{"id":9472,"date":"2022-04-01T11:50:48","date_gmt":"2022-04-01T03:50:48","guid":{"rendered":"https:\/\/www.pyrazoles-derivatives.com\/?p=9472"},"modified":"2022-04-01T11:50:48","modified_gmt":"2022-04-01T03:50:48","slug":"a-new-application-about-25956-17-6","status":"publish","type":"post","link":"https:\/\/www.pyrazoles-derivatives.com\/?p=9472","title":{"rendered":"A new application about 25956-17-6"},"content":{"rendered":"<p>Saha, Tapan Kumar; Bishwas, Raton Kumar; Karmaker, Subarna; Islam, Zinia published an article about the compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate( cas:25956-17-6,SMILESS:O=S(C1=CC=C2C(\/N=N\/C3=CC(C)=C(S(=O)([O-])=O)C=C3OC)=C(O)C=CC2=C1)([O-])=O.[Na+].[Na+] ).<a href=\"https:\/\/www.ambeed.com\/products\/25956-17-6.html\">Quality Control of Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate<\/a>. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:25956-17-6)  through the article.<\/p>\n<p>Allura red AC (ARAC) dye adsorption by natural sawdust (NSD) and hexadecylpyridinium bromide-treated sawdust (MSD) was assessed in aqueous solution as a function of contact time, solution pH, particle size, adsorbent dose, dye concentration, temperature, and ionic strength. Adsorbents were characterized by Fourier transform IR spectroscopy and x-ray diffraction crystallog. Dye adsorption by both adsorbents was confirmed by field emission SEM and energy-dispersive x-ray spectroscopy. The maximum dye adsorption occurred within 120 min at pH 2.0 for NSD and pH 3.0 for MSD, resp., with a 0-75\u03bcm particle size and 0.07 g\/50 mL ARAC dye solution adsorbent dose (50\u03bcmol\/L). Batch adsorption kinetic data were followed by a pseudo-second-order kinetic model vs. pseudo-first-order and Elovich kinetic models. Equilibrium adsorption isotherms were explained by the Langmuir isotherm model, and the maximum extent of adsorption was 52.14\u03bcmol\/g for NSD and 151.88\u03bcmol\/g for MSD at 55\u00b0. Activation energy (Ea) and thermodn. parameters (\u0394G\ue302, \u0394H\ue302, \u0394S\ue302, \u0394G\u00b0, \u0394H\u00b0, \u0394S\u00b0) values proved ARAC dye adsorption by both NSD and MSD sorbents was a spontaneous-endothermic physisorption process. ARAC (98-99%) was released from dye-loaded adsorbents in aqueous solution (pH \u226512) within 120 min. NSD and MSD adsorbents were reused a second time without significant loss of adsorption efficiency.<\/p>\n<p>Compound(25956-17-6)<a href=\"https:\/\/www.ambeed.com\/products\/25956-17-6.html\">Quality Control of Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate<\/a> received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate), if you are interested, you can check out my other related articles.<\/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>Compound(25956-17-6)<a href=\"https:\/\/www.ambeed.com\/products\/25956-17-6.html\">Quality Control of Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate<\/a> received a lot of attention, and I have introduced some compounds in other articles, similar to this compound(Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate), if you are interested, you can check out my other related articles.<\/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-9472","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>A new application about 25956-17-6 | pyrazoles-derivatives<\/title>\n<meta name=\"description\" content=\"Saha, Tapan Kumar; Bishwas, Raton Kumar; Karmaker, Subarna; Islam, Zinia published an article about the compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate( cas:25956-17-6,SMILESS:O=S(C1=CC=C2C(\/N=N\/C3=CC(C)=C(S(=O)([O-])=O)C=C3OC)=C(O)C=CC2=C1)([O-])=O.[Na+].[Na+] ).Quality Control of Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:25956-17-6) through the article.\" \/>\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=9472\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"A new application about 25956-17-6 | pyrazoles-derivatives\" \/>\n<meta property=\"og:description\" content=\"Saha, Tapan Kumar; Bishwas, Raton Kumar; Karmaker, Subarna; Islam, Zinia published an article about the compound: Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate( cas:25956-17-6,SMILESS:O=S(C1=CC=C2C(\/N=N\/C3=CC(C)=C(S(=O)([O-])=O)C=C3OC)=C(O)C=CC2=C1)([O-])=O.[Na+].[Na+] ).Quality Control of Sodium 6-hydroxy-5-((2-methoxy-5-methyl-4-sulfonatophenyl)diazenyl)naphthalene-2-sulfonate. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. 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Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. 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Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. 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Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. 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