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2.3. Characterization
The Fourier transform-infrared (FTIR) spectrum was obtained from a MAGNA 560 FTIR spectrometer (Thermo Nicolet Corporation, USA) using KBr discs in the range from 4000 cm−1 to 400 cm−1. Scanning electron microscopy (SEM) images were obtained using a FEI QUANTA 200 microscope. The swollen resin hydrogel were frozen in liquid nitrogen and immediately snapped and freezedried. The fractured surface of the resin hydrogel was observed.
Differential scanning calorimetry (DSC) was done using a DSC2004 heat flux differential scanning calorimeter (NETZSCH, Germany) at a temperature range from 293 K to 773 K with a heating rate of 10 K/min and an argon gas flow at 40 mL/min.
2.4. Swelling and absorbency of resins in chloride and pH buffer
Solutions NaCl, CaCl2, and AlCl3 solutions were prepared at different concentrations (0.1 mol/L, 0.05 mol/L, and 0.01 mol/L), where 0.1 g of
the resin products was mixed with 200 mL of each salt solution. The water absorbency was measured. Buffer solutions with pH values of 2, 4, 6, 8, 10, and 12 were prepared, where 0.1 g of the resin was mixed with 200 mL of the buffer solution at different pH values. After saturation, filtered and weighed, the hydrogel characteristics were determined, and the absorbency was calculated.
2.5. Determination of biodegradability Resin sheets measuring 1 cm ¡Á 2 cm were weighed and labeled separately. The sheets were then placed in 18 PDA plates containing mycete (six plates each of Penicillium, A. niger, and L. edodes), sealed with tape, and incubated at 30 ◦C. Afterwards, the resin products were filtered, dried, weighed, and the biodegradation was observed
every 3 days.

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