[go: up one dir, main page]

EP0618948A1 - Polylactide containing hot melt adhesive - Google Patents

Polylactide containing hot melt adhesive

Info

Publication number
EP0618948A1
EP0618948A1 EP93922271A EP93922271A EP0618948A1 EP 0618948 A1 EP0618948 A1 EP 0618948A1 EP 93922271 A EP93922271 A EP 93922271A EP 93922271 A EP93922271 A EP 93922271A EP 0618948 A1 EP0618948 A1 EP 0618948A1
Authority
EP
European Patent Office
Prior art keywords
adhesive
weight
poly
ethylene
polylactide
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.)
Ceased
Application number
EP93922271A
Other languages
German (de)
French (fr)
Inventor
Carmine P. Iovine
Thomas F. Kauffman
Jules E. Schoenberg
Paul P. Puletti
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.)
National Starch and Chemical Investment Holding Corp
Original Assignee
National Starch and Chemical Investment Holding Corp
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 US07/968,564 external-priority patent/US5252646A/en
Priority claimed from US08/000,153 external-priority patent/US5312850A/en
Application filed by National Starch and Chemical Investment Holding Corp filed Critical National Starch and Chemical Investment Holding Corp
Publication of EP0618948A1 publication Critical patent/EP0618948A1/en
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • C09J167/00Adhesives based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Adhesives based on derivatives of such polymers
    • C09J167/04Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • 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

Definitions

  • Hot melt adhesives are used commercially for a wide variety of applications.
  • the major advantage of hot melt adhesive systems is the lack of a carrier fluid which eliminates the need for drying the adhesive film once it is applied to the substrate. This elimination of the drying step overcomes hazards associated with solvent usage and also allows for faster production line speeds and lower transportation costs.
  • the degree of tack of the hot melt adhesives may be varied over a wide range to produce adhesives varying from pressure sensitive to non-pressure sensitive in character. Non-pressure sensitive are used, for example, in bookbinding, bag ending, case and carton sealing.
  • Hot melt adhesives have historically been based on petroleum derived polymers such as polyethylene, ethylene-vinyl acetate, styrenic block copolymers, and polypropylene to name a few. These compositions are further tackified, plasticized, and reinforced with a variety of resins, oils and waxes which are derived from both petroleum and naturally occurring feedstocks such as wood, gum and tall oil rosin and terpenes. These classic compositions suffer from the cyclical price cycles common to all oil derived materials, and also are generally very resistant to degradation once the articles employing them are disposed of.
  • the present invention stems from the growing movement away from petroleum derived raw materials to those derived from renewable, natural resources and as part of an effort to utilize raw materials which have demonstrated some level of degradation.
  • the present invention utilizes a class of naturally occurring or synthetically produced thermoplastic, biodegradable .copolymers derived from a non-petroleum feedstock as the base polymer.
  • Such compositions advance the state of the art of hot melt adhesives by alleviating the dependence on petroleum based materials and by allowing for the development of hot melt adhesives which either degrade naturally after coming in contact with the soil or which can be composted.
  • hot melt adhesive compositions suitable for a variety of applications are obtained by use of polylactide (i.e., the bimolecular cyclic ester of lactic acid) or copolymers with other lactones such as glycolide and caprolactone, tackifiers, and optionally, waxes and/or plasticizers.
  • the adhesives may be formulated using conventional additives and may vary from pressure sensitive to non-pressure sensitive in character depending upon the desired application.
  • the present invention is directed to hot melt adhesive compositions comprising 20 to 98% by weight of a polylactide homo- or copolymer where the copolymer contains at least 20 molar percent of the lactide component (1 or d or d,l or meso or mixtures thereof) 2 to 80% by weight of a polar tackifier having a Ring and Ball softening point (as described by ASTM E- 26) greater than about 60°C; 0 to 50% by weight of a plasticizer; 0 to 30% by weight of a wax diluent and 0-3% by weight of a stabilizer.
  • a polar tackifier having a Ring and Ball softening point (as described by ASTM E- 26) greater than about 60°C; 0 to 50% by weight of a plasticizer; 0 to 30% by weight of a wax diluent and 0-3% by weight of a stabilizer.
  • pressure sensitive adhesives can be prepared using 20 to 70% by weight of the polylactide homo- or copolymer, 10 to 60% of a tackifying resin, 10 to 50% plasticizer and 0 to 3% of a stabilizer.
  • Preferred pressure sensitive adhesives are prepared using 30 to 60% of the polylactide homo- or copolymer; 20 to 50% of a tackifying resin, preferably a terpene phenolic resin; and 20 to 30% of a plasticizer, preferably Pycal 94, a phenyl ether of poly(ethylene glycol) from ICI; or Hercolyn D, a methyl ester of hydrogenated rosin from Hercules.
  • Lower levels of plasticizer may also be employed to produce adhesives useful for various end uses such as in construction adhesives for disposable products where some initial degree of tack is needed but no residual pressure sensitive properties are required.
  • non-pressure sensitive adhesives can be prepared using 20-98% by weight of the polylactide homo- or copolymer, 2-80% tackifying resin, 0-30% of a wax-like diluent, 0-30% plasticizer and 0 to 3% of a stabilizer.
  • Preferred non-pressure sensitive adhesives are prepared using 30-80% of the polylactide homo- or copolymer; 10- 40% tackifying resin, preferably terpene-phenolic resins or rosin derivatives; 0-25% of a plasticizer, preferably the phenyl ether of poly(ethylene glycol) or the methyl ester of hydrogenated wood rosin; and 0-20% of a wax-like diluent, preferably hydrogenated castor oil (also known as castor wax) or 12-hydroxystearamide.
  • polymers other than the polylactide may be incorporated into the hot melt adhesives at levels less than about 20% by weight. Representative formulations and applications are discussed hereinbelow and illustrated by the examples, however, these should not be construed as limiting the invention.
  • the major component of the adhesive of the invention present in an amount of 20 to 98% by weight of the adhesive, comprises a homo- or copolymer of polylactide containing at least 20 molar percent of the lactide comonomer.
  • the general structure of the polylactide is shown below:
  • Suitable polymers for use herein have a number average molecular weight (M n ) within the range of 10,000 to 200,000.
  • poly(d,1-lactide) and the meso- are essentially amorphous
  • poly(1-lactide) and poly(d- lactide) is crystalline in nature and has a crystalline melting point of 186°C depending on its molecular weight and stereopurity.
  • the polymers may be prepared by ring- opening polymerization of the bimolecular cyclic ester of lactic acid with acid or base catalysts such as PbO, SnCl 2 , SnCl 4 , ZnCl 2 , SbF 5 , Sb 2 0 3 , or triethylamine using solution, precipitation or melt processes. Alternatively, they may be obtained commercially from Henley Chemicals, Inc. under the Resomer® tradename; from Poly Sciences Inc. or from Ecological Chemical Products Company (EcoChem) .
  • poly(d-lactide) , poly(d,1-lactide) , and poly(meso-lactide) suitable polymers for use herein may also be prepared by copolymerization with other lactones such as glycolide or caprolactone.
  • lactones such as glycolide or caprolactone.
  • poly(d,1-lactide-co-glycolide) polymers containing equimolar amounts of the lactide and glycolide components are available from Henley Chemicals as Resomer RG502, 503, 504, 505 and 506 and are suitable for use herein.
  • poly(d,1-lactide-co- glycolide) polymers known as Resomer RG752, 755 and 756 containing 75% of the lactide component as well as the Resomer 858 polymer which contains 85% lactide are also suitable.
  • the tackifying resins useful in the adhesive compositions are generally polar in nature and have a Ring and Ball softening point greater than 60°C and include rosin and rosin derivatives, terpene phenolics, pure phenolic resins, and the like.
  • the useful tackifying resins include any compatible resins or mixtures thereof such as (1) natural and modified rosins such, for example, as gum rosin, wood rosin, tall oil rosin, distilled rosin, hydrogenated rosin, dimerized rosin, and polymerized rosin; (2) glycerol and pentaerythritol esters of natural and modified rosins, such, for example as the glycerol ester of pale, wood rosin, the glycerol ester of hydrogenated rosin, the glycerol ester of polymerized rosin, the pentaerythritol ester of hydrogenated rosin, and the phenolic-modified pentaerythritol ester of rosin; (3) phenolic modified terpene resins and hydrogenated derivatives thereof such, for example, as the resin product resulting from the condensation, in an acidic medium, of a bicyclic terpene and a phenol;
  • Patent Nos. 4,073,776 and 4,023,826 Mixtures of two or more of the above described tackifying resins, as well as blends of the above resins with small amounts of (e.g., less than about 10% of the adhesive) less compatible resins may be utilized for some formulations. While the tackifier may comprise up to about 80% of the adhesive, it is generally used in amounts of 10 to 60% by weight.
  • compatible plasticizing or extending oils may also be present in the composition.
  • Preferred compatible plasticizers include phthalate plasticizers such as dioctyl phthalate; liquid polyesters such as Dynacol 720 from Huls; benzoate plasticizers such as 1,4- cyclohexane dimethanol dibenzoate (e.g., Benzoflex 352 available commercially from Velsicol) ; phosphate plasticizer such as t-butylphenyl diphenyl phosphate (e.g., Santicizer 154 available commercially from Monsanto) ; poly(ethylene glycols) and derivatives thereof such as the phenyl ether of poly(ethylene glycol) (e.g., Pycal 94 available commercially from ICI) as well as liquid rosin derivatives having Ring and Ball melting points below about 60°C such as the methyl ester of hydrogenated rosin (e.g., Hercolyn D from phthalate plasticizers such as dioctyl phthalate
  • Suitable waxes include 12-hydroxystearamide wax, hydrogenated castor oil, oxidized synthetic waxes, poly(ethylene oxide) having a weight average molecular weight above about 1000 and functionalized synthetic waxes such as carbonyl containing Escomer HlOl from Exxon.
  • adhesive formulations described herein may contain both wax and plasticizer components so that the presence of one or the other is not mutually exclusive.
  • hindered phenols include: 1,3,5- trimethyl-2,4,6-tris(3, 5-di-tert-butyl-4-hydroxy- benzyl)benzene; pentaerythritol tetrakis-3-(3,5-di-tert- butyl-4-hydroxyphenyl)propionate; n-octadecyl 3,5-di- tert-buty1-4-hydroxypheny1) propionate; 4,4'-methylene- bis (2,6-di-tert-butylphenol) ; 4,4'-thiobis (6-tert- butyl-o-cresol) ; 2,6-di-tert-butylphenol; 6-(4-hydroxy- phenoxy)-2,4-bis(n-octylthio)
  • the stabilizer is present in levels of about 0.1 to 3% by weight.
  • Optional additives may be incorporated into the hot melt compositions in order to modify certain properties thereof. Among these additives may be included colorants such as titanium dioxide; and fillers such as talc and clay, etc.
  • colorants such as titanium dioxide
  • fillers such as talc and clay, etc.
  • There may also be present in the adhesive small amounts (e.g. , less than about 20% by weight, and preferably 5 to 20% by weight) of certain thermoplastic polymers such as ethylene vinyl acetate, ethylene acrylic acid, ethylene methyl aerylate and ethylene n-butyl acrylate copolymers containing about 12 to 50% vinyl acetate as well as caprolactone polymers. These polymers are employed in order to impart flexibility, toughness and strength.
  • hot melt adhesive it may be desirable to incorporate into the hot melt adhesive up to 20% by weight of certain hydrophilic polymers such as poly(vinyl alcohol) , hydroxyethyl cellulose, starch, modified starch, poly(vinyl methyl ether) , poly(ethylene oxide) , or poly(hydroxy butyrate/hydroxy valerate) which will function to increase the water sensitivity of the adhesives which may be desired for some applications.
  • hydrophilic polymers such as poly(vinyl alcohol) , hydroxyethyl cellulose, starch, modified starch, poly(vinyl methyl ether) , poly(ethylene oxide) , or poly(hydroxy butyrate/hydroxy valerate) which will function to increase the water sensitivity of the adhesives which may be desired for some applications.
  • hydrophilic polymers such as poly(vinyl alcohol) , hydroxyethyl cellulose, starch, modified starch, poly(vinyl methyl ether) , poly(ethylene oxide) , or poly(hydroxy butyrate/
  • An exemplary procedure involves placing approximately 40% of the total tackifying resin concentration with all the polymer, wax, plasticizers and stabilizers in a jacketed mixing kettle, preferably in a jacketed heavy duty mixer, which is equipped with rotors and thereupon raising the temperature to a range of from up to about 190°C. After the resin has melted, the temperature is lowered to 150° to 165°C. Mixing and heating are continued until a smooth, homogeneous mass is obtained whereupon the remainder of the tackifying resin is thoroughly and uniformly admixed therewith.
  • the adhesives disclosed herein may be employed in a wide variety of uses as are known in the art. The adhesives described herein may be effectively utilized in a variety of packaging and carton sealing applications.
  • the non-pressure sensitive adhesives may also be used to bind a plurality of sheets in a wide range of bookbinding operations. They may also be used for laminating tissue and/or screen-reinforced tissue layers such as are used in individual or roll use applications as in wipers, paper towels, toilet tissue and other consumer or industrial end uses.
  • the resultant adhesives may be used in the assembly or construction of various disposable applications including, but not limited to, sanitary napkins, disposable diapers, hospital gowns, bed pads and the like.
  • adhesives are useful for the assembly of disposable articles using multi-line construction techniques wherein at least one flexible film substrate is bonded to at least one tissue, non- woven, polyolefin or other flexible polymeric film substrate.
  • the adhesives may be useful in the bonding of elastic to polyethylene, polypropylene or non-woven substrate so as, for example, to impart elongation resistant gathers thereto.
  • the adhesive may also be utilized in less demanding disposable construction applications such as for end or perimeter sealing.
  • Peel Temperature Test A bead of test adhesive approximately 1/8 inch in diameter is applied at 325°F to 350°F with a glass rod onto 60 pound/ream kraft paper. A second sheet of the same paper is superimposed on the first sheet within 2 seconds and pressed thereto to form a kraft-to-kraft bond. The bonded sheets are then cut perpendicular to the adhesive line into 1 inch wide strips. Duplicate bonded specimens are placed in an oven with one free end of the specimen attached to a fixed support and a 100 gram load suspended from the other sheet at the same end of the bond. The oven temperature is then increased in 10°F increments at 15 minute intervals.
  • Shear Temperature Test Samples are prepared as in peel temperature test but separate sheets of Kraft at opposite ends of the bonded specimen are suspended and weighted to stress the bond in a shear mode. The temperature of the oven is increased as in peel test until failure occurs.
  • Adhesion Test A molten bead of hot melt at 325°F to 350°F was drawn across the middle (widthwise) of a 1" x 3" strip of Kraft paper. A second strip of Kraft paper was then immediately superimposed upon the first and a 50 gram weight placed on top of the construction. The Kraft to Kraft bonds were then aged 24 hours at either room temperature (RT or 70°F) or at 40°F. After aging, the samples were stressed by hand at the temperature of storage in a 90° peel mode. The presence or absence of fiber tear was then noted.
  • test results presented above show the adhesives to be particularly suitable for packaging applications such as case and carton sealing due to its low viscosity, good fiber tear and acceptable peel and shear values.
  • compositions and test results are shown in Table II.
  • NC 350°F
  • Foral NC is a calcium salt of rosin from Hercules Irganox 1010 is a hindered phenol antioxidant from Ciba Geigy

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

Des compositions de colle thermofusible autoadhésive sont préparées à partir de 20 à 98 % en poids d'un homo- ou copolymère polylactide contenant au moins 20 pour cent en mole du composant lactide; de 2 à 80 % en poids d'une colle polaire présentant un point de ramollissement (tel que décrit par l'ASTM-E 26) supérieur à environ 60 °C; de 0 à 50 % en poids d'un plastifiant; de 0 à 30 % en poids d'un diluant à la cire; de 0 à 3 % par poids d'un stabilisant; et de 0 à 20 % d'un polymère. En utilisant un copolymère biodégradable, thermoplastique, d'origine naturelle comme polymère de base, ces colles constituent un progrès par rapport à la technique antérieure des colles thermofusibles autoadhésives en réduisant la dépendance vis à vis des produits du pétrole et en perfectionnant les colles thermofusibles auto-adhésives qui, soit se dégradent naturellement après avoir été en contact du sol, soit peuvent être compostées.Self-adhesive hot-melt adhesive compositions are prepared from 20 to 98% by weight of a polylactide homopolymer or copolymer containing at least 20 mole percent of the lactide component; from 2 to 80% by weight of a polar adhesive having a softening point (as described by ASTM-E 26) greater than about 60 ° C; from 0 to 50% by weight of a plasticizer; from 0 to 30% by weight of a wax diluent; from 0 to 3% by weight of a stabilizer; and from 0 to 20% of a polymer. By using a biodegradable, thermoplastic, naturally occurring copolymer as the base polymer, these adhesives constitute an improvement over the prior art of self-adhesive hot-melt adhesives by reducing the dependence on petroleum products and by improving self-adhesive hot-melt adhesives. -adhesives which either degrade naturally after being in contact with the ground, or can be composted.

Description

POLYLACTIDE CONTAINING HOT MELT ADHESIVE BACKGROUND OF THE INVENTION Hot melt adhesives are used commercially for a wide variety of applications. The major advantage of hot melt adhesive systems is the lack of a carrier fluid which eliminates the need for drying the adhesive film once it is applied to the substrate. This elimination of the drying step overcomes hazards associated with solvent usage and also allows for faster production line speeds and lower transportation costs. Depending on the desired use, the degree of tack of the hot melt adhesives may be varied over a wide range to produce adhesives varying from pressure sensitive to non-pressure sensitive in character. Non-pressure sensitive are used, for example, in bookbinding, bag ending, case and carton sealing. Pressure sensitive hot melts are used in many applications, and particularly in disposables such as diapers, sanitary products and the like, where room temperature tack and long open time are required. Hot melt adhesives have historically been based on petroleum derived polymers such as polyethylene, ethylene-vinyl acetate, styrenic block copolymers, and polypropylene to name a few. These compositions are further tackified, plasticized, and reinforced with a variety of resins, oils and waxes which are derived from both petroleum and naturally occurring feedstocks such as wood, gum and tall oil rosin and terpenes. These classic compositions suffer from the cyclical price cycles common to all oil derived materials, and also are generally very resistant to degradation once the articles employing them are disposed of.
The present invention stems from the growing movement away from petroleum derived raw materials to those derived from renewable, natural resources and as part of an effort to utilize raw materials which have demonstrated some level of degradation. The present invention utilizes a class of naturally occurring or synthetically produced thermoplastic, biodegradable .copolymers derived from a non-petroleum feedstock as the base polymer. Such compositions advance the state of the art of hot melt adhesives by alleviating the dependence on petroleum based materials and by allowing for the development of hot melt adhesives which either degrade naturally after coming in contact with the soil or which can be composted.
SUMMARY OF THE INVENTION It has been discovered that hot melt adhesive compositions suitable for a variety of applications are obtained by use of polylactide (i.e., the bimolecular cyclic ester of lactic acid) or copolymers with other lactones such as glycolide and caprolactone, tackifiers, and optionally, waxes and/or plasticizers. The adhesives may be formulated using conventional additives and may vary from pressure sensitive to non-pressure sensitive in character depending upon the desired application.
In its broadest aspect, the present invention is directed to hot melt adhesive compositions comprising 20 to 98% by weight of a polylactide homo- or copolymer where the copolymer contains at least 20 molar percent of the lactide component (1 or d or d,l or meso or mixtures thereof) 2 to 80% by weight of a polar tackifier having a Ring and Ball softening point (as described by ASTM E- 26) greater than about 60°C; 0 to 50% by weight of a plasticizer; 0 to 30% by weight of a wax diluent and 0-3% by weight of a stabilizer.
It will be recognized that the general formulations described above can be adapted to include a wide variety of hot melt adhesive compositions, the more precise formulations of which will vary depending upon the specific end use, the knowledge of which is readily available to those skilled in the particular art.
Thus, in general, pressure sensitive adhesives can be prepared using 20 to 70% by weight of the polylactide homo- or copolymer, 10 to 60% of a tackifying resin, 10 to 50% plasticizer and 0 to 3% of a stabilizer. Preferred pressure sensitive adhesives are prepared using 30 to 60% of the polylactide homo- or copolymer; 20 to 50% of a tackifying resin, preferably a terpene phenolic resin; and 20 to 30% of a plasticizer, preferably Pycal 94, a phenyl ether of poly(ethylene glycol) from ICI; or Hercolyn D, a methyl ester of hydrogenated rosin from Hercules. Lower levels of plasticizer may also be employed to produce adhesives useful for various end uses such as in construction adhesives for disposable products where some initial degree of tack is needed but no residual pressure sensitive properties are required.
In general, non-pressure sensitive adhesives can be prepared using 20-98% by weight of the polylactide homo- or copolymer, 2-80% tackifying resin, 0-30% of a wax-like diluent, 0-30% plasticizer and 0 to 3% of a stabilizer. Preferred non-pressure sensitive adhesives are prepared using 30-80% of the polylactide homo- or copolymer; 10- 40% tackifying resin, preferably terpene-phenolic resins or rosin derivatives; 0-25% of a plasticizer, preferably the phenyl ether of poly(ethylene glycol) or the methyl ester of hydrogenated wood rosin; and 0-20% of a wax-like diluent, preferably hydrogenated castor oil (also known as castor wax) or 12-hydroxystearamide. Additionally, polymers other than the polylactide may be incorporated into the hot melt adhesives at levels less than about 20% by weight. Representative formulations and applications are discussed hereinbelow and illustrated by the examples, however, these should not be construed as limiting the invention.
DETAILED DESCRIPTION OF THE INVENTION The major component of the adhesive of the invention, present in an amount of 20 to 98% by weight of the adhesive, comprises a homo- or copolymer of polylactide containing at least 20 molar percent of the lactide comonomer. The general structure of the polylactide is shown below:
Suitable polymers for use herein have a number average molecular weight (Mn) within the range of 10,000 to 200,000.
While poly(d,1-lactide) and the meso- are essentially amorphous, poly(1-lactide) and poly(d- lactide) is crystalline in nature and has a crystalline melting point of 186°C depending on its molecular weight and stereopurity. The polymers may be prepared by ring- opening polymerization of the bimolecular cyclic ester of lactic acid with acid or base catalysts such as PbO, SnCl2, SnCl4, ZnCl2, SbF5, Sb203, or triethylamine using solution, precipitation or melt processes. Alternatively, they may be obtained commercially from Henley Chemicals, Inc. under the Resomer® tradename; from Poly Sciences Inc. or from Ecological Chemical Products Company (EcoChem) .
In addition to homopolymers of poly(1-lactide) , poly (d-lactide) , poly(d,1-lactide) , and poly(meso-lactide) suitable polymers for use herein may also be prepared by copolymerization with other lactones such as glycolide or caprolactone. Thus, poly(d,1-lactide-co-glycolide) polymers containing equimolar amounts of the lactide and glycolide components are available from Henley Chemicals as Resomer RG502, 503, 504, 505 and 506 and are suitable for use herein. In addition, poly(d,1-lactide-co- glycolide) polymers known as Resomer RG752, 755 and 756 containing 75% of the lactide component as well as the Resomer 858 polymer which contains 85% lactide are also suitable.
The tackifying resins useful in the adhesive compositions are generally polar in nature and have a Ring and Ball softening point greater than 60°C and include rosin and rosin derivatives, terpene phenolics, pure phenolic resins, and the like. More particularly, the useful tackifying resins include any compatible resins or mixtures thereof such as (1) natural and modified rosins such, for example, as gum rosin, wood rosin, tall oil rosin, distilled rosin, hydrogenated rosin, dimerized rosin, and polymerized rosin; (2) glycerol and pentaerythritol esters of natural and modified rosins, such, for example as the glycerol ester of pale, wood rosin, the glycerol ester of hydrogenated rosin, the glycerol ester of polymerized rosin, the pentaerythritol ester of hydrogenated rosin, and the phenolic-modified pentaerythritol ester of rosin; (3) phenolic modified terpene resins and hydrogenated derivatives thereof such, for example, as the resin product resulting from the condensation, in an acidic medium, of a bicyclic terpene and a phenol; (4) thermoplastic alkyl phenolic resins such as those described in U.S. Patent Nos. 4,073,776 and 4,023,826. Mixtures of two or more of the above described tackifying resins, as well as blends of the above resins with small amounts of (e.g., less than about 10% of the adhesive) less compatible resins may be utilized for some formulations. While the tackifier may comprise up to about 80% of the adhesive, it is generally used in amounts of 10 to 60% by weight.
Depending on the end-use application, and particularly for uses requiring pressure sensitive properties, various compatible plasticizing or extending oils may also be present in the composition. Preferred compatible plasticizers include phthalate plasticizers such as dioctyl phthalate; liquid polyesters such as Dynacol 720 from Huls; benzoate plasticizers such as 1,4- cyclohexane dimethanol dibenzoate (e.g., Benzoflex 352 available commercially from Velsicol) ; phosphate plasticizer such as t-butylphenyl diphenyl phosphate (e.g., Santicizer 154 available commercially from Monsanto) ; poly(ethylene glycols) and derivatives thereof such as the phenyl ether of poly(ethylene glycol) (e.g., Pycal 94 available commercially from ICI) as well as liquid rosin derivatives having Ring and Ball melting points below about 60°C such as the methyl ester of hydrogenated rosin (e.g., Hercolyn D from Hercules); as well as vegetable and animal oils such as glyceryl esters of fatty acids and polymerization products thereof.
Other applications conventionally employing adhesives based on these polylactide polymers may require the use of wax diluents in order to reduce the melt viscosity or cohesive characteristics of the hot melt adhesive compositions without appreciably decreasing their adhesive bonding characteristics. These waxes are often used in adhesives which do not exhibit pressure sensitive properties.
Suitable waxes include 12-hydroxystearamide wax, hydrogenated castor oil, oxidized synthetic waxes, poly(ethylene oxide) having a weight average molecular weight above about 1000 and functionalized synthetic waxes such as carbonyl containing Escomer HlOl from Exxon.
It should be recognized that some adhesive formulations described herein may contain both wax and plasticizer components so that the presence of one or the other is not mutually exclusive.
Among the applicable stabilizers or antioxidants which may be included herein are high molecular weight hindered phenols and multifunctional phenols such as sulfur and phosphorous-containing phenols. Representative hindered phenols include: 1,3,5- trimethyl-2,4,6-tris(3, 5-di-tert-butyl-4-hydroxy- benzyl)benzene; pentaerythritol tetrakis-3-(3,5-di-tert- butyl-4-hydroxyphenyl)propionate; n-octadecyl 3,5-di- tert-buty1-4-hydroxypheny1) propionate; 4,4'-methylene- bis (2,6-di-tert-butylphenol) ; 4,4'-thiobis (6-tert- butyl-o-cresol) ; 2,6-di-tert-butylphenol; 6-(4-hydroxy- phenoxy)-2,4-bis(n-octylthio)-1,3,5-triazine; di-n- octadecyl-3,5-di-tert-butyl-4-hydroxy-benzylphosphonate; 2-(n-octyl-thio)-ethyl 3,5-di-tert-butyl-4- hydroxybenzoate; and sorbitol hexa[3-(3,5-di-tert-butyl- 4-hydroxyphenyl)propionate] . If used, the stabilizer is present in levels of about 0.1 to 3% by weight. Optional additives may be incorporated into the hot melt compositions in order to modify certain properties thereof. Among these additives may be included colorants such as titanium dioxide; and fillers such as talc and clay, etc. There may also be present in the adhesive small amounts (e.g. , less than about 20% by weight, and preferably 5 to 20% by weight) of certain thermoplastic polymers such as ethylene vinyl acetate, ethylene acrylic acid, ethylene methyl aerylate and ethylene n-butyl acrylate copolymers containing about 12 to 50% vinyl acetate as well as caprolactone polymers. These polymers are employed in order to impart flexibility, toughness and strength. Alternatively and in particular, it may be desirable to incorporate into the hot melt adhesive up to 20% by weight of certain hydrophilic polymers such as poly(vinyl alcohol) , hydroxyethyl cellulose, starch, modified starch, poly(vinyl methyl ether) , poly(ethylene oxide) , or poly(hydroxy butyrate/hydroxy valerate) which will function to increase the water sensitivity of the adhesives which may be desired for some applications. These hot melt adhesive compositions may be formulated using techniques known in the art. An exemplary procedure involves placing approximately 40% of the total tackifying resin concentration with all the polymer, wax, plasticizers and stabilizers in a jacketed mixing kettle, preferably in a jacketed heavy duty mixer, which is equipped with rotors and thereupon raising the temperature to a range of from up to about 190°C. After the resin has melted, the temperature is lowered to 150° to 165°C. Mixing and heating are continued until a smooth, homogeneous mass is obtained whereupon the remainder of the tackifying resin is thoroughly and uniformly admixed therewith. The adhesives disclosed herein may be employed in a wide variety of uses as are known in the art. The adhesives described herein may be effectively utilized in a variety of packaging and carton sealing applications. The non-pressure sensitive adhesives may also be used to bind a plurality of sheets in a wide range of bookbinding operations. They may also be used for laminating tissue and/or screen-reinforced tissue layers such as are used in individual or roll use applications as in wipers, paper towels, toilet tissue and other consumer or industrial end uses. When formulated with plasticizers, the resultant adhesives may be used in the assembly or construction of various disposable applications including, but not limited to, sanitary napkins, disposable diapers, hospital gowns, bed pads and the like. In particular, adhesives are useful for the assembly of disposable articles using multi-line construction techniques wherein at least one flexible film substrate is bonded to at least one tissue, non- woven, polyolefin or other flexible polymeric film substrate. In addition, the adhesives may be useful in the bonding of elastic to polyethylene, polypropylene or non-woven substrate so as, for example, to impart elongation resistant gathers thereto. The adhesive may also be utilized in less demanding disposable construction applications such as for end or perimeter sealing.
In the following illustrative examples all parts are given by weight and all temperatures in degrees Celsius unless otherwise noted. EXAMPLE I
In preparing the following samples, a heavy duty mixer which had been heated to 190°C and which was equipped with a stirring paddle was charged with 40% of the tackifying resin, and/or diluent. After melting of the resins, stirring was then initiated whereupon the polylactide was added slowly at 190°C over a one-half hour period after which the temperature was lowered to 170°C. Heating and stirring were continued until a homogeneous mass was obtained whereupon the remainder of the tackifying resin and/or diluent was admixed therewith. The samples were tested using the following procedures: Viscosity measurements were determined after 30 minutes using a Brookfield viscometer (Spindle 27) at 350°F.
The adhesive was also subjected to Peel/Shear testing such as is conventionally required in the packaging industry. Peel Temperature Test: A bead of test adhesive approximately 1/8 inch in diameter is applied at 325°F to 350°F with a glass rod onto 60 pound/ream kraft paper. A second sheet of the same paper is superimposed on the first sheet within 2 seconds and pressed thereto to form a kraft-to-kraft bond. The bonded sheets are then cut perpendicular to the adhesive line into 1 inch wide strips. Duplicate bonded specimens are placed in an oven with one free end of the specimen attached to a fixed support and a 100 gram load suspended from the other sheet at the same end of the bond. The oven temperature is then increased in 10°F increments at 15 minute intervals. The temperature at which bond delamination occurred is specified as the peel temperature. Shear Temperature Test: Samples are prepared as in peel temperature test but separate sheets of Kraft at opposite ends of the bonded specimen are suspended and weighted to stress the bond in a shear mode. The temperature of the oven is increased as in peel test until failure occurs.
Adhesion Test: A molten bead of hot melt at 325°F to 350°F was drawn across the middle (widthwise) of a 1" x 3" strip of Kraft paper. A second strip of Kraft paper was then immediately superimposed upon the first and a 50 gram weight placed on top of the construction. The Kraft to Kraft bonds were then aged 24 hours at either room temperature (RT or 70°F) or at 40°F. After aging, the samples were stressed by hand at the temperature of storage in a 90° peel mode. The presence or absence of fiber tear was then noted.
The compositions and the results of the testing are shown in Table I.
TABLE I
1 2 3 4 5 6 7 Poly(l- lactidβ)
Poly(l- 21.5 18.0 15.0 15.0 17.0 15.0 15.0 .... lactide)
Hercolyn D 7.5 9.0 9.0 6.0 10.0 9.0 9.0 ____
PEG-200 1.0 3.0 ____ ____ —__ ____ ____ .....
Pycal 94 _____ ____ 3.0 6.0 3.0 3.0 3.0 ....
Nirez 300 ______ ____ 3.0 3.0 -_— ____ ____ ....
Super .... .... 3.0 ._.______-_ .M.M^^
Fluidity
Hylon VII
40% VA, _._--.-- .... .... 3.0 «»_____ ....
EVA
Compat¬ Yes Yes Yes Yes Yes Yes Yes .... ibility
DSC
Tg N/T N/T N/T - 75°C
Tm 47°C 32βC 161° 159° 162° 4°C 31°C 186°C
169° 160° C C C 161° 162°
Viscosity C C 400 N/T 250 C C
(cps) @ N/T 235 80 N/T 100 N/T N/T
350°F N/T 120 >200 N/T >200 120° 120°
Peel N/T >200 F.T. N/T F.T. >200 >200
(°F) N/T F.T. F.T. N/T F.T. 0 O
Shear N/T F.T. F.T. F.T.
(°K) F.T. F.T.
Adhesion
(Kraft)
RT (40°)
Hercolyn D - methyl ester of hydrogenated rosin from Hercules
PEG-200 - polyethylene glycol from Union Carbide
Pycal 94 - phenyl ether of polyethylene glycol from ICI
Nirez 300 - terpene- phenolic resin from Arizona Chemical
N/T - not tested
Super Fluidity Hylon VII - modified starch propionate
The test results presented above show the adhesives to be particularly suitable for packaging applications such as case and carton sealing due to its low viscosity, good fiber tear and acceptable peel and shear values.
Similar performance results would be expected from the use of comparable amounts of poly(d,1-lactide) or copolymers thereof, however, due to the more amorphous nature of the poly(d,1-lactide) the later polymers would be particularly suitable for hot melt pressure sensitive applications.
Another series of hot melt adhesives were formulated and tested as described above. In this series, the adhesives were also tested for thermal stability by storing at 350°F for 72 hours and then noting the appearance of the adhesive.
The compositions and test results are shown in Table II.
TABLE II
8 9 10
Poly(l- 25.0 25.0 25.0 lactide)
Hercolyn D ___ 15.0 15.0
Pycal 94 15.0 ___ ___
Nirez 300 10.0 ___ 10.0
Foral NC ___ 10.0
Irganox 1010 0.1 0.1 0.1
Viscosity @ 335 cps 470 cps 4125 cps
350°F 100 >80°F 140
Peel >200 150 >200
Shear F.T. F.T. F.T.
Adhesion RT F.T. F.T F.T
40βF
Thermal None Yes None
Stability None None None
(72 Brown Black Light hours/350°F) None Yes Brown
Skin None None None
Gel 15 cps None
Color 175 cps
Separation
Char
Final
Viscosity §
350°F Foral NC is a calcium salt of rosin from Hercules Irganox 1010 is a hindered phenol antioxidant from Ciba Geigy
The results presented in Table II indicate that samples 8 and 10 have acceptable thermal stability for most applications. It is also to be noted that the thermal stability may be even further improved by pre- drying of the polylactide polymer since the polymer picks up moisture when stored as a raw material. The results also show that sample 10 would be particularly suitable for industrial bag applications where high heat resistance and relatively higher viscosity are required. Sample 8 shows particular use for case and carton sealing. Sample 9, while not having as high a degree of heat resistance, would nonetheless be suitable for less stringent heat resistant applications such as bottle labelling.

Claims

1. A hot melt adhesive composition comprising 20 to 98% by weight of a polylactide mono- or copolymer containing at least 20 molar percent of the lactide component; 2 to 80% by weight of a polar tackifier having a Ring and Ball softening point (as described by ASTM E-26) greater than about 60°C; 0 to 50% by weight of a plasticizer; 0 to 30% by weight of a wax diluent and 0-3% by weight of a stabilizer.
2. The adhesive of Claim 1 wherein the polylactide is a homopolymer of 1- or d,1-lactide.
3. The adhesive of Claim 1 wherein the polylactide is a co-polymer of (1-lactide) or (d,1-lactide) with glycolide or caprolactone.
4. The adhesive of Claim 1 wherein the polylactide has a number average molecular weight within the range of 10,000 to 200,000.
5. The adhesive of Claim 1 wherein the tackifying resin is selected from the group consisting of (1) natural and modified rosins; (2) glycerol and pentaerythritol esters of natural and modified rosins; (3) phenolic modified terpene resins and hydrogenated derivatives thereof; (4) thermoplastic alkyl phenolic resins; and mixtures thereof.
6. The adhesive of Claim 1 wherein the plasticizer is selected from the group consisting of phthalate plasticizers; liquid polyesters; benzoate plasticizers; phosphate plasticizers; poly(ethylene glycols) and derivatives thereof; and liquid rosin derivatives having Ring and Ball melting points below about 60°.
7. The adhesive of Claim 1 wherein the wax is selected from the group consisting of hydroxy stearamide wax, hydrogenated castor oil, oxidized synthetic waxes, poly(ethylene oxide) having a weight average including weight above about 1000 and functionalized synthetic waxes.
8. The adhesive of Claim 1 wherein there is also present up to 20% by weight of a thermoplastic polymer selected from the group consisting of polycaprolactone ethylene vinyl acetate, ethylene acrylic acid, ethylene methyl acrylate and ethylene n-butyl acrylate copolymers containing 12 to 50% comonomer.
9. The adhesive of Claim 1 wherein there is also present up to 20% by weight of a polymer selected from the group consisting of polyvinyl alcohol, hydroxyethyl cellulose, polyvinyl methyl ether, poly(ethylene oxide) , or poly(hydroxy butyrate hydroxy valerate) .
10. The adhesive of Claim 1 wherein there is also present up to 20% by weight starch or modified starch.
11. A hot melt pressure sensitive adhesive composition comprising 20 to 70% by weight of a polylactide homo- or copolymer containing at least 20 molar percent of the lactide component, 10 to 60% of a tackifying resin, 0 to 3% of a stabilizer and 10 to 50% plasticizer.
12. The adhesive of Claim 11 comprising 30 to 60% of the polylactide copolymer; 20 to 50% of the tackifying resin, 20 to 30% of the plasticizer and 0 to 3% stabilizer.
13. The adhesive of Claim 11 wherein the polylactide polymer is poly(d,1-lactide) or a copolymer thereof.
14. The adhesive of Claim 11 wherein the tackifying resin is a terpene phenolic and the plasticizer is a phenyl ether of poly(ethylene glycol) .
15. The adhesive of Claim 11 wherein there is also present up to 20% by weight of a thermoplastic polymer selected from the group consisting of polycaprolactone ethylene vinyl acetate, ethylene acrylic acid, ethylene methyl acrylate and ethylene n-butyl acrylate copolymers containing 12 to 50% comonomer.
16. The adhesive of Claim 10 wherein there is also present up to 20% by weight of a polymer selected from the group consisting of polyvinyl alcohol, hydroxyethyl cellulose, polyvinyl methyl ether, poly(ethylene oxide) , or poly(hydroxy butyrate hydroxy valerate) .
17. The adhesive of Claim 11 wherein there is also present up to 20% by weight starch or modified starch.
18. A non-pressure sensitive adhesive composition comprising 20-98% by weight of a polylactide homo- or copolymer containing at least 20 molar percent lactide, 2-80% tackifying resin, 0-30% of a wax-like diluent, 0- 25% plasticizer and 0 to 3% stabilizer.
19. The adhesive of Claim 18 wherein the polylactide is poly(1-lactide) or a copolymer thereof.
20. The adhesive of Claim 18 wherein the tackifying resin is a terpene-phenolic resin or rosin derivative, the plasticizer is a phenyl ether of poly(ethylene glycol) or the methyl ester of hydrogenated wood rosin and the wax diluent is hydrogenated castor oil.
21. The adhesive of Claim 18 wherein there is also present up to 20% by weight of a thermoplastic polymer selected from the group consisting of ethylene vinyl acetate, ethylene acrylic acid, ethylene methyl acrylate and ethylene n-butyl acrylate copolymers containing 12 to 50% comonomer as well as polycaprolactone.
22. The adhesive of Claim 18 wherein there is also present up to 20% by weight of a polymer selected from the group consisting of polyvinyl alcohol, hydroxyethyl cellulose, polyvinyl methyl ether, poly(ethylene oxide), or poly(hydroxy butyrate hydroxy valerate).
23. The adhesive of Claim 18 wherein there is also present up to 20% by weight starch or modified starch.
EP93922271A 1992-10-29 1993-09-20 Polylactide containing hot melt adhesive Ceased EP0618948A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US968564 1992-10-29
US07/968,564 US5252646A (en) 1992-10-29 1992-10-29 Polylactide containing hot melt adhesive
US153 1993-01-04
US08/000,153 US5312850A (en) 1993-01-04 1993-01-04 Polylactide and starch containing hot melt adhesive
PCT/US1993/008913 WO1994010257A1 (en) 1992-10-29 1993-09-20 Polylactide containing hot melt adhesive

Publications (1)

Publication Number Publication Date
EP0618948A1 true EP0618948A1 (en) 1994-10-12

Family

ID=26667282

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93922271A Ceased EP0618948A1 (en) 1992-10-29 1993-09-20 Polylactide containing hot melt adhesive

Country Status (5)

Country Link
EP (1) EP0618948A1 (en)
JP (1) JPH07502069A (en)
AU (1) AU659353B2 (en)
CA (1) CA2126849C (en)
WO (1) WO1994010257A1 (en)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6010972A (en) * 1996-04-15 2000-01-04 Kimberly-Clark Worldwide, Inc. Oil-resistant disposable absorbent product
CA2274676A1 (en) 1996-12-31 1998-07-09 James Hongxue Wang Water-responsive polymer compositions and method of making the same
US6552162B1 (en) 1997-07-31 2003-04-22 Kimberly-Clark Worldwide, Inc. Water-responsive, biodegradable compositions and films and articles comprising a blend of polylactide and polyvinyl alcohol and methods for making the same
US6767961B1 (en) 2000-06-19 2004-07-27 Kimberly-Clark Worldwide, Inc. Blends of poly (vinyl alcohol) and poly (ethylene oxide) and articles made therewith
US6958371B1 (en) 2000-06-19 2005-10-25 Kimberly-Clark Worldwide, Inc. Method of making blends of poly(vinyl alcohol) and poly(ethylene oxide)
US6552124B2 (en) 2000-12-29 2003-04-22 Kimberly-Clark Worldwide, Inc. Method of making a polymer blend composition by reactive extrusion
US6500897B2 (en) 2000-12-29 2002-12-31 Kimberly-Clark Worldwide, Inc. Modified biodegradable compositions and a reactive-extrusion process to make the same
US6579934B1 (en) 2000-12-29 2003-06-17 Kimberly-Clark Worldwide, Inc. Reactive extrusion process for making modifiied biodegradable compositions
US7053151B2 (en) 2000-12-29 2006-05-30 Kimberly-Clark Worldwide, Inc. Grafted biodegradable polymer blend compositions
EP1236753A1 (en) 2001-03-02 2002-09-04 Hycail B.V. Environmentally degradable polymeric compounds, their preparation and use as hot melt adhesive
US6890989B2 (en) 2001-03-12 2005-05-10 Kimberly-Clark Worldwide, Inc. Water-responsive biodegradable polymer compositions and method of making same
JP2002097437A (en) * 2001-09-17 2002-04-02 Toyobo Co Ltd Biodegradable polyester adhesive
US8283435B2 (en) 2003-02-21 2012-10-09 Metabolix, Inc. PHA adhesive compositions
JP4724111B2 (en) * 2003-02-21 2011-07-13 メタボリックス インコーポレイティッド PHA blend
DE10358779B4 (en) * 2003-12-12 2007-09-06 Biomet Deutschland Gmbh Biodegradable adhesive composition and its use
WO2005066256A1 (en) 2003-12-30 2005-07-21 Metabolix, Inc. Nucleating agents
JPWO2008044651A1 (en) * 2006-10-06 2010-02-12 国立大学法人大阪大学 Polylactic acid adhesive
US8870871B2 (en) 2007-01-17 2014-10-28 University Of Massachusetts Lowell Biodegradable bone plates and bonding systems
FR2912753B1 (en) * 2007-02-16 2012-10-12 Arkema France COPOLYAMIDE, COMPOSITION COMPRISING SUCH COPOLYAMIDE AND USE THEREOF
FR2937975B1 (en) * 2008-11-06 2011-05-13 Cvlc THERMOFUSIBLE ADHESIVE WITH LOW APPLICATION POLYMER LACTIC ACID TEMPERATURE AND PROCESS FOR PREPARING THE SAME
KR101145374B1 (en) * 2010-11-02 2012-05-15 대상 주식회사 Composition for starch based hot melt adhesive
DE102012202822A1 (en) * 2012-02-24 2013-08-29 Tesa Se Biodegradable pressure-sensitive adhesive
JP5883344B2 (en) 2012-04-26 2016-03-15 ヘンケルジャパン株式会社 Hot melt adhesive
JP5921946B2 (en) * 2012-04-26 2016-05-24 ヘンケルジャパン株式会社 Hot melt adhesive
CN104755538B (en) 2012-08-17 2018-08-31 Cj 第一制糖株式会社 Bio-rubber modifying agent for blend polymer
JP5925094B2 (en) 2012-09-27 2016-05-25 ヘンケルジャパン株式会社 Hot melt adhesive for labels
DE102013205144A1 (en) * 2013-03-22 2014-09-25 Novamelt GmbH Klebstofftechnologie Adhesive composition based on optionally modified polylactide, process for their preparation and use of the adhesive composition
DE102013004909A1 (en) 2013-03-22 2014-10-09 Jowat Ag New adhesive compositions based on renewable raw materials and their use
JP6057837B2 (en) 2013-05-30 2017-01-11 ヘンケルジャパン株式会社 Hot melt adhesive
CN105531308B (en) 2013-05-30 2021-08-10 Cj 第一制糖株式会社 Recycle blends
JP6154725B2 (en) * 2013-10-24 2017-06-28 ヘンケルジャパン株式会社 Hot melt adhesive
ES2820544T3 (en) 2014-03-27 2021-04-21 Cj Cheiljedang Corp Highly charged polymeric systems
KR20160140718A (en) * 2014-03-31 2016-12-07 쓰리엠 이노베이티브 프로퍼티즈 컴파니 Bio-based hot melt adhesives
JP2017521507A (en) * 2014-06-03 2017-08-03 ピュラック バイオケム ビー. ブイ. Non-reactive hot melt adhesive, its manufacture and its use in sealed packages
ES2765700T3 (en) * 2015-10-01 2020-06-10 Purac Biochem Bv Non-reactive hot melt adhesive with setting time improver
JP6531658B2 (en) * 2016-01-28 2019-06-19 東洋インキScホールディングス株式会社 Hot melt adhesive composition and coated article
CN106947403A (en) * 2017-02-27 2017-07-14 东莞市蓝恩科技有限公司 A kind of biodegradable diaphragm
JP6419376B1 (en) * 2018-05-18 2018-11-07 株式会社Bpコンサルティング Method for producing polylactic acid hot melt adhesive
CA3174463A1 (en) * 2020-03-06 2021-09-10 Totalenergies Corbion Bv Multilayer polylactide based structure and articles made therefrom
CN112708257B (en) * 2020-12-31 2022-06-17 宁波能之光新材料科技股份有限公司 High-elasticity wear-resistant outdoor wood-plastic surface layer material and preparation method thereof
ES2942331B2 (en) * 2022-12-29 2023-11-15 Asociacion Investig De Industria Textil Aitex PROCEDURE FOR THE MANUFACTURE OF A HOT FUSE ADHESIVE AND HOT FUSE ADHESIVE OBTAINED BY SUCH PROCEDURE

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4156676A (en) * 1978-03-27 1979-05-29 Chevron Research Company Hot melt adhesives having improved thermal stability
DE3220324C2 (en) * 1981-06-03 1994-02-03 Daicel Chem Mass containing polycaprolactone
EP0428620B1 (en) * 1988-08-08 1999-03-03 Biopak Technology, Ltd. A method of plasticizing lactide polymers.
EP0525245A1 (en) * 1991-08-01 1993-02-03 NOVAMONT S.p.A. Disposable absorbent articles
HU216971B (en) * 1991-05-03 1999-10-28 Novamont S.P.A. Biologically decomposable polymer compositions based on starch and thermoplastic synthetic material
US5169889A (en) * 1992-01-27 1992-12-08 National Starch And Chemical Investment Holding Corporation Poly hydroxybutyrate/hydroxyvalerate based hot melt adhesive

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9410257A1 *

Also Published As

Publication number Publication date
CA2126849C (en) 1999-01-12
AU659353B2 (en) 1995-05-11
WO1994010257A1 (en) 1994-05-11
JPH07502069A (en) 1995-03-02
CA2126849A1 (en) 1994-05-11
AU5133293A (en) 1994-05-24

Similar Documents

Publication Publication Date Title
AU659353B2 (en) Polylactide containing hot melt adhesive
US5252646A (en) Polylactide containing hot melt adhesive
US5312850A (en) Polylactide and starch containing hot melt adhesive
US5169889A (en) Poly hydroxybutyrate/hydroxyvalerate based hot melt adhesive
US5583187A (en) Hot melt adhesives based on hydroxy-functional polyesters
US5574076A (en) Sucrose benzoate as a tackifier for water sensitive or biodegradable hot melt adhesives
US5256717A (en) Hot melt adhesives useful in temporary bonding operations
US5356963A (en) Hydrophilic hot melt adhesives
AU702877B2 (en) Hot melt adhesives based on sulfonated polyesters
AU2001241975B2 (en) Sulfonated copolyester based water-dispersible hot melt adhesive
US5952405A (en) Lactide graft copolymers and hot melt adhesives prepared from same
US4822653A (en) Recyclable hot melt adhesive compositions
JP4620213B2 (en) Use of sulfonated polyesters and anionic or cationic plasticizers in hot melt formulations
AU2001241975A1 (en) Sulfonated copolyester based water-dispersible hot melt adhesive
US5852117A (en) Process for making lactide graft copolymers
EP0699800A2 (en) Hot melt coatings for paper and paperboard

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19940628

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE DK ES FR GB IT NL

17Q First examination report despatched

Effective date: 19951228

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 19970806