K Watanabe, S Okawa, O Miyakawa, S Nakano, N Shiokawa, M Kobayashi
{"title":"[陶瓷烧制过程中非贵金属-陶瓷界面的反应。](3)一种在烧制过程中形成大量氧化铬的商业合金。","authors":"K Watanabe, S Okawa, O Miyakawa, S Nakano, N Shiokawa, M Kobayashi","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>To examine the interface reaction between porcelain and a commercial Ni-Cr dental alloy (containing higher Cr and Mo) during porcelain firing, electron probe microanalyzer (EPMA) and X-ray diffraction have been used to characterize the interface which has emerged by means of selective dissolution of the alloy caused by a bromine-methanol solution. Much Cr oxide was formed at the early stage of firing, and remained in the reaction layer even if the holding time at 960 degrees C was up to 8 minutes. As a result, many Cr atoms diffused into the porcelain layer, most of which was found to form oxides through X-ray diffraction. Moreover, the porcelain layer nearest to the oxide layer was deduced to be modified seriously.</p>","PeriodicalId":77622,"journal":{"name":"Shika zairyo, kikai = Journal of the Japanese Society for Dental Materials and Devices","volume":"9 3","pages":"453-62"},"PeriodicalIF":0.0000,"publicationDate":"1990-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Reactions at the nonprecious metal-ceramic interface during porcelain firing. (3) A commercial alloy forming much Cr oxide during firing].\",\"authors\":\"K Watanabe, S Okawa, O Miyakawa, S Nakano, N Shiokawa, M Kobayashi\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>To examine the interface reaction between porcelain and a commercial Ni-Cr dental alloy (containing higher Cr and Mo) during porcelain firing, electron probe microanalyzer (EPMA) and X-ray diffraction have been used to characterize the interface which has emerged by means of selective dissolution of the alloy caused by a bromine-methanol solution. Much Cr oxide was formed at the early stage of firing, and remained in the reaction layer even if the holding time at 960 degrees C was up to 8 minutes. As a result, many Cr atoms diffused into the porcelain layer, most of which was found to form oxides through X-ray diffraction. Moreover, the porcelain layer nearest to the oxide layer was deduced to be modified seriously.</p>\",\"PeriodicalId\":77622,\"journal\":{\"name\":\"Shika zairyo, kikai = Journal of the Japanese Society for Dental Materials and Devices\",\"volume\":\"9 3\",\"pages\":\"453-62\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1990-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Shika zairyo, kikai = Journal of the Japanese Society for Dental Materials and Devices\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Shika zairyo, kikai = Journal of the Japanese Society for Dental Materials and Devices","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
[Reactions at the nonprecious metal-ceramic interface during porcelain firing. (3) A commercial alloy forming much Cr oxide during firing].
To examine the interface reaction between porcelain and a commercial Ni-Cr dental alloy (containing higher Cr and Mo) during porcelain firing, electron probe microanalyzer (EPMA) and X-ray diffraction have been used to characterize the interface which has emerged by means of selective dissolution of the alloy caused by a bromine-methanol solution. Much Cr oxide was formed at the early stage of firing, and remained in the reaction layer even if the holding time at 960 degrees C was up to 8 minutes. As a result, many Cr atoms diffused into the porcelain layer, most of which was found to form oxides through X-ray diffraction. Moreover, the porcelain layer nearest to the oxide layer was deduced to be modified seriously.