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Premise Liquefied petroleum gas is derived from oil gas, natural gas, the gas production of refinery and petrochemicals. The main components are dimethylmethane, propylene, butane, butylene and such low class hydrocarbon. It's a gas with achromaticity and transparence; LPG is hardly dissolved in water, but dissolved in ethanol and aether, it can dissolve gas production, propagation oil and caoutchouc.

液化石油气(liquefied petroleum gas,LPG)是石油伴生气、天然气、炼油厂及石油化工厂的气体产品,经分离精制而来,其主要成分为丙烷、丙烯、丁烷、丁烯等低分子烃;无色透明,带有微弱的臭味;难溶于水,溶于乙醇和乙醚等,并能溶解石油产品,动植物油和天然橡胶。

In chapter three, the activating agents of ytterbium have been examined. Barbier-type reaction promoted by ytterbium metal was examined. The experimental results shown that the yield of Barbier reaction of imines with allylic bromide promoted by ytterbium is higher than that of aldehydes and ketones with allylic bromide under the same reaction conditions. In this chapter, the reductive cleavage of Se-Se and S-S bond induced by ytterbium metal was also studied.

首先研究了金属镱的活化剂以及活化方法,接着考察了金属镱促进的Barbier反应及其在合成高烯丙基胺和高烯丙基醇中的应用,以及影响该反应的主要因素;究了金属镱促进的二硫醚和二硒醚的S—S键和Se—Se键的还原断裂,继而与氯代烃,胺基甲酰氯反应生成相应的硫醚,硒醚,胺基甲酸硫代酯和硒代酯。

In extracts of source rocks of shahejie 1 group of Gulan low-lying abundant retene, simonellite and cadalene were detected. Their main origin should be lower organisms like algae.

在孤南洼陷沙一段烃源岩抽提物中检测到了较为丰富的惹烯、西蒙内利烯及卡达烯,其主要来源应是藻类等低等植物。

Also useful are oil-soluble copper dithiocarbamates of the general formula Rc Rd z Cu, where z is 1 or 2, and Rc and Rd are the same or different hydrocarbyl radicals containing from 1 to 18, and preferably 2 to 12, carbon atoms, and including radicals such, for example, as alkyl, alkenyl, aryl, aralkyl, alkaryl and cycloaliphatic radicals.

化学通式为Rc Rd z Cu的油溶性二硫代氨基甲酸铜也适用,式中,z为1或2,Rc和Rd是含1~18(以2~12为宜)个碳原子的相同或不同的烃基,这类烃基的实例包括烷基、烯基、芳基、芳烷基、烷芳基和脂环基。

1A series ofω-alkylmercapo acid were synthesized by two methods:one involved the reaction of the appropriateω-bromoalkyl acid with mercaptide under the presence of base;the other method was used only for the long alkyl compound by the reaction ofω-alkenyl acid and alkanethiol in the presence of AIBN.

正是基于以上考虑,本论文探索了合成下沿带有硫醚官能团,而上沿带有偶氮官能团的杯[4]芳烃衍生物的方法,进行了以下研究: 1采用ω-溴代羧酸和烃基硫醇在碱性条件下发生反应,或由ω-烯基羧酸和硫醇在AIBN的存在下反应,得到了ω-硫醚羧酸,使用氯化亚砜将羧酸转化为酰氯。

The reaction performance of Pt-Sn-Li/Al_2O3/FeCrAl catalyst was measured,and the properties of the catalyst were characterized.It was found that reaction temperature,LHSV and the molar ratio of hydrogen to alkane have greatly affected on the catalytic performance of the Pt-Sn-Li/Al_2O_3/FeCrAl catalyst.Under a set of optimal reaction conditions,at 0.1 MPa,470℃,the molar ratio of hydrogen to alkane of 4 and LHSV of 0.14 mL·m~(-2)·h~(-1),the dodecane conversion is 6%,and the dodecene selectivity is about 72%.

结果表明:工业催化剂的催化性能比至今实验室制备的γ-Al_2O_3和SBA-15颗粒负载型颗粒状催化剂的性能好;反应温度、液时空速和氢烃摩尔比对Pt-Sn-Li/Al_2O_3/FeCrAl金属基整体式催化剂脱氢性能都有重要影响,最适宜的反应条件是压力为0.1 MPa,反应温度为470℃,进料氢烃摩尔比为4和LHSV为0.14 mL·m~(-2)·h~(-1),此时十二烷的转化率约为6%,十二烯的选择性约为72%;活性组分涂层与金属基体结合良好。

It was found that the thermodynamically unfavourable isomerization of quadracyclane to norbornadiene could be accomplished in the presence of toluene or durene as a co-sensitizer.

首次发现在甲苯、杜苯等芳烃共敏化下,可以使原来不能进行的、热力学不利的四环烷→降冰片二烯异构化得以进行,并根据CIDNP结果提出这是由于生成了敏化剂/底物/芳烃三元基激络合物使反应的势能面改变造成的并促进单线态的系间窜跃。

Synthesis of organic sulfuric compounds in aqueous media is carried out by: using thio-olefin compounds with carbonyl compounds, acetal/keltone, hydrazone, oxime, osazone and enamine to synthesize mercaptal/keltone compounds in aqueous media; using thio-olefin compounds with alpha-hydroxyaldehyde/keltone or alpha-halogenated aldehyde/keltone to synthesize thia-olefin derivatives in a queous media; using thio-olefin compounds with alpha, beta-unsaturated hydroxy compounds, C-C treble bond, C-N treble bond, C-C double bond, N-N double bond, C-N double bond, C-S double bond, epoxy and its derivatives, aziridine and its derivatives, cyclopropane and its derivatives and halogenated carboxy to synthesize sulfoether compounds in a queous media.

含水介质中有机硫化合物的合成方法,本发明属于有机合成方法,用硫缩烯酮类化合物与羰基化合物、缩醛/酮、腙、肟、脎、烯胺在含水介质中合成缩硫醛/酮化合物,与α-羟基醛/酮或α-卤代醛/酮在含水介质中合成噻烯类衍生物,与α,β-不饱和羰基化合物、碳碳叁键、碳氮叁键、碳碳双键、氮氮双键、碳氮双键、碳硫双键、环氧乙烷及其衍生物、氮杂环丙烷及其衍生物、环丙烷及其衍生物、卤代烃等在含水介质,中合成硫醚化合物。

In an embodiment, the selective hydrogenation catalysts of this disclosure are used in the hydrogenation of highly unsaturated hydrocarbons such as for example and without limitation acetylene, methylacetylene, propadiene or combinations thereof.

在实施方案中,本公开的选择性加氢催化剂被用于高度不饱和烃的加氢中,其中所述高度不饱和烃例如但不限于乙炔、甲基乙炔、丙二烯或它们的组合。

The unsaturated hydrocarbon stream 10 primarily comprises one or more unsaturated hydrocarbons, but it also contains one or more highly unsaturated hydrocarbons such as for example and without limitation acetylene, methylacetylene and propadiene.

所述不饱和烃料流10主要包含一种或多种不饱和烃,但它也含有一种或多种高度不饱和烃例如但不限于乙炔、甲基乙炔和丙二烯。

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