Pharmaceutical Wastewater Treatment Research Articles

Treatment of pharmaceutical industry wastewater for water reuse in Jordan using hybrid constructed wetlands

Developing cost-efficient wastewater treatment technologies for safe reuse is essential, especially in developing countries simultaneously facing water scarcity. This study developed and evaluated a hybrid constructed wetlands (CWs) approach, incorporating tidal flow (TF) operation and utilising local Jordanian zeolite as a wetland substrate for real pharmaceutical industry wastewater treatment. Over 273 days of continuous monitoring, the results revealed that the first-stage TFCWs filled with either raw or modified zeolite performed significantly higher reductions in Chemical Oxygen Demand (COD, 58 %–60 %), Total Nitrogen (TN, 32 %–37 %), and Phosphate (PO4, 46 %–64 %) compared to TFCWs filled with normal sand. Water quality further improved after the second stage of horizontal subsurface flow CWs treatment, achieving log removals of 1.09–2.47 for total coliform and 1.89–2.09 for E. coli. With influent pharmaceutical concentrations ranging from 275 to 2000 μg/L, the zeolite-filled hybrid CWs achieved complete removal (>98 %) for ciprofloxacin, ofloxacin, erythromycin, and enrofloxacin, moderate removal (43 %–81 %) for flumequine and lincomycin, and limited removal (<8 %) for carbamazepine and diclofenac. The overall accumulation of pharmaceuticals in plant tissue and substrate adsorption accounted for only 2.3 % and 4.3 %, respectively, of the total mass removal. Biodegradation of these pharmaceuticals (up to 61 %) through microbial-mediated processes or within plant tissues was identified as the key removal pathway. For both conventional pollutants and pharmaceuticals, modified zeolite wetland media could only slightly enhance treatment without a significant difference between the two treatment groups. The final effluent from all hybrid CWs complied with Jordanian treated industry wastewater reuse standards (category III), and systems filled with raw or modified zeolite achieved over 95 % of samples meeting the highest water reuse category I. This study provides evidence of using hybrid CWs technology as a nature-based solution to address water safety and scarcity challenges.

Artificial intelligence and machine learning for the optimization of pharmaceutical wastewater treatment systems: a review

AbstractThe access to clean and drinkable water is becoming one of the major health issues because most natural waters are now polluted in the context of rapid industrialization and urbanization. Moreover, most pollutants such as antibiotics escape conventional wastewater treatments and are thus discharged in ecosystems, requiring advanced techniques for wastewater treatment. Here we review the use of artificial intelligence and machine learning to optimize pharmaceutical wastewater treatment systems, with focus on water quality, disinfection, renewable energy, biological treatment, blockchain technology, machine learning algorithms, big data, cyber-physical systems, and automated smart grid power distribution networks. Artificial intelligence allows for monitoring contaminants, facilitating data analysis, diagnosing water quality, easing autonomous decision-making, and predicting process parameters. We discuss advances in technical reliability, energy resources and wastewater management, cyber-resilience, security functionalities, and robust multidimensional performance of automated platform and distributed consortium, and stabilization of abnormal fluctuations in water quality parameters.

Progress in bioproduction, characterization and applications of pullulan: a review

AbstractPullulan is a biopolymer produced by various strains of the fungi Aureobasidium pullulans. It is made up of maltotriose units consisting of α-(1,6) and α-(1,4) glycosidic bonds. Pullulan was discovered by Bauer in 1938, characterized by Bernier in 1958 and named as ‘pullulan’ by Bender in 1959. Submerged fermentation is widely employed for pullulan production followed by downstream processing for recovery of pullulan. Factors such as nutrients, minerals, pH, temperature, surfactants, light intensity, and melanin intermediate affect its production. Various optimization methods such as Plackett Burman design, response surface methodology, and artificial neural networks have been utilised for enhancing the yield of pullulan. Pullulan yield as high as 62.52 g/L can be achieved using a 5 L fermenter under optimised conditions. It can be characterized by techniques such as nuclear magnetic resonance, Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy. The biopolymer has remarkable properties which makes it an ideal candidate to be used in various applications such as the biomedical and pharmaceutical sectors, cosmetics, food, and wastewater treatment. Pullulan’s applications can be expanded by chemically modifying to obtain grafted pullulan, polymer blends, nanocomposites and hydrogels which have been gaining importance in recent years. Over the years, many patents using pullulan have been granted for different applications worldwide. This review sheds light on all these aspects of pullulan including its future scope. Graphical abstract

Sequential high-recovery nanofiltration and electrochemical degradation for the treatment of pharmaceutical wastewater

The presence of antibiotics in aquatic ecosystems poses a significant concern for public health and aquatic life, owing to their contribution to the proliferation of antibiotic-resistant bacteria. Effective wastewater treatment strategies are needed to ensure that discharges from pharmaceutical manufacturing facilities are adequately controlled. Here we propose the sequential use of nanofiltration (NF) for concentrating a real pharmaceutical effluent derived from azithromycin production, followed by electrochemical oxidation for thorough removal of pharmaceutical compounds. The NF membrane demonstrated its capability to concentrate wastewater at a high recovery value of 95 % and 99.7 ± 0.2 % rejection to azithromycin. The subsequent electrochemical oxidation process completely degraded azithromycin in the concentrate within 30 min and reduced total organic carbon by 95 % in 180 min. Such integrated treatment approach minimized the electrochemically-treated volume through a low-energy membrane approach and enhanced mass transfer towards the electrodes, therefore driving the process toward zero-liquid-discharge objectives. Overall, our integrated approach holds promises for cost-effective and sustainable removal of trace pharmaceutical compounds and other organics in pharmaceutical wastewater.

Efficient denitrification of pharmaceutical wastewater using a coral-like CuO-ZIF-Co/NF cathode through reasonable matching of nitrate and nitrite reduction

Electrochemical NO3− reduction reaction (NO3RR) is an effective method for removing nitrate from industrial wastewater. The commonly used Cu based cathode can effectively reduce NO3− to NO2−. However, how to achieve a reasonable match between NO3− reduction and subsequent NO2− reduction is a key scientific issue in improving the efficiency of electrochemical NO3RR. A coral-like CuO-ZIF-Co/NF cathode is synthesized through the electrodeposition of Cu particles on the surface of ZIF-Co/NF skeleton combined with annealing. Excessive 2-methylimidazole in ZIF-Co is prone to self-deprotonation which enables effective binding of Co3O4 and CuO on the surface. Electrochemical characterizations reveal that compared to NO3−-N reduction, CuO-ZIF-Co/NF has lower over potential and faster reduction rate for NO2−-N reduction. Further kinetic studies also exhibit that the removal rate of NO2−-N by CuO-ZIF-Co/NF is 1.4 times higher than that of NO3−-N. This difference in reduction rate results in CuO-ZIF-Co/NF exhibiting higher rates of NO3−-N removal (0.97 mg-N (L∙min)-1) and NH4+-N generation (0.37 mg-N (L∙min)-1) than other reported materials at the current density as low as 10 mA cm−2, without any accumulation of NO2−-N during the NO3RR. Moreover, the electrode has shown excellent advantages in the actual pharmaceutical wastewater treatment process. It can not only remove the total nitrogen below the WHO emission limit standard, but also remove hardness and COD from the wastewater simultaneously.

Ultra-efficient decontamination via functionalized reactive electrochemical membrane for peroxymonosulfate activation: High water flux with extremely low energy consumption

A perovskite LaCoO3 functionalized Ti4O7 reactive electrochemical membrane (REM) was developed for electro-enhanced peroxymonosulfate (PMS) activation (E-REM-PMS), addressing limitations in wastewater treatment efficiency, reusability, and interference resistance. It achieved 100% carbamazepine (CBZ) removal at a rate constant of 39.69 min−1, 233 and 23 times of electro-REM (E-REM) system without PMS and REM-PMS system without electricity. In-situ Fourier transform infrared spectroscopy (FTIR) highlighted the promotion of electro-activation on PMS, while density functional theory (DFT) calculations elucidated mechanism differences under three adsorption configurations. 1O2 (2.97×10−9 M), SO4•− (2.09×10−11 M) and •OH (7.36×10−12 M) dominated the E-REM-PMS system, consistent with sequence of reactive species by DFT results. Continuous treatment of pharmaceutical wastewater confirmed 100% CBZ removal and 60%-70% TOC mineralization at ultrahigh water flux (642.86 L/m2·h) with minimal energy consumption (0.01 kWh/m3·order). This work proposed a high-performance and anti-fouling REM, offering an efficient and economical solution for wastewater treatment.

Treatment of pharmaceutical wastewater by a sequential KMnO4/CoFe2O4-mediated catalytic ozonation process

Pharmaceutical compounds, which are of utmost concern, have found their way into natural water bodies, causing numerous problems for both human health and ecosystems. In this study, an integrated system including potassium permanganate (PM) pre-oxidation, followed by a heterogeneous catalytic ozonation process (HCOP) using CoFe2O4 magnetic nanoparticles (CF MNPs), and an activated sludge-based biological treatment (BT) was employed for the first time to treat pharmaceutical wastewater (PWW). In this regard, the effluent from PM pre-oxidation process was used as a batch for the HCOP, and the effluent was used as a batch for the BT process. The results showed that PM pre-treatment of PWW (PM dose = 1264 mg/L and pH = 8.0) reduced the COD content of the PWW from 900 ± 50 to 443 ± 10 mg/L within 120 min of reaction time. The application of HCOP for further treatment of PWW dramatically enhanced COD and TOC removal compared with the single ozonation process (SOP). Under optimum conditions (pH = 10, O3 = 4.0 mg/L, and CF MNPs = 1000 mg/L), HCOP successfully reduced the COD and TOC contents of PWW by 37 % and 46.1 %, respectively, after 120 min of treatment. The consecutive combination of PM pre-treatment followed by HCOP exhibited good potential and reduced COD by over 69 %, resulting in a residual COD of less than 280 mg/L. A biodegradability ratio of over 81 % and residual COD of 54 mg/L for the PWW treated by the PM/HCOP/BT integrated system indicated that biodegradability was enhanced, and a high fraction of refractory organic compounds was effectively removed. In conclusion, the PM/HCOP/BT integrated system is an efficient, synergistic, and easy-to-operate technique for enhancing the biodegradability of PWW.

Kumquat peel-derived biochar to support zeolitic imidazole framework-67 (ZIF-67) for enhancing peracetic acid activation to remove acetaminophen from aqueous solution

This study presents the synthesis of a novel composite catalyst, ZIF-67, doped on sodium bicarbonate-modified biochar derived from kumquat peels (ZIF-67@KSB3), for the enhanced activation of peracetic acid (PAA) in the degradation of acetaminophen (APAP) in aqueous solutions. The composite demonstrated a high degradation efficiency, achieving 94.3% elimination of APAP at an optimal condition of 200 mg L−1 catalyst dosage and 0.4 mM PAA concentration at pH 7. The degradation mechanism was elucidated, revealing that superoxide anion (O2•−) played a dominant role, while singlet oxygen (1O2) and alkoxyl radicals (R–O•) also contributed significantly. The degradation pathways of APAP were proposed based on LC-MS analyses and molecular electrostatic potential calculations, identifying three primary routes of transformation. Stability tests confirmed that the ZIF-67@KSB3 catalyst retained an 86% efficiency in APAP removal after five successive cycles, underscoring its durability and potential for application in pharmaceutical wastewater treatment.

The Solvent Role for the Decomposition of Paracetamol in Distilled and Drinking Water by Pure and Ag-Modified TiO2 Sol-Gel Powders.

In this study, pure TiO2 gels were synthesized by applying the sol-gel method, using Ti(IV) butoxide with the addition of two different solvents, namely ethylene glycol (EG) and isopropanol (isop), with only air moisture present. It was established using XRD that the gel prepared with the addition of EG was amorphous even at 400 °C, while the other gel was amorphous up to 300 °C. It was found that TiO2 (anatase) had a dominant crystalline phase during heating to 600 °C, while at 700 °C, TiO2 (rutile) appeared. The as-obtained powdered materials were annealed at 500 °C and subsequently underwent photocatalytic tests with paracetamol. Additionally, the TiO2 samples were modified with Ag+ co-catalysts (10-2 M), using photofixation by UV illumination. The photocatalytic activity of the Ag-modified powders was also tested in the photodegradation of a commonly used paracetamol in aqueous solution under UV light illumination. The obtained data exhibited that the annealed samples had better photocatalytic efficiency and decomposed paracetamol faster in comparison to the non-annealed sol-gel powders. The highest degradation efficiency was observed for the TBT/isop/Ag material, with degradation efficiencies average values of 65.59% and 75.61% paracetamol achieved after the third cycle of photocatalytic treatment. The co-catalytically modified powders had higher photocatalytic efficiency in comparison to the pure nanosized powders. Moreover, the sol-gel powders of TBT/EG, TBT/EG/Ag (10-2 M), TBT/isop, and TBT/isop/Ag (10-2 M) demonstrated the ability to retain their photocatalytic activity even after three cycles of use, suggesting that they could find practical use in the treatment of pharmaceutical wastewater. The observed photocatalytic efficiency and positive impact of silver make the prepared powders a desirable choice for pharmaceutical drug degradation, helping to promote environmentally friendly and effective wastewater treatment technology.

Novel Ganga-sand-encapsulated polyaniline granules for effective remediation of textile and pharmaceutical wastewater

ABSTRACT This study presents the use of novel Ganga-sand-encapsulated polyaniline granules for effective remediation of textile and pharmaceutical wastewater. The prepared Ganga-sand-encapsulated polyaniline granules were characterised using scanning electron microscope (morphology) and Fourier transform infrared techniques. The effect of adsorbent dose, contact time, pH and concentration influence on the adsorption performance of Ganga-sand-encapsulated polyaniline granules for the removal of methylene blue dye (textile waste) and doxycycline antibiotic (pharmaceutical waste) was studied. Kinetic and isotherm studies were also carried out to investigate the adsorption process further. The maximum adsorptive removal efficacy of methylene blue and doxycycline was found as 98.2% and 85.1%, respectively, at the optimised condition of adsorbent dose: 8 g/L, time: 120 min, pH: 12 and concentration: 50 ppm. From adsorption kinetics, it was established that the adsorption process followed pseudo-second-order (PSO) rather than pseudo-first-order (PFO). The correlation coefficient values for PFO and PSO models were 0.9012 and 0.9992, respectively, for methylene blue dye adsorption on Ganga-sand-encapsulated polyaniline granules. The adsorption isotherm study established that the adsorption process followed the Langmuir model rather than the Freundlich model. This study found that Ganga-sand-encapsulated polyaniline granules can be a promising adsorbent for textile and pharmaceutical wastewater treatment.

Factors affecting the performance of a pharmaceutical wastewater treatment plant: Characterization of effluent and environmental risk

Pharmaceutical industries produce a huge volume of emerging pollutants (EPs) that pose a threat to the aqueous environment. Biological processes have shown their inefficacy in treating many pharmaceutical products. The study assessed physicochemical parameters, EPs, heavy metals in pharmaceutical industrial wastewater, and the removal efficiency (RE) of an aerobic biological treatment plant. The study also assessed the contamination levels and risk using several indices, such as the Canadian Council of Ministers of the Environment Water Quality Index (CCME-WQI), heavy metal pollution index (HPI), heavy metal evaluation index (HEI), and risk quotients index (RQs). The study found that the treated water quality was poor, having antibiotics, nonsteroidal anti-inflammatory drugs, and others, along with several transformation products (TPs) and heavy metals, which were unsafe for consumption with high environmental risk. The analysis results showed that the RE for TSS, BOD5, COD, TDS, and EC were found to be 91.80%, 86.81%, 72.29%, 72.20%, and 65.60%, respectively, where the values of BOD5, COD, NO3−, and PO43− in the effluent were still higher than the permissible limits of the ECR (2023). However, the RE for heavy metals was in the order of Cu (84.62%) > Fe (65.04%) > Mn (63.3%) > Zn (60.58%) > Cd (53.85%) > Ni (54.12%) > Pb (42.42%) > Cr (38%), where Cr and Cd concentrations were still higher than the permissible limit of DoE (2019). The Pearson correlation and PCA suggested that EC, TDS, TSS, DO, BOD5, and COD were the most correlating and contributing variables. This study argued that metal-ligand behaviors mainly affect the removal efficiency of the treatment plant by lowering the removal rate of heavy metals and pharmaceutical products.

Combination of membrane bioreactor with chemical coagulation for the treatment of real pharmaceutical wastewater: Comparison of simultaneous and consecutive pre-treatment of coagulation on MBR performance

In this work, the combination of the coagulation process with the MBR system to reclaim effluent in pharmaceutical industries was investigated. In this research, comparison/concentration optimization of two modes of integrations, including simultaneous; one-step one pot, and consecutive coagulation MBR were investigated. Results showed that COD removal in simultaneous and consecutive modes at optimum values were 85 % and 95.8 %, respectively, which were considerably higher than that of control MBR; 53.89 %. The total fouling ratio for control MBR, simultaneous, and consecutive modes at optimum conditions were 70.69 %, 37.3 %, and 42.5 %, respectively, confirming that the integrated coagulation process and MBR system were considerably effective. Analyzing the secreted metabolite, e.g. protein, carbohydrate, and LB/TB-EPS ratio in the MBR tank as well as on the membrane surface showed that the charge-neutralization and entrapment of bio-foulants by aggregated clots during the coagulation hinder the adhesion of the biofouling agents on the membrane surface, therefore in-line with the flux attenuation trend, lower metabolite concentration results in less membrane fouling. It was found that simultaneous coagulative MBR with 100 mg/L FeCl3 concentration demonstrates better fouling mitigation in comparison with consecutive (even with poly aluminum chloride; PACl as coagulant aid) MBR, while the latter mode shows better performance in terms of wastewater treatment. These findings open avenues for future techno-economic assessments of a coagulation-assisted MBR, providing a cost-effective solution for treating high-strength wastewater on a larger scale.

Phytotoxicity and genotoxicity assessment of organic and inorganic contaminants detected in pharmaceutical industrial wastewaters using Vigna radiata and Allium cepa

The discharged effluent of pharmaceutical industrial wastewater treatment plants (PIWWTPs) exhibits substantial environmental toxicity due to the intricate combination of organic and inorganic pollutants. This study assessed the phytotoxicity, genotoxicity, and cytotoxicity of untreated and treated pharmaceutical industrial wastewater (PIWW). Most of the physicochemical parameters viz. COD, BOD, EC, sulfide, sulfate, nitrate, phosphate, grease, phenols, and metal concentrations viz. B, Cr, Ca, Cd, Cu, Zn, Pb, Hg, and As in untreated wastewater (UTW) were noted beyond the permissible limit and remained higher in treated wastewater (TW). The findings revealed that the performance of PIWWTP was woefully inadequate. The GC-MS spectra of UTW and TW revealed the presence of various organic contaminants. The toxicological studies showed that the UTW had a high degree of phytotoxicity, which persisted even after the treatment as it inhibited the seed germination in Vigna radiata. The seed germination was inhibited up to 70% and 50% tested at 50% concentration of UTW and TW respectively. Genotoxicity was measured by determining mitotic index and chromosomal aberrations in Allium cepa root apex grown in untreated and treated PIWW. Compared to the negative control, the mitotic index dropped to 85% and 75% at the 50% concentrations of UTW and TW, respectively. Chromosomal aberrations were also found in the cellular mass of root apex growing in both UTW and TW. According to the findings, it is unsafe for the environment to release PIWW that has not been properly treated, as this could pose serious risks to environmental health.

In-situ active sites analysis of bifunctional metal-organic frameworks for coupled adsorption and electrochemical oxidation of PPCPs

Pharmaceuticals and personal care products (PPCPs) pose a significant wastewater pollution concern. While electrochemical oxidation is promising, it struggles with slow mass transfer. To address this, we propose a novel strategy utilizing bifunctional metal–organic frameworks (MOFs) that couple an adsorbent with an electrocatalyst. The real active sites within iron-based MOFs responsible for the adsorption of PPCPs are MIL-101(Fe) molecules, while the in-situ formed active sites, α-FeOOH, accelerate the charge transfer under bias, contributing to the electrooxidation of PPCPs. The rapid destruction of adsorbed organics on the dual-functional electrode surface enables to release adsorption sites. This, in turn, paves the way for fast and efficient re-adsorption of PPCPs molecules, consequently promoting mass transfer. Iron-based MOFs exhibit excellent adsorption capacity (∼60 mg g−1 for sulfosalicylic acid, ∼15 mg g−1 for acetaminophen) and electrooxidation ability (94 % removal in 2 h, 31.2 kWh kg−1 COD) with good stability in realistic pharmaceutical wastewater treatment. This study offers a novel strategy for removing PPCPs using molecular electrocatalysts and provides new insights for designing and constructing MOFs for refractory wastewater treatment.

Blighia sapida Waste Biochar in Batch and Fixed-Bed Adsorption of Chloroquine Phosphate: Efficacy Validation Using Artificial Neural Networks.

The present study investigated the potency of biochar prepared from Blighia sapida seedpods (BSSPs) in the uptake of chloroquine phosphate (CQP) from single-component batch and multicomponent fixed-bed adsorption systems. BSSPs presented a highly porous structure with a BET surface area of 1122.05 m2/g, to which adsorption efficiency correlated. The Dubinin-Radushkevich isotherm energy was obtained as 129.09 kJ/mol, confirming the chemisorption nature of the BSSP-CQP adsorption system. The efficiency of the artificial neural network (ANN) was evaluated using the lowest mean square error (MSE = 7.27) and highest correlation coefficient (R2 = 0.9910). A good agreement between the experimental results and the ANN-predicted data indicated the efficiency of the model. The percentage removal of 95.78% obtained for the column adsorption studies indicated the effectiveness of BSSPs in a multicomponent system. The mechanism of the interaction proceeded via hydrogen bonding and electrostatic attraction. This was confirmed by the high desorption efficiency (69.11%) with a HCl eluent. The degree of reversibility was found to be 2.95, indicating the reusability potential of BSSPs. BSSPs are therefore considered multilayered adsorbents with potential applications in pharmaceutical wastewater treatment.

WITHDRAWN: Clean production of a new activated carbon/tungstate composite from olive mill wastewater for the removal of diclofenac and paracetamol: Adsorption mechanism and transition state

A new carbon/tungstate composite based on liquid by-products, in particular olive mill wastewater (OMWW), was used to remove diclofenac and paracetamol, by adsorption. The composite was prepared using a clean method based on the addition of dissociated tungstate in hydrogen peroxide (H2O2), combined with single carbonization at 950 °C for 5 min. To study the effect of tungstate on composite properties, 4 carbon/tungstate combinations, varying as a function of the mass content of tungstate added, were studied: 0, 1, 2 and 3%wt. The optimum combination showed significant porosity, thermal stability and a wealth of sites suitable for adsorption. The adsorption tests showed that the Freundlich and double-layer adsorption models best described the equilibrium relationship, while the pseudo-second-order model best described the kinetics, regardless of adsorbate. Moreover, high saturation adsorption capacities, for diclofenac (712 mg g−1) and paracetamol (517 mg g−1), were obtained. Non-steric results showed a double-layer adsorption in a parallel orientation and an interaction ratio of 3 sites per molecule. The Activation parameters confirmed rapid adsorption kinetics, physical interactions and easy desorption from the surface. The chemical mechanism was governed by bi/tridentate interactions with a predominance of π-π interactions. The treatment of a real pharmaceutical wastewater with a chemical oxygen demand of 8.1 g(O2).L−1 resulted in 89% removal. Overall, this work presents a new clean solution for the capture of pharmaceutical molecules from water and a detailed presentation of adsorption mechanisms, in particular: chemical, physical, non-steric and at the transition state.

Ce/Fe bimetallic MOF derivatives in situ modified bulk carbon aerogel composite cathode for efficient heterogeneous electro-fenton degradation of chloramphenicol

In this study, we utilized a Ce-modified iron-based metal-organic framework derivative to in situ modify bulk CA (Ce/Fe@C-CA) as a bifunctional composite cathode to degrade chloramphenicol (CAP) in the heterogeneous electro-Fenton (EF) process. The composite cathode exhibited satisfactory CAP degradation efficiency, wide pH adaptability (2–9) and low metal leaching. Under the appropriate conditions (pH = 5, current density = 6 mA/cm2), 94.89% of CAP degradation efficiency was obtained within 60 min. The introduction of Ce increased the oxygen vacancy content, enhanced the cathodic electrochemical activity, promoted the production of a variety of reactive oxygen species and participates in the degradation of CAP, of which ·OH and 1O2 were dominant. Meanwhile, the electron transfer and synergistic catalysis between Ce and Fe promoted the regeneration of the metal active site, which was beneficial to improve the reuse stability of the Ce/Fe@C-CA cathode. The degradation pathway of CAP was obtained by DFT calculations and UPLC-MS/MS detection. This study not only proposed a novel bifunctional electro-Fenton cathode, but also provided a effective strategy for the treatment of actual pharmaceutical wastewater.

Reduction characteristic of chlorobenzene by a newly isolated Paenarthrobacter ureafaciens LY from a pharmaceutical wastewater treatment plant.

A highly efficient chlorobenzene-degrading strain was isolated from the sludge of a sewage treatment plant associated with a pharmaceutical company. The strain exhibited a similarity of over 99.9% with multiple strains of Paenarthrobacter ureafaciens. Therefore, the strain was suggested to be P. ureafaciens LY. This novel strain exhibited a broad spectrum of pollutant degradation capabilities, effectively degrading chlorobenzene and other organic pollutants, such as 1, 2, 4-trichlorobenzene, phenol, and xylene. Moreover, P. ureafaciens LY co-metabolized mixtures of chlorobenzene with 1, 2, 4-trichlorobenzene or phenol. Evaluation of its degradation efficiency showed that it achieved an impressive degradation rate of 94.78% for chlorobenzene within 8 h. The Haldane-Andrews model was used to describe the growth of P. ureafaciens LY under specific pollutants and its concentrations, revealing a maximum specific growth rate (μmax ) of 0.33 h-1 . The isolation and characterization of P. ureafaciens LY, along with its ability to degrade chlorobenzene, provides valuable insights for the development of efficient and eco-friendly approaches to mitigate chlorobenzene contamination. Additionally, investigation of the degradation performance of the strain in the presence of other pollutants offers important information for understanding the complexities of co-metabolism in mixed-pollutant environments.

Deciphering the core bacterial community structure and function and their response to environmental factors in activated sludge from pharmaceutical wastewater treatment plants

Pharmaceutical wastewater is recognized for its heightened concentrations of organic pollutants, and biological treatment stands out as an effective technology to remove these organic pollution. Therefore, a comprehensive exploration of core bacterial community compositions, functions, and their responses to environmental factors in pharmaceutical wastewater treatment plants (PWWTPs) is important for understanding the removal mechanism of these organic pollutants. This study comprehensively investigated 36 activated sludge (AS) samples from 15 PWWTPs in China. The results revealed that Proteobacteria (45.41%) was the dominant phylum in AS samples, followed by Bacteroidetes (19.54%) and Chloroflexi (4.13%). While the dominant genera were similar in both aerobic and anaerobic treatment processes, their relative abundances exhibited significant variations. Genera like HA73, Kosmotoga, and Desulfovibrio were more abundant during anaerobic treatment, while Rhodoplanes, Bdellovibrio, and Hyphomicrobium dominated during aerobic treatment. 13 and 10 core operational taxonomic units (OTUs) were identified in aerobic and anaerobic sludge, respectively. Further analysis revealed that core OTUs belonging to genera Kosmotoga, Desulfovibrio, Thauera, Hyphomicrobium, and Chelativorans, were associated with key functions, including sulfur metabolism, methane metabolism, amino acid metabolism, carbohydrate metabolism, toluene degradation, and nitrogen metabolism. Furthermore, this study highlighted the crucial roles of environmental factors, such as COD, NH4+-N, SO42−, and TP, in shaping both the structure and core functions of bacterial communities within AS of PWWTPs. Notably, these factors indirectly affect functional attributes by modulating the bacterial community composition and structure in pharmaceutical wastewater. These findings provide valuable insights for optimizing the efficiency of biochemical treatment processes in PWWTPs.

Efficient treatment of veterinary pharmaceutical industrial wastewater by catalytic ozonation process: degradation of enrofloxacin via molecular ozone reactions.

The study focused on the efficacious performance of bimetallic Fe-Zn loaded 3A zeolite in catalytic ozonation for the degradation of highly toxic veterinary antibiotic enrofloxacin in wastewater of the pharmaceutical industry. Batch experiments were conducted in a glass reactor containing a submerged pump holding catalyst pellets at suction. The submerged pump provided the agitation and recirculation across the solution for effective contact with the catalyst. The effect of ozone flow (0.8-1.55mg/min) and catalyst dose (5-15g/L) on the enrofloxacin degradation and removal of other conventional pollutants COD, BOD5, turbidity was studied. In batch experiments, 10g of Fe-Zn 3A zeolite efficiently removed 92% of enrofloxacin, 77% of COD, 69% BOD5, and 61% turbidity in 1L sample of pharmaceutical wastewater in 30min at 1.1mg/min of O3 flow. The catalytic performance of Fe-Zn 3A zeolite notably exceeded the removal efficiencies of 52%, 51%, 52%, and 59% for enrofloxacin, COD, BOD5, and turbidity, respectively, achieved with single ozonation process. Furthermore, an increase in the biodegradability of treated pharmaceutical industrial wastewater was observed and made biodegradable easily for subsequent treatment.