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公开(公告)号:US20180188159A1
公开(公告)日:2018-07-05
申请号:US15736373
申请日:2016-06-16
Applicant: SHELL OIL COMPANY , CHINA UNIVERSITY OF PETROLEUM
Inventor: Zhichang LIU , Rui ZHANG , Xuan ZHANG , Xianghai MENG , Haiyan LIU , Chunming XU , Peter Anton August KLUSENER
IPC: G01N21/27 , G01N21/3577 , G01N21/79 , C07C2/60 , B01J31/02
CPC classification number: G01N21/272 , B01J31/0279 , B01J2231/32 , C07C2/60 , C07C2531/02 , G01N21/35 , G01N21/3577 , G01N21/79
Abstract: The present invention relates to a process for monitoring the catalytic activity of an ionic liquid and for the regeneration of the ionic liquid in continuous conversion of an olefin in an alkylation. The process includes (a) providing an ionic liquid; (b) reacting a hydrocarbon mixture with the ionic liquid to obtain an ionic liquid phase. In step (d), adding an organic compound to the ionic liquid phase. In step (e), obtaining an absorption peak of a mixture from step (d) and in step (f) repeating until the absorption peak reaches a maximum or a minimum value. In step (g), determining the total amount of the organic compound or the ionic liquid phase added. Next, (h) calculating the catalytic activity of the ionic liquid. Then, (i) adding aluminium halides to the reaction of step (b) such that the activity of step (h) stays above the minimum level.
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公开(公告)号:US20180180555A1
公开(公告)日:2018-06-28
申请号:US15736354
申请日:2016-06-16
Applicant: SHELL OIL COMPANY , CHINA UNIVERSITY OF PETROLEUM
Inventor: Rui ZHANG , Zhichang LIU , Xuan ZHANG , Xianghai MENG , Haiyan LIU , Chunming XU , Peter Anton August KLUSENER
CPC classification number: G01N21/79 , B01J31/0279 , B01J31/0284 , B01J31/4015 , B01J2231/44 , C07C2/68 , C07C2531/02 , C10G29/205 , G01N21/35 , G01N2021/3595
Abstract: The present invention relates to a process for monitoring the catalytic activity of an ionic liquid. In step (a), providing an acidic ionic liquid; (b) providing an organic compound; (c) adding at least a portion of the organic compound to at least a portion of the ionic liquid; (d) recording an infrared spectrum of a mixture from step (c) to obtain at least one absorption peak. In step (e), repeating steps (c) and (d) until at least one absorption peak reaches a maximum value or a minimum value. In step (f), determining at the maximum value or minimum value of step (e): the total amount of the organic compound or the total amount of the ionic liquid added. In step (g), calculating the catalytic activity of the ionic liquid based on: the total amount of the organic compound or the total amount of ionic liquid, as determined in step (f).
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公开(公告)号:US20160207787A1
公开(公告)日:2016-07-21
申请号:US14902423
申请日:2013-12-02
Applicant: CHINA UNIVERSITY OF PETROLEUM-BEIJING
Inventor: Haiyan LIU , Xinyan SUN , Xiaojun BAO , Gang SHI
IPC: C01B39/26
CPC classification number: C01B39/265 , C01B39/26
Abstract: The present invention provides a method for preparing a mordenite, which is a method for preparing the mordenite through a hydrothermal crystallization by using natural aluminosilicate minerals as total silicon sources and total aluminum sources, comprising the steps of: subjecting the natural aluminosilicate minerals to activation treatment which is an activation by sub-molten salt and an activation by thermal treatment; selecting and mixing the activated natural aluminosilicate minerals according to the silicon-to-aluminum ratio of the targeted mordenite, adding thereto deionized water, sodium hydroxide, crystal seed, a templating agent to obtain a reaction mixture; adjusting the reaction mixture by using an inorganic acid to have a pH of 10-13, and then aging it at 40-80° C. for 6-24 hours; and subjecting the aged reaction mixture to hydrothermal crystallization, and then filtering, washing, drying and calcinating the crystallized product to obtain the mordenite. The method for preparing a mordenite provided in the present invention enlarges the sources of raw materials for a molecular sieve, has a low cost and a simple process route, and can largely reduce the cost for synthesizing a molecular sieve.
Abstract translation: 本发明提供一种制备丝光沸石的方法,其是通过使用天然硅铝酸盐矿物作为总硅源和总铝源通过水热结晶制备丝光沸石的方法,包括以下步骤:将天然硅铝酸盐矿物进行活化处理 这是通过次熔盐的活化和通过热处理的活化; 根据目标丝光沸石的硅 - 铝比选择和混合活化的天然硅铝酸盐矿物,加入去离子水,氢氧化钠,晶体种子,模板剂以获得反应混合物; 通过使用无机酸调节反应混合物以使pH为10-13,然后在40-80℃下老化6-24小时; 并对老化的反应混合物进行水热结晶,然后过滤,洗涤,干燥和煅烧结晶产物,得到丝光沸石。 本发明中提供的丝光沸石的制备方法扩大了分子筛原料的来源,成本低,工艺路线简单,能大大降低合成分子筛的成本。
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公开(公告)号:US20240109056A1
公开(公告)日:2024-04-04
申请号:US18156979
申请日:2023-01-19
Applicant: China University of Petroleum - Beijing
Inventor: Tao ZHENG , Rui ZHANG , Zhichang LIU , Haiyan LIU , Xianghai MENG , Chunming XU
Abstract: The present disclosure provides a composite ionic liquid and a preparation method and a use thereof. A first aspect of the present disclosure provides a preparation method of a composite ionic liquid, where an ammonium salt, a first metal salt, a second metal salt, and a third metal salt are sequentially added into a reactor for performing a reaction under different conditions, and the composite ionic liquid is obtained after the reaction is finished. The composite ionic liquid prepared by the method may be used as a catalyst to catalyze an alkylation reaction of isoparaffin with C4 olefin to obtain alkylated oil, which has the advantages of high catalytic activity, long catalytic life, low consumption, and better distribution of the resulting alkylated oil, etc, and thereby significantly reducing the production costs and improving the quality of the resulted alkylated oil.
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公开(公告)号:US20180029894A1
公开(公告)日:2018-02-01
申请号:US15527969
申请日:2014-11-19
Inventor: Xiaojun BAO , Yuanyuan YUE , Jinbiao YANG , Haiyan LIU , Pei YUAN
IPC: C01B39/04
CPC classification number: C01B39/04 , C01P2002/90 , C01P2004/62
Abstract: The present invention provides a preparation method of Beta molecular sieve, comprising: activating a mineral having low silica-to-alumina ratio and a mineral having high silica-to-alumina ratio, respectively, wherein the mineral having low silica-to-alumina ratio is activated via a sub-molten salt medium, and the mineral having high silica-to-alumina ratio is activated via means of high-temperature calcination; mixing the activated minerals with sodium chloride, potassium chloride, water and template agent for hydrothermal crystallization, wherein the charged amounts of the raw materials satisfies a molar ratio of: 0.03-0.18 Na2O:0.01-0.03 K2O:0.1-0.4 (TEA)2O:1 SiO2:0.01-0.5 Al2O3:12-40 H2O; cooling the crystallized product and removing the mother liquor by filtration, washing the resulting filter cake with water to neutral and drying it to obtain the Beta molecular sieve. The method of the present invention broadens the range of raw materials for synthesizing the molecular sieve, greatly reduce the production cost, and significantly improve the environmental friendliness of the synthesis process, thereby having a wide range of application prospects.
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公开(公告)号:US20160185609A1
公开(公告)日:2016-06-30
申请号:US14895481
申请日:2013-12-02
Applicant: CHINA UNIVERSITY OF PETROLEUM-BEIJING
Inventor: Xiaojun BAO , Yuanyuan YUE , Tiesen LI , Haiyan LIU , Gang SHI , Jinbiao YANG
IPC: C01B39/18
CPC classification number: C01B39/18
Abstract: The present invention relates to a synthesis method of zeolite 4A, wherein natural clay mineral, provided as the total silicon source and aluminum source required for molecular sieve synthesis, is activated before they are crystallized under hydrothermal conditions to synthesize zeolite 4A. In the method of the present invention, a simple process is employed and inexpensive raw materials are used, resulting in zeolite 4A having a whiteness of 90% or more and a calcium ion exchange capacity of no less than 310 mg CaCO3/g zeolite. According to the present invention, the range of raw materials for the preparation of molecular sieve materials is broadened, and therefore not only the cost for molecular sieve production is greatly reduced by using the sub-molten salt activation method, but also the greenness in the production process of molecular sieve materials is significantly improved.
Abstract translation: 本发明涉及一种沸石4A的合成方法,其中作为分子筛合成所需的总硅源和铝源提供的天然粘土矿物在水热条件下结晶以合成沸石4A之前被活化。 在本发明的方法中,采用简单的方法,使用廉价的原料,得到沸石4A的白度为90%以上,钙离子交换容量不低于310mg CaCO 3 / g沸石。 根据本发明,用于制备分子筛材料的原料的范围变宽,因此通过使用次熔盐活化方法不仅大大降低了分子筛生产的成本,而且通过使用次熔融盐活化方法, 分子筛材料的生产工艺得到明显改善。
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