基于ZIF-L的微固相萃取技术测定地表水中痕量典型多环芳烃

制备类沸石咪唑酯骨架ZIF-L材料,将其用作微固相萃取吸附剂,处理水中萘、苊、苊烯、芴、菲、蒽、荧蒽、芘等8种痕量典型多环芳烃,再用HPLC测定。试验表明,ZIF-L对上述多环芳烃的萃取效率明显高于商品化萃取材料C 18和多壁碳纳米管。方法在0.100μg/L^200μg/L范围内线性良好,方法检出限为0.02μg/L^0.03μg/L,标准溶液5次测定结果的RSD为4.7%~9.5%,实际水样加标回收率为84.5%~115%。将该方法用于北太湖5个点位水样的测定,测定值为未检出~3.40μg/L。     

水环境中致病菌分子生物学检测技术研究进展

总结了水环境中主要致病菌及其导致的疾病;介绍了检测水环境样品中致病菌的聚合酶链式反应（PCR）、实时定量PCR、等温扩增技术、生物传感器和高通量测序等分子生物学技术研究进展;分析了不同检测技术的优缺点和应用特点;提出了水环境中致病菌分子生物学检测技术的未来发展方向,为水环境中致病菌分析检测和风险控制提供研究思路和技术支撑。     

不同区域城市空气O3和PM2.5累积速率时序模型

利用2017—2018年全国7个区域10个典型城市环境空气O₃和PM_2.5浓度数据,统计污染物累积速率,进而采用回归方法拟合污染物浓度及其累积速率的时间序列模型,分析不同区域污染物时序变化特征差异。结果表明：不同区域O₃浓度时序曲线拟合程度总体高于PM_2.5,石家庄O₃拟合程度最高,西安PM_2.5拟合程度最高。以07：00、14：00分别作为O₃、PM_2.5模拟起点是24 h中的最优模型。不同城市夏季O₃小时浓度时序变化曲线均为单峰形态,O₃浓度及累积速率峰值出现时间可能由城市所处经度决定,太原O₃累积最快,西安O₃消解最快。各城市间冬季PM_2.5小时浓度及其累积速率时序变化曲线形态差异较大,沈阳PM_2.5累积和消解均最快。与浓度相比,城市环境空气O₃和PM_2.5累积速率与光照、扩散条件等有更好的时间相关性。     

Non-microcystin producing Microcystis wesenbergii (Komárek) Komárek (Cyanobacteria) representing a main waterbloom-forming species in Chinese waters

It is well known that several morphospecies of Microcystis, such as Microcystis aeruginosa (Kützing) Lemmermann and Microcystis viridis (A. Brown) Lemmermann can produce hepatotoxic microcystins. However, previous studies gave contradictory conclusions about microcystin production of Microcystis wesenbergii (Komárek) Komárek. In the present study, ten Microcystis morphospecies were identified in waterblooms of seven Chinese waterbodies, and Microcystis wesenbergii was shown as the dominant species in these waters. More than 250 single colonies of M. wesenbergii were chosen, under morphological identification, to examine whether M. wesenbergii produce hepatotoxic microcystin by using multiplex PCR for molecular detection of a region (mcyA) of microcystin synthesis genes, and chemical analyses of microcystin content by ELISA and HPLC for 21 isolated strains of M. wesenbergii from these waters were also performed. Both molecular and chemical methods demonstrated that M. wesenbergii from Chinese waters did not produce microcystin.     

Radiation-induced degradation of methyl orange in aqueous solutions

Degradation of methyl orange under gamma-irradiation was investigated. The reactions followed pseudo first-order kinetics. Apparent degradation rate constant, estimated through linear regression analysis, increased with an increase of dose rate and a decrease of initial methyl orange concentration. Degradation of methyl orange was significantly accelerated under oxidative condition, but was slightly enhanced under reductive condition. However, the result of decoloration was better under reductive condition than oxidative one. An analysis on the intermediates using Fourier transform infrared and gas chromatography/mass spectrometry demonstrates that the radiolytic degradation of methyl orange was processed with different C-N cleavages under oxidative and reductive conditions.     

Sorption of pentachlorophenol on surficial sediments: the roles of metal oxides and organic materials with co-existed copper present

The sorption characteristics of pentachlorophenol (PCP) in the surficial sediments were investigated using a selective extraction procedure. The results show that the Gamma(max) of PCP sorption decreased from 1.60mumolg(-1) to 0.69mumolg(-1) by approximately 60% after selective removal of organic materials from the sediments. The sorption of PCP in the sediments after selective removal of Mn oxides increased nearly up to 600% (from 1.60mumolg(-1) to 11.11mumolg(-1)) and, to a less degree, the PCP sorption in the sediments after simultaneous removal of Fe/Mn oxides (Gamma(max)=3.53mumolg(-1)). The analysis of the data using an additional model indicates that the contribution of Mn oxides to PCP sorption was negative, and Fe oxides and organic materials both have greater potential for sorption of PCP with less contribution from residues including Mn and Fe oxides in the residual fractions determined by a sequential extraction procedure and clay and silicate minerals. The differences in the decreased degrees of PCP sorption with increasing of Cu suggest that competition between Cu and PCP for sorption sites mainly takes place on Fe oxides.     

溶胶凝胶法制备磷钨酸掺杂TiO2薄膜及其光催化性能

以钛酸四丁酯为前驱物,采用溶胶凝胶法制备了磷钨酸掺杂的二氧化钛薄膜。通过XRD、FT-TR对该薄膜进行了表征,研究了薄膜在对氯苯酚光降解中的催化活性。结果表明,当磷钨酸与二氧化钛摩尔比为0.01∶1、薄膜烧结温度600℃、对氯苯酚溶液浓度30 mg/L（pH＝5）、光催化8 h的条件下,对氯苯酚的降解率超过90%,且薄膜可以重复使用。磷钨酸对二氧化钛的光催化活性具有明显的促进作用。     

水体中钼污染物的迁移转化研究进展

水体的重金属钼污染在中国部分地区已经显现,明确钼迁移转化规律是治理钼污染的基础.在总结水体钼污染形成机制的基础上,综述了水体钼污染物迁移转化的研究进展.其中,在水体胶体对钼的吸附研究方面较深入,酸碱条件和胶体种类是钼迁移转化的主要影响因素.而目前的研究,对尾矿中不同种类原钼矿物迁移转化与环境条件相互作用的关系尚不明确.因此,解决实际钼污染同题还需更深入的系统性探索.     

超声波预处理提高污泥好氧消化性能研究

为评价超声波预处理对提高污泥生物消化的作用,采用超声波预处理与好氧消化衔接,测试了污泥消化的溶解性有机物(SCOD)、TSS及蛋白酶变化过程.结果表明,污泥超声波预处理效果较好的能量密度与时间分别为12 kW/L和10 min,此时有机物释放与能量输入之比较优;在此条件下,经预处理后的污泥好氧消化性能明显比未处理的高.消化时间为10.5 d时,经超声波预处理的污泥TSS减量42.7%,而未处理的污泥仅减量20.9%.经超声波预处理后,污泥中的蛋白酶活性明显提高;同时,超声波预处理释放出较多的可溶性物质.因此,增加的可溶性物质与蛋白酶活性使得污泥迅速降解,提高了污泥好氧消化效率,缩短了污泥好氧消化时间.     

Fenton法氧化处理水中土霉素的研究

为了评价Fenton法预处理抗生素生产废水中残留的高浓度土霉素的可行性,对Fenton试剂(Fe2 -H2O2)法催化氧化降解水溶液中的土霉素进行了研究.探讨了H2O2与Fe2 投加比例、投加量以及起始pH值对降解效果的影响,同时考察了土霉素废水中大量共存的草酸根离子对氧化过程的影响.结果表明,当H2O2与Fe2 按照5:1的比例投加时降解效率最高,最佳初始pH值在3.0-4.0之间.在最佳投加比例下,H2O2投加量为0.9 mmol/L,100 mg/L的土霉素可在10 min内得到完全降解.最佳反应条件下经过处理后土霉素水溶液TOC的去除率达40%左右,可生化性(BOD5/COD)也得到明显的改善.水中共存的草酸根离子对氧化效率具有明显的影响,但通过增加亚铁离子的量可以消除草酸的影响.