2022
DOI: 10.1016/j.fochx.2022.100407
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Aggregation of konjac glucomannan by ethanol under low-alkali treatment

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Cited by 14 publications
(7 citation statements)
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“…Ethanol's solvent nature possibly reconfigured the gel network, causing this shrinkage. This aligns with prior research demonstrating solvents' effects on gel structures [28][29][30]. In addition, it has been shown that ethanol has the potential to initiate syneresis, a phenomenon that is supported by a significant connection (r = 0.746; Table 4) between the occurrence of syneresis and the size of the gel.…”
Section: Gel Syneresis Size and Colorimetric Propertiessupporting
confidence: 87%
See 1 more Smart Citation
“…Ethanol's solvent nature possibly reconfigured the gel network, causing this shrinkage. This aligns with prior research demonstrating solvents' effects on gel structures [28][29][30]. In addition, it has been shown that ethanol has the potential to initiate syneresis, a phenomenon that is supported by a significant connection (r = 0.746; Table 4) between the occurrence of syneresis and the size of the gel.…”
Section: Gel Syneresis Size and Colorimetric Propertiessupporting
confidence: 87%
“…Nonetheless, values were still within an appreciable elastic domain [2]. This trend is reminiscent of findings in earlier research, where low Tan δ values have been frequently associated with a robust gel network [8,28]. Nevertheless, the increasing Tan δ values with prolonged ethanol exposure underscore a diminishing elasticity, likely due to ethanol's interference with the intricate network of the starch gel, reducing its size and elastic nature.…”
Section: Rheological Propertiessupporting
confidence: 77%
“…[ 30 ] As shown in Figure 3e, the EB of our material is 26.9% larger than the previously largest EB (i.e., CA(OH) 2 /KGM). Meanwhile, the E of our material is within the order of kPa of Agar/KGM [ 55 ] and much smaller than E of other edible and c‐KGM‐based materials [ 48,49,56–58 ] (Figure 3f). Note that E of Ca(OH) 2 /KGM, [ 30 ] gelatin/KGM, [ 44 ] EC/KGM, [ 46 ] and Ag/KGM [ 57 ] have not been reported, and therefore no comparison is made.…”
Section: Resultsmentioning
confidence: 93%
“…Fourier-transform infrared (FTIR) spectra confirmed the structure and composition of the KGM powder (Figure S2), with results showing a wide absorption band at 3430 cm –1 that is attributed to hydroxyl vibrations (−OH groups) and peaks at 2918 and 2890 cm –1 that are attributed to −CH 2 – stretching vibrations. The absorption peaks at 1728, 1378, and 1243 cm –1 correspond to the stretching vibrations of the CO in the acetyl group, symmetric C–H bending vibrations in the methyl group, and C–O vibrations in the O-acetyl groups, respectively. , The characteristic band at 1026 cm –1 is attributed to the stretching vibrations of the −C–O–C– group, and the broad absorption bands at 872 and 803 cm –1 are attributed to mannose. There is a distinct amphiphilicity in the KGM structure due to the segregation of polar (−OH groups) and nonpolar (−CH groups) patches. Therefore, KGM aggregation and subsequent gel formation are assumed to be driven by hydrophobic contacts and hydrogen bonds.…”
Section: Resultsmentioning
confidence: 99%