NO760856L - - Google Patents

Info

Publication number: NO760856L
Authority: NO; Norway
Prior art keywords: powder; glass bottles; bottles; coating; imidazoline
Prior art date: 1975-03-12

Application number

NO760856A

Other languages

English (en)

Norwegian (no)

Inventor

F Schuelde

J Obendorf

G Doermann

Original Assignee

Veba Chemie Ag

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.)

1975-03-12

Filing date

1976-03-11

Publication date

1976-09-14

1976-03-11 Application filed by Veba Chemie Ag filed Critical Veba Chemie Ag

1976-09-14 Publication of NO760856L publication Critical patent/NO760856L/no

Links

239000000843 powder Substances 0.000 claims description 28
238000000576 coating method Methods 0.000 claims description 26
239000011521 glass Substances 0.000 claims description 25
239000011248 coating agent Substances 0.000 claims description 20
238000000034 method Methods 0.000 claims description 16
238000002844 melting Methods 0.000 claims description 11
230000008018 melting Effects 0.000 claims description 11
239000004848 polyfunctional curative Substances 0.000 claims description 11
-1 cyclic amidine Chemical class 0.000 claims description 10
239000010410 layer Substances 0.000 claims description 7
BKCCAYLNRIRKDJ-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1h-imidazole Chemical compound N1CCN=C1C1=CC=CC=C1 BKCCAYLNRIRKDJ-UHFFFAOYSA-N 0.000 claims description 5
238000010438 heat treatment Methods 0.000 claims description 5
230000001476 alcoholic effect Effects 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
239000011241 protective layer Substances 0.000 claims description 4
238000005245 sintering Methods 0.000 claims description 4
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
238000001035 drying Methods 0.000 claims description 3
239000003292 glue Substances 0.000 claims description 3
229910000077 silane Inorganic materials 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
150000001409 amidines Chemical class 0.000 claims description 2
125000000732 arylene group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
239000000975 dye Substances 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
238000012545 processing Methods 0.000 claims description 2
125000000592 heterocycloalkyl group Chemical group 0.000 claims 1
239000004922 lacquer Substances 0.000 claims 1
125000000547 substituted alkyl group Chemical group 0.000 claims 1
239000002966 varnish Substances 0.000 claims 1
239000000203 mixture Substances 0.000 description 21
229920000647 polyepoxide Polymers 0.000 description 17
239000007787 solid Substances 0.000 description 13
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 12
239000004593 Epoxy Substances 0.000 description 9
150000001875 compounds Chemical class 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 8
150000002118 epoxides Chemical class 0.000 description 7
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 6
239000003822 epoxy resin Substances 0.000 description 6
125000003700 epoxy group Chemical group 0.000 description 4
238000009472 formulation Methods 0.000 description 4
150000002462 imidazolines Chemical class 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000002245 particle Substances 0.000 description 4
229920005989 resin Polymers 0.000 description 4
239000011347 resin Substances 0.000 description 4
239000002253 acid Substances 0.000 description 3
239000000853 adhesive Substances 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
229940083254 peripheral vasodilators imidazoline derivative Drugs 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
238000005406 washing Methods 0.000 description 3
JJUVAPMVTXLLFR-UHFFFAOYSA-N 5-methyl-2-phenyl-4,5-dihydro-1h-imidazole Chemical compound N1C(C)CN=C1C1=CC=CC=C1 JJUVAPMVTXLLFR-UHFFFAOYSA-N 0.000 description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
150000001241 acetals Chemical class 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
235000014171 carbonated beverage Nutrition 0.000 description 2
238000004140 cleaning Methods 0.000 description 2
230000006378 damage Effects 0.000 description 2
RWYFURDDADFSHT-RBBHPAOJSA-N diane Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1.C1=C(Cl)C2=CC(=O)[C@@H]3CC3[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 RWYFURDDADFSHT-RBBHPAOJSA-N 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000011835 investigation Methods 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920000570 polyether Polymers 0.000 description 2
238000011417 postcuring Methods 0.000 description 2
238000007086 side reaction Methods 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
238000012360 testing method Methods 0.000 description 2
ZJXICXCNTQYJNT-UHFFFAOYSA-N 1-(4,5-dihydroimidazol-1-ylmethyl)-4,5-dihydroimidazole Chemical compound C1CN=CN1CN1CCN=C1 ZJXICXCNTQYJNT-UHFFFAOYSA-N 0.000 description 1
DPVAXLIXQRRYKZ-UHFFFAOYSA-N 1-[2-(4,5-dihydroimidazol-1-yl)phenyl]-4,5-dihydroimidazole Chemical compound C1=NCCN1C1=CC=CC=C1N1C=NCC1 DPVAXLIXQRRYKZ-UHFFFAOYSA-N 0.000 description 1
AHTPZXAPHHTTFU-UHFFFAOYSA-N 1-[3-(4,5-dihydroimidazol-1-yl)phenyl]-4,5-dihydroimidazole Chemical compound C1=NCCN1C1=CC=CC(N2C=NCC2)=C1 AHTPZXAPHHTTFU-UHFFFAOYSA-N 0.000 description 1
LOCJFVVULRDEEL-UHFFFAOYSA-N 1-[4-(4,5-dihydroimidazol-1-yl)phenyl]-4,5-dihydroimidazole Chemical compound C1=NCCN1C1=CC=C(N2C=NCC2)C=C1 LOCJFVVULRDEEL-UHFFFAOYSA-N 0.000 description 1
HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical class CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 description 1
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
ZNWOXGIEIAGCQA-UHFFFAOYSA-N 2-(2-methylphenyl)-4,5-dihydro-1h-imidazole Chemical compound CC1=CC=CC=C1C1=NCCN1 ZNWOXGIEIAGCQA-UHFFFAOYSA-N 0.000 description 1
VDGKMJYQQUTBQD-UHFFFAOYSA-N 2-(4-methylphenyl)-4,5-dihydro-1h-imidazole Chemical compound C1=CC(C)=CC=C1C1=NCCN1 VDGKMJYQQUTBQD-UHFFFAOYSA-N 0.000 description 1
QUPKCFBHJFNUEW-UHFFFAOYSA-N 2-ethyl-4,5-dihydro-1h-imidazole Chemical compound CCC1=NCCN1 QUPKCFBHJFNUEW-UHFFFAOYSA-N 0.000 description 1
SHYARJUKNREDGB-UHFFFAOYSA-N 2-ethyl-5-methyl-4,5-dihydro-1h-imidazole Chemical compound CCC1=NCC(C)N1 SHYARJUKNREDGB-UHFFFAOYSA-N 0.000 description 1
VWSLLSXLURJCDF-UHFFFAOYSA-N 2-methyl-4,5-dihydro-1h-imidazole Chemical compound CC1=NCCN1 VWSLLSXLURJCDF-UHFFFAOYSA-N 0.000 description 1
MBRFGGHJIHPHGK-UHFFFAOYSA-N 3-(4,5-dihydro-1h-imidazol-2-yl)pyridine Chemical compound N1CCN=C1C1=CC=CN=C1 MBRFGGHJIHPHGK-UHFFFAOYSA-N 0.000 description 1
MWJNDHSPXOXMIH-UHFFFAOYSA-N 4-(4,5-dihydro-1h-imidazol-2-yl)pyridine Chemical compound N1CCN=C1C1=CC=NC=C1 MWJNDHSPXOXMIH-UHFFFAOYSA-N 0.000 description 1
HDPBBNNDDQOWPJ-UHFFFAOYSA-N 4-[1,2,2-tris(4-hydroxyphenyl)ethyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 HDPBBNNDDQOWPJ-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
208000020564 Eye injury Diseases 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
208000027418 Wounds and injury Diseases 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910001854 alkali hydroxide Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
239000003831 antifriction material Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
150000004984 aromatic diamines Chemical class 0.000 description 1
235000013405 beer Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
MLVSWIXRZNPEKF-UPHRSURJSA-N bis(oxiran-2-ylmethyl) (z)-but-2-enedioate Chemical compound C1OC1COC(=O)\C=C/C(=O)OCC1CO1 MLVSWIXRZNPEKF-UPHRSURJSA-N 0.000 description 1
JRPRCOLKIYRSNH-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) benzene-1,2-dicarboxylate Chemical compound C=1C=CC=C(C(=O)OCC2OC2)C=1C(=O)OCC1CO1 JRPRCOLKIYRSNH-UHFFFAOYSA-N 0.000 description 1
KIKYOFDZBWIHTF-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohex-3-ene-1,2-dicarboxylate Chemical compound C1CC=CC(C(=O)OCC2OC2)C1C(=O)OCC1CO1 KIKYOFDZBWIHTF-UHFFFAOYSA-N 0.000 description 1
XFUOBHWPTSIEOV-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) cyclohexane-1,2-dicarboxylate Chemical compound C1CCCC(C(=O)OCC2OC2)C1C(=O)OCC1CO1 XFUOBHWPTSIEOV-UHFFFAOYSA-N 0.000 description 1
KBWLNCUTNDKMPN-UHFFFAOYSA-N bis(oxiran-2-ylmethyl) hexanedioate Chemical compound C1OC1COC(=O)CCCCC(=O)OCC1CO1 KBWLNCUTNDKMPN-UHFFFAOYSA-N 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
239000011247 coating layer Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
238000004880 explosion Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
238000011049 filling Methods 0.000 description 1
238000005429 filling process Methods 0.000 description 1
238000011010 flushing procedure Methods 0.000 description 1
239000011888 foil Substances 0.000 description 1
235000015203 fruit juice Nutrition 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
125000004404 heteroalkyl group Chemical group 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
208000014674 injury Diseases 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000000463 material Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000011707 mineral Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
230000035515 penetration Effects 0.000 description 1
150000004714 phosphonium salts Chemical group 0.000 description 1
229910000073 phosphorus hydride Inorganic materials 0.000 description 1
239000002985 plastic film Substances 0.000 description 1
229920006255 plastic film Polymers 0.000 description 1
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
150000007519 polyprotic acids Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
239000001294 propane Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000007017 scission Effects 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
239000012815 thermoplastic material Substances 0.000 description 1
JIVZKJJQOZQXQB-UHFFFAOYSA-N tolazoline Chemical compound C=1C=CC=CC=1CC1=NCCN1 JIVZKJJQOZQXQB-UHFFFAOYSA-N 0.000 description 1
JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
PZJJKWKADRNWSW-UHFFFAOYSA-N trimethoxysilicon Chemical compound CO[Si](OC)OC PZJJKWKADRNWSW-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
DIHAURBCYGTGCV-UHFFFAOYSA-N xi-4,5-Dihydro-2,4(5)-dimethyl-1H-imidazole Chemical compound CC1CN=C(C)N1 DIHAURBCYGTGCV-UHFFFAOYSA-N 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/02—Processes for applying liquids or other fluent materials performed by spraying
- B05D1/04—Processes for applying liquids or other fluent materials performed by spraying involving the use of an electrostatic field
- B05D1/045—Processes for applying liquids or other fluent materials performed by spraying involving the use of an electrostatic field on non-conductive substrates
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D23/00—Details of bottles or jars not otherwise provided for
- B65D23/08—Coverings or external coatings
- B65D23/0807—Coatings
- B65D23/0814—Coatings characterised by the composition of the material
- B65D23/0821—Coatings characterised by the composition of the material consisting mainly of polymeric materials
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/28—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
- C03C17/32—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with synthetic or natural resins
- C03C17/326—Epoxy resins
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
- C03C17/3405—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions with at least two coatings of organic materials
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/5046—Amines heterocyclic
- C08G59/5053—Amines heterocyclic containing only nitrogen as a heteroatom
- C08G59/5073—Amines heterocyclic containing only nitrogen as a heteroatom having two nitrogen atoms in the ring
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2203/00—Other substrates
- B05D2203/30—Other inorganic substrates, e.g. ceramics, silicon
- B05D2203/35—Glass

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Materials Engineering (AREA)
Geochemistry & Mineralogy (AREA)
Life Sciences & Earth Sciences (AREA)
General Chemical & Material Sciences (AREA)
Mechanical Engineering (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Surface Treatment Of Glass (AREA)
Paints Or Removers (AREA)
Application Of Or Painting With Fluid Materials (AREA)

NO760856A 1975-03-12 1976-03-11 NO760856L (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2510734A DE2510734B2 (de)	1975-03-12	1975-03-12	Verfahren zum Beschichten von Glasflaschen mit einer transparenten Schutzschicht

Publications (1)

Publication Number	Publication Date
NO760856L true NO760856L (de)	1976-09-14

Family

ID=5941138

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO760856A NO760856L (de)	1975-03-12	1976-03-11

Country Status (15)

Country	Link
JP (1)	JPS51114415A (de)
AT (1)	AT343772B (de)
AU (1)	AU501165B2 (de)
BE (1)	BE839503A (de)
CA (1)	CA1072828A (de)
CH (1)	CH599908A5 (de)
DE (1)	DE2510734B2 (de)
ES (1)	ES446022A1 (de)
FR (1)	FR2303724A1 (de)
GB (1)	GB1545874A (de)
IT (1)	IT1056980B (de)
NL (1)	NL7602557A (de)
NO (1)	NO760856L (de)
SE (1)	SE418848B (de)
ZA (1)	ZA761530B (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2861235D1 (en) *	1977-09-07	1981-12-10	Huels Chemische Werke Ag	Method of coating glass surfaces
DE2748969C2 (de) *	1977-11-02	1987-04-30	Resicoat Gmbh Beschichtungspulver, 7410 Reutlingen	Beschichtung von Blitzlampen
FR2439166A1 (fr) *	1978-10-18	1980-05-16	Duco Sa	Procede de revetement d'objets en verre ou en ceramique
DE19618206A1 (de)	1996-05-07	1997-11-13	Heye Hermann Fa	Verfahren und Vorrichtung zur Beschichtung von Glasbehältern und beschichteter Glasbehälter
WO1999008973A1 (es) *	1997-08-14	1999-02-25	Gallart Gabas Jesus	Procedimiento para el envejecimiento de botellas de vidrio
ES2136556B1 (es) *	1997-08-14	2000-09-01	Gallart Gabas Jesus	Procedimiento para el envejecimiento de botellas de vidrio.
PL377761A1 (pl) *	2003-01-09	2006-02-20	Baxter Healthcare S.A.	Bezpieczny pojemnik do substancji biologicznie czynnych i sposób jego wytwarzania
DE102005006903B4 (de) *	2005-02-16	2010-01-28	Engel Oberflächentechnik GmbH	Verfahren zum Beschichten von Glasflächen und Oberfläche eines Glasgegenstandes

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FR1426058A (fr) *	1960-04-06	1966-01-28	Owens Illinois Glass Co	Flacons en verre pour aérosols et leur procédé de fabrication
FR2293989A1 (fr) *	1974-12-13	1976-07-09	Duco Sa	Procede de revetement de substrats non conducteurs au moyen de produits filmogenes

1975
- 1975-03-12 DE DE2510734A patent/DE2510734B2/de not_active Withdrawn
1976
- 1976-03-10 CH CH294376A patent/CH599908A5/xx not_active IP Right Cessation
- 1976-03-10 IT IT21020/76A patent/IT1056980B/it active
- 1976-03-11 AT AT179476A patent/AT343772B/de not_active IP Right Cessation
- 1976-03-11 GB GB9791/76A patent/GB1545874A/en not_active Expired
- 1976-03-11 NL NL7602557A patent/NL7602557A/xx not_active Application Discontinuation
- 1976-03-11 SE SE7603208A patent/SE418848B/xx unknown
- 1976-03-11 NO NO760856A patent/NO760856L/no unknown
- 1976-03-11 JP JP51026590A patent/JPS51114415A/ja active Pending
- 1976-03-12 AU AU11978/76A patent/AU501165B2/en not_active Expired
- 1976-03-12 FR FR7607237A patent/FR2303724A1/fr active Granted
- 1976-03-12 ZA ZA761530A patent/ZA761530B/xx unknown
- 1976-03-12 CA CA247,749A patent/CA1072828A/en not_active Expired
- 1976-03-12 BE BE165108A patent/BE839503A/xx unknown
- 1976-03-12 ES ES446022A patent/ES446022A1/es not_active Expired

Also Published As

Publication number	Publication date
SE418848B (sv)	1981-06-29
GB1545874A (en)	1979-05-16
FR2303724A1 (fr)	1976-10-08
JPS51114415A (en)	1976-10-08
DE2510734A1 (de)	1976-09-30
AU1197876A (en)	1977-09-15
NL7602557A (nl)	1976-09-14
DE2510734B2 (de)	1979-06-21
ZA761530B (en)	1977-03-30
IT1056980B (it)	1982-02-20
ES446022A1 (es)	1977-06-01
CA1072828A (en)	1980-03-04
CH599908A5 (de)	1978-06-15
AU501165B2 (en)	1979-06-14
BE839503A (fr)	1976-07-01
FR2303724B1 (de)	1980-02-29
ATA179476A (de)	1977-10-15
SE7603208L (sv)	1976-09-13
AT343772B (de)	1978-06-12

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