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炼厂干气制氢新途径 被引量:1
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作者 崔君利 王德利 李向阳 《沈阳化工》 1998年第2期24-28,共5页
通过对轻油制氢和焦化干气制氢的工艺和制氢成本的简单对比,提出采用炼厂干气选择氧化氢制的新工艺,此工艺较烃类-水蒸汽转化法具有明显的优越性,是目前炼厂干气制氢的新途径。
关键词 选择氧化 制氢 石油裂化气
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我国石化工业制氢技术发展的研究与建议 被引量:8
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作者 刘发起 《辽宁化工》 CAS 1997年第3期136-138,共3页
本文综述了石化工业目前几种主要制氢方法及国外制氢技术发展动向,对我国石化工业制氢技术的发展提出几点建议。
关键词 烃类水蒸汽转化 变压吸附 分离 石油裂化气 制氢
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制氢转化催化剂失活原因及处理 被引量:1
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作者 陈哲明 《齐鲁石油化工》 1995年第3期214-216,共3页
关键词 制氢 石油裂化气 催化剂活性
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用新鲜水浸泡法卸制氢装置低温变换催化剂
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作者 吴奋勇 孔庆成 欧阳兴 《石油炼制与化工》 CAS CSCD 北大核心 1999年第2期20-22,共3页
在简单介绍轻烃水蒸气转化制氢工艺中用钝化工艺技术卸低温变换催化剂的基础上,详细叙述了用新鲜水浸泡法卸低温变换催化剂(铜-锌系B202型催化剂)的新工艺,在茂名石油化工公司炼油厂制氢装置上的实际应用表明,该方法与钝化法... 在简单介绍轻烃水蒸气转化制氢工艺中用钝化工艺技术卸低温变换催化剂的基础上,详细叙述了用新鲜水浸泡法卸低温变换催化剂(铜-锌系B202型催化剂)的新工艺,在茂名石油化工公司炼油厂制氢装置上的实际应用表明,该方法与钝化法相比具有工艺简单,操作方便,安全可靠,卸剂时粉尘少,时间短等特点,已收到良好的效益,是一种可行的卸低温变换催化剂的技术。 展开更多
关键词 水浸没 低温变换 催化剂 制氢装置 石油裂化气
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制氢装置PSA吸附剂的失活与再生
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作者 张炳华 《金山油化纤》 1999年第2期39-44,共6页
介绍在制氢装置实施吸附剂再生方案的经过及PSA的工艺过程和吸附剂失活的原因分析;并对吸附剂再生前后氢气回收率和吸附容量作了比较。通过实践,降低了生产成本,提高了装置运转能力。
关键词 PSA 吸附剂 再生 制氢 石油裂化气
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现有制氢装置的低费用技术改造
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作者 杨华琮 《石化译文》 1995年第2期9-14,17,共7页
关键词 制氢装置 技术改造 费用 石油裂化气
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Study on Commercial Application of FP-DSN Sulfur Transfer Additive in FCC Unit 被引量:2
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作者 Gao Siming Han Rongxian Chen Desheng(SINOPEC Qingdao Petrochemical Company,Qingdao 266043) 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2009年第2期15-19,共5页
The FCC unit with addition of various inventories of the FP-DSN type sulfur transfer additive was tested in a commercial scale. The effect of the sulfur transfer additive was analyzed by investigating the indicators r... The FCC unit with addition of various inventories of the FP-DSN type sulfur transfer additive was tested in a commercial scale. The effect of the sulfur transfer additive was analyzed by investigating the indicators related with the regenerator flue gas composition,the dry gas composition before desulfurization,the LPG composition before desulfurization,the acid gas,and the yield of gasoline and diesel. The test results indicated that the sulfur was trans ferred from the feed stream into the dry gas,LPG and acid gas,and the sulfur transfer effect was obvious only when the inventory of sulfur transfer additive exceeded over 2.0% of total FCC catalyst inventory. 展开更多
关键词 catalytic cracking unit sulfur transfer additive commercial application
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Kinetics and Selectivity in Thermal Hydrocracking and Catalytic Hydrocracking of Asphaltenes
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作者 Zhao Yingxian Li Da (Ningbo Institute of Technology,Zhejiang University,Ningbo 315100) 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2011年第1期24-31,共8页
A pentane-insoluble mixture of asphaltenes was processed by thermal hydrocracking and catalytic hydrocracking over Ni-Mo/γ-Al2O3 catalyst in a microbatch reactor at 430 ℃.The experimental data of asphaltene conversi... A pentane-insoluble mixture of asphaltenes was processed by thermal hydrocracking and catalytic hydrocracking over Ni-Mo/γ-Al2O3 catalyst in a microbatch reactor at 430 ℃.The experimental data of asphaltene conversion adequately fit second-order kinetics to give the apparent rate constants of 2.435×10-2 and 9.360×10-2 (wt frac)-1 min-1 for the two processes,respectively.A three-lump kinetic model is proposed to evaluate the rate constants for parallel reactions of asphaltenes producing liquid oil (k1) and gas+coke (k3),and consecutive reaction producing gas+coke (k2) from this liquid oil.The evaluated constants for asphaltenes hydrocracking,in the presence and absence of the catalyst,respectively,show that k1 is 2.430×10-2 and 9.355×10-2 (wt frac)-1 min-1,k2 is 2.426×10-2 and 6.347×10-3 min-1,and k3 is 5.416×10-5 and 4.803×10-5 (wt frac)-1 min-1.As compared with the thermal hydrocracking of asphaltenes,the catalytic hydrocracking of asphaltenes promotes liquid production and inhibits coke formation effectively. 展开更多
关键词 ASPHALTENES thermal hydrocracking catalytic hydrocracking KINETICS SELECTIVITY
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Effect of Metal Contamination on the Performance of Catalyst for Deep Catalytic Cracking Process 被引量:3
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作者 Zhang Zhigang 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2009年第2期37-42,共6页
The effect of different metal contamination levels of catalysts for Deep Catalytic Cracking(DCC) on the distribution and selectivity of DCC products was investigated in a FCC pilot unit. The pilot test results showed ... The effect of different metal contamination levels of catalysts for Deep Catalytic Cracking(DCC) on the distribution and selectivity of DCC products was investigated in a FCC pilot unit. The pilot test results showed that the effects of the metal contamination level of catalyst on the propylene yield,the coke yield,the LPG yield,the gasoline yield,the selectivity of low carbon olefins,and coke selectivity was significant,and that the influence of metal contamination level on the conversion and dry gas yield was minor. 展开更多
关键词 low carbon olefins metal contamination catalytic cracking PETROCHEMICALS
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Geochemical evolution during the cracking of crude oil into gas under different pressure systems 被引量:4
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作者 CHEN ZhongHong ZHANG ShouChun ZHA Ming 《Science China Earth Sciences》 SCIE EI CAS 2014年第3期480-490,共11页
Two comparative simulation experiments(a normal atmospheric-pressure opening system and a 20 MPa closed system)were conducted to study the geochemical evolution of n-alkane,sterane,and terpane biomarkers in the proces... Two comparative simulation experiments(a normal atmospheric-pressure opening system and a 20 MPa closed system)were conducted to study the geochemical evolution of n-alkane,sterane,and terpane biomarkers in the process of oil cracking into gas under different pressures.With an initial experimental temperature set at 300°C,the temperature was increased to 650°C at a heating rate of 30°C/h.The products were tested every 50°C starting at 300°C,and a pressure of 20 MPa was achieved using a water column.The low-maturity crude oil sample was from the Paleogene system in the Dongying sag in eastern China.The threshold temperature obtained for the primary oil cracking process in both pressure systems was 450°C.Before the oil was cracked into gas,some components,including macromolecular n-alkanes,were cracked into medium-or small-sized n-alkanes.The secondary oil cracking of heavy hydrocarbon gases of C2–5to methane mainly occurred between 550°C to 650°C,and the parameters Ln(C1/C2)and Ln(C1/C3),as well as the dry coefficients,increased.Overpressure inhibited the oil cracking process.In the 20 MPa system,the oil conversion rate decreased,the temperature threshold for gas generation rose,and oil cracking was inhibited.Compared with the normal pressure system,high-carbon n-alkanes and other compounds in the 20 MPa pressure system were reserved.Furthermore,the parameters∑C21-/∑22+,Ln(C1/C2),and Ln(C1/C3),as well as the dry coefficients,decreased within the main temperature range.During secondary oil cracking(550°C to 600°C),the Ph/nC18and Pr/nC17decreased.High pressure influenced the evolution of the biomarkers Ts and Tm,C31homohopane,C29sterane,and their related maturity parameters to different extents during oil cracking under different temperature ranges. 展开更多
关键词 crude oil cracking high temperature and high pressure N-ALKANES BIOMARKER geochemical evolution
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