Читать книгу High-Performance Materials from Bio-based Feedstocks - Группа авторов - Страница 36

Graphite is an infinite three‐dimensional (3D) material comprising several stacked layers anchored by weak Van der Waals forces. Each stacked layer is a two‐dimensional (2D) carbon sheet structured in a hexagonal honeycomb lattice called graphene [65, 66]. Graphene was discovered in 2004 and presents astonishing properties. Its appearance is like a soft film, and it has a high Young’s modulus and excellent thermal and electrical properties. Previous research reveals that graphene has a very high surface area of over 2000 m² g⁻¹ and can be easily chemically modified [67]. Within the past decade, numerous investigations have used graphene in various applications along with exploring the practical synthesis procedures of graphene from biomass [68, 69]. Graphene can be synthesized through several methods including micromechanical exfoliation of graphite, chemical vapor deposition (CVD) of graphite, epitaxial graphene growth on silicon carbide, chemical graphitization of graphene oxide, and carbonization of biomass and waste materials [70–74]. Micromechanical exfoliation and CVD of graphite produced good‐quality graphene. The transformation of biomass into graphene can be accomplished via the carbonization of biomass under specific conditions. For example, pyrolysis of camphor leaves at an ultra‐high temperature of 1200 °C under nitrogen or argon atmosphere produced a biochar, which was subsequently reacted with D‐tyrosine as a bio‐based dispersion agent under sonication to obtain graphene [75]. The graphene derived from biomass contained many impurities, whereas the graphene synthesized from graphite is usually purer. To avoid contamination, some researchers used pure lignin to produce fine graphene through a stepwise pyrolysis process [76]. The biomass type may affect the properties of graphene as well. Populus wood was mixed with KOH before carbonization under nitrogen. Surprisingly, the graphene‐like carbon material was found on the structure of the obtained biochar [20]. Sucrose, xylitol, and glucose were also used as starting materials for graphene synthesis. The carbonization of sugar mixed with FeCl₃ generated graphene‐like carbon materials, which presented excellent catalytic activity in the hydrogenation of nitrobenzene [77]. Even though graphene is one of the beneficial carbon materials, the production of graphene from biomass without any impurities remains a challenge.

To meet the requirement to be a heterogeneous catalyst or support, the physicochemical properties and thermal stability of the material are crucial as these dictate the catalytic efficiency. As previously described, bio‐based carbon materials have predominant characteristics that benefit their application as a direct catalyst or catalyst support. Biomass‐derived porous carbon materials with high porosity provide a greater number of active sites. Moreover, the pore size and specific surface area can be tailored via the process parameters (temperature, time, heating rate, type of biomass, activating agent, etc.). Several forms of bio‐based carbon materials including granules, pellets, tubes, and sheets can be produced. A variety of natural oxygenated surface functional groups in bio‐based carbon materials is useful for metal adsorption when used as a support. These functional groups can also enhance reactant adsorption in heterogeneous catalysis. Some bio‐based carbon materials are cheaper than commercial catalysts and supports, e.g. zeolite, silica, and alumina. Before going into the details on the applications of promising bio‐based carbon materials in a field of catalysis, some of their properties are summarized in Table 2.3.

Table 2.3 Comparison of typical physical and chemical properties of bio‐based carbon materials [30, 39, 43, 48].

Bio‐based carbon materials	Surface area (m2 g−1)	Pore volume (cm3 g−1)	Functional groups
Biochar	100–500	0.03–0.25	–COOH, –OH, C–H, C=C, C=O
Hydrochar	1–43	0.007–0.2	–OH, C=C, C=O, C–C, –CH2, –CH3
Activated carbon (chemical treatment)	400–2700	0.3–1.53	–OH, C–H, C=C, C–O
Activated carbon (physical treatment)	300–1000	0.1–0.99	–OH, C=O, C–O
Graphene	800–1800	0.3–0.9	C–H, C–OH, C=C
Sugar‐derived carbon	1–5	—	—
Carbon nanotube	300–600	2.5	–COOH, –OH