with several cylinders for ausgeruestete press for injection moulding: a thermoplastic mass

• 1. 陶瓷粉末-和/或金属粉末-冲压工具、陶瓷粉末-和/或金属粉末-压力机、带有这样的冲压工具的模块化系统、用于组装和用于运行陶瓷粉末-和/或金属粉末-冲压工具或压力机的方法 [P] . 中国专利： CN103384594B . 2016.05.04
• 2. 陶瓷粉末-和/或金属粉末-冲压工具、陶瓷粉末-和/或金属粉末-压力机、带有这样的冲压工具的模块化系统、用于组装和用于运行陶瓷粉末-和/或金属粉末-冲压工具或压力机的方法 [P] . 中国专利： CN103384594A . 2013-11-06
• 3. Toy-brick moulding unit - for mass prodn from thermoplastics combining injection and press moulding units for producing coupling [P] . 德国专利： DE2202061A1 . 1973-07-26

  机译： 玩具砖成型单元-用于热塑性塑料的批量生产，结合了注射成型和冲压成型单元以生产联轴器

• 4. schliesseinheit for hydraulic press, preferably for press for injection moulding: a thermoplastic mass [P] . 德国专利： DE000001627830A . 1971-02-25

  机译： schliesseinheit用于液压机，优选用于注塑机：热塑性物料

• 5. Press cylinder of an injection moulding machine for thermoplastic materials [P] . 英国专利： GB900673A . 1962-07-11

  机译： 用于热塑性材料的注塑机的压缸

• 1. Effect of intramuscular calcitonin injection combined with intra-articular ozone injection on the expression of the IL family and MMPs family of knee osteoarthritis [J] . Liang Luo 海南医科大学学报（英文版） . 2017,第019期
• 2. Effect of intramuscular calcitonin injection combined with intra-articular ozone injection on the expression of the IL family and MMPs family of knee osteoarthritis [J] . Liang Luo 海南医科大学学报(英文版) . 2017,第019期
• 3. In-line compounding of direct long fibre thermoplastics: injection versus compression moulding [C] . M. McLeod, E. Baril, J.-F. Hetu, Joint Canada-Japan workshop on composites . 2011
• 4. Cavity temperature measurement and control in thermoplastics injection moulding. [D] . Manero-Brito, Federico Jose. 1997
• 5. Case Report: Under pressure: progressively enlarging facial mass following high-pressure paint injection injury [O] . Jameel Mushtaq, Abigail Walker, Ben Hunter 2016
• 6. INFLUENCE OF NANOFIBER LOADING AND MOULDING CONDITIONS ON THE JOINING STRENGTH OF THERMOPLASTIC COMPOSITES FABRICATED BY INJECTION OVER-MOULDING PROCESS [O] . KOKI MATSUMOTO, TUKASA NAGASAKA, KENICHI TAKEMURA, 2020

• 1. Elimination of Fuel Pressure Fluctuation and Multi-injection Fuel Mass Deviation of High Pressure Common-rail Fuel Injection System [J] . LI Pimao ,ZHANG Youtong ,LI Tieshuan . 中国机械工程学报 . 2015,第002期
• 2. Numerical Analysis of the Compression Ratio’s Influence, the Nature of the Fuel and the Injection Feed on the Cylinder Pressure [J] . Daniel Roméo Kamta Legue ,Marcel Obounou ,Ekobena Fouda Henri . 能源与动力工程（英文） . 2019,第6期
• 3. 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
• 4. 奥钢联钢铁公司用于AHSS钢生产的新串列式冷轧机的投产结果 [C] . Gregor Nopp ,Gerlinde Djumlija ,Roland Kellermayr . 第五届中国国际钢铁大会 . 2008
• 5. 选择性雌激素受体调节剂--奥培米芬用于治疗绝经后外阴及阴道萎缩的Meta分析 [A] . 颜溪婷 . 2018