Volume 121, Issue 2 pp. 770-776

Finishing of silk by acrylic acid in the presence of sodium citrate and potassium per sulphate as catalysts under thermal treatment

D. Das

Corresponding Author

D. Das

National Institute of Fashion Technology (Ministry of Textiles, Government of India), Salt Lake City, Kolkata 700098, India

National Institute of Fashion Technology (Ministry of Textiles, Government of India), Salt Lake City, Kolkata 700098, India===Search for more papers by this author
A. Mukherjee

A. Mukherjee

National Institute of Fashion Technology (Ministry of Textiles, Government of India), Salt Lake City, Kolkata 700098, India

Search for more papers by this author
P. Bhattacharya

P. Bhattacharya

Chemical Engineering Department, Jadavpur University, Kolkata 700032, India

Search for more papers by this author
D. Chakrabarty

D. Chakrabarty

Department of Polymer Science and Technology, University of Calcutta, Kolkata 700009, India

Search for more papers by this author
First published: 24 February 2011
Citations: 9

Abstract

Silk fabric was finished using acrylic acid (AA) as the finishing agent in the presence of sodium citrate and potassium per oxodisulphate catalysts separately or in selected combinations employing a pad-dry-cure technique. Treatment with 6% AA at 30°C and at pH 7 produced optimum effects; a batching time of 45–60 min at 30°C, followed by drying of the batched fabric at 95°C for 5 min and curing of the dried fabric at 140°C for 5 min produced most balanced improvements in the properties such as wrinkle recovery, extensibility, and moisture regain with retention of more than 80% of original strength. Sodium citrate catalyst allowed esterification of AA with proteineous constituent of silk and potassium per sulfate catalyst allowed radical polymerization of free AA or silk bound AA moieties; the said process ultimately led to some degree of crosslinking of the chain polymers of silk. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.