Optical Response of Mesoporous Silica Layer on Plasmonic Array to Isopropanol Vapor

Author(s):  
Shunsuke Murai ◽  
Hiroyuki Sakamoto ◽  
Koji Fujita ◽  
Katsuhisa Tanaka
Nanomaterials ◽  
2018 ◽  
Vol 9 (1) ◽  
pp. 35 ◽  
Author(s):  
Anna Mutschler ◽  
Vivian Stock ◽  
Lena Ebert ◽  
Emma Björk ◽  
Kerstin Leopold ◽  
...  

Trace-level detection of mercury in waters is connected with several complications including complex multistep analysis routines, applying additional, harmful reagents increasing the risk of contamination, and the need for expensive analysis equipment. Here, we present a straightforward reagent-free approach for mercury trace determination using a novel thin film sampling stick for passive sampling based on gold nanoparticles. The nanoparticles supported on a silicon wafer and further covered with a thin layer of mesoporous silica. The mesoporous silica layer is acting as a protection layer preventing gold desorption upon exposure to water. The gold nanoparticles are created by thermal treatment of a homogenous gold layer on silicon wafer prepared by vacuum evaporation. This gold-covered substrate is subsequently covered by a layer of mesoporous silica through dip-coating. Dissolved mercury ions are extracted from a water sample, e.g., river water, by incorporation into the gold matrix in a diffusion-controlled manner. Thus, the amount of mercury accumulated during sampling depends on the mercury concentration of the water sample, the accumulation time, as well as the size of the substrate. Therefore, the experimental conditions can be chosen to fit any given mercury concentration level without loss of sensitivity. Determination of the mercury amount collected on the stick is performed after thermal desorption of mercury in the gas phase using atomic fluorescence spectrometry. Furthermore, the substrates can be re-used several tens of times without any loss of performance, and the batch-to-batch variations are minimal. Therefore, the nanogold-mesoporous silica sampling substrates allow for highly sensitive, simple, and reagent-free determination of mercury trace concentrations in waters, which should also be applicable for on-site analysis. Successful validation of the method was shown by measurement of mercury concentration in the certified reference material ORMS-5, a river water.


2008 ◽  
Vol 607 ◽  
pp. 30-33 ◽  
Author(s):  
Laszlo Lizkay ◽  
C. Corbel ◽  
P. Perez ◽  
P. Desgardin ◽  
Marie France Barthe ◽  
...  

Positron annihilation gamma energy distribution, lifetime spectroscopy and time-of-flight method were used to study surfactant-templated mesoporous silica films deposited on glass. The lifetime depth profiling was correlated to Doppler broadening and 3γ annihilation fraction measurements to determine the annihilation characteristics inside the films. A set of consistent fingerprints for positronium annihilation, o-Ps reemission into vacuum, and pore size was directly determined. The lifetime measurements were performed in reflection mode with a specially designed lifetime spectrometer mounted on a slow positron beam system. The intensity of the 142 ns vacuum lifetime component was recorded as a function of the energy of the positron beam. In a film with high porosity a reemission efficiency of as high as 40 % was found at low positron energy. Positron lifetime in samples capped by a thin silica layer was used to determine the pore size. The energy of the reemitted o-Ps fraction was measured by a time-of-flight detector, mounted on the same system, allowing determination of both o-Ps re-emission efficiency and energy in the same sample. We demonstrate the potential of the simultaneous use of different positron annihilation techniques in the study of thin porous films.


2019 ◽  
Vol 241 ◽  
pp. 196-204 ◽  
Author(s):  
Tommy Haynes ◽  
Ovidiu Ersen ◽  
Vincent Dubois ◽  
Didier Desmecht ◽  
Keizo Nakagawa ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 12 ◽  
Author(s):  
Xiaohui Wang ◽  
Xin Ding ◽  
Houbing Zou

The channel lengths of mesoporous materials have a crucial impact on the catalytic performances of as-loaded active components. However, it remains a challenge to precisely tune the mesochannel length in a wide range from ≤50 nm to 200 nm. In this paper, we developed a top-down strategy, that is to say, crushing hollow microspheres, for preparing mesoporous silica nanosheets (MSSs) with perpendicular mesochannels and tunable thicknesses. Owing to the heterogeneous growth of the mesoporous silica layer on the surfaces of polystyrene microspheres (hard template), it was achieved to regulate the mesochannel length continuously in the range of 20–200 nm. The obtained materials were characterized by X-ray diffraction (XRD), nitrogen sorption, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The effect of channel lengths on the catalytic activity of metal nanoparticles was then investigated in the selective hydrogenation reaction of nitroarenes. It was found that a short channel not only favored dispersing metal nanoparticles uniformly and then avoiding pore blocking, but also improved the accessibility of metal nanoparticles largely during reactions.


2010 ◽  
Vol 64 (12) ◽  
pp. 1383-1386 ◽  
Author(s):  
Min Zhang ◽  
Xihao Zhang ◽  
Xiwen He ◽  
Langxing Chen ◽  
Yukui Zhang

2017 ◽  
Vol 243 ◽  
pp. 1205-1213 ◽  
Author(s):  
Dániel Sebők ◽  
László Janovák ◽  
Dániel Kovács ◽  
András Sápi ◽  
Dorina G. Dobó ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1073
Author(s):  
Jingxin Zhu ◽  
Haijuan Wu ◽  
Ding Wang ◽  
Yanlong Ma ◽  
Lan Jia

This paper presents a facile and low-cost strategy for fabrication lysozyme-loaded mesoporous silica nanotubes (MSNTs) by using silk fibroin (SF) nanofiber templates. The “top-down method” was adopted to dissolve degummed silk in CaCl2/ formic acid (FA) solvent, and the solution containing SF nanofibrils was used for electrospinning to prepare SF nanofiber templates. As SF contains a large number of -OH, -NH2 and -COOH groups, the silica layer could be easily formed on its surface by the Söber sol-gel method without adding any surfactant or coupling agent. After calcination, the MSNTs were obtained with inner diameters about 200 nm, the wall thickness ranges from 37 ± 2 nm to 66 ± 3 nm and the Brunauer–Emmett–Teller (BET) specific surface area was up to 200.48 m2/g, the pore volume was 1.109 cm3/g. By loading lysozyme, the MSNTs exhibited relatively high drug encapsulation efficiency up to 31.82% and an excellent long-term sustained release in 360 h (15 days). These results suggest that the MSNTs with the hierarchical structure of mesoporous and macroporous will be a promising carrier for applications in biomacromolecular drug delivery systems.


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