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1.
低温压力容器08Ni3DR钢在极低温度下(-100℃)具有较好的强韧性匹配,在实际工程应用中,保障焊接接头的低温冲击韧性一直是压力容器制造过程中的难题之一。对于实际的焊接接头,最薄弱区域的确定以及最薄弱区域的影响对焊接接头的表征具有重要的意义。通过将夏比V型缺口开在母材、焊缝、热影响区不同位置处,系统研究了08Ni3DR压力容器钢焊接接头的组织和韧性。结果表明:焊接接头韧性最薄弱区域为粗晶热影响区,其粗晶热影响区的显微组织为粗大的粒状贝氏体和板条贝氏体组成的复合组织。粗晶热影响区宽度在缺口尖端前沿所占比例越高,试样的冲击吸收能量越低。当粗晶热影响区宽度所占比例达到100%时,冲击吸收能量为27 J,相比于母材冲击韧性损失高达90.7%。以上两个方面充分体现出焊接接头最薄弱区域对冲击韧性有很大的影响。  相似文献   
2.
范祥娟  李文生  崔帅  李建军 《表面技术》2021,50(5):152-159, 191
目的 合理选用摩擦偶件材料,以减缓Ni3Al基涂层宽温域内的摩擦磨损.方法 分别以WC-Co和316L为摩擦偶件,研究25~800℃内其对Ni3Al基涂层润滑和磨损机理的影响.采用高温硬度仪测试摩擦偶件在不同温度时的硬度,采用附带能谱仪的扫描电子显微镜观察磨损表面、磨斑和磨屑的形貌并测试成分,采用拉曼散射仪测试磨损表面和磨斑的成分.结果 在25~800℃,随温度的升高,两种摩擦副的摩擦系数具有一致的变化规律.与WC-Co对摩时,涂层在各温度下均具有低磨损率,且随温度升高,磨损率呈下降趋势.在25~200℃,与316L对摩时,涂层主要表现为粘着磨损和磨粒磨损,而与WC-Co对摩时,涂层在高接触应力下发生塑性变形,抑制Ag润滑相析出和涂层剥落,使其较前者具有高摩擦系数和低磨损率.在400℃,与WC-Co对摩时,高接触应力下产生的摩擦热促使涂层发生轻微的氧化,形成NiO和NiCr2O4,使其减摩性能优于Ni3Al/316L摩擦副.在600~800℃,与316L对摩时,涂层由严重的粘着磨损转变为氧化磨损;而与WC-Co对摩时,涂层由氧化磨损和剥层磨损转变为氧化磨损.此外,800℃时,Ni3Al/316L摩擦副的摩擦磨损发生在光滑润滑膜与粗糙转移膜之间,而Ni3Al/WC-Co摩擦副发生在光滑的润滑膜与转移膜之间.结论 在25~800℃,涂层与316L和WC-Co对摩时均具有良好的减摩性能,且与WC-Co对摩时具有更优的耐磨性能.  相似文献   
3.
4.
基于密度泛函理论(DFT),通过量子化学计算研究了主要的石油卟啉,包括ETIO、DPEP、DI-PEP、RHODO-TIO、RHODO-PEP或RHODO-I-PEP型和Ni2+/VO2+形成的金属卟啉配合物的分子结构、电子特性、解离能等。卟啉环的空腔尺寸、电荷分布、共轭特性均使其易于与Ni2+/VO2+发生络合,且配合物结构稳定。空间效应和竞争吸附使得VO2+卟啉配合物中的V原子和卟啉环不共面,VO2+卟啉环的配位作用弱于Ni2+卟啉环,因此Ni的脱除通常比V困难。Ni2+/VO2+卟啉配合物表现出显著的取代基效应:供电子的环烷基促进了卟啉环和Ni2+/VO2+的配位;吸电子的苯基削弱了卟啉环和Ni2+/VO2+的配位。对原油中Ni2+/VO2+卟啉化合物配位化学特性的研究,对于原油脱Ni/V技术的开发与改进具有一定的理论指导作用。  相似文献   
5.
Significant efforts have been made to develop highly active non-noble metal-based, affordable metallic and stable electro-catalysts for hydrogen evolution reaction (HER). Strong acid and bases are now used in HER operations to achieve large-scale, sustained H2 fuel production. However, few studies have utilized phosphate-buffered neutral electrolytes (PBS) in the field of neutral electrolyte technology. In this work, a certain alloys with a Ni–Cr basis have been produced as favorable components for the HER under neutral conditions. Additionally, the current investigations are emphasizing on the concentration of buffer phosphate species in the HER activity of various materials. By employing polarization and electrochemical impedance spectroscopy (EIS) in neutral solutions, the electro-catalytic activity of new alloys on HER was evaluated. According to the preliminary findings, the examined Ni–Cr-based alloys show superior HER catalytic activity in neutral electrolytes. Additionally, the Ni–Cr alloy matrix with Fe and Mo added enhances HER electrocatalytic efficiency while lowering interfacial charge transfer resistance. Due to its low overpotential of ?297 mV @ 10 mA cm?2 and Tafel slope of 94 mV dec?1 in 1.0 M PBS media, the Ni–Cr–Mo–Fe alloy exhibits an efficient HER, suggesting that the Ni–Cr–Mo–Fe electrode will be a potential noble metal-free electro-catalyst for HER. The Ni–Cr–Mo–Fe cathode is a readily available and affordable material for the production of HER in neutral medium.  相似文献   
6.
采用三辛基甲基氯化铵(Aliquat 336)与薄荷醇组成的疏水性低共熔溶剂(DES)为萃取剂,从硫氰酸钠溶液中分离Co(Ⅱ)和Ni(Ⅱ),考察了SCN-浓度、温度、酸度等条件对萃取分离性能的影响,研究了Co(Ⅱ)和Ni(Ⅱ)的反萃行为,并采用紫外-可见吸收光谱分析了疏水DES萃取Co(Ⅱ)的机理。结果表明,Co(Ⅱ)和Ni(Ⅱ)的分配比随着SCN-浓度的增加而增加,温度和酸度对镍钴的萃取分离性能影响很小,优化条件下Co(Ⅱ)和Ni(Ⅱ)的分离因子大于400。萃入有机相的Ni(Ⅱ)可采用0.1 mol/L NH3?H2O + 0.1 mol/L NH4Cl + 4 mol/L NaCl溶液洗涤到水相,有机相中的Co(Ⅱ)可采用1 mol/L乙二胺完全反萃。该DES体系萃取Co(Ⅱ)的机理符合阴离子交换。  相似文献   
7.
Hydrogen represents the most conventional fuel to feed Solid Oxide Fuel Cells (SOFCs) for green energy production. However, hydrogen has some drawbacks which prevent the large-scale implementation. Research identified ammonia as promising hydrogen vector. Hereby, highly dispersed Ni nanoparticle are deposited on La-doped strontium titanate by exsolution, greatly affecting the electrochemical performance. The exsolved Ni-doped lanthanum strontium titanate (La0·45Sr0·45Ti0·90Ni0.10-δO3 – LSTNOH) was largely characterized. XRD analysis detected 10 mol% of Ni doping has been successfully incorporated in to the perovskite structure and then released when exposed in reducing environment. SEM images show Ni nanoparticles highly dispersed on the surface. XPS confirms the presence of Ni on the surface after the exsolution and allows to exclude other detrimental diffusion towards the bulk. A LSTNOH derived composite based anode has been investigated through impedance spectroscopy using ammonia and hydrogen as fuel. It demonstrates best performances compared to the one obtained by Ni infiltration on LSTO (La0·45Sr0·45TiO3) composite scaffold. Polarization resistance, running on ammonia, decreases raising the temperature and the performances approach those in hydrogen.  相似文献   
8.
《Ceramics International》2022,48(11):15207-15217
SCAPS solar cell simulation program was applied to model an inverted structure of perovskite solar cells using Cu-doped Ni1-xO thin films as hole transport layer. The Cu-doped Ni1-xO film were made by co-sputtering deposition under different deposition conditions. By increasing the amount of the Cu-dopant, the film crystallinity enhanced whereas the bandgap energy decreased. The transmittance of the thin films decreased significantly by increasing the sputtering power of copper. High quality, uniform, compact, and pin-hole free films with low surface roughness were achieved. The structural, chemical, surface morphology, optical, electrical, and electronic properties of the Cu doped Ni1-xO films were used as input parameters in the simulation of Pb-based (MAPbI3-xClx) and Pb-free (MAGeI3) perovskite solar cells. Simulation results showed that the performance of both Pb-based and Pb-free perovskite solar cell devices significantly enhanced with Cu-doped Ni1-xO film. The highest power conversion efficiency (PCE) for the Pb-free perovskite solar cell is 8.9% which is lower than the highest PCE of 17.5% for the Pb-based perovskite solar cell.  相似文献   
9.
《Ceramics International》2022,48(15):21773-21780
In this work, Ni/TiC composites were synthesized by the laser cladding technique (LCT). A scanning electron microscope (SEM), X-ray diffractometer (XRD), microhardness meter, electrochemical workstation, and friction and wear tester examined the microstructure, surface morphology, phase structure, microhardness, wear, and corrosion resistances of the Ni/TiC composites. These results indicated the Ni/40TiC composite contained finer equiaxed crystals than the Ni and Ni/20TiC composites. In addition, numerous TiC particles in the Ni/40TiC composite impeded growth of the nickel crystals, which resulted in the fine microstructure of the Ni/40TiC composite. The Ni, Ni/20TiC, and Ni/40TiC composites exhibited face-centered cubic (f c c) lattices. The average microhardness values of the Ni/20TiC and Ni/40TiC composites were approximately 748 HV and 851 HV, respectively. The Ni/40TiC composite had the lowest friction coefficient (0.43) among all three coatings, and only some shallow scratches appeared on the surface of the Ni/40TiC composite. The corrosion potential (E) of Ni/40TiC exceeded the Ni/20TiC composite, and both were larger than the Ni composite, which indicated the Ni/40TiC composite had outstanding corrosion resistance and the Ni composite had poor corrosion resistance. The corrosion current densities (i) of Ni, Ni/20TiC, and Ni/40TiC composites were 5.912, 4.405, and 3.248 μA/cm2, respectively.  相似文献   
10.
This work investigates selective Ni locations over Ni/CeZrOx–Al2O3 catalysts at different Ni loading contents and their influences on reaction pathways in ethanol steam reforming (ESR). Depending on the Ni loading contents, the added Ni selectively interacts with CeZrOx–Al2O3, resulting in the stepwise locations of Ni over CeZrOx–Al2O3. This behavior induces a remarkable difference in hydrogen production and coke formation in ESR. The selective interaction between Ni and CeZrOx for 10-wt.% Ni generates more oxygen vacancies in the CeZrOx lattice. The Ni sites near the oxygen vacancies enhance reforming via steam activation, resulting in the highest hydrogen production rate of 1863.0 μmol/gcat·min. In contrast, for 15 and 20-wt.% Ni, excessive Ni is additionally deposited on Al2O3 after the saturation of Ni–CeZrOx interactions. These Ni sites on Al2O3 accelerate coking from the ethylene produced on the acidic sites, resulting in a high coke amount of 19.1 mgc/gcat·h (20Ni/CZ-Al).  相似文献   
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