Hard nanocomposite comprising stereoregular syndiotactic polypropylene with chemically bonded gold nanoparticles

An effective method to synthesize directly a hard composite material containing uniformly dispersed nanogold particles chemically bonded with a stereospecific, crystalline polymer matrix has been developed. Syndiotactic polypropylene was synthesized and functionalized to have a hydroxyl terminal group (sPP_OH) via a metallocene catalysis with a selective chain transfer. Next, sPP_OH was activated to react with ethylene sulfide forming the thiol‐terminated polymer, sPP_SH. sPP_SH was then chemically bonded to gold nanoparticles (AuNPs) formed in situ via a reduction of HAuCl₄. The bonding between thiol and AuNP stabilized the AuNPs and led to the formation of sPP_AuNPs composite containing uniformly‐dispersed AuNPs of a 19–40 nm size without noticeable aggregation. Furthermore, the chemical bonding of AuNPs has afforded sPP_AuNPs a thermal degradation temperature (T_D) 49.4 °C higher than the pristine sPP or sPP_OH and 25.7 °C higher than sPP_SH without any adverse effect on the crystalline temperature and melting temperature. In addition, the characteristic UV‐Vis absorption wavelength of sPP_AuNPs remains the same at various temperatures, thus indicating the independence of optical property on temperature as well as the good thermal stability of the sPP_AuNPs composite. ¹H NMR, ¹³C NMR, FESEM, STEM, XPS, TGA and DSC were used to investigate the molecular structure, morphology and thermal properties of the resulting sPP_AuNPs nanocomposite. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010     

Copolyphenylenes with pendant benzimidazolyl and diethanolaminohexyloxy groups: Synthesis and electron‐transporting application in PLEDs

Two new electron‐transporting copolyphenylenes P1NH and P2NH possessing balanced charges crucial to emission efficiency of polymer light‐emitting diodes (PLEDs) have been synthesized and applied as an electron‐transporting layer (ETL). The main chain structure is all para‐linkage for P1NH and both para‐ and meta‐linkage for P2NH , with the same pendant electron‐withdrawing benzimidazolyl and polar diethanolaminohexyloxy groups. Both copolymers possess excellent thermal stability (T _d > 300 °C, T _g > 100 °C) due to their rigid backbones. In addition, the pendant groups effectively lower LUMO (～ ?2.70 eV) and HOMO (～ ?5.70 eV) levels, resulting in improved electron‐transporting and hole‐blocking capabilities. Multilayer yellow‐emitting PLEDs with a configuration of ITO/PEDOT:PSS/SY/ETL/LiF/Al were successfully fabricated by the spin‐coating process. The maximum luminance and maximum current efficiency of the P1NH ‐based device were 12,881 cd/m² and 10.94 cd/A, respectively, superior to the performance of P2NH ‐based device (4938 cd/m², 3.70 cd/A) and the device without ETL (8690 cd/m², 2.78 cd/A). Current results indicate that P1NH is highly effective in enhancing electron transport and device performance. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55 , 2494–2505     

Surrogate-based modeling and dimension reduction techniques for multi-scale mechanics problems

Successful modeling and/or design of engineering systems often requires one to address the impact of multiple "design variables" on the prescribed outcome.There are often multiple,competing objectives based on which we assess the outcome of optimization.Since accurate,high fidelity models are typically time consuming and computationally expensive,comprehensive evaluations can be conducted only if an efficient framework is available.Furthermore,informed decisions of the model/hardware’s overall performance rely on an adequate understanding of the global,not local,sensitivity of the individual design variables on the objectives.The surrogate-based approach,which involves approximating the objectives as continuous functions of design variables from limited data,offers a rational framework to reduce the number of important input variables,i.e.,the dimension of a design or modeling space.In this paper,we review the fundamental issues that arise in surrogate-based analysis and optimization,highlighting concepts,methods,techniques,as well as modeling implications for mechanics problems.To aid the discussions of the issues involved,we summarize recent efforts in investigating cryogenic cavitating flows,active flow control based on dielectric barrier discharge concepts,and lithium(Li)-ion batteries.It is also stressed that many multi-scale mechanics problems can naturally benefit from the surrogate approach for "scale bridging."     

Assessment of conservative weighting scheme in simulating chemical vapour deposition with trace species

Low‐pressure or ultra‐high vacuum chemical vapour deposition often involves important trace species in both gas‐phase and surface reactions. The conservative weighting scheme (J. Thermophys. Heat Transfer 1996; 10 (4) : 579) has been used to deal with the trace species often involved in some non‐reactive physical processes, which is otherwise considered computationally impossible using the conventional DSMC method. This conservative weighting scheme (CWS) improves greatly the statistical uncertainties by decreasing the weighting factors of trace‐species particles and ensures the conservation of both momentum and energy between two colliding particles with large difference of weighting factors. This CWS is further extended to treat reactive processes for gas‐phase and surface reactions with trace species, which is called extended conservative weighting scheme (ECWS). A single‐cell equilibrium simulation is performed for verifying both the CWS and ECWS in treating trace species. The results of using CWS show that it is most efficient and accurate for weight ratio (trace to non‐trace) equal to or less than 0.01 for flows with two and three species. The results of a single‐cell simulation using ECWS for gas‐phase reaction and surface reactions show that only ECWS can produce acceptable results with reasonable computational time. Copyright © 2003 John Wiley & Sons, Ltd.     

Creep crack growth on spent fuel zircaloy cladding in interim storage

The effect of creep failure mechanisms on the creep crack growth is examined on spent fuel Zircaloy cladding in interim storage. Based on the creep fracture mechanics parameter C^* and the strain energy density criteria, the relationship between the creep crack growth rate and the fracture mechanics parameter C^* is established theoretically. The effects of initial crack lengths and storage temperature profiles on cladding failure are discussed in detail. The results show that the initial crack length and the storage temperature profile play an important role in the interim dry storage. When the storage temperature remains at a constant temperature of 400 °C, it will be safe for the cladding which stores in the interim dry storage. The results presented in this study provide a reliable cladding integrity evaluation for spent fuel in the interim dry storage.     

High-speed monitoring of the crystallinity change in poly(lactic acid) during photodegradation by using a newly developed wide area NIR imaging system (Compovision)

We aimed to achieve wide area rapid monitoring of the crystallinity change in poly(lactic acid) (PLA) during photodegradation caused by ultraviolet (UV) light by using a newly developed near-infrared (NIR) camera (Compovison). Several kinds of PLA samples with different crystallinities and their blends with poly[(3)-(R)-hydroxybutyrate] were prepared. Their two-dimensional NIR spectra in the 1,000–2,350-nm region were measured by Compovision at a 5-min interval during photolysis. An intensity decrease of the band in the 1,900-1,925-nm region due to the second overtone of the C = O stretching vibration of PLA was observed during photolysis. This suggests that an anhydride carbonyl is produced during photolysis. The NIR image of the crystallinity change monitored by the band at 1,917 nm in the standard normal variate spectra clearly shows the inhomogeneity of crystal evolution. A logarithmic increase was observed for all identified areas in the PLA film; however, the time to reach the maximum crystallinity was slightly different according to the initial crystallinity of the sample. It is likely that the initial crystallinity of the sample influences the degradation speed more than the degradation amount. These imaging results have provided fundamental chemical insights into the photolytic process for PLA, and at the same time they have demonstrated that the two-dimensional spectral data obtained by Compovision are useful for process monitoring of polymers.     

Active dielectric metasurface based on phase‐change medium

We propose all‐dielectric metasurfaces that can be actively re‐configured using the phase‐change material Ge₂Sb₂Te₅ (GST) alloy. With selectively controlled phase transitions on the composing GST elements, metasurfaces can be tailored to exhibit varied functionalities. Using phase‐change GST rod as the basic building block, we have modelled metamolecules with tunable optical response when phase change occurs on select constituent GST rods. Tunable gradient metasurfaces can be realized with variable supercell period consisting of different patterns of the GST rods in their amorphous and crystalline states. Simulation results indicate a range of functions can be delivered, including multilevel signal modulating, near‐field coupling of GST rods, and anomalous reflection angle controlling. This work opens up a new space in exploring active meta‐devices with broader applications that cannot be achieved in their passive counterparts with permanent properties once fabricated.

     

Recent trends in nanomaterial-based microanalytical systems for the speciation of trace elements: A critical review

Trace element speciation in biomedical and environmental science has gained increasing attention over the past decade as researchers have begun to realize its importance in toxicological studies. Several nanomaterials, including titanium dioxide nanoparticles (nano-TiO₂), carbon nanotubes (CNTs), and magnetic nanoparticles (MNPs), have been used as sorbents to separate and preconcentrate trace element species prior to detection through mass spectrometry or optical spectroscopy. Recently, these nanomaterial-based speciation techniques have been integrated with microfluidics to minimize sample and reagent consumption and simplify analyses. This review provides a critical look into the present state and recent applications of nanomaterial-based microanalytical systems in the speciation of trace elements. The adsorption and preconcentration efficiencies, sample volume requirements, and detection limits of these nanomaterial-based speciation techniques are detailed, and their applications in environmental and biological analyses are discussed. Current perspectives and future trends into the increasing use of nanomaterial-based microfluidic techniques for trace element speciation are highlighted.