Showing papers on "Chromium published in 1990"

Chromium reduction in Pseudomonas putida.

Abstract: Reduction of hexavalent chromium (chromate) to less-toxic trivalent chromium was studied by using cell suspensions and cell-free supernatant fluids from Pseudomonas putida PRS2000. Chromate reductase activity was associated with soluble protein and not with the membrane fraction. The crude enzyme activity was heat labile and showed a Km of 40 microM CrO4(2-). Neither sulfate nor nitrate affected chromate reduction either in vitro or with intact cells.

Interlayer magnetic coupling in Fe/Cr multilayered structures

Abstract: We have calculated the mgnetic coupling of two layers of iron through an intervening layer of chromium. We use the mixing interaction between iron atoms at the interfaces with the conduction electrons of chromium and the band structure of paramagnetic chromium. When we take into account the roughness of the interface, our calculated coupling reproduces the essential features of the coupling found in Fe/Cr superlattices.

Hexavalent chromium interaction with chitosan

Abstract: Chitosan prepared from fresh water crab shells was used for hexavalent chromium removal. Kinetic studies indicated a rapid removal of chromium from aqueous solutions. The first-order rate constant for chromium removal was calculated to be 1.92 h−1. Sorption isothermal data could be interpreted by the Langmuir relationship. Drastic decrease in chromium removal was observed with the increase in pH. Sorption was almost 90% at pH 3 at an initial chromium concentration of 5 mg/L and reduced to 10% at pH 7 and above. Presence of electrolytes and chloride significantly affected the chromium removal, indicating the electrostatic attraction as the main removal mechanism. Regeneration of the sorbent with alkali was not very effective as only 60–65% of sorbed chromium could be recovered.

The effect of chromium picolinate on serum cholesterol and apolipoprotein fractions in human subjects.

Abstract: Chromium has been implicated as a cofactor in the maintenance of normal lipid and carbohydrate metabolism. A deficiency of chromium results from diets low in biologically available chromium. Picolinic acid, a metabolite of tryptophan, forms stable complexes with transitional metal ions, which results in an improved bioavailability of the metal ion chromium. To determine whether or not chromium picolinate is effective in humans, 28 volunteer subjects were given either chromium tripicolinate (3.8 micromol [200 micrograms] chromium) or a placebo daily for 42 days in a double-blind crossover study. A 14-day period off capsules was used between treatments. Levels of total cholesterol, low-density lipoprotein (LDL) cholesterol, and apolipoprotein B, the principal protein of the LDL fraction, decreased significantly while the subjects were ingesting chromium picolinate. The concentration of apolipoprotein A-I, the principal protein of the high-density lipoprotein (HDL) fraction, increased substantially during treatment with chromium picolinate. The HDL-cholesterol level was elevated slightly but not significantly during ingestion of chromium picolinate. Only apolipoprotein B, of the variables measured, was altered significantly during supplementation with the placebo. These observations show that chromium picolinate is efficacious in lowering blood lipids in humans.

Photocurrent Spectroscopic Investigations of Passive Films on Chromium

Abstract: A detailed photoelectrochemical study was carried out in order to identify the nature and the properties of the passive layers on chromium under different experimental conditions. Different compositions of the films, related to various hydration degrees of the Cr(III) oxides, have been inferred on the basis of the bandgap values measured at changing pH, electrode potential, and polarization time. By comparison with air‐grown films, it has been concluded that anhydrous is never formed in acidic solution. The water content in the passive film increases at decreasing potentials and for long polarization times. In some cases, especially at neutral pH values, passive films possess a duplex structure, consisting of two layers with different hydration degrees. The photoelectrochemical study suggests an insulating or a slightly p‐type behavior of the passive layers.

A newly developed chromium(III) gel technology

Abstract: Laboratory testing of a recently developed chromium(III) (Cr(III)) gel technology is reported. The gels can be used in conjunction with a number of oilfield treatments. The single-fluid acrylamide-polymer/Cr(III)-carboxylate aqueous gels are formed by crosslinking acrylamide polymer with a Cr(III)-carboxylate-complex crosslinking agent. Representative gel compositions and associated gel properties are discussed.

Non-linear population processes of Er3+ laser levels in chromium-doped garnet crystals

Abstract: In garnets doped with chromium and rare-earth ions, the processes of energy transfer, including upconversion, were investigated. Their influence on laser properties is established.

Role of Valence State and Solubility of Chromium Compounds on Induction of Cytotoxicity, Mutagenesis, and Anchorage Independence in Diploid Human Fibroblasts

Abstract: We previously showed that carcinogenic nickel, arsenic, and chromium(VI) compounds induced anchorage independence (AI) in diploid human fibroblastic cells (HFC) derived from foreskins (K. A. Biedermann and J. R. Landolph, Cancer Res., 47: 3815-3823, 1987). To elucidate the role of the valence state of chromium and solubility of chromium compounds in inducing AI, we studied the ability of soluble and insoluble hexavalent [chromium(VI)] and trivalent [chromium(III)] chromium compounds to induce mutation and AI in HFC. Chromium(VI) compounds (PbCrO4, CaCrO4, Na2CrO4, and CrO3) were 1000-fold more cytotoxic to HFC (average 50% lethal dose 0.5 microM) than chromium(III) compounds (CrCl3, Cr2O3, Cr2S3; average 50% lethal dose 500 microM). However, equal concentrations (0.1-10.0 microM) of soluble or insoluble chromium compounds in either +6 or +3 valence states induced similar increases in frequencies of AI in HFC (100-200/10(5]. Chromium(VI)- and chromium(III)-induced AI was a stable phenotype. All soluble chromium(VI) and insoluble chromium(III) compounds studied induced mutation to 6-thioguanine resistance at cytotoxic concentrations in HFC. Insoluble PbCr(VI)O4 and a soluble form of Cr(III)Cl3 were inactive in this assay. Mutation induction by chromium(III) compounds only occurred at cytotoxic concentrations (100-1000 microM) 1000-fold greater than those concentrations of chromium(VI) compounds (0.25-1 microM) which were cytotoxic, mutagenic, and induced AI. Soluble hexavalent Na2(51)CrO4 was taken up facilely by cells at concentrations that induced cytotoxicity, mutation, and AI. At concentrations of 0.25-1.0 microM, which induced AI but were not cytotoxic or mutagenic, or concentrations of 1-1000 microM, which were cytotoxic and mutagenic, soluble trivalent 51CrCl3 was not taken up by cells. An insoluble form of CrCl3 was not taken up intracellularly but did avidly associate with cells over the concentration range 1 to 100 microM which induced AI, cytotoxicity, and mutagenicity. Therefore, both chromium(VI) and chromium(III) compounds induced genotoxic effects in human fibroblasts. Cellular uptake, cytotoxicity, mutagenicity, and AI induced by soluble chromium(VI) compounds all occurred at the low concentrations of 0.2 to 1.0 microM; hence mutagenicity and induction of AI may be coupled for soluble chromium(VI) compounds but not for insoluble PbCrO4, which induced AI but was not mutagenic. Cytotoxicity and mutagenicity of insoluble chromium(III) occurred at concentrations of 10-100 microM, but induction of AI occurred at concentrations of 0.1-10 microM, indicating that inductions of mutagenicity and AI were not coupled for chromium(III) compounds.(ABSTRACT TRUNCATED AT 400 WORDS)

Reduction of hexavalent chromium by ascorbic acid and glutathione with special reference to the rat lung.

Abstract: The reduction of 20 microM hexavalent chromium [chromium(VI)] by L-ascorbic acid (AsA) (0.06-2 mM) and/or glutathione (GSH) (2-15 mM) in buffer solutions, cell-free bronchoalveolar lavage fluids or soluble fractions of rat lungs was investigated at physiological pH (37 degrees C). The reduction in AsA solution was pseudo-first-order in a single phase with respect to chromium(VI), but that in GSH solution showed a two-phase process. The half-life of chromium(IV) ranged from seconds to hours. The reducing ability of AsA was markedly higher than that of GSH. Coexistence of equimolar GSH with AsA accelerated the reduction rate slightly, in comparison with that in the corresponding AsA solution. Lavage fluids containing 0.06 mM AsA showed pH-dependent reactions similar to those of the corresponding AsA solutions. The lung-soluble fractions reduced chromium(VI) in a process composed of phase I and phase II, characterized by the reducing ability of AsA-GSH cooperation and of AsA alone, respectively. Reduction in the former was 30-40% more rapid than in the latter. The biological half-life of chromium(VI) in the lung was estimated to be 0.6 min, on the basis of the reducing activity in the first phase. However, the apparent biological half-life of chromium(VI) was about 2 min in rat lungs after intratracheal injection of chromate, involving depletion of AsA, but no significant changes in GSH. The difference is discussed in terms of AsA-induced initiative reduction in the alveolar lining fluid and subsequent obstructive effects of the resulting trivalent species on trans-membrane permeability of chromate anions.(ABSTRACT TRUNCATED AT 250 WORDS)

Acidity as a factor in leaching of copper, chromium and arsenic from CCA-treated dimension lumber

Abstract: Samples of new and weathered utility lumber pressure-treated with chromated copper arsenate (CCA) were tested for leaching of copper, chromium and arsenic by submersion in leaching baths of various pH levels. Accumulation of metals was monitored in leachate at pH 3.5, 4.5, 5.5, 7.0 and 8.5 over a period of 40 d by atomic absorption spectroscopy. Copper, chromium and arsenic were found in the leachate of both new and weathered wood with significantly higher levels of all metals occurring at acidic pH levels. Up to 100% of CCA treatment metals were found to have leached at pH 3.5, whereas a maximum of 9% of metals leached at pH 8.5. Metal leaching was found to be higher in citric acid than in dilute sulfuric acid solutions. Leaching of copper, chromium and arsenic was not proportional to the amount of metal present before leaching.

Chromium addition and environmental embrittlement in Fe3Al

Abstract: Iron aluminides based on Fe[sub 3]Al afford excellent oxidation properties at relatively low cost, making them candidates for use as structural material in corrosive environments. Recently, efforts have been devoted to understanding and improving their ductility through control of grain structure, alloy additions and material processing. Studies at this laboratory have shown that the ambient temperature ductility can be increased significantly by additions of up to 6% Cr. This increase in ductility was earlier attributed to increased cleavage strength, easier cross slip due to lower antiphase boundary (APB) energy, and solid softening. Very recent studies of FeAl and Fe[sub 3]Al in various tensile testing environments have indicated that both alloy systems are relatively more ductile at room temperature when tested in vacuum or dry oxygen. Ductilities of 12--18% were attained in both iron aluminide systems in an oxygen pressure of 6.7 [times] 10[sup 4] Pa, while only 2--4% ductility was achieved in normal laboratory air. It seems appropriate to reexamine the mechanism by which chromium produces improved ductility at room temperature in laboratory air and to correlate it with the environmental effects on mechanical properties. In the current investigation, the authors have evaluated room temperature tensile properties of the binary more » alloy (Fe-28Al, at.%) and ternary alloy containing chromium (Fe-28Al-4Cr) as a function of surface condition and heat treatment. The results indicate that, although chromium may affect cleavage strength and APB energies, its most significant effect on room temperature ductility is to modify the protective surface oxide, resulting in a minimization of environmental embrittlement. « less

Chromium compounds and uses thereof

Abstract: Novel chromlum-containing compounds, such as, for example, chromium pyrrolides, are prepared by forming a mixture of a chromium salt, a metal amide, and an electron pair donor solvent, such as, for example, an ether. These novel chromium-containing, or chromium pyrrolide, compounds can be used either unsupported or supported on an inorganic oxide support to trimerize and/or polymerize olefins.

Reaction of chromium (VI) with hydrogen peroxide in the presence of glutathione: reactive intermediates and resulting DNA damage.

Abstract: The reaction of chromium(VI) with hydrogen peroxide was studied in the presence of glutathione. In vitro, reaction of chromium(VI) with hydrogen peroxide alone led to production of hydroxyl radical as the significant reactive intermediate, while reaction of chromium(VI) with glutathione led to formation of two chromium(V)-glutathione complexes and the glutathione thiyl radical. Incubation of chromium(VI) with glutathione prior to addition of hydrogen peroxide led to formation of peroxochromium(V) species and a dramatic increase in hydroxyl radical production over that detected in the reaction of chromium(VI) with hydrogen peroxide alone. In contrast, addition of chromium(VI) to a preincubated mixture of glutathione and hydrogen peroxide led to a decrease in hydroxyl radical production over that obtained in the reaction of chromium(VI) with hydrogen peroxide. When pBR322 DNA was added to the above reactions, the extent of chromium(VI)-induced DNA strand breakage correlated with the relative amount of hydroxyl radical formed. Reaction of chromium(VI) with calf thymus DNA in the presence of a preincubated mixture of glutathione and hydrogen peroxide led to detection of the 8-hydroxydeoxyguanosine adduct, whose formation correlated with that of hydroxyl radical production. No significant chromium-DNA adduct formation was detected. The results suggest that, in the cellular metabolism of chromium(VI), preformed chromium(V)-glutathione complexes may react with hydrogen peroxide in a Fenton-type manner to produce hydroxyl radical as the DNA-damaging agent. However, if glutathione reacts with hydrogen peroxide prior to exposure to chromium(VI), the amount of hydroxyl radical generated may not be sufficient to cause significant DNA damage.(ABSTRACT TRUNCATED AT 250 WORDS)

Reduction of toxic chromate in an industrial effluent by use of a chromate-reducing strain of Enterobacter cloacae.

Abstract: Detoxification and removal of hexavalent chromium (chromate: CrO4 2−) in an industrial effluent was investigated using Enterobacter cloacae HO1. This bacterium could completely reduce chromate to less toxic trivalent chromium when appropiate nutrients were supplied to the effluent. The reduction rate was strongly dependent on the amount of added carbon and energy sources, and also on cell density. Since the reduced chromium readily formed insoluble chromium hydroxides, about 40% of the reduced chromium could be removed from the treated water by centrifugation.

Characterization of oxide structures formed on nickel-chromium alloy during low pressure oxidation at 500–600°C

Abstract: Low pressure oxidation studies of Ni-18%Cr alloy were carried out at temperatures of 500–600°C for very brief periods. Detailed XPS, AES, SEM, and TEM studies identified four stages in the initial oxidation. These are: (1) formation of a mixed nickel-chromium oxide overlayer; (2) growth of submicron-sized oxide nodules; (3) development of dark “hole-like” patches on the surface; and (4) growth of “second generation” oxide nodules. Both types of nodules consist primarily of a nickel structure depleted in oxygen. Their formation appears to result from a very rapid outward movement of nickel from localized defects in the metal. The dark patches result from the presence of a chromium oxide-rich underlayer, which appears to form by a lateral migration of chromium from adjacent oxide/metal interface regions and from grain boundaries.

Behavior of grain boundary chemistry and precipitates upon thermal treatment of controlled purity alloy 690

Abstract: Grain boundary composition and carbide composition and structure were characterized for various microstructures of controlled purity alloy 690. Heat treatments produced varying degrees of grain boundary chromium depletion and precipitate distributions which were characterizedvia scanning transmission electron microscopy (STEM). Convergent beam electron diffraction revealed that the dominant carbide is M23C6, and energy dispersive X-ray analysis (EDAX) determined that the metallic content was about 90 at. pct chromium. A discontinuous precipitation reaction was observed and is attributed to a high degree of carbon supersaturation. Grain boundary composition measurements confirm that chromium depletion is controlled by volume diffusion of chromium to chromium-rich grain boundary carbides in the temperature range of 873 to 1073 K. Grain boundary chromium levels as low as 18.8 at. pct were obtained by thermal treatment at 873 K for 250 hours and 973 K for 1 hour. A thermodynamic and kinetic model developed for alloy 600 was modified to describe the development of the chromium depletion profile in alloy 690 during thermal treatment. Experimentally measured chromium profiles agree well with the model results for the dependence of the chromium depletion zone width and depth on various input parameters. The establishment of the model for alloy 690 allows the chromium depletion zone width and depth to be computed as a function of alloy composition, grain size, and temperature. The chromium depletion profiles and the precipitate structure and composition of controlled purity 690 are compared to those of controlled purity 600. A thermodynamic analysis of the carbide stability indicates that other factors, such as favorable orientation relationships, play an important role in controlling the precipitation of Cr23C6 in nickel-base alloys.

A method for removal of toxic chromium using dialysis-sac cultures of a chromate-reducing strain of Enterobacter cloacae.

Abstract: A method for removal of toxic hexavalent chromium (chlomate: CrO inf4 sup2− ) was developed by use of dialysis-sac cultures of a chromate-reducing strain of Enterobacter cloacae (HO1). E. cloacae strain HO1 cells were put in dialysis (semipermeable membrane) sacs, and the sacs were submerged in water containing toxic CrO inf4 sup2− . The dialysis sacs allowed CrO inf4 sup2− to diffuse into the culture, and CrO inf4 sup2− was reduced anaerobically in the dialysis sacs by the E. cloacae cells. Because reduced chromium readily formed insoluble chromium hydroxides in the dialysis sacs, the greater part of reduced chromium was unable to diffuse out through the semipermeable membrane. Thus the dialysis culture of E. cloacae strain HO1 could successfully remove toxic chromium from the surrounding water. If the initial concentration of CrO inf4 sup2− was less than 4mM (208 ppm as chromium), about 90% of the total chromium could be removed from water by the described method.

Biological removal of toxic chromium using an Enterobacter cloacae strain that reduces chromate under anaerobic conditions.

Abstract: The present communication is the first report on the potential of chromate-reducing bacteria to remove toxic chromium from wastewater. Dialysis culture systems with the anion-exchange membrane sucessfully removed all the reduced chromium under anaerobic conditions.

Polyhedral oligometallasilasesquioxanes as models for silica-supported catalysts: chromium attached to two vicinal siloxy groups

Abstract: The reaction of [(cyclo-C6H11)7Si7O9(OSiMe3)(OH)2] with CrO3 leads to the formation of [(cyclo-C6H11)7Si7O11(OSiMe3)CrO2], a new crystallographically characterized silyl-chromate complex that catalyses the polymerization of ethylene in the presence of trialkylaluminium reagents.

Highly corrosion and/or oxidation-resistant protective coating containing rhenium

Abstract: A protective coating for metal components formed of nickel or cobalt-based superalloys essentially consists of the following constituents (in percentages by weight): 1 to 20% rhenium, 22 to 50% chromium, 0 to 15% aluminum, the share of chromium and aluminum taken together being at least 25% and at most 53%, 0.3 to 2% in total of at least one reactive element from the group consisting of the rare earths, and 0 to 3% silicon, impurities, as well as the following elective components: 0 to 5% hafnium, 0 to 12% tungsten, 0 to 10% manganese, 0 to 15% tantalum, 0 to 5% titanium, 0 to 4% niobium, and 0 to 2% zirconium, the total share of the elective components being from 0 to a maximum of 15%, and a remainder primarily being at least one of the elements iron, nickel, and cobalt.