The effect of solvent and catalyst concentration, pH and ionic strength on ozone bleaching of commercial eucalyptus kraft pulp in acetone-water solution in the presence of Keggin-type heteropolyanion [PMo(7)V(5)O(40)](8-) (HPA-5) has been examined and compared with conventional (solvent/catalyst free) ozonation systems. The solvent content and medium acidity were found to be the principal factors affecting ozonation efficiency. Increase in acetone concentration from 6% to 60% (w/w) led to gain in pulp brightness by 20.6% and delignification degree by 28.4%. Within the operative pH 1-2 range required for ozonation, the increase in pulp brightness by 7.6% and delignification degree by 18.1% was observed with acidity change from pH 1 to 2. The HPA-5 concentration of 1mM was found to be optimal for effective pulp ozonation in acetone solution. The role of the Donnan effect was examined. Increase in ionic strength (cation concentration) up to 0.25 M caused significant bleaching improvement.
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http://dx.doi.org/10.1016/j.biortech.2010.01.076 | DOI Listing |
Int J Biol Macromol
December 2024
Key Laboratory of Science and Technology of Eco-Textile, Ministry of Education, Jiangnan University, Wuxi, Jiangsu 214122, China. Electronic address:
Int J Biol Macromol
January 2025
College of Light Industry and Food Technology, Zhongkai University of Agriculture and Engineering, Guangzhou 510225, China; Guangdong Provincial Food Green Packaging Engineering Center, Zhongkai University of Agriculture and Engineering, Guangzhou 510225, China. Electronic address:
J Pharm Bioallied Sci
July 2024
Department of Oral Medicine and Radiology, New Horizon Dental College and Research Institute, Bilaspur, Chhattisgarh, India.
Sci Rep
September 2024
Postgraduate Program in Dentistry, University of Grande Rio (UNIGRANRIO), Rio de Janeiro, RJ, Brazil.
Arch Immunol Ther Exp (Warsz)
January 2024
Department of Oral Medicine, Medical University of Lublin, Lublin, Poland.
This study aimed to determine the effect of ozone on the expression of and genes in dental pulp cells. Additionally, the programmed cell death protein 1, programmed death-ligand 1, and CD200 antigens were determined in lymphocytes to assess their surface expression. Dental pulp cells were cultured from extracted healthy third molars and characterized as dental pulp stromal cells.
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