GB1028804A - Paraformaldehyde - Google Patents

Paraformaldehyde

Info

Publication number
GB1028804A
GB1028804A GB28120/63A GB2812063A GB1028804A GB 1028804 A GB1028804 A GB 1028804A GB 28120/63 A GB28120/63 A GB 28120/63A GB 2812063 A GB2812063 A GB 2812063A GB 1028804 A GB1028804 A GB 1028804A
Authority
GB
United Kingdom
Prior art keywords
paraformaldehyde
stabilized
aryl
substituted
formaldehyde
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
GB28120/63A
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.)
Montedison SpA
Original Assignee
Montedison SpA
Montecatini Societa Generale per lIndustria Mineraria e Chimica SpA
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 Montedison SpA, Montecatini Societa Generale per lIndustria Mineraria e Chimica SpA filed Critical Montedison SpA
Publication of GB1028804A publication Critical patent/GB1028804A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08G12/30Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with substituted triazines
    • C08G12/32Melamines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08G12/34Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds and acyclic or carbocyclic compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G12/00Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08G12/02Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
    • C08G12/40Chemically modified polycondensates
    • C08G12/42Chemically modified polycondensates by etherifying
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G14/00Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
    • C08G14/02Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
    • C08G14/04Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
    • C08G14/06Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L61/00Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
    • C08L61/20Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
    • C08L61/26Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
    • C08L61/28Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with melamine

Abstract

The invention comprises stabilized paraformaldehyde having a formaldehyde content higher than 80%, a water solubility at 50 DEG C. of about 95% in 30-40 mins., an average degree of polymerization between 15 and 70 corresponding to an average molecular weight between 450 and 2100 and containing from 0.01 to 5% by weight of a triazine stabilizer having the general formula <FORM:1028804/C2/1> in which R1 is a hydrogen atom or an alkyl, aryl, a partially or completely hydrogenated aryl, aryl ortho-substituted with a guanamine radical or alkylaryl group, or an alkylamino or amino alkenyl group which may be substituted by hydrocarbon groups, and R2 and R3 are the same or different and are hydroxyl or aryl groups which may be hydrogenated or substituted in the benzene ring, or amine groups -NR1R11 in which R1 and R11 are hydrogen atoms or aryl, alkyl or alkenyl groups which may be substituted with hydroxy groups. Solid crystalline paraformaldehyde having a formaldehyde content higher than 96% may be obtained by drying the stabilized paraformaldehyde. Concentrated aqueous formaldehyde solutions having a formaldehyde content of 36-45% by weight, may be obtained by dissolving the stabilized paraformaldehyde in water. The stabilized paraformaldehyde may be obtained by the concentration and cooling of an alkaline formaldehyde solution containing the stabilizer and centrifuging the slurry obtained. The stabilized paraformaldehyde may be obtained in the form of flakes by concentrating the stabilized alkaline formaldehyde solutions to a formaldehyde concentration of at least 80% (by weight) adjusting the pH to 8-10 at a temperature of 80-100 DEG C., quenching on a metal surface and then scraping off the solid paraformaldehyde in the form of flakes. Suitable stabilizers of the above general formula are, for example, benzoguanamine, diallyl melamine and tetrahydrobenzoguanamine. It appears that the stabilizer reacts with the formaldehyde to form methylol groups but the mechanism of the stabilization is not known.ALSO:Stabilized paraformaldehyde having a formaldehyde content higher than 80%, a water-solubility at 50 DEG C. of about 95% in 30-40 mins., an average degree of polymerization between 15 and 70 corresponding to an average molecular weight between 450 and 2100 contains from 0.01-5% by weight of a triazine stabilizer having the general formula <FORM:1028804/C3/1> in which R1 is a hydrogen atom or an alkyl, aryl, a partially or completely hydrogenated aryl, aryl ortho-substituted with a guanamine radical or alkylaryl group or an alkylamino or aminoalkenyl group which may be substituted by hydrocarbon groups, and R2 and R3 are the same or different and are hydroxyl or aryl groups which may be hydrogenated or substituted in the benzene ring, or amine groups -NR1R11 in which R1 and R11 are hydrogen atoms or aryl, alkyl or alkenyl groups which may be substituted by hydroxy groups. Solid crystalline paraformaldehyde having a formaldehyde content higher than 96% may be obtained by drying the stabilized paraformaldehyde. The stabilized paraformaldehyde may be obtained by the concentration and cooling of an alkaline formaldehyde solution containing the stabilizer and centrifuging the slurry obtained. The stabilized paraformaldehyde may be obtained in the form of flakes by concentrating the stabilized alkaline formaldehyde solution to a formaldehyde content of at least 80% (by weight) adjusting the pH to 8-10 at a temperature of 80-100 DEG C., quenching on a metal surface and scraping off the solid paraformaldehyde in the form of flakes. Suitable stabilizers of the above general formula are, for example, benzoguanamine, diallylmelamine and tetrahydrobenzoguanamine.
GB28120/63A 1962-07-17 1963-07-16 Paraformaldehyde Expired GB1028804A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IT1441062 1962-07-17
IT1362663 1963-06-28

Publications (1)

Publication Number Publication Date
GB1028804A true GB1028804A (en) 1966-05-11

Family

ID=26326657

Family Applications (1)

Application Number Title Priority Date Filing Date
GB28120/63A Expired GB1028804A (en) 1962-07-17 1963-07-16 Paraformaldehyde

Country Status (1)

Country Link
GB (1) GB1028804A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5898087A (en) * 1996-03-20 1999-04-27 Celanese International Corporation Addition of amine to improve parafomaldehyde

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5898087A (en) * 1996-03-20 1999-04-27 Celanese International Corporation Addition of amine to improve parafomaldehyde

Similar Documents

Publication Publication Date Title
KR930002402A (en) Modified Melamine-Formaldehyde Resin
GB986925A (en) Stabilising oxymethylene polymers
ES431623A1 (en) Process of preparing aqueous solutions of melamine-formaldehyde condensation products having anionic sulfo groups
GB965006A (en) Anthraquinone dyestuffs free from acid groups imparting water-solubility and a process for their manufacture
KR860003308A (en) Process for preparing low-electrolyte-containing lignosulfonate sodium
GB1028804A (en) Paraformaldehyde
US3301797A (en) Linear triazine polymers
US3852374A (en) Tanning agents
GB1251847A (en)
US2464247A (en) Preparation of guanidine sulfates
US3563987A (en) Preparation of cyanuric acid
US3388172A (en) Water-soluble paraformaldehyde compositions
US3420799A (en) Process for preparing aminoplasts from alkoxyacetaldehyde with an azine
Solomon et al. Polar Factors in Radical Dissociations. Kinetics of Decomposition of meta-Substituted Phenylazotriphenylmethanes1a
US3626024A (en) Stabilized polyacetals and process for their manufacture
GB2056436A (en) Alkylene bis-guanamines and their use for stabilising formaldehyde solutions
US3793280A (en) Stable solutions of melamine-urea-formaldehyde condensates containing a stabilizing aldehyde and processes for their preparation
US3093645A (en) Nu-oxides of amino-s-triazines and process for preparing them
US3207727A (en) Method of stabilizing polyoxymethylene
US3428593A (en) High efficiency stable liquid phenolformaldehyde resin
US2600698A (en) Reaction products from an aldehyde, an aminotriazine, and a mono-nheterocyclic compound
Albert et al. 274. Pteridine studies. Part XI. The decomposition of 2-hydroxypteridine by alkali
GB1187352A (en) New, Sulphur-Containing Derivatives of Aminotriazine-Formaldehyde Condensation products, process for their preparation, and their use as Plasticizing Additives for Quick-Curing and Storage-Stable Aminoplast Moulding Compositions
US3457220A (en) Process for stabilizing copolymers of trioxane and cyclic ethers
US2312699A (en) Triazinyl carboxy-alkyl sulphides and salts thereof