Effects of Wildfire on Soil CO2 Emission and Bacterial Community in Plantations.

In order to study the effects of wildfires on soil carbon dioxide (CO2) emissions and microbial communities in planted forests, Pinus massoniana Lamb. and Cunninghamia lanceolata (Lamb.) Hook. forests were selected as the research subjects. Through a culture test with 60 days of indoor constant temperature, the soil physical and chemical properties, organic carbon mineralization, organic carbon components, enzyme activity, and microbial community structure changes of the two plantations after fire were analyzed. The results showed that wildfires significantly reduced soil CO2 emissions from the Pinus massoniana forests and Cunninghamia lanceolata forests by 270.67 mg·kg-1 and 470.40 mg·kg-1, respectively, with Cunninghamia lanceolata forests exhibiting the greatest reduction in soil CO2 emissions compared to unburned soils. Bioinformatics analysis revealed that the abundance of soil Proteobacteria in the Pinus massoniana and Cunninghamia lanceolata forests decreased by 6.00% and 4.55%, respectively, after wildfires. Additionally, redundancy analysis indicated a significant positive correlation between Proteobacteria and soil CO2 emissions, suggesting that the decrease in Proteobacteria may inhibit soil CO2 emissions. The Cunninghamia lanceolata forests exhibited a significant increase in soil available nutrients and inhibition of enzyme activities after the wildfire. Additionally, soil CO2 emissions decreased more, indicating a stronger adaptive capacity to environmental changes following the wildfire. In summary, wildfire in the Cunninghamia lanceolata forests led to the most pronounced reduction in soil CO2 emissions, thereby mitigating soil carbon emissions in the region.

Channel power management of 400†G transmission system based on C6T + L6†T spectrum and QPSK modulation format.

In the 400 Gbit/s transmission system based on C + L band spectrum and QPSK modulation format, the short-wavelength signal power will be shifted to the long-wavelength signal due to the presence of the stimulated Raman scattering (SRS) effect, which will seriously affect the performance of the transmission system as the transmission span accumulates. The solution is to set the gain and gain slopes of the C-band amplifier and L-band amplifier appropriately at each optical amplifier site, and adjust the signal power of each channel through the WSS at the transmitting end and the WSS at the DGE site, so that the flatness of the channel power at the receiving end can be controlled in a reasonable range, thus guaranteeing the transmission performance of the system. However, the system fault will destroy the originally set channel power, which will seriously affect the transmission performance of the system. In this paper, filling channel device combined with output power locking of amplifiers used in a 400 Gbit/s system based on C + L band and QPSK modulation format to provide the protection for the system is proposed and demonstrated for the first time, which gives different solutions for sudden fault at different locations of the system, and provides a reference for the channel power management of multi-band optical transmission systems in the future.

Damage Evolution and Acoustic Emission Characteristics of Sandstone under Freeze-Thaw Cycles.

The deformation and fracture characteristics of rocks under freeze-thaw cycles were investigated by using uniaxial compression tests with acoustic emission (AE) monitoring. The results showed that the sandstone peak stress and elastic modulus decreased with an increasing number of freeze-thaw cycles, and the strain increased significantly. The rates of increase in the total energy and elastic energy decreased with an increasing number of freeze-thaw cycles. The freeze-thaw damage factor De was directly proportional to the number of freeze-thaw cycles. The total damage factor D was inversely proportional to the freeze-thaw cycles when the freeze-thaw-induced damage and load-induced damage were coupled. By analyzing the AE energy rate, event rate, amplitude, and frequency of the sandstone during damage, it was found that the amplitude varies irregularly with the freeze-thaw cycles and that the AE energy and event rates can better show the development of internal cracks in the sandstone. The peak frequency was the most sensitive and could be used as an index to predict when the sandstone ultimately failed. The increase in the number of freeze-thaw cycles encouraged the development of internal cracks in the sandstone. The crack characteristics change from mixed tensile-shear fractures before they undergo freeze-thaw cycles to tensile fracturing after a high number of freeze-thaw cycles. These research results provide a valuable reference for understanding the mechanisms of rock damage caused by freeze-thaw cycles as well as for making predictions about the safety of engineering structures in cold climates.

On the mechanism of acceptorless dehydrogenation of N-heterocycles catalyzed by tBuOK: a computational study.

The catalytic acceptorless dehydrogenation (ADH) of saturated N-heterocycles has recently gained considerable attention as a promising strategy for hydrogen release from liquid organic hydrogen carriers (LOHCs). Recently, a simple tBuOK base-promoted ADH of N-heterocycles was developed by Yu et al. (Adv. Synth. Catal. 2019, 361, 3958). However, it is still open as to how the tBuOK plays a catalytic role in the ADH process. Herein, our density functional study reveals that the tBuOK catalyzes the ADH of 1,2,3,4-tetrahydroquinoline (THQ) through a quasi-metal-ligand bifunctional catalytic channel or a base-catalyzed pathway with close energy barriers. The hydride transfer in the first dehydrogenation process is determined to be the rate determining step, and the second dehydrogenation can proceed directly from 34DHQ regulated by the tBuOK. In addition, the computational results show that the cooperation of a suitable alkali metal ion with the tBuO- group is so critical that the tBuOLi and the isolated tBuO- are both inferior to tBuOK as a dehydrogenation catalyst.

Model Emulsions Stabilized with Nonionic Surfactants: Structure and Rheology Across Catastrophic Phase Inversion.

The catastrophic phase inversion process of model emulsions (water/Span 80-Tween 80/heptane) from oil-in-water to water-in-oil emulsion was investigated. During this process, the phase inversion of the emulsion was monitored through Fourier transform infrared spectroscopy (FT-IR). In emulsions without NaCl, oil-in-water gel emulsions are formed prior to phase inversion. As the HLB value increases, the oil volume fraction required for phase inversion becomes higher. Polydisperse distribution of the gel emulsion is observed from microscope optical images. The Turbiscan Lab stability analyzer indicates that O/W gel emulsions before the phase inversion has good stability at 50 °C. Rheological measurements reveal that emulsions exhibit non-Newtonian behavior. The viscosity of the gel emulsions increases significantly prior to phase inversion. As the oil volume fraction increases, the storage modulus and loss modulus of the gel emulsion increase to a maximum, at which catastrophic phase inversion occurs. In emulsions with NaCl, there is no oil-in-water gel emulsion formed before phase inversion. The physicochemical properties of the emulsion play a crucial role in whether gel emulsions are produced during catastrophic phase inversion. These gel emulsions have the potential to diversify the applications in crude oil extraction, drug delivery systems, packaging materials, and other fields.

Effect of Fe(III) Species on the Stability of a Water-Model Oil Emulsion with an Anionic Sulfonate Surfactant as an Emulsifier.

The stability of an emulsion has an important effect on enhancing oil recovery. However, the effect of ions with different valences on the stability of the emulsion emulsified by an ionic surfactant is not fully understood. In this study, the effects of Fe(III) species on the stability, microscopic morphology of droplets, interfacial properties, and rheological properties of water-model oil emulsions emulsified by sodium dodecyl benzenesulfonate (SDBS) were explored. The effect of Fe(III) species on the stability of a W/O crude oil emulsion was also explored. The stability experiment results show that the addition of the Fe(III) species impairs the stability of the model oil-in-water (O/W) emulsion, in which the O/W model oil emulsion is inverted to a water-in-model oil (W/O) emulsion at ∼99 ppm. With the increase of Fe(III) species concentration, stable W/O model oil and W/O crude oil emulsions are obtained. The rheological results indicated that the existence of the Fe(III) species has a remarkable effect on the viscosity and viscoelastic behaviors of the water-model oil emulsion. The calculation results based on Derjaguin-Landau-Verwey-Overbeek (DLVO) theory are in accord with the stability experiment results. Furthermore, the addition of EO groups makes the phase inversion point appear at a higher Fe(III) species concentration, forming a more stable W/O model oil emulsion and a more unstable O/W model oil emulsion. The experimental results are helpful to comprehensively understand the effect of Fe(III) species on the stability of an emulsion emulsified by an anionic sulfonate surfactant, which can help to enhance the oil recovery.

Effect of Temperature on Asphaltene Precipitation in Crude Oils from Xinjiang Oilfield.

During the production of crude oil, asphaltenes are prone to precipitate due to the changes of external conditions (temperature, pressure, etc.). Therefore, a series of research studies were designed to investigate the effect of temperature on asphaltene precipitation for two Xinjiang crude oils (S1, S2) so as to reveal the mechanism of asphaltene dissolution. First, the changes of asphaltene precipitation were intuitively observed by using a microscope. The results demonstrated that the asphaltene solubility increased with the increase of temperature and the dispersion rate of asphaltene particles increased with the decrease of particle size. Second, the variation of asphaltene precipitation with temperature was quantified by a gravimetric method. The results suggested that the different asphaltenes showed different sensitivity to temperature within the temperature range 25-120 °C. Third, a hypothesis was proposed to explain these results and proved that the asphaltene aggregate structure was an important factor for asphaltene stability. The crystallite parameters of asphaltenes were obtained by X-ray diffraction (XRD) to describe the structural characteristics. The results revealed that the layer distance between aromatic sheets (d m ) of asphaltenes derived from S1 oil and S2 oil were 0.378 and 0.408 nm, respectively, which implied that the asphaltene aggregates derived from S2 oil were looser than those of S1 oil. Therefore, high temperature could facilitate the penetration of resins into asphaltene aggregates and ultimately improve the dispersion of asphaltenes. Finally, molecular dynamics (MD) simulation was used to verify the conclusions. Based on the molecular dynamics method, asphaltene aggregate models were developed. The compactness and internal energy of each model were calculated. The results showed that the asphaltene dispersion capability was proportional to the porosity and internal energy.

Molybdenum disulfide composite materials with encapsulated copper nanoparticles as hydrogen evolution catalysts.

In the current work, a series of molybdenum disulfide composite MCNTs@Cu@MoS2 materials with high hydrogen evolution performance are prepared. In the hydrogen evolution reaction, their overpotential is as low as 225 mV at a current density of 10 mA cm-2 in 1 M H2SO4 as electrolyte solution. This excellent catalytic activity has been ascribed to its lower electrical impedance and high double layer capacitance. The encapsulation of copper nanoparticles into MoS2 crystals significantly reduces their resistance, enhancing the electron transfer rate during water electrolysis. Thereby, the introduction of conductive nanoparticles into semi-conductive catalyst crystals would be an efficient measure to improve their electrochemical catalytic activity in the hydrogen evolution reaction.

(1-Selenocyanatoethyl)benzene: A Selenocyanation Reagent for Site-Selective Selenocyanation of Inert Alkyl C(sp3)-H Bonds.

A new, simple, yet easily accessible, (1-selenocyanatoethyl)benzene has been designed and applied as a SeCN group transfer reagent for selenocyanation of aliphatic C(sp3)-H bonds for the first time. This protocol is featured with mild reaction conditions and wide substrate scope. Control experiments reveal that a radical-group transfer mechanism might be involved.

Unraveling How the H2 Treatment Helps Improve the Performances of Cu and Ag Loaded Y Zeolites for Adsorptive Desulfurization.

This work seeks for a better understanding on how the gas treatment process affected the structure of metal loaded zeolite Y (MY, M = Ag, Cu) adsorbants and how the structural changes affected the performances of the adsorbents for adsorptive desulfurization. A series of characterization tools including solid-state nuclear magnetic resonance were employed. Compared to the N2 treatment, the H2 treatment on the MY adsorbents led to the reduction of the loaded M components to their metallic state and, consequently, brought several structural changes to the zeolitic framework. The structural changes brought by the H2 treatment can be accounted for the decreased Brönsted acidity over the Lewis acidity of the adsorbents and thus helped in improving their adsorption capacity. This paper provides new insights on how the zeolitic framework changes affected the sulfur adsorption capacity of MY, which is helpful for designing better adsorbents for sulfur removal from oil.

Generation of an optical triangular-shaped pulse train with variable symmetry by using an I/Q modulator.

A setup for an optical triangular-shaped pulse train with variable symmetry is proposed. The key component is an I/Q (I: in-phase, Q: quadrature phase) modulator. By properly setting the three variables, the optical intensity can be expressed by the sum of infinite sinusoidal harmonics, which indicates the possibility to approximate the asymmetrical waveform. It is found that the scheme is capable for generating an optical triangular-shaped pulse train with a tunable symmetrical coefficient (${20}\% \le \delta \le {80}\% $20%≤δ≤80%) and low fitting error ($\eta \le {6}\% $η≤6%).

Investigation on Adsorption and Separation Behavior of Propane/Propene Mixtures in Zeolites.

Propane/propene separation is among the most energy-intensive separation processes in the petrochemical industry. Separation based on adsorption on a nanoporous material (e.g., zeolites) has spawned new ideas for this process. Therefore, we conducted grand canonical ensemble Monte Carlo simulations to investigate the adsorption and separation of propane and propene in one-dimensional (ATS, MOR, and AWO), two-dimensional (MWW, FER, and BOG) and three-dimensional (MFI, BEA, FAU) zeolites. The computation of pure components indicates that the adsorption capacity is affected by the zeolite pore diameter, dimensionality, and isosteric heat. For a given diameter, three dimensional zeolites exhibit better adsorption properties than two or one-dimensional zeolites. Zeolites with diameters ranging from 4.8 Å to 5.4 Å show high propane and propene affinity. In binary mixture simulations, the separation capacity of propane and propene increases with elevated pressure and decreased temperature. Among these zeolites, AWO exhibits the best separation performance due to its eight-ring window channel, which is consistent with experimental results. Thus, our results provide better understanding on propane and propene adsorption and separation in different zeolites, as well as insight into how production conditions could be upgraded.

UiO-66-supported Fe catalyst: a vapour deposition preparation method and its superior catalytic performance for removal of organic pollutants in water.

A vapour deposition (VD) method was established for preparation of the UiO-66-supported Fe (Fe/UiO-66) catalyst, which provided the first case of the metal-organic framework (MOF)-supported Fe catalyst prepared by using the vapour-based method. The Fe loading was around 7.0-8.5 wt% under the present preparation conditions. The crystal structure of UiO-66 was not obviously influenced by the Fe loading, while the surface area significantly decreased, implicating most of the Fe components resided in the pores on UiO-66. The results for the methyl orange (MO) removal tests showed that MO in aqueous solution can be removed by UiO-66 by adsorption, and in contrast, it can be oxidized by H2O2 with the catalysis of Fe/UiO-66. Further catalytic tests showed that Fe/UiO-66 was rather effective to catalyse the oxidation of benzene derivatives like aniline in water in terms of chemical oxygen demand (COD) removal efficiency. The catalytic test results for Fe/UiO-66 were compared to those of Fe/Al2O3 with the same Fe loading and to the catalysts reported in the literature. This paper provides a general strategy for VD preparation of MOF-supported Fe catalyst on the one hand, and new catalysts for removing organic pollutants from water, on the other hand.

Methane activation on nickel oxide clusters with a concerted mechanism: a density functional theory study of the effect of silica support.

The support effect is an important issue in heterogeneous catalysis. A systematic density functional theory (DFT) study was performed to investigate the support effect of a silica model on the initial step of methane activation on NixOx (x =2,3) clusters with a concerted mechanism. Four reactions were examined by exploring their potential energy surfaces (PES): CH4 reacting with unsupported Ni2O2, with silica-supported Ni2O2, with unsupported Ni3O3, and with silica-supported Ni3O3. For each reaction, PES with different spin states were explored. For CH4 activation taking place via a concerted mechanism, the reaction barriers in terms of free energy and reaction free energy increased with the involvement of the model silica support. Only one PES made a major contribution to the overall reaction rate of all four reactions examined. No spin transition process was required for the reactions to undergo their most-favorable pathway from their starting reactants. These results provide a deeper insight into the support effect on C-H bond activation of small alkanes in general, and of methane in particular, on supported transition metal catalysts.

The dependence of surface tension on surface properties of ionic surfactant solution and the effects of counter-ions therein.

In the present paper, we aim to investigate the dependence of surface tension on the surface properties and reveal the counter-ion effects on the adsorption of ionic surfactants on the solution surface. The surface tension, surface excess and surface concentration (defined as the amount of surfactant adsorbed in the surface phase divided by the surface area) of two anionic surfactants, namely dodecyl sulfate sodium and dodecyl sulfate caesium, dissolved in non-aqueous polar solvent formamide have been separately measured at 6 °C through independent experiments. Then, the correlation of surface tension with surface concentration and that of surface tension with surface excess is inspected in detail. It was found that there is a linear relationship between the surface tension and the surface concentration for the pure solutions of each surfactant, but their surface tension and surface excess cannot be correlated linearly. It is striking that the same surface tension-surface concentration linearity holds for two different surfactants, although they have apparently distinct counter-ions. Based on this finding, it is derived that the surface tension is decided by surface concentration of the surface active ions. After analyzing the surface structure, it is concluded that the counter-ions affect the surface tension indirectly through modifying the adsorption amount of the surface active ions in the surface layer.

The fabrication of porous N-doped carbon from widely available urea formaldehyde resin for carbon dioxide adsorption.

N-doped carbon material constitutes abundant of micropores and basic nitrogen species that have potential implementation for CO2 capture. In this paper, porous carbon material with high nitrogen content was simply fabricated by carbonizing low cost and widely available urea formaldehyde resin, and then followed by KOH activation. CO2 capture experiment showed high adsorption capacity of 3.21 mmol g(-1) at 25 °C under 1 atm for UFCA-2-600. XRD, SEM, XPS and FT-IR analysis confirmed that a graphitic-like structure was retained even after high temperature carbonization and strong base activation. Textural property analysis revealed that narrow micropores, especially below 0.8 nm, were effective for CO2 adsorption by physical adsorption mechanism. Chemical evolved investigation revealed that graphitic-like embedded basic nitrogen groups are generated from bridged and terminal amines of urea formaldehyde resin from thermal carbonization and KOH activation treatment, which is responsible for the enrichment of CO2 capacity by chemical adsorption mechanism. The relationship between CO2 adsorption capacity and pore size or basic N species was also studied, which turned out that both of them played crucial role by physical and chemical adsorption mechanism, respectively.

The competitive adsorption of counter-ions at the surface of anionic surfactants solution.

We have determined the surface excess of surface active anion and counter-ions in a non-aqueous polar solution of anionic surfactants blends, as well as their distributions near the solution surface. The blends of two anionic surfactants, sodium dodecyl sulfate (SDS) and cesium dodecyl sulfate (CDS), with different contents were used as solutes to prepare the solutions. According to the isotherms that are separately fitted to the pure SDS and the pure CDS solutions (C. Wang and H. Morgner, Langmuir, 2010, 26, 3121), CDS has a slightly but significantly higher surface excess than SDS (CDS is 14.8% higher) at the concentration of 0.04 molal kg(-1) solvent. Therefore, in this work we chose 0.04 molal kg(-1) solvent as total anion concentration and varied the contents of surfactants. From present experimental results, we found that the surface excess of anion increases slightly with the CDS in the bulk content. Importantly, the fractions of Cs(+) in cationic surface excess are higher than its contents in the bulk for all three solutions. This demonstrates that Cs(+) is more competitive than Na(+) in the adsorption. The surface structure of the solutions have been characterized by concentration-depth profiles, of Cs(+), Na(+) and of sulfur which is used to identify dodecyl sulfate. Those profiles evidence that Cs ions penetrate deeper than sodium ions into the layer formed by the heads of the anions, reducing the electrical potential of the surface more efficiently. This can be used to explain the adsorption competition between those two counter-ions. The cause that makes Cs(+) more competitive than Na(+) in the adsorption can be attributed to its less tightly bound solvation shell, and thus, to its effectively smaller ion size.

Effects of counterions on adsorption behavior of anionic surfactants on solution surface.

The goal of the present paper concerns the effects of counterions on adsorption behavior of anionic surfactants. The surfactants chosen are sodium dodecyl sulfate and cesium dodecyl sulfate, and the polar solvent is formamide. In the investigations, the surface excess and surface tension have been measured independently. On this basis the chemical potential was determined with the help of the Gibbs equation. In addition, the structure of electrical double layer has been investigated. It was determined by the distribution of the oppositely charged ions near the surface. The results evidence that the counterions have profound effects on the adsorption behavior of ionic surfactants on solution surface. The cause can be attributed to the properties of counterions, such as size and solvophilicity.