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181.
182.
Well‐defined poly(3‐alkyl‐4‐benzamide) was synthesized by means of chain‐growth condensation polymerization of phenyl 3‐octyl‐4‐(4‐octyloxybenzyl(OOB)amino)benzoate ( 1c ) from initiator 2 , followed by removal of the OOB groups on amide nitrogen of poly 1c . Polymerization of 1c with phenyl 4‐(trifluoromethyl)benzoate ( 2b ) in the presence of 1,1,1,3,3,3‐hexamethyldisilazide (LiHMDS) and LiCl in THF at ?10 °C gave poly 1c with a narrow molecular weight distribution (Mw/Mn ≤ 1.08) and a well‐defined molecular weight (Mn = 4480–12,700) determined by the feed ratio of monomer to initiator (from 10 to 30). The OOB groups of poly 1c were removed with H2SO4 to give the corresponding N‐unsubstituted poly(p‐benzamide) (poly 1c′ ) with low polydispersity. The solublity of poly 1c′ in polar organic solvents was dramatically higher than that of poly(p‐benzamide), demonstrating that introduction of an alkyl group on the aromatic ring is very effective for improving the solubility of poly(p‐benzamide). © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 360–365  相似文献   
183.
The growth, XRD patterns, spectral properties, and fluorescence decays of Yb:Ca0.28Ba0.72Nb2O6 (Yb:CBN) with doping concentration of 1 at.% and 5 at.% were studied. The peak absorption cross-section and the emission cross-section were calculated. Larger Stark splitting of Yb:CBN offers the prospect of the quasi-four level laser operation.  相似文献   
184.
Oligo(spiroketal)s (OSKs) were synthesized from myo‐inositol, a naturally occurring cyclic compound bearing six hydroxyl groups. The successful synthesis of OSKs was achieved using silyl ethers 2 derived from 1,4‐di‐O‐alkylated myo‐inositol 1 as monomers, which underwent polycondensation with 1,4‐cyclohexanedione (CHD) at 0 °C in the presence of trimethylsilyl triflate as a catalyst. Because of the irreversible nature of the condensation reaction of silyl ethers with ketones, the resulting OSKs 7 had higher molecular weights than previously reported OSKs that were obtained by polycondensation of tetraols 1 with CHD, where backward hydrolysis of the ketal functions occurred. In addition, another series of OSKs, 8, were synthesized using silyl ethers 3 derived from 2,5‐di‐O‐alkylated myo‐inositol 6 , which are more symmetric monomers than silyl ethers 2 . Silyl ethers 3 underwent efficient polycondensation with CHD, whereas tetraol 6 did not, demonstrating that the derivation of such tetraols into the corresponding silyl ethers is a powerful strategy to access OSKs. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 2407–2414  相似文献   
185.
In this paper, we study the following fractional Schrödinger equation with critical or supercritical growth where 0 < s < 1, N > 2s, λ > 0, , , ( ? Δ)s denotes the fractional Laplacian of order s and f is a continuous superlinear but subcritical function. Under some suitable conditions, we prove that the equation has a nontrivial solution for small λ > 0 by variational methods. Our main contribution is related to the fact that we are able to deal with the case .  相似文献   
186.
Solar-driven water splitting to produce clean and renewable hydrogen offers a green strategy to address the energy crisis and environmental pollution. Heterostructure catalysts are receiving increasing attention for photocatalytic hydrogen generation. ZnO/ZnS/CdS and ZnO/CdS heterostructures have been successfully designed and prepared according to two different strategies. By introducing a heterointerface layer of ZnS between ZnO and CdS, a Z scheme charge-transfer channel was promoted and achieved superior photocatalytic performance. A highest hydrogen generation rate of 156.7 μmol g−1 h−1 was achieved by precise control of the thickness of the heterointerface layer and of the CdS shell. These findings demonstrated that heterostructures are promising catalysts for solar-driven water splitting, and that heterointerface engineering is an effective way to improve the photocatalytic properties of heterostructures.  相似文献   
187.
论文针对中密度聚乙烯材料(MDPE),采用平板试样进行了I型疲劳裂纹扩展和单次过载下裂纹扩展试验.发现与金属材料类似,单次拉伸过载对聚乙烯(PE)的疲劳裂纹扩展有明显的迟滞作用,降低了裂纹扩展速率.试验还通过变载荷刻线法获取疲劳裂纹扩展前缘的实际形貌和变化规律,对常规变载荷刻线方法进行了调整和验证,其修正方法对高分子材料的疲劳裂纹扩展前缘刻线具有较好的效果.通过观察发现含楔形塑性区的裂尖钝化是裂纹迟滞的主要原因.过载引入的塑性区内残余应力对裂纹迟滞也起了重要作用.论文利用Dugdale模型计算了塑性区尺寸,使用基于残余应力的Wheeler模型对过载迟滞进行了很好的拟合.  相似文献   
188.
189.
We establish that solutions to the Cauchy–Dirichlet problem
?tu?div(Dξf(x,Du))=0
for functionals f:Ω×RN×n[0,) of linear growth can be obtained as limits of solutions to flows with p-growth in the limit p1. The result can be interpreted on the one hand as a stability result. On the other hand it provides an existence result for general flows with linear growth.  相似文献   
190.
We consider fully nonlinear uniformly elliptic equations with quadratic growth in the gradient, such as
?F(x,u,Du,D2u)=λc(x)u+M(x)Du,Du+h(x)
in a bounded domain with a Dirichlet boundary condition; here λR, c,hLp(Ω), p>n1, c?0 and the matrix M satisfies 0<μ1IMμ2I. Recently this problem was studied in the “coercive” case λc0, where uniqueness of solutions can be expected; and it was conjectured that the solution set is more complex for noncoercive equations. This conjecture was verified in 2015 by Arcoya, de Coster, Jeanjean and Tanaka for equations in divergence form, by exploiting the integral formulation of the problem. Here we show that similar phenomena occur for general, even fully nonlinear, equations in nondivergence form. We use different techniques based on the maximum principle.We develop a new method to obtain the crucial uniform a priori bounds, which permit to us to use degree theory. This method is based on basic regularity estimates such as half-Harnack inequalities, and on a Vázquez type strong maximum principle for our kind of equations.  相似文献   
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