Discrete dynamics of light in an anti-parity-time symmetric photonic lattice in atomic vapors.

We demonstrate the realization of an anti-parity-time (PT)-symmetric photonic lattice in a coherent three-level Λ-type 85Rb atomic system both experimentally and theoretically. Such an instantaneously reconfigurable anti-PT-symmetric photonic lattice is "written" by two one-dimensional coupling fields, which are arranged alternately along the x direction and can modulate the refractive index of the atomic vapor in a spatially periodical manner via controllable atomic coherence. By properly adjusting the relevant atomic parameters, the phase shift between two adjacent lattice channels occurs in the constructed non-Hermitian photonic system. Such a readily reconfigurable anti-PT-symmetric photonic lattice may open the door for demonstrating the discrete characteristics of the optical waves in periodic anti-PT-symmetric photonic systems.

Phase Stability Control of Optical Fiber Partial Discharge Ultrasonic Sensing System.

Optic fiber interferometers are highly sensitive ultrasonic sensors for partial discharge detection. However, low-frequency vibration and environmental noise will disturb the sensors in the field, and cause a phase fading suppression effect that reduces sensitivity. This paper analyzed the problems existing in the phase feedback control system based on PZT, and an improved scheme incorporating a high-frequency carrier phase demodulation is proposed. Based on an acousto-optic modulator, the proposed phase feedback control system overcomes the phase fading suppression effect. A test is carried out on an ultrasonic calibration platform and a transformer oil discharge platform. The test results show that the stability of the improved phase demodulation system has been significantly improved, and meets the requirements of field applications. Compared with the signal-to-noise ratio at the time of phase fading of the system before the improvement, the signal-to-noise ratio of the improved system is improved by 69 dB.

Preparation and photocatalytic performance of UIO-66/La-MOF composite.

To improve the photocatalytic degradation efficiency of photocatalytic materials UIO-66 and La-MOFs under visible-light irradiation, a series of photocatalytic materials with La and Zr as metal centers and terephthalic acid (H2BDC) and 2-amino terephthalic acid (H2ATA) as organic ligands were prepared by solvothermal method. The photocatalytic materials were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible (UV-vis) spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, and Mott-Schottky test. The photocatalytic degradation performance to Rhodamine B of the catalysts was fully investigated. Results show that the H2ATA series had stronger visible-light absorption capacity and better photocatalytic performance. The 0.35 La/Zr-H2ATA composite showed the best photocatalytic degradation. The quenching experiments confirmed that the active species in the photocatalytic degradation were the holes and superoxide radicals. The possible mechanisms of the carrier migration paths in the energy level matching for La/Zr-H2BDC and La/Zr-H2ATA were also discussed in detail.

Synthesis of a novel cost-effective double-ligand Zr-based MOF via an inverted modulator strategy towards enhanced adsorption and photodegradation of tetracycline.

Developing visible-light response photocatalysts with high activity and adsorption alongside sustainability is vitally important to environmental restoration. Here, we fabricated a novel metal organic framework (MOF) with cost-effective double-ligands (fumaric acid and 2-aminoterephthalic acid as ligand precursors, denoted as MA-MOF) via a facile solvothermal method. Specifically, crystalline [Zr6O4(OH)4(fumarate)6] (MOF-801) can be only formed with monocarboxylic acids as modulators. Therefore, in the construction of crystalline double-ligand MA-MOF, the absence of monocarboxylic acid modulators successfully prevents the formation of crystalline MOF-801. Instead, the crystalline double-ligand MA-MOF is formed. Properties of MA-MOFs including the surface area, porosity, charge transfer resistance, and energy level position can be adjusted via altering the ratio of ligands. The optimal sample, MA-MOF2 (prepared with a molar ratio of fumaric acid and 2-aminoterephthalic acid being 2:1), shows a total 94.6% removal of tetracycline via adsorption and photodegradation, far exceeding the corresponding single-ligand counterparts. This work proposes an innovative inverted modulator strategy for constructing double-ligand MOFs.

Tailoring moisture electroactive Ag/Zn@cotton coupled with electrospun PVDF/PS nanofibers for antimicrobial face masks.

Face mask has become an essential and effective apparatus to protect human beings from air pollution, especially the air-borne pathogens. However, most commercial face masks can hardly achieve good particulate matters (PMs) and high bactericidal efficacy concurrently. Herein, a bilayer structured composite filter medium with built-in antimicrobial activities was constructed by combining cotton woven modified by magnetron sputtered Ag/Zn coatings and electrospun poly(vinylidene fluoride)/polystyrene (PVDF/PS) nanofibers. With the benefit of external moisture, an electrical stimulation was generated inside the composite fabric and thus endowed the fabric antimicrobial function. The resultant composite fabric presented conspicuous performance for integrated air pollution control, high filtration performance towards PM0.3 (99.1%, 79.2 Pa) and exceptional interception ratio against Escherichia coli (99.64%) and Staphylococcus aureus (98.75%) within 20 min contact. The high efficiency contact sterilization function of the bilayer fabric could further potentially promote disinfection and reuse of the filter media. This work may provide a new perspective on designing high-performance face mask media for public health protection.

Hydro electroactive Cu/Zn coated cotton fiber nonwovens for antibacterial and antiviral applications.

In this study, Cu/Zn galvanic electrodes were sputtered on the two surfaces of hydrophilic cotton fiber nonwovens (Cotton) to prepare hydro electroactive Cu/Cotton/Zn composites. When the Cu/Cotton/Zn was used as a functional layer in the face mask, the Cu/Zn galvanic electrodes can be spontaneously activated by water vapor molecules exhaled by the human body and generate galvanic current. Based on this, the hydro electroactive Cu/Cotton/Zn demonstrated excellent antibacterial activity against Escherichia coli and Staphylococcus aureus and could deactivate Enterovirus 71 (EV71) virions transmitted through the respiratory tract by 97.72% after 15 min of contact. Moreover, the Cu/Cotton/Zn did not affect the particle filtration efficiency and breathability of the face mask's polypropylene (PP) melt-blown layer. Furthermore, the cytotoxicity assessment of Cu/Cotton/Zn showed no cytotoxicity, indicating good biological security. Overall, the Cu/Cotton/Zn may provide a new approach to increase the antibacterial and antiviral performance of current personnel protective equipment on the market.

Ag/Zn Galvanic Couple Cotton Nonwovens with Breath-Activated Electroactivity: A Possible Antibacterial Layer for Personal Protective Face Masks.

The water vapor exhaled by the human body can severely accelerate the charge dissipation of commercial face masks, thereby reducing the electrostatic adsorption efficiency and increasing the bacterial invasion risk. This study developed an electroactive antibacterial cotton nonwoven (Ag/cotton/Zn) using eco-friendly magnetron sputtering technology. The Ag/Zn electrode constructed on the surface of cotton nonwovens could produce a microelectric field in the moist environment of human respiration, which endowed Ag/cotton/Zn with excellent electroactivity. When Ag/cotton/Zn was used as an additional layer of polypropylene melt-blown nonwovens or polylactic acid nanofibers, the prepared personal protective air filter had a filtration efficiency of up to 96.8% and an appropriate pressure drop and air permeability. The antibacterial results based on bacterial aerosols showed that the antibacterial efficiency against Escherichia coli and Staphylococcus aureus in 20 min was 99.74 and 99.79%, respectively, indicating an excellent electroactive killing efficiency against airborne bacteria. In addition, Ag/cotton/Zn showed excellent biological security. These results shed some light on the design and fabrication of next generation of personal protective air filter materials driven by human breathing.

Emission characteristics and potential toxicity of polycyclic aromatic hydrocarbons in particulate matter from the prebaked anode industry.

The emission factors (EFs) and source profiles of polycyclic aromatic hydrocarbons (PAHs) in particulate matter (PM10 and PM2.5) from the prebaked anode industry were studied to fill the knowledge gap and provide data for emission inventory and source resolution. In 2018, three prebaked anode plants were selected in Central China, each having one calcining chimney as well as one baking chimney, and then 92 samples were collected from the stack gas of the six chimneys. The results of the study are as follows. (1) PM10 and PM2.5 from the prebaked anode industry contained 37-42% water-soluble ions, 16-20% elements, 11-17% organic carbon, and 9.2-14% elemental carbon. (2) The EFs for PAHs of PM10 and PM2.5 were 1146.1 ± 899.7 and 866.2 ± 1179.8 mg/(t aluminum produced), respectively. The EF for BaP was seven times lower than that given by the European Environment Agency (EEA), whereas those of BbF, BkF, and IcdP were 2-13 times higher than those given by the EEA. (3) Seven diagnostic ratios for PAHs, including Ant/(Ant+Phe), Flua/(Flua+Pyr), BaA/(BaA + Chr), IcdP/(IcdP+BghiP), Flu/(Flu+Pyr), Phe/Ant and BaA/Chr were discussed. Just by diagnostic ratio, it is hard to precisely distinguish between calcining and baking in prebaked industry. (4) The toxic equivalence of PMs in the baking stack gas in the prebaked anode industry was five times higher than that in the calcining stack gas, and PM2.5 showed higher potential toxicity risk than PM10.

[Heavy Metal Pollution Characteristics and Ecological and Health Risk Assessment of Atmospheric PM2.5 in a Living Area of Zhengzhou City].

To study the pollution characteristics of atmospheric heavy metal elements in a living area of Zhengzhou City, assess the potential ecological risks, and determine risks to resident health in this city, the Wuhan Tianhong TH-16A Airborne Particles Intelligent Sampler was used to collect atmospheric PM2.5 in Zhengzhou City. The mass concentrations of 17 metal elements were analyzed by ambient air determination of inorganic elements by ambient particle matter wavelength dispersive X-ray fluorescence spectrometry. The source of heavy metals was analyzed by the enrichment factor method and principal component analysis. The ecological risk index method and the US Environmental Protection Agency's health risk assessment method were used to evaluate the potential ecological risks and residents' health risks from Cr, Cd, Cu, Zn, Ni, Pb, As, and other elements. The results showed that metals with higher enrichment factor values were Cd, Sb, Pb, and As, and Cd had the highest enrichment factor value. The sources of metal elements in a living area of Zhengzhou City were mainly crust/burning coal, fuel, garbage burning, metallurgical dust, and vehicle emission. The single factor potential ecological hazard index values of Cd, Pb, Zn, As, Cu, Ni, and Cr were 70420.2, 255.3, 204.6, 71.5, 36.9, 24.0, and 5.1, respectively. Cd, As, and Cr in a living area of Zhengzhou City posed a cancer risk, and Cd was the most harmful. Mn had a non-carcinogenic risk.

[Emission Characteristics Analysis and Health Risk Assessment of Unorganized VOCs in the Carbon Industry, Zhengzhou].

The three typical carbon enterprises in Zhengzhou were selected as research targets, and the emission characteristics of volatile organic compounds (VOCs) and their ozone formation potential (OFP) in different functional areas were studied. The US Environmental Protection Agency (EPA) health risk assessment model was used to evaluate the health risks of VOCs emitted by the carbon industry. The results showed that the concentration of VOCs in the production areas of the three research enterprises was between 89.77-964.60 µg·m-3, and the management area was between 51.46-121.59 µg·m-3. Naphthalene and carbon disulfide were at the highest concentrations in the carbon plants. The ozone formation potential of VOCs in the production area was between 75.42-1416.73 µg·m-3, and in the management area was between 65.32-202.42 µg·m-3, mainly from the contribution of aromatic hydrocarbons and olefins. The carcinogenic health risk (Risk) of VOCs in the production area was 3.5×10-5-2.8×10-3, and in the management area was 2.0×10-5-9.4×10-5, which was higher than the maximum acceptable level recommended by the EPA (10-6). The non-carcinogenic health risk index (HI) of the VOCs in the production area was 3.2-1.4×102, and in the management area was 4.3×10-1-3.8, except for the management area of the first enterprise, which was greater than 1, which may expose the workers. These health factors cause cancer and non-carcinogenic hazards.

Hydrochar production from watermelon peel by hydrothermal carbonization.

Watermelon peel waste was hydrothermally carbonized under 190°C and 260°C for 1h, 6h, and 12h, respectively. The hydrochar and spent liquor were collected and assayed for their properties. The results indicated that hydrochar yield was 2-5% and 46-95% on fresh and dry matter, respectively. Low temperature (190°C) was conducive to high conversion efficiency. The hydrochar had higher C/N ratio (22.19-26.86), more alkyl C, aryl C, and carbonyl C, but lower H/C (0.98-1.22) and O/C ratios (0.13-0.38), and less O-alky C, carboxylic C, compared with feedstock. So the aliphaticity decreased, whereas aromaticity increased significantly, especially under severe conditions. It should be watchful for that the toxic compounds in hydrochar may induce environmental risk while it is amended into soil. The spent liquor with abundant nutrients could be used as a fertilizer. Further work is required for testing the application in soil.