Experimental Determination of the Equilibrium Conditions of Binary Gas Hydrates of Cyclopentane plus Oxygen, Cyclopentane plus Nitrogen, and Cyclopentane plus Hydrogen
文献类型：期刊论文
| 作者 | Du Jianwei; Liang Deqing; Li Dongliang; Li Xinjun |
| 刊名 | industrial & engineering chemistry research
 |
| 出版日期 | 2010-11-17 |
| 卷号 | 49期号:22页码:11797-11800 |
| 关键词 | PHASE-EQUILIBRIUM CLATHRATE HYDRATE METHYL CYCLOHEXANE CARBON-DIOXIDE TETRAHYDROPYRAN |
| ISSN号 | 0888-5885 |
| 产权排序 | [du jianwei; liang deqing; li dongliang; li xinjun(李新军)] cas, key lab renewable energy & gas hydrate, guangzhou inst energy convers, guangzhou 510640, guangdong, peoples r china |
| 通讯作者 | liangdq@ms.giec.ac.cn |
| 中文摘要 | in this work, four-phase hydrate equilibrium data for each of the systems cyclopentane (cp) + water + hydrogen, cp + water + nitrogen, and cp + water + oxygen were measured and are reported in the temperature range of 281.3-303.1 k and the pressure range of 2.27-30.40 mpa. measurements were made using an isochoric method. experimental data on the equilibrium conditions of the two systems nitrogen + water and hydrogen + water with cp are reported over a previously uninvestigated extended temperature span. the hydrate dissociation data for the cp + water + hydrogen system are compared with some selected experimental data from the literature, and the acceptable agreement demonstrates the reliability of the experimental method used in this work. finally, the first quadruple phase equilibrium data in the ternary system cp + water + oxygen have been achieved. |
| 英文摘要 | in this work, four-phase hydrate equilibrium data for each of the systems cyclopentane (cp) + water + hydrogen, cp + water + nitrogen, and cp + water + oxygen were measured and are reported in the temperature range of 281.3-303.1 k and the pressure range of 2.27-30.40 mpa. measurements were made using an isochoric method. experimental data on the equilibrium conditions of the two systems nitrogen + water and hydrogen + water with cp are reported over a previously uninvestigated extended temperature span. the hydrate dissociation data for the cp + water + hydrogen system are compared with some selected experimental data from the literature, and the acceptable agreement demonstrates the reliability of the experimental method used in this work. finally, the first quadruple phase equilibrium data in the ternary system cp + water + oxygen have been achieved. |
| WOS标题词 | science & technology ; technology |
| 学科主题 | engineering |
| 类目[WOS] | engineering, chemical |
| 研究领域[WOS] | engineering |
| 关键词[WOS] | phase-equilibrium ; clathrate hydrate ; methyl cyclohexane ; carbon-dioxide ; tetrahydropyran |
| 收录类别 | SCI |
| 资助信息 | national natural science foundation of china [50876107]; national basic research program of china [2009cb219504]; nsfc-guangdong union foundation [u0733003]; cas [kgcx2-yw-805] |
| 原文出处 | https://dx.doi.org/10.1021/ie101339j |
| 语种 | 英语 |
| WOS记录号 | WOS:000283916700077 |
| 公开日期 | 2014-12-24 |
| 源URL | [http://ir.giec.ac.cn/handle/344007/8467]  |
| 专题 | 中国科学院广州能源研究所 |
| 作者单位 | CAS, Key Lab Renewable Energy & Gas Hydrate, Guangzhou Inst Energy Convers, Guangzhou 510640, Guangdong, Peoples R China |
| 推荐引用方式 GB/T 7714 | Du Jianwei,Liang Deqing,Li Dongliang,et al. Experimental Determination of the Equilibrium Conditions of Binary Gas Hydrates of Cyclopentane plus Oxygen, Cyclopentane plus Nitrogen, and Cyclopentane plus Hydrogen[J]. industrial & engineering chemistry research,2010,49(22):11797-11800. |
| APA | Du Jianwei,Liang Deqing,Li Dongliang,&Li Xinjun.(2010).Experimental Determination of the Equilibrium Conditions of Binary Gas Hydrates of Cyclopentane plus Oxygen, Cyclopentane plus Nitrogen, and Cyclopentane plus Hydrogen.industrial & engineering chemistry research,49(22),11797-11800. |
| MLA | Du Jianwei,et al."Experimental Determination of the Equilibrium Conditions of Binary Gas Hydrates of Cyclopentane plus Oxygen, Cyclopentane plus Nitrogen, and Cyclopentane plus Hydrogen".industrial & engineering chemistry research 49.22(2010):11797-11800. |
入库方式： OAI收割
来源：广州能源研究所
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