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GB1092657A - Improvements relating to the stabilization of aqueous formaldehyde solutions - Google Patents

Improvements relating to the stabilization of aqueous formaldehyde solutions

Info

Publication number
GB1092657A
GB1092657A GB5103364A GB5103364A GB1092657A GB 1092657 A GB1092657 A GB 1092657A GB 5103364 A GB5103364 A GB 5103364A GB 5103364 A GB5103364 A GB 5103364A GB 1092657 A GB1092657 A GB 1092657A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
guanamine
formula
polyhydric alcohol
hydrocarbyl
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
GB5103364A
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.)
Koei Chemical Co Ltd
Original Assignee
Koei Chemical Co Ltd
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 Koei Chemical Co Ltd filed Critical Koei Chemical Co Ltd
Publication of GB1092657A publication Critical patent/GB1092657A/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
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/86Use of additives, e.g. for stabilisation

Landscapes

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

Abstract

Formaldehyde condensates are prepared by reacting under alkaline or acidic conditions: (1) a guanamine of the formula <FORM:1092657/C3/1> in which R is an alkyl or aryl group, with an alkanol and formaldehyde; (2) a hydrocarbyl melamine of the formula <FORM:1092657/C3/2> in which R1 is an alkyl, cycloalkyl, aryl or aralkyl group, with a polyhydric alcohol and formaldehyde; and (3) a guanamine of the above formula, a polyhydric alcohol and formaldehyde. Examples relate to the condensation of formaldehyde, a guanamine or a melamine and methanol, glycerol, sorbitol, triethylene glycol, 1,1,1-trimethylolpropane, 1,2-propylene glycol, ethylene glycol, pentaerythritol, and polypropylene glycol. Example 8 describes the preparation of a condensate of polyvinyl alcohol, formaldehyde and benzoguanamine.ALSO:Aqueous formaldehyde solutions which contain at least 37% by weight formaldehyde are stabilized by dissolving therein less than 1000 p.p.m. by wt. of solution of one or more stabilizing agents selected from (1) alkoxymethylated guanamines obtained under alkaline or acid conditions from an alkanol formaldehyde and a guanamine of the formula <FORM:1092657/C2/1> wherein R is an alkyl or aryl group; (2) a condensation product, obtained under acid or alkaline conditions, of a polyhydric alcohol, formaldehyde and an hydrocarbyl melamine of the formula <FORM:1092657/C2/2> wherein R1 is an alkyl, cycloalkyl, aryl or aralkyl radical; (3) a product obtained by reacting under acid or alkaline conditions, a polyhydric alcohol and an alkoxymethylated hydrocarbyl melamine derived from the hydrocarbyl melamines of Formula II; (4) a product obtained by reacting under acid or alkaline conditions a polyhydric alcohol, formaldehyde or a guanamine of the Formula I; and (5) a product obtained by reacting under acid or alkaline conditions a polyhydric alcohol and an alkoxymethylated guanamine (the guanamine being the same as that stated in (1)). Preferred guanamines are aceto-, propio-, butyro- and benzo-guanamines, preferred hydrocarbyl melamines, methyl-, ethyl-, propyl-butyl-, cyclohexyl-, benzyl- and phenyl-melamines, preferred alkanols, methanol, ethanol, propanol, and butanol and preferred polyhydric alcohols, polyvinyl alcohol (see Division C3), ethylene glycol, 1,2-propylene glycol, polyethylene glycol, polypropylene glycol, glycerol, 1,1,1-trimethylol propane, pentaerythritol and sorbitol. The stabilizers may be prepared and added to the formaldehyde solution, which preferably also contains small amounts of methanol, without prior isolation of the reaction products. Examples are provided.
GB5103364A 1963-12-28 1964-12-15 Improvements relating to the stabilization of aqueous formaldehyde solutions Expired GB1092657A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7103763 1963-12-28

Publications (1)

Publication Number Publication Date
GB1092657A true GB1092657A (en) 1967-11-29

Family

ID=13448909

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5103364A Expired GB1092657A (en) 1963-12-28 1964-12-15 Improvements relating to the stabilization of aqueous formaldehyde solutions

Country Status (8)

Country Link
AT (2) AT265228B (en)
CH (1) CH434224A (en)
DE (1) DE1268608B (en)
FI (1) FI40894B (en)
GB (1) GB1092657A (en)
NL (2) NL6415100A (en)
NO (1) NO117850B (en)
SE (1) SE320961B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20190194523A1 (en) * 2017-12-22 2019-06-27 Clariant International, Ltd. Synergized hemiacetals composition and method for scavenging sulfides and mercaptans
US11530347B2 (en) 2016-07-01 2022-12-20 Clariant International Ltd Synergized acetals composition and method for scavenging sulfides and mercaptans
US11603497B2 (en) 2017-12-22 2023-03-14 Clariant International Ltd Synergized acetals composition and method for scavenging sulfides and mercaptans

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1067560B (en) * 1976-11-19 1985-03-16 Montedison Spa PROCESS FOR THE PREPARATION OF STABLE WATER SUSPENSIONS OF FORMALDEHYDE AND PRODUCTS OBTAINED
DE2919496A1 (en) 1979-05-15 1980-12-04 Degussa NEW BISGUANAMINE

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1336037A (en) * 1962-10-17 1963-08-23 Montedison Spa Stable aqueous solutions of formaldehyde and method of preparation

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11530347B2 (en) 2016-07-01 2022-12-20 Clariant International Ltd Synergized acetals composition and method for scavenging sulfides and mercaptans
US20190194523A1 (en) * 2017-12-22 2019-06-27 Clariant International, Ltd. Synergized hemiacetals composition and method for scavenging sulfides and mercaptans
WO2019120761A1 (en) * 2017-12-22 2019-06-27 Clariant International Ltd Synergized acetals composition and method for scavenging sulfides and mercaptants
CN111163855A (en) * 2017-12-22 2020-05-15 科莱恩国际有限公司 Synergistic acetal compositions and methods for scavenging sulfides and mercaptans
US11555140B2 (en) * 2017-12-22 2023-01-17 Clariant International Ltd Synergized hemiacetals composition and method for scavenging sulfides and mercaptans
US11603497B2 (en) 2017-12-22 2023-03-14 Clariant International Ltd Synergized acetals composition and method for scavenging sulfides and mercaptans

Also Published As

Publication number Publication date
CH434224A (en) 1967-04-30
SE320961B (en) 1970-02-23
AT265228B (en) 1968-10-10
NO117850B (en) 1969-10-06
NL6415100A (en) 1965-06-29
DE1268608B (en) 1968-05-22
FI40894B (en) 1969-03-31
AT264486B (en) 1968-09-10
NL7105917A (en) 1971-07-26

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