A digital miniature x-ray tube with a high-density triode carbon nanotube field emitter

2013 ◽  
Vol 102 (2) ◽  
pp. 023504 ◽  
Author(s):  
Jin-Woo Jeong ◽  
Jun-Tae Kang ◽  
Sungyoul Choi ◽  
Jae-Woo Kim ◽  
Seungjoon Ahn ◽  
...  
2019 ◽  
Vol 53 (15) ◽  
pp. 2091-2104 ◽  
Author(s):  
Gaurav Arora ◽  
Himanshu Pathak ◽  
Sunny Zafar

Carbon nanotubes have been used as reinforcements in polymers due to their high elasticity, flexibility, and thermal conductivity. In this study, pellets of high-density polyethylene +20 wt% carbon nanotube and polypropylene +20 wt% carbon nanotube were cured using microwave energy. X-ray diffraction, differential scanning calorimetry, thermogravimetric analysis, uniaxial tensile test, and scanning electron microscopy was used to study morphology, thermal stability, and mechanical performance of the microwave-cured composites. X-ray diffraction analysis confirmed the bonding between the polymer and carbon nanotube as the peaks shifted and intensified. From the thermal study, it was observed that melting point of the composites is affected by microwave curing and the crystallinity of high-density polyethylene/carbon nanotube and polypropylene/carbon nanotube changed by 57.67% and 47.28%, respectively. Results of the uniaxial tensile test indicated that Young’s modulus of microwave cured high-density polyethylene/carbon nanotube and polypropylene/carbon nanotube composites were improved by 295% and 787.8%, respectively. Scanning electron microscopic fractography shows the stretching of polymer over-lapped on carbon nanotubes in the direction of the applied load.


2016 ◽  
Vol 55 (6S1) ◽  
pp. 06GF10 ◽  
Author(s):  
Shuhei Okawaki ◽  
Satoshi Abo ◽  
Fujio Wakaya ◽  
Hayato Yamashita ◽  
Masayuki Abe ◽  
...  
Keyword(s):  

2016 ◽  
Vol 69 (3) ◽  
pp. 297-303
Author(s):  
Hyun Suk Kim ◽  
Edward Joseph D. Castro ◽  
Choong Hun Lee
Keyword(s):  

2013 ◽  
Vol 111 ◽  
pp. 114-117 ◽  
Author(s):  
Vitaliy A. Guzenko ◽  
Anna Mustonen ◽  
Patrick Helfenstein ◽  
Eugenie Kirk ◽  
Soichiro Tsujino

Author(s):  
Jongmin Lim ◽  
Amar Prasad Gupta ◽  
Hangyeol Park ◽  
Jinho Choi ◽  
Jaeik Jung ◽  
...  
Keyword(s):  
Low Dose ◽  

2015 ◽  
Vol 54 (6S1) ◽  
pp. 06FF10 ◽  
Author(s):  
Shuhei Okawaki ◽  
Satoshi Abo ◽  
Fujio Wakaya ◽  
Masayuki Abe ◽  
Mikio Takai

2003 ◽  
Vol 774 ◽  
Author(s):  
Susan M. Rea ◽  
Serena M. Best ◽  
William Bonfield

AbstractHAPEXTM (40 vol% hydroxyapatite in a high-density polyethylene matrix) and AWPEX (40 vol% apatite-wollastonite glass ceramic in a high density polyethylene matrix) are composites designed to provide bioactivity and to match the mechanical properties of human cortical bone. HAPEXTM has had clinical success in middle ear and orbital implants, and there is great potential for further orthopaedic applications of these materials. However, more detailed in vitro investigations must be performed to better understand the biological interactions of the composites and so the bioactivity of each material was assessed in this study. Specifically, the effects of controlled surface topography and ceramic filler composition on apatite layer formation in acellular simulated body fluid (SBF) with ion concentration similar to those of human blood plasma were examined. Samples were prepared as 1 cm × 1 cm × 1 mm tiles with polished, roughened, or parallel-grooved surface finishes, and were incubated in 20 ml of SBF at 36.5 °C for 1, 3, 7, or 14 days. The formation of a biologically active apatite layer on the composite surface after immersion was demonstrated by thin-film x-ray diffraction (TF-XRD), environmental scanning electron microscopy (ESEM) imaging and energy dispersive x-ray (EDX) analysis. Variations in sample weight and solution pH over the period of incubation were also recorded. Significant differences were found between the two materials tested, with greater bioactivity in AWPEX than HAPEXTM overall. Results also indicate that within each material the surface topography is highly important, with rougher samples correlated to earlier apatite formation.


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