Calcium chromite

Vashook V, Vasylechko L, Zosel J, Gruner W, Ullmann H, Guth U (2004) Crystal structure and electrical conductivity of lanthanum-calcium chromites-titanates Lai xCaxCr] yTiyOa s (x = 0-1, y = 0-1). J Solid State Chem 177 3784-3794... 

Fig. 1. Global distribution of seabed mineral deposits, where x represents chromite + barite titanium, zirconium, hafnium, and thorium tin I gold, platinum, and silver 3 sand and gravel shell, calcium carbonate gems marine polymetaUic sulfides phosphorites Cl cobalt cmsts S sulfur and B...

Recommendations by the ACGIH are classified as threshold limit values (TLV) based on 8-h TWA. Chromium metal and alloys, Cr(II) compounds and Cr(III) compounds, including chromite ore, have a TLV of 0.5 mg/m Cr in air. Water-soluble Cr(VI) compounds have a TLV of 0.05 mg/m Cr. Certain water-insoluble Cr(VI) compounds, ie, the chromates of 2inc, barium, calcium, lead, strontium, sintered chromic acid, and processing chromite ores, also have a TLV of 0.05 mg/m as well as a human carcinogen designation (145). 

When it is desirable to use a weak black, bone black may be substituted for carbon. It is manufactured by calcining animal bones and contains approximately 85% calcium phosphate and calcium carbonate. Black iron oxide (Fe O is stable up to 150°C. Copper chromite black (Cu(Cr02)2) is iuert to all but mbberlike compositions and has been calcined to 600°C. 

The anode material in SOF(7s is a cermet (rnetal/cerarnic composite material) of 30 to 40 percent nickel in zirconia, and the cathode is lanthanum rnanganite doped with calcium oxide or strontium oxide. Both of these materials are porous and mixed ionic/electronic conductors. The bipolar separator typically is doped lanthanum chromite, but a metal can be used in cells operating below 1073 K (1472°F). The bipolar plate materials are dense and electronically conductive. 

Modification of the burning rates, pressure exponents, and temp coefficients of burning rate of the fluorocarbon composites has been accomplished with copper, lead, tin, sodium, ammonium and potassium fluoborates sodium, potassium, lithium, lead, copper and calcium fluorides potassium and ammonium dichromate lead and zinc stearate cesium carbonate potassium and ammonium sulfate copper chromite oxides of magnesium, copper and manganese boron zinc dust and carbon black (Ref 75)... 

In a review of the course and mechanism of the catalytic decomposition of ammonium perchlorate, the considerable effects of metal oxides in reducing the explosion temperature of the salt are described [1], Solymosi s previous work had shown reductions from 440° to about 270° by dichromium trioxide, to 260° by 10 mol% of cadmium oxide and to 200°C by 0.2% of zinc oxide. The effect of various concentrations of copper chromite , copper oxide, iron oxide and potassium permanganate on the catalysed combustion of the propellant salt was studied [2], Similar studies on the effects of compounds of 11 metals and potassium dichromate in particular, have been reported [3], Presence of calcium carbonate or calcium oxide has a stabilising effect on the salt, either alone or in admixture with polystyrene [4],... 

The interconnect material is in contact with both electrodes at elevated temperatures, so chemical compatibility with other fuel cell components is important. Although, direct reaction of lanthanum chromite based materials with other components is typically not a major problem [2], reaction between calcium-doped lanthanum chromite and YSZ has been observed [20-24], but can be minimized by application of an interlayer to prevent calcium migration [25], Strontium doping, rather than calcium doping, tends to improve the resistance to reaction [26], but reaction can occur with strontium doping, especially if SrCr04 forms on the interconnect [27],... 

Lanthanum chromite is a p-type conductor so divalent ions, which act as electron acceptors on the trivalent (La3+ or Cr3+) sites, are used to increase the conductivity. As discussed above, the most common dopants are calcium and strontium on the lanthanum site. Although there is considerable scatter in the conductivities reported by different researchers due to differences in microstrucure and morpohology, the increase in conductivity with calcium doping is typically higher than that with strontium doping [4], The increase in conductivity at 700°C in air with calcium additions is shown in Figure 4.1 [1, 2, 28-44], One of the advantages of the perovskite structure is that it... 

Lanthanum chromite is the most common base for SOFC interconnects, but chromites of other lanthanide elements have also been used [43, 45, 46, 48, 54, 55], Although the conductivity of calcium-doped gadolinium chromite for low calcium contents is in the upper range of conductivities for lanthanum chromite, other nonlanthanum chromites typically have lower conductivities. However, the use of other lanthanides provides benefits in controlling the phase transformation temperature and in potential cost savings [48],... 

Carter JD, Appel CC, and Mogensen M. Reactions at the calcium doped lanthanum chromite-yttria stabilized zirconia interface. J. Sol. St. Chem. 1996 122 407—415. 

Sakai N, Kawada T, Yokokawa H, Dokiya M, and Iwata T. Sinterability and electrical conductivity of calcium-doped lanthanum chromites. J. Mater. Sci. 1990 25-,4531-4534. 

Yasuda I and Hikita T. Electrical conductivity and defect structure of calcium-doped lanthanum chromites. 7. Electrochem. Soc. 1993 140 1699-1704. 

Paulik SW, Baskaran S, and Armstrong TR. Mechanical properties of calcium- and strontium-substituted lanthanum chromite. J. Mater. Sci. 1997 33 2397-2404. 

Marinho EP, Souza AG, de Melo DS, Santos IMG, Melo DMA, and da Silva WJ. Lanthanum chromites partially substituted by calcium strontium and barium synthesized by urea combustion—Thermogravimetric study. J. Thermal Analysis Calorimetry 2007 87 801-804. 

Chick LA, Kiu J, Stevenson JW, Armstrong TA, McCready DE, Maupin GD, Coffey GW, and Coyle CA. Phase transitions and transient liquid-phase sintering in calcium-substituted lanthanum chromite. J. Am. Ceram. Soc. 1997 80 2109-2120. 

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