三氯乙烯在苯酚菌中的共代谢降解性能研究

通过生物降解实验考察三氯乙烯(TCE)在苯酚驯化微生物中的共代谢降解性能,并进行动力学分析。结果表明,苯酚是TCE-苯酚共代谢过程必不可少的共代谢基质;TCE的共代谢降解与苯酚和TCE初始浓度有关。TCE在降解初期会出现一个短暂的迟滞期,TCE的大量降解要在苯酚被利用后才发生;高质量浓度TCE(>9mg/L)对共代谢降解有抑制作用。苯酚/TCE(质量比)在10～15以上时,苯酚菌对TCE的去除率较大。Haldane模型能够很好地拟合苯酚和TCE的比降解速率。动力学分析表明,微生物对苯酚的亲和力要大于TCE,苯酚对TCE共降解具有竞争性抑制作用,TCE对微生物存在毒性抑制作用;结果证实了生物降解实验的结论。     

Assessment of heterogeneity of metal composition of fine particulate matter collected from eight U.S. counties using principal component analysis

The main objectives of this study are to (1) characterize chemical constituents of particulate matter (PM) and (2) compare overall differences in PM collected from eight US. counties. This project was undertaken as a part of a larger research program conducted by the Johns Hopkins Particulate Matter Research Center (JHPMRC). The goal of the JHPMRC is to explore the relationship between health effects and exposure to ambient PM of differing composition. The JHPMRC collected weekly filter-based ambient fine particle samples from eight US. counties between January 2008 and January 2010. Each sampling effort consisted of a 5-6-week sampling period. Filters were analyzed for 25 metals using inductively coupled plasma mass spectrometry (ICP-MS). Overall compositional differences were ranked by principal component analysis (PCA). The results showed that weekly concentrations of each element varied 3-40 times between the eight counties. PCA showed that the first five principal components explained 85% of the total variance. The authors found significant overall compositional differences in PM as the average of standardized principal component scores differed between the counties. These findings demonstrate PCA is a useful tool to identify the differences in PM compositional mixtures by county. These differences will be helpful for epidemiological and toxicological studies to help explain why health risks associated with PM exposure are different in locations with similar mass concentrations of PM.     

零价铁复合有机膨润土处理染料废水的研究

针对目前印染废水处理现状及膨润土在水处理中回收困难等问题,提出将零价铁复合到有机膨润土中制成零价铁复合有机膨润土(ZVI-OB),以达到高效吸附并降解污染物的目的。以染料废水(Orange II) 作为研究对象,考察了废水中染料的初始浓度、pH以及吸附时间对ZVI-OB去除染料效率的影响,并研究了吸附后降解过程中时间和pH对污染物降解的影响以及降解前后膨润土层结构的变化。研究结果表明,ZVI-OB相对于CTMAB改性的有机膨润土而言,其吸附量有所降低,但ZVI-OB在吸附污染物之后能有效降解有机物。ZVI-OB在饱和吸附Orange II后经催化氧化,总有机碳含量降低为原来的19%,可以重复利用。     

几种腐殖填料生物滤池COD去除效能比较研究

分别采用腐殖垃圾、泥炭、煤炭等腐殖填料及河沙构筑生物滤池,处理模拟废水,比较研究其COD去除效能及降解特征,为工艺填料改性提供理论依据。几种填料的扫描电镜分析图显示腐殖垃圾及泥炭以团聚体三维空间结构为主;煤炭与河沙表面粗糙程度较小,且主要由颗粒状物质构成。稀释平板涂布法分离出各生物滤池中发挥主要作用的微生物共3种,各系统菌落数量有差异,但种类相同。3种腐殖填料生物滤池在进水有机物浓度为500 mg/L及1000 mg/L时均有较理想的有机物去除效率。3种腐殖填料生物滤池中泥炭构筑的腐殖填料生物滤池有机物比降解速率最小,因而微生物比增长速率最小,微生物增长和自身氧化最易趋向于动态平衡,对应的饱和水力渗透系数最大,滤池最不易发生堵塞,最有利于腐殖填料生物滤池长期稳定运行,证明泥炭是一种优良的生物介质。     

采用Zn-Se/不锈钢阴极的超声-电解法处理罗丹明B废水

采用超声-电解法考察了Zn-Se/不锈钢阴极处理罗丹明B废水的效果及影响因素。正交实验优化结果表明:在电流密度为2.4A/dm2、废水初始pH为6、超声功率为160W、通气量为10L/h、m(Zn)∶m(Se)为1∶1.5的Zn-Se/不锈钢作阴极、Ti/TiO2和铁网为双阳极的条件下,超声-电解法处理罗丹明B废水120min,废水脱色率为98.97%,COD去除率为88.11%。     

A method of detecting carbonyl compounds in tree leaves in China

Background, aim, and scope  

Carbonyl compounds have been paid more and more attention because some carbonyl species have been proven to be carcinogenic or a risk for human health. Plant leaves are both an important emission source and an important sink of carbonyl compounds. But the research on carbonyl compounds from plant leaves is very scarce. In order to make an approach to the emission mechanism of plant leaves, a new method was established to extract carbonyl compounds from fresh plant leaves.     

Potential physiological effects of pharmaceutical compounds in Atlantic salmon (<Emphasis Type="Italic">Salmo salar</Emphasis>) implied by transcriptomic analysis

Background, aim, and scope  

Pharmaceuticals are emerging pollutants widely used in everyday urban activities which can be detected in surface, ground, and drinking waters. Their presence is derived from consumption of medicines, disposal of expired medications, release of treated and untreated urban effluents, and from the pharmaceutical industry. Their growing use has become an alarming environmental problem which potentially will become dangerous in the future. However, there is still a lack of knowledge about long-term effects in non-target organisms as well as for human health. Toxicity testing has indicated a relatively low acute toxicity to fish species, but no information is available on possible sublethal effects. This study provides data on the physiological pathways involved in the exposure of Atlantic salmon as representative test species to three pharmaceutical compounds found in ground, surface, and drinking waters based on the evaluation of the xenobiotic-induced impairment resulting in the activation and silencing of specific genes.     

可见光响应型CuO/BiVO4的光催化活性研究

采用浸渍法制备了CuO/BiVO4光催化剂,通过X射线衍射(XRD)、热重/差示扫描量热(TG/DSC)和傅立叶红外光谱(FTIR)对其进行了表征,并在可见光照射下考察了其光催化氧化亚甲基蓝(MB)的动力学特性。结果表明,Cu的掺杂并未改变BiVO4的晶型结构;Cu(NO3)2/BiVO4在热处理(30～300℃)过程中,NO3-已经完全分解,Cu最终以CuO的形式存在于CuO/BiVO4光催化剂体系中;掺杂不同量Cu的CuO/BiVO4中的Cu2+/Bi+(摩尔比)实测值与理论值相近,该系列光催化剂的合成过程具有较高的可信度;在可见光照射下,CuO/BiVO4光催化降解MB反应符合表观一级反应动力学特征;当Cu2+/Bi+为0.050时,反应动力学速率常数(k)达到最高值(0.4334h-1),此时的k比单体BiVO4作用下的提高了1.04倍;由于异质结的存在,CuO/BiVO4与单体BiVO4相比,电子和空穴的利用率大大增加,使得CuO/BiVO4的光催化活性较单体BiVO4有了大幅度提高。     

臭氧氧化法深度处理纤维板生产废水的研究

采用臭氧氧化法深度处理纤维板生产废水,探讨了臭氧投加量以及反应时间对COD和色度去除的影响,得到了最佳的工艺参数,并分析了这种处理方法的经济性。结果表明,当臭氧投加量为180mg/L、反应时间为30min时,纤维板生产废水的COD、色度去除率分别为58.3%、98.3%。采用臭氧氧化法深度处理纤维素废水的投资成本为600～700元/t,运行成本为0.8～1.2元/t,较Fenton氧化处理方法而言,在处理效率和经济成本上具有较大优势。     

Kinetic study of the OH reaction with some hydrochloroethers under simulated atmospheric conditions

Using the relative rate technique, rate constants for the gas-phase reactions of hydroxyl radicals with 2-chloroethyl methyl ether (k₁), 2-chloroethyl ethyl ether (k₂) and bis(2-chloroethyl) ether (k₃) have been measured. Experiments were carried out at (298 ± 2) K and atmospheric pressure using synthetic air as bath gas. Using n-pentane and n-heptane as reference compounds, the following rate constants were derived: k₁ = (5.2 ± 1.2) × 10^?12, k₂ = (8.3 ± 1.9) × 10^?12 and k₃ = (7.6 ± 1.9) × 10^?12, in units of cm³ molecule^?1 s^?1. This is the first experimental determination of k₂ and k₃ under atmospheric pressure. The rate constants obtained are compared with previous literature data and the observed trends in the relative rates of reaction of hydroxyl radicals with the ethers studied are discussed. The atmospheric implications of the results are considered in terms of lifetimes and fates of the hydrochloroethers studied.