Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “ROOM”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,567 records · Page 87
All sourcesNASA NTRSDOE OSTI
DOE OSTI2015

Residual-stress-induced grain growth of twinned grains and its effect on formability of magnesium alloy sheet at room temperature

A magnesium alloy sheet was subjected to in-plane compression along with a vertical load to avoid buckling during compression. Pre-compressed specimens machined from the sheet were annealed at different temperatures and the changes in microstructure and texture were observed using electron back scattered diffraction (EBSD). Twinned grains preferentially grew during annealing at 300 °C, so that a strong texture with the < 0001 > direction parallel to the transverse direction developed. EBSD analysis confirmed that the friction caused by the vertical load induced inhomogeneous distribution of residual stress, which acted as an additional driving force for preferential grain growth of twinned grain during annealing. The annealed specimen showed excellent formability. - Highlights: • A magnesium alloy sheet subjected to in-plane compression under a vertical load • The vertical load induced inhomogeneous distribution of the residual stress. • The residual stress acted as an additional driving force for grain growth. • The annealed specimen with strong non-basal texture showed excellent formability.

36 MATERIALS SCIENCE↗
DOE OSTI2022

Quantification of room temperature strengthening of laser shock peened Ni-based superalloy using synchrotron microdiffraction

Laser shock peening (LSP), a surface modification technique, is promising to enhance the strength and wear resistance for Ni-based superalloys. To understand the strengthening mechanism in a laser shock peened Ni-based superalloy DZ417G, we utilize synchrotron poly- and monochromatic X-ray microdiffraction, as well as electron microscopy and microhardness to quantify the local microstructures and mechanical properties at various depths. In the 1.2-mm-deep hardened layer, the microhardness increases monotonically by ~50% from the unaffected interior to the surface. Quantitative microdiffraction analysis shows that large amounts of dislocations are introduced by LSP. High densities of 7.1 × 10 15 m -2 and 11.8 × 10 15 m -2 are seen close to the peened surface for the γ- and γ'-phases, respectively, which are 5 and 20 times of those in the unaffected region. Different gradients of dislocation density are observed for the two phases from interior to surface, and their combined effect accounts well for the hardness increment. Due to the unaltered γ'-precipitates and chemical composition in the LSP affected zone, the large density of dislocations dominates the observed strengthening. Combined poly- and monochromatic X-ray microdiffraction allows quantifying the local microstructures of plastic deformation over a large sampling scale that can hardly be achieved using other materials characterization techniques.

36 MATERIALS SCIENCE↗
DOE OSTI2010

Rapid synthesis of room temperature ferromagnetic Ag-doped LaMnO{sub 3} perovskite phases by the solution combustion method

We report the rapid solution combustion synthesis and characterization of Ag-substituted LaMnO{sub 3} phases at relatively low temperature using oxalyl dihydrazide, as fuel. Structural parameters were refined by the Rietveld method using powder X-ray diffraction data. While the parent LaMnO{sub 3} crystallizes in the orthorhombic structure, the Ag-substituted compounds crystallize in the rhombohedral symmetry. On increasing Ag-content, unit cell volume and Mn-O-Mn bond angle decreases. The Fourier transform infra red spectrum shows two absorption bands corresponding to Mn-O stretching vibration ({nu}{sub s} mode) and Mn-O-Mn deformation vibration ({nu}{sub b} mode) around 600 cm{sup -1} and 400 cm{sup -1} for the compositions, x = 0.0, 0.05 and 0.10, respectively. Electrical resistivity measurements reveal that composition-controlled metal to insulator transition, with the maximum metal to insulator being 280 K for the composition La{sub 0.75}Ag{sub 0.25}MnO{sub 3}. Increase in magnetic moment was observed with increase in Ag-content. The maximum magnetic moment of 35 emu/g was observed for the composition La{sub 0.80}Ag{sub 0.20}MnO{sub 3}.

36 MATERIALS SCIENCE↗
DOE OSTI2011

Solvothermal synthesis of SrMoO{sub 4}:Ln (Ln = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanoparticles and its photoluminescence properties at room temperature

Research highlights: {yields} A facile hydrothermal process was used to fabricate luminescent nanocrystals. {yields} The PL emissions the nanocrystals can be tuned by doping different rare-earth ions. {yields} A possible formation scheme for the as-synthesized nanocrystals was presented. -- Abstract: Rare-earth ions (Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) doped SrMoO{sub 4} nanoparticles were prepared by solvothermal route using oleic acid as surfactant to control the particle shape and size. X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectra (XPS), photoluminescence spectra (PL) and the kinetic decay times were applied to characterize the obtained samples. The XRD patterns reveal that all the doped samples are assigned to the scheelite-type tetragonal structure of SrMoO{sub 4} phase. In addition, the as-synthesized SrMoO{sub 4}:Ln (Ln = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) particles are high purity well crystallized and with the average size of 30-50 nm. The possible formation process of SrMoO{sub 4}:Ln (Ln = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanoparticles have been discussed as well. Upon excitation by ultraviolet radiation, the as-synthesized SrMoO{sub 4}:Ln (Ln = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanoparticles exhibit the characteristic emission lines of corresponding Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}, respectively.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2012

Room temperature novel chemical synthesis of Cu{sub 2}ZnSnS{sub 4} (CZTS) absorbing layer for photovoltaic application

Highlights: Black-Right-Pointing-Pointer Simple and inexpensive method for the synthesis of CZTS films. Black-Right-Pointing-Pointer Structural, morphological and optical properties. Black-Right-Pointing-Pointer Find great application in solar cells with efficiency 0.12%. -- Abstract: Cu{sub 2}ZnSnS{sub 4} (CZTS) thin films have been prepared by a novel chemical successive ionic layer adsorption and reaction (SILAR) method. These films were annealed in vacuum at 673 K and further characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-vis spectroscopy, electrical, and wettability studies. The X-ray diffraction studies showed the formation of kesterite structure of CZTS films. Scanning electron micrograph revealed the formation of densely packed, compact and large grained CZTS films. The CZTS films showed high optical absorption (10{sup 4} cm{sup -1}) exhibiting band gap energy of 1.55 eV. Wettability test revealed the hydrophilic nature of CZTS films. The CZTS thin films showed semiconducting behavior with p-type electrical conductivity. Further photovoltaic activity of these films was studied by forming the photoelectrochemical cell.

36 MATERIALS SCIENCE↗
DOE OSTI2012

Room temperature synthesis of high temperature stable lanthanum phosphate–yttria nano composite

Graphical abstract: A facile aqueous sol–gel route involving precipitation–peptization mechanism followed by electrostatic stabilization is used for synthesizing nanocrystalline composite containing lanthanum phosphate and yttria. Highlights: ► A novel lanthanum phosphate–Y{sub 2}O{sub 3} nano composite is synthesized for the first time using a modified facile sol gel process. ► The composite becomes crystalline at 600 °C and X-ray diffraction pattern is indexed for monoclinic LaPO{sub 4} and cubic yttria. ► The composite synthesized was tested up to 1300 °C and no reaction between the phases of the constituents is observed with the morphologies of the phases being retained. -- Abstract: A facile aqueous sol–gel route involving precipitation–peptization mechanism followed by electrostatic stabilization is used for synthesizing nanocrystalline composite containing lanthanum phosphate and yttria. Lanthanum phosphate (80 wt%)–yttria (20 wt%) nano composite (LaPO{sub 4}–20%Y{sub 2}O{sub 3}), has an average particle size of ∼70 nm after heat treatment of precursor at 600 °C. TG–DTA analysis reveals that stable phase of the composite is formed on heating the precursor at 600 °C. The TEM images of the composite show rod shape morphology of LaPO{sub 4} in which yttria is acquiring near spherical shape. Phase identification of the composite as well as the phase stability up to 1300 °C was carried out using X-ray diffraction technique. With the phases being stable at higher temperatures, the composite synthesized should be a potential material for high temperature applications like thermal barrier coatings and metal melting applications.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Novel method of room temperature ionic liquid assisted Fe{sub 3}O{sub 4} nanocubes and nanoflakes synthesis

Graphical abstract: - Highlights: • First time [Bmim][TfO] IL is used for the Fe{sub 3}O{sub 4} nanoparticle synthesis. • Novel method tunes Fe{sub 3}O{sub 4} nanocubes and nanoflakes forms influenced by the base and IL. • Fe{sub 3}O{sub 4} oxidized topotactically into γ-Fe{sub 2}O{sub 3} nanoparticles by annealing and base. • Uniform morphology with average size of 33 nm negligible superstructure are formed. • Ms values are characterized by thin layer of γ-Fe{sub 2}O{sub 3} on the nanoparticle surface. - Abstract: For the first time, the nanomagnetite superparamagnetic particles are successfully synthesized by precipitation method using 1-n-butyl-3-methylimidazolium trifluoromethane sulfonate [Bmim][TfO] ionic liquid medium/surfactant. The obtained Fe{sub 3}O{sub 4} particles are nanocubes and nanoflakes and this formation is influenced by the base concentration and anisotropic circumstances produced by the ionic liquid and their size varies from 20 nm to 150 × 300 nm (width × length). The synthesized magnetite nanoparticles are characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, Field emission scanning electron microscopy (FE-SEM), Transmission electron microscopy (TEM) and Vibrating sample magnetometer (VSM) studies. The results show that the core of the Fe{sub 3}O{sub 4} nanoparticles is surrounded by a thin layer of γ-Fe{sub 2}O{sub 3} by topotactical partial oxidation, which is remarkably proceed with the subsequent calcination. The magnetite nanocubes have high saturation magnetization value and exhibit superparamagnetic hysteresis loop.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Room temperature multiferroic properties of (Bi{sub 0.95}La{sub 0.05})(Fe{sub 0.97}Mn{sub 0.03})O{sub 3}/NiFe{sub 2}O{sub 4} double layered thin film

Graphical abstract: - Highlights: • Chemical solution deposition of (Bi{sub 0.95}La{sub 0.05})(Fe{sub 0.97}Mn{sub 0.03})O{sub 3}–NiFe{sub 2}O{sub 4} double layered thin film. • Studies on structural, electrical and multiferroic properties. • NiFe{sub 2}O{sub 4} acts as both resistive buffer layer and magnetic source. - Abstract: (Bi{sub 0.95}La{sub 0.05})(Fe{sub 0.97}Mn{sub 0.03})O{sub 3}/NiFe{sub 2}O{sub 4} double layered thin film was prepared on a Pt(111)/Ti/SiO{sub 2}/Si(100) substrate by a chemical solution deposition method. X-ray diffraction and Raman scattering spectroscopy studies confirmed the formation of the distorted rhombohedral perovskite and the inverse spinel cubic structures for the (Bi{sub 0.95}La{sub 0.05})(Fe{sub 0.97}Mn{sub 0.03})O{sub 3}/NiFe{sub 2}O{sub 4} double layered thin film. The (Bi{sub 0.95}La{sub 0.05})(Fe{sub 0.97}Mn{sub 0.03})O{sub 3}/NiFe{sub 2}O{sub 4} double layered thin film exhibited well saturated ferromagnetic (2 M{sub r} of 18.1 emu/cm{sup 3} and 2H{sub c} of 0.32 kOe at 20 kOe) and ferroelectric (2P{sub r} of 60 μC/cm{sup 2} and 2E{sub c} of 813 kV/cm at 866 kV/cm) hysteresis loops with low order of leakage current density (4.5 × 10{sup −6} A/cm{sup 2} at an applied electric field of 100 kV/cm), which suggest the ferroelectric and ferromagnetic multi-layers applications in real devices.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Photoluminescence emission at room temperature in zinc oxide nano-columns

Highlights: • ZnO nanoparticles were obtained by microwave-hydrothermal method. • X-ray diffraction reveals a hexagonal structure. • Photoluminescence emission evidenced two absorption peaks, at around 480 nm and 590 nm wavelengths. - Abstract: Hydrothermal microwave method (HTMW) was used to synthesize crystalline zinc oxide (ZnO) nano-columns at the temperature of 120 °C with a soaking time of 8 min. ZnO nano-columns were characterized by using X-ray analyses (XRD), infrared spectroscopy (FT-IR), thermogravimetric analyses (TG-DTA), field emission gun and transmission electron microscopy (FEG-SEM and TEM) and photoluminescence properties (PL). XRD results indicated that the ZnO nano-columns are free of any impurity phase and crystallize in the hexagonal structure. Typical FT-IR spectra for ZnO nano-columns presented well defined bands, indicating a substantial short-range order in the system. PL spectra consist of a broad band at 590 nm and narrow band at 480 nm corresponding to a near-band edge emission related to the recombination of excitons and level emission related to structural defects. These results show that the HTMW synthesis route is rapid, cost effective, and could be used as an alternative to obtain ZnO nano-columns in the temperature of 120 °C for 8 min.

36 MATERIALS SCIENCE↗
DOE OSTI2014

A facile route to high-purity BN nanoplates with ultraviolet cathodoluminescence emissions at room temperature

Highlights: • We present a novel and simple approach to great-scale fabrication of BN nanoplates. • The as-synthesized products are extensively characterized. • The formation mechanism of BN nanoplates are elucidated based on experimental observations. • A growth model was proposed according to our experimental observations and analysis. • BN nanoplates’ CL performance envisions its applications such as UV emitters. - Abstract: We present a novel and notably simple approach to fabricate BN nanoplates in large scale employing ammonia borane as a single-source precursor. The structure and chemical composition of the as-synthesized products are extensively characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and electron energy-loss spectroscopy (EELS). XRD analysis indicates that the products are hexagonal BN crystal. SEM images confirm that the BN nanoplates have an average diameter of about 200 nm and thickness of tens of nanometers. HRTEM results illustrate the BN nanoplates to be single-crystals. EELS result suggests the nanoplates are composed of boron and nitride elements. The formation mechanism of the BN nanoplates has been elucidated based on our experimental observations, and a growth model has been proposed accordingly. Cathodoluminescence spectroscopic analysis is performed and strong ultraviolet (UV) emissions are detected. Our method provides a simple route towards the large-scale fabrication of high-quality BN nanoplates, for which various promising applications such as compact UV emitters can be envisioned.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Enhanced hydrogen production from water on Pt/g-C3N4 by room temperature electron reduction

Highlights: • A novel way to get efficient Pt/g-C{sub 3}N{sub 4} through glow discharge plasma reduction. • Plasma treatment can be applied to prepare catalyst used for visible light driven reaction. • An alkaline reduction environment can promote the Pt reduction process. - Abstract: An efficient Pt/g-C{sub 3}N{sub 4} photocatalyst was prepared via glow discharge plasma reduction. Based on the hydrogen evolution from water splitting under visible light irradiation, the Pt/g-C{sub 3}N{sub 4} obtained through plasma reduction exhibited enhanced photocatalytic performance with a H{sub 2} evolution rate of 33.9 μmol/h. Among the samples obtained through plasma reduction under different environments, the Pt/g-C{sub 3}N{sub 4} photocatalyst with Pt reduced in NaOH alkaline environment exhibited a markedly increased H{sub 2} evolution rate of 40 μmol/h. The enhanced photocatalytic performance could be attributed to plasma reduction controlling the size of Pt particles and the alkaline environment promoting Pt reduction.

08 HYDROGEN↗
DOE OSTI2018

Highly efficient deep desulfurization of fuels by meso/macroporous H3PW12O40/TiO2 at room temperature

Highlights: • A new kind of meso/macroporous structured HPW/TiO{sub 2} catalyst was prepared by monodispersed polystyrene spheres and quaternary ammonium bromide. • Quaternary ammonium bromide with longer alkyl chains length (STAB) was found to be the best mesostructure-directing agent in the synthesis of meso/macroporous HPW/TiO{sub 2} catalyst. • The influence of dosage of macroporous templates (monodispersed polystyrene spheres) and alkyl chains length of quaternary ammonium bromide on the textural of meso/macroporous HPW/TiO{sub 2} catalyst were investigated. • With proper PS spheres and quaternary ammonium bromide usage, disordered macropores arranged periodicity and led relatively larger pore size and pore volume. • The meso/macroporous HPW/TiO{sub 2} materials exhibited enhanced excellent desulfurization performance of thiophenic sulfur in model fuel than other samples. Dibenzothiophene can be completely removed within 2 h at 30 °C. - Abstract: This paper described the synthesis of meso/macroporous phosphotungstic acid (HPW) /TiO{sub 2} catalyst with quaternary ammonium bromide and monodispersed polystyrene spheres (PS) as dual-template. The synthetic parameters, such as concentration of the templates and the alky chain length of quaternary ammonium bromide was studied carefully and optimized to generate catalyst with regulated porous features. The chemical properties of the catalyst was also investigated, X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) measurements confirmed the Keggin-type HPW were highly dispersed on the TiO{sub 2} framework. The optimal meso/macroporous HPW/TiO{sub 2} catalyst exhibited excellent catalytic activity in the oxidation of refractory sulphur compounds such as benzothiophene (BT), dibenzothiophene (DBT), and 4,6-dimethyldibenzothiophene (4,6-DMDBT). DBT was removed within 2 h at 30 °C under selected reaction conditions and the apparent activation energy for DBT oxidation was calculated to be 45.7 kJ/mol. The high ODS reaction rate of catalyst could be attributed to the combination of unique meso/macroporous architecture allowing for efficient mass transport of reactants and products in pore channel and its high surface area, large mesoporous size, and pore volume enabling sufficient exposure of catalytic active sites. Moreover, the meso/macroporous HPW/TiO{sub 2} catalyst also exhibited excellent reusability with no obviously degradation even after eight cycles.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2011

Interfraction Prostate Rotation Determined from In-Room Computerized Tomography Images

Fiducial markers (FMs) are commonly used as a correction technique for interfraction translations of the prostate. The aim of this investigation was to determine the magnitude of prostate rotations using 2 methods: FM coordinates and the anatomical border of the prostate and rectum. Daily computed tomography (CT) scans (n = 346) of 10 prostate cancer patients with 3 implanted FMs were acquired using the CT on rails. FM coordinates were used to determine rotation in the sagittal, transverse, and coronal planes, and CT contours of the prostate and rectum were used to determine rotation along the sagittal plane. An adaptive technique based on a subset of images (n = 6; planning and first 5 treatment CTs) to reduce systematic rotation errors in the sagittal plane was tested. The standard deviation (SD) of systematic rotation from FM coordinates was 7.6{sup o}, 7.7{sup o}, and 5.0{sup o} in the sagittal, transverse and coronal planes. The corresponding SD of random error was 10.2{sup o}, 15.8{sup o}, and 6.5{sup o}. Errors in the sagittal plane, determined from prostate and rectal contours, were 10.1{sup o} (systematic) and 7.7{sup o} (random). These results did not correlate with rotation computed from FM coordinates (r = -0.017; p = 0.753, n = 337). The systematic error could be reduced by 43% to 5.6{sup o} when the mean prostate position was estimated from 6 CT scans. Prostate rotation is a significant source of error that appears to be more accurately determined using the anatomical border of the prostate and rectum rather than FMs, thus highlighting the utility of CT image guidance.

62 RADIOLOGY AND NUCLEAR MEDICINE↗