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Industrial and agricultural waste streams (waste water, sludges, tailings, etc.) which contain high concentrations of NH4+, PO43–, and transition metals are environmentally harmful and toxic pollutants. At the same time, phosphorous and transition metals constitute highly valuable resources. Typically, separate pathways have been considered to extract hazardous transition metals or phosphate independently from each other. Investigations on the simultaneous removal of multiple components have been carried out only to a limited extent. Here, we report the synthesis routes for Ni- and Co-struvites (NH4MPO4·6H2O, M = Ni2+ and Co2+), which allow for P, ammonia, and metal co-precipitation. By evaluating different reaction parameters, the phase and stability of transition metal struvites as well as their crystal morphologies and sizes could be optimized. Ni-struvite is stable in a wide reactant concentration range and at different metal/phosphorus (M/P) ratios, whereas Co-struvite only forms at low M/P ratios. Detailed investigations of the precipitation process using ex situ and in situ techniques provided insights into the crystallization mechanisms/crystal engineering of these materials. M-struvites crystallize via intermediate colloidal amorphous nanophases, which subsequently aggregate and condense to final crystals after extended reaction times. However, the exact reaction kinetics of the formation of a final crystalline product varies significantly depending on the involved metal cation in the precipitation process: several seconds (Mg) to minutes (Ni) to hours (Co). The achieved level of control over the morphology and size makes precipitation of transition metal struvites a promising method for direct metal recovery and binding them in the form of valuable phosphate raw materials. Under this paradigm, the crystals can be potentially up-cycled as precursor powders for electrochemical or (electro)catalytic applications, which require transition metal phosphates.
The movement of the macroscopic magnetic moment in ferromagnetic systems can be described by the Landau-Lifshitz (LL) or Landau-Lifshitz-Gilbert (LLG) equation. These equations are strictly valid only at absolute zero temperature. To include temperature effects a stochastic version of the LL or LLG equation for a spin density of one per unit cell can be used instead. To apply the stochastic LL to micromagnetic simulations, where the spin density per unit cell is generally higher, a conversion regarding simulation cell size and temperature has to be established. Based on energetic considerations, a conversion for ferromagnetic bulk and thin film systems is proposed. The conversion is tested in micromagnetic simulations which are performed with the Object Oriented Micromagnetic Framework (OOMMF). The Curie temperatures of bulk Nickel, Cobalt and Iron systems as well as Nickel thin-film systems with thicknesses between 6.3 mono layer (ML) and 31ML are determined from micromagnetic simulations. The results show a good agreement with experimentally determined Curie temperatures of bulk and thin film systems when temperature scaling is performed according to the presented model.
The present work deals with Niobcarbid (NbC). Strategic reflections on tungsten carbide and more and more stringent toxicological restrictions for cobalt associated for both with spiraling stock market prices have attracted recently some attention for Niobium carbide as a substitute for tungsten carbide in machining.
The present work deals with Niobcarbid (NbC). Strategic reflections on tungsten carbide and more and more stringent toxicological restrictions for cobalt associated for both with spiraling stock market prices have attracted recently some attention for Niobium carbide as a substitute for tungsten carbide in machining.
The aim of the study presented in this paper is to highlight the potential of niobium carbide cutting tool inserts for machining and to compare their performance to commercially available tungsten carbide inserts. In this work, a comparison between a conventional Wc-Co insert and NbC-Co inserts was carried out under hard machining conditions on specimens made of 100Cr6 bearing steel grade (SAE 52100).
The nature of the bound water in solids with hydrogen-bonded networks depends not only on temperature and pressure but also on the nature of the constituents. The collapse and reorientation of these network structures determines the stability of hydrated solids and transitions to other crystalline or amorphous phases. Here, we study the mechanochemically induced loss of bound water in Co₃(PO₄)₂·8H₂O and compare this process to the behavior under hydrostatic pressure.
The associated phase transition and its kinetics were monitored by X-ray powder diffraction with Synchrotron radiation and quantitative IR spectroscopy. High shearing forces are responsible for the degradation of the hydrogen-bonded network and the concomitant crystalline–amorphous transformation. UV/Vis spectroscopy, extended X-ray absorption spectroscopy (EXAFS), and X-ray absorption near-edge spectroscopy (XANES) provided information about the short-range order in the amorphous solid, and thermal analysis revealed its composition and showed that the moderate charge densities of the Co²⁺ and PO₄³⁻ ions, which make the hydration enthalpy comparable to the binding energy of the counteranions, and the Formation of hydrogen-bonded networks favor multistage crystallization processes associated with the release and uptake of coordinated water. The changes of the Co²⁺ coordination induce a color change from pink to blue; therefore, Co₃(PO₄)₂·8H₂O can be used as an overheat temperature indicator.
In this present study, the mechanical properties (strength, hardness, moduli) and the dry sliding properties of stoichiometric and sub-stoichiometric NbC were compared. Microhardness and elastic properties of NbC depend from the C/Nb ratio, because the binary phase diagram Nb-C shows a region of homogeneity of NbCx of 0,72≤ x ≤1.0. At RT, hard metals of stoichiometric NbC have an elastic modulus E of ~440 GPa, those of substochiometric NbC0,88 an E of 405 GPa. The hot hardness of sub-stoichiometric NbC is above 600°C higher than of WC. The dry sliding wear resistance (0,1-7/10 m/s) of the present Fe3Al-NbC0,94 with ~61 vol.-% NbC as hard phase was close to those known of NbC-based hard metals. No grain pull-outs or fragmentations of the NbC grains were seen in the wear tracks of the Fe3Al-NbC composite (MMC), as a metallurgical interphase was formed between matrix and NbC grains. Stoichiometric and sub-stoichiometric niobium carbides have at RT and 400°C under dry sliding a prone intrinsic wear resistance more or less independent from sliding speed, either as hardmetal or as hard phase in metal matrix composite, associated with an exceptional high load carrying capacity.
Das tribologische Profil von binderlosem NbC und mit 8% bzw. mit 12% Cobalt oder 12% Fe3Al gebundenem NbC wird unter unidirektionaler Gleitreibung (v= 0,1-10 m/s, T= 22°C und 400°C) und unter oszillierender Gleitreibung vergleichend gegenüber Ingenieurkeramiken und Hartmetallen dargestellt. Zusätzlich werden die 4-Punkt-Biegebruchfestigkeit, elastische Eigenschaften (E,G) bis 1.000�C die lastabhängige Mikrohärte sowie die Phasenzusammensetzung und Gefügestrukturen vorgestellt. Die Verschleißkoeffizienten des binderlosen NbC lagen bei T unterhalb von 10-6 mm³/N?m, während diejenigen der cobaltgebundenen NbCs mit ansteigender Gleitgeschwindigkeit von 2-4 10-6 mm³/N?m bei 0,1 m/s auf 5-7 10-7 mm³/N.m bei 10 m/s abnahmen. Die Verschleißkoeffizienten bei 400°C lagen für die NbCs generell unterhalb von 10-6 mm³/N.m. Das tribologische Lasttragevermögen im Trockenlauf, ausgedrückt als PV-Wert, nimmt mit ansteigender Gleitgeschwindigkeit auf 100 W/mm² zu. Bedingt durch die geringe Löslichkeit von NbC in Legierungen offenbarten erste Zerspanversuche mit verschiedenen Stählen eine gegenüber WC-basierten Schneidstoffen signifikant angehobene Zerspanungsvolumina. Somit offenbart NbC in offenen und geschlossenen Tribosystemen Anwendungspotentiale.
The tribological profile of alumina (99.7%) mated against rotating disks made in binder-less niobium carbide (NbC) and cobalt-bonded NbC were determined under unidirectional sliding tests (0.1 m/s to 8.0 m/s; 22 °C and 400 °C) as well as in oscillation tests (f = 20 Hz, Δx = 0.2 mm, 2/50/98% rel. humidity, n = 105/106 cycles) under unlubricated (dry) conditions. In addition, the microstructure and mechanical properties of binderless NbC and NbC bonded with 8% cobalt were determined as well. The reason for testing hot-pressed NbC was to avoid side effects generated by sintering additives and/or second phases. The tribological data obtained were benchmarked with different ceramics, cermets and thermally sprayed coatings. NbC and cobalt-bonded NbC exhibited low wear rates under dry sliding associated with high load carrying capacity. The tribological profile established revealed a strong position of NbC bearing materials under tribological considerations and for closed tribo-systems against traditional references, such as WC, Cr3C2 and (Ti,Mo)(C,N).
The tribological profile of rotating disks made of binder-less niobium carbide (hot-pressed NbC) and cobalt-bonded NbC (NbC-8Co) mated against alumina (99.7%) were determined under unidirectional sliding tests (0.1 m/s to 8.0 m/s; 22°C and 400°C) as well as in oscillation tests (f= 20 Hz, Δx= 0.2 mm, 2/50/98% rel. humidity, n= 105/106 cycles) under un-lubricated (dry) conditions. In addition, the microstructure and mechanical properties of NbC and NbC bonded with 8% cobalt were determined as well. The tribological data obtained were benchmarked with different ceramics, cermets, hard metals and thermally sprayed coatings, where the NbC-8Co presented above 7 m/s the lowest wear rates so far in such a bench mark. NbC and NbC-8Co exhibited low wear rates under dry sliding associated with P·V high load carrying capacity. The tribological profile established revealed a strong position of NbC bearing materials under tribological considerations and for closed tribo-systems against traditional references.