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This study focused on the fabrication of poly(n-butyl methacrylate) (PBMA) nanocomposites with various concentrations of cerium-doped titanium dioxide (Ce–TiO2) nanoparticles via in situ polymerization technique. The structural characterization and the material properties of all the composites were analyzed by UV–visible, FTIR, XRD, SEM, DSC, TG, and tensile strength measurements. The UV–visible and FTIR studies confirmed the effective inclusion of Ce–TiO2 nanoparticles into the PBMA matrix. The change in amorphous morphology of PBMA to a crystalline structure was observed from the XRD pattern. The SEM morphology revealed the attachment of nanoparticles in the polymer matrix. The inclusion of Ce–TiO2 nanoparticles enhanced the glass transition temperature, and thermal stability of the PBMA matrix was revealed from DSC and TG, respectively. The tensile strength of PBMA was greatly enhanced by the addition of Ce–TiO2 nanoparticles. The AC conductivity, dielectric constant, and dielectric loss studies were also performed in the frequency range 102–106 Hz, and it was observed that addition of Ce–TiO2 nanoparticles greatly enhanced the electrical properties of PBMA. The change in dielectric constant with the addition of nanoparticles was correlated with a theoretical modeling study. This work also extended to study the role of Ce–TiO2 nanoparticles in the reinforcing mechanism of the nanocomposite by comparing the actual tensile strength of the composite with different theoretical modeling. The high dielectric constant and tensile strength of composite are beneficial in designing lightweight and highly efficient nanoelectronic materials based on the family of polybutyl acrylates.

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In this research, the effect of cerium dioxide (CeO2) nanoparticles on electrical properties of poly(butyl methacrylate) (PBMA) has been investigated. Polymer nanocomposites reinforced with variable contents of CeO2 nanoparticles (3, 5, 7 and 10 wt%) were fabricated by an in situ polymerization method. The formation of nanocomposites was analyzed by FTIR, XRD, SEM and TEM analysis. Also, the AC and DC conductivities of CeO2 nanoparticles-reinforced PBMA were systematically studied with respect to different loadings of CeO2 fillers. The FTIR, XRD and morphological studies revealed that the nanoparticles were well inserted and uniformly dispersed into the macromolecular chain of PBMA. The AC conductivity of PBMA/CeO2 composite increases not only with the loading of nanoparticles but also with the temperature of the system. The activation energy determined from AC electrical conductivity was found to decrease with the frequency and temperature. DC conductivity of the nanocomposites was increased with the insertion of nanoparticles into PBMA. The DC conductivity of all the composites was greater than pure PBMA. The applicability of different theoretical models such as Scarisbrick, Bueche and McCullough equations was compared with the experimentally determined DC conductivity of PBMA/CeO2 nanocomposites. These models fail to explain the conductivity of polymer composite in the entire loading of fillers. Hence, a new theoretical model is proposed in this study and it shows good agreement with the experimentally observed conductivity values.

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Thermal analysis on organically modified Ca2+-montmorillonite (OMON) and its source materials—octadecylamine (ODA) and Ca2+-montmorillonite (Ca2+-Mon)—was studied using thermally stimulated current (TSC) technique. The appearance of ρ MON peak with the T max = 75 °C shows the ability of the developed TSC system to demonstrate the relaxation effects of dehydration in Ca2+-Mon. It appeared within the temperature range of DSC endothermic peak (30–100 °C) where the T mMON = 58 °C. Segmental motions of ODA chains and structural disruptions in the modifier agent compound produced TSC α ODA, ρ ODA and ρ 1ODA peaks that are comparable to thermal transition and endothermic peaks in DSC profile (T gODA, T m1ODA and T m2ODA). The effect of localized motion in ODA chains as revealed by the TSC βOMON peak (T max = ?23 °C), however, is absent in the DSC profile of OMON. It shows TSC technique has high sensitivity in detecting various relaxation behaviors at molecular level. More evidences are demonstrated by the ρ OMON (T max = 86 °C) and ρ 1OMON (T max = 105 °C) peak originated from the ODA chains structures. These peaks also confirm the intercalation of the modifier cations inside the Ca2+-Mon gallery.  相似文献   
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Four cycloaurated phosphine sulfide complexes, [Au{κ2-2-C6H4P(S)Ph2}2][AuX2] [X=Cl ( 2 ), Br ( 3 ), I ( 4 )] and [Au{κ2-2-C6H4P(S)Ph2}2]PF6 ( 5 ), have been prepared and thoroughly characterized. The compounds were found to be stable under physiological-like conditions and showed excellent cytotoxicity against a broad range of cancer cell lines and remarkable cytotoxicity in 3D tumor spheroids. Mechanistic studies with cervical cancer (HeLa) cells indicated that the cytotoxic effects of the compounds involve the inhibition of thioredoxin reductase and induction of apoptosis through mitochondrial disruption. In vivo experiments in nude mice bearing HeLa xenografts showed that treatment with compounds 4 and 5 resulted in significant inhibition of tumor growth (35.8 and 46.9 %, respectively), better than that of cisplatin (29 %). The newly synthesized gold complexes were also evaluated for their in vitro and in vivo anti-inflammatory activity through the study of lipopolysaccharide (LPS)-activated macrophages and carrageenan-induced hind paw edema in rats, respectively.  相似文献   
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Research on Chemical Intermediates - Metal oxide nanofillers are a special type of additives in rubber composites that impart special qualities such as thermal resistance, tensile strength,...  相似文献   
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Conducting polymer composites of polypyrrole (PPy) and silver doped nickel oxide (Ag-NiO) nanocomposites were synthesised by in situ polymerisation of pyrrole with different contents of Ag-NiO nanoparticles. The formation of nanocomposites were studied by Fourier transform infrared (FTIR) and UV–vis spectroscopy, field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and AC and DC conductivity measurements. The sensitivity of ammonia gas through the nanocomposite was analysed with respect to different contents of nanoparticles. Spectroscopic studies showed the shift in the absorption bands of polymer nanocomposite than that of pure PPy indicating the strong interaction between the nanoparticles and polymer chain. FESEM revealed the uniform dispersion of nanoparticles with spherically shaped metal oxide particles in PPy matrix. The XRD pattern indicated a decrease in amorphous domain of PPy with increase in loading of nanoparticles. The higher thermal stability and glass transition temperature of polymer nanocomposites than that of pure PPy were revealed from the TGA and DSC respectively. The dielectric properties, DC and AC conductivity of nanocomposites were much higher than PPy and these electrical properties increases with the loading of nanoparticles. The nanocomposites showed an enhancement in sensitivity towards ammonia gas detection than PPy.  相似文献   
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