A techno-economic comparison of various process options for the production of 1,1-diethoxy butane
✍ Scribed by Ion Agirre; María Belén Güemez; Anatolie Motelica; Henk M. van Veen; Jaap F. Vente; Pedro L. Arias
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2012
- Tongue
- English
- Weight
- 334 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0268-2575
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
BACKGROUND: Acetals can be considered important bio‐based diesel additives. The production of most of these compounds, from an alcohol and an aldehyde, suffers from low conversion due to thermodynamic limitations. These limitations can be overcome through the removal of the by‐product water. Previous studies showed that the in situ dehydration options of reactive distillation and pervaporation membrane reactor integration offer little advantage or at least not at reasonable unit dimensions. The aim of the present work is the development of a membrane based process and comparison with other alternatives (based on experimental data).
RESULTS: Three different membrane processes were developed. The one in which the reaction mixture is recycled over a first dehydration membrane module and subsequently through a simple distillation column, was found to give the highest overall conversion (100%) at low recycle rates and reasonable membrane area. This process was techno‐economically compared with other possible alternatives: (1) a process based on a conventional tubular reactor and several distillation columns; and (2) a process based on reactive distillation.
CONCLUSIONS: Efficient water removal by membranes avoids possible azeotropes in downstream distillation units making them much simpler, reducing considerably the unit sizes and the energy demand (40% lower). Copyright © 2012 Society of Chemical Industry
📜 SIMILAR VOLUMES
A 42-kDa recombinant protein, PX141, consisting of the trans-activator protein encoded by human T-cell leukemia virus (HTLV-I) (tax, antigen) and the amino-terminal fusion peptide of I 2 amino acid residues of the a-peptide encoded by the plasmid pUC I 9 was produced. In order to investigate the imm