Lithium–sulfur (Li–S) batteries hold great promise to serve as next‐generation energy storage devices. However, the practical performances of Li–S batteries are severely limited by the sulfur cathode regarding its low conductivity, huge volume change, and the polysulfide shuttle effect. The first two issues have been well addressed by introducing mesoporous carbon hosts to the sulfur cathode. Unfortunately, the nonpolar nature of carbon materials renders poor affinity to polar polysulfides, leaving the shuttling issue unaddressed. In this contribution, atomic cobalt is implanted within the skeleton of mesoporous carbon via a supramolecular self‐templating strategy, which simultaneously improves the interaction with polysulfides and maintains the mesoporous structure. Moreover, the atomic cobalt dopants serve as active sites to improve the kinetics of the sulfur redox reactions. With the atomic‐cobalt‐decorated mesoporous carbon host, a high capacity of 1130 mAh gS−1 at 0.5 C and a high stability with a retention of 74.1% after 300 cycles are realized. Implanting atomic metal in mesoporous carbon demonstrates a feasible strategy to endow nanomaterials with targeted functions for Li–S batteries and broad applications.
Additive manufacturing processes like selective laser beam melting of polymers (LBM) are established for production of prototypes and individualized parts. The transfer to serial production currently is hindered by the limited availability of polymer powders with good processability.Within this contribution the effect of powder properties, such as particle size, shape and flowability on the processability in LBM and their influence on device quality is exemplified for polybutylene terephthalate (PBT) materials. A process chain for the production of spherical polymer microparticles has been developed to obtain PBT powder materials. The process chain consists of three steps: First, polymer microparticles are produced by wet grinding.Second, the particle shape is engineered by rounding in a heated downer reactor to improve the flowability of the product. A further improvement of flowability of the still cohesive spherical PBT particles is realized by dry coating with fumed silica.
Within this contribution liquid-liquid phase separation (LLPS) and precipitation from ethanol was studied as an approach to produce polyamide 11 (PA11) powders for selective laser sintering (SLS). To this end, the cloud point and solution temperature curve of the PA11ethanol was determined experimentally via turbidity measurements. The proper range of system composition and temperature for particle formation was deduced. The dependence of particle characteristics on process parameters (polymer concentration, stirring conditions and temperature regime) during LLPS and precipitation was assessed and the products were characterized with respect to their size and morphology. Furthermore, structural, rheological (c.f. viscosity number) and thermal characteristics were analyzed and correlated with process parameters. Rheological characteristics and molecular weight distributions were determined.After removal of fines and dry coating with hydrophobic fumed silica, an optimized PA11 powder with mean particle of several 10 microns showing good flowability for SLS was obtained. SLS processability of this optimized PA11 powder was demonstrated by building multi-layered test specimens in a laser sintering machine. With this contribution, we present a comprehensive workflow for the process development, product characterization and product application of a SLS powder manufactured via precipitation.
Selective laser sintering (SLS) of thermoplastic materials is an additive manufacturing process that overcomes the boundary between prototype construction and functional components. This technique also meets the requirements of traditional and established production processes. Crystallization behavior is one of the most critical properties during the cooling process and needs to be fully understood. Due to the huge influence of crystallization on the mechanical and thermal properties, it is important to investigate this process more closely. A commercial SLS polyamide (PA12) powder was measured with differential scanning calorimetry (DSC) to model a wider temperature range. To model isothermal crystallization between 160 and 168 • C, the Avrami model was used to determine the degree of crystallization. For non-isothermal crystallization between 0.2 and 20 K/min, different models were compared including the Ozawa, Jeziory, and Nakamura equations.
The synthesis of 1-ethyl-3-methyl-4-vinylimidazolium triflate, its polymerization, and ion exchange to yield a family of 4imidazolium polymers with a variety of anions are described. For comparative purposes, the synthesis, polymerization, and ion exchange of an analogous set of 1-vinylimidazolium polymers are also presented. The comparative thermal and dielectric characteristics of the 4-vinyland 1-vinylimidazolium salts were evaluated. The trends in the glass transition (T g ) characteristics of the various 4-vinylimidazolium and 1vinylimidazolium polymers were similar; however, the glass transition temperatures of poly( 4-vinylimidazolium) BF 4 − , PF 6 − , AsF 6 −, and CF 3 SO 3 − salts were significantly higher than those of the corresponding poly(1-vinylimidazolium) salts. This difference and the increase in T g in going from BF 4 − to AsF 6 − in the 4-vinylimidazolium series were attributed to enhanced intramolecular bridging between imidazolium moieties positioned 1,3 or 1,5 along the polymer chain. In the dielectric spectra of 1-vinylimidazolium salts at temperatures in excess of 30 °C, one relaxation mode distinct from that for electrode polarization is observed. The single mode appears to correspond to the α-relaxation peak in poly(3-ethyl-1-vinylimidazolium salts) recently identified and attributed to ion-pair motion by Nakamura et al. In the 4-vinylimidazolium polymer spectra set, at temperatures in excess of 30 °C, two relaxation modes, distinct from that for electrode polarization, are apparent: the α peak also observed in the 1-vinylimidazolium polymer set and a new relaxation peak observed at lower frequency. The lower frequency relaxation peak is identified in this work as the α′-relaxation and is also associated with ion-pair motion. Assuming the relaxation processes to be Arrhenius in nature, the activation energy of the α-relaxation in poly(4-vinylimidazolium) BF 4 − , PF 6 − , CF 3 SO 3 − , TFSI − , and C 2 N 3 − salts ranged from 83 to 28 kJ/mol and appears to scale with the glass transition temperature.
Background: Urinary proteins are predictive and prognostic markers for diabetes nephropathy. Conventional methods for the quantification of urinary proteins, however, are time-consuming, and most require radioactive labeling. We designed a label-free piezoelectric quartz crystal microbalance (QCM) immunosensor array to simultaneously quantify 4 urinary proteins. Methods: We constructed a 2 ؋ 5 model piezoelectric immunosensor array fabricated with disposable quartz crystals for quantification of microalbumin, ␣ 1 -microglobulin,  2 -microglobulin, and IgG in urine. We made calibration curves after immobilization of antibodies at an optimal concentration and then evaluated the performance characteristics of the immunosensor with a series of tests. In addition, we measured 124 urine samples with both QCM immunosensor array and immunonephelometry to assess the correlation between the 2 methods. Results: With the QCM immunosensor array, we were able to quantify 4 urinary proteins within 15 min. This method had an analytical interval of 0.01-60 mg/L. The intraassay and interassay imprecisions (CVs) were <10%, and the relative recovery rates were 90.3%-109.1%. Nonspecificity of the immunosensor was insignificant (frequency shifts <20 Hz). ROC analyses indicated sensitivities were >95.8% and, specificities were
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