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ACS
1. E. Bulemela and Peter R. Tremaine
Standard partial molar volumes of some aqueous alkanolamines and alkoxyamines at temperatures up to 325 °C: functional group additivity in polar organic solutes under hydrothermal conditions
J. Phys. Chem. B, 2008, 112 (18), pp 5626–5645
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http://pubs.acs.org/doi/abs/10.1021/jp711766v2. Espen S. Hamborg, John P. M. Niederer, and Geert F. Versteeg
J. Chem. Eng. Data, 2007, 52 (6), PP 2491–2502
Dissociation constants and thermodynamic properties of amino acids used in co2 absorption from (293 to 353) K
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http://pubs.acs.org/doi/abs/10.1021/je700275v3. David M. Austgen, Gary T. Rochelle, Xiao Peng, Chau Chyun Chen
Model of vapor-liquid equilibria for aqueous acid gas-alkanolamine systems using the electrolyte-nrtl equation
Ind. Eng. Chem. Res., 1989, 28 (7), pp 1060–1073
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http://pubs.acs.org/doi/abs/10.1021/ie00091a028Modeling and experimental study of carbon dioxide absorption in aqueous alkanolamine solutions using a membrane contactor
Ind. Eng. Chem. Res., 2004, 43 (16), pp 4908–4921
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http://pubs.acs.org/doi/abs/10.1021/ie034325a5. R. Blaine Mccleskey
Electrical conductivity of electrolytes found in natural waters from (5 to 90) °C
J. Chem. Eng. Data, 2011, 56 (2), pp 317–327
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http://pubs.acs.org/doi/abs/10.1021/je101012n6. Denis G. Golovanov, Konstantin A. Lyssenko, Mikhail Yu. Antipin, Yakov S. Vygodskii, Elena I. Lozinskaya and Alexander S. Shaplov
Extremely short C–H F contacts in the 1-methyl-3-propyl-imidazolium SiF6 - the reason for ionic “liquid” unexpected high melting point
Cryst. Eng. Comm, 2005, 7, 53-56
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http://dx.doi.org/10.1039/B415742G