USRE30747E - Adhesive applicator crayons - Google Patents
Adhesive applicator crayons Download PDFInfo
- Publication number
- USRE30747E USRE30747E US06/092,376 US9237679A USRE30747E US RE30747 E USRE30747 E US RE30747E US 9237679 A US9237679 A US 9237679A US RE30747 E USRE30747 E US RE30747E
- Authority
- US
- United States
- Prior art keywords
- water
- gel
- forming
- soluble
- 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.)
- Expired - Lifetime
Links
- 239000000853 adhesive Substances 0.000 title claims abstract description 80
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 80
- 239000007788 liquid Substances 0.000 claims abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 15
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims abstract description 13
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 239000003960 organic solvent Substances 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 9
- 239000002585 base Substances 0.000 claims abstract description 7
- 150000003973 alkyl amines Chemical class 0.000 claims abstract description 6
- 229910021529 ammonia Inorganic materials 0.000 claims abstract description 6
- 150000001768 cations Chemical class 0.000 claims abstract description 6
- 239000000126 substance Substances 0.000 claims description 26
- 239000002253 acid Substances 0.000 claims description 8
- 229920000180 alkyd Polymers 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 7
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 229930195729 fatty acid Natural products 0.000 claims description 7
- 150000004665 fatty acids Chemical class 0.000 claims description 7
- 229920002845 Poly(methacrylic acid) Polymers 0.000 claims description 6
- 229920002125 Sokalan® Polymers 0.000 claims description 6
- 229920002472 Starch Polymers 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 6
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 6
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 6
- 239000008107 starch Substances 0.000 claims description 6
- 235000019698 starch Nutrition 0.000 claims description 6
- 229920002554 vinyl polymer Polymers 0.000 claims description 6
- -1 alkali metal salts Chemical class 0.000 claims description 5
- 229920001568 phenolic resin Polymers 0.000 claims description 4
- 239000005011 phenolic resin Substances 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims description 4
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical class ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 claims description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 3
- 229920000881 Modified starch Polymers 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 3
- 150000001241 acetals Chemical class 0.000 claims description 3
- 150000004648 butanoic acid derivatives Chemical class 0.000 claims description 3
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 claims description 3
- 239000004359 castor oil Substances 0.000 claims description 3
- 235000019438 castor oil Nutrition 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000003240 coconut oil Substances 0.000 claims description 3
- 235000019864 coconut oil Nutrition 0.000 claims description 3
- 235000021323 fish oil Nutrition 0.000 claims description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 3
- 239000000944 linseed oil Substances 0.000 claims description 3
- 235000021388 linseed oil Nutrition 0.000 claims description 3
- 235000019426 modified starch Nutrition 0.000 claims description 3
- 229920002401 polyacrylamide Polymers 0.000 claims description 3
- 239000004584 polyacrylic acid Substances 0.000 claims description 3
- 229920002689 polyvinyl acetate Polymers 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- 239000004800 polyvinyl chloride Substances 0.000 claims description 3
- 229920001289 polyvinyl ether Polymers 0.000 claims description 3
- 159000000000 sodium salts Chemical class 0.000 claims description 3
- 239000003549 soybean oil Substances 0.000 claims description 3
- 235000012424 soybean oil Nutrition 0.000 claims description 3
- 239000003784 tall oil Substances 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims 3
- 238000001816 cooling Methods 0.000 claims 2
- 238000002844 melting Methods 0.000 claims 2
- 230000008018 melting Effects 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 238000000465 moulding Methods 0.000 claims 2
- WBHHMMIMDMUBKC-QJWNTBNXSA-N ricinoleic acid Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(O)=O WBHHMMIMDMUBKC-QJWNTBNXSA-N 0.000 claims 2
- 229960003656 ricinoleic acid Drugs 0.000 claims 2
- 229920001567 vinyl ester resin Polymers 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 239000000123 paper Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 240000004760 Pimpinella anisum Species 0.000 description 1
- 235000012550 Pimpinella anisum Nutrition 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 239000004840 adhesive resin Substances 0.000 description 1
- 229920006223 adhesive resin Polymers 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- GLVVKKSPKXTQRB-UHFFFAOYSA-N ethenyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC=C GLVVKKSPKXTQRB-UHFFFAOYSA-N 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000010642 eucalyptus oil Substances 0.000 description 1
- 229940044949 eucalyptus oil Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 238000009950 felting Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000002303 glucose derivatives Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000005349 heatable glass Substances 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940068917 polyethylene glycols Drugs 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940045845 sodium myristate Drugs 0.000 description 1
- JUQGWKYSEXPRGL-UHFFFAOYSA-M sodium;tetradecanoate Chemical compound [Na+].CCCCCCCCCCCCCC([O-])=O JUQGWKYSEXPRGL-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Images
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
- C09J9/00—Adhesives characterised by their physical nature or the effects produced, e.g. glue sticks
- C09J9/005—Glue sticks
-
- 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
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/102—Applications of adhesives in processes or use of adhesives in the form of films or foils in the form of dowels, anchors or cartridges
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/05—Stick
Definitions
- An object of the present invention is the obtention of an adhesive applicator crayon which can be easily spread on foundations to be bonded, which adhesive applicator crayon is age resisting and which lead to a quick adhesion.
- Another object of the invention is the obtention of an adhesive applicator crayon comprising of a shape-giving base consisting of a gel of a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, with a liquid selected from the group consisting of water, water-miscible organic solvents and mixtures thereof, and a content of an adhesive component selected from the group consisting of water-soluble and water-dispersible adhesives.
- an adhesive applicator crayon comprising a shape-giving base consisting of a gel of a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, with a liquid selected from the group consisting of water, water-miscible organic solvents and mixtures thereof, and a content of an adhesive component selected from the group consisting of water-soluble and water-dispersible adhesives.
- FIG. 1 depicts the adhesive applicator crayon of the invention.
- the aliphatic carboxylic acids having from 8 to 36 carbon atoms utilized as the gel-formers can be either branched or straight chain and may contain double bonds or single substituents such as chloro or bromo.
- the aliphatic carboxylic acids having from 8 to 36 carbon atoms should be alkanoic acids, alkenoic acids, alkadienoic acids and their monohalogen substituted acids and particularly fatty acids with 12 to 22 carbon atoms. These can be obtained from natural fats or oils.
- the alkali metal, ammonium or lower alkyl ammonium salts of the carboxylic acids should be water soluble. Particularly favorable results are obtained with sodium stearate.
- the sodium salts of the other fatty acids with 12 to 22 carbon atoms are preferred as well.
- the lithium salts, potassium salts or ammonium salts, possibly substituted by lower alkyl radicals may also be utilized as the gel forming ingredient.
- the alkali metal or ammonium salts of the aliphatic carboxylic acids are disolved in water and/or water-miscible organic solvents.
- water or water-miscible organic solvents alone can be employed.
- Preferred for the preparation of the gel are aqueous systems.
- organic solvents are primarily lower monohydric and polyhydric alcohols for instance, water-miscible lower alkanols, such as methanol, ethanol, isopropanol; water-miscible lower alkanediols, such as ethylenglycol and water-miscible lower alkanetriols, such as glycerine.
- water-miscible lower alkanols such as methanol, ethanol, isopropanol
- water-miscible lower alkanediols such as ethylenglycol
- water-miscible lower alkanetriols such as glycerine.
- Butanol, amyl alcohols and benzyl alcohol as well as dioxane, acetonitrile, tetrahydrofuran, dimethylformamide or dimethylsulfoxide are also useful in small amounts.
- ketones preferably lower alkanones, such as acetone, methylethylketone are also suitable.
- the adhesive component of the adhesive applicator crayons of the invention the known film-forming, water-soluable or water-dispersible adhesives are employed. Both natural as well as synthetic polymeric substances can be used as the water-soluble adhesives. Suitable are, for instance, salts, preferably alkali metal salts of polyacrylic and polymethacrylic acids, polyacrylamides or mixed polymerizates of acrylamide with N-alkyl substituted acrylamides, as well as polyvinylpyrrolidone.
- cellulose derivatives such as methyl and ethyl cellulose, hydroxyethylcellulose, carboxymethylcellulose, degraded water soluble starch and ethoxylated and propoxylated starch derivatives, carboxymethyl starch and the like may be employed as the water-soluble adhesive component.
- water-dispersible adhesives for instance, phenolic resins; alkyd resins; alkyd resins modified with linseed oil, recinic acid, castor oil, soybean oil, coconut oil, tall oil, and fish oil; acrylated alkyd resins; polyvinyl acetals; polyvinyl acetates; polyvinyl butyrates; polyvinyl ethers; polyvinyl chloride; mixed polymerizate of vinyl chloride with vinylidene chlorides; as well as polyacrylic acid esters and polymethacrylic acid esters, may be employed.
- phenolic resins alkyd resins; alkyd resins modified with linseed oil, recinic acid, castor oil, soybean oil, coconut oil, tall oil, and fish oil
- acrylated alkyd resins polyvinyl acetals
- polyvinyl acetates polyvinyl butyrates
- polyvinyl ethers polyvinyl chloride
- the choice of the components of the adhesive applicator crayon should be made in such way that the mass formed is not too soft but, from which material can be easily rubbed off.
- the content of the gel-forming substance that is in particular the alkali metal or ammonium salts of the aliphatic carboxylic acids, should be approximately from 2% to 25%, in particular from 5% to 8%.
- the liquid component of the gel should be approximately from 25% to 80%, in particular from 30% to 70%.
- the amount of the adhesive substance should be between approximately 5% to 40%, in particular 20% to 35%. The percentages given are percents by weight and refer to the total of the gel-forming substance, of the liquid components and of the adhesive substance.
- the adhesive applicator crayon of the invention may as well contain other adjuvants.
- adhesive resins such as colophony, cumarone, indene, furan, ketone, maleate, and sulfonamide resins as well as urea, melamine or phenolic resins.
- plasticizers or moisture retainers such as for instance, tri- and tetraethyleneglycol, sorbitol, mannitol, glycose, ethoxylated glucose and lower molecular weight polyethyleneglycols with a molecular weight up to approximately 4,000 can be employed.
- Glycerine or ethylene glycol also act as plasticizers when employed as the liquid component. These substances are conductive to an easy, soft rubbing.
- the adhesive applicator crayons of the invention contain a minor amount of dyestuffs as well as pigments.
- they may contain odor improving compounds, such as pine-needle oil, eucalyptus oil, aniseed oil, benzaldehyde and the like.
- the adhesive applicator crayons of the invention it is useful to mix the individual components while heating them to temperatures of 60° to 95° C. After a homogeneous mixture has been formed, the hot mass is poured into molds or is molded by means of an extruder into a rope and is cut into pieces.
- the molded adhesive applicator crayons of the invention may be used as such. However, it is preferable to surround the crayon with a type of vapor barrier in order to prevent a rapid evaporation of the liquid component of the gel.
- This vapor barrier may take the form of a paper overwrap as is customary with a common crayon.
- the adhesive applicator crayon may be inserted into a metal or plastic tube which may have a means for exposing the tip of the adhesive applicator crayon as it is used, such as a lipstick tube.
- the adhesive applicator crayon 1 is surrounded by a paper tube 2.
- the adhesive applicator crayons of the invention allow a clean, application of the adhesive substance which application is free from fibers and drips. Due to the soft rubbing off on abrasion, a sufficient application of the adhesive substance is provided which causes a quick felting bond on paper. Thus the mounting of photographs can be carried out without soiling of the picture side of the photograph. Porous materials such as paper of all kinds and all thicknesses as well as thin metal foils can be bonded.
- the adhesive applicator crayons possess an excellent stability of shape but yet can be applied easily.
- the advantage of the gel formation allows the utilization of relatively large amounts of solvent, but moisture retention is improved, drying out is retarded and a good storage stability is obtained.
- the adhesive of the adhesive applicator crayon of the invention could easily be rubbed off, and without pulling any fibers, onto the surface which was to be bonded.
- Typewriter bond was bonded to photographic paper with the above adhesive applicator crayon as well as white cardboard with photographic paper and typewriter bond. After only one minute, a felted bond was formed. Moreover thin foils of brass and aluminum were bonded to one another as well as with letter bond and with cardboard.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Medicinal Preparation (AREA)
Abstract
An adhesive applicator crayon comprising a shape-giving base consisting of a gel of a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, with a liquid selected from the group consisting of water, water-miscible organic solvents and mixtures thereof, and a content of an adhesive component selected from the group consisting of water-soluble and water-dispersible adhesives.
Description
It is known to prepare adhesive applicator crayons from rubber, resin and waxes. Surface layers must be rubbed off these adhesive applicator crayons under relatively high pressures in order to carry out the spreading of the adhesive. Due to the high pressures required for application, it can easily happen that the crayon itself breaks and that those parts which are to be glued together, such as thin paper, are damaged during a rubbing off of a portion of the adhesive applicator crayon material.
An object of the present invention is the obtention of an adhesive applicator crayon which can be easily spread on foundations to be bonded, which adhesive applicator crayon is age resisting and which lead to a quick adhesion.
Another object of the invention is the obtention of an adhesive applicator crayon comprising of a shape-giving base consisting of a gel of a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, with a liquid selected from the group consisting of water, water-miscible organic solvents and mixtures thereof, and a content of an adhesive component selected from the group consisting of water-soluble and water-dispersible adhesives.
These and other objects of the invention will become further apparent as the description proceeds.
It has now been discovered that the problems of the prior art can be overcome in the development of an adhesive applicator crayon comprising a shape-giving base consisting of a gel of a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, with a liquid selected from the group consisting of water, water-miscible organic solvents and mixtures thereof, and a content of an adhesive component selected from the group consisting of water-soluble and water-dispersible adhesives.
FIG. 1 depicts the adhesive applicator crayon of the invention.
The aliphatic carboxylic acids having from 8 to 36 carbon atoms utilized as the gel-formers can be either branched or straight chain and may contain double bonds or single substituents such as chloro or bromo. Preferably the aliphatic carboxylic acids having from 8 to 36 carbon atoms should be alkanoic acids, alkenoic acids, alkadienoic acids and their monohalogen substituted acids and particularly fatty acids with 12 to 22 carbon atoms. These can be obtained from natural fats or oils. The alkali metal, ammonium or lower alkyl ammonium salts of the carboxylic acids should be water soluble. Particularly favorable results are obtained with sodium stearate. Generally, the sodium salts of the other fatty acids with 12 to 22 carbon atoms are preferred as well. However, the lithium salts, potassium salts or ammonium salts, possibly substituted by lower alkyl radicals may also be utilized as the gel forming ingredient.
For the preparation of the gel forming the shape-giving base of the adhesive applicator crayon, the alkali metal or ammonium salts of the aliphatic carboxylic acids are disolved in water and/or water-miscible organic solvents. In addition to mixed aqueous solvents, water or water-miscible organic solvents alone can be employed. Preferred for the preparation of the gel are aqueous systems. The most suitable organic solvents are primarily lower monohydric and polyhydric alcohols for instance, water-miscible lower alkanols, such as methanol, ethanol, isopropanol; water-miscible lower alkanediols, such as ethylenglycol and water-miscible lower alkanetriols, such as glycerine. Butanol, amyl alcohols and benzyl alcohol as well as dioxane, acetonitrile, tetrahydrofuran, dimethylformamide or dimethylsulfoxide are also useful in small amounts. Moreover, as water-miscible organic solvents, ketones, preferably lower alkanones, such as acetone, methylethylketone are also suitable. For the adhesive component of the adhesive applicator crayons of the invention, the known film-forming, water-soluable or water-dispersible adhesives are employed. Both natural as well as synthetic polymeric substances can be used as the water-soluble adhesives. Suitable are, for instance, salts, preferably alkali metal salts of polyacrylic and polymethacrylic acids, polyacrylamides or mixed polymerizates of acrylamide with N-alkyl substituted acrylamides, as well as polyvinylpyrrolidone. Particularly favorable results are obtained with polyvinylpyrrolidone with a molecular weight of approximately 500,000 to 900,000. Furthermore cellulose derivatives such as methyl and ethyl cellulose, hydroxyethylcellulose, carboxymethylcellulose, degraded water soluble starch and ethoxylated and propoxylated starch derivatives, carboxymethyl starch and the like may be employed as the water-soluble adhesive component.
Moreover, as water-dispersible adhesives, for instance, phenolic resins; alkyd resins; alkyd resins modified with linseed oil, recinic acid, castor oil, soybean oil, coconut oil, tall oil, and fish oil; acrylated alkyd resins; polyvinyl acetals; polyvinyl acetates; polyvinyl butyrates; polyvinyl ethers; polyvinyl chloride; mixed polymerizate of vinyl chloride with vinylidene chlorides; as well as polyacrylic acid esters and polymethacrylic acid esters, may be employed.
The choice of the components of the adhesive applicator crayon should be made in such way that the mass formed is not too soft but, from which material can be easily rubbed off. The content of the gel-forming substance, that is in particular the alkali metal or ammonium salts of the aliphatic carboxylic acids, should be approximately from 2% to 25%, in particular from 5% to 8%. The liquid component of the gel should be approximately from 25% to 80%, in particular from 30% to 70%. The amount of the adhesive substance should be between approximately 5% to 40%, in particular 20% to 35%. The percentages given are percents by weight and refer to the total of the gel-forming substance, of the liquid components and of the adhesive substance.
Aside from the above named essential components, the adhesive applicator crayon of the invention may as well contain other adjuvants. As such come into consideration, for instance, adhesive resins such as colophony, cumarone, indene, furan, ketone, maleate, and sulfonamide resins as well as urea, melamine or phenolic resins.
Further as adjuvants, plasticizers or moisture retainers such as for instance, tri- and tetraethyleneglycol, sorbitol, mannitol, glycose, ethoxylated glucose and lower molecular weight polyethyleneglycols with a molecular weight up to approximately 4,000 can be employed. Glycerine or ethylene glycol also act as plasticizers when employed as the liquid component. These substances are conductive to an easy, soft rubbing.
Moreover, it is possible that the adhesive applicator crayons of the invention contain a minor amount of dyestuffs as well as pigments. Finally, they may contain odor improving compounds, such as pine-needle oil, eucalyptus oil, aniseed oil, benzaldehyde and the like.
For the preparation of the adhesive applicator crayons of the invention, it is useful to mix the individual components while heating them to temperatures of 60° to 95° C. After a homogeneous mixture has been formed, the hot mass is poured into molds or is molded by means of an extruder into a rope and is cut into pieces.
The molded adhesive applicator crayons of the invention may be used as such. However, it is preferable to surround the crayon with a type of vapor barrier in order to prevent a rapid evaporation of the liquid component of the gel. This vapor barrier may take the form of a paper overwrap as is customary with a common crayon. Also the adhesive applicator crayon may be inserted into a metal or plastic tube which may have a means for exposing the tip of the adhesive applicator crayon as it is used, such as a lipstick tube.
In the FIGURE, the adhesive applicator crayon 1 is surrounded by a paper tube 2.
The adhesive applicator crayons of the invention allow a clean, application of the adhesive substance which application is free from fibers and drips. Due to the soft rubbing off on abrasion, a sufficient application of the adhesive substance is provided which causes a quick felting bond on paper. Thus the mounting of photographs can be carried out without soiling of the picture side of the photograph. Porous materials such as paper of all kinds and all thicknesses as well as thin metal foils can be bonded.
The adhesive applicator crayons possess an excellent stability of shape but yet can be applied easily. The advantage of the gel formation allows the utilization of relatively large amounts of solvent, but moisture retention is improved, drying out is retarded and a good storage stability is obtained.
The following examples are illustrative of the practice of the invention. They are, however, not to be deemed limitative in any manner.
In a 2-liter three-neck-flask equipped with a stirrer, 470 g. of water, 140 g. of glycerine and 70 g. of sodium stearate were added and heated under reflux to approximately 90° C. with stirring. After approximately 1 hour, the sodium stearate had gone into solution. Subsequently, 320 g. of polyvinylpyrrolidone with a molecular weight of approximately 700,000 were added in portions to the hot solution. The mixture, which at first was nonhomogeneous, was continuously stirred at 90° (6 hours), until a largely transparent adhesive mass free from bubbles was formed. The viscous hot mass was then poured into small glass tubes (10 mm.). Adhesive applicator crayons thus obtained were placed into cases such as are employed, for instance, for lipsticks.
The adhesive of the adhesive applicator crayon of the invention could easily be rubbed off, and without pulling any fibers, onto the surface which was to be bonded. Typewriter bond was bonded to photographic paper with the above adhesive applicator crayon as well as white cardboard with photographic paper and typewriter bond. After only one minute, a felted bond was formed. Moreover thin foils of brass and aluminum were bonded to one another as well as with letter bond and with cardboard.
50 g. of sodium myristate were dissolved in 100 g. of glycerine, 80 g. of water and 470 g. of ethanol and mixed with 300 g. of a mixed polymerisate of vinyl acetate with 20% of vinyl laurate (K-value approximately 51). The preparation of the adhesive mass and the adhesive applicator crayon was carried out as described in Example 1.
In a heatable glass flask which is equipped with a stirrer and a condenser, different mixtures of the components which are listed in the following table were prepared in the way as described in Example 1. In all cases adhesive applicator crayons were obtained from which adhesive material could be easily rubbed off, which after 1 to 3 minutes gave felted bonds on paper.
TABLE
__________________________________________________________________________
Sodium Poly-vinyl- Ethoxylated
Mg-k-Al-
stearate
Glycerine, pyrrolidone,
Ricinicalkyd
glucose OH
silicate.sup.1
Example
gm. gm. Water, gm.
gm. resin, gm.
value 830, gm.
gm.
__________________________________________________________________________
3 ------------
7 --------------
51 32 --------------
10 ------------
4 ------------
8 14 41 30 5 ----------------
2
5 ------------
8 --------------
43 30 5 14 ------------
6 ------------
7 --------------
47 27 5 14 ------------
__________________________________________________________________________
.sup.1 Very finely ground plastorite.
The preceding specific embodiments are illustrative of the practice of the invention. It is to be understood, however, that other expedients known to those skilled in the art or disclosed herein may be employed without departing from the spirit of the invention.
Claims (9)
1. An adhesive applicator crayon comprising a shape-giving base consisting of a gel of a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, in an aqueous liquid selected from the group consisting of water and mixtures of water with water-miscible organic solvents, with a content of from 5% to 40%, based on the total .[.amount of constituents in said crayon.]. .Iadd.of the gel-forming substance, of the liquid components and of the adhesive substance.Iaddend., of a film-forming adhesive component selected from the group consisting of water-soluble and water-dispersable adhesives.
2. The adhesive applicator crayon of claim 1 wherein said gel-forming salt is present in an amount of between 2% and 25% by weight, said liquid is present in an amount of between 25% and 80% by weight and said adhesive component is present in an amount of from 5% to 40% by weight, said percentages relating to the total amount of the aforesaid three components.
3. The adhesive applicator crayon of claim 1 wherein said gel-forming salt is present in an amount of between 5% to 8% by weight, said liquid is present in an amount of between 30% to 70% by weight and said adhesive component is present in an amount of from 20% to 35% by weight, said percentages relating to the total amount of the aforesaid three components.
4. The adhesive applicator crayon of claim 1 wherein said aliphatic carboxylic acid having from 8 to 36 carbon atoms is selected from the group consisting of alkanoic acids, alkenoic acids, alkadienoic acids and monohalogenated derivatives thereof.
5. The adhesive applicator crayon of claim 1 wherein said aliphatic carboxylic acid is a fatty acid having from 12 to 22 carbon atoms.
6. The adhesive applicator crayon of claim 1 wherein said gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms is sodium stearate.
7. The adhesive applicator crayon of claim 1, wherein said film-forming adhesive component is a water-soluble polyvinylpyrrolidone having an average molecular weight of between 500,000 and 900,000.
8. An adhesive applicator crayon comprising a shape-giving base consisting of a gel of a gel-forming sodium salt of a fatty acid having from 12 to 22 carbon atoms in an aqueous liquid selected from the group consisting of water and mixtures of water with water-miscible organic solvents, with a content of from 5% to 40%, based on the total .[.amount of constituents in said crayon.]. .Iadd.of the gel-forming substance, of the liquid components and of the adhesive substance.Iaddend., of a film-forming adhesive component selected from the group consisting of water-soluble alkali metal salts of polyacrylic and polymethacrylic acids, water-soluble polyacrylamides, water-soluble mixed polymerizates of acrylamide and N-alkylacrylamides, water-soluble polyvinylpyrrolidone, water-soluble cellulose derivatives, degraded water-soluble starch, water-soluble ethoxylated and propoxylated starch derivatives, water-soluble carboxymethyl starch, water-dispersible phenolic resins, water-dispersible alkyd resins, water-dispersible alkyd resins modified with linseed oil, ricinic acid, castor oil, soybean oil, coconut oil, tall oil and fish oil, water-dispersible acrylated alkyd resins, water-dispersible polyvinyl acetals, polyvinyl acetates, polyvinyl butyrates, polyvinyl ethers, polyvinyl chloride, water-dispersible mixed polymerizates of vinyl chloride and vinylidene chlorides, water-dispersible mixed polymerizates of vinyl esters of fatty acids and water-dispersible polyacrylic acid esters and polymethacrylic acid esters.
9. The process of preparing an adhesive applicator crayon which comprises the steps of forming a gel from a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, and an aqueous liquid selected from the group consisting of water and mixtures of water with water-miscible organic solvents, melting said gel at a temperature of between 60° C. and 95° C., adding a film-forming adhesive component selected form the group consisting of water-soluble and water-dispersible adhesives in an amount of from 5% to 40%, based on the total .[.amount of constituents in said crayon.]. .Iadd.of the gel-forming substance, of the liquid components and of the adhesive substance.Iaddend., cooling and molding said mixture and recovering said adhesive applicator crayon. .Iadd. 10. An adhesive applicator crayon comprising a shape-giving base consisting of a gel of a gel-forming sodium salt of a fatty acid having from 12 to 22 carbon atoms, in an amount of between 2% and 25% by weight, based on the total of the gel-forming substance, of the liquid components and of the adhesive substance, in an aqueous liquid selected from the group consisting of water and mixtures of water with water-miscible, organic solvents, in an amount of between 25% and 80% by weight, based on the total of the gel-forming substance, of the liquid components and of the adhesive substance, with a content of from 5% to 40% based on the total of the gel-forming substance, of the liquid components and of the adhesive substance, of a film-forming adhesive component selected from the group consisting of water-soluble alkali metal salts of polyacrylic and polymethacrylic acids, water-soluble polyacrylamides, water-soluble mixed polymerizates of acrylamide and N-alkylacrylamides, water-soluble polyvinylpyrrolidone, water-soluble cellulose derivatives, degraded water-soluble starch, water-soluble ethoxylated and propoxylated starch derivatives, water-soluble carboxymethyl starch, water-dispersible phenolic resins, water-dispersible alkyd resins, water-dispersible alkyd resins modified with linseed oil, ricinic acid, castor oil, soybean oil, coconut oil, tall oil and fish oil, water-dispersible acrylated alkyl resins, water-dispersible polyvinyl acetals, polyvinyl acetates, polyvinyl butyrates, polyvinyl ethers, polyvinyl chloride, water-dispersible mixed polymerizates of vinyl chloride and vinylidene chlorides, water-dispersible mixed polymerizates of vinyl esters of fatty acids and water-dispersible polyacrylic acid esters and polymethacrylic acid esters. .Iaddend..Iadd. 11. The process of preparing an adhesive applicator crayon which comprises the steps of forming a gel from a gel-forming salt of an aliphatic carboxylic acid having from 8 to 36 carbon atoms with a cation selected from the group consisting of alkali metals, ammonia and lower alkylamines, in an amount of between 2% and 25% by weight, based on the total of the gel-forming substance, of the liquid components and of the adhesive substance, and an aqueous liquid selected from the group consisting of water and mixtures of water with water-miscible organic solvents, in an amount of between 25% and 80% by weight, based on the total of the gel-forming substance, of the liquid components and of the adhesive substance, melting said gel at a temperature of between 60° C. and 95° C., adding a film-forming adhesive component selected from the group consisting of water-soluble and water-dispersible adhesives, in an amount of from 5% to 40%, based on the total of the gel-forming substance, of the liquid components and of the adhesive substance, cooling and molding said mixture and recovering said adhesive applicator crayon. .Iaddend.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT998/68 | 1968-02-01 | ||
| AT99868A AT297187B (en) | 1968-02-01 | 1968-02-01 | glue stick |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US04785262 Reissue | 1968-12-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE30747E true USRE30747E (en) | 1981-09-22 |
Family
ID=3504585
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US785262A Expired - Lifetime US3576776A (en) | 1968-02-01 | 1968-12-19 | Adhesive applicator crayons |
| US06/092,376 Expired - Lifetime USRE30747E (en) | 1968-02-01 | 1979-11-08 | Adhesive applicator crayons |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US785262A Expired - Lifetime US3576776A (en) | 1968-02-01 | 1968-12-19 | Adhesive applicator crayons |
Country Status (14)
| Country | Link |
|---|---|
| US (2) | US3576776A (en) |
| AT (1) | AT297187B (en) |
| BE (1) | BE727714A (en) |
| BR (1) | BR6906027D0 (en) |
| CH (1) | CH497521A (en) |
| DE (2) | DE1817985C2 (en) |
| DK (1) | DK125481C (en) |
| ES (1) | ES363174A1 (en) |
| FI (1) | FI47492C (en) |
| FR (1) | FR1600973A (en) |
| GB (1) | GB1230884A (en) |
| IE (1) | IE32637B1 (en) |
| NL (2) | NL6900094A (en) |
| SE (1) | SE340498C (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
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Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2054503C2 (en) * | 1970-11-05 | 1982-12-09 | Lingner + Fischer GmbH, 7580 Bühl | Pen for applying glue to documents |
| JPS5028096B1 (en) * | 1970-12-09 | 1975-09-12 | ||
| JPS5034580B1 (en) * | 1970-12-23 | 1975-11-10 | ||
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| US3865770A (en) * | 1972-12-01 | 1975-02-11 | Minnesota Mining & Mfg | Water-dispersible pressure-sensitive adhesive, tape made therewith, and novel tackifiers therefor |
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| JPS529218B2 (en) * | 1973-08-08 | 1977-03-15 | ||
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| IE42162B1 (en) * | 1974-10-11 | 1980-06-18 | Lingner & Fischer Gmbh | Thickening solutions of film-forming polymer |
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| GB8600599D0 (en) * | 1986-01-10 | 1986-02-19 | Lingner & Fischer Gmbh | Composition |
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| DE3606382A1 (en) * | 1986-02-27 | 1987-09-03 | Henkel Kgaa | IMPROVED ADHESIVE PEN |
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| CN109265031A (en) * | 2018-11-02 | 2019-01-25 | 济南大学 | A kind of baric white sulphoaluminate cement clinker and preparation method thereof |
| DE102020109777B3 (en) | 2020-04-08 | 2021-07-29 | Uhu Gmbh & Co. Kg | Adhesive composition for a glue stick and glue stick |
| EP4101885A1 (en) | 2021-06-08 | 2022-12-14 | Henkel AG & Co. KGaA | Dimensionally stable adhesive composition containing enzymatically modified starch |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2368767A (en) * | 1941-02-20 | 1945-02-06 | Hercules Powder Co Ltd | Adhesive composition |
| DE1737097U (en) | 1956-10-30 | 1957-01-03 | Haus Chemikalien G M B H | CUTTER PIN FOR FIXING RUNNING STOCKING STITCHES. |
| US3096202A (en) * | 1960-08-30 | 1963-07-02 | Johnson & Johnson | Polyvinyl pyrrolidone pressure sensitive adhestive and tape containing same |
| US3267052A (en) * | 1963-04-29 | 1966-08-16 | Brennan George Andrew | Adhesive applicator crayon |
| US3313635A (en) * | 1965-06-01 | 1967-04-11 | Daubert Chemical Co | Protective coating compositions for use in airless spray equipment for coating metallic underbodies of automotive vehicles |
| US3338778A (en) * | 1966-09-28 | 1967-08-29 | Eastman Kodak Co | Thermoplastic adhesive of polypropylene, cellulose ester, polyvinyl acetate, sucrose acetate isobutyrate, and polyalkylene glycol |
| US3396128A (en) * | 1962-05-04 | 1968-08-06 | Takeda Chemical Industries Ltd | Method for promoting crystallization of unsaturated polyester resins |
| US3423342A (en) * | 1965-09-16 | 1969-01-21 | Simoniz Co | Adhesive mass substantially free of surface tack |
| US3539481A (en) * | 1968-06-17 | 1970-11-10 | Us Plywood Champ Papers Inc | Adhesive stick |
-
0
- NL NL132208D patent/NL132208C/xx active
-
1968
- 1968-02-01 AT AT99868A patent/AT297187B/en active
- 1968-08-07 SE SE6810633A patent/SE340498C/en unknown
- 1968-11-28 DE DE1817985A patent/DE1817985C2/en not_active Expired
- 1968-11-28 DE DE1811466A patent/DE1811466C3/en not_active Expired
- 1968-12-19 US US785262A patent/US3576776A/en not_active Expired - Lifetime
- 1968-12-24 FR FR1600973D patent/FR1600973A/fr not_active Expired
-
1969
- 1969-01-03 NL NL6900094A patent/NL6900094A/xx unknown
- 1969-01-29 GB GB1230884D patent/GB1230884A/en not_active Expired
- 1969-01-30 FI FI690285A patent/FI47492C/en active
- 1969-01-31 DK DK055769A patent/DK125481C/en active
- 1969-01-31 CH CH157469A patent/CH497521A/en not_active IP Right Cessation
- 1969-01-31 BR BR206027/69A patent/BR6906027D0/en unknown
- 1969-01-31 ES ES363174A patent/ES363174A1/en not_active Expired
- 1969-01-31 BE BE727714D patent/BE727714A/xx not_active IP Right Cessation
- 1969-02-03 IE IE139/69A patent/IE32637B1/en unknown
-
1979
- 1979-11-08 US US06/092,376 patent/USRE30747E/en not_active Expired - Lifetime
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2368767A (en) * | 1941-02-20 | 1945-02-06 | Hercules Powder Co Ltd | Adhesive composition |
| DE1737097U (en) | 1956-10-30 | 1957-01-03 | Haus Chemikalien G M B H | CUTTER PIN FOR FIXING RUNNING STOCKING STITCHES. |
| US3096202A (en) * | 1960-08-30 | 1963-07-02 | Johnson & Johnson | Polyvinyl pyrrolidone pressure sensitive adhestive and tape containing same |
| US3396128A (en) * | 1962-05-04 | 1968-08-06 | Takeda Chemical Industries Ltd | Method for promoting crystallization of unsaturated polyester resins |
| US3267052A (en) * | 1963-04-29 | 1966-08-16 | Brennan George Andrew | Adhesive applicator crayon |
| US3313635A (en) * | 1965-06-01 | 1967-04-11 | Daubert Chemical Co | Protective coating compositions for use in airless spray equipment for coating metallic underbodies of automotive vehicles |
| US3423342A (en) * | 1965-09-16 | 1969-01-21 | Simoniz Co | Adhesive mass substantially free of surface tack |
| US3338778A (en) * | 1966-09-28 | 1967-08-29 | Eastman Kodak Co | Thermoplastic adhesive of polypropylene, cellulose ester, polyvinyl acetate, sucrose acetate isobutyrate, and polyalkylene glycol |
| US3539481A (en) * | 1968-06-17 | 1970-11-10 | Us Plywood Champ Papers Inc | Adhesive stick |
Non-Patent Citations (3)
| Title |
|---|
| Chemical Abstracts, vol. 53, 1959, p. 1648e. * |
| Chemical Abstracts, vol. 53, No. 6, Mar. 25, 1959, p. 5602b. * |
| Chemical Abstracts, vol. 54, No. 15, Aug. 10, 1960, p. 14875bc. * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4366099A (en) | 1979-05-04 | 1982-12-28 | Societe Anonyme Dite: L'oreal | Process for treating cosmetic oils so as to modify their properties and cosmetic compositions containing these oils |
| US4639475A (en) | 1983-08-04 | 1987-01-27 | Henkel Kommanditgesellschaft Auf Aktien | Adhesive stick and a process for its production |
| US5147457A (en) * | 1989-10-12 | 1992-09-15 | Fuekinori Kogyo Kabushiki Kaisha | Correction stick |
| US5433775A (en) * | 1991-07-30 | 1995-07-18 | Henkel Kommanditgesellschaft Auf Aktien | Adhesive stick based on starch ethers |
| US5567753A (en) * | 1995-01-27 | 1996-10-22 | Avery Dennison Corporation | Adhesive composition which changes from colored to colorless upon application to a substrate |
Also Published As
| Publication number | Publication date |
|---|---|
| ES363174A1 (en) | 1970-11-16 |
| NL6900094A (en) | 1969-08-05 |
| FI47492C (en) | 1973-12-10 |
| FI47492B (en) | 1973-08-31 |
| SE340498B (en) | 1971-11-22 |
| AT297187B (en) | 1972-03-10 |
| IE32637L (en) | 1969-08-01 |
| DE1811466C3 (en) | 1980-04-17 |
| BE727714A (en) | 1969-07-31 |
| US3576776A (en) | 1971-04-27 |
| DE1817985A1 (en) | 1976-10-14 |
| IE32637B1 (en) | 1973-10-17 |
| DE1811466A1 (en) | 1969-08-14 |
| FR1600973A (en) | 1970-08-03 |
| NL132208C (en) | |
| DE1817985C2 (en) | 1979-01-25 |
| CH497521A (en) | 1970-10-15 |
| BR6906027D0 (en) | 1973-01-11 |
| DK125481B (en) | 1973-02-26 |
| GB1230884A (en) | 1971-05-05 |
| DK125481C (en) | 1989-12-27 |
| SE340498C (en) | 1981-01-05 |
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