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Ozone (O3) is a critical gas in various industrial applications, particularly in semiconductor manufacturing, where it is used for wafer cleaning and oxidation processes. Accurate and reliable detection of ozone concentration is essential for process control, ensuring product quality, and safeguarding workplace safety. By studying the UV absorption characteristics of O3 and combining the specific operational needs of semiconductor process gas analysis, a pressure-insensitive ozone gas sensor has been developed. In its optical structure, a straight-through design without corners was adopted, achieving a coupling efficiency of 52% in the gas chamber. This device can operate reliably in a temperature range from 0 °C to 50 °C, with only ±0.3% full-scale error across the entire temperature range. The sensor consists of a deep ultraviolet light-emitting diode in a narrow spectrum centered at 254 nm, a photodetector, and a gas chamber, with dimensions of 85 mm × 25 mm × 35 mm. The performance of the sensor has been meticulously evaluated through simulation and experimental analysis. The sensor's gas detection accuracy is 750 ppb, with a rapid response time (t90) of 7 s, and a limit of detection of 2.26 ppm. It has the potential to be applied in various fields for ozone monitoring, including the semiconductor industry, water treatment facilities, and environmental research. [ABSTRACT FROM AUTHOR]

This paper proposes a lens design method for effectively collimating the light emitting from a light-emitting diode (LED). This collimating lens contains two aspherical lens surfaces which can be mathematically characterized using a few designing parameters, and hence is called an analytic collimating lens. An optical ray-tracing algorithm has been developed for these analytic collimating lenses to analyze their optical performance and to optimize their designs. Six high-power and commercially available ultraviolet (UV) LEDs are chosen as examples for demonstrating the optimal collimating lens design. For each UV-LED, the corresponding optical collimating lens is determined by inputting the ray data file provided by the manufacture over a finite-size emitting area. The divergent angles of the six UV-LEDs have been successfully collimated to a narrow range in between 1.56° to 2.84° from their original radiation angle around 46° to 120°. Furthermore, the proposed analytical collimating lenses are suitable for mass-production using standard mold injection methods, and hence possess great potentials for industry applications of LEDs. [ABSTRACT FROM AUTHOR]

Effective and reliable interconnections are crucial for microfluidics to connect with the macro world. Current microfluidic interfaces are still bulky, expensive, or with issues of clogging and material limitation. In this study, a novel ultraviolet (UV)-assisted coaxial three-dimensional (3D) printing approach was proposed to fabricate hollow microfluidic connectors with advantages of rapid prototyping, fixture-free, and materials compatible. An assembled coaxial nozzle was designed to enable co-flow extrusion, where the inner flow (water) served as the sacrificial layer and the outer flow (adhesive) was cured for shell formation. Furthermore, a converged UV-LED light source was attached to the coaxial nozzle for UV curing of adhesives. UV rheological characterizations were performed to study the UV curing kinematics, and the gelation time was employed to describe the state transition behaviors of UV curable adhesives used in the study. To explore requirements for successful hollow connectors direct printing, processing criteria such as co-flow regime and pre-cure time were investigated. The hollow connectors with an inner channel diameter of ~150 μ m and a height of 5 mm were successfully printed on polymethyl methacrylate (PMMA) and glass substrate. The integration feasibility of the proposed method was also demonstrated by the presented microfluidic device with printed hollow connectors. [ABSTRACT FROM AUTHOR]

In this study, we investigated the effects of InGaN/GaN-based interlayer (IL) and electron emitting layer (EEL) consisting of a GaN barrier layer grown with different metal-organic (MO) precursors of gallium (Ga), which were grown underneath the active layer. The growth behavior of GaN with triethyl Ga (TEGa) showed an increasing growth time due to a lower growth rate compared with GaN grown with trimethyl Ga (TMGa), resulting in the formation of columnar domains and grain boundary with reduced defect. UV-A light emitting diode (LED) chips with three types of ILs and EELs, grown with different MO sources, were fabricated and evaluated by light output power (LOP) measurements. The LOP intensity of UVLED-III with the GaN barrier layer-based IL and EEL grown by TEGa was enhanced by 1.5 times compared to that of the IL and EEL grown with TMGa at 300 mA current injection. Use of the GaN barrier layer in ILs and EELs grown by TEGa improved the crystal quality of the post grown InGaN/GaN multiple quantum well, which reduces leakage current. Therefore, for the UV-A LED with ILs and EELs grown with TEGa MO precursors, electrical and optical properties were improved significantly. [ABSTRACT FROM AUTHOR]

Micro light emitting diode (μLED) displays have been in development since 2017, aimed for application in 2020. However, when using three-color, i.e., red, blue, and green LEDs, or blue LEDs that excite red and green phosphors, many challenges arise in mass production, cost, and quality. Our group has devised an ultraviolet (UV)-excited red, green, and blue (RGB) display that excites red, green, and blue phosphors using UV-LEDs. This paper studies how the composition and crystal defects of a light-emitting layer affect the luminous efficiency of a UV μLED chip from the perspective of internal quantum efficiency (IQE). It was confirmed that the luminous efficiency improves by making the LED chips in the near ultraviolet range μ-size. The UV μLED chip emitting at 385 nm exhibited a more linear output than a 400-nm purple μLED chip. [ABSTRACT FROM AUTHOR]

Ultraviolet light emitting diodes (UV-LEDs) have attracted great interest in recent years. They can be used to polymerize coatings, such as those used for prefinished wood flooring. In this project, two lamps were compared for their suitability to be used on a wood flooring finishing line: a UV-microwave and a UV-LED lamp. Low heat emission was found for the UV-LED lamp compared to the UV-microwave one. This study also reveals that the 4 W/cm² UV-LED lamp used is not powerful enough to cure UV high solids acrylate coatings while satisfactory results can be obtained for UV water-based formulations. In fact, conversion percentages were found to be low for the high solids coatings, leaving the coatings tacky. Higher conversion percentages were obtained for the UV water-based formulations. As a result, mass loss, hardness, and scratch resistance found for the samples cured by UV-LED were closed to the ones found for the samples cured using the UV microwave lamp. [ABSTRACT FROM AUTHOR]

As an emerging light source, ultraviolet light emitting diodes (UV-LEDs) are adopted to overcome the shortcomings of the conventional mercury lamp, such as mercury pollution. The degradation of chloramphenicol (CAP) using three UV-LED-based advanced oxidation processes (AOPs)—UV-LED/persulfate (UV-LED/PS), UV-LED/peroxymonosulfate (UV-LED/PMS) and UV-LED/chlorine—was investigated. Results indicate that CAP can be more effectively degraded by the hybrid processes when compared to UV irradiation and oxidants alone. Degradation of CAP using the three UV-LED-based AOPs followed pseudo-first-order kinetics. The degradation rate constants (kobs) for UV-LED/PS, UV-LED/PMS, and UV-LED/chlorine were 0.0522, 0.0437 and 0.0523 min−1, and the CAP removal rates 99%, 98.1% and 96.3%, respectively. The degradation rate constant (kobs) increased with increasing oxidant dosage for UV-LED/chlorine, whereas overdosing reduced CAP degradation using UV-LED/PS and UV-LED/PMS. Ultraviolet wavelength influenced degradation efficiency of the UV-LED based AOPs with maximum CAP degradation observed at a wavelength of 280 nm. The application of UV-LED enhanced the formation DBPs during subsequent chlorination. uUV-LED/PMS produced more disinfection by-products than UV-LED/PS. Compared to UV-LED, UV-LED/PS reduced the formation of dichloroacetonitrile and trichloronitromethane during chlorination owing to its capacity to degrade the nitro group in CAP. The intermediates dichloroacetamide, 4-nitrobenzoic acid, 4-nitrophenol were produced during the degradation of CAP using each of UV-LED, UV-LED/PS and UV-LED/chlorine. The present study provides further evidence supporting the application of UV-LED in AOPs. [ABSTRACT FROM AUTHOR]

We constructed an imaging system to measure the concentration of acetone gas by acetone reduction using secondary alcohol dehydrogenase (S-ADH). Reduced nicotinamide adenine dinucleotide (NADH) was used as an electron donor, and acetone was imaged by fluorescence detection of the decrease in the autofluorescence of NADH. In this system, S-ADH–immobilized membranes wetted with buffer solution containing NADH were placed in a dark box, and UV-LED excitation sheets and a high-sensitivity camera were installed on both sides of the optical axis to enable loading of acetone gas. A hydrophilic polytetrafluoroethylene (H-PTFE) membrane with low autofluorescence was used as a substrate, and honeycomb-like through-hole structures were fabricated using a CO2 laser device. After loading the enzyme membrane with acetone gas standards, a decrease in fluorescence intensity was observed in accordance with the concentration of acetone gas. The degree of decrease in fluorescence intensity was calculated using image analysis software; it was possible to quantify acetone gas at concentrations of 50–2000 ppb, a range that includes the exhaled breath concentration of acetone in healthy subjects. We applied this imaging system to measure the acetone gas in the air exhaled by a healthy individual during fasting. [ABSTRACT FROM AUTHOR]

Polymeric nanofibrous membranes (NFMs) with both high whiteness and high thermal and ultraviolet (UV) stability are highly desired as reflectors for ultraviolet light-emitting diodes (UV-LEDs) devices. In the current work, a semi-alicyclic and fluoro-containing polyimide (PI) NFM with potential application in such kinds of circumstances was successfully fabricated from the organo-soluble PI resin solution via a one-step electrospinning procedure. In order to achieve the target, a semi-alicyclic PI resin was first designed and synthesized from an alicyclic dianhydride, 3,4-dicarboxy-1,2,3,4,5,6,7,8-decahydro-1-naphthalenesuccinic dianhydride (or hydrogenated tetralin dianhydride, HTDA), and a fluoro-containing diamine, 2,2-bis[4-(4-amino-phenoxy)phenyl]hexafluoropropane (BDAF), via an imidization procedure. The derived PI (HTDA-BDAF) resin possessed a number-average molecular weight (Mn) higher than 33,000 g/mol and was highly soluble in polar aprotic solvents, such as N,N-dimethylacetamide (DMAc). The electrospinning solution was prepared by dissolving the PI resin in DMAc at a solid content of 25–35 wt%. For comparison, the conventional high-whiteness polystyrene (PS) NFM was prepared according to a similar electrospinning procedure. The thermal and UV stability of the derived PI and PS NFMs were investigated by exposure under the UV-LED (wavelength: 365 nm) irradiation. Various thermal evaluation results indicated that the developed PI (HTDA-BDAF) NFM could maintain both the high reflectance and high whiteness at elevated temperatures. For example, after thermal treatment at 200 °C for 1 h in air, the PI (HTDA-BDAF) NFM exhibited a reflectance at a wavelength of 457 nm (R457) of 89.0%, which was comparable to that of the pristine PI NMF (R457 = 90.2%). The PI (HTDA-BDAF) NFM exhibited a whiteness index (WI) of 90.88, which was also close to that of the pristine sample (WI = 91.22). However, for the PS NFM counterpart, the R457 value decreased from the pristine 88.4% to 18.1% after thermal treatment at 150 °C for 1 h, and the sample became transparent. The PI NFM maintained good optical and mechanical properties during the high dose (2670 J/cm2) of UV exposure, while the properties of the PS NFM apparently deteriorated under the same UV aging. [ABSTRACT FROM AUTHOR]

Polybrominated diphenyl ethers (PBDEs) are persistent organic pollutants that can arrive to water bodies from their use as flame retardants in a wide range of applications, such as electric and electronic devices or textiles. In this study, the photodegradation of PBDEs in water samples when applying UV-LED radiation was studied. Irradiation was applied at three different wavelengths (255 nm, 265 nm and 285 nm) and different exposure times. The best degradation conditions for spiked purified water samples were at 285 nm and 240 min, resulting in degradations between 67% and 86%. The optimized methodology was applied to real water samples from different sources: river, marine, wastewater (effluent and influent of treatment plants) and greywater samples. Real water samples were spiked and exposed to 4 hours of irradiation at 285 nm. Successful photodegradation of PBDEs ranging from 51% to 97% was achieved for all PBDE congeners in the different water samples with the exception of the marine one, in which only a 31% of degradation was achieved. [ABSTRACT FROM AUTHOR]

More than 1 year has passed since social activities have been restricted due to the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). More recently, novel SARS-CoV-2 variants have been spreading around the world, and there is growing concern that they may have higher transmissibility and that the protective efficacy of vaccines may be weaker against them. Immediate measures are needed to reduce human exposure to the virus. In this study, the antiviral efficacy of deep-ultraviolet light-emitting diode (DUV-LED) irradiation (280 ± 5 nm, 3.75 mW/cm2) against three SARS-CoV-2 variants was evaluated. For the B.1.1.7, B.1.351, and P.1 variant strains, irradiation of the virus stocks for 1 s resulted in infectious titer reduction rates of 96.3%, 94.6%, and 91.9%, respectively, and with irradiation for 5 s, the rates increased to 99.9%, 99.9%, and 99.8%, respectively. We also tested the effect of pulsed DUV-LED irradiation (7.5 mW/cm2, duty rate: 50%, frequency: 1 kHz) under the same output conditions as for continuous irradiation and found that the antiviral efficacy of pulsed and continuous irradiation was the same. These findings suggest that by further developing and optimizing the DUV-LED device to increase its output, it may be possible to instantly inactivate SARS-CoV-2 with DUV-LED irradiation. [ABSTRACT FROM AUTHOR]

In this study, we evaluated the effectiveness of UV-LED-irradiated TiO2 in removing 24 commonly detected PPCPs in two water matrices (municipal wastewater effluent and Suwannee River NOM–synthetic water) and compared their performance with that of ultrapure water. Relatively fast removal kinetics were observed for 29% and 12% of the PPCPs in ultrapure water and synthetic surface water, respectively (kapp of 1–2 min−1). However, they all remained recalcitrant to photocatalysis when using wastewater effluent as the background matrix (kapp < 0.1 min−1). We also observed that the pH-corrected octanol/water partition coefficient (log Dow) correlated well with PPCP degradation rate constants in ultrapure water, whereas molecular weight was strongly associated with the rate constants in both synthetic surface water and wastewater. The electrical energy per order (EEO) values calculated at the end of the experiments suggest that UV-LED/P25 can be an energy-efficient method for water treatment applications (2.96, 4.77, and 16.36 kW h m−3 in ultrapure water, synthetic surface water, and wastewater effluents, respectively). Although TiO2 photocatalysis is a promising approach in removing PPCPs, our results indicate that additional challenges need to be overcome for PPCPs in more complex water matrices, including an assessment of photocatalytic removal under different background water matrices. [ABSTRACT FROM AUTHOR]

The elimination of mercury, low energy consumption, and low heat make the ultraviolet light-emitting diode (UV-LED) system emerge as a promising alternative to conventional UV-mercury radiation coating. Hence, a series of hydrophobic coatings based on urethane acrylate oligomer and fluorinated monomer via UV-LED photopolymerisation was designed in this paper. The presence of fluorine component at 1160 cm−1, 1235 cm−1, and 1296 cm−1 was confirmed by Fourier Transform Infra-Red spectroscopy. A considerably high degree C=C conversion (96–98%) and gel fraction (95–93%) verified the application of UV-LED as a new technique in radiation coating. It is well-accepted that fluorinated monomer can change the surface wettability as the water contact angle of the coating evolved from 88.4° to 121.2°, which, in turn, reduced its surface free energy by 70.5%. Hence, the hydrophobicity of the coating was governed by the migration of the fluorine component to the coating surface as validated by scanning electron and atomic force microscopies. However, above 4 phr of fluorinated monomer, the transparency of the cured coating examined by UV-visible spectroscopy experienced approximately a 16% reduction. In summary, the utilisation of UV-LED was a great initiative to develop green aspect in photopolymerisation, particularly in coating technology. [ABSTRACT FROM AUTHOR]

The photocatalytic degradation of potassium hexacyanoferrate (III) was assessed in a bench-scale compound parabolic collectors (CPC) reactor assisted with a light-emitting diode (LED) UV-A source emitting at 365 nm, and using a modified TiO2 as a catalyst via the hydrothermal treatment of commercial Aeroxide P25. The experiments were performed under oxic and anoxic conditions in order to observe a possible reduction of the iron. The modified TiO2 showed a specific surface area 2.5 times greater than the original Aeroxide P25 and its isotherm and hysteresis indicated that the modified catalyst is mesoporous. The bandgap energy (Eg) of the modified TiO2 increased (3.34 eV) compared to the P25 TiO2 band gap (3.20 eV). A specific reaction rate constant of 0.1977 min−1 and an electrical oxidation efficiency of 7.77 kWh/m3 were obtained in the photocatalytic degradation. Although the TiO2 P25 yields a photocatalytic degradation 9.5% higher than that obtained one with the modified catalyst (hydrothermal), this catalyst showed better performance in terms of free cyanide release. This last aspect is a significant benefit since this can help to avoid the pollution of fresh water by reusing the treated wastewater for gold extraction. A photocatalytic degradation of the cyanocomplex of 93% was achieved when the process occurred under oxic conditions, which favored the removal. Summarizing, the hydrothermal method could be a promising treatment to obtain TiO2-based catalysts with larger specific areas. [ABSTRACT FROM AUTHOR]

The aim of this systematic review was to investigate the effectiveness of various disinfection methods available for stethoscopes. In March 2019, we performed a search in PubMed and Scopus using the search terms: "reducing stethoscopes contamination" and "disinfection stethoscopes"; the Mesh terms used in PubMed were "Decontamination/methods" or "Disinfection/methods" and "Stethoscopes/microbiology". Selection criteria were: English language; at least one disinfection method tested. A total of 253 publications were screened. After title, abstract, and full-text analysis, 17 papers were included in the systematic review. Ethanol at 90%, Ethanol-Based Hands Sanitizer (EBHS), triclosan, chlorhexidine, isopropyl alcohol, 66% ethyl alcohol, sodium hypochlorite, and benzalkonium chloride have been proven to lower the presence of bacteria on stethoscopes' surfaces. In addition, alcohol wipes show effective results. A wearable device emitting ultraviolet C by Light-Emitting Diode (LED) resulted efficacious against common microorganisms involved in Healthcare Associated Infections. The cover impregnated with silver ions seemed to be associated with significantly higher colony counts. Instead, copper stethoscopes surface reduced bacterial load. The disinfection of stethoscopes appears to be essential. There are many valid methods available; the choice depends on various factors, such as the cost, availability, and practicality.

III-nitride-based ultraviolet light emitting diode (UV LED) has numerous attractive applications in air and water purification, UV photolithography, and in situ activation of drugs through optical stimulus, solid state lighting, polymer curing, and laser surgery. However, the unclear failure mechanisms and uncertainty reliability have limited its application. Therefore, a design of an appropriate reliability test plan for UV LEDs has become extremely urgent. Compared to traditional reliability tests recommended in LED lighting industry, the step-stress accelerated degradation test (SSADT) is more cost-effective and time-effective. This paper compares three SSADT testing plans with temperature and driving currents as stepwise increasing loads to determine an appropriate test strategy for UV LEDs. The study shows that: (1) the failure mechanisms among different SSADT tests seem to be very different, since the driving current determines the failure mechanisms of UV LEDs more sensitively, and (2) the stepped temperature accelerated degradation test with an appropriate current is recommended for UV LEDs. [ABSTRACT FROM AUTHOR]

Ultraviolet light-emitting diodes (UV-LEDs) have recently emerged as a viable technology for water disinfection. However, the performance of the technology in full-scale drinking-water treatment systems remains poorly characterised. Furthermore, current UV disinfection standards and protocols have been developed specifically for conventional mercury UV systems and so do not necessarily provide an accurate indication of UV-LED disinfection performance. Hence, this study aimed to test the hypothesis that a full-scale UV-LED reactor can match the Cryptosporidium inactivation efficiency of conventional mercury UV reactors. Male-specific bacteriophage (MS2) was used as the Cryptosporidium spp. surrogate microorganism. The time-based inactivation efficiency of the full-scale reactor was firstly compared to that of a bench-scale (batch-type) UV-LED reactor. This was then related to mercury UV reactors by comparing the fluence-based efficiency of the bench-scale reactor to the USEPA 90% prediction interval range of expected MS2 inactivation using mercury UV lamps. The results showed that the full-scale UV-LED reactor was at least as effective as conventional mercury UV reactors at the water-quality and drive-current conditions considered. Nevertheless, comparisons between the bench- and full-scale UV-LED reactors indicated that improvements in the hydraulic flow profile and power output of the full-scale reactor could help to further improve the efficiency of UV-LED reactors for municipal drinking water disinfection. This represents the world's first full-scale UV-LED reactor that can be applied at municipal water treatment works for disinfection of pathogenic microorganisms from drinking water. [ABSTRACT FROM AUTHOR]

For gold extraction, the most used extraction technique is the Merrill-Crow process, which uses lixiviants as sodium or potassium cyanide for gold leaching at alkaline conditions. The cyanide ion has an affinity not only for gold and silver, but for other metals in the ores, such as Al, Fe, Cu, Ni, Zn, and other toxic metals like Hg, As, Cr, Co, Pb, Sn, and Mn. After the extraction stage, the resulting wastewater is concentrated at alkaline conditions with concentrations up to 1000 ppm of metals. Photocatalysis is an advanced oxidation process (AOP) able to generate a photoreaction in the solid surface of a semiconductor activated by light. Although it is well known that photocatalytic processes can remove metals in solution, there are no compilations about the researches on photocatalytic removal of metals in wastewater with cyanide. Hence, this review comprises the existing applications of photocatalytic processes to remove metal and in some cases recover cyanide from recalcitrant wastewater from gold extraction. The use of this process, in general, requires the addition of several scavengers in order to force the mechanism to a pathway where the electrons can be transferred to the metal-cyanide matrices, or elsewhere the entire metallic cyanocomplex can be degraded by an oxidative pathway. [ABSTRACT FROM AUTHOR]