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Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture

Research output: Contribution to conference - Without ISBN/ISSN Abstractpeer-review

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Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture. / Bhuiyan, Md Masud Rana; Saha, Basu.
2023. 8 Abstract from IChemE Fluid Separations Special Interest Group (FSSIG) organised one day symposium - What’s New in Fluid Separations?, Lancaster, United Kingdom.

Research output: Contribution to conference - Without ISBN/ISSN Abstractpeer-review

Harvard

Bhuiyan, MMR & Saha, B 2023, 'Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture', IChemE Fluid Separations Special Interest Group (FSSIG) organised one day symposium - What’s New in Fluid Separations?, Lancaster, United Kingdom, 28/06/23 - 28/06/23 pp. 8.

APA

Bhuiyan, M. M. R., & Saha, B. (2023). Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture. 8. Abstract from IChemE Fluid Separations Special Interest Group (FSSIG) organised one day symposium - What’s New in Fluid Separations?, Lancaster, United Kingdom.

Vancouver

Bhuiyan MMR, Saha B. Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture. 2023. Abstract from IChemE Fluid Separations Special Interest Group (FSSIG) organised one day symposium - What’s New in Fluid Separations?, Lancaster, United Kingdom.

Author

Bhuiyan, Md Masud Rana ; Saha, Basu. / Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture. Abstract from IChemE Fluid Separations Special Interest Group (FSSIG) organised one day symposium - What’s New in Fluid Separations?, Lancaster, United Kingdom.1 p.

Bibtex

@conference{64914d2527e442fb9a08110a45d6d01c,
title = "Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture",
abstract = "Alkene epoxidation has been established as an important process for chemical synthesis as the resultant epoxide acts as a raw material or intermediate that can be transformed into many useful substances such as plasticizers, perfumes, and epoxy resins. The conventional epoxidation process involves stoichiometric peracids as oxidising agents, but it is not environmentally friendly. In contrast, polymer-supported heterogeneous catalysts with tert-butyl hydroperoxide (TBHP) as an oxidant have demonstrated strong catalytic activity and product selectivity. In this study, an efficient and selective polybenzimidazole-supported molybdenum (VI) complex (PBI.Mo) was used for the batch epoxidation of 1,5-hexadiene and 1,7-octadiene. Response surface methodology (RSM) using Box-Behnken Design (BBD) was employed for designing experimental runs and studying the interaction effect of different variables including reaction feed molar ratio of alkene to TBHP, reaction temperature, catalyst loading, and reaction time on the percentage yield of the reaction. Batch epoxidation of 1,5-hexadiene and 1,7-octadiene with TBHP as an oxidant in the presence of polymer-supported Mo(VI) catalyst was conducted in a classical batch reactor. The products were separated from the batch reaction mixtures and collected at regular intervals from reaction mixtures and analysed using Shimadzu GC-2014 gas chromatography. Design Expert software was used to develop the numerical optimisation step by combining the desirability of each independent variable into a single value and then searching for optimum values for the response goals. To validate the optimal response values of the predicted quadratic equation, batch experiments were performed at optimum conditions. The reusability studies of PBI.Mo catalysts have been performed in order to reduce production costs and consider large-scale industrial applications. Experimental results for epoxidation reaction showed that the catalyst could be used several times without any appreciable decrease in the conversion of TBHP for batch experiments. This study demonstrates that PBI.Mo complex could be used as an effective catalyst for a greener and more efficient epoxidation of alkenes with TBHP as an oxidising reagent.",
keywords = "tert-butyl hydroperoxide (TBHP), epoxidation, polymer-supported Mo(VI) catalyst, Response surface methodology (RSM), 1,5-hexadiene, 1,7-octadiene",
author = "Bhuiyan, {Md Masud Rana} and Basu Saha",
year = "2023",
month = jun,
day = "28",
language = "English",
pages = "8",
note = "IChemE Fluid Separations Special Interest Group (FSSIG) organised one day symposium - What{\textquoteright}s New in Fluid Separations? ; Conference date: 28-06-2023 Through 28-06-2023",
url = "https://www.icheme.org/membership/communities/special-interest-groups/fluid-separations/events/28-06-23-whats-new-in-fluid-separations/",

}

RIS

TY - CONF

T1 - Optimisation of greener alkene epoxidation via response surface methodology for effective separation of epoxides from the reaction mixture

AU - Bhuiyan, Md Masud Rana

AU - Saha, Basu

PY - 2023/6/28

Y1 - 2023/6/28

N2 - Alkene epoxidation has been established as an important process for chemical synthesis as the resultant epoxide acts as a raw material or intermediate that can be transformed into many useful substances such as plasticizers, perfumes, and epoxy resins. The conventional epoxidation process involves stoichiometric peracids as oxidising agents, but it is not environmentally friendly. In contrast, polymer-supported heterogeneous catalysts with tert-butyl hydroperoxide (TBHP) as an oxidant have demonstrated strong catalytic activity and product selectivity. In this study, an efficient and selective polybenzimidazole-supported molybdenum (VI) complex (PBI.Mo) was used for the batch epoxidation of 1,5-hexadiene and 1,7-octadiene. Response surface methodology (RSM) using Box-Behnken Design (BBD) was employed for designing experimental runs and studying the interaction effect of different variables including reaction feed molar ratio of alkene to TBHP, reaction temperature, catalyst loading, and reaction time on the percentage yield of the reaction. Batch epoxidation of 1,5-hexadiene and 1,7-octadiene with TBHP as an oxidant in the presence of polymer-supported Mo(VI) catalyst was conducted in a classical batch reactor. The products were separated from the batch reaction mixtures and collected at regular intervals from reaction mixtures and analysed using Shimadzu GC-2014 gas chromatography. Design Expert software was used to develop the numerical optimisation step by combining the desirability of each independent variable into a single value and then searching for optimum values for the response goals. To validate the optimal response values of the predicted quadratic equation, batch experiments were performed at optimum conditions. The reusability studies of PBI.Mo catalysts have been performed in order to reduce production costs and consider large-scale industrial applications. Experimental results for epoxidation reaction showed that the catalyst could be used several times without any appreciable decrease in the conversion of TBHP for batch experiments. This study demonstrates that PBI.Mo complex could be used as an effective catalyst for a greener and more efficient epoxidation of alkenes with TBHP as an oxidising reagent.

AB - Alkene epoxidation has been established as an important process for chemical synthesis as the resultant epoxide acts as a raw material or intermediate that can be transformed into many useful substances such as plasticizers, perfumes, and epoxy resins. The conventional epoxidation process involves stoichiometric peracids as oxidising agents, but it is not environmentally friendly. In contrast, polymer-supported heterogeneous catalysts with tert-butyl hydroperoxide (TBHP) as an oxidant have demonstrated strong catalytic activity and product selectivity. In this study, an efficient and selective polybenzimidazole-supported molybdenum (VI) complex (PBI.Mo) was used for the batch epoxidation of 1,5-hexadiene and 1,7-octadiene. Response surface methodology (RSM) using Box-Behnken Design (BBD) was employed for designing experimental runs and studying the interaction effect of different variables including reaction feed molar ratio of alkene to TBHP, reaction temperature, catalyst loading, and reaction time on the percentage yield of the reaction. Batch epoxidation of 1,5-hexadiene and 1,7-octadiene with TBHP as an oxidant in the presence of polymer-supported Mo(VI) catalyst was conducted in a classical batch reactor. The products were separated from the batch reaction mixtures and collected at regular intervals from reaction mixtures and analysed using Shimadzu GC-2014 gas chromatography. Design Expert software was used to develop the numerical optimisation step by combining the desirability of each independent variable into a single value and then searching for optimum values for the response goals. To validate the optimal response values of the predicted quadratic equation, batch experiments were performed at optimum conditions. The reusability studies of PBI.Mo catalysts have been performed in order to reduce production costs and consider large-scale industrial applications. Experimental results for epoxidation reaction showed that the catalyst could be used several times without any appreciable decrease in the conversion of TBHP for batch experiments. This study demonstrates that PBI.Mo complex could be used as an effective catalyst for a greener and more efficient epoxidation of alkenes with TBHP as an oxidising reagent.

KW - tert-butyl hydroperoxide (TBHP)

KW - epoxidation

KW - polymer-supported Mo(VI) catalyst

KW - Response surface methodology (RSM)

KW - 1,5-hexadiene

KW - 1,7-octadiene

M3 - Abstract

SP - 8

T2 - IChemE Fluid Separations Special Interest Group (FSSIG) organised one day symposium - What’s New in Fluid Separations?

Y2 - 28 June 2023 through 28 June 2023

ER -