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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 28 (1979), S. 131-136 
    ISSN: 1432-0827
    Keywords: Calcium ; Phosphate ; Citrate ; Precipitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary The influence of citrate ions on the precipitation of crystalline apatitic precipitates with low Ca/P molar ratios [octacalcium phosphate (OCP) and calcium-deficient apatites (DA) (system A)] and of the intercrystalline mixtures of calcium hydrogen phosphate dihydrate (DCPD) and DA (system B) was investigated. Samples were prepared by direct mixing of calcium chloride solutions (A, 6·10−3 mol dm−3; B, 1·10−1 mol dm−3) and sodium phosphate solutions (A, 6·10−3 mol dm−3; B, 2·10−2 mol dm−3) containing citrate (0–2·10−3 mol dm−3) and preadjusted to pH 7.4. In the presence of citrate ions: (a) crystal growth of OCP and DA was slowed down; (b) habit modification of DCPD crystals occurred; and (c) equilibration in intercrystalline mixtures of DCPD and DA's was slowed down. All phenomena were caused by surface adsorption of negatively charged ions, most probably CaC6H5O7-, which is the prevalent calcium citrate species under the given experimental conditions. Habit modification of DCPD was induced by preferential adsorption at the (001) crystal plane.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 8 (1971), S. 142-153 
    ISSN: 1432-0827
    Keywords: Calcium ; Phosphate ; Precipitate ; Electrolyte ; Physiology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé La précipitation de phosphates de calcium, peu solubles, à partir de solutions de chlorure de calcium (3×10−4M à 1×10−1M) et de phosphate de sodium (Ptot. 1×10−3M à 6×10−2M, [NaOH]/[H3PO4]∼1.75, pH 7.4), est étudiée à 25° et à 37°. Les précipités, obtenus 24 heures après mélange, sont identifiés par microscopie optique et électronique, par diffraction électronique et aux rayons X, par analyses chimiques et par leurs indices de réfraction. Dans un large éventail de concentrations des réactifs à 25°, c'est surtout du phosphate octocalcique qui se forme, alors qu'à 37°, on obtient des apatites déficients en calcium. A cette dernière température, l'OCP se différencie seulement à des concentrations faibles, à la limite de précipitation. A des concentrations relativement élevées (Catot.×Ptot.〉10−4)et aux deux températures, des mélanges de dihydrate de phosphate dicalcique (DCPD) et d'apatites sont obtenus, la zone de concentration diminuant avec l'augmentation de la température.
    Abstract: Zusammenfassung Die Ausfällung von schwer löslichen Calciumphosphaten aus wäßrigen Calciumchloridlösungen (3×10−4M bis 1×10−1M) und Natriumphosphatlösungen (Ptot. 1×10−3M bis 6×10−2M, [NaOH]/H3PO4]∼1,75, pH 7,4) wurde bei 25° und bei 37° untersucht. Niederschläge, welche 24 Stunden nach dem Mischen isoliert wurden, konnten mittels Licht- und Elektronenmikroskopie, Röntgenstrahlen und Elektronendiffraktion, chemischen Analysen und Refraktions-Indices identifiziert werden. Über den weitesten Konzentrationsbereich der Versuchssubstanzen wurde bei 25° hauptsächlich Octocalciumphosphat gebildet, während bei 37° calciumarme Apatite entstanden. Bei der letztgenannten Temperatur fiel das OCP nur bei niedrigen Konzentrationsprodukten aus, d.h. an der Ausfällungsgrenze. Bei relativ hohen Konzentrationsprodukten (Catot.×Ptot.〉10−4) und bei beiden Versuchstemperaturen wurden Gemische von Dicalciumphosphatdihydrat (DCPD) und Apatiten erhalten, indem der Konzentrationsbereich bei zunehmender Temperatur abnimmt.
    Notes: Abstract Precipitation of slightly soluble calcium phosphates from aqueous solutions of calcium chloride (3×10−4M to 1×10−1M) and sodium phosphate (Ptot. 1×10−3M to 6×10−2M, [NaOH]/[H3PO4]∼1.75, pH 7.4) was studied at 25° and 37°. Precipitates isolated 24 hours after mixing were identified by means of light and electron microscopy, X-ray and electron diffraction, chemical analyses and refractive indices. Over the widest range of reactant concentrations at 25°, octacalcium phosphate was predominantly formed, while at 37°, calcium deficient apatites were obtained. At the latter temperature OCP separated at very low concentration products only, i.e. at the precipitation boundary. At relatively high concentration products (Catot.×Ptot.〉10−4) and at both temperatures, mixtures of dicalcium phosphate dihydrate (DCPD) and apatites were obtained, the concentration region decreasing with increasing temperature.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 10 (1972), S. 82-90 
    ISSN: 1432-0827
    Keywords: Calcium ; Phosphate ; Precipitation ; Kinetics ; Chemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé La cinétique de la formation et de la transformation des précipités de phosphate de calcium, obtenus en mélangeant de volumes égaux de solutions à 6×10−3 M de calcium total et/ou phosphate total est étudiée à 25°C. Les solutions de phosphate sont préajustées à un pH de 7.4. Les changements de pH et de turbidité des solutions sont suivis simultanément en fonction du temps. Les précipités sont isolés à des intervalles de temps variables et caractérisés par diverses méthodes physico-chimiques. Initialement un précipité avec un rapport molaire Ca/P de 1.5, amorphe aux rayons X et en diffraction électronique, est formé. Le spectre IR indique la présence de PO 4 3− et de HPO 4 2− . Après une période métastable, on observe la précipitation d'un matériel cristallin dans ou sur la phase amorphe. Vingt quatre heures après préparation de l'échantillon les précipités présentent surtout les caractères du phosphate octocalcique.
    Abstract: Zusammenfassung Die Kinetik der Bildung und Transformation von Calciumphosphat-Niederschlägen wurde bei 25°C untersucht. Es wurden dazu gleiche Volumen von Lösungen gemischt, bei einer Konzentration von 6×10−3M totales Calcium und/oder totales Phosphat. Die Phosphatlösungen wurden zuerst auf pH 7,4 eingestellt. Veränderungen des pH und Trübung der Lösungen wurden gleichzeitig als eine Funktion der Zeit aufgezeichnet. Niederschläge wurden in verschiedenen Zeitintervallen isoliert und mit verschiedenen physiko-chemischen Methoden charakterisiert. Am Anfang wurde ein Niederschlag mit einem molaren Ca/P-Verhältnis von 1,5, im Röntgenbild und in der Elektronendiffraktion amorph, gebildet. Infrarotspektren deuteten die Anwesenheit von PO 4 3− - und HPO 4 2− -Ionen an. Nach einer metastabilen Periode erfolgte ein Niederschlag aus kristallinem Material innerhalb oder auf der amorphen Substanz. 24 Std nach der Herstellung der Proben zeigten die Niederschläge in der Hauptsache die Charakteristiken von Octocalciumphosphat.
    Notes: Abstract The kinetics of the formation and transformation of calcium phosphate precipitates obtained by mixing equal volumes of solutions, 6×10−3 M in total calcium and/or total phosphate was investigated at 25°. The phosphate solutions were preadjusted to pH 7.4. Changes of the pH and turbidity of the solutions were followed simultaneously as a function of time. Precipitates were isolated at various time intervals and characterized by different physicochemical methods. Initially a precipitate with a molar Ca/P ratio of 1.5, amorphous to X-ray and electron diffraction was formed. IR spectra indicated the presence of PO 4 3− and HPO 4 2− ions. After a period of metastability, precipitation of a crystalline material within or upon the amorphous matter occurred. Twenty four hours after sample preparation the precipitates showed mainly the characteristics of octacalcium phosphate.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 4 (1970), S. 142-143 
    ISSN: 1432-0827
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 130 (1989), S. 155-167 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The sorption of cesium and cobalt on kaolinite and montmorillonite were followed by radiotracer method. The sorption of cesium can be described by a Freundlich isotherm. Cobalt sorption on clays equilibrated in cesium chloride solutions significantly differs for kaolinite and montmorillonite due to their differences in sites available for cation sorption and changes in solution chemistry. Heterogeneous exchange of cesium ions between clay and the surrounding electrolyte was performed in order to obtain information about clay/electrolyte systems equilibration. An interplay of different processes included in the attainment of true chemical equilibria of clay/electrolyte systems are responsible for the change of clay surface properties and total exchange capacity.
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  • 6
    Publication Date: 1989-03-01
    Print ISSN: 0236-5731
    Electronic ISSN: 1588-2780
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Published by Springer
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  • 7
    Publication Date: 1986-02-01
    Print ISSN: 0022-0248
    Electronic ISSN: 1873-5002
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Published by Elsevier
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  • 8
    Publication Date: 1986-12-01
    Print ISSN: 0022-0248
    Electronic ISSN: 1873-5002
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Published by Elsevier
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  • 9
    Publication Date: 1982-04-01
    Print ISSN: 0022-0248
    Electronic ISSN: 1873-5002
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Published by Elsevier
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  • 10
    Publication Date: 1987-01-01
    Print ISSN: 0166-6622
    Electronic ISSN: 1873-4340
    Topics: Chemistry and Pharmacology , Physics
    Published by Elsevier
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