4.3 Article

Effects of Ultra-sonification Assisting Polyethylene Glycol Pre-treatment on the Crystallinity and Accessibility of Cellulose Fiber

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/10601325.2010.508016

Keywords

Cellulose fiber; cellulosic water absorbent; crystallinity; PEG; pre-treatment

Funding

  1. Ministry of Science and Technology, P. R. China [2006AA100215]
  2. SRF for ROCS
  3. State Education Ministry, P. R. China
  4. China University of Geosciences (Wuhan) [CUGL090223]
  5. State Key Laboratory of Geological Process and Mineral Resources [GPMR200918]

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In order to prepare the advanced cellulosic super-absorbent polymer with high grafting level, we tried the novel ultrasound wave assisting polyethylene glycol (PEG) pre-treatment method to decrease the crystallinity and increase the accessibility of cellulose fiber. The effects of ultrasonification assisting PEG method on the crystallinity and swelling capacity of cellulose fiber were investigated. To optimize the experimental condition, the Taguchi method was employed in the treatment process. The influence factors such as ultrasonic wave power, ultrasonic wave time and PEG molecular weight relative to the crystallinity of cellulose fiber were studied systematically. The degree of crystallinity of cellulose fiber was measured by wide-angle X-ray diffraction (WAXD). The morphology of cellulose fiber was observed by environment scanning electron microscopy (ESEM). The effects of pre-treatment variables on the water absorbency and water retention values of cellulose fiber were also investigated. The research results revealed that, under the optimal experimental condition (ultrasonic powder, 500 W; ultrasonic time, 150 s; PEG molecular weight, 600 g/mol), the crystallinity of cellulose fiber decreased from 72.16 to 42.95%. Accordingly, the absorbency of cellulose fiber increased from 1.436 to 2.063 g/g, and the water retention value increased from 47.21 to 113.4%. However, the morphology of cellulose fiber did not change thoroughly compared with the original cellulose fiber. It can be hypothesized that the original inter- and intra-macromolecular hydrogen bonds in cellulose network were weakened, resulting from the high level dispersion of PEG within cellulose network without breaking the surface morphology of fiber.

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