Process for making formic acid utilizing higher-boiling formate esters

Patent metadata

Field	Value
Publication number	US-10544077-B2
Application number	US-201816043329-A
Country	US
Kind code	B2
Filing date	Jul 24, 2018
Priority date	Aug 2, 2017
Publication date	Jan 28, 2020
Grant date	Jan 28, 2020

Abstract

Disclosed is a process for recovering formic acid from a formate ester that allows for recovery of a formic acid product comprising greater than 75 wt. % formic acid. Disclosed is also a process for producing formic acid by carbonylating a carrier alcohol, hydrolyzing the formate ester of the carrier alcohol, and recovering a formic acid product comprising greater than 70 wt. % formic acid. Discloses are carrier alcohols that enable more favorable hydrolysis equilibriums and/or distillation sequences.

First claim

We claim:

1. A process for recovering formic acid from a formate ester mixture, wherein the process comprises
a) feeding the formate ester mixture and water to a hydrolysis zone, wherein the formate ester mixture comprises a formate ester of a carrier alcohol and the carrier alcohol;
b) hydrolyzing the formate ester mixture in the hydrolysis zone to produce a hydrolysis effluent comprising the formate ester of the carrier alcohol, formic acid, and the carrier alcohol; and
c) feeding the hydrolysis effluent to a distillation zone and removing a formic acid product and an alcohol/ester stream, wherein the formic acid product comprises greater than 75 wt. % formic acid and the alcohol/ester stream comprises less than 5 wt. % formic acid,

wherein the distillation zone comprises a first distillation column and the hydrolysis effluent is fed to the first distillation column,
wherein (1) each of the formate ester of the carrier alcohol, the carrier alcohol, and any azeotrope formed by the formate ester of the carrier alcohol and the carrier alcohol has a boiling point temperature higher than the formic acid/water azeotrope boiling point temperature, (2) the formate ester of the carrier alcohol and formic acid do not form an azeotrope, and (3) the carrier alcohol and formic acid do not form an azeotrope, with (1)-(3) being satisfied at an operating pressure of the first distillation column, and
wherein the carrier alcohol is selected from the group consisting of ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 2,3-butanediol, 1,4-butanediol, 1,2-cyclohexanediol, 1,3-cyclohexanediol, 1,4-cyclohexanediol, 1,2-phenylenedimethanol, 1,3-phenylenedimethanol, 1,4-phenylenedimethanol, 1,2-cyclohexanedimethanol, 1,3-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, 2,2,4-trimethylpentane-1,3-diol, glycerol, trimethylolethane, trimethylolpropane, trimethylolbutane, diethylene glycol, triethylene glycol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monopropyl ether, diethylene glycol monobutyl ether, 1-ethoxy-2-propanol, 1-propoxy-2-propanol, 1-butoxy-2-propanol, 2-ethoxy-1-propanol, 2-propoxy-1-propanol, 2-butoxy-1-propanol, ethylene glycol monoformate, diethylene glycol monoformate, 2-hydroxy-propylformate, [2,2,2]-bicyclo-1,4-octanediol, adamantine-1,3,5,7-tetraol, and adamantane-1,3-diol.

2. The process of claim 1 , wherein the formic acid product comprises greater than 95 wt. % formic acid.

3. The process of claim 1 , wherein the alcohol/ester stream comprises less than 0.5 wt. %, formic acid and less than 200 ppm water.

4. The process of claim 1 , wherein the formate ester mixture comprises at least 50 wt. % formate ester of the carrier alcohol.

5. The process of claim 1 , wherein a molar ratio of water:formate ester of the carrier alcohol fed to the hydrolysis zone ranges from 1:1 to 3:1.

6. The process of claim 1 , wherein the formate ester of the carrier alcohol is selected from the group consisting of formate ester of ethylene glycol, formate ester of diethylene glycol, formate ester of diethylene glycol monomethyl ether, formate ester of 1,2-propanediol, formate ester of 1-propoxy-2-propanol, formate ester of 2-hydroxy-propanol, formate ester of 1-ethoxy-2-propanol and formate ester of 1 butoxy-2-propanol and the carrier alcohol is selected from the group consisting of ethylene glycol, diethylene glycol, diethylene glycol monomethyl ether, 1,2-propanediol, 1-propoxy-2-propanol, 2-hydroxy-propanol, 1-ethoxy-2-propanol and 1-butoxy-2-propanol.

7. The process of claim 1 , wherein a first distillate from the first distillation column comprises a higher weight percent of formic acid than a weight percent of formic acid in a formic acid/water azeotrope at the operating pressure of the first distillation column; the process further comprising
d) feeding the first distillate to a product purification column and removing the formic acid product as a product purification column distillate and removing a product purification column bottoms comprising formic acid in an amount within 7 weight percentage points of an amount of formic acid in a formic acid/water azeotrope at an operating pressure of the product purification column; and
e) feeding the product purification column bottoms to the first distillation column.

8. The process of claim 1 wherein an overall conversion of the formate ester of the carrier alcohol in the formate ester mixture to formic acid in the formic acid product ranges from 40% to 90%.

9. The process of claim 1 , wherein the first distillation column has a base temperature from 60° C. to 150° C., the operating pressure of the first distillation column ranges from 0.4 bara to 4 bara, and the first distillation column comprises from 10 to 40 theoretical stages.

10. A process for producing formic acid, wherein the process comprises,
a) feeding carbon monoxide, a fresh feed, and a catalyst feed to a carbonylation zone, wherein the fresh feed comprises a carrier alcohol, carbonylating the carrier alcohol to produce a formate ester of the carrier alcohol, and removing a carbonylation effluent comprising the formate ester of the carrier alcohol, the carrier alcohol, and a homogeneous catalyst;
b) feeding the carbonylation effluent to a catalyst separation zone and removing a catalyst mixture and a formate ester mixture, wherein the catalyst mixture comprises the homogeneous catalyst and the carrier alcohol, and wherein the formate ester mixture comprises the formate ester of the carrier alcohol;
c) feeding the formate ester mixture and water to a hydrolysis zone, hydrolyzing the formate ester of the carrier alcohol, and removing a hydrolysis effluent comprising the formate ester of the carrier alcohol, formic acid, and the carrier alcohol; and
d) feeding the hydrolysis effluent to a distillation zone and removing a formic acid product and an alcohol/ester stream, wherein the formic acid product comprises greater than 75 wt. % formic acid and the alcohol/ester stream comprises less than 5 wt. % formic acid;

wherein the distillation zone comprises a first distillation column and the hydrolysis effluent is fed to the first distillation column,
wherein (1) each of the formate ester of the carrier alcohol, the carrier alcohol, and any azeotrope formed by the formate ester of the carrier alcohol and the carrier alcohol has a boiling point temperature higher than the formic acid/water azeotrope boiling point temperature, (2) the formate ester of the carrier alcohol and formic acid do not form an azeotrope, and (3) the carrier alcohol and formic acid do not form an azeotrope, with (1)-(3) being satisfied at the operating pressure of the first distillation column, and
wherein the carrier alcohol is selected from the group consisting of ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 2,3-butanediol, 1,4-butanediol, 1,2-cyclohexanediol, 1,3-cyclohexanediol, 1,4-cyclohexanediol, 1,2-phenylenedimethanol, 1,3-phenylenedimethanol, 1,4-phenylenedimethanol, 1,2-cyclohexanedimethanol, 1,3-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, 2,2,4-trimethylpentane-1,3-diol, glycerol, trimethylolethane, trimethylolpropane, trimethylolbutane, diethylene glycol, triethylene glycol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monopropyl ether, diethylene glycol monobutyl ether, 1-ethoxy-2-propanol, 1-propoxy-2-propanol, 1-butoxy-2-propanol, 2-ethoxy-1-propanol, 2-propoxy-1-propanol, 2-butoxy-1-propanol, ethylene glycol monoformate, diethylene glycol monoformate, 2-hydroxy-propylformate, [2,2,2]-bicyclo-1,4-octanediol, adamantine-1,3,5,7-tetraol, and adamant

Assignees

• Eastman Chem Co

Inventors

• Barnicki Scott Donald
• Hembre Robert Thomas
• Chakraborty Sumit
• Osborne Vickie Haygood
• Laningham Michael Richard
• Van De Vyver Stijn

Classifications

• C07C51/12

  on an oxygen-containing group in organic compounds, e.g. alcohols · CPC title

• C07C51/44

  by distillation · CPC title

• C07C51/46

  by azeotropic distillation · CPC title

• C07C51/09 Primary

  from carboxylic acid esters or lactones · CPC title

• C07C53/02

  Formic acid · CPC title