2012
DOI: 10.4028/www.scientific.net/amr.488-489.1404
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Characterization of Chitin Extracted from Waste Sources via XRD, FTIR, and TGA Techniques

Abstract: This work presents the chitin preparation from waste sources, the chitin powders were successfully extracted from shrimp shell, crab shell and squid pen. To prepare chitin powders, all raw materials were washed and grounded using agate mortar, which the particle size of powder is 212–250 μm. Then, the powdered materials were immersed into solution of chloroform and methanol (with 2:1 ratio) at room temperature for removing fat. The deprotienation and decarbonation, the samples were immersed in 50 wt% of NaOH s… Show more

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Cited by 7 publications
(7 citation statements)
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“…The next corresponding peaks at 1645 cm -1 and 1629 cm -1 represents the presence of amide groups of chitin polysaccharides [24]. The next intensity peaks at 1399 cm -1 and 1397 cm -1 corresponds to the asymmetric stretching and vibrations of C = O, which attributes to the presence of CaCO 3 [21,25]. A strong asymmetric stretching of C-N-C is observed at the regions of 1014 cm -1 and 1029 cm -1 [25].…”
Section: Ftir Analysis Of Treated and Untreated Portunus Sanguinolentmentioning
confidence: 92%
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“…The next corresponding peaks at 1645 cm -1 and 1629 cm -1 represents the presence of amide groups of chitin polysaccharides [24]. The next intensity peaks at 1399 cm -1 and 1397 cm -1 corresponds to the asymmetric stretching and vibrations of C = O, which attributes to the presence of CaCO 3 [21,25]. A strong asymmetric stretching of C-N-C is observed at the regions of 1014 cm -1 and 1029 cm -1 [25].…”
Section: Ftir Analysis Of Treated and Untreated Portunus Sanguinolentmentioning
confidence: 92%
“…In order to eliminate the fat content, sieved shell powders were treated with a solution of chloroform and methanol (ratio 2:1) at room temperature for 1 h. Followed by deproteination by immersing in 5 wt% of sodium hydroxide solution for 24 h and then decarbonization of the samples was done using 4 wt% of hydro chloric acid solution for 1 h. Deacetylation was done with 50% sodium hydroxide solution at 100 C for 4 h to get chitosan-based shell powder. At last, filtration was done to remove the solution and dried at normal environmental conditions to get desired treated powder filler, the percentage of chemicals was considered as per the literature findings [20,21]. The photographic images of untreated Portunus sanguinolentus shell powder, Treated Portunus sanguinolentus shell powder and Biwoven Jute fiber mat (fabrics) are shown in Figure 2(a) to (c) and SEM image of treated Portunus sanguinolentus shell powder is shown in Figure 2 the treated Portunus sanguinolentus shell powder which has a rough surface since it is treated with chemicals thereby removing protein and other organic matters from its surface.…”
Section: Methodsmentioning
confidence: 99%
“…It was then filtrated and dried at room temperature to get the final powder. Thus, the complete crab shell powder was successfully processed without any organic compounds, with the help of chemical reagents [16].…”
Section: Methodsmentioning
confidence: 99%
“…Decomposition mainly occurs in three different stages in chemically processed CBS. In the first phase, at 100-250°C, the degradation of protein traces and moisture from the crab shell surface occur, followed by the degradation of the saccharide structure of the molecule at 250-360°C [16,21]. This includes the dehydration of saccharide rings, polymerisation and decomposition of the acetylated and deacetylated units of chitin biopolymeric fibres.…”
Section: Thermal Stability Of Varying Ingredients and Compositesmentioning
confidence: 99%
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