On the viscosity Arrhenius temperature for methanol + N,N-dimethylformamide binary mixtures over the temperature range from 303.15 to 323.15 K

References

• Bhuiyan MMH, Uddin MH. Excess molar volumes and excess viscosities for mixtures of N,N-dimethylformamide with methanol, ethanol and 2-propanol at different temperatures. J Mol Liq. 2008;138:139–146. doi:10.1016/j.molliq.2007.07.006
   Web of Science ®Google Scholar
• Riddick JA, Bunger WB, Sakano TK. Organic Solvents. 4th ed. New York (NY): Wiley Interscience; 1986.
   Google Scholar
• Laesecke A. Comments on “excess molar volumes and excess viscosities for mixtures of N,N-dimethylformamide with methanol, ethanol and 2-propanol at different temperatures” by (M. M. H. Bhuiyan and M. H. Uddin, J. Mol. Liquids, 138(2008)1–3, 139–146). J Mol Liq. 2009;145:51–53.
   Web of Science ®Google Scholar
• Yang C, Sun Y, He Y, Ma P. Volumetric properties and viscosities of binary mixtures of N,N-dimethylformamide with methanol and ethanol in the temperature range (293.15 to 333.15) K. J Chem Eng Data. 2008;53:293–297. doi:10.1021/je700430g
   Web of Science ®Google Scholar
• Bakshi MS, Kaur G. Thermodynamic behavior of mixtures. 4. Mixtures of methanol with pyridine and N,N-dimethylformamide at 25 °C. J Chem Eng Data. 1997;42:298–300. doi:10.1021/je960300p
   Web of Science ®Google Scholar
• Kinart CM. N,N-dimethylformamide-methanol binary mixtures and their assumed internal structures. Phys Chem Liq. 1994;27:115–121. doi:10.1080/00319109408029516
   Web of Science ®Google Scholar
• Bendová M, Řehák K, Matouš J, Novák JP. Liquid–liquid equilibrium in ternary systems N,N-dimethylformamide + 2-methylpentane + methanol and N,N-dimethylformamide + methylcyclohexane + methanol. Fluid Phase Equilib. 2006;239:16–25. doi:10.1016/j.fluid.2005.09.025
   Web of Science ®Google Scholar
• Zhang B, Cai Y, Mou XL, Lou N, Wang X. Density functional and multiphoton ionization studies of N,N-dimethylformamide–(methanol)n clusters. Chem Phys. 2002;280:229–238. doi:10.1016/S0301-0104(02)00560-8
   Web of Science ®Google Scholar
• Rabor JB, Yoshidome T, Mitsushio T, Yoshida K, Sarno BJ, Higo M. Excess molar volumes and excess viscosities for mixtures of N,N-dimethylformamide with methanol, ethanol and 2-propanol at different temperatures. Int Res J Pure Appl Chem. 2013;3:159–181. doi:10.9734/IRJPAC/2013/3442
   Google Scholar
• Hao Y, Zhang S, Yao K. Vapor–liquid equilibrium data for methanol +tert-butylamine +N,N-dimethylformamide and constituent binary systems at atmospheric pressure. J Chem Eng Data. 2012;57:1244–1248. doi:10.1021/je201349k
   Web of Science ®Google Scholar
• Zielkiewicz J. Excess volumes in (N,N-dimethylformamide + methanol + water) at the temperature 313.15 K. J Chem Thermodyn. 1995;27:415–422. doi:10.1006/jcht.1995.0041
   Web of Science ®Google Scholar
• Unger M, Harnacke B, Noda I, Siesler HW. Solvent interactions in methanol/N,N-dimethylamide binary systems studied by Fourier transform infrared-attenuated total reflection (FT-IR/ATR) and two-dimensional correlation spectroscopy (2D-COS). Appl Spectrosc. 2011;65:892–900. doi:10.1366/10-06141
   PubMed Web of Science ®Google Scholar
• Chao JP, Dai M, Wang YX. Studies of thermodynamic properties of binary mixtures containing an alcohol XII. Excess molar enthalpies of an (alkan-1-ol + N, N-dimethylformamide or dimethyl sulfoxide) at 298.15 K. J Chem Thermodyn. 1989;21:1169–1175. doi:10.1016/0021-9614(89)90103-1
   Web of Science ®Google Scholar
• Singh PP, Verma DV, Arora PS. Thermodynamics of binary methanol solutions. Thermochim Acta. 1976;15:267–280. doi:10.1016/0040-6031(76)85080-0
   Web of Science ®Google Scholar
• Hichri M, Das D, Messaâdi A, Bel Hadj Hmida ES, Ouerfelli N, Khattech I. Viscosity Arrhenius activation energy and derived partial molar properties in of N,N-dimethylacetamide + 2-ethoxyethanol binary mixtures at temperatures from 298.15 K to 318.15 K. Phys Chem Liq. 2013;51:721–730.
   Web of Science ®Google Scholar
• Das D, Messaâdi A, Dhouibi N, Ouerfelli N, Hamzaoui AH. Viscosity Arrhenius activation energy and derived partial molar properties in N,N-dimethylacetamide + water binary mixtures at temperatures from 298.15 K to 318.15 K. Phys Chem Liq Phys Chem Liq. 2013;51:677–685.
   Web of Science ®Google Scholar
• Ouerfelli N, Barhoumi Z, Iulian O. Viscosity Arrhenius activation energy and derived partial molar properties in 1,4-dioxane + water binary mixtures from 293.15 to 323.15 K. J Solution Chem. 2012;41:458–474. doi:10.1007/s10953-012-9812-9
   Web of Science ®Google Scholar
• Das D, Ouerfelli N. The relative reduced Redlich-Kister and Herráez equations for correlating excess properties of N,N-dimethylacetamide + formamide binary mixtures at temperatures from 298.15 K to 318.15K. J Solution Chem. 2012;41:1334–1351. doi:10.1007/s10953-012-9878-4
   Web of Science ®Google Scholar
• Das D, Messaâdi A, Barhoumi Z, Ouerfelli N. The relative reduced Redlich–Kister equations for correlating excess properties of N,N-dimethylacetamide + water binary mixtures at temperatures from 298.15 K to 318.15 K. J Solution Chem. 2012;41:1555–1574. doi:10.1007/s10953-012-9888-2
   Web of Science ®Google Scholar
• Das D, Barhoumi Z, Ouerfelli N. The relative reduced Redlich–Kister equations for correlating excess properties of N,N-dimethylacetamide + 2-methoxyethanol binary mixtures at temperatures from 298.15 K to 318.15 K. Phys Chem Liq. 2012;50:346–366. doi:10.1080/00319104.2011.646516
   Web of Science ®Google Scholar
• Das D, Barhoumi Z, Dhouibi N, Sanhoury MAMK, Ouerfelli N. The reduced Redlich–Kister equations for correlating volumetric and viscometric properties of N,N-dimethylacetamide + dimethylformamide binary mixtures at temperatures from 298.15 to 318.15 K. Phys Chem Liq. 2012;50:712–734. doi:10.1080/00319104.2012.713553
   Web of Science ®Google Scholar
• Das D, Messaâdi A, Dhouibi N, Ouerfelli N. Investigations of the reduced Redlich–Kister equations for correlating excess properties of N,N-dimethylacetamide + 2-ethoxyethanol binary mixtures at temperatures from 298.15 K to 318.15 K. Phys Chem Liq. 2012;50:773–797. doi:10.1080/00319104.2012.717893
   Web of Science ®Google Scholar
• Singh M. Survismeter – Type I and II for surface tension, viscosity measurements of liquids for academic, and research and development studies. J Biochem Biophys Methods. 2006;67:151–161. doi:10.1016/j.jbbm.2006.02.008
   PubMedGoogle Scholar
• Chandra A, Patidar V, Singh M, Kale RK. Physicochemical and friccohesity study of glycine, L-alanine and L-phenylalanine with aqueous methyltrioctylammonium and cetylpyridinium chloride from T = (293.15 to 308.15) K. J Chem Thermodyn. 2013;65:18–28. doi:10.1016/j.jct.2013.05.037
   Web of Science ®Google Scholar
• Singh M, Kumar V, Kale RK. Viscous and surface properties of upper critical solution temperatures of immiscible solvents with biomolecules, surfactants and polymer resin. Int J Therm. 2011;14:87–95. doi:10.5541/ijot.345
   Google Scholar
• Ameta RK, Singh M, Kale RK. Synthesis and structure–activity relationship of benzylamine supported platinum (IV) complexes. New J Chem. 2013;37:1501–1508. doi:10.1039/c3nj41141a
   Web of Science ®Google Scholar
• Singh M, Kumar V, Patel JS, Kale RK. Thermodynamics of philicphobic interaction shift in aqueous Tweens 20-80. Int J Therm. 2011;14:135–146.
   Google Scholar
• Singh M, Ameta RK, Kitawat BS, Kale RK. An interaction study of chloro and alkyl substituted benzylamine with DPPH• through UV spectrophotometric and physicochemical methods at T = (298.15, 303.15 and 308.15) K. J Mat Sci Chem Eng. 2014;2:43–51.
   Google Scholar
• Singhal S. Molecular-matrix of PVP derivative with alanine and electron rich core silicic acid, their spectroscopic and thermal characterizations with IR and TGA and their antimicrobial activity. Int J Chemtech Appl. 2013;2:152–161.
   Google Scholar
• Ouerfelli N, Messaâdi A, Bel Hadj Hmida E, Cherif E, Amdouni N. Validity of the correlation-Belda equation for some physical and chemical properties in isobutyric acid + water mixtures near and far away from critical temperature. Phys Chem Liq. 2011;49:655–672.
   Web of Science ®Google Scholar
• Iulian O, Ciocîrlan O. Viscosity and density of systems with water, 1,4-dioxane and ethylene glycol between (293.15 and 313.15) K. I. binary systems. Rev Roum Chim. 2010;55:45–53.
   Web of Science ®Google Scholar
• Herraez JV, Belda R, Diez O, An HM. Equation for the correlation of viscosities of binary mixtures. J Solution Chem. 2008;37:233–248.
   Web of Science ®Google Scholar
• Ouerfelli N, Bouaziz M, Herráez JV. Treatment of Herráez equation correlating viscosity in binary liquid mixtures exhibiting strictly monotonous distribution. Phys Chem Liq. 2013;51:55–74. doi:10.1080/00319104.2012.682260
   Web of Science ®Google Scholar
• Ouerfelli N, Kouissi T, Zrelli N, Bouanz M. Competition of correlation viscosities equations in isobutyric acid + water binary mixtures near and far away from the critical temperature. J Solution Chem. 2009;38:983–1004.
   Web of Science ®Google Scholar
• Cherif E, Ouerfelli N, Bouaziz M. Competition between Redlich–Kister and adapted Herráez equations of correlation conductivities in isobutyric acid + water binary mixtures near and far away from the critical temperature. Phys Chem Liq. 2011;49:155–171. doi:10.1080/00319100903074593
   Web of Science ®Google Scholar
• Ouerfelli N, Kouissi T, Iulian O. The relative reduced Redlich-Kister and Herráez equations for correlating viscosities of 1,4-dioxane + water mixtures at temperatures from 293.15 K to 323.15 K. J Solution Chem. 2010;39:57–75. doi:10.1007/s10953-009-9484-2
   Web of Science ®Google Scholar
• Ouerfelli N, Iulian O, Bouaziz M. Competition between Redlich–Kister and improved Herráez equations of correlation viscosities in 1,4-dioxane +water binary mixtures at different temperatures. Phys Chem Liq. 2010;48:488–513. doi:10.1080/00319100903131559
   Web of Science ®Google Scholar
• Ouerfelli N, Barhoumi Z, Besbes R, Amdouni N. The reduced Redlich–Kister excess molar Gibbs energy of activation of viscous flow and derived properties in 1,4-dioxane + water binary mixtures from 293.15 to 309.15 K. Phys Chem Liq. 2011;49:777–800. doi:10.1080/00319104.2010.521927
   Web of Science ®Google Scholar
• Dallel M, Das D, Bel Hadj Hmida ES, Al-Omair NA, Al-Arfaj AA, Ouerfelli N. Derived partial molar properties investigations of viscosity Arrhenius parameters in formamide + N,N-dimethylacetamide systems at different temperatures. Phys Chem Liq. 2013; in press. doi:10.1080/00319104.2013.871669
   Web of Science ®Google Scholar
• Besbes R, Ouerfelli N, Abderabba M. Study of chemical interactions in binary mixture water-1,4-dioxane: neighbourhood and associated model approach. Mediterr J Chem. 2012;1:289–302. Available from: http://dx.doi.org/10.13171/mjc.1.6.2012.05.06.12
   Google Scholar
• Longuet-Higgins HC. The statistical thermodynamics of multicomponent systems. Proc Roy Soc (London). 1951;205:247–269. doi:10.1098/rspa.1951.0028
   Web of Science ®Google Scholar
• Matsubayashi N, Nakahara M. Dynamics in regular solutions: concentration and viscosity dependence of orientational correlation time of a benzene molecule. J Chem Phys. 1991;94:653–661. doi:10.1063/1.460331
   Web of Science ®Google Scholar
• Nakagawa T. Is viscosity B coefficient characteristic for solute-solvent interaction? J Mol Liq. 1995;63:303–316. doi:10.1016/0167-7322(94)00792-U
   Web of Science ®Google Scholar
• De Ruiz Holgado ME, De Schaefer CR, Araneibia EL. Viscosity study of 1-propanol with polyethylene glycol 350 monomethyl ether systems at different temperatures. J Mol Liq. 1999;79:257–267.
   Web of Science ®Google Scholar
• Falkenhagen H. Theorie der Elektrolyte. Leipzig: Hirzel; 1971.
   Google Scholar
• Eyring H, John MS. Significant Liquid Structure. New York (NY): Wiley; 1969.
   Google Scholar
• Ali A, Nain AK, Hyder S. Ion-solvent interaction of sodium iodide and lithium nitrate in N,N-dimethylformamide + ethanol mixtures at various temperatures. J Indian Chem Soc. 1998;5:501–505.
   Google Scholar
• Leaist DG, MacEwan K, Stefan A, Zamari M. Binary mutual diffusion coefficients of aqueous cyclic ethers at 25 °C. Tetrahydrofuran, 1,3-dioxolane, 1,4-dioxane, 1,3-dioxane, tetrahydropyran, and trioxane. J Chem Eng Data. 2000;45:815–818. doi:10.1021/je000079n
   Web of Science ®Google Scholar