Cationisation of Cotton with Natural Source Based Gelatin for Salt-Free Reactive Dyeing of Cationised Cotton

被引:0
作者
Ahmed, Mohammed [1 ]
Sukumar, Nachiappan [2 ]
Yusuf, Arega [3 ]
Awol, Yasin [4 ]
机构
[1] Wollo Univ, Kombolcha Inst Technol, Dept Text Engn, Amhara Region, Ethiopia
[2] KS Rangasamy Technol, Dept Text Technol, Thiruchengode, Tamil Nadu, India
[3] Wollo Univ, Kombolcha Inst Technol, Dept Leather Engn, Amhara Region, Ethiopia
[4] Wollo Univ, Kombolcha Inst Technol, Dept Chem Engn, Amhara Region, Ethiopia
关键词
Cotton; salt-free dyeing; gelatin; cationization; collagen; fibrous protein; OPTIMIZATION; FABRICS;
D O I
10.1080/15440478.2022.2125920
中图分类号
TB3 [工程材料学]; TS1 [纺织工业、染整工业];
学科分类号
0805 ; 080502 ; 0821 ;
摘要
Cotton fabric was chemically modified with gelatin, extracted from fleshing waste of collagen by thermal hydrolysis process to increase the dyeing capability of reactive dye. Gelatin imparts new functional groups with fabric and develops Ammonia ion in slightly acid conditions to obtain cationized cotton fabric permit salt and alkali-free reactive dyeing with acceptable shade depth. The imparting of gelatin on the cotton fabric was confirmed by FTIR, UV/VIS absorption, and K/S values. The result shows that they have advantage of high dye utilization and better fastness. Color fastness of treated dyed fabric was equal to the untreated dyed fabric and obtained 4/5 washing fastness, 5 rubbing fastnesses, and 4/5 perspiration fastness. The UV/VIS absorption results show 6.4% improvement in exhaustion and K/S results have 7% improvement in fixation and 9.4% in dye utilization to that of untreated dyeing with salt. Cationized fabric not only increased the exhaustion of the dye but also improved the crease resistance angle at 120 degrees due to the formation of cross-linkage between amide group and the carboxylic acid. To obtain the expected results, cationization was done at alkaline media and the optimum parameter was determined, whereas dyeing conducted at slightly acidic media with optimum parameters.
引用
收藏
页码:15353 / 15366
页数:14
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