The increasing demand for high-purity hydrogen (H) as renewable energy sources is driving advancements in membrane technology, which is essential for achieving efficient gas separation. Polyimide (PI) membranes have become an emerging option for H/CO separation due to its excellent thermal stability and stability under harsh conditions. However, the neat PI membrane suffers performance loss due to CO plasticization effect and an encountered trade-off limit between permeability and selectivity. Therefore, membrane modification by crosslinking and blending emerged as a recent strategy to enhance the membrane's performance and properties. This paper provides: (1) An overview of the possible method to do the modification in PI membranes, including the advantages and challenges of the membrane modification types; (2) As blending and crosslinking is the most popular modification for the PI membrane, their roles in enhancing membrane properties for improved H/CO separation are discussed; (3) The critical parameters of the blending and crosslinking processes are also clarified for the optimal purification process; (4) The future outlook for H/CO separation using membrane technology is discussed, aiming to provide commercialization strategy for optimal H/CO separation. Thus, this review could provide guidelines for the readers to implement changes that significantly enhance the membrane's features for high-purity H production.
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http://dx.doi.org/10.3390/polym17050615 | DOI Listing |
RSC Adv
February 2025
Center for Computational Quantum Chemistry, University of Georgia Athens Georgia 30602 USA
The structures and energetics of the binuclear cyclopentadienylmetal alkyne systems CpMCR (M = Ni, Co, Fe; R = Me and NMe) have been investigated using density functional theory. For the CpMC(NMe) (M = Ni, Co, Fe) systems the relative energies of isomeric tetrahedrane CpM(alkyne) structures having intact alkyne ligands and alkyne dichotomy structures CpM(CNMe) in which the C[triple bond, length as m-dash]C triple bond of the alkyne has broken completely to give separate MeNC units depending on the central metal atoms. For the nickel system CpNiC(NMe) as well as the related nickel systems CpNi(MeCNMe) and CpNiCMe the tetrahedrane structures are clearly preferred energetically consistent with the experimental syntheses of several stable CpNi(alkyne) complexes.
View Article and Find Full Text PDFMar Pollut Bull
December 2024
School of Science and Technology, Hong Kong Metropolitan University, Hong Kong; State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong. Electronic address:
Omics technology has been employed in recent research on algicidal bacteria, but previous transcriptomic studies mainly focused on bacteria or algae, neglecting their interaction. This study explores interactions between algicidal bacterium Maribacter dokdonesis P4 and target alga Karenia mikimotoi KMHK using proteomics. Proteomics responses of KMHK after co-culture with P4 in separate compartments of the transwell for 8 and 24 h were evaluated using tandem mass tags (TMT) proteomics, and changes of P4 proteomics were also assessed.
View Article and Find Full Text PDFJ Phycol
February 2024
Laboratory of Molecular Environmental Microbiology, Department of Environmental Science and Ecological Engineering, Korea University, Seoul, Republic of Korea.
Respir Investig
July 2023
Department of Palliative Medicine, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Hyogo 650-0017, Japan.
Background: Supplemental oxygen is widely used for dyspnea relief; however, its efficacy is yet to be verified. This study aimed to determine the efficacy of supplemental oxygen for dyspnea relief in patients with advanced progressive illness.
Methods: In this systematic review, several databases, including MEDLINE and EMBASE, were searched to identify eligible randomized controlled trials (RCTs) on the topic published up to September 23, 2019.
Phys Chem Chem Phys
March 2023
Department of Applied Chemistry, National Chiayi University, Chiayi 60004, Taiwan.
The element effects of Lewis acid (LA) and Lewis base (LB) on the potential energy surfaces of [2+5] cycloaddition reactions of norbornene-based G14/P-based (G14 = group 14 element) and Si/G15-based (G15 = group 14 element) frustrated Lewis pair (FLP)-type molecules with benzaldehyde were theoretically examined density functional theory and several sophisticated methods. The theoretical findings indicated that among the above nine norbornene-linked G14/G15-based FLPs, only the Si/N-Rea, Si/P-Rea, and Si/As-Rea FLP-assisted compounds can readily undergo cycloaddition reactions with doubly bonded organic systems from kinetic and thermodynamic viewpoints. The energy decomposition analysis showed that the bonding interactions between the norbornene-based G14/G15-FLPs and benzaldehyde are better described in terms of the singlet-singlet model (donor-acceptor model) rather than the triplet-triplet model (electron-sharing model).
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