Relevant bibliographies by topics / Phosphates

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Phosphates'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Phosphates"

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Wolschendorf, Frank, Maysa Mahfoud, and Michael Niederweis. "Porins Are Required for Uptake of Phosphates by Mycobacterium smegmatis." Journal of Bacteriology 189, no. 6 (2007): 2435–42. http://dx.doi.org/10.1128/jb.01600-06.

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ABSTRACT Phosphorus is an essential nutrient, but how phosphates cross the mycobacterial cell wall is unknown. Phosphatase activity in whole cells of Mycobacterium smegmatis was significantly lower than that in lysed cells, indicating that access to the substrate was restricted. The loss of the outer membrane (OM) porin MspA also reduced the phosphatase activity in whole cells compared to that in lysed cells. A similar result was obtained for M. smegmatis that overexpressed endogenous alkaline phosphatase, indicating that PhoA is not a surface protein, contrary to a previous report. The uptake
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Asenjo, Ana, Lorena Rodríguez, and Nieves Villanueva. "Determination of phosphorylated residues from human respiratory syncytial virus P protein that are dynamically dephosphorylated by cellular phosphatases: a possible role for serine 54." Journal of General Virology 86, no. 4 (2005): 1109–20. http://dx.doi.org/10.1099/vir.0.80692-0.

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The 241 aa human respiratory synctyial virus (HRSV) Long strain P protein is phosphorylated at serines 116, 117 and/or 119, and 232. Phosphates added to these residues have slow turnover and can be detected in the absence of protein phosphatase inhibition. Inhibition of phosphatases PP1 and PP2A increases the level of phosphorylation at serines 116, 117 and/or 119, suggesting a more rapid turnover for phosphates added to these residues compared to that of S232. High-turnover phosphorylation is detected in the P-protein NH2-terminal region, mainly at S54 and, to a lesser extent, at S39, in the
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Jamroz, Dorota, Agnieszka Gajda-Janiak, Zbigniew Wzorek, Zygmunt Kowalski, and Janusz Kubizna. "Chemical and Biological Characteristics of Different Hydrated Monocalcium Phosphates for Broiler Chickens." Annals of Animal Science 12, no. 2 (2012): 187–200. http://dx.doi.org/10.2478/v10220-012-0016-4.

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Chemical and Biological Characteristics of Different Hydrated Monocalcium Phosphates for Broiler ChickensThree hydrated monocalcium phosphates differing in purity (with or without monetite, or monetite and calcite) and in crystalline structure were used in broiler chickens diets. The performance indices, concentration of Ca, P and Mg and activity of alkaline phosphatase in blood plasma, the content of these mineral elements in bones, and physico-mechanical parameters of femur and tibia bones were recorded. Body weight on 35th day of life, feed intake and mechanical parameters of bone quality w
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de Groot, H., H. de Groot, and T. Noll. "Enzymic determination of inorganic phosphates, organic phosphates and phosphate-liberating enzymes by use of nucleoside phosphorylase-xanthine oxidase (dehydrogenase)-coupled reactions." Biochemical Journal 230, no. 1 (1985): 255–60. http://dx.doi.org/10.1042/bj2300255.

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Coupled enzyme assays are described for measuring inorganic phosphates, organic phosphates and phosphate-liberating enzymes in biological material. The assays all determine Pi by its reaction with inosine, catalysed by nucleoside phosphorylase; this yields ribose 1-phosphate and hypoxanthine. The hypoxanthine is oxidized to uric acid by xanthine oxidase, and may be measured either by the absorbance of the uric acid, or by the formazan formed when a tetrazolium salt is used as the oxidant. The coupled enzyme assays are characterized by high sensitivity, quantitative utilization of phosphates an
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Tang, Xiaoyun, and David N. Brindley. "Lipid Phosphate Phosphatases and Cancer." Biomolecules 10, no. 9 (2020): 1263. http://dx.doi.org/10.3390/biom10091263.

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Lipid phosphate phosphatases (LPPs) are a group of three enzymes (LPP1–3) that belong to a phospholipid phosphatase (PLPP) family. The LPPs dephosphorylate a wide spectrum of bioactive lipid phosphates, among which lysophosphatidate (LPA) and sphingosine 1-phosphate (S1P) are two important extracellular signaling molecules. The LPPs are integral membrane proteins, which are localized on plasma membranes and intracellular membranes, including the endoplasmic reticulum and Golgi network. LPPs regulate signaling transduction in cancer cells and demonstrate different effects in cancer progression
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Kidder, D. L., and K. Swett. "Basal Cambrian reworked phosphates from Spitsbergen (Norway) and their implications." Geological Magazine 126, no. 1 (1989): 79–88. http://dx.doi.org/10.1017/s0016756800006166.

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AbstractSeveral phosphatic zones are associated with the oldest remains of shelly fossils on the arctic island of Spitsbergen. The phosphate occurs as reworked nodules and layers associated with a disconformity. A gap in the acritarch biostratigraphic record supports a hiatus associated with the phosphatic zone. Palaeogeographic positions for Svalbard, both (1) as a single unit, and (2) as three isolated parts prior to Caledonian tectonism are consistent with conditions favourable to at least minimal amounts of upwelling. However, upwelling may not have been a prerequisite for development of t
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Klumpp, Susanne, Jan Hermesmeier, Dagmar Selke, Ralf Baumeister, Roland Kellner, and Josef Krieglstein. "Protein Histidine Phosphatase: A Novel Enzyme with Potency for Neuronal Signaling." Journal of Cerebral Blood Flow & Metabolism 22, no. 12 (2002): 1420–24. http://dx.doi.org/10.1097/01.wcb.0000045041.03034.99.

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The importance of reversible phosphorylation for neuronal signaling and cell survival is well recognized. Knowledge in vertebrates, however, is so far limited to O-phosphates from serine, threonine, and tyrosine. The authors describe an enzyme acting on N-phosphates. It is the first protein histidine phosphatase identified in vertebrates. This histidine phosphatase is ubiquitously expressed in mammalian tissues including brain. Characterization and sequencing showed a yet unknown protein with no similarity to other phosphatases. In Caenorhabditis elegans, the homolog of this histidine phosphat
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Nignan, Iliassou, Jean Ouedraogo, Satoshi Nakamura, Idriss Serme, and Kalifa Coulibaly. "Effets du mode d’application d’engrais phosphatés (CBKCa et TSP) sur la productivité du mil (Pennisetum glaucum (L.) R. Br) au centre ouest du Burkina Faso." International Journal of Biological and Chemical Sciences 17, no. 6 (2024): 2312–24. http://dx.doi.org/10.4314/ijbcs.v17i6.14.

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La distance d’application des phosphatés pourrait influencer la réponse des cultures à la fertilisation phosphatée due à la faible mobilité du phosphore. Ainsi, une étude a été conduite en 2021 et 2022 à Saria, pour évaluer l’effet de la distance d’application de deux engrais phosphatés sur la productivité du mil. Se sont le Burkina Phosphate calciné enrichi en calcium (CBKCa) et triple super phosphate (TSP). Pour ce faire, un dispositif factoriel avec quatre répétitions a été installé. Les phosphates ont été appliquées sur les parcelles principales à trois distances d’application (0 ; 5 et 10
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Höer, A., and E. Oberdisse. "Inositol 1,3,4,5,6-pentakisphosphate and inositol hexakisphosphate are inhibitors of the soluble inositol 1,3,4,5-tetrakisphosphate 3-phosphatase and the inositol 1,4,5-trisphosphate/1,3,4,5-tetrakisphosphate 5-phosphatase from pig brain." Biochemical Journal 278, no. 1 (1991): 219–24. http://dx.doi.org/10.1042/bj2780219.

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The influence of highly phosphorylated inositol phosphates on the Ins(1,3,4,5)P4 3-phosphatase enriched from the soluble fraction of pig brain was tested, using [5-32P]Ins(1,3,4,5)P4 as substrate. Both Ins(1,3,4,5,6)P5 and InsP6 were very potent inhibitors of the Ins(1,3,4,5)P4 3-phosphatase. The Ki values were approximately 60 nM and approximately 3 nM for Ins(1,3,4,5,6)P5 and InsP6 respectively. Ins(1,3,4,5,6)P5 and InsP6 also inhibited the Ins(1,4,5)P3/Ins(1,3,4,5)P4 5-phosphatase. Using Ins(1,3,4,5)P4 as substrate, the Ki values were about 35 microM and 15 microM for Ins(1,3,4,5,6)P5 and I
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SUÁREZ, V. B., L. FRISÓN, M. Z. de BASÍLICO, M. RIVERA, and J. A. REINHEIMER. "Inhibitory Activity of Phosphates on Molds Isolated from Foods and Food Processing Plants." Journal of Food Protection 68, no. 11 (2005): 2475–79. http://dx.doi.org/10.4315/0362-028x-68.11.2475.

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Six commercial phosphates were evaluated for inhibition of the growth of 17 molds isolated from food sources. The assays were performed at neutral and natural (without pH adjustment) pH values, and the molds were streaked on plate count agar with added phosphates. Phosphate concentrations of 0.1, 0.3, 0.5, 1.0, and 1.5% (wt/vol) were used, and the MIC was determined. The resistance of molds to phosphates depended on the species. At a neutral pH, Aspergillus ochraceus and Fusarium proliferatum were resistant to all phosphates at all concentrations assayed, and Byssochlamys nivea, Aureobasidium
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Dissertations / Theses on the topic "Phosphates"

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Keita, Ousainou Ansumana. "The synthesis of new phenylhydroxyiodonium phosphates from (diacetoxyiodobenzene) and dialkyl phosphates and their use in the α-phosphorylation of ketones to mono-ketol phosphates". University of Akron / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=akron1197558427.

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Ashraf, Imran [Verfasser]. "Phosphate ageing in soil and bioavailability of aged phosphates / Imran Ashraf." Gießen : Universitätsbibliothek, 2016. http://d-nb.info/1081302763/34.

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Kong, Anne Mandy 1973. "Cloning and characterisation of a novel 72 kDa inositol polyphosphate 5-phosphatase." Monash University, Dept. of Biochemistry and Molecular Biology, 2001. http://arrow.monash.edu.au/hdl/1959.1/9036.

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Shekhar, Avinash. "REVERSION OF POLY-PHOSPHATES TO ORTHO-PHOSPHATES IN WATER DISTRIBUTION SYSTEMS." Master's thesis, University of Central Florida, 2007. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/2202.

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Orthophosphates and polyphosphates are rarely present at significant levels in raw water source but are purposefully added to the water in various forms to inhibit corrosion, iron oxidation (red water), or calcium carbonate precipitation (scale formation). Orthophosphates serve as building blocks for polyphosphates, which includes structures in linear chain, branched chains (metaphosphate) and "glassy" polyphosphate polymers. The advantage of polyphosphates over ortho phosphates lies in the fact that they slowly revert to orthophosphates and thus provide corrosion inhibition action over longer
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Abderrahim, Mohamed Lofti. "Contribution de l'imagerie numérique à l'analyse des phosphates : application au bassin phosphate de Gafsa (Tunisie)." Saint-Etienne, 1996. http://www.theses.fr/1996STET4015.

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Les techniques orientées vers le traitement des phosphates et en particulier celles relatives à la détermination de la fraction exploitable reposent actuellement sur deux procédés : l'examen au microscope et la détermination par des méthodes analytiques : chimique, physique et physico-chimique (spectrographie, rayon x, etc. ). On identifie ainsi les phases présentes (analyse qualitative) et on effectue un ensemble de mesures (analyse quantitative), tels que taille nombre de grains, pourcentage en phase, etc. Bien qu'ils fournissent des résultats satisfaisants, les deux procédés d'analyse cités
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Ahmadi, Kamran. "Cristallochimie de phosphates microporeux." Poitiers, 1994. http://www.theses.fr/1994POIT2372.

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Chopineaux, Anne-Paule. "Le problème posé par la présence des phosphates dans les eaux." Paris 5, 1995. http://www.theses.fr/1995PA05P102.

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Stock, Joseph R. "Synthesis of BIS(2.2,2-Trifluoroethyl) vinylphosphates." Connect to online version at OhioLINK ETD Connect to online version at Digital.Maag, 1998. http://hdl.handle.net/1989/4785.

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Raynaud, Sylvie. "Synthèse, frittage et propriétés mécaniques de phosphates de calcium dans le système hydroxyapatite - phosphate tricalcique." Limoges, 1999. http://www.theses.fr/1999LIMO0035.

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Des phosphates de calcium de rapport molaire ca/p compris entre 3/2 et 10/6 ont ete synthetises par precipitation en milieu aqueux. Les poudres sont monophasees de structure apatitique mais de stoechiometrie variable en calcium ca 1 0 x@ x(hpo 4) x(po 4) 6 x(oh) 2 x@ x (@ lacune, 0 x 1). Le rapport ca/p varie avec la temperature de synthese, il est maitrise par le controle precis de cette temperature. La calcination entre 400\c et 700\c fait diminuer la surface specifique des poudres sans densification par coalescence des particules. L'accroissement de la concentration en lacunes dans la struc
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Prévôt, Liliane. "Geochemistry, petrography, genesis of Cretaceous-Eocene phosphorites : the Ganntour deposit, Morocco : a type example /." Paris : Société géologique de France, 1990. http://catalogue.bnf.fr/ark:/12148/cb35430903w.

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Texte traduit de: Th. Etat--Sci. nat.--Strasbourg 1, 1988. Titre de soutenance : Géochimie et pétrographie de la formation à phosphate des Ganntour, Maroc ; utilisation pour une explication de la genèse des phosphorites crétacé-éocènes.<br>Résumé en français. Bibliogr. p. 210-218.
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Books on the topic "Phosphates"

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Menon, R. G. Compaction of phosphate rocks with soluble phosphates: An alternative technology to partial acidulation of phosphate rocks with low reactivity : IFDC experience. International Fertilizer Development Center, 1996.

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Burnett, John L. Mineral commodity report, phosphate rock. California Dept. of Conservation, Division of Mines and Geology, 1985.

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Z, Serazetdinov D., ed. Kompleksnai͡a︡ pererabotka fosforitov i fiziko-khimicheskie issledovanii͡a︡ neorganicheskikh materialov. "Gylym", 1991.

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Burnett, John L. Mineral commodity report, phosphate rock. California Dept. of Conservation, Division of Mines and Geology, 1985.

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Karray, Bourane Zenaïdi. Le marché mondial des phosphates et des engrais phosphatés. 2nd ed. Economica, 1987.

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Spence, Hugh S. Investigation of a reported discovery of phosphate in Alberta. Govt. Print. Bureau, 1997.

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Miller, Gregory J., ed. Inositol Phosphates. Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-0167-9.

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Slansky, Maurice. Geology of sedimentary phosphates. North Oxford Academic, 1985.

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Slansky, Maurice. Geology of sedimentary phosphates. North Oxford Academic, 1986.

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Freeman, D. B. Phosphating and metal pre-treatment: A guide to modern processes and practice. Woodhead-Faulkner in association with Pyrene Chemical Services Ltd., 1986.

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Book chapters on the topic "Phosphates"

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Hughes, John M., and John Rakovan. "1. The Crystal Structure of Apatite, Ca5(PO4)3(F,OH,Cl)." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-004.

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Pan, Yuanming, and Michael E. Fleet. "2. Compositions of the Apatite-Group Minerals: Substitution Mechanisms and Controlling Factors." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-005.

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Rakovan, John. "3. Growth and Surface Properties of Apatite." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-006.

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Boatner, Lynn A. "4. Synthesis, Structure, and Properties of Monazite, Pretulite, and Xenotime." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-007.

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Huminicki, Danielle M. C., and Frank C. Hawthorne. "5. The Crystal Chemistry of the Phosphate Minerals." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-008.

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Piccoli, Philip M., and Philip A. Candela. "6. Apatite in Igneous Systems." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-009.

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Spear, Frank S., and Joseph M. Pyle. "7. Apatite, Monazite, and Xenotime in Metamorphic Rocks." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-010.

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Pyle, Joseph M., Frank S. Spear, and David A. Wark. "8. Electron Microprobe Analysis of REE in Apatite, Monazite and Xenotime: Protocols and Pitfalls." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-011.

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Knudsen, Andrew C., and Mickey E. Gunter. "9. Sedimentary Phosphorites—An Example: Phosphoria Formation, Southeastern Idaho, U.S.A." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-012.

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Filippelli, Gabriel M. "10. The Global Phosphorus Cycle." In Phosphates, edited by Matthew J. Kohn, John Rakovan, and John M. Hughes. De Gruyter, 2002. http://dx.doi.org/10.1515/9781501509636-013.

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Conference papers on the topic "Phosphates"

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Sabadash, Vira, Oleh Konovalov, Anna Nowik-Zajac, and Iwona Zawierucha. "Adsorption Properties of Natural and Synthetic Zeolites for Ammonium and Phosphate Removal from Wastewater." In 8th International Congress "Environment Protection. Energy Saving. Sustainable Environmental Management". Trans Tech Publications Ltd, 2025. https://doi.org/10.4028/p-p0hfsd.

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Water resources are crucial in any region's overall natural resource complex. This research focuses on addressing these pollution issues through water treatment processes. The primary objective of this study was to examine the adsorption of phosphates using both natural and synthetic adsorbents, particularly aluminosilicates. Under static and dynamic conditions, the research assessed the sorption characteristics of natural zeolite, specifically clinoptilolite obtained from the Sokyrnytsia mineral deposits. Results indicated that the adsorption of phosphates is more effective in acidic environm
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Brown, V., J. Chalut, and D. Hartwick. "Application Experience with Low Phosphate Cooling Water Treatment." In CORROSION 2004. NACE International, 2004. https://doi.org/10.5006/c2004-04084.

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Abstract Inorganic phosphates have a long history of being effective corrosion inhibitors however, with the trend to lower phosphate levels in cooling water, a new set of operating guidelines are required to minimize the risk of scaling/deposition. This paper will explore the chemistry of this type of program and outline application criteria that should be used to govern the application, in order to balance corrosion and fouling issues. Cases studies will be used to highlight the primary conclusions.
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Minch, Britt A., Mark McGuiness, Tom Oleksiak, et al. "Water Soluble Magnesium and Aluminum Corrosion Inhibitors." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01675.

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Abstract Aluminum and magnesium are prone to surface attack (dark stains) when exposed to aqueous alkaline conditions. Surface active phosphorus and other chemistries have been employed in the industry to passivate these surfaces and prevent staining. Phosphonate and phosphate chemistries have been shown to be effective in controlling surface corrosion. The current work explores alkyl phosphates and investigates how structure impacts the efficacy of the corrosion inhibition. Corrosion inhibition is related not only to the ability of the phosphate to interact with the nonferrous surface, but al
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Suzuki, T., and T. Kawamura. "Corrosion and Scale Inhibitors for Cooling Water Systems." In CORROSION 1989. NACE International, 1989. https://doi.org/10.5006/c1989-89457.

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Abstract The Japanese history of research and development of corrosion and scale inhibitors for open recirculating cooling water systems is reviewed. Chromate based treatment had been mainly used prior to the enforcement of the Water Pollution Control Law in 1970. After that, corrosion inhibitors were changed from chromate to phosphate or phosphates-polymer treatments. At first, polymers were only used for scale control. However, polymers are now used extensively to improve the effect of corrosion inhibitors and to disperse many kinds of suspended solids. The performance of non-phosphorous coo
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Alves, Helena, Friedrich Stenner, D. C. Agarwal, and Antoine Hoxha. "Alloys Suitable for Phosphoric Acid Applications." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06221.

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Abstract More than 95% of the world demand for phosphoric acid is met by the wet-process, which involves the reaction of the phosphate rock with concentrated sulfuric acid. Pure phosphoric acid is only mildly corrosive to metals. However, the presence of impurities in the phosphate ores like chlorides, fluorides and silicates and the free sulfuric acid lead to complex corrosive conditions. The level of impurity depends on the origin of the phosphates and their processing, e.g. washing the ores with sea water further increases the level of chlorides. The corrosive attack is further aggravated b
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Bennett, James P., Kyei-Sing Kwong, Hugh Thomas, Anna Nakano, and Jinichiro Nakano. "Microstructure and Corrosion of Phosphate Containing Cr2o3 Gasifier Refractories." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05974.

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Abstract Gasification is an efficient, environmentally clean technology capable of processing a variety of abundant natural carbon sources or industry wastes/byproducts such as coal, petroleum coke, or biomass into CO and H2 (synthesis gas, or syngas) used in the production of electric power or chemicals. Gasification is considered an important option in future energy or chemical production because of its efficiency and because environmental pollutants such as SO3 and mercury are easily captured. However, the short service life of the Cr2O3 refractory used to protect the outer steel containmen
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Zhao, Wangxuan, Haruto Kobashi, Hiroto Takahashi, et al. "Observation of Time Evolution of Phase Transitions in Calcium Phosphates by Terahertz Spectroscopy." In 2024 49th International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz). IEEE, 2024. http://dx.doi.org/10.1109/irmmw-thz60956.2024.10697559.

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Guruviah, S., and M. Sundaram. "Role of Inhibitive Pigments on the Protection of Metals by Organic Coatings." In CORROSION 1989. NACE International, 1989. https://doi.org/10.5006/c1989-89141.

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Abstract Pigments play an important role in controlling corrosion. Inhibitive pigments are extensively used since they protect the metal surface by modifying the environments. The protective effect of inhibiting pigments is mainly due to the formation of a passive oxide film and soluble inhibitive ions. The evaluations of the paints containing these inhibitive pigments such as chromates, phosphates, red lead and zinc dust by electrochemical, accelerated and field trials are described in this paper.
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Sparrow, G. R., and Christophe Chandler. "The Role of Surface Chemistry and VCI's in Early Stages of Metal Processing." In CORROSION 1995. NACE International, 1995. https://doi.org/10.5006/c1995-95489.

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Abstract Despite massive efforts to control corrosion, it still has major affects on costs, quality, and performance. Unfortunately, corrosion protection is emphasized far too late in manufacturing. Corrosion control before or during earlier stages of manufacturing and processing is not considered. Yet many product failures are caused by contamination or poor corrosion control at stages well before final packaging. Modem surface analytical methods, ISS (Ion Scattering Spectroscopy) and SIMS (Secondary Ion Mass Spectroscopy), can monitor surface corrosion and contamination to trace product fail
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Tysnes, Q.-B., A. J. M. Verhoeven, G. M. Aarbakke, and H. Holmsen. "Phosphoinositide metabolism in resting and thrombin-stimulated human platelets: Evidence for metabolic homogeneity." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644517.

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On the basis of differences in specific radioactivity (SA), separate pools of phosphoinositides have recently been proposed in platelets. Human platelets were labelled for 60 min with [32p]p- and subsequently transferred to a phosphate- and Ca2+free Tyrode’s solution by gel-filtration. Thereafter, the platelets were either incubated at 37°C for 120 min, a condition which induces increase in specific labelling of the diester phosphate of phosphatitylinositol (PI), or stimulated with 0.5 U/ml of thrombin. The changes in SA of both diester and monoester phosphates of the phosphoinositides were de
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Reports on the topic "Phosphates"

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Jinawath, Supatra. Fabrication of porous calcium phosphates. Chulalongkorn University, 2002. https://doi.org/10.58837/chula.res.2002.29.

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The starting materials for this experiment were monocalcium phosphate monohydrate, dicalcium phosphate dihydrate and anhydrous dicalcium phosphate synthesized in-house from the by-product of a local bone-gelatin manufacture. Porous calcium phosphates comprising hydroxyapatite either as a single phase or a composite containing traces of its congeners. i.e., β-TCP were fabricated in the forms of granules and compacts. The characteristics of typical compacts produced were 37 v % apparent porosity with interconnected pores of diameter 1-30 µm, and flexural and compressive strengths of 17.51 and 78
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2

Raghothama, Kashchandra G., Avner Silber, and Avraham Levy. Biotechnology approaches to enhance phosphorus acquisition of tomato plants. United States Department of Agriculture, 2006. http://dx.doi.org/10.32747/2006.7586546.bard.

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Abstract: Phosphorus is one of the least available macronutrient in the soil. The high affinity phosphate transporters are known to be associated with phosphate acquisition under natural conditions. Due to unique interactions of phosphate with soil particles, up to 80% of the applied phosphates may be fixed forcing the farmers to apply 4 to 5 times the fertilizers necessary for crop production. Efficient uptake and utilization of this essential nutrient is essential for sustainability and profitability of agriculture. Many predictions point to utilization/exhaustion of high quality phosphate r
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3

Chandler, F. W., and R. L. Christie. Gîtes stratiformes de phosphates. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1995. http://dx.doi.org/10.4095/207953.

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4

Clearfield, Abraham. Organic Derivatives of Layered Group (4) Phosphates. Defense Technical Information Center, 1988. http://dx.doi.org/10.21236/ada201080.

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5

Moss, Robert A. Cleavage of Phosphates, Phosphonates, Phosphonothioates, and Phosphodiesters. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada416192.

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Sales, B. C., L. A. Boatner, B. C. Chakoumakos, J. C. McCallum, J. O. Ramey, and R. A. Zuhr. Structural analysis of amorphous phosphates using high performance liquid chromatography. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10111962.

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X. Shari Li, W. Yantasee A.R. Courtney, and S.V. Mattigod. TEMPLATED SYNTHESIS OF MESOPOROUS TITANIUM PHOSPHATES FOR THE SEQUESTRATION OF RADIONUCLIDES. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/884953.

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Sasaki, D. Y., T. M. Alam, and R. A. Assink. Synthetic molecular receptors for phosphates and phosphonates in sol-gel materials. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/563827.

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9

Shamsutdinov, Artem, Igor Valtsifer, and Yan Huo. The manufacturing of fire-extinguishing powder materials with specific morphology and hydrophobicity of ammonium phosphates particles. Peeref, 2023. http://dx.doi.org/10.54985/peeref.2307p9690323.

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10

Ewing, R. C. Radiation effects and annealing kinetics in crystalline silicates, phosphates and complex Nb-Ta-Ti oxides. FInal Report. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/459761.

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