process for the manufacture of injection molding, press, study and sinterformen with a galvanoplastisch generated formkörper

• 1. 一种用放电等离子烧结研究镓掺杂氧化锌陶瓷最佳烧结工艺的方法 [P] . 中国专利： CN105669182A . 2016-06-15
• 2. 利用微型烧结试验研究铁矿石烧结性能的方法 [P] . 中国专利： CN102213659A . 2011-10-12
• 3. process for the manufacture of injection molding, press, praege and sinterformen [P] . 德国专利： DE000001208603A . 1966-01-05

  机译： 注塑，冲压，精炼和烧结的制造方法

• 4. Device for manufacturing fiber-reinforced plastic components by injection process, has closing device locking upper part in molding position with respect to lower part, where pressures are retained by closing device during injection process [P] . 德国专利： DE102012022633A1 . 2014-05-22

  机译： 通过注射过程制造纤维增强塑料组件的装置，其关闭装置将上部锁定在相对于下部的模制位置，在注射过程中通过关闭装置保持压力

• 5. Useful for the manufacture of structural components by injection molding, pressure molding or by depositional process. [P] . ES2304047T3 . 2008-09-01

  机译： 可用于通过注射成型，压力成型或沉积工艺制造结构部件。

• 1. RHEOLOGICAL STUDIES ON REACTION INJECTION MOLDING PROCESS WITH A SLIT MEASURING SYSTEM [J] . 江体乾, 李春洲, 方波, 中国化学工程学报：英文版 . 1996,第002期
• 2. Effect of annealing processing on microstructure and properties of Ti-6Al-4V alloy by powder injection molding [J] . 郭世柏, 曲选辉, 向军淮, 中国有色金属学会会刊：英文版 . 2006,第B02期
• 3. New approach to develop a 3D non-isothermal computational framework for injection molding process based on level set method [J] . Xin Zhuang, Jie Ouyang, Chuntao Jiang, 中国化学工程学报（英文版） . 2016,第007期
• 4. An Experimental Study on the Dimensional Characteristics of 7 inch Light Guide Plate Manufactured by Injection/Compression Molding with Rapid Heating of a Mold [C] . Inki Min, Seokkwan Hong, Yongju Lee, Annual technical conference of the Society of Plastics Engineers;ANTEC 2012 . 2012
• 5. A study of the effects of various injection molding processing conditions on nano-scale replication for high-rate manufacturing. [D] . Alabran, Michael W. 2006
• 6. Study of an Online Monitoring Adaptive System for an Injection Molding Process Based on a Nozzle Pressure Curve [O] . Jia-Chen Fan-Jiang, Chi-Wei Su, Guan-Yan Liou, 2021
• 7. A comparative study between melt granulation/compression and hot melt extrusion/injection molding for the manufacturing of oral sustained release thermoplastic polyurethane matrices [O] . G. Verstraete, P. Mertens, W. Grymonpré, 2016

• 1. Gaussian Process Modeling of Process Optimization and Parameter Correlation for Injection Molding [J] . Xiaoping Liao ,Wei Xia ,Fengying Long . 材料科学与工程：中英文版 . 2010,第010期
• 2. 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
• 3. 高超冲压性能计算的疑难杂症及其诊治(对高超冲压推进性能评估方法建立检验标准和行业规范的思考) [C] . 叶中元 . 第四届冲压发动机学术会议 . 2013
• 4. 超高分子量聚乙烯柱塞冲压注塑成型过程的研究 [A] . 张学阳 . 2011