US1067665A - Process for the manufacture of formaldehyde. - Google Patents

Process for the manufacture of formaldehyde. Download PDF

Info

Publication number
US1067665A
US1067665A US51861209A US1909518612A US1067665A US 1067665 A US1067665 A US 1067665A US 51861209 A US51861209 A US 51861209A US 1909518612 A US1909518612 A US 1909518612A US 1067665 A US1067665 A US 1067665A
Authority
US
United States
Prior art keywords
formaldehyde
methyl alcohol
manufacture
yield
catalyzer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US51861209A
Inventor
Methodie Jwanowitsch Kusnezow
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
PERTH AMBOY CHEMICAL WORKS
Original Assignee
PERTH AMBOY CHEMICAL WORKS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by PERTH AMBOY CHEMICAL WORKS filed Critical PERTH AMBOY CHEMICAL WORKS
Priority to US51861209A priority Critical patent/US1067665A/en
Application granted granted Critical
Publication of US1067665A publication Critical patent/US1067665A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/32Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
    • C07C45/37Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups
    • C07C45/38Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of >C—O—functional groups to >C=O groups being a primary hydroxyl group

Definitions

  • the catalytic material is preferably pre pared from a sheet of fine-meshed silverwire netting by coiling it up into rolls or by piling up a considerable number of la yers of the same and compressing them, or by precipitating the silver from a solution of a silver salt, for instance, from an ammoniacal solution of silver nitrate and then applying it to a suitable non-catalytic base or support, such as asbestos-Wool, Woven asbestos-fabric or pumice-stone, which has been first relieved of organic substances by calcination.
  • the catalytic material is introduced into the catalyzing apparatus of usual construction, after which the apparatus is strongly heated and the mixture of methylalcohol vapors and air is conducted over the catalytic material.
  • the external heating of the catalyzer may be interrupted.
  • the reaction mixture is now conducted continuously over the catalytic mass, care being taken, that the temperature of the apparatus will not drop too low (not below 250 C.) because otherwise the reaction would be interrupted unless heat be supplied from outside.
  • the yield is almost equal to the theoretical quantity, which is not ossible in using copper as a catalyzer. I the latter is used, a tolerably good yield may be obtained only by conducting over the cat-alyzer also a large excess of methyl alcohol vapor, a portion of which remains undecomposed, but in that case the methyl alcohol must be separated from the reaction mixture by distillation, entailing expense and Waste of formaldehyde and methyl alcohol. This is at present the general standard of the art of making formaldehyde by oxidizing methyl alcohol by means of a copper catalyzer.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

UNITED sratrnsrarnur UM ICE.
METHODIE JWANOWITSCH xusunzow. or oHARKow, RUSSIA, ASSIGNOR, BY MESNE ASSIGNMENTS, r'o PEB'IH kMBOY CHEMICAL WORKS, A CORPORATION 01 NEW Patented July 15, 11913.
JERSEY.
PROCESS FOR THE MANUFACTURE 01' FORMALDEHYDE.
1 067 665. Specification of Letters Patent.
No Drawing.
Application filed September 20, 19 9. Serial No. 518,612.
To all whom it may concern:
lie it known that I, Mu'rnoois JWANowrrscu Kvsnnzow, chemist, a subject of the lhupcror of Russia, residing at Charkow, Russia. have invented a certain new and useful Process for the llrlanut'acture of Formaldehyde, of which the following is a specification.
The usual process for producing formaldehyde consists in passing heated air through methyl alcohol and conducting the mixture of methyl alcohol vapors and air thus obtained over heated copper. Besides copper, platinum, pumice stone and other materials have been tried as catalyzers, but without success, on account of the interior yield obtained with these substances. I have found that metallic silver is a more advantageous catalyzer than copper and the other materials hitherto used.
The catalytic material is preferably pre pared from a sheet of fine-meshed silverwire netting by coiling it up into rolls or by piling up a considerable number of la yers of the same and compressing them, or by precipitating the silver from a solution of a silver salt, for instance, from an ammoniacal solution of silver nitrate and then applying it to a suitable non-catalytic base or support, such as asbestos-Wool, Woven asbestos-fabric or pumice-stone, which has been first relieved of organic substances by calcination. The catalytic material is introduced into the catalyzing apparatus of usual construction, after which the apparatus is strongly heated and the mixture of methylalcohol vapors and air is conducted over the catalytic material. As soon as the reaction has been started, the external heating of the catalyzer may be interrupted. The reaction mixture is now conducted continuously over the catalytic mass, care being taken, that the temperature of the apparatus will not drop too low (not below 250 C.) because otherwise the reaction would be interrupted unless heat be supplied from outside.
A small portion of the methyl alcohol passes undecomposed through the contact substance, but as the aqueous solution of formaldehyde formed in commerce always contains methyl alcohol, the reaction mixt ure produced may be utilized immediately.
The yield is almost equal to the theoretical quantity, which is not ossible in using copper as a catalyzer. I the latter is used, a tolerably good yield may be obtained only by conducting over the cat-alyzer also a large excess of methyl alcohol vapor, a portion of which remains undecomposed, but in that case the methyl alcohol must be separated from the reaction mixture by distillation, entailing expense and Waste of formaldehyde and methyl alcohol. This is at present the general standard of the art of making formaldehyde by oxidizing methyl alcohol by means of a copper catalyzer. Both the expenses for labor, etc., and the loss of raw material sustained in the various manipulations present considerable ditficulties and objections in commercial practice and render the control of the process very inconvenient, a tolerable yield only being obtained owing to over-oxidation, and hence, the general efiiciency of the copper contact process must be called a moderate one. Contrary to these shortcomings experienced in the commercial ractice of the old process, my invention a ords facilities which cannot be realized by the old process, most painstaking experiments under the various conditions having amply demonstrated that the highest and always reliable yield in formaldehyde loan only be attained by abandoning the present universally adopted copper catalyzer for the metallic silver catalyzer.
. In my process, it is immaterial to the yield, whether one runs the process with only a slight excess of methyl alcohol, or Whether one even operates with a gas mixture the constituents of which exist in practically theoretical proportions.
This fact is of vital importance to the industry of formaldehyde manufacture and represents a great advance, particularly in view of the above cited facts showing that the yield is almost theoretical and that the portion of methyl alcohol which escapes the reaction is so small as to render the reaction mixture immediately available for commercial purposes. The efi'iciency of my process of oxidizing methyl alcohol to formaldehyde by applying silver as a catalyzer is far suover heated metallic silver, substantially as 10 perior to that of any other process known at described. the present time, as the process may be so i In testimony gwhereof I have hereunto set well defined as to guarantee a very high and my hand in presence of'tw'o subscribing wituniform yield.
' lnesses. What I claim is:
METHODIE JWANOWIISCH KUSNEZOW. The proeess'for the manufacture of for- Witnesses: maldehyde, which consists in conducting a PAUL SOROLOFF, mixture of methyl aleohol vapors and air PETER Amuionorr.
US51861209A 1909-09-20 1909-09-20 Process for the manufacture of formaldehyde. Expired - Lifetime US1067665A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US51861209A US1067665A (en) 1909-09-20 1909-09-20 Process for the manufacture of formaldehyde.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US51861209A US1067665A (en) 1909-09-20 1909-09-20 Process for the manufacture of formaldehyde.

Publications (1)

Publication Number Publication Date
US1067665A true US1067665A (en) 1913-07-15

Family

ID=3135906

Family Applications (1)

Application Number Title Priority Date Filing Date
US51861209A Expired - Lifetime US1067665A (en) 1909-09-20 1909-09-20 Process for the manufacture of formaldehyde.

Country Status (1)

Country Link
US (1) US1067665A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2682560A (en) * 1952-11-22 1954-06-29 Eastman Kodak Co Conversion of organic hydroxy compounds to carbonyl derivatives
US4382149A (en) * 1980-11-05 1983-05-03 Borden, Inc. Supported silver catalyst

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2682560A (en) * 1952-11-22 1954-06-29 Eastman Kodak Co Conversion of organic hydroxy compounds to carbonyl derivatives
US4382149A (en) * 1980-11-05 1983-05-03 Borden, Inc. Supported silver catalyst

Similar Documents

Publication Publication Date Title
US2300969A (en) Production of alkinols
US1067665A (en) Process for the manufacture of formaldehyde.
US2527315A (en) Preparation of urea
EP0022697A1 (en) Process for the direct preparation of beta-methylthio-propionaldehyde
FR2760747A1 (en) PROCESS FOR THE MANUFACTURE OF GLYCIDOL OR A GLYCIDYL COMPOUND
US2385549A (en) Production of acrylonitrile
US1911746A (en) And charles f
US1449423A (en) Production of naphthyl amines
US2339348A (en) Process for making dicarbonylic compounds
US1595299A (en) Manufacture of phenols
US2836614A (en) Process for producing unsaturated nitriles
US2042303A (en) Production of aldehydes
US2597698A (en) Nitration of aliphatic hydrocarbons
US2150120A (en) Cycijc process fob the production
US1953548A (en) Preparation of normal propyl alcohol
US1100076A (en) Process of making formaldehyde.
SU944499A3 (en) Process for producing aromatic aldehydes
US1077442A (en) Process of hydrogenizing organic compounds.
US4025526A (en) Process for producing thiazoles
JP2007320944A (en) Method for producing 2-hydroxy-4-methyltetrahydropyran
JPH0427233B2 (en)
US3923903A (en) Oxidation of cyclic mono-olefins to {60 ,{107 -dialdeydes
US2010066A (en) Manufacture of aliphatic ketones
US2003477A (en) Process for effecting organic vapor phase reactions
US1870104A (en) Production of oxygenated aliphatic compounds