藻细胞内外有机物氯消毒后典型消毒副产物的生成潜能

为探究藻细胞内外有机物氯化后典型消毒副产物的生成潜能,选取小球藻为研究对象,采用加氯消毒法研究了在不同生长时期及不同氯投加量下典型含碳类消毒副产物(THMs)和含氮类卤代消毒副产物(TCNM)的生成规律,并对二者的生成势进行了对比.结果表明:细胞外有机物(EOM)和细胞内有机物(IOM)提取液的总有机碳(TOC)和有机氮(DON)较高,而芳香结构和不饱和双键的有机质质量浓度很低;从对数生长期到衰亡期,EOM经氯化后TCNM的生成量逐渐增加,IOM的TCNM生成量则呈现先增加后降低的趋势;THMs的生成规律与TCNM相似,但其生成量明显高于TCNM.增加氯投量,EOM的TCNM生成量逐渐升高,IOM的TCNM生成量则先升高后下降;在氯投量为30 mg/L时,IOM的TCNM生成量最高;稳定生长期小球藻细胞的EOM和IOM在氯投量由20 mg/L升高到30 mg/L时,THMs的生成量稳定增加,当氯投量超过30 mg/L时,THMs的生成势显著升高,且三氯甲烷为THMs的主导物种.     

浮游植物现存量表征指标间相关性研究Ⅰ:叶绿素a与生物量

收集国内、外有关资料,并结合潘家口水库现场围隔实验,主要从实验室内研究水体、野外围隔水体及天然水体三个方面,对浮游植物叶绿素a含量与生物量间的相关性进行探讨。结果表明:在实验室条件下,叶绿素a与生物量一般呈显著正相关关系,但当优势藻种发生明显变更时,二者相关性不明显甚至不相关;现有资料显示,野外围隔实验水中,叶绿素a与生物量一般呈显著正相关。在天然水体中,叶绿素a与生物量可能相关或不相关。叶绿素a与藻密度的关系将在续文中予以讨论。     

环境因子对鱼饵中磷释放影响的实验研究

通过室内模拟实验,分析了环境因子(上覆水、微生物活动、温度、pH、水动力条件)对鱼饵磷释放特征的影响及原因。结果表明:鱼饵在去离子水中总磷和正磷酸盐的平衡释放量约是潘家口水库水中的1.58倍和1.76倍;微生物作用有利于鱼饵中磷向水体释放,前者总磷和正磷酸盐的释放量约为后者的1.55倍和1.28倍;温度升高和水体扰动促进了鱼饵中磷的释放;酸性和碱性条件下鱼饵中磷的释放量高于中性条件下鱼饵中磷的释放量。各环境因子作用下,鱼饵中磷在前3h内的释放速率最大。     

Synthesis of a perfluorooctanoic acid molecularly imprinted polymer for the selective removal of perfluorooctanoic acid in an aqueous environment

Perfluorooctanoic acid (PFOA) contamination in the environment is a global problem. The aqueous phase is the main medium for PFOA because of its moderate solubility. Adsorption is a feasible way to remove PFOA because of its chemical and biological stability. In this study, a new type of molecularly imprinted polymer (MIP) for the selective adsorption of PFOA in aqueous solutions was synthesized by the precipitation polymerization method with PFOA as the template molecule after optimization. The adsorption kinetics and isotherms of the MIP adsorbent toward PFOA were studied, and the effects of the pH and cations on the adsorption were investigated with batch experiments. The results show that acrylamide (AAM) was the best functional monomer, and the optimal molar ratio of PFOA to AAM to ethylene glycol dimethacrylate (crosslinker) was 1:6:25. The optimized MIP adsorbent had a high affinity for PFOA, and the uptake percentage by the MIP adsorbent was 1.3–2.5 times that of the nonimprinted polymer (NIP) when PFOA existed alone. A maximum PFOA sorption capacity of 5.45 mg/g based on the Langmuir isotherm model was achieved with the MIP adsorbent. The MIP adsorbent exhibited a high selectivity for PFOA over competitive compounds (other perfluorinated alkyl carboxylic and sulfonic acids), whereas the NIP did not. Approximately 90% of the PFOA in the mixture was removed by the MIP adsorbent; this was 18 times that of the NIP. Moreover, the regenerability of the MIP adsorbent was confirmed in five sequential adsorption–desorption cycles without a significant reduction in the PFOA uptake. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43192.     

固定化纳米铁/微生物小球去除高氯酸盐性能

从活性污泥中筛选出一株高效高氯酸盐降解菌,对其进行常规的生理生化实验,并结合16S rDNA序列分析,比对结果表明,该菌株与β变形菌纲(Thauera Phenylacetica)的相似性达99％.此菌株和纳米铁以海藻酸钙为载体,制备了纳米铁/微生物小球(NMBs),并研究其微观结构和去除高氯酸盐的性能.同时也考察了不同温度和pH等环境条件下,该体系及其游离体系去除高氯酸盐效果的对比.结果表明,所制备的小球直径为3～5 mm,表面布满孔道,利于物质的进入.小球去除高氯酸盐的过程主要是吸附、化学还原和生物降解三阶段共同作用的结果,其中后两阶段,均符合一级动力学规律.同时还发现,温度适中(30℃左右),中性pH(约7.8)环境下小球体系去除高氯酸盐效果最佳,且该体系对温度和pH适应能力较强,有利于实际污染的原位修复.     

氨基糖氯消毒后典型卤代碳、氮消毒副产物生成势研究

本研究以典型氨基糖类物质D-(+)-葡萄糖胺为研究对象,采用氯消毒方式,探究了D-(+)-葡萄糖胺是否是卤代碳、氮消毒副产物三卤甲烷(THMs)和三氯硝基甲烷(TCNM)的前驱物,明确其THMs和TCNM生成势及投氯量、p H值、溴离子浓度、亚硝酸根离子浓度这对其生成势的影响。结果表明:D-(+)-葡萄糖胺是THMs和TCNM的主要前驱物,三氯甲烷是氯消毒过程中主要的THMs物种。增大投氯量,HNMs和TCNM的生成势均升高;随着p H值的增大,THMs的生成势升高,TCNM的生成势先升高后降低;随着溴离子浓度和亚硝酸根离子浓度的增大,THMs的生成势均为先升高后降低,而TCNM生成势在高溴离子和高亚硝酸根离子浓度下则表现出被抑制的趋势。     

Catalytic activity of nickel nanoparticles in hydrogenation of p-nitrophenol to p-aminophenol

Nickel nanoparticles with different sizes and different structures were prepared by reducing nickel oxalate with hydrazine hydrate in the presence of citric acid, sodium dodecyl sulphonate, Tween 80, PEG 6000, and D-sorbitol as organic modifiers. The type of organic modifiers affected the size and the structure of the resultant nickel nanoparticles. The catalytic activities of the nickel nanoparticles increased with decreasing the particle size in the hydrogenation of p-nitrophenol to p-aminophenol. All the as-prepared nickel nanoparticles showed higher catalytic activity and selectivity than conventional Raney Ni catalyst.     

Remediation of petroleum contaminated soils by joint action of Pharbitis nil L. and its microbial community

The plot-culture experiments were conducted for examining the feasibility of Pharbitis nil L. and its microbial community to remedy petroleum contaminated soils. The petroleum contaminated soil, containing 10% (w/w) of the total petroleum hydrocarbons (TPHs), was collected from the Shengli Oil Field, Dongying City, Shandong Province, China. The collected soil was applied and diluted to a series of petroleum contaminated soils (0.5%, 1.0%, 2.0% and 4.0%). Root length, microbial populations and numbers in the rhizosphere were also measured in this work. The results showed that there was significantly (p < 0.05) greater degradation rate of TPHs in vegetated treatments, up to 27.63-67.42%, compared with the unvegetated controls (only 10.20-35.61%), after a 127-day incubation. Although various fractions of TPHs had an insignificant concentration difference due to the presence of the remediation plants, there was a much higher removal of saturated hydrocarbon compared with other components. The biomass of P. nil L. did not decrease significantly when the concentration of petroleum hydrocarbons in soil was ≤ 2.0%. The trends of microbial populations and numbers in the rhizosphere were similar to the biomass changes, with the exception that fungi at 0.5% petroleum contaminated soil had the largest microbial populations and numbers.     

Adsorption of single-ringed N- and S-heterocyclic aromatics on carbon nanotubes

Adsorption of single-ringed N- and S-heterocyclic aromatics on single-walled carbon nanotubes (SWCNTs) was examined to explore the potential of using carbon nanotubes (CNTs) as drug carriers and environmental adsorbents. Adsorbates included pyrimidine, 2-aminopyrimidine, 4,6-diaminopyrimidine, thiophene, benzene and aniline. Adsorbents included pristine SWCNTs, oxidized SWCNTs, and nonporous graphite. Adsorption of N- and S-heterocyclic aromatics was significantly enhanced by non-hydrophobic interactions. Particularly, the -NH₂-substituted compounds exhibited much stronger (up to 2 orders of magnitude) adsorption affinities to oxidized SWCNTs than benzene, even though they are much less hydrophobic. The π-π coupling or electron donor-acceptor (EDA) interactions are likely adsorption-enhancement mechanisms for all six compounds. The lone-pair electrons of the N heteroatoms and the -NH₂ group can enable n-π EDA interactions with SWCNT surfaces. Lewis acid-base interactions are another significant adsorption-enhancement mechanism for the -NH₂-substituted compounds (and possibly for pyrimidine) on SWCNTs. For the N-heterocyclic aromatics, adsorption affinity is highly dependent on the O-functionality of the SWCNT surface and on solution pH, due to the speciation reactions of both adsorbates and SWCNT surface O-functional groups, indicating that selective adsorption of N-heterocyclic aromatics is possible by combining the surface functionality of CNTs and solution chemistry.