Meanwhile, the quantitative calculation results indicate that the porosity losses by compaction, carbonate cementation, kaolinite cementation, chlorite coatings, and siliceous cementation are 23.5, 3.1, 3.8, 3.0, and 0.8%, respectively. In addition, dissolution is significant to improve the reservoir physical property, and the increase of dissolved porosity is around 3.2%. More significantly, this study uses a detailed and systematic method for analyzing the tightness mechanism and the pore evolution process of the Ch-6 sandstones in the western Jiyuan area, Ordos Basin, China.A sensitive diethyl ether gas sensor based on cataluminescence on nano-Pd/ZnNi3Al2O7 at a temperature lower than 150 °C was reported. The composition of the sensitive material was determined by energy-dispersive spectrometry, and a particle size of less than 50 nm was shown by transmission electron microscopy. When the atomic percentage of Pd in the sensing material is 0.8-1.3%, it is beneficial to the low-temperature and high-selective cataluminescence of diethyl ether. The signal response and recovery of diethyl ether on the sensitive material can be completed quickly in 0.5 s, and the relative standard deviation of the signal within 500 h of continuous operation is not more than 2.5%. There is good linear relationship between the luminescence intensity and the concentration of diethyl ether in the range of 0.08-75 mg/m3. The detection limit (3σ) is 0.04 mg/m3. The working conditions optimized by the response surface methodology were an analytical wavelength of 548.86 nm, a reaction temperature of 109.18 °C, and a carrier gas velocity of 125.88 mL/min. The sensitivity of the method can be increased by 4.5% under the optimized working conditions. The optimization method is universal for many multi-parameter processes.The oxygen evolution reaction (OER) and the hydrogen evolution reaction occurred at the anode and cathode, which depends on the electronic structure, morphology, electrochemically active surface area, and charge-transfer resistance of the electrocatalyst. Transition metals like cobalt, nickel, and iron have better OER and oxygen reduction reaction activities. At the same time, transition-metal oxide/carbon hybrid has several applications in electrochemical energy conversion reactions. The rich catalytic site of transition metals and the excellent conductivity of carbon material make these materials as a hopeful electrocatalyst in OER. Carbon-incorporated LaFe0.8Co0.2O3 was prepared by a simple solution combustion method for the development of the best performance of the electrocatalyst. The catalyst can deliver 10 mA/cm2 current density at an overpotential of 410 mV with better catalytic stability.  https://www.selleckchem.com/products/c188-9.html  The introduction of carbon material improves the dispersion ability of the catalyst and the electrical conductivity. The Tafel slope and onset potential of the best catalyst are 49.1 mV/dec and 1.55 V, respectively.Silk fibroin (SF) has been widely used as wound dressings due to its good biocompatibility. To enhance the antibacterial properties of the dressings, silver (Ag) is often added. However, an overdose of Ag may cause cytotoxicity and inhibit wound healing. Therefore, this study aimed to develop a two-layered membrane to reduce cytotoxicity while maintaining the antibacterial properties of Ag through a simplified layer-by-layer technique. The membranes comprised an Ag-rich SF layer (Ag-SF) and a pure SF layer. The unilateral Ag-loaded membranes showed efficient antibacterial properties at doses above 0.06 mg/mL Ag, and the antibacterial properties were comparable on both sides. In contrast, the SF sides of the membranes showed lower cytotoxicity than the Ag-SF sides of the membranes. Further studies on the thickness ratio of Ag-SF/SF layers revealed that Ag0.12-SF/SF membranes with a ratio of 13 had high cytocompatibility on the SF sides while holding a strong antibacterial property. Besides, the SF sides of the Ag0.12-SF/SF13 membranes promoted the expression levels of collagen I and transforming growth factor-β mRNA in human foreskin fibroblasts. The SF sides of the Ag0.12-SF/SF13 membranes significantly promoted the healing of infected wounds in vivo. Therefore, unilateral loading with the simplified layer-by-layer preparation technique provided an effective method to balance the cytotoxicity and the antibacterial property of Ag-loaded materials and thus form a broader therapeutic window for Ag applications. The unilateral Ag-loaded silk fibroin difunctional membranes have the potential to be further preclinically explored as wound dressings.Because of its high conductivity and intrinsic stability, poly(3,4-ethylenedioxythiophene (PEDOT) has gained great attention both in academic research and industry over the years. In this study, we used the oxidative molecular layer deposition (oMLD) technique to deposit PEDOT from 3,4-ethylenedioxythiophene (EDOT) and a new inorganic oxidizing agent, rhenium pentachloride (ReCl5). We extensively characterized the properties of the films by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy (XPS), energy-dispersive X-ray spectroscopy (EDS), Raman, and conductivity measurements. The oMLD of polymers is based on the sequential adsorption of the monomer and its oxidation-induced polymerization. However, oMLD has been scarcely used because of the challenge of finding a suitable combination of volatile, reactive, and stable organic monomers applicable at high temperatures. ReCl5 showed promising properties in oMLD because it has high thermal stability and high oxidizing ability for EDOT. PEDOT films were deposited at temperatures of 125-200 °C. EDS and XPS measurements showed that the as-deposited films contained residues of rhenium and chlorine, which could be removed by rinsing the films with deionized water. The polymer films were transparent in the visible region and showed relatively high electrical conductivities within the 2-2000 S cm-1 range.Water-insoluble cationic poly(vinyl alcohol) (PVA) films were fabricated using a mixed aqueous solution of PVA and poly([2-(methacryloyloxy)ethyl]trimethylammonium chloride (METAC)-co-methacrylic acid (MAAc)-co-5-methacrylamido-1,2-benzoxaborole (MAAmBO)) copolymer (3D). The surface of the PVA film is typically negatively charged, and simple fabrication methods for water-insoluble PVA films with cationic surface charges are required to expand their application fields. METAC, which has a permanent positive charge owing to the presence of a quaternary ammonium cation, was selected as the cationic unit. The MAAc and MAAmBO units were used as two types of cross-linking structures for the thermal cross-linking of the hydroxy and carboxy groups of the MAAc unit (covalent bonding) as well as the diol and benzoxaborole groups of the MAAmBO unit (dynamic covalent bonding). The films were thermally cross-linked at 135 °C for 4 h without the addition of materials. After immersion in surplus water at 80 °C for 3 h, the cross-linked PVA/3D films retained almost 100% of their weights.