PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

The Preparation of Soluble Cellouronic Acid Sodium Salt by 4-Acetamide-TEMPO Mediated Oxidation of Ultrasound-Pretreated Parenchyma Cellulose from Bagasse Pith

Autorzy
Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The parenchyma cellulose isolated from bagasse pith was used as an alternative resource for preparation of water-soluble cellouronic acid sodium salt (CAS). The influence of ultrasound treatment on the cellulose was investigated for obtaining CAS by regioselective oxidization using 4-acetamide-TEMPO and NaClO with NaClO2 as a primary oxidant in an aqueous buffer at pH 6.0. The yield, carboxylate content and polymerization degree (DP) of CAS were measured as a function of ultrasonic power, agitating time and cellulose consistency by an orthogonal test. The ultrasound-treated conditions were further improved by discussion of ultrasonic power, the most important factor influencing the yield and DP. An optimized CAS yield of 72.9% with DP value (DPv) of 212 was found when the ultrasonic strength is 550 W, agitating time is 3 h and cellulose consistency is 2.0%. The oxidation reactivity of cellulose was improved by ultrasonic irradiation, whereas no significant changes in crystallinity of cellulose were measured after ultrasonic treatment. Moreover, the ultrasound treatment has a greater effect on yielding CAS from parenchyma cellulose than from bagasse fibrous’ one. The CAS was further characterized by Fourier transform infrared spectroscopy (FT-IR) and Scanning electron microscopy (SEM).
Rocznik
Strony
267--275
Opis fizyczny
Bibliogr. 22 poz., fot., tab., wykr.
Twórcy
autor
  • Faculty of Environmental Science and Engineering, Kunming University of Science and Technology 650500, Kunming, China
  • Faculty of Chemical Engineering, Kunming University of Science and Technology 650500, Kunming, China
autor
  • Faculty of Chemical Engineering, Kunming University of Science and Technology 650500, Kunming, China
autor
  • Faculty of Chemical Engineering, Kunming University of Science and Technology 650500, Kunming, China
autor
  • Faculty of Chemical Engineering, Kunming University of Science and Technology 650500, Kunming, China
Bibliografia
  • 1. Biliuta G., FRAS L., STRNAD S., HARABAGIU V., CoSERI S. (2010). Oxidation of cellulose fibers mediated by nonpersistent nitroxyl radicals, Journal of Polymer Science: Part A: Polymer Chemistry, 48, 21, 4790- 4799.
  • 2. BILIUTA G., FRAS L., HARABAGIU V., COSERI S. .(2011) Mild oxidation of cellulose fibers using dioxygen as ultimate oxidizing agent, Digest Journal of Nanomaterials and Biostructures, 6, 1, 291-297.
  • 3. BILIUTA G., FRAS L., DROBOTA M., PERSIN Z., KREZE T., KLEINSCHEK K.S., RIBITSCH V., HARA- BAGUI V., COSERI S. (2013), Comparison study of TEMPO and phthalimide-N-oxy (PINO) radicals on oxidation efficiency toward cellulose, Carbohydrate Polymers, 91, 2, 502-507.
  • 4. CHEN W.S., Yu H.P., Liu Y.X., CHEN P., ZHANG M.X., HAÏ Y.F. (2011a), Individualization of cellulose nanofibers from, wood using high-intensity ul- trasonication combined with, chemical pretreatments, Carbohydrate Polymers, 83, 4, 1804-1811.
  • 5. Chen W.S., Yu H.P., Liu Y.X. (2011b), Preparation, of millimeter- long cellulose I nanofibers with, diameters of 30-80 nm from, bamboo fibers, Carbohydrate Polymers, 86, 2, 453-461.
  • 6. COSERI S., NISTOR G., FRAS S., STRNAD S., HARABAGIU V., SIMIONESCU B.C. (2009), Mild and selective oxidation of cellulose fibers in the presence of N-Hydroxyph.th.ali.m.i.de, Biomacromolecules, 10, 8, 2294-2299.
  • 7. COSERI S., BILIUTA G. (2012), Bromide-free oxidizing system, for carboxylic moiety formation in cellulose chain, Carbohydrate Polymers, 90, 4, 1415-1419.
  • 8. COSERI S., BILIUTA G., SIMIONESCU B.C., KLEIN- SCHEK K.S., RIBITSCH V., HARABAGIU V. (2013), Oxidized cellulose-Survey of the m.ost recent achievements, Carbohydrate Polymers, 93, 1, 207-215.
  • 9. HlROTA M., TAMURA N., SAITO T., ISOGAI A. (2009), Oxidation of regenerated cellulose with. NaClOn catalyzed by TEMPO and NaCIO under acid-neutral conditions, Carbohydrate Polymers, 78, 2, 330-335.
  • 10. IWAMOTO S., KAI W.H., ISOGAI T., SAITO T., ISOGAI A., I WAT A T. (2010), Comparison study of TEMPO-an.alogous compounds on. oxidation efficiency of wood cellulose for preparation of cellulose nanofibrils, Polymer Degradation and Stability, 95, 8, 1394- 1398.
  • 11. JAMBRAK A.R., LELAS V., HERCEG Z., BADAN- JAK M., BATUR V., MUZA M. (2009), Advantages and disadvantages of high, power ultrasound application in the dairy industry, Mljekarstvo, 59, 4, 267-281.
  • 12. KUMAR V., YANG T.R. (2002), HNO3/H3PO4- NANOnm.edi.ated oxidation of cellulose - preparation and characterization of bioabsorbable oxidized celluloses in high, yields and with, different levels of oxidation, Carbohydrate Polymers, 48, 4, 403-412.
  • 13. Liu C.F., SUN R.C., QIN M.H., ZHANG A.P., REN J.K., YE J., LUO W., Cao Z.N. (2008), Suc- cinoylation of sugarcane bagasse under ultrasound ir- raditation, Bioresource Technology, 99, 5, 1465-1473.
  • 14. REINA T., TSUGUYUKI S., AKIRA I. (2012), Cellulose nanofibrils prepared from, softwood cellulose by TEMPO/NaCIO/NaClOnsystem.s in water at pH lh8 or 6.8, International Journal of Biological Macromolecules, 51, 3, 228-234.
  • 15. REN Q.L. (2003), Textbook of Optimization Design and Analysis of Experiments [in Chinese: Higher Education Press, Beijing China.
  • 16. SHlBATA I., ISOGAI A. (2003), Depolymerization of cellouronic acid during TEMPO-mediated oxidation, Cellulose, 10, 2, 151-158.
  • 17. SHINODA R., SAITO T., OKITA Y., ISOGAI A. (2012), Relationship between, length and degree of polymerization of TEMPO-oxidized cellulose nanofibrils, Biomacromolecules, 13, 3, 842-849.
  • 18. SUSLICK K.S. (1990), Sonochemistry, Science, 247, 4949, 1439-1441.
  • 19. TANG A., ZHANG H., CHEN G., XIE G.H., LIANG W.Z. (2005), Influence of ultrasound treatment on. accessibility and regioselective oxidation reactivity of cellulose, Ultrasonics Sonochemistry, 12, 6, 467-472.
  • 20. Yu H., Liu R.G., SHEN D.W., Wu Z.H., HUANG Y. (2008), Arrangement of cellulose microfibrils in. the wheat straw cell wall, Carbohydrate Polymers, 72, 1, 122-127.
  • 21. VILKHU K., MAWSON R., SIMONS L., BATES D. (2008), Applications an.dopportun.iti.es for ultrasound assisted extraction in. the food industry - a review, Innovative Food Science and Emerging Technology, 9,2, 161-169.
  • 22. ZHANG K., FISCHER S., GEISSLER A., BRENDLER E. , Analysis of carboxylate groups in oxidized never-dried cellulose II catalyzed by TEMPO and Jr acetam.i.de-TEMPO, Carbohydrate Polymers, 87, 1, 894-900.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-28c1870f-fb10-4c40-9a58-ebb945622769
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.