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The reaction of acetone with chlorine gas is a rapid chain reaction.

丙酮与氯气反应制取一氯丙酮,是一个快速的连锁反应。

Methods: from prepation of crude drug as start, study the technology of extract and defat with L9 (3~4) orthogonal test. With EtOH extraction and water sed, alkali washing, EtOAC extraction as main methods of eliminate dopant. Finally with alky AlzO3 chromatographic column, rich and gain anticancer active site. The maximum response was achieved at a 40 min extracting time with 10 times volume 90% EtOH added to the sample for the first time and 30 min for the second time. Adding 10 times water will produce precipitation; Place the precipitation into 6 times petroleum benzin to de-fat at 60℃.

云南红豆杉中抗癌活性物制备工艺研究方法:利用正交设计试验L9(3~4)确定原料药提取工艺为:10倍量90%乙醇提取两次,第一次40分钟,第二次30分钟;醇提液用10倍量水沉;沉淀加6倍量石油醚40℃脱脂;用1mol/L的NaOH溶液碱洗,除去酸性杂质;以碱性氧化铝柱,以环己烷/丙酮为洗脱溶剂,在环己烷-丙酮(6:4)段富集到所需活性部位,洗脱剂用量为3VB。

The objective of the present study was to investigate the effect of energy intake during the dry period on the expression of Pyruvate carboxylase and Phosphoenolpyrevate carboxykinase mRNA in the liver of periparturient diary cows.

本研究目的在於观测乾奶期不同能量摄入对围产期健康奶牛肝糖异生关键酶-丙酮酸羧化酶和磷酸烯醇式丙酮酸羧激酶基因表达的影响。

This paper details an efficient method for a one-step transformation of the trityl ether to the acetonide. Treatment of trityl ether with a mixture of trifluoroacetic acid, 2,2-dimethoxy propane and camphorsulfonic acid as catalyst in dichloromethane through detritylation followed by acetonization gave the acetonide in high yield.

介绍了一种新的高效的由三苯甲基醚直接生成丙酮化合物的方法,也就是使三氟乙酸条件下脱三苯甲基的反应和生成丙酮化合物的反应在一个反应瓶中同时进行,使脱三苯甲基作用后生成的醇继续反应得到高产率的丙酮化合物。

Chemiluminescent immunoassay is one of the advanced immunoassay ofnon-radioisotopic immunoassay because of its high sensitivity, wide dynamic range,high accuracy, stable labeled protein, full automation and extensive application field.CLIA using acridinium ester derivatives as chemiluminescent label has advantages oflow background, high signal-to-noise ratio, no need of catalyst and simpleluminescence system. Different aspects associating the DMAE·NHS-based CLIA were studied in thisthesis, including synthesis of acridinium ester, chemiluminescentcharacteristics of DMAE·NHS, labelling antibody or streptavidin with DMAE·NHS,two-site sandwich chemiluminescent immunoassay for TSH, two-sitesandwich chemiluminescent immunoassay involved biotin-streptavidinsystem for TSH, and competitive chemiluminescent immunoassay usingbiotin-streptavidin system for TT〓. The desired acridinium ester, DMAE·NHS, was synthesized according to thereference method with some modifications. The products were identified by IR, NMR,MS and elemental analysis. In our method, KOH was used in place of NaOH tosynthesize benzyl ester of 3,5-dimethyl-4-hydroxybenzoic acid,2',6'-dimethyl-4'-(n-succinimidyloxycarbonyl) phenyl-acridinium-9-carboxylate waspurified on a silica gel column with chloroform/ethylacetate(4:1, v/v) as eluent andfurther purified by triturating with hexane/acetone(2:1, v/v).

DMAE·NHS的合成是本论文的关键和难点,我们对文献方法进行改进:文献方法用氢氧化钠与3,5-二甲基-4-羟基苯甲酸反应制得3,5-二甲基-4-羟基苯甲酸钠,再用3,5-二甲基-4-羟基苯甲酸钠与苄氯作用制备3,5-二甲基-4-羟基苯甲酸苄酯,我们用氢氧化钾代替氢氧化钠,使合成取得成功;在合成2',6'-二甲基-4'-苯基-吖啶-9-甲酸酯时,文献方法对粗产品进行两次硅胶柱层析纯化,第一次柱层析用氯仿/乙酸乙酯(4∶1,V∶V)作溶剂和淋洗剂,第二次柱层析用己烷/丙酮(2∶1,V∶V)作溶剂和淋洗剂,按照文献方法得到的不是所需要的化合物,我们只进行第一次柱层析纯化,然后用己烷/丙酮(2∶1,V∶V)进行研磨,过滤,洗涤,除去溶于己烷/丙酮(2∶1,V∶V)的部分,得到所需要的产品。

For determination of pyruvic acid, we used the ferrocene as an electron transfer mediator and pyruvate oxidase as a catalyzer, and had a systemic research for the immobilization of ferrocene and enzyme on the gold electrode. At last, a pyruvic acid biosensor with good stability and activity of electrochemistry and biocatalysis was constructed. There are two aspects of contents in the paper. The first step, we had an in-depth research for the immobilization of ferrocene on the gold electrode, and fabricated a modified gold electrode by glutaric dialdehyde cross-linked egg white as the matrix of ferrocene immobilization.

本文以研制一种通过对酶催化反应引起的电化学响应进行检测,从而实现对丙酮酸浓度进行检测的方法为目的,选择了二茂铁为电子传递介体,丙酮酸氧化酶为酶催化剂,并对将上述物质固定到金电极表面从而制成一种新型的生物传感器的方法进行了系统而全面的研究,并制得了一种全新的具有良好电化学与生物催化活性和稳定性的丙酮酸生物传感器。

The results showed that (1) The grain size of nanometer YiO_2 was40~80nm.The wavelength corresponding to the maximum absorbency values were observedin the 200~320nm range.The crystal structure of carbon doped TiO_2 photocatalyst is primarilyanatase(22.43% rutile), and the content of carbon is about 4.6%.(2) The relative humidityvaring from 8% to 80%, the photocatalytic degradation degree of benzene increased withincreasing relative humidity; and to toluene, degradation rate was hanced by relative humidityup to 60%, and more or less inhibited above 60%.(3) Scheme and results of orthogonal testswere used by evaluating the photocatalytic performance of the gas phase methanol, acetoneand 1-heptane.The results revealed that their degradation degree reached 84.5%, 93.39% and93.45%, respectively.(4) The 254nm UV lamp showed higher photocatalytic degradation rate.For methanol, acetone and 1-heptane, it was found that photocatalytic degradation reactionoccurs with the light strength of daylight lamp.(5) Under the the same conditions, 15%degradation degree has been obtained for benzene, whilst about 10% degradation degree wasattained by Degussa P25; During the initial phases, the toluene revealed higher photocatalyticactivity, comparing with Degussa P25, the degradation degree of methanol, acetone and1-heptane were slightly lower.

结果表明:(1)CVD法制备的纳米TiO_2光催化剂,颗粒球形度好、粒径在40~80nm之间;最大吸光度值所对应的波长为200~320nm;含碳量约为4.6%;晶型组成主要为锐钛矿型,金红石的含量约为22.43%;(2)在相对湿度为8%~80%范围内,苯的光催化降解率随着相对湿度的增大而增大;甲苯在相对湿度为60%时达到最好降解效果,当相对湿度增大到80%时光催化效果降低;(3)将正交实验设计及实验方案应用于气相甲醇、丙酮和正庚烷光催化降解研究,实验结果表明:三者最高降解率分别为84.5%、93.39%和93.45%;(4)有254nm紫外灯参与的光催化实验可以大大提高有机气体的光催化降解率;在日光灯的照射下,掺碳纳米TiO_2对气相甲醇、丙酮和正庚烷具有一定的光催化氧化能力;(5)较P25粉,在相同的光催化操作条件下:气相苯的平均降解率达15%,高于P25粉10%的降解率;气相甲苯在初始阶段具有较高的反应速率;气相甲醇、丙酮和正庚烷的降解率略低于P25粉。

The products were identified by IR,NMR,MS and elemental analysis. In our method,K.OH was used in place of NaOH to synthesize benzyl ester of 3,5-dimethyl-4-hydroxybenzoic acid,2',6'-dimethyl-4'-(n-succinimidyloxycarbonyl) phenyl-acridinium-9-carboxylate was purified on a silica gel column with chloroform/ethylacetate(4:l,v/v) as eluent and further purified by triturating with hexane/acetone(2:l,v/v).The luminescence produced by DMAE-NHS is a flash light with maximumemission at 0.4s and decay half-time of 0.9s. The luminescence intensity is 6.11x10 cps/mol,which is affected by the composition of trigger and surfactant.

DMAE·NHS的合成是本论文的关键和难点,我们对文献方法进行改进:文献方法用氢氧化钠与3,5-二甲基-4-羟基苯甲酸反应制得3,5-甲基-4-羟基苯甲酸钠,再用3,5-二甲基-4-羟基苯甲酸钠与苄氯作用制备3,5-二甲基-4-羟基苯甲酸苄酯,我们用氢氧化钾代替氢氧化钠,使合成取得成功;在合成2',6'-二甲基-4'-苯基-吖啶-9-甲酸酯时,文献方法对粗产品进行两次硅胶柱层析纯化,第一次柱层析用氯仿/乙酸乙酯(4:1,Ⅴ:Ⅴ)作溶剂和淋洗剂,第二次柱层析用己烷/丙酮(2:1,Ⅴ:Ⅴ)作溶剂和淋洗剂,按照文献方法得到的不是所需要的化合物,我们只进行第一次柱层析纯化,然后用己烷/丙酮(2:1,Ⅴ:Ⅴ)进行研磨,过滤,洗涤,除去溶于己烷/丙酮(2:1,Ⅴ:Ⅴ)的部分,得到所需要的产品。

In order to study the aldol condensation of 2.15-hexadecanedione on the surface of aluminium, the intermolecular condensation mechanism of acetone occurring on aluminum was simulated by using semi-empirical AM1 method embodied in MOPAC 6.0 program package. The optimized structures and geometry parameters of 5 transition complexes and 4 intermediates were given.First, 2 molecules of acetone coordinated with aluminum by electrostatic attraction.One atom of hydrogen of acetone migrated to aluminum because of t...

为了研究2,15-十六烷二酮在氧化铝表面的环合机理,选择小分子丙酮为模型化合物,用量子化学半经验AM1方法研究双分子丙酮在氧化铝表面的醛醇缩合机理,给出了反应过程中的5个过渡态和4个中间体的结构和几何参数,该催化反应可以认为是氧化铝分子与两分子丙酮分子发生静电络合作用,然后借助氧原子的负电荷导致脱氢并实现缩合,根据中间体的能量变化,推测有较稳定的铝复合物生成。

Guanine can quench the phthalhydrazidylazoacetylacetone's ECL in acid medium, and the linear concentration range of guanine relative to the ECL intensity is from 2.0×10~(-6) to 1.0×10~(-5) mol/L.The mechanism of phthalhydrazidylazoacetylacetone's ECL on the surface of ITO glass has been discussed according the experimental phenomenon.The phenomenon of ITO self-luminescence has also been studied.It has been found that the machanism of phthalhydrazidylazoacetylacetone on the surface of ITO in different medium is dissimilarity. The phenomenon of ITO self-luminescence may be caused by the interaction of the active oxygen element and ITO's surface.

鸟嘌呤在弱酸性介质中3-(1-乙酰丙酮偶氮)苯二甲酰肼的电化学发光具有显著的淬灭作用,2.0×10~(-6)~1.0×10~(-5) mol/L浓度范围内,电化学发光强度与鸟嘌呤的浓度成良好的线性关系根据相关试验现象对3-(1-乙酰丙酮偶氮)苯二甲酰肼在氧化铟锡玻璃电极上的电化学发光机理进行了初步探讨,并对氧化铟锡玻璃电极自身发光现象进行了研究,研究发现在不同酸度环境中,3-(1-乙酰丙酮偶氮)苯二甲酰肼在氧化铟锡玻璃电极上电化学发光的机理是显著不同的;ITO自身发光可能是由活性氧系分子与ITO镀膜玻璃电极表面相作用引起的。

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