Microstructure,mechanical, tribological,and oxidizing properties of AlCrSiN/AlCrVN/AlCrNbN multilayer coatings with different modulated thicknesses

Multilayer structure design is one of the most promising methods for improving the comprehensive performance of AlCrN-based hard coatings applied to cutting tools. In this study, four types of AlCrSiN/AlCrVN/AlCrNbN multilayer coatings, with different modulated thicknesses, were deposited to investigate their microstructure, mechanical, tribological, and oxidizing properties. All multilayer coatings exhibited grain growth along the crystallographic plane of (200) with a NaCl-type face-centered cubic (FCC) structure. The results show that, as the modulation thickness decreases from ～35 nm to ～10 nm, (1) the grain refinement effect is increasingly evident; (2) all multilayer coatings show a hardness of >30 GPa and an elastic modulus of >300 GPa. Both the ability to resist elastic strain to failure and the plastic deformation of multilayer coatings increase. In addition, their resistance to cracking reduces; (3) the wear rates of these multilayer coatings reduce successively from 1.78 × 10^?16 m³ N^?1 m^?1 to 7.7 × 10^?17 m³ N^?1 m^?1. This is attributed to an increase in self-lubricating VO_x and a decrease in adhesives from the counterparts; (4) the best high-temperature oxidation resistance was obtained for the multilayer coating with a modulated thickness of ～15 nm.     

Effects of an inhomogeneous electron density distribution on the hydrogen distribution in TiZrTaNbAl multi-principal element alloys

A body-centered cubic equiatomic TiZrTaNbAl multi-principal element alloy (MPEA) with elemental fluctuations was investigated to further understand the relationship between the microstructure and hydrogen distribution. In this study, a composition dependence of the hydrogen distribution was observed in the TiZrTaNbAl MPEA. An inhomogeneous electron density distribution of the MPEA was revealed by advanced differential phase-contrast scanning electron microscopy (DPC-STEM) for the first time. The results showed that the electron density has a significant effect on the hydrogen distribution in TiZrTaNbAl MPEAs. This work provides new insight into the design of materials with high hydrogen storage capacity and high hydrogen embrittlement resistance.     

锑酸消除含氚废空气中的氚

用锑酸作消气材料 ,压制成消氚电极 ,在适当外加条件下 ,考察了锑酸作消氚材料直接将含氚废空气中的氚除去的可能性。对消氚过程中料气中氚的浓度及水分对消氚结果的影响进行了考察 ,给出了消气片中氚的物料平衡。结果表明 :在 3 2L含氚空气中 ,用锑酸制成的消氚材料 ,在 2 0 0min左右可将原料气氛中 80 %以上的氚去除     

被动式氚取样器性能的实验研究

介绍了核设施工作场所和环境空气中氚化水蒸气HTO的监测，被动式氚取样器在国外已经得到非常广泛的应用，所研制的被动式氚取样器，特别适用于7－30d的长期取样，给出该取样周期内空气中HTO浓度的平均值。     

The use of the scanning electron microscope in the determination of the mineral composition of Ballachulish slate

Slate is a fine-grained, low-grade metamorphic rock derived from argillaceous sediments or occasionally volcanic ash. Although most slates contain mainly quartz, chlorite and white mica, they vary considerably in their durability, some lasting centuries while others fail after a few years of service. A detailed characterisation of their mineralogy is required for the assessment of performance, and to establish the provenance of a used slate. A combination of methods was used to examine Ballachulish slates; XRD analysis to determine the principal minerals present, XRF analysis to determine the total chemical composition, and scanning electron microscopy to determine the chemical composition of individual minerals. It was found that the white mica in Ballachulish slate is phengite and the chlorite is ripidolite. Feldspar is present as albite and carbonate as ferroan dolomite. Several accessory minerals were also identified, including chloritoid, monzonite and zircon. There was considerable variation in the ratio of the principal minerals, making it impossible to identify used slates by this criterion. Instead, chemical composition of the individual minerals, and possibly key accessory minerals, should be used to determine the provenance of slates.     

On the elemental effect of AlCoCrCuFeNi high-entropy alloy system

The AlCoCrCuFeNi high-entropy alloy system was synthesized using a well-developed arc melting and casting method. Their elemental effect on microstructures and hardness was investigated with X-ray diffraction, scanning electron microscopy and Vickers hardness testing. The alloys exhibit quite simple FCC and BCC solid solution phases. Co, Cu and Ni elements enhance the formation of the FCC phase while Al and Cr enhance that of the BCC phase in the alloy system. BCC phases form a spinodal structure during cooling. Copper tends to segregate at the interdendrite region and forms a Cu-rich FCC phase. Low copper content renders the interdendrite as a thin film and the as-cast structure like recrystallized grain structure. The formation of BCC phases significantly increases the hardness level of the alloy system. The strengthening mechanism is discussed.     

Standard reference materials for cements

The eight portland cements and two calcium aluminate cements in the Standard Reference Material (SRM) 1880 series are among the most popular SRMs in the catalog of the National Institute of Standards and Technology (NIST) Standard Reference Materials Program. Numerous laboratories rely on them for elemental analysis and qualification for ASTM C 114-00 Standard Test Methods for Chemical Analysis of Hydraulic Cement. NIST has collected new candidate materials from around the world and partnered with Construction Technology Laboratories (CTL) in their preparation and certification. This paper describes the procedures taken at NIST and CTL to prepare and test materials for certification including the homogeneity testing, the X-ray fluorescence methods and the statistical data analysis performed for value assignment.     

手套箱气氛中氚化水处理的工艺研究

分子筛吸附柱和热金属镁床是手套箱气氛中氚化水 (HTO)搜集和分解处理的一种有效手段。测试了分子筛柱对气氛中水的吸附性能和热金属镁床对HTO的分解性能。结果表明 :分子筛柱对气氛中水的吸附效率 >99 99% ,在空气中水含量为 3 4× 1 0 - 3～ 4 2× 1 0 - 3条件下 ,未发现吸附柱水的贯穿现象 ;热金属镁床对HTO的分解率 >99 9% ,当金属镁的消耗量大于 80 %时 ,未见分解率明显降低。     

Chemical control of colloidal fouling of reverse osmosis systems

Fouling of membranes by colloidal organic and inorganic particles continues to be documented as the most common and challenging obstacle in attaining stable continuous operation of reverse osmosis (RO) and ultrafiltration (UF) systems. Much current research is being conducted on physical parameters to mitigate such fouling. The focus has been on membrane synthesis and element design; microfiltration and ultrafiltration pretreatment; electromagnetic devices; correlation with physical factors such as Silt Density Index, zeta potential and critical flux; technique of direct observation of fouling process through a membrane; and classification of macromolecular organics for correlation with fouling characteristics. We report initial successes with chemical control of colloidal fouling. Through screening with a large number of observable coagulations of natural colloids, we have developed a group of proprietary anticoagulants and dispersants that would, at less than 10 ppm dosage to the RO feedwater, control various classes of colloidal foulants. Case studies of the control of humic matter, elemental sulfur and colloidal silicate in problematic RO systems that became stabilized are briefly presented. We conclude that a great need and potential exists in economically controlling the myriads of fouling interactions of colloidal particles during concentration within the brine channels of RO membrane elements. Low dosages of antifoulants can in many cases obviate the need for installation and maintenance of pretreatment unit or operations designed to remove such colloidal foulants from the process stream.     

Trace element loads in the Great Lakes Basin: A reconnaissance

Water quality data for trace elements in the Great Lakes are relatively scarce, complicating the assessment of current trace element baselines and their distribution patterns. Here, we present concentration data for >40 major and trace elements in >100 samples from the Great Lakes connecting channels, surface waters, precipitation and select Canadian tributaries, to establish a high-level assessment of loading rates across the basin. Contrasting upstream-to-downstream trends were observed for the investigated trace elements, ranging from net-decreasing (>5-fold for e.g., Co, Tl, Y) to net-increasing surface water concentrations (>2-fold for e.g., Sb, U, As). Calculated loading rates reveal different, element-specific controls of runoff, connecting channel loads or precipitation on trace element occurrence. Lake-wide elemental mass-balances could be reasonably closed for conservative trace elements (e.g., Li, <53% residual) but not for others (e.g., rare earth elements with up to 5-fold discrepancies), reflective of general data scarcity and uncertainty in loading rates. In line with major water quality trends, spatial distribution patterns in Lakes Erie and Ontario display subtle near-shore to off-shore heterogeneity for a few trace elements (<1 order-of-magnitude for V or Se), but higher variability for trace elements with significant inputs derived from tributaries. This work provides important quantitative baseline data for trace elements in the Great Lakes that may help optimize surveillance and management strategies for the preservation of Great Lakes water quality.