TW495538B - Hydrophobically modified resin compositions and uses thereof - Google Patents

Hydrophobically modified resin compositions and uses thereof Download PDF

Info

Publication number: TW495538B
Authority: TW; Taiwan
Prior art keywords: amine; group; acid; paper; resin composition
Prior art date: 1997-03-04

Application number

TW087103237A

Other languages

English (en)

Chinese (zh)

Inventor

John Charles Gast

Original Assignee

Hercules Inc

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.)

1997-03-04

Filing date

1998-03-05

Publication date

2002-07-21

1998-03-05 Application filed by Hercules Inc filed Critical Hercules Inc

2002-07-21 Application granted granted Critical

2002-07-21 Publication of TW495538B publication Critical patent/TW495538B/zh

Links

239000011342 resin composition Substances 0.000 title claims abstract description 45
238000004513 sizing Methods 0.000 claims abstract description 84
238000006243 chemical reaction Methods 0.000 claims abstract description 64
239000000203 mixture Substances 0.000 claims abstract description 56
239000003795 chemical substances by application Substances 0.000 claims abstract description 54
229920000768 polyamine Polymers 0.000 claims abstract description 35
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 29
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 26
239000007795 chemical reaction product Substances 0.000 claims abstract description 9
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical class NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims abstract description 8
125000003277 amino group Chemical group 0.000 claims description 68
150000001412 amines Chemical class 0.000 claims description 64
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 62
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 52
-1 Amine amine Chemical class 0.000 claims description 40
239000002253 acid Substances 0.000 claims description 34
238000011049 filling Methods 0.000 claims description 28
239000001361 adipic acid Substances 0.000 claims description 26
235000011037 adipic acid Nutrition 0.000 claims description 26
230000002209 hydrophobic effect Effects 0.000 claims description 25
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 22
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 18
238000000034 method Methods 0.000 claims description 18
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 15
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 14
239000004593 Epoxy Substances 0.000 claims description 13
239000004890 Hydrophobing Agent Substances 0.000 claims description 13
230000002079 cooperative effect Effects 0.000 claims description 13
125000000217 alkyl group Chemical group 0.000 claims description 12
229920000642 polymer Polymers 0.000 claims description 11
150000008064 anhydrides Chemical class 0.000 claims description 10
239000000539 dimer Substances 0.000 claims description 10
229920006395 saturated elastomer Polymers 0.000 claims description 9
125000003118 aryl group Chemical group 0.000 claims description 7
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 6
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 6
125000003342 alkenyl group Chemical group 0.000 claims description 6
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 6
239000000126 substance Substances 0.000 claims description 6
150000002148 esters Chemical class 0.000 claims description 5
238000010438 heat treatment Methods 0.000 claims description 5
238000012856 packing Methods 0.000 claims description 5
229920001281 polyalkylene Polymers 0.000 claims description 5
239000000725 suspension Substances 0.000 claims description 5
XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 claims description 5
125000004417 unsaturated alkyl group Chemical group 0.000 claims description 5
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
150000004985 diamines Chemical class 0.000 claims description 4
150000001991 dicarboxylic acids Chemical class 0.000 claims description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 4
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 claims description 4
239000001294 propane Substances 0.000 claims description 4
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 claims description 4
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 3
239000007900 aqueous suspension Substances 0.000 claims description 3
125000004429 atom Chemical group 0.000 claims description 3
125000000392 cycloalkenyl group Chemical group 0.000 claims description 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
YVWGMAFXEJHFRO-UHFFFAOYSA-N halopropane Chemical compound FC(F)C(F)(F)CBr YVWGMAFXEJHFRO-UHFFFAOYSA-N 0.000 claims description 3
229950000188 halopropane Drugs 0.000 claims description 3
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 2
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims description 2
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 2
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
238000004132 cross linking Methods 0.000 claims description 2
238000001035 drying Methods 0.000 claims description 2
239000001530 fumaric acid Substances 0.000 claims description 2
150000007857 hydrazones Chemical class 0.000 claims description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
239000011976 maleic acid Substances 0.000 claims description 2
235000006408 oxalic acid Nutrition 0.000 claims description 2
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 2
229960001124 trientine Drugs 0.000 claims description 2
LBQZVWQOPFFQJI-GGWOSOGESA-N (e)-3-[3-[5-[(e)-2-carboxyethenyl]-2-hydroxy-3-methoxyphenyl]-4-hydroxy-5-methoxyphenyl]prop-2-enoic acid Chemical compound COC1=CC(\C=C\C(O)=O)=CC(C=2C(=C(OC)C=C(\C=C\C(O)=O)C=2)O)=C1O LBQZVWQOPFFQJI-GGWOSOGESA-N 0.000 claims 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical class C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 2
PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 1
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims 1
QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 claims 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
239000004202 carbamide Substances 0.000 claims 1
235000013877 carbamide Nutrition 0.000 claims 1
150000001735 carboxylic acids Chemical class 0.000 claims 1
150000002576 ketones Chemical class 0.000 claims 1
239000007788 liquid Substances 0.000 claims 1
210000003254 palate Anatomy 0.000 claims 1
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 8
XPXMKIXDFWLRAA-UHFFFAOYSA-N hydrazinide Chemical compound [NH-]N XPXMKIXDFWLRAA-UHFFFAOYSA-N 0.000 abstract 3
125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 abstract 3
125000001302 tertiary amino group Chemical group 0.000 abstract 3
239000000123 paper Substances 0.000 description 96
239000000047 product Substances 0.000 description 70
239000007787 solid Substances 0.000 description 49
239000006185 dispersion Substances 0.000 description 36
229920005989 resin Polymers 0.000 description 30
239000011347 resin Substances 0.000 description 30
230000000052 comparative effect Effects 0.000 description 26
239000000243 solution Substances 0.000 description 20
GBBHWGRJHHNAGT-UHFFFAOYSA-N 3-hexadecyloxolane-2,5-dione Chemical compound CCCCCCCCCCCCCCCCC1CC(=O)OC1=O GBBHWGRJHHNAGT-UHFFFAOYSA-N 0.000 description 18
125000002091 cationic group Chemical group 0.000 description 16
239000002245 particle Substances 0.000 description 15
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 11
238000002360 preparation method Methods 0.000 description 11
239000011541 reaction mixture Substances 0.000 description 11
229940014800 succinic anhydride Drugs 0.000 description 11
229920002472 Starch Polymers 0.000 description 9
230000000694 effects Effects 0.000 description 9
239000008107 starch Substances 0.000 description 9
235000019698 starch Nutrition 0.000 description 9
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical class CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 8
239000002904 solvent Substances 0.000 description 8
239000001384 succinic acid Substances 0.000 description 8
ZRALSGWEFCBTJO-UHFFFAOYSA-N anhydrous guanidine Natural products NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 7
238000005259 measurement Methods 0.000 description 7
238000012986 modification Methods 0.000 description 7
230000004048 modification Effects 0.000 description 7
238000010025 steaming Methods 0.000 description 7
SSZWWUDQMAHNAQ-UHFFFAOYSA-N 3-chloropropane-1,2-diol Chemical compound OCC(O)CCl SSZWWUDQMAHNAQ-UHFFFAOYSA-N 0.000 description 6
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
229920000147 Styrene maleic anhydride Polymers 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 5
238000004821 distillation Methods 0.000 description 5
239000000463 material Substances 0.000 description 5
238000010791 quenching Methods 0.000 description 5
PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 4
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 4
235000021355 Stearic acid Nutrition 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
230000000875 corresponding effect Effects 0.000 description 4
239000001046 green dye Substances 0.000 description 4
239000002655 kraft paper Substances 0.000 description 4
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
230000003287 optical effect Effects 0.000 description 4
239000000843 powder Substances 0.000 description 4
230000000171 quenching effect Effects 0.000 description 4
239000008117 stearic acid Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
VDSRDVXCJCFBDO-UHFFFAOYSA-N 2h-pyran-2,3-diamine Chemical compound NC1OC=CC=C1N VDSRDVXCJCFBDO-UHFFFAOYSA-N 0.000 description 3
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
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
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 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
239000005642 Oleic acid Substances 0.000 description 3
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 3
239000006260 foam Substances 0.000 description 3
238000005187 foaming Methods 0.000 description 3
235000019253 formic acid Nutrition 0.000 description 3
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
235000021313 oleic acid Nutrition 0.000 description 3
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
230000035484 reaction time Effects 0.000 description 3
239000011734 sodium Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011122 softwood Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
229920001187 thermosetting polymer Polymers 0.000 description 3
DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 2
RSPWVGZWUBNLQU-FOCLMDBBSA-N 3-[(e)-hexadec-1-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCCCCCCC\C=C\C1CC(=O)OC1=O RSPWVGZWUBNLQU-FOCLMDBBSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 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
238000013019 agitation Methods 0.000 description 2
229940037003 alum Drugs 0.000 description 2
239000012736 aqueous medium Substances 0.000 description 2
239000003125 aqueous solvent Substances 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
238000001816 cooling Methods 0.000 description 2
FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohex-2-enone Chemical class O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 2
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
FLISWPFVWWWNNP-BQYQJAHWSA-N dihydro-3-(1-octenyl)-2,5-furandione Chemical compound CCCCCC\C=C\C1CC(=O)OC1=O FLISWPFVWWWNNP-BQYQJAHWSA-N 0.000 description 2
238000007865 diluting Methods 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
239000000835 fiber Substances 0.000 description 2
239000003292 glue Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
239000011121 hardwood Substances 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
238000009434 installation Methods 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
UTOPWMOLSKOLTQ-UHFFFAOYSA-N octacosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCC(O)=O UTOPWMOLSKOLTQ-UHFFFAOYSA-N 0.000 description 2
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
239000001254 oxidized starch Substances 0.000 description 2
235000013808 oxidized starch Nutrition 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
230000003068 static effect Effects 0.000 description 2
239000002023 wood Substances 0.000 description 2
NGDLSKPZMOTRTR-OAPYJULQSA-N (4z)-4-heptadecylidene-3-hexadecyloxetan-2-one Chemical compound CCCCCCCCCCCCCCCC\C=C1/OC(=O)C1CCCCCCCCCCCCCCCC NGDLSKPZMOTRTR-OAPYJULQSA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
ZOKHGHDRKCYWTH-UHFFFAOYSA-N 1,1-dichloropropan-2-ol Chemical compound CC(O)C(Cl)Cl ZOKHGHDRKCYWTH-UHFFFAOYSA-N 0.000 description 1
IFDLXKQSUOWIBO-UHFFFAOYSA-N 1,3-dichloropropan-1-ol Chemical compound OC(Cl)CCCl IFDLXKQSUOWIBO-UHFFFAOYSA-N 0.000 description 1
HYYJOCXNESGFSB-UHFFFAOYSA-N 1-(oxiran-2-yl)-n-(oxiran-2-ylmethyl)methanamine Chemical class C1OC1CNCC1CO1 HYYJOCXNESGFSB-UHFFFAOYSA-N 0.000 description 1
CHHHXKFHOYLYRE-UHFFFAOYSA-M 2,4-Hexadienoic acid, potassium salt (1:1), (2E,4E)- Chemical compound [K+].CC=CC=CC([O-])=O CHHHXKFHOYLYRE-UHFFFAOYSA-M 0.000 description 1
AHHOLQNVLJNGIP-UHFFFAOYSA-N 3,4-dibutyloxolane-2,5-dione Chemical compound C(CCC)C1C(C(=O)OC1=O)CCCC AHHOLQNVLJNGIP-UHFFFAOYSA-N 0.000 description 1
XRAJHWOOOMPDFP-UHFFFAOYSA-N 3-(16-methylheptadecyl)oxolane-2,5-dione Chemical compound CC(C)CCCCCCCCCCCCCCCC1CC(=O)OC1=O XRAJHWOOOMPDFP-UHFFFAOYSA-N 0.000 description 1
HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 description 1
KAYAKFYASWYOEB-ISLYRVAYSA-N 3-[(e)-octadec-1-enyl]oxolane-2,5-dione Chemical compound CCCCCCCCCCCCCCCC\C=C\C1CC(=O)OC1=O KAYAKFYASWYOEB-ISLYRVAYSA-N 0.000 description 1
SLZVPYKIWGEOHT-UHFFFAOYSA-N 3-hexadecylpyrrolidine-2,5-dione Chemical compound CCCCCCCCCCCCCCCCC1CC(=O)NC1=O SLZVPYKIWGEOHT-UHFFFAOYSA-N 0.000 description 1
ZJFCVUTYZHUNSW-UHFFFAOYSA-N 3-octadecyloxolane-2,5-dione Chemical compound CCCCCCCCCCCCCCCCCCC1CC(=O)OC1=O ZJFCVUTYZHUNSW-UHFFFAOYSA-N 0.000 description 1
YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 description 1
AHURGTOIDVSXCR-UHFFFAOYSA-N CCCCCCCCCCCCC=CC=CC1CC(=O)OC1=O Chemical compound CCCCCCCCCCCCC=CC=CC1CC(=O)OC1=O AHURGTOIDVSXCR-UHFFFAOYSA-N 0.000 description 1
241000283153 Cetacea Species 0.000 description 1
239000009261 D 400 Substances 0.000 description 1
241000545744 Hirudinea Species 0.000 description 1
WZELXJBMMZFDDU-UHFFFAOYSA-N Imidazol-2-one Chemical class O=C1N=CC=N1 WZELXJBMMZFDDU-UHFFFAOYSA-N 0.000 description 1
240000008821 Menyanthes trifoliata Species 0.000 description 1
CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 description 1
235000019482 Palm oil Nutrition 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
235000019483 Peanut oil Nutrition 0.000 description 1
241001237728 Precis Species 0.000 description 1
235000019484 Rapeseed oil Nutrition 0.000 description 1
235000004443 Ricinus communis Nutrition 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000000304 alkynyl group Chemical group 0.000 description 1
239000012431 aqueous reaction media Substances 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
239000010426 asphalt Substances 0.000 description 1
CJGONBSILIMWOA-UHFFFAOYSA-N azane;octadecan-1-amine Chemical compound N.CCCCCCCCCCCCCCCCCCN CJGONBSILIMWOA-UHFFFAOYSA-N 0.000 description 1
239000010480 babassu oil Substances 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
239000003139 biocide Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
229940106189 ceramide Drugs 0.000 description 1
ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
238000010411 cooking Methods 0.000 description 1
125000006165 cyclic alkyl group Chemical group 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000006471 dimerization reaction Methods 0.000 description 1
239000002612 dispersion medium Substances 0.000 description 1
238000002036 drum drying Methods 0.000 description 1
229910001651 emery Inorganic materials 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000003623 enhancer Substances 0.000 description 1
239000003822 epoxy resin Substances 0.000 description 1
150000008376 fluorenones Chemical class 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000002309 gasification Methods 0.000 description 1
238000000265 homogenisation Methods 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
239000004569 hydrophobicizing agent Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
150000002561 ketenes Chemical class 0.000 description 1
238000011068 loading method Methods 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
SNMVRZFUUCLYTO-UHFFFAOYSA-N n-propyl chloride Chemical compound CCCCl SNMVRZFUUCLYTO-UHFFFAOYSA-N 0.000 description 1
VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
239000004006 olive oil Substances 0.000 description 1
235000008390 olive oil Nutrition 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000019865 palm kernel oil Nutrition 0.000 description 1
239000003346 palm kernel oil Substances 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
239000000312 peanut oil Substances 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
150000008442 polyphenolic compounds Chemical class 0.000 description 1
235000013824 polyphenols Nutrition 0.000 description 1
239000004302 potassium sorbate Substances 0.000 description 1
235000010241 potassium sorbate Nutrition 0.000 description 1
229940069338 potassium sorbate Drugs 0.000 description 1
229940088417 precipitated calcium carbonate Drugs 0.000 description 1
238000012545 processing Methods 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
229960003656 ricinoleic acid Drugs 0.000 description 1
FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000013049 sediment Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000758 substrate Substances 0.000 description 1
RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
238000004381 surface treatment Methods 0.000 description 1
239000003760 tallow Substances 0.000 description 1
239000012085 test solution Substances 0.000 description 1
TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
239000009333 tian-xian Substances 0.000 description 1
AZCVFLMXESYPIR-NSCUHMNNSA-N trans-10-dodecenoic acid Chemical compound C\C=C\CCCCCCCCC(O)=O AZCVFLMXESYPIR-NSCUHMNNSA-N 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 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
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/16—Sizing or water-repelling agents
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/028—Polyamidoamines
- C08G73/0286—Preparatory process from polyamidoamines and epihalohydrins
- 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
- D21H17/56—Polyamines; Polyimines; Polyester-imides

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Paper (AREA)
Graft Or Block Polymers (AREA)

TW087103237A 1997-03-04 1998-03-05 Hydrophobically modified resin compositions and uses thereof TW495538B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US81209297A	1997-03-04	1997-03-04

Publications (1)

Publication Number	Publication Date
TW495538B true TW495538B (en)	2002-07-21

Family

ID=25208473

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW087103237A TW495538B (en)	1997-03-04	1998-03-05	Hydrophobically modified resin compositions and uses thereof

Country Status (6)

Country	Link
EP (1)	EP0907672A1 (de)
AU (1)	AU726005B2 (de)
CA (1)	CA2261954A1 (de)
TW (1)	TW495538B (de)
WO (1)	WO1998039376A1 (de)
ZA (1)	ZA981848B (de)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
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
JP2003515006A (ja) *	1999-11-19	2003-04-22	アクゾノーベルエヌ．ブイ．	湿潤強度増強剤およびその製造方法
US6673205B2 (en) *	2001-05-10	2004-01-06	Fort James Corporation	Use of hydrophobically modified polyaminamides with polyethylene glycol esters in paper products
SE522783C2 (sv) *	2001-05-18	2004-03-09	Sca Hygiene Prod Ab	Våtstarkt tissuepapper
CA2461629C (en)	2003-03-24	2012-05-08	Nof Corporation	Paper additive composition and method for producing paper using the same
US7041197B2 (en)	2003-04-15	2006-05-09	Fort James Corporation	Wet strength and softness enhancement of paper products
US8651285B2 (en) †	2009-08-19	2014-02-18	Johns Manville	Performance polymeric fiber webs
AU2012236373B2 (en)	2011-03-31	2016-06-23	Solenis Technologies Cayman, L.P.	Sizing compositions

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3922243A (en) *	1973-08-31	1975-11-25	Hercules Inc	Ketene dimer modified water-dispersible thermosettable cationic resins
US4478682A (en) *	1981-07-02	1984-10-23	Hercules Incorporated	Sizing method and sizing composition for use therein
DE4200715A1 (de) *	1992-01-14	1993-07-15	Bayer Ag	Vinylpolymerisat-dispersionen

1998
- 1998-02-20 EP EP98907552A patent/EP0907672A1/de not_active Withdrawn
- 1998-02-20 CA CA002261954A patent/CA2261954A1/en not_active Abandoned
- 1998-02-20 AU AU63326/98A patent/AU726005B2/en not_active Ceased
- 1998-02-20 WO PCT/US1998/003358 patent/WO1998039376A1/en not_active Ceased
- 1998-03-04 ZA ZA981848A patent/ZA981848B/xx unknown
- 1998-03-05 TW TW087103237A patent/TW495538B/zh active

Also Published As

Publication number	Publication date
EP0907672A1 (de)	1999-04-14
WO1998039376A1 (en)	1998-09-11
ZA981848B (en)	1998-09-04
AU726005B2 (en)	2000-10-26
AU6332698A (en)	1998-09-22
CA2261954A1 (en)	1998-09-11

Publication	Publication Date	Title
CA1135909A (en)	1982-11-23	Ketene dimer paper sizing compositions
US4144123A (en)	1979-03-13	Incorporating a crosslinked polyamidoamine condensation product into paper-making pulp
TW495538B (en)	2002-07-21	Hydrophobically modified resin compositions and uses thereof
JPS6215680B2 (de)	1987-04-08
CN103459719B (zh)	2016-02-03	施胶组合物
PL162951B1 (pl)	1994-01-31	Srodek zaklejajacy i sposób wytwarzania srodka zaklejajacego PL PL PL
NL8000117A (nl)	1981-08-03	Appreteermiddel en werkwijze voor het bereiden hiervan.
CA2086487C (en)	1999-02-16	Cationic polyamines useful as drainage aids and stabilizers for rosin-based sizing agents
US3922243A (en)	1975-11-25	Ketene dimer modified water-dispersible thermosettable cationic resins
US3840486A (en)	1974-10-08	Water-soluble,thermosettable resinous compositions prepared from dicyandiamide,hcho,ammonium salt and a salt of an aminopolyamide and method for preparing the same
EP0054075B1 (de)	1984-08-22	Behandlungsmittel für cellulose sowie damit behandelte papierprodukte
TWI791577B (zh)	2023-02-11	疏水性之含乙烯胺之聚合物組合物及其於製紙應用之用途
JP5751412B2 (ja)	2015-07-22	製紙用ロジン系エマルジョン型サイズ剤およびこれを用いて得られる紙
JP2022140358A (ja)	2022-09-26	製紙用ロジン系サイズ剤、紙
US3988280A (en)	1976-10-26	Water-dispersible thermosettable cationic resins and paper sized therewith
JP2006316388A (ja)	2006-11-24	紙用低密度化剤及び低密度紙の製造方法
US3989659A (en)	1976-11-02	Water-dispersible thermosettable cationic resins and paper sized therewith
JP2003247197A (ja)	2003-09-05	紙用嵩高剤及び嵩高紙の製造方法
US3990939A (en)	1976-11-09	Paper sized with ketene dimer modified water-dispersible thermosettable cationic resins
JP4764107B2 (ja)	2011-08-31	紙用低密度化剤及び低密度紙の製造方法
JP3304584B2 (ja)	2002-07-22	ロジン系エマルション組成物、その製造方法、サイズ剤、サイジング方法
CN118785837A (zh)	2024-10-15	用于改善纸巾和/或毛巾产品的柔软性的组合物
JPH03294596A (ja)	1991-12-25	カチオン性ロジンエマルジヨンサイズ剤
JP2022111417A (ja)	2022-08-01	製紙用エマルジョンサイズ剤、紙
JP2022045340A (ja)	2022-03-18	カチオン性ロジン系エマルジョンサイズ剤、紙