{"id":9599,"date":"2022-04-11T04:48:22","date_gmt":"2022-04-10T20:48:22","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599"},"modified":"2022-04-11T04:48:22","modified_gmt":"2022-04-10T20:48:22","slug":"awesome-and-easy-science-experiments-about-25956-17-6","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599","title":{"rendered":"Awesome and Easy Science Experiments about 25956-17-6"},"content":{"rendered":"<p><a href=\"https:\/\/www.ambeed.com\/products\/25956-17-6.html\">HPLC of Formula: 25956-17-6<\/a>. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Performance evaluation of photolytic and electrochemical oxidation processes for enhanced degradation of food dyes laden wastewater. Author is Sartaj, Seema; Ali, Nisar; Khan, Adnan; Malik, Sumeet; Bilal, Muhammad; Khan, Menhad; Ali, Nauman; Hussain, Sajjad; Khan, Hammad; Khan, Sabir.<\/p>\n<p>Wastewater containing dyes is considered as the top-priority pollutant when discharged into the environment. Herein, we report for the applicability of 254 nm UV light and electrochem. process using a titanium ruthenium oxide anode for the degradation of Allura red and erythrosine dyes. During the photolytic process, 95% of Allura red dye (50 ppm) was removed after 1 h at pH 12 and 35\u00b0C, whereas 90% color removal of erythrosine dye (50 ppm) was achieved after 6 h of treatment at pH 6.0 and 30\u00b0C. On the other hand, 99.60% of Allura red dye (200 ppm) was removed within 5 min by the electrochem. process applying a c.d. (5 mA cm-2) at pH 5.0 and 0.1 mol L-1 sodium chloride (NaCl) electrolytic medium. Similarly, 99.61% of erythrosine dye (50 ppm) degradation was achieved after 10 min at a c.d. of 8 mA cm-2, pH 6.0, and 0.1 mol L-1 of NaCl electrolyte. The min. energy consumption value for Allura red and erythrosine dyes (0.196 and 0.941 kWh m-3, resp.) was calculated at optimum current densities of 5 and 8 mA cm-2. The results demonstrated that the electrochem. process is more efficient at removing dyes in a shorter time than the photolytic process since it generates powerful oxidants like the chlorine mol., hypochlorous acid, and hypochlorite on the surface of the anode and initiates a chain reaction to oxidize the dyes mols.<\/p>\n<p>As far as I know, this compound(25956-17-6)<a href=\"https:\/\/www.ambeed.com\/products\/25956-17-6.html\">HPLC of Formula: 25956-17-6<\/a> can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.<\/p>\n<p>Reference:<br \/><a href=\"https:\/\/en.wikipedia.org\/wiki\/Pyrazole\">Pyrazole &#8211; Wikipedia<\/a>,<br \/><a href=\"https:\/\/www.sciencedirect.com\/topics\/chemistry\/pyrazoles\">Pyrazoles &#8211; an overview | ScienceDirect Topics<\/A><\/p>\n","protected":false},"excerpt":{"rendered":"<p>As far as I know, this compound(25956-17-6)<a href=\"https:\/\/www.ambeed.com\/products\/25956-17-6.html\">HPLC of Formula: 25956-17-6<\/a> can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.<\/p>\n","protected":false},"author":8,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[727,131],"tags":[500],"class_list":["post-9599","post","type-post","status-publish","format-standard","hentry","category-25956-17-6","category-pyrazoles-derivatives","tag-m-w400-500"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Awesome and Easy Science Experiments about 25956-17-6 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"HPLC of Formula: 25956-17-6. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Performance evaluation of photolytic and electrochemical oxidation processes for enhanced degradation of food dyes laden wastewater. Author is Sartaj, Seema; Ali, Nisar; Khan, Adnan; Malik, Sumeet; Bilal, Muhammad; Khan, Menhad; Ali, Nauman; Hussain, Sajjad; Khan, Hammad; Khan, Sabir.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.pyrazoles-derivatives.com\/?p=9599\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Awesome and Easy Science Experiments about 25956-17-6 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"HPLC of Formula: 25956-17-6. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Performance evaluation of photolytic and electrochemical oxidation processes for enhanced degradation of food dyes laden wastewater. Author is Sartaj, Seema; Ali, Nisar; Khan, Adnan; Malik, Sumeet; Bilal, Muhammad; Khan, Menhad; Ali, Nauman; Hussain, Sajjad; Khan, Hammad; Khan, Sabir.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.pyrazoles-derivatives.com\/?p=9599\" \/>\n<meta property=\"og:site_name\" content=\"pyrazoles-derivatives\" \/>\n<meta property=\"article:published_time\" content=\"2022-04-10T20:48:22+00:00\" \/>\n<meta name=\"author\" content=\"Jessica.F\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Jessica.F\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9599\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9599\",\"name\":\"Awesome and Easy Science Experiments about 25956-17-6 | pyrazoles-derivatives\",\"isPartOf\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#website\"},\"datePublished\":\"2022-04-10T20:48:22+00:00\",\"author\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\"},\"description\":\"HPLC of Formula: 25956-17-6. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Performance evaluation of photolytic and electrochemical oxidation processes for enhanced degradation of food dyes laden wastewater. Author is Sartaj, Seema; Ali, Nisar; Khan, Adnan; Malik, Sumeet; Bilal, Muhammad; Khan, Menhad; Ali, Nauman; Hussain, Sajjad; Khan, Hammad; Khan, Sabir.\",\"breadcrumb\":{\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9599#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/www.pyrazoles-derivatives.com\/?p=9599\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/?p=9599#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"\u9996\u9875\",\"item\":\"https:\/\/www.pyrazoles-derivatives.com\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Awesome and Easy Science Experiments about 25956-17-6\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#website\",\"url\":\"https:\/\/www.pyrazoles-derivatives.com\/\",\"name\":\"pyrazoles-derivatives\",\"description\":\"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. Pyrazole derivatives play an important role in antitumor agents.\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/www.pyrazoles-derivatives.com\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Person\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1\",\"name\":\"Jessica.F\",\"image\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/image\/\",\"url\":\"https:\/\/cn.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"contentUrl\":\"https:\/\/cn.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g\",\"caption\":\"Jessica.F\"}}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Awesome and Easy Science Experiments about 25956-17-6 | pyrazoles-derivatives","description":"HPLC of Formula: 25956-17-6. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Performance evaluation of photolytic and electrochemical oxidation processes for enhanced degradation of food dyes laden wastewater. Author is Sartaj, Seema; Ali, Nisar; Khan, Adnan; Malik, Sumeet; Bilal, Muhammad; Khan, Menhad; Ali, Nauman; Hussain, Sajjad; Khan, Hammad; Khan, Sabir.","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599","og_locale":"en_US","og_type":"article","og_title":"Awesome and Easy Science Experiments about 25956-17-6 | pyrazoles-derivatives","og_description":"HPLC of Formula: 25956-17-6. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Performance evaluation of photolytic and electrochemical oxidation processes for enhanced degradation of food dyes laden wastewater. Author is Sartaj, Seema; Ali, Nisar; Khan, Adnan; Malik, Sumeet; Bilal, Muhammad; Khan, Menhad; Ali, Nauman; Hussain, Sajjad; Khan, Hammad; Khan, Sabir.","og_url":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599","og_site_name":"pyrazoles-derivatives","article_published_time":"2022-04-10T20:48:22+00:00","author":"Jessica.F","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Jessica.F","Est. reading time":"2 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599","url":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599","name":"Awesome and Easy Science Experiments about 25956-17-6 | pyrazoles-derivatives","isPartOf":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#website"},"datePublished":"2022-04-10T20:48:22+00:00","author":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1"},"description":"HPLC of Formula: 25956-17-6. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate, is researched, Molecular C18H14N2Na2O8S2, CAS is 25956-17-6, about Performance evaluation of photolytic and electrochemical oxidation processes for enhanced degradation of food dyes laden wastewater. Author is Sartaj, Seema; Ali, Nisar; Khan, Adnan; Malik, Sumeet; Bilal, Muhammad; Khan, Menhad; Ali, Nauman; Hussain, Sajjad; Khan, Hammad; Khan, Sabir.","breadcrumb":{"@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.pyrazoles-derivatives.com\/?p=9599"]}]},{"@type":"BreadcrumbList","@id":"https:\/\/www.pyrazoles-derivatives.com\/?p=9599#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"\u9996\u9875","item":"https:\/\/www.pyrazoles-derivatives.com\/"},{"@type":"ListItem","position":2,"name":"Awesome and Easy Science Experiments about 25956-17-6"}]},{"@type":"WebSite","@id":"https:\/\/www.pyrazoles-derivatives.com\/#website","url":"https:\/\/www.pyrazoles-derivatives.com\/","name":"pyrazoles-derivatives","description":"Several pyrazole derivatives possess important pharmacological activities and they have been proved useful materials in drug research. Pyrazole derivatives play an important role in antitumor agents.","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.pyrazoles-derivatives.com\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Person","@id":"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/d9a9f27bed675392c6f363a01ffd49f1","name":"Jessica.F","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.pyrazoles-derivatives.com\/#\/schema\/person\/image\/","url":"https:\/\/cn.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g","contentUrl":"https:\/\/cn.cravatar.com\/avatar\/2d1cec2a99eeaad5a5b217c9cdbfb610?s=96&d=mm&r=g","caption":"Jessica.F"}}]}},"_links":{"self":[{"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=\/wp\/v2\/posts\/9599","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=9599"}],"version-history":[{"count":0,"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=\/wp\/v2\/posts\/9599\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=9599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=9599"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.pyrazoles-derivatives.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=9599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}