Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “ZIRCONIUM”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 253 records · Page 14Linked to original sources
PubMed1998

Yttrium-partially stabilized zirconium dioxide posts: an approach to restoring coronally compromised nonvital teeth.

In the pursuit of esthetic restorations for nonvital teeth, the introduction of a tooth-colored intraradicular post system is described. Conventional metallic posts can corrode and may cause inflammatory reactions and discoloration of the periodontium. Zirconium dioxide is a chemically stable ceramic with physical and optical properties that make it an ideal choice for the construction of esthetic, life-like restorations. The purpose of this study was to describe the composition, properties, and practical applications of zirconia posts in clinical practice.

Ceramics↗
PubMed1999

Zirconium oxide post and core system for the restoration of an endodontically treated incisor.

Due to their enhanced optical properties (eg, translucency, value, chroma), ceramic systems can provide natural aesthetics for restorations placed in the anterior segment. In endodontically treated teeth with stained dentin, however, the use of translucent ceramic materials may be contraindicated unless the underlying discoloration can be masked. This article describes the use of a zirconium oxide post and core system with an all-ceramic crown for the restoration of an endodontically treated anterior tooth. This contemporary system allows optical and mechanical requisites to be resolved simultaneously.

Ceramics↗
PubMed2002

[Dynamics of accumulation and disappearance of Zirconium-95 in the maize/soil and soybean/soil ecosystem].

The dynamics of accumulation and disappearance of 95Zr in two kinds crop-soil ecosystem was studied by using isotope-tracer techniques for simulated pollutants, and the fitting equation was confirmed by application of the closed tow-compartment model and nonlinear regression method. The results showed: 1. The Zirconium-95 absorbed from soil main retention in root of the maize and soybean, and the specific activity of 95Zr in root increased with time slowly, then tended dynamics balance gradually after a period of time. The specific activity of rest parts was lower, and biggish parts were background activity level, which indicated that the 95Zr absorbed by roots was difficult of transference and transportation in the maize and soybean. 2. The 95Zr in soil main retention in surface layer soil(0-8 cm), and the rate of it's activity and total activity > 97.5%, which indicated that the 95Zr absorbed by surface soil could not readily move downwards with percolating water. 3. The regression equation of accumulation and disappearance of 95Zr in the maize and soybean were Cm(t) = 3.2067(1 - e-0.1582t) and Cb(t) = 3.0925(1- e -0.1363t) by analyzing the experiment data with exponential regression method. The results of squared deviations analyzing indicated that each regression equation could describe the dynamics of accumulation and disappearance of 95Zr in the maize-soil and soybean-soil ecosystems preferably.

Ecosystem↗
PubMed2006

Soft and hard tissue response to zirconium dioxide dental implants--a clinical study in man.

Titanium dental implants have been used successfully in implantology for more than 40 years. Recent research, however, suggests that titanium might have more side effects than previously believed. Zirconia ceramics have been employed in orthopaedic surgery for approximately 30 years and were recently introduced into dentistry as a metal replacement for crown and bridge work as well as implant abutments. Zirconium dioxide has been shown in both in vitro and in vivo studies to have desirable osseointegrative properties. This clinical study shows that dental implants made from zirconia are a feasible alternative to titanium dental implants. In addition to excellent cosmetic results, zirconia implants allow a degree of osseointegration and soft tissue response that is superior to titanium dental implants.

Dental Implantation, Endosseous↗
PubMed1993

Podoconiosis in the Ethiopian Rift Valley. Role of beryllium and zirconium.

A geogenic origin has been proposed in the aetiology of non-filarial elephantiasis of the feet and legs, recently renamed podoconiosis. Soil collected in an area of the Ethiopian Rift Valley, the borough of Ocholo, known for its high prevalence of podoconiosis (5.06%), has been submitted to mineral analysis. High values of sulphur (S), cerium (Ce), lanthanum (La) and neodymium (Nd), typical for basaltic bedrocks, were found. Of special interest were the values for zirconium (Zr) and beryllium (Be), 618 +/- 87 ppm and 4.6 +/- 0.5 ppm respectively, twice as high as those recorded for soils sampled in neighbouring areas where the prevalence of podoconiosis is low. To be noted also, a high content in vanadium, above 250 ppm, in half of the soil samples collected in this region. Year-long exposure of unprotected feet to Zr and Be, known for their ability to induce granuloma formation in the lymphoid tissue of man, and present in a clay rich in colloidal silica particle, highly abrasive to skin, is doubtlessly a factor involved in the development of lymph node sclerosis leading to elephantiasis.

Adolescent↗
PubMed1997

Zirconium-labeled monoclonal antibodies and their distribution in tumor-bearing nude mice.

UNLABELLED: A method to label monoclonal antibodies (MAbs) with 88Zr and 89Zr has been developed and tested on the MAbs 323/A3 and E48. METHODS: The bifunctional chelating agent desferal (Df) was linked through a thioether bond to the MAbs. Labeling was accomplished by addition of the premodified antibodies to isolated Zr. The retention of the in vivo behavior of the MAbs was determined by comparing the biodistribution of 88Zr-labeled MAbs with those of 123I and 99mTc in mice bearing tumor xenografts. RESULTS: The labeling was simple and the yields were high (above 90%). The obtained conjugates retained their immunoreactivity (> 80%). The blood clearance and biodistribution of Zr-labeled MAbs resembled those of the reference conjugates. The Zr-Df-MAb conjugates showed a specific tumor accumulation. Zirconium-89-labeled 323/A3 could be visualized with a PET camera. The absence of large amounts of Zr present in the bone pointed to a good in vivo stability of the Zr-Df-MAb conjugates. CONCLUSION: This method is well suited for labeling MAbs with Zr isotopes. Using 89Zr, the biodistribution of the radioimmunoconjugate can easily be visualized with a PET camera.

Animals↗
PubMed2000

Zirconium-mediated asymmetric baeyer-villiger oxidation.

Combinations of axially chiral C2-symmetric diols were used as ligands in zirconium-mediated Baeyer-Villiger reactions. The in situ preformed Zr-diol species proved effective in the asymmetric oxidation of bicyclic and monosubstituted cyclobutanones when a hydroperoxide was employed as oxidant. Asymmetric induction could be preserved upon replacement of one out of two enantiopure BINOL ligands by conformationally flexible 2,2'-biphenol.

Journal Article↗
PubMed1999

Shaping Solid-State Supramolecular Cavities: Chemically Induced Accordionlike Movement of gamma-Zirconium Phosphate Containing Polyethylenoxide Pillars.

The hydrophilic oxygen atoms of polyethylenoxide chains inserted as pillars in gamma-zirconium phosphate form hydrogen bonds with the acid groups of the host. As a result the pillars are almost perpendicular to the gamma layers. Upon changing the pH level of the supernatant solution the hydrogen bonds are broken and the pillars become almost perpendicular to the layers (shown schematically). Thus there is a reversible enlargement-shortening of the interlayer space.

Journal Article↗
PubMed2000

Characterization of zirconium complexes of interest in spent nuclear fuel reprocessing by electrospray ionization mass spectrometry

Liquid-liquid extraction of zirconium, one of the most important fission products, was followed using electrospray ionization mass spectrometry under conditions simulating reprocessing of nuclear spent fuel. Zr(IV) can precipitate from the organic phase after extraction by dibutylphosphoric acid (HDBP), the most common degradation product of tributylphosphate (TBP) radiolysis. Different complexes were detected with electrospray used in positive or negative ion modes, according to the extraction conditions such as the ligand/metal ratio. Stoichiometry of the Zr(IV) complexes was determined by combining isotopic labeling [H(15)NO(3)] of the aqueous phase in the extraction system and tandem mass spectrometry experiments. These results were compared with the species observed using other techniques reported in the literature. The mechanisms of ionization/desorption of these complexes are proposed depending on the organic ligand character (neutral (L) such as TBP, or acidic (HL') such as HDBP), and the ionization mode used. Copyright 2000 John Wiley & Sons, Ltd.

Journal Article↗
PubMed2001

Zirconium(IV) complexes of oxydiacetic acid in aqueous solution and in the solid state as studied by multinuclear NMR and X-ray crystallography.

The structures of complexes of Zr(IV) and oxydiacetate (ODA2-) in aqueous solutions of pH 0-7 were investigated with the use of 1H, 13C, and 17O NMR spectroscopy. Equilibria of mononuclear [Zr(oda)]2+, [Zr(oda)2], and [Zr(oda)3]2- complexes have been observed. In all complexes ODA2- is bound in a tridentate fashion through the two carboxylate groups and the ether oxygen. No di- or oligonuclear species containing ODA2- were observed. An excess of free Zr(IV) remains in solution, probably as a result of weak electrostatic interactions between negatively charged Zr-ODA complexes or free ODA2- and a positively charged cyclic tetranuclear hydroxy zirconium complex. CP-MAS 13C NMR spectra of solid compounds isolated from the samples indicated that the structures of the [Zr(oda)2] and [Zr(oda)3]2- complexes in solution are similar to those in the solid state. This is corroborated by the single-crystal X-ray structure of Na2[Zr(oda)3] x 5.5 H2O, which was obtained from a solution containing exclusively the [Zr(oda)3]2- complex. In this structure Zr(IV) is nine-coordinate with the three ODA2- ligands bound in a tricapped trigonal prismatic geometry. The negative charge of this [Zr(oda)3]2complex is balanced by two Na+ ions, one of which is on a center of symmetry between delta and lambda enantiomers of [Zr(oda)3]2-. This Na+ is octahedrally coordinated to six (non Zr(IV)-bound) carboxylate oxygen atoms of six different [Zr(oda)3]2- units.

Journal Article↗
PubMed2002

Zirconium-catalyzed amine oxidation: a mechanistic study.

The zirconium-catalyzed oxidation of amines in the presence of hydroperoxides gives the corresponding nitro compounds in high yields. In the present paper, we describe mechanistic details of this three-step oxidation, which was investigated by means of DFT calculations. It is shown that N-oxides, hydroxylamines, and nitroso derivatives are formed as intermediates. These compounds had already been postulated on the basis of synthetic experiments. During the oxidation process, the nitrogen atom changes its electronic character from a strong nucleophilic center to a moderate electrophilic center; this is reflected by the geometry of the transition states of the oxygen-transfer process.

Journal Article↗
PubMed2004

Zirconium-mediated cross-coupling of terminal alkynes and vinyl bromides: selective synthesis of cyclobutene and 1,3-diene derivatives.

A diastereoselective synthesis of 1,3-butadiene or cyclobutene derivatives by a zirconium-mediated reaction of alkenyllithium compounds and vinyl bromides is reported. The key steps involve the generation of zirconocene-alkyne complexes from haloalkenes and subsequent coupling with alkenyl bromides. Thus, formally the process supposes the cross-coupling reaction between a terminal alkyne and an alkenyl bromide. Moreover, the use of butyl vinyl ether instead of vinyl bromide as the unsaturated system allows an alternative access to different 1,3-butadiene regioisomers.

Journal Article↗
PubMed1997

Transport Properties of Aqueous Glycerol and Aqueous Mannitol through the Zirconium Oxide Membrane

The transport properties of aqueous glycerol and aqueous mannitol across a zirconium oxide membrane are, investigated from the point of view of irreversible thermodynamics. The data on hydrodynamic permeability are analyzed in terms of frictional coefficients and entropy of activation. The phenomenological coefficient characterizing the electroosmotic flow and the membrane characteristics are also estimated for the various solutions with the object of determining the efficiencies of electrokinetic energy conversion and zeta potential. Copyright 1997Academic Press

Journal Article↗
PubMed2000

Electrocatalytic Oxidation of Coenzyme NADH at Carbon Paste Electrodes, Modified with Zirconium Phosphate and Some Redox Mediators.

Carbon paste electrodes (CPE), modified with zirconium phosphate (ZrP) along with some redox mediators, were prepared and shown to be active in electrocatalytic oxidation of coenzyme NADH. Nile blue (NB), methylviologen (MV), and benzylviologen (BV) were added to ZrP-containing CPE, showing a shift of their redox potentials toward the positive direction, ranging from ca. 0.20 to 0.35 V. This shift was interpreted in terms of different complexation abilities of oxidized and reduced forms of mediators with the host matrix. The modified electrodes prepared showed electrocatalytic activity for electrooxidation of NADH. The i,c-dependencies for the modified electrodes were shown to follow Michaelis-Menten kinetics. For C:ZrP:NB and C:ZrP:MV electrodes, Michaelis constants of 0.870 +/- 0.012 and 0.153 +/- 0.015 mM, respectively, were obtained. The sensitivity of C:ZrP:NB and C:ZrP:MV electrodes to NADH varied from 19.2 to 60.8 and from 18.4 to 50.9 µA/mM c cm(2), respectively, by changing the working potential from -0.2 to 0.2 V vs. SCE. Copyright 2000 Academic Press.

Journal Article↗
PubMed1996

Evaluation of skin sensitization potential of nickel, chromium, titanium and zirconium salts using guinea-pigs and mice.

Contact sensitization capacity of four metal salts, nickel sulphate (NiSO4), potassium dichromate (K2Cr2O7), titanium chloride (TiCl4) and zirconium chloride (ZrCl4), was evaluated using guinea-pigs and mice. In the guinea-pig sensitization tests, we set up an injection concentration to 1% for all chemicals, and changed the challenge concentration. Guinea-pigs were sensitized with NiSO4, K2Cr2O7 and TiCl4. Among the test metal salts, K2Cr2O7 showed the highest sensitization rate and strongest skin reactions. ZrCl4 did not cause any sensitization responses under our experimental conditions. Minimum challenge concentration to cause a skin response was < 0.25% for K2Cr2O7, 0.5% for NiSO4 and 2% for TiCl4, respectively. A sensitive mouse lymph node assay (SLNA) also determined NiSO4 and K2Cr2O7 as a sensitizer. In the SLNA, TiCl4 caused mild lymph node responses, but was classified as a non-sensitizer as well as ZrCl4. Considering these results, the order of sensitization potential was K2Cr2O7 > NiSO4 > ZrCl4. NiSO4- and K2CrO7-sensitized animals did not show any reactions to ZrCl4 and TiCl4. No cross-reaction among these metal salts was found.

Administration, Topical↗
PubMed2004

A comparative study on textural characterization: cation-exchange and sorption properties of crystalline alpha-zirconium(IV), tin(IV), and titanium(IV) phosphates.

Tetravalent metal phosphates (M=Zr, Ti, and Sn) were prepared and characterized by XRD, surface properties, and TG-DTA. The cation exchange and sorption behavior of these metal phosphates toward transition metal ions such as Cu(2+), Co(2+), and Ni(2+) have been studied comparatively as a function of temperature and concentration. The adsorption process was found to increases with increase in temperature and concentration. The selectivity order for alpha-titanium and alpha-tin phosphates is Cu(2+)>Co(2+)>Ni(2+), whereas for alpha-zirconium phosphate it is Cu(2+)>Ni(2+)>Co(2+). The ion exchange capacity of alpha-titanium phosphate is greater than those of other phosphates, which is explained on the basis of the surface behavior, disorderness of the system, degree of hydrolysis of incoming guest adsorbate metal ions, and structural steric hindrance of the exchangers during adsorption and sorption. The distribution coefficient, Gibbs free energy, enthalpy, and entropy values indicate that the ion-exchange processes are spontaneous.

Journal Article↗
PubMed2006

Cloud point extraction and simultaneous determination of zirconium and hafnium using ICP-OES.

In the present study a simple versatile separation method using cloud point procedure for extraction of trace levels of zirconium and hafnium is proposed. The extraction of analytes from aqueous samples was performed in the presence of quinalizarine as chelating agent and Triton X-114 as a non-ionic surfactant. After phase separation, the surfactant-rich phase was diluted with 30% (v/v) propanol solution containing 1 mol l(-1) HNO3. Then, the enriched analytes in the surfactant-rich phase were determined by inductively coupled plasma-optical emission spectrometry (ICP-OES). The different variables affecting the complexation and extraction conditions were optimized. Under the optimum conditions (i.e. 3.4 x 10(-5) mol l(-1) quinalizarine, 0.1% (w/v) Triton X-114, 55 degrees C equilibrium temperature) the calibration graphs were linear in the range of 0.5-1000 mug l(-1) with detection limits (DLs) of 0.26 and 0.31 microg l(-1) for Zr and Hf, respectively. Under the presence of foreign ions no significant interference was observed. The precision (%RSD) for 8 replicate determinations at 200 microg l(-1) of Zr and Hf was better than 2.9% and the enrichment factors were obtained as 38.9 and 35.8 for Zr and Hf, respectively. Finally, the proposed method was successfully utilized for the determination of these cations in water and alloy samples.

Journal Article↗
PubMed2006

Polarized IR and Raman spectra and ab initio calculations for bis(guanidine) zirconium bis(nitrilotriacetate) hydrate single crystal [C(NH2)3]2[Zr[N(CH2COO)3]2](H2O)--the new laser Raman converter.

Fourier transform polarized IR and Raman spectra of bis(guanidine) zirconium bis(nitrilotriacetate) hydrate single crystal [C(NH(2))(3)](2)[Zr[N(CH(2)COO)(3)](2)](H(2)O) have been measured in the regions 30-4000 and 80-4000 cm(-1) and correlated with X-ray structural data. The factor group analysis has been applied in the discussion of the dichroic dependence of the vibrational modes. The assignment of the internal vibrations for the [Zr(nitrilotriacetate)2]2- complex ion has been based on the ab initio quantum chemical calculations. The usefulness of the studied crystal as Raman laser converter was analyzed basing on the comparison of the spontaneous and stimulated Raman spectra.

Cations↗