Design of Self Priming Venturi Scrubber For The Simultaneous Abatement of HCL Gas and Particulate Matter From The Ue Gas
Design of Self Priming Venturi Scrubber For The Simultaneous Abatement of HCL Gas and Particulate Matter From The Ue Gas
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Manisha Bal a,∗ , Hammad Siddiqi a , Subhrajit Mukherjee a , B.C. Meikap a,b
aDepartment of Chemical Engineering, Indian Institute of Technology (IIT) Kharagpur, West Bengal 721302, India
bDepartment of Chemical Engineering, School of Engineering, Howard College, University of Kwazulu-Natal,
Durban, South Africa
a r t i c l e i n f o a b s t r a c t
Article history: Mostly, HCl gas along with particulate matter are generated from the combustion and waste
Received 19 March 2019 incineration process but exposure of these air pollutants beyond a certain limit is very dan-
Received in revised form 10 June gerous to the human life. Therefore, experimental study of simultaneous removal of HCl
2019 gas and fly ash from the flue gas using self priming venturi scrubber is investigated. Effect
Accepted 7 August 2019 of various parameters like throat gas velocity, inlet fly ash concentration, inlet HCl concen-
Available online 16 August 2019 tration and hydrostatic head of water on the removal of HCl gas and fly ash particle has
been studied. Maximum HCl removal is obtained as 98.3% at 60 m/s of throat gas velocity,
Keywords: 0.77 m of water level height, 500 ppm of inlet HCl loading and 0.3 × 10−3 kg/m3 of inlet fly ash
Self priming venturi scrubber concentration. On the other hand, maximum fly ash removal of 99.91% is achieved at 60 m/s
Particulate and gaseous pollutant of throat gas velocity, 0.77 m of water level height and 0.3 × 10−3 kg/m3 of inlet fly ash con-
removal centration. Empirical model is also developed for the prediction of HCl removal efficiency
Scrubbing in the presence of fly ash and validated with the experimental results. Thus the submerged
Pollution control venturi scrubber is a novel technique which may control the emissions from many process
industries.
© 2019 Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
1. Introduction and literature review according to the World Bank standards (State Compensation Insurance
Fund, 2015; World Bank Group, 1998). Therefore, most importance has
Industrial emitted gases contain different type of air pollutants which been given by the researcher in design and development in the removal
solely depend on the type of process and unit operation. These air pol- technique.
lutants are generally in the form of dangerous gases and particulate Both sequential and simultaneous removal technique have been
matter. Most of the power plant or waste incineration process emits practiced in the past decades for the removal of gaseous pollutants
toxic HCl gas along with fly ash particle (Shemwell et al., 2002; Kameda along with particulate matter. In the sequential method, particulate
et al., 2011). Emission of HCl gas results in coughing, edema, inflam- matter is removed in the 1st step and then the gaseous pollutants are
mation and desquamation of upper respiratory tract in inhalation and removed in the 2nd step. In the simultaneous removal technique, both
irritation of eye. On the other hand, fly ash particles can go deep inside gaseous and particulate matters are separated in one step. Sequential
the lungs and can be the cause of lung cancer and many heart dis- method becomes problematic for the industry to remove the particulate
eases (U.S Environmental Protection Agency, 1999; Azam et al., 2016; laden gaseous pollutants. Therefore simultaneous removal in one sin-
Kim et al., 2015). In light of this adverse effect on humans and the gle step is more viable to achieve techno economic feasibility (Meikap
environment, abatement of HCl gas as well as fly ash particle is very et al., 2002a,b; Bandyopadhyay, 1996). Despite of inherent shortcoming,
necessary in their source. According to the OSHS Board, ceiling value wet scrubbers are only the technique which removes the particulate
of HCl gas is 2 ppm and exposure limit of fly ash particle is 0.050 g/Nm3 matter and HCl gas both efficiently in simultaneous process.
Pollock et al. (1966) first investigated simultaneous removal of fly
ash and SO2 using a wet scrubber with alkali stream and results
∗
Corresponding author. obtained from this investigation are highly appreciated. Particulate
E-mail address: [email protected] (M. Bal). removal efficiency was 98%, whereas SO2 removal efficiency was 95%.
https://doi.org/10.1016/j.cherd.2019.08.005
0263-8762/© 2019 Institution of Chemical Engineers. Published by Elsevier B.V. All rights reserved.
312 Chemical Engineering Research and Design 1 5 0 ( 2 0 1 9 ) 311–319
PHCl present research, we tried to remove HCl gas and particulate matter
Partial pressure of HCl in inlet gas, Pa
from flue gases in a self-priming venturi scrubber for non-submerged
Vimp Volume of impinger solution, L
and submerged condition using 0.005 N NaOH solution as scrubbing
Vair Volume of air, Ml
liquid. In my previous work, HCl removal in this self priming ven-
Vb Velocity of bubble, m/s
turi scrubber has been investigated at different concentration of NaOH
Mair Molecular weight of air, g in scrubbing liquid. 0.005 N NaOH was shown the maximum removal
MCl Molecular weight of chloride ion, mg efficiency of HCl. Thatswhy, 0.005 N NaOH scrubbing liquid has been
air Density of air, g/Ml chosen for present experiments (Bal et al., 2019a). Moreover, variation
l Density of liquid, kg/m3 of effecting parameters such as gas flow rate, inlet HCl loading, inlet
g Density of gas, kg/m3 concentration of fly ash and liquid height in outer cylinder on removal
l Viscosity of scrubbing liquid, Pa-s efficiency was investigated. Empirical model was also developed for
g Viscosity of gas, Pa-s the prediction of HCl removal efficiency of in the presence of fly ash
for the non-submerged and submerged conditions and compared with
KG Overall gas mass transfer coefficient, m/s
the experimental results.
kG Gas side mass transfer coefficient, m/s
kl Liquid side mass transfer coefficient, m/s
E Enhancement factor 2. Material required and experimental
I Stoichiometric mole ratio of NaOH and HCl procedure
surface tension of gas-NaOH solution interface,
N/m 2.1. Material
DNaOH Diffusivity of NaOH in water, m2 /s
DHCl Diffusivity of HCl in water, m2 /s Merck Life Science Pvt. Ltd., India supplied the HCl acid (35%)
DHCl NaOH Diffusivity of HCl in 0.005 N NaOH solution, and solid NaOH. Perspex was used to fabricate the venturi
m2 /s scrubber which was procured by Anupam Enterprise, West
Re g Reynolds number of gas, dimensionless Bengal, India. Sample fly ash was supplied from the Kolaghat
Re b Reynolds number of bubble, dimensionless Thermal Power Station, West Bengal, India.
Sc Schmidt number, dimensionless
flyash-HCl Experimental removal efficiency of flyash in 2.2. Experimental set up and procedure
presence of HCl, %
HCl-flyash Experimental removal efficiency of HCl in Schematic representation of experimental set up is
presence of flyash, % shown in the Fig. 1. In the present research, venturi
HCl-FA NS Predicted removal efficiency of HCl in pres- scrubber is kept inside the vertical perspex column
ence of flyash for non-submerged condition, % (Length × Diameter = 1 m × 0.17 m).Convergent angle and
HCl-FA S1 Predicted removal efficiency of HCl inside ven- divergent angle are 25◦ and 7◦ , respectively. Air stream was
turi scrubber for submerged condition, % passed through a calibrated rotameter to measure the flow
HCl-FA S Predictedremoval efficiency of HCl in presence rate of air and mixed with HCl vapours and fly ash particles
of flyash for submerged condition, % in a venturi shaped mixing tank which produced a uniform
composition of HCl gas and fly ash particles. On the other
hand, 0.005 N NaOH solution was drawn from the liquid tank
to the bottom of the column. Liquid level was maintained at
Chemical Engineering Research and Design 1 5 0 ( 2 0 1 9 ) 311–319 313
Fig. 1 – Schematic diagram of experimental set up for simultaneous removal of HCl gas and fly ash.
desired height. Here, HCl vapours were produced by passing filter (FAS), vacuum pump (VP) and dry gas meter (GM). Fly ash
air through the diluted HCl solution in a round bottomed flask was collected on the glass fibre filter paper which was dried in
and flow rate of air was adjusted by the calibrated rotameter. an air oven at 105 ◦ C and cooled in desiccators. Difference in
Fly ash was fed in a mild steel hopper (Hp ) used as storage weight of initial and final filter paper determines the amount
chamber which was connected to an electric vibrator feeder of fly ash particle collected in filter paper. Amount of sample is
(VB ) to control the flow of fly ash to the mixing tank. Basically, expressed as fly ash collected in filter paper (kg) that is divided
suction was created inside the venturi mixing tank due to by the volume of the air. Here vacuum pump sucked the fly ash
air flow rate which helps to mix the solid in the air stream enabling it to pass through the fly ash collector. Whereas dry
uniformly. Concentration of HCl gas was controlled by the gas meter was used to measure the volume of the air passing
operating valve between the connecting line with volumetric through the fly ash collector. Furthermore after leaving from
flask and mixing tank. Scrubbing liquids entered the venturi the gas meter air was passed through the impinger which was
scrubber at the throat section by the suction generated due to connected with the aspirant bottle. Impinger solution con-
huge pressure drop between the outside hydrostatic pressure taining 100 mL of NaOH solution was selected based on the
of liquid and static pressure of the gas in a venturi scrubber. solubility of HCl. Aspirant bottle was filled with water. It con-
However, the gas collided with the liquid droplets mainly trols the flow rate of gaseous sample collection by the control
by inertial impaction and captured the fly ash particle and valve. Volume of the air passing through the impinger solution
absorbed the HCl gas from the airstream. Here, HCl concen- was evaluated by the volume of water coming out from the
tration was adjusted in the air stream as 100 ppm, 300 ppm, aspirant bottle. Ion chromatography was used to measure the
500 ppm, whereas, fly ash concentration was maintained as Cl− ion concentration (ppm) generated in impinger solution.
(0.003–0.3) × 10−3 kg/m3 . Inlet and outlet concentration of HCl (ppm) were calculated
using the below formula Eq. (1) (Bal et al., 2019a,b).
2.3. Sampling procedure and analysis
Vimp (L) *CCl (ppm) Mair (g)
CHCl (ppm) = *10−6 * g (1)
Sampling was done simultaneously at the inlet and outlet MCl (mg) Vair (mL) *air ( mL )
sampling port by passing the sample 1st through the par-
ticulate sampling assembly and then through the impinger 2.4. Selection of scrubbing liquid
containing absorbing solution. Sampling has been done at
isokinetic condition (Bal et al., 2019a,b; Kurella and Meikap, Selection of scrubbing liquid is very important factor for the
2016). Isokinetic condition is obtained when the velocity of removal of HCl gas in the present system. There are some fac-
the sample captured from the inlet or outlet is equal to the tors that should be kept in mind while choosing the scrubbing
velocity of the sample passing through the scrubbing system. liquid such as high absorption capacity, availability, nontoxic,
In the present study, sample was collected at the sampling low price, low viscosity, low vapour pressure, non-corrosive
flow rate of 0.41–0.83 LPM and for 5–15 min. Particulate sam- and also could be regenerated or disposed of in a simple
pling assembly consists of fly ash collector glass micro fibre way (Bandyopadhyay and Biswas, 2006).In the literature many
314 Chemical Engineering Research and Design 1 5 0 ( 2 0 1 9 ) 311–319
Fig. 2 – Concentration profiles of components for HCl absorption with chemical reaction (Film theory).
absorbents are suggested in removing the HCl gas like sodium Enhancement factor of instantaneous chemical reaction
bicarbonate, methanol, ethanol, Ca(OH)2 ,ether etc. (Kong and for the HCl absorption in NaOH solution can be given by Eq.
Balland, 2011; Pozzo et al., 2018). Absorbing capacity of NaOH (4) (Bal et al., 2019a).
in HCl is extremely high (Brady, 1987) and effluent solutions
from the scrubber can be rejuvenated in the alkali solution by DNaoH CNaOH
E=1+i (4)
reacting normally with lime, i.e., Ca (OH)2 . DHCl CHCl,int
norms.
CHCl−fly ash I − CHCl−fly ash O
HCl−fly ash = × 100 (11)
3.2. XRF analysis CHCl−fly ash I
XRF analysis has been done to determine the sample compo- 5. Results and discussion
sition. Fig. 4 shows the different oxide composition present in
fly ash. 5.1. EDX analysis
4. Removal efficiency study of HCl and fly Dried sample, fly ash was first analysed in EDX and then after
ash scrubbing operation, fly ash was collected in the form of slurry
and accumulated in the settler placed at the bottom of the
4.1. Experimental procedure for simultaneous removal scrubber assembly; fly ash was allowed to settle for 30 min in
efficiency of HCl and fly ash the settler. After that, fly ash was dried in an air oven for 30
mints at 80 ◦ C and then again analysed in EDX. Results of EDX
In the present work the simultaneous removal of HCl and fly analysis for the fly ash before and after scrubbing operation
ash with the help of self-priming venturi scrubber is analysed are shown in Fig. 5a, b respectively. From the figure, the pres-
at different gas flow rate, inlet HCl loading, inlet concentration ence of Cl− in the fly ash is observed. Basically, HCl gas was
5.2. Effect of throat gas velocity and inlet HCl loading means increase in molecular density of HCl gas which dimin-
on HCl removal efficiency in the presence of fly ash particle ishes the distance between the gas molecules. It results in
enhancement of impaction between liquid droplets and gas
The effect of throat gas velocity on HCl gas removal effi- molecules. It causes increase in removal efficiency. Therefore,
ciency at 0.77 m water level in outer cylinder in the presence it can be concluded that the inlet HCl concentration is plays
of 0.3 × 10−3 kg/m3 of fly ash is shown in the Fig. 6. Graphs has important which affects the efficiency significantly. Maximum
been plotted at the H = 0.77 m because maximum efficiency HCl removal efficiency, 98.3% is obtained at the 60 m/s of throat
has obtained at H = 0.77 m. Reason behind this maximum gas velocity, 0.77 m of water height, 500 ppm of inlet HCl con-
efficiency is that longer interaction time of the gas stream centration and 0.3 × 10−3 kg/m3 of inlet fly ash concentration.
when it passes through the water bed surrounding the ven-
turi scrubber in the form of bubbles which does not happen in 5.3. Comparison of removal efficiency of HCl gas in the
a non-submerged condition. presence and absence of fly ash particle
It can be seen from the Fig. 6, even after presence of fly ash
the HCl removal efficiency increases with throat gas velocity. To compare the removal efficiency in the presence of fly ash
The absorption rate of HCl gas in scrubbing liquid is very high and absence of fly ash a graphhas been plotted in the Fig. 7,
in the presence of fly ash. Liquid injected at the throat section, kept at identical condition of throat gas velocity, inlet con-
interaction of high speed contaminated air with the entrant centrations and water height in the outer cylinder. Efficiency
liquid, droplet formation occurs that droplets absorbs the HCl obtained for HCl scrubbing in the presence of fly ash is found
gas from the air. High gas velocity enhances the amount of liq- to be more than the efficiency of scrubber in absence of fly
uid entering at the throat section of the venturi scrubber and ash. This happens may be due to three basic reasons: (1) cat-
relative velocity between air and liquid which is responsible alytic activity of fly ash, or (2) enhancement in pH of scrubbing
for the increment in removal efficiency of HCl. liquid in the presence of fly ash or (3) adherence of fly ash par-
It is also shown in the Fig. 6 that with increase in HCl load- ticles to the gas molecules. In the literature (Rajmohan et al.,
ing, the HCl removal efficiency enhances. High HCl loading 2008), it is reported that the gas liquid system is controlled
Chemical Engineering Research and Design 1 5 0 ( 2 0 1 9 ) 311–319 317
5.5. Effect of throat gas velocity and inlet fly ash Fig. 10 – Effect of inlet HCl loading on fly ash removal
concentration on removal efficiency of fly ash efficiency.
50 Q 1.5
dd = + 91.8( l ) (13)
ug Qg
Simplified dimensionless analysed equation can be written Fig. 11 – Comparison of experimental and predicted from
as below. the developed model in submerged and non-submerged
condition.
a b Ql c Cflyash I
d
HCl−FA NS = k Reg (Sc) ( ) ( ) (15)
Qg g The final equation is given in the Eq. (19)
a1 b1 ticulate matter along with gaseous pollutants which affect
V d DHCl CHCl h c1
l b b the human health and environment severely. So, removal
HCl−FA s1 = K1 NaOH IE
( )
l l db of both particulate matter as well as gaseous pollutants is
d1
e1 very imperative. Therefore, in the present study, simultane-
Cflyash I l ous removal of HCl gas as well as fly ash has been carried
( ) (17)
g g out in a specially designed and fabricated self priming ven-
turi scrubber. Scrubbing of HCl gas and fly ash using 0.005 N
Here, inlet concentration of HCl (CFA IE ) is the outlet HCl con- NaOH solutions as scrubbing liquid was done at various water
centration at the end of diffuser section evaluated from the heights in outer cylinder, throat gas velocities, inlet HCl gas
empirical equation developed for the non-submerged condi- concentrations and inlet fly ash concentrations. Efficiency
tion. h is the distance between the outlet of venturi scrubber in removing of fly ash is found to be function of throat
and liquid height in outer cylinder. Bubble diameter and gas velocity, height of liquid and inlet fly ash concentration.
velocity were calculated by the equation reported in the lit- Maximum HCl removal, 98.3% is achieved at 60 m/s of throat
erature (Bal et al., 2019). gas velocity, 0.77 m of water height, 500 ppm of inlet HCl
concentration and 0.3 × 10−3 kg/m3 of inlet fly ash concentra-
d1
h c1 Cflyash I tion. On the other hand, maximum fly ash removal, 99.91%
HCl−FA s1 = K (Reb )a1 (Sc)b1 ( ) ( ) (18)
db g is obtained at 60 m/s of throat gas velocity, 0.77 m of water
Chemical Engineering Research and Design 1 5 0 ( 2 0 1 9 ) 311–319 319
height and 0.3 × 10−3 kg/m3 of inlet fly ash concentration. Kim, K.H., Kabir, E., Kabir, S., 2015. A review on the human health
Moreover the scrubbing of HCl gas about 7–10% enhancement impact of airborne particulate matter. Environ. Int. 74,
136–143.
in efficiency was observed in the presence of fly ash due to
Kohl, L., Riesenfeld, F.C., 1985. Gas Purification, second ed.
adsorption of HCl gas on the surface of fly ash particle. Exper-
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showed excellent fitting for the prediction of HCl removal effi- Kong, Y., Balland, J.P., 2011. Effective removal of HCl and SO2 with
ciency in the presence of fly ash. Thus it can be concluded dry injection of sodium bicarbonate or trona. Proceedings of
that the desired removal of gaseous pollutants along with the 19th Annual North American Waste-to-Energy Conference
the particulate matter can be achieved in self priming venturi (NAWTEC19).
Kraub, M., Rzehak, R., 2017. Reactive absorption of CO2 in NaOH:
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Acknowledgement Kurella, S., Meikap, B.C., 2016. Removal of fly-ash and dust
particulate matters from syngas produced by gasification of
Present work was supported by Department of Chemical coal by using a multi-stage dual-flow sieve plate wet scrubber.
Engineering, Indian Institute of Technology Kharagpur, West J. Environ. Sci. Health A 51 (10), 870–876.
Bengal, India. Levendis, 1998. Simultaneous Control of SO2 , NO2 , HCl, and
Particulates by In-furnace High-temperature Sorbent Injection
and Particulate Removal, U.S. Patent 5785936. Assigned to
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