Relevant bibliographies by topics / Sulphone chemistry

Contents

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

Academic literature on the topic 'Sulphone chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Sulphone chemistry.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Sulphone chemistry"

1

Nishikubo, Tadatomi, Atsushi Kameyama, Yoshinari Hosono, and Youji Yamada. "Synthesis of Polymers in Aqueous Solutions: Heterogeneous Oxidation of Poly(Amide-Sulphide) in Water." High Performance Polymers 10, no. 1 (March 1998): 23–31. http://dx.doi.org/10.1088/0954-0083/10/1/004.

Full text
Abstract:
The heterogeneous oxidation of N-(2-phenylthioethyl)benzamide in a dispersion of water was performed with twice the amount of hydrogen peroxide at 60 °C for 72 h as a model reaction of the oxidation of poly(amide-sulphide) (polymer 1), and the corresponding N-[2-(phenylsulphoxy)-ethyl]benzamide and N-[2-(phenylsulphonyl)ethyl]benzamide were obtained in 5% and 95% yields respectively. This suggests that the alkyl phenyl sulphide group was easily oxidized with time via the alkyl phenyl sulphoxide group into the alkyl phenyl sulphone group. On the other hand, when heterogeneous oxidation of diphenyl sulphide in a dispersion of water was carried out with twice the amount of hydrogen peroxide at 60 °C for 72 h, the corresponding diphenyl sulphoxide and diphenyl sulphone were obtained in 77% and 23% yields, respectively. Therefore, the oxidation rate of the diphenyl sulphide group was much slower than that of the alkyl phenyl sulphide group, and the heterogeneous oxidation of diphenyl sulphide with excess hydrogen peroxide in a dispersion of water primarily produced diphenyl sulphoxide under the same conditions. On the basis of these model reactions, the heterogeneous oxidation of polymer 1, which was prepared by the polyaddition of bis(4-mercaptophenyl)sulphide with m-phenylenebis(2-oxazoline), was performed with one to three times the amount of hydrogen peroxide in a dispersion of water at 60 °C, and the Tg of the resulting polymers gradually increased with reaction time from 111 °C to 165 °C. When the oxidization was carried out with three times the amount of hydrogen peroxide for 48 h, the polymer with major structure, poly(amide-sulphone) (polymer 3), was obtained. Polymer 3 was also easily prepared by the oxidization of polymer 1 with equivalent amounts of sodium periodate in a dispersion of water at 60 °C for 48 h.
APA, Harvard, Vancouver, ISO, and other styles
2

Giblin, Gerard M. P., Steve H. Ramcharitar, and Nigel S. Simpkins. "Synthesis and stereoselective chemistry of a novel cyclopentadienyl sulphone." Tetrahedron Letters 29, no. 33 (January 1988): 4197–200. http://dx.doi.org/10.1016/s0040-4039(00)80454-2.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Grossert, J. Stuart, Jeffrey Hoyle, T. Stanley Cameron, Stephen P. Roe, and Beverly R. Vincent. "The structures of some sulphur-stabilized carbanions and stereoelectronic requirements for the formation of α-sulphonyl carbanions." Canadian Journal of Chemistry 65, no. 6 (June 1, 1987): 1407–15. http://dx.doi.org/10.1139/v87-238.

Full text
Abstract:
Relatively few structure determinations of α-sulphonyl stabilized carbanions have been reported. The salient features of these are summarized and discussed in the light of the X-ray crystal structures of the potassium salt from bis(methylsulfonyl)-3-(2,6-dimethoxypyridyl)sulfonylmethane (5), the carbon acid bis(methylsulphonyl-4-(1,3-dimethoxyphenyl)sulphonylmethane (6), the triethylammonium salt of 2-methylsulphonyl-2-phenylthio-1-(3-pyridyl)-1-ethanone (7), the carbon acid 2-methyl-sulphonyl-2-phenylthio-1-phenylethanone (8), and its triethylammonium salt (9). Results of these structure determinations show that the α-sulphonyl carbanion has a significantly shorter −C—SO2 bond distance than the free sulphone, but that the S—O bond distances are essentially unchanged. The coordination about the carbanionic carbon atoms is planar; these atoms can be described as interacting with the sulphur atoms in an ylid-like manner, with a barrier to rotation about the −C—SO2 bond. The sulphonyl oxygen atoms do interact to a significant degree with the counterion, but there is no close contact between the counterion and the carbanionic carbon atom. A comparison of the structures of 6 and 5, or of 8 and 9, permits an assessment to be made concerning the stereoelectronics of deprotonation reactions on carbon atoms adjacent to sulphones.
APA, Harvard, Vancouver, ISO, and other styles
4

El-Dean, A. M. Kamal, A. A. Atalla, Th A. Mohamed, and A. A. Geies. "Synthesis of Some Pyrazolopyridine Sulphonamide Derivatives." Zeitschrift für Naturforschung B 46, no. 4 (April 1, 1991): 541–46. http://dx.doi.org/10.1515/znb-1991-0417.

Full text
Abstract:
The diazonium salt of 3-aminopyrazolopyridine when treated with SO2 and CuCl2 produces the corresponding sulphonyl chloride. The sulphonyl chloride chloride easily reacts with hydrazine hydrate, ammonia, aromatic or heterocyclic amines to produce the corresponding sulphohydrazide, sulphonamide or N-sulphonamide derivatives. Sulphohydrazide reacts with acetylacetone to produce pyrazoly pyrazolopyridinyl sulphone which is also obtained by reaction of sulphonyl chloride with dimethylpyrazole. The aminopyrazolopyridine can be converte into pyrazolopyridinthiole by its reacting with ethyl dithioxanthate. The pyrazolopyridinthiole reacts with alkyl halides or acrylonitrile to produce S-alkylated derivatives.
APA, Harvard, Vancouver, ISO, and other styles
5

WahbaErian, Ayman. "1,1-Dicyano-2-Phenyl-3-Phenylsulphonylpropene: A Novel Reagent in Sulphone Chemistry." Synthetic Communications 28, no. 19 (October 1998): 3549–58. http://dx.doi.org/10.1080/00397919808004901.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Vajda, E., I. Hargittai, and D. Hnyk. "Molecular structure of trans- and cis-methylchlorovinyl sulphone." Journal of Molecular Structure 162, no. 1-2 (November 1987): 75–86. http://dx.doi.org/10.1016/0022-2860(87)85024-x.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Janarthanan, V., Frank E. Karasz, and William J. MacKnight. "Miscibility in polybenzimidazole/polyimide sulphone blends: a comparison of blends containing fluorinated and non-fluorinated polyimide sulphone." Polymer 33, no. 16 (January 1992): 3388–93. http://dx.doi.org/10.1016/0032-3861(92)91096-k.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

ABRAHAM, R., I. HAWORTH, A. BUNN, and R. HEARMON. "Substituent effects in the 13C nuclear magnetic resonance spectra of aryl ether copolymers: 2. Ether sulphone/ether ether sulphone and ether sulphone/ether ketone copolymers in deuterated dimethylsulphoxide." Polymer 29, no. 6 (June 1988): 1110–17. http://dx.doi.org/10.1016/0032-3861(88)90024-9.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Cabiddu, Maria G., Salvatore Cabiddu, Claudia Fattuoni, Costantino Floris, Gioanna Gelli, and Stefana Melis. "METALATION REACTIONS. PART XVII. DILITHIATION OF PHENYL ISOPROPYL SULPHONE." Phosphorus, Sulfur, and Silicon and the Related Elements 70, no. 1 (January 1992): 139–43. http://dx.doi.org/10.1080/10426509208049162.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Abraham Joseph, K., and M. Srinivasan. "Synthesis and characterization of polyesters containing sulphide, sulphone or carbonyl groups in their backbones." European Polymer Journal 29, no. 12 (December 1993): 1641–45. http://dx.doi.org/10.1016/0014-3057(93)90259-i.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Sulphone chemistry"

1

Malcolm, Robert Karl. "Tactic poly(olefin sulphone)s." Thesis, Queen's University Belfast, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.295459.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Fee, S. J. G. "Studies of the conformational properties of simple alkyl sulphones and poly(olefin sulphone)s." Thesis, Queen's University Belfast, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373529.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Kneale, Christopher Juan. "Synthetic and mechanistic aspects of organosulphur chemistry." Thesis, University of Oxford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253138.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Al-Jebouri, Hamza Yaseen. "Synthesis of butadiene sulphone derivatives with cyano substituents." Thesis, University of Surrey, 1985. http://epubs.surrey.ac.uk/847181/.

Full text
Abstract:
The vicinal dicyano compounds are good starting materials for the synthesis of macromolecules such as phthalocyanines and tetrazaporphins. The synthesis of cyano compounds and vicinal dicyano compounds, particularly the cyano derivatives of butadiene sulphones have been studied in this work. This thesis is divided into five chapters as follows: The first chapter contains a general introduction about organic cyanides; their preparations, reactions and applications. In the second chapter, the synthesis of butadiene sulphone derivatives leading to mono and dicyano substituents is dealt with. It includes some mechanistic studies as well as spectroscopic studies by means of ir, [1]H nmr and mass spectrometry. Chapter three discusses the synthesis of 3-cyano-and 3,4-dicyanodihydrothiophene. Oxidation of dihydrothiophenes into butadiene sulphones is also discussed in this chapter. The synthesis of alpha,beta-unsaturated nitriles from ketones and aldehydes, and in particular, the synthesis of 2,3-dicyano-1,3-butadiene is discussed in chapter four. The addition of hydrogen cyanide to alpha,beta-unsaturated nitriles is also discussed. Chapter five deals with the multistep synthesis of 2,3-dicyano-1,3-butadiene from phthalic anhydride. It also contains some mechanistic studies.
APA, Harvard, Vancouver, ISO, and other styles
5

Sergis, Andreas Neophytos. "Reactions of sulphone stabilised carbanions with fluorinated aromatic compounds." Thesis, University of Greenwich, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.280469.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Phillipson, Neil. "Ketone homologation via hydroxy sulphone rearrangement - a new method for the synthesis of polyoxygenated carbon frameworks." Thesis, University of York, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.282294.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Denness, James E. "The preparation and characterisation of trifluoromethylated poly(ether sulphone)s and poly(ether ether ketone)s." Thesis, University of York, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306268.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Ngabe, Barnabe. "Physical chemistry of sulphide self-heating." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123024.

Full text
Abstract:
ABSTRACTA prerequisite step towards building a self-heating (SH) model for sulphide materials is the determination of physico-chemical parameters such as the specific heat capacity (Cp), and the energy of activation (Ea). The specific heat capacity of one copper and three nickel concentrates was determined over the temperature range 50 to 80oC in the presence of 6% moisture using the self-heating (SH) apparatus and confirmed by Drop Calorimetry. The Cp values from both techniques were comparable. The Cp values were similar for all concentrates increasing from 0.4 to 1.4 Jg-1K-1 as temperature increased from 50 to 80oC. From the Cp values, the enthalpy change (ΔH), the entropy change (ΔS) and the Gibbs free energy change (ΔG) for self-heating, were determined. The ΔG was negative, demonstrating that self-heating of the concentrates was spontaneous.Using the self-heating apparatus the, activation energy (Ea) was determined for the Ni-and Cu-concentrates and for pairs of sulphide minerals. The Ea ranged from 22 to 30 kJ.mol-1, implying a common reaction. Further support for a common reaction is the strong positive correlation between Ea and ln(QA/Cp) where Q (J.kg-1) is the heat of reaction causing self-heating and A the Arrhenius pre-exponential factor (s-1). Comparing to literature, the Ea values correspond to partial oxidation of hydrogen sulphide, supporting the contention that H2S may be an intermediate product in the self-heating of sulphide minerals. A positive relationship between Ea and the rest potential difference (ΔV) for the sulphide pairs and a negative relationship between Cp and ΔV were demonstrated which support a connection between self-heating and the galvanic effect.
RESUMÉLa réalisation d'un modèle mathématique de l'auto-échauffement des concentrés sulfurés de nickel et de cuivre et des mélanges des minerais sulfurés, enjoint à la détermination des paramètres physico-chimiques tels que les capacités de chaleur spécifiques (Cp), et les énergies d'activation (Ea). Les capacités de chaleur spécifiques d'un concentré de cuivre et de trois concentrés de nickel contenant 6% d'humidité, ont été déterminées par utilisation d'un instrument de mesure de vitesse d'auto – échauffement et validées par la calorimétrie de chute dans l'intervalle de températures allant de 50 à 80oC. Les Cp (0.4 à 1.4 Jg-1K-1) obtenues sont similaires pour tous les échantillons. A partir des valeurs des Cp, les variations de l'enthalpie (ΔH), l'entropie (ΔS) et de l'énergie libre de Gibbs (ΔG) de l'auto échauffement ont été déterminées. La valeur négative de ΔG confirme le caractère spontané de l'auto échauffement des minerais sulfurés.Les énergies d'activation (Ea) pour l'auto-échauffement des concentrés de nickel et cuivre et des paires de minerais sulfurés étaient déterminées en faisant usage de l'appareil d'auto-échauffement. Les Ea ainsi obtenues oscillent entre 22 et 30 kJ.mol-1 : Ce qui est suggestif d'une rèaction chimique commune gouvernant l'auto-échauffement de ces matériaux. Ce fait est corroboré par la forte corrélation obtenue entre Ea et ln(QA/Cp) (Q (J.kg-1) est la chaleur de la rèaction chimique responsable de l'auto-échauffement et A (s-1) la constante d'Arrhenius).Ensuite celles-ci sont similaires à celle de l'oxydation partielle du H2S. Il se pourrait, ce faisant, que H2S soit un composé intermediaire lors de l'auto–échauffement des sulfures.Enfin, la corrélation positive entre Ea et la difference de potential (ΔV) dans les paires de minerais sulfurés et celle negative entre Cp et ΔV sont une preuve qu'il existe bel et bien une connection entre l'auto-échauffement et l'effet galvanique.
APA, Harvard, Vancouver, ISO, and other styles
9

Hewkin, Cheryl T. "New chemistry of sulphonyl substituted small rings." Thesis, University of Newcastle Upon Tyne, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.293576.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Laffey, Thomas Gerard. "Applications of sulphones in organic synthesis." Thesis, University of Oxford, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.276586.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "Sulphone chemistry"

1

Wei, Sun, Wang Dianzuo 1934-, and SpringerLink (Online service), eds. Electrochemistry of Flotation of Sulphide Minerals. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2009.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Gilmore, Elisabeth. The chemistry and transport of particulate matter (PM2.5) sulphate in Toronto, Ontario. Ottawa: National Library of Canada, 2002.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Anderson, Mark Edwin. A Technique for measuring the reactivity of sulphide waste rock: The oxygen consumption. Waterloo, Ont: University of Waterloo, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Knocke, William R. Chlorite ion reduction by ferrous iron addition. Denver, CO: AWWA Research Foundation and American Water Works Association, 1993.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Simpson, W. W. Calcium sulfide precipitation of mercury from gold-silver-cyanide leach slurries. Pittsburgh, Pa. (Cochrans Mill Rd., P.O. Box 18070, Pittsburgh 15236): U.S. Dept. of the Interior, Bureau of Mines, 1986.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Simpson, W. W. Calcium sulfide precipitation of mercury from gold-silver-cyanide leach slurries. Washington, DC: U.S. Bureau of Mines, 1986.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Motov, David Lazarevich. Fiziko-khimii︠a︡ i sulʹfatnai︠a︡ tekhnologii︠a︡ titano-redkometallʹnogo syrʹi︠a︡ = Physico-chemistry and sulphate technology of titanium-rare metal raw materials. Apatity: Institut khimii i tekhnologii redkikh ėlementov i mineralʹnogo syrʹi︠a︡ im. I.V. Tananaeva KNT︠S︡ RAN, 2002.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Saul, Patai, Rappoport Zvi, and Stirling C. J. M, eds. The Chemistry of sulphones and sulphoxides. Chichester [Sussex]: Wiley, 1988.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

H, Greiling, and Scott John E, eds. Keratan sulphate: Chemistry, biology, chemical pathology. London : Biochemical Society, 1989.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

E, Scott John, and Harden Discussion (8th), eds. Dermatan sulphate proteoglycans: Chemistry, biology, chemical pathology. London: Portland Press, 1993.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Book chapters on the topic "Sulphone chemistry"

1

Tolun, Raşit. "Chemistry of Sulphide Mineral Flotation." In Mineral Processing Design, 37–75. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3549-5_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Luptáková, A., and P. Andráš. "Formation of Acid Mine Drainage in Sulphide Ore Deposits." In The Handbook of Environmental Chemistry, 259–76. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/698_2018_313.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Lowe, Gordon. "The Stereochemical Course of Sulphate Activation and Transfer." In Sulfur-Centered Reactive Intermediates in Chemistry and Biology, 239–56. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5874-9_21.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Morse, J. W. "Sedimentary Geochemistry of the Carbonate and Sulphide Systems and their Potential Influence on Toxic Metal Bioavailability." In Chemistry of Marine Water and Sediments, 165–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04935-8_7.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Partridge, S. M., and H. F. Davis. "The Presence in Cartilage of a Complex Containing Chondroitin Sulphate Combined with a Non-Collagenous Protein." In Ciba Foundation Symposium - Chemistry and Biology of Mucopolysaccharides, 93–115. Chichester, UK: John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/9780470719060.ch7.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Majdi, Hooshang, and Hans Persson. "Effects of ammonium sulphate application on the chemistry of bulk soil, rhizosphere, fine roots and fine-root distribution in a Picea abies (L.) Karst. stand." In Nutrient Uptake and Cycling in Forest Ecosystems, 151–60. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0455-5_16.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

"Introduction to Sulphone Chemistry." In Sulphones in Organic Synthesis, 1–4. Elsevier, 1993. http://dx.doi.org/10.1016/b978-0-08-040284-0.50005-0.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

"Chemistry of Cyclic Sulphones." In Sulphones in Organic Synthesis, 290–333. Elsevier, 1993. http://dx.doi.org/10.1016/b978-0-08-040284-0.50012-8.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

"Cycloaddition Chemistry of Unsaturated Sulphones." In Sulphones in Organic Synthesis, 227–53. Elsevier, 1993. http://dx.doi.org/10.1016/b978-0-08-040284-0.50010-4.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

"Sulphoxides and Sulphones." In Lectures on Organic Chemistry, 341–50. IMPERIAL COLLEGE PRESS, 1997. http://dx.doi.org/10.1142/9781848160903_0025.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Sulphone chemistry"

1

Al-Harbi, B. G., A. J. Graham, and K. S. Sorbie. "Zinc and Lead Interactions in Combined Sulphide Scales." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2017. http://dx.doi.org/10.2118/184509-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Williams, H., C. Tortolano, Nalco Champion, and T. Adenuga. "Mechanisms of Environmentally Acceptable Inhibitors for Zinc Sulphide Inhibition." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2015. http://dx.doi.org/10.2118/173771-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Goodwin, Neil, Gordon M. Graham, and Dario M. Frigo. "Ultra HPHT Solubility of Calcium Sulphate and Other Minerals." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2017. http://dx.doi.org/10.2118/184568-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Hall, Christopher. "Scanning Probe Microscopy: Sulphate Minerals in Scales and Cements." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1995. http://dx.doi.org/10.2118/28996-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Stalker, R., G. M. Graham, G. Hellings, Joanne C. Williams, and I. Littlehales. "Downhole Scale Formation and Inhibition in Mild Sulphate Scaling Conditions." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2005. http://dx.doi.org/10.2118/93427-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Evans, Paul. "Reservoir Souring Modelling, Prediction and Mitigation." In ASME 2008 27th International Conference on Offshore Mechanics and Arctic Engineering. ASMEDC, 2008. http://dx.doi.org/10.1115/omae2008-57085.

Full text
Abstract:
The prediction of reservoir souring due to the activity of sulphate-reducing bacteria (SRB) during water injection is an important consideration in material selection for wells and production facilities. A number of reservoir souring models have been developed in the past 16 years or so, with the objective of predicting the timing and magnitude of H2S production. The results of the reservoir souring models are dependent on a number of reservoir geometry, geochemical, microbiological and reservoir geology parameters. For example, the SRB activity is dependent on the availability of essential nutrients such as sulphate and dissolved hydrocarbons in the injection and formation waters. Environmental parameters such as temperature and pressure control in which parts of the reservoir SRB can be active. Water flow path and extent of water breakthrough has a major impact on H2S production. Very low reservoir permeabilities will restrict the movement of SRB into the rock matrix and certain minerals have the ability to scavenge H2S within the reservoir. All of these parameters must be accounted for in a reservoir souring simulation, and this requires the cooperation of reservoir engineers, geologists, production chemists and facilities engineers. Several techniques have been employed in the oil industry to try to control the generation of H2S within the reservoir. These include the application of biocides to control SRB activity, the injection of nitrate to stimulate other bacterial populations to out compete SRB for available food sources and the use of sulphate removal technologies to minimize sulphide production.
APA, Harvard, Vancouver, ISO, and other styles
7

SATIENPERAKUL, SAKCHAI, SAISUNEE LIAWRUANGRATH, and TERENCE J. CARDWELL. "A SIMPLE CHEMILUMINESCENCE FLOW INJECTION ANALYSIS FOR THE DETERMINATION OF SULPHIDE IN AQUEOUS SAMPLES." In Chemistry, Biology and Applications. WORLD SCIENTIFIC, 2007. http://dx.doi.org/10.1142/9789812770196_0033.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Rafferty, Andrew, Christine Stewart-Liddon, Caroline Simpson, Paul Hammonds, Gordon M. Graham, and Phillip Maskell. "Methodology to Evaluate the Performance and Stability of Hydrogen Sulphide Scavengers." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2019. http://dx.doi.org/10.2118/193571-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Shaw, Scott Stewart, and Kenneth Stuart Sorbie. "Scale Inhibitor Consumption in Long-Term Static Barium Sulphate Inhibition Efficiency Tests." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 2013. http://dx.doi.org/10.2118/164052-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Temple, Erin, Myles Jordan, Helen Williams, Sigrid Kjelstrup, Marija Kilibarda, and Kolbjorn Johansen. "Development of a Barium Sulphate Scale Inhibitor for Chalk Solid Loaded Conditions." In SPE International Conference on Oilfield Chemistry. Society of Petroleum Engineers, 2019. http://dx.doi.org/10.2118/193543-ms.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Sulphone chemistry"

1

Ames, D. E., and I. Kjarsgaard. Sulphide and alteration mineral chemistry of low- and high- sulphide Cu-PGE-Ni deposits in the Footwall environment, Sudbury, Canada. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2013. http://dx.doi.org/10.4095/292707.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Herzig, P. M., and G. H. Friedrich. Sulphide mineralization, hydrothermal alteration and chemistry in the drill hole CY-2a, Agrokipia, Cyprus. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1987. http://dx.doi.org/10.4095/122591.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Manor, M. J., J. S. Scoates, G. T. Nixon, and D. E. Ames. Geology, geochronology, mineral chemistry, and geochemistry: Supporting databases for the convergent margin Ni-Cu-PGE deposit study, Giant Mascot magmatic sulphide deposit, Hope, southwestern British Columbia. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2015. http://dx.doi.org/10.4095/297318.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Ames, D. E., and G. Tuba. Epidote-amphibole and accessory phase mineral chemistry as a vector to low-sulphide platinum group element mineralization, Sudbury: laser ablation ICP-MS trace element study of hydrothermal alteration. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2015. http://dx.doi.org/10.4095/296695.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Sulphone chemistry' for particular source types:
Journal articles Dissertations / Theses Books
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography