Academic literature on the topic 'Sulfato complex'
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Journal articles on the topic "Sulfato complex"
Wieghardt, Karl, Stefan Drüeke, Phalguni Chaudhuri, Ulrich Flörke, Hans-Jürgen Haupt, Bernhard Nuber, and Johannes Weiss. "Bioanorganische Modellkomplexe für Metalloproteine des Eisen(III): Synthese, Kristallstrukturen und Magnetismus der zweikernigen Komplexe [L2Fe2III(µ-O)(μ-SO4)2] · 3 H2O und [L2Fe2III(μ-O)(μ-SO3)2] · 5/3 NaClO4 · (H2O)3.67 (L = N,N′N″-Trimethyl-1,4,7-triazacyclononan) / Bioinorganic Model Complexes for Metalloproteins of Iron(III): Syntheses, Crystal Structures, and Magnetism of the Binuclear Complexes [L2Fe2III(μ-O)(μ-SO4)2]·3 Η2O and [L2Fe2III(μ-O)(μ-SO3)2] · 5/3 NaClO4 · (H2O)3.67 (L = N,N′,N″-Trimethyl-1,4,7-triazacyclononane)." Zeitschrift für Naturforschung B 44, no. 9 (September 1, 1989): 1093–101. http://dx.doi.org/10.1515/znb-1989-0916.
Full textKelly, Norman, Marco Wenzel, Thomas Doert, Kerstin Gloe, Jan J. Weigand, Leonard F. Lindoy, and Karsten Gloe. "Unique Occurrence of Cationic and Anionic Bis-1,2-diaminocyclohexane Copper(II) Units in a Double Complex Salt." Australian Journal of Chemistry 69, no. 5 (2016): 533. http://dx.doi.org/10.1071/ch15697.
Full textStoeckli-Evans, Helen, Olha Sereda, Antonia Neels, Sebastien Oguey, Catherine Ionescu, and Yvan Jacquier. "In situsingle-crystal to single-crystal (SCSC) transformation of the one-dimensional polymercatena-poly[[diaqua(sulfato)copper(II)]-μ2-glycine] into the two-dimensional polymer poly[μ2-glycine-μ4-sulfato-copper(II)]." Acta Crystallographica Section C Structural Chemistry 70, no. 11 (October 15, 2014): 1057–63. http://dx.doi.org/10.1107/s2053229614021123.
Full textMezei, Gellert. "Sulfate-bridged dimeric trinuclear copper(II)–pyrazolate complex with three different terminal ligands." Acta Crystallographica Section E Crystallographic Communications 72, no. 8 (July 8, 2016): 1064–67. http://dx.doi.org/10.1107/s2056989016010719.
Full textLiu, Ting, Yi-An Wang, Qing Zang, and Guo-Qing Zhong. "Hydrothermal Synthesis, Structural Characterization, and Interaction Mechanism with DNA of Copper(II) Complex Containing 2,2′-Bipyridine." Bioinorganic Chemistry and Applications 2018 (2018): 1–10. http://dx.doi.org/10.1155/2018/8459638.
Full textZeghouan, Ouahida, Mohamed AbdEsselem Dems, Seifeddine Sellami, Hocine Merazig, and Jean Claude Daran. "A strongly fluorescent NiII complex with 2-(2-hydroxyethyl)pyridine ligands: synthesis, characterization and theoretical analysis and comparison with a related polymeric CuII complex." Acta Crystallographica Section E Crystallographic Communications 74, no. 8 (July 6, 2018): 1042–48. http://dx.doi.org/10.1107/s2056989018009301.
Full textZheng, Yue-Qing, and Jian-Li Lin. "A New Sulfato-bridged Manganese(II) Phenanthroline Complex: [Mn(phen)(H2O)2(SO4)]." Zeitschrift für anorganische und allgemeine Chemie 629, no. 2 (February 2003): 185–87. http://dx.doi.org/10.1002/zaac.200390028.
Full textZasłona, Halina, Piotr Drożdżewski, and Maciej Barys. "A helical coordination polymer of zinc(II), 4-hydroxybenzohydrazide and sulfate ions." Acta Crystallographica Section C Crystal Structure Communications 69, no. 3 (February 5, 2013): 229–31. http://dx.doi.org/10.1107/s0108270113002758.
Full textMatsushima, Yoshiyuki, Akio Matsunaga, Kazuhiro Sakai, and Akitsugu Okuwaki. "Potentiometric Studies on Sulfato Complex of Aluminium(III) in Aqueous Solution at Elevated Temperatures." Bulletin of the Chemical Society of Japan 61, no. 12 (December 1988): 4259–63. http://dx.doi.org/10.1246/bcsj.61.4259.
Full textVicente, C. P., P. Zancan, L. L. Peixoto, R. Alves-Sá, F. S. Araújo, P. A. S. Mourão, and M. S. G. Pavão. "Unbalanced Effects of Dermatan Sulfates with Different Sulfation Patterns on Coagulation, Thrombosis and Bleeding." Thrombosis and Haemostasis 86, no. 11 (2001): 1215–20. http://dx.doi.org/10.1055/s-0037-1616054.
Full textDissertations / Theses on the topic "Sulfato complex"
Sakamoto, Luiz Maçao. "Estudo comparativo entre os aumentos das ferremias, determinados sem a administração prévia de ferro; após as administrações de sulfato ferroso, e complexo ferro-peptídeo." Universidade de São Paulo, 2003. http://www.teses.usp.br/teses/disponiveis/17/17138/tde-15072003-122244/.
Full textIron deficiency and iron-deficiency anemia continue to be major nutritional and public health problems all over the world, affecting about 2 billion people, especially in developing countries. In general, programs for the prevention and treatment of anemia present low adhesion due, among other factors, to the side effects related to the gastrointestinal system resulting from the oral administration of iron-containing compounds, especially ferrous sulfate. Thus, it is necessary to develop new strategies, compounds or release systems presenting high iron bioavailability and minimizing or eliminating side effects. In this respect, the iron-peptide complex (IPC), due to its physicochemical characteristics differing from those of ferrous sulfate (FS), represents a possible alternative as a source of iron. It is an organic complex of low solubility at acid pH and fully soluble at neutral or alkaline pH. Based on these characteristics, on the increased blood iron concentrations (levels of serum iron bound to apotransferrin) occurring in human beings during the diurnal period as observed by Wiltink et al. (1973), and on the similar results obtained with FS and the iron-glycine and ferric EDTA complexes by Dutra-de-Oliveira et al. (1995) in a study on rats, the hypotheses tested in the present study in which the iron-peptide complex was administered orally to healthy men were: 1) the complex induces significant increases in blood iron concentrations compared to control (C) subjects receiving no iron administration; 2) induces significant increases equal to or higher than those obtained after administration of SF used as reference. Thus, in order to test these hypotheses, we compared statistically the variations in control blood iron concentrations and the concentrations induced by the administration of the iron-peptide complex and SF. The variations were determined from the difference between the blood iron concentrations obtained in samples collected from 10 healthy adult men at 30, 60, 120, 240, 480 and 720 minutes () and those obtained at time zero, counted starting from the beginning of collection. Each volunteer was submitted to the following treatments: at time 0, after a 480fast he received at 7 day intervals the following amounts of iron: 0 mg (C), 60 mg (FP1) and 80 mg (FP2) as IPC, and 60 mg as FS. He then fasted for an additional 720 and received 60 mg as IPC together with a diet free of inhibitors of iron absorption during and after administration (FPD). The Dunn test demonstrated significant increases in blood iron concentrations for FSxC [60(p<0.01), 120(p<0.01), 240(p<0.01)], FSxFP1 [120(p<0.01), 240(p<0.05), 480(p<0.05)] and FSxFPD [240(p<0.01), and 480(p<0.05)]. Significant increases occurred in the areas under the curve for the following comparisons at the following intervals: 0240 [FSxC (p<0.01), FSxFP1 (p<0.05)], 240720 [FSxFP1 (p<0.05), FSxFPD (p<0.05)] e 0720 [FSxC (p<0.05), FSxFP1 (p<0.05), and FSxFPD (p<0.05)]. Conclusions: The initial hypotheses were not confirmed since the increase in blood iron concentrations after the administration of the iron-peptide complex was not significant compared to the increase in control blood iron concentration at the respective time points. These increases were significantly lower than those obtained after SF administration, except for those obtained after the administration of the iron-peptide complex at a quantity equivalent to 80 mg iron.
Marzak, Saïd. "Complexes du cuivre (i) construits sur le fragment (ms::(4))**(2-) (m=mo,w) : role du ligand thiocyanate dans l'edification de composes heterometalliques a structure infinie." Paris 6, 1988. http://www.theses.fr/1988PA066401.
Full textJúnior, Antonio Carlos Roveda. "Reatividade química de um novo nitrosilsulfito complexo trans-[Ru(NH3)4(isn)(N(O)SO3)](PF6), e desenvolvimento de filmes de amido doadores de óxido nítrico." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/75/75135/tde-26072016-144608/.
Full textAiming the production of new nitric oxide releasing materials (NORM), this work reports the development of a cassava starch based film, in which a ruthenium nitrosyl complex was impregnated, and evaluate the NO release from this film. Ruthenium nitrosyl complex trans-[Ru(NH3)4(isn)NO](BF4)3 (RuNOisn; isn = isonicotinamide) is able to release NO in a controlled manner through both photolysis (λirr = 310-370 nm) and chemical reduction. The incorporation of such complex into the starch-based films was performed under mild conditions, yielding a new material able to store and release NO, abbreviated as CSx-RuNOisn. Spectroscopic analysis of CSx-RuNOisn indicated that the coordination sphere of RuNOisn remained intact during film production. Exposure of CSx-RuNOisn to long wave UV-light (λirr = 355 nm) leads to NO release and likely to the formation of the paramagnetic photoproduct trans-[RuIII(NH3)4isn(H2O)]3+ in the film. Reaction of this aquoruthenium(III) complex with aqueous nitrite regenerates RuNOisn in the film. Delivery of NO upon photolysis of CSx-RuNO isn was verified and quantified by trapping with oxymyoglobin. The calculated concentration of NO released from the film was 5.02 ± 0.12 μM (10.04 ± 0.24 nmol NO in a 2 mL) after approximately 17 min of irradiation (500 laser pulses at 2 s intervals). Moreover, NO release upon chemical reduction was carried out using L-cysteine as a reductant. Cysteine-mediated NO delivery from CSx-RuNOisn persisted for more than 7 h, during which physiologically relevant NO concentrations were liberated (average flux of 1.9 pmol NO s-1 cm-2 of film). This value is comparable to that produced by endothelial cells (1.67 pmol s-1 cm-2). Preliminary results about the biodegradation of the films in vivo suggest that the films were completely absorbed by the organism in a period of 30 days. These results suggest that CSx-RuNOisn is a promising candidate for use in biological applications. A new nitrosylsulphito complex bearing the ligand (N(O)SO3-) was isolated, trans-[Ru(NH3)4(isn)(N(O)SO3)](X) (isn = isonicotinamide, X = PF6- or SiPF6-), and its structure was determined by X-Ray crystallography. This complex was obtained by the reaction between trans-[Ru(NH3)4(isn)(NO)]3+ and sulfite ions (SO32-). X-Ray results confirmed that the nucleophilic attack of the sulphite anion (SO32-) was on the nitrogen atom of the nitrosyl ligand (NO) coordinated to the ruthenium center ([Ru-NO+]), yielding the ligand O=N-SO3-: [RuNO+]3+ + SO32- → [Ru(N(O)SO3)]+. Complex trans- [Ru(NH3)4(isn)(N(O)SO3)]+ is stable in aqueous solution from pH 7.4 to 5.2, and the decomposition rates (k) (due to the isn labilization) are in the range of k = 0.86-3.07 × 10-5 s-1. In more acidic conditions, (acetate buffer pH 4.2, 3.9, and trifluoroacetic acid solution 1.0 M) complex trans-[Ru(NH3)4(isn)(N(O)SO3)]+ is converted into the respective nitrosyl trans-[RuII(NH3)4(isn)NO+]3+. Reaction of trans-[Ru(NH3)4(isn)(N(O)SO3)]+ and hydroxide ions (OH-) yielded the nitro complex trans-[Ru(NH3)4(isn)(NO2)]+, which was characterized by 15N NMR and electronic spectroscopy. Rate constants for such reaction are k = 6.16 ± 0.22 M-1 s-1 at 25oC, and k = 2.15 ± 0.07 M-1 s-1 at 15oC. In the case of complex trans-[RuII(NH3)4(isn)NO+]3+, its reaction with OH- also yield the nitro complex trans-[Ru(NH3)4(isn)(NO2)]+. The estimated rate constant for such reaction was k = 46.9-57.6 M-1 s-1 at 25oC, and the experimental value obtained at 15oC was k = 10.53 ± 0.29 M-1 s-1. The ion complex trans-[Ru(NH3)4(isn)(N(O)SO3)]+ showed an intense and broad band at 362 nm (ε∼6000 M-1 cm-1) in aqueous solutions, which was assigned by DFT calculations to the following transitions: metal to ligand charge transfer (MLCT) Ru→N(O)SO3 and Ru→isn, and d→d as well. Preliminary photolysis assays (λirrad = 355 nm) performed with complex trans-[Ru(NH3)4(isn)(N(O)SO3)](PF6) in phosphate buffer solution (pH 7,4) suggests that the following species have been formed (in the initial photolysis period): i) NO, ii) SO3•-, and iii) isn (labilized). The whole mechanism to yield such products is still under investigation.
Yvanes-Giuliani, Yliane. "Aluminium geochemistry in coastal lowland acid sulfate soils (CLASS) : speciation, reactivity and mobility." Thesis, Aix-Marseille, 2014. http://www.theses.fr/2014AIXM4364.
Full textThe aim of this thesis was to further understanding on Al geochemistry in coastal lowland acid sulfate soils (CLASS). It was observed that Al was present almost solely (> 98%) as negatively charged complexes in CLASS pore-waters, presumably with natural organic matter. Isotopically exchangeable concentrations (E-values) of Al and extraction solutions used to estimate the exchangeable pool showed that 1 M KCl always underestimated isotopically exchangeable Al concentrations in these soils and that 0.2 M CuCl2 improved agreement between both methodologies but sometimes overestimated corresponding E values. A sequential extraction procedure showed that substantial amounts of Al have already been dissolved from primary aluminosilicates initially present in the soils and remain in the soils mostly as reactive secondary Al minerals. The outcomes of this thesis significantly further our understanding of Al geochemistry in CLASS environments and how this knowledge can be incorporated into land management practices
Estienne, Jacques. "Des halogènes dans les édifices moléculaires étioniques : études cristallographiques, corrélations structure-réactivité, structure-conductivité, modèles structuraux." Aix-Marseille 1, 1986. http://www.theses.fr/1986AIX11001.
Full textIerno, Hélène. "Modélisation chimique de protéines fer-soufre : synthèses et caractérisations physico-chimiques de nouveaux agrégats à ligands imidazoles." Université Joseph Fourier (Grenoble ; 1971-2015), 1995. http://www.theses.fr/1995GRE10151.
Full textYu, Quanwei. "Ionene and ionene alkyl sulfate stoichiometric complexes." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2004. http://nbn-resolving.de/urn:nbn:de:swb:14-1099409249500-35629.
Full textWu, Danjun. "Multifunctional Chitosan-based Complexes for Nanomedicine." Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10294.
Full textThis work is devoted to the elaboration of nano-polyelectrolyte complexes (PECs) systems with improved stability in physiological media and to the establishment of their high potential of applications as bioactive (macro) molecule delivery systems. Chitosan as polycation were complexed with four natural polyanions of different charged groups and densities (-COO- and SO3 - as negative charges), namely hyaluronan (HYA), chondroitin sulfate (ChonS), dextran sulfate (DS) and heparin (HEP). The factors impacting the formation and physical-chemical properties of chitosan-HYA nanocomplexes were investigated. However, these nanovectors lost their colloidal character in physiological media. To improve their colloidal stability in physiological conditions, an innovative stabilization strategy was designed, involving zinc ion. This stabilization strategy proved versatile and was extended to chitosan-ChonS PECs. Though a long-term stability was achieved, this strategy was only applicable to cationic PECs. Therefore, an alternate approach enabled the improvement of the colloidal stability in physiological media of both positive and negative colloids by designing core-shell ternary polyelectrolyte nanocomplexes composed of strong polyacid (DS or HEP)-chitosan PECs as core and a chitosan-HYA complex as shell. Furthermore, all of the stabilized nanocomplexes allowed the encapsulation of active molecules anti-retroviral drug tenofovir and surface functionalization with targeting IgAs. In vitro, these nanovectors exhibited an inhibition of infection of PBMCs by HIV-1 virus which could be superior to the free drug
Ramírez, Rivera Luis Miguel. "Síntese de complexos nanoestruturados formados por óxidos de ferro e sulfato de condroitina." reponame:Repositório Institucional da UnB, 2013. http://repositorio.unb.br/handle/10482/15741.
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O objetivo desde projeto é sintetizar complexos nanoestruturados formados por óxidos de ferro e 4-sulfato de condroitina (4-SC). Dois métodos de síntese química foram empregados. No primeiro, nanopartículas de magnetita foram sintetizadas por meio da técnica de coprecipitação em meio aquoso, funcionalizadas com 4-sulfato de condroitina por meio da técnica de automontagem e em seguida dispersas em pH neutro. Na segunda rota de síntese, as nanopartículas de magnetita foram coprecipitadas na presença do 4-sulfato de condroitina e suspensas em meio aquoso com pH neutro. A espectroscopia Raman foi empregada para identificar a fase do óxido de ferro produzido, cujo resultado confirmou a síntese de magnetita. A análise dos espectros obtidos no infravermelho e dos dados de potencial zeta confirmaram a presença da cobertura de 4-sulfato de condroitina. Em adição, os resultados mostraram também diferenças no modo de interação do 4-SC com a superfície das partículas produzidas por meio dos diferentes métodos de síntese. Também foi realizado um monitoramento da estabilidade coloidal em meio biológico tais como a solução tampão fosfato (PBS) e meio de cultura DMEM. _______________________________________________________________________________________ ABSTRACT
The aim of this study is to produce nanostructured complexes of iron oxides and chondroitin-4-sulphate (C4S). Two synthesis routes were employed. On the first, magnetite nanoparticles were synthetized via the technique of coprecipitation in aqueous media, functionalized with chondroitin-4-sulphate via the layer-by-layer technique and then dispersed in neutral pH. On the second method, the magnetite nanoparticles were precipitated in the presence of chondroitin-4-sulphate and peptized in aqueous media with neutral pH. Raman spectroscopy was used to identify the iron oxide phase, confirming the synthesis of magnetite. The analysis of the infrared spectra and the data from zeta potential confirmed the presence of chondroitin-4-sulphate on the nanoparticles surface. In addition, the results indicated that the attachment of chondroitin-4-sulphate at the nanoparticle surface depends on the synthesis method. The colloidal stability was monitored in biological media, including phosphate buffer solution and DMEM culture medium.
Cukiernik, Fabio D. "Synthèses, études physicochimiques et structurales de nouveaux matériaux moléculaires mésogènes : les carboxylates binucléaires de ruthénium." Grenoble 1, 1993. http://www.theses.fr/1993GRE10134.
Full textBooks on the topic "Sulfato complex"
Kirchman, David L. Processes in anoxic environments. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780198789406.003.0011.
Full textBook chapters on the topic "Sulfato complex"
Pardasani, R. T., and P. Pardasani. "Magnetic properties of a dimeric μ-sulfato-ruthenium(III) complex with bis(diisopropylthiophosphoryl)amide." In Magnetic Properties of Paramagnetic Compounds, 668. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_359.
Full textPardasani, R. T., and P. Pardasani. "Magnetic properties of sulfato bridged dinuclear copper(II) complex containing bis(2-pyridylcarbonyl)-amide anion." In Magnetic Properties of Paramagnetic Compounds, 1115–16. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_586.
Full textHargens, Robert D., Woonza Min, Robert C. Henney, T. M. Brown, and A. Galliart. "Bis(ethylenediamine)sulfito Complexes of Cobalt(III)." In Inorganic Syntheses, 77–81. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132456.ch15.
Full textReed, Gregory A., and Cherukury Madhu. "Peroxide Scavenging by Cu(II) Sulfate and Cu(II) (3,5-Diisopropylsalicylate)2." In Biology of Copper Complexes, 287–98. Totowa, NJ: Humana Press, 1987. http://dx.doi.org/10.1007/978-1-4612-4584-1_22.
Full textBeauregard, M., P. C. Meunier, and R. Popovic. "Differential Sensitivity Toward Sulfate Inhibition Among PSII Complexes in Barley Thylakoids." In Current Research in Photosynthesis, 331–34. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0511-5_71.
Full textHabermann, B., T. Krüger, H. Stephan, K. Hollmann, and K. Gloe. "Novel Bis(phenoxyalkyl)sulfane Podands — Synthesis and Complex Formation with Thiophilic Metals Ions." In Molecular Recognition and Inclusion, 345–48. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_55.
Full textKazachenko, Aleksandr S., Natalya Yu Vasilyeva, and Yuriy N. Malyar. "Numerical Optimization of the Galactomannan Sulfation Process with a Sulfamic Acid-Urea Complex." In Software Engineering Perspectives in Intelligent Systems, 567–74. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-63319-6_52.
Full textGrishkovets, V. I., A. E. Kondratenko, and V. Ya Chirva. "New Preparation of Triterpenoid-3-Sulfates by the Use of SO3-DMSO Complex." In Advances in Experimental Medicine and Biology, 209–10. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0413-5_17.
Full textGülen, Demet, Robert Knox, and Jacques Breton. "Optical effects of sodium dodecyl sulfate treatment of the isolated light harvesting complex of higher plants." In Current topics in photosynthesis, 11–18. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4412-1_2.
Full textPardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) sulfate complex with 6-amino-5-formyl-1, 3-dimethyluracilato-(N6)-benzoylhydrazone." In Magnetic Properties of Paramagnetic Compounds, 616–17. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_314.
Full textConference papers on the topic "Sulfato complex"
Schick, K. P., S. Shapiro, G. Tuszynski, and J. Slawek. "SULFATIDES AND GLYCOLIPIDS IN PLATELETS AND ENDOTHELIAL CELLS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643641.
Full textSappok, Alexander, Sean Munnis, and Victor W. Wong. "Individual and Synergistic Effects of Lubricant Additive Components on Diesel Particulate Filter Ash Accumulation and Performance." In ASME 2012 Internal Combustion Engine Division Spring Technical Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/ices2012-81237.
Full textShifler, David A. "The Increasing Complexity of Hot Corrosion." In ASME Turbo Expo 2017: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/gt2017-65281.
Full textRoque, Claude, Michel Renard, and Nguyen Van Quy. "Numerical Model for Predicting Complex Sulfate Scaling During Waterflooding." In SPE Formation Damage Control Symposium. Society of Petroleum Engineers, 1994. http://dx.doi.org/10.2118/27387-ms.
Full textShifler, David A. "The Increasing Complexity of Corrosion in Gas Turbines." In ASME Turbo Expo 2019: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/gt2019-90111.
Full textJordan, Myles Martin, Ian Ralph Collins, and Eric James Mackay. "Low Sulfate Seawater Injection for Barium Sulfate Scale Control: A Life-of-Field Solution to a Complex Challenge." In SPE International Symposium and Exhibition on Formation Damage Control. Society of Petroleum Engineers, 2006. http://dx.doi.org/10.2118/98096-ms.
Full textHoppensteadt, D., A. Kumar, J. Fareed, and J. Mardigian. "STUDIES ON THE ANTICOAGULANT AND ANTITHROMBOTIC ACTIONS OF DERMATANS AND THEIR SULFATED DERIVATIVES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643241.
Full textPreissner, K. T., and P. Sie. "S PROTEIN/VITRONECTIN NEUTRALIZES THE ANTICOAGULANT ACTIVITY OF GLYCOSAMINOGLYCANS IN THE INHIBITION OF THROMBIN BY HEPARIN COFACTOR II." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643633.
Full textNiederst, P. N., M. Asbach, M. Ott, and R. E. Zimmermann. "IN VITRO REACTION MODELS OF THROMBIN AND ITS PHYSIOLOGICAL INHIBITOR ANTITHROMBIN III IN THE PRESENCE OF HEPARIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644356.
Full textRahardjo, S. B., T. E. Saraswati, A. Masykur, N. N. F. Finantrena, and L. Fatawati. "Complex of tetrakis(2-amino-3-methylpyridine) copper(II) sulfate tetrahydrate for antibacterial." In Proceedings of the 17th International Conference on Ion Sources. Author(s), 2018. http://dx.doi.org/10.1063/1.5054413.
Full textReports on the topic "Sulfato complex"
Y. Xia, J.I. Friese, D.A. Moore, and L. Rao. STABILITY CONSTANTS OF NP(V) COMPLEXES WITH FLOURIDE AND SULFATE AT VARIABLE TEMPERATURES. Office of Scientific and Technical Information (OSTI), July 2005. http://dx.doi.org/10.2172/884904.
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