WO2012136605A1 - Wässrige bindemittel für körnige und/oder faserförmige substrate - Google Patents
Wässrige bindemittel für körnige und/oder faserförmige substrate Download PDFInfo
- Publication number
- WO2012136605A1 WO2012136605A1 PCT/EP2012/055919 EP2012055919W WO2012136605A1 WO 2012136605 A1 WO2012136605 A1 WO 2012136605A1 EP 2012055919 W EP2012055919 W EP 2012055919W WO 2012136605 A1 WO2012136605 A1 WO 2012136605A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- polymer
- monomers
- aqueous
- monomer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N5/00—Roofing materials comprising a fibrous web coated with bitumen or another polymer, e.g. pitch
- D06N5/003—Roofing materials comprising a fibrous web coated with bitumen or another polymer, e.g. pitch coated with bitumen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/02—Cellulose; Modified cellulose
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/02—Starch; Degradation products thereof, e.g. dextrin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/04—Alginic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/06—Pectin; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/08—Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J101/00—Adhesives based on cellulose, modified cellulose, or cellulose derivatives
- C09J101/02—Cellulose; Modified cellulose
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J103/00—Adhesives based on starch, amylose or amylopectin or on their derivatives or degradation products
- C09J103/02—Starch; Degradation products thereof, e.g. dextrin
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J105/00—Adhesives based on polysaccharides or on their derivatives, not provided for in groups C09J101/00 or C09J103/00
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J105/00—Adhesives based on polysaccharides or on their derivatives, not provided for in groups C09J101/00 or C09J103/00
- C09J105/04—Alginic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J105/00—Adhesives based on polysaccharides or on their derivatives, not provided for in groups C09J101/00 or C09J103/00
- C09J105/06—Pectin; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J105/00—Adhesives based on polysaccharides or on their derivatives, not provided for in groups C09J101/00 or C09J103/00
- C09J105/08—Chitin; Chondroitin sulfate; Hyaluronic acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J143/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and containing boron, silicon, phosphorus, selenium, tellurium, or a metal; Adhesives based on derivatives of such polymers
- C09J143/04—Homopolymers or copolymers of monomers containing silicon
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N5/00—Roofing materials comprising a fibrous web coated with bitumen or another polymer, e.g. pitch
Definitions
- Aqueous binders for granular and / or fibrous substrates for granular and / or fibrous substrates
- the present invention relates to an aqueous binder composition
- an aqueous binder composition comprising as essential binder components a) at least one polymer P composed of> 0.1 and ⁇ 15% by weight of at least one acid group-containing ethylenically unsaturated monomer and / or at least one ⁇ , ⁇ -monoethylenic unsaturated C 3 - to C ß mono- or dicarboxylic bonklamids (monomers A)
- the present invention relates to the use of the aforementioned aqueous binder composition as a binder for granular and / or fibrous substrates, processes for the production of moldings using the aqueous binder composition, and the moldings thus produced, in particular bonded fiber webs, which in turn are used for producing bitumen roofing membranes.
- aqueous binder composition for polysaccharide-containing aqueous binder compositions, the following state of the art can be assumed.
- EP-A 649 870 discloses mixtures of polycarboxylic acids and saccharide compounds in a weight ratio of 95: 5 to 20:80 for the production of polymer films with gas barrier action.
- EP-A 91 1 361 discloses aqueous binder systems for granular and / or fibrous substrates comprising a polycarboxy polymer having a weight average molecular weight of at least 1000 g / mol and a polysaccharide having a weight average molecular weight of at least 10,000 g / mol, the amounts thereof are such that the ⁇ quivalenzfug of carboxyl groups to hydroxyl groups is 3: 1 to 1: 20.
- EP-A 1 578 879 discloses aqueous binder compositions for coating glass fibers, comprising a polycarboxy polymer, a polyhydric alcohol having at least two hydroxyl groups and a so-called water-soluble diluent, in particular polysaccharides having an average molecular weight of less than 10,000 g / mol being proposed as the water-soluble diluent.
- WO 2008/150647 discloses aqueous binder systems for the production of fiber mats, comprising a urea / formaldehyde resin and an aqueous copolymer dispersion whose copolymer is essentially composed of styrene, alkyl acrylates or methacrylates, acrylonitrile and an optionally substituted acrylamide.
- the aqueous copolymer dispersion may still contain starch.
- aqueous binder systems for nonwoven fabrics comprising an aqueous copolymer dispersion, the copolymer contains between 5 and 40 wt .-% of at least one carboxylic acid group-containing monomer in polymerized form and a natural binder component selected from the group comprising polysaccharides, vegetable proteins , Lignins and / or ligninsulfonates.
- a disadvantage of the binder systems of the prior art is that they are not always able to fully satisfy in the production of moldings from granular and / or fibrous substrates, in particular with regard to their mechanical properties.
- the object of the present invention was therefore to provide aqueous binder compositions which overcome the disadvantages of the aqueous binder compositions of the prior art and can be made accessible by means of which shaped articles having improved transverse tear strength at room temperature and / or improved heat resistance at elevated temperature.
- the object was achieved by the aforementioned aqueous binder composition.
- An essential constituent of the aqueous binder composition is a polymer compound P which is built up in copolymerized form
- Monomers and / or at least one ⁇ , ⁇ -monoethylenically unsaturated C 3 - to Cß mono- or dicarboxylic acid amide (monomers A)> 8.0 and ⁇ 30 wt .-% of at least one ethylenically unsaturated carboxylic acid nitrile or
- Homopolymer has a glass transition temperature> 50 ° C (monomers F) and which differs from the monomers A to D.
- Suitable monomers A are all ethylenically unsaturated compounds which have at least one acid group [proton donor], for example a sulfonic acid, phosphonic acid or carboxylic acid group, for example vinylsulfonic acid, allylsulfonic acid, styrenesulfonic acid, 2-acrylamidomethylpropanesulfonic acid, vinylphosphonic acid, Al - lylphosphonic acid, styrenephosphonic acid and 2-acrylamido-2-methylpropanephosphonic.
- proton donor for example a sulfonic acid, phosphonic acid or carboxylic acid group
- vinylsulfonic acid allylsulfonic acid, styrenesulfonic acid, 2-acrylamidomethylpropanesulfonic acid, vinylphosphonic acid, Al - lylphosphonic acid, styrenephosphonic acid and 2-acrylamido-2-methylpropanephosphonic.
- the monomers A are ⁇ , ⁇ -monoethylenically unsaturated, in particular C 3 - to CQ-, preferably C 3 - or C 4 -mono- or dicarboxylic acids, for example acrylic acid, methacrylic acid, ethylacrylic acid, itaconic acid, allylacetic acid, crotonic acid , Vinylacetic acid, fumaric acid, maleic acid, 2-methylmaleic acid.
- the monomers A also include the anhydrides of corresponding ⁇ , ⁇ -monoethylenically unsaturated dicarboxylic acids, such as, for example, maleic anhydride or 2-methylmaleic anhydride.
- the acid group-containing monomer A is preferably selected from the group comprising acrylic acid, methacrylic acid, crotonic acid, fumaric acid, maleic acid, maleic anhydride, 2-methylmaleic acid and itaconic acid, with acrylic acid, methacrylic acid and / or itaconic acid being particularly preferred.
- the monomers A also comprise the fully or partially neutralized water-soluble salts, in particular the alkali metal or ammonium salts, of the abovementioned acids.
- Other suitable monomers A are all ⁇ , ⁇ -monoethylenically unsaturated C 3 -C 4 -mono- or dicarboxylic acid amides.
- the monomers A are the abovementioned compounds whose carboxylic acid amide group is substituted by an alkyl or a methylol group.
- Examples of such monomers A are the amides or diamides of the ⁇ , ⁇ -monoethylenically unsaturated C 3 - to CQ-, preferably C 3 - or C 4 -mono- or dicarboxylic acids such as, for example, acrylamide, methacrylamide, ethylacrylamide, itaconic acid mono or diamide, allylacetic acid amide, crotonic acid mono- or diamide, vinylacetic acid amide, fumaric mono- or diamide, maleic acid mono- or diamide and 2-methylmaleic acid mono- or diamide.
- Examples of ⁇ , ⁇ -monoethylenically unsaturated C 3 - to C 6 -mono- or dicarboxylic acid anhydrides whose carboxamide groups are substituted by an alkyl or a methylol group are N-alkylacrylamides and -methacrylamides, for example N-tert-butylacrylamide and -methacrylamide, N-methylacrylamide and -methacrylamide, and N-methylolacrylamide and N-methylolmethacrylamide.
- Preferred amidic monomers A are acrylamide, methacrylamide, N-methylolacrylamide and / or N-methylolmethacrylamide, with methylolacrylamide and / or N-methylolmethacrylamide being particularly preferred.
- Particularly preferred monomers A are acrylic acid, methacrylic acid, crotonic acid, fumaric acid, maleic acid, maleic anhydride, 2-methylmaleic acid, itaconic acid, acrylamide, methacrylamide, N-methylolacrylamide and / or N-methylolmethacrylamide, where acrylic acid, methacrylic acid, itaconic acid, methylolacrylamide and / or N Methylolmethacrylamid are particularly preferred.
- the amount of the monomers A copolymerized in the polymer P is> 0.1 and ⁇ 15% by weight, preferably> 0.5 and ⁇ 10% by weight and particularly preferably> 3.0 and ⁇ 8.5% by weight ,
- Suitable monomers B are all ethylenically unsaturated compounds which have at least one nitrile group.
- the monomers B are the nitriles which are derived from the abovementioned ⁇ , ⁇ -monoethylenically unsaturated, in particular C 3 - to CQ-, preferably C 3 - or C 4 -mono- or dicarboxylic acids, for example Ac - Rylnitril, methacrylonitrile, maleic acid dinitrile and / or fumaronitrile, with acrylonitrile and / or methacrylonitrile being particularly preferred.
- the amount of the monomers B copolymerized in the polymer P is> 8.0 and ⁇ 30% by weight, preferably> 10 and ⁇ 25% by weight and particularly preferably> 10 and ⁇ 20% by weight.
- Suitable monomers C are all compounds which have at least two non-conjugated ethylenically unsaturated groups.
- Examples include two vinyl radicals containing monomers, two vinylidene radicals having monomers and two alkenyl radicals having monomers.
- Particularly advantageous are the diesters of dihydric alcohols with ⁇ , ⁇ -monoethylenically unsaturated monocarboxylic acids, among which acrylic and methacrylic acid are preferred.
- alkylene glycol diacrylates and dimethacrylates such as ethylene glycol diacrylate, 1, 2-propylene glycol diacrylate, 1, 3-propylene glycol diacrylate, 1, 3 Butylene glycol diacrylate, 1, 4-butylene glycol diacrylate and ethylene glycol dimethacrylate, 1, 2-propylene glycol dimethacrylate, 1, 3-propylene glycol dimethacrylate, 1, 3-Butylenglykoldimethacrylat, 1, 4-Butylenglykoldimethacrylat, tri-esters of trihydric alcohols with ⁇ , ⁇ -monoethylenically unsaturated monocarboxylic acids, such as Glycerol triacrylate, glycerol trimethacrylate, trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, and divinylbenzene, vinyl methacrylate, vinyl acrylate
- the amount of the monomers C copolymerized in the polymer P is> 0 and ⁇ 5.0% by weight, preferably> 0 and ⁇ 3.0% by weight and particularly preferably> 0 and ⁇ 1.5% by weight.
- Suitable monomers D are all monoethylenically unsaturated silane-containing compounds.
- the monomers D have a hydrolyzable silane group.
- Hydrolyzable silane groups advantageously contain at least one alkoxy group or one halogen atom, such as, for example, chlorine.
- monomers D are disclosed in WO 2008/150647, page 9, lines 5 to 25. By their express reference, these monomers D as part of the present
- the monomers D are always preferably used when inorganic granular and / or fibrous substrates, such as in particular glass fibers or mineral fiber, for example, asbestos or rock wool to be bound.
- the amount of the monomers D optionally polymerized in the polymer P is in a preferred embodiment> 0 and ⁇ 10 wt .-%, preferably> 0 and ⁇ 5.0 wt .-% and particularly preferably 0 wt .-%.
- the amount of the monomers copolymerized in the polymer P is D> 0.1 and ⁇ 10% by weight, advantageously> 0.1 and ⁇ 5.0 wt .-% and particularly advantageously> 0.5 and ⁇ 2.5 wt .-%.
- Suitable monomers E are all ethylenically unsaturated monomers whose homopolymer have a glass transition temperature ⁇ 30 ° C. and which differ from the monomers A to D.
- suitable monomers E are conjugated aliphatic C 4 to Cg diene compounds, esters of vinyl alcohol and a C 1 to C 10 monocarboxylic acid, C 1 to C 10 alkyl acrylate, C 5 to C 10 alkyl methacrylate, C 5 to C 10 cycloalkyl acrylate and methacrylate, C 1 to C 10 dialkyl maleate and / or C 1 to C 10 dialkyl fumarate, vinyl ethers of C 3 to C 10 alkanols, branched and unbranched C 3 to C 10 olefins.
- monomers E whose homopolymers have Tg values ⁇ 0 ° C.
- monomers E are vinyl acetate, ethyl acrylate, n-propyl acrylate, n-butyl acrylate, isobutyl acrylate, sec-butyl acrylate, n-hexyl acrylate, 2-ethylhexyl acrylate, n-hexyl methacrylate, 2-ethylhexyl methacrylate, di-n-butyl maleate, di- n-butyl fumarate, with 2-ethylhexyl acrylate, n-butyl acrylate, 1, 4-butadiene and / or ethyl acrylate are particularly preferred.
- the amount of the monomer E copolymerized in the polymer P is> 20 and ⁇ 70% by weight, preferably> 25 and ⁇ 65% by weight and particularly preferably> 30 and ⁇ 60% by weight.
- Suitable monomers F are all ethylenically unsaturated monomers whose homopolymerized polymers have a glass transition temperature> 50.degree. C. and which differ from monomers A to D.
- Suitable monomers F are, for example, vinylaromatic monomers and C 4 to C 4 alkyl methacrylates.
- Vinylaromatic monomers are in particular derivatives of styrene or of ⁇ -methylstyrene in which the phenyl rings are optionally substituted by 1, 2 or 3 C 1 to C 4 alkyl groups, halogen, in particular bromine or chlorine and / or methoxy groups. Preference is given to those monomers whose homopolymers have a glass transition temperature> 80 ° C.
- Particularly preferred monomers are styrene, ⁇ -methylstyrene, o- or p-vinyltoluene, p-acetoxystyrene, p-bromostyrene, p-tert-butylstyrene, o-, m- or p-chlorostyrene, methyl methacrylate, tert-butyl acrylate, tert-butylstyrene.
- the amount of monomers F copolymerized in the polymer P is> 25 and ⁇ 71.9% by weight, preferably> 25 and ⁇ 64.5% by weight and particularly preferably> 25 and ⁇ 57% by weight.
- the glass transition temperature Tg it is meant the glass transition temperature limit which it strives for according to G. Kanig (Kolloid-Zeitschrift & Zeitschrift fur Polymere, Vol. 190, page 1, Equation 1) with increasing molecular weight.
- the Tg is determined by the DSC method (differential scanning calorimetry, 20 K / min, midpoint measurement, DIN 53 765).
- the Tg values for the homopolymers of most monomers are known and are listed, for example, in Ullmann's Ecyclopedia of Industrial Chemistry, VCH Weinheim, 1992, Vol. 5, Vol. A21, p. 169; Further sources of glass transition temperatures of homopolymers are, for example, J.
- Cio-alkyl groups are to be understood as meaning linear or branched alkyl radicals having 1 to 10 carbon atoms, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, iso-pentyl, tert-pentyl n-hexyl, 2-ethylhexyl, n-nonyl or n-decyl be understood.
- C 5 -C 10 -cycloalkyl groups are preferably cyclopentyl or cyclohexyl groups, which may optionally be substituted by 1, 2 or 3 C 1
- the aqueous binder compositions advantageously comprise polymers P whose at least one monomer E is selected from the group comprising conjugated aliphatic see C 4 to Cg diene compounds, esters of vinyl alcohol and a C to C 10 monocarboxylic acid, C 1 to C 10 alkyl acrylate, C 5 to C 10 alkyl methacrylate, C 5 to C 10 cycloalkyl acrylate and methacrylate, C 1 to C 10 dialkyl maleinate and / or C 1 to C 10 dialkyl fumarate and whose at least one monomer F is selected from the group comprising vinylaromatic monomer and / or C 4 to C 4 alkyl methacrylate.
- monomers P whose at least one monomer E is selected from the group comprising conjugated aliphatic see C 4 to Cg diene compounds, esters of vinyl alcohol and a C to C 10 monocarboxylic acid, C 1 to C 10 alkyl acrylate, C 5 to C 10 alkyl methacryl
- the aqueous binder compositions comprise polymers P which contain> 0 and ⁇ 1, 5 wt .-% of at least one monomer C in copolymerized form.
- the aqueous binder composition contains a polymer P, which is constructed in copolymerized form
- the aqueous binder composition contains a polymer P, which is constructed in copolymerized form
- the preparation of the polymers P is known in principle to the person skilled in the art and is carried out, for example, by radical polymerization of the monomers A to F by the method of substance, emulsion, solution, precipitation or suspension polymerization, although the free-radically initiated aqueous emulsion polymerization is particularly preferred.
- the polymer P is dispersed in an aqueous medium, i. used in the form of an aqueous polymer dispersion.
- the free-radically initiated aqueous emulsion polymerization is usually carried out by dispersing the ethylenically unsaturated monomers, generally with concomitant use of dispersing aids, such as emulsifiers and / or protective colloids, in aqueous medium and polymerizing them by means of at least one water-soluble free-radical polymerization initiator.
- the residual contents of unreacted ethylenically unsaturated monomers are also chemical and / or physical methods known to the person skilled in the art [see, for example, EP-A 771328, DE-A 19624299, DE-A 19621027, DE-A 19741 184, DE-A 19741 187, DE-A 19805122, DE-A 19828183, DE-A 19839199, DE-A 19840586 and 198471 15], the polymer content by dilution or concentration is adjusted to a desired value or the aqueous polymer dispersion more common Additives such as bactericidal, foaming or viscosity modifying additives added.
- aqueous dispersions of a polymer P which are composed of> 0.1 and ⁇ 15% by weight of at least one monomer A are advantageously used to prepare the aqueous binder compositions
- the total amount of the monomers A to F (total monomer amount) in the aqueous reaction medium can be initially introduced before the initiation of the polymerization reaction.
- the metering of the monomers A to F can be carried out as separate individual streams, as inhomogeneous or homogeneous (part) mixtures or as a monomer emulsion.
- the monomers A to F are advantageously metered in the form of a monomer mixture, in particular in the form of an aqueous monomer emulsion.
- dispersants are used which keep both the monomer droplets and the polymer particles formed dispersed in the aqueous medium and thus ensure the stability of the aqueous polymer dispersion produced.
- Suitable dispersing agents are both the protective colloids customarily used for carrying out free-radical aqueous emulsion polymerizations and emulsifiers.
- Suitable protective colloids are, for example, polyvinyl alcohols, polyalkylene glycols, alkali metal salts of polyacrylic acids and polymethacrylic acids, gelatin derivatives or acrylic acid, methacrylic acid, maleic anhydride, 2-acrylamido-2-methylpropanesulfonic acid and / or 4-styrenesulfonic acid-containing copolymers and their alkali metal salts but also N-vinylpyrrolidone, N-vinylcaprolactam, N-vinylcarbazole, 1-vinylimidazole, 2-vinylimidazole, 2-vinylpyridine, 4-vinylpyridine, acrylamide, methacrylamide, acrylates containing amine groups, methacrylates, acrylamides and / or methacrylamides containing homopolymers and copolymers.
- protective colloids can be found in Houben-Weyl, Methods of Organic Chemistry, Volume XI V / 1, Macromolecular Materials, Georg Thieme Verlag, Stuttgart, 1961, pages 41 1 to 420.
- mixtures of protective colloids and / or emulsifiers can be used.
- dispersants used are exclusively emulsifiers whose relative molecular weights, in contrast to the protective colloids, are usually below 1000. They may be anionic, cationic or nonionic in nature.
- the individual components must be compatible with each other, which can be checked in case of doubt by hand on fewer preliminary tests.
- anionic emulsifiers are compatible with each other and with nonionic emulsifiers.
- cationic emulsifiers while anionic and cationic emulsifiers are usually incompatible with each other.
- An overview of suitable emulsifiers can be found in Houben-Weyl, Methods of Organic Chemistry, Volume XIV / 1, Macromolecular Materials, Georg-Thieme-Verlag, Stuttgart, 1961, pages 192 to 208.
- emulsifiers are used in particular as dispersing aids.
- Nonionic emulsifiers are, for example, ethoxylated mono-, di- and tri-alkylphenols (EO degree: 3 to 50, alkyl radical: C 4 to C 12) and also ethoxylated fatty alcohols (EO degree: 3 to 80, alkyl radical: Ce to C36).
- Lutensol ® A grades C12C1-1- fatty alcohol ethoxylates, EO units: 3 to 8
- Lutensol ® AO grades C 3 -C 5 -Oxoalkoholethoxylate, EO units: 3 to 30
- Lutensol ® AT Ci 6 Ci 8 -Fettalkoholethoxylate, EO degree: 1 1 to 80
- Lutensol ® ON brands Cio-Oxoalkoholethoxylate, EO degree: 3 to 1 1
- Lutensol ® TO brands Ci 3 - Oxo alcohol ethoxylates, EO grade: 3 to 20
- Typical anionic emulsifiers are, for example, alkali metal and ammonium salts of alkyl sulfates (alkyl radical: Ce to C12), of sulfuric monoesters of ethoxylated alkanols (EO degree: 4 to 30, alkyl radical: C12 to Cie) and ethoxylated alkylphenols (EO degree: 3 to 50, Alkyl radical: C 4 to C 12), of alkylsulfonic acids (alkyl radical: C 12 to Cie) and of alkylarylsulfonic acids (alkyl radical: Cg to
- R 1 and R 2 hydrogen atoms or C 4 - mean to C2 4 alkyl, and H atoms are not the same, and may be M 1 and M 2 alkali metal ions and / or ammonium ions, proved to be suitable in the general formula (I
- R 1 and R 2 are preferably linear or branched alkyl radicals having 6 to 18 C atoms, in particular having 6, 12 and 16 C atoms or hydrogen, where R 1 and R 2 are not both simultaneously H atoms.
- M 1 and M 2 are preferably sodium, potassium or ammonium, with sodium being particularly preferred.
- Particularly advantageous compounds (I) are those in which M 1 and M 2 are sodium, R 1 is a branched alkyl radical having 12 C atoms and R 2 is an H atom or R 1 .
- technical mixtures are used which have a proportion of 50 to 90 wt .-% of the monoalkylated product, such as Dowfax ® 2A1 (trademark of the Dow Chemical Company).
- the compounds (I) are well known, for example from US-A 4269749, and commercially available.
- Suitable cationic emulsifiers are generally a primary, secondary, tertiary or quaternary ammonium salts containing CQ to C 18 -alkyl, alkylaryl or heterocyclic, alkanolammonium salts, pyridinium salts, imidazolinium salts, oxazolinium salts, morpholinium salts, thiazolinium salts and salts of amine oxides, quinolinium salts, Isoquinolinium salts, tropylium salts, sulfonium salts and phosphonium salts.
- Examples include dodecylammonium acetate or the corresponding sulfate, the sulfates or acetates of the various 2- (N, N, N-trimethylammonium) ethylparaffinklaer, N-Cetylpyridiniumsulfat, N-Laurylpyridiniumsulfat and N-cetyl-N, N, N-trimethylammonium sulfate, N- Dodecyl-N, N, N-trimethylammonium sulfate, N-octyl-N, N, N-trimethylammonium sulfate, N, N-distearyl-N, N-dimethylammonium sulfate and the gemini surfactant N, N '- (lauryldimethyl) ethylenediamine disulfate, ethoxylated tallow fatty alkyl -N-methyl ammonium sulfate and ethoxylated
- BASF SE about 1 1 ethylene oxide.
- Numerous other examples can be found in H. Stumblee, Tensid-Taschenbuch, Carl-Hanser-Verlag, Kunststoff, Vienna, 1981, and in McCutcheon's, Emulsifiers & Detergents, MC Publishing Company, Glen Rock, 1989.
- anionic counterparts are as possible are low nucleophilic, such as perchlorate, sulfate, phosphate, nitrate and carboxylates such as acetate, trifluoroacetate, trichloroacetate, propionate, oxalate, citrate, benzoate, as well as conjugated anions of organosulfonic acids, such as methylsulfonate, trifluoromethylsulfonate and para-toluenesulfonate , furthermore tetrafluoroborate, tetraphenylborate, tetrakis (pentafluorophenyl) borate, tetrakis [bis (3,5-trifluoromethyl) phenyl] borate, hexafluorophosphate, hexafluoroarsenate or hexafluoroantimonate.
- organosulfonic acids such as methylsulfonate, trifluoromethylsul
- the emulsifiers preferably used as dispersing agents are advantageously in a total amount> 0.005 and ⁇ 10 wt .-%, preferably> 0.01 and ⁇ 5 wt .-%, in particular> 0.1 and ⁇ 3 wt .-%, each based on the total amount of monomers A to F (Geticianmonomerenmenge), used.
- the total amount of the protective colloids used as dispersing aids in addition to or instead of the emulsifiers is often> 0.1 and ⁇ 40% by weight and frequently> 0.2 and ⁇ 25% by weight, in each case based on the total monomer amount.
- anionic and / or nonionic emulsifiers preference is given to using anionic and / or nonionic emulsifiers and, with particular preference, anionic emulsifiers as dispersion auxiliaries.
- the total amount of the dispersing aid in the aqueous reaction medium can be determined before the initiation of the polymerization. be presented. However, it is also possible, if appropriate, to initially introduce only a subset of the dispersing agent in the aqueous reaction medium prior to initiation of the polymerization reaction and then to add continuously or batchwise the total amount or any residual amount of the dispersing assistant remaining under polymerization conditions during the free-radical emulsion polymerization. Preferably, the addition of the main or the total amount of dispersing aid takes place in the form of an aqueous monomer emulsion.
- free-radical polymerization initiator can be both peroxides and azo compounds.
- redoxi nitiatorsysteme come into consideration.
- peroxides may in principle inorganic peroxides, such as hydrogen peroxide or peroxodisulfates, such as the mono- or di-alkali metal or ammonium salts of peroxodisulfuric, such as their mono- and di-sodium, potassium or ammonium salts or organic peroxides, such as alkyl hydroperoxides, for example tert-butyl, p-menthyl or cumyl hydroperoxide, as well as dialkyl or diarylperoxides, such as di-tert-butyl or di-cumyl peroxide are used.
- organic peroxides such as alkyl hydroperoxides, for example tert-butyl, p-menthyl or cumyl hydroperoxide, as well as dialkyl or diarylperoxides, such as di-tert-butyl or di-cumyl peroxide are used.
- an azo compound substantially 2,2 - azobis (is
- Suitable oxidizing agents for redox initiator systems are essentially the abovementioned peroxides.
- Suitable reducing agents may be sulfur compounds having a low oxidation state, such as alkali metal sulfites, for example potassium and / or sodium sulfite, alkali hydrogen sulfites, for example potassium and / or sodium bisulfite, alkali metal metabisulfites, for example potassium and / or sodium metabisulfite, formaldehyde sulfoxylates, for example potassium and / or sodium formaldehyde sulfoxylate, Alkali salts, especially potassium and / or sodium salts, aliphatic sulfinic acids and alkali metal hydrogen sulfides, such as, for example, potassium and / or sodium hydrogen sulfide, salts of polyvalent metals, such as iron (II)
- the amount of the radical initiator used based on the total amount of monomers, 0.01 to 5 wt .-%, preferably 0.1 to 3 wt .-% and particularly preferably 0.2 to 1, 5 wt .-%.
- the total amount of the free-radical initiator in the aqueous reaction medium can be initially introduced before the initiation of the polymerization reaction.
- Initiation of the polymerization reaction starts the polymerization reaction of the monomers present in the polymerization vessel after radical formation of the radical initiator. stood.
- the initiation of the polymerization reaction by adding radical initiator to the aqueous polymerization mixture in the polymerization vessel can be carried out under polymerization conditions.
- a partial or total amount of the free-radical initiator it is also possible for a partial or total amount of the free-radical initiator to be added to the aqueous polymerization mixture containing the initially charged monomers in the polymerization vessel under conditions which are not suitable for initiating a polymerization reaction, for example at low temperature, and then polymerization conditions in the aqueous polymerization mixture be set.
- Polymerization conditions are generally to be understood as meaning those temperatures and pressures below which the free-radically initiated aqueous emulsion polymerization proceeds at an adequate rate of polymerization. They are dependent, in particular, on the radical initiator used.
- the type and amount of the radical initiator, the polymerization temperature and the polymerization pressure are advantageously selected so that the free-radical initiator has a half-life of ⁇ 3 hours, more preferably ⁇ 1 hour and most preferably ⁇ 30 minutes, and there are always enough starting radicals available to effect the polymerization reaction to initiate and maintain.
- the reaction temperature for the free-radical aqueous emulsion polymerization is the entire range from 0 to 170 ° C into consideration. In this case, temperatures of 50 to 120 ° C, preferably 60 to 1 10 ° C and particularly preferably 70 to 100 ° C are applied in the rule.
- the free-radical aqueous emulsion polymerization may be carried out at a pressure less than or equal to 1 atm [1.013 bar (absolute), atmospheric pressure] such that the polymerization temperature may exceed 100 ° C and may be up to 170 ° C. In the presence of monomers A to F having a low boiling point, the emulsion polymerization is preferably carried out under elevated pressure.
- the pressure may be 1, 2, 1, 5, 2, 5, 10, 15 bar (absolute) or even higher values. If the emulsion polymerization is carried out under reduced pressure, pressures of 950 mbar, often 900 mbar and often 850 mbar (absolute) are set.
- the free-radical aqueous emulsion polymerization is advantageously carried out at 1 atm with exclusion of oxygen, in particular under an inert gas atmosphere, for example under nitrogen or argon.
- the aqueous reaction medium may in principle also in minor amounts ( ⁇ 5 wt .-%) include water-soluble organic solvents such as methanol, ethanol, isopropanol, butanols, pentanols, but also acetone, etc.
- water-soluble organic solvents such as methanol, ethanol, isopropanol, butanols, pentanols, but also acetone, etc.
- the process according to the invention is preferably carried out in the absence of such solvents.
- free radical-transferring compounds in order to reduce or control the molecular weight of the polymers P obtainable by the polymerization.
- free radical-transferring compounds such as, for example, n-butyl chloride, n-butyl bromide, n-butyl iodide, methylene chloride, ethylene dichloride, chloroform, bromoform, bromotrichloromethane, dibromodichloromethane, carbon tetrachloride, carbon tetrachloride, benzyl chloride, benzyl bromide, organic thio compounds, such as primary, secondary or tertiary aliphatic thiols, such as, for example, ethanethiol, n-propanethiol, 2- Propanethiol, n-butanethiol
- the total amount of radically alkene-transferring compounds optionally used during the emulsion polymerization, based on the total amount of monomers, is generally ⁇ 5% by weight, often ⁇ 3% by weight and frequently ⁇ 1% by weight.
- a partial or total amount of the optional radical-transferring compound is added to the aqueous reaction medium prior to the initiation of radical polymerization.
- a partial or total amount of the radical chain transferring compound can advantageously also be fed to the aqueous reaction medium together with the monomers A to F during the polymerization.
- the polymers P used according to the invention may in principle have glass transition temperatures Tg in the range of> -70 and ⁇ 150 ° C.
- the monomers A, B, D, E and F are advantageously chosen in type and amount so that the polymers prepared solely from them have a glass transition temperature Tg in the range of> -10 and ⁇ 70 ° C. and advantageously in the range> 5 and ⁇ 50 ° C and particularly advantageous in the range> 15 and ⁇ 45 ° C.
- glass transition temperature Tg is understood to mean the midpoint temperature according to ASTM D 3418-82, determined by differential thermal analysis (DSC) [cf. also U Ilmann 's Encyclopedia of Industrial Chemistry, page 169, Verlag Chemie, Weinheim, 1992 and Zosel in paint and varnish, 82, pages 125 to 134, 1976].
- Glass transition temperatures of each of only one of the monomers 1, 2 n constructed polymers in degrees Kelvin The glass transition temperatures of these homopolymers of most ethylenically unsaturated monomers are known (or can be determined experimentally in a simple manner known per se) and, for example, in J. Brandrup, EH Immergut, Polymer Handbook Is Ed. J. Wiley, New York, 1966, 2nd ed. J. Wiley, New York, 1975 and 3rd Ed. J. Wiley, New York, 1989, and in Ullmann 's Cncyclopedia of Industrial Chemistry, page 169, Verlag Chemie, Weinheim, 1992.
- the free-radically initiated aqueous emulsion polymerization also in the presence of a polymer seed, for example in the presence of 0.01 to 3 wt .-%, often from 0.02 to 2 wt .-% and often from 0.04 to 1, 5 %
- a polymer seed for example in the presence of 0.01 to 3 wt .-%, often from 0.02 to 2 wt .-% and often from 0.04 to 1, 5 %
- a polymer seed is used in particular when the particle size of the polymer particles to be produced by means of a free-radically aqueous emulsion polymerization is to be specifically adjusted (see, for example, US Pat. No. 2,520,959 and US Pat. No. 3,397,165).
- a polymer seed is used whose polymer seed particles have a narrow particle size distribution and weight-average diameters Dw ⁇ 100 nm, frequently> 5 nm to ⁇ 50 nm and often> 15 nm to ⁇ 35 nm.
- the determination of the weight-average particle diameter is known to the person skilled in the art and takes place, for example, via the method of the analytical ultracentrifuge.
- Weight-average particle diameter is understood in this document to mean the weight-average Dw50 value determined by the method of the analytical ultracentrifuge (see, in this regard, SE Harding et al., Analytical Ultracentrifugation in Biochemistry and Polymer Science, Royal Society of Chemistry, Cambridge, Great Britain 1992, Chapter 10, Analysis of Polymer Dispersions with an Eight-Cell AUC Multiplexer: High Resolution Particle Size Distribution and Density Gradient Techniques, W. Gurchtie, pages 147 to 175).
- narrow particle size distribution should be understood as meaning the ratio of the weight-average particle diameter Dw50 and the number-average particle diameter DN50 determined by the method of the analytical ultracentrifuge
- the polymer seed is used in the form of an aqueous polymer dispersion.
- the aforementioned amounts are based on the polymer solids content of the aqueous polymer seed dispersion.
- a foreign polymer seed is understood to mean a polymer seed which was prepared in a separate reaction step and whose monomeric composition is different from the polymer prepared by the free-radical initiated aqueous emulsion polymerization
- the preparation of a foreign polymer seed is familiar to the person skilled in the art and is usually carried out by initially charging a relatively small amount of monomers and a relatively large amount of emulsifiers in a reaction vessel and adding a sufficient amount of polymerization initiator at reaction temperature.
- polymer foreign seed having a glass transition temperature> 50 ° C., frequently> 60 ° C. or> 70 ° C. and often> 80 ° C. or> 90 ° C.
- polystyrene or polymethyl methacrylate polymer seed Particularly preferred is a polystyrene or polymethyl methacrylate polymer seed.
- the total amount of foreign polymer seed can be presented in the polymerization vessel. But it is also possible to submit only a subset of Fremdpolymerse seed in the polymerization and add the remaining amount during the polymerization together with the monomers A to F. If necessary, however, it is also possible to add the total amount of polymer seed in the course of the polymerization. Preferably, the total amount of Fremdpolymersaat is submitted before initiation of the polymerization in the polymerization.
- aqueous polymer P dispersions usually have a polymer solids content of> 10 and ⁇ 70 wt .-%, often> 20 and ⁇ 65 wt .-% and often> 25 and ⁇ 60 wt .-%, each based on the aqueous polymer dispersion, on.
- the number-average particle diameter (cumulant z-average) determined by quasi-elastic light scattering (ISO Standard 13 321) is generally in the range> 10 and ⁇ 2000 nm, frequently in the range> 10 and ⁇ 700 nm and often in the range> 50 to ⁇ 400 nm.
- aqueous polymer P dispersions can in principle also be prepared in the form of so-called secondary polymer dispersions (for the basic preparation of secondary polymer dispersions, see, for example, Eckersley et al., Am Chem Chem, Soc., Polymer Chemistry, 1977, 38 (2), pages 630, 631, US-A 3360599, US-A 3238173, US-A 3726824, US-A 3734686 or US-A 6207756).
- the preparation of the secondary aqueous polymer P dispersions is carried out generally in such a way that the polymers prepared by the method of substance or solution polymerization P dissolved in a suitable organic solvent and to form aqueous polymers / solvent (mini) emulsions in a aqueous medium are dispersed. Subsequent solvent removal provides the corresponding aqueous polymer P dispersions.
- the aqueous binder compositions according to the invention comprise aqueous dispersions of polymers P whose number-average particle diameter is in the range> 10 and ⁇ 2000 nm, advantageously in the range> 10 and ⁇ 700 nm and particularly advantageously in the range> 50 to ⁇ 400 nm.
- An essential constituent of the aqueous binder composition is, in addition to at least one polymer P, at least one saccharide compound S.
- a saccharide compound S is understood as meaning monosaccharides, oligosaccharides, polysaccharides, sugar alcohols and substitution products and derivatives of the abovementioned compounds.
- the monosaccharides are organic compounds of the general formula CnHnOn, where n is an integer 5, 6, 7, 8 or 9. These monosaccharides are also referred to as pentoses, hexoses, heptoses, octoses or nonoses, these compounds being subdivided into the corresponding aldoses which contain an aldehyde group or ketones which have a keto group. Accordingly, the monosaccharides include aldo or ketopentoses, hexoses, heptoses, octoses or nonoses.
- Monosaccharide compounds which are preferred according to the invention are the pentoses and hexoses which also occur in nature, with glucose, mannose, galactose and / or xylose being particularly preferred.
- pentoses and hexoses which also occur in nature, with glucose, mannose, galactose and / or xylose being particularly preferred.
- all stereoisomers of all the abovementioned monosaccharides are also included.
- the sugar alcohols are the hydrogenation products of the aforementioned aldo or ketopentoses, hexoses, heptoses, octoses or nonoses which have the general formula C n H 2n + 20 n , where n is an integer 5, 6, 7 , 8 or 9.
- Preferred sugar alcohols are mannitol, lactitol, sorbitol and / or xylitol.
- all stereoisomers of all the aforementioned sugar alcohols should also be included.
- oligosaccharides are the disaccharides, among which the lactose, maltose and / or sucrose are particularly preferred.
- all stereoisomers of all the aforementioned oligosaccharides should also be included.
- Saccharide compounds which are composed of more than ten monosaccharide structural units are referred to in this document as polysaccharide compounds.
- the polysaccharide compounds may be composed of the structural elements of a monosaccharide (so-called homoglycans) or the structural elements of two or more different monosaccharides (so-called heteroglycans). Homoglycans are preferably used according to the invention.
- the starches composed of ⁇ -D-glucose units are particularly preferred.
- the starches consist of the polysaccharides amylose (D-glucose units which are linked together a-1, 4-glycosidically) and amylopectin (D-glucose units which contain a-1, 4- and in addition to about 4% a-1, 6 glycosidically linked).
- amylose D-glucose units which are linked together a-1, 4-glycosidically
- amylopectin D-glucose units which contain a-1, 4- and in addition to about 4% a-1, 6 glycosidically linked.
- Naturally occurring starch contains about 20 to 30% by weight of amylose and about 70 to 80% by weight of amylopectin.
- Starches which are suitable are all native starches, such as starches from corn, wheat, oats, barley, rice, millet, potatoes, peas, tapioca, sorghum or sago. Also of interest are those natural starches which have a high amylopectin content, such as waxy maize starch and waxy potato starch. The amylopectin content of these starches is> 90% by weight, often> 95% and ⁇ 100% by weight.
- saccharide compound S also includes the substitution products and derivatives of the abovementioned mono-, oligo- and polysaccharide compounds and of the sugar alcohols.
- substitution products of a saccharide compound S are understood as meaning those in which at least one hydroxy group of the saccharide compound S has been functionalized while maintaining the saccharide structure, for example by esterification, etherification, oxidation etc.
- the esterification is carried out, for example, by reacting the saccharide compound S with inorganic or organic acids , their anhydrides or halides. Of particular interest are phosphated and acetylated saccharide compounds.
- the etherification is generally carried out by reacting the saccharide compounds with organic halogen compounds, epoxides or sulfates in an aqueous alkaline solution.
- Known ethers are alkyl ethers, hydroxyalkyl hydroxy esters, carboxyalkyl ethers and allyl ethers.
- the oxidation of at least one hydroxyl group by means of an oxidation agent customary in organic carbohydrate chemistry, such as nitric acid, hydrogen peroxide, ammonium persulfate, peroxyacetic acid, sodium hypochlorite and / or 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) produces the corresponding keto compound (in the oxidation of a secondary hydroxy group), or carboxyl compound (in the oxidation of a primary hydroxy group).
- Derivatives of saccharide compounds S are understood to mean those reaction products of oligosaccharides and polysaccharides which are obtained with cleavage of at least one acetal or ketal group (at least one glycosidic bond) and therefore with degradation of the original saccharide structure.
- Such degradation reactions are familiar to the person skilled in the art and are carried out in particular by exposing an oligosaccharide or polysaccharide compound to thermal, enzymatic, oxidative and / or hydrolytic conditions.
- Starch, cellulose, guar gum, xanthan, alginate, pectin, chitosan, gum arabic, carrageenan, agar and / or gellan and substitution products or derivatives thereof are advantageously used as saccharide compound S.
- starches and / or starch derivatives or their substitution products such as advantageously maltodextrin and / or glucose syrup.
- DE Dextrose Equivalent and denotes the percentage of reducing sugars in the dry matter.
- the DE value is a measure of how far the polymer degradation has taken place.
- low DE starches are high in polysaccharides and low in low molecular weight mono- and oligosaccharides, while high DE starches are mainly composed of low molecular weight mono- or disaccharides.
- the maltodextrins preferred in the context of the present invention have DE values in the range from 3 to 20 and weight-average molecular weights of 15,000 to 30,000 g / mol.
- a glucose syrup which is likewise preferred in the context of the present invention has DE values of 20 to 30 and weight-average molecular weights in the range from 3000 to 9000 g / mol.
- Suitable solutions of maltodextrins have solids contents of from 50 to 70% by weight
- suitable solutions of glucose syrup have solids contents of from 70 to 95% by weight.
- maltodextrins are also available in powder form in spray-dried form.
- modified degraded starches which have DE values of from 1 to 3 and weight-average molecular weights Mw of from 100,000 to 1,000,000 g / mol and are usually obtainable as a solid.
- the saccharide compound S generally has a weight-average molecular weight in the range> 1000 and ⁇ 5000000 g / mol, preferably in the range> 10000 and ⁇ 3 000 000 g / mol and more preferably in the range> 50 000 and ⁇ 1 000 000 g / mol.
- the determination of the weight-average molecular weight is carried out by means of gel permeation chromatography familiar to the person skilled in the art with defined standards.
- the saccharide compound S used according to the invention has a solubility of> 10 g, advantageously> 50 g and particularly advantageously> 100 g per liter of deionized water at 20 ° C. and atmospheric pressure.
- the saccharide compound S also forms whose saccharide compound S has a solubility ⁇ 10 g per liter of deionized water at 20 ° C and atmospheric pressure. Depending on the amount of these saccharide compounds used, they can then also be present in the form of their aqueous suspension.
- saccharide compounds S are used in the manner and amount such that they are in aqueous suspension, it is advantageous if the particles of the saccharide compound S suspended in aqueous medium have an average particle diameter ⁇ 5 ⁇ m, preferably ⁇ 3 ⁇ m and particularly preferably ⁇ 1 ⁇ have.
- the average particle diameter is determined as in the case of the aqueous polymer P dispersions by the quasi-elastic light scattering method (ISO standard 13 321).
- the total amount of the saccharide compound S can be added to the aqueous polymerization medium before or during the emulsion polymerization of the monomers A to F or after completion of the emulsion polymerization of the aqueous dispersion of the polymer P.
- the one part or the total amount of the saccharide compound S is added before or during the emulsion polymerization of the monomers A to F, this can generally assume the function of the protective colloid, as a result of which the amount of other protective colloids and / or emulsifiers is reduced or, if appropriate, completely complete can be waived.
- the amount of saccharide compound S is generally> 10 and ⁇ 400 parts by weight, advantageously> 25 and ⁇ 300 parts by weight and particularly advantageously> 40 and ⁇ 250 parts by weight of saccharide compound S per 100 parts by weight. Parts of polymer P.
- aqueous binder composition according to the invention in addition to the polymer P and the saccharide compound S additionally other familiar to the expert in kind and amount components such as thickeners, pigment dispersers, dispersants, emulsifiers, buffering agents, neutralizing agents, biocides, defoamers, polyol - may contain compounds having at least 2 hydroxy groups and having a molecular weight ⁇ 200 g / mol, film-forming aids, organic solvents, pigments or fillers, etc.
- the aqueous binder composition advantageously contains ⁇ 1% by weight, in particular advantageously ⁇ 0.5% by weight, of a polyol compound having at least 2 hydroxyl groups and having a molecular weight ⁇ 200 g / mol, in particular ⁇ 150 g / mol, such as, for example Ethylene glycol, 1, 2-propanediol, 1, 3-propanediol, 1, 2,3-propanetriol, 1, 2-butanediol, 1, 4-butanediol, 1, 2,3,4-butanetetrol, diethanolamine, triethanolamine, etc ., Based on the sum of the total amounts of polymer P and saccharide compound S.
- a polyol compound having at least 2 hydroxyl groups and having a molecular weight ⁇ 200 g / mol, in particular ⁇ 150 g / mol such as, for example Ethylene glycol, 1, 2-propanediol, 1, 3-propanediol, 1,
- Essential to the invention is that the total amount of additional formaldehyde-containing binder components in the aqueous binder composition ⁇ 50 parts by weight and preferably ⁇ 10 parts by weight per 100 parts by weight of the sum of the total amounts of polymer P and saccharide compound S.
- the binder composition according to the invention contains no formaldehyde-containing binder components.
- formaldehyde-containing binder components are to be understood as meaning those binder components for the production of which formaldehyde has been used. Frequently, the preparation of such formaldehyde-containing binder components by condensation reaction of a reactant with formaldehyde. The problem with these formaldehyde-containing binder components is that they still contain up to 20,000 ppm of unreacted formaldehyde and, moreover, they can additionally release bound formaldehyde during the curing process during the curing process at a temperature ⁇ 250 ° C.
- urea / formaldehyde resins known to the person skilled in the art, melamine / formaldehyde resins, phenol / formaldehyde resins, guanamine / formaldehyde resins, benzoguanamine / formaldehyde resins or acetoguanamine / formaldehyde resins ,
- the aqueous binder composition according to the invention is advantageously suitable for use as a binder for granular and / or fibrous substrates.
- the abovementioned aqueous binder compositions can therefore advantageously be used in the production of shaped bodies from granular and / or fibrous substrates.
- Granular and / or fibrous substrates are familiar to the person skilled in the art.
- these are wood chips, wood fibers, cellulose fibers, textile fibers, plastic fibers, glass fibers, mineral fibers or natural fibers such as jute, flax, hemp or sisal, but also cork chips or sand and other organic or inorganic natural and / or synthetic grainy and / or or fibrous compounds whose longest dimension in the case of granular substrates is ⁇ 10 mm, preferably ⁇ 5 mm and in particular ⁇ 2 mm.
- the term substrate should also include the fiber webs available from fibers, such as so-called mechanically bonded, for example needled or chemically pre-bonded fiber webs with.
- the aqueous binder composition according to the invention is particularly advantageously suitable as a formaldehyde-free binder system for the aforementioned fibers and mechanically bonded or chemically pre-bonded fiber webs.
- the process for producing a shaped body from a granular and / or fibrous substrate and the abovementioned aqueous binder composition is advantageously such that the aqueous binder composition according to the invention is applied to a granular and / or fibrous substrate (impregnation), optionally with the aqueous binder composition treated (impregnated) granular and / or fibrous substrate is brought into shape and then the granular and / or fibrous substrate thus obtained a thermal treatment step at a temperature> 1 10 ° C, advantageously> 130 ° C and particularly advantageously> 150 ° C, wherein the binder composition filmed and cured.
- the essential components of the aqueous binder composition ie the aqueous dispersion of the polymer P and the saccharide compound S, especially in the form of their solution or suspension, prior to application to the granular and / or fibrous substrate, can be homogeneously mixed.
- these two components can be mixed only immediately before application, for example with a static and / or dynamic mixing device.
- Impregnation of the granular and / or fibrous substrate is typically accomplished such that the aqueous binder composition is uniformly applied to the surface of the fibrous and / or granular substrate.
- the amount of aqueous binder composition is chosen such that per 100 g of granular and / or fibrous substrate> 1 g and ⁇ 100 g, preferably> 2 g and ⁇ 50 g and particularly preferably> 5 g and ⁇ 30 g Binders (calculated as the sum of the total amounts of polymer P and saccharide compound S on a solid basis) are used.
- Binders (calculated as the sum of the total amounts of polymer P and saccharide compound S on a solid basis) are used.
- the impregnation of the granular and / or fibrous substrate is familiar to the person skilled in the art and takes place, for example, by impregnation or by spraying the granular and / or fibrous substrate with the aqueous binder composition according to the invention.
- the granular and / or fibrous substrate is optionally brought into the desired shape, for example by introduction into a heatable press or mold. Thereafter, the shaped impregnated granular and / or fibrous substrate is dried and cured in a manner known to those skilled in the art.
- the drying or curing of the optionally shaped impregnated granular and / or fibrous substrate takes place in two temperature stages, wherein the drying stage at a temperature ⁇ 100 ° C, preferably> 20 ° C and ⁇ 90 ° C and particularly preferably> 40 and ⁇ 80 ° C and the curing step at a temperature> 1 10 ° C, preferably> 130 and ⁇ 250 ° C and particularly preferably> 180 ° C and ⁇ 220 ° C.
- the drying step and the curing step of the moldings take place in one step, for example in a molding press.
- the moldings obtainable by the process according to the invention have advantageous properties, in particular an improved breaking strength in the transverse direction and improved heat resistance.
- the aqueous binder composition according to the invention is therefore particularly advantageously suitable for the production of nonwoven polyester and / or fiberglass-based fiber webs, which in turn are particularly suitable for the production of bituminous roofing membranes.
- the production of bitumen roofing membranes is familiar to the person skilled in the art and takes place in particular by applying liquefied, optionally modified bitumen to one or both sides of a polyester and / or glass fiber fleece bound with a binder composition according to the invention.
- the invention will be illustrated by the following non-limiting examples.
- Feed 1 aqueous emulsion
- Feed 2 aqueous solution
- the polymerization mixture was then allowed to postpolymerize for a further 2 hours at 85 ° C. and cooled to room temperature. By adding 25% strength by weight ammonia solution was adjusted to a pH of 7.3.
- the aqueous polymer dispersion obtained had a solids content of 52.5% by weight, based on the total weight of the aqueous dispersion.
- the number average particle diameter determined to be 242 nm.
- the solids contents were generally determined by drying a defined amount of the aqueous polymer dispersion (about 0.8 g) with the aid of the moisture analyzer HR73 from Mettler Toledo at a temperature of 130 ° C. to constant weight (about 2 hours). In each case two measurements were carried out. The specified value represents the mean value of these measurements.
- the number-average particle diameters of the polymer particles were generally determined by dynamic light scattering on a 0.005 to 0.01 weight percent aqueous polymer dispersion at 23 ° C. by means of an Autosizers NC from Malvern Instruments, England.
- the mean diameter of the cumulant analysis (cumulant z average) of the measured autocorrelation function (ISO standard 13321) is given.
- the preparation of the comparative polymer dispersion V2 was carried out analogously to the preparation of comparative polymer dispersion V1, with the difference that in feed 1 289 g instead of 51.0 g of acrylonitrile, 298 g instead of 417 g of n-butyl acrylate and 212 g instead of 331 g of styrene were.
- the aqueous polymer dispersion obtained had a solids content of 52.5% by weight, based on the total weight of the aqueous dispersion.
- Polymer Dispersion K1 The polymer dispersion K1 was prepared analogously to the preparation of the comparative polymer dispersion V1 with the difference that in feed 1 85.0 g instead of 51.0 g of acrylonitrile, 399 g instead of 417 g of n-butyl acrylate and 315 g instead of 331 g Styrene were used.
- the aqueous polymer dispersion obtained had a solids content of 53.2% by weight, based on the total weight of the aqueous dispersion. The number average particle diameter to 233 nm determined.
- the preparation of the polymer dispersion K2 was carried out analogously to the preparation of the polymer dispersion dispersion V1 with the difference that in feed 1 136 g instead of 51.0 g of acrylic nitrile, 374 g instead of 417 g of n-butyl acrylate and 289 g instead of 331 g of styrene were used.
- the aqueous polymer dispersion obtained had a solids content of 52.9% by weight, based on the total weight of the aqueous dispersion.
- Polymer dispersion K3 Polymer Dispersion K3 was prepared analogously to the preparation of comparative polymer dispersion V1 with the difference that in feed 1 187 g instead of 51.0 g of acrylonitrile, 348 g instead of 417 g of n-butyl acrylate and 264 g instead of 331 g Styrene were used.
- the aqueous polymer dispersion obtained had a solids content of 52.7% by weight, based on the total weight of the aqueous dispersion. The number average particle diameter to 234 nm determined.
- the preparation of the polymer dispersion K4 was carried out analogously to the preparation of the comparative polymer dispersion V1 with the difference that in feed 1 238 g instead of 51, 0 g acrylonitrile, 323 g instead of 417 g of n-butyl acrylate and 238 g instead of 331 g of styrene were.
- the aqueous polymer dispersion obtained had a solids content of 52.9% by weight, based on the total weight of the aqueous dispersion.
- the number average particle diameter is determined to be 240 nm.
- the preparation of the impregnating was such that the aqueous polymer dispersions were K1 to K4 and the Polymerisat constituersionen V1 and V2 with the aqueous solution of the hydroxylated potato starch Emsol ® K55 mixed so homogeneous that the weight ratio of the respective solid contents of the aqueous polymer dispersions hydroxylated potato starch 7: 3 (corresponding to 42.9 parts by weight of starch per 100 parts by weight of solid of the aqueous polymer dispersions).
- the resulting homogeneous polymer / starch mixtures were diluted by dilution with deionized Water adjusted to a solids content of 15 wt .-%.
- the correspondingly obtained aqueous dispersions are referred to as impregnating liquors FK1 to FK4 and FV1 and FV2. Production of bonded fiber webs
- a needled polyethylene terephthalate spunbonded nonwoven (40 cm in length, 37 cm in width) having a density of 125 g / m 2 from Freudenberg-Politex was used as the nonwoven.
- the wet entry was adjusted to 162.5 g impregnating liquor (corresponding to a solids content of 24.4 g).
- the impregnated fiber webs obtained were dried in a laboratory dryer LTV with needle frame from Mathis (circulating air operation) and cured.
- the respective impregnated fiber webs were placed on a folded-up needle frame, fixed by folding and then dried for 3 minutes at 200 ° C and cured.
- the bonded nonwoven fabrics obtained are referred to as nonwoven fabrics FK1 to FK4 and FV1 and FV2.
- the determination of the heat resistance of the fiber webs FK1 to FK4 and FV1 and FV2 was based on DIN 18192 by measurements of the elongation in the longitudinal direction and the shrinkage in the transverse direction at 200 ° C. For this purpose, 100 x 340 mm strips were punched out of the fiber webs in the longitudinal direction. On the nonwoven strip in each case starting from the two narrow sides at a distance of 120 mm in each case a center mark was attached, resulting in a measuring distance between the markers of 100 mm. In the middle of this measuring section, the width of the nonwoven strip was checked by measurement. Subsequently, the narrow ends were clamped in clamping rails.
- the tripod required for the measurement and a stainless steel cylinder weighing 8 kg were heated to 200 ° C in a drying oven.
- the marked and measured nonwoven strips by means of a clamping rail to the tripod located in the drying cabinet attached freely suspended.
- the 8 kg heavy stainless steel cylinder was hung on the lower clamping rail, the drying cabinet door closed and leave the so clamped nonwoven fabric for 10 minutes at 200 ° C in a drying oven.
- the laboratory stand was then removed from the drying cabinet together with the loaded nonwoven strip and cooled for 5 minutes at room temperature.
- the stainless steel cylinder was first detached from the lower clamping rail and then the upper clamping rail from the stand (tripod and stainless steel cylinders were placed back in the drying cabinet for temperature control for the next measurement).
- the nonwoven strip was laid flat on the laboratory bench and the respective distance between the two attached markings (in the longitudinal direction) and the respective width at the narrowest point (in the transverse direction) of the nonwoven strips measured. In each case measurements were carried out on 5 separate measuring strips. The values likewise given in Table 1 represent the average values of these measurements. The smaller the elongation in the longitudinal direction and the smaller the shrinkage in the transverse direction, the better the results are to be evaluated. The change in the longitudinal or transverse direction in percent, based on the corresponding distances before the thermal treatment, is given.
- Non-woven fabric [in N / 50 mm] [in%] [in%]
- the fiber webs produced with the binder compositions of the invention have an improved transverse tear strength at room temperature and improved heat resistance at 200 ° C.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polymerisation Methods In General (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Reinforced Plastic Materials (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014503097A JP2014512433A (ja) | 2011-04-04 | 2012-04-02 | 粒状及び/又は繊維状基材のための水性結合剤 |
EP12711881.8A EP2694580B1 (de) | 2011-04-04 | 2012-04-02 | Wässrige bindemittel für körnige und/oder faserförmige substrate |
BR112013025244A BR112013025244A2 (pt) | 2011-04-04 | 2012-04-02 | composição de aglutinante aquosa, uso de uma composição de aglutinante aquosa, processo para a produção de um artigo moldado, artigo moldado, uso de um artigo moldado, e, membrana de telhado betumizada |
CN201280027501.8A CN103582667B (zh) | 2011-04-04 | 2012-04-02 | 用于颗粒状和/或纤维状基底的水性粘合剂 |
KR1020137028663A KR20140021633A (ko) | 2011-04-04 | 2012-04-02 | 과립형 및/또는 섬유성 기재를 위한 수성 결합제 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11161026 | 2011-04-04 | ||
EP11161026.7 | 2011-04-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2012136605A1 true WO2012136605A1 (de) | 2012-10-11 |
Family
ID=45928899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2012/055919 WO2012136605A1 (de) | 2011-04-04 | 2012-04-02 | Wässrige bindemittel für körnige und/oder faserförmige substrate |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP2694580B1 (de) |
JP (1) | JP2014512433A (de) |
KR (1) | KR20140021633A (de) |
CN (1) | CN103582667B (de) |
BR (1) | BR112013025244A2 (de) |
WO (1) | WO2012136605A1 (de) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016008834A1 (de) * | 2014-07-15 | 2016-01-21 | Basf Se | Bindemittel für bodenbelagsklebstoffe |
DE102014012238A1 (de) * | 2014-08-21 | 2016-02-25 | Johns Manville Europe Gmbh | Binderverfestigtes, textiles Flächengebilde, Verfahren zu dessen Herstellung und dessen Verwendung |
WO2017072186A1 (en) * | 2015-10-30 | 2017-05-04 | Knauf Insulation Sprl | Improved binder compositions and uses thereof |
WO2020221605A1 (en) | 2019-05-02 | 2020-11-05 | Basf Se | Aqueous binder composition |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106687525A (zh) | 2014-07-04 | 2017-05-17 | 陶氏环球技术有限责任公司 | 环氧树脂吸收聚合物粒子 |
US20170198180A1 (en) * | 2014-07-15 | 2017-07-13 | Basf Se | Pressure sensitive adhesives |
CN107699156B (zh) * | 2016-08-08 | 2020-10-16 | 陶氏环球技术有限责任公司 | 粘合剂体系组合物 |
WO2021197999A1 (en) * | 2020-03-30 | 2021-10-07 | Freudenberg Performance Materials Se & Co. Kg | Bituminous membranes with biodegradable binder |
CN112388786B (zh) * | 2020-11-05 | 2021-09-21 | 临沂明拓木业有限公司 | 一种废弃木质材料再生利用方法 |
Citations (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2520959A (en) | 1945-11-06 | 1950-09-05 | Goodrich Co B F | Polymerization of vinyl compounds |
US3238173A (en) | 1962-09-27 | 1966-03-01 | Shell Oil Co | Polystyrene-polyisoprene-polystyrene block copolymer latices and process for their preparation |
US3360599A (en) | 1963-11-06 | 1967-12-26 | Shell Oil Co | Preparation of coherent block copolymer films of high tensile strength and extensibility |
US3397165A (en) | 1964-05-04 | 1968-08-13 | Grace W R & Co | Preparation of latex of butadienecontaining copolymers |
US3726824A (en) | 1970-09-16 | 1973-04-10 | Dow Chemical Co | Preparation of film-forming latexes of polyvinylaromatic-polydiene block copolymers |
US3734686A (en) | 1971-08-12 | 1973-05-22 | Cosden Oil & Chem Co | Composition and method for treating carpets and pile fabrics |
US4269749A (en) | 1979-04-30 | 1981-05-26 | The Dow Chemical Company | Method of imparting salt and/or mechanical stability to aqueous polymer microsuspensions |
DE4003422A1 (de) | 1990-02-06 | 1991-08-08 | Basf Ag | Waessrige polyurethanzubereitungen |
EP0575625A1 (de) * | 1992-01-10 | 1993-12-29 | Sumitomo Dow Limited | Verfahren zur herstellung eines copolymer-latices und dessen verwendung |
EP0649870A1 (de) | 1993-10-20 | 1995-04-26 | Kureha Kagaku Kogyo Kabushiki Kaisha | Gassperrefilm und Herstellungsverfahren dafür |
DE19624299A1 (de) | 1995-06-30 | 1997-01-02 | Basf Ag | Verfahren zur Entfernung organischer Verbindungen aus Dispersionen und Vorrichtung zu dessen Durchführung |
EP0771328A1 (de) | 1994-06-03 | 1997-05-07 | Basf Aktiengesellschaft | Verfahren zur herstellung einer wässrigen polymerisatdispersion |
DE19621027A1 (de) | 1996-05-24 | 1997-11-27 | Basf Ag | Verfahren zur Abtrennung flüchtiger organischer Komponenten aus Suspensionen oder Dispersionen |
DE19741187A1 (de) | 1997-09-18 | 1999-03-25 | Basf Ag | Verfahren zur Verminderung des Restmonomerengehalts in wässrigen Polymerdispersionen |
DE19741184A1 (de) | 1997-09-18 | 1999-03-25 | Basf Ag | Verfahren zur Verminderung von Restmonomeren in Flüssigsystemen unter Zugabe eines Redoxinitiatorsystems |
DE19805122A1 (de) | 1998-02-09 | 1999-04-22 | Basf Ag | Verfahren zur Herstellung wässriger Polymerisatdispersionen mit geringem Restmonomerengehalt |
EP0911361A1 (de) | 1997-10-27 | 1999-04-28 | National Starch and Chemical Investment Holding Corporation | Hitzehärtbare Polysaccharide |
DE19828183A1 (de) | 1998-06-24 | 1999-12-30 | Basf Ag | Verfahren zur Entfernung von restflüchtigen Komponenten aus Polymerdispersionen |
DE19839199A1 (de) | 1998-08-28 | 2000-03-02 | Basf Ag | Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen |
DE19840586A1 (de) | 1998-09-05 | 2000-03-09 | Basf Ag | Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen |
DE19847115C1 (de) | 1998-10-13 | 2000-05-04 | Basf Ag | Gegenstrom-Stripprohr |
US6207756B1 (en) | 1998-03-04 | 2001-03-27 | Exxon Chemical Patents, Inc. | Product and method for making polyolefin polymer dispersions |
EP1578879A1 (de) | 2002-12-19 | 2005-09-28 | Owens Corning | Acrylat- bindemittel |
WO2008150647A1 (en) | 2007-05-30 | 2008-12-11 | Georgia-Pacific Chemicals, Llc | Binder compositions for fiber mats, and fiber mats and articles comprising them |
US20090170978A1 (en) | 2007-12-26 | 2009-07-02 | Kelly Michael Dewayne | Curable composition |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3160843B2 (ja) * | 1991-09-27 | 2001-04-25 | 日本エイアンドエル株式会社 | 共重合体ラテックスを含有してなる組成物 |
DE4133190A1 (de) * | 1991-10-07 | 1993-04-08 | Basf Ag | Formkoerper |
JP4674067B2 (ja) * | 2004-08-12 | 2011-04-20 | 関西ペイント株式会社 | 変性澱粉含有樹脂水分散体及び該水分散体の製造方法 |
DE102005037113A1 (de) * | 2005-08-03 | 2007-02-08 | Basf Ag | Verwendung einer thermisch härtbaren wässrigen Zusammensetzung als Bindemittel für Substrate |
FI120695B (fi) * | 2006-03-06 | 2010-01-29 | Upm Kymmene Oyj | Luonnonrasvahappopohjaista akrylaattihybridihartsia sisältävät komposiitit |
-
2012
- 2012-04-02 WO PCT/EP2012/055919 patent/WO2012136605A1/de unknown
- 2012-04-02 BR BR112013025244A patent/BR112013025244A2/pt not_active Application Discontinuation
- 2012-04-02 JP JP2014503097A patent/JP2014512433A/ja active Pending
- 2012-04-02 EP EP12711881.8A patent/EP2694580B1/de active Active
- 2012-04-02 CN CN201280027501.8A patent/CN103582667B/zh active Active
- 2012-04-02 KR KR1020137028663A patent/KR20140021633A/ko active IP Right Grant
Patent Citations (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2520959A (en) | 1945-11-06 | 1950-09-05 | Goodrich Co B F | Polymerization of vinyl compounds |
US3238173A (en) | 1962-09-27 | 1966-03-01 | Shell Oil Co | Polystyrene-polyisoprene-polystyrene block copolymer latices and process for their preparation |
US3360599A (en) | 1963-11-06 | 1967-12-26 | Shell Oil Co | Preparation of coherent block copolymer films of high tensile strength and extensibility |
US3397165A (en) | 1964-05-04 | 1968-08-13 | Grace W R & Co | Preparation of latex of butadienecontaining copolymers |
US3726824A (en) | 1970-09-16 | 1973-04-10 | Dow Chemical Co | Preparation of film-forming latexes of polyvinylaromatic-polydiene block copolymers |
US3734686A (en) | 1971-08-12 | 1973-05-22 | Cosden Oil & Chem Co | Composition and method for treating carpets and pile fabrics |
US4269749A (en) | 1979-04-30 | 1981-05-26 | The Dow Chemical Company | Method of imparting salt and/or mechanical stability to aqueous polymer microsuspensions |
DE4003422A1 (de) | 1990-02-06 | 1991-08-08 | Basf Ag | Waessrige polyurethanzubereitungen |
EP0575625A1 (de) * | 1992-01-10 | 1993-12-29 | Sumitomo Dow Limited | Verfahren zur herstellung eines copolymer-latices und dessen verwendung |
EP0649870A1 (de) | 1993-10-20 | 1995-04-26 | Kureha Kagaku Kogyo Kabushiki Kaisha | Gassperrefilm und Herstellungsverfahren dafür |
EP0771328A1 (de) | 1994-06-03 | 1997-05-07 | Basf Aktiengesellschaft | Verfahren zur herstellung einer wässrigen polymerisatdispersion |
DE19624299A1 (de) | 1995-06-30 | 1997-01-02 | Basf Ag | Verfahren zur Entfernung organischer Verbindungen aus Dispersionen und Vorrichtung zu dessen Durchführung |
DE19621027A1 (de) | 1996-05-24 | 1997-11-27 | Basf Ag | Verfahren zur Abtrennung flüchtiger organischer Komponenten aus Suspensionen oder Dispersionen |
DE19741187A1 (de) | 1997-09-18 | 1999-03-25 | Basf Ag | Verfahren zur Verminderung des Restmonomerengehalts in wässrigen Polymerdispersionen |
DE19741184A1 (de) | 1997-09-18 | 1999-03-25 | Basf Ag | Verfahren zur Verminderung von Restmonomeren in Flüssigsystemen unter Zugabe eines Redoxinitiatorsystems |
EP0911361A1 (de) | 1997-10-27 | 1999-04-28 | National Starch and Chemical Investment Holding Corporation | Hitzehärtbare Polysaccharide |
DE19805122A1 (de) | 1998-02-09 | 1999-04-22 | Basf Ag | Verfahren zur Herstellung wässriger Polymerisatdispersionen mit geringem Restmonomerengehalt |
US6207756B1 (en) | 1998-03-04 | 2001-03-27 | Exxon Chemical Patents, Inc. | Product and method for making polyolefin polymer dispersions |
DE19828183A1 (de) | 1998-06-24 | 1999-12-30 | Basf Ag | Verfahren zur Entfernung von restflüchtigen Komponenten aus Polymerdispersionen |
DE19839199A1 (de) | 1998-08-28 | 2000-03-02 | Basf Ag | Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen |
DE19840586A1 (de) | 1998-09-05 | 2000-03-09 | Basf Ag | Verfahren zur Verminderung der Restmonomerenmenge in wässrigen Polymerdispersionen |
DE19847115C1 (de) | 1998-10-13 | 2000-05-04 | Basf Ag | Gegenstrom-Stripprohr |
EP1578879A1 (de) | 2002-12-19 | 2005-09-28 | Owens Corning | Acrylat- bindemittel |
WO2008150647A1 (en) | 2007-05-30 | 2008-12-11 | Georgia-Pacific Chemicals, Llc | Binder compositions for fiber mats, and fiber mats and articles comprising them |
US20090170978A1 (en) | 2007-12-26 | 2009-07-02 | Kelly Michael Dewayne | Curable composition |
Non-Patent Citations (24)
Title |
---|
"Emulsion Polymerisation", 1965, INTERSCIENCE PUBLISHERS |
"McCutcheon's, Emulsifiers & Detergents", 1989, MC PUBLISHING COMPANY |
"POLYMER HANDBOOK", 1975, J. WILEY |
"POLYMER HANDBOOK", 1975, J.WILEY |
"POLYMER HANDBOOK", 1989, J. WILEY |
"Ull- mann's Encyclopedia of Industrial Chemistry", 1992, VERLAG CHEMIE, pages: 169 |
"Ullmann's Cncyclopedia of Industrial Chemistry", 1992, VERLAG CHEMIE, pages: 169 |
"Ullmann's Ecyclopedia of Industrial Chemistry", vol. A21, 1992, VCH, pages: 169 |
"Ullmann's Encyclopädie der technischen Chemie", vol. 19, 1980, VERLAG CHEMIE, pages: 18 |
D. DIEDERICH, CHEMIE IN UNSERER ZEIT, vol. 24, 1990, pages 135 - 142 |
D.C. BLACKLEY, HIGH POLYMER LATICES, vol. 1, 1966, pages 35 FF |
ECKERSLEY ET AL., AM. CHEM. SOC., DIV. POLYMER CHEMISTRY, vol. 38, no. 2, 1977, pages 630,631 |
ENCYCLOPEDIA OF POLYMER SCIENCE AND ENGINEERING, vol. 8, 1987, pages 659 FF |
F. HÖLSCHER: "Dispersionen synthetischer Hochpolymerer", 1969, SPRINGER-VERLAG |
G. KANIG, KOLLOID-ZEITSCHRIFT & ZEITSCHRIFT FÜR POLYMERE, vol. 190, pages 1 |
H. STACHE: "Tensid-Taschenbuch", 1981, CARL-HANSER-VERLAG |
H. WARSON: "The Applications of Synthetic Resin Emulsions", 1972, pages: 246 FF |
HOUBEN-WEYL: "Methoden der organischen Chemie", vol. XIV/1, 1961, GEORG-THIEME-VERLAG, pages: 192 - 208 |
HOUBEN-WEYL: "Methoden der organischen Chemie", vol. XIV/1, 1961, GEORG-THIEME-VERLAG, pages: 411 - 420 |
J. BRANDRUP; E.H. IMMERGUT: "Polymer Handbook", 1966, J. WILEY |
J. BRANDRUP; E.H. IMMERGUT: "Polymerhandbook", vol. 11, 1989, JOHN WILEY & SONS, pages: 133 - 141 |
S.E. HARDING ET AL.: "Analytical Ultracentrifugation in Biochemistry and Polymer Science", 1992, ROYAL SOCIETY OF CHEMISTRY, article "Analysis of Polymer Dispersions with an Eight-Cell-AUC-Multiplexer: High Resolution Particle Size Distribution and Density Gradient Techniques", pages: 147 - 175 |
T.G. FOX, BULL. AM. PHYS. SOC., vol. 1, 1956, pages 123 |
ZOSEL, FARBE UND LACK, vol. 82, 1976, pages 125 - 134 |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016008834A1 (de) * | 2014-07-15 | 2016-01-21 | Basf Se | Bindemittel für bodenbelagsklebstoffe |
US10344190B2 (en) | 2014-07-15 | 2019-07-09 | Basf Se | Binders for flooring adhesives |
DE102014012238A1 (de) * | 2014-08-21 | 2016-02-25 | Johns Manville Europe Gmbh | Binderverfestigtes, textiles Flächengebilde, Verfahren zu dessen Herstellung und dessen Verwendung |
US10119213B2 (en) | 2014-08-21 | 2018-11-06 | Johns Manville | Binder-consolidated textile fabric, method for producing it, and use thereof |
WO2017072186A1 (en) * | 2015-10-30 | 2017-05-04 | Knauf Insulation Sprl | Improved binder compositions and uses thereof |
US11325985B2 (en) | 2015-10-30 | 2022-05-10 | Knauf Insulation Sprl | Binder compositions and uses thereof |
US11945883B2 (en) | 2015-10-30 | 2024-04-02 | Knauf Insulation Sprl | Binder compositions and uses thereof |
WO2020221605A1 (en) | 2019-05-02 | 2020-11-05 | Basf Se | Aqueous binder composition |
Also Published As
Publication number | Publication date |
---|---|
EP2694580B1 (de) | 2019-07-10 |
CN103582667B (zh) | 2017-03-15 |
BR112013025244A2 (pt) | 2016-12-20 |
KR20140021633A (ko) | 2014-02-20 |
CN103582667A (zh) | 2014-02-12 |
EP2694580A1 (de) | 2014-02-12 |
JP2014512433A (ja) | 2014-05-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2694580B1 (de) | Wässrige bindemittel für körnige und/oder faserförmige substrate | |
EP2681271B1 (de) | Wässrige bindemittel für körnige und/oder faserförmige substrate | |
EP2814885B1 (de) | Wässrige bindemittelzusammensetzung | |
US9187671B2 (en) | Aqueous binders for granular and/or fibrous substrates | |
US9708485B2 (en) | Aqueous binders for granular and/or fibrous substrates | |
EP2744837B1 (de) | Verfahren zur herstellung eines wässrigen bindemittelsystems | |
EP2760898B1 (de) | Verfahren zur herstellung einer wässrigen polymerisatdispersion | |
WO2017097545A1 (de) | Verfahren zur herstellung einer wässrigen polymerisatdispersion | |
EP3169738B1 (de) | Bindemittel für bodenbelagsklebstoffe | |
EP1846524A1 (de) | Verwendung einer wässrigen polymerdispersion als bindemittel für cellulosische fasern sowie zur herstellung von filtermaterialien | |
EP2475692B1 (de) | Verfahren zur herstellung einer wässrigen bindemitteldispersion | |
EP2013239A1 (de) | Verwendung einer wässrigen polymerzusammensetzung als bindemittel für faserförmige oder körnige substrate | |
US20130046055A1 (en) | Process for producing an aqueous binder system | |
WO2005121188A1 (de) | Verfahren zur herstellung wässriger polymerisatdispersionen | |
WO2020221605A1 (en) | Aqueous binder composition | |
DE102011005638A1 (de) | Verfahren zur Herstellung eines Formkörpers aus körnigen und/oder faserförmigen Substraten | |
EP3129414B1 (de) | Verfahren zur herstellung einer wässrigen polymerisatdispersion | |
EP3126432A1 (de) | Verfahren zur herstellung von formkörpern |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12711881 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2014503097 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 20137028663 Country of ref document: KR Kind code of ref document: A |
|
REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: 112013025244 Country of ref document: BR |
|
ENP | Entry into the national phase |
Ref document number: 112013025244 Country of ref document: BR Kind code of ref document: A2 Effective date: 20130930 |