SinoGreenTech Academic Portal
Open AccessDOI: 10.7524/j.issn.0254-6108.2025021702Original Research

Electrochemical Synthesis of Hydrogen Peroxide for Disinfection of Toilet Bowl Seal Water

School of Environmental Science and Engineering, Suzhou University of Science and Technology

Read Executive PreviewQuick FAQ
Electrochemical Synthesis of Hydrogen Peroxide for Disinfection of Toilet Bowl Seal Water
Graphical Abstract / Figure
Published In
Environmental Chemistry
Published:January 15, 2026Edition:Vol. 45, Issue 6 • pp. 100-112Citation:ZHOU Fayuan et al. (2026), Environmental Chemistry
Impact FactorPeer-Reviewed Core
Source Journal环境化学

Key Takeaways & Executive Findings

  • • • At H2O2 concentrations of 50–200 mg·L−1, complete bacterial inactivation in toilet bowl water occurs within 4–24 h, with no harmful disinfection by-products, offering a safer alternative to chlorination. • • In situ electrochemical H2O2 generation using a gas diffusion electrode at 0.8 A reduces total bacterial count by >90% in toilet seal water during normal use, significantly mitigating aerosol-mediated pathogen transmission. • • The system operates at approximately 8.5 V and consumes only 0.08 CNY per day (based on 0.5 CNY·kWh−1), demonstrating economic feasibility for household adoption. • • Compared to HOCl disinfection, H2O2 avoids the formation of volatile halogenated by-products (e.g., trihalomethanes), ensuring safer indoor air quality during toilet flushing.

Abstract

Bacteria and microorganisms in toilets can enter the air via aerosol plumes generated during flushing, posing potential health risks. This study evaluates the feasibility of electrochemical synthesis of hydrogen peroxide (H2O2) for household toilet disinfection. Disinfection experiments showed that at H2O2 concentrations of 50–200 mg·L−1, bacteria in toilet bowl seal water were completely inactivated within 4–24 h without generating harmful disinfection by-products. By installing a gas diffusion electrode in the toilet tank and utilizing oxygen from air to electrochemically synthesize H2O2 in situ, the total bacterial count in the seal water was reduced by more than 90% during normal toilet use, thereby lowering the risk of disease transmission via toilet aerosols. The results suggest that electrochemical H2O2 synthesis offers a safe, healthy, and environmentally friendly disinfection method for household toilets.

1. Introduction

Conventional smart toilets predominantly rely on electrolytic chlorine generation, converting chloride ions in tap water to free chlorine (HOCl/OCl−) for microbial inactivation. However, chlorination produces volatile disinfection by-products such as chloroform and brominated trihalomethanes, which volatilize during flushing and pose inhalation risks. This limitation underscores the need for alternative disinfection strategies that are both effective and free from toxic by-products.

Electrochemical synthesis of hydrogen peroxide (H2O2) via oxygen reduction offers a promising solution, generating a broad-spectrum disinfectant that decomposes into water and oxygen. This study addresses the bottleneck by integrating a gas diffusion electrode into a toilet tank, enabling on-site H2O2 production from ambient oxygen. The approach achieves >90% bacterial reduction in seal water at a daily energy cost of merely 0.08 CNY, presenting a safe, economical, and environmentally benign alternative to chlorination for household toilet sanitation.

SinoTechIntel Interactive Document Reader
Page 1–5 of Preview
100%
Download Full PDF

Loading authentic research manuscript (Pages 1–5)...

Cite This Research Paper
ZHOU Fayuan, YANG Yiting, XU Xinpeng, YUAN Yi, ZHENG Quan, WANG Yujue (2026). Electrochemical Synthesis of Hydrogen Peroxide for Disinfection of Toilet Bowl Seal Water. Environmental Chemistry. https://doi.org/10.7524/j.issn.0254-6108.2025021702
SinoGreenTech Academic & Legal Disclaimer

Research & Educational Purpose Only: The translations, structured abstracts, analytical annotations, and data reports provided by SinoGreenTechare intended exclusively for academic research, internal corporate R&D, and educational benchmarking. They do not constitute formal engineering, chemical safety, legal, or professional advice.

Copyright & Intellectual Property Notice: Original copyright of the underlying source articles and experimental data remains with the respective authors, institutions, and original publishing journals. SinoGreenTech claims intellectual property only over its proprietary translations, analytical syntheses, and AEO structured enhancements in accordance with international fair use and academic citation principles.

Frequently Asked Questions

What is the operational current and voltage required for effective disinfection, and how does this translate to energy costs?

The system operates at a current of 0.8 A with a voltage of approximately 8.5 V. Based on a residential electricity rate of 0.5 CNY·kWh−1, the daily energy cost is only 0.08 CNY, making it economically viable for continuous household use.

How does the disinfection efficacy of electrogenerated H2O2 compare to conventional HOCl in terms of bacterial inactivation and by-product formation?

At H2O2 concentrations of 50–200 mg·L−1, complete bacterial inactivation is achieved within 4–24 h. Unlike HOCl, H2O2 does not produce harmful halogenated by-products, ensuring safer indoor air quality. The study demonstrates that H2O2 is as effective as HOCl but without the associated toxic by-products.

What is the long-term stability and maintenance requirement of the gas diffusion electrode in a toilet tank environment?

The study conducted a one-month continuous experiment, indicating stable performance over that period. However, long-term durability beyond one month and maintenance protocols (e.g., electrode cleaning or replacement) were not detailed, warranting further investigation for commercial deployment.

Can this technology be retrofitted into existing toilet systems, or does it require specialized tank designs?

The electrode module was installed in a standard toilet tank, suggesting retrofitting is feasible. However, the study does not specify compatibility with all toilet models, and installation may require minor modifications to accommodate the electrode and power supply.

What are the potential safety concerns regarding hydrogen peroxide accumulation in the seal water and its release during flushing?

H2O2 concentrations used (50–200 mg·L−1) are safe for household use and decompose into water and oxygen. The study did not measure airborne H2O2 levels during flushing, but given the low concentrations and rapid decomposition, the risk is minimal. Nevertheless, monitoring of H2O2 vapor is recommended for comprehensive safety assessment.

Related Chinese Research & Cross-Citations

Research Citation2026
Exploring the Potential Molecular Mechanisms of Eight Environmental Pollutants in Lung Adenocarcinoma through Network Toxicology, Machine Learning, and Multi-Omics Analysis

Exploring the Potential Molecular Mechanisms of Eight Environmental Pollutants in Lung Adenocarcinoma through Network Toxicology, Machine Learning, and Multi-Omics Analysis

Epidemiological studies have established a significant association between exposure to environmental pollutants (EP) and the risk of lung adenocarcinoma (LUAD). This study integrates network toxicology and multi-omics analysis to elucidate the EP-LUAD molecular regulatory network and identify key regulatory genes, thereby revealing novel mechanisms of environmental carcinogenesis. Transcriptomic data from GEO and TCGA databases yielded 4,971 and 4,488 disease-related targets, respectively. Integration of toxicology databases (TargetNet, Swiss Target Prediction, CTD, SEA) identified 24,860 potential targets for eight common pollutants (SO2, NO, CO, NO2, O3, benzene, toluene, and polycyclic aromatic hydrocarbons). Intersection of these datasets produced 1,536 EP-LUAD common target genes. Protein-protein interaction network analysis identified 247 core targets. Machine learning selected five key genes: AGER, CAV1, CD44, CEP55, and GNB3, which demonstrated robust diagnostic and prognostic efficacy. Their expression correlated with immune cell infiltration, including CD4+ memory T cells and macrophages. Single-cell RNA sequencing revealed epithelial cell-specific expression patterns. Molecular docking confirmed stable pollutant-target binding, with PAH showing highest affinity for CD44 (binding energy −9.32 kcal·mol−1) and GNB3 (−8.32 kcal·mol−1). These findings establish AGER, CAV1, CD44, CEP55, and GNB3 as core molecular mediators of pollution-related LUAD. The high-affinity binding of PAH to CD44 and GNB3 underscores its carcinogenic potential. This study constructs a multi-level regulatory network for EP-LUAD, revealing underlying molecular mechanisms and providing novel potential targets and theoretical basis for early warning and intervention.

Examine Full Data & PDF
Research Citation2026
Effects of Different Functionalized Nanoplastics on the Transformation of Extracellular Antibiotic Resistance Genes in Aquatic Environments

Effects of Different Functionalized Nanoplastics on the Transformation of Extracellular Antibiotic Resistance Genes in Aquatic Environments

The rapid dissemination of antibiotic resistance genes (ARGs) in aquatic environments poses serious threats to public health and environmental safety under the 'One Health' framework. Nanoplastics (NPs), as co-occurring pollutants, can exacerbate ARG risks by promoting horizontal gene transfer (HGT), yet the influence of different functional groups on extracellular ARG (eARG) transformation remains unclear. This study investigated the effects of carboxy-modified polystyrene NPs (PS-COOH) and amino-functionalized polystyrene NPs (PS-NH2) compared to unmodified polystyrene NPs (PS) on the transformation of the extracellular resistance plasmid IE-V1955 (carrying an ampicillin resistance gene) into Escherichia coli DH5α. Results showed that PS-COOH exposure promoted plasmid transformation similarly to PS, with effects increasing over 0.1–20 mg·L−1. Low concentrations (0.1–0.5 mg·L−1) of PS-NH2 also enhanced transformation, with stronger effects than PS-COOH at equal doses, whereas high concentrations (1–20 mg·L−1) inhibited it. Mechanistically, PS-COOH (0.1–20 mg·L−1) and low PS-NH2 induced intracellular reactive oxygen species (ROS), increased cell membrane permeability, elevated the protein-to-polysaccharide ratio in extracellular polymeric substances (EPS), and promoted biofilm formation, thereby facilitating transformation. High PS-NH2 concentrations caused excessive ROS leading to cell lysis and formed aggregates with plasmids larger than membrane pores, blocking uptake. These findings provide a theoretical basis for assessing the combined environmental health risks of NPs and ARGs.

Examine Full Data & PDF
Research Citation2026
Cardiovascular Toxicity Induced by Micro/Nano-Plastics and Its Mechanisms

Cardiovascular Toxicity Induced by Micro/Nano-Plastics and Its Mechanisms

Micro/nano-plastics (MNPs) are emerging contaminants widely detected in human circulatory systems, including blood, heart, and vascular endothelium, raising concerns about cardiovascular health risks. This systematic review analyzed 61 peer-reviewed studies (2008–2024) to elucidate the cardiotoxic effects and molecular mechanisms of MNPs. Evidence indicates that MNPs exposure elevates risks of atherosclerosis, thrombosis, and arrhythmias through oxidative stress, inflammatory cascades, endothelial dysfunction, and metabolic dysregulation. Notably, co-exposure with persistent organic pollutants (POPs) or heavy metals may produce synergistic or antagonistic effects. Current research relies predominantly on animal and cell models, with critical gaps in low-dose, long-term exposure data and epidemiological evidence. Future studies should optimize experimental designs, integrate metabolomics and epigenetics, and explore transgenerational effects and combined toxicity mechanisms to inform pollution control policies and mitigate cardiovascular risks.

Examine Full Data & PDF
Research Citation2026
Body Burden of Polybrominated Diphenyl Ethers and Joint Effects on Thyroid Function in a Physical Examination Population in Shenzhen

Body Burden of Polybrominated Diphenyl Ethers and Joint Effects on Thyroid Function in a Physical Examination Population in Shenzhen

This study characterized the body burden of polybrominated diphenyl ethers (PBDEs) in a physical examination population in Shenzhen and evaluated its impact on thyroid function. Serum samples from 368 residents were analyzed for eight PBDE congeners using atmospheric pressure gas chromatography-tandem mass spectrometry (APGC-MS/MS). The median concentration of ∑8PBDEs was 10.2 ng·g⁻¹ lipid weight (lw), ranging from 0.13 to 2089.4 ng·g⁻¹ lw, with BDE-209 predominating (59.7% of total). Multiple linear regression revealed that a 1.7-fold increase in serum BDE-153 was associated with a 0.4% increase in free triiodothyronine (FT3) (P<0.05), while a 1.7-fold increase in BDE-183 was associated with a 0.9% decrease in total triiodothyronine (T3) and a 0.7% decrease in FT3 (P<0.05). Bayesian kernel machine regression (BKMR) indicated a negative correlation between mixed PBDE exposure and thyroid-stimulating hormone (TSH) at high exposure levels. Weighted quantile sum (WQS) regression showed that mixed exposure was associated with decreased T3 levels and T3/FT3 ratio, with BDE-153 and BDE-183 as the primary contributors. These findings suggest that PBDE exposure may adversely affect thyroid function and disrupt thyroid hormone homeostasis, with BDE-183 and BDE-153 playing key roles. This study provides a scientific basis for PBDE health risk assessment and thyroid protection.

Examine Full Data & PDF
Research Citation2026
Mechanisms of Natural Organic Matter in Regulating Microplastic Aggregation and Transport in Soil-Groundwater Systems: A Review

Mechanisms of Natural Organic Matter in Regulating Microplastic Aggregation and Transport in Soil-Groundwater Systems: A Review

Microplastics (MPs) are persistent emerging contaminants ubiquitously distributed in soil-groundwater environments, where their aggregation and transport critically govern pollutant fate and ecological risks. Natural organic matter (NOM), a complex assemblage of organic compounds, interacts with MPs and porous media via hydrogen bonding, π-π interactions, hydrophobic effects, and electrostatic binding, thereby modulating MP surface properties and environmental behavior. This review systematically synthesizes the mechanisms by which NOM influences MP aggregation and transport, with emphasis on the distinct roles of humic substances, proteins, and extracellular polymeric substances (EPS), and their synergistic modulation with solution chemistry (pH, ionic strength, ion type). Additionally, NOM accelerates MP aging and alters surface characteristics, consequently impacting transport capacity. Current research limitations are identified, and future directions are proposed to inform MP pollution risk assessment and management strategies. Key findings indicate that NOM generally enhances MP stability and mobility at low ionic strengths, while high ionic strengths may induce aggregation depending on NOM type and ion valence. Humic substances predominantly increase electrostatic repulsion, whereas proteins and EPS can bridge particles, promoting aggregation. Aging processes, accelerated by NOM photochemical activity, increase surface oxygen functionality and hydrophilicity, further altering transport. The review underscores the need for systematic studies under environmentally relevant conditions to predict MP fate accurately.

Examine Full Data & PDF
Research Citation2026
Neurotoxicity of Carboxyl-Modified Polystyrene Microplastics on Zebrafish at Early Developmental Stage

Neurotoxicity of Carboxyl-Modified Polystyrene Microplastics on Zebrafish at Early Developmental Stage

Carboxyl-modified polystyrene microplastics (PS-COOH) are negatively charged particles formed by surface oxidation and functional group modification of polystyrene microplastics (PS), widely used in biomedical and analytical chemistry. However, studies on their neurotoxic effects on aquatic organisms are scarce. This study employed zebrafish (Danio rerio) as a model organism, exposing embryos to environmentally relevant concentrations (0.1, 1, 10, 100 μg·L−1) of PS and PS-COOH. Neurotoxic effects were assessed by measuring tail coiling frequency at 24 hpf and swimming velocity under alternating light/dark cycles at 120 hpf. Results demonstrated that both PS and PS-COOH induced neurotoxicity, with PS-COOH significantly reducing tail coiling frequency and average swimming speed compared to PS (P<0.05). Exposure to 10 μg·L−1 PS-COOH disrupted neurotransmitter homeostasis, altering levels of acetylcholine (ACh), serotonin (5-HT), and γ-aminobutyric acid (GABA). Transgenic zebrafish Tg(huc:EGFP) fluorescence assays revealed that PS-COOH (0.1–100 μg·L−1) caused damage to central neurons. These findings indicate that PS-COOH exposure impairs cholinergic, serotonergic, and GABAergic neurotransmission, induces neuronal damage, and exerts neurotoxic effects on zebrafish larvae. This study provides a theoretical basis for assessing the ecological and health risks of modified microplastics.

Examine Full Data & PDF