Method and apparatus for pasteurizing and bottling of beer and other carbonic acid speeds of drinking water standards containing flue sig

• 1. 制备含有大麦浓缩物和啤酒花提取物的未发酵碳酸饮料的方法及由其制备的未发酵碳酸饮料 [P] . 中国专利： CN1903082A . 2007-01-31
• 2. 用于制造含有啤酒花叶或啤酒花茎的发酵饮料的方法 [P] . 中国专利： CN111032847A . 2020-04-17
• 3. A method for the sterile bottling of beer and other carbonic acid speeds of drinking water standards containing flue sig [P] . 德国专利： DE1432368A1 . 1968-12-19

  机译： 一种对含有烟道信号的啤酒和其他碳酸标准饮用水进行无菌装瓶的方法

• 4. A method and device for the sterile bottling of beer and other carbonic acid speeds of drinking water standards containing flue sig [P] . 德国专利： DE1000709B . 1957-01-10

  机译： 用于对含有烟道信号的啤酒和其他碳酸标准饮用水进行无菌装瓶的方法和装置

• 5. seduce and apparatus for bottling of drinking water standards signal flue, in particular beer, in bottles and the like. [P] . 德国专利： DE1121955B . 1962-01-11

  机译： 用于将饮用水标准装瓶的勾引物和设备，用于在瓶等中发出烟道，特别是啤酒。

• 1. Rapid detection of coliforms in drinking water of Arak city using multiplex PCR method in comparison with the standard method of culture (Most Probably Number) [J] . Dehghan fatemeh, Najarian Negin, Kasravi Alii Reza, 亚太热带生物医学杂志（英文版） . 2014,第005期
• 2. Rapid detection of coliforms in drinking water of Arak city using multiplex PCR method in comparison with the standard method of culture(Most probably Number) [J] . Dehghan fatemeh, Zolfaghari Mohammad Reza, Arjomandzadegan Mohammad, 亚太热带生物医学杂志：英文版 . 2014,第005期
• 3. Parasitic Contamination of Drinking Water and Egyptian Standards for Parasites in Drinking Water [J] . Wafaa M. Hikal 生态学期刊（英文） . 2020,第001期
• 4. Method Development in Quantification of Quantification of Iodoacetic Iodoacetic Acids Acids Drinking Water Using in Drinking Water Using GC/EIGC/EI-MS/MS MS/MS [C] . Hannah K. Liberatore, Amy A. Cuthbertson, Susan D. Richardson ASMS Conference on Mass Spectrometry and Allied Topics . 2016
• 5. Particle stabilized water in liquid carbon dioxide and liquid carbon dioxide in water emulsions for ocean and geologic storage: Apparatus and methods [D] . Swett, Peter A. 2008
• 6. Electrolytic hydrogen-generating bottle supplies drinking water with free/combined chlorine and ozone repressed within safety standard under hydrogen-rich conditions [O] . Toshihisa Hatae, Nobuhiko Miwa 2021
• 7. Determination of bromate and chlorinated haloacetic acids in bottled drinking water with chromatographic methods [O] . Liu YJ, Mou S 2004
• 8. Study of Home Drinking Water Treatment Units Containing Activated Carbon for Organics Reduction: Interim Phase 2 Report to Criteria and Standards Division, Office of Drinking Water [R] . 1980

• 1. Treatment of Radon Rich Bottled Water by Granular Activated Carbon Adsorption Method [J] . Saddig D. Jastaniah ,Bassam Z. Shakhreet ,Hanan Y. Abbas . 生物物理学期刊（英文） . 2014,第1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. 基于声音信号的啤酒瓶密封性检测方法 [C] . LI Hong-yu ,李洪宇 ,GONG Xiao-dong . 2013年全国第九届精密工程学术研讨会 . 2013