条件反应

Effects on the reaction of factors such as reactant ratio, reaction time, and reaction temperature were investigated, and optimum reaction conditions were determined as follows: mole ratio of cyanuric chloride to ethylamine to sodium hydroxide to sodium methyl mercaptide was 1:2.1:2.0:1.7, and the temperature and time of the first, second, and third substitution reactions were -2, 0, and 82℃ and 30, 60, and 180 min, respectively.

讨论了原料配比、反应时间和反应温度等因素对反应的影响，获得了较佳的反应条件。较佳反应条件为三聚氯氰：乙胺：氢氧化钠：甲硫醇钠＝l：2.1：2.0：1.7，第一、第二、第三取代反应的反应温度和反应时间分别为-2℃、0℃、82℃和30、60、180min。

For Texaco water gas,the methanol synthesis is based on formyl route under high concentration of CO(15%-16% in volume).

认为合成甲醇在相同的工艺操作条件下，由于反应气体成分的不同，造成了反应途径的区别，即焦炉气制甲醇在高CO2的条件下(体积分数6%～9%)，甲醇合成反应主要是以甲酰基途径合成；徳士古水煤气制甲醇在高CO条件下(体积分数15%～16%)，甲醇合成反应主要是以甲酸基途径合成。

By use of the Fischer-Tropsch reaction in a C-H-O system, we discussed the relationships between inorganic CO〓 and some physical chemistry conditions, such as Oxygen flee degree , temperature, pressure, other objects consistency and catalyzer. a when T=200K～2000K, if f〓＞0, the reaction of generating CO〓 will be dominant, CH〓 hardily exists; b when T＞1000K, CH〓 is not propitious to exist, carbon in system almost exists in form of CO〓; c the more pressure, the more CO〓 is propitious to exist; d the more consistency of CO, O〓 and H〓O, the more CO〓 is propitious to exist, the more consistency of H〓, the more CH〓 is propitious to exist.

依据C-H-O体系费托反应的简化模型，讨论了氧逸度、温度、压强、其它物质浓度、催化剂等物理化学条件对无机成因CO〓生成的影响，从理论上讨论了在地质环境中，无机成因CO〓存在的物理化学条件：1在T＝200K～2000K的温度范围内，体系中一旦氧逸度＞0，生成CO〓的反应将占绝对优势，CH〓几乎不可能存在；2T＞1000K时，不利于CH〓形成，使体系中的碳主要以CO〓的形式存在；3体系压强越大，越有利于CO〓的形成；4反应物CO、O〓、H〓O的浓度越高，越有利与CO〓的存在，H〓的浓度高有利于CH〓的形成。5地质成藏作用可以经历很长的地质年代，这足以补偿矿物岩石中的Ni、Mo、Fe、Co、Ru等催化性能的降低及其它动力学条件的不足，使得费托反应可能发生，从而生成无机成因的CO〓和烃类。

Results show that 4-oxo-β-ionone is the major product with yield of 53.5% under the conditions as follows: reaction temperature 45℃, reaction time 24 h, the molar ratio of n: n(NaClO3): n 20: 100: 3, and pH value of solution in 1-3; on the other hand, 5,6-epoxy-β-ionone is major product with yield of 25.4% when reaction temperature is 40℃, reaction time is 24 h, the molar ratio of n: n(NaClO3): n is 20: 120: 5, and pH values of solution is 3. The excessive β-ionone can be recovered by vacuum distillation for reusing again. 4-oxo-β-ionone and 5,6-epoxy-3-ionone were purified by recrystallization and silica gel column chromatograph respectively with the purity over 98%.

研究结果表明：氯酸钠氧化β-紫罗兰酮的反应主要生成4-氧代－β-紫罗兰酮和5，6-环氧－β-紫罗兰酮，经重结晶和硅胶柱层析分离，纯度高于98%；4-氧代－β-紫罗兰酮的有利合成条件是反应温度为45℃，反应时间为24h，溶液的pH值为1~3，反应物配比n：n(NaClO3)：n为20：100：3，最佳收率为53.5%；5，6-环氧－β-紫罗兰酮有利的合成条件是反应温度为40℃，反应时间为24h，溶液的pH值为3，反应物配比n：n(NaClO3)：n为20：120：5，其收率为25.4%；未反应的β-紫罗兰酮经减压蒸馏回收后可重复使用。

In this research, the activities of CWDE were measured by saccharifying according to the theory that red-brown amino compounds were produced when 3, 5-dinitro salicylic acid and aldehyde were heated together. And the testing conditions were made clear. The activity of Cx should be tested with optimal temperature of 50℃, optimal pH of 4.8, incubation time of 30 min, and optimal substrate of 0.6% CMC-Na. Due to the heat-libality, Cx should be sterilized more than 10 min. The testing conditions of the activity ofβ-G were almost the same with Cx except the substrate of 0.5% salicin and the sterilization time of more than 15 min.

主要取得了一下成果：(1)明确了条锈菌细胞壁降解酶活性测定的条件：羧甲基纤维素酶活性的测定条件为50℃，pH4.8，反应时间30min，底物浓度为0.6%羧甲基纤维素钠，以DNS法测定，且失活酶液的灭活时间应大于10min；β-葡萄糖苷酶活性的测定条件为：50℃，pH4.8，反应时间30min，底物浓度为0.5%水杨苷，以DNS法测定，且失活酶液的灭活时间应大于15min；果胶酶活性的测定条件为：50℃，pH4.8，反应时间1h，底物浓度为0.25%果胶，以DNS法测定，且失活酶液的灭活时间应大于10min。

The test results showed that under low ambient temperature and aphotic storage conditions jet fuel exhibited good color stability.Oxidation reactions,such as photo-catalyzed oxidation and radical oxidation,were the main reaction mechanism of color degradation,and copper played an important role in catalyzing the oxidation reactions.Under static thermal stability testing condi...

试验结果表明，喷气燃料在较低温度、无光储存条件下具有很好的颜色安定性；氧化反应是导致喷气燃料颜色变深的主要反应机理；静态热安定性试验条件下，喷气燃料的颜色随氧化时间呈相对稳定的加深趋势；氧化铝吸附脱除了喷气燃料中的一些原有氧化抑制剂，使喷气燃料在较高温度、有氧条件下易于发生氧化反应；铜在喷气燃料氧化变色反应过程中具有明显的催化作用。

To improve the selectivity, the Co/Mn/Br catalyst system with ethanal as an additive was studied and the reaction conditions were also optimized, which were as follows:the amount of ethanal 10%(mole ration base on the substrate), reaction temperature 100℃,reaction time 30min,the oxygen pressure 0.2MPa, the amount of the composite catalyst Co/Mn/Br 7%,the mass ration of different ingredients 2:2:1. Under these conditions, the yield comes to 24.10% and the selectivity reaches 75.03%.

为了提高反应的选择性，论文初步研究了以乙醛作为添加剂条件下各工艺参数的影响，并进行正交优化，得出最佳条件为：乙醛加入量1：10，反应温度100℃，反应时间30min，氧气压力0.2MPa， Co/Mn/Br混合催化剂加入量7%，质量比2：2：1，在此条件下，反应产率为24.10%，选择性可达75.03%。

Study result suggest: The change of stock in RFCCU directly affect gasoline content. Gasoline content can be reduced through increasing the equilibrium activity of catalyst, controlling reaction level, increasing recirculating rate of gasoline and stability of gasoline level. Conclusions drawn from experiment is that optimization of operating condition has great effect on lowering olefine content of gasoline which can be reduced from 60% to 50%.Reducing reaction temperature is useful for lowering olefine content of gasoline, when the reaction temperature is raised, thermal cracking rate is higher than catalytic cracking rate, so that olefine content is increased. Raising catalyst-to-oil ratio is good for lowering olefine content. With conversion rate increased, the yield of LPG and coke is raised, the yield of gasoline is increased firstly and then decreased slightly, hydrogen transfer index is increased, so the olefine content is decreased.

研究结果表明：催化裂化装置的原料的变化直接影响到催化汽油的烯烃含量；可以通过优化催化装置的操作条件来降低催化汽油中的烯烃含量，其中通过提高催化剂平衡活性、控制反应深度、增加汽油回炼量、汽油深度稳定可以降低催化汽油烯烃含量，优化工艺条件对降低催化汽油烯烃含量有较大作用，汽油烯烃含量由60％降至50％左右；降低反应温度有利于降低催化汽油的烯烃含量，当反应温度的提高，热裂化反应速度提高的幅度大于催化裂化反应速度提高的幅度，汽油烯烃含量增加；剂油比的提高有利于降低催化汽油的烯烃含量，转化率提高，液化气产率提高，汽油收率先增加后略有下降，焦炭产率增加，氢转移反应指数提高，汽油烯烃含量下降；反应时间对产品分布及汽油烯烃含量有影响，增加提升管反应时间，液化汽、汽油产率提高，干气和焦炭产率增加。

To the product yield is mainly studied in the brominating process, and the best synthesizing process conditions is obtained; the effect of the selection, quantity of the solvent, the reaction temperature, reaction time, and the catalyzer to the product yield is researched in the process of ketalization and the relative preferable process conditions has been got.

在脱溴反应中，主要研究了溶剂的用量、溶剂配比、物料配比、反应时间和反应温度等对目标产物得率的影响；在选择性溴化反应中，主要研究了溶剂和溴化剂的选择、物料配比、溶剂的用量等参数对产物质量和得率的影响，最终得到了合成的最佳工艺条件；在缩酮化反应中，主要研究了溶剂的选择、溶剂的用量、反应温度、反应时间和催化剂的选择等参数对产物得率的影响，并得到合成的较佳工艺条件。

The effect of reaction temperature,reaction time,materials ratio on the synthesis of piperidine alcohol benzoate ,hindered amine light stabilizer,from piperidine alcohol and benzoyl chloride by direct condensation were studied,and the proper technological conditions were given as follows:the reaction temperature is 95℃;reaction time is 4 h; the mole ratio of reactants,n∶n is 1∶1.4,the amounts of solvent is 40 mL(based 0.1mol piperidine alcohol),the arerage yield ...

王树清，高崇，苯甲酸哌啶醇酯HALS的合成工艺研究研究了以苯甲酰氯和哌啶醇为原料直接缩合合成苯甲酸哌啶醇酯受阻胺光稳定剂时反应温度、反应时间、原料配比等条件对合成反应的影响，确定了最佳工艺条件。最适宜的工艺条件是：反应温度95℃、反应时间6h、原料摩尔比n∶n为1∶1.4，溶剂用量为70mL(相对于0.1mol哌啶醇)，苯甲酸哌啶醇酯的收率为91.05%，产品纯度98.5%。

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如果你不幸失恋了，请告诉我，我会帮助你摆脱困境，真的，请联系我啦！

China's plan to cut energy intensity by 20 percent and pollutant discharges by 10 percent between 2006 and 2010 is a case in point.

中国计划在2006年到2010间降低20%的能源强度和减少10%的主要污染物排放，就是一个这样的例子。