Conversion of dialkyl ethers into olefins

Conversion of dialkyl ethers into olefins

Patent Manufacture T. Nanba Nok Corp. Jpn. Kokai 1993 of zeolite Tokkyo Koho diphosphonic phonic acid), membranes 95,89,716, Apr. 4, 1995; App...

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Patent

Manufacture T. Nanba Nok Corp. Jpn. Kokai 1993

of zeolite Tokkyo

Koho

diphosphonic phonic acid),

membranes 95,89,716,

Apr.

4, 1995;

Appl.

Sept.

24,

The manufacturing process for producing zeolite membranes involves heating aqueous mixtures containing colloidal SiO,, alumina, alkali metals, tetrapropylammonium salt crystallizing agents, and water at O.l-5Wmin in an autoclave, and hydrothermal crystallization at 160-200°C to give ZSM-5 zeolite membrane.

Solid-state dealumination process mina in the tetrahedral framework gallium, titanium, or zirconium H.K. Beyer; G. Pal-Borbely W.R. Grace and Co. U.S. 5,411,724, May 2, 1995;

for substituting aluof zeolites by silicon,

June

2, 1993

acid, ethylenediaminetetra(methylenephospyrophosphoric acid, and/or their salts.

Hydrocarbon cracking process lysts with hybrid [ALBI-zeolite H.H. Hsing; R.E. Pratt; C.H.M. Texaco Inc. U.S. 5,395,512, Mar. 7, 1995;

employing additives

Tsang Appl.

zeolite

cata-

et al. May

14, 1993

A hydrocarbon feedstock is cracked at an elevated temperature in a zone with a zeolite catalyst. The cracking catalyst is a mixture of a crystalline aluminosilicate zeolite and a hybrid [AI,Blzeolite. In this process the hydrocarbon feedstock is contacted with the zeolite catalyst in, for example, a fluidized bed catalytic cracking unit to yield cracked products containing increased amounts of C&a olefins.

Manufacture Appl.

report

of aromatic

bisialkyl

carbonates)

S. Asaoka; K. Ikeda; K. Ueda et al. Chiyoda Chemical Engineering Construction Co. Jpn. Kokai Tokkyo Koho 95.48,320, Feb. 21, 1995;

The solid-state dealumination process involves forming a solid reaction mixture containing >I of the hvdrated ammonium or alkali metal forms of zeolites with tetrahedral frameworks, and 21 crystalline ammonium fluorohalometallate that is thermally stable at the temperature at which substitution proceeds and small enough to penetrate into the pores of the zeolites. Heating the solid reaction mixture at elevated temperature to remove Al from the zeolite framework produces a corresponding zeolite framework having the aluminum substituted by another element, and a fluorohaloaluminate complex, which is removed.

‘--Aromatic bisfalkyl carbonates) are manufactured by reaction of aromatic dihydroxy compounds and R’-OCO,Ar’ IR’ = lower alkyl; Ar’ = nonreactive group-(un)substituted an/l], over zeolite catalysts containing alkali metal ions and/or alkaline earth metal ions, for example, K ion-exchanged zeolite 3A.

CATALYSIS

A. Tissler; R. Thome; K. Becker et al. VAW Aluminum A.-G. US. 5,407,654, Apr. 18, 1995; Appl. July

Process and zeolitic catalysts alkyl aromatic compounds

for preparing

short

chain

J.M. Bennett; C.D. Chang; J.C. Cheng et al. Mobil Oil Corp. US. 5,371,310, Dec. 6, 1994; Appl. June 19, 1991 Cont.-in-part of U.S. 5,236,575 Relatively short chain alkyl aromatic compounds are prepared by alkylating or transalkylating an aromatic compound with a relatively short chain alkylating or transalkylating agent in the presence of a catalyst comprising zeolite MCM-49. A catalyst was prepared from AI,(SO& xH,O and a silica precursor in the presence of NaOH and hexamethyleneimine and was used to alkylate benzene with ethylene.

Catalytic aromatic

cracking of light hydrocarbons hydrocarbons in the presence

T. Takahashi; S. Kanejima Asahi Chemical Industries Jpn. Kokai Tokkyo Koho Appls. June 4, 1993

94,346,062;

94,346,063,

to olefins of zeolites

and

Dec. 20, 1994;

C,_,, paraffin-based hydrocarbons are converted to ethyleneand propylene-based lower olefins and benzene-, PhMe-, and xylene-based monocyclic aromatic hydrocarbons by using aluminosilicate-zeolites with average primary crystal size 0.01-I pm and SiO,/AI,O, ratio 50-300, for example, zeolite ZSM-5 containing Mg.

Manufacture

of hydrogen

H. Nagashima; T. Tomita; Mitsubishi Gas Chemical Jpn. Kokai Tokkyo Koho Appls. Sept. 1, 1993

peroxide

M. lshiuchi Co. 95,69,604;

et al. 95,69,605,

Mar.

14,

1995;

H,O, is manufactured by hydrogenating 0 in a solvent using Pt-group metal catalysts also containing Zr, Al, Cu, Fe, Ni, and/or Co on a support that may be a crystalline zeolite. Preferably, the Pt group metal is Pd, and the solvent is a halogen-free acid. The solvent may contain a stabilizer for H,O,, selected from aminotri(methylenephosphonic acid), l-hydroxyethylidene-l,l-

Appl.

June

4,

IW?

Synthetic conversion

crystalline aluminosilicates for the catalytic of hydrocarbons in petrochemical processes 6, 1990

The invention relates to synthetic crystalline aluminosilicates of the pentasil type and a method for using them as catalysts or catalyst components in petrochemical processes for the catalytic conversion of hydrocarbons and their derivatives into useful organic compounds and intermediates.

Preparation

of diisopropyl

ether

J.F. Knifton; P.S.E. Dai Texaco Development Corp. Eur. Pat. Appl. 652,200, May

from

10, 1995;

US.

acetone Appl.

Nov.

8, 1993

Diisopropyl ether was prepared from a crude byproduct acetone stream by hydrogenating the crude stream over a bulk metal, Ni-rich catalyst to give an isopropanol-rich intermediate and dehydrating the intermediate in the presence of a strong acid zeolite catalyst. Preferably, the zeolite catalyst used in the second step is a p-zeolite, optionally modified with one or more metals from groups IB, VB, VIB, VIIB. and VIII of the Periodic Table or a dealuminized Y-zeolite.

Preparation of dialkyl zeolite catalysts

carbonates

with

ion-exchanged

T. Kondo; Y. Okada; F. Tanaka et al. Chiyoda Chemical Engineering Construction Co. Jpn. Kokai Tokkyo Koho 95,48,319, Feb. 21, 1995; Appl. 1992

Nov.

20,

Dialkyl carbonates are prepared by treatment of alcohols with cyclic carbonates at 20-200°C in the liquid phase in the presence of zeolites exchanged with alkali metal ions and/or alkaline earth metal ions, for example, zeolite 3A (i.e., K-exchanged A-type zeolite).

Conversion

of dialkyl

ethers

into olefins

G.I. Cox; D.D. Pete; D.D. Rosenfeld Exxon Chemical Patents, Inc. PCT Int. Appl. 95,11,209, Apr. 27, 1995;

U.S. Appl.

Oct.

19, 1993

Dialkyl ethers (e.g., tertiary amyl butyl ether) are converted to the corresponding olefin (e.g., isobutylene) by contacting the ether with a faujasite aluminosilicate catalyst in which 250% of the alkali metal content originally present in the faujasite is ex-

Zeolites

16:316-320,

1996

317

Patent

report

changed by 21 alkaline earth metal (e.g., CaY zeolite) and the catalyst is pretreated with steam which enhances its selectivity and reduces byproduct yields.

Gasoline

upgrading

B. Chawla; D.N. Mazzone; M.S. Sarli et al. Mobil Oil Corp. U.S. 5,411,658, May 2, 1995; Appl. Aug. 15, 1991 Low sulfur gasoline of relatively high octane number is produced from cracked, sulfur-containing olefinic naphthas by hydrodesulfurization followed by treatment over an acidic catalyst comprising zeolite j3 with a metal hydrogenation component, preferably a mild hydrogenation component such as molybdenum. The treatment over the acidic catalyst in the second step restores the octane loss, which takes place as a result of the hydrogenative treatment and results in a low sulfur gasoline product with an octane number comparable to that of the feed naphtha.

Preparation

of glycerol

SEPARATION

PROCESSES

for the separation

for the separation

of diethylnaphthalene

iso-

K. Sato; T. Masuda; F. Matsuda et al. Organ0 K.K.; Shinnittetsu Kagaku Jpn. Kokai Tokkyo Koho 95,61,943, Mar. 7, 1995; Appl. Aug. 25, 1993 A method for the separation of diethylnaphthalene isomers involves the use of a chromatographic process. For example, a mixture containing 2,6-diethylnaphthalene (I) 36 wt%, 1,3diethylnaphthalene (II) 13 wt%, 2,7-diethylnaphthalene (III) 35 wt%, and others 16 wt% was subjected to a separation process using a chromatographic apparatus comprising 12 columns using K-modified Y zeolite and pxylene solvent. The raffinate contained I 67.4 wt%, II 22.2 wt%, Ill 0.8 wt%, and others 9.6 wt%.

Hydrocarbon

adsorbents

for exhaust

gases

H. Yamada; T. Ueoka; A. Takami et al. Mazda Motor Corp. Ger. Offen. 4,435,073, Apr. 6, 1995; Jpn. Appl. Sept. 30, 1993 Powdered silicates of differing pore diameters with lomembered rings and 12.membered rings, supported on zeolites also containing CeO, and Pd (Pt, Rh), are used as hydrocarbon adsorbents in exhaust gas catalysts for NO, removal.

Purification adsorbents

of formaldehyde-containing

gases by zeolite

M. Harada; S. Morishita; Y. Noda et al. Toyo Seikan Kaisha Ltd.; Tosoh Corp.; Tosoo Zeooru K.K. Jpn. Kokai Tokkyo Koho 95,80,248, Mar. 28, 1995; Appl. Sept. 16, 1993 The method comprises contacting HCHO-containing gases with honeycomb adsorbents containing 250 kg/m3 ZSM-5 zeolites

318

Zeolites

16:316-320,

Amino acids and their salts as carbonate zeolite-containing detergents B. Kottwitz; H. Dolhaine; H. Upadek He&e/ K.-G.a.A. Ger. Offen. 4,319,578, Dec. 15, 1994;

Appl.

substitutes

June

in

14, 1993

An amino acid or its salt (e.g., Na glycinate) is used with a zeolite builder in carbonateand phosphate-free laundry detergents, giving reduced incrustations on fabrics and washing appliances compared with detergents containing an alkali metal carbonate instead of the amino acid or salt.

Granular laundry lected builders

detergent

E.J. Pancheri Procter and Gamble U.S. 5,378,388, Jan.

compositions

Co. 3, 1995;

Appl.

June

containing

se-

25, 1993

The title compositions show optimum cleaning performance when thev contain a builder mixture comprising a crystallline aluminosiiicate 3.5-4.5, a crystalline layered Na silicate (e.g., SKS 6) 1, and citric acid (or salt) 1 part.

of mxylene

T. Shioda; H. Yasuda; N. Saito et al. Mitsubishi Kagaku K.K. Jpn. Kokai Tokkyo Koho 95,76,531, Mar. 20, 1995; Appl. Sept. 7, 1993 m-Xylene is separated from a mixture of C, aromatic hydrocarbons by a chromatographic process using a crystalline zeolite adsorbent followed by distillation. For example, a raffinate obtained from a pxylene plant was treated chromatographically using KY zeolite as adsorbent and pseudocumene as solvent to give a m-xylene-rich fraction that was then distilled.

Method mers

DETERGENTS

ethers

C. Dewattines; H. Hinnekens Fina Research S.A. Eur. Pat. Appl. 649,829, Apr. 26, 1995; Belgian Appl. Oct. 15, 1993 A process for the preparation of glycerol ethers comprises condensation of glycerol with a branched olefin (e.g., isobutylene) in the presence of an acidic zeolite with large pores, an interconnected network of channels, and a Si/AI ratio >5.

Method

with SiO,/AI,O, molecular ratio 2100 for 0.2-0.5 s. The method, especially suitable for the treatment of organic solventcontaining gases (e.g., painting waste gases), removes low Iconcentration HCHO efficiently with safety.

1996

Detergent laundering

compositions

E. Smulders; G. Vogt; Henkel K.-G.a.A. Ger. Offen. 4,320,851,

inhibiting

dye transfer

G. Nienhaus Jan.

The title compositions builders selected from layered silicates.

5, 1995; Appl.

contain crystalline

Builder compositions ing incrustations

nonionic zeolites

in laundry

The title compositions comprise a layered a phosphate, and, optionally, a zeolite.

G. Meine; H. Casper; Henkel K.-G.a.A. Ger. Offen. 4,325,880,

with

zeolite

builder

J. Poethkow

et al.

Feb.

9, 1995;

June

23, 1993

surfactant, (e.g., zeolite

detergents

J. Poethkow; B. Kottwitz; B. Stevermann Henkel K.-G.a.A. Ger. Offen. 4,324,807, Jan. 26, 1995; Appl.

Use of cellulase

during

Appl.

soap.. NaA)

and and

for prevent-

July

23, 1993

silicate

(e.g.,

SKS 61,

in detergents

Aug.

2, 1993

A cellulase is used in laundry detergents containing crystalline zeolite builders to reduce incrustations during repeated washing of fabrics.

MISCELLANEOUS Zeolite-containing blended plastics S. Bourgigot; P. Breant; Elf Atochem S.A. Eur. Pat. Appl. 629,678, 1993

APPLICATIONS flame

retardant

R. Delobel Dec.

compositions

for

et al.

21, 1994;

French

Appl.

June

18,

Blended plastics contain 21 dehydrating agent and 21 zeolite. The blended plastics are selected from polyamides and polyolefins. The zeolites are selected from zeolites A, X, Y, L, ZSM. and ZM, and the preferred dehydrating agent is ammonium polyphosphate.