Conditions for shale gas accumulation and the gas-bearing factors of the Wufeng-Longmaxi formation in the Laifeng-Xianfeng area.

In this work, taking wells LD1, LD2, and LY2 in the Laifeng-Xianfeng area as the research target, through core description, intensive core sampling, experimental analysis, imaging logging and other methods, the characteristics of graptolite zone development, organic carbon content, mineral composition, shale reservoir properties and the gas-bearing properties of the Wufeng-Longmaxi Formation shale are systematically analyzed. The main factors affecting the gas-bearing capacity of the Wufeng-Longmaxi Formation shale are extensively evaluated. The results reveal the following: ① The Wufeng-Longmaxi Formation shale, which was deposited in a deep-water shelf environment, has a large thickness (50-60 m) and a stable distribution.

Damage and energy characteristics of coal rock combinations with inclined coal seams under axial loading.

A single load compression test of rock-coal-rock assemblages (RCRs) containing coal bodies with different inclinations was carried out with the research background of mining deep, large-steep coal seams. It was found that the larger the inclination angle of the coal body in the RCR samples, the larger the compaction stage of the samples and the smaller the uniaxial compressive strength value. In addition, both the maximum acoustic emission (AE) energy of the samples and the cumulative AE energy at the moment of destruction decreased with the increase of the inclination angle of the coal body in the form of exponential relativities.

Fracability evaluation of the middle-upper Permian marine shale reservoir in well HD1, western Hubei area.

Taking the HD1 well as the research target, through intensive core sampling, experimental test analysis, comprehensive logging interpretation and other methods, the fracability of shale reservoirs was discussed in this paper. The results show that the Gufeng-Dalong Formation in the HD1 well has a high organic carbon content, and the organic-rich shale developed in the lower part of the Gufeng and Dalong Formations with thicknesses of 30 m and 15 m, respectively. For the low-porosity and ultralow-permeability shale reservoir type, the natural fractures are undeveloped in the lower part of the Dalong Formation, with a lower linear density, while they are well developed in the Xiayao and Longtan Formations and the lower part of the Gufeng Formation, and the interlayer bedding fractures are relatively developed.

Enhancing the thermostability, UV shielding and antimicrobial activity of transparent chitosan film by carbon quantum dots containing N/P.

The chitosan (CS) transparent film has attracted much attention in food and medicine packaging areas due to their biodegradability and good availability. A novel carbon quantum dots compound containing nitrogen and phosphorus (NP-CQDs) was obtained by reacting citric acids, with urea and phytic acids. The density of the film was increased, and the water vapor permeation was reduced by the presence of NP-CQDs.

Reaction kinetics and properties of MDI base poly (urethane-isocyanurate) network polymers.

Since the trimerization of isocyanate occurs easily and controllably to form a clear trifunctional isocyanate ring, this reaction is an ideal candidate for the synthesis of a clear poly(urethane-isocyanurate) network polymer. Poly(urethane-isocyanurate) network polymer (PUI) was prepared from diphenylmethane diisocyanate (MDI) and propylene glycol (PPG) by cyclotrimerization of isocyanate group (NCO). It was proved that the expected product was successfully prepared by NCO determination, fourier transform infrared (FTIR) and gel permeation chromatography (GPC) characterization.

Improved Efficiency in All-Small-Molecule Organic Solar Cells with Ternary Blend of Nonfullerene Acceptor and Chlorinated and Nonchlorinated Donors.

Ternary nonfullerene all-small-molecule organic solar cells (NFSM-OSCs) were developed by incorporating a nonfullerene acceptor (IDIC) and two structurally similar small molecular donors (SM and SM-Cl), where SM-Cl is a novel small molecular donor derived from the reported molecular donor SM. When doping 10% SM-Cl in the SM:IDIC binary system, the power conversion efficiency (PCE) of the ternary solar cell was dramatically increased from 9.39 to 10.

Photocured Materials with Self-Healing Function through Ionic Interactions for Flexible Electronics.

Photocured materials with self-healing function have the merit of long lifetime and environmentally benign preparation process and thus find potential applications in various fields. Herein, a novel imidazolium-containing photocurable monomer, (6-(3-(3(2-hydroxyethyl)-1 H-imidazol-3-ium bromide)propanoyloxy)hexyl acrylate, IM-A), was designed and synthesized. Self-healing polymers were prepared by fast photocuring with IM-A, isobornyl acrylate, 2-(2-ethoxyethoxy)ethyl acrylate, and 2-hydroxyethyl acrylate as the monomers.

[Analysis of the parental origin of MECP2 mutations in patients with Rett syndrome].

Objective: To identify the parental origin of methyl-CpG-binding protein 2 (MECP2) gene mutations in Chinese patients with Rett syndrome.

Methods: Single nucleotide polymorphisms (SNPs) in intron 3 of the MECP2 gene were analyzed by PCR and sequencing in 115 patients with Rett syndrome. Then sequencing of the SNP region was performed for the fathers of the patients who had at least one SNP, to determine which allele was from the father.

X chromosome inactivation in Rett Syndrome and its correlations with MECP2 mutations and phenotype.

Rett syndrome (RTT) is an X-linked dominant neurodevelopment disorder, which is mainly caused by gene mutation of methyl-CpG-binding protein 2 (MECP2). The correlations between genotype, X chromosome inactivation (XCI), and phenotype have been studied, but the results are conflicting. In the present study, XCI patterns in patients and their mothers, parental origin of skewed X chromosome in patients, and the correlations between XCI, genotype, and phenotype were analyzed in 52 cases of RTT with MECP2 mutations, 50 RTT mothers, and 48 normal female controls.

[X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome].

Objective: Rett syndrome (RTT) is a severe childhood neurodevelopmental disorder mainly affecting females. The pathogenic gene is located at Xq28, which codes for the methyl-CpG-binding protein 2. MECP2 gene is affected by X chromosome inactivation (XCI).

[MECP2 gene mutations in twenty-six cases with atypical Rett syndrome].

Objective: Rett syndrome (RTT) is an X-linked progressive neurodeveopmental disorder that almost exclusively affects girls, and is one of the most common causes of mental retardation in females, with an estimated prevalence of approximately 1 in 10,000 - 15,000 female individuals. Mutations in X-linked methyl-CpG-binding protein 2 (MECP2) gene, located on chromosome Xq28, have been found to be a cause of RS. A lot of mutations have been reported to be related to RS recently.