NO130730B - - Google Patents

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Info

Publication number: NO130730B
Authority: NO; Norway
Prior art keywords: polar; residue; solvent; tetracarboxylic acid; organic solvent
Prior art date: 1970-01-31

Application number

NO00251/71A

Other languages

English (en)

Norwegian (no)

Other versions

NO130730C (fr

Inventor

E Behr

Original Assignee

Dynamit Nobel 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.)

1970-01-31

Filing date

1971-01-22

Publication date

1974-10-21

1970-01-31 Priority claimed from DE19702004495 external-priority patent/DE2004495C/de

1971-01-22 Application filed by Dynamit Nobel Ag filed Critical Dynamit Nobel Ag

1974-10-21 Publication of NO130730B publication Critical patent/NO130730B/no

1975-01-29 Publication of NO130730C publication Critical patent/NO130730C/no

Links

238000000034 method Methods 0.000 claims description 22
238000006243 chemical reaction Methods 0.000 claims description 15
239000004952 Polyamide Substances 0.000 claims description 14
229920002647 polyamide Polymers 0.000 claims description 14
125000004432 carbon atom Chemical group C* 0.000 claims description 11
238000003756 stirring Methods 0.000 claims description 10
-1 tetracarboxylic acid dianhydride Chemical class 0.000 claims description 10
239000002904 solvent Substances 0.000 claims description 9
125000003118 aryl group Chemical group 0.000 claims description 7
150000004985 diamines Chemical class 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 5
239000006185 dispersion Substances 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
239000000203 mixture Substances 0.000 claims description 5
239000003960 organic solvent Substances 0.000 claims description 5
229910052799 carbon Inorganic materials 0.000 claims description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
150000001735 carboxylic acids Chemical class 0.000 claims description 3
239000012454 non-polar solvent Substances 0.000 claims description 3
150000000000 tetracarboxylic acids Chemical class 0.000 claims description 3
150000007513 acids Chemical class 0.000 claims description 2
125000003277 amino group Chemical group 0.000 claims description 2
239000008240 homogeneous mixture Substances 0.000 claims description 2
239000003495 polar organic solvent Substances 0.000 claims description 2
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
239000002270 dispersing agent Substances 0.000 description 12
GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 10
150000001732 carboxylic acid derivatives Chemical class 0.000 description 10
239000007787 solid Substances 0.000 description 10
239000000243 solution Substances 0.000 description 10
239000002798 polar solvent Substances 0.000 description 6
HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 4
239000004642 Polyimide Substances 0.000 description 4
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 4
229920001721 polyimide Polymers 0.000 description 4
229920000642 polymer Polymers 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000008064 anhydrides Chemical class 0.000 description 3
238000001816 cooling Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
150000004984 aromatic diamines Chemical class 0.000 description 2
238000005266 casting Methods 0.000 description 2
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
230000001419 dependent effect Effects 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
SFVQZIJMDCZHOY-UHFFFAOYSA-N 2,7-dichloro-1H-naphthalene-1,2,3,4-tetracarboxylic acid Chemical compound ClC1(C(C2=CC(=CC=C2C(=C1C(=O)O)C(=O)O)Cl)C(=O)O)C(=O)O SFVQZIJMDCZHOY-UHFFFAOYSA-N 0.000 description 1
YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
GEYAGBVEAJGCFB-UHFFFAOYSA-N 4-[2-(3,4-dicarboxyphenyl)propan-2-yl]phthalic acid Chemical compound C=1C=C(C(O)=O)C(C(O)=O)=CC=1C(C)(C)C1=CC=C(C(O)=O)C(C(O)=O)=C1 GEYAGBVEAJGCFB-UHFFFAOYSA-N 0.000 description 1
QQGYZOYWNCKGEK-UHFFFAOYSA-N 5-[(1,3-dioxo-2-benzofuran-5-yl)oxy]-2-benzofuran-1,3-dione Chemical compound C1=C2C(=O)OC(=O)C2=CC(OC=2C=C3C(=O)OC(C3=CC=2)=O)=C1 QQGYZOYWNCKGEK-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
MQJKPEGWNLWLTK-UHFFFAOYSA-N Dapsone Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=C1 MQJKPEGWNLWLTK-UHFFFAOYSA-N 0.000 description 1
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
SUAKHGWARZSWIH-UHFFFAOYSA-N N,N‐diethylformamide Chemical compound CCN(CC)C=O SUAKHGWARZSWIH-UHFFFAOYSA-N 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000000010 aprotic solvent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
WOSVXXBNNCUXMT-UHFFFAOYSA-N cyclopentane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C1CC(C(O)=O)C(C(O)=O)C1C(O)=O WOSVXXBNNCUXMT-UHFFFAOYSA-N 0.000 description 1
230000000694 effects Effects 0.000 description 1
AIJZIRPGCQPZSL-UHFFFAOYSA-N ethylenetetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)=C(C(O)=O)C(O)=O AIJZIRPGCQPZSL-UHFFFAOYSA-N 0.000 description 1
239000011888 foil Substances 0.000 description 1
239000012456 homogeneous solution Substances 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
OBKARQMATMRWQZ-UHFFFAOYSA-N naphthalene-1,2,5,6-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 OBKARQMATMRWQZ-UHFFFAOYSA-N 0.000 description 1
DOBFTMLCEYUAQC-UHFFFAOYSA-N naphthalene-2,3,6,7-tetracarboxylic acid Chemical compound OC(=O)C1=C(C(O)=O)C=C2C=C(C(O)=O)C(C(=O)O)=CC2=C1 DOBFTMLCEYUAQC-UHFFFAOYSA-N 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000001301 oxygen Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
230000007306 turnover Effects 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1003—Preparatory processes

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

NO251/71A 1970-01-31 1971-01-22 NO130730C (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19702004495 DE2004495C (de)		1970-01-31	Verfahren zur Herstellung von Polyamidcarbonsauren

Publications (2)

Publication Number	Publication Date
NO130730B true NO130730B (fr)	1974-10-21
NO130730C NO130730C (fr)	1975-01-29

Family

ID=5761117

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO251/71A NO130730C (fr)	1970-01-31	1971-01-22

Country Status (13)

Country	Link
US (1)	US3663492A (fr)
AT (1)	AT309077B (fr)
BE (1)	BE762258A (fr)
BR (1)	BR7100585D0 (fr)
CA (1)	CA941092A (fr)
CH (1)	CH559224A5 (fr)
ES (1)	ES387800A1 (fr)
FR (1)	FR2077433B1 (fr)
GB (1)	GB1345608A (fr)
NL (1)	NL7101218A (fr)
NO (1)	NO130730C (fr)
RO (1)	RO62174A (fr)
SU (1)	SU410592A3 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5512131A (en) *	1978-07-11	1980-01-28	Hitachi Chem Co Ltd	Preparation of polyamic acid for semiconductor treatment
US4487911A (en) *	1979-07-23	1984-12-11	The P. D. George Company	Stable polyamic acids
JPS58180532A (ja) *	1982-04-16	1983-10-22	Sumitomo Chem Co Ltd	芳香族ポリアミドイミドの製造方法
JP2000025873A (ja)	1998-07-09	2000-01-25	Sony Corp	カセット収納ケース
JP2000025875A (ja)	1998-07-09	2000-01-25	Sony Corp	カセット収納ケース

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1162203A (en) *	1966-04-06	1969-08-20	Nat Res Dev	Production of Polyamic Acids and Polyimides

1971
- 1971-01-06 US US104522A patent/US3663492A/en not_active Expired - Lifetime
- 1971-01-22 NO NO251/71A patent/NO130730C/no unknown
- 1971-01-25 SU SU1613264A patent/SU410592A3/ru active
- 1971-01-26 CH CH114471A patent/CH559224A5/xx not_active IP Right Cessation
- 1971-01-28 BR BR585/71A patent/BR7100585D0/pt unknown
- 1971-01-29 CA CA104,051A patent/CA941092A/en not_active Expired
- 1971-01-29 BE BE762258A patent/BE762258A/fr unknown
- 1971-01-29 FR FR717103012A patent/FR2077433B1/fr not_active Expired
- 1971-01-29 AT AT75071A patent/AT309077B/de active
- 1971-01-29 NL NL7101218A patent/NL7101218A/xx unknown
- 1971-01-30 RO RO65747A patent/RO62174A/ro unknown
- 1971-01-30 ES ES387800A patent/ES387800A1/es not_active Expired
- 1971-04-19 GB GB2041471A patent/GB1345608A/en not_active Expired

Also Published As

Publication number	Publication date
CA941092A (en)	1974-01-29
GB1345608A (en)	1974-01-30
FR2077433B1 (fr)	1974-02-22
NO130730C (fr)	1975-01-29
DE2004495B2 (de)	1972-10-19
ES387800A1 (es)	1973-05-16
BR7100585D0 (pt)	1973-04-17
US3663492A (en)	1972-05-16
NL7101218A (fr)	1971-08-03
CH559224A5 (fr)	1975-02-28
PL73005B1 (fr)	1974-08-30
SU410592A3 (fr)	1974-01-05
FR2077433A1 (fr)	1971-10-22
AT309077B (de)	1973-08-10
RO62174A (fr)	1977-05-15
DE2004495A1 (fr)	1971-07-22
BE762258A (fr)	1971-07-01

Publication	Publication Date	Title
Bower et al.	1963	Aromatic polyimides
Frazer et al.	1964	Poly (1, 3, 4‐oxadiazoles): A new class of polymers by cyclodehydration of polyhydrazides
US3875116A (en)	1975-04-01	Polyetherimides
EP0223958B1 (fr)	1990-11-22	Copolyamideimides réticulés et leurs méthode de préparation
US3893811A (en)	1975-07-08	Apparatus for producing polyamide esters
US4098800A (en)	1978-07-04	Process for preparing polyetheramide-acids
DE112007003428B4 (de)	2015-07-23	Lösungsmittel-lösliche Polyimid-Copolymere sowie Verfahren zu deren Herstellung
US3975345A (en)	1976-08-17	Polyamideimides and method for making
US4197396A (en)	1980-04-08	Solvent free or sinterable polyetheramide acid reaction product
US3748304A (en)	1973-07-24	Amide-imide copolymers
JPS5839845B2 (ja)	1983-09-01	ポリアミドカルボンサンノセイホウ
US3407176A (en)	1968-10-22	Polyamide-acids and polyimide from a mixture of dianhydrides
US4073788A (en)	1978-02-14	Partially imidized polyamide-acid polymers, aqueous coating compositions, coated wire and method, and partially imidized intermediate
US3575923A (en)	1971-04-20	Aqueous process for the preparation of polyimide resins
US3705869A (en)	1972-12-12	Soluble polyimides
NO130730B (fr)	1974-10-21
KR840000807B1 (ko)	1984-06-12	폴리이미드-이소인드로퀴나졸린디온-실리콘 공중합체 수지의 제조방법
US3810858A (en)	1974-05-14	Method for recovering polyamide acid values from deteriorated dispersions of polyamide acid
US4189518A (en)	1980-02-19	Cured polymeric coating material, coated substrate, and process of forming
US3546152A (en)	1970-12-08	Process for reducing viscosity of polytrimellitamide-imide solution
US4481339A (en)	1984-11-06	Acid-extended copolyamideimides and method for their preparation
US3516967A (en)	1970-06-23	Polyiminoimide and polyamide nitrile compositions
US4101487A (en)	1978-07-18	Coating medium
US3933758A (en)	1976-01-20	Iminoimidazolidinedione and parabanic acid polymers containing imide groups
US4428977A (en)	1984-01-31	Ammonium salt of partially emidized polyamide acid for aqueous coating composition