GB1058652A - Aminoplast compositions for use in textile finishing - Google Patents
Aminoplast compositions for use in textile finishingInfo
- Publication number
- GB1058652A GB1058652A GB4129463A GB4129463A GB1058652A GB 1058652 A GB1058652 A GB 1058652A GB 4129463 A GB4129463 A GB 4129463A GB 4129463 A GB4129463 A GB 4129463A GB 1058652 A GB1058652 A GB 1058652A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dimethylol
- glycol bis
- acid
- glycerin
- textile
- 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/11—Compounds containing epoxy groups or precursors thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/40—Chemically modified polycondensates
- C08G12/42—Chemically modified polycondensates by etherifying
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/165—Ethers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/55—Epoxy resins
Abstract
A composition for imparting crease-resistance to cellulosic textiles comprises an aqueous solution in which are mixed (a) an aminoplast precondensate derived from formalydehyde which is thermosetting and/or which cross-links with cellulose; (b) an acid or acid-liberating catalyst, and (c) a compound having an average per molecule of (m - n) groups -CH(OH)CH2X and n groups <FORM:1058652/C3/1> where m is at least 2, n is between 0 and 1 inclusive, and X is halogen, and having a boiling point above 170 DEG C. The preferred precondensates (a) are those of formaldehyde with urea, or urea derivatives, or ethers thereof, e.g. ethyleneurea, propyleneurea, dioxyethyleneura, acetylene diurea, hydroxypropyleneurea, N-methyltriazone, N-ethyltriazone, N-propyltriazone, melamine or dicyandiamide. Preferred catalysts (b) are water soluble salts, e.g. chlorides, nitrates, sulphates of polyvalent metals, e.g. Mg, Zn, Al, Zr. The compounds (c) may be ethers of glycidol or glycerin monohalohydrin and an aliphatic polyol of 2-6 C atoms, or acetals of glycidol or a glycerin halohydrin with a C 1-4 aldehyde. The solution should contain (a) sufficient to deposit 1.5-8.5 gm. of (a) per 100 gm. of textile, and (c) sufficient to deposit 5-15 gm. of (c) per 100 gm. of textile, and may also contain brightening, bluing, softening, or finishing agents. Crease resistance may be enhanced by treating the heat-cured textile with a strongly alkaline solution. In examples aqueous solutions are prepared containing (1) dimethylol urea, tetramethyl hexamethylolmelamine, ethylene glycol bis(glycerin chlorohydrin ether) and MgCl2, (2) dimethylol ethylene triazine, a partly hydrolysed glycerol/epichlorhydrin adduct, a polyethylene emulsion octadecyl urea and Zn(NO3)2, (3) dimethylol propyleneurea, 1:4 - dichloro - butane - 2:3 - diol and ZnCl2, (4) dimethylol dioxyethyleneurea, ethylene glycol bis(glycerin chlorohydrin ether), MgCl2 and ethanol, and (5) dimethylolurea, hexamethylolmelamine, butylene glycol bis(glycerin chlorohydrin ether), Zn(NO3)2 and methanol.ALSO:Cellulosic textile materials may be rendered crease-resistant by soaking in a composition comprising an aqueous solution in which are mixed (a) an aminoplast precondensate derived from formaldehyde which is thermosetting and/or which cross-links with cellulose, (b) an acid or acid-liberating catalyst, and (c) a compound containing an average per molecule (m-n) groups -CH(OH)CH2X, and n groups <FORM:1058652/D1-D2/1> , where m is at least 2, n is between O and 1 inclusive, and X is halogen (see Division C3). After the soaking excess composition is removed, the textile is dried and cured by heating at above 120 DEG C. for 1-10 mins. The product may be further treated with a solution of a strong base, e.g. a 2-22% solution of an alkali metal hydroxide or carbonate, at up to 100 DEG C, then rinsed and acidified to remove residual base. The composition may also contain optical brightening, bluing, softening or other finishing agents, e.g. dispersions of low molecular weight polyethylenes, esters of polyacrylic acid, and emulsions of higher fatty acid amines. In Examples (1) mercerized cotton poplin is soaked in an aqueous solution of dimethylolurea, tetramethyl hexamethylolmelamine, ethylene glycol bis (glycerin chlorohydrin ether) MgCl2, then squeezed, dried treated with 8% NaOH, squeezed, let stand, rinsed, acidified, rinsed and dried, (2) cotton cretonne is similarly treated using an aqueous solution of dimethylol ethylenetriazine, a partially dehydrochlorinated glycerol/epichlorhydrin adduct, a polyethylene emulsion, octadecylurea and Zu (NO3)2, (3) cotton-polyester gabardine is similarly treated with 1:4-dichloro-butane-2:3-diol, dimethylol propyleneurea and Zu Cl2 (4) mercerized cotton poplin is similarly treated with dimethylol dioxyethyleneurea, ethylene glycol bis (glycerin chlorohydrin ether), MgCl2, and ethanol, then finally treated with an emulsion of an ester of polyacrylic acid, (5) viscose rayon lining material is similarly treated with dimethylolurea, hexamethylolmelamine, butylene glycol bis (glycerin chlorohydrin ether), Zu(NO3)2 and methanol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEC28744A DE1254116B (en) | 1962-12-22 | 1962-12-22 | Process for finishing textile materials |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1058652A true GB1058652A (en) | 1967-02-15 |
Family
ID=7018744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4129463A Expired GB1058652A (en) | 1962-12-22 | 1963-10-18 | Aminoplast compositions for use in textile finishing |
Country Status (7)
Country | Link |
---|---|
AT (1) | AT240329B (en) |
BE (1) | BE641596A (en) |
CH (1) | CH450346A (en) |
DE (1) | DE1254116B (en) |
GB (1) | GB1058652A (en) |
NL (1) | NL296806A (en) |
SE (1) | SE313288B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2090190A1 (en) * | 1970-05-21 | 1972-01-14 | Sandoz Sa | Strengthening cellulosic fibres - by n-methylol cpds and aluminium nitrate |
US7863405B2 (en) | 2004-09-02 | 2011-01-04 | Eastman Chemical Company | Removal of residual acetaldehyde from polyester polymer particles |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2794754A (en) * | 1956-04-30 | 1957-06-04 | Shell Dev | Treatment of textile materials |
-
0
- NL NL296806D patent/NL296806A/xx unknown
-
1962
- 1962-12-22 DE DEC28744A patent/DE1254116B/en active Pending
-
1963
- 1963-06-19 AT AT490463A patent/AT240329B/en active
- 1963-07-08 CH CH849363A patent/CH450346A/en unknown
- 1963-10-18 GB GB4129463A patent/GB1058652A/en not_active Expired
- 1963-12-10 SE SE13709/63A patent/SE313288B/xx unknown
- 1963-12-20 BE BE641596A patent/BE641596A/xx unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2090190A1 (en) * | 1970-05-21 | 1972-01-14 | Sandoz Sa | Strengthening cellulosic fibres - by n-methylol cpds and aluminium nitrate |
US7863405B2 (en) | 2004-09-02 | 2011-01-04 | Eastman Chemical Company | Removal of residual acetaldehyde from polyester polymer particles |
Also Published As
Publication number | Publication date |
---|---|
CH450346A (en) | 1968-04-30 |
CH849363A4 (en) | 1967-10-14 |
SE313288B (en) | 1969-08-11 |
BE641596A (en) | 1964-04-16 |
DE1254116B (en) | 1967-11-16 |
NL296806A (en) | |
AT240329B (en) | 1965-05-25 |
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