FI62876C - Anjoniska medel foer pappersytlimning - Google Patents
Anjoniska medel foer pappersytlimning Download PDFInfo
- Publication number
- FI62876C FI62876C FI781927A FI781927A FI62876C FI 62876 C FI62876 C FI 62876C FI 781927 A FI781927 A FI 781927A FI 781927 A FI781927 A FI 781927A FI 62876 C FI62876 C FI 62876C
- Authority
- FI
- Finland
- Prior art keywords
- paper
- sizing
- copolymers
- adhesive
- anionic
- Prior art date
Links
- 238000004513 sizing Methods 0.000 description 22
- 239000000853 adhesive Substances 0.000 description 15
- 230000001070 adhesive effect Effects 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- -1 aluminum ions Chemical class 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 6
- 238000004026 adhesive bonding Methods 0.000 description 6
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 229920006301 statistical copolymer Polymers 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 125000005462 imide group Chemical group 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical compound CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
- IUQJDHJVPLLKFL-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)acetate;dimethylazanium Chemical compound CNC.OC(=O)COC1=CC=C(Cl)C=C1Cl IUQJDHJVPLLKFL-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- 235000002566 Capsicum Nutrition 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000006002 Pepper Substances 0.000 description 1
- 235000016761 Piper aduncum Nutrition 0.000 description 1
- 235000017804 Piper guineense Nutrition 0.000 description 1
- 244000203593 Piper nigrum Species 0.000 description 1
- 235000008184 Piper nigrum Nutrition 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 239000004826 Synthetic adhesive Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical group 0.000 description 1
- 229920006320 anionic starch Polymers 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 150000005332 diethylamines Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 150000004680 hydrogen peroxides Chemical class 0.000 description 1
- 150000003949 imides Chemical group 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- 239000013558 reference substance Substances 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/41—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
- D21H17/42—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups anionic
- D21H17/43—Carboxyl groups or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/10—Copolymer characterised by the proportions of the comonomers expressed as molar percentages
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paper (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772727510 DE2727510A1 (de) | 1977-06-18 | 1977-06-18 | Anionische papieroberflaechenleimungsmittel |
| DE2727510 | 1977-06-18 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI781927A7 FI781927A7 (fi) | 1978-12-19 |
| FI62876B FI62876B (fi) | 1982-11-30 |
| FI62876C true FI62876C (fi) | 1983-03-10 |
Family
ID=6011812
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI781927A FI62876C (fi) | 1977-06-18 | 1978-06-16 | Anjoniska medel foer pappersytlimning |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US4200559A (de) |
| EP (1) | EP0000221B1 (de) |
| JP (1) | JPS546911A (de) |
| AT (1) | AT364910B (de) |
| DE (2) | DE2727510A1 (de) |
| DK (1) | DK273178A (de) |
| ES (1) | ES470820A1 (de) |
| FI (1) | FI62876C (de) |
| IT (1) | IT1096705B (de) |
| NO (1) | NO150645C (de) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2905764A1 (de) * | 1979-02-15 | 1980-08-28 | Huels Chemische Werke Ag | Hydroxylgruppenhaltige copolymerisate, verfahren zu ihrer herstellung und ihre verwendung als papierleimungsmittel |
| DE2939293A1 (de) * | 1979-09-28 | 1981-04-09 | Chemische Werke Hüls AG, 4370 Marl | Copolymerisat aus maleinsaeureanhydrid, dicyclopentadien und vinylcyclohexen und dessen verwendung als anionisches papieroberflaechenleimungsmittel |
| DE3148456A1 (de) * | 1981-12-08 | 1983-07-21 | Basf Ag, 6700 Ludwigshafen | Leimungsmittel fuer papier |
| JPS6052700A (ja) * | 1983-09-01 | 1985-03-25 | 東ソー株式会社 | 紙コ−ト用組成物 |
| US4767553A (en) * | 1986-12-24 | 1988-08-30 | Texaco Inc. | Lubricating oil containing dispersant viscosity index improver |
| DE4133123A1 (de) * | 1991-10-05 | 1993-04-08 | Basf Ag | Verwendung von copolymerisaten aus langkettigen olefinen und maleinsaeureanhydrid in form der halbamide mit morpholin als leimungsmittel fuer papier |
| US7041197B2 (en) * | 2003-04-15 | 2006-05-09 | Fort James Corporation | Wet strength and softness enhancement of paper products |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2475731A (en) * | 1944-10-27 | 1949-07-12 | Bakelite Corp | Copolymerization products of styrene and adduct modified glycolmaleate resins |
| US2608550A (en) * | 1947-01-08 | 1952-08-26 | Interchem Corp | Reaction products of unsaturated dicarboxylic acid derivatives with cyclopentadiene polymers |
| US3188303A (en) * | 1961-03-17 | 1965-06-08 | Velsicol Chemical Corp | Process and product relating to the reaction of dicyclopentadiene and alpha, beta di-and tri-carboxylic acids |
| DE1570538A1 (de) * | 1965-02-05 | 1970-01-29 | Hoechst Ag | Verfahren zur Herstellung von hochmolekularen Terpolymeren |
| US3468823A (en) * | 1965-06-14 | 1969-09-23 | Monsanto Co | Maleic interpolymer-starch-rosin sizes |
| JPS5113046B2 (de) * | 1972-10-20 | 1976-04-24 | ||
| JPS5325049B2 (de) * | 1972-11-15 | 1978-07-25 | ||
| US4115331A (en) * | 1973-05-31 | 1978-09-19 | Sanyo Chemical Industries, Ltd. | Surface sizing compositions for paper |
| FR2335535A1 (fr) * | 1975-12-16 | 1977-07-15 | Borg Warner | Copolymeres d'anhydride maleique et de dimeres de dienes conjugues cycliques et leur procede de preparation |
-
1977
- 1977-06-18 DE DE19772727510 patent/DE2727510A1/de not_active Withdrawn
-
1978
- 1978-06-12 IT IT24430/78A patent/IT1096705B/it active
- 1978-06-14 DE DE7878200042T patent/DE2861751D1/de not_active Expired
- 1978-06-14 EP EP78200042A patent/EP0000221B1/de not_active Expired
- 1978-06-15 AT AT0436178A patent/AT364910B/de not_active IP Right Cessation
- 1978-06-15 ES ES470820A patent/ES470820A1/es not_active Expired
- 1978-06-16 DK DK273178A patent/DK273178A/da not_active Application Discontinuation
- 1978-06-16 NO NO782107A patent/NO150645C/no unknown
- 1978-06-16 JP JP7226378A patent/JPS546911A/ja active Pending
- 1978-06-16 FI FI781927A patent/FI62876C/fi not_active IP Right Cessation
- 1978-06-16 US US05/916,124 patent/US4200559A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| NO782107L (no) | 1978-12-19 |
| DK273178A (da) | 1978-12-19 |
| FI62876B (fi) | 1982-11-30 |
| IT1096705B (it) | 1985-08-26 |
| ES470820A1 (es) | 1979-01-16 |
| DE2861751D1 (en) | 1982-06-03 |
| IT7824430A0 (it) | 1978-06-12 |
| NO150645B (no) | 1984-08-13 |
| US4200559A (en) | 1980-04-29 |
| EP0000221A1 (de) | 1979-01-10 |
| EP0000221B1 (de) | 1982-04-21 |
| AT364910B (de) | 1981-11-25 |
| JPS546911A (en) | 1979-01-19 |
| NO150645C (no) | 1984-11-21 |
| ATA436178A (de) | 1981-04-15 |
| FI781927A7 (fi) | 1978-12-19 |
| DE2727510A1 (de) | 1979-01-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: VEBA-CHEMIE AKTIENGESELLSCHAFT |