US2860382A - Textile fiber unit - Google Patents

Textile fiber unit Download PDF

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US2860382A
US2860382A US353307A US35330753A US2860382A US 2860382 A US2860382 A US 2860382A US 353307 A US353307 A US 353307A US 35330753 A US35330753 A US 35330753A US 2860382 A US2860382 A US 2860382A
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resin
plasticizer
ester
weight
parts
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US353307A
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Richard A Garrett
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Armstrong World Industries Inc
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Armstrong Cork Co
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Priority to GB6771/55A priority patent/GB741860A/en
Priority to GB16853/53A priority patent/GB733897A/en
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/244Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01HSPINNING OR TWISTING
    • D01H5/00Drafting machines or arrangements ; Threading of roving into drafting machine
    • D01H5/18Drafting machines or arrangements without fallers or like pinned bars
    • D01H5/70Constructional features of drafting elements
    • D01H5/74Rollers or roller bearings
    • D01H5/80Rollers or roller bearings with covers; Cots or covers
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01HSPINNING OR TWISTING
    • D01H5/00Drafting machines or arrangements ; Threading of roving into drafting machine
    • D01H5/18Drafting machines or arrangements without fallers or like pinned bars
    • D01H5/70Constructional features of drafting elements
    • D01H5/86Aprons; Apron supports; Apron tensioning arrangements
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/244Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
    • D06M13/282Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
    • D06M13/288Phosphonic or phosphonous acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01HSPINNING OR TWISTING
    • D01H2700/00Spinning or twisting machines; Drafting devices
    • D01H2700/245Conception or fabrication of drafting cylinders

Definitions

  • This invention relates to textile fiber working units such as pencil roll covers, long draft aprons, comber detaching rolls, and the like.
  • Pencil roll covers are used in the textile fiber working industry in SacoLowell and similar type machines and serve the purpose ofcon.- trolling fiber draft. In such operation the roll, covers frictionally engage the fibers and; static electricity on the roll surface causes the fibers to be disrupted, resulting in the creation of waste which floats about the mill and collects on the machines, creating a substantial nuisance and' often resulting, in the production of defective' yarn.
  • the textile fibers lie in engagement. with the working.
  • apron or aprons must have a static-free working surface in order to form-high quality yarn.
  • the working surface In aprons, the working surface must be yielding andv resilient, and. the apron structure should be free of any tendency toward excessive growth or stretchingv during operation. It should also be resistant to attack by thev oils enr countered in use. Comber detaching rolls serve to disengage the fibers from the combers, and the presence, of static electricity on the rolls would cause the fine webof fibers to be disrupted and an uneven web to. be formed. Similar problems are encountered in other textile fiber working units such as twister rolls, selfweighted Washburn rolls, and the like.
  • plasticizer for the resin which is compatible with the resin in such proportions at temperatures above 45 F. and renders the composition static-free
  • said plasticizer being selected from the group consisting of: (a) an ester, the acid component of which is selected, from the group consisting of at least one aliphatic acid, phosphoric acid, andphosphonic acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular Weight of said ester, (b) Z-ethylhexyl diester amide, (0) fatty acid nitrile of C -C fatty acids, C4H9OC2H4OC2H4O C2H4OC4H9, and e) mixtures of two or more of the above plasticizers,
  • Such unit may be secured to a roll structure as; in the case, of, the pencil or slip roll covers or may. be formed into a tubular product and severedinto productsz, such. as; aprons or the like.
  • a. reinforcing cord may be provided within the body ofthe unit in, the manner, described in Billmeyer. Patent. 2,470,599; granted May 17, 1949. It hasbeen found, however, that; for some services. the use: of a, reinforcing: COIidf is not. necessary.
  • Figure l is a top plan view of apencil or-sli'p roll.hav-- ing applied thereto a. cover made in accordance with the; present invention
  • Figure 2 is asectional view taken along line II"-II of Figure 1';
  • Figure 3 is an end view of a longdraft apron made in accordance with, the. present, invention. mounted; in. a. typical Casablanca type framewhich has. been diagram! matically shown;
  • Figure 4" is. a perspective view of a, section. of tubing. made in. accordance with the present invention and. adapt: ed for severance into aprons; and,
  • Figure 5 is. a perspective view. showing a pencil or slip. roll cover suitable for mounting upon: the roll structure of Figure 1.
  • the roll body 2 is of conventional shape or configuration and. may beformed of metal. It has a cover 3v mounted thereon made in accordance with; the present. invention, said cover having a workin surface 4,
  • apron 5 is shown as. encircling a;dr i,v .-v ing roll. and. a. front. bar 7.
  • the apron, 5, is shown; as; made from a. tubular body 8 in accordance with, the present invention, andv the apron. has a,- working surface 9 Inthis embodiment.
  • the apron is. not reinforcedg; but; as previously mentioned, a reinforcing cord may b e;pr,o videdl as taught by Billmeyer.
  • FIG 41 a section of tubular stock 10 is shown; which may be severed into. appropriate pieces for as aprons.
  • Figure 5 shows a pencil rollcover 11 Which-isforrneQ without a reinforcement of. any sort, and may be; ad hesively secured to a metal pencil roll. to form a struc ture such asv that, shown in Figures. 1. and 2. i
  • Pencil roll cover composition Parts by weight
  • the resin will be selected from, the group consisting of polyvinyl chloride, the poly merization product of a mixture of vinyl chloride and vinyl' acetate containing about vinyl chloride and about 5% vinyl acetate, and mixtures thereof.
  • the polyvinyl chloride resin may be one sold under the trade designation Koroseal.
  • the polymerization product of the mixture vinyl chloride and vinyl acetate may be the resin sold under the trade designation VYNW, and the mixture may be any proportions of the resins. sold under the trade designations given above.
  • the plasticizer may be any one of the plasticizers for the resin listed below.
  • the first three plasticizers are preferred. Of course, mixtures of the various plasticizers may be used.
  • Fatty acid nitrile of Ca-Czo fatty acids Polyethylene glycol di-Z-ethylhexoate.
  • Plasticizers l-10, 12, 14-16, and 18-21 are in class (a) mentioned previously, i. e., an ester, the acid component of which is selected from the group consisting of at least one aliphatic acid, phosphoric acid, and phosphonic acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular weight of said ester; plasticizer 11 is in class (b), Z-ethylhexyl di-ester amide; plasticizer 13 is in class (c), fatty acid nitrile of C C fatty acids; and plasticizer 17 is in class (d),
  • Plasticizers 1, 2, 4, 8, 14, l5, l6, and 18 are esters of an aliphatic acid and an aliphatic alcohol in which the aliphatic acid component of the ester has 2 to 18 carbon atoms and in which the aliphatic alcohol component of the ester has from 1 to 8 carbon atoms.
  • Plasticizers 6 and 7 are linear polymerized esters of glycol and polycarboxylic acid. Any other plasticizer or mixture of plasticizers selected from classes (a) to (d) mentioned previously and which are compatible in proportions of about 50 to 150 parts for each 100 parts of resin (all parts by weight) at temperatures above F.
  • plasticizer or plasticizers selected will de pend upon the particular type of fiber working unit being prepared, the service conditions which it will encounter, and other variable factors.
  • the quantity of plasticizer used will likewise depend upon such variable factors. For pencil roll covers the amount of plasticizer used will generally be determined by the hardness desired in the finished product and the static resistance of the working surface.
  • parts of plasticizer to 100 parts of resin will be adequate to secure static resistance in all instances except with linear polyester type plasticizer, No. 6, Where about 85 parts by weight of plasticizer to 100 parts of resin are required to provide a static-free working surface. Where this quantity of plasticizer tends to produce a product which is too resilient and yielding for specific uses, one of the other plasticizers such as plasticizer No. 1 listed above will be chosen. Wide latitude is possible in the selection of plasticizers.
  • a preferred filler is the one sold under the trademark Silene EF which is a precipitated calcium silicate.
  • Silene EF other fillers may be substituted, such as clay, whiting, and carbon black. Titanium dioxide and carbon black, such as Gastex," are used principally as color pigments, and in lieu thereof other pigments may be employed.
  • the white lead serves as a heat stabilizer, and in place of it materials such as lead stearate, basic lead silicate, and the like may be substituted.
  • fillers, pigments, and stabilizers used may be varied and are not critical. These compounding ingredients are well known, and those skilled in the art will have no difficulty in compounding with various fillers, pigments, and stabilizers, as required.
  • the various ingredients are mixed in a suitable container or internal mixer.
  • the blended ingredients are then fused on a heated two-roll mill, the temperature of which is in the order of 275 F. to 300 F.
  • the fused compound is then extruded into tubular sections of the desired length.
  • the extruded tubes are then permitted to cool and are subsequently cut into covers, aprons, or the like of the desired dimensions.
  • cover may be mounted upon metal rolls, as shown in Figures 1 and 2 of the drawing, and the outer surface of the cover is ground to the desired diameter and surface smoothness.
  • a composition suitable for fabrication into aprons may be prepared as follows:
  • plasticizer for example, the quantity of plasticizer will be about parts by weight for each parts by weight of resin. Other plasticizers may be used in larger or smaller quantities within the range recited.
  • the mixing, fusing, and extruding steps will be the same as those mentioned above in connection with the pencil roll cover composition.
  • the extruded tube will be as close as possible in dimensions to those required in the finished apron.
  • the tube may then be mounted upon a mandrel having an outer diameter corresponding to the inner diameter of the apron being fabricated, and the assembly may then be heated in an oven at 250 F. for about one hour which will tend to anneal the composition. Thereafter, the tube will be severed into aprons of the desired dimensions; and if found necessary or desirable, the outer surface may be buffed or ground to provide a working sur-' face having the requisite texture.
  • compositions of this invention may be formed from the compositions of this invention; and while the compounding may vary to some extent with the various units, they will in all events include a working surface formed of a composition of a resin selected from the group consisting of polyvinyl chloride, the polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95 vinyl chloride and about 5% vinyl acetate, and mixtures thereof; and they will have incorporated therewith a plasticizer for the resin which renders the composition static-free and which is selected from the classes (a), (b), (c), and (d) above or mixtures of two or more thereof.
  • a plasticizer for the resin which renders the composition static-free and which is selected from the classes (a), (b), (c), and (d) above or mixtures of two or more thereof.
  • fillers, pigments, and stabilizing agents and the like may be incorporated.
  • the proportioning of resin and plasticizer may vary but will fall within the range of 50 to 150 parts by weight of plasticizer for each 100 parts by weight of resin; and the plasticizer will, of course, be compatible with the resin in such proportions at all temperatures above 45 F. encountered in the use of the product.
  • a textile fiber working unit having a static-free Working surface formed of a composition of a resin selected from the group consisting of vinyl chloride, the polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95% vinyl chloride and about 5% vinyl acetate, and mixtures thereof, having incorporated therewith between about 50 parts by weight and about 150 parts by weight for each 100 parts by weight of resin of a plasticizer for the resin which is compatible with the resin in such proportions at temperatures above 45 F.
  • a resin selected from the group consisting of vinyl chloride, the polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95% vinyl chloride and about 5% vinyl acetate, and mixtures thereof, having incorporated therewith between about 50 parts by weight and about 150 parts by weight for each 100 parts by weight of resin of a plasticizer for the resin which is compatible with the resin in such proportions at temperatures above 45 F.
  • said plasticizer being selected from the group consisting of: (a) an ester, the acid component of which is selected from the group consisting of at least one aliphatic acid, phosphoric acid, and phosphonic acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular Weight of said ester, (b) 2-ethylhexyl di ester amide, (0) fatty acid nitrile of C -C fatty acids, (d)
  • a textile fiber working unit in accordance with claim 1 in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about vinyl chloride and about 5% vinyl acetate.
  • a textile fiber working unit in accordance with claim 2 in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95 vinyl chloride and about 5% vinyl acetate and in which the plasticizer consists principally of triethylene glycol ester of C -C fatty acids.
  • a textile fiber Working unit in accordance with claim 1 in which the unit consists of a slip roll cover and in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95 vinyl chloride and about 5% vinyl aectate and in which the resin has incorporated therewith about 50 parts by weight of said plasticizer for each parts by weight of resin.
  • a textile fiber working unit in accordance with claim 1 in which the unit consists of a draft apron in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95% vinyl chloride and about 5% vinyl acetate.
  • a textile fiber working unit in accordance with claim 1 in which the unit consists of a draft apron in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95% vinyl chloride and about 5% vinyl acetate and in which said plasticizer for the resin is resistant to oil extraction.
  • a textile fiber working unit in accordance with claim 2 in which the aliphatic acid component of the ester has 2 to 18 carbon atoms and in which the aliphatic alcohol component of the ester has from 1 to 8 carbon atoms.

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
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  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

Nov. 18, 1958 R. A- GARRETT TEXTILE FIBER UNIT Filed May e. 1953 T W W W. A S R A H m R attouw United States Patent TEXTILE FIBER UNIT Richard A. Garrett, Manor Township, Lancaster County, Pa., assignor to Armstrong Cork Company, Lancaster, Pa., a corporation of Pennsylvania Application May 6, 1953, Serial No. 353,307
16 Claims. (Cl. 19-143) This invention relates to textile fiber working units such as pencil roll covers, long draft aprons, comber detaching rolls, and the like. Pencil roll covers are used in the textile fiber working industry in SacoLowell and similar type machines and serve the purpose ofcon.- trolling fiber draft. In such operation the roll, covers frictionally engage the fibers and; static electricity on the roll surface causes the fibers to be disrupted, resulting in the creation of waste which floats about the mill and collects on the machines, creating a substantial nuisance and' often resulting, in the production of defective' yarn. In. long draft aprons, the textile fibers lie in engagement. with the working. surface af the apron or aprons, and these, too, must have a static-free working surface in order to form-high quality yarn. In aprons, the working surface must be yielding andv resilient, and. the apron structure should be free of any tendency toward excessive growth or stretchingv during operation. It should also be resistant to attack by thev oils enr countered in use. Comber detaching rolls serve to disengage the fibers from the combers, and the presence, of static electricity on the rolls would cause the fine webof fibers to be disrupted and an uneven web to. be formed. Similar problems are encountered in other textile fiber working units such as twister rolls, selfweighted Washburn rolls, and the like.
It is an object of this. invention toprovide a textile composition of a resin selected from the group consist-- ing of polyvinyl chloride, the polymerization product of a mixture of vinyl chloride and vinyl acetate containing; about 95% vinyl chloride and about vinyl acetate,
and mixtures thereof, each 100 parts by weight of the resin having incorporated therewith between about 50;
parts by weight and 150 parts by weight of plasticizer for the resin which is compatible with the resin in such proportions at temperatures above 45 F. and renders the composition static-free, said plasticizer being selected from the group consisting of: (a) an ester, the acid component of which is selected, from the group consisting of at least one aliphatic acid, phosphoric acid, andphosphonic acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular Weight of said ester, (b) Z-ethylhexyl diester amide, (0) fatty acid nitrile of C -C fatty acids, C4H9OC2H4OC2H4O C2H4OC4H9, and e) mixtures of two or more of the above plasticizers,
Patented Nov. 18, 1958 and: (a): m xtur s o o: or re f th bove. plas ticizers. Such unit may be secured to a roll structure as; in the case, of, the pencil or slip roll covers or may. be formed into a tubular product and severedinto productsz, such. as; aprons or the like. If required, a. reinforcing cord may be provided within the body ofthe unit in, the manner, described in Billmeyer. Patent. 2,470,599; granted May 17, 1949. It hasbeen found, however, that; for some services. the use: of a, reinforcing: COIidf is not. necessary.
The attached drawing illustrates a number of'embodh ments of the, invention asfollows:
Figure l is a top plan view of apencil or-sli'p roll.hav-- ing applied thereto a. cover made in accordance with the; present invention;
Figure 2 is asectional view taken along line II"-II of Figure 1';
Figure 3 is an end view of a longdraft apron made in accordance with, the. present, invention. mounted; in. a. typical Casablanca type framewhich has. been diagram! matically shown;
Figure 4" is. a perspective view of a, section. of tubing. made in. accordance with the present invention and. adapt: ed for severance into aprons; and,
Figure 5 is. a perspective view. showing a pencil or slip. roll cover suitable for mounting upon: the roll structure of Figure 1.
In Figure 1, the roll body 2 is of conventional shape or configuration and. may beformed of metal. It has a cover 3v mounted thereon made in accordance with; the present. invention, said cover having a workin surface 4,,
In Eigure,3 an. apron 5 is shown as. encircling a;dr i,v .-v ing roll. and. a. front. bar 7. The apron, 5, is shown; as; made from a. tubular body 8 in accordance with, the present invention, andv the apron. has a,- working surface 9 Inthis embodiment. the apron is. not reinforcedg; but; as previously mentioned, a reinforcing cord may b e;pr,o videdl as taught by Billmeyer.
In Figure 41 a, section of tubular stock 10 is shown; which may be severed into. appropriate pieces for as aprons.
Figure 5 shows a pencil rollcover 11 Which-isforrneQ without a reinforcement of. any sort, and may be; ad hesively secured to a metal pencil roll. to form a struc ture such asv that, shown in Figures. 1. and 2. i
In the preparation, of the composition of the present; invention for use in the fabrication of a pencil roll; cover, the following example is given:
Pencil roll cover composition Parts by weight;
Resin 100- Plasticizer 5'01"50' White lead' 1.5- Filler 20' Titanium dioxide 15 Carbon black 03 In the above example the resin will be selected from, the group consisting of polyvinyl chloride, the poly merization product of a mixture of vinyl chloride and vinyl' acetate containing about vinyl chloride and about 5% vinyl acetate, and mixtures thereof. The polyvinyl chloride resin may be one sold under the trade designation Koroseal. The polymerization product of the mixture vinyl chloride and vinyl acetate may be the resin sold under the trade designation VYNW, and the mixture may be any proportions of the resins. sold under the trade designations given above.
The plasticizer may be any one of the plasticizers for the resin listed below. The first three plasticizers are preferred. Of course, mixtures of the various plasticizers may be used.
Plastlcizer Trade Name Chemical Composition Butyl benzl sebacate. Capryl benzyl sebacate. 2-ethylhexyl di ester amide. Tributyl phosphate.
Triglycol dihexoete.
High M. W. Polyethe High M. W. Polyether ester Dioctyl styryl phosphonate.
Dibutyl benzene phosphonate.
Dioctyl benzene phosphonate.
Fatty acid nitrile of Ca-Czo fatty acids. Polyethylene glycol di-Z-ethylhexoate.
' Di (2-ethylbutyl Cellosolve) succinate.
Plasticizers l-10, 12, 14-16, and 18-21 are in class (a) mentioned previously, i. e., an ester, the acid component of which is selected from the group consisting of at least one aliphatic acid, phosphoric acid, and phosphonic acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular weight of said ester; plasticizer 11 is in class (b), Z-ethylhexyl di-ester amide; plasticizer 13 is in class (c), fatty acid nitrile of C C fatty acids; and plasticizer 17 is in class (d),
Plasticizers 1, 2, 4, 8, 14, l5, l6, and 18 are esters of an aliphatic acid and an aliphatic alcohol in which the aliphatic acid component of the ester has 2 to 18 carbon atoms and in which the aliphatic alcohol component of the ester has from 1 to 8 carbon atoms. Plasticizers 6 and 7 are linear polymerized esters of glycol and polycarboxylic acid. Any other plasticizer or mixture of plasticizers selected from classes (a) to (d) mentioned previously and which are compatible in proportions of about 50 to 150 parts for each 100 parts of resin (all parts by weight) at temperatures above F. may be employed so long as the plasticizer does not deleteriously affect the resin or so alter its physical characteristics as to render the working surface of the article unsatisfactory. The plasticizer or plasticizers selected will de pend upon the particular type of fiber working unit being prepared, the service conditions which it will encounter, and other variable factors. The quantity of plasticizer used will likewise depend upon such variable factors. For pencil roll covers the amount of plasticizer used will generally be determined by the hardness desired in the finished product and the static resistance of the working surface. With the plasticizers listed above, parts of plasticizer to 100 parts of resin will be adequate to secure static resistance in all instances except with linear polyester type plasticizer, No. 6, Where about 85 parts by weight of plasticizer to 100 parts of resin are required to provide a static-free working surface. Where this quantity of plasticizer tends to produce a product which is too resilient and yielding for specific uses, one of the other plasticizers such as plasticizer No. 1 listed above will be chosen. Wide latitude is possible in the selection of plasticizers.
A preferred filler is the one sold under the trademark Silene EF which is a precipitated calcium silicate. In place of Silene EF other fillers may be substituted, such as clay, whiting, and carbon black. Titanium dioxide and carbon black, such as Gastex," are used principally as color pigments, and in lieu thereof other pigments may be employed. The white lead serves as a heat stabilizer, and in place of it materials such as lead stearate, basic lead silicate, and the like may be substituted.
The quantities of the fillers, pigments, and stabilizers used may be varied and are not critical. These compounding ingredients are well known, and those skilled in the art will have no difficulty in compounding with various fillers, pigments, and stabilizers, as required.
In the preparation of the composition, the various ingredients are mixed in a suitable container or internal mixer. The blended ingredients are then fused on a heated two-roll mill, the temperature of which is in the order of 275 F. to 300 F. The fused compound is then extruded into tubular sections of the desired length. The extruded tubes are then permitted to cool and are subsequently cut into covers, aprons, or the like of the desired dimensions. Where roll covers are being fabricated, the covering may be mounted upon metal rolls, as shown in Figures 1 and 2 of the drawing, and the outer surface of the cover is ground to the desired diameter and surface smoothness.
A composition suitable for fabrication into aprons may be prepared as follows:
Apron composition Parts by weight Resin 100 Plasticizer 50-150 White lead 1.5 Titanium dioxide 15 Carbon black 0.3
Nos. 6 or 7 are used, for example, the quantity of plasticizer will be about parts by weight for each parts by weight of resin. Other plasticizers may be used in larger or smaller quantities within the range recited.
In the fabrication of the apron the mixing, fusing, and extruding steps will be the same as those mentioned above in connection with the pencil roll cover composition. The extruded tube will be as close as possible in dimensions to those required in the finished apron. The tube may then be mounted upon a mandrel having an outer diameter corresponding to the inner diameter of the apron being fabricated, and the assembly may then be heated in an oven at 250 F. for about one hour which will tend to anneal the composition. Thereafter, the tube will be severed into aprons of the desired dimensions; and if found necessary or desirable, the outer surface may be buffed or ground to provide a working sur-' face having the requisite texture.
Other textile fiber working units may be formed from the compositions of this invention; and while the compounding may vary to some extent with the various units, they will in all events include a working surface formed of a composition of a resin selected from the group consisting of polyvinyl chloride, the polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95 vinyl chloride and about 5% vinyl acetate, and mixtures thereof; and they will have incorporated therewith a plasticizer for the resin which renders the composition static-free and which is selected from the classes (a), (b), (c), and (d) above or mixtures of two or more thereof. As mentioned above, fillers, pigments, and stabilizing agents and the like may be incorporated. The proportioning of resin and plasticizer may vary but will fall within the range of 50 to 150 parts by weight of plasticizer for each 100 parts by weight of resin; and the plasticizer will, of course, be compatible with the resin in such proportions at all temperatures above 45 F. encountered in the use of the product.
This application is a continuation-in-part of my copending application, Serial No. 148,719, filed March 9, 1950, now abandoned.
-I claim:
1. A textile fiber working unit having a static-free Working surface formed of a composition of a resin selected from the group consisting of vinyl chloride, the polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95% vinyl chloride and about 5% vinyl acetate, and mixtures thereof, having incorporated therewith between about 50 parts by weight and about 150 parts by weight for each 100 parts by weight of resin of a plasticizer for the resin which is compatible with the resin in such proportions at temperatures above 45 F. and which renders the composition static-free, said plasticizer being selected from the group consisting of: (a) an ester, the acid component of which is selected from the group consisting of at least one aliphatic acid, phosphoric acid, and phosphonic acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular Weight of said ester, (b) 2-ethylhexyl di ester amide, (0) fatty acid nitrile of C -C fatty acids, (d)
and (e) mixtures of two or more of the above plasticizers.
2. A textile fiber working unit in accordance with claim 1 in which the principal plasticizer for the resin is an ester of an aliphatic acid and an aliphatic alcohol.
3. A textile fiber working unit in accordance with claim 2 in which the plasticizer consists principally of triethylene glycol ester of C -C fatty acids.
4. A textile fiber working unit in accordance with claim 2 in which the plasticizer consists principally of polyester (linear).
5. A textile fiber working unit in accordance with claim 1 in which the principal plasticizer for the resin is an ester, the acid component of which is at least one aliphatic acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular weight of the ester.
6. A textile fiber Working unit in accordance with claim 1 in which the principal plasticizer for the resin is an ester of phosphoric acid, the molecular weight of the aliphatic portion of said ester representing more than 50% of the total molecular weight of said ester,
7. A textile fiber working unit in accordance with claim 6 in which the plasticizer consists principally of tributoxy ethyl phosphate.
8. A textile fiber Working unit in accordance with claim 1 in which the principal plasticizer for the resin is a phosphonate, the molecular weight of aliphatic portion of which represents more than 50% of the total molecular weight of said phosphonate.
9. A textile fiber working unit in accordance with claim 1 in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about vinyl chloride and about 5% vinyl acetate.
10. A textile fiber working unit in accordance with claim 1 in which the resin consists principally of polyvinyl chloride.
11. A textile fiber working unit in accordance with claim 2 in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95 vinyl chloride and about 5% vinyl acetate and in which the plasticizer consists principally of triethylene glycol ester of C -C fatty acids.
12. A textile fiber Working unit in accordance with claim 1 in which the unit consists of a slip roll cover and in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95 vinyl chloride and about 5% vinyl aectate and in which the resin has incorporated therewith about 50 parts by weight of said plasticizer for each parts by weight of resin.
13. A textile fiber working unit in accordance with claim 1 in which the unit consists of a draft apron in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95% vinyl chloride and about 5% vinyl acetate.
14. A textile fiber working unit in accordance with claim 1 in which the unit consists of a draft apron in which the resin consists principally of the resinous polymerization product of a mixture of vinyl chloride and vinyl acetate containing about 95% vinyl chloride and about 5% vinyl acetate and in which said plasticizer for the resin is resistant to oil extraction.
15. A textile fiber working unit in accordance with claim 2 in which the plasticizer consists principally of linear polymerized ester of glycol and polycarboxylic acid.
16. A textile fiber working unit in accordance with claim 2 in which the aliphatic acid component of the ester has 2 to 18 carbon atoms and in which the aliphatic alcohol component of the ester has from 1 to 8 carbon atoms.
References Cited in the file of this patent UNITED STATES PATENTS 1,935,577 -Reid Nov. 17, 1933 2,010,963 Robertson Aug. 13, 1935 2,278,424 Campbell Apr. 7, 1942 2,597,708 Cresswell May 20, 1952 FOREIGN PATENTS 486,911 Great Britain June 13, 1938

Claims (1)

1. A TEXTILE FIBER WORKING UNIT HAVING A STATIC-FREE WORKING SURFACE FORMED OF A COMPOSITION OF A RESIN SELECTED FROM THE GROUP CONSISTING OF VINYL CHLORIDE, THE POLYMERIZATION PRODUCT OF A MIXTURE OF VINYL CHLORIDE AND VINYL ACETATE CONTAINING ABOUT 95% VINYL CHLORIDE AND ABOUT 5% VINYL ACETATE, AND MIXTURES THEREOF HAVING INCORPORATED THEREWITH BETWEEN ABOUT 50 PARTS BY WEIGHT AND ABOUT 150 PARTS BY WEIGHT FOR EACH 100 PARTS BY WEIGHT OF RESIN OF A PLASTICIZER FOR THE RESIN WHICH IS COMPATIBLE WITH THE RESIN IN SUCH PROPORTION AT TEMPERATURES ABOVE 45*F. AND WHICH RENDERS, THE COMPOSITION STATIC-FREE, SAID PLASTICIZER BEING SELECTED FROM THE GROUP CONSISTING OF: (A) AN ESTER, THE ACID COMPONENT OF WHICH IS SELECTED FROM THE GROUP CONSISTING OF AT LEAST ONE ALIPHATIC ACID, PHOSPHORIC ACID, AND PHOSPHONIC ACID, THE MOLECULAR WEIGHT OF THE ALIPHATIC PORTION OF SAID ESTER REPRESENTING MORE THAN 50% OF THE TOTAL MOLECULAR WEIGHT OF SAID ESTER, (B) 2-ETHYLHEXYL DI ESTER AMIDE, (C) FATTY ACID NITRILE OF C6-C30 FATTY ACIDS, (D)
US353307A 1950-03-09 1953-05-06 Textile fiber unit Expired - Lifetime US2860382A (en)

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GB6771/55A GB741860A (en) 1953-05-06 1953-06-18 Improvements in or relating to textile fiber units
GB16853/53A GB733897A (en) 1950-03-09 1953-06-18 Improvements in or relating to textile fiber units

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2996646A (en) * 1957-01-09 1961-08-15 Eastman Kodak Co Antistatic device
US3133884A (en) * 1960-08-22 1964-05-19 Monsanto Chemicals Coating composition containing a liquid phosphate ester, a thermoplastic resin and asiliceous material
US4346145A (en) * 1981-01-05 1982-08-24 Western Electric Co., Inc. Coating composition and coated articles
US4443573A (en) * 1981-04-15 1984-04-17 Allied Corporation Additive dispersions and process for their incorporation with fiber-forming polymers
US4582867A (en) * 1981-01-05 1986-04-15 At&T Technologies, Inc. Coating composition and coated articles
US5198521A (en) * 1988-08-29 1993-03-30 Armstrong World Industries, Inc. Conductive polyurethane-urea/polyethylene oxide polymer
US5620762A (en) * 1992-10-15 1997-04-15 Armstrong World Industries, Inc. Textile fiber-working units and compositions for their fiber-working surface layer

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE557192A (en) * 1956-05-04

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1935577A (en) * 1928-05-17 1933-11-14 Carbide & Carbon Chem Corp Vinyl resin
US2010963A (en) * 1933-01-25 1935-08-13 Carbide & Carbon Chem Corp Process for making films and the like and products thereby made
GB486911A (en) * 1937-08-18 1938-06-13 Sonoco Products Co Improvements in covered rollers for drawing and feeding textile fibres
US2278424A (en) * 1937-07-22 1942-04-07 Sonoco Products Co Cover for textile rolls and method of making the same
US2597708A (en) * 1948-12-30 1952-05-20 American Cyanamid Co Antistatic agent, treatment of shaped articles therewith, and treated articles

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1935577A (en) * 1928-05-17 1933-11-14 Carbide & Carbon Chem Corp Vinyl resin
US2010963A (en) * 1933-01-25 1935-08-13 Carbide & Carbon Chem Corp Process for making films and the like and products thereby made
US2278424A (en) * 1937-07-22 1942-04-07 Sonoco Products Co Cover for textile rolls and method of making the same
GB486911A (en) * 1937-08-18 1938-06-13 Sonoco Products Co Improvements in covered rollers for drawing and feeding textile fibres
US2597708A (en) * 1948-12-30 1952-05-20 American Cyanamid Co Antistatic agent, treatment of shaped articles therewith, and treated articles

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2996646A (en) * 1957-01-09 1961-08-15 Eastman Kodak Co Antistatic device
US3133884A (en) * 1960-08-22 1964-05-19 Monsanto Chemicals Coating composition containing a liquid phosphate ester, a thermoplastic resin and asiliceous material
US4346145A (en) * 1981-01-05 1982-08-24 Western Electric Co., Inc. Coating composition and coated articles
US4582867A (en) * 1981-01-05 1986-04-15 At&T Technologies, Inc. Coating composition and coated articles
US4443573A (en) * 1981-04-15 1984-04-17 Allied Corporation Additive dispersions and process for their incorporation with fiber-forming polymers
US5198521A (en) * 1988-08-29 1993-03-30 Armstrong World Industries, Inc. Conductive polyurethane-urea/polyethylene oxide polymer
US5620762A (en) * 1992-10-15 1997-04-15 Armstrong World Industries, Inc. Textile fiber-working units and compositions for their fiber-working surface layer

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