GB612108A - Improvements in or relating to pressure sensitive adhesive sheets or tapes - Google Patents

Improvements in or relating to pressure sensitive adhesive sheets or tapes

Info

Publication number
GB612108A
GB612108A GB2983/45A GB298345A GB612108A GB 612108 A GB612108 A GB 612108A GB 2983/45 A GB2983/45 A GB 2983/45A GB 298345 A GB298345 A GB 298345A GB 612108 A GB612108 A GB 612108A
Authority
GB
United Kingdom
Prior art keywords
resin
rubber
phenol
oil
heated
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB2983/45A
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.)
3M Co
Original Assignee
Minnesota Mining and Manufacturing Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Publication of GB612108A publication Critical patent/GB612108A/en
Expired 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/20Adhesives in the form of films or foils characterised by their carriers
    • C09J7/21Paper; Textile fabrics
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • 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
    • C09J7/00Adhesives in the form of films or foils
    • C09J7/30Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38Pressure-sensitive adhesives [PSA]
    • C09J7/381Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • C09J7/383Natural or synthetic rubber

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

A pressure-sensitive adhesive composition is made by heating together rubber that has been degraded or depolymerised by heating or mechanical working or both to a tacky and liquid or pasty state, and an oil-soluble, heat-reactive phenol-aldehyde resin. The depolymerisation of the rubber is effected by prolonged mechanical working in the presence of heat and air or oxygen. The process may be shortened by the addition of small quantities of copper or its salts, succinic acid, the zinc chloride double salt of phenyl hydrazine, naphthyl or xylyl mercaptan. Alternatively scrap rubber, such as red inner tube scrap, may be heated and stirred until it remains a heavy sticky liquid. The oil-soluble phenolaldehyde resins are made from alkyl- or aryl-substituted phenols such as ptert-, amyl- or butyl phenol, p-sec-octyl phenol, and o- or p-phenyl phenol, reacted with 1-2 mols. formaldehyde. The oil-soluble phenol-aldehyde resin and the depolymerized rubber are heated while being mixed, and other ingredients such as hydrogenated indene-coumarone resin, ester gum, rosin, clay, carbon black, zinc or magnesium oxide or resinate, titanium oxide, mineral oil, beta-naphthol may be added during the mixing and heating stage. A petroleum solvent with if desired a small ethyl alcohol content may be added on cooling. The adhesive may be used as an aqueous dispersion. Alternatively the depolymerised rubber and the oil-soluble phenol-aldehyde resin may be mixed cold, applied to a backing, and then heated to promote the reaction between the rubber and resin. The resin may be made by heating together under reflux p-tert.-butyl phenol, aqueous formaldehyde, and ammonia until the free formaldehyde content of the aqueous phase is reduced to 8 per cent. The resulting heavy fluid resin is dehydrated, e.g. by heating under vacuum and then heated at 110 DEG C. until a test drop forms a brittle pill on cooling. Alternatively formaldehyde and sodium hydroxide solutions are mixed and reacted with p-tert.-amyl phenol until the free formaldehyde content is 1 per cent or less. Dilute sulphuric acid is added to reduce the pH value to 1 or 2 when the resin separates. The resin is then washed, dehydrated, and heated.ALSO:A pressure-sensitive adhesive composition is made by heating together rubber that has been degraded or depolymerized by heating or mechanical working or both to a tacky and liquid or pasty state, and an oil soluble, heat-reactive phenol-aldehyde resin. The depolymerization of the rubber is effected by prolonged mechanical working in the presence of heat and air or oxygen. The process may be shortened by the addition of small quantities of copper or its salts, succinic acid, the zinc chloride double salt of phenyl hydrazine, napthyl or xylyl mercaptan. Alternatively scrap rubber, such as red inner tube scrap, may be heated and stirred until it remains a heavy sticky liquid. The oil-soluble phenolaldehyde resins are made from alkyl- or aryl-substituted phenols such as p. tert. amyl or butyl phenol, p. sec. octyl phenol, and o or h phenyl phenol, reacted with 1-2 mols formaldehyde. The oil soluble phenol-aldehyde resin and the depolymerized rubber are heated while being mixed, and other ingredients such as hydrogenated indenecoumarone resin, ester gum, rosin, clay carbon black, zinc or magnesium oxide or resinate, titanium oxide, mineral oil, beta-naphthol may be added during the mixing and heating stage. A petroleum solvent with if desired a small ethyl alcohol content may be added on cooling. The adhesive may be calendered on to the backing without solvents, or may be used as an aqueous dispersion. Alternatively the depolymerized rubber and the oil-soluble phenolaldehyde resin may be mixed cold, applied to a backing, and then heated to promote the reaction between the rubber and resin.
GB2983/45A 1944-04-17 1945-02-06 Improvements in or relating to pressure sensitive adhesive sheets or tapes Expired GB612108A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US612108XA 1944-04-17 1944-04-17
US855296XA 1944-04-17 1944-04-17
US940914XA 1944-04-17 1944-04-17

Publications (1)

Publication Number Publication Date
GB612108A true GB612108A (en) 1948-11-09

Family

ID=27370001

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2983/45A Expired GB612108A (en) 1944-04-17 1945-02-06 Improvements in or relating to pressure sensitive adhesive sheets or tapes

Country Status (2)

Country Link
DE (1) DE855296C (en)
GB (1) GB612108A (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2725981A (en) * 1953-05-04 1955-12-06 Minnesota Mining & Mfg High-temperature masking tape
FR1137453A (en) * 1954-08-13 1957-05-29 Adhesive tapes
DE964628C (en) * 1955-04-04 1957-05-23 Beiersdorf & Co A G P Process for the production of self-adhesive sheets or tapes
DE1032454B (en) * 1955-05-06 1958-06-19 Minnesota Mining & Mfg Process for the production of an adhesive composition from rubber-like diene polymer and phenol aldehyde resins, which is used for the production of pressure-sensitive adhesive tapes
GB822294A (en) * 1955-05-09 1959-10-21 Thomas Howard Shelley Adhesives
DE1054322B (en) * 1956-06-19 1959-04-02 Lohmann K G Process for the production of self-adhesive tapes or blanks
NL243702A (en) * 1959-07-13 1900-01-01
DE1289223B (en) * 1960-09-08 1969-02-13 Ebnoether Method for gluing flat structures
DE102008063036A1 (en) * 2008-12-23 2010-07-01 Tesa Se Process for the preparation of a thermally reactive pressure-sensitive adhesive

Also Published As

Publication number Publication date
DE855296C (en) 1952-11-10

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