Highly Efficient and Recyclable Catalysts for Cellobiose Hydrolysis: Systematic Comparison of Carbon Nanomaterials Functionalized With Benzyl Sulfonic Acids

Utilization of natural polymers has attracted increasing attention because of the consumption and over-exploitation of non-renewable resources, such as coal and oil. The development of green processing of cellulose, the most abundant biorenewable material on Earth, is urgent from the viewpoints of both sustainability and environmental protection. The discovery of the dissolution of cellulose in ionic liquids (ILs, salts which melt below 100 °C) provides new opportunities for the processing of this biopolymer, however, many fundamental and practical questions need to be answered in order to determine if this will ultimately be a green or sustainable strategy. In this critical review, the open fundamental questions regarding the interactions of cellulose with both the IL cations and anions in the dissolution process are discussed. Investigations have shown that the interactions between the anion and cellulose play an important role in the solvation of cellulose, however, opinions on the role of the cation are conflicting. Some researchers have concluded that the cations are hydrogen bonding to this biopolymer, while others suggest they are not. Our review of the available data has led us to urge the use of more chemical units of solubility, such as 'g cellulose per mole of IL' or 'mol IL per mol hydroxyl in cellulose' to provide more consistency in data reporting and more insight into the dissolution mechanism. This review will also assess the greenness and sustainability of IL processing of biomass, where it would seem that the choices of cation and anion are critical not only to the science of the dissolution, but to the ultimate 'greenness' of any process (142 references).

Carbon-based adsorbents such as graphene and its derivatives, carbon nanotubes, activated carbon, and biochar are often used to remove heavy metals from aqueous solutions. One of the important aspects of effective carbon adsorbents for heavy metals is their tunable surface functional groups. To promote the applications of functionalized carbon adsorbents in heavy metal removal, a systematic documentation of their syntheses and interactions with metals in aqueous solution is crucial. This work provides a comprehensive review of recent research on various carbon adsorbents in terms of their surface functional groups and the associated removal behaviors and performances to heavy metals in aqueous solutions. The governing removal mechanisms of carbon adsorbents to aqueous heavy metals are first outlined with a special focus on the roles of surface functional groups. It then summarizes and categorizes various synthesis methods that are commonly used to introduce heteroatoms, primarily oxygen, nitrogen, and sulfur, onto carbon surfaces for enhanced surface functionalities and sorptive properties to heavy metals in aqueous solutions. After that, the effects of various functional groups on adsorption behaviors of heavy metals onto the functionalized carbon adsorbents are elucidated. A perspective of future work on functional carbon adsorbents for heavy metal removal as well as other potential applications is also presented at the end.