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Experimental Investigation of Drillstring Torsional Vibration Effect on Rate of Penetration with PDC Bits in Hard Rock
Polycrystalline diamond compact (PDC) bits have shown tremendous performance compared to roller cone bits and have gained attraction in deep geothermal drilling applications. While PDC bits can reach a higher rate of penetration compared to other bits, they are more prone to drilling vibrations. The scope of this paper is to quantify the effects of drillstring torsional vibrations on PDC bit performance using a laboratory testing facility. Here, the tests were performed with three drillstring configurations to evaluate the effect of drillstring vibrations. The results showed that rigid testing overestimates the bit rate of penetration by 35% due to torsional vibrations.
Quantitative measurement of hard X-ray spectra from laser-driven fast ignition plasma
Abstract not provided
Hard X-ray fluorescence spectroscopy of high pressure cavitating fluids in aluminum nozzles
X-rays are frequently used to study the internal geometry of dense objects, and to measure the density of multiphase flows. However, quantitatively measuring fluid density inside a metallic object such as a high pressure spray nozzle is difficult. X-rays of sufficiently high energy to penetrate a metal object are not appreciably absorbed by the fluid inside. This requires the use of plastic or beryllium test sections, which are not suited to high pressure conditions. We present a high-energy X-ray fluorescence technique which can overcome this problem. The experiments were conducted at the 7-BM beamline of the Advanced Photon Source at Argonne National Laboratory. A hydrocarbon fluid was seeded with cerium nanoparticles. The fluid was pumped at high pressure through aluminum nozzles with inner diameters of 0.36-0.90 mm and wall thicknesses of 2-3 mm. A collimated, monochromatic 42.5 keV X-ray beam excited K-edge fluorescence from the cerium. The K-alpha emission lines at 34-35 keV were recorded by a cryogenic germanium detector. Changes in fluid density due to cavitation of the liquid inside the nozzle were measured by raster scanning the nozzle across the beam. A spatial resolution of 20 x 20 mu m(2) was achieved with a slitted beam, which was improved to 5 x 10 mu m(2) with X-ray focusing mirrors. The uncertainty in the path-integrated vapor fraction was 30-40 mu m at 95% confidence. A limitation of this approach is that for low vapor pressure fluids, the nanoparticles increase the vapor pressure of the fluid and act as additional nucleation sites. These experiments demonstrate a path forward for measurements of multiphase flows inside metal components under conditions that are not feasible in optically accessible materials.
Simulating Knoop hardness anisotropy of aluminum and β-HMX with a crystal plasticity finite element model
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Process optimization and properties of magnetically hard cobalt carbide nanoparticles via modified polyol method
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Substitutional and interstitial doping in LaCo5 system for the development of hard magnetic properties: A first principles study
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Structural evolution and magnetic hardness of (Sm,Zr)(Fe,Co,Ti) 12 alloy particles via reduction-diffusion
The quest for achieving high coercivity in Sm(Fe,Co,Ti) 12 alloys, despite their inherent strong magnetocrystalline anisotropy, has posed significant challenges. Recently, (Sm,Zr)(Fe,Co,Ti) 12 monocrystalline particles have exhibited coercivity μ 0 H c > 1.2 T, showcasing promising prospects and significant potential for both manufacturing and research endeavors. This study delves into the structural evolution of (Sm,Zr)(Fe,Co,Ti) 12 (1:12) alloy particles made via the calciothermic reduction-diffusion synthesis process as influenced by the molar ratios of Ca atoms to O 2- ions (Ca/O), annealing time and annealing temperature. Critical insight that informs conditions to optimize the magnetic response is gained via systematic experimentation and advanced electron microscopy. Complex structural features, including core-shell morphologies and intricate multiphase compositions within individual particles, are unveiled. An optimal Ca/O ratio of 1.30 produces particles with a coercivity up to μ 0 H c = 1.63 T, while higher Ca/O ratios induce the formation of a Sm-rich TbCu 7 -type (1: 7 ) phase, which only partially transforms into the desired 1:12 phase during annealing. Persistent remnants of the 1:7 phase locally impact atomic structure, particle morphology, and coercivity. Furthermore, these findings underscore the complex interplay between synthesis parameters, resulting structures, and magnetic properties, informing the design and optimization of high-performance permanent magnets comprised of the (1:12) compound.
High hardness and oxidation-resistant Cr-containing medium entropy ZrTaW diboride
This study reports the successful synthesis of a Cr-containing (Zr 0.30 Ta 0.34 Cr 0.06 W 0.30 )B 2 medium-entropy boride (MEB) via an in-situ reactive borothermal reduction route from oxide precursors. High-energy ball milling was employed to homogenize the precursor mixture prior to reactive densification. X-ray diffraction confirmed the formation of a predominantly AlB₂-type hexagonal diboride structure together with a secondary (W X , M 1-X )B monoboride phase. Microstructural characterization revealed compositional heterogeneity and localized W-rich regions associated with the secondary phase. The synthesized medium-entropy boride exhibited enhanced mechanical properties, which are attributed to lattice distortion and solid-solution strengthening effects. Thermogravimetric analysis revealed complex multistage oxidation behavior, and the oxidation resistance was compared with conventional ultra-high-temperature diborides. The results demonstrate the strong relationship between oxide-derived processing, compositional complexity, phase evolution, and oxidation behavior, highlighting the potential of medium-entropy borides for high-temperature structural applications
Defect-rich and N-doped hard carbon as a sustainable anode for high-energy lithium-ion capacitors
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Effect of alloying with Sc, Nb and Zr on reduction-diffusion synthesis of magnetically hard Sm(Fe,Co,Ti) 12 -based monocrystalline powders
Powders of Sm(Fe,Co) 11.2 Ti 0.8 alloys modified with Sc, Nb and Zr, as well as with additional Ti were prepared by reducing mechanically activated raw oxides with Ca metal in the furnace preheated to 990–1250 °C. Expansion of the crystal lattice upon introduction of Nb or additional Ti implies that atoms of these elements replace the smaller Fe atoms in the tetragonal ThMn 12 -type structure. On the other hand, contraction of the lattice upon introduction of Sc or Zr was smaller than what was expected for replacement of the Sm atoms, which suggests that the Sc and Zr atoms replace both the Sm and Fe atoms. Washing away the reduction byproducts expands the crystal lattice of the 1:12 particles and increases their coercivity. The lattice expansion associated with the washing is believed to be caused by interstitial H atoms; more research, however, is needed to establish the mechanism(s) of the washing effect on the coercivity. The earlier reported development of a high coercivity in zirconium-modified monocrystalline particles achieved by increasing the reduction annealing temperature to ≈1200 °C was similarly characteristic of the particles modified with Sc (the coercivity reaches 11.5 kOe) and Nb (8.1 kOe), but not for the particles prepared with additional Ti where the maximum coercivity of 8.3 kOe develops for a lower annealing temperature. Furthermore, it is concluded that Sc, Nb and Zr modify the high-temperature phase equilibria of the Sm(Fe,Co) 11.2 Ti 0.8 alloys allowing for an effective high-temperature processing, whereas the alloy coercivity increases with the synthesis temperature through a different, still unknown mechanism which may involve suppression of the defects specific to the 1:12 crystals.