DE1120070B - Verfahren zur Herstellung von faerbbaren Gebilden aus Polypropylen - Google Patents
Verfahren zur Herstellung von faerbbaren Gebilden aus PolypropylenInfo
- Publication number
- DE1120070B DE1120070B DEM35414A DEM0035414A DE1120070B DE 1120070 B DE1120070 B DE 1120070B DE M35414 A DEM35414 A DE M35414A DE M0035414 A DEM0035414 A DE M0035414A DE 1120070 B DE1120070 B DE 1120070B
- Authority
- DE
- Germany
- Prior art keywords
- polypropylene
- threads
- epoxy resin
- water
- dyes
- 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.)
- Pending
Links
- -1 polypropylene Polymers 0.000 title claims description 15
- 239000004743 Polypropylene Substances 0.000 title claims description 14
- 229920001155 polypropylene Polymers 0.000 title claims description 14
- 238000000034 method Methods 0.000 title claims description 6
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000003822 epoxy resin Substances 0.000 claims description 15
- 229920000647 polyepoxide Polymers 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 11
- 238000010521 absorption reaction Methods 0.000 claims description 9
- 239000000975 dye Substances 0.000 claims description 6
- 238000004043 dyeing Methods 0.000 claims description 6
- 239000012932 acetate dye Substances 0.000 claims description 5
- 238000001125 extrusion Methods 0.000 claims description 4
- 239000003431 cross linking reagent Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 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 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 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 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 229960004488 linolenic acid Drugs 0.000 description 2
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229910052979 sodium sulfide Inorganic materials 0.000 description 2
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- 241000031711 Cytophagaceae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C08L23/12—Polypropene
-
- 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
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/46—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyolefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/10—Polyvinyl halide esters or alcohol fiber modification
-
- 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
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/928—Polyolefin fiber
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT1416056 | 1956-09-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1120070B true DE1120070B (de) | 1961-12-21 |
Family
ID=11144876
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEM35414A Pending DE1120070B (de) | 1956-09-27 | 1957-09-23 | Verfahren zur Herstellung von faerbbaren Gebilden aus Polypropylen |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3013998A (en, 2012) |
| BE (1) | BE561156A (en, 2012) |
| CH (1) | CH365176A (en, 2012) |
| DE (1) | DE1120070B (en, 2012) |
| ES (1) | ES237783A1 (en, 2012) |
| FR (1) | FR1187838A (en, 2012) |
| GB (1) | GB866920A (en, 2012) |
| NL (1) | NL221118A (en, 2012) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3312755A (en) * | 1956-12-12 | 1967-04-04 | Montedison Spa | Readily dyeable compositions consisting of isotactic polypropylene and from 0.1 to 200deg. of a member selected from the group consisting of polyamides, polyurethanes, polyesters and polyalkyleneimine reaction products |
| IT610638A (en, 2012) * | 1959-06-09 | |||
| DE1174012B (de) * | 1959-12-18 | 1964-07-16 | Fuji Spinning Co Ltd | Verfahren zur Herstellung von leicht faerbbaren Fasern oder aehnlich geformten Gegenstaenden aus kristallinem Polypropylen |
| BE603385A (en, 2012) * | 1960-05-05 | |||
| BE611524A (en, 2012) * | 1960-12-15 | |||
| NL276258A (en, 2012) * | 1961-03-23 | |||
| NL130157C (en, 2012) * | 1961-06-15 | |||
| US3195975A (en) * | 1961-08-10 | 1965-07-20 | Montedison Spa | Tri-methylol propane diallyl ether treatment of polyolefin-polymeric nitrogenous compound mixtures and fibers and product thereof |
| BE626339A (en, 2012) * | 1961-12-21 | 1900-01-01 | ||
| US3288897A (en) * | 1962-05-18 | 1966-11-29 | Montedison Spa | Dyeable materials |
| US3294864A (en) * | 1962-10-05 | 1966-12-27 | Exxon Research Engineering Co | Polyolefins blended with amineepoxide condensate |
| US3262988A (en) * | 1962-12-11 | 1966-07-26 | Union Carbide Corp | Composition comprising low density polyethylene and a thermoplastic polyhydroxy polyether giving smooth contour at high extrusion speeds |
| GB2264117B (en) * | 1992-02-13 | 1995-07-26 | Shinto Paint Co Ltd | Under-coating composition |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2683130A (en) * | 1950-05-27 | 1954-07-06 | Koppers Co Inc | Polymeric compositions from phenolaldehyde-epoxy resins and resins reactive therewith |
| US2683128A (en) * | 1950-09-29 | 1954-07-06 | Koppers Co Inc | Polymeric compositions |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA470662A (en) * | 1951-01-09 | F. Klein Arthur | Methods of dyeing vinyl polymers and copolymers | |
| BE411266A (en, 2012) * | 1934-09-15 | |||
| US2376511A (en) * | 1941-05-23 | 1945-05-22 | Chrysler Corp | Method of making synthetic resin yarn |
| US2367173A (en) * | 1942-02-26 | 1945-01-09 | Martin Elmore Louis | Process for melt extruding synthetic polymers |
| NL68092C (en, 2012) * | 1947-06-11 | |||
| US2713567A (en) * | 1952-04-14 | 1955-07-19 | Shell Dev | Composition containing glycidyl polyether and a polyvinyl acetal resin |
| US2707709A (en) * | 1952-09-12 | 1955-05-03 | Monsanto Chemicals | Non-electrostatic resinous molding compositions |
-
0
- NL NL221118D patent/NL221118A/xx unknown
-
1957
- 1957-09-16 US US683981A patent/US3013998A/en not_active Expired - Lifetime
- 1957-09-21 CH CH5079657A patent/CH365176A/de unknown
- 1957-09-23 FR FR1187838D patent/FR1187838A/fr not_active Expired
- 1957-09-23 DE DEM35414A patent/DE1120070B/de active Pending
- 1957-09-25 GB GB30098/57A patent/GB866920A/en not_active Expired
- 1957-09-26 ES ES0237783A patent/ES237783A1/es not_active Expired
- 1957-09-26 BE BE561156D patent/BE561156A/xx unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2683130A (en) * | 1950-05-27 | 1954-07-06 | Koppers Co Inc | Polymeric compositions from phenolaldehyde-epoxy resins and resins reactive therewith |
| US2683128A (en) * | 1950-09-29 | 1954-07-06 | Koppers Co Inc | Polymeric compositions |
Also Published As
| Publication number | Publication date |
|---|---|
| US3013998A (en) | 1961-12-19 |
| CH365176A (de) | 1962-10-31 |
| ES237783A1 (es) | 1958-07-01 |
| GB866920A (en) | 1961-05-03 |
| NL221118A (en, 2012) | 1900-01-01 |
| FR1187838A (fr) | 1959-09-16 |
| BE561156A (fr) | 1960-05-20 |
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