Ozone Production Research Articles

Impact of the Indian Ocean Dipole Mode on Planetary Boundary Layer Ozone in China

AbstractThe Indian Ocean Dipole (IOD) mode exerts distinct impacts on the climate in China and can further affect tropospheric ozone. Using long‐term GEOS‐Chem simulations, we found distinct changes in planetary boundary layer ozone throughout China during positive and negative phases of IOD. In summer, ozone shows synchronized increases except in southern China during positive IOD; the ozone increases are dominated by chemical production and transport in northern and western China, respectively. The increased precursor from biogenic emissions contributed to ozone chemical formation in the northern region, and the increased precipitation and decreased solar radiation hindered ozone production in southern China. Ozone changes show good symmetry over most regions during negative IOD. In autumn, the ozone reduction in southern China shares the same reason as summer, while the chemical increase over northern China is affected more by changes in solar radiation and relative humidity than in the precursor emission.

Impacts of tropical cyclone–heat wave compound events on surface ozone in eastern China: comparison between the Yangtze River and Pearl River deltas

Abstract. China has implemented some air pollution management measures in recent years, yet severe ozone pollution remains a significant issue. The southeastern coast of China (SECC) is often influenced by hot extremes and tropical cyclones (TCs), and the two can occur simultaneously (TC–HDs). The compound TC–HDs show a rising trend in the summers of 2014–2019, potentially affecting ozone pollution. Here, we found that surface ozone concentrations over the SECC are more elevated during extremely hot days than the summer climatology. However, compared to extremely hot days alone (AHDs), the maximum 8 h average ozone (MDA8 O3) concentration increases by an average of 6.8 µg m−3 in the Pearl River Delta (PRD) and decreases by 13.2 µg m−3 in the Yangtze River Delta (YRD) during the compound TC–HDs. The meteorological conditions during AHDs favor the chemical production of ozone over the SECC, exhibiting increased temperature and solar radiation and decreased relative humidity. Relative to AHDs, strong northeasterly winds prevail in the SECC during TC–HDs, suggesting the potential of ozone cross-regional transport between YRD and PRD. The process analysis in the chemical transport model (GEOS-Chem) suggests that relative to AHDs, the chemical production of ozone is enhanced in YRD during TC–HDs, while horizontal transport alleviates ozone pollution in YRD but worsens it in PRD through cross-regional transport. The results highlight the significant effects of cross-regional transport in modulating ozone pollution in the two megacity clusters during hot extremes accompanied by TC activities, giving insight into future ozone control measures over the SECC under global warming.

Effects of mineral fertilization (NPK) on combined high temperature and ozone damage in rice

BackgroundIncreasing concern has recently been highlighted regarding crop damage due to extreme weather events caused by global warming and the increased production of ground-level ozone. Several studies have investigated rice growth in response to fertilization conditions under various environmental stress conditions; however, studies on growth development in response to fertilization conditions under combined high-temperature/ozone treatment conditions are scarce. In this study, we aimed investigate the growth and physiological development of rice under combined high temperature and ozone treatment conditions and to reveal the damage-mitigation effects of NPK fertilization treatments.ResultsThe plants were treated with varying levels of NPK [N2 (N-P-K: 9.0-4.5-4.0 kg/a), P2 (4.5-9.0-4.0 kg/a), K2 (4.5-4.5-8.0 kg/a), and control (4.5-4.5-4.0 kg/10a).] under combined high-temperature (35 ℃) and ozone (150 pb) treatment conditions. Analysis of the growth metrics, including plant height, leaf age, dry weight, and the plant height/leaf age (PH/L) ratio were revealed that combined high-temperature/ozone treatment promoted the phenological development indicated by increasing leaf age but decreased the plant height and dry weight indicating its negative effect on quantitative growth. The effects of this combined high-temperature/ozone treatment on growth were alleviated by NPK fertilization, particularly in K2 treatment but worsened in N2 treatment. Visible damage symptoms in rice leaves induced by exposure to the combined stressors was also alleviated by the K2 treatment. At the physiological level, K2 treatment reduced the expression of OsF3H2, which is associated with antioxidant activity, suggesting that potassium improved stress tolerance. Additionally, expression of genes related to abscisic acid (ABA) metabolism showed increased OsNECD (ABA synthesis) and decreased OsCYP707A3 (ABA degradation) in the K2 treatment, promoting a stronger adaptive stress response. Stomatal conductance measurements indicated a slight increase under K2 treatment, reflecting enhanced regulation of stomatal function during stress.ConclusionThe study highlights the potential of potassium fertilization to mitigate combined high-temperature and ozone stress in rice, suggesting it as a strategy to improve crop resilience and optimize fertilization. The findings offer insights into fertilization treatments and can guide future research on stress tolerance in crops.

National and transboundary contributions to surface ozone concentration across European countries

Tropospheric ozone impacts health, climate, and ecosystems. Effective ozone mitigation policies are challenged by limited quantitative understanding of national versus transboundary contributions to surface ozone. This study uses a chemical transport model with a source apportionment algorithm to analyze ozone contributions across Europe from 2015 to 2017 during peak ozone season. We quantify country-level ozone production and imported ozone, distinguishing contributions from 35 European countries, neighboring countries, seas, and hemispheric influences. Results show substantial contributions from outside the 35 European countries, with hemispheric contributions playing a significant role. European contributions are crucial during high ozone episodes, especially from Germany, France, Italy, the UK, Poland, and Spain. Spain, northern Italy, and northwest France are identified as areas where national precursor reductions would be more effective in improving national air quality. Furthermore, 25 of the 35 European countries studied are net importers of cumulative ozone mass, with the Netherlands, Belgium, and the UK acting as major exporters. These findings highlight the need for comprehensive air quality policies and cross-border cooperation.

Analysis of Ozone Pollution and Precursor Control Strategies in the Pearl River Delta During Summer and Autumn Transition Season

To analyze the causes of ozone pollution in the Pearl River Delta （PRD） Region during the summer and autumn transition seasons, a case study was carried out in Guangzhou, which is located in the center of the PRD Region, to analyze the ozone photochemical production and destruction pathways as well as emission reduction scenarios using a box model based on comprehensive observation. The results showed that the stagnant meteorological conditions and high temperature during the observation period were suitable for the photochemical production of ozone, which led to widespread and prolonged ozone pollution. Aromatic hydrocarbons （AHs） contributed the most to the ozone formation potential （OFP）, and m/p-xylene, toluene, and o-xylene were the major three VOC species contributing to the OFP. Box model analysis revealed that the averaged net O3 production rate during the polluted period was 23.2×10-9 h-1 and the peak reached 39.2×10-9 h-1. The HO2·+NO and NO2+·OH reaction pathways contributed the most to the local photochemical ozone production （51.2%） and destruction （47.0%）, respectively. Observed ozone concentration was primarily controlled by both the local photochemical O3 production and the export-dominated transport. The RIR and EKMA analyses showed that O3 formation in Guangzhou during the summer-autumn transition seasons was mainly a VOC-limited regime and AHs showed the greatest sensitivity to O3 production. Toluene, m/p-xylene, o-xylene, n-butane, and propylene were the five key components affecting O3 generation. The analysis of reduction scenarios showed that reducing anthropogenic VOC emissions was the most favorable way to reduce O3 concentrations； however, if NOx emission was controlled after reducing VOCs, the O3 concentration would rebound in a short time. Our results suggested that the synergistic reduction of VOCs and NOx while mainly focusing on VOCs alleviation should be implemented to continuously reduce ozone concentrations in the future.

Development of inductive energy storage pulsed power supply using SiC semiconductor devices for ozone production by streamer discharges

Abstract Inductive energy storage (IES) pulsed power generator driven by the silicon carbide (SiC)-MOSFET with the blocking voltage of 1.2 kV was developed. The IES pulsed power generator consists of a capacitor, a pulsed transformer and the SiC-MOSFET used as an opening switch. The influence of turn ratio of the pulsed transformer on the output voltage was evaluated. The amplitude of output voltage increased with increasing the secondary turn ratio. Under the conditions of no lord , a peak output voltage of 13 kV and a pulse width of 120 ns were obtained with a voltage across the drain-source terminals of the MOSFET of 1kV with no lord. The peak voltage value increased, and the peak current and pulse width value decreased with increasing load resistance and decreased capacitance. The maximum energy transfer efficiency was obtained with 500 Ω and was Approximately 56%.

Apparent effective ionization coefficient in N2 and O2 gas mixtures determined with two separate methods

N2:O2 gas mixtures are important for applications of atmospheric pressure plasmas such as ozone production, air purification from VOCs and NOx and surface treatments. Fundamental parameters such as the effective ionization coefficient are inputs for theoretical plasma models for applications and must thus be accurately known. This work determined the apparent effective ionization coefficient in N2:O2 mixtures in a broad reduced electric field strength E/N range of 150–1200 Td with two separate methods and compared with BOLSIG+ calculations of reduced effective ionization coefficient. Additionally, the equilibrium distance required to establish a steady-state electron energy distribution was estimated from spatial profiles of optical emission.

A multi-perspective assessment of satellite surface Ozone products in China: Spatiotemporal variability, land cover impacts and pollution monitoring capability

Accurate Ozone concentration datasets are essential for comprehensively understanding air quality, climate change, and the health and societal impacts related to Ozone exposure. Currently, there is limited research comparing near-surface Ozone concentration products. In this study, we employed continuous evaluation metrics (R2, RMSE, RB) and classified statistical indicators (POD, FAR, CSI) to comprehensively compare and assess three near-surface Ozone concentration products (CHAP O3, LGAP O3, TAP O3) in China from 2015 to 2020. Our findings indicate that CHAP outperforms other products in estimating near-surface Ozone concentration and monitoring Ozone pollution in China. In terms of temporal scale, the three Ozone products exhibited a strong correlation in specific regions across multiple time scales (R2> 0.6). The RMSE values of the products were lower in CHAP, followed by TAP, and higher in LGAP. Notably, LGAP significantly underestimated Ozone concentrations over time. Regarding spatial scale, CHAP and TAP align closely with ground observations, whereas LGAP shows significant underestimation in latitude and longitude, with the discrepancy increasing gradually along the longitude. All three products exhibited strong correlations with measured data at various sites (R2> 0.6). The RMSE and | RB| distributions of CHAP and TAP were similar and superior to LGAP. CHAP and TAP perform better than LGAP under specific land cover types, especially in urban and vegetation-covered areas, while their performance is relatively poorer in farmland-covered areas. Concerning pollution events, CHAP and TAP exhibit strong detection capabilities for Ozone pollution events in the Beijing–Tianjin–Hebei (BTH) region and other majority areas, with POD values exceeding 0.6, and FAR values below 0.1, showcasing excellent CSI performance. In contrast, LGAP has weaker detection capabilities, with POD values primarily in the 0–0.2 range and lower CSI values. This comprehensive evaluation sheds light on the strengths and weaknesses of different near-surface Ozone concentration products and their implications for assessing Ozone pollution in China.

Ozone production in nanosecond pulsed dielectric barrier discharge in synthetic air: the Effect of Pulse Width

This work investigates the effect of pulse width on the characteristics of electrical discharge, optical emission spectra and ozone production in a water electrode DBD using a modulable nanosecond pulsed power supply. Results show that the increase of pulse width tpw slightly increases the spectral intensity and the rotational temperature Trot, with a typical Trot of 299 ± 5 K at an applied peak voltage Vp of 18.6 kV and a tpw of 400 ns. The electronic excitation temperature Texc increases linearly with Vp and gradually with tpw, while the electron density ne shows a non-linear relationship with tpw. Results also show that an increase in tpw slightly increases the energy density. At low energy densities (SIE < 50 J/L), increasing tpw can improve ozone generation efficiency, reaching a maximum of 99.64 ± 0.87 g/kWh at 33.60 ± 1.53 J/L at a tpw of 900 ns. This investigation provides substantial insight into the nanosecond pulsed ozone production.

A new lightning scheme in the Canadian Atmospheric Model (CanAM5.1): implementation, evaluation, and projections of lightning and fire in future climates

Abstract. Lightning is an important atmospheric process for generating reactive nitrogen, resulting in the production of tropospheric ozone, as well as igniting wildland fires, which result in potentially large emissions of many pollutants and short-lived climate forcers. Lightning is also expected to change in frequency and location with the changing climate. As such, lightning is an important component of Earth system models. Until now, the Canadian Earth System Model (CanESM) did not contain an interactive-lightning parameterization. The fire parameterization in CanESM5.1 was designed to use prescribed monthly climatological lightning. In this study, we have added a logistical regression lightning model that predicts lightning occurrence interactively based on three environmental variables and their interactions in CanESM5.1's atmospheric model, CanAM5.1 (Canadian Atmospheric Model), creating the capacity to interactively model lightning, allowing for future projections under different climate scenarios. The modelled lightning and resulting burned area were evaluated against satellite measurements over the historical period, and model biases were found to be acceptable. Modelled lightning had a small negative bias and excellent land–ocean ratio compared to satellite measurements. The modified version of CanESM5.1 was used to simulate two future climate scenarios (SSP2-4.5 and SSP5-8.5; Shared Socioeconomic Pathway) to assess how lightning and burned area change in the future. Under the higher-emissions scenario (SSP5-8.5), CanESM5.1 predicts almost no change to the global mean lightning flash rate by the end of the century (2081–2100 vs. 2015–2035 average). However, there are substantial regional changes to lightning – particularly over land – such as a mean increase of 6 % in the northern mid-latitudes and decrease of −8 % in the tropics. By the century's end, the change in global total burned area with prescribed climatological lightning was about 2 times greater than that with interactive lightning (42 % vs. 26 % increase, respectively). Conversely, in the northern mid-latitudes the use of interactive lightning resulted in 3 times more burned area compared to that with unchanging lightning (48 % vs. 16 % increase, respectively). These results show that the future changes to burned area are greatly dependent on a model's lightning scheme, both spatially and overall.

Self-supporting three-dimensional CuNi–Sb–SnO2 anode with ultra-long service life for efficient removal of antibiotics in wastewater

Electrochemical ozone production (EOP) is a promising technology for the removal of contaminants in wastewater. However, traditional two-dimensional anodes for EOP are restricted by their reliance on substrates and limited surface area, thus exhibiting poor stability and efficiency. Herein, a novel three-dimensional Sb–SnO2 with Cu and Ni co-doped (3D CuNi-ATO) was synthesized via a facile pressing-sintering method without the Ti substrate. 3D CuNi-ATO had a specific surface area two orders of magnitude higher than conventional CuNi-ATO/Ti, as well as the significant capability of EOP that differs from intrinsic 3D ATO. This endowed 3D CuNi-ATO with the capability to remove tetracycline with a pseudo-first-order rate constant of 0.033 min−1 under a low current density of 5 mA cm−2 within 120 min, which was far more efficient than that by 3D ATO and other two-dimensional anodes reported. The 3D CuNi-ATO was confirmed stable in 100 cycles and had an accelerated service lifetime of over 1100 h versus 83 h of CuNi-ATO/Ti. The degradation of tetracycline in complex matrix and flow-through reactors further revealed the promising potential of 3D CuNi-ATO to be applied in scenarios of practical application and continuous high-rate treatment.

Methylene Blue Degradation Using Non-Thermal Plasma

Methylene blue (C16H18ClN3) dye can be decomposed using non-thermal plasma. However, there is a problem in that the maintenance of electrodes and dielectrics is necessary due to the durability and heat generation problems due to the high temperatures. Therefore, in this study, a comparative experiment was performed between the flat DBD plasma module and the diffuser DBD module under the same conditions. For methylene blue decomposition, the characteristic changes in the air flow rate, ozone production rate, energy consumption rate, and decomposition rate were compared. In the experiment, 7 L water was placed in a 15 L reactor, and measurements were performed for approximately 1 h. We performed the same process by setting the initial methylene blue concentration to 143 mg/L. According to the results, the flat DBD module achieved a decomposition rate of 100% in 40 min, an energy yield of 46.7 g/kWh, and an ozone generation amount of 6.5 g/h. The diffuser DBD module achieved a decomposition rate of 90%, an energy production of 24.6 g/kWh, and an ozone generation of 1.97 g/h in 60 min.

Insights into the long-term (2005–2021) spatiotemporal evolution of summer ozone production sensitivity in the Northern Hemisphere derived with the Ozone Monitoring Instrument (OMI)

Abstract. Tropospheric ozone (O3) formation depends on the relative abundance of precursor species, nitrogen oxides (NOx), and volatile organic compounds (VOCs). Advancements in satellite retrievals of formaldehyde (HCHO) and nitrogen dioxide (NO2) vertical column densities (VCDs), and the corresponding HCHO/NO2 ratios (FNRs), provide the opportunity to diagnose the spatiotemporal evolution of O3 production sensitivity regimes. This study investigates trends of Ozone Monitoring Instrument (OMI)-derived summertime VCD HCHO, NO2, and FNRs in the Northern Hemisphere from 2005 to 2021. FNR trends were analyzed for polluted regions, specifically for 46 highly populated cities, over the entire 17-year period and in 2020 when global anthropogenic emissions were reduced due to COVID-19 lockdown restrictions. It was determined that OMI-derived FNRs have increased on average by ∼ 65 % across cities in the Northern Hemisphere. Increasing OMI-derived FNRs indicates a general transition from radical-limited to NOx-limited regimes. The increasing trend is driven by reduced NO2 concentrations because of emission-control strategies of NOx. OMI FNR trends were compared to ground-based in situ measurements in US cities, and it was determined that they can capture the trends in increasing FNRs (R=0.91) and decreasing NO2 (R=0.98) occurring at the surface. OMI FNRs in urban areas were higher (∼ 20 %) in 2020 for most cities studied here compared to 2019 and 2021. In addition to studying the longest period of OMI FNRs across the Northern Hemisphere to date, the capabilities and challenges of using satellite VCD FNRs to study surface-level O3 production sensitivity regimes are discussed.

Beyond self-healing: stabilizing and destabilizing photochemical adjustment of the ozone layer

Abstract. The ozone layer is often noted to exhibit self-healing, whereby depletion of ozone aloft induces ozone increases below, explained as resulting from enhanced ozone production due to the associated increase in ultraviolet (UV) radiation below. Similarly, ozone enhancement aloft can reduce ozone below (reverse self-healing). This paper considers self-healing and reverse self-healing to manifest a general mechanism we call photochemical adjustment, whereby ozone perturbations lead to a downward cascade of anomalies in UV and ozone. Conventional explanations for self-healing imply that photochemical adjustment is stabilizing, damping perturbations towards the surface. However, photochemical adjustment can be destabilizing if the enhanced UV disproportionately increases the ozone sink, as can occur if the enhanced UV photolyzes ozone to produce atomic oxygen, which speeds up catalytic destruction of ozone. We analyze photochemical adjustment in two linear ozone models (Cariolle v2.9 and LINOZ), finding that (1) photochemical adjustment is destabilizing above 40 km in the tropical stratosphere and (2) self-healing often represents only a small fraction of the total photochemical stabilization. The destabilizing regime above 40 km is reproduced in a much simpler model: the Chapman cycle augmented with destruction of O and O3 by generalized catalytic cycles and transport (the Chapman+2 model). The Chapman+2 model reveals that photochemical destabilization occurs where the ozone sink is more sensitive than the source to perturbations in overhead column ozone, which is found to occur when the window of overlapping absorption by O2 and O3 is optically unsaturated, i.e., when overhead slant column ozone is below approximately 1018 molec. cm−2.

Ozone sensitivity to high energy demand day electricity and onroad emissions during LISTOS

ABSTRACT Using a high-resolution, 1.33 km by 1.33 km coupled Weather Research and Forecasting-Community Multi-scale Air Quality Model (WRF-CMAQ), we quantify the impact of emissions of nitrogen oxides (NOx) from high energy demand day (HEDD) electricity generating units (EGU) and onroad vehicles on ambient ozone air quality in the Long Island Sound Tropospheric Ozone Study (LISTOS) region covering New York City (NYC); Long Island, NY; coastal Connecticut; and neighboring areas. We test sensitivity scenarios to quantify HEDD EGU NOx contributions to ozone: (1) zero out HEDD EGU emissions, (2) dispatch HEDD EGUs starting with the lowest NOx emitting units first, (3) reduce onroad emissions by 90%, (4) combine zero out HEDD EGU emissions and reducing onroad emissions by 90%, and (5) dispatch HEDD EGUs starting with the lowest emitting units coupled with a reduction in onroad emissions by 90%. Results determine that HEDD EGUs lead to highly localized impacts on ambient concentrations of ozone while onroad emission reductions lead to large-scale regional concentration impacts. Further, reducing onroad emissions by 90% leads to spatially smaller VOC-limited regions and spatially larger transitional and NOX-limited regions around NYC. Despite the limited scale at which the EGU emission reductions occur, modifying HEDD EGU NOX emissions still provides substantial benefits in reducing ozone concentrations in the region, particularly at elevated ozone concentrations above 70 ppb. Implications: High-resolution coupled meteorology-chemistry modeling was used to quantify the impacts of high energy demand day (HEDD) electricity generating units (EGUs) and onroad transportation emissions changes on ozone air quality in the LISTOS region. Despite being highly localized and variable, HEDD EGUs NOX emissions sensitivity tests led to quantifiable changes in ozone. Further, reducing onroad emissions by 90% produced large decreases in ozone concentrations and led to a more NOX-sensitive ozone photochemical regime. With a transition to greater NOX-sensitivity, urban NOX-titration weakens and ozone is more likely to decline with the removal of additional NOX from sources like HEDD EGUs.

Variations in summertime ozone in Nanjing between 2015 and 2020: roles of meteorology, radical chain length and ozone production efficiency

Variations in summertime ozone in Nanjing between 2015 and 2020: roles of meteorology, radical chain length and ozone production efficiency

Efficient Electrochemical Ozone and Hydrogen Peroxide Production by Synergistic Effect of Atomically Dispersed Pt, Boron and Nitrogen Doped 2D Diamonds

Efficient Electrochemical Ozone and Hydrogen Peroxide Production by Synergistic Effect of Atomically Dispersed Pt, Boron and Nitrogen Doped 2D Diamonds

The effect of different climate and air quality policies in China on in situ ozone production in Beijing

Abstract. In recent years, clean air policies have led to reductions in air pollution across China. Alongside this, emerging carbon neutrality (CN) policies that aim to address the impacts of climate change may also deliver air quality (AQ) co-benefits or climate penalties. Different CN policies will lead to different changes in volatile organic compound (VOC), NOx and particulate matter (PM) emissions, which will in turn impact the photochemical production of secondary pollutants such as ozone (O3). It is currently unclear how different combinations of AQ and CN policies may impact in situ O3 production across China in the future. A detailed chemical box model incorporating the Master Chemical Mechanism was developed to investigate the impact of combined AQ and CN policies on O3 formation in Beijing. The Multi-resolution Emission Inventory model for Climate and air pollution research (MEIC) and the Dynamic Projection model for Emissions in China (DPEC) were used to estimate future pollutant mixing ratios, relative to ambient observations of 35 VOCs, NOx, CO and aerosol surface area (ASA) during the APHH-Beijing 2017 summer campaign. The most ambitious policy scenario, “Ambitious Pollution 1.5D Goals”, led to the largest reduction in O3 production by 2060 but was not the most impactful scenario for reducing O3 production between 2030–2045. Larger reductions were observed under the “Ambitious Pollution Neutral Goals” policy, which focuses on achieving net zero by 2060. O3 production was found to be most sensitive to changes in the OLE2 group of VOCs (alkenes where kOH&gt;7×104 ppm−1 min−1; a 5 % increase in OLE2 increased simulated O3 production by 1.12 %). However, reducing less reactive but higher concentration species in Beijing (such as short-chain alkanes) led to larger reductions in O3 production under all scenarios. O3 production was not sensitive to changes in ASA, with a 69 % decrease in ASA leading to a change of &lt;1 % in O3. However, doubling biogenic VOCs in the model further increased O3 production in 2060 under all future scenarios by up to 18 %, indicating that the influence of future climate-induced changes in biogenic emissions may have a significant impact on in situ O3 formation in Beijing. This study highlights that the emission trajectories of certain specific VOCs are highly influential in determining possible future O3 air quality effects that may arise from increasing ambient temperatures and decarbonisation in Beijing.

Combating Pathogens Using Carbon-Fiber Ionizers (CFIs) for Air Purification: A Narrative Review

Airborne pathogens, though a minor fraction of airborne particles, can cause infections, intoxications, or allergic reactions through respiration, dermal contact, or ingestion. The SARS-CoV-2 pandemic has underscored the significance of mitigating airborne microbial threats. Traditional air ionization methods, such as dielectric barrier discharge and metal tip corona discharge, produce ozone, a reactive and potentially harmful byproduct. However, carbon-fiber ionizers (CFIs) generate high concentrations of ions with minimal ozone production, making them a safer alternative. Operating at voltages below 5 kV, CFIs are more efficient than their metallic counterparts. This review focuses on the antimicrobial efficacy of CFIs, which produce unipolar ions that can disrupt microbial membranes, leading to cell death. Compared to ultraviolet light sterilization, CFIs are cost-effective and suitable for small spaces. The literature review highlights the need for comprehensive studies to evaluate the real-world application and effectiveness of CFIs. Many existing studies are limited by small-scale testing and insufficient data reporting, complicating comparative analyses. Our work aims to provide a detailed perspective on CFIs, examining their impact on various microorganisms, ion efficacy, ionization outcomes, and ozone generation levels. By addressing these aspects, the review seeks to offer an updated understanding of CFIs’ antimicrobial capabilities and to identify limitations in current research, paving the way for more informed and effective air purification strategies.

Cotransport of 6PPD-Q and pristine/aged microplastics in porous media: An insight based on transport forms and mechanisms

The environmental fate and risks of microplastics (MPs) and their associated contaminants have attracted increasing concern in recent years. In this study, the cotransport of six kinds of pristine and aged MPs and the antiager ozonation product N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine-quinone (6PPD-Q) were investigated via a series of batch and transport experiments, and characteristic analysis (e.g., SEM, FTIR and XPS). Generally, pristine MPs exhibit higher adsorption ability than aged MPs due to the hydrophobic interaction. The 6PPD-Q usually exhibited both free moving and bond-MPs moving during transport process in presence of MPs, but none free 6PPD-Q was detected in presence of pristine PP MPs. The mobility of 6PPD-Q was generally facilitated in presence of MPs by bond-MPs moving due to the hydrogen bonding, halogen bonding, π-π interaction (the maximum total mass recovery of 84.11%), which efficiency was influenced with the combined effect of adsorption ability and mobility of MPs. The pristine PVC MPs showed highest facilitation on 6PPD-Q transport. The retained 6PPD-Q in porous media also was released by various MPs with different mass recovery ranged from 15.72% to 56.26% via surface moving of MPs around porous media. Both the dissolved and retained 6PPD-Q decreased the MPs mobility with the minimum mass recovery of 34.02%. Findings from this study contribute to the prediction and assessment of the combined risks of MPs and 6PPD-Q.