Probing the surface polarity of native celluloses using genuine solvatochromic dyes

被引:18
作者
Fischer, K
Spange, S
Fischer, S
Bellmann, C
Adams, J
机构
[1] Univ Technol Chemnitz, Fac Sci, Inst Chem, D-09111 Chemnitz, Germany
[2] Tech Univ Freiberg, Dept Inorgan Chem, D-08596 Freiberg, Germany
[3] IPF Dresden, D-01069 Dresden, Germany
[4] Tech Univ Clausthal, Inst Phys Chem, D-38678 Clausthal Zellerfeld, Germany
关键词
cellulose; Kamlet-Taft parameters; solvatochromism; surface polarity;
D O I
10.1023/A:1015896629947
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
The surface polarity of native celluloses has been investigated by the following solvatochromic dyes: dicyano-bis (1,10)-phenanthroline iron (II) Fe(phen)(2) (CN)(2) (1), bis(4-N,N-dimethylamino)-benzophenone (2), and cou-marine 153 (3). Linear Solvation Energy (LSE) relationships and the UV/Vis data have been used to characterize the surface polarity of different native cellulose batches in terms of the empirical Kamlet-Taft polarity parameters alpha (hydrogen bond acidity), beta (hydrogen bond basicity), and pi * (dipolarity/polarizability). alpha, beta, pi * and calculated Reichardt's E T (30) values are reported for various native and regenerated cellulose samples with different degrees of crystallinity. The degree of crystallinity of the cellulose samples has been determined by X-ray. The microcrystalline environment of cellulose can be exactly parameterized in terms of the alpha, beta and pi * values. It shows a fairly strong acidity alpha and a low dipolarity/polarizability. For the amorphous sections smaller alpha and larger pi * values are observed. The correspondence of the empirical polarity parameters determined has been discussed in relation to results from pyrene fluorescence and zetapotential measurements.
引用
收藏
页码:31 / 40
页数:10
相关论文
共 41 条
[1]   Linear solvation energy relationships to explain interactions responsible for solute adsorption onto a polar polymeric sorbent [J].
Brune, BJ ;
Payne, GF ;
Chaubal, MV .
LANGMUIR, 1997, 13 (21) :5766-5769
[2]   THE PY SCALE OF SOLVENT POLARITIES [J].
DONG, DC ;
WINNIK, MA .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1984, 62 (11) :2560-2565
[3]  
Fischer K, 2000, MACROMOL CHEM PHYS, V201, P1922, DOI 10.1002/1521-3935(20001001)201:15<1922::AID-MACP1922>3.0.CO
[4]  
2-Y
[5]  
FISCHER K, 2002, UNPUB J POLYM SCI B
[6]  
FISCHER S, 2002, IN PRESS PAPIER
[7]   SOLVENT EFFECTS ON REACTIVITIES OF ORGANOMETALLIC COMPOUNDS [J].
GUTMANN, V .
COORDINATION CHEMISTRY REVIEWS, 1976, 18 (02) :225-255
[8]   RHO-SIGMA-PI ANALYSIS . METHOD FOR CORRELATION OF BIOLOGICAL ACTIVITY + CHEMICAL STRUCTURE [J].
HANSCH, C ;
FUJITA, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1964, 86 (08) :1616-&
[9]   SOLVATOCHROMIC STUDIES OF SOLVATED CHROMATOGRAPHIC STATIONARY PHASES [J].
HELBURN, RS ;
RUTAN, SC ;
POMPANO, J ;
MITCHEM, D ;
PATTERSON, WT .
ANALYTICAL CHEMISTRY, 1994, 66 (05) :610-618
[10]  
ILHARCO LM, 1997, LANGMUIR, V13, P4162