Microwave-Assisted Solvent-Free Acetylation of Cellulose with Acetic Anhydride in the Presence of Iodine as a Catalyst
暂无分享,去创建一个
Tong-Qi Yuan | Jing Bian | Jing Li | Feng Xu | Run-Cang Sun | Feng Peng | Liping Zhang | R. Sun | T. Yuan | Feng Xu | F. Peng | J. Bian | Li-Ping Zhang | Jing Li
[1] H. Behmadi,et al. Synthesis of Phenanthrimidazole from 9,10-Phenanthraquinone and Aldehydes by Molecular Iodine as Catalyst. , 2009 .
[2] Weilin Xu,et al. Microwave-assisted solubilization and solution properties of hyperbranched polysaccharide. , 2008, Carbohydrate research.
[3] Aiqin Hou,et al. Effect of microwave irradiation on the physical properties and morphological structures of cotton cellulose , 2008 .
[4] J. L. Willett,et al. RAPID AND ENVIRONMENTALLY FRIENDLY PREPARATION OF STARCH ESTERS , 2008 .
[5] J. Yadav,et al. Iodine as a mild, efficient, and cost-effective catalyst for the synthesis of thiiranes from oxiranes , 2008 .
[6] R. Sun,et al. Acetylation of wheat straw hemicelluloses in ionic liquid using iodine as a catalyst , 2007 .
[7] A. Idris,et al. Performance of cellulose acetate - polyethersulphone blend membrane prepared using microwave heating for palm oil mill effluent treatment. , 2007, Water science and technology : a journal of the International Association on Water Pollution Research.
[8] M. A. Moharram,et al. X‐ray diffraction methods in the study of the effect of microwave heating on the transformation of cellulose I into cellulose II during mercerization , 2007 .
[9] J. L. Willett,et al. Iodine catalyzed esterification of cellulose using reduced levels of solvent , 2007 .
[10] J. E. Lier,et al. Molecular Iodine in Isopropenyl Acetate (IPA): A Highly Efficient Catalyst for the Acetylation of Alcohols, Amines and Phenols under Solvent-Free Conditions. , 2006 .
[11] R. Sun,et al. Characteristics of cellulose isolated by a totally chlorine-free method from Caragana korshinskii , 2006 .
[12] J. L. Willett,et al. Rapid preparation of starch maleate half-esters , 2006 .
[13] Yuyu Sun,et al. Acetylation of cellulose using recyclable polymeric catalysts , 2006 .
[14] D. Cerqueira,et al. A New Value for the Heat of Fusion of a Perfect Crystal of Cellulose Acetate , 2006 .
[15] J. L. Willett,et al. Solvent-free process to esterify polysaccharides. , 2005, Biomacromolecules.
[16] S. Jovanović,et al. A Comparison of Some Methods for the Determination of the Degree of Substitution of Carboxymethyl Starch , 2005 .
[17] P. Phukan. Iodine as an extremely powerful catalyst for the acetylation of alcohols under solvent-free conditions , 2004 .
[18] J. Yadav,et al. Molecular Iodine‐Catalyzed Highly Stereoselective Synthesis of Sugar Acetylenes. , 2003 .
[19] R. Granet,et al. Rapid homogeneous esterification of cellulose induced by microwave irradiation , 2002 .
[20] S. Mccarthy,et al. Microwave-Assisted Solvent-Free or Aqueous-Based Synthesis of Biodegradable Polymers , 2002 .
[21] R. Malaisamy,et al. CELLULOSE ACETATE AND EPOXY RESIN BLEND ULTRAFILTRATION MEMBRANES: REPARATION, CHARACTERIZATION, AND APPLICATION , 2002 .
[22] Paul A. Rundquist,et al. Advances in cellulose ester performance and application , 2001 .
[23] Vanete Thomaz Soccol,et al. Biotechnological potential of agro-industrial residues. I: sugarcane bagasse , 2000 .
[24] Jianzhang Li,et al. Chemical modification of wood by anhydrides without solvents or catalysts , 2000, Journal of Wood Science.
[25] H. Kono,et al. CPMAS13C NMR and X-ray studies of cellooligosaccharide acetates as a model for cellulose triacetate , 1999 .
[26] K. Pandey. A study of chemical structure of soft and hardwood and wood polymers by FTIR spectroscopy , 1999 .
[27] R. Dart,et al. Preparation, characterization and biodegradation studies on cellulose acetates with varying degrees of substitution , 1997 .
[28] R. Atalla,et al. Solid-State 13C NMR and Raman Studies of Cellulose Triacetate: Oligomers, Polymorphism, and Inferences about Chain Polarity , 1996 .
[29] J. Sassi,et al. Ultrastructural aspects of the acetylation of cellulose , 1995 .
[30] W. MacKnight. Macromolecules. , 1976, Science.
[31] E. Frollini,et al. Sisal cellulose acetates obtained from heterogeneous reactions , 2008 .
[32] Huai N. Cheng,et al. Novel modified soybean oil containing hydrazino-ester: synthesis and characterization , 2007 .
[33] J. Yadav,et al. Molecular Iodine-Catalyzed Highly Stereoselective Synthesis of Sugar Acetylenes , 2003 .
[34] C. Hill,et al. Kinetic and Mechanistic Aspects of the Acetylation of Wood with Acetic Anhydride , 1998 .
[35] D. Satchell. An outline of acylation , 1963 .