Kinetics and performance studies of a switchable solvent TMG (1,1,3,3-tetramethylguanidine)/1-propanol/carbon dioxide system

The rate constants and the activation energies of the reaction between carbon dioxide and 1,1,3,3-tetramethylguanidine (TMG) in 1-propanol solution were measured by a stopped-flow technique at a temperature range of 288--308 K and at a TMG concentration range of 2.5--10.0 wt %. Based on the pseudo-first-order reaction for CO2, the reaction was modeled by a termolecular reaction mechanism, which resulted in a rate constant of 199.30 m3 kmol-1 s-1 at 298 K. The activation energies were 5.19 kJ/mol and 5.26 kJ/mol at 2.5 and 5.0 wt % TMG, respectively. In addition, carbon dioxide absorption capacity was investigated using a gas--liquid contact system. Absorption capacity of the 10.0 wt % TMG/1-propanol system was found to be 0.035 mol CO2/0.035 mol TMG, indicating a favorable loading ratio of 1:1. Repeatability and potential performance losses of this system were analyzed by Fourier transform infrared spectrometry (FTIR) in the range of 400--4000 cm-1. It was found that the FTIR spectra of the rich solvent became virtually identical to the spectra of the lean solvent upon thermal desorption, promising efficient regeneration. It is therefore concluded that the TMG/1-propanol/CO2 system is easily switchable and can be used both for carbon dioxide capture and for other applications that require rapid change of medium from nonionic to ionic liquid.

Kinetics and performance studies of a switchable solvent TMG (1,1,3,3-tetramethylguanidine)/1-propanol/carbon dioxide system

The rate constants and the activation energies of the reaction between carbon dioxide and 1,1,3,3-tetramethylguanidine (TMG) in 1-propanol solution were measured by a stopped-flow technique at a temperature range of 288--308 K and at a TMG concentration range of 2.5--10.0 wt %. Based on the pseudo-first-order reaction for CO2, the reaction was modeled by a termolecular reaction mechanism, which resulted in a rate constant of 199.30 m3 kmol-1 s-1 at 298 K. The activation energies were 5.19 kJ/mol and 5.26 kJ/mol at 2.5 and 5.0 wt % TMG, respectively. In addition, carbon dioxide absorption capacity was investigated using a gas--liquid contact system. Absorption capacity of the 10.0 wt % TMG/1-propanol system was found to be 0.035 mol CO2/0.035 mol TMG, indicating a favorable loading ratio of 1:1. Repeatability and potential performance losses of this system were analyzed by Fourier transform infrared spectrometry (FTIR) in the range of 400--4000 cm-1. It was found that the FTIR spectra of the rich solvent became virtually identical to the spectra of the lean solvent upon thermal desorption, promising efficient regeneration. It is therefore concluded that the TMG/1-propanol/CO2 system is easily switchable and can be used both for carbon dioxide capture and for other applications that require rapid change of medium from nonionic to ionic liquid.

___

  • TMG/1-propanol This work Ozturk et al., 201440 0.98 1 76 61 67 EA(kJ/mol) 0.99 130 23 Experimental
  • Heldebrant, D. J.; Koech, P. K.; Rainbolt, J. E.; Zheng, R. 10th International Conference on Greenhouse Gas Control Technologies, Amsterdam, the Netherlands, 19–23 September 2010; Gale, J.; Hendriks, C.; Turkenberg,
  • W., Eds; Elsevier: Amsterdam, 2011, p. 216–223.
  • Ozturk, M. C.; Ume, C. S.; Alper, E. Chem. Eng. Technol. 2012, 35, 2093–2098.
  • Caplow, M. J. Am. Chem. Soc. 1968, 90, 6795–6803.
  • Danckwerts, P. V. Chem. Eng. Sci. 1979, 34, 443–446.
  • Ume, C. S.; Alper, E.; Gordesli, F. P. Int. J. Chem. Kinet. 2013, 45, 161–167.
  • Davis, R. A.; Sandall, O. C. Chem. Eng. Sci. 1993, 48, 3187–3193.
  • Crooks, J. E.; Donnellan, J. P . J. Chem. Soc. Perk. T. 1989, 2, 331–333.
  • Alper, E. Chem. Eng. J. Bioch. Eng. 1990, 44, 107–111. da Silva, E. F.; Svendsen, H. F. Ind. Eng. Chem. Res. 2004, 43, 3413–3418.
  • Arslan, B. Master of Science Thesis, Faculty of Engineering, Hacettepe University, Turkey, 2012.
  • Alper, E. Ind. Eng. Chem. Res. 1990, 29, 1725–1728.
  • Ozturk, M. C.; Yuksel Orhan O.; Alper, E. Int. J. Greenh. Gas Con. 2014, 26, 76–82.
  • (http://dx.doi.org/10.1016/j.ijggc.2014.04.023).
Turkish Journal of Chemistry-Cover
  • ISSN: 1300-0527
  • Yayın Aralığı: 6
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Synthesis of tetrahydropyrimidinium salts and their in situ catalytic activities towards the Buchwald--Hartwig amination reaction under microwave irradiation

Liangru YANG, Huanyu BIAN, Wenpeng MAI, Pu MAO, Yongmei XIAO, Dong WEI, Lingbo QU

Synthesis and properties of novel magnetic nanoparticles grafted with nitropyridine-substituted calix[4]arene derivative as Cr^{6+} extractant

Serkan SAYIN, Vildan DOĞAN

Synthesis, molecular docking, and antitumoral activity of alnustone-like compounds against estrogen receptor alpha-positive human breast cancer

Kaan KÜÇÜKOĞLU, Hatice SEÇİNTİ, Aykut ÖZGÜR, Hasan SEÇEN, Yusuf TUTAR

Synthesis and characterization of substituted benzimidazole Co(II), Fe(II), and Zn(II) complexes and structural characterization of dichlorobis{1-[2-(1-piperidinyl)ethyl]-1H-benzimidazole-_KN^3} zinc(II)

Hasan KÜÇÜKBAY, Ülkü YILMAZ, Orhan BÜYÜKGÜNGÖR, Mehmet AKKURT

Synthesis, properties, and electrochemistry of a photochromic compound based on dithienylethene and ProDOT

Melek PAMUK ALGI, Atilla CİHANER, Fatih ALGI

Synthesis of methyl 4-(9H-carbazole-9-carbanothioylthio) benzoate: electropolymerization and impedimetric study

Murat ATEŞ, Nesimi ULUDAĞ, Fatih ARICAN, Tolga KARAZEHİR

Synthesis and properties of novel magnetic nanoparticles grafted with nitropyridine-substituted calix[4]arene derivative as Cr6+ extractant

Serkan SAYIN, Vildan DOĞAN

Purification and characterization of NADPH-cytochrome P450 reductase from Lake Van fish liver microsomes and investigation of some chemical and metals' effects on the enzyme activity

Müslüm KUZU, Mehmet ÇİFTCİ

Amperometric biosensing of ethanol based on integration of alcohol dehydrogenase with a Pt/PPy--PVS/MB electrode

Özlem ÇOLAK, Fatma ARSLAN

Reduction behavior of fenoxaprop-p-ethyl and its voltammetric determination

Zeki EŞ, İbrahim Hüdai TAŞDEMİR