Development of a brazing process for Nb-1Zr heat receiver tubes Final report, 1 May 1967 - 31 Jan. 1968
Process developed for brazing niobium-zirconium alloys for heat exchanger tube fabrication
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Process developed for brazing niobium-zirconium alloys for heat exchanger tube fabrication
Diffusion process for preparing niobium stannide superconducting tape stabilized to any level, discussing reaction time, temperature and contamination
Temperature dependent isomer shift and anharmonic binding of Sn 119 in niobium stannide, measuring Mossbauer recoil free fraction
Nickel base alloy with resistance to oxidation at high temperatures and superior stress-rupture properties
Calculation of lower critical fields and comparison with measured values for some niobium-titanium alloys
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Of all the A-15 samples of NbGe alloy examined, DT 094 is unique in that it was at least 99% pure A-15 phase. Also its diffraction peaks were noisy as if there were about a one percent compositional variation on this phase. DT 094, however, was only a large fragment of the drop tube drop, and thus its small sample size may have reduced the intensity, thus enhancing fluctuations enough to explain some of the loss of peak resolution.
The evolution of hydrogen from 347 stainless steel has been studied by using a real time dynamic technique under ultrahigh vacuum conditions. Auger electron spectroscopy was used to determine the surface composition as a function of time and temperature. The surface film on the electropolished samples was found to be approximately 15 A thick and consisted of a carbon-oxygen complex and a metal oxide (FexOy). Upon heating to 400 C, the carbon-oxygen complex desorbed as CO and the remaining oxygen and carbon began to incorporate. Also at this temperature sulfur began to diffuse out of the bulk to the surface and at approximately 800 C formed a complete monolayer. At 900 C, carbon and oxygen virtually disappeared, leaving the monolayer of sulfur as the only surface contaminant. The hydrogen diffusivity was found to follow closely the equation D = 7.01 x 10 to the -7th exp(-48.0/RT) sq m per second over the entire temperature range studied, thus indicating that hydrogen evolution is not significantly affected by the changing surface composition. The somewhat higher value of the diffusivity obtained in this work compared to past measurements in austenitic stainless steels may indicate the importance of sample preprocessing and ultrahigh vacuum conditions in minimizing the effects of surface layers.
Creep rupture tests of electron beam welded PWC-11 sheet were conducted at 1350 K. Full penetration, single pass welds were oriented transverse to the testing direction in 1 mm thick sheet. With this orientation, stress was imposed equally on the base metal, weld metal, and heat-affected zone. Tests were conducted in both the postweld annealed and aged conditions. Unwelded specimens with similar heat treatments were tested for comparative purposes. It was found that the weld region is stronger than the base metal for both the annealed and aged conditions and that the PWC-11 material is stronger in the annealed condition than in the aged condition.
Isotope and trace element geochemistry of Precambrian mantle derived rocks and implications for the formation of the continental crust is discussed. Epsilon Nd values of Archean komatiites are variable, but range up to at least +5, suggesting that the Archean mantle was heterogeneous and, in part, very depleted as far back as 3.4 to 3.5 Ga. This may be taken as evidence for separation of continental crust very early in Earth history. If these komatiite sources were allowed to evolve in a closed system, they would produce modern day reservoirs with much higher epsilon Nd values than is observed. This implies recycling of some sort of enriched material, perhaps subducted sediments, although other possibilities exist. Archean volcanics show lower Nb/Th than modern volcanics, suggesting a more primitive mantle source than that observed nowadays. However, Cretaceous komatiites from Gorgona island have similar Nb/Th to Archean volcanics, indicating either the Archean mantle source was indeed more primitive, or Archean magmas were derived from a deep ocean island source like that proposed for Gorgona.
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Modified-CPF and CASSCF/multireference-CI theoretical calculations are presented for the ground and low-lying states of YO and YS, ZrO and ZS, and NbO and NbS. The techniques employed are explained, and the calculated spectroscopic constants are presented in extensive tables. Good agreement is found with published experimental data on the oxides, and it is inferred that the sulfide results are accurate as well. Particular attention is given to the high-lying quartet manifold of states in YO and the (1) 3Pi-a3Delta transition of ZrS (possibly the source of the IR Keenan bands seen in S-star spectra).
Due to its high strength at temperatures up to 1600 K, fabrication of niobium base alloy WC-3009 (Nb30Hf9W) by traditional methods is difficult. Powder metallurgy (P/M) processing offers an attractive fabrication alternative for this high strength alloy. Spherical powders of WC-3009 produced by electron beam atomizing (EBA) process were successfully consolidated into a one inch diameter rod by vacuum hot pressing and swaging techniques. Tensile strength of the fully dense P/M material at 300-1590 K were similar to the arc-melted material. Creep rupture tests in vacuum indicated that WC-3009 exhibits a class 1 solid solution (glide controlled) creep behavior in the 1480 to 1590 K temperature range and stress range of 14 to 70 MPa. The creep behavior was correlated with temperature and stress using a power law relationship. The calculated stress exponent n, was about 3.2 and the apparent activation energy, Q, was about 270 kJ/mol. The large creep ductility exhibited by WC-3009 was attributed to its high strain rate sensitivity.
A new Cu-based alloy possessing high strength, high conductivity, and good stability at elevated temperatures was recently produced. This paper details the melting of the master alloys, production of rapidly solidified ribbon, and processing of the ribbon to sheet by hot pressing and hot rolling.
A new Cu-based alloy possessing high strength, high conductivity, and good stability at elevated temperatures was recently produced. This paper details the melting of the master alloys, production of rapidly solidified ribbon, and processing of the ribbon to sheet by hot pressing and hot rolling.
In order to use sulfur-containing resources economically and with minimal environmental damage, it is important to understand the desulfurization processes. Hydrodesulfurization, for example, is carried out on the surface of a heterogeneous metal sulfide catalyst. Studies of simple, soluble inorganic systems provide information regarding the structure and reactivity of sulfur-containing compounds with metal complexes. Further, consistent with recent trends in materials chemistry, many model compounds warrant further study as catalyst precursors. The reactivity of low-valent organometallic sandwich pi-complexes toward dithiocarboxylic acids is described. For example, treatment of bisbenzene vanadium with CH3CSSH affords a divanadium tetrakis(dithioacetate) complex. The crystallographically determined V-V bond distance, 2.800(2), is nearly the same as the V-V bond distance in a V(mu-nu squared-S2)2V' unit in the mineral patonite (VS4)n. The stability of the V2S4 core in the dimer is demonstrated by evidence of V2S4(+) in the mass spectrum (70 eV, solid probe) of the vanadium dimer. Several other systems relevant to HDS catalysis are also discussed.
Titanium aluminide metal matrix composites are prominent materials systems being considered for high temperature aerospace applications. One of the major problems with this material is the reactivity between existing reinforcements and the matrix after prolonged thermal exposure. This paper presents results from an investigation of reaction kinetics between Ti-14Al-21Nb (wt pct) and SCS-6 fibers and SiC fibers with surface coatings of TiB2, TiC, TiN, W, and Si. Microstructural evaluation of the reaction layers as well as matrix regions around the fibers is presented.