| 1 |
Van Der Klashorst G H.,The chemical properties of the lignin present in three industrial spent pulping liquors and the implication of these properties on the possible utilization of these lignin's, SIR Special report HOUT, 26 (1985)
|
| 2 |
Glasser W. G., Saraf V. P. & Newman W. H., Hydroxyl propylated lignin-isocyanate combination as bonding agents for wood and cellulose fibers, J. Adhesion, 14, 233-255 (1982)
DOI
ScienceOn
|
| 3 |
Yasuda S. & Asano K.,Preparation of strongly acidic cation-exchange resins from gymnosperm acid hydrolysis lignin, J. Wood Sci, 46: 477-479 (2000)
DOI
ScienceOn
|
| 4 |
Yasuda S., Ito K., Nhamaguchi E. &Matsushita Y, Ready chemical conversion ofacid hydrolysis lignin into water-soluble lignosulfonate I. Successive treatment of acid hydrolysis lignin by phenolation, hydroxymethylation and Sulfonation, Mokuzai Gakkaishi, 43 (I): 68-74 (1997)
|
| 5 |
Yasuda S., Tachi M. & Takagi Y., Penalization of red pine sulfuric acid lignin and Guaiacyl sulfuric acid lignin model in the Presence of sulfuric catalyst, Mokuzai Gakkaishi, 35 (6): 513-520 (1989)
|
| 6 |
Seiichi Y., Motoyoshi T. & Yasuo T.,Penalizations of Red pine sulfuric acid Lignin and Guaiacyl sulfuric acid lignin model in the presence ofsulfuric acid catalyst, Mokuzai Gakkaishi, 35 (6): 513-520 (1989)
|
| 7 |
Nada A. M., EL-Saied H., Ibrahem A. A. & YousefM. A., Waste liquors from cellulosic industries, IV. Lignin as a component in phenol-formaldehyde resoles resin, J. of Appl. Polym. Sci., 33: 2915-2924 (1987)
DOI
ScienceOn
|
| 8 |
Johns W. E.,Isocyanates as wood binders- a review, J. Adhesion, 15: 59-67 (1982)
DOI
|
| 9 |
Yoshino Y., Ion exchange resin, Maruzen, Tokyo, 171-1172(1956)
|
| 10 |
EL-Saied H., Nada A. M., Ibrahem A. A. & Yousef M. A., Waste liquors from cellulosic industries, Ⅲ. Lignin from soda-spent Liquors as a component in phenol- formaldehyde resin, Die Angewadte Makromolekulare Chemie, 122: 169-181 (1984)
DOI
|
| 11 |
Mansour O.Y., Nagaty A. & Nagieb Z. A., Structure of alkali lignin's fractionated from Ricinus communes and bagasse. 3. IR spectra, J Macromol Sci-Chern, A21 (6&7): 801-823 (1984)
|
| 12 |
Sudo K. & Shimizu K., A New Carbon Fiber from lignin, J. of Appl. Polym. Sci. 44: 127-134 (1992)
DOI
|
| 13 |
Jun'lchi H., Atsuo K., Katsuhiko M. & PAUsL W. A., Preparation of activated ca.bon from lignin by chemical activation. Carbon, 38: 1873-1878 (2000)
DOI
ScienceOn
|
| 14 |
Mark H. F., Gaylord N. G., & Bikales N. M., In Encyclopedia of polymer science and technology. Interscience publishers / John Wiley and Sons Inc, New York USA, 7: 704-705 (1967)
|
| 15 |
Maldas D. & Kokta B. V., Studies on the preparation and properties of particleboard made from bagasse and PVC:Ⅱ.Influence of the addition of coupling agents, Bioresource Technology, 35: 251-261 (1991)
DOI
ScienceOn
|
| 16 |
Zoumpoulakis L & Simitzis, Ion exchange resins from phenol/formaldehyde resin- modified lignin, Polym Int, 50: 277-283 (2001)
DOI
ScienceOn
|
| 17 |
Brauns F. E, The Chemistry of Lignin, Academic Press, New York, 479 (1952)
|
| 18 |
Mathiasson A. & Kubat D. G., Lignin as binder in particle boards using high frequency heating, Holz als Roh-und Werkstoff, 52: 9-18 (1994)
DOI
ScienceOn
|
| 19 |
Yasuda S., Terashima N. & Ito K., Chemical structures ofsulfuric acid lignin. IV. Reaction ofarylglycerol-aryl ether with seventy-two percent sulfuric acid, Mokuzai Gakkaishi, 27: 879-884 (1981)
|
webmaster
