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ConclusionThere is good cytotoxicity of the ethyl acetate and acetone extracts from Alocasia macrorrhiza to tumor cells, and no obvious acute toxicity has been observed. Therefore these two parts have good anti-tumor prospects.

结论醋酸乙酯和丙酮提取物有较好的细胞毒活性,没有明显的急性毒性,这两部分有较好的抗肿瘤前景。

The obvious acute toxicities were not observed for the ethyl acetate and acetone extracts of Alocasia macrorrhiza under the treatment doses of 60g·kg-1 and 36.5 g·kg-1 respectively.

海芋的丙酮和醋酸乙酯提取物分别在60 g·kg-1和36.5 g·kg-1的给药剂量下没有显示明显的急性毒性。

The group of low migration nucleases were prepared by ammonium carbonate processing +acid denaturation + thermal denaturation + acetone extraction.

在提取过程中产生两组核酸酶,在SDS-PAGE-DNA功能胶中迁移率较慢的一组采用碳酸铵处理+酸变性+热变性+丙酮沉淀的提取方法来获得较好的层析样品。

With this standard method, simultaneous quantification of DMC, MPC, DPC, phenol and anisole can be achieved accurately, which provide the standard methods for evaluation of different catalysts and control of the reaction process. The microwave-aided catalytic technique was applied in the transesterification of DMC and phenol.

分别以苯甲酸乙酯和丙酮为内标物,实现了对酯交换反应塔釜产品和塔顶馏分的同时定量,为评价催化剂活性的高低和工艺条件的优劣提供了标准化分析方法。

Methods The immobilizing conditions of neutrophil alkaline phosphatase staining were detected by the stationary liquid of 40%, 60% and 80% acetone-citric acid, and at the same time, the staining conditions were detected at 10, 15 and 20 minutes in the matrix liquid prepared respectively with 2-amino-2-methyl-1.3-propylene glycol (PH9.4-9.6) buffer, barbital (PH9.2) buffer and Tris (PH9.2) buffer.

用40%、60%、80%的丙酮-枸缘酸固定液对中性粒细胞碱性磷酸酶染色固定条件进行测定。同时用2-氨基-2-甲基-1.3-丙二醇(pH9.4-9.6)缓冲液、巴比妥(pH9.2)缓冲液、Tris(pH9.2)缓冲液配制的基质液分别在10、15、20分钟的染色条件进行测定。

The results showed that the first canonical correlation coefficient between aldehydes, ketones, esters and the total quantity of each kind of ingredient and smoking quality achieved 5 % or 1 % remarkable level. And their correlation depended mainly in the correlation between phenylacetaldehyde, furfural, megastigmatrienone-1, megastigmatrienone-3, geranylacetone,β-damascenone, keto-isophorone, dihydroactinidiolide and smoking quality.

结果表明:醛类成分、酮类成分、酯类成分与香气质、香气量的第一典型相关系数达到5%或1%显著水平,各类成分总量与香气质、香气量的第一典型相关系数达到1%极显著水平,其相关关系主要表现在苯乙醛、糠醛、巨豆三烯酮1、巨豆三烯酮3、香叶基丙酮、β-大马酮、氧化异佛尔酮、二氢猕猴桃内酯等成分与香气质、香气量的相关上。

The activity of pyruvate carboxylase depends on the presence of acetyl CoA so that more oxaloacetate os made when acetyl CoA levels rise.

丙酮酸羧化酶的活性依赖于乙酰-CoA 的存在。因此,当乙酰-CoA,水平上升时,会产生更多的草酰乙酸。

The preparing process is described as follows:(1) the raw materials are dispersed in the solvent;(2) the solution is arranged between two electrodes;(3) alternating current with a voltage of 5 V-100V and a frequency of 10Hz-1000Hz is applied to both ends of the electrodes for 5minutes to one hour;(4) the product obtained after being washed with deionized water and pump filtrated or after centrifugal treatment is dried by being heated to 40 centigrade to 100 centigrade to get the nanometer grain, wherein the raw materials in the first step are micrometer materials or nanometer materials such as sulphide, selenide, telluride and oxide; without special requirement on shape or appearance, the materials can be in the shape of a rod, a fork, a star, a block or a sphere; the solvent in the first step can be water, ethanol, acetone, benzene or tetra chloromethane.

步骤为:1将原料分散于溶剂中;2使制成的溶液处于两电极之间;3在电极两端的加交流电,电压为5V-100V,频率为10Hz-1000Hz,时间为5min-1h;将产物用去离子水洗涤、抽滤,或进行离心处理后;4将所得到产物加热到40~100℃进行干燥,得到纳米颗粒。步骤1中原料为硫化物、硒化物、碲化物、氧化物等微米或纳米材料,其形貌不限,可以为棒状、枝状、星状、块状、球形等多种形状。步骤1中的溶剂可以为水、乙醇、丙酮、苯或四氯化碳。

In the asymmetric hydrogenation of ethyl pyruvate catalyzed by 0 5% Rh/PVP TiO 2, the chiral modifier cinchonidine not only induces the enantioselectivity, but also accelerates the reaction rate greatly.

研究了辛可尼定作手性修饰剂修饰的负载型纳米铑簇合物催化剂(0 5 %Rh/PVP TiO2 )催化丙酮酸乙酯不对称氢化反应,在该反应中手性修饰剂辛可尼定不仅具有对产物生成的手性诱导作用,而且对反应具有明显加速作用;在优化反应条件后,反应的TOF和对映选择性分别可以达到 5 8 0min-1和

The condensation reaction of citral with acetone catalyzed by aqueous sodium hydroxide solution to give pseudoionone was studied in detail.

前言 丙酮和柠檬醛在氮氧比钠水溶液的催化作用「生成假性紫罗兰酮是国内外应用得较为f一泛的合成紫罗兰酮的方法。

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