A method for the production and processing a lagerfaehigen polymerizable press mass for the preparation of any desired form body, in particular of plastic plates

• 1. 生产发泡塑料材料的方法,特别是基于PVC的聚合物泡沫体和用于实施所述方法的聚合物共混物的制剂 [P] . 中国专利： CN103025805B . 2014.06.25
• 2. 生产发泡塑料材料的方法,特别是基于PVC的聚合物泡沫体和用于实施所述方法的聚合物共混物的制剂 [P] . 中国专利： CN103025805A . 2013-04-03
• 3. A method for the production and processing a lagerfaehigen polymerizable press mass for the preparation of any desired form body, in particular of plastic plates [P] . 德国专利： DE1569339B2 . 1974-10-17

  机译： 一种用于生产和加工可用于生产任何期望的成型体，特别是塑料板的可贮藏啤酒的可聚合压块的方法

• 4. A method for the production and processing a lagerfaehigen polymerizable press mass for the preparation of any desired form body, in particular of plastic plates [P] . 德国专利： DE1569339A1 . 1969-08-21

  机译： 一种用于生产和加工可用于生产任何期望的成型体，特别是塑料板的可贮藏啤酒的可聚合压块的方法

• 5. A method for the production of the form bodies from a plastic, polymerizable press mass [P] . 德国专利： DE1059174B . 1959-06-11

  机译： 一种由可聚合的塑料压制成型体的方法

• 1. “Giant pressure shadow” structure and ore-finding method of tectonic stress field in the Tongchang Cu-Au polymetallic orefield,Shaanxi,China：Ⅱ.Dynamics of tectonic ore-forming processes and prognosis of concealed ores [J] . HAN Runsheng, WANG Lei, MA Deyun, 中国地球化学学报：英文版 . 2010,第004期
• 2. Decreased Gastric Body Mucosa Obestatin Expression in Abdominal Obesity Patients With Normal Body Mass Index [J] . GAO Xin Yuan, KUANG Hong Yu, LIU Xiao Min, 生物医学与环境科学（英文版） . 2014,第005期
• 3. Process Control of Forming the Surface Quality Parameters of Parts According to a Desired Law by Methods of Surface Plastic Deformation [C] . Nagorkin M. N., Fedorov V. P., Kovalyova E. V. International Conference on Aviamechanical Engineering and Transport . 2019
• 4. Comparison of two loading surface preparation methods on rat vertebral bodies for compression testing [D] . Schumacher, Yvonne. 2013
• 5. Identification of Anaerobic Bacteria by Bruker Biotyper Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry with On-Plate Formic Acid Preparation [O] . Bryan H. Schmitt, Scott A. Cunningham, Aaron L. Dailey, 2013
• 6. BACKGROUND TO THE ARRANGEMENT OF AUTOMATING AND VOLVOUS PROCESSES IN THE FORM-FORMING MACHINES WHEN TREATING THE PREPARATIONS AND DETAILS BY THE PLASTIC DEFORMATION METHOD [O] . A.D. Uchitel, Yu.A. Malinovsky, A.N. Panchenko, 2018

• 1. 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
• 2. Processing of AM60 magnesium alloy by hydrostatic cyclic expansion extrusion at elevated temperature as a new severe plastic deformation method [J] . Farshad Samadpour ,Ghader Faraji ,Armin Siahsarani . 矿物冶金与材料学报：英文版 . 2020,第5期
• 3. Effects of preparation methods on the performance of Cu-Mo-Fe-O_x in the hydrogen production from water [J] . Si Chen ,Wei Chu ,Xu Liu . 天然气化学杂志：英文版 . 2011,第5期
• 4. 啤酒生产技术的突破和革新——探讨一种新型环保和绿色的啤酒生产技术 [C] . 陈明 . “食品加工与安全”学术研讨会暨2010年广东省食品学会年会 . 2010
• 5. 用于啤酒生产线上验瓶机监控系统 [A] . 查进 . 2009