Biodegradable polymers have been more attractive for membrane materials, especially poly(lactic acid) (PLA) because they degrade in natural environment after use. In this study, the membranes were developed from a polymer blend of PLA and other biodegradable polymers, such as poly(butylene succinate) (PBS), poly(butylene adipate-co-terphthalate) (PBAT) and Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV). The membranes were formed via nonsolvent induced phase separation process using n-methyl-2-pyrrolidone (NMP) as a solvent and water as a nonsolvent. The pure water flux and BSA rejection were tested to determine the filtration performance of membranes. The microstructures and tensile strength of membranes were characterized by field emission scanning electron microscope (FE-SEM) and universal testing machine (UTM), respectively. All of membranes appeared finger-like and sponge-like structures in cross-section, and porous structure on surface. PLA/PHBV blend membranes had pure water flux and BSA rejection as high as PLA/PBS and PLA/PBAT blend membranes. The pure water flux and BSA rejection of the blend ratio (PLA/PHBV/NMP) of 15:1:84 were 65 l/m2•h and 79%, respectively.
Dental resin composite cements were prepared with simply mixing method of Part A and Part B. The material components in Part A were composed of Bis-GMA, TEDGMA, 4-META, SiO2 nanopowders and BPO. The components in Part B were Bis-GMA, TEDGMA, 4-META, SiO2 nanopowders and 2,2¢-(4-methylphenylimino) diethanol. Before using SiO2 nano-filler in the formulation of Part A and Part B, it had to be coated with methacryloxypropyltrimethoxysilane (MPS) which served as a silane coupling agent. Therefore, the optimum amount of MPS (1, 1.2, 1.5 and 2%) and SiO2 nano-filler (20, 27.27 and 33.33 wt%) used to fabricate the composites were investigated. The homogeneous mixture of Part A and Part B at mass fraction of 1:1 was formed into the bar shape with dimension of 25 mm x 2.0 mm x 2.0 mm and then cured under light source for 20 s. Then flexural strength was measured using the universal testing machine. Depth of cure was tested using mould which was perforated in cylindrical shape of 6 mm in depth and of 4 mm in diameter. The result showed that composite with 27.27 wt% of salinized SiO2 nanopowders by 1.5% of MPS showed the highest flexural strength of 65 MPa and depth of cure of more than 5 mm which were accepted according to ISO 4049. This study could be concluded that using a proper amount of MPS to silanize SiO2 nanopowders and using an optimum amount of SiO2 nanopowders significantly improved the flexural strength of dental resin composite cements.
In the natural gas separation plant, triethylene glycol (TEG) is used as a liquid desiccant dehydrator to absorb water vapor from the gas stream. Even though TEG can be recovered and reused in the process by evaporation and distillation, some of TEG still remains in wastewater of this recovery process. In this work, the polyethersulfone (PES-NTR 7450) membrane was chosen to test for TEG removal capacity on both cross-flow filtration and pervaporation systems. The morphology of membrane and the content of TEG were characterized by scanning electron microscope (SEM) and gas chromatography (GC), respectively. The synthesis wastewater with average TEG content of 5%, 10%, and 20% were used as feed. The increase of feed concentration was trend to increase of TEG rejection (17.49%, 43.29%, and 62.22%). In case of industrial wastewater, the average TEG content of 10.7% was monitored for feed. The high effectiveness of PES-NTR 7450 membrane to remove TEG was performed in pervaporation system. TEG rejection of 99% was achieved at the operation condition of feed temperature 28ºC and applied pressure 1 kg/cm2.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.