DE1144482B - Verfahren zur Herstellung von haertbaren hoehermolekularen Kondensationsprodukten - Google Patents
Verfahren zur Herstellung von haertbaren hoehermolekularen KondensationsproduktenInfo
- Publication number
- DE1144482B DE1144482B DEF33568A DEF0033568A DE1144482B DE 1144482 B DE1144482 B DE 1144482B DE F33568 A DEF33568 A DE F33568A DE F0033568 A DEF0033568 A DE F0033568A DE 1144482 B DE1144482 B DE 1144482B
- Authority
- DE
- Germany
- Prior art keywords
- molecular weight
- hours
- solution
- curable
- aldehydes
- 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
- 238000000034 method Methods 0.000 title claims description 12
- 239000007859 condensation product Substances 0.000 title claims description 5
- 238000004519 manufacturing process Methods 0.000 title description 2
- -1 aliphatic amines Chemical class 0.000 claims description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 8
- 239000004202 carbamide Substances 0.000 claims description 8
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 claims description 7
- 229950005308 oxymethurea Drugs 0.000 claims description 7
- 125000003277 amino group Chemical group 0.000 claims description 5
- 150000007824 aliphatic compounds Chemical class 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 238000002955 isolation Methods 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 2
- 239000000243 solution Substances 0.000 description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 21
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 13
- 238000003756 stirring Methods 0.000 description 11
- 239000008098 formaldehyde solution Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 150000001299 aldehydes Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000000839 emulsion Substances 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- NQGIJDNPUZEBRU-UHFFFAOYSA-N dodecanoyl chloride Chemical compound CCCCCCCCCCCC(Cl)=O NQGIJDNPUZEBRU-UHFFFAOYSA-N 0.000 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 description 3
- 239000002904 solvent Substances 0.000 description 3
- QWDQYHPOSSHSAW-UHFFFAOYSA-N 1-isocyanatooctadecane Chemical compound CCCCCCCCCCCCCCCCCCN=C=O QWDQYHPOSSHSAW-UHFFFAOYSA-N 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- XLOOEGCMPAYAID-UHFFFAOYSA-N 6-(1,3,5-triazin-2-yl)-1h-1,3,5-triazin-2-one Chemical compound N1C(=O)N=CN=C1C1=NC=NC=N1 XLOOEGCMPAYAID-UHFFFAOYSA-N 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical group ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 2
- 229920002866 paraformaldehyde Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- XEPXDIORGSIWCI-UHFFFAOYSA-N 1-chloro-1-(1-chloropentadecoxy)pentadecane Chemical compound CCCCCCCCCCCCCCC(Cl)OC(Cl)CCCCCCCCCCCCCC XEPXDIORGSIWCI-UHFFFAOYSA-N 0.000 description 1
- QMNWYGTWTXOQTP-UHFFFAOYSA-N 1h-triazin-6-one Chemical group O=C1C=CN=NN1 QMNWYGTWTXOQTP-UHFFFAOYSA-N 0.000 description 1
- TXPYHRFTMYVSLD-UHFFFAOYSA-N 2,3,4-tris(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=C(O)C(CC(C)C)=C1CC(C)C TXPYHRFTMYVSLD-UHFFFAOYSA-N 0.000 description 1
- QBJWYMFTMJFGOL-UHFFFAOYSA-N 2-hexadecyloxirane Chemical compound CCCCCCCCCCCCCCCCC1CO1 QBJWYMFTMJFGOL-UHFFFAOYSA-N 0.000 description 1
- ZAXCZCOUDLENMH-UHFFFAOYSA-N 3,3,3-tetramine Chemical compound NCCCNCCCNCCCN ZAXCZCOUDLENMH-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000008050 dialkyl sulfates Chemical class 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LTXYFELJDAARCU-UHFFFAOYSA-N ethyl n-(hydroxymethyl)carbamate Chemical compound CCOC(=O)NCO LTXYFELJDAARCU-UHFFFAOYSA-N 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 150000003977 halocarboxylic acids Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000001302 tertiary amino group Chemical group 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
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
-
- 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
- C08G12/30—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with substituted triazines
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
- C08G18/3842—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring
- C08G18/3851—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing heterocyclic rings having at least one nitrogen atom in the ring containing three nitrogen atoms in the ring
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/71—Monoisocyanates or monoisothiocyanates
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C11/00—Surface finishing of leather
- C14C11/003—Surface finishing of leather using macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C14—SKINS; HIDES; PELTS; LEATHER
- C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
- C14C9/00—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Paper (AREA)
Priority Applications (17)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL296101D NL296101A (d) | 1961-04-01 | ||
| NL276562D NL276562A (d) | 1961-04-01 | ||
| NL120875D NL120875C (d) | 1961-04-01 | ||
| BE615894D BE615894A (d) | 1961-04-01 | ||
| BE635833D BE635833A (d) | 1961-04-01 | ||
| DEF33568A DE1144482B (de) | 1961-04-01 | 1961-04-01 | Verfahren zur Herstellung von haertbaren hoehermolekularen Kondensationsprodukten |
| US182939A US3173895A (en) | 1961-04-01 | 1962-03-27 | Process for preparing hardenable condensation products from bistriazinones |
| GB12438/62A GB1000663A (en) | 1961-04-01 | 1962-03-30 | Process for preparing hardenable aminoplasts |
| CH394262A CH439739A (de) | 1961-04-01 | 1962-03-30 | Verfahren zur Herstellung von härtbaren Bistriazinon-Aldehyd-Kondensationsprodukten |
| FR893010A FR1337234A (fr) | 1961-04-01 | 1962-04-02 | Procédé de préparation de produits de condensation durcissables dérivés de bistriazinones et d'aldéhydes |
| DEF37531A DE1181909B (de) | 1961-04-01 | 1962-08-04 | Verfahren zur Herstellung von haertbaren hoeher-molekularen Kondensationsprodukten |
| US298601A US3211730A (en) | 1961-04-01 | 1963-07-30 | Process for preparing hardenable condensation products |
| CH955463A CH496748A (de) | 1961-04-01 | 1963-08-01 | Verfahren zur Herstellung von härtbaren Bistriazinon-Aldehyd-Kondensationsprodukten |
| GB30820/63A GB1044306A (en) | 1961-04-01 | 1963-08-02 | Process for preparing hardenable aminoplasts |
| AT623663A AT242370B (de) | 1961-04-01 | 1963-08-02 | Verfahren zur Herstellung härtbarer Kondensationsprodukte |
| FR943725A FR84128E (fr) | 1961-04-01 | 1963-08-05 | Procédé de préparation de produits de condensation durcissables dérivés de bis-triazinones et d'aldéhydes |
| SE8595/63A SE305956B (d) | 1961-04-01 | 1963-08-05 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF33568A DE1144482B (de) | 1961-04-01 | 1961-04-01 | Verfahren zur Herstellung von haertbaren hoehermolekularen Kondensationsprodukten |
| FR893010A FR1337234A (fr) | 1961-04-01 | 1962-04-02 | Procédé de préparation de produits de condensation durcissables dérivés de bistriazinones et d'aldéhydes |
| DEF37531A DE1181909B (de) | 1961-04-01 | 1962-08-04 | Verfahren zur Herstellung von haertbaren hoeher-molekularen Kondensationsprodukten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1144482B true DE1144482B (de) | 1963-02-28 |
Family
ID=62597278
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF33568A Pending DE1144482B (de) | 1961-04-01 | 1961-04-01 | Verfahren zur Herstellung von haertbaren hoehermolekularen Kondensationsprodukten |
| DEF37531A Pending DE1181909B (de) | 1961-04-01 | 1962-08-04 | Verfahren zur Herstellung von haertbaren hoeher-molekularen Kondensationsprodukten |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEF37531A Pending DE1181909B (de) | 1961-04-01 | 1962-08-04 | Verfahren zur Herstellung von haertbaren hoeher-molekularen Kondensationsprodukten |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US3173895A (d) |
| AT (1) | AT242370B (d) |
| BE (2) | BE615894A (d) |
| CH (2) | CH439739A (d) |
| DE (2) | DE1144482B (d) |
| FR (2) | FR1337234A (d) |
| GB (2) | GB1000663A (d) |
| NL (3) | NL276562A (d) |
| SE (1) | SE305956B (d) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4104444A (en) | 1975-09-04 | 1978-08-01 | Hoechst Aktiengesellschaft | Fiber reinforced chemically modified protein articles |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2654418A1 (de) * | 1976-12-01 | 1978-06-08 | Hoechst Ag | Verfahren zur herstellung von formkoerpern auf basis von chemisch modifiziertem cell ilosehydrat |
| DE2654417A1 (de) * | 1976-12-01 | 1978-06-08 | Hoechst Ag | Formkoerper, insbesondere verpackungsmaterial, auf basis von chemisch modifiziertem cellulosehydrat sowie verfahren zur herstellung der formkoerper |
| US7777035B2 (en) * | 2005-06-22 | 2010-08-17 | Chemocentryx, Inc. | Azaindazole compounds and methods of use |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2641584A (en) * | 1951-10-26 | 1953-06-09 | Du Pont | Adhesive compositions, including an amylaceous material and a triazone |
| US2729617A (en) * | 1952-04-14 | 1956-01-03 | Allied Chem & Dye Corp | Production of thermosetting synthetic resins capable of imparting improved wet strength to paper |
| US2950553A (en) * | 1957-01-16 | 1960-08-30 | Rohm & Haas | Method of producing wrinkle resistant garments and other manufactured articles of cotton-containing fabrics |
| US3035942A (en) * | 1958-07-15 | 1962-05-22 | American Cyanamid Co | Composition and process for treating cellulose containing textile material |
-
0
- NL NL120875D patent/NL120875C/xx active
- BE BE635833D patent/BE635833A/xx unknown
- BE BE615894D patent/BE615894A/fr unknown
- NL NL296101D patent/NL296101A/xx unknown
- NL NL276562D patent/NL276562A/xx unknown
-
1961
- 1961-04-01 DE DEF33568A patent/DE1144482B/de active Pending
-
1962
- 1962-03-27 US US182939A patent/US3173895A/en not_active Expired - Lifetime
- 1962-03-30 CH CH394262A patent/CH439739A/de unknown
- 1962-03-30 GB GB12438/62A patent/GB1000663A/en not_active Expired
- 1962-04-02 FR FR893010A patent/FR1337234A/fr not_active Expired
- 1962-08-04 DE DEF37531A patent/DE1181909B/de active Pending
-
1963
- 1963-07-30 US US298601A patent/US3211730A/en not_active Expired - Lifetime
- 1963-08-01 CH CH955463A patent/CH496748A/de unknown
- 1963-08-02 GB GB30820/63A patent/GB1044306A/en not_active Expired
- 1963-08-02 AT AT623663A patent/AT242370B/de active
- 1963-08-05 FR FR943725A patent/FR84128E/fr not_active Expired
- 1963-08-05 SE SE8595/63A patent/SE305956B/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4104444A (en) | 1975-09-04 | 1978-08-01 | Hoechst Aktiengesellschaft | Fiber reinforced chemically modified protein articles |
Also Published As
| Publication number | Publication date |
|---|---|
| NL276562A (d) | 1900-01-01 |
| BE635833A (d) | 1900-01-01 |
| CH439739A (de) | 1967-07-15 |
| AT242370B (de) | 1965-09-10 |
| SE305956B (d) | 1968-11-11 |
| BE615894A (d) | 1900-01-01 |
| GB1044306A (en) | 1966-09-28 |
| NL296101A (d) | 1900-01-01 |
| US3173895A (en) | 1965-03-16 |
| GB1000663A (en) | 1965-08-11 |
| DE1181909B (de) | 1964-11-19 |
| NL120875C (d) | 1900-01-01 |
| US3211730A (en) | 1965-10-12 |
| CH496748A (de) | 1970-09-30 |
| FR1337234A (fr) | 1963-09-13 |
| FR84128E (fr) | 1964-11-27 |
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