METHOD OF DETERMINING PHOSPHORUS CONTENT IN STABILISING AGENT USED IN PROCESSING OF PLASRICS, ESPECIALLY OF POLIVINYL CHLORIDE

• 1. 一种聚氯乙烯塑料加工中掺杂轻稀土无毒热稳定剂的复配方法 [P] . 中国专利： CN101831120B . 2012.05.23
• 2. 一种聚氯乙烯塑料加工中掺杂轻稀土无毒热稳定剂的复配方法 [P] . 中国专利： CN101831120A . 2010-09-15
• 3. METHOD OF DETERMINING PHOSPHORUS CONTENT IN STABILISING AGENT USED IN PROCESSING OF PLASRICS, ESPECIALLY OF POLIVINYL CHLORIDE [P] . PL172314B1 . 1997-09-30

  机译： 测定塑料加工中稳定剂中磷含量的方法，尤其是聚氯乙烯

• 4. METHOD FOR DETERMINING AND CONTROLLING OR REGULATING THE PHOSPHORUS CONTENT IN A METALLIC MELT DURING THE REFINING PROCESS OF A METALLIC MELT IN A METALLURGICAL REACTOR [P] . WO2021116324A1 . 2021-06-17

  机译： 在冶金反应器中金属熔体的精炼过程中确定和控制金属熔体中磷含量的方法

• 5. Method for deactivating a Chain Transfer Agent Soluble in Water content in the aqueous filtrate of a polymerization process of vinyl enemulsion oil in water or in suspension acuosA, and processes for the polymerization of Vinyl Chloride [P] . AR012604A1 . 2000-11-08

  机译： 使乙烯基乳化油在水中或在悬浮液a中的聚合过程的水性滤液中的水含量可溶的链转移剂失活的方法，以及氯乙烯的聚合过程

• 1. Establishment of the Determination Methods of Total Anthraquinone Content in Different Processed Products of Rhubarb [J] . Jiangcun WEI, Xiumei MA, Chunli TANG, 药用植物：英文版 . 2021,第001期
• 2. Effect of Different Processing Methods on Content ofβ-Asarone in the Zhuang Medicine Rhizoma Acori Tatarinowii [J] . Peng YANG, Jiangcun WEI, Wen ZHONG, 药用植物：英文版 . 2020,第005期
• 3. Effects of Cooking and Processing Methods on Nitrate Content in Leafy Vegetables [J] . Huihe LI 农业生物技术：英文版 . 2019,第003期
• 4. Effect of Several Common Processing Methods on Content Changes of Resistant Starch and Main Nutrients in ‘Luotian Chestnut＇ [J] . Linling LI, Bingjie HUANG, Hua CHENG, 农业生物技术：英文版 . 2018,第005期
• 5. Methods for Determining Nitrogen, Phosphorus, and Potassium (NPK) Nutrient Content Using Scale-Invariant Feature Transform (SIFT) [C] . Raden Sumiharto, Ristya Ginanjar Putra, Samuel Demetouw International Conference on Information and Communication Technology . 2020
• 6. Hafnium solvent extraction from chloride solutions using organophosphorus reagents (Cyanex 923, 925). [D] . El-Ammouri, Elias G. 1994
• 7. Contribution of Food Additives to Sodium and Phosphorus Content of Diets Rich in Processed Foods [O] . Anna Carrigan, Andrew Klinger, Suzanne S. Choquette, -1
• 8. The Effect of Carcinogenic Agents on the Phosphorus Content of Hair Bulbs and Epidermis The Effect of X-Rays on the Phosphorus Content of the Hair Bulbs1 [O] . Holló Z.M., Zlatarov S. 1956
• 9. Alternative Potentiometric Method for Determining Chloride Content in Concrete Samples from Reinforced Concrete Bridges [R] . Clemena, G. G., Apusen, C. M. 2002

• 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. ICP-AES法测定碳钢中硅锰磷铬镍铜含量与标准方法的偏离评估 [C] . 周秋红 ,翟晓东 . 中国金属学会第十三届分析测试学术年会——冶金及材料分析测试学术报告会 . 2006
• 3. 原子吸收光谱法测定人发中微量元素的方法研究及自闭症患儿头发中微量元素含量的测定与比较 [A] . 解蕾 . 2010