-
公开(公告)号:GB1082432A
公开(公告)日:1967-09-06
申请号:GB5046564
申请日:1964-12-11
Applicant: BASF AG
Inventor: VESCIA MICHELE , SCHWINDT WOLFGANG , DIETRICH WERNER , PERKUHN ULRICH , FAULHABER GERHARD , WOLF HANS , WILHELM HANS
IPC: C03C25/10 , C03C25/475 , D06P1/38
Abstract: Glass fibres are dyed or printed with pigments using as a binder a film-forming polymer which becomes cross-linked under the influence of a proton-acceptor and using an amino-silane or a hydrocarbon wax as an agent having hydrophobic action to promote adhesion between the binder and the glass surface, the process being carried out in the presence of a proton-acceptor, and the treated fibres being finally dried and heated. The polymers are those having groups, for example amino or hydroxy groups, which by means of proton acceptors can enter into covalent bonds with themselves or other groups. The preferred polymers are copolymers bearing hydrocarbon radicals as side chains in which a halogen atom and a hydroxyl group are attached to two adjacent carbon atoms, particularly a polymer obtained by co-polymerising 2-hydroxy-3-chloropropyl acrylate with other monomers. The proton-acceptor may be an alkali metal hydroxide, carbonate or bicarbonate, amonia or an organic amine; it may be provided as the alkali present in the glass. The glass fibres may be treated as such, mixed with other fibres or in the form of fabric. In the treatment, the various components can be applied separately or in combination. Examples illustrate the use of copper phthalocyanine, azo dyes and carbon black as the pigments.
-
公开(公告)号:FR1318627A
公开(公告)日:1963-02-22
申请号:FR877720
申请日:1961-11-02
Applicant: BASF AG
Inventor: LUETZEL GERHARD , ROHLAND WERNER , TARTTER ARNOLD , BARTS GUENTER , DIETRICH WERNER , FEDERKIEL WILHELM , MUELLER ROLAND
IPC: D06P1/00
-
公开(公告)号:GB838691A
公开(公告)日:1960-06-22
申请号:GB3301558
申请日:1958-10-16
Applicant: BASF AG
Inventor: DIETRICH WERNER , KRACHT MANFRED , FUNK HANS
IPC: D06P5/20
Abstract: In the dyeing of textile materials by the "molten metal" technique wherein the textile is drawn through the aqueous dye liquor, e.g. a vat dyestuff liquor, and then through a molten metal bath containing tin, lead, cadmium or bismuth on the surface of which the dye liquor floats, corrosion of the metal is prevented by adding to the dye liquor an acetylenic monohydric or polyhydric alcohol such as propargyl alcohol, butine-(2)-ol-(1), pentine-(2)-ol-(1) and butine-(2)-diol-(1,4).
-
公开(公告)号:CA675862A
公开(公告)日:1963-12-10
申请号:CA675862D
Applicant: BASF AG
Inventor: MUELLER ROLAND , BARTS GUENTER , LUETZEL GERHARD , DIETRICH WERNER , TARTTER ARNOLD , FEDERKIEL WILHELM
-
公开(公告)号:FR1419126A
公开(公告)日:1965-11-26
申请号:FR998477
申请日:1964-12-14
Applicant: BASF AG
Inventor: VESCIA MICHELE , SCHWIND WOLFGANG , DIETRICH WERNER , PERKUHN ULRICH , FAULHABER GERHARD , WOLF HANS , WILHELM HANS
IPC: C03C25/10 , C03C25/475 , D06P1/38
-
公开(公告)号:BE609825A
公开(公告)日:1962-02-15
申请号:BE609825
申请日:1961-10-31
Applicant: BASF AG
Inventor: LUETZEL GERHARD , ROHLAND WERNER , TARTTER ARNOLD , DIETRICH WERNER , BARTS GUENTER , FEDERKIEL WILHELM , MUELLER ROLAND
IPC: C09B62/443 , D06L3/12
-
公开(公告)号:BE579294A
公开(公告)日:1959-12-03
申请号:BE579294
申请日:1959-06-03
Applicant: BASF AG
Inventor: BLUM ADOLF , WILHELM ERNST , DIETRICH WERNER , KUPPERS WILHELM
IPC: D06P
-
公开(公告)号:FR1207983A
公开(公告)日:1960-02-19
申请号:FR1207983D
申请日:1958-11-14
Applicant: BASF AG
Inventor: DIETRICH WERNER , KRACHT MANFRED , FUNK HANS
IPC: C23F11/12
-
公开(公告)号:CA772061A
公开(公告)日:1967-11-21
申请号:CA772061D
Applicant: BASF AG
Inventor: WOLF HANS , WILHELM HANS , SCHWINDT WOLFGANG , PERKUHN ULRICH , FAULHABER GERHARD , VESCIA MICHELE , DIETRICH WERNER
-
10.
公开(公告)号:GB923162A
公开(公告)日:1963-04-10
申请号:GB3886361
申请日:1961-10-31
Applicant: BASF AG
Inventor: LUETZEL GERHARD , ROHLAND WERNER , TARTTER ARNOLD , BARTS GUENTER , DIETRICH WERNER , FEDERKIEL WILHELM , MUELLER ROLAND
IPC: C09B62/443 , D06L3/12
Abstract: Compounds of the formula: are obtained from hexahydro-1,3,5-tri-(b -chloropropionyl)-s-triazine by the action of tertiary amines such as pyridine, quinoline, N-methylimidazole or N-vinylimidazole. Polyamides are obtained by reaction of 2 moles acrylic acid chloride with 1 mole of ethylene, propylene, butylene or hexamethylene diamine or 1,4-diaminobenzene-2-sulphonic acid, or by reaction of 3 moles of acrylic acid chloride with 1 mole of diethylene or dipropylene triamine, or by reaction of 4 moles acrylic acid chloride with 1 mole of triethylene tetramine. Alternatively instead of acrylic acid chloride the following chlorides may be used: b -chloropropionyl, b -sulphato-propionic acid, b -methoxypropionic acid, b -phenoxypropionic acid, b -(4-chlorothiophenyl)-propionic acid or b -phenylsulphone propionic acid chloride. Those compounds containing the b -chloro-propionyl radical may be quaternised with a tertiary amine. Methylene-bis-acrylamide of the formula: is obtained by reaction of 2 moles acrylamide with 1 mole formaldehyde. The above compound may be converted into cyclic compounds with dialdehydes, e.g. with glyoxal to a compound of the formula: ALSO:Textile materials are dyed, printed and/or optically brightened in the presence of an alkaline agent with (a) a dye or optical brightener having one or more reactive hydrogen atoms preferably attached by way of N, O or S atoms or which is capable of making such hydrogen atoms available during the process and (b) a polyfunctional colourless non-fluorescent compound which bears two or more CH2 = CH-CO-groups attached through nitrogen or which is capable of forming such groups during the process. The textile materials may be of acrylic polymers, linear aromatic polyesters, polyamides or especially of cellulosic materials such as cotton or rayon. The alkaline agents specified are sodium and potassium hydroxide, carbonate and bicarbonate, disodium and trisodium phosphate. The dyes or brighteners (a) may bear 1-11 reactive H atoms in the form of 1 DEG or 2 DEG amino groups, sulphonic acid amide, alkylamide and arylamide groups, carboxylic acid amide and alkylamide groups, hydroxyl and sulphydryl groups but particularly -alkylene-OH, -alkylene-NH2, -SO2-NH2, -CH2CH2-OH, -CH2CH2-NH2, -SO2-NH-CH2CH2-OH and -SO2-NH-CH3 groups. Dyestuffs containing methylene ether and ester groups which are converted into methylol groups during the process are also suitable. The dyes may be water-soluble or insoluble and are preferably of low substantivity but may be of the reactive type. (a) and (b) are said to react in the manner of the Michael reaction. The specified compounds (b) are: hexahydro-1, 3, 5-triacryloyl-s-triazine obtainable by reaction of acrylonitrile and formaldehyde, hexahydro-1, 3, 5-tri-(p-chloropropionyl)-s-triazine and its derivatives quaternated with pyridine, quinoline, N-methylimidazole or N-vinylimidazole, the reaction products of 2 moles acrylic acid chloride with 1 mole ethylene, propylene, butylene or hexamethylene diamine or 1, 4-diaminobenzene-2-sulphonic acid, the reaction products of 3 moles acrylic acid chloride with 1 mole of diethylene or dipropylene triamine and the reaction product of 4 moles acrylic acid chloride with 1 mole of triethylene tetramine. Instead of acrylic acid chloride in the above products there may be used the following acyl chlorides: b -chloropropionyl, b -sulphatoethylpropionic acid, b -methoxypropionic acid, b -phenoxypropionic acid, b -(4-chlorothio-phenyl)-propionic acid or b -phenylsulphone-propionic acid chloride. Those compounds containing the b -chloropropionyl radical may be quaternized as above. Also suitable are methylene-bis-acryloylamide obtainable by reaction of 2 moles acrylamide with 1 mole formaldehyde and its condensation product with glyoxal of the formula Fixation may be accomplished at room temperature but preferably at 70 DEG -150 DEG C. by steaming or dry heating for about 5-10 minutes. (a) and (b) may be applied in either sequence but are preferably applied simultaneously from a single bath or paste also containing the alkaline agent by means of jiggers, vats, winch becks, high temperature dyeing apparatus or especially by padding or printing. Resin finishing may be carried out simultaneously. Compounds (b) may be used together with dispersing agents and/or protective colloids as aqueous solutions or dispersions or as solutions in water miscible solvents such as dimethylformamide (preferred), dimethylacetamide, N-methyl-2-pyrrolidone, glycol ethyl ether, tetrahydrofuran, methanol, ethanol, isopropanol, acetone, formic or acetic acid. Many other adjurants are specified among which are dispersing agents such as lignin sulphonate and a naphthalene-2-sulphonic acid/formaldehyde condensate, protective colloids such as carboxymethyl-cellulose, acetylated polyvinyl alcohol or polyvinyl pyrrolidone both of k-value 30, antioxidants such as hydroquinone; wetting agents such as the sodium salt of sulphonated oleic acid N-methylcyclohexylamide, migration inhibitors such as sodium acetate and thickening agents such as sodium alginate. Examples are given of dyeing and printing in which a great variety of dyestuffs is employed; some of them are described in Specifications 520,199, 771,320, 811,221, 811,222, 824,300, 827,568 and 900,764 and German Specifications 335,809, 742,932, 742,939 and 908,068. Other dyestuffs referred to include and Specifications 520,301 and 805,548 also are referred to.
-
-
-
-
-
-
-
-
-