GB917643A - Manufacture of pure formaldehyde - Google Patents
Manufacture of pure formaldehydeInfo
- Publication number
- GB917643A GB917643A GB44040/59A GB4404059A GB917643A GB 917643 A GB917643 A GB 917643A GB 44040/59 A GB44040/59 A GB 44040/59A GB 4404059 A GB4404059 A GB 4404059A GB 917643 A GB917643 A GB 917643A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alcohol
- formaldehyde
- boiling
- semi
- formal
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/02—Saturated compounds having —CHO groups bound to acyclic carbon atoms or to hydrogen
- C07C47/04—Formaldehyde
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/36—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
- C07C29/38—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/30—Compounds having groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/002—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by dehydrogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/32—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen
- C07C45/37—Preparation 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
- C07C45/38—Preparation 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C07C45/75—Reactions with formaldehyde
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
- C07C45/82—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation by distillation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Pure formaldehyde is produced by the thermal splitting of a semi-formal into formaldehyde and alcohol, by heating a semi-formal derived from formaldehyde and an alcohol which melts below 100 DEG C. and boils above 100 DEG C., washing the mixture of vapours formed with a hydrocarbon, as a first auxiliary liquid, which has a good solvent power for the alcohol split off from the semi-formal and little or no solvent power for the formaldehyde and has a boiling point below that of the alcohol, passing the remaining vapours through a condenser and washing them with another hydrocarbon, as a second auxiliary liquid, which is a good solvent for the alcohol and has little or no solvent power for the formaldehyde but has a boiling-point above that of the alcohol the two auxiliary liquids not forming azeotropic mixtures with the alcohol and having boiling points which enable them to be readily separated from the alcohol by distillation. Suitable alcohol components of the semi-formals are, for example, cyclohexanol, methylcyclohexanols, butane-diol-1,4, pentanols, hexanols and octanols. Suitable first auxiliary liquids are hydrocarbons boiling in the range 180-350 DEG C. Suitable second auxiliary liquids are hydrocarbons and hydrocarbon mixtures boiling in the range 80-200 DEG C. The process may be carried out continuously or discontinuously.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1958F0027380 DE1139825B (en) | 1958-12-27 | 1958-12-27 | Process for the preparation of pure alcohol-free formaldehyde. |
Publications (1)
Publication Number | Publication Date |
---|---|
GB917643A true GB917643A (en) | 1963-02-06 |
Family
ID=7092420
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB44040/59A Expired GB917643A (en) | 1958-12-27 | 1959-12-28 | Manufacture of pure formaldehyde |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE586089A (en) |
DE (1) | DE1139825B (en) |
GB (1) | GB917643A (en) |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE560841A (en) * | 1953-07-16 |
-
1958
- 1958-12-27 DE DE1958F0027380 patent/DE1139825B/en active Pending
-
1959
- 1959-12-28 BE BE586089A patent/BE586089A/en unknown
- 1959-12-28 GB GB44040/59A patent/GB917643A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BE586089A (en) | 1960-06-28 |
DE1139825B (en) | 1962-11-22 |
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