CA1074192A - Pellicules ou feuilles enrobees d'un pare-vapeur, et mode de preparation - Google Patents

Pellicules ou feuilles enrobees d'un pare-vapeur, et mode de preparation

Info

Publication number: CA1074192A
Authority: CA; Canada
Prior art keywords: pol; coating; monomers; mil; gas
Prior art date: 1975-01-20
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

CA321,910A

Other languages

English (en)

Inventor

Michael R. Samuels

Richard M. Ikeda

Richard N. Blomberg

Fritz P. Boettcher

Rudolph J. Angelo

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.)

EIDP Inc

Original Assignee

EI Du Pont de Nemours and 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.)

1975-01-20

Filing date

1979-02-20

Publication date

1980-03-25

1975-11-12 Priority claimed from US05/630,996 external-priority patent/US4104438A/en

1976-01-14 Priority claimed from CA243,649A external-priority patent/CA1071035A/fr

1979-02-20 Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co

1979-02-20 Priority to CA321,910A priority Critical patent/CA1074192A/fr

1980-03-25 Application granted granted Critical

1980-03-25 Publication of CA1074192A publication Critical patent/CA1074192A/fr

Status Expired legal-status Critical Current

Links

239000011888 foil Substances 0.000 title abstract description 4
238000000034 method Methods 0.000 title description 7
238000002360 preparation method Methods 0.000 title description 2
238000000576 coating method Methods 0.000 claims abstract description 25
239000011248 coating agent Substances 0.000 claims abstract description 22
229920001721 polyimide Polymers 0.000 claims abstract description 6
239000004760 aramid Substances 0.000 claims abstract 3
229920003235 aromatic polyamide Polymers 0.000 claims abstract 3
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 20
239000000758 substrate Substances 0.000 claims description 12
229920000139 polyethylene terephthalate Polymers 0.000 claims description 10
239000005020 polyethylene terephthalate Substances 0.000 claims description 10
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 8
-1 polyethylene terephthalate Polymers 0.000 claims description 7
239000000178 monomer Substances 0.000 abstract description 24
239000012808 vapor phase Substances 0.000 abstract description 5
239000004642 Polyimide Substances 0.000 abstract description 4
239000003701 inert diluent Substances 0.000 abstract description 3
229920000343 polyazomethine Polymers 0.000 abstract description 2
239000004962 Polyamide-imide Substances 0.000 abstract 1
230000008021 deposition Effects 0.000 abstract 1
229920002312 polyamide-imide Polymers 0.000 abstract 1
238000012643 polycondensation polymerization Methods 0.000 abstract 1
229920000642 polymer Polymers 0.000 description 20
125000003118 aryl group Chemical group 0.000 description 12
FDQSRULYDNDXQB-UHFFFAOYSA-N benzene-1,3-dicarbonyl chloride Chemical compound ClC(=O)C1=CC=CC(C(Cl)=O)=C1 FDQSRULYDNDXQB-UHFFFAOYSA-N 0.000 description 11
239000002253 acid Substances 0.000 description 9
150000002500 ions Chemical class 0.000 description 9
150000001875 compounds Chemical class 0.000 description 6
239000003921 oil Substances 0.000 description 5
150000001408 amides Chemical class 0.000 description 4
239000000047 product Substances 0.000 description 4
239000004698 Polyethylene Substances 0.000 description 3
239000004743 Polypropylene Substances 0.000 description 3
238000009833 condensation Methods 0.000 description 3
230000005494 condensation Effects 0.000 description 3
238000007796 conventional method Methods 0.000 description 3
ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 3
239000007789 gas Substances 0.000 description 3
150000003949 imides Chemical class 0.000 description 3
239000011261 inert gas Substances 0.000 description 3
IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
UOACKFBJUYNSLK-XRKIENNPSA-N Estradiol Cypionate Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H](C4=CC=C(O)C=C4CC3)CC[C@@]21C)C(=O)CCC1CCCC1 UOACKFBJUYNSLK-XRKIENNPSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
241000282337 Nasua nasua Species 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
150000004984 aromatic diamines Chemical class 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
239000002243 precursor Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
BGRJTUBHPOOWDU-UHFFFAOYSA-N sulpiride Chemical compound CCN1CCCC1CNC(=O)C1=CC(S(N)(=O)=O)=CC=C1OC BGRJTUBHPOOWDU-UHFFFAOYSA-N 0.000 description 2
229910052718 tin Inorganic materials 0.000 description 2
239000006200 vaporizer Substances 0.000 description 2
125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
229920002799 BoPET Polymers 0.000 description 1
KSSJBGNOJJETTC-UHFFFAOYSA-N COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC Chemical compound COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC KSSJBGNOJJETTC-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
241000861718 Chloris <Aves> Species 0.000 description 1
JZUFKLXOESDKRF-UHFFFAOYSA-N Chlorothiazide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC2=C1NCNS2(=O)=O JZUFKLXOESDKRF-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
241000243251 Hydra Species 0.000 description 1
241000283986 Lepus Species 0.000 description 1
241001024304 Mino Species 0.000 description 1
101100270435 Mus musculus Arhgef12 gene Proteins 0.000 description 1
101100219404 Mus musculus Calcrl gene Proteins 0.000 description 1
101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
229920002396 Polyurea Polymers 0.000 description 1
101150107341 RERE gene Proteins 0.000 description 1
241000283984 Rodentia Species 0.000 description 1
SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical compound NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 description 1
241000193803 Therea Species 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
239000000956 alloy Substances 0.000 description 1
229910045601 alloy Inorganic materials 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
150000001412 amines Chemical class 0.000 description 1
235000001014 amino acid Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
229940047583 cetamide Drugs 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000010924 continuous production Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
239000000539 dimer Substances 0.000 description 1
229940113088 dimethylacetamide Drugs 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
210000005069 ears Anatomy 0.000 description 1
238000010292 electrical insulation Methods 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001914 filtration Methods 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000001307 helium Substances 0.000 description 1
229910052734 helium Inorganic materials 0.000 description 1
SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
VHOGYURTWQBHIL-UHFFFAOYSA-N leflunomide Chemical compound O1N=CC(C(=O)NC=2C=CC(=CC=2)C(F)(F)F)=C1C VHOGYURTWQBHIL-UHFFFAOYSA-N 0.000 description 1
229960000681 leflunomide Drugs 0.000 description 1
239000000155 melt Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
239000012071 phase Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920001470 polyketone Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
101150081985 scrib gene Proteins 0.000 description 1
GFWRVVCDTLRWPK-KPKJPENVSA-N sofalcone Chemical compound C1=CC(OCC=C(C)C)=CC=C1\C=C\C(=O)C1=CC=C(OCC=C(C)C)C=C1OCC(O)=O GFWRVVCDTLRWPK-KPKJPENVSA-N 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007858 starting material Substances 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
LXEJRKJRKIFVNY-UHFFFAOYSA-N terephthaloyl chloride Chemical group ClC(=O)C1=CC=C(C(Cl)=O)C=C1 LXEJRKJRKIFVNY-UHFFFAOYSA-N 0.000 description 1
239000011135 tin Substances 0.000 description 1
239000013638 trimer Substances 0.000 description 1
VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1

Landscapes

Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Materials For Medical Uses (AREA)

CA321,910A 1975-01-20 1979-02-20 Pellicules ou feuilles enrobees d'un pare-vapeur, et mode de preparation Expired CA1074192A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA321,910A CA1074192A (fr)	1975-01-20	1979-02-20	Pellicules ou feuilles enrobees d'un pare-vapeur, et mode de preparation

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
US54223775A	1975-01-20	1975-01-20
US05/630,996 US4104438A (en)	1975-01-20	1975-11-12	Gas-barrier coated films, sheets or foils and method of preparation
CA243,649A CA1071035A (fr)	1975-01-20	1976-01-14	Revetement antigaz pour pellicules, toles, feuilles de metal et mode de preparation
CA321,910A CA1074192A (fr)	1975-01-20	1979-02-20	Pellicules ou feuilles enrobees d'un pare-vapeur, et mode de preparation

Publications (1)

Publication Number	Publication Date
CA1074192A true CA1074192A (fr)	1980-03-25

Family

ID=27425881

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA321,910A Expired CA1074192A (fr)	1975-01-20	1979-02-20	Pellicules ou feuilles enrobees d'un pare-vapeur, et mode de preparation

Country Status (1)

Country	Link
CA (1)	CA1074192A (fr)

1979
- 1979-02-20 CA CA321,910A patent/CA1074192A/fr not_active Expired

Legal Events

Date	Code	Title	Description
1997-03-25	MKEX	Expiry

Publication	Publication Date	Title
US4180614A (en)	1979-12-25	Gas-barrier coated films, sheets or foils and method of preparation
US4104438A (en)	1978-08-01	Gas-barrier coated films, sheets or foils and method of preparation
Takahashi et al.	1987	Synthesis of aromatic polyimide film by vacuum deposition polymerization
EP0189643B1 (fr)	1992-12-30	Solution de polyamide-acide et film de polyimide préparé à partir de celle-ci
US5089593A (en)	1992-02-18	Polyimide containing 4,4'-bis(4-amino-2-trifluoromethylphenoxy)-biphenyl moieties
CA1071035A (fr)	1980-02-05	Revetement antigaz pour pellicules, toles, feuilles de metal et mode de preparation
TW574261B (en)	2004-02-01	Method of producing through-hole in aromatic polyimide film
Uekita et al.	1988	Heat-stable aromatic polymer precursors as Langmuir-Blodgett film materials
JP5734069B2 (ja)	2015-06-10	フィルムコンデンサ素子及びフィルムコンデンサ並びにフィルムコンデンサ素子の製造方法
US4839217A (en)	1989-06-13	Aromatic polyimide film
US5576398A (en)	1996-11-19	Thermosetting resin composition
EP0684082B1 (fr)	2000-07-12	Système de couche insulaire avec solvant diminué
CA1074192A (fr)	1980-03-25	Pellicules ou feuilles enrobees d'un pare-vapeur, et mode de preparation
JP3863934B2 (ja)	2006-12-27	高分子薄膜の形成方法
US4562100A (en)	1985-12-31	Polyimide coating compositions from diesterified anhydride and aromatic diamine
WO1994012726A1 (fr)	1994-06-09	Procede de couchage du papier avec un copolyester et produit ainsi obtenu
US6008311A (en)	1999-12-28	Aromatic polycarbodiimide and film thereof
JP2002275619A (ja)	2002-09-25	有機高分子薄膜の製造装置および有機高分子薄膜の作製方法
JP3231373B2 (ja)	2001-11-19	合成樹脂被膜の形成装置及び形成方法
US5223603A (en)	1993-06-29	Copolyoxamide oxygen barrier
US5906886A (en)	1999-05-25	Aromatic polyimide article having amorphous layer
JP2821907B2 (ja)	1998-11-05	ポリイミド樹脂被膜の形成方法
US6793995B2 (en)	2004-09-21	Use of a structure based on poly(dimethylketene) and objects comprising this structure
Kubono et al.	1993	Molecular orientation of alkyl-aromatic polyimide thin films prepared by vapour deposition polymerization
JPH09176306A (ja)	1997-07-08	芳香族ポリアミドフィルム及び磁気記録媒体