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Gas Phase Thermal cis-trans Isomerization Reaction of 1-Bromopropene

机译:1-溴丙烯的气相热反式异构化反应

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The kinetics of thermnal cis-trans isomerization reaction of 1-bromopropene(1-BP) was studied at temperatures from 620.8 to 753.15 K over the pressure range 0.17-50.3 Torr. Both the inhibition effect by cyclohexene or propene and the catalytic effect by HBr showed a radical process as the main mechanism of the isomerization. In the suppression of the radical process by the inhibitors, the molecular process also contributed to overall reaction rate. The reactions demonstrated the first order kinetics under both uninhibited and inhibited conditions and could be represented by the expressions (R = 1.987 cal/mol/K) kun/s-1 = (3.45【1.50)】1011exp[(- 48100【 2000)/RT] kinhs-1 = (2.98【1.40)】1012exp[(- 55800【 1800)/RT] where kun is the observed rate constant of cis-1-bromopropene(1-BPc) to trans-1-bromopropene(1-BPt) under uninhibited condition at initial pressure of 50 Torr and kinh is the rate constant under maximal inhibition by cyclohexene. The ratio of rate constants for bromine atom elimination from the allylic hydrogen of reactant(1-BP) and from the inhibitors, propene and cyclohexene, were measured from the observed rates of the uninhibited and inhibited reactions. The inhibition efficiencies of cyclohexene and propene were compared kinetically from the rate constants and shown to give good agreement with the previous results reported from other alkyl bromide pyrolyses.
机译:在620.8至753.15 K的温度和0.17-50.3 Torr的温度下研究了1-溴丙烯(1-BP)的热顺式异构化反应动力学。环己烯或丙烯的抑制作用和HBr的催化作用均显示出自由基过程是异构化的主要机理。在通过抑制剂抑制自由基过程中,分子过程也有助于整体反应速率。该反应在未抑制和抑制条件下均表现出一级动力学,并且可以由以下表达式表示:(R = 1.987 cal / mol / K)kun / s-1 =(3.45【1.50)】1011exp [(-48100【2000) / RT] kinhs-1 =(2.98【1.40)】1012exp [(-55800【1800)/ RT]其中kun是顺式-1-溴丙烯(1-BPc)与反式-1-溴丙烯(1 -BPt)在50 Torr和kinh的初始压力下不受抑制的条件下,是最大受环己烯抑制的速率常数。根据观察到的未抑制和抑制反应的速率,测量了从反应物(1-BP)的烯丙基氢以及抑制剂,丙烯和环己烯中除去溴原子的速率常数的比率。从速率常数上动力学比较了环己烯和丙烯的抑制效率,显示出与其他烷基溴热解所报道的先前结果非常吻合。

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