Reactive Distillation, Catalytic Distillation

Distillation ◽  
2021 ◽  
pp. 283-312
2015 ◽  
Vol 1113 ◽  
pp. 733-738
Author(s):  
Sudibyo Sudibyo ◽  
Muhamad Nazri Murat ◽  
Norashid Aziz

Reactive distillation is a process that combines both reactor and distillation column in one unit process. The reactive distillation is normally applied in MTBE production in order to achieve high reaction conversion and purity of the MTBE. Controlling such reactive distillation is a challenging task due to its highly nonlinear behavior and the existence of strong interactions among control variables. In this work, a Neural Wiener based model predictive control (NWMPC) is designed and implemented to control the tray temperature of MTBE reactive distillation. The Reduced SQP (RSQP) has been embedded as an optimizer in the NWMPC proposed. The MTBE reactive distillation has been modeled using aspen dynamic and the control study has been simulated using Simulink (Matlab) which is integrated with Aspen dynamic model. The results achieved show that the NWMPC is able to maintain tray temperatures at desired set points, able to reject the disturbance and robust toward robustness test conducted.


Catalysts ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1464
Author(s):  
Su Yang ◽  
Xiaoxuan Guo ◽  
Xiaomei Pan ◽  
Liuyu Gu ◽  
Xueping Liu ◽  
...  

Concentrated sulfuric acid is generally used as a catalyst for producing brominated alkanes in traditional methods, but is highly corrosive and difficult to separate. This work reports the preparation of bromopropane from n-propanol based on a reactive distillation strategy combined with alumina-modified sulfated zirconia (Al2O3/SO42−/ZrO2) as a heterogenous catalyst. As expected, under the optimum reaction conditions (110 °C), the yield of bromopropane was 96.18% without side reactions due to the reactive distillation strategy. Meanwhile, the microscopic morphology and performance of Al2O3/SO42−/ZrO2 were evaluated by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Brunner–Emmet–Teller (BET), Fourier transform infrared spectroscopy (FT–IR), and other characterization methods. The results confirmed that the morphology of zirconia sulfate is effectively regulated by the modification method of alumina, and more edges and angles provide more catalytic acid sites for the reaction. Furthermore, Al2O3/SO42−/ZrO2 exhibited high stability and remarkable reusability due to the strong chemical bond Zr–Al–Zr. This work provides a practical method for the preparation of bromopropane and can be further extended to the preparation of other bromoalkanes.


Author(s):  
B Saha ◽  
H T R Teo ◽  
A Alqahtani

With ever-growing environmental concerns, petrochemical and fine chemical industries face an omnipresent issue in recovering dilute acetic acid from its aqueous solutions. Catalytic distillation holds an ascendancy over conventional physical separation methods such as distillation and extraction. Distillation is associated with the high costs involved in vaporising the more volatile water that exists in high proportions and possesses a high latent heat of vaporisation. Extraction is limited in view of the distribution of the components in the reacting system. The implementation of catalytic distillation reduces capital and operating costs, and allows for a wider range of operating conditions. Catalytic distillation is receiving increasing attention and holds a huge potential for the recovery of acetic acid. Through the application of catalytic distillation via the reaction of acetic acid with iso-amyl alcohol, a useful ester in the form of iso-amyl acetate could be produced.In the present work towards further process development, the synthesis of iso-amyl acetate via reactive distillation is studied using Katamax® catalyst packing in the catalytic reactive section. The reactive distillation experiments were carried out at laboratory scale in a 50 mm diameter column with a catalytic packing section of 1 m and non-reactive packed enriching and stripping sections of about 1 m each. A cation exchange resin catalyst, Purolite® CT-175, was used. The experiments were conducted with the aim of achieving an optimum column configuration as well as process conditions for the synthesis of iso-amyl acetate in a reactive distillation column (RDC). Several variants of the RDC set-up e.g. total feed mole ratio, reflux ratio, location of feed points, reflux configuration and acid concentrations were explored for the recovery of dilute acetic acid and to achieve a high purity value added product, iso-amyl acetate.


Energies ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 1152
Author(s):  
Le Cao Nhien ◽  
Nguyen Van Duc Long ◽  
Moonyong Lee

Furfural is only derived from lignocellulosic biomass and is an important chemical used in the plastics, agrochemical, and pharmaceutical industries. The existing industrial furfural production process, involving reaction and purification steps, suffers from a low yield and intensive energy use. Hence, major improvements are needed to sustainably upgrade the furfural production process. In this study, the conventional furfural process based on a continuous stirred tank reactor and distillation columns was designed and optimized from an actual aqueous xylose solution via a biomass pretreatment step. Subsequently, a reactive distillation (RD) and extraction/distillation (ED) configuration was proposed for the reaction and purification steps, respectively, to improve the process efficiency. RD can remove furfural instantly from the reactive liquid phase and can separate heavy components from the raw furfural stream, while the ED configuration with toluene and butyl chloride used as extracting solvents can effectively separate furfural from a dilute aqueous stream. The results showed that the hybrid RD-ED process using a butyl chloride solvent saves up to 51.8% and 57.4% of the total investment costs and total annual costs, respectively, compared to the conventional process. Furthermore, environmental impacts were evaluated and compared for all structural alternatives.


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