Native and structurally modified gum arabic: Exploring the effect of the gum's microstructure in obtaining electroactive nanoparticles

被引:12
作者
Cornelsen, Patricia A. [1 ]
Quintanilha, Ronaldo C. [1 ]
Vidotti, Marcio [1 ]
Gorin, Philip A. J. [2 ]
Simas-Tosin, Fernanda F. [1 ,2 ]
Riegel-Vidotti, Izabel C. [1 ]
机构
[1] Univ Fed Parana UFPR, Dept Quim, Grp Pesquisa Macromol & Interfaces, BR-81531980 Curitiba, PR, Brazil
[2] Univ Fed Parana UFPR, Dept Bioquim & Biol Mol, BR-81531980 Curitiba, PR, Brazil
基金
巴西圣保罗研究基金会;
关键词
Gum arabic; Structural modification; Polyaniline nanoparticles; Electroactive properties; FREE REDUCING OLIGOSACCHARIDES; POLYANILINE; POLYMERIZATION; NANOCOMPOSITES; ASSIGNMENTS; STABILITY; POLYMERS; EXUDATE;
D O I
10.1016/j.carbpol.2014.11.020
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Electroactive nanoparticles combining gum arabic (GA) and polyaniline (PANI) were prepared by chemical synthesis. The gum consists of highly branched anionic polysaccharides with some protein content. GA was structurally modified by Smith controlled degradation, in order to reduce its degree of branching (GAD), aiming the elucidation of the relationship between the structure and the properties of complex polysaccharides. The modification was studied by SEC, GC-MS, C-13 NMR and colorimetric methods. GAD has lower molecular mass, lower degree of branching and lower uronic acid content. Besides it is enriched in galactose and protein when compared with GA. The obtained composites (GA-PANI and GAD-PANI) were thoroughly characterized. Although the use of both polysaccharides (GA and GAD) produced highly stable electroactive nanoparticles, the best combination of properties was achieved for GA-PANI. The sample GAD was not able to prevent the occurrence of crosslinking between PANI chains, possibly due to its lower microstructural complexity which diminishes the occurrence of hydrogen bonds between the polymers. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:35 / 43
页数:9
相关论文
共 44 条
[1]   NMR-SPECTROSCOPY IN THE STRUCTURAL ELUCIDATION OF OLIGOSACCHARIDES AND GLYCOSIDES [J].
AGRAWAL, PK .
PHYTOCHEMISTRY, 1992, 31 (10) :3307-3330
[2]   Acacia stabilized polyaniline dispersions: preparation, properties and blending with poly(vinyl alcohol) [J].
Amarnath, C. A. ;
Palaniappan, S. ;
Rannou, P. ;
Pron, A. .
THIN SOLID FILMS, 2008, 516 (10) :2928-2933
[3]   A review study of (bio)sensor systems based on conducting polymers [J].
Ates, Murat .
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2013, 33 (04) :1853-1859
[4]   The chemical and colloidal stability of polyaniline dispersions [J].
Blinova, NV ;
Sapurina, I ;
Klimovic, J ;
Stejskal, J .
POLYMER DEGRADATION AND STABILITY, 2005, 88 (03) :428-434
[5]  
Cheng DM, 2005, J NANOSCI NANOTECHNO, V5, P466, DOI [10.1166/jnn.2005.058, 10.1166/jnm.2005.058]
[6]   An arabinogalactan isolated from the medicinal plant Maytenus ilicifolia [J].
Cipriani, TR ;
Mellinger, CG ;
Gorin, PAJ ;
Iacomini, M .
JOURNAL OF NATURAL PRODUCTS, 2004, 67 (04) :703-706
[7]   A SIMPLE AND RAPID METHOD FOR THE PERMETHYLATION OF CARBOHYDRATES [J].
CIUCANU, I ;
KEREK, F .
CARBOHYDRATE RESEARCH, 1984, 131 (02) :209-217
[8]  
Cochet M, 2000, J RAMAN SPECTROSC, V31, P1029, DOI 10.1002/1097-4555(200011)31:11<1029::AID-JRS640>3.0.CO
[9]  
2-A
[10]  
Cochet M, 2000, J RAMAN SPECTROSC, V31, P1041, DOI 10.1002/1097-4555(200012)31:12<1041::AID-JRS641>3.0.CO