| Title of Invention | "PROCESS FOR THE PREPARATION OF STABLE AQUEOUS POLYCARBODIIMIDE DISPERSIONS TO BE USED AS CROSSLINKING AGENT WHICH IS FREE OF ORGANIC SOLVENTS" |
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| Abstract | A process for the preparation of stable aqueous polycarbodiimide dispersions, to be used as crosslinking agent, which are free of organic solvents is described. Said process is characterized in: reacting a polyisocyanate in the presence of a carbodiimide catalyst to form a polycarbodiimide, terminating and/or chain extending the polycarbodiimide chain by the addition of a compound containing ahydrophilic group and one or more amine and/or hydroxyl functions during or after the polycarbodiimide formation dispersion of the resulting compound in water, wherein pH is adjusted to a value between 9 and 14 by the addition of a base and/or a buffer to the water used for the dispersion and/or to the obtained aqueous dispersion. According to the present process said terminating or chain extending with the compound containing a hydrophilic group and one or more amine functions may also occur during or after the dispersion of the polycarbodiimide in water. The preferred pH of the polycarbodiimide dispersions is between I I and 13. furthermore the invention relates to a coating mixture comprising the polycarbodiimide dispersions obtained by the invention as crosslinking agent and an aqueous resin containing carboxylic acid functions. Finally the invention comprises cured material obtained by applying said coating mixture to a substrate, and evaporating the water. |
| Full Text | Process for the preparation of stable polycarbodiimide dispersions in water, which are free of organic solvents and may be used as crosslinking agent. Polycarbodiimides are well known crosslinking agents for aqueous resins containing carboxylic acid functions. Most commercially available polycarbodiimide crosslinkers are dissolved in an organic solvent, which is disadvantageous for environmental reasons. Further, they have to be mixed with either water, or'water and a surfactant, before they can be mixed with the aqueous resin. Generally, these aqueous dispersions are not stable and have to be freshly prepared daily. Only aqueous tet-ramethylxylene diisocyanate based polycarbodiimides are stable in water as described in US 5688875 (=EP 0686626) and US 5859166. However, a disadvantage of these polycarbodiimides is that the conditions for the carbodiimide formation from tetramethylxylene diisocyanate are rather •extreme: 22 hrs at 180°C are required and 2 % of a carbodiimide catalyst. Further tetramethylxylene diisocyanate based polycarbodiimides are slower and less efficient crosslinkers than isophorone diisocyanate or 4,4'-dicyclohexylmethane diisocyanate based crosslinkers. Aqueous polycarbodiimide dispersions obtained from isophorone diisocyanate and from 4,4'-dicyclohexylmethane diisocyanate as described in US 5856014, US 5958516, US 6127029, US 6127477, are not stable. The carbodiimide amounts from commercial aqueous polycarbodiimide products (Carbodilites from Nisshinbo Industries) decrease in a stability test at 50° within 6 weeks to 15-70 % of the original value. The object.of the present invention is to provide a process in which the disadvantages mentioned above are eliminated. Description of the invention According to the present invention there is pro- vided a process for the preparation of stable aqueous polycarbodiimide dispersions, to be used as crosslinking agent, which are free of organic solvents, characterised in: - --v reacting a polyisocyanate in the presence of a car-bodiimide catalyst to form a polycarbodiimide, terminating and/or chain extending the polycarbodiimide chain by the addition of a compound containing a hydrophilic group and one or more amine and/or hydroxy functions during or after the polycarbodiimide formation, dispersion of the resulting compound in water, wherein the pH is adjusted between 9 and 14 by the addition of a base or a buffer to the water used for the dispersion and/or to the obtained aqueous dispersion. Alternatively stable aqueous polyisocyanate based polycarbodiimide dispersions can be obtained when the capping or chain extension with the compound containing a hydrophilic group and one or more amine functions is not effected during or. after the polycarbodiimide formation, but occurs during or after the dispersion of the polycarbodiimide in water. Surprisingly the stability of the polycarbodiimide dispersions was significantly increased at higher pH values and the carbodiimide concentration was not decreased within 8 weeks at 50°C. Preferrably at the end of the process the pH will be adjusted to a value between 11 and 13. Conventional carbodiimide catalysts as described in EP 878496 may be used. Surprisingly, it appeared that the reaction temperature and the reaction time could be reduced when 1-methylphospholene-l-oxide was used as catalyst and for this reason this catalyst is preferred. The polyisocyanate which is used to prepare the polycarbodiimide is a conventional polyisocyanate and may be toluene-2,4-diisocyanate, toluene-2,6- diisocyanate and mixtures thereof, diphenylmethane-4,4-diisocyanate, 1,4-phenylenediisocyanate, dicyclohexylmethane-4, 4 ' - diisocyanate, 3-isocyanatomethyl-3,5,5- trimethylcyclohexylisocyanate, 1,6-hexyldiisocyanate, 1,4-cyclohexyl-diisocyanate , norbonyldiisocyanate diisocyanate, or a mixture thereof and is preferably dicyclohexyl-methane-4,4'-diisocyanate. "X. The base which is used to adjust the pH may be an alkali hydroxide such as lithium hydroxyde, sodium hy-droxyde, potassium hydroxide, or a trialkylamine or a tri-alkylamine containing hydroxyl functions. Optionally, the base or part of the base may be incorporated in the poly-carbodiimide chain by capping the polycarbodiimide chain with a dialkylaminoalkyl-amine or alcohol, and/or by the addition of 0.01-0.3 equivalents regarding to the diisocyanate of a tertiary amine containing polyol or polyamine during or after the polycarbodiimide formation. A buffer may be used to fix the pH value. Useful buffers are those with an effective pH range between 9 and 14. The compound containing a hydrophilic group and one or more amine and/or hydroxyl functions is a polyeth-oxy mono- or diol, a polyethoxy/polypropoxy mono- or diol, a polyethoxy mono- or diamine, a polyethoxy/polypropoxy mono- or diamine, a diol or diamine with a polyalkoxy side chain, an hydroxy- or ajnine alkylsulfonate, or a dialkyla-minoalkyl- alcohol or amine. The polycarbodiimide dispersions of the invention may be used as a crosslinker for carboxylic group containing resins in a conventional way: a coating mixture comprising the polycarbodiimide dispersion of the invention and an aqueous resin containing carboxylic acid functions, is prepared. The material is cured by applying the coating mixture to a substrate, for example leather or artificial leather, and evaporating the water. Many additional ingredients may be present, for example fillers, colorants, pigments, silicons, surfactants and the like. For several applications it is advantageous when the distance between the carbodiimide functions in the molecule is increased. In this way the crosslinking is less rigid, the coatings will be more flexible and problems such as greying, which is an effect that the coating is turning greyish and mat at stretching, or brittleness of the coatings may be prevented. Therefore flexible segments may be incorporated in the polycarbodiimide chain as a "spacer" to separate the carbodiimide functions, For this interest 0.01-0.30 equivalents of a mono- or polyol or a mono- or polyamine regarding to the polyisocyanate are added before, during or after the polycarbodiimide formation, which polyol or polyamine is for example a mono or polyhydroxy-alkane, a polyether mono-or polyol, a polyester polyol, a polycarbonate polyol, a polycaprolactam polyol, a mono- or polyamino-alkane, a polyether mono-or polyamine. The polycarbodiimide dispersions of the invention have several advantages: - the dispersions are stable -the polycarbodiimide is an aqueous dispersion and can be easily mixed with an aqueous resin containing carboxylic acid functions - the products are solvent free and no volatile organic vapours escape during the application - the carbodiimide formation with 4,4'- dicyclohexylmethylene diisocyanate (and isophorone diisocyanate) with 1-methylphospholene-1-oxide as carbodiimide catalyst takes less extreme condition's than the procedure with the diiso-cyanates described in US 5688875 and US 5859166. Examples Examples 1A-1F The preparation of aqueous dispersions of polycarbodiimi- des based on dicyclohexylmethane-4,4' -diisocyanate. Under a nitrogen atmosphere 262 g of dicyclohexylmethane-4, 4' -diisocyanate (in the following indicated as HMDI) and 4 g of 1-methylphospholene-l-oxide were heated while stirring to 140°C and heating was continued until an isocyanate content of 8.20 was obtained. Then the mixture was cooled to 90-100°C. The reaction time was 8 hrs. Hydrophilic compounds were added as indicated in Table 1. 0.01 weight % of dibutyl tin laureate was added as a catalyst when hydroxy functional hydrophilic compounds were used and the mixtures were reacted further at 90-100°C until the NCO-signal in the IR-spectrum was disappeared. In the case of Example IE the amine functional compound was added after 1 hr of reaction time. The mixtures were^ cooled down to 60-65°C and dispersed in water of 60-65°C while the solids amount was adjusted to 35 %. In the case of Example IF the amine functional compound was added to the dispersion afterwards and the mixture was stirred for 10 min. A 10 % solution of a base in water as presented in Table 1 was added until the pH was 11-12. The samples were subjected to a stability test at 50°C. Every 2 weeks the carbodiimide amount was checked. The products were stable for at least 8 weeks at 50°C. (Table Removed) a) M-PEG-350 is a polyethoxy ethanol with a mean'molecu lar weight of 350 b) DMEA is N-dimethylethanolamine c) Na-taurine is sodium 2-aminoethylsulfonate Examples 2A-2G The preparation of aqueous dispersions of polycarbodiimi- des based on HMDI. The examples of example 1 A-1F were repeated with the exception that the water was replaced by a 0.01 M di-sodiumphosphate buffer solution. The samples were subjected to a stability test at 50°C. Every 2 weeks the carbo- diimide amount was checked. The products were stable for at least 8 weeks at 50°C. Example 3 The preparation of an aqueous dispersion of a polycarbodi- imide based on HMDI. The example of 1 A was repeated with the exception that 15 g of butanediol was added to the diisocyanate before the catalyst for the carbodiimide formation was added. The reaction was continued until an isocyanate content of 7.01 was obtained and the amount of M-PEG was 148.61 g. Example 4 The preparation of an aqueous dispersion of a po-lycarbodiimide based on HMDI. Under a nitrogen atmosphere 262 g of HMDI and 4 g of 1-methylphospholene-1-oxide were heated while stirring to 140°C and heating was continued until an isocyanate con-.tent of 14.26 was obtained and the mixture was cooled to 90°C. Polyols were added as presented in Table II plus 0.01 weight % of dibutyl tin laureate. Stirring was continued for 30 min at 90°C and 147 g of M-PEG-350 was added. Stirring was continued-at 90°C till no NCO-signal was observed in the IR-spectrum. The 'mixtures were cooled down to 60-65°C and dispersed in water of 60-65°C While the solids amount was adjusted to 40 %. A 10 % solution of NaOH in water was added until the pH was 11. The sample was subjected to the stability test as mentioned above. The products were stable for at least 8 weeks at 50°C. (Table Removed) a) PPG-425 is a propyleneglycol with a mean molecular weight of 425 Example 5 The'xpreparation of aqueous dispersions of polycarbodiimi- des based on diphenylmethane-4,4'-diisocyanate. Under a nitrogen atmosphere 150 g of diphenylmethane-4, 4' -diisocyanate and 140 g M-PEG-350 were heated to 80°C and the mixture was stirred for 60 min at 80°C. 0,4 g of 1-methylphospholene-l-oxide was added and heated and stirring at 80°C was continued until the NCO-signal in the IR-spectrum was disappeared. The reaction time was 3 hrs. The mixtures were cooled down to 60-65°C and dispersed in water of 60-65°C while the solids amount was adjusted to 40 %. 5 % Of a 1 molar solution of sodium carbonate in water was added and the obtained mixture was stirred until . homogenous and then a 10% solution of sodium hydroxyde in water was added until the pH was 11-12. We claim: 1. A process for the preparation of stable aqueous polycarbodiimide dispersions, to be used as crosslinking agent in an aqueous resin containing carboxylic acid functions, which are free of organic solvents, the process comprising the steps of: - reacting a polyisocyanate in the presence of a carbodiimide catalyst to form a polycarbodiimide; - terminating and /or chain extending the polycarbodiimide chain by the addition of a compound containing a hydrophilic group and one or more amine and/or hydroxyl functions during or after the polycarbodiimide formation; - dispersing the resulting compound in water, characterized in that, the pH is adjusted to a value between 9 and 14 by the addition of a base, a buffer, or a base and a buffer, to the water used for the dispersion, to the obtained aqueous dispersion, or to the water used for the dispersion plus to the obtained aqueous dispersion. 2. A process as claimed in claim 1, wherein said terminating or chain extending with the compound containing a hydrophilic group and one or more amine functions occurs during or after the dispersion of the polycarbodiimide in water. 3. A process as claimed in claims 1 and 2, wherein the pH of the polycarbodiimide dispersions is adjusted to a value between 11 and 13. 4. A process as claimed in claims 1-3, wherein said carbodiimide-forming catalyst is 1-methylphospholene-1-oxide. 5. A process as claimed in claims 1-4, in which the polyisocyanate which is used to prepare the polycarbodiimide is toluene-2,4-diisocyanate, toluene-2,6-diisocyanate and mixtures thereof, diphenylmethane-4,4'-diisocyanate, 1,4-phenylenediisocyanate, dicyclohexylmethane-4,4'diisocyanate, 3-isocyanatomethyl-3,5,5-trimethylcyciohexylisocyanate, 1,6-hexyldiisocyanate, 1,4-cyclohexyldiisocyanate, norbonyldiisocyanate, or a mixture thereof. 6. A process as claimed in claims 1-5, wherein the polyisocyanate is dicyclohexylmethane-4,4'-diisocyanate. 7. A process as claimed in claims 1-6, wherein said base is an alkali hydroxide such lithium hydroxide, sodium hydroxide, potassium hydroxide or a trialkylamine or a trialkylamine containing hydroxyl functions. 8. A process as claimed in claims 1-7, wherein the compound containing a hydrophilic group and one or more amine and/or hydroxyl functions of claim 1 contains a tertiary amine functions which contributes to increasing of the pH, which compound is dialkylaminoalkyl-amine or alcohol, and / or 00.1-0.3 equivalents regarding to the diisocyanate of a tertiary amine containing polyol or polyamine. 9. A process as claimed in claims 1-8, wherein the effective pH range of the buffer is between 9 and 14. 10. A process as claimed in claims 1-9, wherein the compound containing a hydrophilic group and one or more amine and /or hydroxyl functions of claim 1 is a polyethoxy mono- or diol, a polyethoxy / polypropoxy mono-or diol, a polyethoxy mono- or diamine, a polyehtoxy / polypropoxy mono- or diamine, a diol or diamine with a polyalkoxy side chain, an hydroxy- or amine alkylsulfonate or a dialkylaminoalkyl- alcohol or amine or a mixture thereof. 11. A process as claimed in claims 1-10, wherein 0.01-0.30 equivalents of a mono- or polyol or a mono- or polyamine regarding to the polyisocyanate are added in addition before, during or after the polycarbodiimide formation, which polyol or polyamine is a mono- or polyhydroxy-alkane, a polyether mono- or polyol, a polyester polyol, a polycarbonate polyol, a polycaprolactam polyol, a mono- or polyamino-alkane, a polyether mono-or polyamine. 12. An aqueous polycarbodiimide dispersion whenever prepared by the process of claims 1-11 which is used as crosslinking agent in an aqueous resin containing carboxylic acid functions. 13. A process for the preparation of stable aqueous polycarbodiimide dispersions substantially as herein described with reference to the foregoing examples and the accompanying tables 1 and II. |
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16-DELNP-2006-Abstract-(01-09-2008).pdf
16-DELNP-2006-Claims-(01-09-2008).pdf
16-DELNP-2006-Claims-(24-03-2009).pdf
16-DELNP-2006-Correspondence-Others-(01-09-2008).pdf
16-DELNP-2006-Correspondence-Others-(16-03-2011).pdf
16-DELNP-2006-Correspondence-Others-(24-03-2009).pdf
16-DELNP-2006-Correspondence-Others-(26-03-2009).pdf
16-DELNP-2006-Correspondence-Others.pdf
16-DELNP-2006-Description (Complete)-(24-03-2009).pdf
16-delnp-2006-description(complete)-01-09-2008.pdf
16-delnp-2006-description(complete).pdf
16-DELNP-2006-Form-1-(01-09-2008).pdf
16-DELNP-2006-Form-1-(26-03-2009).pdf
16-delnp-2006-form-13-(01-09-2008).pdf
16-DELNP-2006-Form-2-(01-09-2008).pdf
16-DELNP-2006-Form-2-(26-03-2009).pdf
16-DELNP-2006-Form-27-(16-03-2011).pdf
16-DELNP-2006-Form-3-(01-09-2008).pdf
16-DELNP-2006-Form-5-(01-09-2008).pdf
16-DELNP-2006-Form-5-(26-03-2009).pdf
16-DELNP-2006-GPA-(01-09-2008).pdf
16-DELNP-2006-GPA-(24-03-2009).pdf
16-DELNP-2006-Petition-137-(24-03-2009).pdf
| Patent Number | 233427 | ||||||||||||
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| Indian Patent Application Number | 16/DELNP/2006 | ||||||||||||
| PG Journal Number | 13/2009 | ||||||||||||
| Publication Date | 27-Mar-2009 | ||||||||||||
| Grant Date | 30-Mar-2009 | ||||||||||||
| Date of Filing | 02-Jan-2006 | ||||||||||||
| Name of Patentee | STAHL INTERNATIONAL B.V. | ||||||||||||
| Applicant Address | SLUISWEG 10, 5145 PE WAALWIJK, THE NETHERLANDS. | ||||||||||||
Inventors:
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| PCT International Classification Number | C08G 18/02 | ||||||||||||
| PCT International Application Number | PCT/NL2004/000470 | ||||||||||||
| PCT International Filing date | 2004-07-02 | ||||||||||||
PCT Conventions:
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