Reversible formation-melting of nano-crystals in supercooled oxyfluoride germanate liquids

The nanocrystals play a critical role in generating and affecting functionalities of glass materials. Therefore, scientists have made considerable efforts in clarifying microscopic mechanisms of nanocrystal formation in glass to obtain the desired type of nanocrystals. However, the phase transitions of nanocrystals during heating have not been well understood. Here we report on a discovery of the reversible melting-formation of nanocrystals in an oxyfluoride germanate glass during heating-cooling circles. Using a differential scanning calorimetry (DSC), we detected a striking endothermic event at 925 K during heating, after the glass underwent a DSC upscan to a temperature between 925–986 K and subsequent cooling. Based on Raman spectroscopy, X-ray diffraction and transmission electron microscopy, the endotherm is attributed to the melting of nano-crystal BaGeF₆ (˜20 nm). An exothermal response was observed at 890 K during the DSC downscan, implying the re-formation of BaGeF₆ nano-crystals. This suggests that the melting-formation of BaGeF₆ nano-crystals is a typical first-order transition.     

Mg gas infiltration for the fabrication of MgB2 pellets using nanosized and microsized B powders

MgB₂ superconductor pellets were synthesized through Mg gas infiltration method using nanosized- and microsized B powders. There was a marked difference in the superconducting properties of the two samples, particularly in the pinning force and dominant pinning mechanism. The microstructures of the samples were observed using HR-TEM and STEM-HAADF, and the results showed that the primary reason for the difference in the superconducting properties is the distribution of the nanosized second-phase particle MgO. Additionally, a feasible reaction model for the Mg gas infiltration method was established. Compared to the Mg liquid infiltration method, the gas infiltration showed better penetrability ability with a small amount of residual Mg. This study presents a novel synthesis process to fabricate an MgB₂ pellet with superior density and superconducting properties. This method can be used in multiple applications such as superconducting bearings, compact superconductor magnets, and magnetic shielding.     

化妆品用改性山茶油制备工艺研究

以山茶油水解产物和聚乙二醇600(PEG600)为原料,在高温下进行酯化反应制备改性山茶油。考察了催化剂种类和用量、反应温度、投料比及反应时间对酯化反应的影响。根据单因素试验得出制备改性山茶油的最佳工艺条件为:预热温度80℃,预热时间5 min,4 ?型分子筛为催化剂,催化剂用量0. 4%,反应温度160℃,投料比(PEG600与山茶油水解产物摩尔比) 1∶1. 2,反应时间6. 5 h。在最佳工艺条件下,酯化率为93. 16%,产物改性山茶油能与水以任意比例互溶。对产物分离纯化后,经定性试验以及红外光谱和超高效液相色谱-质谱(UPLC-MS)分析,发现改性山茶油的主要成分是聚乙二醇单、双酯。同时对产物的各项性能进行测试,其含水率为0. 67%、皂化值(KOH)为110. 2 mg/g、过氧化值为4. 6 mmol/kg、临界胶束浓度为1. 5 g/L(此时表面张力为32. 01mN/m)、HLB值为14、乳化最大分水时间为9. 8 min。     

Effects of chemical etching on structure and properties of Y0.5Gd0.5Ba2Cu3O7-z coated conductors

Corrosion resistance is a crucial property to achieve successful superconducting joints of Y_0.5Gd_0.5Ba₂Cu₃O_7-z (YGdBCO) coated conductors (CCs). Cu and Ag metallic layers need to be fully removed from the area of conductor to be joint to allow for a superconducting path across the joint. Therefore, when using a wet etching process to remove the metallic layers, the joint performance can be significantly influenced by the etching conditions. The effects of chemical etching with ammonia water and hydrogen peroxide mixture on crystal structure, surface microstructure and critical current (I_c) of YGdBCO CCs were systematically investigated. We found the set of etching parameters that does not affect conductor performance, leaving the I_c of the YGdBCO conductor unchanged upon etching. However, when the etching conditions are not optimal, decrease in I_c was found and the underlying reasons driving the degradation were investigated. Raman spectroscopy and XRD analysis indicated that the reduced I_c is mainly due to oxygen deficiency in the YGdBCO crystal lattice.     

Correction to: Parallel optimization of the ray-tracing algorithm based on the HPM model

The Journal of Supercomputing - A correction to this paper has been published: https://doi.org/10.1007/s11227-021-03680-0     

基于自监督学习的病理图像层次分割

在苏木精-伊红(HE)染色病理图像中，细胞染色分布的不均匀和各类组织形态的多样性给病理图像的自动分割带来极大挑战。为解决该问题，提出了一种基于自监督学习的病理图像三步层次分割方法，对病理图像中各类组织进行由粗略到精细的全自动逐层分割。首先，根据互信息的计算结果在RGB色彩空间中进行特征选择；其次，采用K-means聚类将图像初步分割为各类组织结构的色彩稳定区域与模糊区域；然后，以色彩稳定区域为训练集采用朴素贝叶斯分类对模糊区域进行进一步分割，得到完整的细胞核、细胞质和胞外间隙这三类组织结构；最后，对细胞核部分进行结合形状和色彩强度的混合分水岭分割得到细胞核间的精确边界，进而量化计算细胞核个数、核占比、核质比等指标。对脑膜瘤HE染色病理图像的分割实验结果表明，所提方法对于染色和细胞形态差异保持较高的鲁棒性，各类组织区域分割误差在5%以内，在细胞核分割精度的对比实验中平均正确率在96%以上，满足临床自动图像分析的要求，其量化结果可以为定量病理分析提供依据。     

Lewis acid-oxygen vacancy interfacial synergistic catalysis over SO42−/Ce0.84Zr0.16O2–WO3–ZrO2 for N,N-diethylation of aniline with ethanol

Herein, a new mechanism involving Lewis acid-oxygen vacancy interfacial synergistic catalysis for aniline N,N-diethylation with ethanol was proposed, and the SO₄²⁻/Ce_0.84Zr_0.16O₂–WO₃–ZrO₂ catalyst (SCWZ) with both Lewis acid sites and oxygen vacancies was synthesized by the hydrothermal method, which shows better catalytic activity than the reported solid acidic catalysts. Besides, the SO₄²⁻/ZrO₂ (SZ) and SO₄²⁻/WO₃–ZrO₂ (SWZ) catalysts were also prepared and compared with SCWZ to investigate the synergistic effect of each component. The SO₄²⁻ and WO₃ mainly generate Lewis acid by bonding with ZrO₂, which is beneficial for the fracture of the N–H bond in aniline. The Ce_0.84Zr_0.16O₂ solid solution mainly plays a vital role in generating the oxygen vacancies as the interface active species, which can participate in stripping –OH from ethanol, then the carbocation will also be released, which only needs 1.3805 kcal/mol energy, calculated by density functional theory (DFT), to be input. In comparison, the traditional reaction mechanism needs the Brønsted acidic sites to promote the protonation of ethanol, then dehydration and subsequent formation of carbocation followed, and 108.6846 kcal/mol energy needs to be input, which is far higher than that of the new mechanism. The apparent activation energy (E_a) over SCWZ was measured by experiment to be 34.09 kJ/mol, which is much lower than that of SWZ (47.10 kJ/mol) and SZ (54.37 kJ/mol), illustrating comparatively preferable kinetics for SCWZ than that of SWZ and SZ. Besides, the conversion of aniline and selectivity to N,N-diethylaniline over SCWZ reach almost 100% and 73%, respectively. The SCWZ can be renewed for 4 times without rapid deactivation, and the longevity of SCWZ is longer than that of SWZ and SZ, as the loaded SO₄²⁻ and tetragonal ZrO₂ are stabilized by Ce_0.84Zr_0.16O₂ and WO₃, respectively.     

The Crystal Structure and Superconducting Property of (Li0.8Fe0.2)OHFeSe1-xTex

Journal of Superconductivity and Novel Magnetism - (Li0.8Fe0.2)OHFeSe is a superconductor with high superconducting transition temperature (43 K) and stable in air, which is conducive to...     

Mn4+-activated KLaMgWO6: A new high-efficiency far-red phosphor for indoor plant growth LEDs

Novel Mn⁴⁺-activated KLaMgWO₆ red phosphors with different Mn⁴⁺ concentrations were successfully synthesized via a high-temperature solid-state reaction method. The phase formation, microstructure, photoluminescence properties, decay lifetimes and internal quantum efficiency were discussed to analyze the properties of the as-prepared phosphors. The samples belonged to monoclinic crystal system with enough WO₆ octahedrons that provided suitable sites for Mn⁴⁺ ions. Upon the excitation of 348?nm, KLaMgWO₆:Mn⁴⁺ phosphors gave bright far-red emission around 696?nm due to the ²E_g→⁴A_2g transition of Mn⁴⁺ ions. The critical concentration of Mn⁴⁺ was 0.6?mol% and the concentration quenching mechanism belonged to electric multipolar interaction. Besides, the CIE chromaticity coordinates of the KLaMgWO₆:0.6%Mn⁴⁺ phosphor were (0.7205, 0.2794) which located in deep red range, and its color purity reached up to 96.6%. The KLaMgWO₆:0.6%Mn⁴⁺ sample also exhibited high internal quantum efficiency of 43%. All of the admirable optical properties indicate that the KLaMgWO₆:Mn⁴⁺ phosphors can be applied to indoor plant growth illumination.     

Recycling spent lead acid batteries into aqueous zinc-ion battery material with ultra-flat voltage platforms

The harmless disposal of lead paste in the spent lead-acid batteries (LABs) remains an enormous challenge in traditional pyrometallurgical recycling. Here, we introduced a hydrometallurgical method for the recycling of the spent LABs’ waste to obtain the β-PbO as a novel zinc ion batteries (ZIBs) active material. The obtained β-PbO exhibits ultra-flat charge/discharge voltage platforms (0.21 mV/(mAh g^?1)) and stable specific capacity. During the charge/discharge, the β-PbO spontaneously triggers the formation of (ZnSO₄)[Zn(OH)₂]₃·5H₂O (ZHS) micro-sheets as a surface passivation layer. Moreover, the ex-situ X-ray spectra reveal that the reversible phase transformation occurs between PbSO₄ and Pb with the assistance of ZHS by adjusting the PH value on the electrode-electrolyte interface. The synergistic two-phase-reaction mechanism generates ultra-flat voltage platforms upon the charge/discharge. This “energy-saving and environment-friendly” recycling route eliminates the major source of emission of pollution particulates/gases compared to the traditional pyrometallurgical recycling, while at the same time replacing energy-consuming and environmentally detrimental processes of synthesis of current ZIBs cathodes.