Method for purification of phenol
    5.
    发明授权
    Method for purification of phenol 失效
    苯酚纯化方法

    公开(公告)号:US5502259A

    公开(公告)日:1996-03-26

    申请号:US290258

    申请日:1994-08-15

    摘要: The invention relates to a method for purification of phenol and specifically to a method for purification of phenol produced within the process of joint phenol and acetone production by cumene method.The aim of the invention is to develop a catalyst which has high activity for phenol purification from organic mico-impurities with regeneration of the catalyst and which has high mechanical strength and stability with long catalyst life.This result is obtained by phenol purification using a heterogeneous zeolite catalyst. The acidity of the catalyst measured by butane cracking (K.sub.A) is more than 10.It is preferable to use zeolites which are designated according to the classification of the International Zeolite Association by indices FAU (zeolites X, Y), MFI (for example, ZSM-5), MOR (mordenite), MAZ (omega), BEA (beta), FER (ferrierite) and others. These zeolites can be used with binders (aluminum oxide, silica gel, aluminosilicates or aluminophosphates) and without them. It is preferable to use zeolite of the Y type with an aluminosilicate binder and a the value of K.sub.A =50-80 cm.sup.3 /min*g and Si/Al ratio more than 3. The concentration of sodium, potassium and other alkali agents on the basis of their oxides does not exceed 2 wt %, preferably not more than 0.3 wt %. It is preferable to use zeolites with medium and large pores. Size of zeolites pores should be within the range 4 .ANG. in diameter and more. The most preferable zeolites are with large pores (>6 .ANG. in diameter) such as Y and mordenite.

    摘要翻译: 本发明涉及一种纯化苯酚的方法,特别涉及通过异丙苯法在联苯酚和丙酮生产过程中产生的苯酚纯化方法。 本发明的目的是开发一种催化剂,该催化剂具有较高的活性,用于有机微杂杂质的纯化,催化剂的再生,并具有较高的机械强度和稳定性以及较长的催化剂寿命。 该结果通过使用非均相沸石催化剂的苯酚纯化获得。 通过丁烷裂解(KA)测量的催化剂的酸度大于10.优选使用根据国际沸石协会的分类指定的沸石,通过指数FAU(沸石X,Y),MFI(例如, ZSM-5),MOR(丝光沸石),MAZ(ω),BEA(β),FER(镁碱沸石)等。 这些沸石可以与粘合剂(氧化铝,硅胶,硅铝酸盐或铝磷酸盐)一起使用,没有它们。 优选使用Y型沸石与铝硅酸盐粘合剂,KA = 50-80cm 3 / min * g,Si / Al比大于3。钠,钾和其他碱剂的浓度 其氧化物的基数不超过2重量%,优选不大于0.3重量%。 优选使用具有中孔和大孔的沸石。 沸石孔隙的大小应在直径4 ANGSTROM以内。 最优选的沸石具有大孔(直径大于等于6埃),例如Y和丝光沸石。

    Process for the obtainment of a light paraffin isomerization catalyst
    6.
    发明授权
    Process for the obtainment of a light paraffin isomerization catalyst 失效
    获得轻链烷烃异构化催化剂的方法

    公开(公告)号:US5264648A

    公开(公告)日:1993-11-23

    申请号:US742602

    申请日:1991-08-08

    IPC分类号: B01J29/20 C07C5/27 C07C5/13

    摘要: The invention refers to a process for the obtainment of a catalyst useful in the isomerization of light paraffins, fundamentally based on acid treatment of a synthetic mordenite at temperatures between 40.degree. and 100.degree. C. followed by treatment with steam-air at temperatures between 300.degree. and 600.degree. C. which make it possible to optimize the SiO.sub.2 /Al.sub.2 O.sub.3 framework ratio and the amount of extraframework aluminum of the zeolite. The mordenite thus obtained is mixed with an inorganic refractory oxide such as Al.sub.2 O.sub.3 and a metal of group VIII, basically Pt, is added in an amount between 0.1 and 0.5% by weight referred to the final catalyst.The catalyst has been tested in the isomerization of light refinery fractions (C.sub.5 and C.sub.6) and has a high activity and selectivity of branched isomers with a low production of gases and a high octane number for the light gasoline obtained.

    摘要翻译: 本发明涉及获得可用于轻链烷烃异构化的催化剂的方法,其基本上是基于在40℃至100℃之间的合成丝光沸石的酸处理,然后在300℃的温度下用蒸汽 - 空气处理 DEG和600℃,这使得可以优化SiO 2 / Al 2 O 3骨架比和沸石的粉末铝量。 由此获得的丝光沸石与无机耐火氧化物如Al 2 O 3和基本上Pt的金属基本上相加,以与最终催化剂相关的0.1至0.5重量%的量加入。 催化剂已经在轻馏分馏分(C5和C6)的异构化中进行了测试,并且具有高分子异构体的活性和选择性,其中所得到的轻质汽油具有低产气和高辛烷值。

    Catalytic decomposition of N.sub.2 O
    7.
    发明授权
    Catalytic decomposition of N.sub.2 O 失效
    催化分解N2O

    公开(公告)号:US5171553A

    公开(公告)日:1992-12-15

    申请号:US790611

    申请日:1991-11-08

    CPC分类号: B01D53/8628 Y02C20/10

    摘要: The invention describes a highly efficient catalytic pollution control process for removing N.sub.2 O from gaseous mixtures. The catalytic process, which is substantially unaffected by the presence of oxygen, comprises contacting an N.sub.2 O-containing gaseous mixture with a catalyst comprising a crystalline zeolite which, at least in part, is composed of five membered rings having a structure type selected from the group consisting of BETA, MOR, MFI, MEL and FER wherein the crystalline zeolite has been at least partially ion-exchanged with a metal selected from the group consisting of copper, cobalt, rhodium, iridium, ruthenium and palladium under conditions sufficient to convert the N.sub.2 O into gaseous nitrogen and gaseous oxygen.

    Production of high octane gasoline
    9.
    发明授权
    Production of high octane gasoline 失效
    生产高辛烷值汽油

    公开(公告)号:US4676887A

    公开(公告)日:1987-06-30

    申请号:US825294

    申请日:1986-02-03

    CPC分类号: C10G65/12 C10G47/16 C10G69/02

    摘要: A moderate pressure hydrocracking process is disclosed in which substantially dealkylated heavy distillate feedstocks are processed directly to high octane gasoline over a catalyst, preferably comprising a crystalline silicate zeolite hydrocracking component having a Constraint Index less than 2. The bottoms fraction produced from the contacting may be passed to an FCC unit for further processing. In another embodiment, the substantially dealkylated heavy distillate feedstock may be fractionated into a lighter boiling stream and a heavier boiling stream for better ease of processing.

    摘要翻译: 公开了一种中等压力的加氢裂化方法,其中基本上脱烷基化的重质馏出物原料通过催化剂直接加工成高辛烷值汽油,优选包含约束指数小于2的结晶硅酸盐沸石加氢裂化组分。由接触产生的塔底馏分可以是 传递到FCC单元进行进一步处理。 在另一个实施方案中,基本上脱烷基化的重质馏出物原料可以分馏成更轻的沸腾流和较重的沸腾流,以更好地加工。

    Manufacture of naphthenic type lubricating oils
    10.
    再颁专利
    Manufacture of naphthenic type lubricating oils 失效
    制造环烷型润滑油

    公开(公告)号:USRE30529E

    公开(公告)日:1981-02-24

    申请号:US78616

    申请日:1979-09-24

    IPC分类号: B01J29/20 B01J29/26 C10G45/64

    摘要: A process for making naphthenic type lubricating oils from a low VI waxy crude which comprises distilling said low VI waxy crude to 500.degree. to 650.degree. F. at atmospheric pressure to separate distillable fractions therefrom, subjecting the residue to a vacuum distillation at about 25 to about 125 mm Hg absolute pressure to obtain one or more gas oil fractions, optionally hydrotreating said gas oil fractions in the presence of a Ni/Mo catalyst at 550.degree. to 650.degree. F., 0.25 to 1.0 LHSV, and 700-1500 psig, and catalytically dewaxing said distillates in the presence of a H.sup.+ form mordenite catalyst containing a Group VI or Group VIII metal at 550.degree. to 750.degree. F., 500 to 1500 psig and 0.25 to 5.0 LHSV, to obtain said naphthenic type oils having pour points of from about -60.degree. to +20.degree. F.