WO2009115382A2 - Système de résine réactionnelle à deux composants - Google Patents

Système de résine réactionnelle à deux composants Download PDF

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Publication number
WO2009115382A2
WO2009115382A2 PCT/EP2009/051842 EP2009051842W WO2009115382A2 WO 2009115382 A2 WO2009115382 A2 WO 2009115382A2 EP 2009051842 W EP2009051842 W EP 2009051842W WO 2009115382 A2 WO2009115382 A2 WO 2009115382A2
Authority
WO
WIPO (PCT)
Prior art keywords
resin system
reaction resin
component
epoxy
water
Prior art date
Application number
PCT/EP2009/051842
Other languages
German (de)
English (en)
Other versions
WO2009115382A3 (fr
Inventor
Andreas Eisenreich
Steffen Wache
Wilhelm Graf
Original Assignee
Construction Research & Technology Gmbh
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 Construction Research & Technology Gmbh filed Critical Construction Research & Technology Gmbh
Publication of WO2009115382A2 publication Critical patent/WO2009115382A2/fr
Publication of WO2009115382A3 publication Critical patent/WO2009115382A3/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/04Portland cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/40Compounds containing silicon, titanium or zirconium or other organo-metallic compounds; Organo-clays; Organo-inorganic complexes
    • C04B24/42Organo-silicon compounds
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/06Aluminous cements
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • C08L83/04Polysiloxanes
    • C08L83/06Polysiloxanes containing silicon bound to oxygen-containing groups
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04Polysiloxanes
    • C09D183/06Polysiloxanes containing silicon bound to oxygen-containing groups
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00034Physico-chemical characteristics of the mixtures
    • C04B2111/00068Mortar or concrete mixtures with an unusual water/cement ratio
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00663Uses not provided for elsewhere in C04B2111/00 as filling material for cavities or the like
    • C04B2111/00672Pointing or jointing materials

Definitions

  • the present invention is a reaction resin system consisting of a resin and a hardener component, both of which are present separately before processing.
  • Two-component reaction resin systems are well known in the art. Also described above is the use of such systems in connection with the coating of surfaces or in the general field of application of construction chemistry.
  • WO 98/32792 A1 describes a composition based on epoxy polysiloxane polymers.
  • this composition contains a non-aromatic epoxy resin and a biofunctional Aminosilanhär- ter. This system is used for the production of protective coatings, wherein they show a pronounced weathering stability especially against the action of sunlight and a good resistance to chemicals and corrosion influences.
  • a two-component epoxy-based coating agent for cement-bound substrates describes the patent EP 0 991 688 B1.
  • the protected coating agent consists of a resin component A containing an epoxy resin, a reactive diluent, a solid filler and other additives such as pigments, additives and liquid fillers; also a hardener component B, which is a combination of m-xylenediamine and an adducting resin.
  • This coating agent is used for the surface treatment of cast ashes as well as mechanically and / or highly chemically resistant cement-based substrates.
  • EP 0 921 106 A1 discloses a building material mixture with an alkali silicate binder component and a powder component for coating and grouting.
  • This building material mixture is preferably made of potassium silicate as a binder component and a water-binding powder component in the presence of water, which is a mixture of an activated silica component and an activated alumina component.
  • This mixture is said to have excellent chemical resistance in acidic and alkaline Milieu and have a high mechanical strength; It is fire resistant and hardens without cracking. It is also possible to use this building material mixture for coatings and joints.
  • binder systems which are used for the production of jointing mortar.
  • the most widely used are hydraulically hardening grouts, whereby the simple processing faces the material-specific low chemical resistance.
  • contaminants can penetrate the surfaces, causing aesthetic and hygienic deterioration.
  • Coatings, as described in the already mentioned patent application EP 092 106 A1 are, however, unsuitable for the production of jointing mortars, since they are not sufficiently stable in case of early exposure to water and to alkaline solutions.
  • the present invention has found the object of providing a novel reaction resin system which consists of a resin component and a hardener component, both of which are present separately before being processed.
  • This reaction resin system should show a high chemical resistance after its processing, be little polluted in the cured state, be easy to clean and, in particular, meet the requirements of the processing in jointing mortars.
  • the polyorganosiloxane components of the resin component (A) may particularly represent a compound represented by the general formula (I)
  • R 1 is an epoxy-functional C 2 -alkyl group
  • R 2 is a C 2-4 alkoxy, C 1-12 alkyl, C 6-12 aryl, C 3-8 aralkyl or haloalkyl group, which may be the same or different
  • R is a C 1-4 alkyl group and a, b, c and d are each, independently of one another, a positive integer, where c can also be 0.
  • this radical is an epoxy-functional C 3-6 -alkyl group and in particular a glycidoxypropyl radical
  • R 2 may preferably be ethoxy, methyl, ethyl or propyl, benzyl, phenyl or fluoroalkyl
  • R is in particular an ethyl group.
  • Polyglycidyl ethers of a polyhydric alcohol or of phenol are preferred epoxy functional components, which ether may also be blended with at least one reactive diluent.
  • Preferred representatives of the polyglycidyl ethers are those based on ethylene glycol, glycerol, trimethylolpropane and in particular bisphenol A and / or F and / or novolak.
  • the present invention also provides as a preferred variant that the epoxy-functional component with a monofunctional reactive diluent and in particular with a Ci2-14-glycidyl ether, butyl-phenyl-glycidyl ether, cresyl-phenyl-glycidyl ether, and / or a difunctional glycidyl ether, in particular with a Hexanediol diglycidyl ether, butanediol diglycidyl ether and / or cyclohexanedimethanol diglycidyl ether.
  • the epoxy equivalent weights should be between 130 and 2,000, and preferably between 250 and 1,000.
  • the ratio of the polysiloxane component to the epoxy-functional component is not limited; However, it has proved to be favorable if the claimed reaction resin system has a preferred ratio of polyorganosiloxane to the epoxy-functional component which is 1: 5 to 95 and preferably 1: 20 to 60.
  • the hydraulic binder which is another essential part of the invention of the resin component (A) is subject to no restriction.
  • cements according to DIN 1164 and in particular Portland cements and cements according to DIN EN 14647 and / or special cements, in particular in the form of expansion cements develop favorable properties in the system according to the invention, which is why they are to be regarded as preferred.
  • Particularly suitable in this context are aluminate cements and / or so-called white cements.
  • white cements with a particularly low iron content are to be preferred.
  • a ratio of water to hydraulic binder should be considered, which is ⁇ 0.4 and more preferably ⁇ 0.25.
  • the individual components of the proposed reaction resin system are selected so that the mixture to be processed gives a w / o emulsion. This ensures that the alkoxy groups contained in the preferred polyorganosiloxane can be hydrolyzed and the resulting silanol groups can condense and moreover the amount of water in such proportions is present that it can be completely bound by the hydraulic binder.
  • the resin component (A) of the present invention may additionally contain at least one additive which is selected from the series of emulsifiers, antifoams, flow control agents and accelerators or retarders the hydraulic reaction.
  • at least one additive which is selected from the series of emulsifiers, antifoams, flow control agents and accelerators or retarders the hydraulic reaction.
  • lithium carbonate and / or citric acid are particularly recommended.
  • an emulsifier be used as a further additive, it should have an HLB value ("hydrophilic-lipophilic-balance") of 3 to 8.
  • the hardener component (B) can also be varied within wide limits within the scope of the present invention, whereby the entire claimed system experiences a considerable range of application.
  • suitable representatives of the polyamine component are aliphatic, cycloaliphatic or arylaliphatic amines, where alkylene polyamines and / or a Mannich base are suitable as are particularly preferred to look at.
  • Amines proposed in the series are ethylenediamine, isophoronediamine, propylenediamine, hexamethylenediamine, trimethylhexamethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, xylenediamine and / or condensation products of polyamines with aldehydes and at least monohydric phenols and in particular condensation products which as polyamine are polyalkylenepolyamines and / or formaldehyde as aldehydes are particularly suitable.
  • the present invention provides that this is contained in the hardener component (B) in an amount which ensures at least the hydrolysis of the alkoxy groups contained in the preferred polyorganosiloxane and at the same time corresponds at most to the maximum ratio to the hydraulic binder , In combination with the already discussed ratio of water to hydraulic binder, the water not required for hydrolysis and excess water can be completely hydraulically bound in this way.
  • the lowest amount of water is based on the stoichiometric hydrolysis of the alkoxy groups contained in the preferred polyorganosiloxane and the highest possible amount of water at the ratio of water to hydraulic binder, which, as already stated, ⁇ 0.5 and preferably ⁇ 0.4 should be.
  • the hardener component (B) may also contain further components in addition to the proportions of polyamine and water essential to the invention.
  • the present invention provides for adding to the hardener component (B) at least one catalyst which additionally influences the hydrolysis and / or the condensation of alkoxy / silanol groups and / or addition reactions.
  • organotin catalysts or tertiary amines in question.
  • the present invention comprises a variant in which the resin and / or hardener component additionally contains at least one additive of the series quartz, sand, chalk, barium sulfate, corundum, kaolin, fibers, pigments, and as further additives rheological aids and / or thixotropic agents.
  • the hardener component (B) should be present as a w / o emulsion, which is also included in the present invention.
  • the present invention also includes its special use as jointing mortar, in particular in this system, the advantageous properties of the reaction resin system come into play.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Epoxy Resins (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)

Abstract

L'invention concerne un système de résine réactionnel comprenant un composant de résine et un composant durcisseur, les deux composants étant séparés avant traitement. Le composant de résine A renferme un polysiloxane, un composant fonctionnel époxy, et un liant hydraulique, et le composant durcisseur B renferme une polyamine et de l'eau, le rapport de l'eau au liant hydraulique dans le système de résine réactionnelle étant = 0,5. Pour ledit système, dans lequel les poids équivalents époxy sont compris entre 130 et 2000, le rapport de polysiloxane au composant fonctionnel époxy est de 1 : 5 à 95, et le rapport poids équivalent époxy à poids équivalent poly devrait s'élever à 1 : 0,5 à 1,5; de ce fait, il est recommandé d'ajuster un rapport eau/liant hydraulique à = 0,4. Principalement, lorsqu'on utilise ce système de résine réactionnelle comme mortier de joint, les avantages obtenus sont les suivants : aptitude au nettoyage améliorée, tendance à l'encrassement réduite, résistance élevée vis-à-vis des influences chimiques et climatiques, et stabilité de coloration notablement élevée.
PCT/EP2009/051842 2008-03-15 2009-02-17 Système de résine réactionnelle à deux composants WO2009115382A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102008014526.2 2008-03-15
DE102008014526A DE102008014526A1 (de) 2008-03-15 2008-03-15 Zweikomponentiges Reaktionsharz-System

Publications (2)

Publication Number Publication Date
WO2009115382A2 true WO2009115382A2 (fr) 2009-09-24
WO2009115382A3 WO2009115382A3 (fr) 2009-11-19

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PCT/EP2009/051842 WO2009115382A2 (fr) 2008-03-15 2009-02-17 Système de résine réactionnelle à deux composants

Country Status (2)

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DE (1) DE102008014526A1 (fr)
WO (1) WO2009115382A2 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112789254A (zh) * 2018-10-01 2021-05-11 Sika技术股份公司 双组分环氧水泥砂浆

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2019101740A1 (fr) * 2017-11-21 2019-05-31 Sika Technology Ag Composition à deux constituants à base d'eau à durcissement chimique

Citations (5)

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US6084020A (en) * 1994-08-16 2000-07-04 Decora, Incorporated Non-stick polymer-coated articles of manufacture, and process and coatings for the production thereof
US20040132952A1 (en) * 2000-12-29 2004-07-08 Martial Deruelle Use of an epoxy-and/or carboxy-functionalised polyorganosiloxane, as active material in a liquid silicone composition for water repellency treatment of building materials
US20050154170A1 (en) * 2002-05-03 2005-07-14 Klaassens Lars Ivar I. Epoxy modified organopolysiloxane resin based compositions useful for protective coatings
WO2006068674A2 (fr) * 2004-12-20 2006-06-29 Tnemec Company, Inc. Composition de revetement epoxy adhesif a l'eau et procede
US20070224362A1 (en) * 2004-12-20 2007-09-27 Remi Briand Two-part waterborne epoxy coating composition and method

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DE3213798A1 (de) 1982-04-15 1983-10-20 Hoechst Ag, 6230 Frankfurt Elektrofotografisches kopierverfahren zum abtragen von entwicklerfluessigkeit von einer fotoleiteroberflaeche
US5804616A (en) 1993-05-19 1998-09-08 Ameron International Corporation Epoxy-polysiloxane polymer composition
DE19726263C2 (de) 1997-06-20 2003-02-27 Reaku Hobein Gmbh Zweikomponenten-Beschichtungsmittel auf Epoxidharz-Basis für zementgebundene Untergründe sowie dessen Verwendung
EP0921106A1 (fr) 1997-12-05 1999-06-09 Crc Chemical Research Company Ltd. Mélange pour matériaux de construction à liant contenant un silicate de métal alcalin et composant pulvérulent pour revêtement et jointoiement
DE10107985C1 (de) * 2001-02-19 2002-04-18 3M Espe Ag Polymerisierbare Zubereitungen auf der Basis von Siliziumverbindungen mit aliphatischen und cycloaliphatischen Epoxidgruppen und deren Verwendung
EP1359197A1 (fr) * 2002-05-03 2003-11-05 SigmaKalon Group B.V. Compositions de resines epoxy polysiloxanes pour revêtements

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6084020A (en) * 1994-08-16 2000-07-04 Decora, Incorporated Non-stick polymer-coated articles of manufacture, and process and coatings for the production thereof
US20040132952A1 (en) * 2000-12-29 2004-07-08 Martial Deruelle Use of an epoxy-and/or carboxy-functionalised polyorganosiloxane, as active material in a liquid silicone composition for water repellency treatment of building materials
US20050154170A1 (en) * 2002-05-03 2005-07-14 Klaassens Lars Ivar I. Epoxy modified organopolysiloxane resin based compositions useful for protective coatings
WO2006068674A2 (fr) * 2004-12-20 2006-06-29 Tnemec Company, Inc. Composition de revetement epoxy adhesif a l'eau et procede
US20070224362A1 (en) * 2004-12-20 2007-09-27 Remi Briand Two-part waterborne epoxy coating composition and method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112789254A (zh) * 2018-10-01 2021-05-11 Sika技术股份公司 双组分环氧水泥砂浆
CN112789254B (zh) * 2018-10-01 2022-12-16 Sika技术股份公司 双组分环氧水泥砂浆

Also Published As

Publication number Publication date
WO2009115382A3 (fr) 2009-11-19
DE102008014526A1 (de) 2009-09-17

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