Degradation Kinetics of MEA and DEA by Fenton’s Reagent with Biological Post-Treatment

Harimurti, Sabtanti Harimurti (2009) Degradation Kinetics of MEA and DEA by Fenton’s Reagent with Biological Post-Treatment. Masters thesis, UNIVERSITI TEKNOLOGI PETRONAS.

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Abstract

Alkanolamines in aqueous solutions are commonly used for scrubbing of
carbon dioxide from natural gas, synthesis gas and other gas mixtures. Large
quantities of amines appear in the wastewater during cleaning and maintenance as
well as shutdown of the absorption and desorption columns. The amines are not
readily biodegradable and such wastewater cannot be treated in the conventional
treatment facility. Advanced Oxidation Processes (AOP), such as oxidation by
Fenton’s reagent, UV-H2O2 and UV-Ozone offer a class of techniques of treatment or
partial degradation of recalcitrant organics which are not readily amenable to
conventional biological oxidation. Degradation of alkanolamines by Fenton’s reagent
has been investigated in this work. Mono- and di-ethanolamines have been selected as
two model alkanolamines. Fenton’s oxidation experiments were conducted in a
jacketed glass reactor and the effects of process parameters such as dosing of the
reagents (H2O2 and FeSO4;7H2O), pH, initial concentration of the amine as well as the
mode of addition of the reagents have been studied in details. Since the degradation
process involves a number of intermediates, not all of which could be identified, the
chemical oxidation demand (COD) of the amine solution is selected as a measure of
the extent of degradation. Determination of the COD was done by Hach 5000
spectrophotometer following the standard procedure. FTIR Spectrometer and HPLC
were used for identification and analysis of the degradation fragments. Amine
concentrations upto 20,000 ppm was used since it is characteristic of the effluents
from a natural gas treating plant. It was observed that only a fraction of the COD
could be removed by using a moderate quantity of the reagents. Also, for a solution
having a higher initial amine concentration, the degradation process was very fast.
Most of the total COD removal was attained within a few minutes from the start of the
reaction. This was followed by a very slow rate of COD removal. The reaction rate as
well as the extent of reaction was most favored at a pH of 3. Also the rate of
degradation passes through a maximum with increase of H2O2 dosing and the
Fe2+/H2O2 ratio. Continuous addition of the Fenton’s reagent is much more effective
with better utilization of the H2O2 than one-time addition. Besides COD, time
evolution of the concentrations of the amine and hydrogen peroxide were measured to
monitor the course of the reaction. A rapid fall of H2O2 concentration accompanied
the fast COD reduction. But COD removal was less steep for continuous reagent
addition experiments. The trends were very much similar for both MEA and DEA.
They showed closely similar behavior.
Although it was not possible to identify all the degradation products of the
amines, the formation of glycine as one of the intermediates was decisively
established. This indicates that the alcohol group of an alkanolamine might be more
vulnerable to electrophilic attack by the HO• radicals than the α-carbon atom with
respect to the alcohol group. A plausible reaction pathway is suggested and a rate
equation for MEA degradation was developed.
A high dose of Fenton’s reagent was not of help to increase the COD
reduction. With addition of the stoichiometric quantities of the regent, the degradation
amounted to only about 60% COD removal even though about 98% of H2O2 as
hydroxyl radical source was utilized. Oxidation of one of the degradation products
namely glycine using Fenton’s oxidation was investigated separately. The degradation
rate was slower than the pure substrate. Since 40-50% of the COD remains in the
Fenton-treated solution, we explored the biodegradability of the organic fragments
and oxidation products. The biodegradability test was carried out in an aerobic batch
reactor prescribed by the materials and methods specifications in the Zahn-
Wellens/EMPA Test according to the US Environmental Protection Agency (EPA)
method OPPTS 835.3200. Partially degraded alkanolamines after about 40% COD
removal by Fenton’s oxidation was used to study the biodegradability. The biological
oxidation of untreated alkanolamine was done in parallel. The COD in solution as
well as the biomass concentration was monitored to follow the course of the reaction.
The pH of the medium ranged between 6.5 – 8. No attempt to maintain a constant pH
by buffering was made in order to ascertain the usefulness of the method under
industrial operating conditions. ‘Activated sludge’ from the central wastewater
treatment unit of this university was used for seeding the batch bioreactor. The results
show that the acclimatization time for biological oxidation of a partially degraded
amine sample was about the half of that of the ‘pure’ amine. The time of maximum
COD removal was also shorter for the former sample. The kinetics of biomass growth
could be fitted by the Monod equation. The kinetic constants were evaluated.
Emission of ammonia from the reactor was detected and an ammonia probe
was used to monitor the formation of ammonia during the biodegradation process. It
appears that ammonia formation per unit COD of the partially degraded sample was
more than that of a ‘pure’ amine. This observation is compatible with the formation of
more oxygenated degradation products such as amino-acids during Fenton’s
oxidation. The results of this study are expected to be useful for developing a practical
strategy of treatment of amine-laden wastewater in natural gas-treating plants.

Item Type: Thesis (Masters)
Departments / MOR / COE: Engineering > Chemical
Depositing User: Users 5 not found.
Date Deposited: 04 Jun 2012 10:13
Last Modified: 25 Jan 2017 09:44
URI: http://utpedia.utp.edu.my/id/eprint/2938

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