The graphene film with high thermal conductivity has garnered considerable attention in recent years as an ideal material for dissipating heat in high-power electronic devices. Thermal conductivity is a crucial parame...
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The graphene film with high thermal conductivity has garnered considerable attention in recent years as an ideal material for dissipating heat in high-power electronic devices. Thermal conductivity is a crucial parameter for evaluating its fundamental performance. High-precision measurement holds significant importance for understanding its basic properties, fabrication optimization, and industrial applications. However, it is difficult to simultaneously achieve efficient, accurate, and reliable measurements with existing commercial thermal conductivity testing methods. The development of a convenient, high-precision, and reliable measurement approach remains a great challenge. Here, we introduce a thermal conductivity testing methodology with superior accuracy and excellent efficiency based on an improved steady-state electric heating method, refined through the optimization of heat transfer principles, experimental operation, and data analysis, supported by finite element simulation. The accuracy of measurements is affected by four factors: heat loss calibration, sample size, device design, and data treatment. The experimental results show that the heat loss caused by heat radiation and heat convection affects the temperature distribution and the measurements of the sample, which should be strictly controlled by sample size and temperature rise. Reasonable screening and preprocessing of data are also necessary to improve measurement accuracy. Through the comparative analysis of the temperature distribution and thermal conductivity measurements of samples under different conditions, we propose feasible operational guidance and a standardized testing protocol to minimize measurement error. The measurement error is less than 3.0%, and uncertainty is reduced to 0.5%. Simulation results confirm that the response time of this method is down to milliseconds, correlating well with the experiment, which can effectively improve test efficiency. Considering the combined meri
Optically active α-phenyl-ααethyl-β-propiolactone of high optical purity was prepared and polymerized by homogeneous anionic initiation to the isotactic polyester. The racemic and isotactic polymers had apparently...
Optically active α-phenyl-ααethyl-β-propiolactone of high optical purity was prepared and polymerized by homogeneous anionic initiation to the isotactic polyester. The racemic and isotactic polymers had apparently different crystalline properties suggesting that the former may be syndiotactic or may crystallize with unit cells containing both R and S blocks. Similar attempts to prepare α-methyl-α-isopropyl-β-propiolactone of high optical purity were unsuccessful although a partially crystalline polymer was obtained from the racemic monomer.
We systematically investigated the development of film morphology and crystallinity of methyl-ammonium bismuth (Ⅲ) iodide (MA3Bi2I9) through one- step spin-coating on TiO2-deposited indium tin oxide (ITO)/glass...
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We systematically investigated the development of film morphology and crystallinity of methyl-ammonium bismuth (Ⅲ) iodide (MA3Bi2I9) through one- step spin-coating on TiO2-deposited indium tin oxide (ITO)/glass. The precursor solution concentration and substrate structure have been demonstrated to be critically important in the active-layer evolution of the MA3Bi2I9-based solar cell. This work successfully improved the cell efficiency to 0.42% (average: 0.38%) with the mesoscopic architecture of ITO/compact-TiOdmesoscopic-TiO2 (meso-TiO2)/ MA3Bi2I9/2,2',7,7'-tetrakis(N,N-di-4-methoxyphenylamino)-9,9'spiro-bifluorene (spiro-MeOTAD)/MoO3/Ag under a precursor concentration of 0.45 M, which provided the probability of further improving the efficiency of the BiB+-based lead-free organic-inorganic hybrid solar cells.
The purpose of this study was to prepare iron-based catalysts supported on silica by autocombustion method for directly using for Fischer-Tropsch synthesis(FTS) without a reduction step. The effect of different citr...
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The purpose of this study was to prepare iron-based catalysts supported on silica by autocombustion method for directly using for Fischer-Tropsch synthesis(FTS) without a reduction step. The effect of different citric acid(CA):iron nitrate(N) molar ratios and acid types on the FTS performance of catalysts were investigated. The CA:N molar ratios had an important influence on the formation of iron active phases and FTS activity. The iron carbide(FexC), which is known to be one of the iron active phases, was demonstrated by the X-ray diffraction and X-ray photoelectron spectroscopy. Increasing the CA:N molar ratios up to 0.1 increased CO conversion of catalyst to 86.5%, which was then decreased markedly at higher CA:N molar ratios. An excess of CA resulted in carbon residues covering the catalyst surface and declined FTS activity. The optimal catalyst(CA:N molar ratio = 0.1) achieved the highest CO conversion when compared with other autocombustion catalysts as well as reference catalyst prepared by impregnation method, followed by a reduction step. The autocombustion method had the advantage to synthesize more efficient catalysts without a reduction step. More interestingly, iron-based FTS catalysts need induction duration at the initial stage of FTS reaction even after reduction, because metallic iron species need time to be transformed to FexC. But here, even if without reduction, FexC was formed directly by autocombustion and induction period was eliminated during FTS reaction.
The antioxidant N-isopropyl-N'-phenyl-p-phenylenediamine(4010NA)was dissolved in ethanol and impregnated into silica aerogel(SAG)via vacuum-pressure cycles,yielding composite particles(A-N)with enhanced sustained-...
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The antioxidant N-isopropyl-N'-phenyl-p-phenylenediamine(4010NA)was dissolved in ethanol and impregnated into silica aerogel(SAG)via vacuum-pressure cycles,yielding composite particles(A-N)with enhanced sustained-release and reinforcing *** effect of A-N on the mechanical properties and thermal-oxidative aging resistance of styrene-butadiene rubber(SBR)vulcanizates was *** and BET assessments indicated that the loading efficiency of 4010NA in SAG reached 14.26%within ethanol's solu bility *** A-N into SBR vulcanizates significantly elevated tensile strength by 17.5%and elongation at break by 41.9%over those with fumed silica and ***,A-N notably enhanced the thermal-oxidative aging resistance of *** aging for 96 h at 100℃,the tensile strength and elongation at break of SBR with A-N sustained 70.09%and 58.61%of their initial values,respectively,with the retention rate of elongation at break being 62.8%higher than that of SBR with fumed silica and free *** study revealed that A-N composite particles significantly inhibited the crosslinking in SBR's molecular chains,reducing hardening and embrittlement during later thermal-oxidative aging stages.
Inflammation plays a key role in cartilage damage that occurs in osteoarthritis (OA). However, in vitro assessments of tissue-engineered constructs for cartilage regeneration generally do not consider their performanc...
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Mesoporous aluminosilicate (Al-MS) with different morphology and porosity is synthesized using a combination of sol-gel and hydrothermal methods by controlling the ratio between P123 and nanocellulose (NCC). The role ...
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Blade coating is the most common method of coating paper, and it is applied in coating magnetic suspensions and adhesives. Typically, the blade's upstream edge is clamped into a rigid holder so that the blade and ...
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Blade coating is the most common method of coating paper, and it is applied in coating magnetic suspensions and adhesives. Typically, the blade's upstream edge is clamped into a rigid holder so that the blade and substrate form a converging wedge. The translating substrate drags liquid into the wedge, where liquid forces develop and deflect the elastic blade, but it is loaded externally to counteract the deflection. Liquid dragged past the blade and thus the coating thickness depend on the elastohydrodynamic interaction among blade, liquid, and loading. Shell theory and lubrication flow theory describe the interaction by means of differential equations that are shown to be equivalent to Saita and Scriven's (1985) earlier formulation but that lead to a computationally more efficient analysis. Predictions computed agree with those of the earlier formulation and with experiments. Moreover, the new predictions illustrate effects of normal force loading and broaden the theory of blade coating.
Poly(vinyl alcohol)(PVA)is usually processed and used in a form of aqueous dispersion.A large number of inter-and intramolecular hydrogen bonds make it very difficult to obtain suitable rheological behavior for *** th...
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Poly(vinyl alcohol)(PVA)is usually processed and used in a form of aqueous dispersion.A large number of inter-and intramolecular hydrogen bonds make it very difficult to obtain suitable rheological behavior for *** this study,carbon particles with different topological shapes were added into PVA aqueous dispersion to tune the steady and dynamic rheological *** results show that the zero-dimensional particles(carbon black,CB)increase monotonically the zero-shear viscosity of PVA dispersion,while the one-dimensional particles(carbon nanotubes,CNTs)make it first increase,and then decrease and rise again,like an N-shape,and the two-dimensional particles(graphene oxide,GO)can make it first decrease and then increase,exhibiting a *** is believed that the topological shape of the carbon particles brought about these *** zero-dimensional particles mainly act as physical crosslinking points due to their small *** at a certain content,both CNTs and GO can destroy the intermolecular hydrogen bonds between PVA chains because the PVA chains can twine around the slim CNTs and the large planar size of GO prevents the adsorbed PVA from forming hydrogen bond with other *** high hydroxyl value of carbon particle surface could strengthen this *** is expected that the viscosity of polymer dispersion can be regulated by particles with different topological shape and the surface characteristic,so as to widen the operable concentration range during preparing composite functional materials.
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