程相比,THMs生成量减少了78.08%.     

水体冻结过程中卤乙酸前体物在水-冰体系中的分配研究

通过室内模拟试验,研究了水体冻结过程中,水体中溶解性有机物(DOM)和卤乙酸前体物在水-冰体系中的分配规律.按照DOM在XAD树脂上的吸附特性将其分为5个部分:疏水性有机酸(HPO-A),疏水性中性有机物(HPO-N),过渡亲水性有机酸(TPI-A),过渡亲水性中性有机物(TPI-N)和亲水性有机物(HPI).结果表明:在水体冻结过程中,5种DOM组分在水相中的DOC浓度均随冷冻时间的增长而增加,呈现冷冻浓缩效应.与溶解性有机碳(DOC)所表征的整体有机物相比,5种DOM组分中的卤乙酸(HAAs)前体物更倾向于停留在水相中浓缩.在5种DOM组分中,HPI是主要的HAAs前体物.5种DOM组分在未冻结水中的UV-254与HAAFP均表现出一定相关性,其中HPO-A, TPI-A和HPI的UV-254与HAAFP达到极显著水平.然而在融冰水中,这5种DOM组分的UV-254与HAAFP的相关性均不显著.     

BIODEGRADATION OF DISINFECTION BYPRODUCTS AS A POTENTIAL REMOVAL PROCESS DURING AQUIFER STORAGE RECOVERY1

ABSTRACT: The biodegradation potential of two drinking water disinfection byproducts was investigated using aquifer materials obtained from approximately 100 and 200 meters below land surface in an aerobic aquifer system undergoing aquifer storage recovery of treated surface water. No significant biodegradation of a model trihalomethane compound, chloroform, was observed in aquifer microcosms under aerobic or anaerobic conditions. In contrast, between 16 and 27 percent mineralization of a radiolabeled model haloacetic acid compound, chloroacetic acid, was observed. These results indicate that although the potential for biodegradation of chloroacetic acid exists in deep aquifer systems, chloroform entrained within these aquifers or formed in situ will tend to persist. These results have important implications for water managers planning to meet anticipated lowered permissible levels of trihalomethanes in drinking water.