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    • 1. 发明授权
    • Naphtha upgrading
    • 石脑油升级
    • US5414172A
    • 1995-05-09
    • US184902
    • 1994-01-21
    • Arthur A. ChinNick A. CollinsMohsen N. HarandiRobert T. ThomsonRobert A. Ware
    • Arthur A. ChinNick A. CollinsMohsen N. HarandiRobert T. ThomsonRobert A. Ware
    • C10G59/02C07C2/66C07C4/06
    • C10G59/02
    • A process for upgrading low octane naphthas to produce gasoline products with low levels of benzene and aromatics while retaining a high pool octane uses a paraffinic naphtha reformer feed which is dehexanized to provide a C.sub.7 + fraction which is fed to the reformer and a C.sub.6 fraction which is fed together with the C.sub.6 fraction from the reformer effluent to a catalytic upgrading step where the low octane components from the naphtha and the benzene from the reformate are converted to a low benzene, high octane gasoline by alkylation of the benzene and other aromatics present in the reformate. The process has the advantage that benzene make in the reformer is reduced by the partial by-passing of the C.sub.6 benzene precursors around the reformer; in addition, improved benzene alkylation results from the presence of additional light olefins generated by the cracking of paraffins from the paraffinic naphtha. the reaction is preferably carried out in a turbulent fluidized bed reaction zone.
    • 一种用于升级低辛烷值的石脑油以生产具有低含量苯和芳族化合物的汽油产品同时保留高残留辛烷值的方法使用石蜡石脑油重整器原料,该进料被脱脂以提供进料至重整器的C 7+馏分, 与来自重整器流出物的C6馏分一起进料到催化升级步骤,其中来自石脑油的低辛烷值成分和来自重整产物的苯通过苯和其它芳族化合物的烷基化转化为低苯,高辛烷值汽油 重组。 该方法的优点是在重整器周围的C6苯前体的部分旁路减少了重整器中的苯; 此外,改进的苯烷基化是由于由链烷烃石脑油裂解石蜡产生的另外的轻质烯烃的存在。 该反应优选在湍流流化床反应区中进行。
    • 3. 发明授权
    • Fluid bed catalytic upgrading of reformate
    • 流化床催化升级改质
    • US5395513A
    • 1995-03-07
    • US106690
    • 1993-08-16
    • Arthur A. ChinMohsen N. HarandiKaren M. MillaneRobert A. WareJames S. Warwick
    • Arthur A. ChinMohsen N. HarandiKaren M. MillaneRobert A. WareJames S. Warwick
    • C10G35/09C10G35/095
    • C10G35/09
    • A continuous process for upgrading reformate feedstock or the like to reduce benzene content and increase octane fuel rating. The improved process comprises maintaining a fluidized bed of regenerable acid solid medium pore zeolite catalyst particles in a turbulent regime reaction zone, preferably maintained with a superficial gas velocity of 0.1 to 1 meter/sec. with reformate feedstock being introduced at a bottom portion of the reaction zone at a weight hourly space velocity (WHSV) of 0.1 to 5, based on active catalyst solids; reaction zone total pressure being less than 2000 kPa. The preferred catalyst particles have an average particle size of 20 to 100 microns (.mu.), with about 10 to 25% of the catalyst particles comprising fine particles having a particle size less than 30 microns; and the preferred zeolite catalyst comprises shape selective medium pore aluminosilicate zeolite having a constraint index of 1 to 12. The benzene is reacted by contacting reformate feedstock, such as C.sub.6 distillation heart cut containing at least 70 wt % compounds having six carbon atoms, including benzene, n-hexane and isohexane, with said catalyst particles at reaction temperature of 370.degree. to 540.degree. C. and at benzene partial pressure of at least 200 kPa under reformate conversion conditions sufficient to convert at least 40% of feedstock benzene per pass, thereby producing a high octane fuel product containing less than 10 wt % C.sub.10.sup.+ components.
    • 用于升级重整原料等以降低苯含量和提高辛烷值的连续方法。 改进的方法包括将可再生酸固体中孔沸石催化剂颗粒的流化床保持在湍流状态反应区,优选以0.1至1米/秒的表观气体速度保持。 其中重整原料以基于活性催化剂固体的0.1至5的重时空速(WHSV)引入反应区的底部; 反应区总压力小于2000 kPa。 优选的催化剂颗粒具有20至100微米(μm)的平均粒度,约10至25%的催化剂颗粒包含粒径小于30微米的细颗粒; 并且优选的沸石催化剂包括具有1至12约束指数的形状选择性中孔硅铝酸盐沸石。苯通过使重整油原料接触而反应,例如含有至少70重量%的具有6个碳原子的化合物的C6蒸馏心切,包括苯 正己烷和异己烷,所述催化剂颗粒在370〜540℃的反应温度和至少200kPa的苯分压下,在重整转化条件下,足以每道次转化至少40%的原料苯,由此 产生含有少于10重量%的C10 +组分的高辛烷值燃料产物。
    • 4. 发明授权
    • Isoparaffin/olefin alkylation
    • 异链烷烃/烯烃烷基化
    • US5625113A
    • 1997-04-29
    • US365334
    • 1994-12-28
    • Mohsen N. HarandiJames H. Beech, Jr.Albin Huss, Jr.Robert A. WareAltaf Husain
    • Mohsen N. HarandiJames H. Beech, Jr.Albin Huss, Jr.Robert A. WareAltaf Husain
    • C07C2/58C07C2/62C07C9/16
    • C07C2/58C07C2/62C07C9/16C07C2527/054C07C2529/70
    • A process is disclosed for alkylating an isoparaffin with an olefin comprising the steps of:(a) reacting an isoparaffin having from 4 to 8 carbon atoms with an olefin having from 2 to 12 carbon atoms in a first alkylation reaction stage at temperature from about -40.degree. C. to about 500.degree. C. and overall isoparaffin:olefin feed weight ratio of from about 1:1 to about 250:1 with a solid alkylation catalyst comprising a synthetic porous crystalline material characterized by an X-ray diffraction pattern including values substantially as set forth in Table I of the specification and having a composition comprising the molar relationshipX.sub.2 O.sub.3 :(n)YO.sub.2,wherein n is less than about 35, X is a trivalent element and Y is a tetravalent element;(b) mixing the effluent from said first alkylation stage with additional olefin to evolve an intermediate stream having an isoparaffin:olefin weight ratio of from about 2:1 to about 100:1; and(c) reacting said intermediate stream in a second alkylation stage in the absence of intermediate fractionation with a liquid acid catalyst comprising H.sub.2 SO.sub.4 to produce C.sub.5 + alkylate.
    • 公开了一种用烯烃烷基化异链烷烃的方法,该方法包括以下步骤:(a)使第一烷基化反应阶段中具有4至8个碳原子的异链烷烃与具有2至12个碳原子的烯烃反应, 40℃至约500℃,总异构链烷烃:烯烃进料重量比为约1:1至约250:1,其中固体烷基化催化剂包含合成多孔结晶材料,其特征在于X射线衍射图包括值 基本上如说明书的表I所述,并且具有包含摩尔关系X 2 O 3:(n)YO 2的组成,其中n小于约35,X是三价元素,Y是四价元素; (b)将来自所述第一烷基化阶段的流出物与另外的烯烃混合以产生具有约2:1至约100:1的异链烷烃:烯烃重量比的中间料流; 和(c)在不与中间分级分离的第二烷基化阶段中使所述中间物流与包含H 2 SO 4的液体酸催化剂反应,以产生C5 +烷基化物。
    • 5. 发明授权
    • Process for the conversion of C5 linear olefins to tertiary alkyl ethers
    • 将C5直链烯烃转化为叔烷基醚的方法
    • US5420360A
    • 1995-05-30
    • US112286
    • 1993-08-27
    • Arthur A. ChinRoland B. SaegerJames A. StoosRobert A. Ware
    • Arthur A. ChinRoland B. SaegerJames A. StoosRobert A. Ware
    • C07C41/06
    • C07C41/06C07C41/42Y02P20/127
    • A process is disclosed for producing alkyl tertiary alkyl ether such as TAME from alkanol and hydrocarbon feedstock containing linear olefins, iso-olefins, linear alkanes and iso-alkanes such as C5 streams from FCC. The process selectively etherifies iso-olefins in a plural stage etherification zone whose linear olefin-containing effluent is treated by distillation to remove iso-alkanes, and alkanol before passing to a skeletal isomerization zone using constrained intermediate pore size zeolite catalyst such as ZSM-22, ZSM-23, or ZSM-35, which converts linear olefins to iso-olefins which are cycled for etherification. The use of distillation to remove iso-alkanes and alkanol reduces mass flow to the etherification process and minimizes skeletal isomerization catalyst poisoning by alkanol, without resort to water extraction processes which require subsequent treatment of the isomerization zone feed to remove water.
    • 公开了一种从链烷醇生产烷基叔烷基醚如TAME的方法,以及含有直链烯烃,异烯烃,直链烷烃和异烷烃如FCC的C5流的烃原料。 该方法选择性地醚化多级醚化区中的异烯烃,其直链烯烃流出物通过蒸馏处理以除去异烷烃,和链烷醇在使用约束的中等孔径沸石催化剂如ZSM-22进入骨架异构化区之前 ,ZSM-23或ZSM-35,其将线性烯烃转化为异烯烃,其循环用于醚化。 使用蒸馏来除去异烷烃和链烷醇减少了醚化过程的质量流动,并且使骨架异构化催化剂由链烷醇中毒最小化,而不用采用需要随后处理异构化区域进料以除去水的水提取方法。
    • 9. 发明授权
    • Catalytic hydrodesulfurization
    • 催化加氢脱硫
    • US5011593A
    • 1991-04-30
    • US442870
    • 1989-11-20
    • Robert A. WareStephen S. Wong
    • Robert A. WareStephen S. Wong
    • B01J29/78C10G45/12C10G45/54F02B3/06
    • C10G45/12B01J29/7815B01J2229/26B01J2229/42F02B3/06
    • A hydrodesulfurization process for catalytically hydrosulfurizing highly aromatic feeds, especially catalytically cracked feeds such as light cycle oils from catalytic cracking processes and aromatic extracts, employs a hydrodesulfurization catalyst containing zeolite beta. The zeolite beta based catalyst is more effective for effecting desulfurization than comparable amorphous catalysts or catalysts based on other large pore size zeolite and is capable of achieving a high degree of desulfurization at relatively low levels of conversion. The hydrodesulfurization catalyst comprises a transition metal hydrogenation component, preferably Co/Mo, on zeolite beta together with an inert matrix. The zeolite beta based catalyst may be mixed with amorphous catalyst such as Co/Mo/alumina. The low sulfur products are useful as blending components for road diesel fuels and other distillate fuels.
    • 用于催化加氢硫化高芳族化合物进料,特别是催化裂化进料如来自催化裂化方法的轻质循环油和芳族萃取物的加氢脱硫方法使用含有β沸石的加氢脱硫催化剂。 基于沸石β的催化剂与基于其它大孔径沸石的可比无定形催化剂或催化剂相比,更有效地实现脱硫,并且能够在相当低的转化水平下实现高度脱硫。 加氢脱硫催化剂在沸石β上与惰性基质一起包含过渡金属氢化组分,优选Co / Mo。 沸石β型催化剂可与无定形催化剂如Co / Mo /氧化铝混合。 低硫产品可用作道路柴油燃料和其他馏出燃料的混合组分。
    • 10. 发明授权
    • Process configuration for producing high viscosity lubricating oils
    • 生产高粘度润滑油的工艺配置
    • US4913794A
    • 1990-04-03
    • US379511
    • 1989-07-13
    • Quang N. LeRobert A. WareStephen S. Wong
    • Quang N. LeRobert A. WareStephen S. Wong
    • C10G27/12C10G71/00
    • C10G71/00C10G2400/10
    • A process is disclosed for improving the Viscosity Index of a hydrocarbon lubricating oil comprising the steps of providing a flow reactor having separate first and second inlet ports for the separate co-injection of lubricating oil and an organic peroxide, charging said lubricating oil and said organic peroxide of said flow reactor through said first and second inlet ports respectively, controlling the relative flowrates of said lubricating oil and organic peroxide reactants together with the total volumetric flowrate through said flow reactor to maintain a flow regime which favors diffusional mixing between said organic peroxide and said lubricating oil, and maintaining said organic peroxide and said lubricating oil under conversion conditions including temperatures of between about 50.degree. and 300.degree. C. and pressure sufficient to maintain said lubricating oil and said organic peroxide substantially in the liquid phase. Controlling the flow regime to favor diffusional rather than convective mixing between the lubricating oil and the organic peroxide has surprisingly been found to markedly enhance Viscosity Index improvement.
    • 公开了一种用于改进烃类润滑油的粘度指数的方法,该方法包括以下步骤:提供具有单独的第一和第二入口的流动反应器,用于单独共同注入润滑油和有机过氧化物,将所述润滑油和所述有机物 所述流动反应器分别通过所述第一和第二入口过氧化物,控制所述润滑油和有机过氧化物反应物的相对流速以及通过所述流动反应器的总体积流量,以保持有利于所述有机过氧化物和 所述润滑油,并且在包括约50℃至300℃的温度的转化条件下保持所述有机过氧化物和所述润滑油以及足以使所述润滑油和所述有机过氧化物基本上处于液相的压力。 令人惊讶地发现控制流动状态以有利于润滑油和有机过氧化物之间的扩散而不是对流混合,显着提高了粘度指数的改善。