1, 3-butadiene separating material, and separation method using said separating material

Patent metadata

Field	Value
Publication number	US-9856190-B2
Application number	US-201414906919-A
Country	US
Kind code	B2
Filing date	Jul 1, 2014
Priority date	Jul 26, 2013
Publication date	Jan 2, 2018
Grant date	Jan 2, 2018

Abstract

A separating material superior to conventional separating materials, and a separation method are provided, with which 1,3-butadiene is selectively separated and recovered from a mixed gas including 1,3-butadiene and C4 hydrocarbons other than 1,3-butadiene. A metal complex, which comprises a dicarboxylic acid compound (I) (see (I) below) represented by general formula (I), an ion of a metal such as beryllium, and a bipyridyl compound (II) represented by general formula (II), namely L-Z-L (II) (see (L) below), is characterized by including, as the dicarboxylic acid compound (I), at least two different dicarboxylic acid compounds (I). The metal complex is used as a 1,3-butadiene separating material. Formula (I) L is represented by any of the compounds below. Formula (L).

First claim

The invention claimed is:

1. A 1,3-butadiene separating material that selectively adsorbs 1,3-butadiene from a mixed gas containing 1,3-butadiene and a hydrocarbon having four carbon atoms other than 1,3-butadiene, comprising a metal complex consisting of:
a dicarboxylic acid compound (I) represented by the following general formula (I):

wherein X represents a carbon atom or nitrogen atom, Y represents a hydrogen atom, optionally substituted alkyl group having 1 to 4 carbon atoms, alkenyl group having 2 to 4 carbon atoms, alkoxy group having 1 to 4 carbon atoms, formyl group, acyloxy group having 2 to 4 carbon atoms, hydroxyl group, alkoxycarbonyl group having 2 to 4 carbon atoms, nitro group, cyano group, amino group, monoalkylamino group having 1 to 4 carbon atoms, dialkylamino group having 2 to 4 carbon atoms, acylamino group having 2 to 4 carbon atoms, sulfo group, sulfonate group, carboxyl group or halogen atom in the case X represents a carbon atom or Y is not present in the case X represents a nitrogen atom, and R 1 , R 2 and R 3 respectively and independently represent a hydrogen atom, optionally substituted alkyl group having 1 to 4 carbon atoms or halogen atom;
an ion of at least one type of metal selected from the group consisting of beryllium, magnesium, calcium, strontium, barium, titanium, vanadium, chromium, manganese, iron, ruthenium, cobalt, rhodium, nickel, palladium, platinum, copper, zinc and cadmium; and
a dipyridyl compound (II) represented by the following general formula (II):
L-Z-L  (II)

wherein L is represented by any of the following formulas:

wherein R 4 , R 5 , R 6 and R 7 respectively and independently represent a hydrogen atom, alkyl group having 1 to 4 carbon atoms or a halogen atom, and Z represents —CR8R9-CR10R11- (wherein R 8 , R 9 , R 10 and R 11 respectively and independently represent a hydrogen atom, alkyl group having 1 to 4 carbon atoms, hydroxyl group or halogen atom), an alkylene group having 3 to 4 carbon atoms, —CH═CH—, —C≡C—, —S—S—, —N═N—, —O—CH 2 —, —NH—CH 2 — or —NHCO—); wherein
two or more different types of the dicarboxylic acid compound (I) are contained as the dicarboxylic acid compound (I),
wherein the dicarboxylic acid compound (I) comprises two or more dicarboxylic acids selected from the group consisting of isophthalic acid, 5-methylisophthalic acid 5-tert-butylisophthalic acid, 5-methoxyisophthalic acid, 5-nitroisophthalic acid, sodium 5-sulfoisophthalate, lithium 5-sulfoisphthalate and trimesic acid, and
wherein the metal complex has a structure that is a triply interpenetrating pseudo-diamondoid framework.

2. The 1,3-butadiene separating material according to claim 1 , wherein a combination of the dicarboxylic acid compounds (I) is 5-nitroisophthalic acid and sodium 5-sulfoisophthalate, 5-nitroisophthalic acid and lithium 5-sulfoisophthalate, or 5-nitroisophthalic acid and 5-tert-butylisophthalic acid.

3. The 1,3-butadiene separating material according to claim 1 , wherein the dipyridyl compound (II) is at least one selected from the group consisting of 1,2-di(4-pyridyl)ethylene, 1,2-di(4-pyridyl)ethane, 4,4′-azobispyridine and 4,4′-dipyridyl disulfide.

4. The 1,3-butadiene separating material according to claim 1 , wherein the metal ion is at least one selected from the group consisting of a cobalt ion, nickel ion and zinc ion.

5. The 1,3-butadiene separating material according to claim 1 , wherein the hydrocarbon having four carbon atoms other than 1,3-butadiene is at least one selected from the group consisting of 1-butene, isobutene, trans-2-butene, cis-2-butene, isobutane and n-butane.

6. A 1,3-butadiene separation method comprising: an adsorption step for contacting a separating material with a mixed gas containing 1,3-butadiene and a hydrocarbon having four carbon atoms other than 1,3-butadiene and selectively adsorbing 1,3-butadiene onto the separating material, followed by a regeneration step for desorbing the 1,3-butadiene adsorbed onto the separating material from the separating material and capturing the released 1,3-butadiene, wherein the separating material comprises a metal complex consisting of:
a dicarboxylic acid compound (I) represented by the following general formula (I):

wherein X represents a carbon atom or nitrogen atom, Y represents a hydrogen atom, optionally substituted alkyl group having 1 to 4 carbon atoms, alkenyl group having 2 to 4 carbon atoms, alkoxy group having 1 to 4 carbon atoms, formyl group, acyloxy group having 2 to 4 carbon atoms, hydroxyl group, alkoxycarbonyl group having 2 to 4 carbon atoms, nitro group, cyano group amino group, monoalkylamino group having 1 to 4 carbon atoms, dialkylamino group having 2 to 4 carbon atoms, acylamino group having 2 to 4 carbon atoms, sulfo group, sulfonate group, carboxyl group or halogen atom in the case X represents a carbon atom or Y is not present in the case X represents a nitrogen atom, and R 1 , R 2 and R 3 respectively and independently represent a hydrogen atom, optionally substituted alkyl group having 1 to 4 carbon atoms or halogen atom,
an ion of at least one type of metal selected from the group consisting of beryllium, magnesium, calcium, strontium, barium, titanium, vanadium, chromium, manganese, iron, ruthenium, cobalt, rhodium, nickel, palladium, platinum, copper, zinc and cadmium; and
a dipyridyl compound (II) represented by the following general formula (II)
L-Z-L  (II)

wherein L is represented by any of the following formulas:

wherein R 4 , R 5 , R 6 and R 7 respectively and independently represent a hydrogen atom, alkyl group having 1 to 4 carbon atoms or a halogen atom, and Z represents —CR 8 R 9 CR 10 R 11 — (wherein R 8 , R 9 , R 10 , R 11 respectively and independently represent a hydrogen atom, alkyl group having 1 to 4 carbon atoms, hydroxyl group or halogen atom), an alkylene group having 3 to 4 carbon atoms, —CH═CH—, —C≡C—, —S—S—,—N═N—, —O—CH 2 —, —NH—CH 2 — or —NHCO—); wherein
two or more different types of the dicarboxylic acid compound (I) are contained as the dicarboxylic acid compound (I).

7. The 1,3-butadiene separation method according to claim 6 , wherein the separation method is pressure swing adsorption.

8. The 1,3-butadiene separation method according to claim 6 , wherein the separation method is temperature swing adsorption.

9. A 1,3-butadiene separation method, comprising: contacting a mixed gas containing 1,3-butadiene and a hydrocarbon having four carbon atoms other than 1,3-butadiene with a separation membrane and selectively allowing the 1,3-butadiene to pass through the separation membrane to obtain a gas having a higher 1,3-butadiene concentration than the mixed gas, wherein the separation membrane comprises a porous support and a 1,3-butadiene separating material attached to the surface of the porous support, wherein the 1,3-butadiene separating material comprises a metal complex consisting of:
a dicarboxylic acid compound (I) represented h the following general formula (I);

wherein X represents a carbon atom or nitrogen atom, Y represents a hydrogen atom, optionally substituted alkyl group having 1 to 4 carbo

Assignees

• Showa Denko Kk

Inventors

• Kishida Keisuke
• Watanabe Yoshihiro
• Okumura Yoshikuni

Classifications

• B01J20/3491

  by pressure treatment · CPC title

• B01D69/10

  Supported membranes; Membrane supports · CPC title

• B01D53/0462

  Temperature swing adsorption · CPC title

• B01D2256/24

  Hydrocarbons · CPC title

• B01J20/3425

  of sorbents or filter aids comprising organic materials · CPC title