Effect of Diluents on Extraction Equilibrium of trans-Aconitic Acid-Reference-Cited by-同舟云学术

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Effect of Diluents on Extraction Equilibrium of trans-Aconitic Acid

Published:2019-06-18 Issue:7 Volume:64 Page:2985-2996
ISSN:0021-9568
Container-title:Journal of Chemical & Engineering Data
language:en
Short-container-title:J. Chem. Eng. Data

Author:

Nimmakayala Rajesh¹,Pal Dharm¹^ORCID

Affiliation:

1. Department of Chemical Engineering, National Institute of Technology Raipur, Raipur 492010, Chhattisgarh, India

Funder

Chhattisgarh Council of Science and Technology

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jced.9b00059

Reference43 articles.

1. Cane molasses fermentation for continuous ethanol production in an immobilized cells reactor by Saccharomyces cerevisiae

2. Collier, D. W. Process of Treating Aconitic Acid Containing Plant Extracts. U.S. Patent 2,513,287, 1950.

3. Zapata, N. Aconitic Acid from Sugarcane: Production and Industrial Application. Ph.D. Dissertation, Louisiana State University, Baton Rouge, 2007.

4. Separation of aconitic acid from molasses by solvent extraction

5. FAO (2012) http://www.fao.org/fileadmin/templates/est/meetings/sugar_fiji_2012/Kaison_Chang_-_FAO_Policy_Overview.pdf (accessed on Feb 1, 2013).

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1. Reactive extraction for Succinic acid separation from model fermentation broth with tributylamine in 1-decanol;AIP Conference Proceedings;2024

2. Sustainable sugarcane vinasse biorefinement for trans-aconitic acid-based biopolymer synthesis and bioenergy generation;Bioresource Technology Reports;2021-09

3. Modeling and optimization of reactive extraction equilibria and kinetic study of gallic acid using tributyl phosphate in isoamyl alcohol;Separation Science and Technology;2020-04-20

4. Rapid microwave controlled polyesterification of aconitic acid and ethylene glycol;Polymer International;2020-03-06

5. Reactive separation of gallic acid using tributyl phosphate dissolved in 2-octanone, laurylalcohol and heptane;Chemical Data Collections;2020-02

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