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Process development for dimethylacetal synthesis: Thermodynamics and reaction kinetics

Title
Process development for dimethylacetal synthesis: Thermodynamics and reaction kinetics
Type
Article in International Scientific Journal
Year
2005
Authors
Ganesh K. Gand
(Author)
FEUP
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Viviana M. T. M. Silva
(Author)
FEUP
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Alírio E. Rodrigues
(Author)
FEUP
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Journal
Pages: 7287-7297
ISSN: 0888-5885
Indexing
Publicação em ISI Proceedings ISI Proceedings
Publicação em ISI Web of Science ISI Web of Science
COMPENDEX
Scientific classification
FOS: Engineering and technology
CORDIS: Technological sciences > Engineering > Chemical engineering
Other information
Authenticus ID: P-000-1CG
Abstract (EN): The synthesis of acetaldehyde dimethylacetal was studied in a batch reactor by the acetaldehyde and methanol reaction in the liquid phase, using the acid resin Amberlyst-15 as the catalyst. Acetal synthesis was also performed with Y-type zeolite in order to compare the results for both catalysts. The reaction equilibrium constant was determined experimentally in the temperature range 293.15-333.15 K at 1.0 MPa: K-eq = 0.0143 exp[2142.5/T(K)]. The standard molar reaction properties were obtained at 298.15 K: Delta S degrees = -35.34 J mol(-1) K-1, Delta H degrees = -17.81 kJ mol(-1), and Delta G degrees = -7.28 M mol(-1). Kinetic experiments were carried out in the temperature range 293.15-313.15 K at 0.6 MPa. A two-parameter model based on a Langmnir-Hinshelwood rate expression was considered, using activity coefficients from the UNIFAC method, which can describe the experimental kinetic results. The kinetic law is R = k(C)[a(A)a(B) - a(C)a(D)/(K(eq)a(A))]/(1 + K(sD)a(D))(2), and the parameters are k(C) = 6.91 x 10(13) exp[-8 702.6/T(K)] mol g(-1) min(-1) and K-D = 2.37 x 10(32) exp[-22 713/T(K)]. The activation energy of reaction for the synthesis of acetal is 72.35 kJ mol(-1). The relationship between the effectiveness factor and the Thiele modulus was determined.
Language: English
Type (Professor's evaluation): Scientific
Contact: arodrig@fe.up.pt
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