排序方式: 共有15条查询结果,搜索用时 46 毫秒
1.
Mona Akbar Muhammad Farooq Saleem Khan Ling Qian Hui Wang 《Frontiers of Environmental Science & Engineering》2020,14(6):98
2.
3.
4.
Acrylamide (AA) is a potential human carcinogen, genotoxicant, and neurotoxicant. Thus, the aim of this study was to examine the ability of mercapto flavor compounds to remove AA released from consumer packaging into food products. Four mercapto flavor compounds including 1,2-ethanedithiol, 1-butanethiol, 2-methyl-3-furanthiol, and 2-furanmethanethiol were employed to extract AA in model system using high temperature and low humidity. Our study showed that mercaptans were effective in eliminating AA in our model system. In order to remove 0.2 μmol AA, the optimal conditions in the reaction system were mercaptan flavor chemicals at 5 μmol, temperature 180 °C, and reaction time 25 min. In the presence of a higher pH, the greater was the amount of AA eliminated. Evidence indicates that employment of mercapto flavor chemicals under certain temperature and pH conditions is a reliable method to remove any unwanted AA from food products. 相似文献
5.
武耀锋 《再生资源与循环经济》2014,(7):32-35
研究pH值、温度、反应物比率对生成三元接枝共聚物的影响,三元接枝共聚物接枝率与接枝效率的计算,以及三元接枝共聚物对铜离子的吸附效果.实验与计算结果表明:生成三元接枝共聚物的最佳反应条件为引发剂(NH4)2S2O8用量6 mmol/L,反应温度50℃,壳聚糖(CTS):丙烯酰胺(AM):丙烯酸(AA)=1∶2.7∶0.3,pH值=7,反应时间5h;在相同条件下,三元接枝共聚物对铜离子去除效果比壳聚糖有了明显的改善,对铜离子去除率最高达到90.06%,比壳聚糖对铜离子的去除率高49.72%. 相似文献
6.
以粘度和产率为表征,研究不同引发剂、温度、单体丙烯酰胺用量、反应时间对木质素磺酸钠与丙烯酰胺接枝共聚反应的影响,并对木质素磺酸钠接枝共聚条件进行优化。结论:K2S2O8引发的接枝反应产物具有较大粘度和产率,而(NH4)2S2O8、Na2S2O3·5H2O引发体系得到共聚物粘度和产率相对较小,所以该研究采用K2S2O8作为引发剂;通过三因素三水平的正交试验得出对共聚物的产率与粘度的影响顺序为单体丙烯酰胺用量大于反应温度大于反应时间;接枝共聚反应的优化条件是K2S2O8引发剂浓度6×10-3mol/L,反应温度为45℃,反应时间为4 h,单体丙烯酰胺与木钠比为4:1,蒸馏水与木钠比5:1。 相似文献
7.
8.
Yasemin Aydin 《毒物与环境化学》2018,100(2):247-257
Acrylamide, which is commonly used in various industries, may also form in food products cooked in high temperatures. Glycidamide, the ultimate genotoxic metabolite of acrylamide, is generated within cells through CYP4502E1-mediated epoxidation. Recent studies have shown that acrylamide and/or glycidamide may cause infertility by disrupting spermatogenesis, decreasing germ cell production and sperm fertilization ability due to their toxic effects on the male reproductive system. This study aimed to determine some direct effects of acrylamide and glycidamide on antioxidant defenses and on steroidogenic enzymes of Leydig and Sertoli cells. For this purpose, mouse Leydig and Sertoli cells were exposed to acrylamide (0.01 or 1?mmol/L) or to glycidamide (0.001 or 0.5?mmol/L) for 24?h. Following the exposure, antioxidant enzyme activities (catalase, superoxide dismutase, glutathione peroxidase and γ-glutamyl transpeptidase), cellular antioxidant levels (glutathione) and steroidogenic enzyme activities (3β-hydroxysteroid dehydrogenase and 17β-hydroxysteroid dehydrogenase) were calculated. It was shown that acrylamide and glycidamide may cause inhibition of antioxidant and steroidogenic enzymes in Leydig and Sertoli cells. In conclusion, acrylamide and glycidamide may alter testicular function, thereby disrupting male reproduction. 相似文献
9.
Marta Batoryna Magdalena Semla-Kurzawa Bartłomiej Zyśk Bartosz Bojarski Grzegorz Formicki 《Journal of environmental science and health. Part. B》2013,48(9):745-751
The aim of the experiment was to study the influence of acrylamide (ACR) on major antioxidants in the lungs of Swiss mice. The experiment was conducted on male mice that were 8 weeks old. The mice were exposed to ACR at a single dose of 26 µg per animal, which was administered orally. Mice were anesthetized 3, 24, and 48 h after the ACR gavage. Next, histopathological and biochemical analyses of GSH concentration and the activities of SOD, GPx, and CAT were performed in the lungs. Animals exposed to ACR showed demonstrated symptoms of inflammation in lungs, hypertrophy of bronchiolar epithelium, and hyperplasia of alveolar epithelium. GSH concentration was significantly decreased 3 h after ACR gavage, which was followed by a significant increase 48 h after ACR gavage. Similarly, SOD and GPx demonstrated decreased activities 3 h after exposure to ACR, followed by increased activities 48 h after exposure to ACR. CAT activity was significantly increased 24 and 48 h after exposure to ACR. We conclude that oral exposure of mice to ACR results in alterations of lung microstructure, accompanied by the symptoms of redox imbalance. 相似文献
10.