Efficient and sustainable photocatalytic inactivation of E. coli by an innovative immobilized Ag/TiO2 photocatalyst with peroxymonosulfate (PMS) under visible light.

A novel catalytic system for effective photocatalytic inactivation of Escherichia coli (E. coli) was constructed by anchoring Ag nanoparticles (AgNPs) on silane coupling agent (SCA) pretreated TiO2 nano-tube arrays (Ag/SCA/TiO2NTAs). Morphology and structural analyses revealed that SCA could disperse AgNPs evenly on TiO2NTAs, thus inducing a superior surface plasmon resonance (SPR) effect. Ag/SCA/TiO2NTAs catalyst exhibited excellent inactivation performance when in the presence of peroxymonosulfate (PMS) and visible light (VL), with 6-log E. coli was completely inactivated within 60 min, which was 5.3, 12.5 and 13.2 times higher than that of Ag/SCA/TiO2NTAs/VL, PMS/VL and Ag/SCA/TiO2NTAs/PMS/dark systems, respectively. Additionally, the photocatalyst exhibited a highly reusable property, with the inactivation performance almost unchanged after ten cycles of uses with minimal Ag leaching. The inactivation mechanism analysis demonstrated that both radical (SO4•-, OH) and non-radical (h+, 1O2) pathways involved in E. coli inactivation, and SCA played a pivotal role in the production of reactive species. Chloride ions (Cl-) greatly enhanced the inactivation efficiency, while bicarbonate (HCO3-) and phosphate (H2PO4-) showed an inhibitory effect. Humic acid (HA) displayed a dual effect on inactivation performance, where the low concentration of HA facilitated the bacteria inactivation, while the higher dose suppressed bacteria inactivation. Moreover, the system exhibited excellent inactivation performance in tap water. This work first used SCA as the binder to fix AgNPs on TiO2NTAs for VL photocatalytic inactivation of bacteria with the assistance of PMS, which was expected to provide some insights into the practical treatment of drinking water.

An Effective Approach to the Disinfection of Pathogens: Cationic Conjugated Polyelectrolytes and Oligomers.

The synthetic cationic conjugated polyelectrolytes and oligomers have demonstrated great effectiveness and versatility as antimicrobial materials. They have the ability to eliminate or render inactive various pathogens, including viruses like SARS-CoV-2, bacteria, and fungi. These pathogens can be rapidly eradicated when the polyelectrolytes and oligomers are applied as sprays, wipes, or coatings on solid surfaces. Inactivation of the pathogens occurs through two distinct processes: a non-light-activated process similar to Quats, and a more efficient and faster process that is triggered by light. These materials possess fluorescence and photosensitizing properties, enabling prolonged protection when coated on surfaces. The level of fluorescence exhibited by samples applied to nonfluorescent surfaces serves as an indicator of the coating's integrity and viability, making it easily detectable. Importantly, these materials demonstrate low toxicity towards mammalian cells and human skin, allowing for their safe use. While they can serve as durable coatings for pathogen protection, extended exposure to visible or ultraviolet light leads to their photochemical degradation. Our research also suggests that these materials act against pathogens through nonspecific mechanisms, minimizing the likelihood of pathogens developing resistance and rendering the materials ineffective.

Effect of thermosonication on bioactive compounds, enzymatic and microbiological inactivation in nectar with strawberry by-products.

The aim of this study was to evaluate whether the addition of strawberry by-products (pulp and achene) and thermosonication offers a nectar with a potential contribution of health and safety benefits. Strawberry nectar with 0, 10 and 20% of strawberry by-products (SB) was subjected to thermosonication (24 kHz) at 70 and 80% for 8 min at 50 °C. Total soluble solids, pH, polyphenol oxidase (PO) and pectin methylesterase (PME) activities, total soluble phenols (TSP), ascorbic acid (AA), anthocyanins and antioxidant capacity (AOX) were evaluated. Microbiological reduction and inactivation of Escherichia coli was also determined. A limited activity was observed in PO and PME related to the SB percentage added. TSP, AA, anthocyanins, and AOX were increased due to the different percentages of SB added to the nectar. A reduction of aerobic mesophiles (1.28 Log CFU/mL), molds and yeast counts (1.23 Log CFU/mL) were achieved by thermosonication. E. coli inactivation was approximately 1 log CFU/mL in 20% SB nectar at 80% amplitude, 8 min at 50 °C, but increased during storage at 6 °C (0.915-5.86 Log CFU/mL). Thermosonication showed the possibility of employing strawberry by-products in nectars, improving the use of agro-industrial residues by non-thermal technologies.

Effect of turbulence, dispersion, and stratification on Escherichia coli disinfection in a subtropical maturation pond.

Sunlight disinfection is important for treatment of wastewater within maturation ponds. This study analyses the movement of Escherichi coli within a slice of a maturation pond, being affected by stratification, sunlight attenuation and mixing driven by wind shear and natural convection using computational fluid dynamics (CFD). Since the exposure to ultraviolet light is most effective in the near-surface region of the pond, natural convective mixing mechanisms to transport the pathogens from the lower parts of the pond are critical for disinfection efficacy. Different turbulence models are considered for closure of the momentum conservation equations and compared with a laminar flow simulation and a completely stirred tank reactor (CSTR) model. The effect of turbulence and stratification is shown to be significant for thermal and velocity distributions, and predictions of E. coli die-off. Greater volume-averaged E. coli die-off was predicted by the computationally convenient CSTR model than the CFD turbulence and laminar models. The simulation results are compared with experimental data and show that complete vertical mixing occurs in a diurnal pattern aiding die-off in sunlight-attenuating water. Practical applications of the model can assist in management strategies for maturation ponds such as off-take locations/times and evaluating seasonal variations in sunlight disinfection.

Understanding the Structural-Dependent Photocatalytic Antibacterial Activity: a Case Study of Ag Modified BiVO4.

In this work, Ag/BiVO4 heterostructural photocatalysts were developed in order to reveal exceptional structural-dependent photoinduced charge migration kinetics as well as the underlying photocatalytic antibacterial dynamic process. The structure-dependent interface of BiVO4 and Ag nanoparticles was successfully constructed to improve the photoinduced interface charge transfer efficiency and interface correlation. DFT calculation indicated that a net charge of about 0.33 e between Ag and tz-BiVO4 was achieved by extraordinary interface charge transfer, being far larger than that between Ag and ms-BiVO4. Larger net charge has consequences on mobility of charge carriers of tz-BiVO4 that can raise the migration and separation of charge carriers for Ag/tz-BiVO4 heterojunction. Fine interfacial contact between Ag and tz-BiVO4 led to the optimized photocatalytic performance toward E. coli inactivation, being predominately higher than that of tz-BiVO4, ms-BiVO4, and Ag/ms-BiVO4 catalysts. Besides photocatalytic activity, the thermocatalytic inactivation activity of Ag/tz-BiVO4 also exhibited a factor of about 7.2 and 3.1 times higher than that of tz-BiVO4 and Ag/ms-BiVO4. Trapping and EPR measurements suggested that the structural-dependent photocatalytic activity of Ag/BiVO4 mainly originated from the pronounced variation of the capability to produce H2O2 active species, where the capability of generating H2O2 over Ag/tz-BiVO4 is highly accelerated. Moreover, it cannot be ignored that this study provides an ideal candidate for many aspects, such as environmental and water pollution caused by pathogenic microorganisms and disinfection of medical materials, food packaging, household materials, and public places, etc.

Visible light driven CuBi2O4/Bi2MoO6 p-n heterojunction with enhanced photocatalytic inactivation of E. coli and mechanism insight.

Here, a novel CuBi2O4/Bi2MoO6 (CBO/BMO) p-n heterojunction was fabricated and exhibited markedly improved photocatalytic inactivation capacity of E. coli cells under visible light excitation (λ > 420 nm) compared with pure CuBi2O4 and Bi2MoO6. The CBO/BMO-0.5 hybrid displayed the highest photoinactivation ability which could completely inactivate the E. coli cellswithin 4 h. The mechanism of photocatalytic disinfection towards E. coli of CBO/BMO heterojunctions was attributed to the disruption of cell-membrane, leakage and damage of cellular content including total protein and DNA as verified with SEM, fluorescence-base dead/live stain, sodium dodecyl sulfate polyacrylamide gel electropheresis (SDS-PAGE) and agarose gel electrophoresis (AGE). Additionally, the scavenge experiments showed that the reactive species h+, e- and •O2-play the predominant role in the photocatalytic system of CBO/BMO hybrids. The improved photocatalytic activity of CBO/BMO composites was mainly attributed to the promotion of spatial separation and migration rate of photoproduced electron-hole pairs, enhancement of visible light absorption and more generation of reactive species (•O2-) on the interface of catalyst and water which was demonstrated by nitroblue tetrazolium (NBT) and EPR. Our work indicated that construction of CuBi2O4/Bi2MoO6 p-n heterostructure photocatalyst is a promising environmental friendly alternative method to deal with the biohazards of pathogenic microorganisms.

Enhanced visible-light-driven photocatalytic disinfection using AgBr-modified g-C3N4 composite and its mechanism.

In this study, novel AgBr-modified g-C3N4 (AgBr/g-C3N4) photocatalysts were prepared by an adsorption-deposition method and characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET), and ultraviolet-visible spectroscopy (UV-vis). Furthermore, the photocatalytic disinfection performance on Escherichia coli (ATCC 15597) was investigated. The as-prepared photocatalysts exhibited well crystalline structures and morphologies with C3N4 and exhibited a stronger bacterial inactivation than that of pristine g-C3N4. The disinfection efficiency reached up to 4.80 log under 150 min of visible light irradiation when AgBr-modified g-C3N4 was prepared at a molar ratio of 1:5 (AgBr: g-C3N4), which was a 4.2 log increase compared with that of pristine g-C3N4 under the same experimental conditions. The enhancement of the photocatalytic activity of AgBr/g-C3N4 was attributed to the effective production and transfer of the photo-induced electrons under visible light irradiation, since the AgBr modification reduced the bandgap energy and boarded the visible light area. Furthermore, h+ was found to be the dominant contributor for bacterial inactivation. The h+ and photo-generated reactive oxygen species (ROSs) damaged the cell membranes and destroyed metabolic processes, resulting in leakage of potassium ions and proteins, lipid peroxidation, degradation of intracellular protein, and a reduction of the ATP levels, which finally lead to bacterial death. These results provide a theoretical basis for the development of low-cost, high-efficiency photocatalysts for green/sustainable water disinfection.

Continuous efficient removal and inactivation mechanism of E. coli by bismuth-doped SnO2/C electrocatalytic membrane.

The Bi-SnO2/C electrocatalytic membrane was fabricated via a simple electrochemical reduction and hydrothermal method. Under the action of electric field, the Sn2+ and Bi3+ were firstly adsorbed and reduced to metallic Sn and Bi on the carbon membrane surface by cathodic reduction reaction, and the Bi-SnO2/C membrane was obtained subsequently through hydrothermal oxidation process. Confirmed by SEM, TEM, XRD, and XPS characterizations, the nano-Bi-SnO2 is homogeneously distributed on the membrane surface and is firmly attached to the carbon membrane via C-O-Sn chemical bond. Through CV, LSV, and EIS electrochemical analysis, the Bi-SnO2/C membrane possesses the higher electrocatalytic activity and stability than carbon membrane. Therefore, the Bi-SnO2/C membrane could continuously efficiently remove and inactivate Escherichia coli in water through flow-through mode. As a result, the sterilization efficiency can reach more than 99.99% under the conditions of cell voltage 4 V, flow rate 1.4 mL/min, and E. coli initial concentration 1.0 × 104 CFU/mL, owing to the synergistic effect of the membrane separation and electrocatalytic oxidation. Moreover, it was found that the oxidation groups of ⋅OH radicals generated by Bi-SnO2/C membrane play the crucial role for bactericidal performance. This work presents a low-cost, highly active, and stable electrocatalytic membrane towards continuous bacterial inactivation, which exhibits promising potential in water disinfection and is beneficial for practical large-scale applications.

Build-up and impact of volatile fatty acids on E. coli and A. lumbricoides during co-digestion of urine diverting dehydrating toilet (UDDT-F) faeces.

This study examined the potential of Escherichia coli (E. coli) and Ascaris lumbricoides (A. lumbricoides) eggs inactivation in faecal matter coming from urine diverting dehydrating toilets (UDDT-F) by applying high concentrations of volatile fatty acids (VFAs) during anaerobic stabilization. The impact of individual VFAs on E. coli and A. lumbricoides eggs inactivation in UDDT-F was assessed by applying various concentrations of store-bought acetate, propionate and butyrate. High VFA concentrations were also obtained by performing co-digestion of UDDT-F with organic market waste (OMW) using various mixing ratios. All experiments were performed under anaerobic conditions in laboratory scale batch assays at 35±1 °C. A correlation was observed between E. coli log inactivation and VFA concentration. Store bought VFA spiked UDDT-F substrates achieved E. coli inactivation up to 4.7 log units/day compared to UDDT-F control sample that achieved 0.6 log units/day. In co-digesting UDDT-F and organic market waste (OMW), a ND-VFA concentration of 4800-6000 mg/L was needed to achieve E. coli log inactivation to below detectable levels and complete A. lumbricoides egg inactivation in less than four days. E. coli and A. lumbricoides egg inactivation was found to be related to the concentration of non-dissociated VFA (ND-VFA), increasing with an increase in the OMW fraction in the feed substrate. Highest ND-VFA concentration of 6500 mg/L was obtained at a UDDT-F:OMW ratio 1:1, below which there was a decline, attributed to product inhibition of acidogenic bacteria. Results of our present research showed the potential for E. coli and A. lumbricoides inactivation from UDDT-F up to WHO standards by allowing VFA build-up during anaerobic stabilization of faecal matter.

Innovative Ti1- xNb xN-Ag Films Inducing Bacterial Disinfection by Visible Light/Thermal Treatment.

This study presents innovative Ti1- xNb xN-Ag films obtained by a suitable combination of low-energy and high-energy sputtering leading to bacterial inactivation. The bacterial inactivation kinetics by the TiNbN layers was drastically enhanced by the addition of 6-7% Ag and proceeded to completion within 3 h after the film autoclaving. By X-ray photoelectron spectroscopy (XPS), the samples after autoclaving presented in their upper layers TiO2, Nb2O5 and Ag2O with a surface composition of Ti0.81Nb0.19N0.99Ag0.068. Surface potential/pH changes in the Ti1- xNb xN-Ag films were monitored during bacterial inactivation. Surface redox processes during the bacterial inactivation were detected by XPS. The diffusion of Ag in the Ti1- xNb xN-Ag films was followed at 50 and 70 °C pointing. The beneficial thermal treatment points out to the bifunctional bacterial inactivation properties of these films and their potential application in healthcare facilities. Interfacial charge transfer (IFCT) under light irradiation between Ag2O, Nb2O5 and TiO2 is suggested consistent with the data found during the course of this study. The TiO2/Nb2O5 lattice mechanism is discussed in the framework of the Verwey's controlled valence model. The surface properties of the Ti1- xNb xN-Ag films were investigated by X-ray diffraction, atomic force microscopy, and scanning electron microscopy.

A control system for ultrasound devices utilized for inactivating E. coli in wastewater.

Sonochemical processes applied to wastewater treatment have an influence on the behavior of ultrasonic systems. This is especially due to the load characteristic of the sonochemical process itself and the temperature increase caused by internal damping within the converter. Hence, a controlling device is needed to guarantee the operation in resonance and to keep the vibration amplitude constant. This paper presents a digital control system for the operation of weak to strong damped ultrasonic devices and its application for inactivating Escherichia coli in wastewater. In an experimental investigation, the electric data during a sonochemical process to inactivate E. coli in wastewater is taken into account to analyze the efficacy of the treatment process and the reaction of the vibration system to the process. Frequency response measurements depict that the resonance frequency changes with the sonicated medium and the vibration amplitude decreases with driving current. In addition to a common continuous operation of the system, different pulsed modes are investigated. The experiments prove the common dependencies between inactivation and power level or treatment time. Additionally, it is pointed out that the control of the sonochemical device is of utmost importance to guarantee an efficient treatment of water, because fast process changes, especially in pulsed operation modes, need to be controlled to a steady state as fast as possible. Although a water treatment efficiency increase using pulsed modes was not proved, it is shown, that the performance of the control unit is capable of using different driving modes in water treatment.

Antibacterial properties of TiO2 modified with reduced graphene oxide.

In this paper, the antibacterial activity of titanium dioxide modified with reduced graphene oxide (rGO) was presented. TiO2/rGO photocatalysts were prepared by the hydrothermal method under elevated pressure at 180°C and heated at 100°C in Ar flow. The obtained photocatalysts were characterized by means of XRD, FTIR/DRS, UV-vis/DR, Raman spectroscopy and scanning electron microscopy (SEM). The carbon content was also examined. FTIR/DRS and Raman analysis confirmed the presence of rGO in the TiO2 structure, suggesting a successful modification. The antimicrobial photoactivity of photocatalysts was conducted against E. coli under an artificial solar light. The results show that all TiO2/rGO photocatalysts exhibited an antibacterial activity higher than unmodified TiO2. The best result was found for sample with 1.5wt% additive of reduced graphene oxide. In this case, total inactivation of E. coli was noticed after 75min of irradiation. It was found that the presence of rGO in sample improves the antimicrobial activity.

Iron oxide-mediated semiconductor photocatalysis vs. heterogeneous photo-Fenton treatment of viruses in wastewater. Impact of the oxide particle size.

The photo-Fenton process is recognized as a promising technique towards microorganism disinfection in wastewater, but its efficiency is hampered at near-neutral pH operating values. In this work, we overcome these obstacles by using the heterogeneous photo-Fenton process as the default disinfecting technique, targeting MS2 coliphage in wastewater. The use of low concentrations of iron oxides in wastewater without H2O2 (wüstite, maghemite, magnetite) has demonstrated limited semiconductor-mediated MS2 inactivation. Changing the operational pH and the size of the oxide particles indicated that the isoelectric point of the iron oxides and the active surface area are crucial in the success of the process, and the possible underlying mechanisms are investigated. Furthermore, the addition of low amounts of Fe-oxides (1mgL-1) and H2O2 in the system (1, 5 and 10mgL-1) greatly enhanced the inactivation process, leading to heterogeneous photo-Fenton processes on the surface of the magnetically separable oxides used. Additionally, photo-dissolution of iron in the bulk, lead to homogeneous photo-Fenton, further aided by the complexation by the dissolved organic matter in the solution. Finally, we assess the impact of the presence of the bacterial host and the difference caused by the different iron sources (salts, oxides) and the Fe-oxide size (normal, nano-sized).

Beneficial effect of Cu on Ti-Nb-Ta-Zr sputtered uniform/adhesive gum films accelerating bacterial inactivation under indoor visible light.

This article presents the evidence for the significant effect of copper accelerating the bacterial inactivation on Ti-Nb-Ta-Zr (TNTZ) sputtered films on glass up to a Cu content of 8.3 at.%. These films were deposited by dc magnetron co-sputtering of an alloy target Ti-23Nb-0.7Ta-2Zr (at.%) and a Cu target. The fastest bacterial inactivation of E. coli on this later TNTZ-Cu surface proceeded within ∼75min. The films deposited by magnetron sputtering are chemically homogenous. The film roughness evaluated by atomic force spectroscopy (AFM) on the TNTZ-Cu 8.3 at.% Cu sample presented an RMS-value of 20.1nm being the highest RMS of any Cu-sputtered TNTZ sample. The implication of the RMS value found for this sample leading to the fastest interfacial bacterial inactivation kinetics is also discussed. Values for the Young's modulus and hardness are reported for the TNTZ films in the presence of various Cu-contents. Evaluation of the bacterial inactivation kinetics of E. coli under low intensity actinic hospital light and in the dark was carried out. The stable repetitive bacterial inactivation was consistent with the extremely low Cu-ion release from the samples of 0.4 ppb. Evidence is presented by the bacterial inactivation dependence on the applied light intensity for the intervention of Cu as semiconductor CuO during the bacterial inactivation at the TNTZ-Cu interface. The mechanism of CuO-intervention under light is suggested based on the pH/and potential changes registered during bacterial disinfection.

Quasi-Instantaneous Bacterial Inactivation on Cu-Ag Nanoparticulate 3D Catheters in the Dark and Under Light: Mechanism and Dynamics.

The first evidence for Cu-Ag (50%/50%) nanoparticulate hybrid coatings is presented leading to a complete and almost instantaneous bacterial inactivation in the dark (≤5 min). Dark bacterial inactivation times on Cu-Ag (50%/50%) were observed to coincide with the times required by actinic light irradiation. This provides the evidence that the bimetal Cu-Ag driven inactivation predominates over a CuO/Cu2O and Ag2O oxides inducing a semiconductor driven behavior. Cu- or Ag-coated polyurethane (PU) catheters led to bacterial inactivation needing about ∼30 min. The accelerated bacterial inactivation by Cu-Ag coated on 3D catheters sputtered was investigated in a detailed way. The release of Cu/Ag ions during bacterial inactivation was followed by inductively coupled plasma mass-spectrometry (ICP-MS) and the amount of Cu and Ag-ions released were below the cytotoxicity levels permitted by the sanitary regulations. By stereomicroscopy the amount of live/dead cells were followed during the bacterial inactivation time. By Fourier transform infrared spectroscopy (FTIR), the systematic shift of the -(CH2) band stretching of the outer lipo-polysaccharide bilayer (LPS) was followed to monitor the changes leading to cell lysis. A hydrophobic to hydrophilic transformation of the Cu-Ag PU catheter surface under light was observed within 30 min followed concomitantly to a longer back transformation to the hydrophobic initial state in the dark. Physical insight is provided for the superior performance of Cu-Ag films compared to Cu or Ag films in view of the drastic acceleration of the bacterial inactivation observed on bimetal Cu-Ag films coating PU catheters. A mechanism of bacterial inactivation is suggested that is consistent with the findings reported in this study.

Coupling of narrow and wide band-gap semiconductors on uniform films active in bacterial disinfection under low intensity visible light: implications of the interfacial charge transfer (IFCT).

This study reports the design, preparation, testing and surface characterization of uniform films deposited by sputtering Ag and Ta on non-heat resistant polyester to evaluate the Escherichia coli inactivation by TaON, TaN/Ag, Ag and TaON/Ag polyester. Co-sputtering for 120 s Ta and Ag in the presence of N2 and O2 led to the faster E. coli inactivation by a TaON/Ag sample within ∼40 min under visible light irradiation. The deconvolution of TaON/Ag peaks obtained by X-ray photoelectron spectroscopy (XPS) allowed the assignment of the Ta2O5 and Ag-species. The shifts observed for the XPS peaks have been assigned to AgO to Ag2O and Ag(0), and are a function of the applied sputtering times. The mechanism of interfacial charge transfer (IFCT) from the Ag2O conduction band (cb) to the lower laying Ta2O5 (cb) is discussed suggesting a reaction mechanism. The optical absorption of the TaON and TaON/Ag samples found by diffuse reflectance spectroscopy (DRS) correlated well with the kinetics of E. coli inactivation. The TaON/Ag sample microstructure was characterized by contact angle (CA) and by atomic force microscopy (AFM). Self-cleaning of the TaON/Ag polyester after each disinfection cycle enabled repetitive E. coli inactivation.

Studies on the electrochemical disinfection of water containing Escherichia coli using a Dimensionally Stable Anode

The aim of this work was to investigate the disinfectant effect of electrolysis on chlorine-free water, artificially contaminated with Escherichia coli (CCT-1457) and to evaluate the bactericidal activity of electrolysis and kinetic behavior of a single-cell reactor, with a DSA (Dimensionally Stable Anode) electrode to develop a scaled-up system. A high-density E. coli suspension (10(6) CFU mL-1) was electrolyzed in this reactor at 25, 50 and 75 mA cm-2 for up to 60 min, at flow rates of 200 and 500 L h-1. Bacterial survival fell by 98.9 percent without addition of chlorinated compounds and a power consumption rate not more than 5.60 kWh m-3 at flow rate of 200 L h-1 and 75 mA cm-2. The process produced a germicidal effect that reached this inactivation rate within a relatively short contact time. Also, a solution of electrolyzed 0.08 M Na2SO4 added to the inoculum showed residual bactericidal effect. The efficiency of disinfection was regulated by both the contact time and current density applied, and a kinetic function for the survival rate was developed for the purpose of scaling up.

Água contaminada é uma das maiores origens de doenças em seres humanos. Em todo o mundo, a cloração é o método mais utilizado para promover desinfecção em águas de abastecimento devido ao seu efeito residual, quando adequadamente calculado. Contudo, se a água apresentar matéria orgânica, pode haver a geração de organoclorados, os quais são genotóxicos e carcinogênicos. Sob esta óptica, investigamos o efeito bactericida da aplicação da eletrólise em água sem cloro contaminada com Escherichia coli (CCT-1457). O objetivo deste estudo foi avaliar o poder de desinfecção e o comportamento cinético da eletrólise realizada em reator de compartimento único e usando eletrodos ADE (Anodo Dimensionalmente Estável), visando ampliação de escala. Uma suspensão contendo elevada concentração de E. coli (10(6) UFC mL-1) foi submetida ao tratamento no reator em 25, 50 e 75 mA cm-2 durante 60 min, em vazões de 200 e 50 Lh-1. A taxa de inativação foi aproximadamente 99 por cento para a solução isenta de compostos clorados, com consumo de energia elétrica menor que 5,60 kWh m-3 em 200 L h-1 e 75 mA cm-2. Uma solução de Na2SO4 0,08M eletrolisada e adicionada posteriormente ao inoculo apresentou efeito residual bactericida. A eficiência da desinfecção foi regida pelo tempo de contato e pela densidade de corrente aplicada, e foi realizado um estudo cinético que permite a ampliação de escala.