scholarly journals Proton Conductive, Low Methanol Crossover Cellulose-Based Membranes

Membranes ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 539
Author(s):  
Jamaliah Aburabie ◽  
Boor Lalia ◽  
Raed Hashaikeh

This work describes the development of sulfated cellulose (SC) polymer and explores its potential as an electrolyte-membrane for direct methanol fuel cells (DMFC). The fabrication of our membranes was initiated by the preparation of the novel sulfated cellulose solution via controlled acid hydrolysis of microcrystalline cellulose (MCC). Ion-conductive crosslinked SC membranes were prepared following a chemical crosslinking reaction. SC solution was chemically crosslinked with glutaraldehyde (GA) and cured at 30 °C to produce the aforementioned membranes. Effects of GA concentration on methanol permeability, proton conductivity, water uptake and thermal stabilities were investigated. The crosslinking reaction is confirmed by FTIR technique where a bond between the primary OH groups of cellulose and the GA aldehyde groups was achieved, leading to the increased hydrophobic backbone domains in the membrane. The results show that the time of crosslinking reaction highly affects the proton conduction and methanol permeability. The proton conductivity and methanol crossover (3M) of our GA crosslinked SC membranes are 3.7 × 10−2 mS cm−1 and 8.2 × 10−9 cm2 s−1, respectively. Crosslinked sulfated cellulose films have lower ion conductivity than the state-of-the-art Nafion (10.2 mS cm−1); however, the methanol crossover is three orders of magnitude lower than Nafion membranes (1.0 × 10−5 cm2 s−1 at 1 M). Such biofilms with high methanol resistivity address the major hurdle that prevents the widespread applications of direct alcohol fuel cells.

Nanomaterials ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 1292 ◽  
Author(s):  
Gutru Rambabu ◽  
Santoshkumar D. Bhat ◽  
Filipe M. L. Figueiredo

A membrane electrolyte that restricts the methanol cross-over while retaining proton conductivity is essential for better electrochemical selectivity in direct methanol fuel cells (DMFCs). Extensive research carried out to explore numerous blends and composites for application as polymer electrolyte membranes (PEMs) revealed promising electrochemical selectivity in DMFCs of carbon nanomaterial-based polymer composites. The present review covers important literature on different carbon nanomaterial-based PEMs reported during the last decade. The review emphasises the proton conductivity and methanol permeability of nanocomposite membranes with carbon nanotubes, graphene oxide and fullerene as additives, assessing critically the impact of each type of filler on those properties.


2009 ◽  
Vol 81 (12) ◽  
pp. 2309-2316 ◽  
Author(s):  
Yong Fang ◽  
Ruiying Miao ◽  
Tongtao Wang ◽  
Xindong Wang

A series of novel composite membranes was prepared by using poly(vinyl alcohol) (PVA) with polyimide (PI) as base material and 8-trimethoxysilylpropyl glycerine ether-1,3,6-pyrenetrisulfonic acid (TSGEPS) as proton conductor for direct methanol fuel cells (DMFCs). The parameters of membranes, including water sorption, hydrolysis stability, dimensional stability, proton conductivity, and methanol permeability were studied. The proton conductivity of the membranes is in the order of 10–2 S/cm, and the membranes show better resistance to methanol permeability (1.51 × 10–7 cm2 s–1) and better selectivity (20.6 × 104 S cm–3 s) than those of Nafion115 under the same measurement conditions.


2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
Apiradee Sanglimsuwan ◽  
Narumon Seeponkai ◽  
Jatuphorn Wootthikanokkhan

Electrolyte nanocomposite membranes for proton exchange membrane fuel cells and direct methanol fuel cells were prepared by carrying out a sulfonation of poly(vinyl alcohol) with sulfosuccinic acid and adding a type of organically modified montmorillonite (layered silicate nanoclay) commercially known as Cloisite 93A. The effects of the different concentrations (0, 2, 4, 6, 8 wt. %) of the organoclay in the membranes on water uptake, ion exchange capacity (IEC), proton conductivity, and methanol permeability were measured, respectively, via gravimetry, titration, impedance analysis, and gas chromatography techniques. The IEC values remained constant for all concentrations. Water uptakes and proton conductivities of the nanocomposite membranes changed with the clay content in a nonlinear fashion. While all the nanocomposite membranes had lower methanol permeability than Nafion115, the 6% concentration of Cloisite 93A in sulfonated poly(vinyl alcohol) membrane displayed the greatest proton conductivity to methanol permeability ratio.


2021 ◽  
pp. 095400832110394
Author(s):  
Yan Ma ◽  
Kaixu Ren ◽  
Ziqiu Zeng ◽  
Mengna Feng ◽  
Yumin Huang

To improve the performances of sulfonated poly (arylene ether nitrile) (SPEN)–based proton exchange membranes (PEMs) in direct methanol fuel cells (DMFCs), the copper phthalocyanine grafted graphene oxide (CP-GO) was successfully prepared via in situ polymerization and subsequently incorporated into SPEN as filler to fabricate a series of SPEN/CP-GO-X (X represents for the mass ratio of CP-GO) composite membranes. The water absorption, swelling ratio, mechanical properties, proton conductivity, and methanol permeability of the membranes were systematically studied. CP-GO possesses good dispersion and compatibility with SPEN matrix, which is propitious to the formation of strong interfacial interactions with the SPEN, so as to provide more efficient transport channels for proton transfer in the composite membranes and significantly improve the proton conductivity of the membranes. Besides, the strong π–π conjugation interactions between CP-GO and SPEN matrix can make the composite membranes more compact, blocking the methanol transfer in the membranes, and significantly reducing the methanol permeability. Consequently, the SPEN/CP-GO-1 composite membrane displayed outstanding tensile strength (58 MPa at 100% RH and 25°C), excellent proton conductivity (0.178 S cm−1 at 60°C), and superior selectivity (5.552 × 105 S·cm−3·s). This study proposed a new method and strategy for the preparation of high performance PEMs.


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