Accepted Manuscript Performance evaluation of a lab-scale moving bed biofilm reactor (MBBR) using polyethylene as support material in the treatment of wastewater contaminated with terephthalic acid
Jiawei Liu, Jie Zhou, Ning Xu, Aiyong He, Fengxue Xin, Jiangfeng Ma, Yan Fang, Wenming Zhang, Shixun Liu, Min Jiang, Weiliang Dong PII:
S0045-6535(19)30638-1
DOI:
10.1016/j.chemosphere.2019.03.186
Reference:
CHEM 23500
To appear in:
Chemosphere
Received Date:
21 November 2018
Accepted Date:
29 March 2019
Please cite this article as: Jiawei Liu, Jie Zhou, Ning Xu, Aiyong He, Fengxue Xin, Jiangfeng Ma, Yan Fang, Wenming Zhang, Shixun Liu, Min Jiang, Weiliang Dong, Performance evaluation of a lab-scale moving bed biofilm reactor (MBBR) using polyethylene as support material in the treatment of wastewater contaminated with terephthalic acid, Chemosphere (2019), doi: 10.1016/j. chemosphere.2019.03.186
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ACCEPTED MANUSCRIPT
Performance evaluation of a lab-scale moving bed biofilm reactor (MBBR) using polyethylene as support material in the treatment of wastewater contaminated with terephthalic acid Jiawei Liua, Jie Zhoua,b, Ning Xua,c, Aiyong Hec, Fengxue Xina,b, Jiangfeng Maa,b, Yan Fanga,b, Wenming Zhanga,b, Shixun Liua, Min Jianga,b*, Weiliang Donga,b,*
aState
Key Laboratory of Materials-Oriented Chemical Engineering, College of
Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, 211800, P.R. China bJiangsu
National Synergetic Innovation Center for Advanced Materials (SICAM),
Nanjing Tech University, Nanjing, 211800, P.R. China cJiangsu
Key Laboratory for Biomass-based Energy and Enzyme Technology,
Huaiyin Normal University, Huaian, 223300, P. R. China
*Correspondence: Nanjing Tech University, Puzhu South Road No. 30, Nanjing 211800, P. R. China. Tel.: +86 25 58139933; Fax: +86 25 58139933 E-mail address:
[email protected] (W.L. Dong);
[email protected] (M. 1
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Jiang)
2
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Abstract
2
Untreated terephthalic acid (TPA) wastewaters with high organic loads will
3
cause severe environmental pollution problems. In this study, a lab-scale moving bed
4
biofilm reactor, where biomass of Delftia sp. WL-3 is attached to polypropylene
5
carrier elements, has been tested for TPA bioremediation at 25-27°C. The system
6
achieved stable operation after a short 15-day start-up period. During the operation
7
period of 65 days, stable chemical oxygen demand (COD) and TPA removal
8
efficiencies of 68% and 76% were maintained with an organic load rate (OLR) and
9
hydraulic retention time of 2.5 kg COD·(m3·d)-1 and 24 h, respectively. In addition,
10
the Scanning Electron Microscope (SEM) showed that high-densities of WL-3
11
biomass accumulated on the surface of the carrier and formed a rich biofilm,
12
indicating polypropylene carrier can improve the degradation efficiency. On the
13
contrary, the biodegradation ability of stain WL-3 without the polypropylene carrier
14
declined significantly with removal efficiencies of 10% and 15% for COD and TPA.
15
Furthermore, the system exhibited excellent robustness to different OLR and influent
16
matrix ratios, indicating its potential for applications in the treatment of
17
TPA-containment wastewater in the field.
18 19
Keywords
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Polypropylene carrier; moving bed biofilm reactor; TPA wastewater; Delftia sp.
21
WL-3. 3
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Highlights
27
28 29
the first time .
30 31
34
Polyethylene was used as the support material to enhance TPA biotreatment processes.
32 33
MBBR and Delftia sp. WL-3 were used for the treatment of TPA wastewater for
This reactor exhibited excellent adaptability to perturbations of different environmental factors.
This reactor indicated its potential for applications in the treatment of TPA-containing wastewater.
35 36 37 38 39 40 41 42 4
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1.
Introduction
49
Terephthalic acid (TPA) is one of the most important chemical products in the
50
world. It is widely used in the manufacture of polyester fibers, molded resin and
51
polyethylene terephthalate (PET) bottles (Kleerebezem et al. 2000). TPA manufacture
52
consumes a large amount of water in in the process of production, resulting in 3-10 m3
53
wastewater generation per ton of TPA produced. This wastewater has a chemical
54
oxygen demand (COD) of 5-20 kg·m3, and contains other chemical contaminants such
55
as terephthalate, acetate, benzoate and p-toluate (Kleerebezem et al., 1997; Macarie et
56
al., 1992).
57
TPA wastewaters with high organic loads can cause severe environmental
58
pollution problems (Young et al., 2000), inhibiting the growth of aquatic organisms
59
including fish and algae and having teratogenic and mutagenic effects on animals.
60
They can even harm human health through food chain enrichment, thereby causing
61
bladder cancer, damaging kidneys, liver and testes, as well as causing other organ
62
dysfunctions (Karthik et al., 2008). Consequently, the American Environmental
63
Protection Agency (EPA) has listed TPA as one of the priority environmental 5
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pollutants in 1978 (Kim et al., 2012). However, the treatment of TPA-containing
65
wastewater remains an urgent problem to be solved even forty years later
66
et al., 2008).
(Karthik
67
Bioreactors have advantages over physical and chemical processes, because they
68
can effectively remove a wide range of pollutants from wastewater in an
69
environmentally sound and cost-effective manner (Wang et al., 1998; Jaafari et al.,
70
2014; Seyedsalehi et al., 2018). The biological anaerobic reactors used to treat TPA
71
wastewater can be divided into up-flow anaerobic sludge blanket reactors (UASB),
72
anaerobic baffled reactors (ABR) and fluidized bed reactors (FBR) (Macarie et al.,
73
1992; Young et al., 2000; Karthik et al., 2008). However, anaerobic processes have
74
several disadvantages, including low biomass, low COD removal capacity, and
75
complex operation control systems. The moving-bed biofilm reactor (MBBR), which
76
uses an aerobic activated sludge process, has attracted considerable attention in recent
77
years (Calderón et al., 2012; Biswas et al., 2014; Chhetri et al., 2015).
78
Moving-bed biofilm reactor (MBBR), a completely mixed and continuously
79
operated biofilm reactor with much advantages of high sludge retention time while
80
requiring comparatively low HRTs, good tolerance to organic loading shocks, no
81
major sludge bulking issues and low risks regarding the clogging of carrier media,
82
was introduced about 30 years ago and is now used in large-scale operations all over
83
the world (Delnavaz et al., 2010; Jafari et al., 2013; Malovanyy et al., 2015). In
84
addition, the MBBR can support a higher biofilm density while maintaining favorable 6
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mass transfer characteristics by raising the amount of moving carrier or using a carrier
86
with a large effective biofilm surface area (Biswas et al., 2014; Canziani et al., 2006).
87
Therefore, the MBBR process has been recently implemented to treat wastewater with
88
a number of highly toxic pollutants, including landfill leachate (Chen et al., 2008),
89
aniline (Delnavaz et al., 2010), ammonium from saline wastewater (Bassin et al.,
90
2011), coal gasification wastewater (Li et al., 2011), thiocyanate (Jeongc et al., 2006)
91
and pharmaceutical wastewater from antibiotic fermentations (Xing et al., 2013).
92
However, we are not aware of any publications on the treatment of TPA wastewater
93
using a MBBR.
94
In this study, an aerobic MBBR with polyethylene as the support material and
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Delftia sp. WL-3 as bacterial sludge was used for the biodegradation of
96
TPA-containment wastewater. The performance of the aerobic reactor system was
97
evaluated under different operating conditions, including different influent TPA
98
concentrations, hydraulic retention time (HRT) values and sudden change factors.
99 100
2.
Materials and methods
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2.1
Simulated wastewater
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The synthetic TPA wastewater was prepared by adding the following reagents
103
into tap water (per liter of final liquid volume): 134 mg of NH4Cl, 65 mg of
104
K2HPO4·3H2O, 700 mg of TPA. A trace metal solution of 0.1% (v/v) was added
105
everyday, which contained 50, 50, 50, 50, 50, 50, 50, 30 mg·L-1 for H3BO3, ZnCl2, 7
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MnSO4H2O,
107
respectively (Feng et al., 2015). The prepared simulated wastewater had a COD of
108
1000 mg·L-1 and a COD:N:P ratio of 100:5:1. All chemical reagents were of
109
analytical grade or higher and were purchased from Sinopharm Chemical Reagent Co.
110
Ltd (Shanghai, China). The polypropylene carrier was obtained from KingFa Co. Ltd
111
(Guangzhou, China).
112
2.2
(NH4)6Mo7O244H2O,
AlCl3,
CoCl26H2O,
NiCl2,
and
CuCl2,
Lab-scale aerobic reactor system
113
The reactor was analogous to the industrial MBBR reactor system and was
114
developed for the continuous treatment of TPA wastewater. A schematic diagram of
115
the system is shown in Fig. 1. The 2.3-L reactor was made of organic glass with a
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diameter of 10 cm and height of 30 cm. The wastewater in the reactor was circulated
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from the top to the bottom to expand the bacterial sludge biomass, resulting in a
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working volume of 1.5 L. The recirculation flow rate of influent wastewater was
119
controlled by a variable-speed peristaltic pump, and was mixed in a TPA tank (T-I)
120
prior to introducing it into the reactor. The oxygen was provided by an oxygen pump
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connected to the reactor. The reactor was filled with the carrier to 45% of its active
122
volume, and the total amount of carrier was 0.675 L. The observed physical properties
123
of the polypropylene carriers were as follows: mean diameter (ɸ) 8.7 mm, specific dry
124
density 4.2 kg·m3 and specific surface area (Sa) 900 (m2·m-3). The system was tested
125
at various OLRs to achieve the most effective performance of the reactor. During the
126
experiments, the reactor was maintained at room temperature (25–27°C). 8
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2.3
Reactor set-up, inoculation and start-up
128
The reactor was filled with the simulated wastewater containing TPA as a carbon
129
source and inoculated with the WL-3 bacterial sludge. The WL-3 bacterial sludge was
130
composed of Delftia sp. strain WL-3, which was isolated from a secondary settling
131
tank in Sinopec Yangzi Petrochemical Co. Ltd (Nanjing, China) (Liu et al., 2018),
132
precultured in LB medium for 12 h and harvested by centrifugation at 6000 × g for 10
133
min, followed by washing twice with sterilized water. An aliquot comprising 7.50 g of
134
the bacterial sludge was used to inoculate 1 L of TPA wastewater, after which the
135
bacteria-wastewater mixture was slowly feed with the oxygen for several days and
136
then fed into the reactor at a low flow rate. The initial concentration of TPA in the
137
simulated wastewater was 500 mg·L-1. An oxygen pump was used in the reactor to
138
provide oxygen for the growth of the strain WL-3, which is aerobic. The biomass was
139
immobilized on the carriers and acclimatized though continuous feeding of TPA
140
wastewater over a period of 15 d. A reactor inoculated with the WL-3 bacterial sludge
141
without the carrier served as a control. The reactors with and without carrier material
142
were denoted as S1 and S2, respectively.
143
2.4 Experimental procedures
144
2.4.1 Determining the effect of influent COD concentration on the reactor
145
During the operation period, the reactor (S1) was started with 1.0 kg
146
COD·(m3·d)-1 OLR, 24 h HRT, under the conditions of varying COD values (1000,
147
1500, 2000, 2500 mg·L-1). The concentrations of TPA corresponding to the COD 9
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were 700, 1050, 1400 and 1750 mg·L-1 respectively. Each time the influent
149
concentration of COD was changed, an adaptation period of two days was provided,
150
followed by determination of COD and TPA concentration in the third day, and all
151
experiments were performed in triplicate.
152
2.4.2 Determining the effect of HRT on the reactor
153
During the operation period, the reactor (S1) was started with 2500 mg·L-1
154
influent COD concentration. The COD:N:P ratio was 100:5:1, and the HRT was
155
varied (24, 20, 16 and 12 h). Each time the HRT operating conditions were changed,
156
an adaptation period of two days was provided, followed by the determination of the
157
COD and TPA concentration in the third day and all experiments were performed in
158
triplicate.
159
2.4.3 Determining the effect of simultaneous changes of hydraulic retention time and
160
influent matrix ratio on the reactor
161
During the operation period, the reactor (S1) was started with 2500 mg·L-1
162
influent COD concentration, 24 h HRT and a COD:N:P ratio of 100:5:1. The influent
163
matrix ratio (COD:N:P) was changed from 100:5:1 to 300:5:1, and the HRT was
164
changed from 24 h to 12 h at the same time to examine the ability of the reactor to
165
resist simultaneous perturbations of multiple factors. The influent matrix ratio and
166
HRT were subsequently returned to the same value as before to examine the system’s
167
ability of self-recovery after damage. Concentrations of COD and TPA were
168
determined in the operation period and all experiments were performed in triplicate. 10
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2.5
Analytical methods
170
The concentration of TPA in the wastewater was measured by high performance
171
liquid chromatography (HPLC). Samples were collected at regular intervals, and
172
supernatant was harvested by centrifugation at 10000 × g for 10 min and then filtered
173
through a 0.22-μm nylon membrane for HPLC analysis using a Kromasil 100-5C18
174
column (4.6 mm × 250 mm; Agilent Technologies, China) with a mobile phase
175
comprising methanol:water (80:20, vol/vol) at a flow rate of 0.8 mL·min-1. The
176
detection wavelength was 240 nm, and the injection volume was 5 µL. The
177
concentration of COD was measured by the potassium dichromate method which used
178
potassium dichromate as oxidant (Jaafari et al., 2017).
179
The carrier samples were mildly washed with a 50 mM phosphate buffer (pH
180
7.0), fixed with glutaraldehyde in the phosphate buffer solution (2.5% w/v, pH 7.0)
181
and laid aside for 12 h. The fixed carrier samples were dehydrated with ethanol, dried
182
in a constant-temperature drying oven at 35°C (Kleerebezem et al., 2015). The
183
structure of the biofilm in the carrier samples finally observed via SEM (TM3000;
184
Hitachi, Tokyo, Japan) at a beam energy of 15 kV. Before examination, samples were
185
coated with a thin layer of gold using a sputter coater (Quorum Q 150 RS, Quorum
186
Technologies).
187
3. Results and discussion
188
3.1
189
Reactor design A schematic representation of the TPA wastewater treatment system consisted of 11
ACCEPTED MANUSCRIPT 190
the MBBR reactor, oxygen pump, feed tank and diaphragm metering pump is shown
191
in Fig. 1. The MBBR reactor was inoculated with a bacterial sludge comprising
192
Delftia sp. WL-3, which was identified in a previous study to have excellent TPA
193
degradation ability (Liu et al., 2018). Polypropylene material was selected as carrier
194
in the MBBR reactor because of its excellent abrasion resistance, longevity under
195
reactor conditions, and low price. Therefore, carriers do not need to be replaced
196
frequently, which simplifies the operability in the field and reduces the running costs.
197
In addition, the carrier is designed with a cross structure in the center, which can
198
increase the internal surface area of the carrier for microorganism attachment. When
199
the system was started, the carrier was mostly suspended in the upper middle of the
200
reactor after being soaked in the aqueous phase, while only a small amount settled at
201
the bottom of the reactor. Consequently, fluidization of the reactor bed can be
202
achieved with lower energy inputs. It is worth mentioning that this is the first time
203
that a MBBR is used for a TPA wastewater treatment system.
204
3.2
Start-up operation period of the reactor
205
During the start-up period (Fig. 2), both reactors (S1 and S2) were operated at a
206
low OLR (0.33 kg COD·(m3·d)-1) and a long HRT (36 h) to ensure microbial
207
adaptation and growth. On day 7 after the start of operation, the TPA-degrading strain
208
WL-3 could not adapt the reactor system with high COD in short order. Therefore, the
209
biofilm on the carriers was had difficulties forming, which resulted in poor removal
210
efficiencies of COD and TPA, which were lower than 30%. In the second stage (day 8 12
ACCEPTED MANUSCRIPT 211
to 15), the removal efficiencies of COD and TPA gradually increased to maximum of
212
66% and 78% respectively. The main reason is that the WL-3 sludge adapted to the
213
internal environment of the reactor, started to grow quickly and formed a mature
214
biofilm on the surface of carriers. Thus, both the biodegradation system and the
215
degradation ability of TPA reached equilibrium and stability. Finally, the MBBR
216
reactor containing polypropylene as carrier and Delftia sp. WL-3 as degrader strain
217
worked effectively after 15 days of running. By contrast, the corresponding removal
218
efficiencies of COD and TPA in reactor S2 reached only about 10% and 15%, after 15
219
days, which was significantly lower than that of reactor S1 (Fig. 2). It might be the
220
strains were taken out from the water outlet by the water flow easily in the reactor
221
without carriers. While in the reactor with carriers, the strains attached to the carrier,
222
then the increased the ventilation make them grow faster and they formed a mature
223
biofilm finally. These results also indicated that the polypropylene carriers play a key
224
role for improving the robustness and degradability of the system in the wastewater
225
purification process.
226
The start-up behavior is crucial for sewage treatment systems, because a shorter
227
start-up period can drastically improve the process economics (Chhetri et al., 2015).
228
The start-up period of the anaerobic fluidized bed reactor using brick beads and
229
porous ceramics as support materials was 34 d and 18 d, respectively (Chhetri et al.,
230
2015). In addition, a continuous stirred-tank reactor (CSTR) with selectively enriched
231
acidogenic mixed consortia needs 25 d to start up (Yan et al., 2004). A two-stage 13
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up-flow anaerobic sludge blanket (UASB) process which was investigated as an
233
efficient configuration option for the treatment of purified TPA wastewater takes 40 d
234
to start up (Kim et al., 2012). However, the reactor concept developed in this study
235
needs only 15 days to enter the stable operation period, which offers great advantages
236
during the start-up period for biodegradation of TPA wastewater.
237
3.3
Microscopy studies of the carrier
238
After 15 d, the surface of the polypropylene carrier in the reactor S1 was
239
observed using SEM. As shown in Fig. 3, the high-density strain WL-3 accumulated
240
and formed a dense biofilm on the surface of the polypropylene carrier while the
241
surface of the control polypropylene carrier not inoculated with strain WL-3 was
242
smooth and without biofilm. The polypropylene carrier provided a medium with a
243
large surface area for the formation and growth of biofilm. Therefore, the
244
polypropylene carrier is essential for the formation of a biofilm by strain WL-3 in the
245
TPA wastewater treatment system, which in turn improved the removal efficiency of
246
TPA. It was also reported that a mature biofilm on the carrier plays a key role in the
247
removal of organic contaminants (Yan et al., 2004).
248
3.4
249
3.4.1 Effect of influent COD concentration on the reactor
Steady-state operation period of the reactor
250
This study simulated a medium-strength TPA wastewater and evaluated the
251
effect of environmental perturbations on the reactor by changing the concentration of
252
influent COD, which was divided into four stages according to different COD 14
ACCEPTED MANUSCRIPT 253
concentrations.
254
The first stage is the start-up and stabilization period of the reactor with an
255
average concentration of influent COD of 1000 mg·L-1. During this stage, the
256
microorganisms could not adapt to the high-pollution environment, which resulted in
257
slow growth and difficulty in forming a biofilm, resulting in a low removal efficiency
258
of COD which fluctuated between 31.5% and 66.6%. Subsequently, the average COD
259
concentration of the influent was increased to 1500 and 2000 mg·L-1 in the second
260
and third stages, respectively. The removal efficiencies of COD and TPA in the two
261
stages were in a stable up-ward trend. However, the reactor still could not achieve the
262
ideal biodegradation effect. The main reason is that the microorganisms attached to
263
the surface of the carrier or in the suspended state have not yet reached their maximal
264
biomass, in which limited the removal efficiencies of COD and TPA. When the
265
reactor entered the fourth stage, the average COD concentration of the influent was
266
raised to 2500 mg·L-1, which was realistic for organically contaminated wastewater in
267
the field. In this stage, the removal efficiencies of COD and TPA were nearly ideal,
268
reaching 68% and 76%, respectively (Fig. 4). In summary, the change of influent
269
COD concentration did not have a negative impact on the system and the biomass in
270
the carrier reacted with a significant increase.
271
3.4.2 Effect of HRT on the reactor
272
HRT, which refers to the average residence time of the sewage to be treated in
273
the reactor, is one of the most important parameters of biological sewage treatment, 15
ACCEPTED MANUSCRIPT 274
which. It is the average reaction time of the sewage and the microorganisms in the
275
bioreactor (Fernández et al., 2008). As shown in Fig. 5a, the effluent COD
276
concentration gradually decreases as the hydraulic retention time increased, and the
277
average removal efficiency increased from 36% at 12 h to 68% at 24 h. At the same
278
time, the removal efficiency of COD increased significantly from 12 to 20 h with an
279
average value of 66%. Furthermore, the COD removal efficiency tended to be
280
relatively stable from 20 to 24 h. Similarly, the degradation trend of TPA was
281
consistent with that of COD as the HRT increased. As shown in Fig. 5b, the average
282
removal efficiency of TPA increased from 40% at 12 h to 76% at 24 h, after which it
283
tended to be stable.
284
3.4.3 Effect of simultaneous change of HRT and influent matrix ratio on the reactor
285
When the ratio of COD:N:P was changed to 300:5:1 and the HRT reduced from
286
24 to 12 h at the same time, the removal efficiencies of COD and TPA drastically
287
decreased. The respective average values dropped from 68% and 75% to 50% and
288
60%, respectively, indicating that the simultaneous change of two environmental
289
factors had an extremely adverse effect on the system. When the COD:N:P ratio was
290
changed to 100:5:1 and HRT was changed to 24 h, the same as the previous
291
conditions, the removal efficiency of COD and TPA increased to 65% and 72%,
292
respectively. Thus, while the concomitant changes of multiple conditions had a
293
serious impact on the system, it did not collapse, and actually retained the capacity for
294
self-repair when returned to the previous conditions. 16
ACCEPTED MANUSCRIPT 295
Compared with other TPA wastewater reactor treatment systems (Table 1),
296
Continuous stirred-tank reactor demonstrated higher OLR and lower HRT while the
297
COD removal efficiency is relatively lower of 45%. Although the MBBR
298
demonstrated a lower OLR and higher HRT, it had a higher COD removal efficiency
299
of 68%. Moreover, this moderate OLR and HRT are still believed to be acceptable
300
considering that a MBBR has never been reported to treat TPA wastewaters. If the
301
working volume of the MBBR could be increased, the OLR could have been much
302
improved. As a lab-scale moving bed biofilm reactor, expansion of the installation
303
will be helpful in improving the performance during wastewater treatment and more
304
data on using the reactor for the degradation of true industrial TPA-containing
305
wastewater should be gathered in future studies.
306
4. Conclusions
307
In this study, a lab-scale moving bed biofilm reactor with polypropylene
308
elements as carriers for bacterial sludge comprising Delftia sp. WL-3 was designed
309
for the treatment of TPA-containing wastewater. The system had a start-up period of
310
15 days, and showed stable operation during 65 days with COD and TPA removal
311
efficiencies of 68% and 76% at OLR and HRT of 2.5 kg COD·(m3·d)-1 and 24 h,
312
respectively. Furthermore, the system exhibited excellent adaptability to perturbations
313
of different environmental factors, including influent TPA concentration and HRT, as
314
well as sudden changes of factors, indicating its potential for applications in the
315
treatment of TPA-containing wastewater. 17
ACCEPTED MANUSCRIPT 316 317
Acknowledgements
318
This work was supported by the National Natural Science Foundation of China
319
(31700092, 21706125, 21727818 and 21706124), the Jiangsu Province Natural
320
Science Foundation for Youth (BK20170997, BK20170993), the Jiangsu Synergetic
321
Innovation Center for Advanced Bio-Manufacture (XTE1834), the Key Science and
322
Technology Project of Jiangsu Province (BE2016389), Project of State Key
323
Laboratory of Materials-Oriented Chemical Engineering (KL17-09), the China
324
Postdoctoral Innovative Talents Support Program (BX20180140), the Open
325
Foundation of Jiangsu Key Laboratory for Biomass-Based Energy and Enzyme
326
Technology (BEETKB1801) and Postgraduate Research & Practice Innovation
327
Program of Jiangsu Province (KYCX18-1114).
328 329
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ACCEPTED MANUSCRIPT Credit Author Statement: Jiawei Liu, Jie Zhou, Ning Xu, Weiliang Dong did the experiments and writed this manuscript. Aiyong He, Fengxue Xin, Jiangfeng Ma and Wenming Zhang analyzed the data and made the figures and tables. Jiawei Liu, Jie Zhou and Weiliang Dong drafted the manuscript. Shixun Liu and Min Jiang revised the review. All authors read and approved the final version.
ACCEPTED MANUSCRIPT Figure Captions Figure 1. Schematic diagram of the lab-scale MBBR system. Figure 2. COD and TPA removal efficiencies in the reactor with polypropylene carriers (S1) and without polypropylene carriers (S2) during the start-up period. (a) COD removal efficiency; (b) TPA removal efficiency. Figure 3. Scanning electron micrograph of the surface of the polypropylene carrier. (a) The surface of polypropylene carriers not inoculated with strain WL-3; (b) the surface of polypropylene carriers inoculated with strain WL-3. Figure 4. Effect of different influent COD and TPA concentrations on the reactor S1 during the operation period. (a) The concentrations of influent and effluent COD; (b) the concentrations of influent and effluent TPA. Figure 5. Effect of different HRT on the reactor S1 during the operation period. (a) The concentrations of influent and effluent COD; (b) the concentrations of influent and effluent TPA. Figure 6. Effect of simultaneously changing HRT and the influent matrix ratio on the reactor S1.
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2 3 4 5 6 7 8 9 10 11 12 13 14 15
Figure 1
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18 19 20 21 22 23
Figure 2
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25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40
Figure 3
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42 43 44 45 46 47
Figure 4
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49 50 51 52 53 54 55 56
Figure 5
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Figure 6
ACCEPTED MANUSCRIPT Highlights
MBBR and Delftia sp. WL-3 were used for the treatment of TPA wastewater for the first time .
Polyethylene was used as the support material to enhance TPA biotreatment processes.
This reactor exhibited excellent adaptability to perturbations of different environmental factors.
This reactor indicated its potential for applications in the treatment of TPAcontaining wastewater.
Table 1. Performance of different reactor systems treating TPA wastewater
Anaerobic fixed film fixed bed
Influent COD
OLR
HRT
(mg·L-1)
(kg COD·(m3·d)-1)
(h)
5,000
4-5
24
COD removal efficiency (%) 62
reactor Anaerobic filter
References (Pophali et al., 2007)
-
5.05
50
79
(Joung et al., 2009)
Internal circulation anaerobic reactor
1,100-1,600
-
10
50
(Huang et al., 2009)
Continuous stirred-tank reactor
4,000
16
6
45
(Zhu et al., 2010)
Anaerobic sludge blanket reactor
-
2.6
3
46.4
(Guyot et al., 1990)
Moving bed biofilm reactor
2500
2.5
24
68
This study