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281.
通过虾夷马粪海胆胚胎暴露实验,研究了常见石油烃零号柴油对海胆胚胎发育时间以及发育时期内海胆胚胎的SOD、CAT、GPx及谷胱甘肽转移酶(GST)四种酶活性的影响。结果表明,不同浓度的零号柴油水溶组分对海胆胚胎发育的各个时期具有不同程度的延迟效应,低浓度对海胆胚胎中的四种酶表现出不同程度的诱导效应;四种酶活性的变化程度比较,对GPx和GST酶活力的影响要明显大于对CAT和SOD的影响;随着浓度的不断增大,四种酶活性受到不同程度的抑制作用,高浓度对酶活性的抑制作用尤为显著;囊胚期对影响最为敏感,可作为生物标志物。 相似文献
282.
采用零价铁(Fe0)还原降解土壤中的硝基苯,考察土壤理化性质对还原效果的影响。结果显示,当2 g土壤中NB含量约为2.5×10-6mol/g,铁粉用量为50 mg,土壤含水量为75%时,控温25℃条件下反应1 h,硝基苯在松砂土和中壤土中的还原率分别可达到82.9%和91.1%。硝基苯在2种土壤中的还原率表现出中壤土〉松砂土的规律;土壤微生物和土壤有机质含量升高有利于反应进行;粒径偏小的中壤土中硝基苯还原较彻底。NB在土壤中的老化时间对Fe0还原效果影响较小。 相似文献
283.
LnMnO3+σ (Ln0;=0;La, Pr, Nd, Sm, Eu, Gd or Dy) perovskites synthesized by sol-gel method were employed for gaseous elemental mercury (Hg0) removal from coal-fired flue gas. Characterization results revealed the structure of the perovskites presented a phase transition process from rhombohedral system to O- and O'-orthorhombic structure with the change of A-site rare earth elements. The perovskites showed satisfactory Hg0 removal capacity in a narrow temperature range of 100–150°C. NdMnO3+σ with an O-O’ orthorhombic structure presented the best Hg0 removal performance, which markedly depends on four factors: crystal structure, oxygen vacancy density, Mn4+/Mn3+ ratio and surface element segregation. The Hg0 removal mechanism was illustrated based on the mercury temperature programmed desorption experiment and X-ray photoelectron spectroscopy characterization. Both chemisorption and catalytic oxidation played a role in the Hg0 removal process. Chemisorption dominated the Hg0 removal, due to the slow catalytic oxidation rate at low temperature. This work preliminarily established the relation between the structure of rare earth manganese perovskite and Hg0 removal performance. 相似文献
284.
To assess the capacity of the natural environment for degrading plastics, the populations of poly(0mn6522p2826/xxlarge946.gif" alt="beta" align="MIDDLE" BORDER="0">-hydroxybutyrate)(PHB)-and poly(0mn6522p2826/xxlarge949.gif" alt="epsi" align="BASELINE" BORDER="0">-caprolactone)(PCL)-degrading aerobic microorganisms and their ratios to the total number of microorganisms in soil samples were estimated by the plate count method with agar medium containing emulsified PHB or PCL. The numbers of the degrading microorganisms were determined by counting colonies that formed clear zones on the plate. It was found that PHB- and PCL-degrading (depolymerizing) microorganisms are distributed over many kinds of material, including landfill leachate, compost, sewage sludge, forest soil, farm soil, paddy soil, weed field soil, roadside sand, and pond sediment. Of total colony counts, the percentages of PHB and PCL degrading microorganisms were 0.2013;11.4 and 0.8013;11.0%, respectively. The results suggest that many kinds of degrading microorganisms are present in each environment and that specific consortia differing in biodegradation capacity are constructed. 相似文献
285.
Physical properties and biodegradability of blends containing poly(ε-caprolactone) and tropical starches 总被引:1,自引:0,他引:1
Hardaning Pranamuda Yutaka Tokiwa Hideo Tanaka 《Journal of Polymers and the Environment》1996,4(1):1-7
In order to assess feasibility of tropical starches (sago and cassava starches) as biodegradable plastic materials, blending with poly(0">-caprolactone) (PCL), a biodegradable polymer, was carried out. It was confirmed that the physical properties (tensile strength and elongation) of PCL/sago and PCL/cassava blends were similar to those of PCL/corn blend, suggesting that sago and cassava starches can also be blended with PCL for production of biodegradable plastic. However, the properties of all PCL/starch blends were still low compared with those of polyethylene. Enzymatic degradability evaluation showed that lipase degradation of PCL and0">-amylase degradation of starch increased as the starch content in the blend increased. Burial test of the blends for 1, 3, and 5 months was carried out and the rate of degradation of the PCL/sago blend was confirmed to be slower than those of PCL/corn and PCL/cassava blends. Observation of the film blends structure by scanning electron microscope revealed that the starch was dispersed in a PCL continuous phase. Furthermore, changes in the film surface before and after enyzme treatments were observed. 相似文献
286.
Emo Chiellini Andrea Corti Arianna Giovannini Piero Narducci Anna M. Paparella Roberto Solaro 《Journal of Polymers and the Environment》1996,4(1):37-50
The results of an investigation aimed at evaluation of the biodegradability of blends of poly(0">-caprolactone) (PCL) with poly(ethylene terephthalate) (PET) as the major component are reported. Specimens of the blends, as melt extruded films and/or powders, were submitted to degradation tests under different environmental conditions including full-scale composting, soil burial, bench-scale accelerated aerobic degradation, and exposure to axenic cultures and esterolytic enzymes. Indications have been gained that blending in the melt gives rise to insertion of PCL segments in the PET chain. Copolymers thus attained acted as macromolecular compatibilizers, allowing for a complete miscibility of PCL and PET. The biodegradation detected on the blend samples was, however, well below the values expected from chemical composition and behavior of individual homopolymers under the same environmental conditions. The presence of PET as the major component in PET/PCL blends apparently reduces the propensity of PCL to be degraded, at least in the investigated composition range. The degradation data collected under different environmental conditions indicate that the full-scale composting system is the most efficient among the tested degradation procedures. 相似文献
287.
Rasmus Renstad Sigbritt Karlsson Åsa Sandgren Ann-Christine Albertsson 《Journal of Polymers and the Environment》1998,6(4):209-221
Melt-pressed films of polycaprolactone (PCL) and poly(lactic acid) (PLA) with processing additives, CaCO3, SiO2, and erucamide, were subjected to pure fungal cultures Aspergillus fumigatus and Penicillium simplicissimum and to composting. The PCL films showed a rapid weight loss with a minor reduction in the molecular weight after 45 days in A. fumigatus. The addition of SiO2 to PCL increased the rate of (bio)erosion in A. fumigatus and in compost. The use of a slip additive, erucamide, was shown to modify the properties of the film surface without decreasing the rate of bio(erosion). Both the rate of weight loss and the rate of molecular weight reduction of PCL increased with decreasing film thickness. The addition of CaCO3 to PLA significantly reduced the thermal degradation during processing, but it also reduced the rate of the subsequent (bio)degradation in the pure fungal cultures. PLA without additives and PLA containing SiO2 exhibited the fastest (bio)degradation, followed by PLA with CaCO3. The degradation of the PLA films was initially governed by chemical hydrolysis, followed by an acceleration of the weight change and of the molecular weight reduction. PLA film subjected to composting exhibits a rapid decrease in molecular weight, which then remains unchanged during the measurement period, probably because of crystallization. 相似文献
288.
289.
Bruce A. Ramsay Ilie Saracovan Juliana A. Ramsay Robert H. Marchessault 《Journal of Polymers and the Environment》1994,2(1):1-7
A simple method was developed for the preparation of an autoclavable, long-side-chain poly (0">-hydroxyalkanoate) (LSC-PHA) colloidal suspension, which was used as a substrate for enzymatic degradation and to prepare agar overlay plates for the isolation of microorganisms producing extracellular LSC-PHA depolymerase. Six cultures producing extracellular LSC-PHA depolymerase were isolated from a composted hydrocarbon-contaminated soil. All were pseudomonads or related bacteria. All (with the possible exception ofXanthomonas maltophilia) could produce LSC PHA. Except forX. maltophilia none could hydrolyze poly (0">-hydroxybutyrate). Screening of sevenPseudomonas strains known to accumulate LSC PHA showed that all were negative for extracellular LSC-PHA depolymerase production. It was concluded that extracellular LSC-PHA depolymerase producers are found mostly in the genusPseudomonas but that they are relatively uncommon. 相似文献
290.
Thomas M. Scherer R. Clinton Fuller Robert W. Lenz 《Journal of Polymers and the Environment》1994,2(4):263-269
The bacterial polyester, poly(00h3p1/xxlarge946.gif" alt="beta" align="MIDDLE" BORDER="0">-hydroxybutyrate-co-00h3p1/xxlarge946.gif" alt="beta" align="MIDDLE" BORDER="0">-hydroxyvalerate) (PHB/V), was cross-linked with 1, 5, 7, 10, 20, and 30 wt% benzoyl peroxide by thermal decomposition reactions. Solvent extractions were carried out to determine the cross-linked fractions of the films. The sol/gel data were used to estimate cross-link densities. Films of PHB/V cross-linked with 10% benzoyl peroxide were placed in contact with purified depolymerase A secreted byP. lemoignei. These samples exhibited weight loss rates which were half that of un-cross-linked PHB/V, but the network was degraded completely by the enzyme. The results of this study suggest that anendo-type enzymatic degradation may occur, in addition to theexo-type activity, which is normally presumed to occur with theP. lemoignei depolymerase system. 相似文献