ES447465A1 - Aqueous solutions of etherified melamine formaldehyde resins - Google Patents

Aqueous solutions of etherified melamine formaldehyde resins

Info

Publication number
ES447465A1
ES447465A1 ES447465A ES447465A ES447465A1 ES 447465 A1 ES447465 A1 ES 447465A1 ES 447465 A ES447465 A ES 447465A ES 447465 A ES447465 A ES 447465A ES 447465 A1 ES447465 A1 ES 447465A1
Authority
ES
Spain
Prior art keywords
phase
degrees centigrade
formaldehyde
melamine
temperature
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
ES447465A
Other languages
Spanish (es)
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.)
Saint Gobain Industries SA
Compagnie de Saint Gobain SA
Original Assignee
Saint Gobain Industries SA
Compagnie de Saint Gobain SA
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 Saint Gobain Industries SA, Compagnie de Saint Gobain SA filed Critical Saint Gobain Industries SA
Publication of ES447465A1 publication Critical patent/ES447465A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10Coating
    • C03C25/24Coatings containing organic materials
    • C03C25/26Macromolecular compounds or prepolymers
    • C03C25/32Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C03C25/34Condensation polymers of aldehydes, e.g. with phenols, ureas, melamines, amides or amines
    • 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
    • C08G12/424Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds
    • C08G12/425Chemically modified polycondensates by etherifying of polycondensates based on heterocyclic compounds based on triazines
    • C08G12/427Melamine
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins
    • D06M15/427Amino-aldehyde resins modified by alkoxylated compounds or alkylene oxides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Textile Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Materials Engineering (AREA)
  • Phenolic Resins Or Amino Resins (AREA)

Abstract

"Procedure for obtaining aqueous solutions of etherified melamino-formaldehyde resins, with a long shelf life and a low proportion of free formaldehyde", characterized in that in a first phase, melamine is reacted with formaldehyde, gradually adding and stirring the melamine under solid form, to a solution obtained by mixing a solution containing thirty to fifty percent, and preferably about thirty-six percent formaldehyde, in an amount corresponding to a formaldehyde/melamine molecular ratio between 5 and 11, preferably between 6.5 and 10; of one or more polyols in an amount corresponding to a polyol-melamine molecular ratio comprised between 3 and 5, preferably between 3.5 and 4.0; of triethanolamine in an amount corresponding to a triethanolamine/melamine molecular ratio, comprised between 0.2 and 0.6, preferably between 0.3 and 0.4, at a temperature between 60 and 70 degrees Celsius, preferably between 63 and 68 degrees Celsius, the pH after the addition of the melamine is between 8.5 and 9.5 and preferably between 8.8 and 9.2, and the reaction is achieved by rapid cooling to a temperature between 20 and 40 degrees centigrade, preferably between 33 and 37 degrees centigrade, when the cloud point occurs between 40 and 65 degrees centigrade, preferably between 45 and 55 degrees centigrade; in a second phase, etherification is carried out by lowering the pH of the reaction mixture resulting from the first phase by gradually adding a pure acid or in concentrated aqueous solution, to a value between 1.5 and 3.0, all while maintaining the temperature from the end of the first phase, and at the end of the etherification reaction, the solution obtained is neutralized by adding a base; in a third phase, the solution obtained at the end of the second phase is matured, keeping it for a period of between two and five hours at a temperature of between 50 and 90 degrees centigrade, preferably between 70 and 85 degrees centigrade; in a fourth phase the proportion of free formaldehyde in the solution obtained at the end of the third phase is reduced to a final proportion in free formaldehyde not exceeding 6 weight percent. (Machine-translation by Google Translate, not legally binding)
ES447465A 1975-04-30 1976-04-29 Aqueous solutions of etherified melamine formaldehyde resins Expired ES447465A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7513569A FR2309575A1 (en) 1975-04-30 1975-04-30 AQUEOUS SOLUTIONS OF ETHERIFIED MELAMINE-FORMALDEHYDE RESINS WITH A LONG SHELF LIFE AND LOW FREE FORMALDEHYDE CONTENT

Publications (1)

Publication Number Publication Date
ES447465A1 true ES447465A1 (en) 1977-07-01

Family

ID=9154670

Family Applications (1)

Application Number Title Priority Date Filing Date
ES447465A Expired ES447465A1 (en) 1975-04-30 1976-04-29 Aqueous solutions of etherified melamine formaldehyde resins

Country Status (28)

Country Link
JP (1) JPS5853648B2 (en)
AT (1) AT344993B (en)
AU (1) AU501880B2 (en)
BE (1) BE841304A (en)
BR (1) BR7602672A (en)
CA (1) CA1091836A (en)
CH (1) CH603737A5 (en)
CS (1) CS191304B2 (en)
DD (1) DD128380A5 (en)
DE (1) DE2617232C2 (en)
ES (1) ES447465A1 (en)
FI (1) FI62547C (en)
FR (1) FR2309575A1 (en)
GB (1) GB1501534A (en)
HU (1) HU177034B (en)
IE (1) IE43271B1 (en)
IT (1) IT1059948B (en)
LU (1) LU74857A1 (en)
MX (1) MX3319E (en)
NL (1) NL190286C (en)
NO (1) NO142444C (en)
NZ (1) NZ180713A (en)
PL (1) PL105541B1 (en)
RO (1) RO70306A (en)
SE (1) SE419229B (en)
TR (1) TR19067A (en)
YU (1) YU37352B (en)
ZA (1) ZA762575B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2715020C2 (en) * 1977-04-04 1983-04-28 Cassella Ag, 6000 Frankfurt Process for the preparation of aqueous melamine / urea resin solutions
GB2136008B (en) * 1983-02-07 1986-06-25 Enigma Nv Formaldehyde binder
GB2170208B (en) * 1985-01-29 1988-06-22 Enigma Nv A formaldehyde binder
DE19633625A1 (en) * 1996-08-21 1998-02-26 Basf Ag Process for the preparation of aqueous concentrated solutions of N-methylol ethers suitable for the finishing of cellulose-containing textile materials
CN110042701B (en) * 2019-03-29 2023-09-15 广东福美新材料科技有限公司 Moistureproof flame-retardant impregnated paper and preparation method thereof
RU2019134226A (en) * 2019-10-25 2021-04-26 Общество с ограниченной ответственностью "Комберри" TRANSPARENT GEL-POLYMER ELECTROLYTES OF INCREASED CONDUCTIVITY BASED ON TRIAZINE COPOLYMERS

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1012319A (en) * 1962-06-01 1965-12-08 British Industrial Plastics Water-soluble modified melamine-formaldehyde resins
DE2005166C3 (en) * 1970-02-05 1975-05-15 Chemische Fabrik Pfersee Gmbh, 8900 Augsburg Process for the production of water-soluble, etherified methylolmelamines
GB1317774A (en) * 1970-06-02 1973-05-23 British Industrial Plastics Melamine formaldehyde condensation products

Also Published As

Publication number Publication date
PL105541B1 (en) 1979-10-31
NL190286B (en) 1993-08-02
FR2309575B1 (en) 1980-01-11
LU74857A1 (en) 1977-02-08
AU501880B2 (en) 1979-07-05
CA1091836A (en) 1980-12-16
DD128380A5 (en) 1977-11-16
FI62547C (en) 1983-01-10
DE2617232A1 (en) 1976-11-11
RO70306A (en) 1982-04-12
YU37352B (en) 1984-08-31
HU177034B (en) 1981-06-28
JPS5853648B2 (en) 1983-11-30
ATA316676A (en) 1977-12-15
NZ180713A (en) 1978-09-20
TR19067A (en) 1978-05-01
NO142444C (en) 1980-08-20
FI62547B (en) 1982-09-30
SE7604717L (en) 1976-10-31
AU1346476A (en) 1977-11-03
FR2309575A1 (en) 1976-11-26
IE43271L (en) 1976-10-30
YU108476A (en) 1983-04-27
NL190286C (en) 1994-01-03
IE43271B1 (en) 1981-01-28
GB1501534A (en) 1978-02-15
FI761168A (en) 1976-10-31
DE2617232C2 (en) 1987-03-26
BR7602672A (en) 1976-11-23
CS191304B2 (en) 1979-06-29
AT344993B (en) 1978-08-25
NO761499L (en) 1976-11-02
SE419229B (en) 1981-07-20
MX3319E (en) 1980-09-22
BE841304A (en) 1976-10-29
JPS51131593A (en) 1976-11-16
NL7604581A (en) 1976-11-02
IT1059948B (en) 1982-06-21
ZA762575B (en) 1977-04-27
NO142444B (en) 1980-05-12
CH603737A5 (en) 1978-08-31

Similar Documents

Publication Publication Date Title
Fainberg et al. Correlation of Solvolysis Rates. V. 1 α-Phenylethyl Chloride2
ES267248A1 (en) Pyrazolo-pyrimidines and process for preparing same
ES395835A1 (en) Cosmetic compositions and their use
ES447465A1 (en) Aqueous solutions of etherified melamine formaldehyde resins
ES400927A1 (en) Dentrifrices
JPS5356288A (en) Preparation of phenolic resin
ES416496A1 (en) Dyestuff powders
ES381138A1 (en) 1-methyl-2-substituted 5-nitroimidazoles
GB660534A (en) Diazotype photoprinting material
GB1412240A (en) Process for the preparation of 3- o,o-diethyldithiophosphorylmethyl -6-chlorobenzoxazolone
GB822929A (en) Process for the production of stable solutions of hardenable condensation products of melamine, thiourea and formaldehyde
GB1250257A (en)
SU717083A1 (en) Method of preparing concentrated ures formaldehyde resin
GB1133388A (en) Production of pure anhydrous dioxolane-(1,3)
ES367383A1 (en) Procedure for the preparation of diffusion aliphatic sulphonates. (Machine-translation by Google Translate, not legally binding)
JPS5653122A (en) Preparation of polyoxymethylene
KR830008988A (en) Method for preparing di-alpha-amino-1, 4-cyclohexadienyl-1-acetic acid
ES364069A1 (en) Procedure for obtaining tetracycline salts. (Machine-translation by Google Translate, not legally binding)
JPS565476A (en) Polyalkyl-2- 2,4-dihydroxyphenyl -7-hydroxychroman and its preparation
JPS5464588A (en) Preparation of water-soluble resol resin
GB834100A (en) Improvements in the preparation of mixed aldols
JPS5657815A (en) Preparation of resorcinol co-condensation resin
ES461252A1 (en) Preparation of gamma-pyrones
ES373486A1 (en) New mixed acetals and process for the production of mixed acetals
ES290018A1 (en) Water-soluble paraformaldehyde compositions