scholarly journals Preparation of Triple-Functionalized Montmorillonite Layers Promoting Thermal Stability of Polystyrene

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2170
Author(s):  
Chengcheng Yu ◽  
Xu Hu ◽  
Shichao Lu ◽  
Yangchuan Ke ◽  
Jianbin Luo

The objective of this study was to investigate the effect of three different treatments on the morphology, microstructure, and the thermal characteristics of a montmorillonite (Mt) sample, by using hydrochloric acid (HCl), tributyl tetradecyl phosphonium chloride (TTPC) surfactant, and γ-methacryloxypropyltrimethoxysilane (γ-MPS). The resultant nanofillers were characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD), transmission electron microscopy (TEM), nitrogen adsorption–desorption analysis, X-ray fluorescence spectrometry (XRF), and thermogravimetric analysis (TGA). The results showed that the amount of chemical grafting of the γ-MPS was increased after the acid treatment, whereas the amount of intercalation of the TTPC surfactant was decreased. The preintercalation of TTPC or silylation of γ-MPS, for the Mt sample, had a certain hindrance effect on its subsequent silylation or intercalation treatments. Furthermore, the effect of four different nanofillers on the thermal stability properties of the polystyrene (PS) matrix were also investigated. The results showed an increase in thermal stability for the triple-functionalized Mt, compared with the double-functionalized samples. The onset decomposition temperatures and the maximum mass loss temperatures of the PS nanocomposites were increased by 27 °C and 32 °C, respectively, by the incorporation of triple-modified Mt, as a result of the good exfoliation and dispersion of the nanolayers, more favorable polymer–nanofiller interaction, as well as the formation of a more remarkable tortuous pathway in the continuous matrix.

2005 ◽  
Vol 20 (10) ◽  
pp. 2682-2690 ◽  
Author(s):  
Yufang Zhu ◽  
Weihua Shen ◽  
Xiaoping Dong ◽  
Jianlin Shi

A stable mesoporous multilamellar silica vesicle (MSV) was developed with a gallery pore size of about 14.0 nm. A simulative enzyme, hemoglobin (Hb), was immobilized on this newly developed MSV and a conventional mesoporous silica material SBA-15. The structures and the immobilization of Hb on the mesoporous supports were characterized with x-ray diffraction, transmission electron microscopy, N2 adsorption-desorption isotherms, Fourier transform infrared, ultraviolet-visible spectroscopy, and so forth. MSV is a promising support for immobilizing Hb due to its large pore size and high Hb immobilization capacity (up to 522 mg/g) compared to SBA-15 (236 mg/g). Less than 5% Hb was leached from Hb/MSV at pH 6.0. The activity study indicated that the immobilized Hb retained most peroxidase activity compared to free Hb. Thermal stability of the immobilized Hb was improved by the proctetive environment of MSV and SBA-15. Such an Hb-mesoporous support with high Hb immobilization capacity, high activity, and enhanced thermal stability will be attractive for practical applications.


1998 ◽  
Vol 514 ◽  
Author(s):  
M. F. Wu ◽  
A. Vantomne ◽  
S. Hogg ◽  
H. Pattyn ◽  
G. Langouche ◽  
...  

ABSTRACTThe Nd-disilicide, which exists only in a tetragonal or an orthorhombic structure, cannot be grown epitaxially on a Si(111) substrate. However, by adding Y and using channeled ion beam synthesis, hexagonal Nd0.32Y0.68Si1.7 epilayers with lattice constant of aepi = 0.3915 nm and cepi = 0.4152 nm and with good crystalline quality (χmin of Nd and Y is 3.5% and 4.3 % respectively) are formed in a Si(111) substrate. This shows that the addition of Y to the Nd-Si system forces the latter into a hexagonal structure. The epilayer is stable up to 950 °C; annealing at 1000 °C results in partial transformation into other phases. The formation, the structure and the thermal stability of this ternary silicide have been studied using Rutherford backscattering/channeling, x-ray diffraction and transmission electron microscopy.


2017 ◽  
Vol 373 ◽  
pp. 299-302
Author(s):  
Bo Zhou ◽  
Chong Yang Li ◽  
Ning Qi ◽  
Zhi Quan Chen

Porous ZnO were synthesized with soft template method using zinc acetate Zn (CH3COO)2·2H2O as precursor and block copolymer F127 as the surfactant. Nitrogen adsorption-desorption measurements indicate that the ZnO sample contains large pores with mean diameter of about 30 nm. However, both small-angle X-ray diffraction and transmission electron microscope measurements indicate that the pore ordering is missing. Positron lifetime measurements reveal two long lifetime components in the porous ZnO. The longest lifetime τ4 (75 ns) corresponds to ortho-positronium (o-Ps) annihilation in large pores. The pore size estimated from τ4 is about 10.6 nm. This is much smaller than that estimated from Nitrogen adsorption-desorption measurements. In addition, the intensity I4 is only about 2.2%. This is probably due to the chemical quenching and/or inhibition of positronium formation induced by ZnO, which reduces o-Ps lifetime and intensity, and leads to under estimation of the pore size.


2013 ◽  
Vol 779-780 ◽  
pp. 201-204
Author(s):  
Miao Li ◽  
Hong Wang ◽  
Xian Qing Li ◽  
Jin Rong Liu

Ordered hexagonally mesoporous molecular sieve Al-MCM-41 with Si/Al (atom) ratio=9 was prepared by hydrothermal synthesis using raw kaolin. X-ray diffraction (XRD), Nitrogen adsorption desorption, Transmission Electron Microscope (TEM) and Energy Dispersive X-ray Detector (EDX) were employed to characterise raw kaolin, calcined kaolin, as-synthesized and calcined Al-MCM-41. The results indicated that characteristic reflections of raw kaolin disappeared after calcination, both of as-synthesized and calcined Al-MCM-41 exhibited well ordered hexagonally mesoporous molecular sieve structure.


NANO ◽  
2013 ◽  
Vol 08 (05) ◽  
pp. 1350050
Author(s):  
MIN GUAN ◽  
HAI-PENG BI ◽  
ZUYUAN WANG ◽  
SHAOHUA BU ◽  
LING HUANG ◽  
...  

Mesoporous silicas SBA-15 are modified with β-Cyclodextrins (β-CD) by simple grafting method. β-CD functionalized SBA-15 was characterized by Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), powder X-ray diffraction (PXRD), nitrogen adsorption–desorption measurements, thermogravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS). Furthermore, the applicability of it is investigated through studying the adsorption properties of clenbuterol. It showed better adsorption capacities of clenbuterol than pure SBA-15. β-CD functionalized SBA-15 material has the potential applications in the treatment of clenbuterol contamination in food and environment science.


2012 ◽  
Vol 616-618 ◽  
pp. 1797-1800
Author(s):  
Yu Mei Gong ◽  
Qing Liang ◽  
Jing Chuan Song ◽  
Ling Ming Xia

This paper presents the preparation of bimodal crystalline macro-/mesoporous titania powders by using a pluronic polymer (EO20PO70EO20, P123) as a template through a hydrothermal treatment. The as-prepared powders were characterized by X-ray diffraction (XRD), nitrogen adsorption-desorption, scanning electron microscope (SEM) and transmission electron microscope (TEM). The results reveal that the amount of P123 has a significant effect on the surface area of the mesoporous titania. When the mass ratio of P123:TBOT is 1:14, the crystalline macro-/mesoporous titania has the largest surface area (120.96 m2/g), the average pore diameter of this sample reaches a minimum of 6.67 nm.


1993 ◽  
Vol 8 (10) ◽  
pp. 2600-2607 ◽  
Author(s):  
M. Brunel ◽  
S. Enzo ◽  
M. Jergel ◽  
S. Luby ◽  
E. Majkova ◽  
...  

Tungsten/silicon multilayers with tungsten layers of a thickness of 1–2 nm were prepared by means of electron beam deposition. Their structure and thermal stability under rapid thermal annealing were investigated by a combination of x-ray diffraction techniques and cross-sectional transmission electron microscopy. The crystallization behavior was found to depend on the interdiffusion and mixing at the tungsten/silicon interfaces during deposition as well as during annealing. The as-deposited tungsten/silicon multilayers were amorphous and remained stable after annealing at 250 °C/40 s. Interdiffusion and crystallization occurred after annealing all samples from 500 °C/40 s up to 1000 °C/20 s. By performing the same heat treatment in the tungsten/silicon multilayers, the formation of body-centered cubic W was observed with a layer thickness ratio δW/δsi = 1, whereas tetragonal WSi2 was detected in tungsten/silicon multilayers with a layer thickness ratio of δw/δsi ∼0.25. This dependence of the crystallization products on the layer thickness ratio δw/δsi originates from the different phenomena of interdiffusion and mixing at the tungsten/silicon interfaces. The possible formation of bcc tungsten as a first stage of crystallization of tungsten-silicon amorphous phase, rich in tungsten, is discussed.


2010 ◽  
Vol 160-162 ◽  
pp. 117-122 ◽  
Author(s):  
Zhi Hong Li ◽  
Ji Min Wu ◽  
Shu Jie Huang ◽  
J. Guan ◽  
Xi Zheng Zhang

Strontium hydroxyapatite powders was prepared by the hydrothermal method using Sr(NO3)2 and (NH4)2HPO4 as reagents. Fourier transform infrared spectroscopy, X-ray diffraction, Transmission electron microscope, Energy dispersive X-ray, and Thermogravimetric-differential thermal analysis were employed to investigate the crystalline phase, chemical composition, morphology, and thermal stability of the Strontium hydroxyapatite. And the cytotoxicity of Strontium hydroxyapatite was analyzed through MTT assay. Results showed that Strontium hydroxyapatite prepared by hydrothermal Method has excellent crystal structure, good dispersion, high purity, and rod-like morphology with dimensions 200-500 nm in length and 20 nm in diameter. Meanwhile, the apatite has poor thermal stability. However, the apatite is cytocompatible and may have better biocompatibility, which can serve as strontium source incorporation into calcium phosphate cement and for bone repair.


2010 ◽  
Vol 150-151 ◽  
pp. 386-390
Author(s):  
Yuan Xun Li ◽  
Ying Li Liu ◽  
Huai Wu Zhang ◽  
Wei Wei Ling

The rod-shaped polyaniline (PANI)-barium ferrite nanocomposites were synthesized by in situ polymerization of aniline in the presence of BaFe12O19 nanoparticles with diameters of 60-80 nm. The composites obtained were characterized by infrared spectra (IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The thermal stability and the composition of the composites were investigated by TG-DTG analysis. The results indicate that the thermal stability of the composites is higher than that of the pure PANI which can be attributed to the interactions existed between PANI chains and ferrite particles.


2013 ◽  
Vol 22 (3) ◽  
pp. 096369351302200
Author(s):  
N. Ivashchenko ◽  
V. Tertykh ◽  
J. Skubiszewska-Zięba ◽  
R. Leboda ◽  
S. Khainakov ◽  
...  

Palladium nanoparticles with controlled size were synthesized within the pores of the mesoporous SBA-15 and SBA-16 silicas with grafted silicon hydride groups. Nitrogen adsorption-desorption method, X-ray diffraction and transmission electron microscopy (TEM) were used for characterization of palladium-containing composites. Results of material study clearly revealed that Pd nanoparticles prepared by this method were located inside the porous channels and were quite uniform in size (mostly 5–6 nm). The influence of metal content on the particles size and porous structure of supports was investigated.


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