last update: 2/11/24
             
                 Ethanol chemistry
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Ethanol to ethylene
Etanol to butadiene


Ethanol  ===> Ethylene

2012 study
ethanol to ethylene



 process flow diagram :(complete article)
ethanol to C2H2 process flow diagram


2021 update   2021 update:technip energy)



Ethanol  ===>  butadiene

Lebedev  process
 2 CH3-CH2OH =====> CH2=CH2-CH2=CH2  + 2 H2O  + H2
catalyst :  mix of various metal oxide /  doped zeolit / ....
temperature 450°c

Ostromisslensky process
CH3-CH2OH + CH3-CHO  ====> CH2=CH2-CH2=CH2 +2H2O

process description  :

1,3-Butadiene (BD), the monomer of synthetic rubbers and polymers, is one of the most
important unsaturated hydrocarbons. There are two methods of BD production: Lebedev -
conversion of ethanol (EtOH) over one catalyst in one reactor, and Ostromisslensky - conversion
of a mixture of EtOH and acetaldehyde (AA), which is produced over a catalyst in the first
reactor and then converted to BD over another catalyst in the second reactor. 



Some new developments


https://www.sciencedirect.com/science/article/abs/pii/S0263876223001880#preview-section-abstract

Highlights
  • The yield of one-stage ETB (Lebedev) process is 0.3 kg butadiene / kg-ethanol versus the theoretical value of 0.587.
  • The reaction takes place in two adiabatic fixed-bed reactors with radial flow and interstage heating.
  • Butadiene separation can be achieved by cryogenic distillation and DMF absorption.
  • Use of inert gas to lower ethanol partial pressure has a negative impact on the profitability.
  • The two-stage (Ostromislensky) process has better economics.

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https://hal.sorbonne-universite.fr/hal-01437547v1

Highlights

 Tantalum-containing SiBEA zeolite with isolated framework mononuclear Ta(V) doped with Ag, Cu and Zn were prepared and characterized by XRD, XPS, DR UV-VIS and FTIR (with pyridine, 2,6-di-tert-butylpyridine, pyrrole and deuterated chloroform). The conversion of ethanol as renewable raw material into 1,3-butadiene by Lebedev method over these zeolite catalysts was investigated. The doping of TaSiBEA with Ag, Cu and Zn changes its catalytic properties in ethanol conversion into 1,3-butadiene as a result of modification of acid-base properties with formation of additional dehydrogenation sites. Such modification allows accelerating ethanol dehydrogenation to acetaldehyde and subsequent steps of the ethanol-to-butadiene process. Ethanol conversion and butadiene selectivity over the catalysts increase in the order: TaSiBEA < ZnTaSiBEA < AgTaSiBEA < CuTaSiBEA. Higher selectivity to butadiene (73 %) was achieved over CuTaSiBEA (at 88% ethanol conversion, T = 598 К, WHSV = 0.5 h-1).


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