GB989801A - Process for the production of anhydrous formaldehyde - Google Patents
Process for the production of anhydrous formaldehydeInfo
- Publication number
- GB989801A GB989801A GB2858361A GB2858361A GB989801A GB 989801 A GB989801 A GB 989801A GB 2858361 A GB2858361 A GB 2858361A GB 2858361 A GB2858361 A GB 2858361A GB 989801 A GB989801 A GB 989801A
- Authority
- GB
- United Kingdom
- Prior art keywords
- trimethylol
- hemiacetal
- formaldehyde
- propane
- alcohol
- 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
- 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
-
- 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
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/515—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an acetalised, ketalised hemi-acetalised, or hemi-ketalised 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
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/85—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to a chemical modification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Substantially anhydrous, monomeric formaldehyde is produced by reacting an aqueous formaldehyde solution with an alcohol which contains at least three hydroxyl groups in the molecule and which has been obtained by condensation of an aliphatic aldehyde with formaldehyde, dehydrating the resulting hemiacetal-water mixture by distillation, and subsequently thermally decomposing the hemiacetal into formaldehyde gas and said alcohol, and recovering the formaldehyde thus obtained. Alcohols specified for forming the hemiacetal are 1,1,1 - trimethylol - ethane, 1,1,1 - trimethylol - propane, 1,1,1 - trimethylol - butane, 1,1,1 - trimethylol - 2 - hydroxypropane and pentaerythritol. The dehydration of the hemiacetal-water mixture is preferably carried out in a vacuum of 15 to 25 mm. Hg and may be effected discontinuously or continuously. The thermal decomposition of the hemiacetate may also be discontinuous or continuous and with the hemiacetal of 1,1,1-trimethylol-propane, for example, may be effected at a temperature of 140 DEG to 180 DEG C.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2858361A GB989801A (en) | 1961-08-08 | 1961-08-08 | Process for the production of anhydrous formaldehyde |
FR870456A FR1301078A (en) | 1961-08-08 | 1961-08-09 | Anhydrous formaldehyde manufacturing process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2858361A GB989801A (en) | 1961-08-08 | 1961-08-08 | Process for the production of anhydrous formaldehyde |
Publications (1)
Publication Number | Publication Date |
---|---|
GB989801A true GB989801A (en) | 1965-04-22 |
Family
ID=10277904
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2858361A Expired GB989801A (en) | 1961-08-08 | 1961-08-08 | Process for the production of anhydrous formaldehyde |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB989801A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0543226A2 (en) * | 1991-11-16 | 1993-05-26 | BASF Aktiengesellschaft | Process for the preparation of anhydrous and from impurities depleted formaldehyde |
CN114057543A (en) * | 2020-07-29 | 2022-02-18 | 山东辰信新能源有限公司 | Recovery method of ineffective carrier in DMMn synthesis process |
-
1961
- 1961-08-08 GB GB2858361A patent/GB989801A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0543226A2 (en) * | 1991-11-16 | 1993-05-26 | BASF Aktiengesellschaft | Process for the preparation of anhydrous and from impurities depleted formaldehyde |
EP0543226A3 (en) * | 1991-11-16 | 1993-06-30 | Basf Aktiengesellschaft | Process for the preparation of anhydrous and from impurities depleted formaldehyde |
CN114057543A (en) * | 2020-07-29 | 2022-02-18 | 山东辰信新能源有限公司 | Recovery method of ineffective carrier in DMMn synthesis process |
CN114057543B (en) * | 2020-07-29 | 2023-09-15 | 山东辰信新能源有限公司 | Recovery method of failure carrier in DMMn synthesis process |
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