浅述汽车加油站油气回收系统监测研究

加油站油气回收系统是由卸油油气回收系统、汽油密闭储存、加油油气回收系统、在线监测系统和油气排放处理装置组成。该系统的作用是将加油站在卸油、储油和加油过程中产生的油气,通过密闭收集、储存和送入油罐汽车的罐内,运送到储油库集中回收变成汽油,以达到在汽车加油、油料储运过程中油汽不外泄,不污染周边环境的目的。根据中华人民共和国《加油站大气污染物排放标准》(GB 20952-2007)中第六条的规定,长三角地区的改造项目应在2010年1月1日进行,因此对加油站油气回收系统的监测显得十分紧迫。     

固相萃取-原子荧光光谱法测定土壤中的砷

采用硝酸-氢氟酸-盐酸体系微波消解土壤并结合On-Guard ⅡH柱去除消解液中重金属,原子荧光光谱法测定土壤中的砷。本方法前处理操作过程简单、省时、省力、酸用量少,砷的加标回收率为94.4％～105.6％,能够满足环境监测分析的要求。     

三峡库区库中干流及支流水体夏季二氧化碳分压及扩散通量

以三峡库区库中干流以及主要支流——梅溪河为研究区,于2013年5月对该区域水体中溶解二氧化碳分压(pCO2)进行了走航观测.结果表明,夏季梅溪河表层pCO2为6.8~7.5 Pa,三峡库区库中长江干流表层pCO2为201.4~210.2 Pa.在库区干、支流交汇的过渡区水体剖面上,表层水体pCO2最低为53.5 Pa,随着水深增加,pCO2急剧增大,在3 m处达到约210Pa后基本保持不变.通过计算,库区支流梅溪河和库区干流表层水体的CO2释放通量分别为-7.48 mmol·(m2·d)-1和39.58 mmol·(m2·d)-1.结果表明,库区支流梅溪河表现为大气中CO2的"汇",而库区干流表现为CO2的"源",库区干、支流水体在CO2的释放上有显著差异.     

泄爆导管对球形容器内气体爆炸泄放过程影响的试验

设计了球形容器内气体爆炸通过导管泄爆的试验系统,选用体积分数为10%(特殊说明除外)的甲烷和空气预混气体开展试验,研究了泄爆导管长度、容器容积、点火位置、气体体积分数、破膜压力等因素的影响。结果表明:泄爆导管越长,容器内的正压力峰值和负压力峰值越大;密闭爆炸时,球形容器的容积对爆炸压力峰值几乎无影响;不同容积球形容器内气体爆炸通过相同导管泄爆时(导管长度均为6 m,直径均为0.06 m),容积大的容器内的压力锋值为小容器压力值的3.3倍,且大容器内的压力上升速率也明显高于密闭爆炸的情况;有泄爆导管存在时,尾部点火容器内的压力峰值高于中心点火;泄爆导管的存在使得容器内的压力峰值高于直接泄爆时的压力峰值;无论有、无泄爆导管,容器内的压力峰值均随破膜压力增加而增加,但差值越来越小,说明导管的存在对容器爆炸泄爆过程的影响趋向缓和,但导管的存在总是阻碍了泄爆过程,增加了爆炸的严重程度,因此,在泄爆设计时要充分考虑导管的影响,适当提高容器自身的耐压强度。     

In-situ surfactant/surfactant-nutrient mix-enhanced bioremediation of NAPL (fuel)-contaminated sandy soil aquifers

SCOPE AND BACKGROUND: Contamination of soils, aquifers and groundwater by nonaqueous phase liquid (NAPL) pollutants constitutes a major environmental issue of concern, worldwide. The residual (biodegradation-resistant) hydrophobic fuel hydrocarbons entrapped in the soil porous matrix, possess a particular bioremediation challenge due to their becoming virtually immobile, nor desorbable, or water dispersible. Consequently, they are not available as substrates to the micro-organism-based biodegradation. MATERIALS AND METHODS: Our research involves the development of economically feasible, surfactant/surfactant-nutrient mix (SSNM)-enhanced bioremediation methodologies for sustainable, in situ bioremediation of fuel-contaminated aquifers. This requires, methodologically, (a) the optimization, via in vitro 'flow' (columns) lab experiments and screening processes, of an effective mixture for the intended SSNM-enhanced bioremediation; and (b) the study of the combined effect of the optimized SSNM on the solubilization/mobilization and biodegradation of NAPL (fuel) in in vitro site/aquifer-simulated bioremediation. RESULTS AND DISCUSSION: The essence of our findings: (1) kerosene's maximum enhanced mobilization - f = 3.6, compared with that of deionized water, was achieved with an SSNM having the composition of linear alkylbenzene sulfonate (LABS): coco-amphodiacetate (containing N): surfactant-nutrient X (containing both N and P) = 0.15: 0.15: 0.05 g/L, respectively; (2) 62-64% of the initial amount of kerosene in the initially saturated soil matrix, 'packed' in a column, has been eluted from it during approximately 30 days, compared with 68% of kerosene biodegradation in 'vessel' settings, in 21 days. CONCLUSIONS: (1) The indigenous microorganisms present in th vadose zones of fuel-contaminated sandy soil aquifers are potentially capable of unassisted removal of approximately 80% of the initially contained fuel (kerosene), during a period of about 42 days; (2) the major effects of the SSNM addition are (a) enhanced mobilization of the bulky NAPL; and (b) enhanced desorbtion/ solubilization/dispersion of the entrapped NAPL which, in turn, facilitate their enhanced biodegradation. RECOMMENDATIONS AND PERSPECTIVE: Our findings suggest that pre-optimized, biodegradable SSNM is essential for surfactants-based bioremediation of NAPL-contaminated aquifers, in order to make this in-situ methodology both technologically and economically feasible.     

微纳米气液分散体系吸收NO

以模拟烟气为气源,去离子水为水源,通过微纳米气泡发生器形成微纳米气液分散体系,吸收模拟烟气中的NO,考察了多种因素对脱硝率(η)和气相体积总传质系数(KGa)的影响,分析了微纳米气液分散体系吸收NO的反应机理。结果表明:η和KGa随着进气NO体积分数和十二烷基苯磺酸钠(SDBS)质量浓度的提高而下降;随着吸收液初始pH的提高先降低后升高;随着进气O_2体积分数的增大而提高;随着吸收液温度的升高先提高后降低;控制进气NO体积分数为0.06%时,在吸收液初始pH为2.0、吸收剂为去离子水、吸收液温度为25℃、进气O_2体积分数为10%的最佳条件下,脱硝率可达81.0%。微纳米气液分散体系是通过产生羟基自由基从而对NO进行氧化吸收的。     

根据具体情况优化EPA8310中色谱分离条件

运用Agilent（安捷伦）1200系列高效液相色谱和多环芳烃专用柱ZORBAX Eclipse PAH（4.6×250mm、5μm,P.N.959990-918,S.N.USPAB01066）,对16种多环芳烃化合物混合溶液进行分析,根据具体实验条件优化EPA8310中色谱分离条件并得到了更节省时间、分离效率更好的流动相梯度变化程序。     

Evaluating peats for their capacities to remove odorous compounds from liquid swine manure using headspace “solid‐phase microextraction”

Abstract

This paper reports on research designed to investigate the capacities of different highly characterized peats to remove odorous compounds from liquid swine manure (LSM). Peat types representing a wide range of properties were tested in order to establish which chemical and physical properties might be most indicative of their capacities to remediate odors produced by LSM. Eight percent slurries (of peat/LSM) were measured for odor changes after 24 hours using odor panel and GC/MS‐Solid‐phase microextraction (GC/MS‐SPME) analysis.

The GC/MS‐SPME and odor panel results indicated that, although all peats tested in this study were found to be effective at removing odor‐causing compounds found in LSM, some peats tended to work better than others. Overall, the peats that were the most effective at removing odor‐causing compounds tended to have lower bulk densities, ash contents, fulvic acids contents, and guaiacyl lignins contents,and higher water holding capacities, hydraulic conductivities, “total other lignins”; contents, hydrogen contents, carbon contents, and total cellulose contents.

GC/MS‐SPME analysis was found to be a reasonably inexpensive and efficient way of conducting this type of research. It allows one to identify a large number of the odor‐causing compounds found in LSM, and more importantly, to detect with some precision specific differences in the amounts of these compounds between peat types.     

Improved Gas Chromatographic method for analysis of trichlorfon insecticide in soil and turfgrass thatch

Abstract

An improved Gas Chromatographic method utilizing simple extraction and one‐step purification on solid phase extraction tubes was developed for analysis of trichlorfon as an intact insecticide compound in turfgrass thatch and soil. A Gas Chromatograph/Mass Spectrum (GC/MS) was used for confirmation of trichlorfon structure. The method readily determines trichlorfon in the presence of dichlorvos. Using an electron capture (EC) detector, the detection limits were 0.02 ppm in soil, 0.04 ppm in turfgrass thatch, and 0.09 ppm in soil, and 0.2 ppm in turfgrass thatch using an nitrogen phosphorus (NP) detector.