{"title":"2铁皮船建造中材料的形状、尺寸与重量的关系","authors":"E. Reed","doi":"10.1098/rspl.1867.0060","DOIUrl":null,"url":null,"abstract":"this nitrile is converted into an acid which M. Merz describes under the name of naphthaline-carboxylic acid. The opinion expressed by this chemist, that his acid might be identical with the one observed by myself, I am inclined to adopt, although there are still some few discrepancies in our observations to be elucidated. M. Merz states that the fusing-point of his acid is at 140°, whilst the acid examined by myself fuses at 160°. In order to remove, if possible, this discrepancy, I have, since I saw M. Merz’s paper, again and repeatedly taken the fusing-point of menaphthoxylic acid, but always with the same result. Possibly the fusingpoint of the acid prepared by means of a sulphonaphthylate may be found somewhat higher when the compound is carefully purified by repeated crystallization from alcohol. 306 Mr. Reed on the Form, Dimensions, [Mar. 19}","PeriodicalId":20661,"journal":{"name":"Proceedings of the Royal Society of London","volume":"1 1","pages":"306 - 310"},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1098/rspl.1867.0060","citationCount":"0","resultStr":"{\"title\":\"II. On the relation of form and dimensions to weight of material in the construction of iron-clad ships\",\"authors\":\"E. Reed\",\"doi\":\"10.1098/rspl.1867.0060\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"this nitrile is converted into an acid which M. Merz describes under the name of naphthaline-carboxylic acid. The opinion expressed by this chemist, that his acid might be identical with the one observed by myself, I am inclined to adopt, although there are still some few discrepancies in our observations to be elucidated. M. Merz states that the fusing-point of his acid is at 140°, whilst the acid examined by myself fuses at 160°. In order to remove, if possible, this discrepancy, I have, since I saw M. Merz’s paper, again and repeatedly taken the fusing-point of menaphthoxylic acid, but always with the same result. Possibly the fusingpoint of the acid prepared by means of a sulphonaphthylate may be found somewhat higher when the compound is carefully purified by repeated crystallization from alcohol. 306 Mr. Reed on the Form, Dimensions, [Mar. 19}\",\"PeriodicalId\":20661,\"journal\":{\"name\":\"Proceedings of the Royal Society of London\",\"volume\":\"1 1\",\"pages\":\"306 - 310\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1098/rspl.1867.0060\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Proceedings of the Royal Society of London\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1098/rspl.1867.0060\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the Royal Society of London","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1098/rspl.1867.0060","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
II. On the relation of form and dimensions to weight of material in the construction of iron-clad ships
this nitrile is converted into an acid which M. Merz describes under the name of naphthaline-carboxylic acid. The opinion expressed by this chemist, that his acid might be identical with the one observed by myself, I am inclined to adopt, although there are still some few discrepancies in our observations to be elucidated. M. Merz states that the fusing-point of his acid is at 140°, whilst the acid examined by myself fuses at 160°. In order to remove, if possible, this discrepancy, I have, since I saw M. Merz’s paper, again and repeatedly taken the fusing-point of menaphthoxylic acid, but always with the same result. Possibly the fusingpoint of the acid prepared by means of a sulphonaphthylate may be found somewhat higher when the compound is carefully purified by repeated crystallization from alcohol. 306 Mr. Reed on the Form, Dimensions, [Mar. 19}