Relevant parameters for assessing the environmental impact of some pyridinium, ammonium and pyrrolidinium based ionic liquids

Several physico-chemical properties relevant to determine the environmental impact of ionic liquids - aqueous solubility, octanol/water partition coefficient, chromatographically derived lipophilicity and infinite dilution diffusion coefficients in water - were measured in ionic liquids based on pyridinium, ammonium and pyrrolidinium cations with bis(trifluoromethylsulfonyl)imide anions. The influence of the presence of hydroxyl or ester groups in the physico-chemical properties of these liquids was checked. It appeared that the presence of functional oxygenated moieties reduces the lipophilicity of ionic liquids and so decreases the risk of bioaccumulation in environment.     

海洋灾害中政府承灾力脆弱性研究

信息扩散方法可以将一个分明值的样本点变成一个模糊集,把单值点变成集值样本点.这种方法对于海洋灾害呈现的非连续、样本点个数少的情况尤其适用,可以最大程度挖掘数据本身携带的信息.本文以市级区域作为研究对象,利用信息扩散原理建立政府承灾力脆弱性评价模型,通过对政府承灾系数的超越概率分析来评价海洋灾害中政府承灾力的脆弱性.进而对海洋灾害政府承灾力的脆弱度进行系统聚类分析,并以山东省为例进行实证研究,最终得到山东省沿海各市风暴潮灾害政府承灾力脆弱度的风验区划图.研究结果表明,威海、烟台、东营、日照的政府承灾力脆弱度较重,青岛、滨州次之,而潍坊的政府脆弱度最小.究其差异原因,各市不尽相同,主要表现在各市灾害发生概率、经济发展水平以及重视程度的不同.长期来看,海洋灾害中政府承灾力的提高依赖于最大程度减少海洋灾害带来的经济损失以及最大程度保障政府应对灾害的资金准备,为各级政府提高抗灾减灾能力提供了一定参考.     

Retention time profiling of all 136 tetra- through octa- chlorinated dibenzo-p-dioxins and dibenzofurans on a variety of Si-Arylene gas chromatographic stationary phases

The applicability of three different Silphenylene Silicone co-polymer (Si-Arylene) GC stationary phases (J&W Scientific DB-5ms, Varian VF-5ms, and VF-Xms) has been evaluated for the separation of all 136 tetra- through the octa- chlorinated dibenzo-p-dioxins (PCDD) and chlorinated dibenzofurans (PCDF) from closely eluting isomers using gas chromatography/high resolution mass spectrometry (GC/HRMS). Their relative performance data are compared to the “conventional” 5% diphenyl 95% dimethylpolysiloxane GC column (Supelco Equity-5) and to each other based on absolute retention times, visualized mass chromatograms, and the separation of 2,3,7,8-substituted isomers. VF-Xms GC column was able to demonstrate a better performance towards separation of 2,3,7,8-substituted PCDD/PCDF compared to other Si-Arylene GC columns tested, where only 2,3,4,7,8-PnCDF can not be resolved from 1,2,3,6,9-PnCDF and 2,3,4,6,7,8-/1,2,3,6,8,9-HxCDF and 1,2,3,7,8,9-/1,2,3,4,8,9-HxCDF can be at least partially resolved. These data suggest that the development of a single GC column for the separation of all 17 2,3,7,8-substituted dioxins and furans is feasible, which therefore could be used as a standard tool for the PCDD/PCDF methods globally including USEPA methods 1613b, 8290A, 8280B, European Standard Method EN 1948, Canadian methods DFPCB-E3418, EPS 1/RM/19, Japanese methods JIS K0311 and JIS K0312. Having one specific GC column to separate all 2,3,7,8-substituted PCDD/PCDF will significantly improve the data quality, comparability by the various methods and assessment techniques while simultaneously leading to a more cost and time efficient operation.     

电除尘器斜气流状态下粉尘沉降试验研究

针对电除尘器在实际运行过程中出现的除尘效率下降问题,提出斜气流这一新型技术,对均匀气流与斜气流分布状态进行可视化研究;在两种气流状态下进行粉尘沉降试验,对试验结果进行对比分析、总结相应规律;对我国电除尘器气流技术的发展提出了建议。     

大气超细颗粒物观测和扩散模拟研究进展

总结了近年来不同地区对不同环境下大气超细颗粒物的观测和扩散模拟研究进展。大量的观测研究结果表明,大气超细颗粒物的时空分布、组成特征、形成和成长的特性因观测地区的不同而存在很大差异,受气象因素和局部污染源的影响很大;其来源主要包括固定、移动燃烧源的直接排放和大气中颗粒成核现象,前一种来源一般是局部的,而后一种来源则是区域性的。目前,大多数关于大气超细颗粒物扩散的模拟研究都是针对其质量浓度的,对其数浓度扩散的模拟研究主要集中在小范围(机动车排放烟云的研究方面),在城市区域范围上的研究和应用还很少。最后,探讨和展望了大气超细颗粒物今后的主要研究方向和研究中面临的挑战。     

Microwave-assisted stripping of oil contaminated drill cuttings

The application of microwave heating technology to conventional gas stripping processes has been investigated in the remediation of contaminated drill cuttings. The technical feasibility and limitations of nitrogen and steam stripping processes are demonstrated, and it is shown that the combination of microwave heating with the stripping process offers a step change in performance. Order of magnitude improvements in processing time are shown for the microwave-assisted processes, as well as greatly improved levels of remediation. The mechanisms of contaminant removal are discussed, along with the phenomena which occur with microwave heating processes. The energy requirements of each of pure gas and microwave-assisted processes are also discussed, and the potential applications of each technology are highlighted relative to the overall remediation requirements.     

Crosslinking and stabilization of high fractional free volume polymers for gas separation

Crosslinkable poly(4-methyl-2-pentyne) (PMP) membranes were cast from carbon tetrachloride solutions containing PMP and either 4,4′-diazidobenzophenone or 4,4′-(hexafluoroisopropylidene)diphenyl azide. The composite membranes were transparent and homogeneous and were crosslinked by UV irradiation at room temperature or thermal treatment at 180 °C. Low levels of the bis(aryl azide) (1–4.5 wt%) were effective in rendering the membranes insoluble in cyclohexane and carbon tetrachloride, both are good solvents for PMP, thus PMP can easily be converted to mechanically stable membranes with permeabilities and selectivities comparable or higher than those of the well-known poly(dimethylsiloxane) (PDMS). The permeabilities of O₂, N₂, H₂, CH₄ and CO₂ were measured. Compared to pure PMP, the crosslinked membranes containing bis(aryl azide) had lower permeabilities and higher selectivities, consistent with a reduction in free volume.     

Laboratory longitudinal diffusion tests: 1. Dimensionless formulations and validity of simplified solutions

To obtain reliable diffusion parameters for diffusion testing, multiple experiments should not only be cross-checked but the internal consistency of each experiment should also be verified. In the through- and in-diffusion tests with solution reservoirs, test interpretation of different phases often makes use of simplified analytical solutions. This study explores the feasibility of steady, quasi-steady, equilibrium and transient-state analyses using simplified analytical solutions with respect to (i) valid conditions for each analytical solution, (ii) potential error, and (iii) experimental time. For increased generality, a series of numerical analyses are performed using unified dimensionless parameters and the results are all related to dimensionless reservoir volume (DRV) which includes only the sorptive parameter as an unknown. This means the above factors can be investigated on the basis of the sorption properties of the testing material and/or tracer. The main findings are that steady, quasi-steady and equilibrium-state analyses are applicable when the tracer is not highly sorptive. However, quasi-steady and equilibrium-state analyses become inefficient or impractical compared to steady state analysis when the tracer is non-sorbing and material porosity is significantly low. Systematic and comprehensive reformulation of analytical models enables the comparison of experimental times between different test methods. The applicability and potential error of each test interpretation can also be studied. These can be applied in designing, performing, and interpreting diffusion experiments by deducing DRV from the available information for the target material and tracer, combined with the results of this study.     

炸药爆炸条件下释放气溶胶扩散研究

针对炸药爆炸事故造成的气溶胶污染物为瞬时体源的特点,根据事故应急时效性的原则,利用后置虚拟源等效的方法和点源扩散的高斯公式,探讨了炸药爆炸事故造成的气溶胶污染物扩散范围和浓度的计算方法,并分析干沉积和物质放射性衰变等因素对扩散浓度的影响。运用该方法对钚气溶胶扩散进行了计算和分析,其结果表明:该计算方法具有一定的有效性和实用价值,能为该类事故早期实施各种应急计划和措施提供参考依据。     

Determination of dithiocarbamate fungicide propineb and its main metabolite propylenethiourea in airborne samples

A simple, rapid and sensitive GC–MS method for the determination of dithiocarbamate fungicide propineb [polymeric zinc propylenebis (dithiocarbamate)] and an improved HPLC procedure for the simultaneous determination of its main metabolite, propylenethiourea, and ethylenethiourea, the main metabolite of all ethylenedithiocarbamates, in airborne samples are described. The method for the analysis of propineb involves the evolution of carbon disulfide (CS₂), under acidic conditions in the presence of stannous chloride, extraction of the generated CS₂ into a layer of isooctane which is then analyzed for CS₂ content by GC–MS in SIM mode. Under the optimum conditions, the retention time of CS₂ was 1.89 min and the total time of chromatographic analysis was 5 min. Recoveries from spiking glass microfibre filters (GF/A) and silica gel filters were 86 ± 7 (n = 9) and 89 ± 4 (n = 9), respectively. The limit of detection is 0.7 ng per filter, which is equivalent to about 0.8–1.0 ng m⁻³ in air. In parallel, an HPLC method with ultraviolet detection is presented for the simultaneous analysis of the metabolites. Separation of the two metabolites was attained in less than 5 min. Recoveries from spiking GF/A and silica gel filters for ethylenethiourea were 100 ± 1 (n = 3) and 98 ± 2 (n = 3), respectively, while for propylenethiourea were 102 ± 1 (n = 3) and 98 ± 1 (n = 3), respectively. The detection limits are about 36–43 and 40–49 ng m⁻³ in air for ethylenethiourea and propylenethiourea, respectively. All the analytes spiked in the filters are proven to be stable for more than one month, at −4 °C.