DE1937710A1 - Nassfeste Harze - Google Patents
Nassfeste HarzeInfo
- Publication number
- DE1937710A1 DE1937710A1 DE19691937710 DE1937710A DE1937710A1 DE 1937710 A1 DE1937710 A1 DE 1937710A1 DE 19691937710 DE19691937710 DE 19691937710 DE 1937710 A DE1937710 A DE 1937710A DE 1937710 A1 DE1937710 A1 DE 1937710A1
- Authority
- DE
- Germany
- Prior art keywords
- resin
- parts
- acid
- paper
- acrylamide
- 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
- 229920005989 resin Polymers 0.000 title claims description 95
- 239000011347 resin Substances 0.000 title claims description 95
- 239000000203 mixture Substances 0.000 claims description 36
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical group O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 claims description 22
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 14
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 229940015043 glyoxal Drugs 0.000 claims description 11
- 229920001744 Polyaldehyde Polymers 0.000 claims description 8
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 8
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 8
- 239000001361 adipic acid Substances 0.000 claims description 7
- 235000011037 adipic acid Nutrition 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 239000004952 Polyamide Substances 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 238000006482 condensation reaction Methods 0.000 claims description 4
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 4
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 4
- 239000000725 suspension Substances 0.000 claims description 4
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical group O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims description 3
- 150000003926 acrylamides Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
- 230000036651 mood Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 description 59
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 41
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 39
- 239000000123 paper Substances 0.000 description 37
- 239000007787 solid Substances 0.000 description 34
- 239000002655 kraft paper Substances 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- 229940037003 alum Drugs 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 229920001131 Pulp (paper) Polymers 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- -1 propylenetriamine Chemical compound 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical class CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 description 3
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- IZALUMVGBVKPJD-UHFFFAOYSA-N benzene-1,3-dicarbaldehyde Chemical compound O=CC1=CC=CC(C=O)=C1 IZALUMVGBVKPJD-UHFFFAOYSA-N 0.000 description 2
- 230000003750 conditioning effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 150000007519 polyprotic acids Polymers 0.000 description 2
- 239000013055 pulp slurry Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000001384 succinic acid Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical class OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- WVUYYXUATWMVIT-UHFFFAOYSA-N 1-bromo-4-ethoxybenzene Chemical compound CCOC1=CC=C(Br)C=C1 WVUYYXUATWMVIT-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- XWSGEVNYFYKXCP-UHFFFAOYSA-N 2-[carboxymethyl(methyl)amino]acetic acid Chemical compound OC(=O)CN(C)CC(O)=O XWSGEVNYFYKXCP-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- HCUZVMHXDRSBKX-UHFFFAOYSA-N 2-decylpropanedioic acid Chemical compound CCCCCCCCCCC(C(O)=O)C(O)=O HCUZVMHXDRSBKX-UHFFFAOYSA-N 0.000 description 1
- WWMIMRADNBGDHP-UHFFFAOYSA-N 2-hydroxyhexanedial Chemical compound O=CC(O)CCCC=O WWMIMRADNBGDHP-UHFFFAOYSA-N 0.000 description 1
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 241000173529 Aconitum napellus Species 0.000 description 1
- UMHJEEQLYBKSAN-UHFFFAOYSA-N Adipaldehyde Chemical compound O=CCCCCC=O UMHJEEQLYBKSAN-UHFFFAOYSA-N 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- 241000234479 Narcissus Species 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 229920002472 Starch Polymers 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229940023019 aconite Drugs 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000011128 aluminium sulphate Nutrition 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- 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 1
- 235000021240 caseins Nutrition 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- LNGJOYPCXLOTKL-UHFFFAOYSA-N cyclopentane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)C1 LNGJOYPCXLOTKL-UHFFFAOYSA-N 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
- 230000003292 diminished effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000009189 diving Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- JGEMYUOFGVHXKV-OWOJBTEDSA-N fumaraldehyde Chemical compound O=C\C=C\C=O JGEMYUOFGVHXKV-OWOJBTEDSA-N 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 238000002803 maceration Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
- KHARCSTZAGNHOT-UHFFFAOYSA-N naphthalene-2,3-dicarboxylic acid Chemical compound C1=CC=C2C=C(C(O)=O)C(C(=O)O)=CC2=C1 KHARCSTZAGNHOT-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- UVTBHNQYDPSCPO-UHFFFAOYSA-N pentane-1,1,5-tricarboxylic acid Chemical class OC(=O)CCCCC(C(O)=O)C(O)=O UVTBHNQYDPSCPO-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000005031 sulfite paper Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- UVZICZIVKIMRNE-UHFFFAOYSA-N thiodiacetic acid Chemical compound OC(=O)CSCC(O)=O UVZICZIVKIMRNE-UHFFFAOYSA-N 0.000 description 1
- 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 1
- MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 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
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
- D21H17/55—Polyamides; Polyaminoamides; Polyester-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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74709068A | 1968-07-24 | 1968-07-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1937710A1 true DE1937710A1 (de) | 1970-01-29 |
Family
ID=25003617
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19691937710 Pending DE1937710A1 (de) | 1968-07-24 | 1969-07-24 | Nassfeste Harze |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3607622A (OSRAM) |
| BE (1) | BE736513A (OSRAM) |
| BR (1) | BR6910808D0 (OSRAM) |
| DE (1) | DE1937710A1 (OSRAM) |
| ES (1) | ES369800A1 (OSRAM) |
| FR (1) | FR2013630A1 (OSRAM) |
| GB (1) | GB1269567A (OSRAM) |
| NL (1) | NL6911321A (OSRAM) |
| SE (1) | SE361048B (OSRAM) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10134156B4 (de) * | 2000-08-22 | 2009-08-27 | Uzin Tyro Ag | Verwendung einer Selbstklebefolie |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3853816A (en) * | 1965-07-12 | 1974-12-10 | American Cyanamid Co | Water-soluble thermosetting glyoxalated carbamoylalkyl alkyleneamino polymers and paper having a content thereof |
| US3728215A (en) * | 1971-03-12 | 1973-04-17 | Hercules Inc | Aminopalyamide{13 acrylamide{13 polyaldehyde resins employing an alpha, beta-unsaturated monobasic carboxylic acid or ester to make the aminopolyamide and their utility as wet and dry strengthening agents in papermaking |
| LU68901A1 (OSRAM) * | 1973-11-30 | 1975-08-20 | ||
| US4060507A (en) * | 1975-08-01 | 1977-11-29 | General Mills Chemicals, Inc. | Aminopolyamide-acrylamide-glyoxal resin |
| CA1096540A (en) * | 1976-02-12 | 1981-02-24 | Terence W. Rave | GLYOXAL MODIFIED POLY(.beta.-ALANINE) STRENGTHENING RESINS FOR USE IN PAPER |
| DE3274357D1 (en) * | 1981-04-27 | 1987-01-08 | Dow Chemical Co | Branched polyamidoamines, method for their preparation and method of improving the wet strength of paper using them |
| US4416729A (en) * | 1982-01-04 | 1983-11-22 | The Dow Chemical Company | Ammonium polyamidoamines |
| LU84268A1 (fr) * | 1982-07-13 | 1984-03-22 | Oreal | Poly beta-alanine reticulee et ses differentes applications |
| JPS61197008A (ja) * | 1985-02-27 | 1986-09-01 | Mitsubishi Chem Ind Ltd | 微細鉱物粒子を含む廃水処理用アニオン性凝集剤 |
| US4714736A (en) * | 1986-05-29 | 1987-12-22 | The Dow Chemical Company | Stable polyamide solutions |
| US5386040A (en) * | 1992-05-27 | 1995-01-31 | National Starch And Chemical Investment Holding Corporation | Low molecular weight polyacetals and polyaldehydes |
| US5382323A (en) * | 1993-01-08 | 1995-01-17 | Nalco Chemical Company | Cross-linked poly(aminoamides) as yankee dryer adhesives |
| US5427652A (en) * | 1994-02-04 | 1995-06-27 | The Mead Corporation | Repulpable wet strength paper |
| US5567798A (en) * | 1994-09-12 | 1996-10-22 | Georgia-Pacific Resins, Inc. | Repulpable wet strength resins for paper and paperboard |
| DE69603539T2 (de) | 1995-05-18 | 2000-01-13 | Fort James Corp., Richmond | Neue adhesive Zusammensetzungen zum Kreppen, Verfahren zum Kreppen und gekrepptes fibröses Gewebe |
| US6689250B1 (en) | 1995-05-18 | 2004-02-10 | Fort James Corporation | Crosslinkable creping adhesive formulations |
| US6197919B1 (en) | 1997-05-30 | 2001-03-06 | Hercules Incorporated | Resins of amphoteric aldehyde polymers and use of said resins as temporary wet-strength or dry-strength resins for paper |
| US6075082A (en) * | 1997-12-03 | 2000-06-13 | Nalco Chemical Company | Cross-linked polymide binders for ceramics manufacture |
| US5908889A (en) * | 1997-12-03 | 1999-06-01 | Nalco Chemical Company | Polyamide binders for ceramics manufacture |
| US6153106A (en) * | 1999-03-03 | 2000-11-28 | Nalco Chemical Company | Method for inhibiting the formation and deposition of silica scale in water systems |
| US6702923B1 (en) * | 1999-11-19 | 2004-03-09 | Akzo Nobel Nv | Wet strength agent and method for production thereof |
| US20020096281A1 (en) | 1999-11-19 | 2002-07-25 | Hans Wallenius | Wet-strong tissue paper |
| RU2223972C1 (ru) * | 1999-11-19 | 2004-02-20 | Акцо Нобель Н.В. | Агент для повышения влагопрочности и способ его получения |
| US20050261404A1 (en) * | 2004-05-20 | 2005-11-24 | Georgia-Pacific Resins, Inc. | Thermosetting adhesive compositions comprising a protein-based component and a polymeric quaternary amine cure accelerant |
| US20050257888A1 (en) * | 2004-05-20 | 2005-11-24 | Georgia-Pacific Resins, Inc. | Phenolic resin-based adhesives and methods of using same in preparing laminated veneer lumber (LVL) |
| US7736559B2 (en) * | 2004-05-20 | 2010-06-15 | Georgia-Pacific Chemicals Llc | Binding wood using a thermosetting adhesive composition comprising a protein-based component and a polymeric quaternary amine cure accelerant |
| US20060231968A1 (en) * | 2005-04-13 | 2006-10-19 | Georgia-Pacific Resins, Inc. | Protein-modified isocyanate-functional adhesive binder for cellulosic composite materials |
| US7589153B2 (en) * | 2005-05-25 | 2009-09-15 | Georgia-Pacific Chemicals Llc | Glyoxalated inter-copolymers with high and adjustable charge density |
| CN101316878B (zh) * | 2005-09-27 | 2013-07-31 | 巴科曼实验室国际公司 | 降低聚合物中有机杂质含量的方法和由其制得的产品 |
| US7863395B2 (en) * | 2006-12-20 | 2011-01-04 | Georgia-Pacific Chemicals Llc | Polyacrylamide-based strengthening agent |
| US8252866B2 (en) * | 2007-10-19 | 2012-08-28 | Georgia-Pacific Chemicals Llc | Azetidinium-functional polysaccharides and uses thereof |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2616818A (en) * | 1948-11-18 | 1952-11-04 | Hercules Powder Co Ltd | Paper coating |
| US2886557A (en) * | 1954-07-22 | 1959-05-12 | Nobel Francaise Soc | Glyoxal cross-linked acrylamide copolymers |
| US3420735A (en) * | 1967-03-31 | 1969-01-07 | Scott Paper Co | Wet-strength resins and a process for improving the wet-strength of paper |
-
1968
- 1968-07-24 US US747090A patent/US3607622A/en not_active Expired - Lifetime
-
1969
- 1969-07-17 BR BR210808/69A patent/BR6910808D0/pt unknown
- 1969-07-18 SE SE10203/69A patent/SE361048B/xx unknown
- 1969-07-23 ES ES369800A patent/ES369800A1/es not_active Expired
- 1969-07-23 GB GB37154/69A patent/GB1269567A/en not_active Expired
- 1969-07-23 NL NL6911321A patent/NL6911321A/xx unknown
- 1969-07-24 BE BE736513D patent/BE736513A/xx unknown
- 1969-07-24 DE DE19691937710 patent/DE1937710A1/de active Pending
- 1969-07-24 FR FR6925368A patent/FR2013630A1/fr not_active Withdrawn
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10134156B4 (de) * | 2000-08-22 | 2009-08-27 | Uzin Tyro Ag | Verwendung einer Selbstklebefolie |
Also Published As
| Publication number | Publication date |
|---|---|
| BR6910808D0 (pt) | 1973-02-15 |
| GB1269567A (en) | 1972-04-06 |
| FR2013630A1 (OSRAM) | 1970-04-03 |
| ES369800A1 (es) | 1971-12-16 |
| BE736513A (OSRAM) | 1970-01-26 |
| NL6911321A (OSRAM) | 1970-01-27 |
| US3607622A (en) | 1971-09-21 |
| SE361048B (OSRAM) | 1973-10-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1937710A1 (de) | Nassfeste Harze | |
| EP0074558B1 (de) | Verfahren zur Herstellung von wasserlöslichen, stickstoffhaltigen Kondensationsprodukten und deren Verwendung bei der Papierherstellung | |
| DE2951507C2 (OSRAM) | ||
| DE1802435C3 (de) | Verfahren zur Herstellung von vernetzten Harzen auf der Basis von basischen Polyamidoaminen und deren Verwendung als Entwässerungs-, Retentions- und Flockungsmittel bei der Papierherstellung | |
| DE3000502C2 (OSRAM) | ||
| DE2710061A1 (de) | Verfahren zur herstellung geleimten papiers und mittel zu seiner durchfuehrung | |
| DE1795392A1 (de) | Kationaktive,wasserloesliche Polyamide | |
| DE1595791A1 (de) | Verfahren zur Herstellung eines kationischen,waermehaertenden Harzes | |
| EP0061173B1 (de) | Verfahren zum Färben von Papier | |
| DE69400997T2 (de) | Zusammensetzung für die Herstellung von nassverfestigtem Papier | |
| DE2156215C3 (de) | Verfahren, zur Erhöhung der Retention und Retentionshilfsmittel | |
| DE2031947A1 (de) | Polyäthylenimin-Fettsäure-Epihalohydrin-Produkt | |
| EP0031899B1 (de) | Selbstvernetzende wasserlösliche Reaktionsprodukte, Verfahren zur Herstellung von Bindemitteln aus solchen Produkten und Verwendung der Produkte zur Erhöhung der Nassfestigkeit von Papier | |
| DE2210972A1 (de) | Naßfeste Harze | |
| EP0131200B1 (de) | Wasserlösliche, von Esterbindungen weitgehend freie Reaktionsprodukte aus Epihalogenhydrin und wasserlöslichen basischen Polyamidoaminen, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE19607641A1 (de) | Wasserlösliche Kondensationsprodukte aus Aminogruppen enthaltenden Verbindungen und halogenfreien Vernetzern, Verfahren zu ihrer Herstellung und ihre Verwendung | |
| DE1012165B (de) | Verfahren zum Leimen von Papier | |
| EP0129689A2 (de) | Copylmere und ihre Verwendung als Leimungsmittel | |
| DE1812416C3 (de) | Verfahren zur Oberflächen- und/oder Masseleimung von Papier | |
| DE1495195A1 (de) | Kondensationsprodukte | |
| DE2819039A1 (de) | Leimungsmittel fuer papier | |
| CH642385A5 (en) | Process for the preparation of novel cationic, water-soluble, polymeric reaction products | |
| DE2031293B2 (de) | Verfahren zum leimen von papier | |
| DE2705873A1 (de) | Glyoxalmodifizierte poly-(beta-alanin)-verfestigungsharze zur anwendung in papier | |
| EP0123196A2 (de) | Verfahren zur Herstellung von wasserlöslichen kationischen Harnstoff-Formaldehyd-Harzen und deren Verwendung bei der Papierherstellung |