Annealing of mesoporous silica loaded with silver nanoparticles within its pores from isothermal sorption

1998 ◽  
Vol 13 (10) ◽  
pp. 2888-2895 ◽  
Author(s):  
Weiping Cai ◽  
Lide Zhang ◽  
Huicai Zhong ◽  
Guoliang He

Influences of annealing on the structure of mesoporous silica loaded with silver (Ag) nanoparticles, and on the coarsening of Ag particles within pores of the host were investigated from isothermal sorption. Doping a small amount of Ag nanoparticles into pores of silica and subsequent annealing decreases the measured values of specific surface area and pore volume of porous silica significantly. This is attributed to the presence and coarsening of Ag particles within pores or channels between pores, which result in more and more isolated and unmeasured free spaces. The measured value of a specific surface area for the doped samples cannot represent the real value, which is, in fact, unable to be measured directly. During additional annealing, Ag particles within silica coarsen mainly according to the mechanism of formation of Ag adatoms on pore wall and diffusion of the adatoms along with pore walls. Only the larger particles located in the larger pores can continuously grow. The smaller particles and those located in the channels or pores with smaller dimension will disappear. The activation energy of the ripening process was estimated to be about 0.60 eV, and the migration barrier of Ag adatom on the pore wall of silica is about 0.10 eV.

2020 ◽  
Vol 1 (9) ◽  
pp. 3556-3564
Author(s):  
Lan She ◽  
Miao Sun ◽  
Xinfang Li ◽  
Anfeng Kang ◽  
Feng Yang ◽  
...  

Results indicated that the effect of MSNRs on cell viability and cellular oxidative stress was related to specific surface area.


2011 ◽  
Vol 22 (3) ◽  
pp. 731-739 ◽  
Author(s):  
Huanjun Zhou ◽  
Xiaohui Wu ◽  
Jie Wei ◽  
Xun Lu ◽  
Shuo Zhang ◽  
...  

2019 ◽  
Vol 280 ◽  
pp. 133-143 ◽  
Author(s):  
Laura M. Henning ◽  
Diego Díaz Cubas ◽  
Maria G. Colmenares ◽  
Johannes Schmidt ◽  
Maged F. Bekheet ◽  
...  

Energies ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 3445 ◽  
Author(s):  
Donghyeon Kim ◽  
Youngjin Seo ◽  
Juhyun Kim ◽  
Jeongmin Han ◽  
Youngsoo Lee

Coalbed methane (CBM) content is generally estimated using the isotherm theory between pressure and adsorbed amounts of methane. It usually determines the maximum content of adsorbed methane or storage capacity. However, CBM content obtained via laboratory experiment is not consistent with that in the in-situ state because samples are usually ground, which changes the specific surface area. In this study, the effect of the specific surface area relative to CBM content was investigated, and diffusion coefficients were estimated using equilibrium time analysis. The differences in adsorbed content with sample particle size allowed the determination of a specific surface area where gases can adsorb. Also, there was an equilibrium time difference between fine and lump coal, because more time is needed for the gas to diffuse through the coal matrix and adsorb onto the surface in lump coal. Based on this, we constructed a laboratory-scale simulation model, which matched with experimental results. Consequently, the diffusion coefficient, which is usually calculated through canister testing, can be easily obtained. These results stress that lump coal experiments and associated simulations are necessary for more reliable CBM production analysis.


2004 ◽  
Vol 77 (2) ◽  
pp. 214-226 ◽  
Author(s):  
G. R. Hamed ◽  
K.-C. Hua

Abstract A carboxylated nitrile rubber (XNBR) and a carboxylated SBR (XSBR) were mixed with zinc oxide particles of different specific surface areas (“S”, 35 m2/g; “M”, 3.5m2/g; “L”, 0.5 m2/g) and cure behavior at 165 ºC studied using oscillating disc rheometry. Without added zinc oxide, both raw rubbers slowly stiffen over many hours of heating. This is probably due to condensation of carboxyl groups to form anhydride crosslinks. XNBR compositions containing the finely divided “S” crosslink much more rapidly. Full cure is reached after about 10 minutes of heating. Cure rate decreases markedly as the specific surface area of the ZnO decreases. A composition containing “M” at twice stoichiometry requires about an hour to cure well, while with “L”, about 10 hours are required. In contrast, curing of the XSBR depends little on the specific surface area of the ZnO, either with “S” or “L”, curing is essentially complete after 30 minutes. After simply mixing ZnO into either rubber, it remains as a dispersed particulate. With XNBR, curing appears to be controlled by the rate of dissolution and diffusion of ZnO, while, with XSBR, reaction is not diffusion limited and may be confined to regions near particle surfaces.


2016 ◽  
Vol 123 ◽  
pp. 76-82 ◽  
Author(s):  
Zhu Shu ◽  
Tiantian Li ◽  
Jun Zhou ◽  
Yun Chen ◽  
Zimo Sheng ◽  
...  

2021 ◽  
Author(s):  
Qiang Chen ◽  
Kai Chen ◽  
Feng Yu ◽  
Aixia Guo ◽  
Siqing Zou ◽  
...  

Abstract High surface area mesoporous silica (SiO2) nanospheres has been considered an ideal material for the catalytic, adsorption and drug delivery. However, synthesis of ultra-high specific surface area mesoporous silica nanoparticles with well-defined sphere structure and small particle size (< 200 nm) is still challenging. Here, a two-stream confined jet impingement continuous microchannel reactor is proposed to produce novel mesoporous silica nanospheres (MSNs) with ultra-high specific surface area (SSA) and abundant worm-like meso-porosity. The as-obtained MSNs with worm-like mesoporous structure were produced with average particle diameter of 142 ~ 207 nm, high SSA of 1347 ~ 1854 m2/g, total pore volume of 0.86 ~ 1.23 cm3/g and pore diameter of 2.6 ~ 3.3nm. Moreover, the shear force field in the microchannel reactor on the mesoscopic structure of MSNs was simulated by mesoscopic kinetics. Additionally, MSNs was used as the silicon source to synthesize lithium silicate (Li4SiO4), which enhanced carbon dioxide (CO2) adsorption of 27.18 wt% at 650 ℃.


2021 ◽  
Author(s):  
Liangcai Wang ◽  
Xin Feng ◽  
Huanhuan Ma ◽  
Jielong Wu ◽  
Yu Chen ◽  
...  

Abstract This work provides an idea for efficient and harmless utilization of lignin and further evaluated the textural properties of lignin-derived activated carbon/specific capacitance relationship. The yield of cellulose-doped apricot shell lignin (ASLC) was 30.42%. H3PO4/KOH was used to assist the preparation of ASLC-derived activated carbon (AAC) for capacitors. The specific surface areas of the as-obtained AAC-P-3 and AAC-K-2 were 1475.16 m2/g and 2136.56 m2/g, respectively. The specific capacitances of AAC-P-3 and AAC-K-2 were 169.14 F/g and 236.00 F/g, respectively, upon the current density of 0.50 A/g. In capacitors containing aqueous KOH as the electrolyte, the AR2 (0.983) between specific surface area and specific capacitance was highest, followed by the AR2 (0.978) between Vmicro/Vmeso and specific capacitance, the AR2 (0.975) between pore-wall thickness and specific capacitance. Consequently, the specific capacitances of the AACs depend not only the specific surface area, but also on the Vmicro/Vmeso, pore-wall thickness, and Vmicro.


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