Method of manufacture of chains and apparatus for injection moulding permettantla implementation of the process

• 1. 机具用的链条、用于制造链条用的销栓的方法和用于制造链条用的传动器件的方法 [P] . 中国专利： CN104942888B . 2020.03.06
• 2. 机具用的链条、用于制造链条用的销栓的方法和用于制造链条用的传动器件的方法 [P] . 中国专利： CN104942888A . 2015-09-30
• 3. AN INJECTION MOULDING APPARATUS, AND AN IMPLEMENT FOR AN INJECTION MOULDING APPARATUS [P] . 世界知识产权组织专利： WO2012028674A1 . 2012-03-08

  机译： 注射模制设备以及注射模制设备的实现

• 4. An injection moulding apparatus, and an implement for an injection moulding apparatus [P] . 欧洲知识产权局专利： EP2425953A1 . 2012-03-07

  机译： 注射成型设备以及用于注射成型设备的工具

• 5. Method of manufacturing footwear articles such as injection-moulding as well as the footwear articles obtained by implementing the process [P] . 法国专利： FR2555025B3 . 1986-06-13

  机译： 制造鞋类物品的方法，例如注射成型以及通过实施该方法获得的鞋类物品

• 1. Optimization of Injection Moulding Process Parameters for Manufacturing Plastic Components (PBT) Using Taguchi Method (TM) [C] . Rajendra Khavekar, Hari Vasudevan, Gosar Vimal International Conference on Recent Advances in Materials and Manufacturing Technologies . 2019
• 2. Development of an injection and moulding subsystem for a microcellular plastic manufacturing process. [D] . Ozolins, Christopher. 2001
• 3. Investigation of a Short Carbon Fibre-Reinforced Polyamide and Comparison of Two Manufacturing Processes: Fused Deposition Modelling (FDM) and Polymer Injection Moulding (PIM) [O] . Elena Verdejo de Toro, Juana Coello Sobrino, Alberto Martínez Martínez, 2020
• 4. Injection moulding process: CFD evaluation on the orientation of polymeric chains for manufacturing heart valves. [O] . De Gaetano, F, Serrani, M, Brubert, J, 2015
• 5. Metal Injection Moulding: A Near Net Shape Fabrication Method for the Manufacture of Turbine Engine Component [R] . Julien, B., Despres, M. 2006

• 1. High-quality manufacturing method of complicated castings based on multi-material hybrid moulding process [J] . Li-min Liu ,Zhong-de Shan ,Feng Liu . 中国铸造 . 2018,第005期
• 2. Strain Rate Effects on Tensile Properties of HDPE-PP Composite Prepared by Extrusion and Injection Moulding Method [J] . Harekrushna Sutar ,Himanshu Sekhar Maharana ,Chiranjit Dutta . 材料科学与应用期刊（英文） . 2019,第3期
• 3. Analysis of the Manufactured Tolerances with the Three-Dimensional Method of Angular Chains of Dimensions Applied to a Cylinder Head of Car Engine [J] . Aida Mezghani ,Alain Bellacicco ,Jamel Louati . 工程（英文）（1947-3931） . 2010,第10期
• 4. BACKGROUND： Vibrio vulnifi cus inside the body could activate the NF-!B signaling pathwayand initiate the inflammatory cascade. The lung is one of the earliest organs affected by sepsisassociated with acute lung injury. High mobility group protein B1 （HMGB1） is an important late-actingpro-infl ammatory cytokine involving in the pathophysiology of sepsis. It is also involved in the injuryprocess in the lung, liver and intestine. There has been no report on the involvement of HMGB1 inVibrio vulnifi cus sepsis-induced lung injury.METHODS： Sixty rats were randomly divided into a normal control group （group A, n=10） anda Vibrio vulnificus sepsis group （group B, n=50）. Sepsis was induced in the rats by subcutaneousinjection of Vibrio vulnificus （concentration 6×108 cfu/mL, volume 0.1 mL/100g）） into the left lowerlimbs. The rats in group B were sacrifi ced separately 1, 6, 12, 24, and 48 hours after the infection.Their lungs were stored as specimens, lung water content was measured, and lung pathology wasobserved under a light microscope. The expressions of the HMGB1 gene and protein in the lungswere detected by RT-PCR and Western blot. Data were analyzed with one-way analysis of variance（ANOVA） and the LSD method for pair-wise comparison between the two groups. P〈0.05 wasconsidered statistically signifi cant.RESULTS： Compared to group A （0.652±0.177）, HMGB1 mRNA expression in the lungs ofgroup B was signifi cantly higher at 0 hour （1.161±0.358, P=0.013）, 24 hours （1.679±0.235, P=0.000）,and 48 hours （1.258±0.274, P=0.004） （P〈0.05）, and peaked at 24 hours. Compared to group A（0.594±0.190）, HMGB1 protein expression at 6 hours （1.408±0.567, P=0.026） after infection wassignificantly increased （P〈0. 05）, and peaked at 24 hours （2.415±1.064, P=0.000） after infection.Compared to group A （0.699±0.054）, lung water content was significantly increased at 6 hours（0.759±0.030, P=0.001）,12 hours （0.767±0.023, P=0.000）, 24 hours （0.771±0.043, P=0.000） and 48hours （0.789±0.137, P=0.000） after infection （P〈0.05）. Compared to group A, pathological changesat 12 hours in group B indicate marked pulmonary vascular congestion, interstitial edema andinfl ammatory infi ltration. Alveolar cavity collapse and boundaries of the alveolar septum could not beclearly identifi ed.CONCLUSION： Vibrio vulnifi cus sepsis can lead to injury in rat lungs, and increased HMGB1expression in lung tissue may be one of the mechanisms for injury from Vibrio vulnifi cus sepsis. [J] . Qiao-meng Qiu ,Zhong-wang Li ,Lu-ming Tang . 世界急诊医学杂志(英文) . 2011,第4期
• 5. Study on the Measurement Systems and Implementation Methods of Strategic Distributor's Core Competence Under Supply Chain Management [J] . YANG Jianhua Department of Business AdministrationShandong Institute of Business and TechnologyYantai 264005China . 武汉理工大学学报 . 2006,第S3期
• 6. GERDC:用于多代设备成熟数据中心的绿色设备更新方法 [C] . PAN Yue-Dou ,潘月斗 ,WANG Hong-Rui . 第十届中国计算机图形学大会暨第十八届全国计算机辅助设计与图形学会会议 . 2014
• 7. 用于微纳注塑成型的镍模板的制造 [A] . 张晓霞 . 2020