DE420442C - Process for the production of formaldehyde from methyl alcohol - Google Patents

Process for the production of formaldehyde from methyl alcohol

Info

Publication number
DE420442C
DE420442C DEB113023D DEB0113023D DE420442C DE 420442 C DE420442 C DE 420442C DE B113023 D DEB113023 D DE B113023D DE B0113023 D DEB0113023 D DE B0113023D DE 420442 C DE420442 C DE 420442C
Authority
DE
Germany
Prior art keywords
formaldehyde
methyl alcohol
production
methanol
contact
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
Application number
DEB113023D
Other languages
German (de)
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.)
BASF SE
Original Assignee
BASF SE
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 BASF SE filed Critical BASF SE
Priority to DEB113023D priority Critical patent/DE420442C/en
Application granted granted Critical
Publication of DE420442C publication Critical patent/DE420442C/en
Expired 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

Description

Verfahren zur Gewinnung von Formaldehyd aus Methylalkohol. Bei der Verwendung von synthetisch, d. h. durch katalytische Reduktion der Oxyde de.-Kohlenstoff s unter Druck hergestelltem Methanol für die Gewinnung von Formaldehyd durch katalytische Oxydation haben sich Schwierigkeiten herausgestellt, indem die Ausbeuten vielfach unbefriedigend waren. ja sogar die Kontaktmasse öfters in kurzer Zeit völlig unwirksam wurde. Wie sich ergeben hat, beruht dieser Übelstand darauf, daß selbst in dem destilliertcn synthetischen Methanol sehr häufig kleine Mengen flüchtiger Eisenverbindungen, insbesondere Eisencarbonyl (z. B. i bis 5 mg Fe im Liter), enthalten sind, und daß diese leicht den Kohltakt verderben. Tatsächlich erhält man sofort gute Ausbeuten, wenn das Methanol, etwa durch gründliche Fraktionierung, von den flüchtigen Eisenverbindungen befreit worden ist.Process for obtaining formaldehyde from methyl alcohol. In the Use of synthetic, d. H. by catalytic reduction of the oxides of carbon s methanol produced under pressure for the recovery of formaldehyde by catalytic Oxidation problems have been found by increasing the yields many times over were unsatisfactory. even the contact compound often becomes completely ineffective in a short time became. As has been shown, this deficiency is due to the fact that even in that synthetic methanol very often small amounts of volatile iron compounds, in particular Iron carbonyl (e.g. 1 to 5 mg Fe per liter) are included, and that these easily spoil the cabbage clock. In fact, good yields are obtained immediately if the methanol, for example through thorough fractionation, freed from the volatile iron compounds has been.

Man kann jedoch, wie sich weiter gezeigt hat, auch Eisencarbonyl u. dgl. enthaltendes synthetisches Methanol ohne weiteres für die katalytische Gewinnung von Formaldehyd verwenden. wenn man den zweckmäßig bereits mit Luft vermischten Methylalkoholdampf auf dem Wege zum Kontakt durch eine auf etwa 150 bis 300° gehaltene Schicht eines indifferenten Materials leitet; auf diesem scheidet sich das Eisen in Form von Eisenoxyd ab, %vährend der Methylalkoholdampf mit der Luft hindurchgeht. Der so gereinigte Methylalko; hol liefert dann bei der Oxydation zu Formaldehyd befriedigende Ausbeuten. Die Schicht indifferenten Materials kann z. B. aus Glas, Quarz, Porzellanstücken u. dgl. bestehen und etwa 2o bis 8o cm lang sein.However, as has also been shown, iron carbonyl and the like can also be used. The like. Containing synthetic methanol readily for catalytic recovery use of formaldehyde. if you already mixed it with air Methyl alcohol vapor on its way to contact by a held at about 150-300 ° Layer of an indifferent material conducts; on this the iron separates in the form of iron oxide,% while the methyl alcohol vapor passes through with the air. The methyl alcohol thus purified; hol then yields formaldehyde during the oxidation satisfactory yields. The layer of indifferent material can, for. B. made of glass, Quartz, pieces of porcelain and the like are made and about 20 to 8o cm long.

Die Wirkung des vorliegenden Verfahrens wird durch folgende Vergleichsversuche verdeutlicht Reines Methanol wurde vergast und im Gemisch mit Luft über einen zur Oxydation des Methanols zu Formaldehyd geeigneten Kontakt ,geleitet. Es wurden Ausbeuten an Formaldehyd von 83 bis 85 Prozent erzielt. Methanol, das i9 mg Eisen als Eisencarbonyl im Liter enthielt, lieferte bei gleicher Behandlung nur eine Ausbeute an Formaldehyd von 55,8 Prozent, und die Kontaktmasse war nach kürzer Zeit unbrauchbar. Wurde jedoch das Gemisch von eisencarbonylhaltigem Methanoldampf und Luft, selbst wenn das Methanol einen noch wesentlich höheren Gehalt an Eisencarbonyl aufwies, über indifferentes, auf i 5o bis 3oo° erhitztes Material geleitet, bevor es an den Katalysator gelangte, so wurden Ausbeuten an Formaldehyd von 83 bis 8:1 Prozent erhalten, und der Katalysä'or behielt seine gute Wirksamkeit unverändert bei.The effect of the present method is demonstrated by the following comparative tests clarified Pure methanol was gasified and mixed with air via a to Oxidation of the methanol to formaldehyde-suitable contact, passed. There were yields in formaldehyde of 83 to 85 percent. Methanol, the 19 mg of iron as iron carbonyl contained in the liter, gave only a yield of formaldehyde with the same treatment of 55.8 percent, and the contact mass was unusable after a short time. However, it was the mixture of iron carbonyl-containing methanol vapor and air, even if the methanol had an even higher content of iron carbonyl than indifferent, material heated to 150 ° to 300 ° C. passed before it reached the catalyst, so yields of formaldehyde of 83 to 8: 1 percent were obtained, and the catalyst retained its good effectiveness unchanged.

Claims (2)

PATEN T-ANSPRTIcHR: i. Verfahren zur Gewinnung von Formaldehyd aus Methylalkohol, dadurch gekennzeichnet, daß man bei der Verwendung von synthetischem Methanol dieses sorgfältig von flüchtigen Eisenverbindungen befreit. PATEN T-CLAIM: i. Process for the production of formaldehyde from methyl alcohol, characterized in that, when synthetic methanol is used, it is carefully freed from volatile iron compounds. 2. Ausführungsform des Verfahrens nach Anspruch i, dadurch gekennzeichnet, daß man den Dampf des Methylalkohols vor oder zweckmäßig nach der Vermischung mit Luft vor dem Auftreffen auf den Kontakt durch eine auf ungefähr i 5o bis 3oo° gehaltene Schicht indifferenten Materials leitet.2nd embodiment of the method according to claim i, characterized in that the vapor of the methyl alcohol before or, appropriately, after mixing with air before it comes into contact with the contact by a layer of indifferent material held at about 150 to 300 degrees directs.
DEB113023D 1924-02-29 1924-02-29 Process for the production of formaldehyde from methyl alcohol Expired DE420442C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEB113023D DE420442C (en) 1924-02-29 1924-02-29 Process for the production of formaldehyde from methyl alcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEB113023D DE420442C (en) 1924-02-29 1924-02-29 Process for the production of formaldehyde from methyl alcohol

Publications (1)

Publication Number Publication Date
DE420442C true DE420442C (en) 1925-10-24

Family

ID=6993371

Family Applications (1)

Application Number Title Priority Date Filing Date
DEB113023D Expired DE420442C (en) 1924-02-29 1924-02-29 Process for the production of formaldehyde from methyl alcohol

Country Status (1)

Country Link
DE (1) DE420442C (en)

Similar Documents

Publication Publication Date Title
EP0071787B1 (en) Ruthenium/carbon-hydrogenation catalysts, their preparation and their use in the selective hydrogenation of unsaturated carbonyl compounds
DE2235326A1 (en) METHOD FOR CLEANING UP 1,2-UNSATATULATED CARBONIC ACIDS
DE515678C (en) Process for the production of mainly esters among other organic compounds
DE1271115C2 (en) Process for the purification of reducible, cyclic, organic compounds by distillation
DE420442C (en) Process for the production of formaldehyde from methyl alcohol
DE829890C (en) Process for the preparation of terpene formylation products
DE879985C (en) Process for the purification of aldehydes and ketones
DE534118C (en) Process for the production of strongly adsorbing, high molecular weight products by catalytic polymerisation and / or condensation of acetylene
DE1277236B (en) Process for the production of butyraldehyde
DE814739C (en) Process for purifying synthetic aldehyde products
DE1248642B (en) Process for the production of acrylonitrile by reacting propylene with oxygen and ammonia
DE489280C (en) Process for the purification of mixtures of oxygen-containing organic compounds obtained by hydrogenating the oxides of carbon
DE880746C (en) Process for the production of cobalt carbonyl hydrogen and optionally cobalt carbonyl
DE858403C (en) Process for the production of phenols
DE579033C (en) Process for the production of a solution of coal in mineral oils or tars
DE890948C (en) Manufacture of oxidation products containing carboxylic acid
DE1231231B (en) Process for removing cobalt from oxosynthetic mixtures
DE430623C (en) Process for the purification synthetically from the oxides of carbon by treating with hydrogen compounds such as methanol, higher alcohols, esters and the like. like
DE552008C (en) Process for the preparation of ethylene from acetylene
DE857373C (en) Processing method for aqueous solutions of acrylonitrile
DE734621C (en) Process for the preparation of hydrogenation products of the follicular hormone
DE712693C (en) Process for the production of a paraffin mixture from high molecular weight paraffins
DE206330C (en)
DE539476C (en) Process for the oxidation of organic compounds in the liquid phase by means of gases containing oxygen
DE186881C (en)