EP2625213A1 - Réduction de la teneur en monomères présentant des groupes isocyanate dans des compositions de polyuréthane durcissant à l'humidité - Google Patents

Réduction de la teneur en monomères présentant des groupes isocyanate dans des compositions de polyuréthane durcissant à l'humidité

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Publication number
EP2625213A1
EP2625213A1 EP11764579.6A EP11764579A EP2625213A1 EP 2625213 A1 EP2625213 A1 EP 2625213A1 EP 11764579 A EP11764579 A EP 11764579A EP 2625213 A1 EP2625213 A1 EP 2625213A1
Authority
EP
European Patent Office
Prior art keywords
isocyanate groups
composition
silicon dioxide
groups
composition according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP11764579.6A
Other languages
German (de)
English (en)
Inventor
Laila Hossain
Dario Veghini
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sika Technology AG
Original Assignee
Sika Technology AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sika Technology AG filed Critical Sika Technology AG
Priority to EP11764579.6A priority Critical patent/EP2625213A1/fr
Publication of EP2625213A1 publication Critical patent/EP2625213A1/fr
Withdrawn legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3893—Low-molecular-weight compounds having heteroatoms other than oxygen containing silicon
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3893—Low-molecular-weight compounds having heteroatoms other than oxygen containing silicon
    • C08G18/3895—Inorganic compounds, e.g. aqueous alkalimetalsilicate solutions; Organic derivatives thereof containing no direct silicon-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00—Specific properties of additives
    • C08K2201/002—Physical properties
    • C08K2201/005—Additives being defined by their particle size in general
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00—Use of pretreated ingredients
    • C08K9/04—Ingredients treated with organic substances
    • C08K9/06—Ingredients treated with organic substances with silicon-containing compounds

Definitions

  • the invention is in the field of moisture-curing polyurethane compositions, which are used in particular as elastic adhesives, sealants and coatings. State of the art
  • compositions based on isocyanate group-containing polyurethane polymers have been used for quite some time as elastic adhesives, sealants and coatings.
  • the polyurethane polymers containing isocyanate groups are typically prepared by reacting polyols with an excess of polyisocyanates. Due to the production, the isocyanate group-containing polyurethane polymer has a residual content of polyisocyanates, ie monomers having isocyanate groups.
  • the polyurethane polymers having isocyanate groups prepared are customarily used without further processing in moisture-curing polyurethane compositions, with the remainder of isocyanate group-containing monomers also remaining in the composition.
  • isocyanate group-containing monomers may have some beneficial effect on the composition, in many applications it is desirable or necessary to reduce the level of isocyanate group-containing monomers in moisture-curing polyurethane compositions.
  • WO 03/046040 A1 describes, for example, the reduction of the fraction of isocyanate group-containing monomers by distillation of the polyurethane polymers having isocyanate groups obtained reaction product, wherein the starting materials used in the preparation are distilled off.
  • the distillation of polymer compositions is complicated and expensive.
  • the object of the present invention is therefore to provide a composition comprising at least one polyurethane polymer containing isocyanate groups, which has a lower proportion of isocyanate group-containing monomers.
  • Silica having on its surface functional groups which are reactive toward isocyanate groups a reduction in the proportion of isocyanate group-containing monomers in compositions containing at least one isocyanate group-containing polyurethane polymer brings about without affecting the composition thereby.
  • composition comprising
  • At least one silica having on its surface functional groups which are reactive towards isocyanate groups at least one silica having on its surface functional groups which are reactive towards isocyanate groups.
  • the silica is present in the form of particles which have an average particle size of ⁇ 100 ⁇ m and a specific surface area of> 100 m 2 / g.
  • the functional groups of the silica are at least partially reacted with isocyanate groups of the isocyanate group-containing monomer.
  • polymer in the present document comprises, on the one hand, a collective of chemically uniform, but different in terms of degree of polymerization, molecular weight and chain length macromolecules, which was prepared by a polyreaction (polymerization, polyaddition, polycondensation)
  • a polyreaction polymerization, polyaddition, polycondensation
  • Such a group of macromolecules from polyreactions ie compounds which have been obtained by reactions, such as additions or substitutions, of functional groups on predetermined macromolecules and which may be chemically uniform or chemically non-uniform oligomeric pre-adducts whose functional groups are involved in the construction of macromolecules.
  • polyurethane polymer encompasses all polymers which are prepared by the so-called diisocyanate-polyaddition process, including those polymers which are almost or completely free of urethane groups.
  • polyurethane polymers are polyether polyurethanes, polyester polyurethanes, Polyether polyureas, polyureas, polyester-polyureas, polyisocyanurates and polycarbodiimides.
  • Organicsilane compounds which have on the one hand at least one, usually two or three, via Si-O bonds, directly attached to the silicon atom alkoxy groups or acyloxy groups, and on the other hand at least one, bonded via a Si-C bond directly to the silicon atom
  • Such silanes are also known to the person skilled in the art as organoalkoxysilanes or organoacyloxysilanes.
  • Tetraalkoxysilanes consequently do not represent organosilanes according to this definition.
  • aminosilanes or "mercaptosilanes” denotes organosilanes whose organic radical has an amino group or a mercapto group.
  • molecular weight is meant herein the molecular weight average M n (number average).
  • room temperature is meant a temperature of 23 ° C.
  • the isocyanate group-containing polyurethane polymer contained in the composition is typically obtainable from the reaction of at least one polyol with at least one polyisocyanate, as is well known to those skilled in the art.
  • Suitable polyols are in particular polyether polyols, polyester polyols and polycarbonate polyols and mixtures of these polyols,
  • polyoxyethylene polyol in particular polyoxyethylene polyol, polyoxypropylene polyol and polyoxypropylene polyoxyethylene polyol, preferably polyoxyethylene diol, polyoxypropylene diol, polyoxyethylene triol, polyoxypropylene triol, polyoxypropylene polyoxyethylene diol and polyoxypropylene polyoxyethylene triol.
  • Suitable polyols preferably have an average molecular weight of 250 to 30 ⁇ 00 g / mol, in particular of 400 to 8000 g / mol, and an average OH functionality in the range of 1 .6 to 3.
  • Suitable polyols are commercially available, for example, under the trade name Acclaim® 4200 N from Bayer MaterialScience AG, Germany.
  • Suitable polyisocyanates are commercially available aliphatic, cycloaliphatic or aromatic polyisocyanates. Particularly suitable are diisocyanates such as 1,6-hexamethylene diisocyanate (HDI), 2,2,4- and 2,4,4-
  • TMDI Trimethyl 1,6-hexamethylene diisocyanate
  • IPDI isophorone diisocyanate
  • TDI tolylene 2,4- and 2,6-diisocyanate
  • MDI 4,4'-MDI
  • Particularly suitable are technical mixtures of MDI with a high content of 4,4'-MDI.
  • Suitable polyols and polyisocyanates are, for example, those described for the preparation of the polyurethane polymer PUP in the patent application WO 2010/049516 A1, the disclosure of which is hereby incorporated by reference.
  • compositions may also comprise a plurality of different isocyanate group-containing polyurethane polymers prepared using different polyisocyanates.
  • the composition comprises at least one
  • Isocyanate group-containing polyurethane polymer of a polymeric diol and MDI as diisocyanate and an isocyanate groups having
  • Polyurethane polymer of a polymeric diol and TDI as a diisocyanate preferably have an average molecular weight of from 1000 to 50 ⁇ 00 g / mol, in particular of 2,000 to 30 ⁇ 00 g / mol, and an average NCO functionality in the range of 1 .8 to 3 on.
  • composition according to the invention contains at least one isocyanate group-containing monomer, the isocyanate groups of which are at least partially reacted with the functional groups of the silicon dioxide.
  • Isocyanate group-containing monomer having the functional groups of the silica is formed upon combining the composition with the silica.
  • the at least one isocyanate group-containing monomer contained in the composition is typically a diisocyanate and is derived from the preparation of the isocyanate group-containing polyurethane polymer as described above. Accordingly, the monomer having isocyanate groups is generally a starting material for the preparation of the polyurethane polymer, which is obtained in particular since, in order to prepare an isocyanate-group-terminated polyurethane polymer, the diisocyanate is stoichiometric relative to the polyol
  • the composition When the composition is one containing a plurality of different isocyanate group-containing polyurethane polymers prepared using different polyisocyanates, the composition typically also includes different isocyanate group-containing monomers. For example, these are MDI and TDI, as previously described.
  • the proportion of isocyanate group-containing monomer which remains in the composition is in particular ⁇ 1 .5 wt .-%, preferably ⁇ 1 wt .-%, based on the weight of the total composition.
  • the proportion of MDI is in particular ⁇ 0.1 wt .-%, based on the weight of the total composition.
  • composition according to the invention comprises at least one silicon dioxide which has on its surface functional groups which are reactive towards isocyanate groups, the functional groups of the silica being at least partially reacted with isocyanate groups of the isocyanate group-containing monomer.
  • the silica is present in the form of particles which have an average particle size of ⁇ 100 pm.
  • the average particle size is> 1 pm, preferably in the range from 50 to 60 pm.
  • the particles may have any desired shape, for example spheres, chips, flakes and the like.
  • the particles have a specific surface of
  • the particles have a specific surface area of> 300 m 2 / g, preferably in the range of 400 to 800 m 2 / g.
  • the silica is in the form of particles which are porous, the pores having a size in the range of 0.4 to 50 nm, in particular 1 to 20 nm. Particularly suitable are particles having a pore size of 5 to 10 nm.
  • the specific surface area is measured by means of nitrogen adsorption with a gas adsorption device from Beckman Coulter, Inc., USA, according to the BET method (EN ISO 18757).
  • the pore size distribution can be calculated from the adsorption curve, which results from the measurement of the specific surface area.
  • porous particles with a large specific surface have the advantage that they have a large number of functional groups
  • Groups may have per particle.
  • they have the advantage that their functional groups react selectively with the isocyanate groups of the isocyanate group-containing monomer and only to a small extent with the isocyanate groups of the isocyanate group-containing polyurethane polymer. Due to the porosity, the functional groups of the silicon dioxide for the polyurethane polymer are only accessible with difficulty.
  • the silica is functionalized on its surface with functional groups that are reactive toward isocyanate groups, that is, the surface of the silica is chemically modified.
  • the functional groups, which are reactive towards isocyanate groups are enriched via adsorption of suitable compounds on the surface of the silica. Also possible is the presence of adsorptively and covalently bound functional groups.
  • the functional groups which are reactive toward isocyanate groups are in particular amino-, mercapto, carboxyl, or
  • Thiourea groups preferably amino groups.
  • silica functionalized with amino groups is that amino groups have a particularly high reactivity towards isocyanate groups.
  • the silica is functionalized with an organosilane, the organic radical of which has at least one functional group, which is reactive towards isocyanate groups.
  • the functionalization of the silica is known to the person skilled in the art and is carried out in particular by combining silica with the organosilane.
  • Particularly suitable organosilanes are aminosilanes or
  • suitable organosilanes are 3-aminopropyltrimethoxysilane, N-butyl-3-aminopropyltrimethoxysilane, N-phenyl-3-amino-propyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane and also analogs of said organosilanes with ethoxy or isopropoxy groups instead of the methoxy groups on the silicon.
  • organosilanes are di- or triamino-functional organosilanes, for example N- (2-aminoethyl) -3-aminopropyltrimethoxysilane or N- (2-aminoethyl) -N '- [3- (trimethoxysilyl) propyl] ethylene diamine.
  • compositions containing at least one isocyanate group-containing polyurethane polymer By using a silica as described above in compositions containing at least one isocyanate group-containing polyurethane polymer, the balance of isocyanate group-containing monomers remaining in the composition, particularly due to the preparation of the isocyanate group-containing polyurethane polymer, can be removed or reduced.
  • silica has the advantage of the described silica is that its functional groups react very selectively with the isocyanate groups of the monomer and thus the isocyanate groups of the polyurethane polymer are available for curing the composition.
  • Particularly suitable functionalized silica is commercially available, for example, under the tradename QuadraSil TM AP, MP or TA from Johnson Matthey, plc, Great Britain.
  • the proportion of silica having on its surface functional groups which are reactive towards isocyanate groups is in particular 0.01 to 10 wt .-%, in particular 0.5 to 5 wt .-%, preferably 0.5 to 3 wt .-%, based on the total weight of the composition.
  • composition according to the invention may contain further constituents which are known in polyurethane chemistry and in particular in the field of moisture-curing adhesives and sealants based on
  • Polyurethane polymers are common and well known to those skilled in the art.
  • such other ingredients include fillers, catalysts, adhesion promoters, rheology modifiers, plasticizers, reactive diluents, desiccants, and the like.
  • composition according to the invention additionally contains at least one filler.
  • Suitable fillers are inorganic and organic fillers, for example, natural ground or precipitated calcium carbonates, which optionally are coated with fatty acids, particularly stearic acid, barium sulphate (BaS0 4, also called baryta or barite), calcined
  • Kaolins aluminum oxides, aluminum hydroxides, silicic acids, in particular finely divided silicas from pyrolysis processes, Russian, in particular industrially produced carbon black (Russ carbon black), PVC powder or hollow spheres.
  • Preferred fillers are calcium carbonates, calcined kaolins, carbon black, finely divided silicas and flame-retardant fillers, such as hydroxides or hydrates, in particular hydroxides or hydrates of aluminum, preferably aluminum hydroxide.
  • a suitable amount of filler is for example in the range of 10 to 70 wt .-%, in particular 15 to 60 wt .-%, preferably 30 to 60 wt .-%, based on the total composition.
  • the present invention relates to a method for
  • composition comprising at least one polyurethane polymer having isocyanate groups and at least one isocyanate group-containing monomer
  • composition with a silica which has on its surface functional groups which are reactive towards isocyanate groups, the silica being in the form of particles having an average particle size of ⁇ 100 pm and a specific surface area of> 100 m 2 / g ,
  • This inventive method leads to a reduction of the proportion of isocyanate group-containing monomers in the composition.
  • the composition contains at least one
  • Isocyanate group-containing polyurethane polymer and at least one isocyanate group-containing monomer to a composition which directly and without further workup from the preparation of
  • Isocyanate group-containing polyurethane polymer emerges.
  • Such a composition typically comprises the isocyanate group-containing polyurethane polymer as the reaction product, residual proportions of the starting materials used, and any other components known to those skilled in the art which are required for the preparation of the polyurethane polymer.
  • silica used may remain in the composition for its further use after the reaction of its functional groups with the isocyanate group-containing monomers or it may be removed from the composition, for example by filtration.
  • the silica used after the reaction of its functional groups with the isocyanate group-containing monomers should not remain in the composition, the bringing together of the composition containing at least one isocyanate polyurethane polymer and at least one isocyanate group-containing monomer with the functionalized silica by means of passage the composition by a pad or packing of a described silica, typically in a solid or
  • the composition comprising at least one polyurethane polymer having isocyanate groups and at least one isocyanate group-containing monomer is a composition as is known from the preparation of the invention
  • Isocyanate group-containing polyurethane polymer wherein the composition already comprises further constituents conventionally used for the use of the composition as an adhesive, sealant or as a coating, as mentioned above.
  • the combination of the functionalized silica with the silica is carried out in particular in a vacuum mixer at temperatures in the range from 20 ° C to 100 ° C.
  • the advantage of this embodiment of the process is that the process can in principle also be used on already ready-to-use compositions based on polyurethane polymers containing isocyanate groups for reducing the proportion of isocyanate group-containing monomers.
  • a composition which arises directly and without further workup from the preparation of the polyurethane polymer having isocyanate groups is provided and combined with the functionalized silicon dioxide, as described in the first embodiment of the process.
  • this embodiment is that the reduction of the monomer content is very effective.
  • this embodiment has the advantage that it can be selectively used for the reduction of the proportion of a particular monomer in compositions comprising a plurality of different isocyanate group-containing polyurethane polymers.
  • the inventive method is suitable for reducing the proportion of symmetrical diisocyanates such as MDI, typically in compositions containing at least one polyurethane polymer containing isocyanate groups of a polymeric diol and MDI as diisocyanate.
  • the invention relates to a composition obtained by a process for reducing the proportion of isocyanate group-containing monomers in compositions containing at least one polyurethane polymer containing isocyanate groups and at least one isocyanate group-containing monomer, as described above.
  • compositions described above are preferably made and stored in the absence of moisture.
  • the composition is storage stable, that is, it can in the absence of moisture, in a suitable package or arrangement, such as a keg, a bag or a bag
  • Cartridge over a period of several months to a year and longer, without being changed in their application properties or in their properties after curing in a relevant for their use to the extent.
  • the present invention relates to the use of a previously described composition as a moisture-curing adhesive, sealant or coating, which can be applied in particular at room temperature or at elevated temperature, for example to 100 ° C.
  • the invention also relates to a cured composition which is obtainable from the reaction of a composition as described above with water, in particular in the form of atmospheric moisture.
  • the present invention relates to the use of silica having on its surface functional groups which are reactive towards isocyanate groups, for reducing the proportion of isocyanate group-containing monomers in compositions containing at least one isocyanate group-containing polyurethane polymer and at least one isocyanate group-containing monomer.
  • the silica is present in the form of particles which have an average particle size of ⁇ 100 ⁇ m and a specific surface area of> 100 m 2 / g.
  • Humidity cured films with a thickness of 2 mm Humidity cured films with a thickness of 2 mm.
  • the shear modulus (also G-modulus) was determined according to DIN 54451, with two aluminum specimens (70 x 25 x 5 mm) which is 204 N (available from Sika Switzerland AG) pretreated with Sika ® primer, in an area of 10 x 25 mm glued with an adhesive layer thickness of 1 .75 mm and cured for 7 days at 23 ° C and 50% relative humidity.
  • the shear modulus is measured at 10% slip.
  • the adhesives were filled in internally painted aluminum cartridges. After conditioning for 12 hours at 23 ° C, the cartridges were opened and squeezed out by means of a squeezer. For this, a nozzle with 5 mm inner diameter was screwed onto the cartridge. A press release (Zwick / Roell Z005) was used to determine the force needed to squeeze out the sealant at a squeezing speed of 60 mm / min. The value given is an average of the forces measured after an extrusion stroke of 22 mm, 24 mm, 26 mm and 28 mm. After 45 mm Auspressweg the measurement was stopped.
  • the monomer content for MDI and TDI was determined as follows: Approx. Weighed 150 mg of the sample into a 10 ml volumetric flask and dissolved it with dry acetonitrile. After derivatization with 1% by volume of N-propyl-4-nitrobenzylamine in acetonitrile (volume ratio 1: 1) The sample was allowed to stand for 30 minutes and then filtered through a nylon membrane (pore size 0.2 pm).
  • HPLC PDA detector HPLC system: Varian ProStar LC system; detector: Varian ProStar 330 photodiode array; column: Kinetex 100 PFP, 2.6 pm 100x3 mm; column oven: 30 ° C; Mobile Phase A) : 0.04 M sodium acetate (pH 4.5); Mobile phase C: acetonitrile; HPLC method: SOP-390C;
  • P1 has a monomer content of MDI of 2.38% by weight.
  • the reduction in the proportion of isocyanate group-containing monomers was determined by measuring the monomer content in P1 and then combining P1 with QuadraSil TM AP, a
  • the adhesives were prepared as follows, the respective proportions of the individual constituents in Table 1 being indicated in parts by weight:
  • the isocyanate-containing polyurethane polymer P1 was initially charged in a vacuum mixer. At room temperature, add the QuadraSil TM AP or QuadraSil TM AP (denatured) and stir for 30 minutes. The mixture was then warmed to 60 ° C and the DIDP was added. Subsequently, carbon black and chalk were added and further stirred at 60 ° C, then cooled to 50 ° C. Finally, the catalyst was added and the mixture was made into a homogeneous paste for a further 10 minutes at 50 ° C, then cooled to room temperature and flooded with nitrogen. The adhesives produced were then filled into internally painted aluminum Sp Rudkolbenkartuschen.
  • Example 1 does not contain QuadraSil TM AP.
  • the QuadraSil TM AP was added along with the plasticizer, ie without separate stirring, and stirred only for 5 minutes.
  • the QuadraSil TM AP was added immediately after the catalyst. Examples 1 and 8 are reference examples.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

L'invention concerne une composition qui comprend au moins un polymère de polyuréthane contenant des groupes isocyanate, au moins un monomère contenant des groupes isocyanate, ainsi qu'au moins un dioxyde de silicium présentant à sa surface des groupes fonctionnels réactifs vis-à-vis des groupes isocyanate. Ici, le dioxyde de silicium est présent sous forme de particules ayant une taille moyenne ≤ 100 µm et une aire de surface spécifique ≥ 100 m²/g. En outre, les groupes fonctionnels du dioxyde de silicium réagissent au moins en partie avec des groupes isocyanate du monomère contenant des groupes isocyanate.
EP11764579.6A 2010-10-06 2011-10-06 Réduction de la teneur en monomères présentant des groupes isocyanate dans des compositions de polyuréthane durcissant à l'humidité Withdrawn EP2625213A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP11764579.6A EP2625213A1 (fr) 2010-10-06 2011-10-06 Réduction de la teneur en monomères présentant des groupes isocyanate dans des compositions de polyuréthane durcissant à l'humidité

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP20100186742 EP2439219A1 (fr) 2010-10-06 2010-10-06 Réduction de la part de monomères comprenant des groupes isocyanates dans des compositions de polyuréthane durcissant à l'humidité
EP11764579.6A EP2625213A1 (fr) 2010-10-06 2011-10-06 Réduction de la teneur en monomères présentant des groupes isocyanate dans des compositions de polyuréthane durcissant à l'humidité
PCT/EP2011/067478 WO2012045821A1 (fr) 2010-10-06 2011-10-06 Réduction de la teneur en monomères présentant des groupes isocyanate dans des compositions de polyuréthane durcissant à l'humidité

Publications (1)

Publication Number Publication Date
EP2625213A1 true EP2625213A1 (fr) 2013-08-14

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EP20100186742 Withdrawn EP2439219A1 (fr) 2010-10-06 2010-10-06 Réduction de la part de monomères comprenant des groupes isocyanates dans des compositions de polyuréthane durcissant à l'humidité
EP11764579.6A Withdrawn EP2625213A1 (fr) 2010-10-06 2011-10-06 Réduction de la teneur en monomères présentant des groupes isocyanate dans des compositions de polyuréthane durcissant à l'humidité

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EP20100186742 Withdrawn EP2439219A1 (fr) 2010-10-06 2010-10-06 Réduction de la part de monomères comprenant des groupes isocyanates dans des compositions de polyuréthane durcissant à l'humidité

Country Status (4)

Country Link
US (1) US20130158210A1 (fr)
EP (2) EP2439219A1 (fr)
CN (1) CN103124755A (fr)
WO (1) WO2012045821A1 (fr)

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WO2019140447A1 (fr) * 2018-01-15 2019-07-18 Becker Iv John C Revêtement à ultra-haute résistance et composites
DE102018209444B3 (de) 2018-06-13 2019-07-25 Fresenius Medical Care Deutschland Gmbh Verfahren zum Vergießen von Hohlfasermembranen, Hohlfasermembranfilter und isocyanatgruppenhaltiges Addukt
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