Spectroscopic analysis of a dye-mineral composite - a Raman and FT-IR study

被引:20
作者
Manciu, F. S. [1 ]
Ramirez, A. [2 ,3 ]
Durrer, W. [1 ]
Govani, J. [1 ]
Chianelli, R. R. [2 ,3 ]
机构
[1] Univ Texas El Paso, Dept Phys, El Paso, TX 79968 USA
[2] Univ Texas El Paso, Dept Chem, El Paso, TX 79968 USA
[3] Univ Texas El Paso, Mat Res & Technol Inst, El Paso, TX 79968 USA
基金
美国国家科学基金会;
关键词
Raman spectroscopy; infrared absorption; surface properties;
D O I
10.1002/jrs.1979
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
In this investigation, we address the question of how organic thioindigo binds to inorganic palygorskite to form a pigment similar to Maya Blue. We also address how such binding, if it occurs, might be affected by varying the proportion of dye relative to that of the mineral, and by varying the length of heating time used in preparation of the pigment. In addition to samples of palygorskite and thioindigo both alone, four synthetic pigment samples were prepared; two samples of 8 wt.% dye, one heated at 170 degrees C for 3 h and one at 170 degrees C for 9 h, and two samples of 16 wt.% dye, one heated at 170 degrees C for 3 h and one at 170 degrees C for 9 h. All samples were examined using Fourier transform-infrared (FT-IR) and FT-Raman spectroscopy. For the pigment samples, FT-IR peaks at 1627 cm(-1) are attributed to a downshifted C=O stretching mode of thioindigo due to dye-clay interaction. This interpretation is corroborated by FT-Raman C=O peaks with 14 cm(-1) shifts to lower wavenumber for the pigment relative to thioindigo alone. Additional Raman scattering between 550 cm(-1) and 650 cm(-1) also suggests dye-clay interaction through metal-oxygen bonding. We are thus led to the possibility of mostly hydrogen bonding between silanol and carbonyl at lower dye concentration, with a predominance of metal-oxygen bonding at higher dye concentration. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:1257 / 1261
页数:5
相关论文
共 17 条
[1]  
CHIANELLI RR, 2006, Patent No. 7052541
[2]   Crystal structure refinements of palygorskite and Maya Blue from molecular modelling and powder synchrotron diffraction [J].
Chiari, G ;
Giustetto, R ;
Ricchiardi, G .
EUROPEAN JOURNAL OF MINERALOGY, 2003, 15 (01) :21-33
[3]   Dehydroindigo:: A new piece into the Maya Blue puzzle from the voltammetry of microparticles approach [J].
Doménech, A ;
Doménech-Carbó, MT ;
Pascual, MLVD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (12) :6027-6039
[4]  
GETTENS RJ, 1946, PAIN MAT SHORT ENCY
[5]   Maya blue: A computational and spectroscopic study [J].
Giustetto, R ;
Xamena, FXLI ;
Ricchiardi, G ;
Bordiga, S ;
Damin, A ;
Gobetto, R ;
Chierotti, MR .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (41) :19360-19368
[6]   THE COORDINATION OF ALUMINUM IONS IN THE PALYGORSKITE STRUCTURE [J].
GUVEN, N ;
DELACAILLERIE, JBD ;
FRIPIAT, JJ .
CLAYS AND CLAY MINERALS, 1992, 40 (04) :457-461
[7]   SYNTHESIS, LOCATION, AND PHOTOINDUCED TRANSFORMATION OF ZEOLITE-ENCAGED THIOINDIGO [J].
HOPPE, R ;
SCHULZEKLOFF, G ;
WOHRLE, D ;
KIRSCHHOCK, C ;
FUESS, H .
LANGMUIR, 1994, 10 (05) :1517-1523
[8]   Structural study of Maya Blue: Textural, thermal and solidstate multinuclear magnetic resonance characterization of the palygorskite-indigo and sepiolite-indigo adducts [J].
Hubbard, B ;
Kuang, WX ;
Moser, A ;
Facey, GA ;
Detellier, C .
CLAYS AND CLAY MINERALS, 2003, 51 (03) :318-326
[9]  
KEBLER R, 1967, J STUD CONSERV, V12, P41
[10]  
Leona M., 2004, J AM INT CONSERV, V43, P37