US20040040681A1 - Bulky flexible paper and process for producing the same - Google Patents
Bulky flexible paper and process for producing the same Download PDFInfo
- Publication number
- US20040040681A1 US20040040681A1 US10/416,552 US41655203A US2004040681A1 US 20040040681 A1 US20040040681 A1 US 20040040681A1 US 41655203 A US41655203 A US 41655203A US 2004040681 A1 US2004040681 A1 US 2004040681A1
- Authority
- US
- United States
- Prior art keywords
- paper
- bulk
- increasing
- softening agent
- melting point
- 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.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims description 24
- 239000004902 Softening Agent Substances 0.000 claims abstract description 104
- 238000001035 drying Methods 0.000 claims abstract description 41
- 238000002844 melting Methods 0.000 claims abstract description 37
- 230000008018 melting Effects 0.000 claims abstract description 37
- -1 ester compound Chemical class 0.000 claims abstract description 27
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 17
- 239000000194 fatty acid Substances 0.000 claims abstract description 17
- 229930195729 fatty acid Natural products 0.000 claims abstract description 17
- 239000007788 liquid Substances 0.000 claims abstract description 17
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 10
- 239000007787 solid Substances 0.000 claims abstract description 10
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 10
- 125000005210 alkyl ammonium group Chemical group 0.000 claims abstract description 6
- 239000004094 surface-active agent Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 abstract description 23
- 238000007639 printing Methods 0.000 abstract description 4
- 239000000123 paper Substances 0.000 description 164
- 230000000052 comparative effect Effects 0.000 description 26
- 239000000835 fiber Substances 0.000 description 22
- 230000000694 effects Effects 0.000 description 16
- 239000000839 emulsion Substances 0.000 description 16
- 239000003153 chemical reaction reagent Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 239000002270 dispersing agent Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 7
- 239000000945 filler Substances 0.000 description 7
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 230000002209 hydrophobic effect Effects 0.000 description 6
- 229920001131 Pulp (paper) Polymers 0.000 description 5
- 230000007613 environmental effect Effects 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 4
- 230000001965 increasing effect Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 238000004513 sizing Methods 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- FSEJJKIPRNUIFL-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-octadecanoyloxypropyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCCCCCCCCCCCC FSEJJKIPRNUIFL-UHFFFAOYSA-N 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 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 3
- 239000002655 kraft paper Substances 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- FHYUZZZBYFIZFH-NBTZWHCOSA-N (9Z,12Z)-octadeca-9,12-dienoic acid propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O FHYUZZZBYFIZFH-NBTZWHCOSA-N 0.000 description 2
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004166 Lanolin Substances 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 description 2
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- UXFNXQOUKCRBHD-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-(16-methylheptadecanoyloxy)propyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCCCCCCCCCC(C)C UXFNXQOUKCRBHD-UHFFFAOYSA-N 0.000 description 2
- BJXXCOMGRRCAGN-XPWSMXQVSA-N [2,2-bis(hydroxymethyl)-3-[(e)-octadec-9-enoyl]oxypropyl] (e)-octadec-9-enoate Chemical compound CCCCCCCC\C=C\CCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCC\C=C\CCCCCCCC BJXXCOMGRRCAGN-XPWSMXQVSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- UWLPCYBIJSLGQO-UHFFFAOYSA-N dodecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCC(O)=O UWLPCYBIJSLGQO-UHFFFAOYSA-N 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 239000011121 hardwood Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229940039717 lanolin Drugs 0.000 description 2
- 235000019388 lanolin Nutrition 0.000 description 2
- QLPMKRZYJPNIRP-UHFFFAOYSA-M methyl(trioctyl)azanium;bromide Chemical compound [Br-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC QLPMKRZYJPNIRP-UHFFFAOYSA-M 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 229940093625 propylene glycol monostearate Drugs 0.000 description 2
- 239000013055 pulp slurry Substances 0.000 description 2
- 235000011071 sorbitan monopalmitate Nutrition 0.000 description 2
- 239000001570 sorbitan monopalmitate Substances 0.000 description 2
- 229940031953 sorbitan monopalmitate Drugs 0.000 description 2
- 239000001587 sorbitan monostearate Substances 0.000 description 2
- 235000011076 sorbitan monostearate Nutrition 0.000 description 2
- 229940035048 sorbitan monostearate Drugs 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- VMPHSYLJUKZBJJ-UHFFFAOYSA-N trilaurin Chemical compound CCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC VMPHSYLJUKZBJJ-UHFFFAOYSA-N 0.000 description 2
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- HBOQXIRUPVQLKX-BBWANDEASA-N 1,2,3-trilinoleoylglycerol Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/C\C=C/CCCCC)COC(=O)CCCCCCC\C=C/C\C=C/CCCCC HBOQXIRUPVQLKX-BBWANDEASA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 description 1
- DNACJYZYGAJDBK-UHFFFAOYSA-N 16-methylheptadecanoic acid propane-1,2,3-triol Chemical compound OCC(O)CO.CC(C)CCCCCCCCCCCCCCC(O)=O.CC(C)CCCCCCCCCCCCCCC(O)=O DNACJYZYGAJDBK-UHFFFAOYSA-N 0.000 description 1
- WZUNUACWCJJERC-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)butyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CC)(CO)CO WZUNUACWCJJERC-UHFFFAOYSA-N 0.000 description 1
- JNAYPSWVMNJOPQ-UHFFFAOYSA-N 2,3-bis(16-methylheptadecanoyloxy)propyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCCCCCCCC(C)C JNAYPSWVMNJOPQ-UHFFFAOYSA-N 0.000 description 1
- ASKIVFGGGGIGKH-UHFFFAOYSA-N 2,3-dihydroxypropyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(O)CO ASKIVFGGGGIGKH-UHFFFAOYSA-N 0.000 description 1
- IENIFXNJFLJZGP-UHFFFAOYSA-N 2-(16-methylheptadecanoyloxy)ethyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCC(C)C IENIFXNJFLJZGP-UHFFFAOYSA-N 0.000 description 1
- OATHWIHWTWDNLJ-UHFFFAOYSA-N 2-(16-methylheptadecanoyloxy)propyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(C)OC(=O)CCCCCCCCCCCCCCC(C)C OATHWIHWTWDNLJ-UHFFFAOYSA-N 0.000 description 1
- SRHFAJHKZRUNCK-MAZCIEHSSA-N 2-[(9z,12z)-octadeca-9,12-dienoyl]oxyethyl (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCCOC(=O)CCCCCCC\C=C/C\C=C/CCCCC SRHFAJHKZRUNCK-MAZCIEHSSA-N 0.000 description 1
- ONXCNBUPZHJDCQ-QYCRHRGJSA-N 2-[(9z,12z)-octadeca-9,12-dienoyl]oxypropyl (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC ONXCNBUPZHJDCQ-QYCRHRGJSA-N 0.000 description 1
- UMHYVXGZRGOICM-AUYXYSRISA-N 2-[(z)-octadec-9-enoyl]oxypropyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(C)OC(=O)CCCCCCC\C=C/CCCCCCCC UMHYVXGZRGOICM-AUYXYSRISA-N 0.000 description 1
- IKVCSHRLYCDSFD-UHFFFAOYSA-N 2-hexadecanoyloxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCC IKVCSHRLYCDSFD-UHFFFAOYSA-N 0.000 description 1
- KKNRLFRQWDXUQD-HZJYTTRNSA-N 2-hydroxyethyl (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCCO KKNRLFRQWDXUQD-HZJYTTRNSA-N 0.000 description 1
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 1
- GTRGFUCVDQMYKO-UHFFFAOYSA-N 2-hydroxyethyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCCO GTRGFUCVDQMYKO-UHFFFAOYSA-N 0.000 description 1
- CTXGTHVAWRBISV-UHFFFAOYSA-N 2-hydroxyethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCO CTXGTHVAWRBISV-UHFFFAOYSA-N 0.000 description 1
- BXCRLBBIZJSWNS-UHFFFAOYSA-N 2-hydroxyethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCO BXCRLBBIZJSWNS-UHFFFAOYSA-N 0.000 description 1
- ZVTDEEBSWIQAFJ-KHPPLWFESA-N 2-hydroxypropyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(C)O ZVTDEEBSWIQAFJ-KHPPLWFESA-N 0.000 description 1
- BJRXGOFKVBOFCO-UHFFFAOYSA-N 2-hydroxypropyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(C)O BJRXGOFKVBOFCO-UHFFFAOYSA-N 0.000 description 1
- VCNPGCHIKPSUSP-UHFFFAOYSA-N 2-hydroxypropyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(C)O VCNPGCHIKPSUSP-UHFFFAOYSA-N 0.000 description 1
- JEMDXOYRWHZUCG-UHFFFAOYSA-N 2-octadecanoyloxypropyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)OC(=O)CCCCCCCCCCCCCCCCC JEMDXOYRWHZUCG-UHFFFAOYSA-N 0.000 description 1
- NRRPJRVSNIJDAP-UHFFFAOYSA-N 2-tetradecanoyloxypropyl tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OCC(C)OC(=O)CCCCCCCCCCCCC NRRPJRVSNIJDAP-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-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
- 239000004953 Aliphatic polyamide Substances 0.000 description 1
- FEAPLHZEJWLJRC-RGLFHLPNSA-N C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)OCC(COC(CCCCCCC\C=C/C\C=C/CCCCC)=O)(COC(CCCCCCC\C=C/C\C=C/CCCCC)=O)COC(CCCCCCC\C=C/C\C=C/CCCCC)=O Chemical compound C(CCCCCCC\C=C/C\C=C/CCCCC)(=O)OCC(COC(CCCCCCC\C=C/C\C=C/CCCCC)=O)(COC(CCCCCCC\C=C/C\C=C/CCCCC)=O)COC(CCCCCCC\C=C/C\C=C/CCCCC)=O FEAPLHZEJWLJRC-RGLFHLPNSA-N 0.000 description 1
- ONJPCDHZCFGTSI-NJYHNNHUSA-N CC(C)CCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC(C)C)[C@H]1OC[C@H](O)[C@H]1O Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC(C)C)[C@H]1OC[C@H](O)[C@H]1O ONJPCDHZCFGTSI-NJYHNNHUSA-N 0.000 description 1
- QMCRGOJVEJJFKM-NBTZWHCOSA-N CC(O)CO.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O Chemical compound CC(O)CO.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O QMCRGOJVEJJFKM-NBTZWHCOSA-N 0.000 description 1
- JNSGYXHNMZDPSI-MAZCIEHSSA-N CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCC\C=C/C\C=C/CCCCC Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCC\C=C/C\C=C/CCCCC JNSGYXHNMZDPSI-MAZCIEHSSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- AZLIXMDAMOHKAG-CVBJKYQLSA-N OCC(O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O Chemical compound OCC(O)CO.CCCCCCCC\C=C/CCCCCCCC(O)=O.CCCCCCCC\C=C/CCCCCCCC(O)=O AZLIXMDAMOHKAG-CVBJKYQLSA-N 0.000 description 1
- NYIIDPYDLJYGAY-GRVYQHKQSA-N OCC(O)CO.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O Chemical compound OCC(O)CO.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O NYIIDPYDLJYGAY-GRVYQHKQSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- NKSOSPOXQKNIKJ-CLFAGFIQSA-N Polyoxyethylene dioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCOC(=O)CCCCCCC\C=C/CCCCCCCC NKSOSPOXQKNIKJ-CLFAGFIQSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 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
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920001938 Vegetable gum Polymers 0.000 description 1
- 235000008853 Zanthoxylum piperitum Nutrition 0.000 description 1
- 244000131415 Zanthoxylum piperitum Species 0.000 description 1
- AQKOHYMKBUOXEB-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-(16-methylheptadecanoyloxy)oxolan-2-yl]-2-(16-methylheptadecanoyloxy)ethyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCC(C)C)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCC(C)C AQKOHYMKBUOXEB-RYNSOKOISA-N 0.000 description 1
- IJCWFDPJFXGQBN-RYNSOKOISA-N [(2R)-2-[(2R,3R,4S)-4-hydroxy-3-octadecanoyloxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCCCC IJCWFDPJFXGQBN-RYNSOKOISA-N 0.000 description 1
- TTZKGYULRVDFJJ-GIVMLJSASA-N [(2r)-2-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-[(z)-octadec-9-enoyl]oxyethyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1O TTZKGYULRVDFJJ-GIVMLJSASA-N 0.000 description 1
- PZQBWGFCGIRLBB-NJYHNNHUSA-N [(2r)-2-[(2s,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-octadecanoyloxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCCCCCCCCCCCC)[C@H]1OC[C@H](O)[C@H]1O PZQBWGFCGIRLBB-NJYHNNHUSA-N 0.000 description 1
- DNTMJTROKXRBDM-UUWWDYFTSA-N [(2r,3r,4s)-2-[(1r)-1-hexadecanoyloxy-2-hydroxyethyl]-4-hydroxyoxolan-3-yl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)O[C@H](CO)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCCCCCCCCCC DNTMJTROKXRBDM-UUWWDYFTSA-N 0.000 description 1
- NVANJYGRGNEULT-BDZGGURLSA-N [(3s,4r,5r)-4-hexadecanoyloxy-5-[(1r)-1-hexadecanoyloxy-2-hydroxyethyl]oxolan-3-yl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)O[C@H](CO)[C@H]1OC[C@H](OC(=O)CCCCCCCCCCCCCCC)[C@H]1OC(=O)CCCCCCCCCCCCCCC NVANJYGRGNEULT-BDZGGURLSA-N 0.000 description 1
- CYCUQBHCRPDWQM-UHFFFAOYSA-N [2,2-bis(dodecanoyloxymethyl)-3-hydroxypropyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CO)(COC(=O)CCCCCCCCCCC)COC(=O)CCCCCCCCCCC CYCUQBHCRPDWQM-UHFFFAOYSA-N 0.000 description 1
- DAIYEXZQVXSNAT-UHFFFAOYSA-N [2-(dodecanoyloxymethyl)-3-hydroxy-2-(hydroxymethyl)propyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CO)(CO)COC(=O)CCCCCCCCCCC DAIYEXZQVXSNAT-UHFFFAOYSA-N 0.000 description 1
- WXZIMZQDEGUSQL-UHFFFAOYSA-N [2-(hydroxymethyl)-3-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-2-[[(9Z,12Z)-octadeca-9,12-dienoyl]oxymethyl]propyl] (9Z,12Z)-octadeca-9,12-dienoate Chemical compound C(CCCCCCCC=C/CC=C/CCCCC)(=O)OCC(COC(CCCCCCCC=C/CC=C/CCCCC)=O)(COC(CCCCCCCC=C/CC=C/CCCCC)=O)CO WXZIMZQDEGUSQL-UHFFFAOYSA-N 0.000 description 1
- WOMIGYWYSKWGFG-UCTUUELPSA-N [2-(hydroxymethyl)-3-[(e)-octadec-9-enoyl]oxy-2-[[(e)-octadec-9-enoyl]oxymethyl]propyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C\CCCCCCCC(=O)OCC(CO)(COC(=O)CCCCCCC\C=C\CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC WOMIGYWYSKWGFG-UCTUUELPSA-N 0.000 description 1
- FWCDLNRNBHJDQB-UHFFFAOYSA-N [2-(hydroxymethyl)-3-octadecanoyloxy-2-(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(CO)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC FWCDLNRNBHJDQB-UHFFFAOYSA-N 0.000 description 1
- LPGFSDGXTDNTCB-UHFFFAOYSA-N [3-(16-methylheptadecanoyloxy)-2,2-bis(16-methylheptadecanoyloxymethyl)propyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCC(C)C)(COC(=O)CCCCCCCCCCCCCCC(C)C)COC(=O)CCCCCCCCCCCCCCC(C)C LPGFSDGXTDNTCB-UHFFFAOYSA-N 0.000 description 1
- QTIMEBJTEBWHOB-PMDAXIHYSA-N [3-[(z)-octadec-9-enoyl]oxy-2,2-bis[[(z)-octadec-9-enoyl]oxymethyl]propyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(COC(=O)CCCCCCC\C=C/CCCCCCCC)(COC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC QTIMEBJTEBWHOB-PMDAXIHYSA-N 0.000 description 1
- QWSLXWOHIYWPGZ-HZJYTTRNSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] (9z,12z)-octadeca-9,12-dienoate Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(=O)OCC(CO)(CO)CO QWSLXWOHIYWPGZ-HZJYTTRNSA-N 0.000 description 1
- QQVGEJLUEOSDBB-KTKRTIGZSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(CO)(CO)CO QQVGEJLUEOSDBB-KTKRTIGZSA-N 0.000 description 1
- FWGDUBYAYWFEHL-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCC(=O)OCC(CO)(CO)CO FWGDUBYAYWFEHL-UHFFFAOYSA-N 0.000 description 1
- ZJLATTXAOOPYRU-UHFFFAOYSA-N [3-hydroxy-2,2-bis(hydroxymethyl)propyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(CO)(CO)CO ZJLATTXAOOPYRU-UHFFFAOYSA-N 0.000 description 1
- OCKWAZCWKSMKNC-UHFFFAOYSA-N [3-octadecanoyloxy-2,2-bis(octadecanoyloxymethyl)propyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)(COC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC OCKWAZCWKSMKNC-UHFFFAOYSA-N 0.000 description 1
- 229920003231 aliphatic polyamide Polymers 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 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
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- QBEUXDWEKIOSIL-UHFFFAOYSA-N benzyl 5-amino-1h-pyrazole-4-carboxylate Chemical compound N1N=CC(C(=O)OCC=2C=CC=CC=2)=C1N QBEUXDWEKIOSIL-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- GZWGEAAWWHKLDR-JDVCJPALSA-M dimethyl-bis[(z)-octadec-9-enoyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC(=O)[N+](C)(C)C(=O)CCCCCCC\C=C/CCCCCCCC GZWGEAAWWHKLDR-JDVCJPALSA-M 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- VSZKZIHQDZUZER-UHFFFAOYSA-N dodecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCC(O)=O.CCCCCCCCCCCC(O)=O VSZKZIHQDZUZER-UHFFFAOYSA-N 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 238000007644 letterpress printing Methods 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- XKBGEWXEAPTVCK-UHFFFAOYSA-M methyltrioctylammonium chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC XKBGEWXEAPTVCK-UHFFFAOYSA-M 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- UQDVHJGNIFVBLG-UHFFFAOYSA-N octadecanoic acid;propane-1,2,3-triol Chemical compound OCC(O)CO.CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O UQDVHJGNIFVBLG-UHFFFAOYSA-N 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229940010310 propylene glycol dioleate Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 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
- SBHRWOBHKASWGU-UHFFFAOYSA-M tridodecyl(methyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(CCCCCCCCCCCC)CCCCCCCCCCCC SBHRWOBHKASWGU-UHFFFAOYSA-M 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- 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
- D21H21/22—Agents rendering paper porous, absorbent or bulky
-
- 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
- D21H25/00—After-treatment of paper not provided for in groups D21H17/00 - D21H23/00
- D21H25/04—Physical treatment, e.g. heating, irradiating
- D21H25/06—Physical treatment, e.g. heating, irradiating of impregnated or coated paper
Definitions
- This invention relates to a bulky flexible paper and a method for producing such paper.
- the methods used to increase paper bulk include those that employ cross-linked pulp (Japanese Patent Application Laid-open No. 4-185792, etc.), those that add synthetic fiber to the paper mixture (Japanese Patent Application Laid-open No. 3-269199, etc.), those that fill the space between pulp fibers with inorganic material or other filler (Japanese Patent Application Laid-open No. 3-124895, etc.), and those that use foaming granules (Japanese Patent Application Laid-open Nos. 5-230798, 11-200282, etc.).
- softening agent containing di-longchain alkyl-based quaternary ammonium salt, glycerin and water or fatty alcohol of carbon number 4 or below Japanese Patent Application Laid-open No. 4-100995
- softening agent containing lanolin and lanolin derivative Japanese Patent Application Laid-open No. 53-147803
- softening agent containing urethane alcohol or its quaternary compound Japanese Patent Application Laid-open No. 60-139897
- softening agent containing cationic oligomer Japanese Patent Application Laid-open No.
- One purpose of the present invention is to provide a method for the production of a printing paper that offers sufficient bulk and flexibility by optimizing the effect of the bulk-increasing/softening agent.
- Another purpose of the present invention is to provide a printing paper that offers sufficient bulk and flexibility, even when the temperature of the paper surface has been low in the drying process during paper-making.
- the inventors have carried out extensive studies in order to identify ways of achieving the above purposes, and have found that the relationship between the melting point of the bulk-increasing/softening agent and the temperature of the paper surface during the preheating drying period (a period during the drying process before the temperature of the wet paper becomes constant) is important. Moreover, the inventors have found that raising the temperature of the paper surface to the melting point of the bulk-increasing/softening agent or above would produce a sufficient bulk-increasing/softening effect. In other words, drying the wet paper under conditions in which the temperature of the paper surface remains at or above the melting point of the bulk-increasing/softening agent results in a paper offering sufficient bulk and excellent flexibility.
- the bulk5 increasing/softening agent to be used should desirably be an ester compound of polyhydric alcohol and higher fatty acid or long-chain alkyl ammonium salt. Additionally, the bulk-increasing/softening agent should preferably be added to between 0.1 weight-% and 5.0 weight-%, inclusive, of the material pulp. To add bulk and flexibility without changing the properties of the paper, it is even better to limit the amount of bulk-increasing/softening agent to between 0.2 weight-% and 2.0 weight-%, inclusive.
- the inventors have also found a way to produce a paper that offers sufficient bulk and excellent flexibility, even when the temperature of the paper surface drops for some reason in the drying process during paper-making. Specifically, the inventors found a way to produce a bulky flexible paper containing a bulk15 increasing/softening agent, which has a HLB of 6 or below and is either a liquid or a solid with a melting point of 40° C.
- the desired choice of said bulk-increasing/softening agent is an ester compound of polyhydric alcohol and higher unsaturated fatty acid and/or higher branched-chain fatty acid, with a surfactant added in an amount not greater than 10.0 weight-% of the bulk-increasing/softening agent.
- the bulk-increasing/softening agent should preferably be added to between 0.1 weight-% and 5.0 weight-%, inclusive, of the material pulp.
- the amount of bulk-increasing/softening agent should be limited to between 0.2 weight-% and 2.0 weight-%, inclusive, of the material pulp, so as to add bulk and flexibility without a significant change in the properties of the paper.
- the process of drying in a paper-making machine involves the use of a cylinder dryer or hot-air dryer.
- a cylinder dryer or hot-air dryer To meet the demand for a faster paper-making process and/or coating process, in recent years the IR dryer, flotation dryer and other types of dryers have been used to increase the drying capability. All dryers use heated air as a drying heat source. Heated air is blown onto the paper sheet to raise the surface temperature and thus efficiently vaporize the moisture within the paper.
- the heated air used for drying is subsequently discharged from the dryer, together with the steam from the paper sheet.
- heated air has a relatively small thermal capacity because there is no latent heat of condensation. Therefore, it takes some time before the paper reaches a constant rate of drying (condition in which the evaporation rate of steam is constant).
- the heated air present following the drying process contains generated steam and therefore stores a lot of thermal energy. However, this energy is often not recovered/reused but is instead discarded directly. Nevertheless, to shorten the time needed for the paper to achieve a constant rate of drying, it is effective to increase the thermal energy used in the drying process. To increase the thermal energy beyond the level provided by the heated air present following the drying process, it is important to increase the partial pressure of steam or raise the wet-bulb temperature.
- the specific methods for this include adjusting the exhaust volume from the dryer in order to increase the partial pressure of steam within the dryer, or using superheated steam or a gas that contains a lot of superheated steam as a heat source.
- superheated steam contacts the paper sheet within the dryer, a portion of it is condensed and becomes liquid.
- the latent heat of condensation causes the surface temperature of the paper sheet to rise rapidly, thereby allowing the paper to achieve a constant rate of drying within a shorter period of time.
- the surface temperature of the paper is said to be between 40° C. and 55° C. until the temperature of the wet paper becomes constant (preheating drying period), after which the temperature rises to between 55° C. and 80° C.
- the mechanism by which the paper increases in bulk and becomes flexible is not clear.
- the currently available bulk-increasing/softening agents do not have the same chemical composition, it is thought that bulk and flexibility are created when the bulk-increasing/softening agent is fixed onto the pulp fibers and increases the bonding distance between fibers.
- the bulk-increasing/softening agent dissolves when it receives heat during the preheating drying period, whereupon it coats the fiber surface. This has a hydrophobic effect on the fibers themselves and inhibits the hydrogen bonding between fibers, which usually occurs when the paper is dried, thus enhancing the paper's bulk and flexibility.
- a bulk-increasing/softening agent with a melting point of 55° C. or higher is used, the agent does not dissolve sufficiently and its coatability drops. This reduces the hydrophobic effect on the fibers and the fibers undergo hydrogen bonding, which in turn reduces the paper's bulk and flexibility.
- the paper should preferably be dried under conditions in which the paper's surface temperature is at least 10° C. higher than the melting point of the bulk-increasing/softening agent. In other words, the surface temperature of the paper should preferably be sufficiently higher than the melting point of the bulk-increasing/softening agent during the preheating drying period.
- the surface temperature of the paper during the preheating drying period should preferably be 40° C. or above.
- the drying should take place with the surface temperature of the paper being at least 10° C. higher than the melting point of the agent.
- the inventors examined the relationship between the surface temperature of the paper, especially during the preheating drying period, on one hand and the bulk and flexibility of paper on the other, and have found that a sufficient hydrophobic property could be added to the fiber surface and a low-density paper offering improved flexibility could be produced through the use of a bulk-increasing/softening agent that is liquid at room temperature or a solid with a melting point of 40° C. or below that easily dissolves under a small amount of heat. The inventors also found that such a bulk-increasing/softening agent should desirably have a HLB of 6 or below.
- a printing paper offering sufficient bulk and excellent flexibility could be obtained using a bulk-increasing/softening agent, even when the surface temperature of the paper drops for some reason in the drying process during paper-making.
- a bulky flexible paper containing a bulk-increasing/softening agent with a HLB of 6 or below, wherein said agent is either a liquid or a solid with a melting point of 40° C. or below can be obtained.
- the bulk-increasing/softening agent used in the present invention has both a hydrophobic group and a hydrophilic group in the molecule, which is a well-known property of surfactants.
- suitable surfactants include higher alcohol and higher fatty acid containing alkylene oxide, but the bulk-increasing/softening agent should not be limited to surfactant as long as the chemical is able to add bulk and flexibility to the paper. It is also known that certain aliphatic polyamide amine compounds produce a bulk-increasing/softening effect.
- the bulk-increasing/softening agents currently available on the market include Sursol VL by BASF, Bayvolum P Liquid by Bayer, Reactopaque (opacity-improving agent) by Sansho, and KB-08T and KB-115 by Kao.
- the ester compound of polyhydric alcohol and higher fatty acid which is used as a bulk-increasing/softening agent in the present invention, should preferably be an ester compound of polyhydric alcohol and higher unsaturated fatty acid or ester compound of polyhydric alcohol and higher branched-chain fatty acid. Specific examples of these compounds are listed as follows:
- Higher unsaturated fatty-acid esters include ethylene glycol monooleate, ethylene glycol dioleate, ethylene glycol monolinolate, ethylene glycol dilinolate, glycerin monooleate, glycerin dioleate, glycerin trioleate, glycerin monolinolate, glycerin dilinolate, glycerin trilinolate, propylene glycol monooleate, propylene glycol dioleate, propylene glycol monolinolate, propylene glycol dilinolate, pentaerythritol monooleate, pentaerythritol dioleate, pentaerythritol trioleate, pentaerythritol tetraoleate, pentaerythritol monolinolate, pentaerythritol dilinolate, pentaerythritol dil
- Higher branched-chain fatty-acid esters include ethylene glycol monoisostearate, ethylene glycol diisostearate, glycerin monoisostearate, glycerin diisostearate, glycerin triisostearate, propylene glycol monoisostearate, propylene glycol diisostearate, pentaerythritol monoisostearate, pentaerythritol diisostearate, pentaeriythritol triisostearate, pentaerythritol tetraisostearate, sorbitan diisostearate, sorbitan triisostearate and sorbitan tetraisostearate, but are not limited to these compounds.
- Ester compounds of polyhydric alcohol and higher fatty acid include ethylene glycol monolaurate, ethylene glycol dilaurate, ethylene glycol monopalmitate, ethylene glycol dipalmitate, glycerin monostearate, glycerin distearate, glycerin tristearate, glycerin monolaurate, glycerin dilaurate, glycerin trilaurate, propylene glycol monostearate, propylene glycol distearate, propylene glycol monomyristate, propylene glycol dimyristate, pentaerythritol monolaurate, pentaerythritol dilaurate, pentaerythritol trilaurate, pentaerythritol tetraraurate, pentaerythritol monostearate, pentaerythritol distearate, pentaerythritol tristea
- long-chain alkyl ammonium salt include the following compounds: lauryl trimethyl ammonium chloride, cetyl trimethyl ammonium bromide, stearyl trimethyl ammonium chloride, dimethyl distearyl ammonium chloride, dioleoyl dimethyl ammonium chloride, tridodecyl methyl ammonium chloride, trioctyl methyl ammonium chloride and trioctyl methyl ammonium bromide, but are not limited to these compounds.
- higher fatty-acid esters are mostly solid at normal temperature.
- a majority of higher unsaturated fatty-acid esters and higher branched-chain fatty-acid esters are liquid at normal temperature.
- Higher unsaturated fatty-acid esters and higher branched-chain fatty-acid esters that are solid at normal temperature have, in most cases, a melting point of 40° C. or below.
- a bulk-increasing/softening agent with a high HLB and thus insufficient hydrophobic property may not produce the desired bulk-increasing/softening effect because it cannot provide sufficient hydrophobicity to the fibers. If the HLB is low, specifically 6 or below in regard to the present invention, the fibers can be provided with sufficient hydrophobicity.
- surfactants that can be used in conjunction with the bulk-increasing/softening agent in the present invention include the following compounds: anionic surfactants such as Pelex OT-P (Kao), Demol EP (Kao), Disper TL (Meisei Chemical Works), Gohseran L-3266 (Nippon Synthetic Chemical Industry) and Aron T-40 (Toa Gosei Kagaku); nonionic surfactants such as Emulgen A-60 (Kao) and Emulmin 50 (Sanyo Chemical); and cationic surfactants such as Cation DS (Sanyo Chemical), Quartamin 86W (Kao) and Quartamin D86P (Kao), but are not limited to these products.
- anionic surfactants such as Pelex OT-P (Kao), Demol EP (Kao), Disper TL (Meisei Chemical Works), Gohseran L-3266 (Nippon Synthetic Chemical Industry) and Aron T-40 (Toa Go
- the bulky flexible paper provided through the present invention is produced from various types of pulp through the normal paper-making process.
- Material pulps include chemical pulp (bleached or unbleached kraft pulp from softwood, bleached or unbleached kraft pulp from hardwood, etc.), mechanical pulp (groundwood pulp, thermomechanical pulp, chemi-thermomechanical pulp, etc.), or recycled, ink-removed pulp, wherein these material pulps may be used alone or in combination at arbitrary ratios of blending.
- the pH level of the pulp slurry may be in the acid, neutral or alkali range.
- the bulky flexible paper provided through the present invention may contain filler.
- fillers must or must not be used, and common fillers can be employed.
- examples include inorganic fillers such as clay, fired clay, silicious marl, talc, kaolin, fired kaolin, delaminated kaolin, heavy calcium carbonate, light calcium carbonate, magnesium carbonate, barium carbonate, titanium dioxide, zinc oxide, silicon oxide, amorphous silica, aluminum hydroxide, calcium hydroxide, magnesium hydroxide and zinc hydroxide; and organic fillers such as urea-formalin resin, polystyrene resin, phenol resin and fine hollow grains, wherein such fillers can be used alone or in any combination.
- inorganic fillers such as clay, fired clay, silicious marl, talc, kaolin, fired kaolin, delaminated kaolin, heavy calcium carbonate, light calcium carbonate, magnesium carbonate, barium carbonate, titanium dioxide, zinc oxide, silicon oxide, amorphous silica, aluminum hydroxide, calcium hydroxide, magnesium hydroxide and zinc
- various nonionic or cationic internal auxiliaries traditionally used in the paper-making process such as retention-aiding agent, freeness-improving agent, paper-strength enhancer and sizing agent, may be selected and used as appropriate.
- Internal auxiliaries normally used in the paper-making process include aluminum sulfate; aluminum chloride; sodium aluminate; basic aluminum compounds such as basic aluminum chloride and basic aluminum polyhydroxide; water-soluble aluminum compounds such as alumina sol that dissolve easily in water; polyvalent metals such as ferrous sulfate and ferric sulfate; and silica sol.
- the sizing agent can be chosen from various types, including alkyl ketene dimer compounds, alkenyl succinate anhydride compounds, styrene-acryl compounds, higher fatty acid compounds, petroleum resin-based sizing agents, and rosin-based sizing agents.
- auxiliaries normally used in the paper-making process include various starches, polyacrylamide, urea resin, melamine resin, epoxy resin, polyamide resin, polyamide, polyamine resin, polyamine, polyethylenimine, vegetable gum, polyvinyl alcohol, latex, polyethylene oxide and hydrophilic-crosslinked-polymer-particle dispersion, as well as their derivatives and transformed versions.
- dye, fluorescent whitener, pH regulator, defoaming agent, pitch controller, slime controller and other agents normally used in the paper-making process may be added as appropriate for the given application.
- the method of producing paper provided through the present invention applies to all papers made using different schemes, including papers produced in the acid range of around pH 4 to 5 or those produced in the neutral range of around pH 6 (weak acidity) to 9 (weak alkalinity), wherein the slurry usually contains calcium carbonate or other alkali filler.
- the paper-making machine may be a Fourdrinier paper machine, twin-wire machine, Yankee machine, or a machine of another suitable type.
- the bulky flexible paper obtained in the manner explained above is ideal, for example, as a product for offset printing. It can also be used as a letterpress printing paper, electrophotographic paper, ink-jet printing paper, thermal paper, pressure-sensitive paper or other type of paper used for the recording of information.
- the paper obtained through the present invention is also suitable as the base paper of a coated stock.
- the present invention is not limited to these examples.
- the prepared hand-made paper sheets were dried using two types of dryers. Specifically, a fan dryer was used when the condition assumed that the temperature of the paper's surface would be normal to lower during the preheating drying period, and an environmental tester was used when the condition assumed that the temperature of the paper's surface would be normal to higher.
- the initial temperature of the paper's surface was used as the surface temperature during the preheating drying period.
- Clark stiffness In conformance with JIS P 8143
- HLB of bulk-increasing/softening agent Calculated through the following formula:
- HLB 20 ⁇ (Molecular weight of hydrophilic group)/(Total molecular weight)
- a bulk-increasing/softening agent comprising 10.0 g of pentaerythritol distearate (reagent by Tokyo Kasei Kogyo; melting point 51° C., HLB 4.0) and a dispersant comprising 0.1 g of Pelex OT-P (Kao) were mixed thoroughly and added to 1,000 g of water. The mixture was agitated for 10 minutes at a speed of 10,000 rpm using an emulsifier to prepare an emulsion of bulk-increasing/softening agent. Bleached kraft pulp from hardwood (CSF freeness 350 ml) was used as the pulp content.
- CSF freeness 350 ml was used as the pulp content.
- the aforementioned emulsion of bulk-increasing/softening agent was then added to the pulp to 1.0 weight-% to prepare a paper material. Thereafter, a round manual paper-making tool was used to produce a paper with a grammage of 60 g/m 2 , which was then pressed under an effective pressure of 4.18 kg/cm 2 . The pressed paper was dried for one hour in an environmental tester (initial temperature of paper surface at 70° C.) to obtain a bulky flexible paper.
- a bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of glycerin monolaurate (reagent by Tokyo Kasei Kogyo; melting point 63° C., HLB 6.6) and a dispersant comprising 0.2 g of Emulgen A-60 (Kao).
- a bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of sorbitan monopalmitate (reagent by Aldrich; span #40, melting point 46° C., HLB 8.1) and a dispersant comprising 0.25 g of Emulgen A60 (Kao).
- a bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of sorbitan monostearate (reagent by Aldrich; melting point 56° C., HLB 7.6) and a dispersant comprising 0.15 g of Cation DS (Sanyo Chemical).
- a bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of propylene glycol monostearate (prepared by the inventors; melting point 50° C., HLB 4.4) and a dispersant comprising 0.3 g of Cation DS (Sanyo Chemical).
- a bulk-increasing/softening agent comprising 10.0 g of propylene glycol monostearate (prepared by the inventors; melting point 50° C., HLB 4.4) and a dispersant comprising 0.3 g of Cation DS (Sanyo Chemical).
- a bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 3.0 g of trioctyl methyl ammonium bromide (reagent by Aldrich; melting point 37° C., HLB 1.6) and a dispersant comprising 0.1 g of Emulgen A60 (Kao).
- a bulky flexible paper was obtained in the same manner as described in Example 6, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- a bulky flexible paper was obtained in the same manner as described in Example 1, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- a bulky flexible paper was obtained in the same manner as described in Example 2, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- a bulky flexible paper was obtained in the same manner as described in Example 3, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- a bulky flexible paper was obtained in the same manner as described in Example 4, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- a bulky flexible paper was obtained in the same manner as described in Example 5, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- Example 1 A hand-made paper sheet was obtained in the same manner as described in Example 1, except that no bulk-increasing/softening agent was added.
- TABLE 1 Initial temper- ature Paper property data Melting of paper Breaking Clark point HLB surface Density length stiffness (° C.) ( ⁇ ) (° C.) (g/cm 3 ) (km) (cm 3 /100)
- Example 1 51 4.0 70 0.51 2.79 43.0
- Example 2 63 6.6 70 0.53 2.88 47.9
- Example 3 46 8.1 70 0.52 2.80 46.8
- Example 4 56 7.6 70 0.51 2.72 45.4
- Example 5 50 4.4 70 0.50 2.59 44.9
- Example 6 37 1.6 70 0.49 2.41 42.2
- Example 7 37 1.6 40 0.53 2.82 48.0 Comparative 51 4.0 40 0.54 2.91 52.3 example 1 Comparative 63 6.6 40 0.56 3.01 56.2
- Comparative 46 8.1 40 0.57 3.16 59.1
- Comparative 56 7.6 40 0.56
- Table 1 shows that a more bulky flexible paper could be obtained when the wet paper was dried in a condition where the initial surface temperature of the paper was higher than the melting point of the bulk-increasing/softening agent (examples 1 through 7), compared with when it was dried in a condition where the initial temperature of paper surface was lower (comparative examples 1 through 6).
- the initial temperature of paper surface must be sufficiently higher than the bulk-increasing/softening agent while the wet paper is being dried in order for the agent to effectively enhance the paper's bulk and flexibility.
- a bulk-increasing/softening agent comprising 10.0 g of pentaerythritol dioleate (reagent by Tokyo Kasei Kogyo; liquid, HLB 4.0) and a dispersant comprising 0.1 g of Pelex OT-P (Kao) were mixed thoroughly and added to 1,000 g of water. The mixture was agitated for 10 minutes at a speed of 10,000 rpm using an emulsifier to prepare an emulsion of bulk-increasing/softening agent. LBKP (CSF freeness 350 ml) was used as the pulp content.
- the aforementioned emulsion of bulk-increasing/softening agent was then added to the pulp to 1.0 weight-% to prepare a paper material. Thereafter, a round manual paper-making tool was used to produce a paper with a grammage of 60 g/m 2 , which was then pressed under an effective pressure of 4.18 kg/cm 2 . The pressed paper was dried for one hour in a fan dryer (initial temperature of paper surface at 40° C.) and an environmental tester (initial temperature of paper surface at 70° C.) to obtain a bulky flexible paper.
- a bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of glycerin trioleate (reagent by Tokyo Kasei Kogyo; liquid, HLB 2.0) and a dispersant comprising 0.2 g of Emulgen A-60 (Kao).
- a bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of glycerin monolinolate (reagent by Tokyo Kasei Kogyo; liquid, HLB 5.1) and a dispersant comprising 0.15 g of Cation DS (Sanyo Chemical).
- a bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 0.3 g of pentaerythritol diisostearate (prepared by the inventors; liquid, HLB 4.0).
- a bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising pentaerythritol distearate (reagent by Tokyo Kasei Kogyo; melting point 51° C., HLB 4.0).
- Example 8 A hand-made paper sheet was obtained in the same manner as described in Example 8, except that no bulk-increasing/softening agent was added.
- TABLE 2 Low-temperature dryer High-temperature dryer Clark Clark Break- stiff- Break- stiff- ing ness ing ness HLB Density length (cm 3 / Density length (cm 3 / ( ⁇ ) (g/cm 3 ) (km) 100) (g/cm 3 ) (km) 100)
- Example 8 4.0 0.49 2.62 36.3 0.51 2.65 36.1
- Example 9 2.0 0.49 2.55 38.0 0.50 2.49 35.1
- Example 10 5.1 0.50 2.59 37.8 0.50 2.56 35.2
- Example 11 4.0 0.51 2.69 38.7 0.51 2.55 37.6 Comparative 4.0 0.54 2.91 44.3 0.51 2.79 36.2 example 7 Comparative 9.4 0.56 3.01 47.2 0.55 2.98 42.3 example 8 Comparative — 0.58 3.43 48.3 0.59 3.52 49.0 example 9
- the initial temperature of paper surface must be sufficiently high to achieve any meaningful bulk-increasing/softening effect. From the comparison of Examples 7 through 11 and Comparative Example 8, it has been verified that a sufficient bulk-increasing/softening effect can be achieved if the HLB of the bulk-increasing/softening agent is 6 or below.
- the present invention allows for the production of a paper offering sufficient bulk and flexibility even when the paper's surface temperature drops in the initial drying process, by using a bulk-increasing/softening agent with a HLB of 6 or below, wherein said agent is either a liquid or a solid with a melting point of 40° C. or below.
Landscapes
- Paper (AREA)
Abstract
Produce a printing paper that offers sufficient bulk and flexibility by using a bulk-increasing/softening agent with a HLB of 6 or below, which is either a liquid or a solid with a melting point of 40° C. or below, wherein the agent may be an ester compound of polyhydric alcohol and higher fatty acid or a long-chain alkyl ammonium salt, and by adjusting the surface temperature of the paper during a preheating drying period (a period during a drying process before the temperature of a wet paper becomes constant) to at least 10° C. higher than the melting point of the bulk-increasing/softening agent.
Description
- This invention relates to a bulky flexible paper and a method for producing such paper.
- Comic books and paperbacks have been flourishing at a rapid pace in recent years, reflecting the decreasing number of book readers-a trend that is forcing the industry to print more visually appealing, inexpensive books. Lighter, more flexible papers are therefore required for use in the production of comic books/paperbacks. Here, “lighter” means reduced weight at a fixed thickness, i.e., higher bulk (lower density). Given the public's increasing awareness of environmental problems, the production of lighter papers is essential, as it facilitates the effective use of paper pulps produced from wood resources. “Flexible” refers to the flexural rigidity of paper at a fixed thickness, i.e. the pliability of paper that makes it easy to keep the book open instead of allowing the pages to close naturally.
- The methods used to increase paper bulk include those that employ cross-linked pulp (Japanese Patent Application Laid-open No. 4-185792, etc.), those that add synthetic fiber to the paper mixture (Japanese Patent Application Laid-open No. 3-269199, etc.), those that fill the space between pulp fibers with inorganic material or other filler (Japanese Patent Application Laid-open No. 3-124895, etc.), and those that use foaming granules (Japanese Patent Application Laid-open Nos. 5-230798, 11-200282, etc.). However, the use of cross25 linked pulp and synthetic fiber makes it impossible to recycle the paper, while applying a filler between the pulp fibers or using foaming granules reduces the paper's strength significantly. Methods that use general surfactants (publication of WO patent application No. 98/03730; Japanese Patent Application Laid-open Nos. 11-200283, 11-200284, 11-200285, 11-269799, 11-350380, etc.) have also been reported.
- Contrastingly, the flexibility of paper is believed to manifest in accordance with the fiber type, paper density, moisture content of paper and other factors that interact with paper fibers. Paper products used in the home, such as toilet paper and facial tissue, require a certain level of flexibility to suit their purposes. Numerous softening agents have been developed to date, and glycerin, polyethylene glycol, urea, emulsified paraffin, quaternary ammonium salt and other substances are known to add flexibility to paper. Additionally, a softening agent containing di-longchain alkyl-based quaternary ammonium salt (Japanese Patent Application Laid-open Nos. 63-165597, 8-296197, etc.), softening agent containing di-longchain alkyl-based quaternary ammonium salt, glycerin and water or fatty alcohol of carbon number 4 or below (Japanese Patent Application Laid-open No. 4-100995), softening agent containing lanolin and lanolin derivative (Japanese Patent Application Laid-open No. 53-147803), softening agent containing urethane alcohol or its quaternary compound (Japanese Patent Application Laid-open No. 60-139897), softening agent containing cationic oligomer (Japanese Patent Application Laid-open No. 63-251049), softening agent containing polyamide derivative (Japanese Patent Application Laid-open No. 51-38600), and pyrolidone carboxylic acid or its salt (Japanese Patent Application Laid-open No. 7-189170) are also reported. However, these bulk-increasing agents or softening agents have often failed to exhibit sufficient bulk-increasing effect or softening effect or have only exhibited low repeatability of the bulk-increasing/softening effect in the paper-making process.
- One purpose of the present invention is to provide a method for the production of a printing paper that offers sufficient bulk and flexibility by optimizing the effect of the bulk-increasing/softening agent.
- Another purpose of the present invention is to provide a printing paper that offers sufficient bulk and flexibility, even when the temperature of the paper surface has been low in the drying process during paper-making.
- The inventors have carried out extensive studies in order to identify ways of achieving the above purposes, and have found that the relationship between the melting point of the bulk-increasing/softening agent and the temperature of the paper surface during the preheating drying period (a period during the drying process before the temperature of the wet paper becomes constant) is important. Moreover, the inventors have found that raising the temperature of the paper surface to the melting point of the bulk-increasing/softening agent or above would produce a sufficient bulk-increasing/softening effect. In other words, drying the wet paper under conditions in which the temperature of the paper surface remains at or above the melting point of the bulk-increasing/softening agent results in a paper offering sufficient bulk and excellent flexibility. The bulk5 increasing/softening agent to be used should desirably be an ester compound of polyhydric alcohol and higher fatty acid or long-chain alkyl ammonium salt. Additionally, the bulk-increasing/softening agent should preferably be added to between 0.1 weight-% and 5.0 weight-%, inclusive, of the material pulp. To add bulk and flexibility without changing the properties of the paper, it is even better to limit the amount of bulk-increasing/softening agent to between 0.2 weight-% and 2.0 weight-%, inclusive.
- In the above study process, the inventors have also found a way to produce a paper that offers sufficient bulk and excellent flexibility, even when the temperature of the paper surface drops for some reason in the drying process during paper-making. Specifically, the inventors found a way to produce a bulky flexible paper containing a bulk15 increasing/softening agent, which has a HLB of 6 or below and is either a liquid or a solid with a melting point of 40° C. or below, wherein the desired choice of said bulk-increasing/softening agent is an ester compound of polyhydric alcohol and higher unsaturated fatty acid and/or higher branched-chain fatty acid, with a surfactant added in an amount not greater than 10.0 weight-% of the bulk-increasing/softening agent. Additionally, the bulk-increasing/softening agent should preferably be added to between 0.1 weight-% and 5.0 weight-%, inclusive, of the material pulp. Better yet, the amount of bulk-increasing/softening agent should be limited to between 0.2 weight-% and 2.0 weight-%, inclusive, of the material pulp, so as to add bulk and flexibility without a significant change in the properties of the paper.
- The bulky flexible paper provided through the use of the present invention, as well as its production method, are detailed below.
- Generally, the process of drying in a paper-making machine involves the use of a cylinder dryer or hot-air dryer. To meet the demand for a faster paper-making process and/or coating process, in recent years the IR dryer, flotation dryer and other types of dryers have been used to increase the drying capability. All dryers use heated air as a drying heat source. Heated air is blown onto the paper sheet to raise the surface temperature and thus efficiently vaporize the moisture within the paper.
- The heated air used for drying is subsequently discharged from the dryer, together with the steam from the paper sheet. Normally, heated air has a relatively small thermal capacity because there is no latent heat of condensation. Therefore, it takes some time before the paper reaches a constant rate of drying (condition in which the evaporation rate of steam is constant). On the other hand, the heated air present following the drying process contains generated steam and therefore stores a lot of thermal energy. However, this energy is often not recovered/reused but is instead discarded directly. Nevertheless, to shorten the time needed for the paper to achieve a constant rate of drying, it is effective to increase the thermal energy used in the drying process. To increase the thermal energy beyond the level provided by the heated air present following the drying process, it is important to increase the partial pressure of steam or raise the wet-bulb temperature.
- The specific methods for this include adjusting the exhaust volume from the dryer in order to increase the partial pressure of steam within the dryer, or using superheated steam or a gas that contains a lot of superheated steam as a heat source. When superheated steam contacts the paper sheet within the dryer, a portion of it is condensed and becomes liquid. At this time, the latent heat of condensation causes the surface temperature of the paper sheet to rise rapidly, thereby allowing the paper to achieve a constant rate of drying within a shorter period of time.
- Given the general drying process in a paper-making machine, the surface temperature of the paper is said to be between 40° C. and 55° C. until the temperature of the wet paper becomes constant (preheating drying period), after which the temperature rises to between 55° C. and 80° C. However, the mechanism by which the paper increases in bulk and becomes flexible is not clear. Although the currently available bulk-increasing/softening agents do not have the same chemical composition, it is thought that bulk and flexibility are created when the bulk-increasing/softening agent is fixed onto the pulp fibers and increases the bonding distance between fibers. Specifically, the bulk-increasing/softening agent dissolves when it receives heat during the preheating drying period, whereupon it coats the fiber surface. This has a hydrophobic effect on the fibers themselves and inhibits the hydrogen bonding between fibers, which usually occurs when the paper is dried, thus enhancing the paper's bulk and flexibility. However, if a bulk-increasing/softening agent with a melting point of 55° C. or higher is used, the agent does not dissolve sufficiently and its coatability drops. This reduces the hydrophobic effect on the fibers and the fibers undergo hydrogen bonding, which in turn reduces the paper's bulk and flexibility.
- Even when the melting point of the bulk-increasing/softening agent is between 55° C. and 60° C., if the crystallization property of the agent is high and the agent does not receive thermal energy sufficient for it to dissolve, then hydrogen bonding will occur between the fibers before the bulk-increasing/softening agent dissolves. When this happens, the paper does not have sufficient bulk or flexibility. Therefore, the paper should preferably be dried under conditions in which the paper's surface temperature is at least 10° C. higher than the melting point of the bulk-increasing/softening agent. In other words, the surface temperature of the paper should preferably be sufficiently higher than the melting point of the bulk-increasing/softening agent during the preheating drying period. For example, if the melting point of the bulk-increasing/softening agent is 40° C., the surface temperature of the paper during the preheating drying period should preferably be 40° C. or above. However, to ensure the bulk and flexibility of the paper, the drying should take place with the surface temperature of the paper being at least 10° C. higher than the melting point of the agent.
- After studying the relationship between the surface temperature of the paper, especially during the preheating drying period, on one hand and the bulk and flexibility of paper on the other, it was found that by keeping the paper's surface temperature at or above the melting point of the bulk-increasing/softening agent while the paper is being dried, the fiber surface could be efficiently covered by a hydrophobic compound, thus enabling the production of a low-density paper having improved flexibility. Consequently, this finding led to the present invention. It was also revealed that if, due to a drop in drying efficiency for some reason, the paper's surface temperature cannot be raised to a sufficient level in the drying process during paper-making, the bulk-increasing/softening agent will not dissolve and the coatability will drop. This produces a reduction in the hydrophobic effect on the fibers and the fibers undergo hydrogen bonding, which in turn reduces the paper's bulk and flexibility. Even if the bulk-increasing/softening agent does dissolve, hydrogen bonding between fibers could still occur prior to dissolution if the paper does not receive sufficient heat. This also reduces the paper's bulk and flexibility. Given a general drying process in a paper-making machine, the surface temperature of the paper is between 40° C. and 55° C. until the temperature of the wet paper becomes constant (preheating drying period), after which the wet paper temperature rises to between 55° C. and 80° C. Generally, bulk and flexibility are created during the preheating drying period before bonding between the fibers takes place.
- Based on these findings, the inventors examined the relationship between the surface temperature of the paper, especially during the preheating drying period, on one hand and the bulk and flexibility of paper on the other, and have found that a sufficient hydrophobic property could be added to the fiber surface and a low-density paper offering improved flexibility could be produced through the use of a bulk-increasing/softening agent that is liquid at room temperature or a solid with a melting point of 40° C. or below that easily dissolves under a small amount of heat. The inventors also found that such a bulk-increasing/softening agent should desirably have a HLB of 6 or below.
- In other words, the inventors have found that a printing paper offering sufficient bulk and excellent flexibility could be obtained using a bulk-increasing/softening agent, even when the surface temperature of the paper drops for some reason in the drying process during paper-making. In this case, a bulky flexible paper containing a bulk-increasing/softening agent with a HLB of 6 or below, wherein said agent is either a liquid or a solid with a melting point of 40° C. or below, can be obtained.
- The bulk-increasing/softening agent used in the present invention has both a hydrophobic group and a hydrophilic group in the molecule, which is a well-known property of surfactants. Examples of suitable surfactants include higher alcohol and higher fatty acid containing alkylene oxide, but the bulk-increasing/softening agent should not be limited to surfactant as long as the chemical is able to add bulk and flexibility to the paper. It is also known that certain aliphatic polyamide amine compounds produce a bulk-increasing/softening effect. The bulk-increasing/softening agents currently available on the market include Sursol VL by BASF, Bayvolum P Liquid by Bayer, Reactopaque (opacity-improving agent) by Sansho, and KB-08T and KB-115 by Kao.
- Generally, long-chain alkyl ammonium salt and ester compound of a certain polyhydric alcohol and higher fatty acid are solid in most cases, and are also prone to the effects of the paper's surface temperature in the initial stage of the drying process due to a wide range of melting points.
- The ester compound of polyhydric alcohol and higher fatty acid, which is used as a bulk-increasing/softening agent in the present invention, should preferably be an ester compound of polyhydric alcohol and higher unsaturated fatty acid or ester compound of polyhydric alcohol and higher branched-chain fatty acid. Specific examples of these compounds are listed as follows:
- Higher unsaturated fatty-acid esters include ethylene glycol monooleate, ethylene glycol dioleate, ethylene glycol monolinolate, ethylene glycol dilinolate, glycerin monooleate, glycerin dioleate, glycerin trioleate, glycerin monolinolate, glycerin dilinolate, glycerin trilinolate, propylene glycol monooleate, propylene glycol dioleate, propylene glycol monolinolate, propylene glycol dilinolate, pentaerythritol monooleate, pentaerythritol dioleate, pentaerythritol trioleate, pentaerythritol tetraoleate, pentaerythritol monolinolate, pentaerythritol dilinolate, pentaerythritol trilinolate, pentaerythritol tetralinolate, sorbitan dioleate, sorbitan trioleate, sorbitan tetraoleate, sorbitan dilinolate, sorbitan trilinolate and sorbitan tetralinolate, but are not limited to these compounds.
- Higher branched-chain fatty-acid esters include ethylene glycol monoisostearate, ethylene glycol diisostearate, glycerin monoisostearate, glycerin diisostearate, glycerin triisostearate, propylene glycol monoisostearate, propylene glycol diisostearate, pentaerythritol monoisostearate, pentaerythritol diisostearate, pentaeriythritol triisostearate, pentaerythritol tetraisostearate, sorbitan diisostearate, sorbitan triisostearate and sorbitan tetraisostearate, but are not limited to these compounds.
- Ester compounds of polyhydric alcohol and higher fatty acid include ethylene glycol monolaurate, ethylene glycol dilaurate, ethylene glycol monopalmitate, ethylene glycol dipalmitate, glycerin monostearate, glycerin distearate, glycerin tristearate, glycerin monolaurate, glycerin dilaurate, glycerin trilaurate, propylene glycol monostearate, propylene glycol distearate, propylene glycol monomyristate, propylene glycol dimyristate, pentaerythritol monolaurate, pentaerythritol dilaurate, pentaerythritol trilaurate, pentaerythritol tetraraurate, pentaerythritol monostearate, pentaerythritol distearate, pentaerythritol tristearate, pentaerythritol tetrastearate, sorbitan monopalmitate, sorbitan dipalmitate, sorbitan tripalmitate, sorbitan tetrapalmitate, sorbitan monostearate, sorbitan distearate, sorbitan tristearate and sorbitan tetrastearate, but are not limited to these compounds.
- Specific examples of long-chain alkyl ammonium salt include the following compounds: lauryl trimethyl ammonium chloride, cetyl trimethyl ammonium bromide, stearyl trimethyl ammonium chloride, dimethyl distearyl ammonium chloride, dioleoyl dimethyl ammonium chloride, tridodecyl methyl ammonium chloride, trioctyl methyl ammonium chloride and trioctyl methyl ammonium bromide, but are not limited to these compounds.
- Generally, higher fatty-acid esters are mostly solid at normal temperature. On the other hand, a majority of higher unsaturated fatty-acid esters and higher branched-chain fatty-acid esters are liquid at normal temperature. Higher unsaturated fatty-acid esters and higher branched-chain fatty-acid esters that are solid at normal temperature have, in most cases, a melting point of 40° C. or below.
- In the present invention, a bulk-increasing/softening agent with a high HLB and thus insufficient hydrophobic property may not produce the desired bulk-increasing/softening effect because it cannot provide sufficient hydrophobicity to the fibers. If the HLB is low, specifically 6 or below in regard to the present invention, the fibers can be provided with sufficient hydrophobicity.
- However, excessive hydrophobicity inhibits the efficient dispersion of water, which in turn prevents the uniform attachment of bulk-increasing/softening agent to the fibers. As a result, a sufficient bulk-increasing/softening effect cannot be achieved. Therefore, when using a bulk-increasing/softening agent with high hydrophobicity, it is important to produce a uniform emulsion by adding a surfactant offering excellent dispersibility. Some bulk-increasing/softening agents have a self-emulsification property. However, when a bulk-increasing/softening agent with high hydrophobicity is used, it is preferable that a surfactant be added to 10.0 weight-% or less of the bulk-increasing/softening agent.
- Specific examples of surfactants that can be used in conjunction with the bulk-increasing/softening agent in the present invention include the following compounds: anionic surfactants such as Pelex OT-P (Kao), Demol EP (Kao), Disper TL (Meisei Chemical Works), Gohseran L-3266 (Nippon Synthetic Chemical Industry) and Aron T-40 (Toa Gosei Kagaku); nonionic surfactants such as Emulgen A-60 (Kao) and Emulmin 50 (Sanyo Chemical); and cationic surfactants such as Cation DS (Sanyo Chemical), Quartamin 86W (Kao) and Quartamin D86P (Kao), but are not limited to these products.
- The addition of a bulk-increasing/softening agent inhibits the bonding of pulp fibers, which generally results in lower paper strength and the increased bulk/flexibility of paper. However, the effect of adding a bulk-increasing/softening agent hits a plateau at a certain amount. In other words, it is preferable that a bulk-increasing/softening agent be added to between 0.1 weight-% and 5.0 weight-%, inclusive, of the material pulp. It is even better to limit the amount of bulk-increasing/softening agent to between 0.2 weight-% and 2.0 weight-%, inclusive, since an excessive addition of such agent may affect the general paper properties, for example by triggering a substantial change in the friction coefficient of the paper, while an insufficient amount may not fully produce the desired bulk-increasing/softening effect, depending on the type of bulk-increasing/softening agent used.
- The bulky flexible paper provided through the present invention is produced from various types of pulp through the normal paper-making process. Material pulps include chemical pulp (bleached or unbleached kraft pulp from softwood, bleached or unbleached kraft pulp from hardwood, etc.), mechanical pulp (groundwood pulp, thermomechanical pulp, chemi-thermomechanical pulp, etc.), or recycled, ink-removed pulp, wherein these material pulps may be used alone or in combination at arbitrary ratios of blending. The pH level of the pulp slurry may be in the acid, neutral or alkali range. The bulky flexible paper provided through the present invention may contain filler.
- There are no limitations as to which fillers must or must not be used, and common fillers can be employed. Examples include inorganic fillers such as clay, fired clay, silicious marl, talc, kaolin, fired kaolin, delaminated kaolin, heavy calcium carbonate, light calcium carbonate, magnesium carbonate, barium carbonate, titanium dioxide, zinc oxide, silicon oxide, amorphous silica, aluminum hydroxide, calcium hydroxide, magnesium hydroxide and zinc hydroxide; and organic fillers such as urea-formalin resin, polystyrene resin, phenol resin and fine hollow grains, wherein such fillers can be used alone or in any combination.
- To obtain a paper containing a bulk-increasing/softening agent as defined in the present invention, add a bulk-increasing agent or its emulsion internally during the normal paper-making process (as opposed to applying the agent to the exterior of the paper after it has been made). Addition of bulk-increasing agent may take place at any step, as long as the uniform mixing of agent and pulp slurry can be achieved.
- When producing a bulky flexible paper as defined in the present invention, various nonionic or cationic internal auxiliaries traditionally used in the paper-making process, such as retention-aiding agent, freeness-improving agent, paper-strength enhancer and sizing agent, may be selected and used as appropriate.
- Internal auxiliaries normally used in the paper-making process include aluminum sulfate; aluminum chloride; sodium aluminate; basic aluminum compounds such as basic aluminum chloride and basic aluminum polyhydroxide; water-soluble aluminum compounds such as alumina sol that dissolve easily in water; polyvalent metals such as ferrous sulfate and ferric sulfate; and silica sol.
- The sizing agent can be chosen from various types, including alkyl ketene dimer compounds, alkenyl succinate anhydride compounds, styrene-acryl compounds, higher fatty acid compounds, petroleum resin-based sizing agents, and rosin-based sizing agents.
- Other auxiliaries normally used in the paper-making process include various starches, polyacrylamide, urea resin, melamine resin, epoxy resin, polyamide resin, polyamide, polyamine resin, polyamine, polyethylenimine, vegetable gum, polyvinyl alcohol, latex, polyethylene oxide and hydrophilic-crosslinked-polymer-particle dispersion, as well as their derivatives and transformed versions.
- Additionally, dye, fluorescent whitener, pH regulator, defoaming agent, pitch controller, slime controller and other agents normally used in the paper-making process may be added as appropriate for the given application. The method of producing paper provided through the present invention applies to all papers made using different schemes, including papers produced in the acid range of around pH 4 to 5 or those produced in the neutral range of around pH 6 (weak acidity) to 9 (weak alkalinity), wherein the slurry usually contains calcium carbonate or other alkali filler. The paper-making machine may be a Fourdrinier paper machine, twin-wire machine, Yankee machine, or a machine of another suitable type.
- The bulky flexible paper obtained in the manner explained above is ideal, for example, as a product for offset printing. It can also be used as a letterpress printing paper, electrophotographic paper, ink-jet printing paper, thermal paper, pressure-sensitive paper or other type of paper used for the recording of information. The paper obtained through the present invention is also suitable as the base paper of a coated stock.
- Examples of the present invention are explained below in detail. Note that the present invention is not limited to these examples. As a means of simulating the temperature of the paper's surface during the normal paper-making process, the prepared hand-made paper sheets were dried using two types of dryers. Specifically, a fan dryer was used when the condition assumed that the temperature of the paper's surface would be normal to lower during the preheating drying period, and an environmental tester was used when the condition assumed that the temperature of the paper's surface would be normal to higher. In the following examples the initial temperature of the paper's surface was used as the surface temperature during the preheating drying period.
- Low-temperature drying: Fan dryer (initial temperature of paper surface 40° C., heating temperature 105° C.)
- High-temperature drying: Environmental tester (initial temperature of paper surface 70° C., heating temperature 105° C.)
- The following items were measured and evaluated on the flexible papers with higher bulk produced in the examples and comparative examples. The results are shown in Table 1.
- Density: In conformance with JIS P 8118
- Tensile strength: In conformance with JIS P 8113
- Clark stiffness: In conformance with JIS P 8143
- HLB of bulk-increasing/softening agent: Calculated through the following formula:
- HLB=20×(Molecular weight of hydrophilic group)/(Total molecular weight)
- Of the examples given below, Examples 1 through 7 and Comparative Examples 1 through 6 relate to the present invention, while Examples 11 through 14 and Comparative Examples II through 13 relate to the present invention.
- A bulk-increasing/softening agent comprising 10.0 g of pentaerythritol distearate (reagent by Tokyo Kasei Kogyo; melting point 51° C., HLB 4.0) and a dispersant comprising 0.1 g of Pelex OT-P (Kao) were mixed thoroughly and added to 1,000 g of water. The mixture was agitated for 10 minutes at a speed of 10,000 rpm using an emulsifier to prepare an emulsion of bulk-increasing/softening agent. Bleached kraft pulp from hardwood (CSF freeness 350 ml) was used as the pulp content. The aforementioned emulsion of bulk-increasing/softening agent was then added to the pulp to 1.0 weight-% to prepare a paper material. Thereafter, a round manual paper-making tool was used to produce a paper with a grammage of 60 g/m 2, which was then pressed under an effective pressure of 4.18 kg/cm2. The pressed paper was dried for one hour in an environmental tester (initial temperature of paper surface at 70° C.) to obtain a bulky flexible paper.
- A bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of glycerin monolaurate (reagent by Tokyo Kasei Kogyo; melting point 63° C., HLB 6.6) and a dispersant comprising 0.2 g of Emulgen A-60 (Kao).
- A bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of sorbitan monopalmitate (reagent by Aldrich; span #40, melting point 46° C., HLB 8.1) and a dispersant comprising 0.25 g of Emulgen A60 (Kao).
- A bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of sorbitan monostearate (reagent by Aldrich; melting point 56° C., HLB 7.6) and a dispersant comprising 0.15 g of Cation DS (Sanyo Chemical).
- A bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of propylene glycol monostearate (prepared by the inventors; melting point 50° C., HLB 4.4) and a dispersant comprising 0.3 g of Cation DS (Sanyo Chemical).
- A bulky flexible paper was obtained in the same manner as described in Example 1, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 3.0 g of trioctyl methyl ammonium bromide (reagent by Aldrich; melting point 37° C., HLB 1.6) and a dispersant comprising 0.1 g of Emulgen A60 (Kao).
- A bulky flexible paper was obtained in the same manner as described in Example 6, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- A bulky flexible paper was obtained in the same manner as described in Example 1, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- A bulky flexible paper was obtained in the same manner as described in Example 2, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- A bulky flexible paper was obtained in the same manner as described in Example 3, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- A bulky flexible paper was obtained in the same manner as described in Example 4, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- A bulky flexible paper was obtained in the same manner as described in Example 5, except that a fan dryer (initial temperature of paper surface at 40° C.) was used.
- A hand-made paper sheet was obtained in the same manner as described in Example 1, except that no bulk-increasing/softening agent was added.
TABLE 1 Initial temper- ature Paper property data Melting of paper Breaking Clark point HLB surface Density length stiffness (° C.) (−) (° C.) (g/cm3) (km) (cm3/100) Example 1 51 4.0 70 0.51 2.79 43.0 Example 2 63 6.6 70 0.53 2.88 47.9 Example 3 46 8.1 70 0.52 2.80 46.8 Example 4 56 7.6 70 0.51 2.72 45.4 Example 5 50 4.4 70 0.50 2.59 44.9 Example 6 37 1.6 70 0.49 2.41 42.2 Example 7 37 1.6 40 0.53 2.82 48.0 Comparative 51 4.0 40 0.54 2.91 52.3 example 1 Comparative 63 6.6 40 0.56 3.01 56.2 example 2 Comparative 46 8.1 40 0.57 3.16 59.1 example 3 Comparative 56 7.6 40 0.56 3.03 57.2 example 4 Comparative 50 4.4 40 0.55 2.90 54.1 example 5 Comparative — — 70 0.59 3.50 66.8 example 6 - Table 1 shows that a more bulky flexible paper could be obtained when the wet paper was dried in a condition where the initial surface temperature of the paper was higher than the melting point of the bulk-increasing/softening agent (examples 1 through 7), compared with when it was dried in a condition where the initial temperature of paper surface was lower (comparative examples 1 through 6). In other words, it has been verified the initial temperature of paper surface must be sufficiently higher than the bulk-increasing/softening agent while the wet paper is being dried in order for the agent to effectively enhance the paper's bulk and flexibility.
- A bulk-increasing/softening agent comprising 10.0 g of pentaerythritol dioleate (reagent by Tokyo Kasei Kogyo; liquid, HLB 4.0) and a dispersant comprising 0.1 g of Pelex OT-P (Kao) were mixed thoroughly and added to 1,000 g of water. The mixture was agitated for 10 minutes at a speed of 10,000 rpm using an emulsifier to prepare an emulsion of bulk-increasing/softening agent. LBKP (CSF freeness 350 ml) was used as the pulp content. The aforementioned emulsion of bulk-increasing/softening agent was then added to the pulp to 1.0 weight-% to prepare a paper material. Thereafter, a round manual paper-making tool was used to produce a paper with a grammage of 60 g/m 2, which was then pressed under an effective pressure of 4.18 kg/cm2. The pressed paper was dried for one hour in a fan dryer (initial temperature of paper surface at 40° C.) and an environmental tester (initial temperature of paper surface at 70° C.) to obtain a bulky flexible paper.
- A bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of glycerin trioleate (reagent by Tokyo Kasei Kogyo; liquid, HLB 2.0) and a dispersant comprising 0.2 g of Emulgen A-60 (Kao).
- A bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 10.0 g of glycerin monolinolate (reagent by Tokyo Kasei Kogyo; liquid, HLB 5.1) and a dispersant comprising 0.15 g of Cation DS (Sanyo Chemical).
- A bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising 0.3 g of pentaerythritol diisostearate (prepared by the inventors; liquid, HLB 4.0).
- A bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising pentaerythritol distearate (reagent by Tokyo Kasei Kogyo; melting point 51° C., HLB 4.0).
- A bulky flexible paper was obtained in the same manner as described in Example 8, except that the emulsion of bulk-increasing/softening agent was prepared from a bulk-increasing/softening agent comprising sorbitan monolaurate (reagent by Tokyo Kasei Kogyo; span #20, liquid, HLB 9.4).
- A hand-made paper sheet was obtained in the same manner as described in Example 8, except that no bulk-increasing/softening agent was added.
TABLE 2 Low-temperature dryer High-temperature dryer Clark Clark Break- stiff- Break- stiff- ing ness ing ness HLB Density length (cm3/ Density length (cm3/ (−) (g/cm3) (km) 100) (g/cm3) (km) 100) Example 8 4.0 0.49 2.62 36.3 0.51 2.65 36.1 Example 9 2.0 0.49 2.55 38.0 0.50 2.49 35.1 Example 10 5.1 0.50 2.59 37.8 0.50 2.56 35.2 Example 11 4.0 0.51 2.69 38.7 0.51 2.55 37.6 Comparative 4.0 0.54 2.91 44.3 0.51 2.79 36.2 example 7 Comparative 9.4 0.56 3.01 47.2 0.55 2.98 42.3 example 8 Comparative — 0.58 3.43 48.3 0.59 3.52 49.0 example 9 - From Table 2, the result of comparison between Examples 8 through 11 and Comparative Example 7 shows that when a higher unsaturated fatty-acid ester or higher branched-chain fatty-acid ester, which is liquid at normal temperature, is used as a bulk-increasing/softening agent, then a paper with low Clark stiffness can be obtained even when the initial temperature of paper surface is lower than when a higher saturated fatty-acid ester with a higher melting point is used. In other words, while the examples achieved a sufficient bulk-increasing/softening effect regardless of the drying temperature (initial temperature of paper surface), in the comparative examples (using a bulk-increasing/softening agent with a melting point of 40° C. or above) the initial temperature of paper surface must be sufficiently high to achieve any meaningful bulk-increasing/softening effect. From the comparison of Examples 7 through 11 and Comparative Example 8, it has been verified that a sufficient bulk-increasing/softening effect can be achieved if the HLB of the bulk-increasing/softening agent is 6 or below.
- Industrial Field of Application
- Subject to the present invention, as shown in Table 1, a more bulky flexible paper was obtained when the wet paper was dried in a condition where the paper's initial surface temperature was high, compared with when it was dried in a condition where the paper's initial surface temperature was low (comparative examples 1 through 6). In other words, it has been verified the initial temperature of the paper's surface must be sufficiently higher than the bulk-increasing/softening agent while the wet paper is being dried in order for the agent to effectively enhance the paper's bulk and flexibility.
- When a higher unsaturated fatty-acid ester or higher branched-chain fatty-acid ester, which is liquid at normal temperature, was used as a bulk-increasing/softening agent, a bulk paper with lower Clark stiffness was obtained even when the paper's initial surface temperature was lower than when a higher saturated fatty-acid ester with a higher melting point was used. In other words, a sufficient bulk-increasing/softening effect was achieved in the examples regardless of the drying temperature (initial temperature of paper surface), which leads to a conclusion that achieving any meaningful bulk-increasing/softening effect requires a sufficiently high initial temperature of the paper's surface.
- As explained above, the present invention allows for the production of a paper offering sufficient bulk and flexibility even when the paper's surface temperature drops in the initial drying process, by using a bulk-increasing/softening agent with a HLB of 6 or below, wherein said agent is either a liquid or a solid with a melting point of 40° C. or below.
Claims (11)
1. A method for producing bulky flexible paper using a bulk-increasing /softening agent, wherein the surface temperature of said paper during a preheating drying period (a period during a drying process before the temperature of a wet paper becomes constant) is adjusted to or above the melting point of said bulk-increasing softening agent.
2. The method as recited in claim 1 , wherein said bulk-increasing/softening agent is an ester compound of polyhydric alcohol and higher fatty acid and/or a long-chain alkyl ammonium salt.
3. (Amended) The method as recited in claim 1 , wherein said bulk-increasing/softening agent has a HLB of 6 or below and is either a liquid or a solid with a melting point of 40° C. or below.
4. (Amended) The method as recited in claim 1 , wherein the surface temperature of said paper is adjusted to at least 10° C. higher than the melting point of said bulk-increasing/softening agent.
5. (Amended) A bulky flexible paper comprising at least one selected from the group consisting of an ester compound of polyhydric alcohol and higher fatty acid, and a long-chain alkyl ammonium salt as a bulk-increasing/softening agent.
7. (Amended) The bulky flexible paper as recited in claim 5 , wherein a surfactant is added to 10.0 weight-% of said bulk-increasing/softening agent or less.
8. (New) The method as recited in claim 2 , wherein said bulk-increasing/softening agent has a HLB of 6 or below and is either a liquid or a solid with a melting point of 40° C. or below.
9. (New) The method as recited in claim 2 , wherein the surface temperature of said paper is adjusted to at least 10° C. higher than the melting point of said bulk-increasing/softening agent.
10. (New) The method as recited in claim 3 , wherein the surface temperature of said paper is adjusted to at least 10° C. higher than the melting point of said bulk-increasing/softening agent.
11. (New) The method as recited in claim 8 , wherein the surface temperature of said paper is adjusted to at least 10° C. higher than the melting point of said bulk-increasing/softening agent.
12. (New) The bulky flexible paper as recited in claim 6, wherein a surfactant is added to 10.0 weight-% of said bulk-increasing/softening agent or less.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000345848A JP2002155495A (en) | 2000-11-13 | 2000-11-13 | Method for producing bulky and soft paper |
| JP2000345848 | 2000-11-13 | ||
| JP2000345847 | 2000-11-13 | ||
| JP2000345847A JP2002155494A (en) | 2000-11-13 | 2000-11-13 | Bulky and soft paper |
| PCT/JP2001/009908 WO2002038862A1 (en) | 2000-11-13 | 2001-11-13 | Bulky flexible paper and process for producing the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20040040681A1 true US20040040681A1 (en) | 2004-03-04 |
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ID=26603894
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/416,552 Abandoned US20040040681A1 (en) | 2000-11-13 | 2001-11-13 | Bulky flexible paper and process for producing the same |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20040040681A1 (en) |
| AU (1) | AU2002224036A1 (en) |
| CA (1) | CA2428505A1 (en) |
| DE (1) | DE10196875B4 (en) |
| FI (1) | FI121819B (en) |
| WO (1) | WO2002038862A1 (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040121158A1 (en) * | 2002-12-20 | 2004-06-24 | Kimberly-Clark Worldwide, Inc. | Wiping products having a low coefficient of friction in the wet state and process for producing same |
| US20050103458A1 (en) * | 2003-11-14 | 2005-05-19 | Hiroshi Ono | High-bulk, wood containing printing paper |
| US6994770B2 (en) | 2002-12-20 | 2006-02-07 | Kimberly-Clark Worldwide, Inc. | Strength additives for tissue products |
| US20060075630A1 (en) * | 2004-10-07 | 2006-04-13 | Seth Valentine | Manufacture of unitized electrode assembly for PEM fuel cells |
| US20070054100A1 (en) * | 2005-09-07 | 2007-03-08 | Oji Paper Co., Ltd. | Coated paper |
| US20110048661A1 (en) * | 2009-09-01 | 2011-03-03 | Armstrong World Industries, Inc. | Cellulosic product forming process and wet formed cellulosic product |
| US20130137534A1 (en) * | 2011-11-29 | 2013-05-30 | Dunlop Sports Co. Ltd. | Resin composition for golf ball and golf ball |
| US20210047529A1 (en) * | 2018-01-29 | 2021-02-18 | Mitsubishi Pencil Company, Limited | Aqueous ink composition for writing instrument |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006013903A1 (en) * | 2006-03-25 | 2007-09-27 | Metsä Tissue Oyj | Production of wadding products useful as a towel from tissue- and/or tissue like material by a material web with a top and bottom side, comprises applying oil and an emulsifier on the top and/or bottom of the material web |
| CN103821030B (en) * | 2014-03-12 | 2016-01-20 | 彭运福 | Pre-preserved material of a kind of paper grade (stock) and preparation method thereof and a kind of papery industrial packaging production technology |
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- 2001-11-13 DE DE10196875T patent/DE10196875B4/en not_active Expired - Fee Related
- 2001-11-13 CA CA002428505A patent/CA2428505A1/en not_active Abandoned
- 2001-11-13 US US10/416,552 patent/US20040040681A1/en not_active Abandoned
- 2001-11-13 WO PCT/JP2001/009908 patent/WO2002038862A1/en not_active Ceased
- 2001-11-13 AU AU2002224036A patent/AU2002224036A1/en not_active Abandoned
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| US20110048661A1 (en) * | 2009-09-01 | 2011-03-03 | Armstrong World Industries, Inc. | Cellulosic product forming process and wet formed cellulosic product |
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Also Published As
| Publication number | Publication date |
|---|---|
| FI20030704A7 (en) | 2003-07-14 |
| WO2002038862A1 (en) | 2002-05-16 |
| AU2002224036A1 (en) | 2002-05-21 |
| FI121819B (en) | 2011-04-29 |
| FI20030704A0 (en) | 2003-05-12 |
| DE10196875B4 (en) | 2007-05-24 |
| CA2428505A1 (en) | 2002-05-16 |
| DE10196875T1 (en) | 2003-12-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: NIPPON PAPER INDUSTRIES CO., LTD., JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:OHASHI, REIJI;RYU, YUKIKO;NAKAMURA, MITSUTOSHI;AND OTHERS;REEL/FRAME:014451/0952;SIGNING DATES FROM 20030611 TO 20030623 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |