Quasi-3D slope stability analysis of waste dump based on double wedge failure.

The double wedges sliding along the weak layer of the foundation can be observed on the slope of the waste dump and the sliding body is divided into the active wedge and passive wedge by the weak foundation and the failure surfaces of the waste dump. Because the conventional limit equilibrium slice method cannot reflect the polygonal slip surface of the slope of the waste dump with weak foundation, this study proposed a double wedge calculation method for the slope of the waste dump with weak foundation. The limit equilibrium analysis is performed on double wedges by considering the direction and values of the interaction force between double wedges to obtain the safety factor of the slope of the waste dump. Meanwhile, the quasi-3D double wedges stability analysis method of the waste dump slope with weak foundation is proposed by considering the influence of the geometry and sliding direction of the slope surface on the slope stability. The safety factor of the inverted dump slope is 0.82, the volume of the sliding body is 6.43 million m3, and the main sliding direction is 20° south by east. The shear strain rate cloud diagram of the section is 'y' type distribution, and the sliding body is divided into two independent blocks. The safety factor of the sliding body section obtained by the double wedge method is between 0.76 and 0.92, and the closer to the boundary of the sliding body, the greater the safety factor of the section. The quasi-three-dimensional safety factor obtained by theoretical analysis is 0.817. The results show that the calculation results of quasi-3D double wedge are basically consistent with the calculation results of strength reduction method, while the proposed method is simpler. It can be used as a quick method to evaluate slope stability in engineering practice.

Comparative analysis of fracture characteristics between rock and rock-like materials.

In order to investigate the characteristics of rock and rock-like materials during the fracture process, notched semi-circular bending (SCB) experiments of 3 rocks and 2 rock-like materials were conducted in this paper. The process of the crack mouth opening was measured with a clip gauge. Acoustic emission was used to analyze the damage and failure mode of the specimens. Meanwhile, the fracture process zone (FPZ) was analyzed with the digital image correlation (DIC). Finally, the differences in the fracture process between rocks and rock-like materials were observed with a polarized microscope, and the formation mechanism of FPZ was discussed. The results indicate that the sequence from brittleness to plasticity is gypsum, marble, granite, concrete and fine sandstone. The crack opening velocity of gypsum, marble, and granite reaches 0.02-0.025 mm/s, far exceeding that of sandstone and concrete at 0.003 mm/s and 0.005 mm/s. The stronger the brittleness of geomaterials, the less significant their acoustic emission effect. Only a few acoustic emissions occur during the fracture process of gypsum with 8 hits. Its fracture occurs instantaneously rather than through a process of damage to fracture and the failure mode is tensile failure. Sandstone has the strongest plasticity, with a large count of acoustic emissions before and after fracture, with a hit number of 5062, which is 630 times of pure gypsum. The fracture is a process of damage accumulation with 94% of sandstone, 89% of concrete, 80% of granite, and 60% of marble showing a tensile and shear failure mode except gypsum. In addition, the stronger the brittleness of geomaterials, the smaller their FPZ size. The FPZ of gypsum is only about 3 mm, which can be considered as lacking, while other materials are about 6-11 mm. The formation of FPZ depends on whether an interlocking structure can be formed inside the material, which is related to the base material and crystalline or aggregate particle size.

Antimicrobial Resistance and Genomic Characterization of Two mcr-1-Harboring Foodborne Salmonella Isolates Recovered in China, 2016.

The mcr-1 gene mediating mobile colistin resistance in Escherichia coli was first reported in China in 2016 followed by reports among different species worldwide, especially in E. coli and Klebsiella. However, data on its transmission in Salmonella are still lacking. This study analyzed the antimicrobial resistance (AMR) profiles and the mcr-1 gene presence in 755 foodborne Salmonella from 26 provinces of mainland, China in 2016. Genomic features of two mcr-1-carrying isolates, genome sequencing, serotypes and further resistance profiles were studied. Among the 755 Salmonella tested, 72.6% were found to be resistant to at least one antimicrobial agent and 10% were defined as multi-drug resistant (MDR). Salmonella Derby CFSA231 and Salmonella Typhimurium CFSA629 were mcr-1-harboring isolates. Both expressed an MDR phenotype and included a single circular chromosome and one plasmid. Among the 22 AMR genes identified in S. Derby CFSA231, only the mcr-1 gene was localized on the IncX4 type plasmid pCFSA231 while 20 chromosomal AMR genes, including four plasmid-mediated quinolone resistance (PMQR) genes, were mapped within a 64 kb Salmonella genomic island (SGI) like region. S. Typhimurium CFSA629 possessed 11 resistance genes including an mcr-1.19 variant and two ESBL genes. Two IS26-flanked composite-like transposons were identified. Additionally, 153 and 152 virulence factors were separately identified in these two isolates with secretion system and fimbrial adherence determinants as the dominant virulence classes. Our study extends our concern on mcr-1-carrying Salmonella in regards to antimicrobial resistance and virulence factors, and highlight the importance of surveillance to mitigate dissemination of mcr-encoding genes among foodborne Salmonella.

Emergence of a Salmonella enterica serovar Typhimurium ST34 isolate, CFSA629, carrying a novel mcr-1.19 variant cultured from egg in China.

OBJECTIVES: This study aimed to characterize the genomic features of a Salmonella enterica serovar Typhimurium ST34 isolate, CFSA629, which carried a novel mcr-1 variant, designated as mcr-1.19, mapped to an ESBL-encoding IncHI2 plasmid. METHODS: Antimicrobial susceptibility assays as well as WGS were carried out on isolate CFSA629. The complete closed genome was obtained and then explored to obtain genomic features. Plasmid sequence comparison was performed for pCFSA629 with similar plasmids and the mcr-1 genetic environment was analysed. RESULTS: S. Typhimurium ST34 CFSA629 expressed an MDR phenotype to six classes of compound and consisted of a single circular chromosome and one plasmid. It possessed 11 resistance genes including 2 ESBL genes that mapped to the chromosome and the plasmid; an IS26-flanked composite-like transposon was identified. A novel mcr-1 variant (mcr-1.19) was identified, which had a unique SNP (G1534A) that gave rise to a novel MCR-1 protein containing a Val512Ile amino acid substitution. Plasmid pCFSA629 possessed a conjugative plasmid transfer gene cluster as well as an antimicrobial resistance-encoding gene cluster-containing region that contained two IS26 composite-like transposonal modules, but was devoid of any plasmid-mediated quinolone resistance genes. The background of mcr-1.19 consisted of an ISApl1-mcr-1-PAP2-ter module. CONCLUSIONS: We report on an MDR S. Typhimurium ST34 CFSA629 isolate cultured from egg in China, harbouring an mcr-1.19 variant mapped to an IncHI2 plasmid. This highlights the importance of surveillance to mitigate dissemination of mcr-encoding genes among foodborne Salmonella. Improved surveillance is important for tackling the dissemination of mcr genes among foodborne Salmonella around the world.

Cellulose modified by citric acid reinforced polypropylene resin as fillers.

The greatest challenge hindering the use of cellulose as a reinforcing filler in polymeric composites is its poor compatibility due to the inherent hydrophilicity of cellulose and the hydrophobic nature of polymeric matrices. To solve this issue, we demonstrate an effective water-based method to render the cellulose surface with high carboxyl content through the esterification of hydroxyl groups with citric acid in a solid phase reaction without the use of noxious solvents. The modified cellulose was then further hydrophobized by grafting magnesium stearate to the surface. Consequently, the flexural properties of PP composites reinforced by the hydrophobized cellulose fillers were greatly improved compared to those of composites containing hydrophilic cellulose and pure PP resin. The surface modification conditions and filler proportions in composites were optimized. Because of the innocuity and cost-efficiency of citric acid, we believe that citric acid-modified cellulose has immense potential as a sustainable and cost-effective reinforcing filler.

A Versatile Protein and Cell Patterning Method Suitable for Long-Term Neural Cultures.

Herein, we present an easy-to-use protein and cell patterning method relying solely on pipetting, rinsing steps and illumination with a desktop lamp, which does not require any expensive laboratory equipment, custom-built hardware or delicate chemistry. This method is based on the adhesion promoter poly(allylamine)-grafted perfluorophenyl azide, which allows UV-induced cross-linking with proteins and the antifouling molecule poly(vinylpyrrolidone). Versatility is demonstrated by creating patterns with two different proteins and a polysaccharide directly on plastic well plates and on glass slides, and by subsequently seeding primary neurons and C2C12 myoblasts on the patterns to form islands and mini-networks. Patterning characterization is done via immunohistochemistry, Congo red staining, ellipsometry, and infrared spectroscopy. Using a pragmatic setup, patterning contrasts down to 5 µm and statistically significant long-term stability superior to the gold standard poly(l-lysine)-grafted poly(ethylene glycol) could be obtained. This simple method can be used in any laboratory or even in classrooms and its outstanding stability is especially interesting for long-term cell experiments, e.g., for bottom-up neuroscience, where well-defined microislands and microcircuits of primary neurons are studied over weeks.

Bacterial Inhibition and Osteoblast Adhesion on Ti Alloy Surfaces Modified by Poly(PEGMA- r-Phosmer) Coating.

We have synthesized and immobilized PEGMA500-Phosmer to Ti6Al4V surfaces by a simple procedure to reduce bacteria-associated infection without degrading the cell response. Adhered bacteria coverage was lessened to 1% on polymer-coated surfaces when exposed to Escherichia coli, Staphylococcus epidermidis, and Streptococcus mutans. Moreover, PEGMA500-Phosmer and homoPhosmer coatings presented better responses to MC3T3-E1 preosteoblast cells when compared with the results for PEGMA2000-Phosmer-coated and raw Ti alloy surfaces. The behavior of balancing bacterial inhibition and cell attraction of the PEGMA500-Phosmer coating was explained by the grafted phosphate groups, with an appropriate PEG brush length facilitating greater levels of calcium deposition and further fibronectin adsorption when compared with that of the raw Ti alloy surface.

Anti-biofouling phosphorylated HEMA and PEGMA block copolymers show high affinity to hydroxyapatite.

Four types of phosphorylated 2-hydroxyethyl methacrylate and poly(ethylene glycol) methyl ether methacrylate (PEGMA) block copolymers were synthesized by reversible addition fragmentation chain transfer (RAFT) polymerization and post-phosphorylation. These polymers were composed of different phosphate segments and similar PEG brushes. Polymers with defined phosphate segments were investigated to determine the optimal bonding affinity to hydroxyapatite (HAp). Polymers containing short phosphate segments (as low as 23 mer) were capable of immobilizing on HAp surfaces in situ in a short coating time with considerable durability. After surface modification, the dense PEG brushes altered the interfacial properties of HAp. The protein adsorption on the polymer-grafted HAp was drastically reduced compared with the bare HAp. Furthermore, the presence of the PEG brushes on the HAp surface resulted in bacterial inhibition. The polymer with the shortest phosphate segment (23 mer) showed superior inhibition ability.

Inhibition of Bacterial Adhesion on Hydroxyapatite Model Teeth by Surface Modification with PEGMA-Phosmer Copolymers.

Modification of the interface properties on hydroxyapatite and tooth enamel surfaces was investigated to fabricate bacterial resistance in situ. A series of copolymers containing pendants of poly(ethylene glycol) methyl ether methacrylate (PEGMA) and ethylene glycol methacrylate phosphate (Phosmer) were polymerized by conventional free radical polymerization and changing the feed ratio of monomers. The copolymers were immobilized on hydroxyapatite and tooth enamel via the affinity of phosphate groups to hydroxyapatite to form the stable and durable polymer brushes on the surfaces. The amounts of polymer immobilized depended on the phosphate group ratio in the copolymers. Surface modification altered the interfacial properties of hydroxyapatite and inhibited bacterial adhesion. Copolymers containing 40-60% PEGMA segments showed a significant inhibitory effect on bacterial adhesion of S. epidermidis both in the presence and absence of plaque model biomacromolecules.