DE2720534A1 - ADDITIVES TO ELASTIC SEALING COMPOUNDS AND ADHESIVE MATERIALS - Google Patents
ADDITIVES TO ELASTIC SEALING COMPOUNDS AND ADHESIVE MATERIALSInfo
- Publication number
- DE2720534A1 DE2720534A1 DE19772720534 DE2720534A DE2720534A1 DE 2720534 A1 DE2720534 A1 DE 2720534A1 DE 19772720534 DE19772720534 DE 19772720534 DE 2720534 A DE2720534 A DE 2720534A DE 2720534 A1 DE2720534 A1 DE 2720534A1
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- Prior art keywords
- polyethylene
- polypropylene
- mixtures
- powder
- elastic
- 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.)
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1025—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by non-chemical features of one or more of its constituents
- C09K3/1028—Fibres
-
- 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
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
-
- 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
-
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions 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
- C08L83/04—Polysiloxanes
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1012—Sulfur-containing polymers, e.g. polysulfides
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1018—Macromolecular compounds having one or more carbon-to-silicon linkages
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1021—Polyurethanes or derivatives thereof
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/02—Inorganic compounds
- C09K2200/0278—Fibres
- C09K2200/0286—Asbestos
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2200/00—Chemical nature of materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K2200/06—Macromolecular organic compounds, e.g. prepolymers
- C09K2200/0615—Macromolecular organic compounds, e.g. prepolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C09K2200/0625—Polyacrylic esters or derivatives thereof
Description
Dr. F. Zumstein sen. - Dr. E. Assmann - Dr. R. Koenigsberger Dipl.-Phys. R. Holzhauer - Dipl.-!na. F. KJL^seisen Dr. F. Zumstein jun. Dr. F. Zumstein Sr. - Dr. E. Assmann - Dr. R. Koenigsberger Dipl.-Phys. R. Holzhauer - Dipl.-! Na. F. KJL ^ seisen Dr. F. Zumstein jun.
PATENTANWÄLTEPATENT LAWYERS
2 7 20S342 7 20S34
Case En/PP
14/hUCase En / PP
14 / hU
Polychemie GmbH, 89OO Augsburg Zusätze zu elastischen Dichtungsmassen und KlebwerkstoffenPolychemie GmbH, 89OO Augsburg Additives to elastic sealants and adhesives
Gegenstand der Erfindung sind elastische Dichtungsmassen und Klebwerkstoffe mit einem Zusatz von feinverteilten Pulvern aus Polyäthylen oder Polypropylen bzw. einem Gemisch dieser beiden Stoffe.The invention relates to elastic sealing compounds and adhesive materials with an addition of finely divided powders Polyethylene or polypropylene or a mixture of these two substances.
Elastische Dichtungsrnassen und Klebwerkstoffe z.B. zur Abdichtung von Dehn- und Anschlußfugen im Bauwesen, zur Randabdichtung von -Isolierglasscheiben, zur Glasfalzversiegelung und zur Verklebung verschiedener Materialien im Maschinenbau werden hauptsächlich auf einer Harzbasis von Polysulfiden, Slliconen, Polyurethanen, aber auch aus anderen Harzen wie z.B. Butylkautschuken, Acrylpolymerisaten (Co- und Terpolymerisaten) oder deren Gemischen hergestellt.Elastic sealing compounds and adhesive materials, e.g. for sealing of expansion and connection joints in construction, for sealing the edges of insulating glass panes, for sealing glass rebates and for Bonding of various materials in mechanical engineering is mainly based on a resin base of polysulphides, silicones, Polyurethanes, but also made from other resins such as butyl rubbers, Acrylic polymers (copolymers and terpolymers) or their mixtures are produced.
Die für die genannten Anwendungsbereiche aufgeführten Dichtungsmassen und Klebwerkstoffe enthalten neben den entsprechenden synthetischen Polymeren oder Vorprodukten der zu bildenden Polymere noch Weichmacher, Füllstoffe wie z.B. Calcite, Schwerspate oder Quarz, Pigmente wie z.B. Titandioxid oder Ruß, Alterungsschutzmittel und Katalysatoren. Je nach dem Härtungsmechanismus härten sie durch Einwirkung der Luftfeuchtigkeit, durch Oxidation, Polyaddition oder Trocknung.The sealants and adhesives listed for the named areas of application contain the corresponding synthetic polymers or precursors of the polymers to be formed, plasticizers, fillers such as calcite, heavy spar or quartz, pigments such as titanium dioxide or carbon black, anti-aging agents and catalysts. Depending on the hardening mechanism they harden through the action of humidity, through oxidation, Polyaddition or drying.
609845/0476609845/0476
Gut formulierte elastische Dichtungsmassen und Klebwerkstoffe sollen sich problemlos verarbeiten lassen und elastische Verbindungen mit hoher Alterungs- und Witterungsbeständigkeit, guter Haftung und hoher praktischer Dehnfähigkeit ergeben. Insbesondere bei Fugenabdichtungen ist eine optisch einwandfreie, auf Dauer kleb- und rissefreie Oberfläche ohne Inhomogenitäten erforderlich.Well formulated elastic sealants and adhesives should be easy to process and elastic connections with high aging and weather resistance, good adhesion and high practical elasticity. A visually flawless, permanently tack-free and crack-free surface without inhomogeneities required.
Um die Forderung nach optisch homogenen Oberflächen zu erfüllen, ist ein vollständiger Aufschluß und damit eine gute Verteilbarkeit der Füllstoffe während der Produktion der elastischen Produkte erforderlich. Trotz intensiver Durchmischung ist auch bei hochwertigen Produkten die Zerteilung vorhandener Füllstoffagglomerate nicht immer vollständig, so daß in der fertig ausgebildeten Fuge oder Klebestelle sich diese Zusarnmenballungen störend bemerkbar machen.In order to meet the requirement for optically homogeneous surfaces, a complete digestion and thus good distributability is essential of the fillers required during the production of the elastic products. Despite intensive mixing is also In the case of high-quality products, the breaking up of existing filler agglomerates not always completely, so that these agglomerations form in the fully formed joint or adhesive point make disturbing noticeable.
Bei qualitativ hochwertigen, handelsüblichen, elastischen Dichtungsmassen und Klebwerkstoffen werden die oben aufgeführten Forderungen nach guter Haftung und hoher praktischer Dehnfähigkeit weitgehend erfüllt. Infolge der Elastizität der eingesetzten Produkte kann es dennoch in der Praxis zu Adhäsionsfehlern oder Rissen innerhalb der Massen kommen. Ursache der Abrisse an den Fugenflanken oder anderen Untergründen und der Rißbildung innerhalb der elastischen Produkte bei höherer^ Dehnung, die z.B. durch Temperaturschwankungen hervorgerufen werden, sind die zu hohen Kohäsionskräfte zwischen den einzel-. nen Partikeln und den Polymerketten. Auf die Fugenflanken wirken bei Dehnbeanspruchungen zu hohe Spannungen ein, die zu Abrissen führen.In the case of high-quality, commercially available, elastic sealing compounds and adhesive materials, those listed above are used Requirements for good adhesion and high practical elasticity are largely met. As a result of the elasticity of the However, in practice there may be adhesion defects or cracks within the masses. root cause the tears on the joint flanks or other substrates and the formation of cracks within the elastic products at higher ^ Expansion, e.g. caused by temperature fluctuations, is the excessive cohesive forces between the individual. nen particles and the polymer chains. Excessive stresses act on the joint flanks when they are stretched Lead demolition.
Nachdem die Ursache dieses Mangels erkannt worden war, wurden verschiedene Versuche zur Qualitätsverbesserung durchgeführt und Produkte, bei denen gezielt die Kohäsionskräfte erniedrigt wurden, angeboten. Bei derartigen Produkten wurde die Elastizität der Dichtungsmassen und Klebwerkstoffe durch Zugabe erhöhter Mengen an Weichmachern herabgesetzt, so daß die Unter-After the cause of this deficiency had been identified, various attempts to improve quality were carried out and products in which the cohesive forces were deliberately reduced. In such products, the elasticity the sealing compounds and adhesives are reduced by adding increased amounts of plasticizers, so that the under-
8098A5/04768098A5 / 0476
grundhaftung erhöht und die Rißbildung innerhalb der elasti- · sehen Masse verringert wurde. Diese Massen besitzen ihrerseits allerdings die Nachteile, daß sie Weichmacher an die umgebenden Werkstoffe abgeben und zur permanenten Klebrigkeit neigen, womit eine erhöhte Verschmutzungsanfälligkeit verbunden ist.Basic adhesion is increased and the formation of cracks within the elastic mass has been reduced. These masses own in turn however, the disadvantages that they release plasticizers to the surrounding materials and tend to be permanently sticky, which is associated with an increased susceptibility to soiling.
Es wurde nun gefunden, daß durch elastische Dichtungsmassen und Klebwerkstoffe gemäß der Erfindung die genannten Nachteile weitgehend vermieden werden und Produkte mit sehr guten anwendungstechnischen Eigenschaften, insbesondere deutlich verbesserten Haftungseigenschaften, geringerer Neigung zur Rißbildung und einwandfreier Produktionsmöglichkeit resultieren.It has now been found that elastic sealing compounds and adhesive materials according to the invention overcome the disadvantages mentioned largely avoided and products with very good application properties, in particular significantly improved Adhesion properties, a lower tendency to form cracks and perfect production possibilities result.
Die erfindungsgemäßen elastischen Dichtungsmassen und Klebwerkstoffe sind dadurch gekennzeichnet, daß sie einen Zusatz von 1 bis 40 Gew.-# an feinverteilten Pulvern aus Polyäthylen und/ oder Polypropylen mit einem Molekulargewicht von 1000 bis 10 000, vorzugsweise von 2000 bis 5000 oder einem Gemisch mit beliebigem Mischungsverhältnis der beiden Bestandteile enthalten. Es können auch Mischungen von feinverteilten Polyäthylen- und/oder Polypropylenpulvern verschiedener Molekulargewichte in einer Formulierung sowie Mischpolymerisate des Äthylens oder Propylene mit Olefinen mit 2 bis 6 Kohlenstoffatomen im Molekül eingesetzt werden. Die vorgesehenen Polyäthylen- und Polypropylenpulver können in den erfindungsgemäßen elastischen Dichtungsmassen undv Klebwerkstoffen in einem Verteilungsgrad von 0 bis 200 u, vorzugsweise von 0 bis 50 μ vorliegen. Als Polyäthylen kommt Hoch- sowie Niederdruckpolyäthylen in Frage, wobei letzteres bevorzugt ist. The elastic sealants and adhesives according to the invention are characterized in that they contain an addition of 1 to 40 wt .- # of finely divided powders of polyethylene and / or polypropylene with a molecular weight of 1000 to 10,000, preferably from 2000 to 5000 or a mixture of any Mixing ratio of the two ingredients included. Mixtures of finely divided polyethylene and / or polypropylene powders of different molecular weights can also be used in one formulation, as well as copolymers of ethylene or propylene with olefins having 2 to 6 carbon atoms in the molecule. The measures provided for polyethylene and polypropylene powder may preferably be present from 0 to 50 μ in the inventive elastic sealants and v Klebwerkstoffen in a degree of distribution from 0 to 200 u. High-pressure and low-pressure polyethylene are suitable as polyethylene, the latter being preferred .
Bei Konzentrationen oberhalb k0 Gew.-% treten bei permanenter, dynamischer Beanspruchung Ermüdungserscheinungen im Material auf. Unterhalb von 1 Gew.-^ sind die vorstehend beschriebenen Vorteile nicht vorhanden. Ein bevorzugter Bereich ist 5 bis 50, insbesondere I5 bis 20 Gew.-%. At concentrations above k0 wt -.% Occur in permanent, dynamic stress fatigue to the material. Below 1 wt .- ^ the advantages described above are not available. A preferred range is 5 to 50, in particular 15 to 20% by weight .
809845/0476809845/0476
Feinverteilte Polyäthylenwachse wurden bisher z.B. in Lacken und Druckfarben zur Erzielung von Matteffekten, zur Verbesserung der Partikelverteilung, zur Viskositätssteigerung und zur Vermeidung der Sedimentation eingesetzt (siehe hierzu Farbe und Lack/82. Jahrgang/Nr. 11/1976).Up to now, finely divided polyethylene waxes have been used, for example, to improve paints and printing inks to achieve matt effects particle distribution, to increase viscosity and to avoid sedimentation (see 82. Year / no. 11/1976).
Der wesentliche Vorteil der erfindungsgemäßen Dichtungsmassen und Klebwerkstoffe besteht darin, daß die mit ihnen aufgezeichneten Kraft-Längenänderungs-Diagramme nach DIN 53 455 in allen Fällen einen deutlich flacheren Kurvenverlauf ergeben. Es sind folglich bei allen Längenänderungen (Dehnungen) geringere Kräfte aufzuwenden; die Kohäsionskräfte werden erniedrigt und die Spannungen ayil· die Fugenflanken bzw. anderen Untergründe ' werden abgebaut.The main advantage of the sealing compounds and adhesive materials according to the invention is that the force-elongation diagrams recorded with them according to DIN 53 455 give a clearly flatter curve in all cases. As a result, lower forces have to be used for all changes in length (expansion); the cohesive forces are reduced and the tensions ayil ' the joint flanks or other substrates' are reduced.
Die praktische Konsequenz dieses meßbaren Effektes ist eine deutlich geringere Häufigkeit eines Adhäsions- oder Kohäsionsfehlers. Darüberhinaus werden die oben aufgeführten Nachteile eliminiert, die sich dadurch ergeben, daß sich bei der Produktion elastischer Dichtungsmassen und Klebwerkstoffe die eingesetzten Füllstoffe nicht völlig aufschließen lassen. Der unvollständige Aufschluß kann insbesondere dann zwangsläufig eintreten, wenn eine bestimmte Prozeßführung, bei der z.B. die Einwirkung hoher Scherkräfte vermieden werden muß, unumgänglich ist. Die mit Polyäthylen- oder Polypropylenpulvern hergestellten elastischen Dichtungsmassen und Klebwerkstoffe sind auch unter ungünstigen Produktionsbedingungen völlig homogen.The practical consequence of this measurable effect is a significantly lower frequency of an adhesion or cohesion failure. In addition, the disadvantages listed above are eliminated, which result from the fact that during production elastic sealants and adhesives do not allow the fillers used to fully break down. The incomplete digestion can inevitably occur, in particular, when a certain process management in which E.g. the action of high shear forces must be avoided, is inevitable. Those with polyethylene or polypropylene powders Manufactured elastic sealants and adhesives are even under unfavorable production conditions completely homogeneous.
Die in den erfindungsgemäßen Dichtungsmassen und Klebwerkstoffen enthaltenen feinverteilten Polyäthylen- oder Polypropylenpulver müssen selbstverständlich auch mit den übrigen Bestandteilen der Formulierung, wie z.B. mit Weichmachern, Füllstoffen, Katalysatoren, Pigmenten, Stabilisatoren usw. verträglich sein. Den Bindemitteln gegenüber sind sie chemisch inert, d.h. sie gehen mit ihnen keine chemischen Wechselwirkungen ein.Those in the sealing compounds and adhesive materials according to the invention The finely divided polyethylene or polypropylene powder contained must of course also be used with the rest Components of the formulation, e.g. with plasticizers, fillers, catalysts, pigments, stabilizers, etc. be compatible. They are chemically inert to the binders, i.e. they do not interact with them chemically a.
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Die Anwendung der erfindungsgemäßen Dichtungsmassen und Klebwerkstoffe erfolgt in üblicher Weise.The use of the sealing compounds and adhesive materials according to the invention takes place in the usual way.
In den folgenden Beispielen soll der Anmeldungsgegenstand näher erläutert werden, ohne daß dadurch eine Beschränkung erfolgt.The subject of the application is to be explained in more detail in the following examples, without thereby imposing any restriction he follows.
Elastischer Dichtstoff für Isolierglasscheiben, zweikomponentig. Komponente IElastic sealant for insulating glass panes, two-component. Component I.
40,00 g Polysulfid (Thiokol Typ LP 32)40.00 g polysulphide (Thiokol type LP 32)
15,00 g Dibutylphthalat15.00 grams of dibutyl phthalate
15>00 g Polypropylenpulver, Molekulargewicht:15> 00 g polypropylene powder, molecular weight:
10 000, Teilchengröße: 1 bis 5 μ 0,30 g kolloidaler Schwefel10,000, particle size: 1 to 5 μ 0.30 g colloidal sulfur
29,70 g natürliche, kristalline Kreide, Korngröße 1 bis 5 U29.70 g natural, crystalline chalk, grain size 1 to 5 U
100,00 g100.00 g
Komponente II 4,00 g Mangandioxid.Component II 4.00 g of manganese dioxide.
Das eingesetzte Polysulfid besitzt eine Viskosität von 400 bis 500 Poise, einen Wassergehalt von max. 0,2 $> und ein Molekulargewicht von 2000 bis 50 000 (Hauptanteil 10 000). Es ist Gegenstand der US-PS 2 466 963 der Thiotol Corp., Patrick, J.S. u* Ferguson H.R.. · .■ -The polysulfide used has a viscosity of 400 to 500 poise, a water content of max. 0.2 $> and a molecular weight from 2000 to 50,000 (main fraction 10 000). It is the subject of US Pat. No. 2,466,963 to Thiotol Corp., Patrick, JS and Ferguson HR. ·. ■ -
Anmeldungsgemäß weiterhin generell verwendbare Polysulfide sowie Zusatzstoffe, insbesondere Füllstoffe sind den US-Patentschriften 3 123 495 und 3 297 630 zu entnehmen.According to the application, polysulfides and additives, in particular fillers, which can also be used in general, can be found in the US patents 3 123 495 and 3 297 630 can be found.
809845/0476809845/0476
Elastischer Dichtstoff zur Sanitärverfugung, einkomponentig»Elastic sealant for sanitary jointing, one-component »
4o,o g ei ,<^> -Hydroxy-polydimethylsiloxan, Viskosität: ca. 5o ooo cP4o, o g ei, <^> -Hydroxy-polydimethylsiloxane, viscosity: approx. 50,000 cP
2o,o g Siliconöl, Viskosität: ca. 1 ooo cP 15,o g Polyäthylen-Pulver, Molekulargew.: 3 ooo,2o, o g silicone oil, viscosity: approx. 1 ooo cP 15, o g polyethylene powder, molecular weight: 3,000,
Teilchengröße: 1 - 15 ja Particle size: 1 - 15 yes
5fo g pyrogene Kieselsäure, Oberfläche: ca. 15o m /g 16,ο g natürliche, kristalline Kreide, Korngröße 1 - 2o .u 4,ο g Methyl-tri-cyclohexylamino-silan5 f og fumed silica, surface: approx. 15o m / g 16, o g natural, crystalline chalk, grain size 1 - 2o .u 4, o g methyl-tri-cyclohexylamino-silane
Ιοο,ο gΙοο, ο g
Elastischer Dichtstoff zur Rahmenanschlußverfugung, zweilcomponen-Elastic sealant for frame connection jointing, two-component
tig. Komponente I tig. Component I.
35,o g Polysulfid (Thiokcl Type LP 32) 2o,o g Dibutylphthalat 15,ο g Polyäthylen-Pulver, Mol.-Gew.: 5 ooo,35, o g polysulphide (Thiokcl Type LP 32) 2o, o g dibutyl phthalate 15, ο g polyethylene powder, mol.wt .: 5,000,
Teilchengröße: 5 - 4o ja Particle size: 5 - 4o yes
lo#o g Polyäthylenpulver, Mol.-Gew.: 3 ooo, x lo # og polyethylene powder, mol.wt .: 3,000, x
^ Teilchengröße: 5 - 4o ju^ Particle size: 5 - 4o ju
o,l g Triäthylendiamin 19,9 g Kaolin, Korngröße 1 - 4o u0.1 g triethylenediamine 19.9 g kaolin, grain size 1 - 40 u
Ιοο,ο gΙοο, ο g
3,ο g Cumolhydroperoxid, phlegmatisiert.3, ο g cumene hydroperoxide, phlegmatized.
809845/0476809845/0476
Beispiel 4 : - Example 4 : -
Elastische Spachtelmasse zur Rißabdichtung, zveHfompnrientigElastic filler for sealing cracks, zveHfompnrientig
Komponente I ■ Component I ■
• 2,4 g Hexandiol 46,9 g chloriertes Paraffin, 56 Gew.-% Chlor, flüssig 1,2 g Bleioctoat : • 2.4 g hexanediol 46.9 g chlorinated paraffin, 56% by weight chlorine, liquid 1.2 g lead octoate :
2»4 g pyrogene Kieselsäure, Oberfläche: ca. 15o m /g2 »4 g of fumed silica, surface area: approx. 150 m / g
47,1 g Polypropylen-Pulver, Mol.-Gew.: 5 ooo, 47.1 g of polypropylene powder, molar weight: 5,000,
Teilchengröße: 2ö - 4o Ai Particle size: 2ö - 4o Ai
Ιοο,ο g Ιοο, ο g
Komponente II ' . ■" Component II '. ■ "
33,8 g Addukt aus Glycerin und ca. 5o Molen Propylenoxid 6,1 g Toluylendiisocyanat. - 33.8 g adduct of glycerol and approx. 50 moles of propylene oxide 6.1 g of tolylene diisocyanate. -
Zähharter Fliesenkleber, einkomponentig.Tough and hard tile adhesive, one-component.
28,ο g Diphenylmethandiisocyanat28, ο g diphenylmethane diisocyanate
52,ο g Addukt aus Glycerin und ca. 25 Molen Propylenoxid 5,ο g Asbestfaser, Faserlänge: ca. 2o u lo,o g Polyäthylen-Pulver, Mol.-Gew.: Io ooo,52, ο g adduct of glycerine and approx. 25 moles of propylene oxide 5, ο g asbestos fiber, fiber length: approx. 2o u lo, o g polyethylene powder, molar weight: Io ooo,
Teilchengröße: 1 - 5 ja Particle size: 1 - 5 yes
5,ο g Xylol · 5, ο g xylene
Ιοο,ο g Ιοο, ο g
809845/0478809845/0478
Elastischer Dichtstoff für Hochbaufugen, Komponente I Elastic sealant for building construction joints, component I.
35,o g Polysulfid (Thiokol Type LP 32) 5,o g Polypropylen-Pulver, Mol.-Gew.: 3ooo,35, o g polysulphide (Thiokol Type LP 32) 5, o g polypropylene powder, mol.wt .: 3ooo,
Teilchengröße: 1 - 15 μ Particle size: 1 - 15 μ
2o,o g chloriertes Paraffin, 56 Gew.-% Chlor, flüssig l,o g Eisenoxidschwarz2o, o g chlorinated paraffin, 56% by weight chlorine, liquid l, o g iron oxide black
o,2 g kolloidaler Schwefel lo,o g Titandioxid
28,8 g natürliche, kristalline Kreide, Korngröße 3o - 4oo, 2 g colloidal sulfur lo, og titanium dioxide
28.8 g natural, crystalline chalk, grain size 3o - 4o
Ιοο,ο g . "Ιοο, ο g. "
4,ο g Bleidioxid.4, ο g lead dioxide.
Flexibler Isolierkleber, zweikomponentig. Komponente I .Flexible insulating adhesive, two-component. Component I.
. lo,o g Diisodecylphthalat 3o,o g Polypropylen-Pulver, Mol.-Gew.: 5ooo,. lo, o g diisodecyl phthalate 3o, o g polypropylene powder, mol.wt .: 5ooo,
Teilchengröße: Io - 3o uParticle size: Io - 3o u
6o,o g 2.2.-DiIΐlethyl-propandiol-1.3.6o, o g 2.2.-DiIΐlethyl-propanediol-1.3.
Ιοο,ο gΙοο, ο g
Komponente II ' Component II '
195,ο g Benzoldiisocyanat 58o,o g Addukt aus Glycerin und ca. 25 Molen Propylenoxid,195, o g benzene diisocyanate 58o, o g adduct of glycerine and approx. 25 moles of propylene oxide,
809845/0476809845/0476
Beispiel 8 - . Example 8 -.
Elastischer Dichtstoff zur Glasfalzversiegelung,einkomponentig«Elastic sealant for glass rebate sealing, one-component "
4o#o g *i ,CJ -Hydroxy-polydimethyl-siloxan, 4o # o g * i , CJ -hydroxy-polydimethyl-siloxane,
Viskosität: ca. 5o 000 cPViscosity: approx. 5o,000 cP
12,o g Polyäthylen-Pulver, Mol.-Gew.: 5ooo, 12, o g polyethylene powder, mol.wt .: 5ooo,
Teilchengröße: 5 - Ao Al Particle size: 5 - Ao Al
8,o g Polypropylen-Pulver, Mol.-Gew,,: 3ooo8, o g of polypropylene powder, molar weight: 3ooo
Teilchengröße: 2 - 2oyuParticle size: 2 - 2oyu
7#o g pyrogene Kieselsäure, Oberfläche ca. 15o m
3,o g Triacetoxi-silan
3o#o g Siliconöl, Viskosität ca, 1 000 cP7 # og fumed silica, surface about 15o m 3 o g Triacetoxi-silane
3o # o g silicone oil, viscosity approx. 1,000 cP
Ιοο,ο gΙοο, ο g
Piasto-elastische Versiegelungsmasse Pias to-elastic sealing compound
60,0 g Acrylterpolymer z„B. Paraloid CS 1 der Firma 60.0 g of acrylic terpolymer, e.g. Paraloid CS 1 from the company
Rohm and Haas, Philadelphia lo,o g XylolRohm and Haas, Philadelphia 100,000 grams of xylene
19fo g Polypropylen-Pulver, Mol.-Gew.: 25oo ,19 f og of polypropylene powder, mol wt .: 25oo,
Teilchengröße: 3o - 4o μ Particle size: 3o - 4o μ
2,ο g pyrogene Kieselsäure, Oberfläche ca. 15o τατ/g
2,o g Xthylenglykol
7,o g Pine-Öl 2, o g fumed silica, surface approx. 15o τατ / g 2, o g ethylene glycol
7, above pine oil
Ιοο,ο gΙοο, ο g
809845/0*76809845/0 * 76
Claims (4)
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2720534A DE2720534B2 (en) | 1977-05-06 | 1977-05-06 | Use of polyethylene and / or polypropylene powder for the production of elastic sealing compounds and adhesive materials and such sealing compounds and adhesive materials |
CH485578A CH641826A5 (en) | 1977-05-06 | 1978-05-03 | Sealants and adhesives for elastic seals and adhesions |
AT327078A AT355699B (en) | 1977-05-06 | 1978-05-05 | ELASTIC SEALANTS AND ADHESIVES |
FR7813373A FR2389665B1 (en) | 1977-05-06 | 1978-05-05 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2720534A DE2720534B2 (en) | 1977-05-06 | 1977-05-06 | Use of polyethylene and / or polypropylene powder for the production of elastic sealing compounds and adhesive materials and such sealing compounds and adhesive materials |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2720534A1 true DE2720534A1 (en) | 1978-11-09 |
DE2720534B2 DE2720534B2 (en) | 1981-07-30 |
Family
ID=6008279
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2720534A Withdrawn DE2720534B2 (en) | 1977-05-06 | 1977-05-06 | Use of polyethylene and / or polypropylene powder for the production of elastic sealing compounds and adhesive materials and such sealing compounds and adhesive materials |
Country Status (4)
Country | Link |
---|---|
AT (1) | AT355699B (en) |
CH (1) | CH641826A5 (en) |
DE (1) | DE2720534B2 (en) |
FR (1) | FR2389665B1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3217516A1 (en) * | 1982-05-10 | 1983-11-10 | Teroson Gmbh, 6900 Heidelberg | BUTYL RUBBER AND / OR POLYISOBUTYLENE SEALANTS |
US5242977A (en) * | 1986-07-08 | 1993-09-07 | Bayer Aktiengesellschaft | Poly-α-olefin/polyurethane block copolymers, processes for their production and their use |
WO1999031179A1 (en) * | 1997-12-18 | 1999-06-24 | The B.F. Goodrich Company | A polysiloxane having a copolymer dispersed therein and sealants containing the same |
RU2521440C1 (en) * | 2012-12-28 | 2014-06-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Саратовский государственный технический университет имени Гагарина Ю.А." | Casting compound |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3211067A1 (en) * | 1982-03-25 | 1983-09-29 | Siemens AG, 1000 Berlin und 8000 München | FOAMABLE MELT GLUE |
DE3525340A1 (en) * | 1985-07-16 | 1987-01-22 | Ara Werk Kraemer Gmbh & Co | HUMIDITY CURABLE BY HUMIDITY |
Citations (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB544359A (en) * | 1940-10-08 | 1942-04-09 | Cyril Leonard Child | Composition for attaching polythene to other materials |
GB772088A (en) * | 1953-06-24 | 1957-04-10 | Gen Electric | Improvements relating to organopolysiloxanes |
GB814320A (en) * | 1955-06-10 | 1959-06-03 | Ruhrchemie Ag | Process for the production of moulded articles or compact masses from polyethylene powder |
US2940888A (en) * | 1955-10-11 | 1960-06-14 | B B Chem Co | Thermoplastic rod adhesives and method of bonding metallic sheet material therewith |
US2975150A (en) * | 1956-06-11 | 1961-03-14 | B B Chem Co | Thermoplastic adhesive compositions and supply articles |
GB1077083A (en) * | 1962-07-30 | 1967-07-26 | Eastman Kodak Co | Polymerizable compositions for bonding articles and other purposes |
FR1514532A (en) * | 1966-03-12 | 1968-02-23 | Polymer Corp | Compositions for waterproofing and their production |
DE1941059A1 (en) * | 1968-08-12 | 1970-02-19 | Protective Treat S Inc | Rubber-like sealants |
US3497570A (en) * | 1966-08-19 | 1970-02-24 | Dow Corning | Stabilized silicone elastomers |
DE1719171A1 (en) * | 1966-11-28 | 1971-09-02 | Polymer Corp | Vulcanizable sealants |
DE2156356A1 (en) * | 1970-11-12 | 1972-05-25 | Loctite Corp | Thixotropic anaerobic mass |
DE2309508A1 (en) * | 1972-03-20 | 1973-09-27 | Goodyear Tire & Rubber | POLYURETHANE |
DE2335569A1 (en) * | 1972-07-14 | 1974-01-31 | Shinetsu Chemical Co | VULCANIZABLE ORGANOPOLYSILOXANE COMPOUNDS AND THEIR USE AS A KITTE, PASTING, SEALING, CALKING, ADHESIVE AND COATING COMPOUNDS |
GB1354204A (en) * | 1970-06-11 | 1974-06-05 | Johnson & Johnson | Adhesive composition |
DE2320105A1 (en) * | 1973-04-19 | 1974-11-14 | Siemens Ag | Thermosetting fillers for hollow bodies - contain aliphatic diisocyanates, castor oil and polyolefin powder |
US3911185A (en) * | 1974-09-26 | 1975-10-07 | Du Pont | High ring and ball softening point hot melt backsize adhesive composition |
DE2534737A1 (en) * | 1975-08-04 | 1977-02-24 | Rudolf Hinterwaldner | Microencapsulated adhesives with good storage stability - contain carboxylic acid (deriv) and curing agent encapsulated separately |
US4105715A (en) * | 1976-07-14 | 1978-08-08 | Loctite (Ireland) Limited | Cyanoacrylate adhesive paste compositions |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU7304174A (en) * | 1973-11-19 | 1976-04-08 | Aluminum Co Of America | Retortable materials |
-
1977
- 1977-05-06 DE DE2720534A patent/DE2720534B2/en not_active Withdrawn
-
1978
- 1978-05-03 CH CH485578A patent/CH641826A5/en not_active IP Right Cessation
- 1978-05-05 AT AT327078A patent/AT355699B/en not_active IP Right Cessation
- 1978-05-05 FR FR7813373A patent/FR2389665B1/fr not_active Expired
Patent Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB544359A (en) * | 1940-10-08 | 1942-04-09 | Cyril Leonard Child | Composition for attaching polythene to other materials |
GB772088A (en) * | 1953-06-24 | 1957-04-10 | Gen Electric | Improvements relating to organopolysiloxanes |
GB814320A (en) * | 1955-06-10 | 1959-06-03 | Ruhrchemie Ag | Process for the production of moulded articles or compact masses from polyethylene powder |
US2940888A (en) * | 1955-10-11 | 1960-06-14 | B B Chem Co | Thermoplastic rod adhesives and method of bonding metallic sheet material therewith |
US2975150A (en) * | 1956-06-11 | 1961-03-14 | B B Chem Co | Thermoplastic adhesive compositions and supply articles |
GB1077083A (en) * | 1962-07-30 | 1967-07-26 | Eastman Kodak Co | Polymerizable compositions for bonding articles and other purposes |
FR1514532A (en) * | 1966-03-12 | 1968-02-23 | Polymer Corp | Compositions for waterproofing and their production |
US3497570A (en) * | 1966-08-19 | 1970-02-24 | Dow Corning | Stabilized silicone elastomers |
DE1719171A1 (en) * | 1966-11-28 | 1971-09-02 | Polymer Corp | Vulcanizable sealants |
DE1941059A1 (en) * | 1968-08-12 | 1970-02-19 | Protective Treat S Inc | Rubber-like sealants |
GB1354204A (en) * | 1970-06-11 | 1974-06-05 | Johnson & Johnson | Adhesive composition |
DE2156356A1 (en) * | 1970-11-12 | 1972-05-25 | Loctite Corp | Thixotropic anaerobic mass |
GB1362407A (en) * | 1970-11-12 | 1974-08-07 | Loctite Corp | Thixotropic anaerobic composition |
DE2309508A1 (en) * | 1972-03-20 | 1973-09-27 | Goodyear Tire & Rubber | POLYURETHANE |
DE2335569A1 (en) * | 1972-07-14 | 1974-01-31 | Shinetsu Chemical Co | VULCANIZABLE ORGANOPOLYSILOXANE COMPOUNDS AND THEIR USE AS A KITTE, PASTING, SEALING, CALKING, ADHESIVE AND COATING COMPOUNDS |
DE2320105A1 (en) * | 1973-04-19 | 1974-11-14 | Siemens Ag | Thermosetting fillers for hollow bodies - contain aliphatic diisocyanates, castor oil and polyolefin powder |
US3911185A (en) * | 1974-09-26 | 1975-10-07 | Du Pont | High ring and ball softening point hot melt backsize adhesive composition |
DE2534737A1 (en) * | 1975-08-04 | 1977-02-24 | Rudolf Hinterwaldner | Microencapsulated adhesives with good storage stability - contain carboxylic acid (deriv) and curing agent encapsulated separately |
US4105715A (en) * | 1976-07-14 | 1978-08-08 | Loctite (Ireland) Limited | Cyanoacrylate adhesive paste compositions |
Non-Patent Citations (4)
Title |
---|
Kunststoff Rundschau 1974, S.448 * |
Lehrbuch der Lacke und Beschichtungen, Bd.II, Pigmente, Füllstoffe, Farbstoffe, 1974, S.443/444 * |
ULLMANN: Enzyklopädie der technischen Chemie, 3.Aufl., Bd.15, S.769, 1964 * |
ULLMANN: Enzyklopädie der technischen Chemie, 4.Aufl., a) Bd.7, S.85, 1974, b) Bd.14, S.233, 234, 1977, c) Bd.19, S.8, 21, 1980 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3217516A1 (en) * | 1982-05-10 | 1983-11-10 | Teroson Gmbh, 6900 Heidelberg | BUTYL RUBBER AND / OR POLYISOBUTYLENE SEALANTS |
US5242977A (en) * | 1986-07-08 | 1993-09-07 | Bayer Aktiengesellschaft | Poly-α-olefin/polyurethane block copolymers, processes for their production and their use |
WO1999031179A1 (en) * | 1997-12-18 | 1999-06-24 | The B.F. Goodrich Company | A polysiloxane having a copolymer dispersed therein and sealants containing the same |
US6403711B1 (en) | 1997-12-18 | 2002-06-11 | Noveon Ip Holdings Corp. | Polysiloxane having a copolymer dispersed therein and sealants containing the same |
AU751067B2 (en) * | 1997-12-18 | 2002-08-08 | Tremco Incorporated | A polysiloxane having a copolymer dispersed therein and sealants containing the same |
RU2521440C1 (en) * | 2012-12-28 | 2014-06-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Саратовский государственный технический университет имени Гагарина Ю.А." | Casting compound |
Also Published As
Publication number | Publication date |
---|---|
CH641826A5 (en) | 1984-03-15 |
FR2389665B1 (en) | 1980-10-24 |
AT355699B (en) | 1980-03-10 |
ATA327078A (en) | 1979-08-15 |
DE2720534B2 (en) | 1981-07-30 |
FR2389665A1 (en) | 1978-12-01 |
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Legal Events
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OAP | Request for examination filed | ||
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8263 | Opposition against grant of a patent | ||
8230 | Patent withdrawn |