2014
DOI: 10.1016/j.memsci.2014.07.022
|View full text |Cite
|
Sign up to set email alerts
|

Study on characterization and pervaporation performance of interfacially polymerized polyamide thin-film composite membranes for dehydrating tetrahydrofuran

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
16
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 37 publications
(16 citation statements)
references
References 31 publications
0
16
0
Order By: Relevance
“…Subsequently, the solution was cast on the glass substrate with a casting knife, and the glass substrate was immediately immersed in a water bath. The obtained membrane was left in deionized water overnight to completely remove the residual solvent . Thickness of the PAN‐based membranes was maintained at 0.22 ± 0.02 mm.…”
Section: Methodsmentioning
confidence: 99%
“…Subsequently, the solution was cast on the glass substrate with a casting knife, and the glass substrate was immediately immersed in a water bath. The obtained membrane was left in deionized water overnight to completely remove the residual solvent . Thickness of the PAN‐based membranes was maintained at 0.22 ± 0.02 mm.…”
Section: Methodsmentioning
confidence: 99%
“…For instance, Lai and co-workers [5] used ethylenediamine (EDA), m-phenylenediamine (MPD), piperaine (PIP) and 1,6-hexanediamine (HDA) as reactant amines for interfacial reaction with trimesoyl chloride (TMC) to produce membranes for isopropanol dehydration, and they reported that the EDA/TMC membrane showed the best pervaporation performance among the membranes produced with the various amines [5]. They also prepared polyamide TFC membranes by reacting 1,3-diaminopropane (DAPE), 1,3-cyclohexanediamine (CHDA) and MPD with TMC for use in dehydration of tetrahydrofuran, and the DAPE/TMC membrane was found to exhibit the desirable pervaporation performance [6]. In addition, novel amines (e.g., 2,2′-dimethylbenzidine hydrochloride (m-tolidine-H) [7]) and acyl chlorides (e.g., 5-nitrobenzene-1,3-dioyl dichloride and 5-tert-butylbenzene-1,3-dioyl dichloride [8]) have been synthesized to produce interfacially polymerized membranes for ethanol dehydration.…”
Section: Introductionmentioning
confidence: 99%
“…For the CRF post-treatment at 30 °C, abundant pores in the membrane cross-section contributed to the water molecules quickly moving into the CRF coating and to the easy release of small urea molecules from the pores, which resulted in a high rate of nutrient release. High surface roughness of the membrane also led to low hydrophobicity 30 and increased water contact with the higher surface area of the membrane 31 , which also accelerated nutrient release. Post-treatment duration did not affect the controlled-release behavior, mainly because pore size and membrane cross-section thickness did not change significantly at the relative low temperature; although aziridine ring groups of the cross-linker can react with –COOH in waterborne polyacrylate emulsion at room temperature (e.g., 30 °C).…”
Section: Discussionmentioning
confidence: 99%