CA1062829A - High performance hot melt adhesive backsizing compositions and carpet made therewith - Google Patents

High performance hot melt adhesive backsizing compositions and carpet made therewith

Info

Publication number
CA1062829A
CA1062829A CA236,286A CA236286A CA1062829A CA 1062829 A CA1062829 A CA 1062829A CA 236286 A CA236286 A CA 236286A CA 1062829 A CA1062829 A CA 1062829A
Authority
CA
Canada
Prior art keywords
weight percent
carpet
composition
ethylene
vinyl ester
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
Application number
CA236,286A
Other languages
French (fr)
Inventor
George E. Smedberg
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US509562A external-priority patent/US3914489A/en
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Priority to CA314,854A priority Critical patent/CA1066834A/en
Application granted granted Critical
Publication of CA1062829A publication Critical patent/CA1062829A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L101/00Compositions of unspecified macromolecular compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/01Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013Fillers, pigments or reinforcing additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/01Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/014Stabilisers against oxidation, heat, light or ozone
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/08Copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L57/00Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L65/00Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J123/00Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
    • C09J123/02Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
    • C09J123/04Homopolymers or copolymers of ethene
    • C09J123/08Copolymers of ethene
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, 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
    • D06N7/00Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
    • D06N7/0063Floor 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
    • D06N7/0071Floor 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
    • D06N7/0078Floor 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 a hot melt
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, 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
    • D06N2203/00Macromolecular materials of the coating layers
    • D06N2203/04Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N2203/042Polyolefin (co)polymers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, 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
    • D06N2203/00Macromolecular materials of the coating layers
    • D06N2203/06Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06N2203/061Polyesters
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06NWALL, 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
    • D06N2205/00Condition, form or state of the materials
    • D06N2205/06Melt
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/23979Particular backing structure or composition
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/23986With coating, impregnation, or bond
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/23907Pile or nap type surface or component
    • Y10T428/23993Composition of pile or adhesive

Abstract

ABSTRACT OF THE DISCLOSURE
Hot melt backsize compositions having high tensile elongation which result in tufted carpets having improved tuft bind comprise a blend of ethylene/vinyl ester copolymer, hydrocarbon resin, and, optionally, low molecular weight polyethylene, paraffin wax, anti-oxidant and filler.

Description

BACKGROUND OF THE INVENTION
Field of the Invention - This invent~ion relates to carpet backsizing, ana more particularly it relates to hot melt backsizing compositions which result in carpets having high tuft bind.

Descri tion of the Prior Art p Backsizing of tufted carpets with hot melt backsize adhesives has been known now for some years.
U. S. Patent 3,551,231 discloses a process for applying a hot melt backsize adhesive blend of ethylene/vinyl ester copolymer, petroleum wax, and a thermoplastic resin.
Satisfactory carpets are made by applying a critical pressure on the tufted structure while it is in contact with the hot melt adhesive applicator rol~. The necessity of maintaining such critical pressure during the adhesive application detracts from process flexi- -b~lity.
U. S. Patent 3,684,600 discloses the applica-tion of a low viscosity precoat adhesive to the back-side of the tufted structure prior to the application of the hot melt backsize adhesive composition. ~y using the precoat adhesive, the necessity of maintaining a critical pressure on the carpet during the hot melt adhesive ~pplication can be eliminated. The backsize - adhesive composition contains ethylene/vinyl ester co-polymer, low molecular weight, low density polyethylene, microcrystalline wax, aliphatic thermoplastic hydrocarbon resin, dicyclopentadiene alkylation polymer, antioxidant and filler.

U. S. Patent 3,S83,935 discloses a hot melt backsize adhesive composition comprising an ethylene/
v~nyl ester or acrylate polymer, a wax of sufficiently high melting point to yield a blend softer.ing point of at least 190F., a blend of aliphatic thermoplastic hydrocarbon resin and a dicyclopentadiene alkylation polymer, and optionally a filler.
, U. S. Patent 3,745,054 relates to high filler content hot melt backsize adhesive compositions comprising ethylene/vinyl ester copolymer, paraffin wax, micro-crystalline wax, aliphatic thermoplastic hydrocarbon resin, dicyclopentadiene alkylation polymer, antioXidant and filler.
Previously, filler containing hot melt blends have been used to produce carpets having tuft binds which generally average in the 6 to 1~ lb. range. While this is generally adequate for domestic carpet (used in the home), higher tuft bind values will ensure greater durability. Considerably higher tuft binds (18 lb.
average or greater), which up to the present has not been attainable, are desired by the carpet industry for contract carpet (used in schools, hotels, churches, industry, etc.) to ensure meeting typically severe ~ervice requirements.
SUMMARY OF THE INVENTION
~ he present invention provides hot melt blends which offer higher strength, as described below, than has been obtainable with hot melt blends developed and used heretofore. The key to the invention is the application of a novel tackifier resin system, which enhances the ~06Z8Z9 tensile elongation of the blends 8t equivalent tackifier cost and quantity. This in turn provides a substantial lncrease in the tuft bind values attainable for the final carpet as sold to consumers.
The new blend has utility in both the domestic carpet and contract carpet markets. Carpet for domestic use does not encounter severe wear conditions; hence, tuft bind values, etc., can be less than is essential for carpets for schools, motels and hotels, industrial buildings, etc where traffic is severe. It is common in industry to use higher standards, requiring higher costs, for contract carpets. The present invention recognizes this distinction, and is applicable in both end use areas.
According to the present invention there is provided a composition having a tensile elongation of about 700-1500 percent, preferably at least about 900 percent comprising (A) about 15-30 (preferably a~out 18-22) weight percent ethylene/vinyl ester co-polymer having a melt index of about 2 to 100 (preferably about 10-25), a copolymerized ethylene content of about 67 to 84 (preferably about 74-77) weight percent, a copolymerized vinyl ester content of about 16 to 33 (preferably about 23-26) weight percent, wherein the acid moiety of said vinyl ester contains 1-4 (preferably
2-3) carbon atoms, (B) about 30-70 (preferably about 40-50) weight percent of a hydrocarbon resin or a mixture of several hydrocarbon resins having a ring and ball softening point of about 50C.-70C. and a viscosity of 0.5 to 1.5 poise at 135C., and optionally (C) 0 to about S weight percent of a low molecular weight ethylene homopolymer having a molecular weight of about 1500-4000, density of 0.91-0.96 g./cm.3 and a melting point of about 220Y.-270F., (D) 0 to about 5 weight percent of a paraffin wax, (E) an effective amount of an antioxidant, and (F) 0 to about 40 weight percent filler. This composition is intended for lamination of contract carpets, however, it is technically suited to lamination of domestic carpets also, but is too~
costly for this market.
According to the present invention there are further provided contract-type carpets having improved tuft bind, at least an average of 18 pounds, obtained by the use of the above compositions and carrying out the backsizing according to the process of U. S. Patent
3,551,231.
According to the present invention there is further provided a composition having a tensile elongation of about 50 to 400 percent, preferably at least about 200 percent, comprising ~A) about 3 to 15 (preferably about 5 to 10) weight percent ethylene/
vinyl ester copolymer having a melt index of about 2 to 100 (preferably about 10-25), a copolymerized ethylene content of about 67 to ~ (preferably about 74-77) weight percent, a copolymerized vinyl ester content of about 10 to 33 (preferably about 23-26) weight percent, wherein the acid moiety of said vinyl ester contains 1-4 (preferably 2-3) carbon atoms, (B) about 15 to 40 (pre-ferably about 25 to 35) ~eight percent of a hydrocarbon resin or a mixture of several hy~rocarbon resins having a ring and ball softening point of abo~t 50C.-70C. and a viscosity of 0.5 to 1.5 poise at 135C., and optionally ~C) 0 to about 3 weight percent of a low molecular weight ethylene homopolymer having a molecular weight of about 1500-4000, density of 0.91-0.96 g./cm.3 and a melting point of about 220F.-270F., (D) 0 to about 3 weight percent of a paraffin wax, (E) an effective amount of an an~ioxidant, and (F) about 40 to 75 weight percent filler. This composition is intended for lamination of domestic carpets.
According to the present invention there are further provided carpets for domestic uses having im-proved tuft bind, at least an average of 10 pounds, ob-tained by the use of the compositions of the preceding - paragraph and carrying out the backsizing according to the process of U. S. Patent 3,551,231.
DETAILED DESCRIPTION OF THE INVEWTION
It has been discovered that a hot melt formation as described above will produce contract-type carpets having high tuft binds which have not been possible with the type of hot melt blends previously available for ;carpet backsizing. When more filler is added and the blend ingr,edient levels are adjusted to a serviceable viscosity range, a domestic carpet with tuft binds superior to those currently being sold is attained. The higher performance is attributed to the type of hy~rocarbon resin [Component (B)] used and the resultant higher tensile elongation of the hot melt composition.
Hydrocarbon resins suitabie for use in the high performance hot melt backsize compositions are .. . .

10628Zg classified as low molecular weight alkyl-aromatic hydrocarbon resins of the non-reactive, thermoplastic hydrocarbon types. Generally, they range in ring and ball softening point, as measured by ASTM E 28-67, from about 10C.-120C. and have viscosities measured at 135C. of about 0.5-1.5 poises. Certain of these are low molecular weight dicyclopentadiene alkylation polymers and may be prepared according to U. S. Patent 3,023,200.
Included in this type are the ~Piccovar" resins. The ~0 softening point of the resin, or of the mixture of resins, if more than one is employed, has to be between about 50C.-70C. If the softening point of the resin(s) is less than about 50C. the blend viscosity and tensile ~trength are too low. If the softening point is hlgher than about 70C. the blend viscosity is too high and the blend tensile elongation is too low to yield the desired high tuft bind.
~ ables A and B list some of the commercially available hydrocarbon resins which, when used in the hot melt blend, yield the desired specifications for a high performance hot melt blend. The resins shown in Table A
can be used alone, while others (Table B) must be used in admixture with one or more of the resins to obtain the desired physical properties in the final hot melt blend.

t ~062829 C:, ., i p Zl ~ "
1~U ~ . ~

~I H a I ~ ~
~ I ~, 0 ~ I ^ -- ~ a) ,I h u~ I ~ N ~

~ 1~ _~ ~ C ~

H t~ c~
~ ,,1 0 ~

X ~ ~_ ~ ~ .C . 'I
, O O~ Y,' I ` o ~ O ~
~ ~ ~ I C ~ ~ -I ~ 0 ~ o.

i P ~rl u y u a ~ s ,, 0 ~ Lq 0 U~

In Table I are presented data showing tensile elongation and other physical properties of hot melt ~dhesive compositions prepared with the indicated hydrocarbon resins.

~06Z8Z9 . , o~ oO g g O $ ~ 8 o a ¦ o ~ j ~ ~ ~ o ~ ~
~1 Z Iq~o I
~ ~ O O ~ ~ ~ O ~ u~ o c~ o Ja ¦ '3 ~ ~1 N ~ ~ C`~ C`l ~ N ~ ~ C`~l C'.l g ~ ;Ç~
~ C~ . ' ) ~
c~ X_,~ O O O O O O cr~ ~ ~ ~ O ~
I V ~ ~ U~ ~ ~ o U~ o_ ~aiC ~o~ ,oo~ C
.' I - . , ~
N ¦ ~ 0 O O O ~ I~ C~ O O
a D N ~`1 N N ~1 ~I N t~

O ~ n ,~ 0 o ~ h ~1 '1 0 5 ~ 2 I ~j; V b~ U U Cl 0 ~ h ~ ~ ~1 ~ ~ ;3 a 3D ~o o o o u~ n ~ ~ ~ ~ 4 :.
~, O ~ O O ~ O O U~ ~ ~ ~ ~ CO N O~ ~1 U ~~, ~ ~ O ~ ~0 ~ ~ ~ ~ ~ ~ u~ ~ ~ 3 ~ 3 T~
. ,-~a ~ o ~ so cJ~

~06Z8Z9 Etbylene copolymers most useful ih the present invention are copolymers of ethylene with vinyl esters of lower carboxylic acids. Such ethylene/vinyl ester copolymers can be prepared by known techniques, such as illustrated in U. S. Patent 2,200,429 and U. S. Patent 2,703,794. While an ethylene/vinyl acetate copolymer is preferred, other ethylene copolymers, such as those of vinyl formate, vinyl propionate, and vinyl butyrate, are useful as well.
The ethylene copolymers have melt indexes, as ~easured by ASTM 1238-52T, of about 2-100 (preferably 10-25) with polymerized ethylene content of about 67-84 tpreferably 74-77) weight percent. Correspondingly, the polymerized ester content of useful ethylene co-polymers is about 16-23 (preferably 23-26) weight percent.
Additionally, ethylene copolymers containing minor amounts (i.e., up to about 3 weight percent) of polymerizable copolymers, such as acrylic acid, methacrylic acid, ~taconic acid, acrylamide, isobutyl acrylate, beta dimethylaminoethyl methacrylate, beta hydroxyethyl acrylate, diallyl maleate, diallyl phthalate, diallyl ether, or ethylene glycol dimethacrylate, are useful as well.
For contract carpet use the ethylene copolymer should be present in the hot melt blend in about 15-30 weight percent, preferably about 18-22 weight percent.
Blends intended for domestic carpet application should contain about 3 to 15 weight percent, preferably about 5 to 10 weight percent, of the ethylene copolymer.

The optional low molecular weight polyethylene i8 pre~ent in the compositions of the present invention ~n sufficient amount to raise the softening point to a desired level. Thus a higher softening point, e.g., 235F.-240F., is of benefit to the carpet installer if $t becomes necessary to heat-seam two adjacent carpet sections. This ingredient does not appreciably affect the elongation of the composition nor the tuft bind of the finished carpet.
Optionally, an additional ingredient of suitable backsize adhesive compositions of this invention i5 paraffin wax. Paraffin waxes having a melting point of about 146F. to 158F., low needle point penetration (6-24 at 77F.) and low oil content (0.1 to 0.25 percent) are preferred. Generally, their presence up to about 5 weight percent for contract carpet use and up to about 3 weight percent for domestic carpet use is suitable to facilitate application of the blend to the carpet by adjusting the melt-viscosity of the composition to the required level.
The ùse of an antioxidant, such as butylated hydroxytoluene, in about 0.1-0.3 weight percent is advantageous.
Fiilers, such as calci~m carbonate, aluminum hydrate, etc., in about 0-75 weight percent concentration may optionally be incorporated into the compositions of the present invention as a low cost extender which improves carpet hand by providing additional bulk to the carpet. When compounding blends for contract carpet backsizing, care must be taken not to add more than . .

~06Z8Z9 about 40 weight percent filler so as not to reduce the elongation of the bac~size adhesive composition or the tuft bind of the carpet below the required levels.
~ he particular manner in which the ingredients are added to formulate the composition of the present invention is not critical and can be accomplished by any of the well-known techniques.
The high strength of the carpet (in terms of tuft bind) made with compositions of the present inYentiOn is a significant advantage since in many uses (such as contract carpet) it is important to have a very high resistance to tuft pull out. A small child can readily damage a carpet having only a 5-10 pound tuft bind but would find it difficult or impossible to pull out tufts from a carpet having a 15 to 20 pound tuft bind. Quite likely the yarn would break before more than one or two tufts could be pulled out. Similarly, in applications such as hotel lobbies, theaters, etc., where a single tuft might readily be caught accidentally 2~ by users of the carpet, the high strength hot melt blend of the present invention would be of advantage~
Tuft bind, expressed in pounds, is measured by ASTM p 1335 or in some cases by a minor-modification which gives comparable results. Values reported herein - are the average of about 8-10 determinations. It will be appreciated that preparation of the carpet samples, following the teachings of U. S. Patent 3,551,231, may lead to some variability in the tuft bind values because of the many variables that can affect the evenness of the coating and the uniformity of penetration of the ~06Z8Z9 hot melt into the carpet tufts. For prior art carpets, the spread is usually about 5-7 pounds while for carpets of the present invention the spread is usually about 3-4 pounds.
- The following examples, wherein all parts and percentages are by weight, except where otherwise specified, further illustrate the advantages of the present invention. Two separate series of examples are given below. Series I covers blends intended 10 primarily for contract carpet types. Series ~I covers blends intended primarily for domestic carpet use.
SERIES I - CONTRACT CARPETS
COMPARATIVE EXAMPLES Cl TO C4 Reference Blend A, which is representative of the more successful filled prior art blends, was pre-pared:
Reference Blend A - Contract Carpets 15.0% ethylene/vinyl acetate copolymer, melt index -- 1.7-2.3, 25% vinyl acetate, 1.8% low molecular weight polyethylene, 3500 molecular weight, 240F. melting point, ~AC" 8, available from Allied Chemical Company, 10.2% microcrystalline wax, melting point I60F., nShellmax" 400, available from Shell Chemical Company, 17.2% unsaturated aliphatic thermoplastic hydro-:carbon resin, melting point 100C.
(~Piccopale" 100SF, available from Hercules Inc.), 25.6% dicyclopentadiene alkylation polymer, melting point 77F. ("Piccovar" AP 25, available from Hercules Inc.), 0.2% butylated hydroxytoluene (BHT), 30.0~ calcium carbonate filler (No. 9 "~hiting").

--1~--Blend A had the following properties:
Ring and ball softening point, F. 210 V~scosity,- cps. at 310F. 14,000 Tensile, lb./in.2 400-500 Tensile Elongation, % 10-lS
Strength characteristics of the carpet back-sized with the above blend according to the process of U. S. Patent 3,551,231 are given in ~able II.
TAB~E II

10 Properties of Contract-Type Carpets Made Using Reference Blend A

Carpet Backsize Tuft Scrim Bond, No. oz./yd.2 Bind,_lb. lb./3n(l) Cl 27.0 13.0 28.0 C2 18.0 10.0 16.0 ~1) determined by ASTM D-2724-13.
Data in Table II show that tuft bind values are good for many uses, but are below the ultimate goal - a carpet which cannot readily be harmed by accident, heavy wear, or a mischievous child.
An unfilled prior art blend, wherein the filler was omitted to maximize the amount of resinous binder and to improve the tuft bind thereby, was prepared. This composition is designated Reference Blend B~
Reference Blend B - Contract Carpet 31.5~ ethylene/vinyl acetate sopolymer (10-25 melt index, 25% vinyl acetate ), 3.5% paraffin wax, melting point 146F.
("Pacemaker" 53, available from Cities Service Oil Company), 2.6% low molecular weight polyethylene (2000 molecular weiaht, 0.96 gm.~m.3 density) (nPolywax" 2000, available from Petrolite Corp., Eareco Div.l, .

.

11.5% microcrystalline wax, 160F. melting point 25.4% unsaturated aliphatic thermoplastic hydro-carbon resin, melting point 100C.
25.4% dicyclopentadiene alkylation poly~er, meit-ing point 77F., 0.1% butylated hydroxytoluene.
Blend B had the following properties:
Ring and ball softening point, F. 209 Viscosity, cps. at 310F. 10,300 ~ensile, lb./in.2 400-500 Tensile elongation, % 20-25 Strength characteristics of the carpet back-sized with the above blend according to the process of U. S. Patent 3,551,231 are given in Table III.
~LE III
~roperties of Contract-Type Carpets Made Using Unfilled Reference Blend B

Carpet Backsize Tuft Scrim Bond, No. oz./Yd.2 Bind, lb. lb./3"
C3 18.7 14.5 26.2 C4 25.0 14.6 40.0 Data in Table III show a modest improvement in - properties compared to the filled, less costly blend A
which was used for the samples in Table II. However, the small improvement is not adequate to justify the higher cost for most users.
The higher strength hot melt blends of the present invention are illustrated in Examples 1 and 2, intended for contract carpet use, which follow:
.

~igh-Strength Blend - 30% Filled - For Contract CarPet 19.8% ethylene/vinyl acetate copolymer, melt index 17-21, vinyl acetate content 25%, 2.2% paraffin wax, melting point of about 146F.

2.9% low molecular weight (2000) polyethylene, density 0.96 g./cm.3, ring and ball soften-ing point (ASTM-E28) 257F., 45.0% hydrocarbon resin, 60C. ring and ball softening point, viscosity of 1.0 poise at 135C. ("Piccovar" L60, available from ~ercules Inc.), 0.1% butylated hydroxytoluene, 30.0% calcium carbonate.
Physical properties of this blend are given under Blend No. 1 in Table I. The key physical property -tensile elongation - was 950 percent.
Table IV shows the typical carpet properties attained by use of Blend No. 1:
TABLE IV

Properties of Contract-Type Carpets Made Usinq Blend No. 1 Carpet Backsize Tuft Scrim Bond, No. oz.~yd.2 Bind, lb. lb./3"
1 22.2 18.5 27.8 2 27.6 21.3 31.8 3 25.7 18.9 29.3 All tuft bind values were in excess of 18 lbs., a marked improvement over the 10-13 lbs.
values obtained with the corresponding filled prior art ~lend (cf. Table II). In many cases, this level of tuft bind will be near the breaking strength of the carpet yarn. In a few cases, where the ultimate in tuft bind value is desired, further improvement (at added cost) can be secured by elimination of filler, as shown in Example 2. The tuft bind value is above 27 lbs./tuft.
ExAMæLE 2 Unfilled High Strength Blend For Contract Carpet .
28.3% ethylene/vinyl acetate copolymer, melt index of 17-21, vinyl acetate content 25%, 3.1% paraffin wax, melting point of about 1~6F.,
4.0% low molecular weight (2000) polyethylene, density 0.96 g./cm.3, ring and ball soften-ing point (ASTM-E28) 257F., 64.5% hydrocarbon resin, 60C. ring and ball softening point, viscosity of 1.0 poise at 135C., 0.1% butylated hydroxytoluene.
Physical properties of this blend are as follows: .
Ring and ball softening point, F.238 Viscosity, cps. at 310F. 5,337 Tensile, lb./in.2 335 Tensile elongation, % 1090 Typical properties of carpet backsized by the above hot melt blend are shown in Table V.
TABLE V

Properties of Contract-~ype Carpet Made Using Example 2 Blend Carpet Backsize Tuft Bind Scrim Bond No. oz /yd 2 lb. lb./3"
4 25.7 27.6 36.8 This value is above the breaking strength for the yarns used in many carpets sold in today's markets, and is almost double the value obtained by the use of .
.

the corresponding unfilled prior art blend ~i.e., ~4.5-14.6 lbs. cf. Table III).
SERIES II - DOMESTIC CARPETS
Blends described heretofore, intended primarily for contract carpet, are also technically highly desirable for use in domestic carpet backsizing, but costs are prohibitive. However, these blends can be modified to include substantial amounts of inert filler to render the cost more attractive and still retain the improvement in tuft bind. Accordingly, the highly filled blend of the present invention employing the novel tackifier resin 8y5tem yields considerably higher tuft bind than a corresponding highly filled blend employing a widely-used prior art tackifier resin, although, of course, absolute values for both the blends of the present invention and of the prior art will be lower than for less-highly-filled blends of similar composition.
To Sllustrate the benefits of the invention when applied to highly-filled systems, Reference Blend C, and the blends of Examples 3 and 4 were prepared, all at 60% filler level:
Reference Blend C - Domestic Carpets 5WidelY-Used Good Quality Prior Art Blend) (Reference: U. S. Patent 3,745,054) 8.1% ethylene/vinyl acetate copolymer, melt index 17-21, vinyl acetate content 25%.
0.9% paraffin wax, melting point of about 146F.

1.3% low molecular weight polyethy.ene (3500 molecular weight, 240F. melting point, 0.93 gm./cm.3 density3.
5.4% microcrystalline wax, melting point 160F.

12.1% unsaturated aliphatic thermoplastic hydrocarbon resin, melting point 100C.
12.1~ dicyclopentadiene alkylation polymer, melting point 77F.
0.1% butylated hydroxytoluene.
60.0% calcium carbonate.

Domestic Carpet Blend - 60% Filled - Based on Im~roved Tackifier Resin System 8.1% ethylene/vinyl acetate copolymer, melt index 17-21, vinyl acetate content 25%.
0.9~ paraffin wax, melting point of about 146F.
1.8% low molecular weight polyethylene (3500 molecular weight, 240F. melting point, 0.93 gm./cm.3 density).
29.0% hydrocarbon resin, 60C. ring and ball soften-ing point, viscosity of 1.0 poise at 135C.
0.2% butylated hydroxytoluene.
60.0% calcium carbonate.
- 20 ~XAMPLE 4 Domestic Carpet Blend - 60~ Filled - Based on Alternate Improved Tackifier Resin System 7.2% ethylene/vinyl acetate copolymer, melt index 17-21, vinyl acetate content 25~.
0.8% paraffin wax, melting point of about 146F.
1.9% low molecular weight polyethyle3ne (2000 molecular weight, 0.96 gm./cm. density, ring and ball softening point 257F.).
29.6% hydrocarbon resin, 64C. ring and ball softening point, viscosity of 1.0 poise at 135 C.
60.5% calcium carbonate.
The relative merits of the prior art blend and the improved blends of the present invention siven in Examples 3 and 4 are exhibited in two ways. Table VI
provides comparative physical properties for the three blends; the reference blend clearly has a far lower tensile elongation percentage than does the Example 3 or Example 4 blend. The tensile strength for the reference blend is highest, but, as shown below, this does not result in good tuft bind performance.
Table VII shows clearly that the benefit of the high tensile elongation percentage noted in Table VI
carry through, and confer a definite benefit on carpets made with the improved blends. Both tuft bind values and scrim bond values for the carpets made using Example 3 and Example 4 blends are clearly superior to comparable values for the reference blend, even though the carpet ~tyle is common and the backsize coating weights are essentially equal.

- ~oGZ8Z9 n o ~1 C~ O
U;~ O
U .

o .. . ~ m~ o ,~ u~
~o ,~ ~
~:

~1 ~ ~ N . o ~ C~ O O O
~ E~
~ . . '~ ~

~ ~ m ~ ~ S::

~06Z829 os m ~ ~ ~ ,, ~ u~ ~ ~
~ ~ ~ C~ o U~
o .
U~ .

I ~O O ~ O u~ ~O
m ,Q O
~o ~ ~
m 0 ~a E~
P
- ~cq a~ O N . C~ C~ l ~ O ~ C~.l 0 ~ ~ U~ O ~O
~1 ~ ~: ,~J ~ C~ ~ CY C~ ~ CY C`~
C t~S N
~ ~ mo m o~
I _~ ~ .
- ¦ P. o C~ ~
0~ td ~D
P.
o S,. ~ m m m s: ~ ~1> 0 ~ ~ *
_1 O ' O ~
m ~ v ~ -,

Claims (10)

The embodiments of the invention in which an exclu-sive property or privilege is claimed are defined as follows:-
1. A composition having a tensile elongation of about 700 to 1500 percent comprising (A) about 15 to 30 weight percent ethylene/vinyl ester copolymer having a melt index of about 2 to 100, a copolymerized ethylene content of about 67 to 84 weight percent, a copolymerized vinyl ester content of about 16 to 33 weight percent, wherein the acid moiety of said vinyl ester contains 1 to 4 carbon atoms, (B) about 30 to 70 weight percent of one hydrocarbon resin or a mixture of two or more hydrocarbon resins wherein said one hydrocarbon resin or said mixture has a ring and ball softening point of about 50°C. to 70°C. and a viscosity of about 0.5 to 1.5 poise at 135°C., (C) 0 to about 5 weight percent of an ethylene homopolymer having a molecular weight of about 1500 to 4000, density of about 0.91 to 0.96 g./cm.3, and a melting point of about 220°F. to 270°F., (d) 0 to about 5 weight percent of a paraffin wax, (E) 0 to about 0.3 weight percent of an antioxidant, and (F) 0 to about 30 weight percent filler.
2. The composition of Claim 1 having a tensile elongation of at least 900 percent.
3. The composition of Claim 1 wherein said ethylene/vinyl ester copolymer is present in about 18 to 22 weight percent and has a melt index of about 10 to 25.
4. The composition of Claim 3 wherein said copolymerized vinyl ester content is about 23 to 26 weight percent and the acid moiety thereof contains 2 to 3 carbon atoms.
5. The composition of Claim 4 wherein said hydrocarbon resin is present in about 40 to 50 weight percent.
6. The composition of Claim 5 having a tensile elongation of at least about 900 percent.
7. The composition of Claim 6 wherein said vinyl ester is vinyl acetate.
8. A carpet comprised of a primary backing material stitched with closely spaced erect loops of yarn to form a tufted structure, the bottom surface of the tufted structure having as a tuft bonding backsize adhesive coating the composition of Claim 1, said carpet having an average tuft bind of at least 18 pounds.
9. A carpet comprised of a primary backing material stitched with closely spaced erect loops of yarn to form a tufted structure, the bottom surface of the tufted structure having as a tuft bonding backsize adhesive coating the composition of Claim 4, said carpet having an average tuft bind of at least 18 pounds.
10. A carpet comprised of a primary backing material stitched with closely spaced erect loops of yarn to form a tufted structure, the bottom surface of the tufted structure having as a tuft bonding backsize adhesive coating the composition of Claim 7, said carpet having an average tuft bind of at least 18 pounds.
CA236,286A 1974-09-26 1975-09-24 High performance hot melt adhesive backsizing compositions and carpet made therewith Expired CA1062829A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA314,854A CA1066834A (en) 1974-09-26 1978-10-30 High performance hot melt adhesive backsizing compositions and carpet made therewith

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US509562A US3914489A (en) 1974-09-26 1974-09-26 High performance hot melt adhesive backsizing compositions and carpet made therewith
US05/597,140 US4012547A (en) 1974-09-26 1975-07-18 High performance hot melt adhesive backsizing compositions and carpet made therewith

Publications (1)

Publication Number Publication Date
CA1062829A true CA1062829A (en) 1979-09-18

Family

ID=27056590

Family Applications (1)

Application Number Title Priority Date Filing Date
CA236,286A Expired CA1062829A (en) 1974-09-26 1975-09-24 High performance hot melt adhesive backsizing compositions and carpet made therewith

Country Status (7)

Country Link
US (1) US4012547A (en)
JP (1) JPS6023704B2 (en)
CA (1) CA1062829A (en)
DE (1) DE2543137C2 (en)
FR (1) FR2286167A1 (en)
GB (1) GB1514959A (en)
NL (1) NL182408C (en)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4146521A (en) * 1977-09-02 1979-03-27 Eastman Kodak Company Polyethylene containing hot melt adhesives
US4180490A (en) * 1977-09-22 1979-12-25 National Distillers And Chemical Corporation Antiblock system and process aid for vulcanized vinyl acetate ethylene copolymers
FR2438700A2 (en) * 1978-10-13 1980-05-09 Rhone Poulenc Textile Pile fabric carrier - is a flexible plastic grid with pattern for hand pile insertion (NL 15.4.80)
US4335034A (en) * 1978-12-18 1982-06-15 J. P. Stevens & Co., Inc. Thermoplastic compositions and automotive carpeting backed therewith
US4242395A (en) * 1978-12-18 1980-12-30 J. P. Stevens & Co., Inc. Thermoplastic compositions and automotive carpeting backed therewith
IT1130781B (en) * 1979-06-01 1986-06-18 Union Carbide Corp THERMOFORMABLE COMPOSITION FOR BOTTOMS OF CARPETS
US4235761A (en) * 1979-06-22 1980-11-25 M. Argueso & Co., Inc. Water-insoluble thermoplastic compositions for rigidly holding or supporting articles during machining
US4456649A (en) * 1979-10-02 1984-06-26 Manville Service Corporation Low-cost, highly filled, wax-based hot melt adhesives and coatings
JPS56501285A (en) * 1979-10-02 1981-09-10
US4508771A (en) * 1979-11-19 1985-04-02 Exxon Research & Engineering Co. Extruded carpet backing with resin and elastomer components
JPS5832678A (en) * 1981-08-21 1983-02-25 Nippon Oil Co Ltd Hot-melt composition
GR77638B (en) * 1981-09-22 1984-09-25 Milliken Res Corp
US4552794A (en) * 1983-06-30 1985-11-12 Hercules Incorporated Composition for tufted carpets containing azidosulfonyl silane crosslinker
US4501846A (en) * 1983-06-30 1985-02-26 Hercules Incorporated Composition for tufted carpets
GB8401567D0 (en) * 1984-01-20 1984-02-22 Exxon Research Engineering Co Polyethylene wax
US4571410A (en) * 1985-02-07 1986-02-18 Magic Seal Corporation Caulking composition
US4623677A (en) 1985-08-08 1986-11-18 Magic Seal Corporation Summer blend caulking composition
US4752634A (en) * 1986-04-17 1988-06-21 Hercules Incorporated Heat resistant hot melt precoat and adhesive compositions
DE3636023A1 (en) * 1986-10-23 1988-05-05 Atochem Werke Gmbh THERMOPLASTIC POLYMER
US4939036A (en) * 1987-10-14 1990-07-03 Amoco Corporation Method for preparing tufted pile carpet and adhesive therefor
US4844765A (en) * 1987-10-14 1989-07-04 Amoco Corporation Method for preparing tufted pile carpet and adhesive therefor
DE3802881A1 (en) * 1987-11-16 1989-05-24 Utz Ag Georg MICROWAVE-ACTIVATABLE MELT ADHESIVE
US5560972A (en) * 1988-07-25 1996-10-01 Interface, Inc. Latex fusion bonded pile carpets and carpet tile
KR0183464B1 (en) * 1992-05-14 1999-04-01 우에나까 마사노리 Carpet tile and method for producing the same
US5855836A (en) * 1995-09-27 1999-01-05 3D Systems, Inc. Method for selective deposition modeling
HUP0002052A3 (en) 1997-02-28 2000-12-28 Dow Chemical Co Filled polyethylene compositions
US20030211280A1 (en) * 1997-02-28 2003-11-13 Shaw Industries, Inc. Carpet, carpet backings and methods
US7338698B1 (en) 1997-02-28 2008-03-04 Columbia Insurance Company Homogeneously branched ethylene polymer carpet, carpet backing and method for making same
WO1998038375A2 (en) * 1997-02-28 1998-09-03 Shaw Industries, Inc. Carpet, carpet backings and methods
US5874148A (en) * 1997-04-21 1999-02-23 Reichhold Chemicals, Inc. Water resistant textile coating and method of using the same
US6162855A (en) * 1999-02-18 2000-12-19 Reynolds Metals Company Bauxite filler for carpet backings
US20050112320A1 (en) * 2003-11-20 2005-05-26 Wright Jeffery J. Carpet structure with plastomeric foam backing
WO2006019491A2 (en) * 2004-07-19 2006-02-23 Barrier-Bac, Inc. Synthetic turf and method for applying adhesive
JP2007203919A (en) * 2006-02-02 2007-08-16 Suminoe Textile Co Ltd Floor carpet for automobile, and manufacturing method thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3583936A (en) * 1969-01-07 1971-06-08 Du Pont Backsizing adhesive compositions
US3914489A (en) * 1974-09-26 1975-10-21 Du Pont High performance hot melt adhesive backsizing compositions and carpet made therewith

Also Published As

Publication number Publication date
JPS5157747A (en) 1976-05-20
NL182408B (en) 1987-10-01
NL7511385A (en) 1976-03-30
FR2286167A1 (en) 1976-04-23
FR2286167B1 (en) 1981-11-13
NL182408C (en) 1988-03-01
DE2543137A1 (en) 1976-04-15
DE2543137C2 (en) 1985-03-28
JPS6023704B2 (en) 1985-06-08
GB1514959A (en) 1978-06-21
US4012547A (en) 1977-03-15

Similar Documents

Publication Publication Date Title
CA1062829A (en) High performance hot melt adhesive backsizing compositions and carpet made therewith
US3914489A (en) High performance hot melt adhesive backsizing compositions and carpet made therewith
US3745054A (en) High filler content hot melt backsize adhesive compositions
CA1062828A (en) High ring and ball softening point hot melt backsize adhesive composition
US3583936A (en) Backsizing adhesive compositions
US3940525A (en) Tufted carpet having a polyolefin film as the secondary backing
US3390035A (en) Method for manufacturing tufted carpets
US4752634A (en) Heat resistant hot melt precoat and adhesive compositions
US4239563A (en) Process for the use of vinyl acetate-ethylene copolymer emulsions to adhere fibers to carpet backing
US9885149B2 (en) Carpet and carpet backing
US3982051A (en) Backsizing carpet with hot melt composition of ethylene copolymer, atactic polypropylene and vulcanized rubber
EP2231805B1 (en) Use of polyolefins comprising atactic structural elements in floor coverings
US4323626A (en) Heat-adhesive composite fibers
US4072735A (en) Hot melt pressure sensitive adhesives
US3676280A (en) Tufted carpet backsized with polymeric composition
US5021257A (en) Hot-melt adhesive composition
US3887738A (en) Carpet backsized with hot melt adhesive and method
WO1992008614A1 (en) Low melting hot-melt adhesive or coating composition
WO2002102914A1 (en) Hot melt adhesive composition
US3770558A (en) Tufted carpet
US5401791A (en) Bookbinding adhesives; processes for production of bookbinding adhesives; and methods of bookbinding
US5702796A (en) Modified multiphase bitumen composition and floor covering
CA2517864C (en) Vinyl acetate/ethylene and vinyl chloride polymer blends as binders for nonwoven products
US3645948A (en) Automotive carpet backsizing composition
GB2284152A (en) Tufted pile carpet and method of preparation