GB688173A - Adhesive compositions - Google Patents
Adhesive compositionsInfo
- Publication number
- GB688173A GB688173A GB12441/51A GB1244151A GB688173A GB 688173 A GB688173 A GB 688173A GB 12441/51 A GB12441/51 A GB 12441/51A GB 1244151 A GB1244151 A GB 1244151A GB 688173 A GB688173 A GB 688173A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymers
- parts
- rubber
- polymer
- class consisting
- 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
Links
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
- C09J121/00—Adhesives based on unspecified rubbers
-
- 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
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
- C08L2666/08—Homopolymers or copolymers according to C08L7/00 - C08L21/00; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
An adhesive composition particularly suitable for bonding polythene film comprises (1) a normally liquid organic solvent having a boiling-point below 150 DEG C. of the class consisting of dialkyl ethers, alkyl esters of alkanoic acids, and dialkyl ketones; (2) a dispersed polymer of the class consisting of natural and synthetic rubbers and rubber-like polymers; (3) a dissolved polymer of the class consisting of natural and synthetic rubbers and rubber-like polymers; and (4) a tackifier comprising wood rosin, hydrogenated wood rosin, a diethylene glycol ester of polymerized wood rosin, a polycyclic aromatic hydrocarbon having a molecular weight of 500 to 2,000, a maleic anhydride-modified ester gum or a coumarone indene resin. The solvents preferably have a B.P. below 120 DEG C. and may be methyl formate, ethyl acetate, methyl prof pionate, propyl acetate, acetone, diethyl ketones ethyl methyl ketone, n-butyl ether, or isopropyether. The dispersed and dissolved polymers may be the same material, the state of solubility depending on the method of preparation of the polymer including the degree of polymerization. The polymers may be chloropolythene, ethylenevinyl ester interpolymers, crepe rubber, reclaimed rubber, neoprene, butadiene-styrene copolymer, butadiene-acrylonitrile copolymer, polythene, or polybutene. Other substances which may be added are high boiling esters of aliphatic or aromatic acids with C4-C9 alcohols such as dinonyl diglycolate, dioctylphthalate, dinonyl adipate, pentamethylene glycol oleate; hydro-abietyl alcohol, dibasic lead phosphite, phenyl glycidyl ether, dibutyl tin maleate, diglycidyl ether of bis-phenol, lead salts of organic or inorganic acids, barium or cadmium salts of naphthenic or ricinoleic acid, hydroquinone, lecithin, propyl gallate, lauryl thiodipropionate, 2,3 - dimethyl - 1,4 - di - (3,4 - dihydroxyphenyl) - butane, butylated hydroxy anisole, diphenylamine, alpha-phenyl naphthylamine or betaphenyl naphthylamine. Preferably 10-25 parts of the dispersed polymer, 3-15 parts of the dissolved polymer, and 25-50 parts of the tackifier is used per 100 parts of organic solvent. The adhesive may be applied to a polythene film and the surfaces lightly pressed together, the solvent being removed by standing at room temperature for 3-14 days, or by heating at 50 DEG C. for a few hours.ALSO:An adhesive composition particularly suitable for bonding polythene film comprises (1) a normally liquid organic solvent having a boiling point below 150 DEG C. of the class consisting of dialkyl ethers, alkyl esters of alkanoic acids, and dialkyl ketones; (2) a dispersed polymer of the class consisting of natural and synthetic rubbers and rubber-like polymers; (3) a dissolved polymer of the class consisting of natural and synthetic rubbers and rubber-like polymers; and (4) a tackifier comprising wood rosin, hydrogenated wood rosin, a diethylene glycol ester of polymerised wood rosin, a polycyclic aromatic hydrocarbon having a molecular weight of 500 to 2,000, a maleic anhydride-modified ester gum or a coumarone indene resin. The solvents preferably have a B.P. below 120 DEG C. and may be methyl formate, ethyl acetate, methyl propionate, propyl acetate, acetone, diethyl ketone, ethyl methyl ketone, n. butyl ether, or isopropyl ether. The dispersed and dissolved polymers may be the same material the state of solubility depending on the method of preparation of the polymer including the degree of polymerisation. The polymers may be chloropolythene, ethylene-vinyl ester interpolymers, cr<\>zepe rubber, reclaimed rubber, neoprene, butadienestyrene copolymer, butadiene-acrylonitrile copolymer, polythene, or polybutene. Other substances which may be added are high boiling esters of aliphatic or aromatic acids, with C4-C9 alcohols such as dinonyl diglycolate, dioctylphthalate, dinonyl adipate, pentamethylene glycol oleate; hydro-abietyl alcohol, dibasic lead phosphite, phenyl glycidyl ether, dibutyl tin maleate, diglycidyl ether of bis-phenol, lead salts or organic or inorganic acids, barium or cadmium salts of naphthenic or ricinoleic acid, hydroquinone, lecithin, propyl gallate, lauryl thiodipropionate, 2,3 dimethyl-1,4 di(3,4-dihydroxyphenyl) butane, butylated hydroxy anisole, diphenylamine, alpha phenyl naphthylamine or beta phenyl naphthylamine. Preferably 10-25 parts of the dispersed polymer, 3-15 parts of the dissolved polymer, and 25-50 parts of the tackifier are used per 100 parts of organic solvent. The adhesive may be applied to a polythene film and the surfaces lightly pressed together, the solvent being removed by standing at room temperature for 3-14 days, or by heating at 50 DEG C. for a few hours.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US688173XA | 1950-05-29 | 1950-05-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB688173A true GB688173A (en) | 1953-02-25 |
Family
ID=22084878
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12441/51A Expired GB688173A (en) | 1950-05-29 | 1951-05-28 | Adhesive compositions |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB688173A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3527729A (en) * | 1964-06-22 | 1970-09-08 | Minnesota Mining & Mfg | Glare-free coating compositions of elastomeric particles in an elastomeric film-former |
US7193004B2 (en) | 2003-06-30 | 2007-03-20 | The Goodyear Tire & Rubber Company | Pneumatic tire having a component containing low PCA oil |
-
1951
- 1951-05-28 GB GB12441/51A patent/GB688173A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3527729A (en) * | 1964-06-22 | 1970-09-08 | Minnesota Mining & Mfg | Glare-free coating compositions of elastomeric particles in an elastomeric film-former |
US7193004B2 (en) | 2003-06-30 | 2007-03-20 | The Goodyear Tire & Rubber Company | Pneumatic tire having a component containing low PCA oil |
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