Role of pore structure on the activity and stability of sulfide catalyst

2020 ◽  
Author(s):  
W. Chen ◽  
H. Nie ◽  
X. Long ◽  
M. Li ◽  
L. Zhang ◽  
...  
2020 ◽  
Vol 40 (7) ◽  
pp. 591-599
Author(s):  
Yaling Tian ◽  
Kai Liang ◽  
Yali Ji

AbstractThe citrate-based thermoset elastomer is a promising candidate for bone scaffold material, but the harsh curing condition made it difficult to fabricate porous structure. Recently, poly (1, 8-octanediol-co-Pluronic F127 citrate) (POFC) porous scaffold was creatively fabricated by chitin nanofibrils (ChiNFs) supported emulsion-freeze-casting. Thanks to the supporting role of ChiNFs, the lamellar pore structure formed by directional freeze-drying was maintained during the subsequent thermocuring. Herein, bioactive glass (BG) was introduced into the POFC porous scaffolds to improve bioactivity. It was found the complete replacement of ChiNF particles with BG particles could not form a stable porous structure; however, existing at least 15 wt% ChiNF could ensure the formation of lamellar pore, and the interlamellar distance increased with BG ratios. Thus, the BG granules did not contribute to the formation of pore structure like ChiNFs, however, they surely endowed the scaffolds with enhanced mechanical properties, improved osteogenesis bioactivity, better cytocompatibility as well as quick degradation rate. Reasonably adjusting BG ratios could balance the requirements of porous structure and bioactivity.


2010 ◽  
Vol 24 (5) ◽  
pp. 766-776 ◽  
Author(s):  
T. Rivas ◽  
E. Alvarez ◽  
M.J. Mosquera ◽  
L. Alejano ◽  
J. Taboada
Keyword(s):  

2018 ◽  
Author(s):  
Dong Feng ◽  
Xingfang Li ◽  
Chaojie Zhao ◽  
Jing Li ◽  
Qing Liu ◽  
...  

2020 ◽  
Vol 8 (1) ◽  
pp. 102921 ◽  
Author(s):  
Shinta Amelia ◽  
Wahyudi Budi Sediawan ◽  
Imam Prasetyo ◽  
Macarena Munoz ◽  
Teguh Ariyanto

2018 ◽  
Vol 8 (24) ◽  
pp. 6346-6359 ◽  
Author(s):  
Ji-Eun Min ◽  
Sungtak Kim ◽  
Geunjae Kwak ◽  
Yong Tae Kim ◽  
Seung Ju Han ◽  
...  

In a complex reaction system, in which gas, liquid, and solid catalysts work together, understanding the impact of mass transfer that varies with the catalyst pore structure is very challenging but also essential to designing selective catalysts.


2020 ◽  
Vol 7 (2) ◽  
pp. 38
Author(s):  
Leila Dehabadi ◽  
Abdalla H. Karoyo ◽  
Majid Soleimani ◽  
Wahab O. Alabi ◽  
Carey J. Simonson ◽  
...  

The role of chemical modification of pristine linen fiber (LF) on its physicochemical and adsorption properties is reported in this contribution. The surface and textural properties of the pristine LF and its peroxyacetic acid- (PAF) and chlorite-treated (CF) fiber forms were characterized by several complementary methods: spectroscopy (SEM, TEM, FT-IR, and XPS), thermal analysis (DSC and TGA), gas/water adsorption isotherms, and zeta potential (ξ). The results obtained reveal that the surface charge and textural properties (surface area and pore structure) of the LF material was modified upon chemical treatment, as indicated by changes in the biomass composition, morphology, ξ-values, and water/dye uptake properties of the fiber samples. Particularly, the pristine LF sample displays preferential removal efficiency (ER) of methylene blue (MB) dye with ER ~3-fold greater (ER~62%) as compared to the modified materials (CF or PAF; ER~21%), due to the role of surface charge of pectins and lignins present in pristine LF. At higher MB concentration, the relative ER values for LF (~19%) relative to CF or PAF (~16%) reveal the greater role of micropore adsorption sites due to the contributing effect of the textural porosity observed for the modified flax biomass at these conditions. Similar trends occur for the adsorption of water in the liquid vs. vapour phases. The chemical treatment of LF alters the polarity/charge of the surface functional groups, and pore structure properties of the chemically treated fibers, according to the variable hydration properties. The surface and textural properties of LF are altered upon chemical modification, according to the variable adsorption properties with liquid water (l) vs. water vapor (g) due to the role of surface- vs. pore-sites. This study contributes to an understanding of the structure-adsorption properties for pristine and oxidized flax fiber biomass. The chemical conversion of such biomass yields biomaterials with tunable surface and textural properties, as evidenced by the unique adsorption properties observed for pristine LF and its modified forms (CF and PAF). This study addresses knowledge gaps in the field by contributing insight on the relationship between structure and adsorption properties of such LF biomass in its pristine and chemically modified forms.


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