Bench-scale Studies Research Articles

High-performance of anti-bacterial composite membrane prepared from polyethersulfone-polyethylene glycol-silver nanoparticles

A bench-scale study of river water treatment using composite polyethersulfone (PES) membrane was carried out. Polyethylene glycol-silver nanoparticles (PEG-AgNPs) additive was designed to support the simultaneous filtration and disinfection performance of PES membranes via in situ incorporation. Significant improvements in the PES membranes after modification with PEG-AgNPs were observed. The experimental results showed that the PEG-AgNPs increased the PES membrane water flux from 2.87 to 172.84 L/m2·h. The anti-fouling test of the PES membrane toward humic acid molecules after the addition of PES/PEG-AgNPs increased the reversible fouling and decreased the irreversible fouling. In terms of filtration performance, the PES/PEG-AgNP membranes showed high filtration performance, with a water disinfection ability of 99.99 %. Moreover, the leach of silver particles from the PES membrane forced by ultrasonication was <50 ppb, indicating the security and stability of the PES/PEG-AgNP membrane.

Carbon capture via electrochemically mediated alkaline absorption: Lab-scale continuous operation

Energy-efficient capture technologies need to be deployed by 2050 to abate global warming caused by excessive carbon dioxide (CO2) emissions. CO2 capture using alkaline solutions and absorbent regeneration mediated through bipolar membrane electrodialysis (BMED) have been tested previously as a standalone technology. However, the continuous operation of an integrated system remains largely unclear. Here, a bench-scale study was conducted using an integrated prototype to analyze the performance of CO2 capture and electrochemical regeneration using potassium hydroxide (KOH) aqueous solution. A wide range of current densities from 150 to 1000 A/m2 was applied to demonstrate the continuous operation of the CO2 capture system emphasizing the stability in attainable high rich carbon loading and CO2 desorption. The electrochemical regeneration module achieved CO2 desorption efficiency of 70% and absorbent recovery up to 89% under industrial relevant current densities of 500–1000 A/m2. The absorbent recovery has been identified to be a result of the combined effect of load ratio and rich carbon loading. The observed inefficient CO2 separation indicates significant potential to enhance energy efficiency. These results represent a pivotal step forward in electrochemically mediated CO2 capture technology, with promising potential for rapid industrial scale-up in the near future.

Pilot-scale evaluation of a dynamic body-feed filtration system for primary clarification of snake antivenoms produced by the caprylic acid method

The performance of dynamic body-feed filtration (DBF) in the removal of bulky solids produced during the manufacturing of snake antivenoms using the caprylic acid method was evaluated. For this purpose, diatomites with different filterability properties were compared in a bench-scale study to assess their effectiveness in removing the precipitated material formed after the addition of caprylic acid to equine hyperimmune plasma. C1000 diatomite at a concentration of 90 g/L of precipitated plasma showed the best performance. Then, the process was scaled up to three batches of 50 L of hyperimmune horse plasma. At this pilot scale, 108 ± 4% of the immunoglobulins present following plasma precipitation were recovered after DBF. The antivenoms generated using this procedure met quality specifications. When compared to open filtration systems commonly used at an industrial scale by many antivenom manufacturers, DBF has a similar yield and produces filtrates with comparable physicochemical characteristics. However, DBF ensures the microbiological quality of the primary clarification in a way that open systems cannot. This is because: 1) DBF is performed in a single-use closed device of depth filters which prevents microbial contamination, and 2) DBF removes bulky material in few minutes instead of the more than 24 h needed by open filtration systems, thus reducing the risk of contamination. It was concluded that DBF is a cost-effective, easily validated, and GMP-compliant alternative for primary clarification following caprylic acid precipitation of plasma in snake antivenom production.

Bio-based remediation of heavy metals contaminated industrial soil by organic amendments: A bench scale study

Bio-based remediation of heavy metals contaminated industrial soil by organic amendments: A bench scale study

A Wet Scrubber and Electrooxidation System for the Efficient Removal of Odor: A Bench-Scale Study

A Wet Scrubber and Electrooxidation System for the Efficient Removal of Odor: A Bench-Scale Study

Pilot-scale electrochemical advanced oxidation (EAOP) system for the treatment of Ni-EDTA-containing wastewater

Electrochemical advanced oxidation processes (EAOP) have shown great potential for the abatement of complexed heavy metals, such as metal-EDTA complexes, in recent studies. While removal of metal-EDTA complexes has been extensively examined in bench-scale reactors, much less attention has been given to the efficacy of this process at larger scale. In this study, we utilize a 72 L pilot-scale continuous flow system comprised of six serpentine flow channels and 90 pairs of flow-through electrodes for the degradation of Ni-EDTA complexes and removal of Ni from solution. The influence of a range of key operating parameters including flow rate, current density and initial Ni-EDTA concentration on rate and extent of Ni-EDTA degradation and Ni removal were examined. Our results showed that at a feed flow rate of 36 L h−1, current density of 5 mA cm−2 and initial Ni-EDTA concentration of 1 mM, the pilot-scale system achieved 74 % total Ni removal, 78 % total EDTA removal and 40 % TOC removal with energy consumption of 13.6 kWh m−3 order−1 and energy efficiency of 7.9 g kWh−1 for total Ni removal. A mechanistically-based kinetic model, which was developed in our previous bench-scale study, provides a satisfactory description of the experimental results obtained in the pilot-scale unit. Long term operation of the pilot-scale unit resulted in corrosion of PbO2 anode along with inorganic scaling as well as organic fouling on the PbO2 surface resulting in an obvious decline in Ni-EDTA degradation. Overall, the results of this study suggest that large scale anodic oxidation of wastewaters containing metal-organic complexes is an effective means of degrading organic ligands thereby enabling removal of the metal at the cathode. However, additional efforts are required to enhance the durability of the anode material and reduce material costs and energy consumption.

Magnetic coagulant derived from Cassia fistula seed for real textile wastewater treatment: A pilot-scale study

Cassia fistula (C. fistula) seed-derived coagulants have demonstrated substantial potential for treating dye-based wastewater. Such coagulants exhibit notable coagulating-flocculating activity and are environmentally friendly. However, recovering these natural coagulants from aqueous media poses challenges. In this study, we introduce a novel plant-derived magnetic coagulant that is a combination of C. fistula seed gum with magnetic spinel ferrite. This research includes a pilot-scale study to simulate full-scale textile wastewater treatment using this composite. Material characterisations revealed that spherical CoFe2O4 particles could be effectively coated with the active coagulant, C. fistula gum. The saturation magnetisation of the composite, measured at 54.11 emu/g, facilitates its convenient separation from aqueous solutions using an external magnetic field. Bench-scale studies showed that initial pH and coagulant dosage substantially affect the removal efficiency of colour and chemical oxygen demand (COD). In the pilot-scale study, the C. fistula–CoFe2O4 composite demonstrated promising coagulant properties. It achieved a colour removal percentage of 94.0 % with a volume of 30 L and a coagulant dosage of 12.3 g L− 1. Using this coagulation–flocculation process as a primary treatment step, possibly followed by biological or membrane methods, can help meet Vietnamese environmental standards.

Novel Oxidation Strategies for the In Situ Remediation of Chlorinated Solvents from Groundwater—A Bench-Scale Study

Industrial chlorinated solvents continue to be among the most significant issues in groundwater (GW) pollution worldwide. This study assesses the effectiveness of eight novel oxidation treatments, including persulfate (PS), ferrous sulfate, sulfidated nano-zero valent iron (S-nZVI), and potassium ferrate, along with their combinations, for the potential in situ remediation of GW polluted with chlorinated solvents (1,2-dichloroethylene, trichloroethylene, and tetrachloroethylene). Our bench-scale results reveal that the combined addition of PS and S-nZVI can effectively eliminate trichloroethylene (10 µg/L), achieving removal rates of up to 80% and 92% within 1 h, respectively, when using synthetic GW. In the case of real GW, this combination achieved removal rates of 69, 99, and 92% for cis-1,2-dichloroethylene, trichloroethylene, and tetrachloroethylene, respectively, within 24 h. Therefore, this proposed remediation solution resulted in a significant reduction in the environmental risk quotient, shifting it from a high-risk (1.1) to a low-risk (0.2) scenario. Furthermore, the absence of transformation products, such as vinyl chloride, suggests the suitability of employing this solution for the in situ remediation of GW polluted with chlorinated solvents.

222 nm far-UVC light markedly reduces the level of infectious airborne virus in an occupied room

An emerging intervention for control of airborne-mediated pandemics and epidemics is whole-room far-UVC (200–235 nm). Laboratory studies have shown that 222-nm light inactivates airborne pathogens, potentially without harm to exposed occupants. While encouraging results have been reported in benchtop studies and in room-sized bioaerosol chambers, there is a need for quantitative studies of airborne pathogen reduction in occupied rooms. We quantified far-UVC mediated reduction of aerosolized murine norovirus (MNV) in an occupied mouse-cage cleaning room within an animal-care facility. Benchtop studies suggest that MNV is a conservative surrogate for airborne viruses such as influenza and coronavirus. Using four 222-nm fixtures installed in the ceiling, and staying well within current recommended regulatory limits, far-UVC reduced airborne infectious MNV by 99.8% (95% CI: 98.2–99.9%). Similar to previous room-sized bioaerosol chamber studies on far-UVC efficacy, these results suggest that aerosolized virus susceptibility is significantly higher in room-scale tests than in bench-scale laboratory studies. That said, as opposed to controlled laboratory studies, uncertainties in this study related to airflow patterns, virus residence time, and dose to the collected virus introduce uncertainty into the inactivation estimates. This study is the first to directly demonstrate far-UVC anti-microbial efficacy against airborne pathogens in an occupied indoor location.

Predictive modelling of methane yield in biochar-amended cheese whey and septage co-digestion: Exploring synergistic effects using Gompertz and neural networks

This study performed bench scale studies on anaerobic co-digestion of cheese whey and septage mixed with biochar (BC) as additive at various dosages (0.5 g, 1 g, 2 g and 4 g) and total solids (TS) concentrations (5%, 7.5%, 10%,12.5% and 15%). The experimental results revealed 29.58% increase in methane yield (486 ± 11.32 mL/gVS) with 27% reduction in lag phase time at 10% TS concentration and 50 g/L of BC loading. The mechanistic investigations revealed that BC improved process stability by virtue of its robust buffering capacity and mitigated ammonia inhibition. Statistical analysis indicates BC dosage had a more pronounced effect (P < 0.0001) compared to the impact of TS concentrations. Additionally, the results were modelled using Gompertz model (GM) and artificial neural network (ANN) algorithm, which revealed the outperformance of ANN over GM with MSE 17.96, R2 value 0.9942 and error 0.27%. These findings validated the practicality of utilizing a high dosage of BC in semi-solid anaerobic digestion conditions.

EcoGenoRisk: Developing a computational ecological risk assessment tool for synthetic biology

The expanding field of synthetic biology (synbio) supports new opportunities in the design of targeted bioproducts or modified microorganisms. However, this rapid development of synbio products raises concerns surrounding the potential risks of modified microorganisms contaminating unintended environments. These potential invasion risks require new bioinformatic tools to inform the design phase. EcoGenoRisk is a newly constructed computational risk assessment tool for invasiveness that aims to predict where synbio microorganisms may establish a population by screening for habitats of genetically similar microorganisms. The first module of the tool identifies genetically similar microorganisms and potential ecological relationships such as competition, mutualism, and inhibition. In total, 520 archaeal and 32,828 bacterial complete assembly genomes were analyzed to test the specificity and accuracy of the tool as well as to characterize the enzymatic profiles of different taxonomic lineages. Additionally, ecological relationships were analyzed to determine which would result in the greatest potential overlap between shared functional profiles. Notably, competition displayed the significantly highest overlap of shared functions between compared genomes. Overall, EcoGenoRisk is a flexible software pipeline that assists environmental risk assessors to query large databases of known microorganisms and prioritize follow-up bench scale studies.

Deactivation by coking of industrial ZSM-5 catalysts used in LDPE pyrolysis and regeneration by ozonation process – Bench scale studies

Study of the catalytic deactivation during successive uses of ZSM-5 catalysts in bench-scale pyrolysis of low-density polyethylene (200:20 g LDPE:ZSM-5) has been carried out in a semi-batch reactor at 450 °C. The correlation between coke formation over catalyst properties and selectivity during pyrolysis is observed. The loss of catalytic performances translates into a significant drop of aromatics and an increase of waxes in pyrolysis products. The observed deactivation is due to the formation of heavy coke over the catalysts, causing surface hindering, porosity blockage and acid sites diminution. The capacity of ozonation process to regenerate such coked catalysts around 100 °C is demonstrated using a fixed bed reactor. Different times of exposure are investigated to evaluate ozonation efficiency. By using this coke oxidizing treatment during 48 h, regenerated catalysts recovered their initial textural and chemical characteristics (porous volume and acidity) as well as their catalytic performances (similar aromatics proportion as the first pyrolysis).

Impact of orthophosphate on the solubility and properties of lead orthophosphate nanoparticles.

Orthophosphate (PO4) is a commonly used corrosion control treatment to reduce lead (Pb) concentrations in drinking water. PO4 reduces Pb concentrations by forming relatively insoluble lead phosphate (Pb-PO4) minerals. In some cases, however, Pb-PO4 minerals have been observed to form nanoparticles, and if suspended in water, these nanoparticles can be mobile and reach consumer taps. Although recent research on Pb-PO4 particles has been performed, there remains a need to improve our understanding of the nature of Pb-PO4 nanoparticles. For that reason, Pb precipitation experiments were conducted to generate Pb-PO4 nanoparticles in bench scale studies for analysis. The study objective was to observe how pH, dissolved inorganic carbon (DIC), and PO4 impacted the properties of Pb-PO4 particles. Specifically, particle size, surface charge, mineralogy, and solubility were analysed. Hydrocerussite was precipitated when no PO4 was present, hydroxypyromorphite (Pb5(PO4)3OH) nanoparticles (<100 nm diameter) were precipitated when excess PO4 relative to Pb necessary to completely precipitate the mineral was present, and a mixture of the two minerals was precipitated when an insufficient amount of PO4 was present. Hydroxypyromorphite particles were less soluble than hydrocerussite by up to two orders of magnitude. The estimated K sp,OH of 10-66.87 in this work closely aligned with previous K sp,OH estimates that ranged from 10-66.77 to 10-62.79. Hydroxypyromorphite particles would not settle in water which was likely due to their small size and high negative charge. The mobility and size of these particles indicates that there are potential implications for such particulate Pb to remain suspended in water and thus be present in the tap water.

Emerging investigator series: mitigation of harmful algal blooms by electrochemical ozonation: from bench-scale studies to field applications

Harmful algal blooms threaten ecosystems and water safety, necessitating rapid treatment strategies. This study developed an electrochemical ozonation process to realize simultaneous cyanobacteria inactivation and microcystin removal.

Water Purification Using Active Charcoal with Microbes and Chelated Iron Soaked into Its Micropores

Urbanization in China has led to a significant increase in surface water pollution, posing a threat to the health and safety of residents and hindering sustainable economic development. Individual traditional methods have been used to purify polluted water, including the use of bamboo-derived activated charcoal, microbial material, and zero-valent iron. However, these methods have been found to have certain limitations. This study investigates the effects of an activated charcoal material combined with beneficial microbes and chelated nano-iron in removing nitrates. The experiments were conducted at various scales, including a bench-scale study, and studies of a small river, sewage plant tailwater, and artificially constructed wetlands. The microbes used included Bacillus spp., Lactobacillus spp., and yeasts. During the fermentation process, nano-scale iron powder was added, resulting in the formation of bivalent iron ions under anaerobic conditions. These ions were subsequently chelated by organic acids. Bamboo-derived activated charcoal was then soaked in the fermented liquid, allowing the microbes, chelated iron ions, and organic acids to infiltrate the pores of the activated charcoal. This activated charcoal material, containing microbes and chelated iron ions, demonstrated effective nitrate removal in laboratory experiments and sewage plant tailwater treatment, and water purification in wetlands and rivers. It is important to note that this research solely focused on the removal of nitrates, and further studies are required to confirm its effectiveness in other aspects of water purification.

Analysis of the effects of bench-scale cell culture platforms and inoculum cell concentrations on PSC aggregate formation and culture.

Introduction: Human pluripotent stem cells (hPSCs) provide many opportunities for application in regenerative medicine due to their ability to differentiate into cells from all three germ layers, proliferate indefinitely, and replace damaged or dysfunctional cells. However, such cell replacement therapies require the economical generation of clinically relevant cell numbers. Whereas culturing hPSCs as a two-dimensional monolayer is widely used and relatively simple to perform, their culture as suspended three-dimensional aggregates may enable more economical production in large-scale stirred tank bioreactors. To be more relevant to this biomanufacturing, bench-scale differentiation studies should be initiated from aggregated hPSC cultures. Methods: We compared five available bench-scale platforms for generating undifferentiated cell aggregates of human embryonic stem cells (hESCs) using AggreWell™ plates, low attachment plates on an orbital shaker, roller bottles, spinner flasks, and vertical-wheel bioreactors (PBS-Minis). Thereafter, we demonstrated the incorporation of an hPSC aggregation step prior to directed differentiation to pancreatic progenitors and endocrine cells. Results and discussion: The AggreWell™ system had the highest aggregation yield. The initial cell concentrations had an impact on the size of aggregates generated when using AggreWell™ plates as well as in roller bottles. However, aggregates made with low attachment plates, spinner flasks and PBS-Minis were similar regardless of the initial cell number. Aggregate morphology was compact and relatively homogenously distributed in all platforms except for the roller bottles. The size of aggregates formed in PBS-Minis was modulated by the agitation rate during the aggregation. In all cell culture platforms, the net growth rate of cells in 3D aggregates was lower (range: -0.01-0.022h-1) than cells growing as a monolayer (range: 0.039-0.045h-1). Overall, this study describes operating ranges that yield high-quality undifferentiated hESC aggregates using several of the most commonly used bench-scale cell culture platforms. In all of these systems, methods were identified to obtain PSC aggregates with greater than 70% viability, and mean diameters between 60 and 260mm. Finally, we showed the capacity of hPSC aggregates formed with PBS-Minis to differentiate into viable pancreatic progenitors and endocrine cell types.

A Short Review on Dye-Wastewater Valorization Using Up-Flow Anaerobic Sludge Blanket Reactors

Dye-containing effluent generated in textile industries is polluting and complex wastewater. It should be managed adequately before its final destination. The up-flow anaerobic blanket (UASB) reactor application is an ecofriendly and cost-competitive treatment. The present study briefly reviews the UASB application for dye-containing wastewater valorization. Bioenergy and clean-water production potential during dye-containing wastewater treatment are emphasized to promote resource recovery in textile industries. Hydraulic retention time (HRT), organic loading rate (OLR), pH, temperature, and hydraulic mixing influence sludge granulation, microbial activity, and dye removal. HRT and OLR ranges of 6–24 h and 1–12 kg m−3 d−1 of chemical oxygen demand (COD) at a mesophilic temperature (30–40 °C) are recommended for efficient treatment. In these conditions, efficiencies of color and COD of 50–97% and 60–90% are reported in bench-scale UASB studies. Complex dye structures can hinder biomineralization. Pretreatment may be necessary to reduce dye concentration. Carbon-source and redox mediators are added to the UASB reactor to expedite kinetic reactions. A biogas yield of 1.48–2.70 L d−1 in UASB, which treats dye-containing effluents, is documented. Cotreatment of dye wastewater and locally available substrate could increase biogas productivity in UASB reactors. Organic waste generated in the textile industry, such as dye sludge, cotton, and starch, is recommended to make cotreatment cost competitive. Bioenergy production and water reuse allow environmental and economic benefits. Studies on combined systems integrating UASB and membrane processes, such as ultrafiltration and nanofiltration, for the production of reusable water and pretreatment of wastewater and sludge for improvements in biogas production might realize the complete potential for resource recovery of UASB technology. UASB bioenergy usage for integrated treatment trains can reduce operating costs and assist process sustainability in the textile industry.

Toxic effects of thallium (Tl+) on prokaryotic alga Microcystis aeruginosa: Short and long-term influences by potassium and humic acid

Thallium (Tl) is a priority pollutant regulated by the US EPA. It is also a critical element commonly used in high technology industries; with an increasing demand for semiconductors nowadays, wastewater discharges from manufacturing plants or metal mining activities may result in elevated levels of thallium in receiving water harming aquatic organisms. Regarding the impact of thallium on freshwater algae, little attention has been paid to prokaryotic physiology through various exposure periods. In this bench-scale study, prokaryotic alga Microcystis aeruginosa PCC 7806 was cultured in modified BG11 medium and exposed to Tl+ (TlNO3) ranging from 250 to 1250 μg/L for 4 and 14 days. Throughout the experiment using flow cytometry assays, algal population, cell membrane integrity, oxidation stress level, and chlorophyll fluorescence were exacerbated following the exposure to 750 μg Tl/L (approximately 4-day effective concentration of Tl+ for reducing 50% of algal population). Potassium and humic acid (HA) (1–5 mg/L) were added to study their influences on the thallium toxicity. With the additions of potassium, thallium toxicities to algal population and physiology were not significantly changed within 4 days, while they were alleviated within 14 days. With the addition of HA at 1 mg/L, cell membrane integrity was significantly attenuated within 4 days; ameliorating effects on algal population and oxidative stress were not observed until day 14. Thallium toxicities on oxidative stress level and photosynthesis activity were exacerbated in the presence of HA at 3–5 mg/L. The study provides useful information for further studies on the mode of toxic action of Tl+ in prokaryotic algae; it also demonstrates the necessity of considering short and long-term exposure durations while incorporating water chemistry into assessment of thallium toxicity to algae.

Pharmaceutically active compounds in aqueous environment: recent developments in their fate, occurrence and elimination for efficient water purification.

The existence of pharmaceutically active compounds (PhACs) in the water is a major concern for environmentalists due to their deleterious effects on living organisms even at minuscule concentrations. This review focuses on PhACs such as analgesics and anti-inflammatory compounds, which are massively excreted in urine and account for the majority of pharmaceutical pollution. Furthermore, other PhACs such as anti-epileptics, beta-blockers and antibiotics are discussed because they also contribute significantly to pharmaceutical pollution in the aquatic environment. This review is divided into two parts. In the first part, different classes of PhACs and their fate in the wastewater environment are presented. In the second part, recent advances in the removal of PhACs by conventional wastewater treatment plants, including membrane bioreactors (MBRs), activated carbon adsorption and bench-scale studies concerning a broad range of advanced oxidation processes (AOPs) that render practical and appropriate strategies for the complete mineralization and degradation of pharmaceutical drugs, are reviewed. This review indicates that drugs like diclofenac, naproxen, paracetamol and aspirin are removed efficiently by conventional systems. Activated carbon adsorption is suitable for the removal of diclofenac and carbamazepine, whereas AOPs are leading water treatment strategies for the effective removal of reviewed PhACs.

Impact of corrosion inhibitors on antibiotic resistance, metal resistance, and microbial communities in drinking water.

Corrosion inhibitors, including zinc orthophosphate, sodium orthophosphate, and sodium silicate, are commonly used to prevent the corrosion of drinking water infrastructure. Metals such as zinc are known stressors for antibiotic resistance selection, and phosphates can increase microbial growth in drinking water distribution systems (DWDS). Yet, the influence of corrosion inhibitor type on antimicrobial resistance in DWDS is unknown. Here, we show that sodium silicates can decrease antibiotic resistant bacteria (ARB) and antibiotic-resistance genes (ARGs), while zinc orthophosphate increases ARB and ARGs in source water microbial communities. Based on controlled bench-scale studies, zinc orthophosphate addition significantly increased the abundance of ARB resistant to ciprofloxacin, sulfonamides, trimethoprim, and vancomycin, as well as the genes sul1, qacEΔ1, an indication of resistance to quaternary ammonium compounds, and the integron-integrase gene intI1. In contrast, sodium silicate dosage at 10 mg/L resulted in decreased bacterial growth and antibiotic resistance selection compared to the other corrosion inhibitor additions. Source water collected from the drinking water treatment plant intake pipe resulted in less significant changes in ARB and ARG abundance due to corrosion inhibitor addition compared to source water collected from the pier at the recreational beach. In tandem with the antibiotic resistance shifts, significant microbial community composition changes also occurred. Overall, the corrosion inhibitor sodium silicate resulted in the least selection for antibiotic resistance, which suggests it is the preferred corrosion inhibitor option for minimizing antibiotic resistance proliferation in DWDS. However, the selection of an appropriate corrosion inhibitor must also be appropriate for the water chemistry of the system (e.g., pH, alkalinity) to minimize metal leaching first and foremost and to adhere to the lead and copper rule. IMPORTANCE Antibiotic resistance is a growing public health concern across the globe and was recently labeled the silent pandemic. Scientists aim to identify the source of antibiotic resistance and control points to mitigate the spread of antibiotic resistance. Drinking water is a direct exposure route to humans and contains antibiotic-resistant bacteria and associated resistance genes. Corrosion inhibitors are added to prevent metallic pipes in distribution systems from corroding, and the type of corrosion inhibitor selected could also have implications on antibiotic resistance. Indeed, we found that sodium silicate can minimize selection of antibiotic resistance while phosphate-based corrosion inhibitors can promote antibiotic resistance. These findings indicate that sodium silicate is a preferred corrosion inhibitor choice for mitigation of antibiotic resistance.