SE456912B - Vattenloesliga polyamidoaminpolyamin och foerfarande foer framstaellning av en cellulosafiberbaserad arkprodukt - Google Patents

Vattenloesliga polyamidoaminpolyamin och foerfarande foer framstaellning av en cellulosafiberbaserad arkprodukt

Info

Publication number: SE456912B
Authority: SE; Sweden
Prior art keywords: polyamine; product; polyamidoamine; molecular weight; reaction
Prior art date: 1983-06-09

Application number

SE8403075A

Other languages

English (en)

Swedish (sv)

Other versions

SE8403075D0 (sv

SE8403075L (sv

Inventor

P E A Hansson

F Jachimowicz

Original Assignee

Grace W R & Co

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.)

1983-06-09

Filing date

1984-06-07

Publication date

1988-11-14

1984-06-07 Application filed by Grace W R & Co filed Critical Grace W R & Co

1984-06-07 Publication of SE8403075D0 publication Critical patent/SE8403075D0/xx

1984-12-10 Publication of SE8403075L publication Critical patent/SE8403075L/

1988-11-14 Publication of SE456912B publication Critical patent/SE456912B/sv

Links

229920000768 polyamine Polymers 0.000 title claims description 129
238000000034 method Methods 0.000 title claims description 12
239000000835 fiber Substances 0.000 title claims description 8
239000000047 product Substances 0.000 claims description 112
229920000962 poly(amidoamine) Polymers 0.000 claims description 99
239000000463 material Substances 0.000 claims description 48
238000007056 transamidation reaction Methods 0.000 claims description 41
238000006243 chemical reaction Methods 0.000 claims description 34
150000001412 amines Chemical class 0.000 claims description 28
150000001875 compounds Chemical class 0.000 claims description 25
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 23
239000003795 chemical substances by application Substances 0.000 claims description 16
125000003277 amino group Chemical group 0.000 claims description 15
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 15
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 15
125000001931 aliphatic group Chemical group 0.000 claims description 14
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 14
-1 aliphatic saturated dicarboxylic acid Chemical class 0.000 claims description 13
239000000203 mixture Substances 0.000 claims description 12
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 10
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 9
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims description 9
239000007795 chemical reaction product Substances 0.000 claims description 8
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 6
238000009833 condensation Methods 0.000 claims description 6
230000005494 condensation Effects 0.000 claims description 6
125000001302 tertiary amino group Chemical group 0.000 claims description 6
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 5
239000000654 additive Substances 0.000 claims description 5
229910021529 ammonia Inorganic materials 0.000 claims description 5
230000015572 biosynthetic process Effects 0.000 claims description 5
239000007859 condensation product Substances 0.000 claims description 5
239000000945 filler Substances 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
125000002947 alkylene group Chemical group 0.000 claims description 4
239000000049 pigment Substances 0.000 claims description 4
229920000233 poly(alkylene oxides) Polymers 0.000 claims description 4
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims description 3
AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 claims description 2
239000002002 slurry Substances 0.000 claims 3
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 1
NHWGPUVJQFTOQX-UHFFFAOYSA-N ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium Chemical compound CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC NHWGPUVJQFTOQX-UHFFFAOYSA-N 0.000 claims 1
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 claims 1
230000014759 maintenance of location Effects 0.000 description 32
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XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
229920000642 polymer Polymers 0.000 description 13
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
125000003368 amide group Chemical group 0.000 description 9
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 8
238000005227 gel permeation chromatography Methods 0.000 description 8
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238000004519 manufacturing process Methods 0.000 description 6
229920001223 polyethylene glycol Polymers 0.000 description 6
239000004952 Polyamide Substances 0.000 description 5
239000002202 Polyethylene glycol Substances 0.000 description 5
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238000003776 cleavage reaction Methods 0.000 description 5
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238000003756 stirring Methods 0.000 description 5
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NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 4
239000001361 adipic acid Substances 0.000 description 4
235000011037 adipic acid Nutrition 0.000 description 4
150000001408 amides Chemical class 0.000 description 4
150000001991 dicarboxylic acids Chemical class 0.000 description 4
230000000694 effects Effects 0.000 description 4
238000001914 filtration Methods 0.000 description 4
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
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230000001747 exhibiting effect Effects 0.000 description 3
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VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000002994 raw material Substances 0.000 description 3
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239000011541 reaction mixture Substances 0.000 description 3
238000005891 transamination reaction Methods 0.000 description 3
229960001124 trientine Drugs 0.000 description 3
KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 2
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
101100298295 Drosophila melanogaster flfl gene Proteins 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
CREXVNNSNOKDHW-UHFFFAOYSA-N azaniumylideneazanide Chemical group N[N] CREXVNNSNOKDHW-UHFFFAOYSA-N 0.000 description 2
VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
125000002843 carboxylic acid group Chemical group 0.000 description 2
239000000470 constituent Substances 0.000 description 2
230000008878 coupling Effects 0.000 description 2
238000010168 coupling process Methods 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
230000018044 dehydration Effects 0.000 description 2
238000006297 dehydration reaction Methods 0.000 description 2
150000004985 diamines Chemical class 0.000 description 2
239000013051 drainage agent Substances 0.000 description 2
239000012467 final product Substances 0.000 description 2
238000005188 flotation Methods 0.000 description 2
235000010299 hexamethylene tetramine Nutrition 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
238000013383 initial experiment Methods 0.000 description 2
150000003951 lactams Chemical class 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000012434 nucleophilic reagent Substances 0.000 description 2
150000002894 organic compounds Chemical class 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 2
238000012958 reprocessing Methods 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
238000004062 sedimentation Methods 0.000 description 2
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239000011122 softwood Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000010561 standard procedure Methods 0.000 description 2
239000007858 starting material Substances 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
239000000725 suspension Substances 0.000 description 2
JEQDSBVHLKBEIZ-REOHCLBHSA-N (2s)-2-chloropropanoyl chloride Chemical compound C[C@H](Cl)C(Cl)=O JEQDSBVHLKBEIZ-REOHCLBHSA-N 0.000 description 1
HFBHOAHFRNLZGN-LURJTMIESA-N (2s)-2-formamido-4-methylpentanoic acid Chemical compound CC(C)C[C@@H](C(O)=O)NC=O HFBHOAHFRNLZGN-LURJTMIESA-N 0.000 description 1
125000006557 (C2-C5) alkylene group Chemical group 0.000 description 1
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
YHRUOJUYPBUZOS-UHFFFAOYSA-N 1,3-dichloropropane Chemical compound ClCCCCl YHRUOJUYPBUZOS-UHFFFAOYSA-N 0.000 description 1
OVISMSJCKCDOPU-UHFFFAOYSA-N 1,6-dichlorohexane Chemical compound ClCCCCCCCl OVISMSJCKCDOPU-UHFFFAOYSA-N 0.000 description 1
FYBFGAFWCBMEDG-UHFFFAOYSA-N 1-[3,5-di(prop-2-enoyl)-1,3,5-triazinan-1-yl]prop-2-en-1-one Chemical compound C=CC(=O)N1CN(C(=O)C=C)CN(C(=O)C=C)C1 FYBFGAFWCBMEDG-UHFFFAOYSA-N 0.000 description 1
XAZDZMUGHYYPQM-UHFFFAOYSA-N 1-chloro-3-(3-chloro-2-hydroxypropoxy)propan-2-ol Chemical class ClCC(O)COCC(O)CCl XAZDZMUGHYYPQM-UHFFFAOYSA-N 0.000 description 1
PVBMXMKIKMJQRK-UHFFFAOYSA-N 1-chloro-4-(4-chlorobutoxy)butane Chemical compound ClCCCCOCCCCCl PVBMXMKIKMJQRK-UHFFFAOYSA-N 0.000 description 1
MSSMDWAXCNWOGU-UHFFFAOYSA-N 2-(dichloromethyl)-3-methyloxirane Chemical compound CC1OC1C(Cl)Cl MSSMDWAXCNWOGU-UHFFFAOYSA-N 0.000 description 1
SVDDJQGVOFZBNX-UHFFFAOYSA-N 2-chloroethyl carbonochloridate Chemical compound ClCCOC(Cl)=O SVDDJQGVOFZBNX-UHFFFAOYSA-N 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 1
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FRXLFVNGTPQFEJ-UHFFFAOYSA-N 3-bromopropanoyl bromide Chemical compound BrCCC(Br)=O FRXLFVNGTPQFEJ-UHFFFAOYSA-N 0.000 description 1
LFEAJBLOEPTINE-UHFFFAOYSA-N 4-(chloromethyl)-1,3-dioxolan-2-one Chemical compound ClCC1COC(=O)O1 LFEAJBLOEPTINE-UHFFFAOYSA-N 0.000 description 1
SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
UQXNEWQGGVUVQA-UHFFFAOYSA-N 8-aminooctanoic acid Chemical compound NCCCCCCCC(O)=O UQXNEWQGGVUVQA-UHFFFAOYSA-N 0.000 description 1
ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 description 1
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VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-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
MHTONRWSEQKWDM-UHFFFAOYSA-N N'-[[3-[(3-aminopropylamino)methyl]phenyl]methyl]propane-1,3-diamine Chemical compound NCCCNCC1=CC(=CC=C1)CNCCCN MHTONRWSEQKWDM-UHFFFAOYSA-N 0.000 description 1
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NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
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FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
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DYUCNAMTUNGLAB-UHFFFAOYSA-N n,n'-bis(2-aminoethyl)hexane-1,6-diamine Chemical compound NCCNCCCCCCNCCN DYUCNAMTUNGLAB-UHFFFAOYSA-N 0.000 description 1
KVKFRMCSXWQSNT-UHFFFAOYSA-N n,n'-dimethylethane-1,2-diamine Chemical compound CNCCNC KVKFRMCSXWQSNT-UHFFFAOYSA-N 0.000 description 1
ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
239000011368 organic material Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229920000333 poly(propyleneimine) Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920000867 polyelectrolyte Polymers 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
238000010791 quenching Methods 0.000 description 1
230000000171 quenching effect Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000011084 recovery Methods 0.000 description 1
238000004064 recycling Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000012260 resinous material Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000003330 sebacic acids Chemical class 0.000 description 1
238000001542 size-exclusion chromatography Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
229910001388 sodium aluminate Inorganic materials 0.000 description 1
239000011343 solid material Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
150000003504 terephthalic acids Chemical class 0.000 description 1
238000010998 test method Methods 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
VSRBKQFNFZQRBM-UHFFFAOYSA-N tuaminoheptane Chemical compound CCCCCC(C)N VSRBKQFNFZQRBM-UHFFFAOYSA-N 0.000 description 1
229960003986 tuaminoheptane Drugs 0.000 description 1
238000000108 ultra-filtration Methods 0.000 description 1
229960000834 vinyl ether Drugs 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000002351 wastewater Substances 0.000 description 1
238000005303 weighing Methods 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)
Polyamides (AREA)
Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Paper (AREA)
Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)

SE8403075A 1983-06-09 1984-06-07 Vattenloesliga polyamidoaminpolyamin och foerfarande foer framstaellning av en cellulosafiberbaserad arkprodukt SE456912B (sv)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US50255183A	1983-06-09	1983-06-09

Publications (3)

Publication Number	Publication Date
SE8403075D0 SE8403075D0 (sv)	1984-06-07
SE8403075L SE8403075L (sv)	1984-12-10
SE456912B true SE456912B (sv)	1988-11-14

Family

ID=23998324

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE8403075A SE456912B (sv)	1983-06-09	1984-06-07	Vattenloesliga polyamidoaminpolyamin och foerfarande foer framstaellning av en cellulosafiberbaserad arkprodukt

Country Status (12)

Country	Link
JP (2)	JPH0610264B2 (de)
AT (1)	AT385276B (de)
BE (1)	BE899880A (de)
BR (1)	BR8402805A (de)
CH (1)	CH663792A5 (de)
DE (1)	DE3421557A1 (de)
FR (1)	FR2547303B1 (de)
GB (1)	GB2141130B (de)
IT (1)	IT1180183B (de)
NL (1)	NL8401825A (de)
NO (1)	NO161378C (de)
SE (1)	SE456912B (de)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS62104725A (ja) *	1985-10-31	1987-05-15	Meiki Co Ltd	真空引きベント式射出成形機
JPS62124923A (ja) *	1985-11-26	1987-06-06	Kishimoto Sangyo Kk	改良されたベント式射出成形機
US5223097A (en) *	1986-01-09	1993-06-29	W. R. Grace Ab	Method for controlling pitch on a paper-making machine
US5626720A (en) *	1986-01-09	1997-05-06	W.R. Grace & Co.-Conn.	Method for controlling pitch on a papermaking machine
US4722964A (en) *	1986-06-20	1988-02-02	Borden, Inc.	Epoxidized polyalkyleneamine-amide wet strength resin
DE3721057C2 (de) *	1987-06-26	1996-08-22	Bayer Ag	Wasserlösliche, basische Polykondensate, Verfahren zu ihrer Herstellung, diese enthaltende Retentionsmittel und ihre Verwendung zur Herstellung von Papier
GB2254345B (en) *	1991-03-28	1995-06-14	Grace W R & Co	Creping aid
TW334493B (en) *	1996-05-14	1998-06-21	Sugatsune Kogyo	Damper for opening or closing a door
AU2008206098B2 (en) *	2007-01-19	2013-01-17	Solenis Technologies Cayman, L.P.	Creping adhesives made from amine-terminated polyamidoamines
US20120247697A1 (en) *	2011-03-29	2012-10-04	Kemira Oyj	Polyamine Polyamidoamine Epihaloohydrin Compositions and Processes for Preparing and Using the Same
CN103987894A (zh)	2011-09-30	2014-08-13	凯米罗总公司	纸张和造纸方法
US9777434B2 (en)	2011-12-22	2017-10-03	Kemira Dyj	Compositions and methods of making paper products
WO2013179139A1 (en) *	2012-05-30	2013-12-05	Kemira Oyj	Compositions and methods of making paper products
CN105452563B (zh) *	2012-09-26	2018-06-29	凯米罗总公司	吸收剂材料、包括吸收剂材料的产品、组合物和制备吸收剂材料的方法

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1771043C3 (de) *	1968-03-27	1979-05-23	Bayer Ag, 5090 Leverkusen	Selbstvernetzende wasserlösliche Produkte und deren Verwendung als Naßfestmittel für Papier
DE1802435C3 (de) *	1968-10-11	1979-01-18	Basf Ag, 6700 Ludwigshafen	Verfahren zur Herstellung von vernetzten Harzen auf der Basis von basischen Polyamidoaminen und deren Verwendung als Entwässerungs-, Retentions- und Flockungsmittel bei der Papierherstellung
US3793279A (en) *	1972-11-08	1974-02-19	Diamond Shamrock Corp	Mono primary polyamine and organic dihalide modified,epoxidized polyamide for paper wet strength resin
DE2736651A1 (de) *	1977-08-13	1979-02-15	Wolff Walsrode Ag	Hilfsmittel zur verbesserung der retention, entwaesserung und aufbereitung, insbesondere bei der papierherstellung
DE2756469A1 (de) *	1977-12-17	1979-06-21	Bayer Ag	Amidgruppenhaltige polyamine
DE2756431C2 (de) *	1977-12-17	1985-05-15	Bayer Ag, 5090 Leverkusen	Amidgruppenhaltige Polyamine
DE2949870A1 (de) *	1979-12-12	1981-06-19	Hoechst Ag, 6230 Frankfurt	Kondensationsprodukte zur erhoehung der nassfestigkeit von papier
JPS6046130B2 (ja) *	1981-03-30	1985-10-14	星光化学工業株式会社	製紙用添加剤の製造法
DE3135830A1 (de) *	1981-09-10	1983-03-24	Basf Ag, 6700 Ludwigshafen	Verfahren zur herstellung von wasserloeslichen, stickstoffhaltigen kondensationsprodukten und deren verwendung bei der papierherstellung
JPH03199546A (ja) *	1989-12-27	1991-08-30	Meiwa Kk	電波シールドパネル構造体
JP3008839U (ja) *	1994-06-01	1995-03-20	株式会社エポック社	バーコードサッカーゲーム機

1984
- 1984-06-05 GB GB08414268A patent/GB2141130B/en not_active Expired
- 1984-06-07 SE SE8403075A patent/SE456912B/sv not_active IP Right Cessation
- 1984-06-07 DE DE19843421557 patent/DE3421557A1/de not_active Withdrawn
- 1984-06-08 FR FR8409043A patent/FR2547303B1/fr not_active Expired
- 1984-06-08 NO NO842328A patent/NO161378C/no unknown
- 1984-06-08 IT IT21332/84A patent/IT1180183B/it active
- 1984-06-08 BE BE0/213114A patent/BE899880A/fr not_active IP Right Cessation
- 1984-06-08 JP JP59116769A patent/JPH0610264B2/ja not_active Expired - Lifetime
- 1984-06-08 BR BR8402805A patent/BR8402805A/pt unknown
- 1984-06-08 CH CH2816/84A patent/CH663792A5/de not_active IP Right Cessation
- 1984-06-08 NL NL8401825A patent/NL8401825A/nl not_active Application Discontinuation
- 1984-06-12 AT AT0191984A patent/AT385276B/de active
1993
- 1993-08-02 JP JP5208150A patent/JPH0713357B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
NO161378B (no)	1989-05-02
GB8414268D0 (en)	1984-07-11
NO161378C (no)	1989-08-09
IT1180183B (it)	1987-09-23
SE8403075D0 (sv)	1984-06-07
JPS6018528A (ja)	1985-01-30
AT385276B (de)	1988-03-10
BR8402805A (pt)	1985-05-21
DE3421557A1 (de)	1985-01-10
FR2547303B1 (fr)	1988-03-18
GB2141130B (en)	1986-11-12
CH663792A5 (de)	1988-01-15
NL8401825A (nl)	1985-01-02
FR2547303A1 (fr)	1984-12-14
JPH06240597A (ja)	1994-08-30
IT8421332A0 (it)	1984-06-08
JPH0610264B2 (ja)	1994-02-09
JPH0713357B2 (ja)	1995-02-15
BE899880A (fr)	1984-12-10
SE8403075L (sv)	1984-12-10
GB2141130A (en)	1984-12-12
ATA191984A (de)	1987-08-15
NO842328L (no)	1984-12-10

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1995-01-31

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Publication	Publication Date	Title
CA1058794A (en)	1979-07-17	Crosslinked polyamidoamine condensation products for papermaking
KR100468801B1 (ko)	2005-07-11	아미노기를함유하는수용성축합물과부가생성물의제조방법및이축합물과부가생성물의용도
US3642572A (en)	1972-02-15	Cross-linked polyamide-imine polymer for papermaking
CA1196454A (en)	1985-11-12	Preparation of water-soluble, nitrogen-containing condensates and their use in papermaking
SE456912B (sv)	1988-11-14	Vattenloesliga polyamidoaminpolyamin och foerfarande foer framstaellning av en cellulosafiberbaserad arkprodukt
FI64179B (fi)	1983-06-30	Vattenloesliga amidgrupper innehaollande polyaminer och deras anvaendning
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US3215654A (en)	1965-11-02	Process for preparing aqueous solutions of alkylated aminopolyamide-epichlorohydrin resins and use of same as retention aids
GB1284934A (en)	1972-08-09	Improvements in or relating to the manufacture of paper
US3932363A (en)	1976-01-13	Polyamines containing acid groups
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US4093605A (en)	1978-06-06	Auxiliary agent for improving retention, drainage and treatment
US4267059A (en)	1981-05-12	Auxiliary for improving retention, dewatering and working up, particularly in the manufacture of paper
FI64178B (fi)	1983-06-30	Amidgrupper innehaollande vattenloesliga icke-sjaelvtvaerbindande polyaminer och deras anvaendning
US4036821A (en)	1977-07-19	Manufacture of modified basic polyaminoamide with ammonium compound
US4673729A (en)	1987-06-16	Paper auxiliary from condensation product of aliphatic polyol-ether-amine and compound polyfunctional toward amino groups
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CN1125277A (zh)	1996-06-26	寡酰胺-表氯醇树脂用作脱水助剂
FI83226B (fi)	1991-02-28	Polyamidoaminpolyaminer.
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JP2003053400A (ja)	2003-02-25	汚泥脱水剤及び汚泥脱水方法
US4166002A (en)	1979-08-28	Polyamines containing acid groups that are useful in papermaking
DE19621300A1 (de)	1997-12-04	Verfahren zur Erhöhung der Wirksamkeit von wasserlöslichen, Aminogruppen enthaltenden Kondensaten und Additionsprodukten und ihre Verwendung