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291.
292.
Enhanced electron field emission (EFE) behavior of a core–shell heterostructure, where ZnO nanorods (ZNRs) form the core and ultrananocrystalline diamond needles (UNCDNs) form the shell, is reported. EFE properties of ZNR‐UNCDN core–shell heterostructures show a high emission current density of 5.5 mA cm?2 at an applied field of 4.25 V μm?1, and a low turn‐on field of 2.08 V μm?1 compared to the 1.67 mA cm?2 emission current density (at an applied field of 28.7 V μm?1) and 16.6 V μm?1 turn‐on field for bare ZNRs. Such an enhancement in the field emission originates from the unique materials combination, resulting in good electron transport from ZNRs to UNCDNs and efficient field emission of electrons from the UNCDNs. The potential application of these materials is demonstrated by the plasma illumination measurements that lowering the threshold voltage by 160 V confirms the role of ZNR‐UNCDN core–shell heterostructures in the enhancement of electron emission.  相似文献   
293.
The residual thicknesses of the skin and the inner layers are important quality indicators of water‐assisted co‐injection molding (WACIM) process or overflow WACIM (O‐WACIM) parts. At the curved section, the residual thicknesses change significantly. A numerical simulation program based on the computational fluid dynamics method was developed to simulate the O‐WACIM process. After the numerical simulation program was validated with the experimental results, it was used to study the effects of the bending radii and bending angles on the residual thicknesses of the skin and inner layers of O‐WACIM parts. The results showed that the penetration of the inner melt and water was always close to the inner concave side due to the higher local pressure gradient and temperature. The effects of processing parameters on the residual thicknesses of the skin and inner layers were investigated using the orthogonal simulation method. It was found that the residual thicknesses of the skin/inner layer at the inner concave/outer convex side are mainly influenced by different parameters. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42468.  相似文献   
294.
Biodegradable polylactic acid (PLA) was compounded with thermoplastic polyurethane (TPU) by twin‐screw extrusion at weight ratios of 90/10, 80/20, 70/30, and 60/40. The blends were investigated based on their phase morphology, thermal and mechanical properties, and shape memory properties. The tensile results showed that PLA was successfully toughened by TPU. When the TPU content was 40%, the elongation‐at‐break increased to 400%. The SEM morphology showed that TPU was dispersed uniformly in the PLA matrix; DMA and DSC results indicated that the two polymers were immiscible. Most interestingly, it was found that the blends exhibited a shape memory behavior and, unlike most of the existing shape memory polymers (SMPs), the PLA/TPU blends could be deformed at room temperature without an extra heating and cooling step. During the deformation process, TPU acted as a toughening agent that prevented the PLA/TPU blends from breaking; thus, the temporary shape could be kept and internal stress was stored in the blends. Upon heating to above the glass transition temperature of PLA (about 60°C), the deformed parts regained their original shapes quickly along with the release of the stress. POLYM. ENG. SCI., 55:70–80, 2015. © 2014 Society of Plastics Engineers  相似文献   
295.
Pooled nucleic acid amplification test is a promising strategy to reduce cost and resources for screening large populations for infectious disease. However, the benefit of pooled testing is reversed when disease prevalence is high, because of the need to retest each sample to identify infected individual when a pool is positive. Split, Amplify, and Melt analysis of Pooled Assay (SAMPA) is presented, a multicolor digital melting PCR assay in nanoliter chambers that simultaneously identify infected individuals and quantify their viral loads in a single round of pooled testing. This is achieved by early sample tagging with unique barcodes and pooling, followed by single molecule barcode identification in a digital PCR platform using a highly multiplexed melt curve analysis strategy. The feasibility is demonstrated of SAMPA for quantitative unmixing and variant identification from pools of eight synthetic DNA and RNA samples corresponding to the N1 gene, as well as from heat-inactivated SARS-CoV-2 virus. Single round pooled testing of barcoded samples with SAMPA can be a valuable tool for rapid and scalable population testing of infectious disease.  相似文献   
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