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Julien Estager

Publications -  7
Citations -  386

Julien Estager is an academic researcher. The author has contributed to research in topics: Dimethyl carbonate & Pervaporation. The author has an hindex of 7, co-authored 7 publications receiving 200 citations.

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Continuous Flow Upgrading of Selected C2-C6 Platform Chemicals Derived from Biomass.

TL;DR: The aim of this review is to illustrate the various aspects of upgrading bio-based platform molecules toward commodity or specialty chemicals using new process concepts that fall under the umbrella of continuous flow technology and that could change the future perspectives of biorefineries.
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Sustaining the Transition from a Petrobased to a Biobased Chemical Industry with Flow Chemistry

TL;DR: This review considers representative continuous flow processes which utilize a selection of currently popular platform molecules that target industrially relevant building blocks, including commodity chemicals, specialty and fine chemicals, and fuels and fuel additives.
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Sorption and pervaporation study of methanol/dimethyl carbonate mixture with poly(etheretherketone) (PEEK-WC) membrane

TL;DR: In this article, a dense membrane prepared by using a modified poly ether ether ketone (PEEK-WC) polymer was studied for the pervaporation separation of a binary mixture of DMC and methanol.
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Supported ionic liquid membranes for the separation of methanol/dimethyl carbonate mixtures by pervaporation

TL;DR: In this paper, two supported ionic liquid membranes (SILM) based on 1-octyl-3methylimidazolium bis(trifluoromethanesulfonyl)imide ([C8MIM][NTf2]) and N-Octyl-N-methylpyrrolidinium bis (triuoromethemulfoenyl)imides ([C 8C 1Pyrr][NT f2]) were prepared and studied for the pervaporation separation of binary mixtures of DMC/m
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Versatile and scalable synthesis of cyclic organic carbonates under organocatalytic continuous flow conditions

TL;DR: In this article, cyclic organic carbonates are prepared according to alternative sustainable and intensified continuous flow conditions from the corresponding 1,2-diols, using dimethyl carbonate (DMC) as a low toxicity carbonation reagent and relying on the organocatalytic activity of widely available and cheap organic ammonium and phosphonium salts.