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1.
Abstract

PBAT/PMMA/MA/TCP composites were prepared by melt blending and characterized by FTIR, XRD, SEM and in vitro bioactivity studies using SBF and cell viability tests. SBF studies revealed good bioactivity nature which was observed in SEM and confirmed by EDAX. Cell viability test revealed an excellent viability of squamous cells within 2?h than the control. Soil burial tests of the composites show fast degradation within 50 days under natural conditions. The tensile and hardness properties is marginally increased than that of PBAT/PMMA blend. These biocomposites can be used for the fabrication of medical devices by melt blending and injection molding process.  相似文献   
2.
In the present work, the feasibility of friction stir welding (FSW) of poly(methyl methacrylate) sheets was studied experimentally and theoretically by employing thermomechanical simulations. The effect of processing parameters including tool plunge depth, tilt angle, tool rotational speed (w), and transverse velocity (v) was investigated to determine suitable conditions to attain sound and defect-free joints. It is shown that a low tool plunge depth of 0.2?mm and a tilt angle of 2° provide suitable material flow to gain sound joints. By controlling the heat input into stir zone by increasing the tool rotational speed and decreasing linear velocity, the formation of defects can be minimised. Mechanical examinations in both longitudinal (LS) and transverse (TS) directions indicate that the highest joint strength of 57?MPa (for LS) and 42?MPa (for TS) are obtained at processing conditions of w?=?25?mm?min?1 and v?=?1600?rev?min?1. The measured tensile strengths are 81 and 60% of the base polymer, respectively.  相似文献   
3.
The hydrolytic degradation of poly(l ‐lactic acid)/poly(methyl methacrylate) (PLLA/PMMA) blends was carried out by the immersion of thin films in buffer solutions (pH = 7.24) in a shaking water bath at 60 °C for 38 days. The PLA/PMMA blends (0/100; 30/70; 50/50; 70/30; 100/0) were obtained by melt blending using a Brabender internal mixer and shaped into thin films of about 150 µm in thickness. Considering that PMMA does not undergo hydrolytic degradation, that of PLLA was followed via evolution of PLA molecular weight (recorded by size exclusion chromatography), thermal parameters (differential scanning calorimetry (DSC)) and morphology of the films (scanning transmission electron microscopy). The results reveal a completely different degradation pathway of the blends depending on the polymethacrylate/polyester weight ratio. DSC data suggest that, during hydrolysis at higher PMMA content, the polyester amorphous chains, more sensitive to water, are degraded before being able to crystallize, while at higher PLLA content, the crystallization is favoured leading to a sample more resistant to hydrolysis. In other words, and quite unexpectedly, increasing the content of water‐sensitive PLLA in the PLLA/PMMA blends does not mean de facto faster hydrolytic degradation of the resulting materials. © 2018 Society of Chemical Industry  相似文献   
4.
In this study, maghemite/PMMA nano-fibrous composites have been successfully fabricated by using the electrospinning process. PMMA nano-fibres have been selected to be used as the matrix; the PMMA was dissolved in three diverse solvents (Acetone, THF and DMF) in order to obtain fine PMMA nano-fibres. As a result, the PMMA–DMF proved to be the most appropriate polymer solution among the three solvents, with its impressive defect-free surface morphology results. The production of maghemite using Massart’s procedure resulted in nano-particles with an average diameter of 4.98 ± 0.13 nm (using transmission electron microscopy (TEM)). Maghemite nano-particle were then mixed with a prepared polymer solution in order to fabricate maghemite/PMMA nano-fibrous composite. Furthermore, the investigation of the morphology and structure of the composite was carried out using field emission scanning electron microscopy (FESEM), Energy-dispersion X-ray spectroscopy (EDX), Alternating Gradient Magnetometer (AGM), Fourier transform infrared spectrometer (FTIR), X-ray diffraction (XRD) and tensile strength measurement devices. The results indicated that there was a great amount of maghemite, both in and on the composite’s surface, which can be utilized in the purpose of magnetic applications.  相似文献   
5.
采用自由基聚合法制备了纯的和添加了1.5%(质量分数)沥青的聚甲基丙烯酸甲酯(PMMA),用热重(TG)分析和锥形量热仪测试了其热分解和燃烧性能并研究了其热分解动力学。TG分析结果表明,添加质量分数为1.5%的沥青,PMMA在氮气中和空气中的失重速率最大时温度分别由纯PMMA的379.2℃和308.9℃提高至386.2℃和354.7℃,热降解表观活化能显著提高;锥形量热仪测试结果表明沥青使PMMA的点燃时间缩短,燃烧更平稳,加入沥青后,点燃后300 s内的质量损失速率和热释放速率平均值分别由纯PMMA的0.212 g/s和569 k W/m2降至0.191 g/s和514 k W/m2,CO产率和烟释放速率平均值分别由0.009 9 kg/kg和0.027 0 m2/s增至0.012 0 kg/kg和0.036 8 m2/s。沥青提高PMMA燃烧性能的主要原因是抑制了PMMA的热分解。  相似文献   
6.
7.
探究透明PMMA(聚甲基丙烯酸甲酯)厚度和4种不同恒定热流对材料表面温度、质量损失率、着火时间及着火温度的影响。利用反演模型并结合部分实验数据得到PMMA的热物性参数,将其他工况模拟结果与实验测量值及理论分析值相互对比,验证了数值模型和理论分析的准确性和可靠性。结果表明,PMMA着火时间的下降趋势随热流的增大而逐渐变缓。PMMA厚度小于3 mm时,表面温度和质量损失率随厚度增大而减小。PMMA厚度大于3 mm时,着火温度的平均值为(628±20) K,其着火特性几乎不随厚度的变化而变化,故着火温度可作为PMMA着火判据。  相似文献   
8.
A facile route was adopted to blend the matrix. The PMMA/PEG blend was reinforced with three types of nanofillers, i.e., pristine MWCNT (P-CNT), amine functionalized MWCNT (PDA-EA-CNT) and nanobifiller i.e. nanodiamond functional MWCNT (PDA-EA-CNT-ND) to yield three different types of nanocomposites i.e. PMMA/PEG/P-CNT, PMMA/PEG/PDA-EA-CNT and PMMA/PEG/PDA-EA-CNT-ND. These nanocomposites were reinforced with nanofiller loading (1 wt. %, 3 wt. %, 5 wt. %, 10 wt. %, 30 wt. % and 50 wt. %) by solution casting method. Structure of composite and nanofillers was confirmed by FTIR. FESEM imaging revealed that nanocomposites have micro porous morphology. At high magnification, distribution of functionalized CNT/ND appears to be protruding out of the polymeric matrix. The TGA result suggests that the thermal stability of the nanocomposites was enhanced in comparison to PMMA due to grafting of filler molecules with PMMA/PEG macromolecules. The DTG results showed that the bifiller nanocomposites (PMMA/PEG/PDA-EA-CNT-ND) exhibited improved thermal stability with Tmax (431°C) as compared to P-CNT and amine functionalized CNT (PMMA/PEG/PDA-EA-CNT) with Tmax of 395°C and 418°C respectively. XRD results showed fine interaction between filler and the polymeric matrix. As the filler loading was increased the composites showed pronounced XRD peak at 25.9°, corresponding to (002) reflection of nanotubes. Significant improvement in the mechanical properties of composites was recorded with the reinforcement of fillers as compared to the neat matrix. The most significant improvement in tensile strength and elastic modulus was observed for the bifiller nanocomposites with 5 wt. % PDA-EA-CNT-ND. They showed a tensile strength and elastic modulus of 29.9 MPa and 1474.31 MPa respectively as compared to amine functionalized CNT with tensile strength (25.7) and elastic modulus (1466.99 MPa)and P-CNT with tensile strength(25 MPa) and elastic modulus (1155.75 MPa).  相似文献   
9.
用分散聚合法制备聚甲基丙烯酸甲酯(PMMA)微球,以聚乙烯吡咯烷酮(PVP)为分散剂,依次用葡萄糖和硼氢化钠还原银氨溶液,在微球表面化学镀银,得到表面覆银的PMMA-Ag微球,对其进行了表征和分析。结果表明,微球分散性好,银层光滑致密,粒径较均匀,直径约2μm;XRD图谱显示无银以外的其它物相存在;红外光谱显示银与PMMA微球的表面可能存在相互作用,是银还原沉积的影响因素;热重分析表明,PMMA-Ag耐热性有所提高(26℃);制备使用的硝酸银占PMMA微球质量分数为55%时,样品的导电率最大(330 S/cm)。  相似文献   
10.
《Ceramics International》2022,48(9):12112-12117
Gallium oxide (Ga2O3) is a promising candidate for next-generation solar-blind photodetectors (PDs) because of its large bandgap of 4.9 eV. Its single-crystal nanorod structure improves its photoelectric performance, which promotes carrier transformation and separation. However, Ga2O3 nanorods fabricated by the hydrothermal method have many oxygen vacancies, which largely enhance the dark current and reduce the on/off ratio of PDs, restricting application of such devices. Therefore, in this paper, dual strategies are applied to reduce the dark current of a metal–semiconductor–metal-structured Ga2O3 nanorod PD fabricated by the hydrothermal method. Through these dual strategies, which include annealing treatment and the application of a polymethyl methacrylate (PMMA) coating, the dark current of the PD is reduced from 1.34 × 10?7 to 2.04 × 10?9 A at 1 V, resulting in the on/off ratio of the PD reaching as high as 3.24 × 104. Besides, the responsivity and detectivity of the device reach 1.73 A/W and 2.53 × 1012 Jones respectively, which represents better performance than those of other reported Ga2O3 nanorod array PDs. Results have shown that the new strategy adopted can greatly improve the performance of Ga2O3-based ultraviolet photodetectors.  相似文献   
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