Search

During the initial period of straw return, a suitable straw return technology can lay the foundation for long-term soil fertility improvement. This study focused on the issues of backward straw return technology and blind fertilizer application in the southern part of the maize-producing area in the Northeast Plain of China. In this study, two straw return modes (2-year no-tillage straw cover + 1-year deep loosening and burying straw returning mode, NPT; 3-year rotary tillage and burying straw returning mode, RT), with RT mode as a control, were combined with different N fertilizer application rates (0, 192, 240 kg/ha). The changes in soil organic carbon (SOC) and its active components (MBC, DOC, and LOC) in the 0–40 cm soil layer were analyzed, and the carbon stratification rate, carbon pool index (CPI), SOC storages of each component, and maize yield were calculated to evaluate the short-term (3-year) differences in soil organic carbon quantity and quality in order to find suitable straw return methods and nitrogen application rate combinations. The results showed that the NPT mode increased the SOC and MBC content in the 20–30 cm soil layer, with an increase of 16.2% to 37.8% and 23.0% to 50.3%, respectively, compared with the RT mode. Under the NPT mode, the carbon pool stability was higher after nitrogen fertilizer addition, with a CPI value of 10.2% to 37.8% higher in the 20–40 cm soil layer compared with the RT mode. The differences in maize yield were not significant (p < 0.05) between the nitrogen application rates of 192 kg/ha and 240 kg/ha, but the SOC storages did not show significant changes. The MBC storage had the highest value under the nitrogen application rate of 192 kg/ha. Therefore, we thought that, in the early stage of straw return, the organic carbon priming effect caused by increased microbial activity was higher under the nitrogen application rate of 192 kg/ha. Considering the aspects of not affecting maize yield and improving SOC stability, it is recommended to use the NPT mode with the application of a 240 kg/ha nitrogen fertilizer rate for straw return.

As a prerequisite for pollution control, monitoring air pollutants is crucial. In recent years, all walks of life are developing toward intelligence, and the concept of intelligent ports is also the development direction of current port planning. A lot of work such as loading and unloading of port cargo and planning has now achieved intellectual development, and the monitoring of air pollutants in ports also needs to be developed towards intelligence. However, at present, there are not many air pollutant monitoring systems for ports. In order to find monitoring equipment and models that are better suited to the port environment, this paper focuses on the main components of air pollutants in ports (SO2, NOX, PM, etc.) and their sources and describes the monitoring methods and principles for these pollutants in ports and on ships, respectively. Regarding monitoring methods, the current application of DOAS (Differential Optical Absorption Spectroscopy) equipment and the monitoring system based on various gas sensors have great development prospects and advantages, based on the monitoring system being more intelligent. At the same time, the use of the same monitoring principle for a variety of pollutants monitoring equipment to a certain extent can save the cost and efficiency of monitoring. In terms of monitoring mode, the combination of manual analysis and automatic analysis will be perfect for the port’s air pollutant monitoring system. This mode can alleviate the embarrassment of the low life of the sensor-based monitoring system to a certain extent, and the data monitored by this mode will be more accurate.

Studies of the interfacial behavior of pure aqueous nanoparticles have been limited due tothe difficulty of making contaminant-free nanoparticles while also providing narrow size distribution. Colloidal unimolecular polymers (CUPs) are a new type of single-chain nanoparticle with a particle size ranging from 3 to 9 nm, which can be produced free of surfactants and volatile organic contents (VOCs). CUP particles of different sizes and surface charges were made. The surface tension behavior of these CUP particles in water was studied using a maximum bubble pressure tensiometer. The equilibrium surface tension decreased with increasing concentration and the number of charges present on the surface of the CUP particles influences the magnitude of the interfacial behavior. The effect of electrostatic repulsion between the particles on the surface tension was related. At higher concentrations, surface charge condensation started to dominate the surface tension behavior. The dynamic surface tension of CUP particles shows the influence of the diffusion of the particles to the interface on the relaxation time. The relaxation time of the CUP polymer was 0.401 s, which is closer to the diffusion-based relaxation time of 0.133s for SDS (sodium dodecyl sulfate).

Colloidal unimolecular polymer (CUP) particles were made using polymers with different ratios of hydrophobic and hydrophilic monomers via a self-organization process known as water reduction. The water-reduction process and the collapse of the polymer chain to form a CUP were tracked using viscosity measurements as a function of composition. A vibration viscometer, which allowed for viscosity measurement as the water was being added during the water-reduction process, was utilized. The protocol was optimized and tested for factors such as temperature control, loss of material, measurement stability while stirring, and changes in the solution volume with the addition of water. The resulting viscosity curve provided the composition of Tetrahydrofuran (THF)/water mixture that triggers the collapse of a polymer chain into a particle. Hansen as well as dielectric parameters were related to the polymer composition and percentage v/v of THF/water mixture at the collapse point. It was observed that the collapse of the polymer chain occurred when the water/THF composition was at a water volume of between 53.8 to 59.3% in the solvent mixture.

In this study, four kinds of phospholipase A1-metal (Al/Co/Cu/Mn) hybrid nanostructures were prepared for enhancing the stability of the free PLA1. The formed hybrid complexes were characterized by scanning electron microscope (SEM), Fourier infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The stability and substrate specificity of immobilized enzymes were subsequently determined. After immobilization, the temperature tolerance of PLA1–metal hybrid nanostructures was enhanced. The relative activity of PLA1–Al/Co/Cu hybrid nanostructures remained above 60% at 50 °C, while that of free enzyme was below 5%. The thermal transition temperature measured by differential scanning calorimetry (DSC) was found to increase from 65.59 °C (free enzyme) to 173.14 °C, 123.67 °C, 96.31 °C, and 114.79 °C, referring to PLA1–Cu/Co/Al/Mn hybrid nanostructures, respectively. Additionally, after a storage for fourteen days at 4 °C, the immobilized enzymes could exhibit approximately 60% of the initial activity, while the free PLA1 was inactivated after four days of storage. In brief, using Co2+, Cu2+, Al3+, and Mn2+ as the hybridization materials for immobilization could improve the catalytic properties and stability of the free PLA1, suggesting a promising method for a wider application of PLA1 in many fields such as food, cosmetics, and the pharmaceutical industry.

In this study, silicon oxide (SiO2) films were deposited by remote plasma atomic layer deposition with Bis(diethylamino)silane (BDEAS) and an oxygen/argon mixture as the precursors. Oxygen plasma powers play a key role in the quality of SiO2 films. Post-annealing was performed in the air at different temperatures for 1 h. The effects of oxygen plasma powers from 1000 W to 3000 W on the properties of the SiO2 thin films were investigated. The experimental results demonstrated that the SiO2 thin film growth per cycle was greatly affected by the O2 plasma power. Atomic force microscope (AFM) and conductive AFM tests show that the surface of the SiO2 thin films, with different O2 plasma powers, is relatively smooth and the films all present favorable insulation properties. The water contact angle (WCA) of the SiO2 thin film deposited at the power of 1500 W is higher than that of other WCAs of SiO2 films deposited at other plasma powers, indicating that it is less hydrophilic. This phenomenon is more likely to be associated with a smaller bonding energy, which is consistent with the result obtained by Fourier transformation infrared spectroscopy. In addition, the influence of post-annealing temperature on the quality of the SiO2 thin films was also investigated. As the annealing temperature increases, the SiO2 thin film becomes denser, leading to a higher refractive index and a lower etch rate.

Studies of the evaporation of aqueous nanoparticle solutions have been limited due to lack of homogeneity of the solution, difficulties in obtaining reproducible samples and stability of substrates, as well as the effect of other volatile components or contaminants such as surfactants. Colloidal unimolecular polymer (CUP) is a spheroidal nanoparticle with charged hydrophilic groups on the surface, and the particle size ranges from 3 to 9 nm. The large amount of surface water on the CUP surface provides the opportunity to evaluate the evaporation of surface water, which may contribute to the investigation the factors that affect the evaporation rate in solutions of ultra-small particles, like protein, micelle, colloidal, etc. Six CUP systems were evaluated by thermogravimetric analysis (TGA) with respect to time and solids content. The evaporation rate of water was initially enhanced due to the deformation of the air-water interface at low to moderate concentration due to particle charge repulsive forces. At higher concentrations, above 20%, surface charge condensation and increasing viscosity began to dominate. At higher concentration where the CUP reached the gel point the rate of diffusion controlled the evaporation. The final drying point was the loss of three waters of hydration for each carboxylate on the CUP surface.

In this study, aluminum-doped zinc oxide (Al:ZnO) thin films were grown by high-speed atmospheric atomic layer deposition (AALD), and the effects of air annealing on film properties are investigated. The experimental results show that the thermal annealing can significantly reduce the amount of oxygen vacancies defects as evidenced by X-ray photoelectron spectroscopy spectra due to the in-diffusion of oxygen from air to the films. As shown by X-ray diffraction, the annealing repairs the crystalline structure and releases the stress. The absorption coefficient of the films increases with the annealing temperature due to the increased density. The annealing temperature reaching 600 °C leads to relatively significant changes in grain size and band gap. From the results of band gap and Hall-effect measurements, the annealing temperature lower than 600 °C reduces the oxygen vacancies defects acting as shallow donors, while it is suspected that the annealing temperature higher than 600 °C can further remove the oxygen defects introduced mid-gap states.

Zinc oxide (ZnO) has drawn much attention due to its excellent optical and electrical properties. In this study, ZnO film was prepared by a high-deposition-rate spatial atomic layer deposition (ALD) and subjected to a post-annealing process to suppress the intrinsic defects and improve the crystallinity and film properties. The results show that the film thickness increases with annealing temperature owing to the increment of oxide layer caused by the suppression of oxygen vacancy defects as indicated by the X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) spectra. The film transmittance is seldom influenced by annealing. The refractive index increases with annealing temperature at 300–700 °C, possibly due to higher density and crystallinity of the film. The band gap decreases after annealing, which should be ascribed to the decrease in carrier concentration according to Burstein–Moss model. The carrier concentration decreases with increasing annealing temperature at 300–700 °C since the oxygen vacancy defects are suppressed, then it increases at 800 °C possibly due to the out-diffusion of oxygen atoms from the film. Meanwhile, the carrier mobility increases with temperature due to higher crystallinity and larger crystallite size. The film resistivity increases at 300–700 °C then decreases at 800 °C, which should be ascribed primarily to the variation of carrier concentration.

Colloidal Unimolecular Polymer (CUP) particles are spheroidal, 3–9 nm with charged groups on the surface and a hydrophobic core, which offer a larger surface water fraction to improve the analysis of its characteristics. Differential scanning calorimetry (DSC) was performed to determine the characteristics of surface water. These properties include the amount of surface water, the layer thickness, density, specific heat of the surface water above and below the freezing point of water, melting point depression of free water, effect of charge density and particle size. The charge density on the CUP surface was varied as well as the molecular weight which controls the particle diameter. The surface water is proportional to the weight fraction of CUP

Fused deposition modeling (FDM) is a rapidly growing 3D printing technology. However, printing materials are restricted to acrylonitrile butadiene styrene (ABS) or poly (lactic acid) (PLA) in most Fused deposition modeling (FDM) equipment. Here, we report on a new high-performance printing material, polyether-ether-ketone (PEEK), which could surmount these shortcomings. This paper is devoted to studying the influence of layer thickness and raster angle on the mechanical properties of 3D-printed PEEK. Samples with three different layer thicknesses (200, 300 and 400 μm) and raster angles (0°, 30° and 45°) were built using a polyether-ether-ketone (PEEK) 3D printing system and their tensile, compressive and bending strengths were tested. The optimal mechanical properties of polyether-ether-ketone (PEEK) samples were found at a layer thickness of 300 μm and a raster angle of 0°. To evaluate the printing performance of polyether-ether-ketone (PEEK) samples, a comparison was made between the mechanical properties of 3D-printed polyether-ether-ketone (PEEK) and acrylonitrile butadiene styrene (ABS) parts. The results suggest that the average tensile strengths of polyether-ether-ketone (PEEK) parts were 108% higher than those for acrylonitrile butadiene styrene (ABS), and compressive strengths were 114% and bending strengths were 115%. However, the modulus of elasticity for both materials was similar. These results indicate that the mechanical properties of 3D-printed polyether-ether-ketone (PEEK) are superior to 3D-printed ABS.

Polyphenylene sulfide (PPS) is a high-performance semi-crystalline thermoplastic polymer that is widely used in the automotive, electronics, and aerospace industries, as well as other fields. However, PPS introduces several challenges in fused deposition modeling owing to its inherent properties of crystallization and thermal crosslinking. The present study demonstrates the effects of the thermal processing and heat treatment conditions on the accuracy and mechanical properties of PPS samples three-dimensionally printed through fused deposition modeling. By measuring the degree of crystallinity and thermal crosslinking of three-dimensionally printed PPS samples, we found that the thermal history affects the three-dimensionally printed PPS properties. Results show that the accuracy of three-dimensionally printed PPS samples can be improved by means of air-forced cooling in fused deposition modeling. The balance between mechanical strength and ductility was regulated by altering the heat treatment conditions. This approach is applicable to eliminating the warpage of semi-crystalline polymer in three-dimensional printing (not only for PPS) and provides a method of improving the mechanical properties of three-dimensionally printed PPS samples.

The success of the 3D-printing process depends upon the proper selection of process parameters. However, the majority of current related studies focus on the influence of process parameters on the mechanical properties of the parts. The influence of process parameters on the shape-memory effect has been little studied. This study used the orthogonal experimental design method to evaluate the influence of the layer thickness H, raster angle θ, deformation temperature Td and recovery temperature Tr on the shape-recovery ratio Rr and maximum shape-recovery rate Vm of 3D-printed polylactic acid (PLA). The order and contribution of every experimental factor on the target index were determined by range analysis and ANOVA, respectively. The experimental results indicated that the recovery temperature exerted the greatest effect with a variance ratio of 416.10, whereas the layer thickness exerted the smallest effect on the shape-recovery ratio with a variance ratio of 4.902. The recovery temperature exerted the most significant effect on the maximum shape-recovery rate with the highest variance ratio of 1049.50, whereas the raster angle exerted the minimum effect with a variance ratio of 27.163. The results showed that the shape-memory effect of 3D-printed PLA parts depended strongly on recovery temperature, and depended more weakly on the deformation temperature and 3D-printing parameters.