In Situ Solvent Recovery by Organic Solvent Nanofiltration

2014 ◽  
Vol 2 (10) ◽  
pp. 2371-2379 ◽  
Author(s):  
Jeong F. Kim ◽  
Gyorgy Szekely ◽  
Marc Schaepertoens ◽  
Irina B. Valtcheva ◽  
Maria F. Jimenez-Solomon ◽  
...  
2018 ◽  
Vol 6 (45) ◽  
pp. 22987-22997 ◽  
Author(s):  
Yi Li ◽  
Shushan Yuan ◽  
Chen Zhou ◽  
Yan Zhao ◽  
Bart Van der Bruggen

Fabrication of a high flux organic solvent nanofiltration (OSN) membrane from aramid nanofibers (ANFs) with in situ incorporation of ANF/polyethyleneimine (PEI) microspheres.


2020 ◽  
Vol 8 (31) ◽  
pp. 15891-15899 ◽  
Author(s):  
Chenxu Wang ◽  
Chenxuan Li ◽  
Evan R. C. Rutledge ◽  
Sai Che ◽  
Jongbok Lee ◽  
...  

Organic solvent nanofiltration (OSN) membranes composed of aromatic porous polymer networks are fabricated by in situ cross-linking. They exhibit excellent chemical/structural stability, molecular-sieving selectivity, and high permeability for OSN.


2021 ◽  
Vol 420 ◽  
pp. 129338
Author(s):  
Pengpeng He ◽  
Song Zhao ◽  
Chenyue Mao ◽  
Ying Wang ◽  
Guangqing Ma ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1317
Author(s):  
Alena Krupková ◽  
Klára Kubátová ◽  
Lucie Červenková Šťastná ◽  
Petra Cuřínová ◽  
Monika Müllerová ◽  
...  

Three series of poly(ionic) carbosilane dendrimers peripherally functionalized with imidazolium groups substituted on N-3 with methyl, isopropyl and 2,6-diisopropylphenyl (Dipp) were prepared up to the 3rd generation together with model monovalent imidazolium iodides and used as N-heterocyclic carbene (NHC) precursors. Catalytic activity of model and dendritic NHCs generated in situ by deprotonation with DBU was tested in redox esterification of α,β-unsaturated aldehydes and the influence of substitution, dendrimer generation, temperature and substrate structure on the reaction outcome was evaluated. Dipp substituted NHCs showed high activity and selectivity in the reaction with primary alcohols. Effectiveness of organic solvent nanofiltration for the recycling of dendritic NHCs was demonstrated on the 1st generation Dipp substituted catalyst in model redox esterification of cinnamaldehyde with benzyl alcohol. A marked increase in both activity and selectivity in the first four reaction runs was observed and this improved performance was preserved in the following catalytic cycles.


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