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용제를 사용한 Rubia cordifolia의 색소 추출 및 Silk 염색

Dye Extraction and Silk Dyeing of Rubia Cordifolia Using Solvents

  • Lim, Jee Young (Dept. of Clothing & Textiles, Pusan National University) ;
  • Jang, Jeong Dae (Dept. of Clothing & Textiles, Pusan National University)
  • 투고 : 2013.01.17
  • 심사 : 2013.05.09
  • 발행 : 2013.06.30

초록

Rubia cordifolia L (Indian madder) contains red color purpurin (65-67%) and yellow color munjistin (10-12%) as well as nordamncanthal (9-10%). Purpurin is a traditional red dye. The purpose of this research is to increase the dyeability of silk and light fastness of dyed silk fabric. We dyed silk fabrics after pretreatment to remove the yellow component of madder using various solvents such as ethyl acetate, ethanol, methanol, chloroform, and acetone. The total K/S value was the highest in the case of chloroform and reflectance was the lowest at the red color region from 470nm to 530nm. Chloroform dissolved the yellow color of Rubia cordifolia; in addition, we found that the total K/S value increased and the ${\Delta}E$ value decreased by chloroform pretreatment for silk dyeing.

키워드

참고문헌

  1. Ahn, C. S., & Obendorf, S. K. (2003). Separation of chromophoric substance from madder plant under different extraction and analytical conditions. Journal of the Korean Society of Clothing and Textiles, 27(11), 1350-1357.
  2. Ahn, C. S., & Obendorf, S. K. (2004). Comparison of TLC and GC-MS method in the analysis of dye extracted from madder plant. The research Journal of the Costume Culture, 12(4), 579-590.
  3. Cronquist, A. (1981). An intergrated system of classification of flowering plants. New York: Columbia University press.
  4. Gupta, D., Gulrajani, M. L., & Kumari, S. (2004). Light fastness of naturally occurring anthraquinone dyes on nylon. Coloration Technology, 120(5), 205-212. doi:10.1111/j.1478-4408.2004.tb00119.x
  5. Gupta, D., Kumari, S., & Gulrajani, M. (2001a). Dyeing studies with hydroxyanthraquinones extracted from Indian madder. Part 1: Dyeing of nylon with purpurin. Coloration Technology, 117(6), 328-332. doi: 10.1111/j.1478-4408.2001.tb00084.x
  6. Gupta, D., Kumari, S., & Gulrajani, M. (2001b). Dyeing studies with hydroxyanthraquinones extracted from Indian madder. Part 2: dyeing of nylon and polyester with nordamncanthal. Coloration Technology, 117(6), 333-336. doi:10.1111/j.1478-4408.2001.tb00085.x
  7. Joe, K. L. (1996). 염색이론과 실제 [Theory of dyeing and experiment]. Seoul: Hyeongseol publisher.
  8. Jose, C., Publio, P., & Jose, V. (1992). The dyeing of textile materials. Textilia, 428-429.
  9. Karadag, R., & Dolen, E. (2007). Re-examination of Turkey red. Societa Chimica Italiana, 97(7), 583-589.
  10. Kim, K. J., & Lee, J. M. (2005). 염료 화학 [Dye chemistry]. Seoul: Green.
  11. Lee, H. S., & Ko, S. M. (2010). Dyeability of silk fabrics using extracts of Ligustrum Japonicum Thunb fruit. Textile Coloration and Finishing, 22(1), 71-76. https://doi.org/10.5764/TCF.2010.22.1.071
  12. Melchior, H. (1964). A Engler's syllabus der pflanzenfamilien (12th ed.). [The plant classification system (12th ed.)]. Berlin: Gebruder Borntraeger.
  13. Ministry of Commerce. (2000). 천연염료의 안정화 및 염색의 재현성 확립기술개발 [Establishment technology development about stabilization of natural dyes and dyeing reproducibility]. Daegu: Kyungpook National University.
  14. Perkin, A. G., & Everset, A. E. (1918). The natural organic colouring matter. London: Longmans Green.
  15. Schweppe, H. (1989). Identification of red madder and insect dyes by thin-layer chromatography. In S. H. Zeronian & H. L. Needles (Eds.), Historic textile and paper materials II: Conservation and characterization (pp. 188-219). Washington DC: American chemical society.
  16. Thomson, R. H. (1971). Naturally occurring quinones (2nd ed.). London: Academic press.
  17. Vankar, P. S., Shanker, R., Mahanta, D., & Tiwari, S. C. (2008). Ecofriendly sonicator dyeing of cotton with Rubia cordifolia Linn. using biomordant. Dyes and Pigments, 76, 207-212. doi:10.1016/j.dyepig.2006.08.023

피인용 문헌

  1. Dyeability of Fabrics Using Indian Dyestuffs of Madder, Marigold and Pomegranate vol.38, pp.6, 2014, https://doi.org/10.5850/JKSCT.2014.38.6.929
  2. High Light-Fastness Acid Dyes Synthesized from Corresponding Anthraquinone Chromophore Utilizing a Sulfonation Reaction. I. Dye Synthesis and Characterization vol.19, pp.9, 2018, https://doi.org/10.1007/s12221-018-7947-z
  3. A Study for the Conformity Assessment on the Natural Dye by HPLC (1) vol.20, pp.6, 2018, https://doi.org/10.5805/SFTI.2018.20.6.752