DE893585C - Process for the production of floor, table, wall and other covering materials - Google Patents
Process for the production of floor, table, wall and other covering materialsInfo
- Publication number
- DE893585C DE893585C DED8207A DED0008207A DE893585C DE 893585 C DE893585 C DE 893585C DE D8207 A DED8207 A DE D8207A DE D0008207 A DED0008207 A DE D0008207A DE 893585 C DE893585 C DE 893585C
- Authority
- DE
- Germany
- Prior art keywords
- parts
- floor
- polyvinyl
- wall
- production
- 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.)
- Expired
Links
Classifications
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/04—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06N3/06—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with polyvinylchloride or its copolymerisation products
- D06N3/065—PVC together with other resins except polyurethanes
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L31/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
- C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
- C08L31/04—Homopolymers or copolymers of vinyl acetate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L57/00—Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
- C08L93/04—Rosin
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Verfahren zur Herstellung von Fußboden-, Tisch-, Wand-und anderen Belagstoffen Es ist bekannt, Fußboden-, Tisch-, Wand -und andere. Belagstoffe aus vernetzten Polyestern und Polyvi@nyl ,erbinidun(geln herzustellen. Es ist ferner bekannt, daß .die Plastifiz.ierung von Polyvinylchl.ori,d; in der Hauptsache mit Hilfe flüssiger Weichmacher bei Temperaturen um 1C5° C .durchgeführt wind. Diese Weichmacher sind meist hochsiedende Ester :der Phosphors@äu;te, wie z. B. Trikresylphosphat, oder auch Ester aus zweibasischen Säuren, wie z. B. Pht!h:al.säure, und langkettigen einwertigen Alkoholen, wie z. B. B:utylallcdh@ol, Hexylalkohol, Octylalkohol und andere, oder aber Estler .au;s einbas!i.achen höheren Bettsäwren und mehrwertigen Alkoholen, wie Glykole, Pentaerythrit und; .andere. Diese Weichmacher haben zwar einen verhältnismäßig hohen Siedepunkt, siind jedoch schon bei Raumtemperatur mehr oder weniger flüchtig, so daß d er agewfvnschte Weichheitsgrad dcer plastischen Massen sich nicht auf die Dauer erhalten läßt. Weiterhin sind :die meisten .dieser Weichmacher in Benzinköhle:nwa:sserst:offen löslich. Diese Ei,gen@s@chaft wirkt sich bei Fußbodenbelägen nachteilig aus, da die gebräuchlichen Bohnermassen Benzinkohlenwasserstoffe enthalten. Durch die dauernde Verwendung dieser Böhnermassen wind dem Belag Weichmacher entzogen, wodurch seine Gesdhmei.d!ig.1 :eit im Laufe der Zeit ebenfalls nachläßt.Process for the manufacture of floor, table, wall and other Covering materials It is known to floor, table, wall and others. Coverings from cross-linked polyesters and polyvinyl, compounding gels to produce. It is also known that .the plasticization of polyvinylchloride, d; mainly with Using liquid plasticizers at temperatures around 1C5 ° C. Carried out wind. These Plasticizers are mostly high-boiling esters: the phosphorus exterior, such as B. tricresyl phosphate, or esters of dibasic acids, such as. B. Pht! H: al.acid, and long-chain monohydric alcohols, such as. B. B: utylallcdh @ ol, hexyl alcohol, octyl alcohol and others, or else Estler .au; s monobasic! i, higher bed acids and polyvalent ones Alcohols such as glycols, pentaerythritol and; .other. These plasticizers do have have a relatively high boiling point, but are already higher at room temperature or less volatile, so that the desired degree of softness is plastic Masses cannot be preserved in the long run. Furthermore: most of these Plasticizer in gasoline cave: nwa: extremely: freely soluble. This egg, gen @ s @ chaft works are disadvantageous in floor coverings, since the common polishing compounds are petrol hydrocarbons contain. Due to the constant use of this flooring compound, the flooring becomes softener withdrawn, whereby his Gesdhmei.d! ig.1: e also diminishes in the course of time.
Als Weichmacher für benzinfeste Po:lyvin:ylchloriidmasisen eignen sich besonders Kochmole kulare, lineare Kondensationsprodukte, ihrer chemischen Natur ,nach Polyester aus zweibas,i,schen Säuren unid zweiwertiigen Alkoholen, wie z. B. Adipsns:äure und Butyl,englylcol. Diese sind flüssige bis zälhflüsis-ige: Körper von sehr geringer Flüchtigkeit, die jedoch ;bei erhöhter Temperatur d *innflüssig werden. Die Herstellung von Bindemitteln aus Polyv1nylch:l.orid- mit solchen linearen Polyestern ist ohne Zusatz von flüssigen Weichmachern nicht zweckmäßig, da einerseits die Festigkeit des Plastiku:ins und auch. ,das Bindevermögen @desselben darunter leidet, ande-rerseits aber heben die Zusätze flüssiger Weichmacher die gewonnene Bezinfestigkeit wieder zum Teil auf.Suitable as a plasticizer for petrol-resistant polyvinyl chloride masks cooking mole cular, linear condensation products, their chemical ones Nature, like polyester from dibasic acids and dihydric alcohols, such as z. B. Adipsns: acid and butyl, englylcol. These are liquid up viscous: bodies of very low volatility, which, however; with increased Temperature d * become fluid. The production of binders from Polyv1nylch: l.orid- with such linear polyesters is not possible without the addition of liquid plasticizers expedient, since on the one hand the strength of the plastic and also. , the binding capacity @ The same suffers from it, but on the other hand the additives of liquid plasticizers increase the recovered petrol resistance partially up again.
Plasins.che Massen auf Basis Polyvinylchilorvd als Bindemittel, die a)ueschließlich mit flüssigen Weichmachern herg°tellt sind, weisen .außerdem eine schlechte Aufna:h.mefäh-iigkeit für Fülls,boffe auf. Es ist daher praktisch nicht gelungen, mit diesen plastischen Massen hochwertige, mit Füllstoffen gefüllte Belägeherzustellen.Plasins.che masses based on polyvinylchloride as a binder, the a) are manufactured exclusively with liquid plasticizers, also have a poor reception, i.e. the ability to fill up. It is therefore practical not succeeded in using these plastic masses to produce high-quality coverings filled with fillers.
Es ist weiter bekannt, daß sich Polyvinyl@chlo@rid mit und ohne Zusatz flüssiger Weichmacher mit linearen und vernetzten Polyestern kombinieren läßt bzw.,daß B.ind!ennittel auf Basis von vernetzten Polvestern die Mitverwendun:g von Polyvinylverbindungen gestatten.It is also known that polyvinyl chloride with and without additives Liquid plasticizer can be combined with linear and crosslinked polyesters or that For example, the use of polyvinyl compounds based on cross-linked Polvestern is an option allow.
:Neue eingehende Untersuchungen und Versuche habenjed@och ergeben, daß man Beläge mit guten Eigenschaften mit einem Bindemittel aus Polyv inylverbindungen und flüssigen Weichmachern herstellen kann, das mindestens 150% seines. Gelvichtes an Füllstoffen, die überwiegend aus organischen Füllstoffen, wie Korkmehl und Holzmehl, bestehen, .aufnimmt, wenn man als Bindemittel ein, Gemisch von Polyvin.ylchlorid und Polyvinylacetat oder ein Misch:polymerisat aus dien entsprechenden Monomeren mit flüssigen Weichmachern und vernetzten Polyestern verwendet.: New in-depth investigations and experiments have shown that you coverings with good properties with a binder made of Polyv inylverbindungen and liquid plasticizers that can produce at least 150% of its. Gelvichtes of fillers, which mainly consist of organic fillers, such as cork flour and wood flour, exist, .absorbs, if one is used as a binder, mixture of Polyvin.ylchlorid and polyvinyl acetate or a mixed polymer from the corresponding monomers used with liquid plasticizers and crosslinked polyesters.
Geeignete vernetzte Polyester werden erh.altem durch Kondensation von zweibasischen Säuren, wie z. B. Ad ipinsäure, Sebacins-äure, Bernsteinsäure und andere mit idirei- und mehrwertigen Alkoholen, z. B. Hexantriol, Butantriol, Trimethylolpropan, Pentaarythrit und .andiene. Die delbei zum Einsatz gelangenden Mischungen der fFolyvinylvenbindungen können (durch einfache Mischung der einzelnen Polymerisate hergestellt wenden, andererseits aber auch (schon: ih einem besonderenMisch-bzw. Copolymei--isations.verfafhren angefertigt sein.Suitable crosslinked polyesters are obtained by condensation of dibasic acids, such as. B. Ad ipic acid, sebacic acid, succinic acid and others with idirei and polyhydric alcohols, e.g. B. hexanetriol, butanetriol, Trimethylolpropane, pentaarythritol and .andiene. The delbei used Mixtures of the polyvinyl vene compounds can (by simply mixing the individual Turn polymers produced, on the other hand also (already: ih a special mixing or Copolymei - izations.
Das besondere Kennzeichen solcher Bin;de:mittelkompos itionen ist eine erhöhte Fiill-stoffaufnahmiefähigkeit, .die mit den üblichen weichgemachten Polyvinvlverbindungen nicht erzielt wird. Um eine optimale Füllfstoffaufnahme zu erreichen, muß .die Konfdensation. dies Polyesters bei einem bestimmten Vernetzungsgrad unterbrochen sein. Die Vernetzung muß jedoch bereits soweit fortgeschritten sein,. daß ein bei Raumtemperatur zäh-elastisches Material erhalten, wird, das aber bei den Verarbeitungstempenatu@ren von 130 bis 16r01° C plastisch ist, ohne flüssig zu werden. Wird ,das Material bei den Verarbeitungstemperaturen flüssig, so genügt der Vernetzungsgrad noch nicht. Zu weit vernetzte Produkte dragegen lassen, sich nur schwer verarbeiten, da diese Materialien bei den: Verarbeitungstemperaturen nicht mehr plastisch sind. lau wenig und zu.stamk vernetzte Produkte! bewirken auch nur eine ungenügende Füllstoffaufnahme. Die endgültige Auskondensation erfolgt erst im fertigen Belag durch Nachheizen bei Temperaturen von 6o bis ioo° C. .The special characteristic of such bindings is an increased filler absorption capacity, which cannot be achieved with the usual plasticized polyvinyl compounds. In order to achieve an optimal filler absorption, the condensation must. this polyester be interrupted at a certain degree of crosslinking. The networking must, however, have progressed so far. that a material which is tough and elastic at room temperature is obtained, but which is plastic at the processing temperatures of 130 to 160 ° C. without becoming liquid. If the material becomes liquid at the processing temperatures, the degree of crosslinking is not yet sufficient. On the other hand, products that are crosslinked too far are difficult to process because these materials are no longer plastic at the processing temperatures. lukewarm little and too strong networked products! also only cause insufficient filler absorption. The final condensation only takes place in the finished surface by reheating at temperatures of 60 to 100 ° C.
Durch Zusätze von Kolophonium, Kolophoniumestern b@zw. Abietinsäure oder Abieti.nsäureestern lassen sich. die Eigenschaften der Beläge. weitgehend variieren. Diese Stoffe können bei der Herstellung des Plastiksims aus Polyvinylchl,ori,d, und Polyvinylacetat wie oben bei dem Mischvorgang mit den Füllstoffen oder auch bei der vorangegangenen Ankondensation der Polyester zugesetzt werden.By adding rosin, rosin esters b @ zw. Abietic acid or Abieti.nsäureestern can be. the properties of the coverings. vary widely. These materials can be used in the manufacture of the plastic sill from polyvinylchl, ori, d, and polyvinyl acetate as above in the mixing process with the fillers or else the polyesters are added during the previous condensation.
Weiterhin ist es. möglich, dier Mischung bzw. dem Misch:polymerisat aus Polyvinylchlori,d- und Polyv inylacetat auch ,andere Polymerisate bzw. Mi,sc'h@ polymerisabe zuzusetzen, wie z. B. Polyacrylisä@uree.ster, Polystyrol, Polyvi.nyläther. Beispiel i 15 Teile Polyvinylchlorid, 5 Teile Polyvi@nylacetat, io Teile Phtha1.säure:diibutylester und io Teile Kondeneatiomsprodukt aus. 5o Teilen Adipins@äure, 3o Teilen Hexantriol und 2o Teilen Kolophonium werden in einem Knetwerk bei 13o° zum Plastiku.m verknetet. Hierauf setzt man 25 Teile- Korkrriehl, 25 Teile Holzmehl und io Teile Farben en. Die erhaltene Mischm,a.ss,e läßt sich durch Walzen oder Pressen zu Belagplatten verformen. Beispiel 2 22 Teile eines Mischpolymerisates aus 9o Teilen Vinylchlori,d und io Teilen Vinylacetat werden, wie unter i .beschrieben, bei 15o° mit 8 Teilen Phenolester auss:ulfochlorierten Fischer-Tropsch-Kohlenwasserstoffen, 3 Teilen AbietinsäurepentaeTythritester und 7 Teil-en Polyester aus q:3 Teilen Adipinsäure, 17,5 Teilen Bernsteinsäure und' 39,5 Teilen Trsme#ühylolprop:an zu einem Plastikum verarbeitet, das ebenfalls als Bindemittel für Belagstoffe eingesetzt werden kann.Furthermore it is. possible, the mixture or the mixed: polymer also made of polyvinylchloride, d- and polyvinyl acetate, other polymers or Mi, sc'h @ add polymerisabe, such as. B. Polyacrylisä@uree.ster, polystyrene, polyvinyl ether. Example i 15 parts of polyvinyl chloride, 5 parts of polyvinyl acetate, 10 parts of phthalic acid: diibutyl ester and io parts condensate product. 50 parts of adipic acid, 30 parts of hexanetriol and 20 parts of rosin are kneaded in a kneading machine at 130 ° to form plastic. 25 parts of corkscrew, 25 parts of wood flour and 10 parts of paint are placed on this. The mixture obtained, a.ss, e can be converted into covering panels by rolling or pressing deform. Example 2 22 parts of a copolymer of 90 parts of vinyl chloride, i.e. and 10 parts of vinyl acetate are, as described under i., at 15o ° with 8 parts Phenol esters made from: sulfochlorinated Fischer-Tropsch hydrocarbons, 3 parts of abietic acid pentetythritol ester and 7 parts of polyester from q: 3 parts of adipic acid, 17.5 parts of succinic acid and ' 39.5 parts of Trsme # ühylolprop: an processed into a plastic, which is also used as Binder for covering materials can be used.
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DED8207A DE893585C (en) | 1951-03-17 | 1951-03-17 | Process for the production of floor, table, wall and other covering materials |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DED8207A DE893585C (en) | 1951-03-17 | 1951-03-17 | Process for the production of floor, table, wall and other covering materials |
Publications (1)
Publication Number | Publication Date |
---|---|
DE893585C true DE893585C (en) | 1953-10-19 |
Family
ID=7032486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DED8207A Expired DE893585C (en) | 1951-03-17 | 1951-03-17 | Process for the production of floor, table, wall and other covering materials |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE893585C (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1028329B (en) * | 1955-06-01 | 1958-04-17 | Teroson Werk Erich Ross | Process for the production of foams |
DE970857C (en) * | 1954-01-24 | 1958-11-06 | Herberts & Co Gmbh Dr Kurt | Process for the production of storable, polyester-bound, fiber-containing structures which can be hardened under the action of pressure and heat |
-
1951
- 1951-03-17 DE DED8207A patent/DE893585C/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE970857C (en) * | 1954-01-24 | 1958-11-06 | Herberts & Co Gmbh Dr Kurt | Process for the production of storable, polyester-bound, fiber-containing structures which can be hardened under the action of pressure and heat |
DE1028329B (en) * | 1955-06-01 | 1958-04-17 | Teroson Werk Erich Ross | Process for the production of foams |
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