CH416108A - Verfahren zur Herstellung eines neuen harzartigen Kondensationsproduktes sowie dessen Verwendung bei der Herstellung von länglichen geformten Artikeln - Google Patents

Verfahren zur Herstellung eines neuen harzartigen Kondensationsproduktes sowie dessen Verwendung bei der Herstellung von länglichen geformten Artikeln

Info

Publication number: CH416108A
Authority: CH; Switzerland
Prior art keywords: dependent; condensation product; mixture; epichlorohydrin; amine
Prior art date: 1959-05-26

Application number

CH601360A

Other languages

German (de)

English (en)

Inventor

Caldo Cornelio

Cantatore Giuseppe

Original Assignee

Montedison Spa

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.)

1959-05-26

Filing date

1960-05-25

Publication date

1966-06-30

1960-05-25 Application filed by Montedison Spa filed Critical Montedison Spa

1962-07-23 Priority to CH880262A priority Critical patent/CH470442A/de

1966-06-30 Publication of CH416108A publication Critical patent/CH416108A/de

Links

239000007859 condensation product Substances 0.000 title claims description 43
238000004519 manufacturing process Methods 0.000 title claims description 12
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 69
239000000203 mixture Substances 0.000 claims description 66
239000000835 fiber Substances 0.000 claims description 65
-1 polyethylene Polymers 0.000 claims description 44
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 36
238000000034 method Methods 0.000 claims description 32
239000004743 Polypropylene Substances 0.000 claims description 31
229920001155 polypropylene Polymers 0.000 claims description 31
238000009833 condensation Methods 0.000 claims description 22
230000005494 condensation Effects 0.000 claims description 22
239000000047 product Substances 0.000 claims description 22
229920005989 resin Polymers 0.000 claims description 17
239000011347 resin Substances 0.000 claims description 17
150000001412 amines Chemical class 0.000 claims description 16
229920000642 polymer Polymers 0.000 claims description 16
229920000768 polyamine Polymers 0.000 claims description 15
239000002904 solvent Substances 0.000 claims description 15
239000007787 solid Substances 0.000 claims description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
125000004432 carbon atom Chemical group C* 0.000 claims description 11
229920001577 copolymer Polymers 0.000 claims description 10
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 9
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims description 9
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims description 9
229920000098 polyolefin Polymers 0.000 claims description 9
238000009987 spinning Methods 0.000 claims description 8
125000001931 aliphatic group Chemical group 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 7
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 6
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 5
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 5
239000004698 Polyethylene Substances 0.000 claims description 5
239000002270 dispersing agent Substances 0.000 claims description 5
229920000573 polyethylene Polymers 0.000 claims description 5
238000003825 pressing Methods 0.000 claims description 5
150000003335 secondary amines Chemical class 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 4
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 claims description 4
FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 claims description 3
KUYPVEUMNFJTGI-UHFFFAOYSA-N N,N,N',N'-tetrakis(ethenyl)hexane-1,6-diamine Chemical group C=CN(C=C)CCCCCCN(C=C)C=C KUYPVEUMNFJTGI-UHFFFAOYSA-N 0.000 claims description 3
150000004982 aromatic amines Chemical class 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 claims description 3
239000000155 melt Substances 0.000 claims description 3
150000003141 primary amines Chemical class 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
239000004753 textile Substances 0.000 claims description 3
BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 2
150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
150000001336 alkenes Chemical class 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 claims description 2
150000002466 imines Chemical class 0.000 claims description 2
239000012442 inert solvent Substances 0.000 claims description 2
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
230000001419 dependent effect Effects 0.000 claims 17
230000029936 alkylation Effects 0.000 claims 2
238000005804 alkylation reaction Methods 0.000 claims 2
238000006254 arylation reaction Methods 0.000 claims 2
150000001348 alkyl chlorides Chemical class 0.000 claims 1
150000001500 aryl chlorides Chemical class 0.000 claims 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 1
229920001083 polybutene Polymers 0.000 claims 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
229920001059 synthetic polymer Polymers 0.000 claims 1
235000019441 ethanol Nutrition 0.000 description 40
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 39
239000000975 dye Substances 0.000 description 35
230000002378 acidificating effect Effects 0.000 description 25
238000002074 melt spinning Methods 0.000 description 24
239000000243 solution Substances 0.000 description 23
238000004804 winding Methods 0.000 description 23
238000000605 extraction Methods 0.000 description 18
238000010992 reflux Methods 0.000 description 16
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
239000003054 catalyst Substances 0.000 description 14
230000000707 stereoselective effect Effects 0.000 description 14
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 12
238000004043 dyeing Methods 0.000 description 12
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 12
238000003756 stirring Methods 0.000 description 12
238000001035 drying Methods 0.000 description 11
238000010438 heat treatment Methods 0.000 description 11
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
239000000126 substance Substances 0.000 description 8
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 7
238000001125 extrusion Methods 0.000 description 7
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
239000012932 acetate dye Substances 0.000 description 6
239000002253 acid Substances 0.000 description 6
150000001875 compounds Chemical class 0.000 description 6
238000001816 cooling Methods 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
229920002239 polyacrylonitrile Polymers 0.000 description 6
210000002268 wool Anatomy 0.000 description 6
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 5
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 5
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
JROURLWMOZCGJV-UHFFFAOYSA-N alizarin blue Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C1=CC=CN=C1C(O)=C2O JROURLWMOZCGJV-UHFFFAOYSA-N 0.000 description 5
QGJOPFRUJISHPQ-UHFFFAOYSA-N carbon disulphide Natural products S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
150000001298 alcohols Chemical class 0.000 description 4
JBTHDAVBDKKSRW-UHFFFAOYSA-N chembl1552233 Chemical compound CC1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 JBTHDAVBDKKSRW-UHFFFAOYSA-N 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
WPPDXAHGCGPUPK-UHFFFAOYSA-N red 2 Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=2C=3C4=CC=C5C6=CC=C7C8=C(C=9C=CC=CC=9)C9=CC=CC=C9C(C=9C=CC=CC=9)=C8C8=CC=C(C6=C87)C(C=35)=CC=2)C4=C1C1=CC=CC=C1 WPPDXAHGCGPUPK-UHFFFAOYSA-N 0.000 description 4
239000012265 solid product Substances 0.000 description 4
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
238000010521 absorption reaction Methods 0.000 description 3
229960000583 acetic acid Drugs 0.000 description 3
238000009835 boiling Methods 0.000 description 3
235000014510 cooky Nutrition 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
238000005406 washing Methods 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
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VUQPJRPDRDVQMN-UHFFFAOYSA-N 1-chlorooctadecane Chemical compound CCCCCCCCCCCCCCCCCCCl VUQPJRPDRDVQMN-UHFFFAOYSA-N 0.000 description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 description 2
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CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
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XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
150000001502 aryl halides Chemical class 0.000 description 2
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
235000019646 color tone Nutrition 0.000 description 2
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QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
HKUFIYBZNQSHQS-UHFFFAOYSA-N n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCC HKUFIYBZNQSHQS-UHFFFAOYSA-N 0.000 description 2
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150000002484 inorganic compounds Chemical class 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
229940107698 malachite green Drugs 0.000 description 1
239000000463 material Substances 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
150000002829 nitrogen Chemical class 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
235000020075 ouzo Nutrition 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
229940037312 stearamide Drugs 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
229940099259 vaseline Drugs 0.000 description 1
235000019235 yellow 2G Nutrition 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/55—Epoxy resins
- 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
- C08G73/02—Polyamines
- 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
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
- C08G73/022—Preparatory process from polyamines and epihalohydrins
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/18—Homopolymers or copolymers of nitriles
- C08L33/20—Homopolymers or copolymers of acrylonitrile
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/02—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F6/04—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyolefins
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/227—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/12—Applications used for fibers

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
General Chemical & Material Sciences (AREA)
Manufacturing & Machinery (AREA)
Artificial Filaments (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Coloring (AREA)
Compositions Of Macromolecular Compounds (AREA)

CH601360A 1959-05-26 1960-05-25 Verfahren zur Herstellung eines neuen harzartigen Kondensationsproduktes sowie dessen Verwendung bei der Herstellung von länglichen geformten Artikeln CH416108A (de)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CH880262A CH470442A (de)	1959-05-26	1962-07-23	Verfahren zur Herstellung eines harzartigen Kondensationsproduktes sowie dessen Verwendung zur Herstellung von länglichen geformten Artikeln

Applications Claiming Priority (12)

Application Number	Priority Date	Filing Date	Title
IT1884059		1959-05-26
IT890259		1959-05-26
IT1761959		1959-10-22
IT2232959		1959-10-22
IT2352359		1959-12-10
IT2060359		1959-12-10
IT117960		1960-02-22
IT299960		1960-02-22
IT1280060		1960-07-20
IT398561		1961-03-03
IT960461		1961-05-24
IT1389461		1961-07-27

Publications (1)

Publication Number	Publication Date
CH416108A true CH416108A (de)	1966-06-30

Family

ID=27583087

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CH601360A CH416108A (de)	1959-05-26	1960-05-25	Verfahren zur Herstellung eines neuen harzartigen Kondensationsproduktes sowie dessen Verwendung bei der Herstellung von länglichen geformten Artikeln
CH833061A CH469770A (de)	1959-05-26	1961-07-15	Verfahren zur Herstellung eines harzartigen Kondensationsproduktes sowie dessen Verwendung zur Herstellung von Textilfasern

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
CH833061A CH469770A (de)	1959-05-26	1961-07-15	Verfahren zur Herstellung eines harzartigen Kondensationsproduktes sowie dessen Verwendung zur Herstellung von Textilfasern

Country Status (10)

Country	Link
AT (1)	AT238367B (fr)
BE (2)	BE620706A (fr)
CH (2)	CH416108A (fr)
DD (1)	DD47738A (fr)
DE (2)	DE1469105A1 (fr)
DK (2)	DK106584C (fr)
GB (3)	GB950852A (fr)
NL (5)	NL251988A (fr)
OA (1)	OA02364A (fr)
SE (2)	SE308167B (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL286686A (fr) *	1961-12-19
US4301104A (en) *	1980-03-12	1981-11-17	American Cyanamid Company	Process for self-crimping acrylic fiber from a melt of two non-compatible polymers
US9439294B2 (en)	2014-04-16	2016-09-06	Rohm And Haas Electronic Materials Llc	Reaction products of heterocyclic nitrogen compounds polyepoxides and polyhalogens

0
- NL NL281157D patent/NL281157A/xx unknown
- NL NL135464D patent/NL135464C/xx active
- NL NL129127D patent/NL129127C/xx active
- BE BE591201D patent/BE591201A/xx unknown
- BE BE620706D patent/BE620706A/xx unknown
- NL NL267126D patent/NL267126A/xx unknown
- DD DD47738D patent/DD47738A/xx unknown
- NL NL251988D patent/NL251988A/xx unknown
1960
- 1960-05-23 GB GB18101/60A patent/GB950852A/en not_active Expired
- 1960-05-25 DK DK251461AA patent/DK106584C/da active
- 1960-05-25 DK DK205760AA patent/DK102482C/da active
- 1960-05-25 CH CH601360A patent/CH416108A/de unknown
- 1960-05-25 SE SE5186/60A patent/SE308167B/xx unknown
- 1960-05-25 DE DE19601469105 patent/DE1469105A1/de active Pending
1961
- 1961-07-15 CH CH833061A patent/CH469770A/de unknown
- 1961-07-17 GB GB25901/61A patent/GB992011A/en not_active Expired
1962
- 1962-07-23 AT AT592662A patent/AT238367B/de active
- 1962-07-23 GB GB28227/62A patent/GB1006581A/en not_active Expired
- 1962-07-25 DE DE1962M0053683 patent/DE1469110A1/de not_active Withdrawn
- 1962-07-26 SE SE8257/62A patent/SE322862B/xx unknown
1967
- 1967-03-28 OA OA52829A patent/OA02364A/fr unknown

Also Published As

Publication number	Publication date
DK106584C (da)	1967-02-20
GB992011A (en)	1965-05-12
OA02364A (fr)	1970-05-05
NL267126A (fr)	1900-01-01
SE322862B (fr)	1970-04-20
DK102482C (da)	1965-08-30
CH469770A (de)	1969-03-15
DE1469105A1 (de)	1968-11-28
DD47738A (fr)	1900-01-01
NL281157A (fr)	1900-01-01
NL129127C (fr)	1900-01-01
NL135464C (fr)	1900-01-01
NL251988A (fr)	1900-01-01
GB950852A (en)	1964-02-26
SE308167B (fr)	1969-02-03
GB1006581A (en)	1965-10-06
DE1469110A1 (de)	1968-11-07
BE591201A (fr)	1900-01-01
AT238367B (de)	1965-02-10
BE620706A (fr)	1900-01-01

Publication	Publication Date	Title
US3098697A (en)	1963-07-23	Dichloroethane
DE2660699C2 (de)	1985-03-07	Poly-(2,2,6,6-tetraalkyl-4-piperidyl)-amine sowie Verfahren zu deren Herstellung
DE931732C (de)	1955-08-16	Verfahren zur Herstellung eines fuer die Verarbeitung auf geformte Gegenstaende geeigneten Kopolymeren
DE1570890A1 (de)	1970-01-29	Polymerisate aus Diaminobenzaniliden
DE1118970B (de)	1961-12-07	Verfahren zur Herstellung wasserloeslicher oder leicht in Wasser dispergierbarer polymerer quaternaerer Ammoniumverbindungen
DE2047858A1 (de)	1971-04-22	Basische Polyamide, ihre Herstellung und ihre Verwendung
DE1295749B (de)	1969-05-22	Verfahren zur Herstellung von Textilfasern oder Folien mit verbesserter Anfaerbbarkeit
DE1469105A1 (de)	1968-11-28	Verbesserte Textilfaeden und Verfahren zu ihrer Herstellung
DE1469105C (de)	1971-06-03	Textilfaden oder fasern aus einem Gemisch aus Olefinpolymeren ider Acryl nitrilpolymeren mit einer basichen poly meren Stickstoffverbindung sowie Ver fahren zur Herstellung dieser Textil faden oder fasern
US3182105A (en)	1965-05-04	Process of rendering polyolefins more dye receptive by mixing with organic compoundshaving phenolic hydroxy groups
DE1469107A1 (de)	1968-11-07	Spinn- und leicht anfaerbbare polymere Masse
DE1469105B (fr)
US3661821A (en)	1972-05-09	Resinous condensation products and method of preparing same
AT233162B (de)	1964-04-25	Verfahren zur Herstellung färbbarer Textilfasern
DE1246659B (de)	1967-08-10	Verfahren zur Verbesserung der Anfaerbbarkeit von Faeden oder Fasern aus Polyolefinen
AT228380B (de)	1963-07-10	Verfahren zur Herstellung von färbbaren Textilfasern
DE1469106C (de)	1972-01-27	Verfahren zum Verbessern der Anfärb barkeit von Faden aus Polyolefinen
AT219186B (de)	1962-01-10	Verfahren zur Herstellung von Textilfasern auf Basis von kristallinen Polyolefinen
CH391360A (de)	1965-04-30	Rotierbares Bearbeitungsglied zum Versetzen am Boden liegenden Materials
DE2127081C3 (de)	1980-12-18	Färbbare polymere Zusammensetzung
DE1469110C (de)	1971-11-18	Textilfaden mit verbesserter Anfärbbarkeit und Verfahren zu ihrer Herstellung
DE1238214B (de)	1967-04-06	Verfahren zur Herstellung von stickstoffhaltigen Kondensationsprodukten
DE2240534A1 (de)	1973-02-22	Faerbbare kunststoffe auf polyolefinbasis
AT233727B (de)	1964-05-25	Verfahren zur Herstellung von Formgebilden, insbesondere von Fäden, Filmen, Bändern od. dgl. mit verbesserter Färbbarkeit
DE1494659C (de)	1971-11-25	Verfahren zum Herstellen von Textilfaden, Folien und Bändern aus modifizierten Polyolefinen