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Enhanced Proton Conductivity in Sulfonated Poly(ether ether ketone) Membranes by Incorporating Sodium Dodecyl Benzene
Shaoxiong Zhai1, Wenxu Dai2, Jun Lin3
1Beijing Key Laboratory of Energy Safety and Clean Utilization, North China Electric Power University, Beijing 102206, China. ncepuzhaisx@163.com.
Abstract:
It is of great importance to improve the proton conductivity of proton exchange membranes by easy-handling and cost-efficient approaches. In this work, we incorporated a commercially obtained surfactant, sodium dodecyl benzene sulfonate (SDBS), into sulfonated poly(ether ether ketone) (SPEEK) through solution casting to prepare SPEEK/SDBS membranes. When no more than 10 wt % SDBS was added, the SDBS was well dissolved into the SPEEK matrix, and the activation energy for the proton transfer in the SPEEK/SDBS membranes was greatly reduced, leading to significant enhancement of the membrane proton conductivity. Compared with the SPEEK control membrane, the SPEEK/SDBS membrane with 10 wt % SDBS showed a 78% increase in proton conductivity, up from 0.051 S cm-1 to 0.091 S cm-1, while the water uptake increased from 38% to 62%. Moreover, the SPEEK/SDBS membrane exhibited constant proton conductivity under a long-term water immersion test.
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Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent...
Crown Ethers
Physical Properties of Ethers
An ether molecule has a net dipole moment due to the polarity of C–O bonds. Subsequently, boiling points of ethers are lower than those of alcohols of comparable molecular weight and slightly higher than those of hydrocarbons of comparable molecular weight (Table 1).
Ethers can act as hydrogen bond acceptors, making them more water-soluble than hydrocarbons, but since ethers cannot act as hydrogen bond donors, they are much less soluble in water than alcohols. Ethers are considered...
Autoxidation of Ethers to Peroxides and Hydroperoxides

