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Process optimization with acid functionalised activated carbon derived from corncob for production of 4-hydroxymethyl-2,2-dimethyl-1,3-dioxolane and 5-hydroxy-2,2-dimethyl-1,3-dioxane

In this article, a two-step activated carbon preparation technique from corncob has been elucidated. The derived catalysts AAC-CC has been characterized using various techniques for the determination of their structural properties and compared with AC-CC, already reported with another article. The c...

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Detalles Bibliográficos
Autores principales: Kaur, Jaspreet, Sarma, Anil Kumar, Gera, Poonam, Jha, Mithilesh Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060369/
https://www.ncbi.nlm.nih.gov/pubmed/33883575
http://dx.doi.org/10.1038/s41598-021-87622-z
Descripción
Sumario:In this article, a two-step activated carbon preparation technique from corncob has been elucidated. The derived catalysts AAC-CC has been characterized using various techniques for the determination of their structural properties and compared with AC-CC, already reported with another article. The conjugated boat structure of AAC-CC resulted in a very high surface area (779.8 m(2)/g) and high pore volume (0.428 cc/g). This unveils the suitability of AAC-CC as better among the two catalytic pathways for solketal production. The activated carbons so prepared have been used for the valorization of glycerol to produce 2,2-Dimethyl-1,3-dioxolane-4-methanol (solketal), oxygenated additives to fuel. The face-centered composite design (FCCD) of RSM was applied for the optimization of the reaction parameters for the ketalisation reaction using AAC-CC as a catalyst. From the optimized results, the acidic catalyst AAC-CC resulted in a glycerol conversion, i.e. 80.3% under the actual laboratory experiment. Moreover, the catalyst could be reused for three consecutive batch reactions without (< 5%) much reduction of activity and no distinctive structural deformity.