大气降尘中水溶性有机物组成与含量的研究

本文为了研究各个地区大气降尘中水溶性有机物的组成与含量,从离地表２０ 米处的电网绝缘子表面采集九个大气降尘样品,对其水溶性部分用有机溶剂进行有机物的分离萃取,求出有机物的含量,采用ＸＲＰＤ 进行物相鉴定,确定有机物的组成可分为有机酸、有机酸钾盐、有机碱·盐酸盐加合物,尿素与尿素·硝酸盐加合物等四类,并对其影响ＣａＳＯ４·２Ｈ２Ｏ 的溶解度进行一系列实验,结果表明这四类有机物对ＣａＳＯ４·２Ｈ２Ｏ 溶解度的提高均有显著影响,可提高４０ ％ － ６０ ％ ,与实际降尘样品中其溶解度平均提高５０ ％ 左右相一致。由于大气降尘中普遍存在来自土壤与燃煤飞灰所排放的ＣａＳＯ４·２Ｈ２Ｏ,研究有机物的组成与含量,这对了解局部地区环境酸化（ 湿沉降） 有其重要性。     

超临界流体萃取技术及其在环境保护中的应用

超临界流体萃取技术是20世纪70年代末兴起的一种新型分离、精制技术,近年来发展迅速,被广泛应用于化工、食品、医药、生物技术、材料制备等领域.将超临界流体萃取技术用于环境保护则是一个新的研究方向,因此,文章综述了超临界流体萃取技术的基本原理及其在环境保护方面的应用.     

超临界流体技术在环境保护中的应用

简要介绍了超临界流体萃取和超临界水氧化的基本原理及优点 ,综述了超临界流体技术在废水处理、固体废物处理及污染监测中的开发和应用     

共存离子对硫酸盐还原菌（SRB）处理含铬废水的影响研究

报道了用硫酸盐还原菌（ＳＲＢ）处理含铬（ＶＩ）废水时，共存离子Ｓｒ＾２＋，Ｃｄ＾２＋，Ｚｎ＾２＋，ＵＯ＾２＋２，Ａｇ＾＋和Ｃｌ＾－，ＳＯ２－４，ＣＯ＾２－３，ＳｉＦ＾２－６，ＥＤＴＡ柠檬酸根等存在的时的影响，在铬（ＶＩ）为５０μｇ／ｍＬ，菌量一定的条件下，铬的去除率可达８５％以上，共存离子与铬（ＶＩ）的摩尔比为４时影响较为显著，Ｃｄ＾２＋和Ａｇ＾＋使铬的去除量降低，ＵＯ＾２＋２，Ｓｒ＾２＋，Ｚｎ＾     

掺入CO催化活化CO2加氢合成甲醇的研究

用ＴＰＤ,ＴＰＳＲ－ＭＳ活性评价等方法,用Ｃｕ－Ｚｎ－Ａｌ催化剂,对ＣＯ２加氢合成甲醇的原料气掺入适量ＣＯ２进行了研究。结果表明ＣＯ２能占据催化剂表面部分ＣＯ２的吸附位,能抑制ＣＯ２加氢的逆水汽变换反应和促进甲醇合成,从而大大提高了ＣＯ２加事成甲醇的选择性和收率。     

超临界水氧化法处理高浓度有机发酵废水

对酒精废水和乙酰螺旋素废水进行了超临界氧化降解的研究,结果表明,超临界水氧化法是处理高浓度有面废水的一种有效方法,在实验的条件范围内,废水ＣＯＤ的去除率最高可达９９．２％。     

超临界技术的发展现状与前景展望

简要介绍了超临界流体的基本性质,综述了超临界技术在萃取分离、环境保护、材料科学、反应工程、生物技术、清洗工业等方面的发展状况,并对超临界技术的发展前景作了展望。     

超临界流体技术的环境保护中的应用

简要介绍了超临界流体萃取和超临界水氧化的基本原理及优点，综述了超临界流体在废水处理、固体废物处理及污染监测中的开发和应用。     

H-酸的催化湿式氧化反应过程研究

湿式氧化（ＷＡＯ）和催化湿式氧化（ＣＷＡＯ）都能有效地处理染料中间体－－Ｈ－酸。所有的Ｈ－酸在５ｍｉｎ内均被支除和形成一些中间产物。在不同反应时间段测定了ｐＨ值及阴、阳离子和小分子有机酸等中间产物。分析表明,ｐＨ值与ＣＯＤ的去除及有机酸的产生有密切的联系,Ｈ－酸被氧化成ＮＨ４＾＋、ＳＯ４＾２－、ＨＣＯＯＨ和ＣＨ２ＣＯＯＨ。ＷＡＯ法的瓜速率慢而且氧化乙酸困难。而ＣＷＡＯ法的反应速率不但快而且能有效地     

电化学法去除SO2／NOx的研究进展

本文对采用电化学方法去除ＳＯ２／ＮＯｘ废气这一新的研究方法进行了综述,在用酞花青钴（ＣｏＰｃ）修饰的碳气体扩散电极上,ＳＯ２在空气中的体积百分数在２０％以下时可以完全被氧化为硫酸,以连二硫酸盐（Ｓ２Ｏ４＾２－４）作还原剂,Ｆｅ＾２＋－ＥＤＴＡ作络合剂时,ＮＯ可以９０％以上的程度还原为ＮＨ＾＋４与ＮＨ２（ＳＯ３Ｈ）等低价含氮化合物,产物中未见Ｎ２、Ｎ２Ｏ与ＮＯ２等气体,氧化产物ＳＯ＾２－３（或ＨＳＯ     

Biosorption of copper(II) from aqueous solutions by pre-treated biomass of marine algae Padina sp

Biosorption of heavy metals can be an effective process for the removal and recovery of heavy metal ions from aqueous solutions. The biomass of marine algae has been reported to have high uptake capacities for a number of heavy metal ions. In this paper, the adsorption properties of a pre-treated biomass of marine algae Padina sp. for copper(II) were investigated. Equilibrium isotherms and kinetics were obtained from batch adsorption experiments. The biosorption capacities were solution pH dependent and the maximum capacity obtained was 0.80 mmol/g at a solution pH of about 5. The biosorption kinetics was found to be fast, with 90% of adsorption within 15 min and equilibrium reached at 30 min. The effects of light metal ions on copper(II) uptake were studied and the presence of light metal ions did not affect copper(II) uptake significantly. Fixed-bed breakthrough curves for copper(II) removal were also obtained. This study demonstrated that the pre-treated biomass of Padina sp. could be used as an effective biosorbent for the treatment of copper(II) containing wastewater streams.     

超临界水无害化共处理PVC和医疗垃圾焚烧飞灰的可行性探讨

采用超临界水氧化降解PVC同时无害化处理医疗垃圾焚烧飞灰,利用PVC脱氯形成的中间产物盐酸提取医疗垃圾焚烧飞灰中的重金属,达到飞灰无害化的目的。结果显示,超临界水可以将飞灰颗粒打碎,从而提高盐酸提取重金属的速率和效果,但是在超临界水中还存在重金属的固定过程,过长的反应时间和过高的反应温度都会降低重金属的提取效率。在提取过程中,Cu和Zn优先于Pb被盐酸浸出,而Pb被浸出后很容易被超临界水进一步固定。综合考虑重金属在超临界水中的变化特性,总结出超临界水处理飞灰和PVC的最佳条件为:PVC与飞灰质量比0.5:1,温度400℃,提取时间90 min。处理后的飞灰再次经过水洗后,其重金属浸出浓度低于USEPA规定的限制值。本研究为飞灰的无害化处理提供一条新的思路。     

Evaluation of geochemical methods for discrimination of metal contamination in Antarctic marine sediments: a case study from Casey Station

Detecting anthropogenic metal contamination in regional surveys can be particularly difficult when there is a lack of pre-disturbance data, especially when trying to differentiate low to moderate levels of contamination from background values. Furthermore, comparisons with other regional studies are confounded by differing analytical methods used and variations in sediment properties such as grainsize. Several types of geochemical technique, including weak acid partial extraction, strong acid extractions and total digestion have been used. Attempts have been made to overcome the influence that grainsize has on chemical concentrations in heterogeneous environments by analysing the fines, typically the mud fraction (<63 microm), in an attempt to improve the detection of anthropogenic contamination. Here we compare a weak acid partial extraction using 1M HCl and total digestion methods for a regional survey of reference and impacted sites in Antarctica using both whole sediment (<2 mm) and mud (<63 microm) fractions. The 1M partial extraction on whole sediment (<2 mm) most closely distinguished weakly, or moderately, impacted sites from reference locations. It also identified small scale within-location spatial variation in metal contamination that the total digest did not detect. Compared with total digests or analysis of the <63 microm fraction alone, this method minimised the possibility of a Type II statistical error in the regional survey - that is, failing to identify a site as being contaminated when it has elevated metal concentrations. To allow inter-regional comparison of sediment chemistry data from elsewhere in Antarctica, and also more generally, we recommend a 1M HCl partial extraction on whole sediment (<2 mm).     

Removal of Ni(II) and Cu(II) ions using native and acid treated Ni-hyperaccumulator plant Alyssum discolor from Turkish serpentine soil

Alyssum discolor biomass was collected from serpentine soil and was used for removal of metal ions. The plant species grown on serpentine soils are known to be rich with metals ions and thus have more capability for accumulating heavy metals. Native and acid-treated biomass of A. discolor (A. discolor) were utilized for the removal of Ni(II) and Cu(II) ions from aqueous solutions. The effects of contact time, initial concentration, and pH on the biosorption of Ni(II) and Cu(II) ions were investigated. Biosorption equilibrium was established in about 60 min. The surface properties of the biomass preparations were varied with pH, and the maximum amounts of Ni(II) and Cu(II) ions on both A. discolor biomass preparations were adsorbed at pH 5.0. The maximum biosorption capacities of the native, and acid-treated biomass preparations for Ni(II) were 13.1 and 34.7 mg g⁻¹ and for Cu(II) 6.15 and 17.8 mg g⁻¹ dry biomass, respectively. The biosorption of Ni(II) and Cu(II) ions from single and binary component systems can be successfully described by Langmuir and Freundlich isotherms. When the heavy metal ions were in competition, the amounts of biosorbed metal ions on the acid treated plant biomass were found to be 0.542 mmol g⁻¹ for Ni(II) and 0.162 mmol g⁻¹ for Cu(II), the A. discolor biomass was significantly selective for Ni(II) ions. The information gained from these studies was expected to indicate whether the native, and acid-treated forms can have the potential to be used for the removal and recovery of Ni(II) ions from wastewaters.     

Retrieval of heavy metal ions from solution via ferritisation

The paper summarises the results of the studies on retrieval of heavy metal ions in solution by ferritisation and its potential application in waste-water treatment. The optimum procedure for ferritisation of heavy metal ions in solution has been evolved with respect to pH, concentration of Fe2+, rate and time of aeration and temperature. The recommended procedure consists of controlled aeration of the solution containing heavy metal ions and ferrous ions at pH 9.5-10.5 at about 50 degrees C, until the black, granular, magnetic ferrite separates out. The metal ferrites can also be formed, even without heating or forced aeration, by ageing the mixed metal hydroxide precipitate at pH 10 to 11. The metal ferrites formed have been characterised by X-ray diffractometry. The laboratory-scope experiments conducted with synthetic heavy metal solutions as well as actual wastewater from a tanning industry showed that heavy metal ions can be effectively removed from solution to sub-ppm levels. The metal ferrites thus recovered may find commercial application as microwave absorbers, catalysts, metal scavengers, etc. This technique seems to have potential application in simultaneous, one step removal of different heavy metal ions from industrial wastewaters.     

Cu~(2+)、Zn~(2+)对生物脱氮系统的影响

Cu2+和Zn2+是污水处理工艺中经常遇到的金属离子.在驯化好的活性污泥系统中,研究了金属离子Cu2+和Zn2+在0～100 mg/L浓度下对活性污泥牛物脱氮系统的影响.试验发现Cu2+＞5 mg/L、Zn2+＞30 ms/L时,对硝化过程具有明显的抑制作用,在同样浓度的试验条件下Cu2+对硝化过程的抑制作用比Zn2+大.Cu2+≤0.5 mg/L时对反硝化过程具有一定的促进作用,有助于提高TN的去除效果;Cu2+＞0.5 mg/L时,对反硝化产牛抑制作用,随着浓度的增加,TN去除率逐渐下降.Zn2+不影响反硝化过程,仅在大于30 mg/L时,对硝化过程产生抑制作用.重金属Cu2+对生物脱氮系统的影响明显强于Zn2+.     

Biochemical and biological assays of endocrine disrupting compounds in various manure matrices

Wastes generated by animal agriculture have complex matrices and present a significant challenge for achieving accurate measurements of estrogens. The objective of this study was to compare two different extraction methods and two different biochemical and biological estrogen assays on two dairy manure matrices. The two extraction methods studied in this research were a two-step base-toluene extraction and a one-step cyclohexane extraction. The two assays assessed were an enzyme-linked immunosorbent assay (ELISA) and a yeast estrogen screen (YES) bioassay. Estrogenic activity was measured directly as 17beta-estradiol (E2) through the ELISA method or as E2 equivalents (E2-eq) through the YES bioassay. Both extraction methods yielded reasonable recoveries from distilled water in the absence of matrix interferences. In manure samples, ELISA resulted in recoveries slightly higher than 100% in two types of dairy manures, but YES recoveries varied. The YES bioassay detected much higher estrogenic activities in dairy manure compared to the E2 concentrations measured by ELISA. The base-solvent extraction yielded higher E2 concentrations in dairy manure compared to the one-step cyclohexane extraction. These results suggest that manure matrices vary sufficiently that extraction methods must be optimized for specific assays utilized to quantify estrogens in manures.     

Selectivity in the complexation of actinides by humic substances

The interactions of a range of actinide elements (Th, U, Np, Pu, Am) with humic substances from the Needle's Eye natural analogue site were studied by gel permeation chromatography. Bulk humic substances were isolated by ammonia extraction, followed by dialysis against distilled water and freeze-drying. The gel permeation results suggest that Needle's Eye humic substances can be fractionated into three incompletely resolved fractions with average molecular weights determined by analytical ultracentrifugation around 49 000 for Fraction 1, around 14 700 for Fraction 2 and around 8000 for Fraction 3. Although there are significant differences between the organic matter elution patterns in individual gel permeation experiments, presumably due to differences in column packing, these are much smaller than the differences between metal ions. The uranium that is naturally present in these humic substances is largely bound in the late-eluting fraction. Spikes of the early actinides, including Np and Pu in controlled valency states, have been added to the humic substances, and gel permeation of the spiked humic substances shows that the three humic fractions vary greatly in their effectiveness and selectivity as ligands for early actinides.     

Green pre-concentration techniques during pesticide analysis in food samples

The ever-increasing demand for determining pesticides at low concentration levels in different food matrices requires a preliminary step of pre-concentration which is considered a crucial stage. Recently, the parameter of “greenness” during sample pre-concentration of pesticides in food matrices is as important as selectivity in order to avoid using harmful organic solvents during sample preparation. Developing new green pre-concentration techniques is one of the key subjects. Thus, to reduce the impact on the environment during trace analysis of pesticides in food matrices, new developments in pre-concentration have gone in three separate directions: the search for more environmentally friendly solvents, miniaturization and development of solvent-free pre-concentration techniques. Eco-friendly solvents such as supercritical fluids, ionic liquids and natural deep eutectic solvents have been developed for use as extraction solvents during pre-concentration of pesticides in food matrices. Also, miniaturized pre-concentration techniques such as QuEChERS, dispersive liquid–liquid micro-extraction and hollow-fiber liquid-phase micro-extraction have been used during trace analysis of pesticides in food samples as well as solvent-free techniques such as solid-phase micro-extraction and stir bar sorptive extraction. All these developments which are aimed at ensuring that pesticide pre-concentration in different food matrices is green are critically reviewed in this paper.