Damage analysis and optimal design of micro-structure milling cutter based on peridynamics.

H13 die steel has the characteristics of high hardness, strong toughness, and good heat resistance, and is a typical difficult to process materials material. During the cutting process, it is prone to accelerate tool wear and cause thermal deformation. By reasonably designing micro-grooves, the comprehensive performance of the tool can be effectively improved.

Influence of Microgroove Structure on Cutting Performance and Chip Morphology during the Turning of Superalloy Inconel 718.

This study designed a new microgroove cutting tool to machine Inconel 718 and focused on the effect of microgroove structure on the cutting performance and chip morphology during the turning. A comparative analysis of the cutting force, cutting temperature, tool life, tool wear, and chip morphology of the microgroove cutting tool and the original cutting tool was conducted. The main cutting force and temperature of the microgroove cutting tool were reduced by 12% and 12.

Forming process and evaluation of chip in machining of high-strength steel by an independent-developed microgroove turning tool.

Chip morphology is one of the evaluation indexes of cutting performance of cutting tools, and chip forming process has a direct and important influence on chip morphology. High-strength steel 40CrMnMo is one of typical oil country tubular goods (OCTG) and difficult-to-cut materials, and its chip morphology represents the machining quality of OCTG. The chip forming process of a new independent-developed microgroove turning tool for turning oil country tubular goods 40CrMnMo is researched, combining machining experiments with theoretical analysis.

The effect of microRNA-330 replacement on inhibition of growth and migration in renal cancer cells.

This study was conducted to scrutinize microRNA-330 (miR-330) role in growth, migration, and the expression of metastatic genes in renal cell carcinoma (RCC) in vitro. Following transfection of the cells with miR-330 mimic, cell proliferation using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, cell migration by wound healing assay, and apoptosis by flow cytometry were evaluated. Quantitative real-time PCR was conducted to assess expression levels of matrix metalloproteinase 2 (MMP2), MMP9, a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS), Kirsten rat sarcoma virus (K-Ras), cellular Myc (c-Myc), and C-X-C chemokine receptor type 4 (CXCR-4) as metastatic genes in the progression of RCC.