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The thermodynamic functions of NO removal by low carbon hydrocarbons such as methane, ethane, ethene, ethine, propane and propene are calculated,and enthalpy changes of reaction producing activated particles from low carbon hydrocarbons in electric field are calculated to find out the appropriate low carbon hydrocarbons for removing NO.

通过计算甲烷、乙烷、乙烯、乙炔、丙烷和丙烯等低碳烃与NO反应的热力学函数和低碳烃在电场作用下产生活性粒子的反应焓变,找出合适的低碳烃作为脱除NO的添加剂。

The process of adding hydrogen gas in fuel gas of ethylidene chloride pyrolyzer and its effects were introduced.

介绍了在二氯乙烷裂解炉燃料气中添加氢气的工艺过程和效果。

The construction in the future: 6 produce 10000 tons of HFC-152a, the substitute of ODS and 4000 tons of HCFC-142b a year; 7 produce 7000 tons of HCFC-123 and 3000 tons of-113a; 8 build PEVE rosin production with annual output of 5000 tons; 9 produce 3000 tons of PVDF a year; 10 produce 2000 tons of fluorobenzene and 1000 tons of dichlor fluorbenzene a year; and 11 fluoride salt combine device with annual output of 3000 tons.

远期建设:6、ODS替代品HFC-152a年产1万吨联产HCFC-142b4000吨;7、年产HCFC-123产品7000吨、联产二氯三氟乙烷-113a产品3000吨;8、年产PEVE树脂5000吨生产线;9、年产3000吨PVDF氟碳涂料树脂;10、年产2000吨氟苯,二氯氟苯1000吨;11、年产3000吨氟化盐联产装置。

The thermal behaviors of CL-20 mixed with three binders (NC+NC, PET and PBT at 160-200℃ were investigated by NBK LAWA gasometric measuring system. The thermal behaviors were described from the changes of evolved gases and decomposition kinetics. Results show that the apparent activation energies of CL-20 and its mixed systems with, PET and PBT are 176.68, 176.31, 136.12 and 127.0 kJmol^(-1), respectively.

用NBK型&拉瓦&量气测试系统研究了较高温度(160~200℃)下六硝基六氮杂异伍兹烷(CL-20)与硝化棉和硝化甘油双基吸收药、环氧乙烷与四氢呋喃共聚醚、3,3-双叠氮甲基氧杂环丁烷与四氢呋喃共聚物三种黏合剂的全分解过程,从放气规律和动力学的变化阐述了CL-20及其与三种黏合剂混合体系的热行为。

Both star copolymer precursors are hydrolyzed in the acidic conditions, then the corresponding recovered star copolymers of EO and glycidol with multi pending hydroxylmethyls are esterified with 2-bromoisobutyryl bromide to produce the ATRP macroinitiators with multi pending bromoisobutyryl groups . Then the latters initiate the polymerization of styrene to form the corresponding amphiphilic three- and four-arm star PEO-g-PS.

在阴离子共聚EPEE单体和环氧乙烷单体的过程中,通过变换引发剂体系中的醇的结构(由原来的二元醇变成多元醇,如三羟甲基丙烷和季戊四醇),合成了星形结构的共聚物,通过水解反应脱去保护基团后,再与2-溴异丁酰溴反应,得到链的侧端挂有很多2-溴异丁酸酯基的星形大分子引发剂,通过ATRP聚合机理引发苯乙烯聚合得到PEO为主链,PS为侧链的星形一接枝共聚物。

For example, solvent polarity strength, on activato colors surfacesf fat…etc, such as adsorption octadecylarnine ingredients solutions of the order is: ethlene-methylbenzenesulfonic? heptoxide? mixtrue.

例如,溶剂的极性不弱度不不不不差别,不不不不不差活性剂颜料暗不天的吸附也有所不不不不差别,如不一八烷基胺在各组份溶剂洋吸附度的挨次是:甲苯﹥二氯乙烷﹥搀和溶剂。

Amino-6-nitrobenzodifuroxan was prepared through a three-step reaction from starting material 3, 5-dinitrobenzoic acid:(1)3, 5-dinitroaniline (1) was synthesized from the reaction of DNBA and hydrazoic acid in inert solvent 1, 2-dichioroethane through Schmidt rearrangement with yield of 89.6%;(2) 1 was subjected to nitration to prepare pentanitroaniline (2) with yield of 51.1%;(3) The title compound was prepared from 2 and sodium azide in acetic acid through denitrogenation and then Schmidt rearrangement with yield of 86.8%, m.p.204℃~206℃.

以3,5-二硝基苯甲酸为原料经过3步反应合成了7-氨基6-硝基苯并二氧化吠咱:第1步反应,在二氯乙烷惰性溶剂中,DNBA与叠氮酸反应并发生Schmidt重排反应生成3,5-二硝基苯胺(1),产率89.6%;第2步反应,1在含100%硫酸的硝硫混酸中硝化生成五硝基苯胺(2),产率51.1%;第3步反应,2与叠氮酸反应,不经分离直接进行热解脱氮、Schmidt重排反应,得到目标化合物, m.p.204℃~ 206℃,产率86.8%。

The iodination of fluorinated ylide-anions using element iodine or 1,2-diiodoethane wassuccessfully underwent and a series of of perfluoroalkylated α-iodo-α,β-unbsaturated nitriles were prepared.

成功地进行了含氟叶立德阴离子的碘化反应,通过用不同的碘化试剂即单质碘或〓, 2-二碘乙烷制备了一系列全氟烷基化的α—碘代—α,β-不饱和腈。

Ionization was accomplished by using iodoethane and γ-propane sultone respectively.

通过碘乙烷和v-丙磺酸内酯对上述样品进行季铵化,合成了阳离子型及双离子型离聚物。

The influence of different modifier contents,n∶n,reaction temperature and reaction time on aliphatic aqueous dispersion of blocked polyisocyanate were discussed while using methyl ethyl ketoxime as blocker and monohydroxyl poly as hydrophilic modifier.

以甲乙酮肟为封闭剂,以单羟基聚环氧乙烷为亲水改性剂,分别考察了不同改性剂用量、n∶n、反应温度、反应时间对脂肪族水分散封闭型多异氰酸酯合成的影响。

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