CA1065240A - Artificial fibers preparation - Google Patents
Artificial fibers preparationInfo
- Publication number
- CA1065240A CA1065240A CA227,949A CA227949A CA1065240A CA 1065240 A CA1065240 A CA 1065240A CA 227949 A CA227949 A CA 227949A CA 1065240 A CA1065240 A CA 1065240A
- Authority
- CA
- Canada
- Prior art keywords
- sulfur
- plasticized
- fibers
- article
- manufacture
- 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
- 229920002994 synthetic fiber Polymers 0.000 title description 3
- 238000002360 preparation method Methods 0.000 title description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 64
- 239000011593 sulfur Substances 0.000 claims abstract description 60
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 60
- 239000000835 fiber Substances 0.000 claims abstract description 22
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 239000011159 matrix material Substances 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 30
- -1 polypropylene Polymers 0.000 claims description 15
- 239000004743 Polypropylene Substances 0.000 claims description 12
- 239000003365 glass fiber Substances 0.000 claims description 12
- 229920001155 polypropylene Polymers 0.000 claims description 12
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 claims description 10
- 239000000454 talc Substances 0.000 claims description 7
- 229910052623 talc Inorganic materials 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 239000005077 polysulfide Substances 0.000 claims description 5
- 229920001021 polysulfide Polymers 0.000 claims description 5
- 150000008117 polysulfides Polymers 0.000 claims description 5
- 239000004677 Nylon Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 229920001778 nylon Polymers 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 229920000742 Cotton Polymers 0.000 claims 1
- 229920002635 polyurethane Polymers 0.000 claims 1
- 239000004814 polyurethane Substances 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 19
- 238000000034 method Methods 0.000 abstract description 2
- 238000002425 crystallisation Methods 0.000 description 7
- 230000008025 crystallization Effects 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- 239000004033 plastic Substances 0.000 description 7
- 239000013521 mastic Substances 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 244000025254 Cannabis sativa Species 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- VKCLPVFDVVKEKU-UHFFFAOYSA-N S=[P] Chemical class S=[P] VKCLPVFDVVKEKU-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000013066 combination product Substances 0.000 description 1
- 229940127555 combination product Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002991 molded plastic Substances 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 238000009732 tufting Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H11/00—Non-woven pile fabrics
-
- E—FIXED CONSTRUCTIONS
- E01—CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
- E01C—CONSTRUCTION OF, OR SURFACES FOR, ROADS, SPORTS GROUNDS, OR THE LIKE; MACHINES OR AUXILIARY TOOLS FOR CONSTRUCTION OR REPAIR
- E01C13/00—Pavings or foundations specially adapted for playgrounds or sports grounds; Drainage, irrigation or heating of sports grounds
- E01C13/08—Surfaces simulating grass ; Grass-grown sports grounds
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Architecture (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Carpets (AREA)
- Road Paving Structures (AREA)
- Nonwoven Fabrics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
An article of manufacture comprising a plurality of fibers partially embedded in a solidified plasticized sulfur matrix with one end of the fibers extending outward from the matrix to form a turf or carpet-like surface. By the process of embedding, the steps of cementing or providing a backing with cementing are obviated, thus yielding a simpler made article than conventional materials of the broad class.
An article of manufacture comprising a plurality of fibers partially embedded in a solidified plasticized sulfur matrix with one end of the fibers extending outward from the matrix to form a turf or carpet-like surface. By the process of embedding, the steps of cementing or providing a backing with cementing are obviated, thus yielding a simpler made article than conventional materials of the broad class.
Description
~065Z40 BACKGROUND OF T~E INV~NTION
.
The present invention relates to a synthetic turf or carpet-like manufacture comprising a plasticized sulfur i matrix.
Prior patents disclosing synthetic turfs include U.S. Patents 3,422,615; 3,332,828; 3,157,557; 2,515,~47;
.
The present invention relates to a synthetic turf or carpet-like manufacture comprising a plasticized sulfur i matrix.
Prior patents disclosing synthetic turfs include U.S. Patents 3,422,615; 3,332,828; 3,157,557; 2,515,~47;
2,061,750; and 1,939,846.
U.S. Patent 3,422,615 discloses a synthetic turf-like material which i5 referred to as a pile fabric. Fibers which are indicated as being suitable for making the yarns used to make the pile fabric of USP 3,422,615 are said to include olefins, particularly polypropylene, nylon, vinyl, vinylidene chloride, polyvinyl chloride, polyethylene, polyester, polyacrylonitrile, acetate, triacetate, rayon (cellulosics), and glass.
U.S. Patent 3,332,828 relates to artificial turf preferably produced by weaving synthetic fibers on a Wilton cut-pile loom to form a structure consisting of a woven backing having a cut-pile face extending from one surface thereof and then applying a suitable latex formation on the other surface of the backing to render the complete ~tructure dimensionally stable.
U.S. Patent 3,157,557 discloses an integrally molded plastic sod simulating natural grass and comprising a flat flexible base of a thick plastic material having a multiplicity of closely-spaced blade-like plastic stems molded integral with the base.
U.S. Patent 2,515,847 discloses a surfacing structure suitable for use as a putting green for golf. The surfacing structure includes a top layer of rug material having a nap.
:~ -- . .
, . . . .
~065Z40 The rug ~aterial is supported on center layers of sponge rubber-like material. The supported rug material is placed upon the earth.
United States Patent 2,061,750 relates to grass mats prepared by stitching grass simulated material to a base.
United States Patent 1,939,846 discloses distributing - : -, :
fibrous material evenly over the top of a sheet of rubber composi-tion and then vulcanizing the fibers to the sheet in a heat press.
Plasticized sulfur has been disclosed in various references, for example by J. I. Jin in "Chemistry of Plastic-ized Sulfur", Petroleum Division, A. C. S. Symposium, Vol. 19, No. 2, March 1974, pp. 234-241 and by C. Kinney Hancock in "Plasticized Sulfur Compositions for Traffic Marking", Industrial and Engineering Chemistry, Vol. 46, No. 11, November 1954, pp. 2431-2435. Exemplary patents disclosing plasticized sulfur include USP 3,316,115 "Marking Compositions"; USP 3,434,852 "Plasticized Sulfur Compositions"; USP 3,447,941, "Sprayable ; Sulfur Road Marking Compositions"; USP 3,459,717 "Sulfur Based Plastic Composition"; USP 3,560,451 "Plastic and Nonflammable Sulfur Composition"; USP 3,453,125 "Plasticized Sulfur Compositions";
; USP 3,674,525 "Plasticized Sulfur Compositions"; and USP 3,676,166 "Plasticized Sulfur Compositions". Also United States Patent
U.S. Patent 3,422,615 discloses a synthetic turf-like material which i5 referred to as a pile fabric. Fibers which are indicated as being suitable for making the yarns used to make the pile fabric of USP 3,422,615 are said to include olefins, particularly polypropylene, nylon, vinyl, vinylidene chloride, polyvinyl chloride, polyethylene, polyester, polyacrylonitrile, acetate, triacetate, rayon (cellulosics), and glass.
U.S. Patent 3,332,828 relates to artificial turf preferably produced by weaving synthetic fibers on a Wilton cut-pile loom to form a structure consisting of a woven backing having a cut-pile face extending from one surface thereof and then applying a suitable latex formation on the other surface of the backing to render the complete ~tructure dimensionally stable.
U.S. Patent 3,157,557 discloses an integrally molded plastic sod simulating natural grass and comprising a flat flexible base of a thick plastic material having a multiplicity of closely-spaced blade-like plastic stems molded integral with the base.
U.S. Patent 2,515,847 discloses a surfacing structure suitable for use as a putting green for golf. The surfacing structure includes a top layer of rug material having a nap.
:~ -- . .
, . . . .
~065Z40 The rug ~aterial is supported on center layers of sponge rubber-like material. The supported rug material is placed upon the earth.
United States Patent 2,061,750 relates to grass mats prepared by stitching grass simulated material to a base.
United States Patent 1,939,846 discloses distributing - : -, :
fibrous material evenly over the top of a sheet of rubber composi-tion and then vulcanizing the fibers to the sheet in a heat press.
Plasticized sulfur has been disclosed in various references, for example by J. I. Jin in "Chemistry of Plastic-ized Sulfur", Petroleum Division, A. C. S. Symposium, Vol. 19, No. 2, March 1974, pp. 234-241 and by C. Kinney Hancock in "Plasticized Sulfur Compositions for Traffic Marking", Industrial and Engineering Chemistry, Vol. 46, No. 11, November 1954, pp. 2431-2435. Exemplary patents disclosing plasticized sulfur include USP 3,316,115 "Marking Compositions"; USP 3,434,852 "Plasticized Sulfur Compositions"; USP 3,447,941, "Sprayable ; Sulfur Road Marking Compositions"; USP 3,459,717 "Sulfur Based Plastic Composition"; USP 3,560,451 "Plastic and Nonflammable Sulfur Composition"; USP 3,453,125 "Plasticized Sulfur Compositions";
; USP 3,674,525 "Plasticized Sulfur Compositions"; and USP 3,676,166 "Plasticized Sulfur Compositions". Also United States Patent
3,823,019, which has been offered for license by the United States Bureau of Mines, discloses plasticized sulfur compositions.
According to the present invention a manufacture is provided comprising a plurality of fibers partially embedded in a solidified plasticized sulfur matrix with one end of the fibers extending outward from the matrix to form a turf or carpet-like i~ surface.
:
_ 3 _ ~)65Z40 According to a preferred embodiment of the present invention the sulfur is plasticized with dicyclopentadiene, aliphatic polysulfide, aromatic polysulfide, or mixtures thereof.
The term "fiber" is used herein to include mono-filament strands as well as polyfilament strands (yarns and threads and yarns made by twisting a fibrillated thermoplastic tape). Preferably yarn is used to form the product of the present invention. The yarn can be produced by twisting filaments together by methods known in the carpet-producing art. In this regard, see, for example, U.S. Patent 3,422,615.
Materials which can be used as the monofilament strands or as the polyfilament strands, that is~ yarns, include synthetic plastic materials as well as animal-derived materials'such as wool. Preferably, synthetic materials are used, i.e., synthetic plastic materials capable of being formed into filaments and yarns, for example by extruding into a pellicle and then cut or shredded into filaments which can in turn be converted to yarns. Polypropylene is a particularly preferred synthetic "20 plastic material for forming fibers for use herein, and a particularly preferred polypropylene yarn is made by twisting fibrillated polypropylene tapes. Other materials which can be used include other polyolefins, polyethylene terephthalate, polyacrylonitrile, viscose rayon, cellulose acetate, nylon, polyvinyl chloride, and fibrous glass.
In addition to U.S. Patent 3,422,615, U.S. Patents 3,177,557, 3,242,035 and 3,332,828 disclose materials which can be used to produce monofilament strands as well as poly-filament strands (yarns) for making artificial turf.
Among other factors the present invention is based on my finding of the surprisingly advantageous adherence of - ~ - .
1()65Z40 solidified plasticized sulfur to fibers, especially fibcrs such as polypropylene, and especially polypropylene in the form of pieces of yarn. ~lso the combination product of the present invention has been found to poss~ss particularly attractive durability and serviceability characteristics so that it can advantageously be used in surfaces subjected to abusive foot traffic.
Plasticized sulfur as the term is used herein usually has a lower melting point and a higher viscosity than elemental sulfur. Furthermore, plasticized sulfur requires a longer time to crys~allize; i.e., the rate of crystallization of plasticized sulfur is slower than that - of elemental sulfur. One useful way to measure the rate of crystallization is as follows: the test material (0.040 g) is melted on a microscope slide at 130C. and is then covered with a square microscope slide cover slip. The slide is transferred to a hot-plate and is kept at a temperature of 78+2C., as measured on the glass slide using a surface pyrometer. One corner of the melt is seeded with a crystal of test material. The time required ~or complete crystal-lization is measured. Plasticized sulfur, then, ic sulfur containing an additive which increases the crystallization time within experimental error, i.e., the average crystalli-zation time of the plasticized sulfur is greater than the average crystallization time of the elemental sulfur feedstock.
For the present application, plasticizers are those substances which, when added to molten, elemental sulfur, cause an increase in crystallization time in reference to the elemental sulfur itself. ~n one set of experiments, elemental sulfur required 0.44 minute to crystallize under the above conditions, whereas sulfur containing 3.8% of a phenol-sulfur adduct (as described - . .
~65Z40 in United States Patent 3,892,686) required 2.9 minutes. Sulfur containing 6.6% and 9.9% of the same phenol-sulfur adduct required 5.7 and 22 minutes, respectively.
Inorganic plasticizers include iron, arsenic and phosphorus sulfides, but the particularly preferred plasticizers are organic compounds which can react with sulfur to give sulfur-containing materials, such as styrene, alphamethylstyrene, dicyclopentadiene, vinyl cyclohexene, the aromatic compound-sulfur adducts of United States Patent 3,892,686 as well as the aromatic compounds used to produce these adducts, aromatic or ali-phatic liquid polysulfides (e.g., those sold under the trade mark of ThiokolLP-3 or LP-32), and the viscosity control agents described in United States ~- Patents 3,674,525, 3,453,125 and 3,676,166. The preferred aromatic plastic-izing compounds are styrene and the phenol-sulfur adduct of the aforesaid United States Patent 3,892,686. The preferred aliphatic compound is dicyclopentadiene.
One preferred plasticized sulfur substance contains dicyclo-pentadiene, sulfur, glass fiber and talc.
The elemental sulfur may be either crystalline or amorphous and may contain small amounts of impurities such as those normally found in commercial grades of sulfur. Optimum proportions of sulfur, as well as of the other components of the composition may vary considerably. However, proportions of sulfur of about 73 to 97%, by weight, are generally satisfact-ory~
; Dicyclopentadiene is readily available commercially, gener-ally at a purity of about 96% or greater. Preferably it is used in the above preferred plasticized sulfur composition in an amount of about 1 to 7% by ;~
weight.
The glass fiber of the preferred plasticized sulfur compo-. . .
sition is preferably employed in the form of milled fibers, with the fibers generally ranging from about 1/32 to 1/4" in `~4 .
: ' ' . : ' . ' :
1~5Z40 length, preferably with an average length of about l/16".
These fibers, which generally consist of high-silica glass, are readily available co~nercially, often coated with a starch binder. The type of glass is, however, not critical, as long as it provides the resulting composition with adequate shear strength, preferably a shear strength of about 400 to 800 psi.
The glass fiber preferably constitutes about l to 5% by weight of the composition of the invention.
The talc used in the preferred dicyclopentadiene-lQ sulfur-glass fiber-talc composition prefera~ly is a foliated type, or a compact variety such as steatite. Impure varieties such as soapstone can also be used. This ingredient is preferably used in an amount of about l to 15~ by weight of the composition, and serves the dual function of providing thixotropy to the mixture and of dispersing the glass fiber throughout the composition, thereby preventing agglomeration of the fibers.
The preferred composition is used as a fluid mixture of the ingredients, with the sulfur and dicyclopentadiene in molten form and the glass fiber and talc distributed throughout the molten material. Thus the composition is prepared by homogeneous mixing of the ingredients at elevated temperature sufficient to maintain the sulfur and dicyclopentadiene in a molten state. A temperature of about 240 to 320~. is satisfactory, with about 275 to 320F. being preferred. Any conventional vessel or reactor capable of providing the required temperature and mixing means may be used for preparation of the composition.
DRAWING
The drawing is a schematic illustration of an embodiment of the present invention. As shown in the drawing the plasticized sulfur rests on the soil or floor, and yarns or 1~65Z40 fibers are embedded into the plasticized sulfur. The thickness of the plasticized sulfur can vary but typically is between abou~ 1/4" to 3", more usually between about 1/2" and 2" thick. One advantage in preparing the product of the present invention is that it can be prepared for outdoor applications on the site as well as being capable of being prepared in modules or sections in a plant. Usually the product is prepared by im-mersing or embedding fibers in the molten plasticized sulfur and then - removing a backing or o~her means which might be used to hold the fibers or yarn elements in place when they are embedded in the molten plasticized sulfur and during the solidification of the plasticized sulfur. Means for implanting fibers into molten plasticized sulfur are also discussed in my joint inventorship and commonly assigned United States Patent 3,944,452.
EXAMPLES
Example 1 -- Plasticized Sulfur Mastic as a Carpet Base A plasticized sulfur mastic was prepared by heating a mixture of 3 parts of dicyclopentadiene and 100 parts of molten sulfur until there was a noticeable increase in viscosity. Next, 10 parts of talc and 3 parts of glass fiber (milled to 1/8" lengths) were added and the .;.
whole mixture was stirred until it was homogenous. This material was then ; 20 poured onto a flat 12" x 18" area of ground covered with small-sized gravel to a depth of 3/8". Before the sulfur mastic hardened, a sheared or cut-pile indoor-outdoor carpet, made by tufting polypropylene yarn into a polypropylene primary backing and without any latex or other secondary backing, was laid on the mastic. When the mastic had hardened, a corner of the backing -: ~
.
1~65Z40 was pried loose, and then the entire backing was pulled upward, through the cut piles, leaving the tufts securely anchored in the smooth, hard mastic surface. The finished installation had the appearance of a grassy lawn.
One unexpected beneficial advantage of thc product was the excellent adherence and retention of the polypropylene fibers or yarn by the plasticized sulfur.
~xample 2--Non-Plasticized Sulfur ~lastic as a Carpet Base (a) A small (4" x 4") piece of polypropylene tufted o indoor-outdoor carpet was immersed upside down (about 1/4") into a molten sulfur-glass fiber mixture 1/2" deep. When the sulfur had hardened, the carpet backing was cut off, leaving a grass-like structure held in place by the solidified sulfur-glass fiber mixture.
(b) The same experiment was repeated except that the glass fibers were replaced by sand. The results were the same.
The above experiment indicates that sulfur, with or without an added material such as talc or sand or glass fiber, can be used in the present invention instead of plasticized . 2d sulfur. However, my other experimental work indicates that plasticized sulfur performs better in the present invention.
' .
, .
According to the present invention a manufacture is provided comprising a plurality of fibers partially embedded in a solidified plasticized sulfur matrix with one end of the fibers extending outward from the matrix to form a turf or carpet-like i~ surface.
:
_ 3 _ ~)65Z40 According to a preferred embodiment of the present invention the sulfur is plasticized with dicyclopentadiene, aliphatic polysulfide, aromatic polysulfide, or mixtures thereof.
The term "fiber" is used herein to include mono-filament strands as well as polyfilament strands (yarns and threads and yarns made by twisting a fibrillated thermoplastic tape). Preferably yarn is used to form the product of the present invention. The yarn can be produced by twisting filaments together by methods known in the carpet-producing art. In this regard, see, for example, U.S. Patent 3,422,615.
Materials which can be used as the monofilament strands or as the polyfilament strands, that is~ yarns, include synthetic plastic materials as well as animal-derived materials'such as wool. Preferably, synthetic materials are used, i.e., synthetic plastic materials capable of being formed into filaments and yarns, for example by extruding into a pellicle and then cut or shredded into filaments which can in turn be converted to yarns. Polypropylene is a particularly preferred synthetic "20 plastic material for forming fibers for use herein, and a particularly preferred polypropylene yarn is made by twisting fibrillated polypropylene tapes. Other materials which can be used include other polyolefins, polyethylene terephthalate, polyacrylonitrile, viscose rayon, cellulose acetate, nylon, polyvinyl chloride, and fibrous glass.
In addition to U.S. Patent 3,422,615, U.S. Patents 3,177,557, 3,242,035 and 3,332,828 disclose materials which can be used to produce monofilament strands as well as poly-filament strands (yarns) for making artificial turf.
Among other factors the present invention is based on my finding of the surprisingly advantageous adherence of - ~ - .
1()65Z40 solidified plasticized sulfur to fibers, especially fibcrs such as polypropylene, and especially polypropylene in the form of pieces of yarn. ~lso the combination product of the present invention has been found to poss~ss particularly attractive durability and serviceability characteristics so that it can advantageously be used in surfaces subjected to abusive foot traffic.
Plasticized sulfur as the term is used herein usually has a lower melting point and a higher viscosity than elemental sulfur. Furthermore, plasticized sulfur requires a longer time to crys~allize; i.e., the rate of crystallization of plasticized sulfur is slower than that - of elemental sulfur. One useful way to measure the rate of crystallization is as follows: the test material (0.040 g) is melted on a microscope slide at 130C. and is then covered with a square microscope slide cover slip. The slide is transferred to a hot-plate and is kept at a temperature of 78+2C., as measured on the glass slide using a surface pyrometer. One corner of the melt is seeded with a crystal of test material. The time required ~or complete crystal-lization is measured. Plasticized sulfur, then, ic sulfur containing an additive which increases the crystallization time within experimental error, i.e., the average crystalli-zation time of the plasticized sulfur is greater than the average crystallization time of the elemental sulfur feedstock.
For the present application, plasticizers are those substances which, when added to molten, elemental sulfur, cause an increase in crystallization time in reference to the elemental sulfur itself. ~n one set of experiments, elemental sulfur required 0.44 minute to crystallize under the above conditions, whereas sulfur containing 3.8% of a phenol-sulfur adduct (as described - . .
~65Z40 in United States Patent 3,892,686) required 2.9 minutes. Sulfur containing 6.6% and 9.9% of the same phenol-sulfur adduct required 5.7 and 22 minutes, respectively.
Inorganic plasticizers include iron, arsenic and phosphorus sulfides, but the particularly preferred plasticizers are organic compounds which can react with sulfur to give sulfur-containing materials, such as styrene, alphamethylstyrene, dicyclopentadiene, vinyl cyclohexene, the aromatic compound-sulfur adducts of United States Patent 3,892,686 as well as the aromatic compounds used to produce these adducts, aromatic or ali-phatic liquid polysulfides (e.g., those sold under the trade mark of ThiokolLP-3 or LP-32), and the viscosity control agents described in United States ~- Patents 3,674,525, 3,453,125 and 3,676,166. The preferred aromatic plastic-izing compounds are styrene and the phenol-sulfur adduct of the aforesaid United States Patent 3,892,686. The preferred aliphatic compound is dicyclopentadiene.
One preferred plasticized sulfur substance contains dicyclo-pentadiene, sulfur, glass fiber and talc.
The elemental sulfur may be either crystalline or amorphous and may contain small amounts of impurities such as those normally found in commercial grades of sulfur. Optimum proportions of sulfur, as well as of the other components of the composition may vary considerably. However, proportions of sulfur of about 73 to 97%, by weight, are generally satisfact-ory~
; Dicyclopentadiene is readily available commercially, gener-ally at a purity of about 96% or greater. Preferably it is used in the above preferred plasticized sulfur composition in an amount of about 1 to 7% by ;~
weight.
The glass fiber of the preferred plasticized sulfur compo-. . .
sition is preferably employed in the form of milled fibers, with the fibers generally ranging from about 1/32 to 1/4" in `~4 .
: ' ' . : ' . ' :
1~5Z40 length, preferably with an average length of about l/16".
These fibers, which generally consist of high-silica glass, are readily available co~nercially, often coated with a starch binder. The type of glass is, however, not critical, as long as it provides the resulting composition with adequate shear strength, preferably a shear strength of about 400 to 800 psi.
The glass fiber preferably constitutes about l to 5% by weight of the composition of the invention.
The talc used in the preferred dicyclopentadiene-lQ sulfur-glass fiber-talc composition prefera~ly is a foliated type, or a compact variety such as steatite. Impure varieties such as soapstone can also be used. This ingredient is preferably used in an amount of about l to 15~ by weight of the composition, and serves the dual function of providing thixotropy to the mixture and of dispersing the glass fiber throughout the composition, thereby preventing agglomeration of the fibers.
The preferred composition is used as a fluid mixture of the ingredients, with the sulfur and dicyclopentadiene in molten form and the glass fiber and talc distributed throughout the molten material. Thus the composition is prepared by homogeneous mixing of the ingredients at elevated temperature sufficient to maintain the sulfur and dicyclopentadiene in a molten state. A temperature of about 240 to 320~. is satisfactory, with about 275 to 320F. being preferred. Any conventional vessel or reactor capable of providing the required temperature and mixing means may be used for preparation of the composition.
DRAWING
The drawing is a schematic illustration of an embodiment of the present invention. As shown in the drawing the plasticized sulfur rests on the soil or floor, and yarns or 1~65Z40 fibers are embedded into the plasticized sulfur. The thickness of the plasticized sulfur can vary but typically is between abou~ 1/4" to 3", more usually between about 1/2" and 2" thick. One advantage in preparing the product of the present invention is that it can be prepared for outdoor applications on the site as well as being capable of being prepared in modules or sections in a plant. Usually the product is prepared by im-mersing or embedding fibers in the molten plasticized sulfur and then - removing a backing or o~her means which might be used to hold the fibers or yarn elements in place when they are embedded in the molten plasticized sulfur and during the solidification of the plasticized sulfur. Means for implanting fibers into molten plasticized sulfur are also discussed in my joint inventorship and commonly assigned United States Patent 3,944,452.
EXAMPLES
Example 1 -- Plasticized Sulfur Mastic as a Carpet Base A plasticized sulfur mastic was prepared by heating a mixture of 3 parts of dicyclopentadiene and 100 parts of molten sulfur until there was a noticeable increase in viscosity. Next, 10 parts of talc and 3 parts of glass fiber (milled to 1/8" lengths) were added and the .;.
whole mixture was stirred until it was homogenous. This material was then ; 20 poured onto a flat 12" x 18" area of ground covered with small-sized gravel to a depth of 3/8". Before the sulfur mastic hardened, a sheared or cut-pile indoor-outdoor carpet, made by tufting polypropylene yarn into a polypropylene primary backing and without any latex or other secondary backing, was laid on the mastic. When the mastic had hardened, a corner of the backing -: ~
.
1~65Z40 was pried loose, and then the entire backing was pulled upward, through the cut piles, leaving the tufts securely anchored in the smooth, hard mastic surface. The finished installation had the appearance of a grassy lawn.
One unexpected beneficial advantage of thc product was the excellent adherence and retention of the polypropylene fibers or yarn by the plasticized sulfur.
~xample 2--Non-Plasticized Sulfur ~lastic as a Carpet Base (a) A small (4" x 4") piece of polypropylene tufted o indoor-outdoor carpet was immersed upside down (about 1/4") into a molten sulfur-glass fiber mixture 1/2" deep. When the sulfur had hardened, the carpet backing was cut off, leaving a grass-like structure held in place by the solidified sulfur-glass fiber mixture.
(b) The same experiment was repeated except that the glass fibers were replaced by sand. The results were the same.
The above experiment indicates that sulfur, with or without an added material such as talc or sand or glass fiber, can be used in the present invention instead of plasticized . 2d sulfur. However, my other experimental work indicates that plasticized sulfur performs better in the present invention.
' .
, .
Claims (5)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. An article of manufacture comprising a plurality of fibers partially embedded in a solidified plasticized sulfur matrix with one end of the fibers extending outward from the matrix to form a turf or carpet-like surface.
2. An article of manufacture in accordance with claim 1 wherein the sulfur is plasticized with dicyclopentadiene, aliphatic polysulfide, aromatic polysulfides, or mixtures thereof.
3. An article of manufacture in accordance with claim 1 wherein the fibers are wool, cotton, nylon, polypropylene, polyethylene, polyurethane, or mixtures thereof.
4. An article of manufacture in accordance with claim 1 wherein the fibers are polypropylene.
5. An article of manufacture in accordance with claim 1 wherein the plasticized sulfur comprises, by weight, about 73 to 97%
sulfur, about 1 to 7% dicyclopentadiene, about 1 to 5% glass fiber, and about 1 to 15% talc.
sulfur, about 1 to 7% dicyclopentadiene, about 1 to 5% glass fiber, and about 1 to 15% talc.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47445774A | 1974-05-29 | 1974-05-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1065240A true CA1065240A (en) | 1979-10-30 |
Family
ID=23883606
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA227,949A Expired CA1065240A (en) | 1974-05-29 | 1975-05-28 | Artificial fibers preparation |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS512227A (en) |
| CA (1) | CA1065240A (en) |
| DE (1) | DE2523177C2 (en) |
| ES (1) | ES438000A1 (en) |
| FR (1) | FR2272836B1 (en) |
| GB (1) | GB1521981A (en) |
| IT (1) | IT1038477B (en) |
| MX (1) | MX3491E (en) |
| NL (1) | NL161210C (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0437923Y2 (en) * | 1989-09-22 | 1992-09-07 | ||
| GB2390807A (en) * | 2002-07-17 | 2004-01-21 | Bonar Floors Ltd | Surface covering |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2100122A1 (en) * | 1971-01-04 | 1972-07-27 | Möckel, Siegfried, 7912 Weißenhorn | Economical floor covering - in the form of an artificial lawn |
| US3892686A (en) * | 1972-05-15 | 1975-07-01 | Chevron Res | Cellular products produced by foaming and cross-linking aromatic polysulfides |
-
1975
- 1975-05-16 MX MX77675U patent/MX3491E/en unknown
- 1975-05-21 FR FR7515875A patent/FR2272836B1/fr not_active Expired
- 1975-05-23 GB GB2274675A patent/GB1521981A/en not_active Expired
- 1975-05-26 NL NL7506174A patent/NL161210C/en not_active IP Right Cessation
- 1975-05-26 DE DE19752523177 patent/DE2523177C2/en not_active Expired
- 1975-05-28 ES ES438000A patent/ES438000A1/en not_active Expired
- 1975-05-28 JP JP6397275A patent/JPS512227A/en active Pending
- 1975-05-28 IT IT2382175A patent/IT1038477B/en active
- 1975-05-28 CA CA227,949A patent/CA1065240A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2272836B1 (en) | 1979-06-08 |
| JPS512227A (en) | 1976-01-09 |
| NL161210B (en) | 1979-08-15 |
| AU8143575A (en) | 1976-11-25 |
| NL7506174A (en) | 1975-12-02 |
| FR2272836A1 (en) | 1975-12-26 |
| NL161210C (en) | 1980-01-15 |
| MX3491E (en) | 1980-12-16 |
| DE2523177C2 (en) | 1983-04-28 |
| GB1521981A (en) | 1978-08-23 |
| IT1038477B (en) | 1979-11-20 |
| ES438000A1 (en) | 1977-01-16 |
| DE2523177A1 (en) | 1975-12-11 |
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