{"title":"Gas-Driven Porosity Control in Cellulose Acetate Membranes: Comparing Nitrogen and Carbon Dioxide for Micropore Formation.","authors":"Haram Ryu, Sang Wook Kang","doi":"10.1021/acs.biomac.5c00257","DOIUrl":null,"url":null,"abstract":"<p><p>Cellulose acetate (CA) is a widely used porous material in various industrial applications, and its processing methods have evolved. This study presents a novel approach to enhancing pore formation efficiency by substituting nitrogen (N<sub>2</sub>) with carbon dioxide (CO<sub>2</sub>), a gas with a higher quadrupole moment. This method was employed to fabricate lactic acid-plasticized CA membranes coated on polypropylene substrates, enabling control over pore size and porosity. Surface morphology was analyzed using scanning electron microscopy to observe structural changes before and after gas permeation, with respect to the type of gas used. Fourier-transform infrared spectroscopy was used to assess molecular changes induced by lactic acid addition and to investigate gas-specific differences in pore formation. Thermal stability was evaluated via thermogravimetric analysis in relation to pore development. Additionally, the porosity, Gurley values, and gas permeance were measured to compare the effects of N<sub>2</sub> and CO<sub>2</sub> on the physical properties of the membranes.</p>","PeriodicalId":30,"journal":{"name":"Biomacromolecules","volume":" ","pages":""},"PeriodicalIF":5.5000,"publicationDate":"2025-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomacromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.biomac.5c00257","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Cellulose acetate (CA) is a widely used porous material in various industrial applications, and its processing methods have evolved. This study presents a novel approach to enhancing pore formation efficiency by substituting nitrogen (N2) with carbon dioxide (CO2), a gas with a higher quadrupole moment. This method was employed to fabricate lactic acid-plasticized CA membranes coated on polypropylene substrates, enabling control over pore size and porosity. Surface morphology was analyzed using scanning electron microscopy to observe structural changes before and after gas permeation, with respect to the type of gas used. Fourier-transform infrared spectroscopy was used to assess molecular changes induced by lactic acid addition and to investigate gas-specific differences in pore formation. Thermal stability was evaluated via thermogravimetric analysis in relation to pore development. Additionally, the porosity, Gurley values, and gas permeance were measured to compare the effects of N2 and CO2 on the physical properties of the membranes.
期刊介绍:
Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine.
Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.