Homogeneous Synthesis and Characterization of Quaternized Cellulose Derivatives in NaOH-urea Aqueous

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Quaternized cellulose( QC) derivatives were synthesized by reacting cellulose with 3-chloro-2-hydroxypropyl trimethyl ammonium chloride( CHPTAC) in an aqueous solution of Na OH-urea. The chemical structures and physical properties of the obtained QC derivatives were characterized using nitrogen content analysis,Fourier transform infrared spectroscopy( FT-IR),~1H-nuclear magnetic resonance(1H-NMR),X-ray diffraction( XRD),and thermal gravity analysis( TGA). The FT-IR and ~1H-NMR results confirmed the successful introduction of cationic quaternary ammonium groups into the main chain of cellulose. A series of QC derivatives with the degree of substitution( DS) values ranging from 0. 33 to 0. 80 were derived by adjusting the molar ratio of CHPTAC to anhydroglucose unit( AGU) of cellulose,concentration of cellulose in the Na OH-urea solution,as well as reaction temperature and time. According to the DS values of the QC derivatives,the optimized synthetic conditions were as follows: 25℃ reaction temperature,3% cellulose in Na OH-urea solution,the molar ratio of etherification agent to glycosidic cellulose of 15∶ 1,and 12 h reaction time. The TGA and XRD results revealed that the crystalline structure was destroyed during etherification,and the thermal stability of the QC derivatives was lower than that of cellulose. Quaternized cellulose (QC) derivatives were synthesized by reacting cellulose with 3-chloro-2-hydroxypropyl trimethyl ammonium chloride (CHPTAC) in an aqueous solution of Na OH-urea. The chemical structures and physical properties of the obtained QC derivatives were characterized using nitrogen content analysis, Fourier transform infrared spectroscopy (FT-IR), 1H nuclear magnetic resonance (1H-NMR), X-ray diffraction and thermal gravity analysis (TGA) results confirmed the successful introduction of cationic quaternary ammonium groups into the main chain of cellulose. A series of QC derivatives with the degree of substitution (DS) values ​​ranging from 0. 33 to 0. 80 were derived by adjusting the molar ratio of CHPTAC to anhydroglucose unit (AGU) of cellulose, concentration of cellulose in the Na OH-urea solution, as well as reaction temperature and time. According to the DS values ​​of the QC derivatives, the optimized synthetic conditions were as follows: rea ction temperature, 3% cellulose in Na OH-urea solution, the molar ratio of etherification agent to glycosidic cellulose of 15: 1, and 12 h reaction time. The TGA and XRD results revealed that the crystalline structure was destroyed during etherification, and the thermal stability of the QC derivatives was lower than that of cellulose.
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