PROCESS FOR TREATING HYDROCARBON LIQUID COMPOSITIONS
    61.
    发明申请
    PROCESS FOR TREATING HYDROCARBON LIQUID COMPOSITIONS 有权
    处理液体液体组合物的方法

    公开(公告)号:US20080296204A1

    公开(公告)日:2008-12-04

    申请号:US11757542

    申请日:2007-06-04

    CPC classification number: C10G25/00 C10G25/003 C10G25/02 C10G25/05

    Abstract: A process for treating a hydrocarbon liquid composition to improve its storage and/or transportation stability, comprises contacting the hydrocarbon liquid composition with a polar trap, wherein the conductivity of the hydrocarbon liquid composition is not reduced by said contacting with a polar trap. The polar trap may be a clay treater containing attapulgus clay. The process may include sequentially passing the hydrocarbon liquid composition through a dehydrator and a clay treater at a flow rate of between about 100 and about 1000 m3 per hour. Advantageously, the hydrocarbon liquid composition is refined and in particular, may be a Merox™-treated jet fuel.

    Abstract translation: 一种用于处理烃液体组合物以改善其储存和/或运输稳定性的方法,包括使烃液体组合物与极性捕集器接触,其中通过与极性阱接触,烃液体组合物的导电性不会降低。 极性陷阱可以是含有attapulgus粘土的粘土处理器。 该方法可以包括以约100至约1000m 3 /小时的流速依次使烃液体组合物通过脱水器和粘土处理器。 有利地,烃液体组合物被精制,特别是可以是经Merox TM处理的喷气燃料。

    Process for deep desulphurization of cracking gasolines with a small loss of octane number
    63.
    发明申请
    Process for deep desulphurization of cracking gasolines with a small loss of octane number 有权
    裂解汽油的深度脱硫方法,辛烷值的损失小

    公开(公告)号:US20080128328A1

    公开(公告)日:2008-06-05

    申请号:US11984329

    申请日:2007-11-15

    Abstract: The invention relates to a treatment process of a sulphur-containing hydrocarbon fraction, comprising the following steps: a) a hydrodesulphurization step of said hydrocarbon fraction to produce a sulphur-depleted effluent, consisting of passing said hydrocarbon fraction mixed with hydrogen over at least one hydrodesulphurization catalyst. b) a step of separation of the partially desulphurized hydrocarbon fraction from the hydrogen introduced in excess, as well as the H2S formed in step a). c) a step of collecting the sulphurous compounds, consisting of placing the partially desulphurized hydrocarbon fraction originating in step b) in contact with an adsorbent comprising at least one element chosen from the group constituted by the elements of groups VIII, IB, IIB and IVA, the adsorbent being used in reduced form in the absence of hydrogen at a temperature above 40° C., the metal content in the reduced form of the adsorbent being above 25% by weight.

    Abstract translation: 本发明涉及含硫烃馏分的处理方法,其包括以下步骤:a)所述烃馏分的加氢脱硫步骤以产生贫硫流出物,其包括将所述烃馏分与氢气混合至少一个 加氢脱硫催化剂。 b)将部分脱硫的烃馏分与过量引入的氢以及步骤a)中形成的H 2 S分离的步骤。 c)收集含硫化合物的步骤,其包括将来自步骤b)的部分脱硫的烃馏分与包含至少一种选自由VIII,IB,IIB和IVA族元素组成的组的元素的吸附剂接触 ,在不存在氢气的情况下,在高于40℃的温度下使用还原形式的吸附剂,还原形式的吸附剂中的金属含量高于25重量%。

    Method for sulfur compounds removal from contaminated gas and liquid streams
    64.
    发明申请
    Method for sulfur compounds removal from contaminated gas and liquid streams 有权
    从污染气体和液体流中除去硫化合物的方法

    公开(公告)号:US20070193939A1

    公开(公告)日:2007-08-23

    申请号:US10559734

    申请日:2003-06-06

    Abstract: Abstract Described is a desorption process and a process for producing a catalytically deactivated formed zeolitic adsorbent, whereby both processes are suitable to improve the lifetime of a formed zeolithic adsorbant in the removal of sulfur compounds from sulfur contaminated gas and liquid feed streams. The adsorbent is in particular a synthetic 13X or LSX faujasite with a silica to alumina ratio from 1.9:1.0 to about 3.0:1.0. The cations of the faujasite include alkali and alkaline earth metals. The formed zeolite mixture is preferably catalytically deactivated due to a phosphate treatment. The desorption is carried out thermally, wherein the heat treatment is done at different temperature stages to avoid decomposition of the organic sulfur compounds.

    Abstract translation: 摘要描述了一种解吸过程和一种生产催化失活的沸石吸附剂的方法,由此两种方法都适合于改善形成的沸石吸附剂在从硫污染的气体和液体进料流中除去硫化合物的寿命。 吸附剂特别是二氧化硅与氧化铝比为1.9:1.0至约3.0:1.0的合成的13X或LSX八面沸石。 八面沸石的阳离子包括碱金属和碱土金属。 形成的沸石混合物由于磷酸盐处理而优选被催化失活。 解吸热进行,其中热处理在不同的温度阶段进行,以避免有机硫化合物的分解。

    Process for the removal of sulfur-oxidated compounds from a hydrocarbonaceous stream
    67.
    发明申请
    Process for the removal of sulfur-oxidated compounds from a hydrocarbonaceous stream 有权
    从烃流中除去硫氧化化合物的方法

    公开(公告)号:US20050218040A1

    公开(公告)日:2005-10-06

    申请号:US10813250

    申请日:2004-03-30

    CPC classification number: C10G25/003 C10G25/05 C10G25/12

    Abstract: A process for the removal of sulfur-oxidated compounds from a hydrocarbonaceous stream containing sulfur-oxidated compounds wherein the hydrocarbonaceous stream containing sulfur-oxidated compounds is contacted with an adsorbent which selectively adsorbs sulfur-oxidated compounds from the hydrocarbonaceous stream to produce an adsorbent having adsorbed sulfur-oxidated compounds. The loaded adsorbent containing sulfur-oxidated compounds is contacted with a desorbent to produce a desorbent containing sulfur-oxidated compounds and an adsorbent having a reduced content of sulfur-oxidated compounds. The regenerated adsorbent is then used to remove additional sulfur-oxidated compounds.

    Abstract translation: 一种从含硫氧化化合物的含烃流中除去硫氧化化合物的方法,其中含有硫氧化化合物的烃物流与选择性吸附来自烃物流的硫氧化化合物以产生吸附剂的吸附剂接触 硫氧化化合物。 负载的含硫氧化化合物的吸附剂与解吸剂接触以产生含硫氧化化合物的解吸剂和具有降低的硫氧化化合物含量的吸附剂。 然后再生的吸附剂用于除去附加的硫氧化化合物。

    Liquid-phase adsorption process for removing and concentrating heteroatom compounds in hydrocarbons
    69.
    发明授权
    Liquid-phase adsorption process for removing and concentrating heteroatom compounds in hydrocarbons 失效
    用于去除和浓缩烃中杂原子化合物的液相吸附方法

    公开(公告)号:US06790344B1

    公开(公告)日:2004-09-14

    申请号:US09719463

    申请日:2000-12-11

    Abstract: Disclosed is a liquid phase adsorption process for removing and concentrating heteroatom compounds in hydrocarbons (HCH), comprising the steps of adsorption, copurging and regeneration. In the adsorption step, a liquid hydrocarbon stream is fed to an adsorber, which adsorbs HCH and returns adsorption effluent. In the copurging step, HCH, which are extracted from the previous regeneration, are applied to the adsorber, displacing the copurging effluent. In the regeneration step, a polar solvent is flowed through the adsorber, purging HCH. Most of the HCH are then set aside for use in the next copuring step, while a small amount of the HCH are taken out from the process as HCH product. The present invention is economically advantageous in effectively removing HCH from hydrocarbon streams and increasing the concentration of HCH within an HCH product.

    Abstract translation: 公开了一种用于除去和浓缩烃(HCH)中的杂原子化合物的液相吸附方法,包括吸附,复合和再生的步骤。 在吸附步骤中,将液体烃流送入吸附器,吸附HCH并返回吸附流出物。 在复合步骤中,从先前的再生提取的HCH被施加到吸附器上,从而移出复合流出物。 在再生步骤中,极性溶剂流过吸附器,吹扫HCH。 然后将大部分HCH放置在下一个复合步骤中使用,同时将少量的HCH作为HCH产物从该方法中取出。 本发明在有效地从烃流中去除HCH并增加HCH产物内HCH的浓度方面具有经济上的优势。

    Selective sorbents for purification of hydrocarbons
    70.
    发明申请
    Selective sorbents for purification of hydrocarbons 有权
    用于净化烃的选择性吸附剂

    公开(公告)号:US20030163013A1

    公开(公告)日:2003-08-28

    申请号:US10234681

    申请日:2002-09-04

    CPC classification number: C10G25/03 B01J20/186 C10G25/05

    Abstract: CuY and AgY zeolites as selective sorbents for desulfurization of liquid fuels. Thiophene and benzene were used as the model system, and vapor phase isotherms were measured. Compared with NaY, CuY and AgY adsorbed significantly larger amounts of both thiophene and benzene at low pressures. It is hypothesized that this is due to null-complexation with Cunull and Agnull. On a per-cation basis, more thiophene was adsorbed by Cunull than by Agnull, eg. 0.92 molecule/Cunull versus 0.42 molecule/Agnull at 2null10null5 atm and 120null C. Molecular orbital calculations confirmed the relative strengths of null-complexation: thiophene>benzene and Cunull>Agnull. The experimental heats of adsorption for null-complexation are in qualitative agreement with theoretical predictions. The invention further comprises a process and sorbents for removal of aromatics from hydrocarbons.

    Abstract translation: CuY和AgY沸石作为液体燃料脱硫的选择性吸附剂。 使用噻吩和苯作为模型系统,并测量气相等温线。 与NaY相比,CuY和AgY在低压下吸收显着较大量的噻吩和苯。 假设这是由于与Cu +和Ag +的π络合。 在阳离子基础上,更多的噻吩被Cu +吸附,而不是Ag +,例如。 分子轨道计算证实了π络合:噻吩>苯和Cu +> Ag +的相对强度,分子/ Cu +与0.42分子/ Ag +在2x10-5atm和120℃。 pi络合的吸附实验热量与理论预测的定性一致。 本发明还包括从烃中除去芳族化合物的方法和吸附剂。

Patent Agency Ranking