{"id":47133,"date":"2020-03-01T22:20:11","date_gmt":"2020-03-01T22:20:11","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/estudio-en-el-ultravioleta-de-las-posibilidades-analiticas-de-las-reacciones-del-fenol-con-interhalogenos-y-otros-reactivos\/"},"modified":"2020-03-01T22:20:11","modified_gmt":"2020-03-01T22:20:11","slug":"estudio-en-el-ultravioleta-de-las-posibilidades-analiticas-de-las-reacciones-del-fenol-con-interhalogenos-y-otros-reactivos","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/estudio-en-el-ultravioleta-de-las-posibilidades-analiticas-de-las-reacciones-del-fenol-con-interhalogenos-y-otros-reactivos\/","title":{"rendered":"Estudio en el ultravioleta de las posibilidades analiticas de las reacciones del fenol con interhalogenos y otros reactivos."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Guillermina Font Perez <\/strong><\/h2>\n<p>Para la obtencion de un producto de reaccion mas cuantitativamente extraible en disolventes poco polares y de coeficiente de absortividad molar mas elevado en el ultravioleta que el del fenol  se llevaron a cabo ensayos empleando como reactivos  bromo  n-bromosuccinimida monocloruro de iodo y monobromuro de iodo entre otros.  para la eliminacion del exceso de reactivo se ensayaron diversos reductores y como disolvente para la extraccion ciclohexano en base a experiencias anteriores. El monobromuro de iodo es el reactivo que mejores posibilidades analiticas ofrece para la determinacion de fenol por la alta sensibilidad de su reaccion. De los reductores ensayados sulfato de hidrazina era el mas idoneo para la eliminacion del exceso de reactivo. La reaccion tiene lugar a ph acido siendo la concentracion optima de acido clorhidrico de 0 02 m a 0 05 m. La ley de beer se cumple aceptablemente entre 8 y 160 ppb.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Estudio en el ultravioleta de las posibilidades analiticas de las reacciones del fenol con interhalogenos y otros reactivos.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Estudio en el ultravioleta de las posibilidades analiticas de las reacciones del fenol con interhalogenos y otros reactivos. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Guillermina Font Perez <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Universitat de val\u00e9ncia (estudi general)<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1980<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Francisco Bosch Serrat<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Francisco Bosch Reig <\/li>\n<li>Francisco Salinas L\u00f3pez (vocal)<\/li>\n<li>Jos\u00e9 Vi\u00f1a Giner (vocal)<\/li>\n<li>Francisco Bosch Serrat (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Guillermina Font Perez Para la obtencion de un producto de reaccion mas cuantitativamente extraible en disolventes poco [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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