EP0209810B1 - Verfahren zur Herstellung von Boden- oder Wandbelag mit Risseffekt und so erzeugtes Produkt - Google Patents
Verfahren zur Herstellung von Boden- oder Wandbelag mit Risseffekt und so erzeugtes Produkt Download PDFInfo
- Publication number
- EP0209810B1 EP0209810B1 EP86109523A EP86109523A EP0209810B1 EP 0209810 B1 EP0209810 B1 EP 0209810B1 EP 86109523 A EP86109523 A EP 86109523A EP 86109523 A EP86109523 A EP 86109523A EP 0209810 B1 EP0209810 B1 EP 0209810B1
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- EP
- European Patent Office
- Prior art keywords
- die
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- oder
- daß
- dadurch gekennzeichnet
- 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
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
- B05D5/06—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
- B05D5/061—Special surface effect
- B05D5/062—Wrinkled, cracked or ancient-looking effect
-
- 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
- D06N7/00—Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
- D06N7/0005—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface
- D06N7/0028—Floor covering on textile basis comprising a fibrous substrate being coated with at least one layer of a polymer on the top surface characterised by colour effects, e.g. craquelé, reducing gloss
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
- Y10T428/24471—Crackled, crazed or slit
Definitions
- the present invention relates to a process for producing floor coverings or wall coverings, of the synthetic coverings type, with a cracked effect. It also extends to the products obtained by this process.
- Document FR-A-2 126 658 discloses a method for applying an emulsion coating material to produce cracking patterns.
- a lower coating synthetic material containing a mineral material having a high swelling property is deposited, this lower coating material is dried and then a cured coating material containing a silicon dioxide sol is applied.
- the lower coating material absorbs the water contained in the hardened coating material, simultaneously causing it to contract, and also, jointly, cracks.
- a drawback of the process lies in the fact that there are two different layers of particular composition to be used, which require intermediate drying. This process is necessarily slow and expensive.
- Document FR-A-2 247 494 relates to a cracked film of polymer based on PVC and at least one plasticizer distributed in a homogeneous manner. It also claims a coating consisting of a conventional support coated with such a film as well as a process for the preparation thereof.
- the process uses a two-phase system, namely polymer / plasticizer and water. However, this process does not allow sufficient control of the formation of cracks and the opening thereof. Furthermore, this process requires high amounts of water.
- Document US-A-2 612 456 also relates to a process for the manufacture of a decorative and protective coating which has a cracked appearance in which an organosol is used comprising particles of a copolymer of organic vinyl chloride and of acetate, dispersed in a volatile organic liquid.
- the liquid used must have a swelling effect on the polymer particles. This process is also difficult to control and makes it difficult to obtain a dense network of cracks. Furthermore, this process also requires high amounts of solvent.
- An object of the present invention is to provide a process for the production of floor coverings or wall coverings, with a cracked effect requiring only a single layer to obtain said cracked effect.
- Another object of the present invention is to provide a process for the production of cracked floor or wall coverings, in which the amounts of solvent or water required are significantly reduced compared to the state of the art.
- Another object of the present invention is to provide a process for producing deep cracked floor or wall coverings, that is to say in substantially the whole mass of at least one layer of the covering.
- the aim is to provide a new product, that is to say a new floor or wall covering having a cracked effect, of random nature.
- the process of the invention makes it possible to achieve the aims of the invention and in particular makes it possible to produce a coating with a cracked effect, in which the cracks extend randomly, in depth, in the mass.
- the invention also resides in the choice of the sorbent agent / solvent pair used in the particular conditions of the process of the invention.
- the solvent does not disturb the plasticizing effect of the other additives of the synthetic material used for the manufacture of the coating according to the invention. It is obvious that a solvent which does not participate in the plasticization is preferably used, although the use of such a solvent cannot be excluded.
- the absorbent agent is a silica or a silicate, preferably having a specific surface according to BET of between 250 and 700 m 2 / g, preferably of the order of 300 at 400 m 2 / g.
- the coating composition advantageously comprises 0.5 to 15% by weight of sorbent agent.
- a solvent is used whose vapor pressure is very high at the formation temperature of the synthetic film, so that the sorbent shrinks by desorption of the solvent once the film is formed, in order to " tear "forming cracks.
- the temperature at which the solvent has a high vapor pressure, or the boiling temperature of the solvent must be close to the film-forming temperature, because, if this temperature is too high, it does not there will be no cracking, due to the fusion and the surface tension of the synthetic coating. On the other hand, if this temperature is too low, there is evaporation before the film is formed. It is, of course, necessary to ensure that the retraction force is greater than the cohesive force of the film.
- a solvent such as the hydrocarbon fractions and in particular white spirit is used at a rate of the order of 15 to 35% by weight of the plastisol coating.
- the temperature for forming the plastisol coating film is chosen between 110 and 160 ° C.
- the coating can be subjected subsequently, for example at a temperature of the order of 200 ° C. for 1 minute to 2 minutes 30 seconds if it is desired to modify the initial opening of the cracks without affecting their number.
- the gel-forming resin in the presence of water can be chosen from a wide range of commercial products.
- a solvating agent such as ethyl glycol
- water is particularly useful in causing the gel-forming resin to swell.
- the additives necessary for stabilizing the aqueous dispersion are well known in the art and a large amount of commercial products are available. It will preferably be added to the preparation in addition to surface-active agents serving for the stabilization of the anti-foaming agents to facilitate the preparation of the dispersion and to be able to carry out a regular coating.
- the preparation of the dispersion advantageously includes the presence of fillers, pigmented or not, which act in particular on the extent of the cracks or cracks observed.
- the drying heat treatment temperature is chosen between 180 and 210 ° C.
- the coating can subsequently be subjected, for example to a temperature of the order of 20 ° C for 1 minute to 2 minutes 30 seconds if it you want to change the initial opening of the cracks without affecting their number.
- the support on which the plastisol coating composition containing said sorbent / solvent couple is applied or the aqueous dispersion of a dry mixture of PVC and plasticizer containing a gel-forming resin in water may consist of a conventional support which possibly already includes one or more deposits of synthetic material, possibly provided with a print.
- a coating of plastisol for example on the coating obtained, so as to fill the cracks with a suitable material.
- a suitable material for example, a plastisol containing up to 30% of carbon black on the product obtained or optionally an aqueous emulsion of plasticized PVC and conductive carbon black, so as to fill the cracks by a material conducting the electric current.
- Such a coating is particularly suitable for avoiding the formation of static electricity for coatings intended for operating rooms, computer rooms, etc.
- the use of such a composition containing carbon black makes it possible to increase to a value of the order of 10 8 ohm.cm the electrical transverse resistance of the coating obtained which is normally 10 14 ohm.cm.
- the shape, depth and opening of the cracks can be controlled by the temperature of the heat treatment, by the choice of the sorbent / solvent couple and of the resin forming gel in water and by the quantity of solvent used. It should be noted, however, that the depth and the opening of the cracks can be markedly modified later, notably by heat treatment, unless these have been coated beforehand.
- Aerosil 300® and of solvent are respectively 2.68% and 26.31% in the plastisol coating.
- the coating thus obtained is applied to a conventional support having possibly already received at least one coating and / or one impression.
- the product thus obtained is subjected to a heat treatment so as to create cracks, which advantageously consists of passing, for 2 minutes 30 seconds, at a temperature between 110 and 120 ° C, obtained by heating in particular using a forced air oven or infrared radiation or a combination of the two, for example.
- the product obtained is then optionally subjected to an impression of a decoration, according to a process known per se.
- the product can also be subjected to a second heat treatment which allows the opening of already formed cracks.
- a heat treatment consists in passing, for 1 minute to 2 minutes 30 seconds, at a temperature of the order of 200 ° C.
- the product is then passed under a rubber doctor blade which penetrates, inside the cracks, a pigmented fluid plastisol which then undergoes pre-gelification.
- the whole is covered with a coating of PVC plastisol serving as a wear layer and the product obtained is subjected to a gelling operation, for 2 minutes 30 seconds, at a temperature of the order of 190 ° C.
- the rate of Barosil O and white spirit in the coating is, respectively, 12.5% and 28.7%.
- the coating thus obtained is deposited on a conventional support which is subjected to a heat treatment so as to create cracks.
- Said heat treatment consists of a passage of 2 minutes at 110 - 120 ° C, in an oven for example.
- the product thus obtained is then passed under a doctor blade so as to penetrate, inside the cracks, a PVC paste containing 30% carbon black.
- a final baking heat treatment is then carried out.
- a so-called "homogeneous" coating is obtained, the transverse electrical surface resistance of which is lowered to a value of the order of 108 ohm.cm (whereas it is 10 14 ohm.cm for PVC) and which therefore makes it possible to disperse local electrical charges.
- Such a coating could be used in an environment with high sensitivity to local loads such as computer rooms.
- a compact plastisol "composition is prepared according to Example 1.
- FIGS. 3 and 6 relate to a composition as mentioned below in which the gel has been prepared beforehand, that is to say:
- the gel consists of 63 parts of Aerosil® 300 and 637 parts of white spirit.
- the annular pumping makes it possible to express the viscosity as a function of the speed gradient.
- the white spirit is not preferentially adsorbed by the silica but is also distributed in the medium and therefore has a viscosity-lowering effect on the plastisol.
- the solvent swelled the inert charge and remained there even after mixing in the final medium. It has not been used to lower the general viscosity of plastisol. It is only the heat treatment which will make it possible to desorb the solvent from the silica by causing it to shrink.
- Example 6 aqueous dispersion.
- a dry PVC mixture is prepared consisting of:
- An aqueous suspension prepared in a mixer (Moltini type) consists of: This aqueous suspension is deposited with a doctor blade on a support composed of a glass veil coated with a PVC plastisol gelified on a drum and which has the following formulation:
- This coating is dried and baked in a hot air oven between 130 and 210 ° C.
- Example 7 aqueous dispersion
- This suspension is scraped on a support identical to that of Example 1, dried and baked in a hot air oven under the same conditions.
- the various aqueous suspensions can be colored in the mass by adding an adequate pigment to their formulation.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Building Environments (AREA)
- Floor Finish (AREA)
Claims (17)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT86109523T ATE44559T1 (de) | 1985-07-22 | 1986-07-11 | Verfahren zur herstellung von boden- oder wandbelag mit risseffekt und so erzeugtes produkt. |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LU86014 | 1985-07-22 | ||
LU86014A LU86014A1 (fr) | 1985-07-22 | 1985-07-22 | Procede de production de revetements de sol ou muraux a effet craquele et produit obtenu |
LU86088 | 1985-09-23 | ||
LU86088A LU86088A1 (fr) | 1985-09-23 | 1985-09-23 | Procede de production de revetements de sol ou muraux a effet craquele et produit obtenu |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0209810A1 EP0209810A1 (de) | 1987-01-28 |
EP0209810B1 true EP0209810B1 (de) | 1989-07-12 |
Family
ID=26640312
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86109523A Expired EP0209810B1 (de) | 1985-07-22 | 1986-07-11 | Verfahren zur Herstellung von Boden- oder Wandbelag mit Risseffekt und so erzeugtes Produkt |
Country Status (15)
Country | Link |
---|---|
US (1) | US4764411A (de) |
EP (1) | EP0209810B1 (de) |
AU (1) | AU583640B2 (de) |
BE (1) | BE905074A (de) |
CA (1) | CA1260329A (de) |
DE (1) | DE3664346D1 (de) |
DK (1) | DK162925C (de) |
ES (1) | ES2000535A6 (de) |
FR (1) | FR2585027B1 (de) |
GR (1) | GR861901B (de) |
IE (1) | IE57461B1 (de) |
IT (1) | IT1196520B (de) |
NO (1) | NO165690C (de) |
NZ (1) | NZ216844A (de) |
PT (1) | PT83028B (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1264027A (en) * | 1985-10-03 | 1989-12-27 | John B. Jalbert | Heat and pressure consolidated laminate |
US4880689A (en) * | 1985-10-18 | 1989-11-14 | Formica Corporation | Damage resistant decorative laminate |
DE4242356A1 (de) * | 1992-12-15 | 1994-06-16 | Sandoz Ag | Monomerzubereitungen für die Bauindustrie |
US7862835B2 (en) * | 2004-10-27 | 2011-01-04 | Boston Scientific Scimed, Inc. | Method of manufacturing a medical device having a porous coating thereon |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR530658A (fr) * | 1920-08-05 | 1921-12-28 | Clement Et Riviere | Procédé d'obtention d'effets craquelés applicable à la décoration d'objets divers de formes et de matières quelconques |
US2612456A (en) * | 1948-07-29 | 1952-09-30 | Ncr Co | Process for applying an ornamental and protective crackle coating to a base |
US2866720A (en) * | 1955-10-24 | 1958-12-30 | American Marietta Co | Decorative coating and method of making same |
JPS5125442B1 (de) * | 1971-02-10 | 1976-07-31 | ||
FR2247494A1 (en) * | 1973-10-11 | 1975-05-09 | Bat Applic Revetements Plastiq | Polyvinyl chloride decorative film with cracked appearance - prepd by heating layer contg plastisol and dispersed water |
FR2413940A1 (fr) * | 1978-01-10 | 1979-08-03 | Renault | Constitution d'un revetement de sol, notamment pour l'habitacle d'un vehicule automobile |
JPS5840376A (ja) * | 1981-09-03 | 1983-03-09 | Sugita:Kk | 皺模様を有する合成樹脂被膜を製品表面に形成する方法 |
US4605584A (en) * | 1984-12-03 | 1986-08-12 | Armstrong World Industries, Inc. | Decorative materials comprising crinkled chips |
-
1986
- 1986-07-08 IE IE1836/86A patent/IE57461B1/en not_active IP Right Cessation
- 1986-07-08 BE BE6/48236A patent/BE905074A/fr not_active IP Right Cessation
- 1986-07-11 DE DE8686109523T patent/DE3664346D1/de not_active Expired
- 1986-07-11 EP EP86109523A patent/EP0209810B1/de not_active Expired
- 1986-07-14 NZ NZ216844A patent/NZ216844A/xx unknown
- 1986-07-14 CA CA000513680A patent/CA1260329A/en not_active Expired
- 1986-07-15 FR FR8610262A patent/FR2585027B1/fr not_active Expired
- 1986-07-18 IT IT21173/86A patent/IT1196520B/it active
- 1986-07-18 NO NO862913A patent/NO165690C/no not_active IP Right Cessation
- 1986-07-18 AU AU60314/86A patent/AU583640B2/en not_active Ceased
- 1986-07-21 ES ES8600427A patent/ES2000535A6/es not_active Expired
- 1986-07-21 US US06/887,271 patent/US4764411A/en not_active Expired - Lifetime
- 1986-07-21 PT PT83028A patent/PT83028B/pt not_active IP Right Cessation
- 1986-07-21 DK DK346386A patent/DK162925C/da not_active IP Right Cessation
- 1986-07-21 GR GR861901A patent/GR861901B/el unknown
Also Published As
Publication number | Publication date |
---|---|
IT8621173A0 (it) | 1986-07-18 |
FR2585027A1 (fr) | 1987-01-23 |
FR2585027B1 (fr) | 1988-02-26 |
IT1196520B (it) | 1988-11-16 |
DK346386D0 (da) | 1986-07-21 |
DE3664346D1 (en) | 1989-08-17 |
GR861901B (en) | 1986-11-24 |
EP0209810A1 (de) | 1987-01-28 |
ES2000535A6 (es) | 1988-03-01 |
DK162925B (da) | 1991-12-30 |
BE905074A (fr) | 1986-11-03 |
CA1260329A (en) | 1989-09-26 |
PT83028B (pt) | 1992-08-31 |
NO165690B (no) | 1990-12-10 |
NZ216844A (en) | 1989-03-29 |
NO862913L (no) | 1987-01-23 |
US4764411A (en) | 1988-08-16 |
DK162925C (da) | 1992-05-25 |
NO165690C (no) | 1991-03-20 |
AU583640B2 (en) | 1989-05-04 |
AU6031486A (en) | 1987-01-29 |
DK346386A (da) | 1987-01-23 |
NO862913D0 (no) | 1986-07-18 |
IE57461B1 (en) | 1993-02-24 |
PT83028A (fr) | 1986-08-01 |
IE861836L (en) | 1987-01-22 |
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