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天然气水化物的非凡前景与挑战
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作者 Allen Lowrie 李乐中 纪常杰 《国外油田工程》 2000年第8期34-35,38,共3页
本文介绍甲烷水化物作为一种潜在资源愈加引起人们兴趣的基本原因 ,讨论何为水化物 ,其形成和被发现的方式、地点及其易碎特征所产生的地理危险性。作者进一步讨论目前世界对之关注、勘探和地缘政治影响的情况。
关键词 天然气水化物 甲烷水化物 天然气勘探
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恐龙灭绝新说
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《北京档案》 北大核心 1999年第12期43-43,共1页
关键词 恐龙灭绝 小行星 甲烷水化物 次全球性 冲击波 高压环境 白垩纪 墨西哥湾 闪电击 佛罗里达州
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天然可燃冰开采试验获得成功
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《国土资源与环境》 2002年第4期5-5,共1页
关键词 甲烷水化物 海洋 永久冻土带 天然可燃冰 开采
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Measurements of Hydrate Equilibrium Conditions for CH4, CO2, and CH4+C2H6+C3H8 in Various Systems by Step-heating Method 被引量:8
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作者 陈立涛 孙长宇 +3 位作者 陈光进 聂运强 孙占松 刘延涛 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2009年第4期635-641,共7页
Phase equilibrium conditions of gas hydrate in several systems were measured by the step-heating method using the cylindrical transparent sapphire cell device.The experimental data for pure CH4 or CO2+deionized water ... Phase equilibrium conditions of gas hydrate in several systems were measured by the step-heating method using the cylindrical transparent sapphire cell device.The experimental data for pure CH4 or CO2+deionized water systems showed good agreement with those in the literatures.This kind of method was then applied to CH4/CO2+sodium dodecyl sulfate(SDS)aqueous solution,CH4/CO2+SDS aqueous solution+silica sand,and(CH4+C2H6+C3H8)gas mixture+SDS aqueous solution systems,where SDS was added to increase the hydrate formation rate without evident influence on the equilibrium conditions.The feasibility and reliability of the step-heating method,especially for porous media systems and gas mixtures systems were determined.The experimental data for CO2+silica sand data shows that the equilibrium pressure will change significantly when the particle size of silica sand is less than 96μm.The formation equilibrium pressure was also measured by the reformation of hydrate. 展开更多
关键词 equilibrium condition HYDRATE step-heating sodium dodecyl sullate silica sand
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气体水合物研究进展
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作者 侯力群 《国外科技新书评介》 2006年第10期7-7,共1页
本书是2003年春季美国化学工程协会召开的“气体水合物讨论会”的论文集,共收录16篇论文。气体水合物是一种非常特殊的化学组成,它是由水分子(主体分子)包裹着气体分子(客体分子)在低温高压条件下形成的一种无化学键的晶体物质。... 本书是2003年春季美国化学工程协会召开的“气体水合物讨论会”的论文集,共收录16篇论文。气体水合物是一种非常特殊的化学组成,它是由水分子(主体分子)包裹着气体分子(客体分子)在低温高压条件下形成的一种无化学键的晶体物质。通常的气体水合物是甲烷水合物,在常温常压下,甲烷水合物中包含的甲烷气体是甲烷水化物本身的180倍。作为一种替补能源,气体水合物的研究已经越来越受到人们的重视。 展开更多
关键词 气体水合物 甲烷水合物 甲烷水化物 化学工程 化学组成 晶体物质 高压条件 客体分子
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二十一世纪新能源
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作者 阎萍 《天津煤气》 1999年第2期29-32,共4页
关键词 能源 新能源 甲烷水化物 天然气火箭
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Gas hydrate formation in fine sand 被引量:10
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作者 ZANG XiaoYa LIANG DeQing WU NengYou 《Science China Earth Sciences》 SCIE EI CAS 2013年第4期549-556,共8页
Gas hydrate formation from two types of dissolved gas (methane and mixed gas) was studied under varying thermodynamic conditions in a novel apparatus containing two different natural media from the South China Sea. Th... Gas hydrate formation from two types of dissolved gas (methane and mixed gas) was studied under varying thermodynamic conditions in a novel apparatus containing two different natural media from the South China Sea. The testing media consisted of silica sand particles with diameters of 150-250 μm and 250-380 μm. Hydrate was formed (as in nature) in salt water that occupies the interstitial space of the partially water-saturated silica sand bed. The experiments demonstrate that the rate of hydrate formation is a function of particle diameter, gas source, water salinity, and thermodynamic conditions. The initiation time of hydrate formation was very short and pressure decreased rapidly in the initial stage. The process of mixed gas hydrate formation can be divided into three stages for each type of sediment. Sand particle diameter and water salinity also can influence the formation process of hydrate. The conversion rate of water to hydrate was different under varying thermodynamic conditions, although the formation processes were similar. The conversion rate of methane hydrate in the 250-380 μm sediment was greater than that in the 150-250μm sediment. However, the sediment grain size has no significant influence on the conversion rate of mixed gas hydrate. 展开更多
关键词 formation kinetics water conversion rate natural porous media thermodynamic condition
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Pre-activation based stereoselective glycosylations: Stereochemical control by additives and solvent 被引量:1
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作者 WASONGA Gilbert 《Science China Chemistry》 SCIE EI CAS 2011年第1期66-73,262-278,共8页
Stereochemical control is an important issue in carbohydrate synthesis.Glycosyl donors with participating acyl protective groups on 2-O have been shown to give 1,2-trans glycosides reliably under the pre-activation ba... Stereochemical control is an important issue in carbohydrate synthesis.Glycosyl donors with participating acyl protective groups on 2-O have been shown to give 1,2-trans glycosides reliably under the pre-activation based reaction condition.In this work,the effects of additives and reaction solvents on stereoselectivity were examined using donors without participating protective groups on 2-O.While several triflate salt additives did not have major effects,the amount of AgOTf was found to significantly impact the reaction outcome.Excess AgOTf led to lower stereochemical control presumably due to its coordination with the glycosyl triflate intermediate and a more SN1 like reaction pathway.In contrast,the stereoselectivity could be directed by reaction solvents,with diethyl ether favoring the formation of glycosides and dichloromethane leading to β isomers.The trend of stereochemical dependence on reaction solvent was applicable to a variety of building blocks including the selective formation of β-mannosides. 展开更多
关键词 STEREOSELECTIVITY pre-activation based glycosylation ADDITIVES solvent effects
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