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

被引:0
|
作者
Jaspreet Kaur
Anil Kumar Sarma
Poonam Gera
Mithilesh Kumar Jha
机构
[1] Dr. B. R. Ambedkar National Institute of Technology,Department of Chemical Engineering
[2] Sardar Swaran Singh National Institute of Bio-Energy (An Autonomous Institute of MNRE,Chemical Conversion Division
[3] Government of India),undefined
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
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 m2/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.
引用
收藏
相关论文
共 50 条
  • [1] 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
    Kaur, Jaspreet
    Sarma, Anil Kumar
    Gera, Poonam
    Jha, Mithilesh Kumar
    SCIENTIFIC REPORTS, 2021, 11 (01)
  • [2] Conformational Analysis of 5-Ethyl-5-hydroxymethyl-2,2-dimethyl-1,3-dioxane
    Raskildina, G. Z.
    Spirikhin, L. V.
    Zlotskij, S. S.
    Kuznetsov, V. V.
    RUSSIAN JOURNAL OF ORGANIC CHEMISTRY, 2019, 55 (04) : 502 - 507
  • [3] Conformational Analysis of 5-Ethyl-5-hydroxymethyl-2,2-dimethyl-1,3-dioxane
    G. Z. Raskildina
    L. V. Spirikhin
    S. S. Zlotskij
    V. V. Kuznetsov
    Russian Journal of Organic Chemistry, 2019, 55 : 502 - 507
  • [4] ON THE SYNTHESIS AND ENANTIOMERIC PURITY OF (S)-4-ACETYL-2,2-DIMETHYL-1,3-DIOXOLANE
    TANNER, D
    SOMFAI, P
    SYNTHETIC COMMUNICATIONS, 1986, 16 (12) : 1517 - 1522
  • [5] 4R,5R)-bis(hydroxydimethylmethyl)-2,2-dimethyl-1,3-dioxolane
    Boyle, Grant A.
    Kruger, Hendrik G.
    Maguire, Glenn E. M.
    Rademeyer, Melanie
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2006, 62 : O4339 - O4341
  • [6] Synthesis of (+)-2,8-dihydroxyethyl-1,4,7,10-tetraoxaspiro[5.5]undecane from (R)-4-hydroxymethyl-2,2-dimethyl-1,3-dioxane
    SauretCladiere, S
    Jeminet, G
    TETRAHEDRON-ASYMMETRY, 1997, 8 (03) : 417 - 423
  • [7] Chiral capillary gas chromatography for the separation of the enantiomers of 4-chloromethyl-2,2-dimethyl-1,3-dioxolane
    Zhang Zhenyong
    CHINESE JOURNAL OF CHROMATOGRAPHY, 2023, 41 (12) : 1135 - 1140
  • [8] Synthesis of 5-tert-butyl-5-(1-hydroxy-2-methylpropyl)-2,2-dimethyl-1,3-dioxane
    Ju, XL
    Xiang, WS
    Fan, ZJ
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2005, 25 (03) : 332 - 334
  • [9] Microwave Dielectric Permittivity and the Relaxation of 1,3-Dioxolane and 2,2-Dimethyl-1,3-dioxolane-4-methanol Aqueous Solutions
    Lyashchenko, A. K.
    Balakaeva, I. V.
    Smirnova, N. A.
    Safonova, E. A.
    RUSSIAN JOURNAL OF PHYSICAL CHEMISTRY A, 2021, 95 (01) : 90 - 96
  • [10] Microwave Dielectric Permittivity and the Relaxation of 1,3-Dioxolane and 2,2-Dimethyl-1,3-dioxolane-4-methanol Aqueous Solutions
    A. K. Lyashchenko
    I. V. Balakaeva
    N. A. Smirnova
    E. A. Safonova
    Russian Journal of Physical Chemistry A, 2021, 95 : 90 - 96