CH430207A - Verfahren zur Herstellung fester, lagerbeständiger, wasserlöslicher, Kondensationsharze aus Harnstoff, Formaldehyd und Polyaminen - Google Patents

Verfahren zur Herstellung fester, lagerbeständiger, wasserlöslicher, Kondensationsharze aus Harnstoff, Formaldehyd und Polyaminen

Info

Publication number: CH430207A
Authority: CH; Switzerland
Prior art keywords: resin; parts; additive; formaldehyde; condensation
Prior art date: 1961-12-15

Application number

CH1319262A

Other languages

German (de)

English (en)

Inventor

Hans Brandeis

Rolf Fikentscher

Lenz Johann

Kirmse Herbert

Original Assignee

Basf 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.)

1961-12-15

Filing date

1962-11-12

Publication date

1967-02-15

1962-11-12 Application filed by Basf Ag filed Critical Basf Ag

1967-02-15 Publication of CH430207A publication Critical patent/CH430207A/de

Links

229920005989 resin Polymers 0.000 title claims description 82
239000011347 resin Substances 0.000 title claims description 82
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 title claims description 70
238000009833 condensation Methods 0.000 title claims description 38
230000005494 condensation Effects 0.000 title claims description 29
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title claims description 15
239000004202 carbamide Substances 0.000 title claims description 15
229920000768 polyamine Polymers 0.000 title claims description 14
238000004519 manufacturing process Methods 0.000 title claims description 8
239000007787 solid Substances 0.000 title claims description 7
238000000034 method Methods 0.000 title claims description 6
239000000243 solution Substances 0.000 claims description 53
239000000654 additive Substances 0.000 claims description 29
230000000996 additive effect Effects 0.000 claims description 28
239000000843 powder Substances 0.000 claims description 24
239000002253 acid Substances 0.000 claims description 11
238000003860 storage Methods 0.000 claims description 11
150000001875 compounds Chemical class 0.000 claims description 9
239000007864 aqueous solution Substances 0.000 claims description 7
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 6
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 5
125000001931 aliphatic group Chemical group 0.000 claims description 4
238000001035 drying Methods 0.000 claims description 4
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
235000019253 formic acid Nutrition 0.000 claims description 3
150000001449 anionic compounds Chemical class 0.000 claims description 2
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 42
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 18
235000013877 carbamide Nutrition 0.000 description 13
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 8
230000002378 acidificating effect Effects 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
239000000203 mixture Substances 0.000 description 8
238000001694 spray drying Methods 0.000 description 8
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 7
BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 6
239000005457 ice water Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
150000007513 acids Chemical class 0.000 description 4
229920002678 cellulose Polymers 0.000 description 4
239000001913 cellulose Substances 0.000 description 4
239000000499 gel Substances 0.000 description 4
OGNSCSPNOLGXSM-UHFFFAOYSA-N (+/-)-DABA Natural products NCCC(N)C(O)=O OGNSCSPNOLGXSM-UHFFFAOYSA-N 0.000 description 3
229960003692 gamma aminobutyric acid Drugs 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
229910052943 magnesium sulfate Inorganic materials 0.000 description 3
235000019341 magnesium sulphate Nutrition 0.000 description 3
238000006386 neutralization reaction Methods 0.000 description 3
HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 2
ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
229920001807 Urea-formaldehyde Polymers 0.000 description 2
239000012670 alkaline solution Substances 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
239000005018 casein Substances 0.000 description 2
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
235000021240 caseins Nutrition 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
239000000047 product Substances 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 2
XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 2
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
VGGLHLAESQEWCR-UHFFFAOYSA-N N-(hydroxymethyl)urea Chemical compound NC(=O)NCO VGGLHLAESQEWCR-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
238000004026 adhesive bonding Methods 0.000 description 1
230000032683 aging Effects 0.000 description 1
235000004279 alanine Nutrition 0.000 description 1
229960003767 alanine Drugs 0.000 description 1
GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
150000003973 alkyl amines Chemical group 0.000 description 1
229940037003 alum Drugs 0.000 description 1
229960004050 aminobenzoic acid Drugs 0.000 description 1
229960002684 aminocaproic acid Drugs 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000006735 deficit Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002169 ethanolamines Chemical group 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000008098 formaldehyde solution Substances 0.000 description 1
235000013922 glutamic acid Nutrition 0.000 description 1
229960002989 glutamic acid Drugs 0.000 description 1
239000004220 glutamic acid Substances 0.000 description 1
235000013905 glycine and its sodium salt Nutrition 0.000 description 1
159000000011 group IA salts Chemical class 0.000 description 1
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 1
239000007788 liquid Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
230000020477 pH reduction Effects 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
DJEHXEMURTVAOE-UHFFFAOYSA-M potassium bisulfite Chemical compound [K+].OS([O-])=O DJEHXEMURTVAOE-UHFFFAOYSA-M 0.000 description 1
229940099427 potassium bisulfite Drugs 0.000 description 1
235000010259 potassium hydrogen sulphite Nutrition 0.000 description 1
BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
235000019252 potassium sulphite Nutrition 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
239000013049 sediment Substances 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000005728 strengthening Methods 0.000 description 1
229950000244 sulfanilic acid Drugs 0.000 description 1
229960003080 taurine Drugs 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
239000004753 textile Substances 0.000 description 1
UHLICHJXSLXXRV-UHFFFAOYSA-N triazinan-4-one Chemical class O=C1CCNNN1 UHLICHJXSLXXRV-UHFFFAOYSA-N 0.000 description 1
210000002700 urine Anatomy 0.000 description 1
238000010792 warming Methods 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
- 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
- C08G12/40—Chemically modified polycondensates
- 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
- C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08G12/043—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with at least two compounds covered by more than one of the groups C08G12/06 - C08G12/24
- C08G12/046—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with at least two compounds covered by more than one of the groups C08G12/06 - C08G12/24 one being urea or thiourea
- 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

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (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)
Paper (AREA)
Biological Depolymerization Polymers (AREA)
Compositions Of Macromolecular Compounds (AREA)

CH1319262A 1961-12-15 1962-11-12 Verfahren zur Herstellung fester, lagerbeständiger, wasserlöslicher, Kondensationsharze aus Harnstoff, Formaldehyd und Polyaminen CH430207A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DEB0065199		1961-12-15

Publications (1)

Publication Number	Publication Date
CH430207A true CH430207A (de)	1967-02-15

Family

ID=6974676

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1319262A CH430207A (de)	1961-12-15	1962-11-12	Verfahren zur Herstellung fester, lagerbeständiger, wasserlöslicher, Kondensationsharze aus Harnstoff, Formaldehyd und Polyaminen

Country Status (8)

Country	Link
AT (1)	AT242954B (fr)
BE (1)	BE626115A (fr)
CH (1)	CH430207A (fr)
DE (1)	DE1445264C3 (fr)
FR (1)	FR1343190A (fr)
GB (1)	GB1020764A (fr)
NL (1)	NL133087C (fr)
SE (1)	SE305541B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1991002762A1 (fr) *	1989-08-23	1991-03-07	Basf Aktiengesellschaft	Resines cationiques uree-formaldehyde, procede de preparation et utilisation dans l'industrie de fabrication du papier

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2627067C3 (de) *	1976-06-16	1981-06-19	Nišnetagilskij zavod plastmass, Nišnij Tagil, Sverdlovskaja oblast'	Verfahren zur Herstellung von mit aliphatischen Polyaminen modifizierten wasserlöslichen Harnstoff-Formaldehydharzen
US4407976A (en) *	1980-06-16	1983-10-04	Ciba-Geigy Corporation	Anionic adsorbent

0
- BE BE626115A patent/BE626115A/fr unknown
1961
- 1961-12-15 DE DE19611445264 patent/DE1445264C3/de not_active Expired
1962
- 1962-11-12 CH CH1319262A patent/CH430207A/de unknown
- 1962-11-29 SE SE1286862A patent/SE305541B/xx unknown
- 1962-12-10 GB GB4646762A patent/GB1020764A/en not_active Expired
- 1962-12-13 NL NL286692A patent/NL133087C/xx active
- 1962-12-14 AT AT978162A patent/AT242954B/de active
- 1962-12-14 FR FR918668A patent/FR1343190A/fr not_active Expired

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1991002762A1 (fr) *	1989-08-23	1991-03-07	Basf Aktiengesellschaft	Resines cationiques uree-formaldehyde, procede de preparation et utilisation dans l'industrie de fabrication du papier
US5554718A (en) *	1989-08-23	1996-09-10	Basf Aktiengesellschaft	Catonic urea/formaldehyde resins, their preparation and their use in the paper industry

Also Published As

Publication number	Publication date
DE1445264C3 (de)	1974-02-21
SE305541B (sv)	1968-10-28
DE1445264B2 (de)	1973-06-28
GB1020764A (en)	1966-02-23
NL286692A (nl)	1965-02-10
FR1343190A (fr)	1963-11-15
AT242954B (de)	1965-10-11
NL133087C (nl)	1971-12-15
BE626115A (fr)	1963-06-14
DE1445264A1 (de)	1969-04-10

Publication	Publication Date	Title
DE1645536C3 (de)	1979-03-08	Verfahren zur Herstellung von wasserlöslichen, hitzehärtbaren Polymeren
DE1937710A1 (de)	1970-01-29	Nassfeste Harze
AT150002B (de)	1937-06-25	Verfahren zur Herstellung von Aldehyd-Kondensationsprodukten.
DE2928878C2 (de)	1986-08-28	Wäßrige Lösung eines wärmehärt- oder -fixierbaren Harzes, Verfahren zu ihrer Herstellung und ihre Verwendung in einer Papierstreichmasse
CH430207A (de)	1967-02-15	Verfahren zur Herstellung fester, lagerbeständiger, wasserlöslicher, Kondensationsharze aus Harnstoff, Formaldehyd und Polyaminen
DE2353430C2 (de)	1982-04-15	Verfahren zur Herstellung von kationischen Polyaminopolyamiden und deren Verwendung als Papiererzeugungshilfsmittel
EP0489055B1 (fr)	1994-11-02	Resines cationiques uree-formaldehyde, procede de preparation et utilisation dans l'industrie de fabrication du papier
DE3505575A1 (de)	1985-08-29	Harnstoff-formaldehydharz und verfahren zu seiner herstellung
DE2756469A1 (de)	1979-06-21	Amidgruppenhaltige polyamine
DE1103582B (de)	1961-03-30	Verfahren zur Herstellung haertbarer Aminotriazin-Kondensations-produkte
EP0123196B1 (fr)	1988-06-29	Procédé pour la préparation de résines d'urée-formaldéhyde cationiques solubles dans l'eau, et leur utilisation pour la fabrication de papier
DE1595336A1 (de)	1970-09-03	Verfahren zur Herstellung wasserloeslicher kationischer Polykondensate
DE69821745T2 (de)	2004-12-02	Bildung von superabsorbierendem polymer
DE911436C (de)	1954-05-13	Verfahren zur Herstellung von Kondensationsprodukten
US2786824A (en)	1957-03-26	Cationic urea-formaldehyde resins and preparation thereof
DE1908094C3 (de)	1978-11-09	Verwendung wäßriger Lösungen von Aminoplast-Harzkondensaten als Trankharzlösungen
DE2403443A1 (de)	1975-07-31	Verfahren zur herstellung von kationischen kondensationsprodukten
US2803564A (en)	1957-08-20	Acetylene diurea-formaldehyde reaction product and treatment of textiles therewith
DE865975C (de)	1953-02-09	Verfahren zur Herstellung alkaliloeslicher, harzartiger Kondensationsprodukte
AT163630B (de)	1949-07-25	Verfahren zur Herstellung wasserlöslicher methylierter Methylolmelamine
AT167122B (de)	1950-11-10	Verfahren zur Herstellung von Zelluloseerzeugnissen mit verbresserter Naßfestigkeit
AT212016B (de)	1960-11-25	Verfahren zur Herstellung nicht härtbarer kationischer Kondensationsprodukte
DE813210C (de)	1951-09-10	Verfahren zur Herstellung eines waermehaertenden harzartigen Produktes
AT240159B (de)	1965-05-10	Verfahren zur Herstellung von Papier mit verbesserter Naßfestigkeit
DE1017367B (de)	1957-10-10	Verfahren zur Herstellung von hochmolekularen, festen, in neutralem oder schwach saurem Wasser loeslichen, kationenaktiven Harnstoff-Formaldehyd-Kondensationsprodukten