118 resultados para AK6-435
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A review based on 94 cited original papers describes recent achievements in application of different electrochemical detection in flow analysis, injection techniques of flow analysis, liquid chromatography and capillary electrophoresis.
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采用特异性引物 ,以菲、芘降解菌株ZL5的代谢性质粒为模板 ,扩增出邻苯二酚 2 ,3-双加氧酶 (C2 3O)基因 .将该基因和表达载体pET - 30a(+)连接 ,转化E .coliJM10 9(DE3) ,获得了高效表达的转化子 .SDS -PAGE结果表明 ,转化子的C2 3O蛋白不仅在细胞内存在 ,而且能被分泌到胞外 ,薄层扫描显示 ,转化子细胞内和细胞外表达蛋白总量占细胞总蛋白的 4 2 % .酶活分析表明 ,分布在转化子细胞内、外的表达蛋白都具有较高的C2 3O比活力 .Southern杂交将菌株ZL5的C2 3O基因定位在内生质粒的不同酶切片段上 .图 5表 1参 12
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通过模拟试验研究了鸡粪和奶牛粪肥堆腐过程中有机酸的种类、含量和变化规律。结果表明 ,鸡粪腐熟过程中会形成和累积大量的有机酸 ,在堆腐的第 5周 ,最高含量可达 88 2cmol/kg ,DW ;不挥发性有机酸在堆腐的第 3周和第 5周分别达到两个高峰 ,挥发性有机酸在第 6周和第 9周分别达到高峰 ,到第 9周后 ,鸡粪中的有机酸大大降低。鸡粪中除了存在大量的芳香酸如苯二酸及其衍生物外 ,在堆腐的过程中还有大量的丁二酸及其衍生物等多元脂肪酸生成。奶牛粪肥的有机酸以不挥发性有机酸为主 ,总酸量最高可达 2 9 38cmol/kg ,DW ;奶牛粪肥中的不挥发有机酸主要是苯二羧酸的衍生物和长链脂肪酸。堆腐过程中有机酸的种类和数量变化较大。堆腐的第 6周 ,产生了多种激素类物质
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全球大气CO2浓度升高对土壤微生物生态系统的影响已引起广泛关注。本文从土壤微生物群落结构、微生物区系、土壤呼吸、微生物生物量以及土壤酶活性方面对大气高浓度CO2的响应进行了综述。由于提供高浓度CO2的实验系统、所选植物材料以及土壤特性等的不同,大气CO2浓度升高对土壤微生物群落结构、微生物区系、土壤呼吸、微生物生物量以及土壤酶活性的影响并未得出一致结论。但高浓度CO2对土壤微生物生态系统的影响是存在的。
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评价了沈阳张士灌区土壤及稻田的重金属污染状况.结果表明,研究区镉污染仍很严重,样品糙米含镉量为0.435~0.855mg.kg-1,均超过国家食品卫生标准,该浓度与20年前相比有上升的趋势,增加了335%~755%.回归分析表明,土壤的pH值与糙米含镉量呈显著负相关,生物有效态镉与糙米含镉量呈显著正相关.土壤pH值下降使土壤酸化,导致土壤中的镉更多地转变为生物有效态镉,占总量的22.8%~52.0%,易被作物吸收,导致水稻含镉量超标.重金属污染物随着地表径流、地下水及飘尘等移动方式发生迁移转化,使污染范围逐渐扩大.
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从不同侧面综述了当前国内外生化一体化反应器的研究进展情况,并结合在沈阳环境工程重点实验室的相关研究,提出了一体化反应器应用中存在的关键问题和主要解决途径。
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Mg-8Gd-0.6Zr-1RE (RE = La or Ce, wt.%) alloys were prepared by casting. The microstructures, age hardening behavior and mechanical properties were investigated. The results show that the addition of 1 wt.% La or Ce to a Mg-8Gd-0.6Zr alloy reduces the dendrite arm spacing and slightly improves the mechanical properties and age hardening response.
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应用高效液相色谱和电喷雾质谱技术,通过分析生、制川乌单煎及其与生、法半夏共煎液中乌头碱类生物碱的含量和转变途径,发现生半夏在与川乌共煎时对乌头类剧毒生物碱的转化表现出明显的抑制作用,而法半夏却能很好的促进乌头碱类剧毒生物碱的转化,说明川乌与半夏是否可以共用与半夏的炮制与否和炮制方法存在着密切联系。
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The crystal structure of a ternary Tm(DBM)(3)phen complex (DBM - dibenzoylmethane; phen = 1. 10-phenanthroline) and the synthesis of hybrid mesoporous material in which the complex covalently bonded to mesoporous MCM-41 are reported. Crystal data: Tm(DBM)(3)phen C59H47N2O7Tm, monoclinic P21/c, a = 19.3216(12) A, b = 10.6691(7) A, c = 23.0165(15)A, alpha = 90, beta = 91.6330(10), gamma = 90, V = 4742.8(5) A(3), Z = 4. The properties of the Tm(DBM)(3)phen complex and the corresponding hybrid mesoporous material [Tm(DBM)(3)phen-MCM-41] have been studied. The results reveal that the Tm(DBM)(3)phen complex is successfully covalently bonded to MCM-41.
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本论文对异辛酸铁(Fe)-亚磷酸二乙酯(P)-三异丁基铝/三乙基铝(Al)催化体系进行研究, 合成熔点低于130℃的间同1,2-聚丁二烯热塑性弹性体,并且发现三异丁基铝与三乙基铝比例对聚合活性有较大的影响。放大实验合成的间同1,2-聚丁二烯熔点为126℃ ,其1,2-结构含量为84%,间同度为81%;数均分子量13万,重均分子量40万,分子量分布为3.0;300%定伸应力为14.2MPa,拉伸强度20.5MPa,扯断伸长率420%,断裂强度20.4MPa,硬度为94邵尔A,热分解温度435℃,具有良好的力学性能和热稳定性。
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Ce and MgO were added simultaneously to La-Sr-Ni-O catalyst and a substantial enhancement of activity for NO decomposition was observed, which may be attributed to the formation of a new highly active site caused by the addition of Ce and MgO.
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The effects of diluents, temperature, acidity, and ionic strength of the aqueous phase on the interfacial properties of DEHEHP have been extensively investigated using the Du Nouy ring method. In addition, the effect of cerium(IV) concentration loaded in the organic phase on the interfacial tension has also been studied. With the increase of DEHEHP concentration, the value of interfacial tension (gamma) decreases in the studied system, which shows that DEHEHP has interfacial activity as a kind of surfactant. The surface excess at the saturated interface (Gamma(max)) and the minimum bulk concentration of the extractant necessary to saturate the interface (C-min) under the different conditions are calculated according to two adsorption equations such as the Gibbs and Szyszkowski functions to be presented in comprehensive tables and figures. The relationship between the interfacial activity of DEHEHP and cerium(IV) extraction kinetics by DEHEHP has been discussed by considering different factors such as the effects of diluents and temperature. However, the interfacial activity parameter of extractant only is a qualitative parameter, but cannot provide strong enough evidence to quantitatively explain the relationship between extraction kinetics and interfacial properties of an extractant.