US20020006990A1 - Pressure sensitive cohesive - Google Patents
Pressure sensitive cohesive Download PDFInfo
- Publication number
- US20020006990A1 US20020006990A1 US09/904,858 US90485801A US2002006990A1 US 20020006990 A1 US20020006990 A1 US 20020006990A1 US 90485801 A US90485801 A US 90485801A US 2002006990 A1 US2002006990 A1 US 2002006990A1
- Authority
- US
- United States
- Prior art keywords
- cohesive
- latex
- weight
- pressure sensitive
- sensitive adhesive
- 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.)
- Abandoned
Links
- 229920000126 latex Polymers 0.000 claims abstract description 69
- 239000004816 latex Substances 0.000 claims abstract description 69
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 39
- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims abstract description 34
- 229920001971 elastomer Polymers 0.000 claims abstract description 34
- 239000005060 rubber Substances 0.000 claims abstract description 33
- 244000043261 Hevea brasiliensis Species 0.000 claims abstract description 31
- 229920003052 natural elastomer Polymers 0.000 claims abstract description 31
- 229920001194 natural rubber Polymers 0.000 claims abstract description 31
- 229920001897 terpolymer Polymers 0.000 claims abstract description 25
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 23
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229920002472 Starch Polymers 0.000 claims abstract description 18
- 239000008107 starch Substances 0.000 claims abstract description 17
- 235000019698 starch Nutrition 0.000 claims abstract description 17
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 claims abstract description 16
- JAMNSIXSLVPNLC-UHFFFAOYSA-N (4-ethenylphenyl) acetate Chemical compound CC(=O)OC1=CC=C(C=C)C=C1 JAMNSIXSLVPNLC-UHFFFAOYSA-N 0.000 claims abstract description 15
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims abstract description 15
- 229910002027 silica gel Inorganic materials 0.000 claims abstract description 14
- 239000000741 silica gel Substances 0.000 claims abstract description 14
- 239000000178 monomer Substances 0.000 claims abstract description 12
- 239000002174 Styrene-butadiene Substances 0.000 claims abstract description 10
- QUEICCDHEFTIQD-UHFFFAOYSA-N buta-1,3-diene;2-ethenylpyridine;styrene Chemical compound C=CC=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=N1 QUEICCDHEFTIQD-UHFFFAOYSA-N 0.000 claims abstract description 10
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229920006173 natural rubber latex Polymers 0.000 claims abstract description 10
- 229920001084 poly(chloroprene) Polymers 0.000 claims abstract description 10
- 239000011115 styrene butadiene Substances 0.000 claims abstract description 10
- 229920003048 styrene butadiene rubber Polymers 0.000 claims abstract description 10
- 239000011236 particulate material Substances 0.000 claims abstract description 9
- YAAQEISEHDUIFO-UHFFFAOYSA-N C=CC#N.OC(=O)C=CC=CC1=CC=CC=C1 Chemical compound C=CC#N.OC(=O)C=CC=CC1=CC=CC=C1 YAAQEISEHDUIFO-UHFFFAOYSA-N 0.000 claims abstract description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 6
- 239000000835 fiber Substances 0.000 claims description 35
- 239000002245 particle Substances 0.000 claims description 19
- 230000001070 adhesive effect Effects 0.000 claims description 13
- 239000000853 adhesive Substances 0.000 claims description 12
- 238000007789 sealing Methods 0.000 claims description 9
- 230000003078 antioxidant effect Effects 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000001590 oxidative effect Effects 0.000 claims 1
- 238000009472 formulation Methods 0.000 abstract description 13
- 239000000203 mixture Substances 0.000 abstract description 13
- 239000000314 lubricant Substances 0.000 abstract description 6
- 229920001296 polysiloxane Polymers 0.000 abstract description 6
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 abstract description 5
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 abstract description 4
- AOJOEFVRHOZDFN-UHFFFAOYSA-N benzyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1=CC=CC=C1 AOJOEFVRHOZDFN-UHFFFAOYSA-N 0.000 abstract description 4
- 229940119545 isobornyl methacrylate Drugs 0.000 abstract description 4
- -1 polysiloxane Polymers 0.000 abstract description 3
- 239000000377 silicon dioxide Substances 0.000 description 12
- 238000002360 preparation method Methods 0.000 description 9
- 235000012239 silicon dioxide Nutrition 0.000 description 9
- 230000000903 blocking effect Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000003384 imaging method Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 238000000576 coating method Methods 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 1
- MKALOVJHPRAZRE-UHFFFAOYSA-N 5-phenylpenta-2,4-dienoic acid;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=CC=CC1=CC=CC=C1 MKALOVJHPRAZRE-UHFFFAOYSA-N 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
- 229920013625 Synpol Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- HKPHPIREJKHECO-UHFFFAOYSA-N butachlor Chemical compound CCCCOCN(C(=O)CCl)C1=C(CC)C=CC=C1CC HKPHPIREJKHECO-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
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
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F253/00—Macromolecular compounds obtained by polymerising monomers on to natural rubbers or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F287/00—Macromolecular compounds obtained by polymerising monomers on to block polymers
-
- 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
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/006—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to block copolymers containing at least one sequence of polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/04—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to rubbers
-
- 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
- C09J153/00—Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J153/02—Vinyl aromatic monomers and conjugated dienes
-
- 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
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture
- Y10T156/10—Methods of surface bonding and/or assembly therefor
- Y10T156/1002—Methods of surface bonding and/or assembly therefor with permanent bending or reshaping or surface deformation of self sustaining lamina
- Y10T156/1043—Subsequent to assembly
- Y10T156/1049—Folding only
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture
- Y10T156/10—Methods of surface bonding and/or assembly therefor
- Y10T156/1002—Methods of surface bonding and/or assembly therefor with permanent bending or reshaping or surface deformation of self sustaining lamina
- Y10T156/1051—Methods of surface bonding and/or assembly therefor with permanent bending or reshaping or surface deformation of self sustaining lamina by folding
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
- Y10T428/31895—Paper or wood
Definitions
- U.S. Pat. Nos. 4,918,128 and 5,190,818, provide pressure sensitive adhesives/cohesives that are revolutionary in their utility when utilized with mailers or like type documents or business forms. These patented adhesives have allowed the practical implementation in the mailer industry of mailers which may be quickly and effectively produced and sealed without the drawbacks associated with conventional heat or moisture activated adhesives.
- the cohesive according to the present invention contains a natural rubber graft, an appropriate acrylate monomer or monomers such as methyl methacrylate (or cyclohexyl methacrylate, or benzyl methacrylate, or isobornyl methacrylate), finely divided hard particles such as silica, and preferably also starch.
- the cohesive according to the present invention also includes acrylic acid and/or 4-acetoxystyrene, and optionally ethyl hexyl acrylate.
- a pressure sensitive adhesive/cohesive comprising the following components: 100 parts by weight natural rubber. About 5-35%, by weight of the rubber, acrylate monomer. About 0.5-8%, by weight of the rubber, acrylic acid and/or about 1-10% by weight of rubber 4-acetoxystyrene. About 0-20%, by weight of the rubber, ethyl hexyl acrylate. 1-50%, by weight of the rubber, a finely divided hard particulate material having substantially no thermoplasticity. 0-50%, by weight of the rubber, starch.
- carboxylated styrene-butadiene latex or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex or pre-crosslinked natural rubber latex, or a tackifier, or combinations thereof.
- grafted rubber has built-in antioxidant as a result of hydrolysis of acetoxy group which provides the cohesive antioxidant property helping its shelf life as a coated cohesive by acting as a free radical scavenger.
- the pressure sensitive adhesive/cohesive according to the present invention is typically coated on a piece of paper. More typically, since the material according to the invention is best as a cohesive, it is coated on two portions of a piece of paper, the cohesive portions in contact with each other as a result of folding the paper (such as by forming a mailer), or bringing a like sheet in contact therewith, and pressure sealed together (such as by running through conventional pressure sealing equipment, such as “Speedisealer®” equipment available from Moore USA of Lake Forest, Ill.), so as to cause paper fiber tear if attempted to be pulled apart.
- conventional pressure sealing equipment such as “Speedisealer®” equipment available from Moore USA of Lake Forest, Ill.
- the adhesive/cohesive comprises at least 1% ethyl hexyl acrylate, and at least 1% starch; e.g. about 10-30% starch (such as about 20% starch) having an average particle size of about 5-25 microns.
- the hard particulate material preferably comprises silica gel, e.g. about 10-30% (such as about 20%), the silica gel having an average particle size of about 0.2-20 microns (e.g. about 0.3-0.4 microns), or a fumed silica (e.g. 0.1-0.3 microns).
- carboxylated styrene-butadiene latex there also may be at least 5% carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or pre-crosslinked natural rubber latex, or a styrene-acrylate-acrylonitrile latex, or a tackifier, or combinations thereof.
- the acrylic monomer preferably comprises methyl methacrylate, e.g.
- the modified natural rubber latex is preferably electrosterically stabilized natural rubber graft and block terpolymer.
- a method of making a mailer type business form comprises: (a) applying cohesive as cooperating patterns cohesive to a sheet of paper so that when the sheet is folded, or brought into contact with a like sheet, the patterns move into contact with each other, the cohesive comprising a pressure sensitive cohesive including: 100 parts by weight natural rubber; about 5-35% by weight of the rubber acrylate monomer; about 0-8% (preferably about 0.5-8%) by weight of the rubber acrylic acid and/or about 0-10% (preferably about 1-10%) by weight 4-acetoxystyrene; about 0-20% by weight of the rubber ethyl hexyl acrylate; 1-50% by weight of the rubber a finely divided hard particulate material having substantially no thermoplasticity; 0-50% by weight of the rubber starch; and 0-40% by weight of the rubber carboxylated styrene-butadiene latex, styrene-acrylate-acrylonitrile latex
- the method may comprise the further steps of: (b) folding the paper to move the cohesive patterns into contact with each other, and (c) applying a sealing pressure of at least about 100 lbs/lineal inch (e.g. about 200 lbs/lineal inch) to the patterns to seal the cohesive together so as to cause fiber tear if attempted to be pulled apart.
- the terpolymer latex in this example is referred to as latex 1, and the formulation preparation in this example will be referred to as cohesive 1.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with 3% by weight of acrylic acid and about 28% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.4 ⁇ m in an amount of about 20% by weight and a starch, with a specified range of about 10 ⁇ m average particle diameter in an amount of about 14.5 weight % per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive.
- the terpolymer latex in this Example 2 is referred to as latex 2, and the formulation preparation in this example will be referred to as cohesive 2.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 1.5% by weight of acrylic acid and about 23% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3 ⁇ 0.4 ⁇ m in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive.
- the terpolymer latex in this example is referred to as latex 4, and the formulation preparation in this example will be referred to as cohesive 4.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 1.5% by weight of acrylic acid and about 20% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3 ⁇ 0.4 , ⁇ m in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive.
- the terpolymer latex in this example is referred to as a latex 5, and the formulation preparation in this example will be referred to as cohesive 5.
- Electrosterically stabilized latex of rubber graft and block terpolymer with about 1.5% by weight of acrylic acid and about 16% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3 ⁇ 0.4 ⁇ m in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive.
- the terpolymer latex in this example is referred to as latex 6, and the formulation preparation in this example will be referred to as cohesive 6.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 2.5% by weight of acrylic acid and about 15% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3 ⁇ 0.4 ⁇ m in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive.
- the terpolymer latex in this example is referred to as latex 7, and the formulation preparation in this example will be referred to cohesive 7.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 3% by weight of 4-acetoxystyrene and about 15% by weight of methyl methacrylate and 0% by weight of acrylic acid was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3 ⁇ 0.4 ⁇ m in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive.
- 4-acetoxystyrene rubber has a built-in antioxidant in the polymer chain helping the polymer against oxidation.
- the terpolymer latex in this example is referred to as latex 8, and the formulation preparation in this example will be referred to as cohesive 8.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 1.5% by weight of 4-acetoxystyrene and about 15% by weight of methyl methacrylate and 0% by weight of acrylic acid was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3 ⁇ 0.4 ⁇ m in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive.
- 4-acetoxystyrene rubber has a built-in antioxidant in the polymer chain helping the polymer against oxidation.
- the terpolymer latex in this example is referred to as latex 9, and the formulation preparation in this example will be referred to as cohesive 9.
- cohesive 10 Commercially available cohesive (TN-124) referred to as cohesive 10.
- cohesive 11 Commercially available cohesive (TN-124F) referred to as cohesive 11.
- Electrostatically stabilized latex of natural rubber graft and block terpolymer with 4% by weight of cyclohexyl methacrylate and about 12% by weight of methyl methacrylate and 0% by weight of acrylic acid was admixed with fumed/or precipitated silicon dioxide/or silica 5 gel with an average particle diameter of about 0.3 ⁇ 0.4 ⁇ m in amount of about 20% by weight per 100 parts by weight of modified electrostatically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive.
- the terpolymer latex in this example is referred to as latex 9
- the formulation preparation in this example is referred to as cohesive 12.
- Cohesives I, II, IV, V, VI, VII, VIII, IX and XII were applied to 24 pound paper to form a film by an applicator no. 4 Meyer rod and dried in an oven to form a thin film about 7 ⁇ 9 ⁇ m thick for a 24 pound paper (12 samples each).
- samples each with TN-124 and TN-124F (commercially available) were prepared by coating with an applicator no. 4 Meyer rod and dried in an oven to form a thin film of about 7 ⁇ 9 ⁇ m thickness for 24 pound paper. Two minutes after the samples were sealed, the samples were peeled to examine the sealing quality and also it was observed that dried samples were not at all tacky.
- the carboxylated styrene-butadiene latex may be from Ameripol-Synpol, and/or the carboxylated polychloroprene latex from Butachlor XL 415 from Enichem Elastomers America, and/or the vinyl-pyridine styrene-butadiene latex from Pliocord Vp-5622 from Goodyear and/or styrene-acrylate-acrylate latex from OMNOVA Inc.
- the details of the acrylic acid, ethyl hexyl acrylate, cyclohexyl methacrylate, benzyl methacrylate, isobornyl methacrylate, 4-acetoxystyrene, the range of percentage for the various components, and the average particle diameter for the starch and finely divided hard particulate material having substantially no thermal plasticity (preferably silica gel), are as described above in the Background and Summary of the Invention.
- Other modifications are also possible, including coatings on other types of paper besides 20 lb. and 24 lb., and 28 lb. and mailers of all different types may be made, including V-fold, Z-fold, and C-fold, as are conventional, or sheets of paper mated face-to-face.
- the documents/sheets of paper may be preprinted before being fed to a laser (or like) printer or the like, the laser printer imprinting variable and/or non-variable indicia thereon, by applying toner.
- the invention also specifically includes all narrower ranges within a broad range.
- 1-10% means 2-9%, 1.9-3%, 6-9.5%, and all other narrower ranges within the broad range.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Adhesive Tapes (AREA)
- Cephalosporin Compounds (AREA)
- Credit Cards Or The Like (AREA)
- Graft Or Block Polymers (AREA)
Abstract
A pressure sensitive adhesive/cohesive exhibits excellent cohesive body properties, and other desirable features, even when exposed to heat and polysiloxane based lubricants, such as in a laser printer. The formulation comprises 100 parts by weight natural rubber (e.g. electrosterically stabilized natural rubber graft and block terpolymer), and expressed as percentages by weight of the rubber the following components: about 5-35% (e.g. about 28%) acrylate monomer or monomers (such as methyl methacrylate, cyclohexyl methacrylate, benzyl methacrylate, and/or isobornyl methacrylate); about 0.5-8% acrylic acid and/or about 1-10% 4-acetoxystyrene; about 0-20% ethyl hexyl acrylate; about 1-50% (e.g. about 10-30%) finely divided hard particulate material (such as silica gel); 0-50% (preferably about 10-30%) starch; and 0-40% (preferably at least about 5%) carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or a styrene-acrylate-acrylonitrile latex, or vinyl-pyridine styrene-butadiene latex, or pre-crosslinked natural rubber latex, or a tackifier, or combinations thereof. The cohesive is coated onto paper and seals to like cohesive upon the application of a force of at least 100 lbs per lineal inch.
Description
- U.S. Pat. Nos. 4,918,128 and 5,190,818, provide pressure sensitive adhesives/cohesives that are revolutionary in their utility when utilized with mailers or like type documents or business forms. These patented adhesives have allowed the practical implementation in the mailer industry of mailers which may be quickly and effectively produced and sealed without the drawbacks associated with conventional heat or moisture activated adhesives.
- While the adhesives in the above identified patents are extremely effectively, it is desirable to be able to produce an adhesive that has even better properties. While the adhesives in the above identified patents are not tacky after the application to paper, and do not adhere/seal unless a high level of pressure is applied (which prevents the adhesive from blocking during the printing, which would slow down the processing due to paper jams or the like), sometimes the adhesive action may be hampered by contamination of the printing surface and adhesive with silicone lubricants used in conventional printers (particularly laser printers). The adhesive according to the present invention, when coated on paper or like substrates used in mailer type business forms, or the like, has the same advantageous properties as the adhesives in the above identified patents and also has enhanced functionality when contaminated by silicone lubricants.
- Like the preferred embodiments in the above identified patents, the cohesive according to the present invention contains a natural rubber graft, an appropriate acrylate monomer or monomers such as methyl methacrylate (or cyclohexyl methacrylate, or benzyl methacrylate, or isobornyl methacrylate), finely divided hard particles such as silica, and preferably also starch. The cohesive according to the present invention also includes acrylic acid and/or 4-acetoxystyrene, and optionally ethyl hexyl acrylate.
- According to the present invention a pressure sensitive adhesive/cohesive is provided comprising the following components: 100 parts by weight natural rubber. About 5-35%, by weight of the rubber, acrylate monomer. About 0.5-8%, by weight of the rubber, acrylic acid and/or about 1-10% by weight of rubber 4-acetoxystyrene. About 0-20%, by weight of the rubber, ethyl hexyl acrylate. 1-50%, by weight of the rubber, a finely divided hard particulate material having substantially no thermoplasticity. 0-50%, by weight of the rubber, starch. And 0-40%, by weight of the rubber, carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex or pre-crosslinked natural rubber latex, or a tackifier, or combinations thereof.
- In the case of 4-acetoxystyrene as a comonomer in the graft/block of the rubber, grafted rubber has built-in antioxidant as a result of hydrolysis of acetoxy group which provides the cohesive antioxidant property helping its shelf life as a coated cohesive by acting as a free radical scavenger.
- The pressure sensitive adhesive/cohesive according to the present invention is typically coated on a piece of paper. More typically, since the material according to the invention is best as a cohesive, it is coated on two portions of a piece of paper, the cohesive portions in contact with each other as a result of folding the paper (such as by forming a mailer), or bringing a like sheet in contact therewith, and pressure sealed together (such as by running through conventional pressure sealing equipment, such as “Speedisealer®” equipment available from Moore USA of Lake Forest, Ill.), so as to cause paper fiber tear if attempted to be pulled apart.
- Preferably, the adhesive/cohesive comprises at least 1% ethyl hexyl acrylate, and at least 1% starch; e.g. about 10-30% starch (such as about 20% starch) having an average particle size of about 5-25 microns. The hard particulate material preferably comprises silica gel, e.g. about 10-30% (such as about 20%), the silica gel having an average particle size of about 0.2-20 microns (e.g. about 0.3-0.4 microns), or a fumed silica (e.g. 0.1-0.3 microns). There also may be at least 5% carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or pre-crosslinked natural rubber latex, or a styrene-acrylate-acrylonitrile latex, or a tackifier, or combinations thereof. The acrylic monomer preferably comprises methyl methacrylate, e.g. about 5-30%, or 0.5-8% of 4-acetoxystyrene, cyclohexyl methacrylate, benzyl methacrylate, or isobornyl methacrylate; and the acrylic acid typically is between about 0.5-4%, and the 4- acetoxystyrene between about 1-3%. The modified natural rubber latex is preferably electrosterically stabilized natural rubber graft and block terpolymer.
- According to another aspect of the present invention a method of making a mailer type business form is provided. The method comprises: (a) applying cohesive as cooperating patterns cohesive to a sheet of paper so that when the sheet is folded, or brought into contact with a like sheet, the patterns move into contact with each other, the cohesive comprising a pressure sensitive cohesive including: 100 parts by weight natural rubber; about 5-35% by weight of the rubber acrylate monomer; about 0-8% (preferably about 0.5-8%) by weight of the rubber acrylic acid and/or about 0-10% (preferably about 1-10%) by weight 4-acetoxystyrene; about 0-20% by weight of the rubber ethyl hexyl acrylate; 1-50% by weight of the rubber a finely divided hard particulate material having substantially no thermoplasticity; 0-50% by weight of the rubber starch; and 0-40% by weight of the rubber carboxylated styrene-butadiene latex, styrene-acrylate-acrylonitrile latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or pre-crosslinked natural rubber latex, or a tackifier, or combinations thereof.
- The method may comprise the further steps of: (b) folding the paper to move the cohesive patterns into contact with each other, and (c) applying a sealing pressure of at least about 100 lbs/lineal inch (e.g. about 200 lbs/lineal inch) to the patterns to seal the cohesive together so as to cause fiber tear if attempted to be pulled apart.
- It is a primary object of the present invention to provide a pressure sensitive cohesive/adhesive which exhibits excellent adhesive bonding, cohesive bonding, resistance to heat, blocking resistance, resistance to abrasion, non-tackiness, good creep properties, and substantially no loss in adhesion/cohesion upon exposure to heat and polysiloxane based lubricants. This and other objects of the invention will become clear from an inspection of the detailed description of the invention and from the appended claims.
- The general invention as described above will now be set forth with respect to some specific examples.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 1.5% by weight of acrylic acid and about 28.5% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate, was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average aggregate particle size of from about 0.2 μm to 0.6 μm in an amount about 20% by weight and a starch, with a specified range of about 10 μm average particle diameter in an amount of about 14.5 weight % per 100 parts by weight of modified electrosterically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive. The terpolymer latex in this example is referred to as latex 1, and the formulation preparation in this example will be referred to as cohesive 1.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with 3% by weight of acrylic acid and about 28% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.4 μm in an amount of about 20% by weight and a starch, with a specified range of about 10 μm average particle diameter in an amount of about 14.5 weight % per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive. The terpolymer latex in this Example 2 is referred to as latex 2, and the formulation preparation in this example will be referred to as cohesive 2.
- The cohesives of Examples 1 and 2, namely cohesive I and 11, were coated on 20 pound paper using a No. 4 Meyer rod.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 1.5% by weight of acrylic acid and about 23% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3˜0.4 μm in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive. The terpolymer latex in this example is referred to as latex 4, and the formulation preparation in this example will be referred to as cohesive 4.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 1.5% by weight of acrylic acid and about 20% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3˜0.4 , μm in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive. The terpolymer latex in this example is referred to as a latex 5, and the formulation preparation in this example will be referred to as cohesive 5.
- Electrosterically stabilized latex of rubber graft and block terpolymer with about 1.5% by weight of acrylic acid and about 16% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3˜0.4 μm in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber to prepare a pressure sensitive adhesive/cohesive. The terpolymer latex in this example is referred to as latex 6, and the formulation preparation in this example will be referred to as cohesive 6.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 2.5% by weight of acrylic acid and about 15% by weight of methyl methacrylate and 0% by weight of ethyl hexyl acrylate was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3˜0.4 μm in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive. The terpolymer latex in this example is referred to as latex 7, and the formulation preparation in this example will be referred to cohesive 7.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 3% by weight of 4-acetoxystyrene and about 15% by weight of methyl methacrylate and 0% by weight of acrylic acid was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3˜0.4 μm in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive. 4-acetoxystyrene rubber has a built-in antioxidant in the polymer chain helping the polymer against oxidation. The terpolymer latex in this example is referred to as latex 8, and the formulation preparation in this example will be referred to as cohesive 8.
- Electrosterically stabilized latex of natural rubber graft and block terpolymer with about 1.5% by weight of 4-acetoxystyrene and about 15% by weight of methyl methacrylate and 0% by weight of acrylic acid was admixed with fumed/or precipitated silicon dioxide (silica gel) with an average particle diameter of about 0.3˜0.4 μm in an amount of about 20% by weight per 100 parts by weight of modified electrosterically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive. 4-acetoxystyrene rubber has a built-in antioxidant in the polymer chain helping the polymer against oxidation. The terpolymer latex in this example is referred to as latex 9, and the formulation preparation in this example will be referred to as cohesive 9.
- Commercially available cohesive (TN-124) referred to as cohesive 10.
- Commercially available cohesive (TN-124F) referred to as cohesive 11.
- Electrostatically stabilized latex of natural rubber graft and block terpolymer with 4% by weight of cyclohexyl methacrylate and about 12% by weight of methyl methacrylate and 0% by weight of acrylic acid was admixed with fumed/or precipitated silicon dioxide/or silica 5 gel with an average particle diameter of about 0.3˜0.4 μm in amount of about 20% by weight per 100 parts by weight of modified electrostatically stabilized natural rubber, to prepare a pressure sensitive adhesive/cohesive. The terpolymer latex in this example is referred to as latex 9, and the formulation preparation in this example is referred to as cohesive 12.
FORMULATION OF COHESIVES I, II, III, IV, V, VI, VII, VIII, IX, XII INGREDIENTS SUPPLIER PHR Latex 1 or 2 or 4 or 5 or 6 or 7 Moore 100 or 8 or 9 or 12 Silica Cabotex A-2095 Cabot 20.1 Wheat Starch ADM 14.5 Surfactant Surfynol GA Air Products % 1.72 Chemicals Co. Thickener Cellusize Union Carbide 1.08 Antiseptic Nalco 7635 Nalco 0.49 Defoamer SN-381 Sun Nopco 0.74 Total 138.56 - The resulting formulations Cohesives I, II, IV, V, VI, VII, VIII, IX and XII were applied to 24 pound paper to form a film by an applicator no. 4 Meyer rod and dried in an oven to form a thin film about 7˜9 μm thick for a 24 pound paper (12 samples each).
- Two of the samples were sealed with PS-4 Speedisealer® equipment available from Moore North America, Inc., Lake Forest, Ill., with 200 PLI pressure without exposure to the imaging environment. Two minutes after the samples were sealed, the samples were peeled. All samples sealed properly and showed a fiber tear and also it was observed that dried samples were not at all tacky.
- Out of remaining 10 samples, 5 samples were run through a Xerox 4050 Laser printer and 5 samples were run through a Xerox 4635 printer in order to expose the cohesive film to heat and silicone lubricants. After waiting for 2 minute all 10 samples were sealed with a PS-4 Speedisealer® equipment with 200 PLI pressure. Two minutes after the samples were sealed, the samples were peeled to examine the sealing quality and also it was observed that dried samples were not at all tacky. Also after running through the Xerox 4050 and Xerox 4635 printers, the samples showed no sign of blocking, or jamming in the Xerox printers.
- Along with the above mentioned samples, for comparison 12 samples each with TN-124 and TN-124F (commercially available) were prepared by coating with an applicator no. 4 Meyer rod and dried in an oven to form a thin film of about 7˜9 μm thickness for 24 pound paper. Two minutes after the samples were sealed, the samples were peeled to examine the sealing quality and also it was observed that dried samples were not at all tacky.
- All the testing data is summarized in Table 1.
SEALING AFTER SEALING AFTER IMAGING THROUGH IMAGING THROUGH THICKNESS SEALING WITHOUT XEROX 4050 2 MIN XEROX 4635 2 MIN BLOCKING IN THE RUBBING μm SILICONE LUBRICANT DELAY DELAY LASER PRINTER TEST Cohesive 1 7˜9 μm Very strong, fiber tear Very strong, fiber tear poor No pass Cohesive 2 7˜9 μm Very strong, fiber tear Very strong, fiber tear poor No pass Cohesive 3 7˜9 μm Very strong, fiber tear Very strong, fiber tear poor No pass Cohesive 4 7˜9 μm Very strong, fiber tear Very strong, fiber tear fair No pass Cohesive 5 7˜9 μm Very strong, fiber tear Very strong, fiber tear fair No pass Cohesive 6 7˜9 μm Very strong, fiber tear Very strong, fiber tear Very strong, fiber tear No pass Cohesive 7 7˜9 μm Very strong, fiber tear Very strong, fiber tear Very strong, fiber tear No pass Cohesive 8 7˜9 μm Very strong, fiber tear Very strong, fiber tear Very strong, fiber tear No pass Cohesive 9 7˜9 μm Very strong, fiber tear Very strong, fiber tear Very strong, fiber tear No pass Cohesive 10 7˜9 μm Very strong, fiber tear Good, fiber tear poor No pass Cohesive 11 7˜9 μm Very strong, fiber tear Very strong, fiber tear Very strong, fiber tear No pass Cohesive 12 7˜9 μm Very strong, fiber tear Very strong, fiber tear Very strong, fiber tear No pass - If used, the carboxylated styrene-butadiene latex may be from Ameripol-Synpol, and/or the carboxylated polychloroprene latex from Butachlor XL 415 from Enichem Elastomers America, and/or the vinyl-pyridine styrene-butadiene latex from Pliocord Vp-5622 from Goodyear and/or styrene-acrylate-acrylate latex from OMNOVA Inc. The details of the acrylic acid, ethyl hexyl acrylate, cyclohexyl methacrylate, benzyl methacrylate, isobornyl methacrylate, 4-acetoxystyrene, the range of percentage for the various components, and the average particle diameter for the starch and finely divided hard particulate material having substantially no thermal plasticity (preferably silica gel), are as described above in the Background and Summary of the Invention. Other modifications are also possible, including coatings on other types of paper besides 20 lb. and 24 lb., and 28 lb. and mailers of all different types may be made, including V-fold, Z-fold, and C-fold, as are conventional, or sheets of paper mated face-to-face. Other types of sealing equipment, as well as conventional folding equipment, can be utilized, in the practice of the method of the invention, and in the production of business forms pursuant to the invention. Also, other types of products can be produced aside from mailer type business forms. The documents/sheets of paper may be preprinted before being fed to a laser (or like) printer or the like, the laser printer imprinting variable and/or non-variable indicia thereon, by applying toner.
- The invention also specifically includes all narrower ranges within a broad range. For example 1-10% means 2-9%, 1.9-3%, 6-9.5%, and all other narrower ranges within the broad range.
- It will thus be seen that according to the present invention a highly advantageous pressure sensitive adhesive/cohesive, mailer-type business forms and/or pieces of paper coated thereby, have been provided as well as a method of making mailer type business forms. While the invention has been herein shown and described in what is presently conceived to be the most practical and preferred embodiment thereof, many modifications may be made within the scope of the invention, which scope is to be accorded the broadest interpretation of the appended claims so as to encompass all equivalent products, formulations, and methods.
Claims (21)
1. A pressure sensitive adhesive/cohesive comprising:
100 parts by weight natural rubber;
about 5-35% by weight of the rubber at least one acrylate monomer;
about 0-8% by weight of the rubber acrylic acid and/or about 0-10% by weight of rubber 4-acetoxystyrene;
about 0-20% by weight of the rubber ethyl hexyl acrylate;
1-50% by weight of the rubber a finely divided hard particulate material having substantially no thermoplasticity;
0-50% by weight of the rubber starch; and
0-40% by weight of the rubber carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or styrene-acrylate-acrylonitrile latex, or pre-crosslinked natural rubber latex, or a tackifier, or combinations thereof.
2. A pressure sensitive adhesive/cohesive as recited in claim 1 wherein the natural rubber is electrosterically stabilized latex of natural rubber graft and block terpolymer, and wherein the adhesive/cohesive is coated on a piece of paper.
3. A pressure sensitive adhesive/cohesive as recited in claim 2 coated on two portions of a piece of paper, said cohesive portions in contact with each other as a result of folding the paper, and pressure sealed together, so as to cause paper fiber tear if attempted to be pulled apart.
4. A pressure sensitive adhesive/cohesive as recited in claim 2 having a built-in antioxidant in the electrosterically stabilized latex of natural rubber graft and block terpolymer when 4-acetoxystyrene is used as a comonomer in grafting which gives an oxidative stability to the pressure sensitive adhesive/cohesive.
5. A pressure sensitive adhesive/cohesive as recited in claim 1 comprising at least 1% ethyl hexyl acrylate.
6. A pressure sensitive adhesive/cohesive as recited in claim 1 comprising at least 1% starch, and wherein the natural rubber comprises an electrosterically stabilized natural graft and block terpolymer.
7. A pressure sensitive adhesive/cohesive as recited in claim 1 comprising about 10-30% starch having an average particle size of about 5-25 microns.
8. A pressure sensitive adhesive/cohesive as recited in claim 7 wherein the hard particulate material comprises about 10-30% silica gel having an average particle size of about 1-20 microns.
9. A pressure sensitive adhesive/cohesive as recited in claim 1 comprising at least 5% carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or pre-crosslinked natural rubber latex, or a styrene-acrylate-acrylonitrile latex, or a tackifier, or combinations thereof.
10. A pressure sensitive adhesive/cohesive as recited in claim 1 comprising about 1.5-4% acrylic acid, and wherein the acrylic monomer comprises about 15-35% methyl methacrylate.
11. A pressure sensitive adhesive/cohesive as recited in claim 8 wherein the acrylic monomer comprises methyl methacrylate.
12. A pressure sensitive adhesive/cohesive as recited in claim 3 comprising at least 1% starch, and wherein the natural rubber comprises an electrosterically stabilized natural graft and block terpolymer.
13. A pressure sensitive adhesive/cohesive as recited in claim 3 comprising about 10-30% starch having an average particle size of about 5-25 microns.
14. A pressure sensitive adhesive/cohesive as recited in claim 3 wherein the hard particulate material comprises about 10-30% silica gel having an average particle size of about 0.3-0.4 microns.
15. A pressure sensitive adhesive/cohesive as recited in claim 3 comprising at least 5% carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or pre-crosslinked natural rubber latex, or a styrene-acrylate-acrylonitrile latex, or a tackifier, or combinations thereof.
16. A pressure sensitive adhesive/cohesive as recited in claim 3 comprising about 1.5-4% acrylic acid, and wherein the acrylic monomer comprises about 5-30% methyl methacrylate.
17. A pressure sensitive adhesive/cohesive as recited in claim 2 comprising at least 1% starch.
18. A pressure sensitive adhesive/cohesive as recited in claim 17 comprising at least 1% ethyl hexyl acrylate, and wherein the natural rubber comprises an electrosterically stabilized natural graft and block terpolymer.
19. A pressure sensitive adhesive/cohesive as recited in claim 16 comprising at least 5% carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or pre-crosslinked natural rubber latex, or a styrene-acrylate-acrylonitrile latex, or a tackifier, or combinations thereof.
20. A method of making a mailer type business form, comprising:
(a) applying cohesive as cooperating patterns to a sheet of paper so that when the sheet is folded or moved into contact with a like coated sheet, the patterns move into contact with each other, the cohesive comprising a pressure sensitive cohesive including: 100 parts by weight natural rubber; about 5-35% by weight of the rubber at least one acrylate monomer; about 0.5-8% by weight of the rubber acrylic acid and/or about 1 -1 0% by weight of the rubber 4-acetoxystyrene; about 0-20% by weight of the rubber ethyl hexyl acrylate; 1-50% by weight of the rubber a finely divided hard particulate material having substantially no thermoplasticity; 0-50% by weight of the rubber starch; and 0-40% by weight of the rubber carboxylated styrene-butadiene latex, or carboxylated polychloroprene latex, or vinyl-pyridine styrene-butadiene latex, or styrene-acrylate-acrylonitrile latex, or pre-crosslinked natural rubber latex, or a tackifier, or combinations thereof.
21. A method as recited in claim 20 further comprising: (b) folding the paper to move the cohesive patterns into contact with each other, and (c) applying a sealing pressure of at least about 100 lbs/lineal inch to the patterns to seal the cohesive together so as to cause fiber tear if attempted to be pulled apart.
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| US09/904,858 Abandoned US20020006990A1 (en) | 2000-02-22 | 2001-07-16 | Pressure sensitive cohesive |
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| EP (1) | EP1175468B1 (en) |
| JP (1) | JP2003524058A (en) |
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| CN105219322A (en) * | 2015-11-14 | 2016-01-06 | 际华三五一五皮革皮鞋有限公司 | Novel environment friendly note pressure footwear use tackiness agent and preparation method thereof |
| CN106398583A (en) * | 2016-08-30 | 2017-02-15 | 无锡万能胶粘剂有限公司 | All-purpose adhesive being able to control bugs |
| EP4317350A3 (en) | 2017-12-14 | 2024-03-27 | Avery Dennison Corporation | Pressure sensitive adhesive with broad damping temperature and frequency range |
| CN109913141A (en) * | 2019-01-21 | 2019-06-21 | 苏州义铠轩电子科技有限公司 | Processing procedure is with can the inharmonious adhesive tape of heavy industry heat and preparation method thereof |
| WO2022221408A1 (en) * | 2021-04-13 | 2022-10-20 | The Regents Of The University Of Michigan | Preparation of pressure sensitive adhesives from post-consumer superabsorbent polymers |
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| US4107109A (en) * | 1977-03-22 | 1978-08-15 | E. I. Du Pont De Nemours And Company | Reactive compositions and polymers made therefrom |
| US4644026A (en) | 1985-07-18 | 1987-02-17 | Dennison Manufacturing Company | Readhering and removable adhesive |
| JPH0686585B2 (en) | 1986-01-20 | 1994-11-02 | 三井東圧化学株式会社 | Flame retardant adhesive |
| JP2847366B2 (en) | 1987-12-25 | 1999-01-20 | トッパン・フォームズ株式会社 | Printing sheet for pressure-sensitive bonding |
| JP2685229B2 (en) * | 1988-06-25 | 1997-12-03 | シャープ株式会社 | Photoconductor |
| CA1341126C (en) | 1988-06-28 | 2000-10-24 | Albert I. Everaerts | Pressure-sensitive adhesive |
| JP2916190B2 (en) | 1990-01-25 | 1999-07-05 | 三井化学株式会社 | Method for producing synthetic rubber latex adhesive |
| AU633410B2 (en) | 1990-04-20 | 1993-01-28 | Toppan Forms Co., Ltd. | Adhesive composition for temporary adhesive bonding of paper sheets |
| US5143972A (en) | 1990-05-17 | 1992-09-01 | Minnesota Mining And Manufacturing Company | Pressure-sensitive adhesive composition |
| US5229206A (en) | 1990-05-17 | 1993-07-20 | Minnesota Mining And Manufacturing Company | Pressure-sensitive adhesive composition |
| JPH0569687A (en) * | 1991-09-13 | 1993-03-23 | Toppan Moore Co Ltd | Releasable pressure-sensitive adhesive composition and information carrier sheet coated with this pressure-sensitive adhesive composition |
| US5424122A (en) | 1991-12-09 | 1995-06-13 | Minnesota Mining And Manufacturing Company | Nonionic, Ph-neutral pressure sensitive adhesive |
| JP2728329B2 (en) * | 1992-01-09 | 1998-03-18 | 門井 弘 | Cold sealant composition |
| JP3677685B2 (en) * | 1992-03-31 | 2005-08-03 | トッパン・フォームズ株式会社 | Information carrier sheet |
| US5314944A (en) | 1992-10-01 | 1994-05-24 | Moore Business Forms | Pressure sensitive adhesive |
| JP3220279B2 (en) | 1993-05-11 | 2001-10-22 | 社団法人マリノフォーラム二十一 | Submarine tillage device and submarine tillage method |
| US5427851A (en) * | 1994-02-16 | 1995-06-27 | The Standard Register Company | Pressure sensitive adhesive and adhesive coated product |
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| JPH101654A (en) * | 1996-06-19 | 1998-01-06 | Matsumoto Yushi Seiyaku Co Ltd | Removable pressure-sensitive adhesive |
| JPH11198593A (en) * | 1997-12-15 | 1999-07-27 | Minnesota Mining & Mfg Co <3M> | Application film for heat-transfer mark |
-
2000
- 2000-02-22 US US09/507,932 patent/US6383653B1/en not_active Expired - Lifetime
-
2001
- 2001-02-22 DE DE60119445T patent/DE60119445T2/en not_active Expired - Fee Related
- 2001-02-22 US US09/789,532 patent/US6602944B2/en not_active Expired - Lifetime
- 2001-02-22 WO PCT/US2001/005457 patent/WO2001062866A1/en not_active Ceased
- 2001-02-22 CN CNB018002757A patent/CN1204219C/en not_active Expired - Fee Related
- 2001-02-22 NZ NZ514854A patent/NZ514854A/en unknown
- 2001-02-22 AT AT01911017T patent/ATE325853T1/en not_active IP Right Cessation
- 2001-02-22 EP EP01911017A patent/EP1175468B1/en not_active Expired - Lifetime
- 2001-02-22 CA CA2369443A patent/CA2369443C/en not_active Expired - Lifetime
- 2001-02-22 AU AU38562/01A patent/AU772135B2/en not_active Ceased
- 2001-02-22 JP JP2001562641A patent/JP2003524058A/en active Pending
- 2001-02-22 BR BR0104589-0A patent/BR0104589A/en not_active Application Discontinuation
- 2001-07-16 US US09/904,858 patent/US20020006990A1/en not_active Abandoned
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090184157A1 (en) * | 2008-01-18 | 2009-07-23 | Xerox Corporation | Use of silane promoter to modify pressure sensitive adhesive for use in pressure seal mailers printed on igen3 |
| EP2100936A3 (en) * | 2008-01-18 | 2014-08-20 | Xerox Corporation | Use of silane promoter to modify pressure sensitive adhesive for use in pressure seal mailers printed on igen3 |
| US8980388B2 (en) | 2008-01-18 | 2015-03-17 | Xerox Corporation | Use of silane promoter to modify pressure sensitive adhesive for use in pressure seal mailers printed on IGEN3 |
| WO2016008814A1 (en) | 2014-07-15 | 2016-01-21 | Basf Se | Pressure sensitive adhesives |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001062866A1 (en) | 2001-08-30 |
| NZ514854A (en) | 2003-11-28 |
| US20010023738A1 (en) | 2001-09-27 |
| AU772135B2 (en) | 2004-04-08 |
| BR0104589A (en) | 2002-01-08 |
| EP1175468B1 (en) | 2006-05-10 |
| CA2369443A1 (en) | 2001-08-30 |
| US6602944B2 (en) | 2003-08-05 |
| CN1204219C (en) | 2005-06-01 |
| CA2369443C (en) | 2010-12-21 |
| DE60119445D1 (en) | 2006-06-14 |
| DE60119445T2 (en) | 2007-05-24 |
| US6383653B1 (en) | 2002-05-07 |
| ATE325853T1 (en) | 2006-06-15 |
| JP2003524058A (en) | 2003-08-12 |
| EP1175468A1 (en) | 2002-01-30 |
| CN1362984A (en) | 2002-08-07 |
| AU3856201A (en) | 2001-09-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |