Search Results (603)

A predictive gate-to-gate life cycle assessment (LCA) of plasma-assisted ammonia synthesis at TRL 4 is presented according to ISO 14040/44 standards. General plasma-assisted synthesis was evaluated through a mini-review‚ sensitivity analysis‚ and predictive LCA. The specific DBD needle-to-plate configuration LCA is performed using previously published experimental data. Two distinct scenarios were investigated. In the literature-based baseline scenario derived from sensitivity analysis, electricity consumption was 533 kWh/kg NH₃, giving a carbon footprint of 26.65–639.60 kg CO₂-eq/kg NH₃; electricity contributed 98.5% of total emissions, and impacts remained about 2.05 times higher than conventional Haber–Bosch. In contrast, the experimental DBD case study required 63,450 kWh/kg NH₃, showing reactor efficiency as the dominant driver of environmental performance. The BCS (≈1.39 kWh/kg NH₃) suggests that optimized plasma systems could potentially surpass conventional ammonia synthesis in energy efficiency. The environmental performance of plasma-assisted ammonia synthesis is affected by NH₃, NO_x, N₂O, and hydrogen emissions due to impacts on climate, air quality, water systems, and biodiversity. Future improvements may come from reactor and electrode optimization, catalyst integration, alternative plasma sources, and better process and heat integration, although deployment will likely depend on major efficiency gains and may be limited to niche decentralized applications. Full article

This study investigates the simultaneous elimination of ethyl acetate (EA), a representative volatile organic compound (VOC), and Escherichia coli aerosols from indoor air using a continuous-flow dielectric barrier discharge (DBD) plasma reactor coupled with a photocatalytic luminous textile system (Cu/TiO₂-coated fibers). The effects of applied voltage, relative humidity, and air-flow rate on pollutant removal and disinfection performance were systematically evaluated. Optimal DBD operation at 18 kV, 1 m³ h⁻¹ airflow, and 70% relative humidity achieved single-process removal efficiencies of 77% for EA and 2 log reduction (CFU mL⁻¹) for E. coli. When photocatalysis was coupled with DBD plasma, a significant combined effect was observed, increasing EA degradation to 87% and bacterial inactivation to 3.8 log (CFU mL⁻¹). The coupling enhanced active-species generation, improved CO₂ selectivity (up to 53%), and reduced residual ozone concentration. Humidity positively affected microbial inactivation due to °OH radical formation but slightly decreased VOC degradation by limiting ozone regeneration. Results demonstrate the efficiency and scalability of the DBD–photocatalysis hybrid system for multi-pollutant indoor air purification, offering rapid, low-temperature treatment suitable for industrial-scale applications. Full article

Plasma-catalytic oxidation is a promising approach for the abatement of volatile organic compounds (VOCs), yet its efficiency is often limited by the ineffective utilization of plasma-generated reactive oxygen species and incomplete oxidation pathways. In this work, a composite catalyst was constructed by integrating spinel-type NiCo₂O₄ with three-dimensional cubic mesoporous KIT-6 to couple efficient mass transfer with redox-active surface functionality for plasma-catalytic degradation of toluene. The performance of NiCo/KIT-6 was systematically evaluated in a dielectric barrier discharge (DBD) reactor and compared with Ni/KIT-6, Co/KIT-6, and NTP-only systems. XPS, O₂-TPD, H₂-TPR, and apparent dielectric measurements were employed to elucidate catalyst properties relevant to plasma–surface interactions. NiCo/KIT-6 exhibits superior overall performance in terms of toluene conversion, CO_x selectivity, and CO₂ selectivity over a wide range of specific input energies. This enhancement is closely associated with the integrated regulation of surface redox properties, oxygen activation capability, and apparent dielectric response by the NiCo₂O₄/KIT-6 composite structure, which may promote reactive oxygen utilization and facilitates effective plasma–surface redox processes. These results provide insights into the rational design of composite catalysts for plasma-assisted oxidation of aromatic VOCs. Full article

In the renewable energy-driven “green electricity–green hydrogen–green ammonia” pathway, the development of low-temperature and low-energy-consumption ammonia synthesis technologies is of great significance. In this work, a plasma-catalytic ammonia synthesis system was established using a coaxial dielectric barrier discharge (DBD) reactor. The effects of different catalysts, including Ag, Cu, γ-Al₂O₃, BaTiO₃ and Co/BaTiO₃, Ni/BaTiO₃ on ammonia synthesis performance were systematically investigated. The reaction process was analyzed using voltage–current waveforms, Lissajous figures, and optical emission spectroscopy (OES). The results show that different catalytic systems have a significant influence on ammonia synthesis performance, with the promotional effect ranked as follows: Ni/BaTiO₃ > Co/BaTiO₃ > BaTiO₃ > Ag > γ-Al₂O₃ > Cu. Among them, Ni/BaTiO₃ exhibited the best performance. Under the conditions of N₂:H₂ = 1:1 and a gas flow rate of 2.5 L/min, the NH₃ synthesis rate reached 259.48 μmol/min, and the maximum energy efficiency reached 1.40 g-NH₃/kWh. Catalyst characterization results indicate that the BaTiO₃ support maintained a stable crystal structure, while the loaded metal species were highly dispersed and uniformly distributed on the support surface, which is beneficial for the adsorption and conversion of reactive species on the catalyst surface. Discharge characteristic analysis shows that the introduction of BaTiO₃ enhanced the local electric field and improved the uniformity of micro-discharges, while the further incorporation of metal active components strengthened the micro-discharge behavior. OES results reveal that the intensities of characteristic emission lines, such as NH, N₂⁺, and Hα, were significantly enhanced in the Ni/BaTiO₃ system, facilitating the formation and conversion of NH_x intermediates. The superior performance of Ni/BaTiO₃ is attributed to the coupling between BaTiO₃-induced dielectric enhancement and Ni-promoted surface hydrogenation and NH₃ desorption. This work provides mechanistic insight into catalyst-dependent DBD plasma-catalytic ammonia synthesis and offers an experimental basis for the further optimization of plasma-based ammonia production. Full article

Buildings account for a significant share of global energy consumption and carbon emissions, creating an urgent need for advanced energy retrofit technologies. This review critically examines the role of plasma-modified textile polymer materials in improving the energy efficiency and durability of building retrofit systems. Various textile polymers, including polyester (polyethylene terephthalate, PET), polypropylene (PP), polytetrafluoroethylene (PTFE), polyamide (PA), and fiber-reinforced composites, are evaluated in relation to plasma surface engineering approaches, including atmospheric plasma, dielectric barrier discharge (DBD), and plasma jet treatment. Reported studies demonstrate that plasma treatment significantly alters surface morphology and chemistry, resulting in increased surface roughness, enhanced wettability, improved coating adhesion, and superior hydrophobic behavior. Water contact angles increased from approximately 70° to 145° depending on polymer type and plasma conditions, while reflective coating performance improved with solar reflectance enhancements of approximately 10–15%. Plasma-treated reflective roofing and shading textiles also showed reductions in building cooling energy demand of approximately 18–25% and roof temperature decreases of 10–15 °C. Furthermore, plasma-induced surface activation improved durability, ultraviolet (UV) resistance, and weather stability of textile membranes used in facade and roofing applications. The review also discusses industrial challenges related to scalability, plasma aging effects, energy consumption, and long-term performance. Plasma-modified systems demonstrate strong potential for multifunctional, lightweight, and sustainable building envelope technologies for future energy-efficient construction. Full article

Microplastic contamination in soils is an emerging environmental challenge requiring effective and scalable remediation strategies. This review synthesizes advances in physical, chemical, biological, and hybrid approaches, focusing on mechanisms, performance, and practical applicability. Physical methods, particularly adsorption using biochar, achieve removal efficiencies exceeding 86% for 1 μm polystyrene microplastics and maintain > 85% efficiency after multiple reuse cycles, demonstrating strong durability. Filtration and aggregation systems, such as permeable reactive barriers, reach up to 81.55% removal but are less effective in co-contaminated conditions. Chemical strategies exhibit the highest efficiencies. Dielectric barrier discharge plasma achieves 96.5–98.7% degradation within 30–60 min, while electrochemical coagulation reaches ~98% removal via flocculation. Thermal treatments, including pyrolysis, enable near-complete microplastic removal (~100%) at ≥400 °C, although high energy demands limit in situ application. Chemical amendments also improve soil quality, increasing organic matter by ~7.35% and enhancing nutrient availability. Biological approaches offer sustainable but slower remediation. Microbial degradation achieves up to ~60% breakdown within 21 days, while enzyme–microbe systems reach ~21.4% over 60 days. Earthworm activity enhances fragmentation and nutrient cycling (up to 36.1%), whereas phytoremediation alone shows minimal direct degradation (<1% over 12 months). Hybrid strategies, particularly biochar-based systems, provide the most practical solutions by combining adsorption, microbial stimulation, and soil restoration, but their effectiveness in degrading microplastics needs further verification. These systems enhance microbial biomass (up to 57.67%), nutrient availability (up to 66.02%), and crop yield (up to 81.41%). Overall, physicochemical methods ensure rapid removal (>90%), biological approaches support long-term degradation, and hybrid systems offer scalable, sustainable remediation for field applications. Full article

Plasma polymerization offers a solvent-free route to functional polymer materials, but the structural integrity and accessibility of functional groups in plasma-derived networks remain insufficiently validated. Herein, N-vinylimidazole (NVI) was polymerized using atmospheric-pressure dielectric barrier discharge (DBD) plasma in a liquid-film configuration to generate a chemically heterogeneous poly(N-vinylimidazole)-like material that could be recovered and evaluated in aqueous solution. ATR–FTIR and ¹H NMR spectroscopy indicate substantial vinyl-group consumption with retention of imidazole functionality. Functional behavior was probed using chromium(III) (Cr³⁺) as a model metal ion. UV–Vis spectroscopy revealed systematic changes in the Cr³⁺ d–d transition region (~580–600 nm) with increasing polymer concentration, consistent with ligand-field perturbation arising from interactions with imidazole donor sites. A monotonic increase in absorbance with an increasing ligand-to-metal ratio was observed, followed by plateau behavior at higher ratios, indicating saturation of accessible coordination environments. These results demonstrate that plasma-polymerized material retains chemically accessible imidazole functionalities capable of coordinating transition-metal ions in solution, establishing atmospheric-pressure plasma polymerization as a viable route to functional imidazole-containing materials. Full article

Plasma actuators are promising devices for near-wall flow control; however, conventional actuators often produce jets and forcing regions with excessive wall-normal spread, which reduces near-wall actuation selectivity. In this study, micro plasma actuator arrays with SDBD and pulsed-DC configurations were experimentally characterized to examine jets and forcing patterns confined closer to the wall. Micro actuator arrays consisting of eight integrated elements with sub-millimeter electrodes (0.5 mm exposed width) were fabricated by photolithography. Mean velocity fields were evaluated by conventional particle image velocimetry (PIV), while near-electrode flow structures were examined by single-pixel PIV. In addition, the streamwise body-force distribution was estimated from the high-spatial-resolution velocity fields. The results showed that the micro actuator arrays formed jets confined closer to the wall than the conventional actuators, with repeated re-acceleration along the electrode array. The estimated body-force distribution showed that the SDBD configuration retained a reverse-sign forcing pattern near the wall, whereas the pulsed-DC configuration formed a more concentrated near-wall positive forcing pattern with a weaker reverse-sign region and a lower positive peak location (0.54 mm, compared with 1.38 mm for the SDBD configuration). Under the tested quiescent-air characterization conditions, the pulsed-DC configuration produced a more wall-confined positive estimated-forcing pattern. Full article

Direct current (DC) surface flashover on polystyrene (PS) remains a critical bottleneck that impedes its reliable application in high-voltage insulation apparatus. To circumvent the protracted processing durations and stringent film-forming conditions inherent in conventional surface modification techniques, this study proposes a novel “liquid-film-assisted in situ rapid plasma curing” strategy. By harnessing atmospheric-pressure dielectric barrier discharge (DBD) technology within an argon ambient, the rapid (<6 min) and efficient deposition of a fluorosilane (FAS-13) functional coating onto the substrate was achieved. Microscopic characterizations coupled with isothermal surface potential decay (SPD) measurements reveal that this coating substantially mitigates the detrapping and surface migration of charge carriers. Macroscopic DC flashover testing corroborates that, under the optimal modification ratio, the surface breakdown voltage of PS is elevated to 14.04 kV, yielding an insulation gain of 26.94%. To elucidate the underlying physical mechanisms, density functional theory (DFT) calculations were conducted, revealing that the energy band misalignment between the wide-bandgap fluorinated layer and the substrate facilitates the construction of a high-density deep trap network (with a depth of ~0.8 eV) at the coating–substrate interface. By robustly anchoring primary electrons and inducing the formation of a homopolar space charge shielding layer, these deep traps physically arrest the evolution of the secondary electron emission avalanche (SEEA). Consequently, this work not only establishes a viable engineering framework for the rapid, large-scale surface reinforcement of DC insulation equipment but also provides profound quantum chemical insights into interfacial trap regulation within all-organic dielectrics. Full article

Low-temperature atmospheric plasma (LTP) is widely used in industrial processes, such as disinfection, surface modification and wastewater treatment. The dielectric barrier discharge (DBD) is regarded as one of the most robust and reliable methods for generating LTP in ambient air. Compared to conventional AC excitation, pulsed powering offers several advantages (i.e., lower energy use and heat production). The present trend is to use short and fast pulses (in the nano- and picosecond range). In this review, the key design parameters of a DBD (barrier thickness, relative permittivity and gap distance) are discussed. Material-specific phenomena like surface charging and degradation are analyzed. The complex interactions between the pulse source and DBD are examined. By mapping the interdependencies, this review aims to support the rational design and optimization of pulsed DBD systems, and to facilitate their broader industrial use. Full article

In this study, bean starch films were developed and treated with dielectric barrier discharge (DBD) cold plasma (5 min (DBD5), 10 min (DBD10), and 15 min (DBD15)) and pulsed light (PL) radiation (4 J cm⁻² (PL4), 8 J cm⁻² (PL8), and 12 J cm⁻² (PL12)), and the effects of these treatments on the physical, barrier, mechanical, morphological, and structural properties were evaluated, as well as the practical application of the films in bread storage for 7 days. Both treatments significantly modified the film properties (p < 0.05). Film thickness decreased from 95 µm (control) to 87 µm (PL12), while solubility was reduced from 39.40% (control) to 25.32% (PL12), indicating improved water resistance. Reductions in water vapor permeability (WVP) were also observed, with a more pronounced effect for PL12 (approximately 55% reduction compared to the control). The contact angle increased from 58.30° (control) to 67.76° (PL12), indicating a moderate increase in surface hydrophobicity. The DBD cold plasma treatment increased tensile strength (up to 16.05 MPa in DBD15) and reduced elongation (44.72%), whereas PL, especially at PL8, increased flexibility (60.36%). Morphological analyses indicated increased surface roughness for DBD-treated films, while structural analyses suggested subtle changes in molecular organization rather than the formation of well-defined crystalline domains. During bread storage, the treated films, particularly PL12, were significantly more effective than the control in delaying bread staling (final firmness of 6.67 N vs. 11.82 N), reducing mass loss (5.66% vs. 12.66%), and maintaining higher water activity, thereby better preserving product quality. Overall, both treatments showed potential for tailoring film properties: DBD was more effective in enhancing mechanical strength, while PL promoted improvements in barrier properties and practical performance. Therefore, physical treatments, particularly PL, represent promising strategies to overcome intrinsic limitations of starch-based films and to develop packaging materials with potential applications in bakery product preservation. Full article

The antimicrobial resistance crisis necessitates innovative systems for delivering oxidising agents. This study reports the development of a Carbopol^® 940 hydrogel functionalised with plasma-activated water (PAW) for the stabilisation and controlled release of reactive oxygen species (ROS). PAW was synthesised using a dielectric barrier discharge (DBD) reactor with continuous flow of water. The hydrogel’s architecture was characterised via SEM and FTIR, revealing a self-organised nanoporous structure (~1433 nm) that acts as a chemical reservoir. This architecture resulted in 100% retention of O₃ and H₂O₂ for 90 min, significantly extending the biological activity window compared with liquid PAW, and maintaining therapeutic concentrations (3 ppm of H₂O₂) beyond 45 h. In vitro antibacterial potency against Escherichia coli was validated, yielding a clear 25 mm inhibition zone. Subsequently, a clinical proof-of-concept was conducted in a patient with a recalcitrant Wagner Grade 2 diabetic foot ulcer (DFU). The hydrogel as monotherapy—without systemic antibiotics—achieved complete infection remission and full wound closure within 60 days. While this n = 1 case demonstrates translational feasibility, further validation through an ongoing controlled clinical trial is required. In conclusion, the PAW–Carbopol^® 940 hydrogel is a disruptive, low-cost therapeutic platform that effectively eradicates infection and promotes tissue repair through oxidative eustress, positioning it as a sustainable alternative for the advanced management of complex chronic wounds and regenerative medicine. Full article

Plasma-assisted ammonia (NH₃) decomposition is a promising strategy for hydrogen production. However, reactor geometry remains a key factor limiting its hydrogen yield per energy input (${\mathrm{Y}}_{{\mathrm{H}}_2}$). This study systematically investigates H₂ production in outer-dielectric (OD), inner-dielectric (ID), and double-dielectric (DD) coaxial DBD reactors. The results show that the ammonia decomposition performance of OD- and ID-coaxial DBDs is significantly higher than that of the DD-coaxial DBD. OD- and ID-coaxial DBDs generate abundant micro-discharge pulses, enabling effective discharge energy deposition at lower peak voltages. Consequently, the reduced electric fields E/N are maintained within the optimal kinetic window for NH₃ dissociation and H₂ production. Moreover, by balancing residence time and energy density, the 8 cm length electrode achieves a peak ${\mathrm{Y}}_{{\mathrm{H}}_2}$ of 1.22–1.24 gH₂/kWh in the OD-coaxial DBD. For the ID-coaxial DBD, a 1 mm dielectric thickness yields a maximum capacitance of 86 pF, achieving a peak ${\mathrm{Y}}_{{\mathrm{H}}_2}$ of ~1.35 gH₂/kWh at the optimum E/N. In contrast, the DD-coaxial DBD exhibits the lowest ${\mathrm{Y}}_{{\mathrm{H}}_2}$ (≤0.82 gH₂/kWh) with minimal temperature rise. This is caused by the reduced current pulse numbers and the deviation of E/N from the optimal range with elevated operating voltages. This work provides guidance for the optimization of DBD reactors in plasma-assisted NH₃ decomposition for efficient H₂ production. Full article

Oil-contaminated wastewater generated in oil-producing regions requires effective treatment methods capable of degrading persistent petroleum hydrocarbons and reducing the overall organic load. This study investigated plasma–ozone treatment of model oil-contaminated water representative of Kumkol-associated wastewater, with emphasis on reactive oxygen species formation and pollutant degradation. Experiments were carried out in a dielectric barrier discharge plasma reactor operating at 8–15 kV, 10–30 kHz, and 100–300 W. The plasma process generated ozone in the range of 3–18 mg/L and hydrogen peroxide in the range of 4–25 mg/L. For model wastewater containing 100–500 mg/L petroleum hydrocarbons, plasma–ozone treatment for 30 min achieved 70–90% hydrocarbon degradation. At the same time, COD decreased from 180–600 to 60–180 mg O₂/L, while TOC decreased from 60–250 to 20–90 mg/L. These results indicate that plasma–ozone treatment provides effective oxidation of petroleum hydrocarbons together with simultaneous reduction in key water quality indicators, demonstrating its potential for the treatment of oil-contaminated wastewater. Full article

Controlling carbon dioxide (CO₂) emissions remains a central challenge in Indonesia’s energy transition and its commitment to achieving net-zero emission targets. Carbon Capture and Storage (CCS) and Carbon Capture, Utilization, and Storage (CCUS) are widely recognized as important mitigation pathways, particularly for energy and industrial sectors where rapid decarbonization remains difficult. In parallel, cold plasma technology has emerged in the recent scientific literature as an early-stage, non-thermal approach for CO₂ activation under relatively low bulk temperature conditions, attracting interest as a potential long-term research pathway. This paper examines cold plasma technology within the broader CCS/CCUS landscape in Indonesia from a policy and technology perspective. The study adopts a qualitative and descriptive approach, synthesizing the selected academic literature on plasma-based CO₂ conversion, global CCUS development trends, and Indonesia’s regulatory, infrastructural, and energy system context. Rather than assessing techno-economic feasibility, the analysis focuses on identifying structural constraints, performance trade-offs, and policy-relevant considerations. The findings indicate that across plasma configurations, including dielectric barrier discharge, gliding arc, microwave, and radio frequency plasmas, current research outcomes remain constrained by low energy efficiency, limited scalability, and low technology readiness for large-scale applications. Reported performance metrics are largely derived from laboratory-scale studies under controlled conditions and cannot yet be extrapolated to real-world emission sources without a comprehensive system-level evaluation. Compared with established CCS and CCUS pathways, cold plasma technologies remain exploratory and lack the maturity required for near-term deployment. From a policy and research perspective, cold plasma should therefore be regarded as a long-term research option rather than an implementable mitigation solution for Indonesia, with its potential contribution lying in informing future research agendas, technology monitoring, and innovation planning, particularly in relation to CO₂ utilization concepts and decentralized energy systems, contingent upon significant advances in energy performance, system integration, and standardized evaluation frameworks. Full article