A systematic rheological study of alkyl amine surfactants for fluid mobility control in hydrocarbon reservoirs
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1995-8226
- Extent
-
Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
A systematic rheological study of alkyl amine surfactants for fluid mobility control in hydrocarbon reservoirs ; day:10 ; month:2 ; year:2018 ; pages:1-14
Petroleum science ; (10.2.2018), 1-14
- Classification
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Technische Chemie
- Creator
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Liebum, Madalyn M.
- Contributor
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Hirasaki, George
Nguyen, Quoc P.
SpringerLink (Online service)
- DOI
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10.1007/s12182-018-0217-2
- URN
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urn:nbn:de:1111-201804035216
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:47 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Liebum, Madalyn M.
- Hirasaki, George
- Nguyen, Quoc P.
- SpringerLink (Online service)
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Rhodium-catalyzed direct alkylation of benzylic amines using alkyl bromides
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
Palladium-Catalyzed γ-C(sp3)–H Bond Activation of Tertiary Alkyl Amines
Two-dimensional spreading properties and sealing characteristics of fluorocarbon surfactants on several typical hydrocarbon fuels
Multicomponent synthesis of α-branched amines using organozinc reagents generated from alkyl bromides
Self-aggregation of cationic gemini surfactants with amide groups in the spacer and variable alkyl chain length
Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources
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Foaming epoxy-amine-carbamate : The effect of different neat amines on rheological and cellular morphology
Rhodium-catalyzed direct alkylation of benzylic amines using alkyl bromides
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General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
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Self-aggregation of cationic gemini surfactants with amide groups in the spacer and variable alkyl chain length
Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources
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