USRE48818E1 - Hot-melt adhesive substance - Google Patents
Hot-melt adhesive substance Download PDFInfo
- Publication number
- USRE48818E1 USRE48818E1 US16/237,506 US200716237506A USRE48818E US RE48818 E1 USRE48818 E1 US RE48818E1 US 200716237506 A US200716237506 A US 200716237506A US RE48818 E USRE48818 E US RE48818E
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- US
- United States
- Prior art keywords
- melt adhesive
- hot melt
- hygiene article
- fiber material
- diaper
- 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.)
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- 0 [1*]C([2*])([3*])[4*] Chemical compound [1*]C([2*])([3*])[4*] 0.000 description 5
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives 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
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
- C09J123/0807—Copolymers of ethene with unsaturated hydrocarbons only containing more than three carbon atoms
- C09J123/0815—Copolymers of ethene with aliphatic 1-olefins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/58—Adhesives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives 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
- C09J123/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions 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
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
- C08L23/22—Copolymers of isobutene; Butyl rubber; Homopolymers or copolymers of other iso-olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition 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
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
Definitions
- the invention relates to a hot melt adhesive for adhesively bonding fibrous materials such as random fiber nonwovens or woven textiles to smooth substrate surfaces such as plastic films or metal foils.
- panty diapers comprise an inner layer which is readily permeable to liquids, then a fibrous inner layer, preferably a nonwoven, which contains absorbent materials such as superabsorbents and finally an outer plastic film which is impermeable to water and liquids of all types.
- the multilayer materials have to be joined to one another sufficiently strongly for them not to delaminate or slip during their intended use and also for them to offer sufficiently good comfort when worn.
- the adhesives in particular the adhesives for adhesively bonding the surface of the nonwoven to the water-impermeable film have to meet demanding requirements.
- the adhesive bond has to be very strong and durable even at elevated temperatures, it has to withstand considerable mechanical stresses and it must not be water-sensitive.
- the elasticity and flexibility of the various materials in the hygiene article and also their use properties must not be impaired by the presence of the adhesive.
- solvent-free adhesives which can be applied or sprayed on in very thin layers and have a high adhesive strength even in very small amounts by weight are required.
- the manufacture of particularly light articles having good comfort when worn should be made possible in this way.
- Hot melt adhesives containing styrene-isoprene-containing or styrene-butadiene-containing block copolymers are prior art.
- Styrene block copolymers as such without additional tackifiers are not sticky (do not have tack).
- resins or oils are added to the styrene-containing block copolymers. These additives are permanently sticky and difficult for the user to handle. In addition, they tend to penetrate through the nonwoven, which can lead to colored spots and a less favorable optical appearance of the hygiene articles.
- relatively thick nonwoven materials are necessary when such hot melt adhesives are used, which runs counter to the consumers' desire for thin and light hygiene articles.
- WO 01/14487 describes hot melt adhesives and their use as construction adhesives in the production of diapers.
- the hot melt adhesives contain copolymers of ethylene and C 3 -C 20 -alpha-olefins prepared in the presence of metallocene as catalyst, in particular ethylene-1-butene copolymers as are obtainable, for instance, under the trade name EXACT or ethylene-1-octene copolymers as are obtainable under the trade names AFFINITY and ENGAGE.
- EXACT ethylene-1-butene copolymers
- AFFINITY and ENGAGE ethylene-1-octene copolymers
- hot melt adhesives containing polyolefin waxes prepared using metallocene compounds as catalysts and their use describe hot melt adhesives containing polyolefin waxes prepared using metallocene compounds as catalysts and their use. These references also disclose that such polyolefin waxes have glass transition temperatures T g of less than or equal to ⁇ 10° C. It was therefore an object of the present invention to develop a hot melt adhesive which is solvent-free, odorless and both toxicologically and ecotoxicologically acceptable.
- the hot melt adhesive sought should have a viscosity of less than 15 000 mPa ⁇ s at a temperature of 150° C. and be able to be sprayed and applied uniformly as a very thin film at temperatures in the range from 100 to 180° C., without penetrating completely through the nonwoven material. Furthermore, a hot melt adhesive which displays its full adhesive effect and develops a very good adhesive strength even at a weight per unit area of less than 6 g/m 2 is desired.
- a hot melt adhesive of the type mentioned at the outset whose characterizing feature is that it contains at least one polyolefin which has been prepared by polymerization in the presence of metallocene as catalyst and has a ring/ball softening point in the range from 50 to 165° C. and a melt viscosity measured at a temperature of 170° C. in the range from 20 to 40 000 mPa ⁇ s.
- the hot melt adhesive of the invention is particularly suitable as hot melt adhesive for adhesively bonding fiber materials such as nonwoven material to films and for laminating hygiene articles when it contains one or more polyolefin(s) having a glass transition temperature T g of not more than ⁇ 10° C. and a melt flow index MFI of greater than 30 g/10 min, measured in accordance with ISO 1133 at a temperature of 190° C. and under a load of 2.16 kg.
- the hot melt adhesive of the invention can also be used advantageously for the adhesive bonding of textile materials, e.g. woven fabrics.
- the hot melt adhesive of the invention has outstanding properties in respect of its adhesive strength to the respective substrates even at temperatures in the range from 37 to 50° C. and it can, especially at viscosities in the range from 200 to 10 000 mPa ⁇ s at 150° C., be sprayed in a very thin layer onto surfaces. It surprisingly shows no tendency to penetrate through fibrous material such as nonwoven material or textile layers.
- the hot melt adhesive of the invention is not permanently sticky but becomes sticky only on processing from the melt and is therefore easy to handle for a user in the manufacture of hygiene articles of all types.
- the hot melt adhesive of the invention has good internal elasticity which is retained even at low temperatures and easily withstands the repeated deformations of the nonwoven and film materials adhesively bonded by means of it. It is water-insoluble, so that undesirable detachment phenomena cannot occur in the presence of water or high atmospheric humidity.
- Another advantage is the comparatively low viscosity at 100-180° C. of the hot melt adhesive of the invention, which makes particularly low processing temperatures possible. Shrinkage effects which can easily occur every now and again at high processing temperatures are thus avoided.
- the hot melt adhesive of the invention preferably contains polyolefin(s) having melt viscosities measured at a temperature of 170° C. of from 50 to 30 000 mPa ⁇ s, particularly preferably from 100 to 20 000 mPa ⁇ s.
- the hot melt adhesive of the invention is water- and solvent-free and also does not contain any plasticators and/or plasticizers.
- a hot melt adhesive containing the abovementioned polyolefins when these have a number average molar mass M n in the range from 500 to 20 000 g/mol, preferably from 800 to 10 000 g/mol, particularly preferably from 1000 to 5000 g/mol, and a weight average molar mass M w in the range from 1000 to 40 000 g/mol, preferably from 1600 to 30 000 g/mol and particularly preferably from 2000 to 20 000 g/mol.
- the molar mass is determined by gel permeation chromatography.
- the polyolefins present in the hot melt adhesive of the invention are homopolymers of propylene or higher 1-olefins or copolymers of olefins comprising propylene and/or higher 1-olefins and also, if appropriate, ethylene.
- higher 1-olefins preference is given to using linear or branched olefins having from 4 to 20 carbon atoms, preferably from 4 to 6 carbon atoms. These olefins can have an aromatic substituent conjugated with the olefinic double bond.
- 1-olefins examples are 1-butene, 1-hexene, 1-octene and 1-octadecene and also styrene.
- the copolymers preferably comprise from 70 to 99.9% by weight, particularly preferably from 80 to 99% by weight, of one type of olefin. Two or more of the olefins mentioned can be used for preparing the copolymers.
- the polyolefin present in the hot melt adhesive of the invention is a copolymer of propylene with at least one or more further monomers selected from among ethylene and linear or branched 1-olefins having from 4 to 20 carbon atoms, preferably from 4 to 10 carbon atoms, with the content of structural units derived from propylene preferably being from 70 to 99.9% by weight, particularly preferably from 80 to 99% by weight.
- the polyolefin present in the hot melt adhesive is a copolymer of ethylene and at least one branched or unbranched 1-olefin having from 3 to 20 carbon atoms, with the content of structural units derived from ethylene being from 70 to 99.9% by weight.
- the polyolefin present in the hot melt adhesive is a copolymer of propylene with from 0.1 to 30% by weight, in particular from 1 to 20% by weight, of ethylene.
- the hot melt adhesive of the invention preferably contains the polyolefin or polyolefins in an amount of from 2 to 100% by weight, preferably from 30 to 95% by weight, particularly preferably from 50 to 85% by weight, very particularly preferably from 70 to 80% by weight.
- the hot melt adhesive of the invention additionally contains one or more tackifier(s) selected from the group of resins.
- Aliphatic and cycloaliphatic or aromatic hydrocarbon resins are possible. These can be prepared by polymerization of particular resin oil fractions obtained in the refining of petroleum. Such resins, which can, for example, be modified by hydrogenation or functionalization, are obtainable, for example, under the trade names Eastoflex, RegalREZ, Kristalex, Eastotac, Piccotac (Eastman Chemical Company) or Escorez (ExxonMobil Chemical Company).
- resins are polyterpene resins prepared by polymerization of terpenes, for example pinene, in the presence of Friedel-Crafts catalysts, likewise hydrogenated polyterpenes, copolymers and terpolymers of natural terpenes, for example styrene-terpene or ⁇ -methylstyrene-terpene copolymers.
- Further possibilities are natural and modified rosins, in particular resin esters, glyceryl esters of tree resins, pentaerithrityl esters of tree resins and tall oil resins and hydrogenated derivatives thereof and also phenol-modified pentaerithrityl esters of resins and phenol-modified terpene resins.
- the resins mentioned are present in the hot melt adhesive of the invention either individually or in any combination in amounts, based on the total weight of the hot melt adhesive, in the range from 0 to 60% by weight, preferably from 10 to 50% by weight, particularly preferably from 15 to 30% by weight.
- the hot melt adhesive contains one or more of the above-described polyolefins and additionally a tackifier selected from among amorphous poly-alpha-olefins, e.g. of the grades of the Vestoplast® series (Degussa) or the “Rextac” grades from Huntsman, aliphatic, cycloaliphatic or aromatic hydrocarbon resins as are obtainable, for example, under the trade name “Escorez” from ExxonMobil, also polyisobutylene obtainable, for example, under the trade name “Oppanol” from BASF.
- a tackifier selected from among amorphous poly-alpha-olefins, e.g. of the grades of the Vestoplast® series (Degussa) or the “Rextac” grades from Huntsman, aliphatic, cycloaliphatic or aromatic hydrocarbon resins as are obtainable, for example, under the trade name “Escorez” from ExxonMo
- polyolefins such as low-pressure polyethylenes as are available, for example, under the name “Affinity” from Dow Chemical can also be present, also high-pressure polyethylenes including those containing polar comonomers, e.g. ethylene-vinyl acetate.
- the total mixture of the hot melt adhesive obtained in this way has a viscosity in the range from 100 to 10 000 mPa ⁇ s at 170° C., preferably from 120 to 9000 mPa ⁇ s at 170° C., particularly preferably from 130 to 8000 mPa ⁇ s at 170° C.
- pigments, antioxidants, odor binders, antimicrobial agents or colorants and fragrances can additionally be present.
- the hot melt adhesive of the invention is used in the production of various hygiene articles such as diapers, panty diapers, incontinence products, panty liners and sanitary towels, in particular for laminating fiber materials such as nonwoven materials to film.
- the hot melt adhesive of the invention is used in amounts of from 1 to 6 g/m 2 , preferably from 3 to 5.5 g/m 2 , for adhesively bonding nonwoven to film.
- fibrous materials in particular as nonwoven materials, preferably for diaper nonwovens, for total diaper construction and for incontinence products, it is possible to use natural or synthetic fiber materials composed of, for example, cotton, wool, silk, cellulose, linen, polyamide, for example Nylon or Perlon, polyester, for example polyethylene terephthalate or polypropylene terephthalate, polyvinyl chloride, polypropylene, polyethylene and also mixtures of these materials.
- the films can comprise customary materials such as polyethylene terephthalate, polycarbonate, polyethylene, polypropylene, polyvinyl chloride or polystyrene, but the hot melt adhesive of the invention is also suitable for joining fibrous materials to metal surfaces composed of aluminum or iron-containing metals.
- woven textiles as fibrous materials.
- such woven textiles can be adhesively bonded to one another or to nonwoven material or films.
- the invention further provides hygiene articles, preferably diapers, incontinence products, panty liners and sanitary towels, containing the hot melt adhesive of the invention.
- the metallocene polyolefins present in the hot melt adhesive of the invention are prepared using metallocene compounds of the formula I as catalysts.
- M 1 is a metal of group IVb, Vb or VIb of the Periodic Table, for example titanium, zirconium, hafnium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, preferably titanium, zirconium and hafnium.
- R 1 and R 2 are identical or different and are each a hydrogen atom, a C 1 -C 10 -, preferably C 1 -C 3 -alkyl group, in particular methyl, a C 1 -C 10 -, preferably C 1 -C 3 -alkoxy group, a C 6 -C 10 -, preferably C 6 -C 8 -aryl group, a C 6 -C 10 -, preferably C 6 -C 8 -aryloxy group, a C 2 -C 10 -, preferably C 2 -C 4 -alkenyl group, a C 7 -C 40 -, preferably C 7 -C 10 -arylalkyl group, a C 7 -C 40 -, preferably C 7 -C 12 -alkylaryl group, a C 8 -C 40 -, preferably C 8 -C 12 -arylalkenyl group or a halogen, preferably chlorine atom.
- R 3 and R 4 are identical or different and are each a monocyclic or polycyclic hydrocarbon radical which can form a sandwich structure with the central atom M 1 .
- R 3 and R 4 are preferably cyclopentadienyl, indenyl, tetrahydroindenyl, benzoindenyl or fluorenyl, with the basic molecules also being able to bear additional substituents or be bridged to one another.
- one of the radicals R 3 and R 4 can be a substituted nitrogen atom, where R 24 has the meaning of R 17 and is preferably methyl, tert-butyl or cyclohexyl.
- R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are identical or different and are each a hydrogen atom, a halogen atom, preferably a fluorine, chlorine or bromine atom, a C 1 -C 10 , preferably C 1 -C 4 -alkyl group, a C 6 -C 10 -, preferably C 6 -C 8 -aryl group, a C 1 -C 10 -, preferably C 1 -C 3 -alkoxy group, a —NR 16 2 , —SR 16 , —OSiR 16 3 , —SiR 16 or —PR 16 2 radical, where R 16 is a C 1 -C 10 -, preferably C 1 -C 3 -alkyl group or a C 6 -C 10 -, preferably C 6 -C 8 -aryl group or in the case of Si- or P-containing radicals can also be a halogen atom, preferably a chlorine
- R 13 is
- R 17 , R 18 and R 19 are identical or different and are each a hydrogen atom, a halogen atom, preferably a fluorine, chlorine or bromine atom, a C 1 -C 30 -, preferably C 1 -C 4 -alkyl group, in particular a methyl group, a C 1 -C 10 -fluoroalkyl, preferably CF 3 group, a C 6 -C 10 -fluoroaryl group, preferably a pentafluorophenyl group, a C 6 -C 10 -, preferably C 6 -C 8 -aryl group, a C 1 -C 10 -, preferably C 1 -C 4 -alk
- M 2 is silicon, germanium or tin, preferably silicon or germanium.
- R 13 is preferably ⁇ CR 17 R 18 , ⁇ SiR 17 R 18 , ⁇ GeR 17 R 18 , —O—, —S—, ⁇ SO, ⁇ PR 17 or ⁇ P(O)R 17 .
- R 11 and R 12 are identical or different and have the meaning given for R 17 .
- m and n are identical or different and are each zero, 1 or 2, preferably zero or 1, where m plus n is zero, 1 or 2, preferably zero or 1.
- R 14 and R 15 have the meanings of R 17 and R 18 .
- Suitable cocatalysts for metallocenes of the formula I are organoaluminum compounds, in particular aluminoxanes or else aluminum-free systems such as R 20 x NH 4-x BR 21 4 , R 20 x PH 4-x BR 21 4 , R 20 3 CBR 21 4 or BR 21 3 .
- x is from 1 to 4, the radicals R 20 are identical or different, preferably identical, and are each C 1 -C 10 -alkyl or C 6 -C 18 -aryl or two radicals R 20 together with the atom connecting them form a ring and the radicals R 21 are identical or different, preferably identical, and are each C 6 -C 18 -aryl which may be substituted by alkyl, haloalkyl or fluorine.
- R 20 is ethyl, propyl, butyl or phenyl and R 21 is phenyl, pentafluorophenyl, 3,5-bistrifluoromethylphenyl, mesityl, xylyl or tolyl.
- Organoaluminum compounds such as triethylaluminum, tributylaluminum and others and also mixtures of these are suitable for this purpose.
- EP-A-0 321 851 EP-A-0 321 852, EP-A-0 384 264, EP-A-0 571 882 and EP-A-0 890 584.
- the melt viscosities were determined in accordance with DIN 53019 using a rotational viscosimeter, the dropping points were determined in accordance with ASTM D3954, the ring/ball softening points were determined in accordance with ASTM D3104.
- the weight average molar mass M w and the number average molar mass n were determined by gel permeation chromatography at a temperature of 135° C. in 1,2-dichloro-benzene.
- polyolefins 1 to 4 which were used according to the invention and are shown in Table 1 were prepared by methods of the prior art as described in EP 0 384 264 or EP 0 571 882.
- polyolefins 1 to 4 which are described in detail above were melted together with the additional components shown in Table 2 in the mixing ratios indicated and mixed at a temperature of 170° C.
- nonwoven material BBA Style 717D (16.9 gsm) was adhesively bonded to a polyethylene film Clopay DH-203 PE by means of each of the hot melt adhesives as per illustrative formulations 1 to 10 at 25° C., with in each case 6.2 g/m 2 of hot melt adhesive being sprayed onto the nonwoven material and the sprayed nonwoven and the film then being promptly pressed together by means of rollers.
- the specimens were stored for 24 hours at a temperature of 25° C. under standard conditions and then peeled at a speed of 12 inches/min and a peel angle of 180° at 25° C.
- test results show, by way of the initial peel values, a sometimes very large increase in the adhesive strength of the hot melt adhesives containing the polyolefins used according to the invention, compared to hot melt adhesives of the prior art (see Examples 5, 6, 7 and 8). Consequently, a satisfactory adhesive action can be achieved even when using the hot melt adhesives of the invention in amounts of less than 6 g/m 2 .
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Materials Engineering (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hematology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Absorbent Articles And Supports Therefor (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
Abstract
Description
| TABLE 1 |
| Polyolefins used |
| Polyolefin 1 | Polyolefin 2 | Polyolefin 3 | Polyolefin 4 | |
| Preparation | EP 0 384 264 | EP 0 384 264 | EP 0 571 882 | EP 0 384 264 |
| according to | general | general | Ex. 3 | general |
| method | method | method | ||
| Ex. 1-161) | Ex. 1-162) | Ex. 1-163) | ||
| Type | Propylene- | Propylene- | Propylene | Propylene- |
| ethylene | ethylene | homopolymer | ethylene | |
| copolymer | copolymer | copolymer | ||
| Softening | 834) | 88 | 1454) | 106 |
| point (° C.) | ||||
| Viscosity at | 180 | 11500 | 101 | 4300 |
| 170° C. | ||||
| (mPa · s) | ||||
| Mn | 2760 | 8250 | 1980 | 5320 |
| Mw | 6320 | 19110 | 3900 | 12030 |
| 1)Polymerization data: total ethylene usage 400 g, polymerization temp. 75° C. | ||||
| 2)Total ethylene usage 350 g, polymerization temp. 65° C. | ||||
| 3)Total ethylene usage 200 g, polymerization temp. 50° C. | ||||
| 4)Dropping point | ||||
| TABLE 2 |
| Illustrative formulations and comparative formulations |
| (reported in % by weight) and resulting initial peel values in N/mm2, |
| measured at 37° C. |
| Example |
| 1 | 2 | 3 | 4 | 5 | |
| Polyolefin 1 | 80 | ||||
| Polyolefin 2 | 80 | ||||
| Polyolefin 3 | 5 | ||||
| Polyolefin 4 | 75 | 80 | |||
| Affinity GA-1900 | 60 | ||||
| Escorez 5637 | 20 | 20 | 20 | 20 | 40 |
| Oppanol B11 | |||||
| Vestoplast 828 | |||||
| Initial peel | — | 364 | 544 | — | 205 |
| Example |
| 6 | 7 | 8 | 9 | 10 | |
| Comparison I SIS based | 100 | ||||
| Comparison II SIS based | 100 | ||||
| Huntsman RT-2730 | 100 | ||||
| Polyolefin 3 | 70 | 30 | |||
| Escorez 5400 | 40 | ||||
| Escorez 5637 | 20 | ||||
| Oppanol B11 | 10 | ||||
| Vestoplast 828 | 30 | ||||
| Initial peel | 192 | 205 | 166 | 473 | 392 |
| Affinity GA-1900 | Polyethylene (Dow Chemical Corp.) |
| Escorez 5637 | Hydrocarbon resin (ExxonMobil) |
| Escorez 5400 | Hydrocarbon resin (ExxonMobil) |
| Oppanol B11 | Polyisobutene (BASF) |
| Vestoplast 828 | amorphous poly-alpha-olefin (Degussa) |
| Huntsman RT-2730 | amorphous poly-alpha-olefin (Huntsmann) |
| Comparison I SIS based | hot melt adhesive formulation comprising |
| styrene-isoprene block copolymer, oil, resin | |
| (H B Fuller) | |
| Comparison II SIS based | hot melt adhesive formulation comprising |
| styrene-isoprene block copolymer, oil, resin | |
| (National Starch) | |
Claims (94)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16/237,506 USRE48818E1 (en) | 2006-10-18 | 2007-10-06 | Hot-melt adhesive substance |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006049089A DE102006049089A1 (en) | 2006-10-18 | 2006-10-18 | Hotmelt |
| DE102006049089 | 2006-10-18 | ||
| US16/237,506 USRE48818E1 (en) | 2006-10-18 | 2007-10-06 | Hot-melt adhesive substance |
| US12/445,913 US8487026B2 (en) | 2006-10-18 | 2007-10-06 | Hot-melt adhesive substance |
| PCT/EP2007/008691 WO2008046536A1 (en) | 2006-10-18 | 2007-10-06 | Hot-melt adhesive substance |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE48818E1 true USRE48818E1 (en) | 2021-11-16 |
Family
ID=38826453
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12/445,913 Ceased US8487026B2 (en) | 2006-10-18 | 2007-10-06 | Hot-melt adhesive substance |
| US16/237,506 Active 2028-05-23 USRE48818E1 (en) | 2006-10-18 | 2007-10-06 | Hot-melt adhesive substance |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12/445,913 Ceased US8487026B2 (en) | 2006-10-18 | 2007-10-06 | Hot-melt adhesive substance |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US8487026B2 (en) |
| EP (1) | EP2081609B1 (en) |
| JP (1) | JP5565937B2 (en) |
| DE (1) | DE102006049089A1 (en) |
| DK (1) | DK2081609T3 (en) |
| ES (1) | ES2382366T3 (en) |
| PL (1) | PL2081609T3 (en) |
| PT (1) | PT2081609E (en) |
| SI (1) | SI2081609T1 (en) |
| WO (1) | WO2008046536A1 (en) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006049089A1 (en) | 2006-10-18 | 2008-04-30 | Clariant International Limited | Hotmelt |
| CA2830645C (en) * | 2011-03-24 | 2018-09-04 | Henkel Corporation | Stretch film lamination adhesive |
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Also Published As
| Publication number | Publication date |
|---|---|
| DK2081609T3 (en) | 2012-06-25 |
| ES2382366T3 (en) | 2012-06-07 |
| US8487026B2 (en) | 2013-07-16 |
| JP2010506983A (en) | 2010-03-04 |
| PL2081609T3 (en) | 2012-08-31 |
| EP2081609A1 (en) | 2009-07-29 |
| DE102006049089A1 (en) | 2008-04-30 |
| US20100305531A1 (en) | 2010-12-02 |
| SI2081609T1 (en) | 2012-07-31 |
| EP2081609B1 (en) | 2012-03-21 |
| PT2081609E (en) | 2012-05-24 |
| WO2008046536A1 (en) | 2008-04-24 |
| JP5565937B2 (en) | 2014-08-06 |
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