Chromium -modified

Figure 3.6 Experimental X-ray reflectivity curves for a virgin-coated substrate indicative curves in air for gold- and chromium-modified of a metal layer that is not perturbed by the...

Leger, C., Bach, S., and Pereira-Ramos, J.P. 2001. The sol-gel chromium-modified VT),, as a cathodic material for lithium batteries. Journal of Solid State Electrochemistry 11, 71-76. 

In order to elucidate the reasons for the dependence of the catalytic properties of these samples on their preparation method, we studied the acid surface properties of cobalt- and chromium-modified Zr02 catalysts by ammonia thermoprogrammed desorption and IR-spectroscopy. Our results again indicated that the activity of these catalysts in the SCR of NOx by hydrocarbons is a function both of the surface acidity and content of the active metal. The acid site concentration of the starting Zr02 samples prepared by various methods is significant (0.13 and 0.23 mmol/g) but these samples are inactive, while 10% CriOilZtOi prepared by the sol-gel method displays considerable activity in the reaction studied with lower surface acidity. The acid site concentration of the sample with the same composition prepared by the precipitation method is reduced by a factor of 2.5 and, thus, this catalyst has much lower activity in the selective catalytic reduction. 

After reviewing existing information [ ] on the use of strain gauges under conditions similar to those of interest here, it was decided that strain gauges using nickel-chromium (modified Karmat) strain-sensing foils were most applicable. 

French DN, Metallurgical Failures in Fossil Fired Boilers, 2nd ed. John Wiley Sons Inc., NY, USA, 1993. Gleeson B, Cheung WH, Da Costa W and Young DJ, The hot-corrosion behavior of novel co-deposited chromium-modified aluminide coatings. Oxidation of Metals, 1992, 38(3-5) 407-424. 

Carbon content is usually about 0.15% but may be higher in bolting steels and hot-work die steels. Molybdenum content is usually between 0.5 and 1.5% it increases creep—mpture strength and prevents temper embrittlement at the higher chromium contents. In the modified steels, siUcon is added to improve oxidation resistance, titanium and vanadium to stabilize the carbides to higher temperatures, and nickel to reduce notch sensitivity. Most of the chromium—molybdenum steels are used in the aimealed or in the normalized and tempered condition some of the modified grades have better properties in the quench and tempered condition. 

Nickel—Iron. A large amount of nickel is used in alloy and stainless steels and in cast irons. Nickel is added to ferritic alloy steels to increase the hardenabihty and to modify ferrite and cementite properties and morphologies, and thus to improve the strength, toughness, and ductihty of the steel. In austenitic stainless steels, the nickel content is 7—35 wt %. Its primary roles are to stabilize the ductile austenite stmcture and to provide, in conjunction with chromium, good corrosion resistance. Nickel is added to cast irons to improve strength and toughness. 

Most catalysts for solution processes are either completely soluble or pseudo-homogeneous all their catalyst components are introduced into the reactor as Hquids but produce soHd catalysts when combined. The early Du Pont process employed a three-component catalyst consisting of titanium tetrachloride, vanadium oxytrichloride, and triisobutjlalurninum (80,81), whereas Dow used a mixture of titanium tetrachloride and triisobutylalurninum modified with ammonia (86,87). Because processes are intrinsically suitable for the use of soluble catalysts, they were the first to accommodate highly active metallocene catalysts. Other suitable catalyst systems include heterogeneous catalysts (such as chromium-based catalysts) as well as supported and unsupported Ziegler catalysts (88—90). 

Chromium Oxide-Based Catalysts. Chromium oxide-based catalysts were originally developed by Phillips Petroleum Company for the manufacture of HDPE resins subsequendy, they have been modified for ethylene—a-olefin copolymerisation reactions (10). These catalysts use a mixed sihca—titania support containing from 2 to 20 wt % of Ti. After the deposition of chromium species onto the support, the catalyst is first oxidised by an oxygen—air mixture and then reduced at increased temperatures with carbon monoxide. The catalyst systems used for ethylene copolymerisation consist of sohd catalysts and co-catalysts, ie, triaLkylboron or trialkyl aluminum compounds. Ethylene—a-olefin copolymers produced with these catalysts have very broad molecular weight distributions, characterised by M.Jin the 12—35 and MER in the 80—200 range. 

Leather Taiming. Oxahc acid is used as a pH modifier in leather tanning by tannin and basic chromium sulfate. It also functions as a bleaching agent for leather (qv). 

HTS catalyst consists mainly of magnetite crystals stabilized using chromium oxide. Phosphoms, arsenic, and sulfur are poisons to the catalyst. Low reformer steam to carbon ratios give rise to conditions favoring the formation of iron carbides which catalyze the synthesis of hydrocarbons by the Fisher-Tropsch reaction. Modified iron and iron-free HTS catalysts have been developed to avoid these problems (49,50) and allow operation at steam to carbon ratios as low as 2.7. Kinetic and equiUbrium data for the water gas shift reaction are available in reference 51. 

The physical and mechanical properties of steel depend on its microstmcture, that is, the nature, distribution, and amounts of its metaHographic constituents as distinct from its chemical composition. The amount and distribution of iron and iron carbide determine most of the properties, although most plain carbon steels also contain manganese, siUcon, phosphoms, sulfur, oxygen, and traces of nitrogen, hydrogen, and other chemical elements such as aluminum and copper. These elements may modify, to a certain extent, the main effects of iron and iron carbide, but the influence of iron carbide always predominates. This is tme even of medium alloy steels, which may contain considerable amounts of nickel, chromium, and molybdenum. 

Alkyds. Alkyd resins (qv) are polyesters formed by the reaction of polybasic acids, unsaturated fatty acids, and polyhydric alcohols (see Alcohols, POLYHYDRic). Modified alkyds are made when epoxy, sUicone, urethane, or vinyl resins take part in this reaction. The resins cross-link by reaction with oxygen in the air, and carboxylate salts of cobalt, chromium, manganese, zinc, or zirconium are included in the formulation to catalyze drying. 

The reactions are generally run at room temperature or below. With steroids the product is usually isolated by addition of the reaction mixture to water followed by filtration or extraction. The inorganic product of the reaction, chromium III, is soluble in neutral or aqueous acid solutions and can be removed by washing. When steroidal amines are oxidized, the work-up is usually modified such that the steroid may be extracted from the insoluble basic chromium III salts. °... 

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