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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Maximizing Ether Oxygen Content in Polymers for Membrane CO2 Removal from Natural Gas
Junyi Liu1, Gengyi Zhang1, Krysta Clark1
1Department of Chemical and Biological Engineering , University at Buffalo, The State University at New York , Buffalo , New York 14260 , United States.
New rubbery polymers offer superior carbon dioxide (CO2) removal from natural gas. These materials overcome limitations of traditional glassy polymers, providing high CO2/methane (CH4) selectivity unaffected by contaminants.
Area of Science:
- Materials Science
- Chemical Engineering
- Polymer Chemistry
Background:
- Glassy polymers are standard for CO2/CH4 separation but face challenges.
- Competitive sorption and physical aging reduce efficiency and lifespan.
Purpose of the Study:
- To design novel rubbery polymers for CO2 removal from natural gas.
- To overcome limitations of existing glassy polymer membranes.
Main Methods:
- Synthesized rubbery polymers with high ether/ester oxygen to carbon ratios (up to 0.8) using 1,3-dioxolane and 1,3,5-trioxane.
- Incorporated polar groups in short branches to ensure amorphous and rubbery characteristics.
- Tested polymer performance in simulated natural gas with varying hexane content at 50 °C.
Main Results:
- Developed a polymer (P71) with an O/C ratio of 0.71 exhibiting high CO2 permeability (320 Barrers) and CO2/CH4 selectivity (21).
- Achieved solubility-selective CO2/gas separation unaffected by heavy hydrocarbons.
- Demonstrated stable gas permeability over time, avoiding physical aging issues.
Conclusions:
- The novel rubbery polymers exhibit excellent CO2/CH4 separation performance exceeding the upper bound limit.
- These materials offer a promising solution for efficient and durable CO2 capture from natural gas.
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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.
Crown Ethers
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...
Stereotype Content Model

