Polyacrylonitrile/Aminated Polymeric Nanosphere Nanofibers as Efficient Adsorbents for Cr(VI) Removal

In this work, polyacrylonitrile/aminated polymeric nanosphere (PAN/APN) nanofibers were prepared by electrospinning of monodispersed aminated polymeric nanospheres (APNs) for removal of Cr(VI) from aqueous solution. Characterization results showed that obtained PAN/APNs possessed nitrogen functionalization. Furthermore, the adsorption application results indicated that PAN/APN nanofibers exhibited a high adsorption capacity of 556 mg/g at 298 K for Cr(VI) removal. The kinetic data showed that the adsorption process fits the pseudo-second order. A thermodynamic study revealed that the adsorption of Cr(VI) was spontaneous and endothermic. The coexisting ions Na⁺, Ca²⁺, K⁺, Cl⁻, NO₃⁻ and PO₄³⁻ had little influence on Cr(VI) adsorption, while SO₄²⁻ in solution dramatically decreased the removal performance. In the investigation of the removal mechanism, relative results indicated that the adsorption behavior possibly involved electrostatic adsorption, redox reaction and chelation. PAN/APN nanofibers can detoxify Cr(VI) to Cr(III) and subsequently chelate Cr(III) on its surface. The unique structure and nitrogen functionalization of PAN/APN nanofibers make them novel and prospective candidates in heavy metal removal.     

Surface enrichment of Ir on the IrRu alloy for efficient and stable water oxidation catalysis in acid

Inducing the surface enrichment of active noble metal can not only help to stabilize the catalyst but also modify the catalytic performance of the catalyst through electronic and geometric effects. Herein, we report the in situ surface enrichment of Ir on IrRu alloy during the oxygen evolution reaction (OER). The surface enrichment of Ir was probed by ex situ high-resolution transmission electron microscopy (HRTEM), in situ X-ray absorption spectroscopy (XAS), and electrochemical Cu stripping, leading to complementary characterizations of the dynamic reconstruction of the IrRu alloy during OER. Guided by the density functional theory (DFT), an IrRu alloy with low Ir content (20 wt%) was constructed, which displayed a low overpotential of only 230 mV to deliver an OER current density of 10 mA cm⁻² in 0.1 M HClO₄ solution and maintained stable performance for over 20 h. To investigate the practical application potential, a proton exchange membrane (PEM) water electrolyzer using the IrRu alloy as the anode catalyst was assembled, which required a low cell voltage of only 1.48 V to generate a current density of 1 A cm⁻².

Inducing the surface enrichment of active noble metal can not only help to stabilize the catalyst but also modify the catalytic performance of the catalyst through electronic and geometric effects.     

A Comprehensive Review on the Benefits and Problems of Curcumin with Respect to Human Health

Curcumin is the most important active component in turmeric extracts. Curcumin, a natural monomer from plants has received a considerable attention as a dietary supplement, exhibiting evident activity in a wide range of human pathological conditions. In general, curcumin is beneficial to human health, demonstrating pharmacological activities of anti-inflammation and antioxidation, as well as antitumor and immune regulation activities. Curcumin also presents therapeutic potential in neurodegenerative, cardiovascular and cerebrovascular diseases. In this review article, we summarize the advancements made in recent years with respect to curcumin as a biologically active agent in malignant tumors, Alzheimer’s disease (AD), hematological diseases and viral infectious diseases. We also focus on problems associated with curcumin from basic research to clinical translation, such as its low solubility, leading to poor bioavailability, as well as the controversy surrounding the association between curcumin purity and effect. Through a review and summary of the clinical research on curcumin and case reports of adverse effects, we found that the clinical transformation of curcumin is not successful, and excessive intake of curcumin may have adverse effects on the kidneys, heart, liver, blood and immune system, which leads us to warn that curcumin has a long way to go from basic research to application transformation.     

Palladium-catalyzed hydrosilylation of ynones to access silicon-stereogenic silylenones by stereospecific aromatic interaction-assisted Si–H activation

Hydrosilylation is one of the most important reactions in synthetic chemistry and ranks as a fundamental method to access organosilicon compounds in industrial and academic processes. However, the enantioselective construction of chiral-at-silicon compounds via catalytic asymmetric hydrosilylation remained limited and difficult. Here we report a highly enantioselective hydrosilylation of ynones, a type of carbonyl-activated alkynes, using a palladium catalyst with a chiral binaphthyl phosphoramidite ligand. The stereospecific hydrosilylation of ynones affords a series of silicon-stereogenic silylenones with up to 94% yield, 20:1 regioselectivity and 98:2 enantioselectivity. The density functional theory(DFT) calculations were conducted to elucidate the reaction mechanism and origin of high degree of stereoselectivity, in which the powerful potential of aromatic interaction in this reaction is highlighted by the multiple C–H-π interaction and aromatic cavity-oriented enantioselectivitydetermining step during desymmetric functionalization of Si–H bond.     

Na2S-Mediated One-Pot Selective Deoxygenation of α-Hydroxyl Carbonyl Compounds including Natural Products

A practical method for the deoxygenation of α-hydroxyl carbonyl compounds under mild reaction conditions is reported here. The use of cheap and easy-to-handle Na₂S·9H₂O as the reductant in the presence of PPh₃ and N-chlorosuccinimide (NCS) enables the selective dehydroxylation of α-hydroxyl carbonyl compounds, including ketones, esters, amides, imides and nitrile groups. The synthetic utility is demonstrated by the late-stage deoxygenation of bioactive molecule and complex natural products.     

Pattern-adaptive error diffusion algorithm for improved phase-only hologram generation

The bidirectional error diffusion(BERD) algorithm is free from random phase modulation that introduces speckle noise on the reconstructed images, compared with other computer-generated phase-only hologram(POH) approaches. During the POH generation process, the amplitudes of all pixels are traditionally set to one for diffusing the errors to their neighborhood of unprocessed pixels. In this paper, we reveal that the reconstruction quality depends on the uniform amplitude value for different object pattern. The pattern-adaptive BERD(PA-BERD) algorithm is proposed for high-quality holographic reconstruction. The optimized amplitude value can be acquired for each object pattern and each propagation distance.The PA-BERD-based POHs have shown higher reconstruction quality than traditional BERD-based POHs in simulations as well as optical experiments.     

Unraveling hydridic-to-protonic dihydrogen bond predominance in monohydrated dodecaborate clusters

Hydridic-to-protonic dihydrogen bonds (DHBs) are involved in comprehensive structural and energetic evolution, and significantly affect reactivity and selectivity in solution and solid states. Grand challenges exist in understanding DHBs’ bonding nature and strength, and how to harness DHBs. Herein we launched a combined photoelectron spectroscopy and multiscale theoretical investigation using monohydrated closo-dodecaborate clusters B₁₂X₁₂²⁻·H₂O (X = H, F, I) to address such challenges. For the first time, a consistent and unambiguous picture is unraveled demonstrating that B–H⋯H–O DHBs are superior to the conventional B–X⋯H–O HBs, being 1.15 and 4.61 kcal mol⁻¹ stronger than those with X = F and I, respectively. Energy decomposition analyses reveal that induction and dispersion terms make pronounced contributions resulting in a stronger B–H⋯H–O DHB. These findings call out more attention to the prominent roles of DHBs in water environments and pave the way for efficient and eco-friendly catalytic dihydrogen production based on optimized hydridic-to-protonic interactions.

A joint gas-phase ion spectroscopic and multiscale theoretical study reveals unequivocally the predominance of the hydridic-to-protonic dihydrogen bond over the prototypical strong hydrogen bond in monohydrated dodecaborate clusters.     

导电性磁流变弹性体的研究进展

磁流变弹性体(magnetorheological elastomer,MRE)因其独特的场相关性能在工程应用领域引起了广泛关注.论文介绍了MRE的最新发展,重点介绍导电性MRE在材料设计、力学行为和实际应用等方面的研究现状.论文从高性能导电性MRE的研制开始,讨论了材料与结构设计中涉及的关键问题;介绍了导电性MRE材料在磁场作用下的磁、力、电学行为的耦合作用机理和相关物理模型;之后对导电性MRE器件的研究现状进行了总结;最后展望了导电性MRE的发展潜力和面临的挑战.     

轴承自供能监测的径向电磁式能量俘获建模与实验研究

无线网络和低功耗微电子技术的进步推动着设备健康监测技术的网联化和智能化发展.轴承作为旋转设备的关键部件,对国防、轨道交通、风电等重大装备的健康状态起到了非常重要的作用,实现轴承状态监测的微型化和自供能是装备智能化的重要技术基础.论文针对于轴承无线传感器网络的供能问题,提出了一种用于轴承自供能监测的径向电磁式旋转能量俘获建模方法,并通过引入环形Halbach永磁阵列增强了线圈中的磁场强度,提高了能量俘获系统的输出性能.基于磁荷理论和空间坐标变换给出了环形Halbach永磁阵列的径向磁场计算方法,进而利用电磁感应原理建立了电磁式旋转能量俘获系统的输出电压模型,仿真分析了不同参数对系统输出电压的影响.有限元仿真和不同转速下的实验结果验证了所建立模型预测输出电压的准确性,同时功率测试实验表明设计的俘能系统在1000 rpm转速下可实现81.2 mW的输出功率.     

椭圆形孔扩张弹性分析

圆孔扩张理论作为一种相对成熟的理论工具已经广泛运用于岩土工程中的各类问题,但是对于初始孔为椭圆孔的扩孔问题,圆孔扩张理论并不适用.基于保角变换的方法将原物理平面上初始椭圆孔洞的外部映射到像平面上的单位圆外部,将原物理平面上由于椭圆孔洞扩张所产生的位移边界条件转换到像平面上,利用平面复变弹性理论,得到初始椭圆形孔洞孔扩张的弹性解.将论文椭圆孔扩张的退化解与传统圆孔扩张的弹性解进行对比分析,验证椭圆孔扩张弹性解的正确性.续而,针对一算例详细分析了椭圆孔扩张的弹性力学特性.研究结果表明,椭圆孔的退化解与传统的圆孔扩张弹性解完全一致,椭圆孔在弹性扩张过程中长轴方向比短轴方向较难扩张,长轴方向需要的扩张压力比短轴方向的要大.此外,当扩张率a2/a1=0.11/0.1=1.1时,扩张的影响半径为10倍的孔径左右.