US3383243A - Method of preparing a partially collapsed latex foam backed carpet - Google Patents
Method of preparing a partially collapsed latex foam backed carpet Download PDFInfo
- Publication number
- US3383243A US3383243A US654534A US65453467A US3383243A US 3383243 A US3383243 A US 3383243A US 654534 A US654534 A US 654534A US 65453467 A US65453467 A US 65453467A US 3383243 A US3383243 A US 3383243A
- Authority
- US
- United States
- Prior art keywords
- rug
- composition
- backing
- binder
- latex
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 title description 18
- 229920001821 foam rubber Polymers 0.000 title description 3
- 239000011230 binding agent Substances 0.000 description 36
- 239000000203 mixture Substances 0.000 description 28
- 239000000463 material Substances 0.000 description 20
- 229920000126 latex Polymers 0.000 description 15
- 238000000576 coating method Methods 0.000 description 13
- 239000011248 coating agent Substances 0.000 description 11
- 239000006260 foam Substances 0.000 description 11
- 239000004816 latex Substances 0.000 description 10
- 239000000945 filler Substances 0.000 description 9
- 229920001971 elastomer Polymers 0.000 description 8
- 239000000047 product Substances 0.000 description 6
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 5
- 239000008199 coating composition Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- 235000016976 Quercus macrolepis Nutrition 0.000 description 3
- 244000305267 Quercus macrolepis Species 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- -1 e.g. Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000003349 gelling agent Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 238000004073 vulcanization Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 241000276489 Merlangius merlangus Species 0.000 description 2
- 229920013620 Pliolite Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000007761 roller coating Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- XQESJWNDTICJHW-UHFFFAOYSA-N 2-[(2-hydroxy-5-methyl-3-nonylphenyl)methyl]-4-methyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC(C)=CC(CC=2C(=C(CCCCCCCCC)C=C(C)C=2)O)=C1O XQESJWNDTICJHW-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241000221020 Hevea Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 230000003679 aging effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 239000001099 ammonium carbonate Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920003211 cis-1,4-polyisoprene Polymers 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000010073 coating (rubber) Methods 0.000 description 1
- 244000221110 common millet Species 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QDTDJKTWCDVRKH-UHFFFAOYSA-N o-butyl butylsulfanylmethanethioate Chemical compound CCCCOC(=S)SCCCC QDTDJKTWCDVRKH-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 description 1
- 229940048086 sodium pyrophosphate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 235000019818 tetrasodium diphosphate Nutrition 0.000 description 1
- 239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000009732 tufting Methods 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- PGNWIWKMXVDXHP-UHFFFAOYSA-L zinc;1,3-benzothiazole-2-thiolate Chemical compound [Zn+2].C1=CC=C2SC([S-])=NC2=C1.C1=CC=C2SC([S-])=NC2=C1 PGNWIWKMXVDXHP-UHFFFAOYSA-L 0.000 description 1
Images
Classifications
-
- 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
- D06N3/10—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 styrene-butadiene copolymerisation products or other synthetic rubbers or elastomers except polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/30—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof by mixing gases into liquid compositions or plastisols, e.g. frothing with air
-
- 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
- D06N7/0063—Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf
- D06N7/0071—Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf characterised by their backing, e.g. pre-coat, back coating, secondary backing, cushion backing
- D06N7/0073—Floor covering on textile basis comprising a fibrous top layer being coated at the back with at least one polymer layer, e.g. carpets, rugs, synthetic turf characterised by their backing, e.g. pre-coat, back coating, secondary backing, cushion backing the back coating or pre-coat being applied as an aqueous dispersion or latex
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2321/00—Characterised by the use of unspecified rubbers
-
- 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
- D06N2205/00—Condition, form or state of the materials
- D06N2205/04—Foam
-
- 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
- D06N2205/00—Condition, form or state of the materials
- D06N2205/04—Foam
- D06N2205/045—Froth
-
- 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
- D06N2205/00—Condition, form or state of the materials
- D06N2205/20—Cured materials, e.g. vulcanised, cross-linked
-
- 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
- D06N2207/00—Treatments by energy or chemical effects
- D06N2207/08—Treatments by energy or chemical effects using gas
-
- 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
- D06N2209/00—Properties of the materials
- D06N2209/10—Properties of the materials having mechanical properties
- D06N2209/106—Roughness, anti-slip, abrasiveness
Definitions
- a non-skid rug is formed by applying a frothed binder composition to a rug backing and then partially collapsing the froth and drying the binder composition.
- the finished rug includes a backing having a binder layer wherein the binder layer is characterized by a density gradient from the surface to the center.
- the present invention is concerned with rug coatings and more particularly with processes for producing rugs having improved non-skid properties.
- rugs In the production of rugs, whether they be of the woven type wherein the yarn is woven into a backing sheet, e.g., velvets, axminsters, etc., or of the tufted type wherein a plurality of loops or strands of the yarn are deposited in the backing sheet by tufting m chines, it has generally become the practice to lock the yarns in place with a hinder or backing layer.
- binder or backing layers comprise a natural and/or synthetic polymer latex and can be cured or uncured, as desired. Further, they often contain moderate to large amounts of inert fillers, primarily as extenders but also to stiffen or rigidity the latex backing. Although these coatings anchor the yarn firmly, they often have an adverse effect upon the non-skid properties of the rug.
- foamed rubber backing material provides little, if any, locking of the stitches of the tufted rug; therefore, this method also requires a two step operation; one to bind the stitches and another to provide the non-skid characteristics by means of the foamed binder material.
- non-skid properties can be achieved in rugs by aerating (with air or other gases) binder materials, applying a layer of said binder material to a rug backing and then partially collapsing the thus-formed foam. If desired, vulcanization can be carried out simultaneously with the collapse of the foam.
- the binder material By applying the binder material to the rug backing as a froth or foam relatively low weight of binder material is employed, while at the same time the valleys, that is the depressions and irregularities in the rug backing, will be readily penetrated by the frothed binder material. More efiicient coverage of the rug backing will provide a greater degree of non-skid properties since more non-skid rug area is exposed to the floor.
- the controlled collapse of the frothed material is achieved by heating the coated rug. As mentioned above, this can be accomplished during the vulcanization step.
- the absence of the gelling agent in the binder material results in the collapse of the foam to provide better penetration into the rug backing than prior art foam.
- the overall density of the backing layer of the present invention is less than that achieved with a conventional nonfoamed binder material.
- the degree of collapse of the foam is time and temperature dependent and, therefore, various combinations of conditions can be employed to obtain the desired end products.
- the froth or foam is preferably collapsed to to 90% of its original volume, more preferably to In the final product, a density gradient exists in the binder layers, with a relatively high density at the outer surfaces of the layer and a relating low density in the intermediate portion of the layer. Where a relatively low degree of collapse is achieved, the center of the layer generally contains an irregular, relatively small cell structure.
- the finished rug possesses the advantages of both the rugs prepared using conventional binders and rugs prepared using foamed binders while the same time lacking the deficiencies of both.
- the novel rugs of the present invention possess backings that are uniformly covered with binder material; employ a lower coating weight than prior art rugs and employ only a single binder material applied in a single, continuous, simple operation.
- the binder material of the present invention is applied to the rug as a foam which is subsequently collapsed, a relatively thick skin is formed on the surface of the binder material opposite that surface which contacts the rug backing. It is this relatively thick, tough skin which provides the advantageous non-skid properties.
- the surface of binder material next to the rug backing forms an extremely secure bond with the backing because it can obtain intimate contact with the fibers and stitches by means of better penetration achieved during partial collapse of the froth thereby insuring a secure grip after curing.
- the binder compositions of the present invention employ natural and/or synthetic latices.
- a combination of natural and synthetic latices is used.
- Useful synthetic latices included Pliolite 5355 and Pliolite 151 (trade names of Goodyear Tire and Rubber Company for butadiene styrene latices).
- a prefered natural latex is centrifuged Hevea latex.
- the binder material is aerated prior to its application to the rug backing.
- air air
- the froth or foam is prepared by simply beating air or other gases, e.g., butane, fluorocarbons, and the like into the coating composition using conventional apparatus such, for example, as an Oakes mixer or a Firestone foamer.
- Another method for preparing the froth comprises the employment of blowing agents, which when activated, e.g., thermally, chemically, etc., generate gases such as carbon dioxide, ammonia, nitrogen, etc.
- blowing agents which are well known to the art may be applied directly to the coating solution and may be activated either before the coating is applied to the rug or after it is applied but before it is fully cured.
- the amount of aeration and the resulting density of the binder composition may be varied to suit the particular needs.
- the density of the coating solution is less than 1.0 gm./c.c. and, more particularly, less than 0.80.
- the density was between about 0.60 and about 0.8.
- the binder composition of the present invention is applied in any convenient manner; for example, by brushing, spreading, and the like using conventional equipment such as roll coaters.
- the amount applied to the rug varies over a relatively wide range depending upon the desired result. Generally the use of about six to sixteen ounces per yard, preferably twelve ounces per yard is employed.
- the water may be removed by well known techniques, e.g., evaporation, coagulation, and the like. It is during the removal of the water, that is, the drying of the binder composition, that the controlled collapse of the froth is achieved.
- Vulcanizers and accelerators are added to the binder composition to provide vulcanization simultaneously with the partial collapse of the froth; if desired.
- FIG- URE 1 shows a rug having tufts 12 imbedded in a backing fabric 14.
- FIGURE 2 shows the frothed latex com position 16 applied to the backing.
- the binder layer 18 is composed of tough outer skin 20 which provides the non-skid characteristics to the rug and inner skin 24 which provides the binding characteristics to the stitches and fibers of the backing.
- Center portion 22 of the binder layer is composed of an area of lower density than the outer faces.
- the process of the present invention are especially useful in providing the non-skid properties of rugs wherein the binder composition contains fillers.
- the non-skid properties of the rugs will vary inversely with the amount of filler present.
- useful fillers mention may be made of whiting or calcium carbonate, diatomaceous earth, clays, aluminum silicate and aluminum hydrate.
- the amount of filler used in such a coating varies over a considerable range. As much as two or even three parts of the filler may be employed per part, by weight, of the dry rubber.
- the effectiveness of the present invention was especially pronounced when the filler was present in at least a 0.8 to 1 ratio and more particularly a 1 to '1 ratio of filler to dry rubber.
- the coating compositions of the present invention may also contain surfactants, preservatives, deodorants, pigments, dispersing agents, suspending agents, vulcanizing agents, accelerators, thickeners, and the like.
- surfactants preservatives, deodorants, pigments, dispersing agents, suspending agents, vulcanizing agents, accelerators, thickeners, and the like.
- the presence of a surface active agent is especially useful in aerating the coating solutions and the presence of the thickener is especially helpful in maintaining the binder 4 composition in an aerated condition during application to the rug.
- EXAMPLE A latex coating composition was made up in two parts.
- Material Percent Dry Wet Solids Weight Weight Part A comprised:
- Pliolite 5355 (a butadiene-styrene la 1 60 60.0 90. 01
- Pliolite 151 a butadiene-styrene latex, high in styrene) 53 25.0 47.17
- Aeintol DLR S eeial (Potassium salt of a mixed rosin fatty acid soap manufactured by Arizona Chemical 00.)"-.. 21. 5 1.
- Ultrawet DS an alkylbenzene sodium sulfonate surfactant produced by Atlantie Refining Co. 30 0. 60 2.
- Centrifuged Natural Latex 62 40. 0 (i4.
- Part B was added to Part A with gentle agitation and the resultant mixture had a density of about 1.30.
- composition was applied by roller coating to tufted goods at about 12 ounces/ sq. yd. and dried for 12 minutes at 290 F.
- the finished coating thickness was 0.050 inch. This represented a conventional, single, unfoamed binder application.
- the composition was added to an Oakes mixture and air was introduced until the product, as discharged, had a density of about 0.6 to 0.8.
- the frothed composition was applied by roller coating to tufted goods at an about 12 oz./sq. yd. and dried for 12 minutes at 290 F. during which the froth partially collapsed.
- the finished coating thickness was 0.065 inch. This represented the process of the invention.
- composition was treated as in (2) above except that 5 parts of a gelling agent, ammonium acetate, was added, whereby the foam structure was maintained after drying was complete.
- the thickness of the coating was 0.155 inch.
- the Oakes continuous mixer which was used above, is a self-contained machine consisting essentially of a mixing head or chamber, a positive displacement pump to handle the product being mixed, and means to introduce air or other gases into the system for incorporation into the product.
- a Wide range of densities may be obtained.
- a process for preparing rugs which comprises frotli ing in the absence of a gelling agent a latex composition selected from the group consisting of natural and synthetic latices, coating said frothed composition onto the back of a tufted rug, heating said frothed composition to a temperature and for a time suificient to affect partial collapse of said frothed composition of from 50 to 90 percent of its original volume and to affect drying of said frothed composition; whereby said rug is provided with a backing characterized by tough, relatively thick skins of collapsed froth at the rug-composition interface and at the exposed face of said composition and by a relatively low density uncollapsed foam structure intermediate said thick skins.
- composition contains at least about one part by weight of said filter per part of dry rubber.
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Description
May 14, 1968 F. A. DI GIOIA METHOD OF PREPARING A PARTIALLY COLLAPSED LATEX FOAM BACKED CARPET Filed July 19, 1967 FIG. 2
FIG. 3
00 mm E O v T m .Q/%T na A K N F United States Patent 3,383,243 METHOD 0F PREPARING A PARTEALLY QGLLAPSED LATEX FOAM BACKED CARPET Frank A. Di Gioia, Dalton, (2a., assignor to Generai Latex & (Ihernicai Corporation of Georgia, Dalton, (2a., a corporation of Georgia Continuation-in-pm of application Ser. No. 330,655, Dec. 16, 1963. This application July 19, 1967, Ser. No. 654,534
5 Claims. (Cl. 117-161) ABSTRACT OF THE DICLOSURE A non-skid rug is formed by applying a frothed binder composition to a rug backing and then partially collapsing the froth and drying the binder composition. The finished rug includes a backing having a binder layer wherein the binder layer is characterized by a density gradient from the surface to the center.
This application is a continuation-in-part of application Ser. No. 330,655, filed Dec. 16, 1963, now abandoned.
The present invention is concerned with rug coatings and more particularly with processes for producing rugs having improved non-skid properties.
In the production of rugs, whether they be of the woven type wherein the yarn is woven into a backing sheet, e.g., velvets, axminsters, etc., or of the tufted type wherein a plurality of loops or strands of the yarn are deposited in the backing sheet by tufting m chines, it has generally become the practice to lock the yarns in place with a hinder or backing layer. Generally such binder or backing layers comprise a natural and/or synthetic polymer latex and can be cured or uncured, as desired. Further, they often contain moderate to large amounts of inert fillers, primarily as extenders but also to stiffen or rigidity the latex backing. Although these coatings anchor the yarn firmly, they often have an adverse effect upon the non-skid properties of the rug.
In the past, one method of achieving non-skid properties in rugs has been by first applying a binder layer to secure the fibers of the backing fabric and then applying a second rubber coating to provide the desired non-skid properties. Such two layer systems are taught in US. Patents Nos. 1,823,131 and 3,227,574. It can be readily seen that this application of two specialized layers of rubber adds considerably to the processing operation and the cost of the rug.
The art has also employed a foamed rubber backing material to achieve the desired non-skid properties. However, foamed backing material provides little, if any, locking of the stitches of the tufted rug; therefore, this method also requires a two step operation; one to bind the stitches and another to provide the non-skid characteristics by means of the foamed binder material.
A novel process has now been found whereby the single application of the binder material can both provide the desired locking of the stitches of the tufted rug while at the same time providing efiicient non-skid characteristics.
It has now been found that non-skid properties can be achieved in rugs by aerating (with air or other gases) binder materials, applying a layer of said binder material to a rug backing and then partially collapsing the thus-formed foam. If desired, vulcanization can be carried out simultaneously with the collapse of the foam.
By applying the binder material to the rug backing as a froth or foam relatively low weight of binder material is employed, while at the same time the valleys, that is the depressions and irregularities in the rug backing, will be readily penetrated by the frothed binder material. More efiicient coverage of the rug backing will provide a greater degree of non-skid properties since more non-skid rug area is exposed to the floor.
The controlled collapse of the frothed material is achieved by heating the coated rug. As mentioned above, this can be accomplished during the vulcanization step. The absence of the gelling agent in the binder material results in the collapse of the foam to provide better penetration into the rug backing than prior art foam. However, the overall density of the backing layer of the present invention is less than that achieved with a conventional nonfoamed binder material. The degree of collapse of the foam is time and temperature dependent and, therefore, various combinations of conditions can be employed to obtain the desired end products. The froth or foam is preferably collapsed to to 90% of its original volume, more preferably to In the final product, a density gradient exists in the binder layers, with a relatively high density at the outer surfaces of the layer and a relating low density in the intermediate portion of the layer. Where a relatively low degree of collapse is achieved, the center of the layer generally contains an irregular, relatively small cell structure.
The finished rug possesses the advantages of both the rugs prepared using conventional binders and rugs prepared using foamed binders while the same time lacking the deficiencies of both. Thus, the novel rugs of the present invention possess backings that are uniformly covered with binder material; employ a lower coating weight than prior art rugs and employ only a single binder material applied in a single, continuous, simple operation.
Because the binder material of the present invention is applied to the rug as a foam which is subsequently collapsed, a relatively thick skin is formed on the surface of the binder material opposite that surface which contacts the rug backing. It is this relatively thick, tough skin which provides the advantageous non-skid properties. The surface of binder material next to the rug backing forms an extremely secure bond with the backing because it can obtain intimate contact with the fibers and stitches by means of better penetration achieved during partial collapse of the froth thereby insuring a secure grip after curing.
The binder compositions of the present invention employ natural and/or synthetic latices. In a prefered embodiment, a combination of natural and synthetic latices is used. Useful synthetic latices included Pliolite 5355 and Pliolite 151 (trade names of Goodyear Tire and Rubber Company for butadiene styrene latices). A prefered natural latex is centrifuged Hevea latex. Preferably the binder material is aerated prior to its application to the rug backing. Such an embodiment allows the use of the lowest cost blowing agent (air) and permits the operator to determine the density of the coating composition before it is applied to the rug. The froth or foam is prepared by simply beating air or other gases, e.g., butane, fluorocarbons, and the like into the coating composition using conventional apparatus such, for example, as an Oakes mixer or a Firestone foamer.
Another method for preparing the froth comprises the employment of blowing agents, which when activated, e.g., thermally, chemically, etc., generate gases such as carbon dioxide, ammonia, nitrogen, etc.
Such blowing agents which are well known to the art may be applied directly to the coating solution and may be activated either before the coating is applied to the rug or after it is applied but before it is fully cured. As examples of such materials mention may be made of ammonium bicarbonate, urea, or dinitroso-pentamethylenetetraamine.
The amount of aeration and the resulting density of the binder composition may be varied to suit the particular needs. In a preferred embodiment the density of the coating solution is less than 1.0 gm./c.c. and, more particularly, less than 0.80. In a particularly preferred embodiment, the density was between about 0.60 and about 0.8.
The binder composition of the present invention is applied in any convenient manner; for example, by brushing, spreading, and the like using conventional equipment such as roll coaters. The amount applied to the rug varies over a relatively wide range depending upon the desired result. Generally the use of about six to sixteen ounces per yard, preferably twelve ounces per yard is employed. Subsequent to coating, the water may be removed by well known techniques, e.g., evaporation, coagulation, and the like. It is during the removal of the water, that is, the drying of the binder composition, that the controlled collapse of the froth is achieved. Vulcanizers and accelerators are added to the binder composition to provide vulcanization simultaneously with the partial collapse of the froth; if desired.
Turning now to the dnawing, which illustrates the novel product and the method of preparation, FIG- URE 1 shows a rug having tufts 12 imbedded in a backing fabric 14. FIGURE 2 shows the frothed latex com position 16 applied to the backing. After the application of heat partially collapse the froth, and if desired, cure the rubber, the binder layer 18, as shown in FIG- URE 3, is composed of tough outer skin 20 which provides the non-skid characteristics to the rug and inner skin 24 which provides the binding characteristics to the stitches and fibers of the backing. Center portion 22 of the binder layer is composed of an area of lower density than the outer faces.
The process of the present invention are especially useful in providing the non-skid properties of rugs wherein the binder composition contains fillers. Usually the non-skid properties of the rugs will vary inversely with the amount of filler present. As examples of useful fillers, mention may be made of whiting or calcium carbonate, diatomaceous earth, clays, aluminum silicate and aluminum hydrate. The amount of filler used in such a coating varies over a considerable range. As much as two or even three parts of the filler may be employed per part, by weight, of the dry rubber. The effectiveness of the present invention was especially pronounced when the filler was present in at least a 0.8 to 1 ratio and more particularly a 1 to '1 ratio of filler to dry rubber.
The coating compositions of the present invention may also contain surfactants, preservatives, deodorants, pigments, dispersing agents, suspending agents, vulcanizing agents, accelerators, thickeners, and the like. The presence of a surface active agent is especially useful in aerating the coating solutions and the presence of the thickener is especially helpful in maintaining the binder 4 composition in an aerated condition during application to the rug.
The following non-limiting example illustrates the processes of the present invention.
EXAMPLE A latex coating composition was made up in two parts.
Material Percent Dry Wet Solids Weight Weight Part A comprised:
Pliolite 5355 (a butadiene-styrene la 1 60 60.0 90. 01 Pliolite 151 (a butadiene-styrene latex, high in styrene) 53 25.0 47.17 Aeintol DLR S eeial (Potassium salt of a mixed rosin fatty acid soap manufactured by Arizona Chemical 00.)"-.. 21. 5 1. 01 7. 50 Ultrawet DS (an alkylbenzene sodium sulfonate surfactant produced by Atlantie Refining Co.) 30 0. 60 2. 00 Centrifuged Natural Latex 62 40. 0 (i4. 52 Naugawhite (a dispersion of an antioxidant made by Naugatuek Chemical Co.) 39. 6 1. 79 3. 00 Dispersed Sulfur. 09. 7 0.10 0.15 Zine Dibutyl Dithiocarbonate (dispersion) 52 2. 08 4. 00 Zenite Special (A dispersion of zinc mereapto benzothiozole accelerator produced by Du Pont).. 51. 5 1. 03 2.00 Zinc Oxide Dispersion. 52. 4 5. 24 10.0 Titanium Dioxide Dispe on 63. 6 5. 30 8. 33 Water 70.0 'letra Sodium Pyrophosphate. 100 1.00 1.00 Whiting 100 175. 00 175. 00 Parailin Oil Emulsion 69.6 5.22 7. 5 Karaya Gum Solution 3 0. 30 10.0 Polyacrylate 'lhickener... 10 0. 50 5. 0
Total 324.8 508 1 Part B comprised:
Dispersed Sulphur 52. 3 2. 62 5. 00 Arquad 12-50 (Dodeeyltrimethyl ammonium chloride produced by Armour) 50. 0 1. 00 2. 00
Total 3.62 7. 00
Just prior to use, Part B was added to Part A with gentle agitation and the resultant mixture had a density of about 1.30.
For comparative purposes the above-described composition was then employed as follows:
(1) The composition was applied by roller coating to tufted goods at about 12 ounces/ sq. yd. and dried for 12 minutes at 290 F. The finished coating thickness was 0.050 inch. This represented a conventional, single, unfoamed binder application.
(2) The composition was added to an Oakes mixture and air was introduced until the product, as discharged, had a density of about 0.6 to 0.8. The frothed composition was applied by roller coating to tufted goods at an about 12 oz./sq. yd. and dried for 12 minutes at 290 F. during which the froth partially collapsed. The finished coating thickness was 0.065 inch. This represented the process of the invention.
(3) The composition was treated as in (2) above except that 5 parts of a gelling agent, ammonium acetate, was added, whereby the foam structure was maintained after drying was complete. The thickness of the coating was 0.155 inch.
From the foregoing it will be noted that an increase in thickness of coverage of about 30% is achieved over a binder composition which is not foamed and then collapsed. While the foamed and gelled binder had a greater thickness then that of this invention the adhesion to the backing is not as great nor are the aging properties of the product as satisfactory.
When the non-skid properties of the rug of the present invention were compared with one which was not frothed in an inclined plane test, it was found that the angle of the plane could be raised 60 to higher for the rug of the present invent-ion before slipping took place.
The Oakes continuous mixer, which was used above, is a self-contained machine consisting essentially of a mixing head or chamber, a positive displacement pump to handle the product being mixed, and means to introduce air or other gases into the system for incorporation into the product. By controlling the latex flow rate and the air flow rate a Wide range of densities may be obtained.
Since changes may be made in the above process and product without departing from the scope of the invention herein involved, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.
What is claimed is:
1. A process for preparing rugs which comprises frotli ing in the absence of a gelling agent a latex composition selected from the group consisting of natural and synthetic latices, coating said frothed composition onto the back of a tufted rug, heating said frothed composition to a temperature and for a time suificient to affect partial collapse of said frothed composition of from 50 to 90 percent of its original volume and to affect drying of said frothed composition; whereby said rug is provided with a backing characterized by tough, relatively thick skins of collapsed froth at the rug-composition interface and at the exposed face of said composition and by a relatively low density uncollapsed foam structure intermediate said thick skins.
2. The process as defined in claim 1 wherein said composition contains a filler.
3. The process as defined in claim 11 wherein said composition is frothed by the introduction of air to said composition.
4. The method as defined in claim 1 employing said composition at a relative density of less than 1.0.
5. A process as defined in claim 2 wherein said composition contains at least about one part by weight of said filter per part of dry rubber.
References (Iited UNITED STATES PATENTS 2,567,951 9/1951 Lewis l56---78 XR 2,629,919 3/1953 Golden.
2,641,296 6/1953 Marco 161-67 XR 2,649,391 8/1953 Alderfer 15678 XR OTHER REFERENCES Noble; Latex in Industry, 2nd ed., Rubber Age, 1953, TS 1890 M75, PP. 603608, 612, 613.
ROBERT F. BURNETT, Primary Examiner.
R. H. CRISS, Assistant Examiner.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US654534A US3383243A (en) | 1967-07-19 | 1967-07-19 | Method of preparing a partially collapsed latex foam backed carpet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US654534A US3383243A (en) | 1967-07-19 | 1967-07-19 | Method of preparing a partially collapsed latex foam backed carpet |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3383243A true US3383243A (en) | 1968-05-14 |
Family
ID=24625257
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US654534A Expired - Lifetime US3383243A (en) | 1967-07-19 | 1967-07-19 | Method of preparing a partially collapsed latex foam backed carpet |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3383243A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3513046A (en) * | 1966-08-09 | 1970-05-19 | Polymer Corp | Manufacture of double-backed tufted carpets |
| US5373028A (en) * | 1991-08-20 | 1994-12-13 | The Dow Chemical Company | Polyurethane foams having reduced visible emissions during curing |
| US5654065A (en) * | 1994-07-01 | 1997-08-05 | Reittec Co., Ltd. | Composite elastic layer |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2567951A (en) * | 1948-04-07 | 1951-09-18 | Ohio Commw Eng Co | Sponge rubber-textile combination material |
| US2629919A (en) * | 1952-06-25 | 1953-03-03 | Golden Victor | Method of applying foamed rubber latex to a permeable backing |
| US2641296A (en) * | 1950-06-19 | 1953-06-09 | Marco John | Machine for the continuous application of foam rubber cushioning to a carpet |
| US2649391A (en) * | 1950-04-15 | 1953-08-18 | Edward D Andrews | Sponge rubber product |
-
1967
- 1967-07-19 US US654534A patent/US3383243A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2567951A (en) * | 1948-04-07 | 1951-09-18 | Ohio Commw Eng Co | Sponge rubber-textile combination material |
| US2649391A (en) * | 1950-04-15 | 1953-08-18 | Edward D Andrews | Sponge rubber product |
| US2641296A (en) * | 1950-06-19 | 1953-06-09 | Marco John | Machine for the continuous application of foam rubber cushioning to a carpet |
| US2629919A (en) * | 1952-06-25 | 1953-03-03 | Golden Victor | Method of applying foamed rubber latex to a permeable backing |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3513046A (en) * | 1966-08-09 | 1970-05-19 | Polymer Corp | Manufacture of double-backed tufted carpets |
| US5373028A (en) * | 1991-08-20 | 1994-12-13 | The Dow Chemical Company | Polyurethane foams having reduced visible emissions during curing |
| US5654065A (en) * | 1994-07-01 | 1997-08-05 | Reittec Co., Ltd. | Composite elastic layer |
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