Methanol production from methane and carbon dioxide

Information

  • Patent Grant
  • 10040737
  • Patent Number
    10,040,737
  • Date Filed
    Tuesday, July 14, 2015
    8 years ago
  • Date Issued
    Tuesday, August 7, 2018
    5 years ago
  • Inventors
  • Examiners
    • Bakshi; Pancham
    • Luderer; Mark R
    Agents
    • Young Basile Hanlon & MacFarlane, P.C.
Abstract
Carbon dioxide is reacted with methane in a free radical reaction to produce methanol and carbon monoxide. A system for producing carbon dioxide as a feed ingredient for the process through electric power generator is disclosed.
Description
FIELD OF THE INVENTION

Existing technology relates to a process for the production of methanol wherein carbon dioxide is reacted with methane.


BACKGROUND

Existing technology is capable of producing methanol from methane and carbon dioxide, however it is a long, tedious and expensive undertaking. Multiple reactions are required for which dedicated equipment is needed. Like many organic preparations, conversions are low and repeated separations are involved. At the heart of the process is the generation of synthesis gas with all that such chemistry implies: high pressure, elevated temperatures and finicky catalysts.


To illustrate the known procedures for producing methanol, the following equations are helpful.

CO2+3 H2→CH3OH+H2O  1.
CH4+H2O→CO+3 H2  2.


Equation no. 1 represents the classical reaction for producing methanol from synthesis gas. The reaction requires moderate temperature, high pressure and a catalyst based on a copper-zinc compound.


Equation no. 2 shows the formation of synthesis gas by methane steam reforming. High temperatures are required as well as a catalyst typically comprising nickel.


When equations 1 and 2 are combined, the following relationship is obtained.

CH4+CO2→CH3OH+CO  3.


The expression represents the goal of the exercise, namely, the production of methanol from methane and carbon dioxide. Nevertheless, the procedure is indirect and necessitates substantial investment.


Because widespread recovery of carbon dioxide is not practiced, a source of oxygen is required for current operations. Thus, air separation units are needed to provide oxygen to existing methanol facilities. This requirement presents an added cost.


As priorities begin to shift toward more environmentally friendly practices, carbon dioxide will likely assume greater attention. Its recovery and disposition may become mandatory. With this trend in mind, there is an incentive to develop improved technology for the production of methanol using carbon dioxide as a feedstock. This and other objectives of the present invention will become apparent from the discussion that follows and the illustration therewith.





BRIEF DESCRIPTION OF THE DRAWING


FIG. 1 is a rendering of the process indicating the feed streams to a reactor and the product produced; and



FIG. 2 shows a practical application of the present invention in the production of electric power.





DETAILED DESCRIPTION

The present invention takes advantage of two factors: first, the perceived urgency to recover and sequester large quantities of carbon dioxide to mitigate the effects of global warming; second, the availability of new supplies of cheap natural gas from fracking, take advantage of these two factors by reacting. carbon dioxide with methane gas to make methanol.


The chemistry works in favor of a useful product. The free radical reactions that take place by combining methane with carbon dioxide are shown as follows.

CH4—+CH3+H  4.
CH4+OH—+CH30H+H  5.
CO2+H—+CO+OH  6.
CH3+OH—+CH30H  7.


In the above series of equations, equation no. 4 represents the initiation reaction. Equation nos. 5 and 6 represent the chain reactions. And equation no. 7 is the terminal reaction.


As in any free radical phenomena, the overall reaction is extremely fast because the chain reactions occur with lightning speed. No catalyst is required under these conditions.


When equation nos. 5 and 6 are combined, the net result is the following.

CH4+CO2→CH3OH+CO  8.


This is the same outcome as can be obtained by existing technology (equation no. 3), except that the present invention achieves the result in a one-step process that proceeds with high efficiency.


In the free radical reactions that take place, the radicals H and OH are the same ones that occur in the combustion of fuels. The methanol product is relatively stable as suggested by the process for formaldehyde, which requires a catalyst at 600° to 650° C. to decompose methanol. Finally, carbon monoxide can be thought of as a sink in the reaction mechanism. The bond dissociation energy for C—O is 1076.5 kJ/mol, exceeding by far other bond energies.


The conditions for the free radical reaction of the present invention are critical. Near atmospheric pressure is assumed. This mirrors combustion reactions. The temperatures of the reaction must be sufficiently high to sever the chemical bonds. From experience, the temperature is in the range of 600° to 1000° C. The holding time at this temperature is extremely short, thus requiring a flow reactor design.


The simplicity of the present invention is illustrated by FIG. 1. Reactor 1, for example, comprises a coil of hollow tubing through which the reactants flow. This coil is heated in a furnace. The exit gases are quenched and product is separated at 3 from carbon monoxide.


An application of the present invention is shown in FIG. 2 for electric power generation. Turbine 4 is driven by combustion gases. Absorption Column 5 and Stripping Column 6 recover carbon dioxide from the flue gas. Methane and carbon dioxide produce methanol and carbon monoxide in Reactor 7. The separate units are integrated so that the only product is methanol.


SUMMARY

Methyl alcohol or methanol is produced from methane and carbon dioxide in a free radical reaction. In the process, the two reactants are mixed and heated to a high temperature and rapidly quenched, thereby producing methanol and carbon monoxide. The methanol is separated and purified from any byproducts by, for example, distillation.


While the invention has been described in connection with what is presently considered to be the most practical and preferred embodiment, it is to be understood that the invention is not to be limited to the disclosed embodiments but, on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims, which scope is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures as is permitted under the law.

Claims
  • 1. A process for the production of methanol and carbon monoxide from methane and carbon dioxde in a single step using a flow reactor and comprising a non-catalytic free radical reaction involving CH3• and H•, ØH• as reactive free radicals conducted at about one atmosphere pressure and at a temperature in the range of 600° C. to 1000° C.
  • 2. A process for the production of methanol comprising the steps of: a. mixing carbon dioxide with methane at a temperature of between about 600° C. and 1000° C. using a flow reactor and in the absence of a catalyst in a free radical reaction to produce methanol and carbon monoxide; andb. separating the carbon monoxide from the methanol.
  • 3. The process of claim 2 wherein the reactants carbon dioxide and methane are quenched after high temperature mixing.
  • 4. A process for the production of electric powers comprising the steps of: a. driving a turbine by combustion gas to produce flue gases;b. recovering carbon dioxide from flue gases produced in step (a); andc. using the carbon dioxide in the process of claim 3 to produce methanol.
US Referenced Citations (36)
Number Name Date Kind
1849844 Joseph et al. Mar 1932 A
2276192 Hanford et al. Mar 1942 A
3497436 Burleson et al. Feb 1970 A
4364915 Proctor Dec 1982 A
4562174 Stiles Dec 1985 A
4825004 Rutzen et al. Apr 1989 A
4913842 Yoneoka et al. Apr 1990 A
5070016 Hallberg Dec 1991 A
5395991 Scarlett et al. Mar 1995 A
5449696 Dandekar et al. Sep 1995 A
5453412 Deckers et al. Sep 1995 A
5663429 Yamaseki et al. Sep 1997 A
6114279 Fukui et al. Sep 2000 A
6140545 Merger et al. Oct 2000 A
6274108 Fujii et al. Aug 2001 B1
6452058 Schweizer et al. Sep 2002 B1
6486368 Zhou et al. Nov 2002 B1
6632330 Colley et al. Oct 2003 B1
7199276 Sher et al. Apr 2007 B2
7214721 Eastland May 2007 B2
7288689 Janssen et al. Oct 2007 B2
7696390 Stauffer Apr 2010 B2
7906559 Olah Mar 2011 B2
7977272 Miller et al. Jul 2011 B2
8323602 Wright et al. Dec 2012 B2
8440868 Stauffer May 2013 B2
8512460 Moniwa et al. Aug 2013 B2
8581010 Stauffer Nov 2013 B2
8728423 Iijima et al. May 2014 B2
8795415 Katz et al. Aug 2014 B2
8961664 Nakayama et al. Feb 2015 B2
9155991 Ogawa et al. Oct 2015 B2
20070282018 Jenkins et al. Dec 2007 A1
20080269519 Miller et al. Oct 2008 A1
20100261125 Olah et al. Oct 2010 A1
20120259145 Stauffer Oct 2012 A1
Foreign Referenced Citations (3)
Number Date Country
362746 Oct 1922 DE
WO2008080767 Jul 2008 WO
WO2014096226 Jun 2014 WO
Non-Patent Literature Citations (3)
Entry
European Search Report, EP 09 25 1524, dated Sep. 1, 2009.
International Search Report, PCT/EP2007/063570, dated Dec. 3, 2008.
V.N. Ipatieff, G. S. Monroe: “Synthesis of Methanol from Carbon Dioxide and Hydrogen over Copper-Alumina Catalysts. Mechanism of Reaction” J. AM. Chem. Soc., vol. 67, No. 12, Dec. 1945 (Dec. 1945), pp. 2168-2171, SP002543626.
Related Publications (1)
Number Date Country
20170015611 A1 Jan 2017 US