CaCuO2颗粒尺寸对双粉法制备Bi系高温超导带材性能的影响

本文通过基于共沉淀工艺的双粉法制备了Bi_1.76Pb_0.34Sr_1.93Ca_2.0Cu_3.06O_8+d (Bi-2223)前驱体粉末。在这一过程中,首先单独制备了Bi_1.76Pb_0.34Sr_1.93CaCu_2.06O_8+d (Bi-2212)和CaCuO₂(实际相组成为Ca₂CuO₃和CuO)粉末,并分别进行了烧结。通过调节共沉淀工艺过程中的pH值,获得了颗粒尺寸不同的CaCuO₂粉末,然后将Bi-2212与其按照相组成相组成为1:1进行混合,并装入Ag包套中,通过一系列的旋锻、拉拔和轧制工艺,获得设计尺寸的Bi-2223带材。比表面积测试表明随着pH值从3.0增加到5.0和6.5,获得CaCuO₂粉末的平均颗粒尺寸从1.1减小到0.75和0.60 mm。通过扫描电镜对不同尺寸CaCuO₂颗粒制备的Bi-2223生带、第一次热处理和后处理之后带材的相组成和分布进行了表征。结果表明,适当尺寸的CaCuO₂颗粒可以避免团聚现象的出现,因此有利于高载流性能带材的获得。最终通过进一步调节带材的尺寸,1#带材的性能最高,达到了12200 Acm^_-2。     

Process−microstructure−properties relationship in Al−CNTs−Al2O3 nanocomposites manufactured by hybrid powder metallurgy and microwave sintering process

Al−2CNTs−xAl₂O₃ nanocomposites were manufactured by a hybrid powder metallurgy and microwave sintering process. The correlation between process-induced microstructural features and the material properties including physical and mechanical properties as well as ultrasonic parameters was measured. It was found that physical properties including densification and physical dimensional changes were closely associated with the morphology and particle size of nanocomposite powders. The maximum density was obtained by extensive particle refinement at milling time longer than 8 h and Al₂O₃ content of 10 wt.%. Mechanical properties were controlled by Al₂O₃ content, dispersion of nano reinforcements and grain size. The optimum hardness and strength properties were achieved through incorporation of 10 wt.% Al₂O₃ and homogenous dispersion of CNTs and Al₂O₃ nanoparticles (NPs) at 12 h of milling which resulted in the formation of high density of dislocations and extensive grain size refinement. Also both longitudinal and shear velocities and attenuation increase linearly by increasing Al₂O₃ content and milling time. The variation of ultrasonic velocity and attenuation was attributed to the degree of dispersion of CNTs and Al₂O₃ and also less inter-particle spacing in the matrix. The larger Al₂O₃ content and more homogenous dispersion of CNTs and Al₂O₃ NPs at longer milling time exerted higher velocity and attenuation of ultrasonic wave.     

Graphite powder coated polyurethane sponge hollow tube as a high-efficiency and cost-effective oil-removal materials for continuous oil collection from water surface

In this study, the cost-effective graphite powder (GPd)-coated polyurethane (PGPd-PU) sponge hollow tube (PGPd-PUHT) was prepared for high-efficient continuous oil removal, the hydrophobicity-superoleophilicity PGPd-PU sponge was fabricated through a simple dip-coating method, which dipping PU sponge into GPd dispersion and drying, then coating polydimethylsiloxane (PDMS) on sponge skeleton, as-prepared sponge could selectively absorb a variety of oils up to 34 times of its own weight for dimethyl sulfoxide (DMSO). The PGPd-PUHT was prepared via wrapping PGPd-PU sponge on porous tubular support. The obtained PGPd-PUHT could continuously collect various types of oils from water surface with flux as high as 1.52 kL/m²h, and excellent separation efficiency (up to 97.7%) for toluene, as well as remarkable reusability. Moreover, a continuous floating oil collection device based on PGPd-PUHT was designed which showed excellent floating oil collection ability. In addition, our strategy possesses the advantages of low cost, simple preparation, highly efficient, and easily scale-up, showing a great potential for dealing with practical oil spill remediation. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48921.     

A comparative study of Ni catalysts supported on Al2O3, MgO–CaO–Al2O3 and La2O3–Al2O3 for the dry reforming of ethane

CO₂ utilization through the activation of ethane, the second largest component of natural and shale gas, to produce syngas, has garnered significant attention in recent years. This work provides a comparative study of Ni catalysts supported on alumina, alumina modified with CaO and MgO, as well as alumina modified with La₂O₃ for the reaction of dry ethane reforming. The calcined, reduced and spent catalysts were characterized employing XRD, N₂ physisorption, H₂-TPR, CO₂-TPD, TEM, XPS and TPO. The modification of the alumina support with alkaline earth oxides (MgO and CaO) and lanthanide oxides (La₂O₃), as promoters, is found to improve the dispersion of Ni, enhance the catalyst's basicity and metal-support interaction, as well as influence the nature of carbon deposition. The Ni catalyst supported on modified alumina with La₂O₃ exhibits a relatively stable syngas yield during 8 h of operation, while H₂ and CO yields decrease substantially for Ni/Al₂O₃.     

Techno-economic-environmental evaluation of a combined tri and dry reforming of methane for methanol synthesis with a high efficiency CO2 utilization

Production of methanol, as a green energy, from syngas is coming into focus. However, natural gas based methanol plants, which are used steam reforming of methane for syngas production, have a high CO₂ emission resulting in the global warming. In this study, a novel process for methanol synthesis is proposed to reduce CO₂ emission. In this regard, natural gas and flue gas are fed to a parallel-series system with tri and dry reforming of methane for syngas production with the optimized stoichiometric number. Then, the produced syngas is converted to methanol in a reactor. Finally, the produced methanol is purified by two distillation towers. The proposed method is compared to a referenced method in the view of technological, economic and environmental metrics. The techno-economic-environmental analysis of the processes reveals that not only the proposed method, as compared to the referenced one, increases CO₂ conversion from 20.93% to 99.22%, but also it is more economical and environmentally friendly. In addition, the global warming potential of the proposed method is almost 60% lower than that for the referenced method due to the lower CO₂ emission. Therefore, the proposed method can save above MUS$ 8 a year by CO₂ capture.     

Effect of Si/Ti additions on physico-mechanical and chemical properties of FeNiCrCo high entropy alloys manufactured by powder metallurgy technique

FeNiCrCoSi_x and FeNiCrCoTi_x (x=0, 0.3, 0.6, and 0.9 wt.%) high entropy alloys (HEAs) were prepared via the powder metallurgy technique. A homogenous distribution of the elements in all alloys due to the formation of a solid solution phase is observed. The density and hardness of the prepared HEAs are improved by Si and Ti additions, compared to FeNiCrCo HEA. The wear rate of the prepared alloys was studied at different loads and the results indicate that the alloys that contain 0.3 wt.% Si and 0.9 wt.% Ti have the lowest wear rates. X-ray diffraction, SEM, and EDX were used to understand the phases, grain sizes, and microstructures in different investigated HEAs. The effects of Si and Ti content on the corrosion behavior and surface morphologies of sintered FeNiCrCoSi_x and FeNiCrCoTi_x HEAs were studied by immersion in H₂SO₄, HNO₃, and HCl solutions. Uniform corrosion and localized pitting are observed in different sizes in the corrosive media used. Because of the smaller pit size and the reduced pit density, the FeNiCrCoSi_0.3 HEA has an excellent microstructure.     

Effect of coral sand powders and seawater salinity on the impact mechanical properties of cemented coral sand

Coral sand is one kind of the important building materials in coral reef engineering practice. The use of cement as a stabilizing agent can significantly improve the mechanical properties of coral sands and is widely applied in the subbase engineering construction in coral reef islands. Cement-stabilized coral sand structures may contain high contents of fine coral particles and salinity because of the high crushability of coral sands and the existence of seawater surrounding them. In this study, the effects of coral sand powders and seawater salinity on the dynamic mechanical properties of cemented coral sand (CCS) were investigated through the split Hopkinson pressure bar (SHPB) tests and Scanning Electron Microscope (SEM) analysis. It was found that the strength (i.e., the peak stress) of CCS specimens increased firstly and then decreased with the increase of powder content. The specimens reached the maximum peak stress when 3% powder content was included. The initial improvement of CCS strength was attributed to the pore-filling effect of coral powders, namely, the micro pores of the CCS specimens could be more effectively filled with higher percentages of coral powders being used in the experiments. However, excessive coral powders resulted in the reduction of specimen strength because these powders could easily be cemented into agglomerates by absorbing water from the specimens. These agglomerates could reduce the cementation strength between the coarse coral particles and the cement. Meanwhile, the peak stress of CCS specimens was found to be negatively correlated with the average strain rate and the ultimate strain. The degree of specimen fracture was found to be correlated with the amount of specific energy absorption during the tests. Furthermore, the “sulfate attack” caused by the inclusion of salinity of water had different influences on the CCS specimens with different coral powder contents. The ettringite and gypsum produced in “sulfate attack” could fill the pores and lead to cracking of the specimens, significantly affecting the specimen strength.     

X射线荧光光谱在铜矿石分析中的应用文献评介

作者收集了我国用X射线荧光光谱(XRF)分析技术进行铜矿石(含铜精矿)分析的文献共计51篇,其中野外现场分析文献21篇,实验室内分析文献30篇。实验室内方法文献包括熔融制样法12篇,粉末压片制样的15篇,其他方法3篇。文章用列表方式对文献要点进行了介绍,对其中的多元素分析方法文献进行了重点评介,也特别讨论了X射线荧光光谱分析的技术条件、制样方法选取、标准物质与标准方法等问题。文献表明:XRF已成为铜矿石主次痕量分析最强有力的技术方法之一,并随着社会对环境需求的增长,直接粉末压片制样的XRF方法必将具有更广阔的发展前景。全篇引文89篇。     

Synthesis of Invar 36 type alloys from elemental and prealloyed powders by mechanical alloying

Invar 36 (Fe₆₄Ni₃₆) nanocrystalline powders were successfully obtained by the mechanical alloying process. The mechanically alloyed Invar 36 powders were obtained from both, Fe–Ni elemental and Fe–Ni₃Fe prealloyed powders. XRD, DSC and magnetic measurements were used to characterise the Invar 36 powders. The lattice parameter evolution versus temperature of Invar 36 powders was investigated by in-situ high-temperature X-ray diffraction (HT-XRD). For both, Invar 36 (Fe, Ni) and Invar 36 (Fe, Ni₃Fe) powders, the lattice parameter values are constant up to about 350°C. The magnetic measurement also indicated that the Invar 36-type alloys are formed after 16?h of milling.     

Reactions of microcrystalline fullerene C60 with amino and aza macrocyclic ligands under solvent-free conditions

We evaluated the reactivity under solvent-free conditions of 2-aminomethyl-15-crown-5 (AM15C5), 2-aminomethyl-18-crown-6 (AM18C6), 1,4,8,12-tetraazacyclopentadecane (TACPD) and rac-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane (tet b) with microcrystalline fullerene C₆₀. The reactions of nucleophilic addition were carried out at temperatures of about 160°C for 5 h in the case of crown ethers and TACPD, and at 180–190°C for 24 h in the case of tet b. Characterization of the products obtained was performed by using Fourier-transform infrared (FTIR) and Raman spectroscopy, laser desorption/ionization time-of-flight (LDI-TOF) mass spectroscopy, scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). To provide an additional insight into the reactivity of macrocyclic compounds with C₆₀ molecules, we employed theoretical calculations in the frame of density functional theory (DFT). According to the results of SEM imaging, macrocyclic reagents are generally unable to deeply penetrate into the bulk of fullerene microcrystals (with a possible exception of TACPD). According to TGA measurements, the reaction efficiency is very low for tet b, whereas the average content of organic fraction in C₆₀-AM15C5 and C₆₀-AM18C6 reaches about 29%, and in C₆₀-TACPD, almost 40%. According to LDI-TOF mass spectral analysis, the products of TACPD, tet b and AM15C5 reactions with fullerene have oligomeric or polymeric structure. By using DFT theoretical calculations, the latter observation was explained by enhanced reactivity of secondary amino groups toward nucleophilic addition onto fullerene cage.