共查询到19条相似文献,搜索用时 93 毫秒
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本文利用环境测试舱法对硝基清漆中苯系物的释放特征及影响因素进行了研究,在不同温度、相对湿度和空气流速下测试苯系物释放,并采用一阶衰减模型进行模拟.结果表明,苯系物的初始释放速率和衰减速率均与温度和空气流速呈线性正相关关系,而相对湿度并不影响苯系物的初始释放速率和衰减速率;温度和空气流速在释放初始阶段对释放的影响较大,随着苯系物的不断挥发,其影响逐渐变小,因此,增加温度和空气流速有助于加速苯系物的释放,缩短苯系物的释放周期,达到控制苯系物浓度的目的. 相似文献
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耐低温混菌降解苯系物的特性及菌种鉴定研究 总被引:1,自引:0,他引:1
以吉化双苯厂被硝基苯、苯系物(BTEX)污染的土壤为菌源,经过筛选驯化得到一组在低温条件(10℃)下可降解苯系物(BTEX)的混菌。室内研究表明,在10℃,pH=6.8,苯系物(BTEX)总质量浓度200mg·L^-1的条件下,84h后该菌对苯、甲苯、乙苯、二甲苯的降解率依次为93.2%、95.6%、91%、88.4%、对6种质量浓度的苯系物(BTEX)污染物中最难降解的苯进行降解动力学曲线模拟,当苯质量浓度小于17.48mg·L-1时,降解符合一级降解动力学,当苯的质量浓度为17.48~195.30mg·L^-1时,降解符合零级降解动力学、该混菌降解效果稳定、适应环境能力强,经80次传代后仍能保持良好的降解效果,且在6个不同地区含有不同背景组成的地下水中降解效果稳定、应用Biolog细菌自动鉴定系统和16SrDNA序列分析方法对降解率较高的3株菌B2、B4、B6作菌种鉴定,B2为嗜麦芽糖寡养单胞菌(Stenotrophomonas maltophilia),B4为斑生假单胞菌(Pseudomonas maculicola),B6为多刺假单胞菌(Pseudomonas spinosa)。 相似文献
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在重庆地区利用苏马罐系统和气相色谱质谱分析方法对加油站及其周边空气中苯系物进行了初步监测。结果发现,几种苯系物均有检出,各监测点苯系物总体浓度介于0.34-11.33 mg/m3之间,其中苯浓度最高,各点浓度为0.07-3.57 mg/m3,二甲苯其次,苯乙烯最低。从不同监测点来看,卸油区和加油区苯系物浓度普遍较高,环境敏感点相对较低。 相似文献
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本法经硝化、蒸馏除去二硫化碳中的苯系物,然后用处理后的二硫化碳作原油的稀释剂,水和大气中苯系物的浓缩剂。用邻苯二甲酸二壬醇(2.5%) 有机皂土(3%)作固定液,硅烷化101白色担体(60—80目)作载体,填充在2米长的不锈钢管中作为苯系物的分离柱,用氢火焰离子化鉴定器测定。最后用1毫克/升左右的苯系物标准样按外标法进行定性定量分析。其灵敏度对水中苯系物可达0.005毫克/升,准确度在90以上。 相似文献
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2009年北京市苯系物污染水平和变化特征 总被引:5,自引:0,他引:5
采用Tenax-TA/吸附热解吸、光离子化气相色谱法(GC-PID)对北京市大气中苯系物(BTEX)的小时平均浓度进行了为期1年的观测.结果表明,苯、甲苯、乙苯、间/对-二甲苯和邻二甲苯的年平均浓度分别为:4.43、7.03、2.27、4.18和2.06μg.m-3.苯系物之间具有很好的同源性,其浓度存在明显的日变化和季节变化,这些变化特征与交通尾气排放、采暖期化石燃料燃烧、光化学反应活性等密切相关.苯与甲苯特征比值(B/T)的分析表明,交通尾气排放是北京市大气中苯系物的主要来源,冬季和早春采暖期化石燃料燃烧也是北京市大气中BTEX的重要来源之一.乙苯与二甲苯比值(E/X)的季节变化为:夏季>春季>秋季>冬季,与北京市大气光化学反应活性季节变化趋势相似.2009年北京夏季总苯系物的平均浓度比2004年夏季减少了2/3,表明北京市政府为改善空气质量所采取的一系列控制措施十分有效. 相似文献
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This study focused on the sorption isotherms of 1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane (p,p'-DDT) and 1,1-dichloro-2,2-bis(p-chlorophenyl) ethylene (p,p'-DDE) on different original clays (i.e., zeolite, montmorillonite and attapulgite) and organoclay complexes. Sorption of organic pollutants was determined using gas chromatographic (GC) techniques to investigate the sorption behavior, and characterize the effect of, different organic cations. The original clays only sorbed low amounts of p,p'-DDT and p,p'-DDE, and the sorptive curves can be classified as L-shaped. Organoclays exhibited higher amounts of p,p'-DDT and p,p'-DDE sorption. The p,p'-DDT and p,p'-DDE sorption increased with increasing total organic carbon (OC) content of the organoclays. For hexadecyltrimethylammonium (HDTMA)-modified organoclays, the dominant adsorptive medium showed the partitioning sorption of hydrophobic-hydrophobic interaction, indicating no competitive sorption. The sorptive curves can be classified as C-shaped of constant partition (CP). However, benzyltrimethylammonium (BTMA)-modified organoclays exhibited competitive sorption. The sorption isotherm curves can be classified as S-shaped. The sorptive capacity of the HDTMA-modified organoclays for p,p'-DDT were higher than those for p,p'-DDE, but the BTMA-modified organoclays showed a reverse trend. This can be attributed to the different structures and shapes of organic cations, giving different sorptive mechanisms. The p,p'-DDT and p,p'-DDE sorption onto HDTMA-modified organoclays were caused by chemical interaction, with the BTMA modified organoclays occuring due to physical sorption. 相似文献
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Current knowledge of sorption processes in tropical soils is reviewed. Landscapes throughout the tropics are dominated by oxisols which occupy extensive areas of potentially highly productive soils. These soils are dominated by low-activity sesquioxide minerals and clays that have variable charge surfaces. The limited information on tropical soils available suggests that the composition of the ambient soil solution can influence sorption through changes in particle surface-charge density. Thus the observed decrease in sorption in the presence of divalent index cations may be related to the effect of ionic charge on the double-layer thickness which is manifested through a change in surface-charge characteristics. However, much work needs to be done to differentiate the effect of cation charge on surface-charge density from the competitive effect between the index cation and heavy-metal ions for the sorption sites. The effects of inorganic and organic ligands on adsorption of Cd by variable charge surfaces are also reviewed. 相似文献
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有机物在水/有机膨润土界面的化学行为 总被引:8,自引:0,他引:8
研究了苯酚、苯胺、对硝基苯酚等极性或可离子化有机物在不/有机膨润土界面的化学行为,定量描述了表面吸附和分配作用对双阳离子有机膨润土吸附作用的相对贡献率及影响因素。结果表明,表面吸附和分配作用的相对贡献率大小与改性时加入的双阳离子表面活性剂的组成与配比有关。双阳离子有机膨润土40TMAB/60DTAB和40TMAB/200TMAB对苯酚的吸附,在低浓度时以表面吸附为主,在高浓度时以分配作用为主。 相似文献
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Celso de Sousa Figueiredo Gomes 《Environmental geochemistry and health》2018,40(5):1739-1765
The use of clay by humans for medicinal and wellness purposes is most probably as old as mankind. Within minerals, due to its ubiquitous occurrence in nature and easy availability, clay was the first to be used and is still used worldwide. Healing clays have been traditionally used by man for therapeutic, nutritional and skin care purposes, but they could impart some important health and skin care risks. For instance, clay particles could adsorb and make available for elimination or excretion any potential toxic elements or toxins being ingested or produced, but they could adsorb and make available for incorporation, through ingestion or through dermal absorption, toxic elements, e.g. heavy metals. Edible clays, a particular case of healing clays, have been traditionally used by man for nutritional and therapeutic purposes. Geophagy, the deliberate soil eating, earth eating, clay eating and pica (medical condition or eating disorder shown by individuals addicted to eat earth substances), has been observed in all parts of the world since antiquity, reflecting cultural practice, religious belief and physiological needs, be they nutritional (dietary supplementation) or as a remedy for disease. This paper pretends to review historical data, basic concepts and functions, as well as benefits and risks of the use of healing clays, in general, for therapeutic and cosmetic purposes, and of edible clays, in particular, for therapeutic purposes. 相似文献
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Shubo Deng Danmeng Shuai Qiang Yu Jun Huang Gang Yu 《Frontiers of Environmental Science & Engineering》2009,3(2):171-177
Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics, isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS on the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS. 相似文献
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Markus Hildenbrand Ludwig Luckner Ulf Jenk Jochen Schreyer 《Environmental Sciences Europe》1997,9(6):333-338
As a result of former in situ leaching activities with sulfphuric acid, nitroaromatic compounds have invaded into cenomanian and turonian sandstone aquifers and mining waters in parts of the uranium mining of Königstein, Germany (Saxony). In the mining area contamination levels of nitrobenzene, mononitrotoluene and dinitrotoluene lead to a partial excess in the drining water guide values. For environmental protection, control and remediation efforts by flooding, more knowledge about contaminant mobility in sandstone, and in intercalated clays and silts, is demanded. A selected experimental area has been flooded to realize and study transport processes under real mining conditions. In this work, we have examined the mobilization of nitroaromatic compounds by flooding waters. The interactions between the nitroaromatic compounds, which are dissolved in the mining water, and the host rocks are discussed. The existing data for strata of varying lithologic conditions suggest that the sorption processes of the compounds investigated are negligible in pure sandstone aquifer layers and significant in the lithologic conditions with a complex mixture of mudstone, siltstone and clay. Several lithologic conditions are demonstrated in contaminant sinks and sources caused by adsorption processes and mobilization of newly connected stagnant pore waters. 相似文献
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Shalini Srivastava Kumar Rohit Raj Abhishek Kardam 《Environmental Chemistry Letters》2013,11(1):47-53
This article reports the synthesis of an efficient, low-cost material from maize powder to depollute arsenic-contaminated water. Arsenic is toxic for humans and other organisms even at low concentrations. The most well-known and severe case of arsenic poisoning through drinking water has been found in India and Bangladesh. Numerous inorganic materials have been tested for the removal of arsenic from water bodies over the last two decades. However, all such materials have several disadvantages such as unpredictable arsenic ion removal, high cost and the generation of toxic sludge that is often more difficult to manage. Alternatively, organic material from agricultural waste may be modified to enrich functional groups responsible for As sorption and, in turn, used to depollute contaminated waters. Here, Zea mays cob powder has been modified to remove arsenic species from water. Two modified materials were produced: an aminated maize powder and a thiolated maize powder. Amination was done using epichlorohydrin and dimethylamine. Thiolation was done using thioglycolic acids. Amination increased As (III) sorption from 70 to 75.8 % and As (V) sorption from 85 to 94.42 %, compared with unmodified maize powder. Thiolation increased As (III) sorption from 70 to 81.7 % and As (V) sorption from 85 to 90 %. Amination increased usability cycles from 3 to 5. Thiolation increased usability cycles from 3 to 6. The novel modified maize biosorbent has enough potential for the development of a low-cost technological pre-treatment step, prior to high-tech chemical treatments. 相似文献
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Safety assessments for radioactive waste disposal require estimations of the migration of radionuclides in soils. The influence
of humic acid (HA) on the sorption of uranium in its +4 oxidation state to kaolin has been examined from pH 4 to 8, with HA
concentrations of 15–200 ppm. In the absence of HA, 20–40% of the U(IV) was in solution, with more sorption occurring at higher
pH. The presence of HA solubilised up to 90% of the uranium with higher solubilities at higher HA concentrations and higher
pH values. Uranium sorption was mapped against HA sorption, and it was found that there was a lower level of U(IV) sorption
than can be accounted for by just measuring HA sorption. However, this effect got less marked as the pH rose. Sensitivity
analysis indicated that the fraction of surface-bound HA is the controlling parameter for modelling in these systems. 相似文献
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A. R. Strom 《Marine Biology》1979,51(1):33-40
Live copepods, Calanus finmarchicus (Gunnerus) and C. hyperboreus (Krøyer), exposed to dissolved 14C-labeled trimethylamine (TMA) in seawater, oxidized TMA to trimethylamine oxide (TMAO), which accumulated in the organisms. The amount of TMAO synthesized was dependent on the time of exposure to TMA and the concentration of TMA in the seawater. It was inferred that copepods can produce TMAO by oxidation of TMA found in their plant food. Choline and methionine did not appear to be of importance as precursors of TMAO. There were large seasonal changes in TMA monooxygenase activity of both copepods. The activity was high in spring, and decreased through summer and autumn to a winter low in October to March. The changes in TMAO content of C. finmarchicus were, in comparison, small (this aspect was not tested for C. hyperboreus). 相似文献