有机溶剂对苏云金芽孢杆菌(Bacillus thuringiensis)几丁质酶的影响

以苏云金芽孢杆菌(Bt)的发酵液为材料,经硫酸铵分级分离、DEAE-32离子交换柱层析分离,获得部分纯化的Bt几丁质酶(EC3. 2. 1. 14)制剂.研究了几种有机溶剂对Bt几丁质酶的影响.结果表明,甲醇、丙三醇、甲醛和戊二醛对几丁质酶有抑制作用;乙醇、丙醇、乙二醇和二甲亚砜在低浓度时对酶有激活作用,随着浓度的升高表现出抑制作用;二氧六环的浓度低于 5%时,对酶的影响不明显,而高于 5%时,对酶则有激活作用;丙酮对酶有激活作用. 图 1参 10     

Cosolvent effects on sorption isotherm linearity

Sorption-desorption hysteresis, slow desorption kinetics, and other nonideal phenomena have been attributed to the differing sorptive characteristics of the natural organic polymers associated with soils and sediments. In this study, aqueous and mixed solvent systems were used to investigate the effects of a cosolvent, methanol, on sorption isotherm linearity with natural organic matter (NOM), and to evaluate whether these results support, or weaken, the rubbery/glassy polymer conceptualization of NOM. All of the sorption isotherms displayed some nonlinear character. Our data indicates that all of the phenanthrene and atrazine isotherms were nonlinear up to the highest equilibrium solution concentration to solute solubility in water or cosolvent ratios (Ce/Sw,c) used, approximately 0.018 and 0.070, respectively. Isotherm linearity was also observed to increase with volumetric methanol content (fc). This observation is consistent with the NOM rubbery/glassy polymer conceptualization: the presence of methanol in NOM increased isotherm linearity as do solvents in synthetic polymers, and suggests that methanol is interacting with the NOM, enhancing its homogeneity as a sorptive phase so that sorption is less bimodal as fc increases. When the equilibrium solution concentration was normalized for solute solubility in water or methanol-water solutions, greater relative sorption magnitude was observed for the methanol-water treatments. This observation, in conjunction with the faster sorption kinetics observed in the methanol-water sediment column systems, indicates that the increase in relative sorption magnitude with fc may be attributed to the faster sorption kinetics in the methanol-water systems, and hence, greater relative sorptive uptake for the rubbery polymer fraction of NOM at similar time scales.     

Aerobic biodegradation of vinyl chloride and cis-1,2-dichloroethylene in aquifer sediments

Laboratory batch experiments have been performed with sediment and groundwater obtained from two sites in Denmark to study the aerobic biodegradation of vinyl chloride (VC) and cis-1,2-dichloroethylene (c-1,2-DCE) to assess the natural aerobic biodegradation potential at two sites. The experiments revealed that VC was degraded to below the detection limit within 204 and 57 days at the two sites. c-1,2-DCE was also degraded in the experiments but not completely. At the two sites 50% and 35% was removed by the end of the experimental period of 204 and 274 days. The removal of c-1,2-DCE seems to occur concomitantly with VC indicating that the biodegradation of c-1,2-DCE may depend on the biodegradation of VC. However, in both cases natural groundwater was mixed with sediment and consequently there may be other compounds (e.g. ammonium, natural organic compound etc.) that serves as primary substrates for the co-metabolic biodegradation of c-1,2-DCE. At one of the sites methane was supplied to try to enhance the biodegradation of VC and c-1,2-DCE. That was successful since the time for complete biodegradation of VC decreased from 204 days in the absence of methane to 84 days in the presence of methane. For c-1,2-DCE the amount that was biodegraded after 204 days increased from 50% to 90% as a result of the addition of methane. It seems like a potential for natural biodegradation exists at least for VC at these two sites and also to some degree for c-1,2-DCE.     

超(近)临界流体溶剂在反应和分离技术中的应用

超(近)临界流体(S/NCF)具有可调性,通过调节压力和温度或加入共溶剂能够提高S/NCF溶剂中反应和分离的效率,使之具有可控性,有利于改善环境和提高经济效益本文以超临界CO₂和近临界水为例,总结了S/NCF溶剂在可持续反应和分离中的应用和研究进展.     

Application of the Method of Organizational Congruencies in Substituting Organic Solvents With Vegetable Agents for the Cleaning of an Offset Printing Machine

The aim of this research is the application of the Method of Organizational Congruencies before and after the substitution of organic solvents with vegetable agents for the cleaning of an offset printing machine in order to assess the organizational changes. A solvent-free process is the goal of the Subsprint Project (Technology Transfer Program of the European Community). This, study shows how human and environmental health is improved by using vegetable agents, though this change may lead to some other organizational constraints such as an increase of tbe time needed, monotony, and repetitiveness of the technical actions involved. The authors underline that the knowledge of the impact of the new technology on health helps a better understanding of the resistance to the change and its further amelioration.     

A preliminary investigation on the use of organic ionic liquids as green solvents for acylation and oxidation reactions

Different organic ionic liquids (OILs) have been used as green solvents in Friedel–Crafts acylation and alcohol oxidation reactions. Specifically, three OILs were employed, 1-ethyl-3-methylimidazolium chloride, tetraethylammonium bromide, and 1-butyl-3-methylimidazolium chloride, and four reactions studied, acylation of toluene by acetyl chloride, acylation of benzene by propionyl chloride, oxidation of benzyl alcohol by N-methylmorpholine N-oxide, and oxidation of salicylic alcohol by o-iodoxybenzoic acid. The reactions were carried out, at room temperature, in a well-stirred lab-scale glass batch reactor, under inert atmosphere and for reaction times ranging from 5 to 90 min. Gas chromatography was employed to characterize the reaction products. First of all, the desired products yield as a function of the reaction time was investigated. Moreover, simple kinetic models were built for the interpretation of the experimental results. Additional tests were carried out to assess the possibility of recycling the OILs employed. The results of this preliminary study were satisfactory as the OILs investigated proved to be good media in which to carry out the reactions studied in this work (desired products yield greater than 90% were achieved). Moreover, the reaction rate expressions of the kinetic models were able to satisfactorily predict the experimental results. Finally, the possibility of recycling the OIL (in one of the reactions) was proved to be feasible and this suggests the use of recycled OIL together with a fresh make-up, to match high yield values with economical/ecological advantages.     

Distribution of volatile organohalogen compounds in petrochemical plant water streams

The study assesses halogenated volatile organic compound concentrations in the water and wastewater streams of a petrochemical plant. Water samples were collected at 11 sampling points during 5 sampling campaigns. The samples were collected from the oil dewaxing unit and in the wastewater treatment plant. Dichloromethane and 1,2-dichloroethane were the most frequently determined compounds. Tetrachloroethene was also detected at the wastewater treatment plant inlets. The concentrations of halogenated volatile organic compounds dropped significantly at wastewater discharge points compared to wastewater treatment plant inlets. The application of 1,2-dichloroethane/dichloromethane ratio as a tool to assess evaporation processes is discussed.     

Using slow-release permanganate candles to remove TCE from a low permeable aquifer at a former landfill

Past disposal of industrial solvents into unregulated landfills is a significant source of groundwater contamination. In 2009, we began investigating a former unregulated landfill with known trichloroethene (TCE) contamination. Our objective was to pinpoint the location of the plume and treat the TCE using in situ chemical oxidation (ISCO). We accomplished this by using electrical resistivity imaging (ERI) to survey the landfill and map the subsurface lithology. We then used the ERI survey maps to guide direct push groundwater sampling. A TCE plume (100-600 μg L⁻¹) was identified in a low permeable silty-clay aquifer (K_h = 0.5 m d⁻¹) that was within 6 m of ground surface. To treat the TCE, we manufactured slow-release potassium permanganate candles (SRPCs) that were 91.4 cm long and either 5.1 cm or 7.6 cm in dia. For comparison, we inserted equal masses of SRPCs (7.6-cm versus 5.1-cm dia) into the low permeable aquifer in staggered rows that intersected the TCE plume. The 5.1-cm dia candles were inserted using direct push rods while the 7.6-cm SRPCs were placed in 10 permanent wells. Pneumatic circulators that emitted small air bubbles were placed below the 7.6-cm SRPCs in the second year. Results 15 months after installation showed significant TCE reductions in the 7.6-cm candle treatment zone (67-85%) and between 10% and 66% decrease in wells impacted by the direct push candles. These results support using slow-release permanganate candles as a means of treating chlorinated solvents in low permeable aquifers.     

Investigation of the Organic Solvent Resistance Mechanisms in Rhodococcus and Lysinibacillus Using Several Molecular Forensic Tools

Rhodococcus erythropolis IBB_Po5 (KM405337) and Lysinibacillus xylanilyticus IBB_Po7 (KM405338) showed good tolerance to 5% (v/v) organic solvents (alkanes, aromatics). However, 5% (v/v) alkanes (i.e., cyclohexane, n-hexane, n-decane) were less toxic for R. erythropolis IBB_Po5 and L. xylanilyticus IBB_Po7 cells, compared with 5% (v/v) aromatics (i.e., toluene, o-xylene, ethylbenzene). The high organic solvent tolerance of these two Gram-positive bacteria could be due to the presence in their genome of some catabolic (alkB1, todM, xylM) and trehalose-6-phosphate synthase (otsA1) genes. R. erythropolis IBB_Po5 possesses three catabolic genes (i.e., alkB1, todM, xylM), while L. xylanilyticus IBB_Po7 possesses only one catabolic gene (i.e., alkB1). Numerous adaptations involved in organic solvents tolerance were depicted in R. erythropolis IBB_Po5 and L. xylanilyticus IBB_Po7 cells exposed to 5% (v/v) alkanes and aromatics (i.e., changes in the cell growth rate, membrane permeability, cell morphology, biosurfactant emulsification index, carotenoids profile, DNA fingerprinting). Therefore, microbiological, biochemical, and DNA fingerprinting studies of the bacteria isolated from polluted environments could provide valuable information that may complement or supplement other forensic investigations.     

Formation of multiple trimethylsilyl derivatives in the derivatization of 17α-ethinylestradiol with BSTFA or MSTFA followed by gas chromatography-mass spectrometry determination

N,O-bis(trimethylsily)trifluoroacetamide (BSTFA) and N-methyl-N(trimethylsily) trifluoroacetamide (MSTFA) are common derivatization reagents used in the GC-MS analysis of estrogen steroids such as estrone (E1) and 17(-ethinylestradiol (EE2). In this study, three trimethylsilyl (TMS) steroid derivatives, mono-and di-trimethylsilyl EE2 and mono-trimethylsilyl E1, were observed during the derivatization of EE2 with BSTFA or MSTFA and/or GC separation. Factors influencing the production of multiple TMS derivatives and their relative abundance were examined. It was found that both methanol and bisphenol A competed with estrogenic esteroids when reacting with silylation reagents, and thus affected the formation of TMS derivatives and their relative abundance in the derivatization products. Methanol was found to be more reactive than bisphenol A with the BSTFA reagent. None of the three solvents tested in this study could prevent the generation of multiple TMS derivatives during the derivatization of EE2 with BSTFA, followed by GC analysis. A similar result was observed using MSTFA as the derivative reagent followed by GC analysis. Thus, the suitability of BSTFA or MSTFA as the derivatization reagent for the determination of E1 and EE2 by GC-MS, under the conditions reported here, is questionable. This problem can be solved by adding trimethylsilylimidaz (TMSI) in the BSTFA reagent as recommended, and the performance of the method has been proved in this study.