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41.
Akihiko Sakurai Mina Masuda Mikio Sakakibara 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2003,78(9):952-958
The removal of phenol by peroxidase‐catalysed polymerization was examined using Coprinus cinereus peroxidase in the presence of surfactants. The non‐ionic surfactants with poly(oxyethene) residues, Triton X‐100, Triton X‐405 and Tween 20, enhanced the phenol removal efficiency at a level similar to high relative molecular mass poly(ethylene glycol) (relative molecular mass 3000). Although the improvement in the removal efficiency was less than that of Triton X‐100, Span 20, sodium lauryl sulfate (SDS) and lauryl trimethylammonium bromide (DTAB) also enhanced the removal efficiency. The requirement of the enzyme for almost 100% removal of 100 mg dm?3 phenol decreased to one‐fourth by the addition of 30 mg dm?3 Triton X‐100. Triton X‐100, Triton X‐405, Tween 20 and DTAB could reactivate the enzyme precipitated with the phenol polymer, leading to the restarting of the phenol removal reaction. Copyright © 2003 Society of Chemical Industry 相似文献
42.
The catalytic activity of fresh Pd and Pt catalysts supported on γ-alumina in the complete oxidation of CH4 traces under lean-burn conditions was studied in the presence or the absence of water or H2S. Steam-aged catalysts were also studied in order to simulate long-term ageing in real lean-burn natural gas fuelled vehicles (NGVs) exhaust conditions. Without water or H2S added to the feed, Pd catalysts exhibit a superior catalytic activity in methane oxidation compared to Pt ones, whatever the catalysts were fresh or aged. The addition of 10 vol.% water vapour to the feed strongly affects the activity of the fresh Pd catalyst, thus being only slightly more efficient than the fresh Pt one. H2S has a strong poisoning effect on the catalytic activity of Pd catalysts, while Pt catalysts are more resistant. The fresh H2S-poisoned Pd/Al2O3 catalyst was studied by TPD in O2/He. Poisoning species decompose above 873 K as SO2 and O2 in relative concentrations consistent with the decomposition of surface sulphate species. However, a treatment in O2/He at temperatures as high as 923 K does not allow the complete regeneration of the catalytic activity of H2S-poisoned Pd/Al2O3. A mechanism involving the poisoning of PdO by sulphate species is proposed. Different diffusion processes by which these sulphate species can migrate back and forth between PdO and the support, depending on the experimental conditions, are suggested. 相似文献
43.
ABSTRACT: The absorbance of 2,2-diphenyl-1-picrylhydrazyl (DPPH) at 517 nm in methanol and acetone decreased by 20 and 35% for 120 min at 25 °C under light, respectively; in the dark it did not change significantly for 150 min. Decomposition of DPPH under 21% oxygen after 90 min under light was significantly higher than that under 1% oxygen. Absorbance of DPPH in pH 4 buffer solution in methanol, and in pH 10 buffer solution in acetone, decreased by 55 and 80%, respectively, under light for 120 min. The evaluation of antioxidant activity by the changes of DPPH absorbance should be carefully interpreted since the absorbance of DPPH at 517 nm is decreased by light, oxygen, pH, and type of solvent in addition to the antioxidant. 相似文献
44.
织物-树脂复合材料层压板的准静态侵彻机理 总被引:4,自引:1,他引:3
本文利用MTS得到了芳纶和高强维纶织物复合材料层压板受尖头侵彻体穿孔的准静态侵彻曲线 ,比较和分析了不同类型纤维集合体与热固性树脂和热塑性树脂复合材料的破坏模式 ,并考察了芳纶织物复合材料层压板侵彻的逐步破坏过程 ,揭示了复合材料层压板的准静态侵彻机理。 相似文献
45.
模拟计算表明:采用活性趋于表层的分布,可以较明显地提高国产中温变换催化剂的内表面利用率,有效地节省催化剂用量,而对“热点”温度没有多大影响。 相似文献
46.
47.
《西安建筑科技大学学报(自然科学版)》1994,(4)
论述复合脱氧剂的一般化学特性,并以碳化硅和硅铝铁两种复合脱氧剂为例,讨论其对改善钢的质量,进行纯净钢生产的影响。 相似文献
48.
单元系T—p相图的数学结构 总被引:1,自引:0,他引:1
作者以化学元素的稳定单质为基准,推演出了任意物质M_i(相态Ω)的热力学生成活度{相态Ω)的函数形式:?D_Ω数值的大小体现着相态Ω的热力学相对稳定性.根据集合论原理沿D(稳定性)座标取极大值的方法把物理性质互不连续的各个异相态连结在一起,建立了单元系在T-p面上的优势分布方程(PSDE):■作者以H_2O为实例,计算了T-p相图,与实验相图基本一致. 相似文献
49.
钨铜合金药型罩及其性能 总被引:3,自引:0,他引:3
钨铜合金药型罩的应用可以提高射流对均质钢靶的侵彻能力.这一提高得益于射流密度的提高以及断裂时间的延长. 本文对钨铜合金射流及其断裂形态通过X光照像进行了研究.它的旋转效应及其炸高特性也进行了实验研究. 钨铜合金药型罩的威力实验在φ30 mm的破甲弹上进行.在相同装药条件下与紫铜罩相比,威力提高20~30%. 相似文献
50.
Y. C. Wu Darning Feng W. F. Koch 《Journal of research of the National Institute of Standards and Technology》1991,96(6):757-762
Ionic interactions in the two systems NaCl-HEPES (N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid) and NaCl-MOPSO (3-(N-Morpholino)-2-hydroxypropanesulfonic acid) have been studied in terms of their mutual influence on the respective activity coefficients of each component. Activity coefficients for each component of the two systems and for corresponding buffers are calculated from emf measurements of solutions containing NaCl, the aminosulfonic acid, and its conjugate base in a NalSE/solution/AgCl-Ag cell at 5, 15, 25, and 37 °C. 相似文献