Ordered reticulated-structured carbon foams via surfactant-addition into the polymerization medium of bio-based polyols


YARGIÇ A. Ş.

Chemical Engineering and Processing - Process Intensification, cilt.158, 2020 (SCI-Expanded) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 158
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1016/j.cep.2020.108204
  • Dergi Adı: Chemical Engineering and Processing - Process Intensification
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Chemical Abstracts Core, Chimica, Compendex, INSPEC
  • Anahtar Kelimeler: Bio-based carbon foams, non-ionic surfactants, self-foaming, solvolytic liquefaction
  • Bilecik Şeyh Edebali Üniversitesi Adresli: Evet

Özet

© 2020 Elsevier B.V.In the solvolytic liquefaction reaction of biomass, biopolymers are produced by bond-breakage in the complex lignocellulosic composition using the appropriate solvent and functionalizing the related fragments under mild conditions. The utilization of these bio-polyols as carbon sources has enhanced the conspicuous relevance in the handling of agroforestry by-products as an alternative to fossil fuel-based sources, taking into account the terms sustainability and environmental impact. In this study, a green and inexpensive method based on the resinification and subsequent foaming of bio-polyols produced by solvolytic liquefaction of the tree bark was adopted to synthesize carbon foams with a well-developed hierarchical porous structure. The novelty of this study to brighten the studies in the literature was to examine the characteristics of biomass-based carbon foams produced by adding two types of non-ionic surfactants (P123 and PEG3000) into the synthesis medium at different surfactant/biomass ratios (0.15 and 0.20 w/w). This study comprises a promising technique that promotes self-foaming in the existence of non-ionic surfactants to produce reticulated carbon foams from forest industry wastes with porous graphitic structure, high surface area (up to 758 m2/g), and controlled pore size distribution in the micro-pore region (dp<2 nm).