SOME STUDIES ON NATURAL DYES
by DEEPTI BAHL
A thesis submitted in
fulfilment of the requirements for the award of the degree of
DOCTOR OF PHILOSOPHY
Department of Textile Technology INDIAN INSTITUTE OF TECHNOLOGY, DELHI
December, 1994
TO MY HUSBAND
...
WITH LOVECERTIFICATE
This is to certify that the thesis entitled Some Studies on Natural Dyes being submitted by Ms. Deepti Bahl to the Indian Institute of Technology, Delhi for the award of the degree of Doctor of Philosophy is a record of bonafide research work carried out by her under my guidance and supervision.
To the best of my knowledge this thesis has reached the required standard. The material presented in this thesis,, in part or full has not been submitted to any other University or any other Institute for the award of degree or diploma.
M.L.Gulrajani Professor
Department of Textile Technology Indian Institute of Technology New Delhi - 110016
ACKNOWLEDGEMENTS
It is with a deep sense of gratitude that I thank my project supervisor Prof. M.L.Gulrajani, without whose foresight and continued guidance, this work could not have been undertaken or completed successfully.
Sincere thanks are due to Prof R.C.D Kaushik, Director TIT&S, Bhiwani for granting me leave and providing other facilities to continue with the experimental and writing work while at the Institute.
I thank Dr. Khanna, Vice President, Ranbaxy R&D Centre for allowing me full use of all facilities at their centre and Dr.
J.Singh and other scientists for helping out so enthusias- tically with the chromatographic and characterization studies.
I express my thanks to Dr. Raghavan of Physics department and Dr. G.S.Kapoor, Ms Anju Khanna and all other friends, colleagues and technical staff of Chemistry Department, who helped me with small and big things all through this work.
I am grateful to Dr. Sushil Kumar, Director CIMAP and Dr. K.0 Gupta of GBPUA&T, for helping out with literature survey.
Thanks are due to the faculty members of Textile Department for providing valuable guidance, whenever required. To my colleagues Sheetal, Deepali, Shailja and Kannanji for the memorable lunch and tea sessions. Also to Mr. V.A. Passi, Mr.
Rajender Prasad, Mr. Prakash Chand, Mr. Shiv Charan,, Jagdish, Suresh and Ashok of Textile Chemistry Lab; to Mr. Didarmal, Mr. Padam and Mr. Prabhu for rendering timely assistance.
Special thanks to Mr. Rajesh Arora for typing this manuscript always in time with my schedule.
I thank my parents and my mother and brother-in-law for their unwavering support and co-operation throughout. Finally, I thank my husband for believing in me, for being so patient and for everything else that helped make all these years of work so enjoyable. Last, but not the least, I thank my little daughter for sparing me the time, which was rightfully hers, to complete this manuscript.
E I
ABSTRACT
In recent years, the world has become increasingly aware of the environmental issues. Synthetic dyestuffs, in particular, have come under severe criticism for they are highly polluting in their stage of manufacturing as well as application. At the same time there has been a renewal of interest in the use of natural colouring matters for dyeing of textiles.
Many empirical studies have been conducted on colour charac- teristics, fastness properties and dyeing methods used for dyeing with indigenously available natural dye materials.
Studies are also being conducted for identification, preserva- tion and restoration of the natural dyes present on ancient museum textiles. Systematic scientific studies in this field are few.
This thesis is an attempt to study in detail, the mechanism of dyeing various textile fibres with natural dyes; to standar- dise a method for separation and purification of colouring compounds present in a selected plant material and to charac- terize and identify them; to comprehensively review natural dyes and their fastness properties to test and document the fastness properties of some prominent Indian dyes and to study the kinetics of light fading of a particular dye.
Lawsone (2-hydroxy-1,4-naphthoquinone) is the colouring compound found in henna leaves. The dye, possessing the char- acteristics of a disperse dye was used to conduct thermo- dynamic and kinetic studies on six different textile fibres
and at three different temperatures. Results showed that rate of dyeing is directly related to the denier and diffusion coefficient of fibres. The mechanism of dyeing on all fibres resembled the partition mechanism corresponding to the Nernst isotherm at 70 and 1000C. However, at 50°C isotherms were curved, indicating the attainment of a pseudo equilibrium - caused most probably by the aggregation of dye in solution at that temperature. Excessive uptake of dye was observed for all fibres. Experimental evidence showed that this was due to the aggregation of dye molecules inside the fibre. Standard affinity was seen to increase with increase in temperature and heat of dyeing H was positive indicating an exothermic reaction in all cases except wool. On wool, affinity was found to be independent of temperature change. Mordanting with A13+
ions did not appear to affect the equilibrium dye uptake by wool and silk fibres.
Identical studies, as for lawsone, were conducted with juglone - the 5-hydroxy isomer of lawsone. It is the pigment extrac- ted from the rind of green walnuts. Results of the study were quite similar to those for lawsone. Diffusion coefficient was directly related to the diameter of fibres.
Adsorption isotherms were linear at both 50°C and 100°C for all fibres and the standard affinity increased with temperature.. Juglone, in general, showed higher affinity for hydrophobic fibres, as compared to hydophilic fibres but there is little difference in the affinity of individual fibres in each class.
Dye extracted from the roots of dolu or Himalayan rhubarb gives a variety of deep and bright shades on wool and silk. A literature survey showed that the roots contain several deri- vatives of hydroxy anthraquinones which are responsible for the colouring power. Thus it was decided to develop a proce- dure to separate the pigments, purify and identify them, and study their dyeing mechanism. TLC analysis of the extract established the presence of five coloured species and some colourless impurities in the extract. Two solvent systems were standardised as mobile phases for preparative column chromato- graphy. Flash chromatographic technique was employed to elute the columns.
Compounds collected from columns were recrystallized for further purification. HPLC analysis of crude extract and the purified fractions (A,B,C,D and E) estimated the purity of the five compounds as 100%, 97.5%, 98%, 99.44% and 91% respec- tively.
The melting point, Ultra violet and visible spectrum, Infrared spectrum, mass spectrum and Proton NMR spectrum of the frac- tions were recorded, interpreted and compared with reported data to arrive at their structure. First three compounds were identified as - chrysophanic acid (3-methyl, 1,8-dihydroxy anthraquinone), physcion (1,8-dihydroxy, 3-methyl, 6-methoxyl, anthraquinone) and emodin (1,3,8-trihydroxy, 6-methyl anthra- quinone).
Dyeing studies, similar to those conducted with lawsone and juglone were conducted on polyester with the purified dye chrysophanic acid separated from rhubarb extract. The dye exhibited no affinity for silk fibres. Linear isotherm was obtained at 130°C but at 100°C the isotherm was curved - indicating the establishment of a pseudo-equilibrium.
Extensive light and wash fastness tests were conducted on wool and silk fabrics dyed with some prominent yellow, red and brown dyes of India and their fastness ratings recorded as per ISO standards. No natural yellow dye was found to have a fastness grade more than 4 as most yellow dyes are based on the flavonoid molecule which is sensitive to light. Also, several yellow shades turn brown instead of bleaching on exposure to light. Red dyes, in comparison exhibit better fastness, as they are mostly anthraquinone based mordant dyes.
Brown and black dyes mostly obtained from combining tannins with ferrous salt also exhibit moderate to good light fastness. Wash fastness of most dyes was good, ranging between 3-4 grade. But good fastness to light was not always found in dyes having good fastness to washing.
Kinetics of light fading tests showed interesting results. On silk samples the rate of fading curve showed an initial darkening of shades followed by no fading. On wool samples, the curves were near horizontal, indicating little or no fading. The rate, or nature of fading was neither influenced by humidity nor mordanting. The rate of change in colour (DE) was retarded by ferrous mordanting on silk. Unmordanted and
alum mordanted wool samples showed a much higher rate of change in colour than the other mordanted samples.
Spectral curves of silk samples showed increased absorbance in the entire visible region after exposure. On wool samples there were very little change in the spectral curve after exposure. All samples in general turned redder on exposure to light. From these results it could be concluded that the dye is present in a highly associated form in the fibre, due to which it is highly resistant to colour change when exposed to light.
CONTENTS
ABSTRACT
1. INTRODUCTION TO NATURAL DYES ... 1 1.1 CHEMICAL CLASSIFICATION ... 3 1.1.1 Quinones
1.1.2 Indigoids
1.1.3 Pyridine Based Dye 1.1.4 Carotenoids
1.1.5 Diaroyl Methane Based Dye 1.1.6 Dihydropyran Based Dyes 1.1.7 Flavonoids
1.1.8 Tannins
1.2 CLASSIFICATION ON THE BASIS OF APPLICATION METHODS ... 71 1.2.1 Mordant Dyes
1.2.2 Vat Dyes 1.2.3 Direct Dyes 1.2.4 Acid Dyes 1.2.5 Basic Dyes 1.2.6 Disperse Dyes
2. STUDIES ON DYEING WITH NAPHTHOQUINONE DYES ... 78 2A. INTRODUCTION ...80 2A.1 INTRODUCTION TO PHYSICAL CHEMISTRY OF DYEING MECHANISMS . 80 2A.1.1 Kinetics of Dyeing
2A.1.2 The Dyeing System in Equilibrium
2A.2 STUDIES ON MECHANISM OF DYEING WITH NATURAL DYES ... 88 2B. STUDIES WITH LAWSONE ...90 2B.1 EXPERIMENTAL ...91 2B.1.1 Fibres
2B.1.2 The Dye
2B.1.3 Fibre Pretreatment 2B.1.4 Test Methods
2B.1.5 Dyeing Studies 2B.1.6 Mordanting Studies
2B.2 RESULTS AND DISCUSSION ...95 2B.2.1 The dye
2B.2.2 Fibre Characterization 2B.2.3 Kinetic Studies
2B.2.5 Mordanting Studies 2B.2.6 Desorption Study
2C. STUDIES ON DYEING WITH JUGLONE
...
114 2C.1 EXPERIMENTAL...
1142C.1.1 Fibres 2C.1.2 Dye
2C.1.3 Fibre Pretreatment 2C.1.4 Dyeing Studies
2C.2 RESULTS AND DISCUSSION
...
115 2C.2.1 Spectral Studies2C.2.2 Kinetic Studies
2C.2.3 Thermodynamic Studies
2D. CONCLUSIONS
...
126 3. STUDIES WITH HIMALAYAN RHUBARB (Rheum emodi)...
128 3A. EXTRACTION AND CHROMATOGRAPHIC SEPARATION OFCOMPONENTS OF RHUBARB EXTRACT
...
134 3A.1 EXPERIMENTAL...
136 3A.1.1 Dye Extraction3A.1.2 Thin Layer Chromatographic Procedure 3A.1.3 Column Procedure
3A.1.4 HPLC Procedure
3A.2 RESULTS AND DISCUSSION
...
1393A.2.1. TLC Analysis
3A.2.2 Preparative Column Chromatography
3A.2.3 Purification of the Separated Compounds 3A.2.4 HPLC Analysis
3A.3 CONCLUSIONS
...
1493B. CHARACTERIZATION DATA AND STRUCTURE ASSIGNMENT
OF COMPOUNDS ISOLATED FROM RHUBARB EXTRACT
...
1503B.1 EXPERIMENTAL
...
1533B.1.1 Instrumentation
3B.2 RESULTS AND DISCUSSION
...
1543B.2.1 Fraction A 3B.2.2 Fraction B 3B.2.3 Fraction C 3B.2.4 Fraction D 3B.2.5 Fraction E
3B.3 CONCLUSIONS
...
1663C. DYEING OF POLYESTER WITH COMPOUND A (CHRYSOPHANIC ACID) . 169 3C.1 EXPERIMENTAL.
...
1693C.1.1 Fibre 3C.1.2 Dye
3C.1.3 Preparation of dye liquor 3C.1.4 Dyeing
3C.2 RESULTS AND DISCUSSION
...
1703C.2.1 Rate of Dyeing
3C.2.2 Diffusion Coefficient 3C.2.3 Thermodynamic Studies
3C.3 CONCLUSIONS
...
173 4. FASTNESS PROPERTIES OF NATURAL DYES...
175 4A. INTRODUCTION TO THE CONCEPT OF COLOURFASTNESS ANDREVIEW OF LITERATURE ON FASTNESS PROPERTIES OF
NATURAL DYES
...
...176 4A.1 MECHANISM OF FADING...
...176 4A.2 LIGHT FASTNESS PROPERTIES OF DYES ...177 4A.2.1 Chemical Structure of the Colorant4A.2.2 Dye Concentration
4A.2.3 Nature of Incident Light 4A.2.4 Nature of Fibre
4A.2.5 Temperature and Humidity 4A.2.6 Atmospheric Contaminants 4A.2.7 Effect of Mordants
4A.2.8 Presence of Foreign Substances
4A.3 WASHFASTNESS PROPERTIES OF DYES ...182 4A.3.1 State of Dye Inside the Fibre
4A.4 CHEMICAL STRUCTURE OF NATURAL DYES AND THEIR
FASTNESS TO LIGHT
...
1844A.4.1 Yellow and Orange Dyes 4A.4.2 Red Dyes
4A.4.3 Blue Dyes 4A.4.4 Black Dyes 4A.4.5 Brown Dyes
4B. TESTING OF LIGHT AND WASHFASTNESS OF SOME PROMINENT
NATURAL DYES OF INDIA
...
1934B.1 DYES
...
1934B-.2 EXPERIMENTAL
...
1934B.2.1 Fabric
4B.2.2 Dyebath preparation 4B.2.3 Mordanting and dyeing 4B.2.4 Testing and Analysis
4B.3 RESULTS AND DISCUSSION
...
1964B.4 CONCLUSIONS
...
...205 4C. LIGHT FADING MECHANISM OF RHUBARB DYED WOOL AND SILK ....207 4C.1 MATERIALS AND METHODS...
...210 4C.1.1 Lightfastness tests4C.2 RESULTS AND DISCUSSION
...
2124C.2.1 Light Fading Behaviour of Rhubarb Dyed Silk 4C.2.2 Light Fading Behaviour of Rhubarb Dyed Wool
5. CONCLUSIONS
...
230REFERENCES APPENDIX PUBLICATIONS
