{"id":1127,"date":"2016-06-21T13:19:32","date_gmt":"2016-06-21T16:19:32","guid":{"rendered":"https:\/\/www.nachodelatorre.com.ar\/mosconi\/?p=1127"},"modified":"2016-06-21T13:19:32","modified_gmt":"2016-06-21T16:19:32","slug":"un-estudio-de-las-propiedades-de-detonacion-impulso-sensibilidad-al-impacto-y-sintesis-de-anta-nitrada-y-derivados-de-nto","status":"publish","type":"post","link":"https:\/\/www.fie.undef.edu.ar\/ceptm\/?p=1127","title":{"rendered":"Un estudio de las propiedades de detonaci\u00f3n, impulso, sensibilidad al  impacto y s\u00edntesis de ANTA nitrada y derivados de NTO"},"content":{"rendered":"<p>Los derivados nitrados del 5-amino- 3-nitro- 1,2,4-triazol (ANTA) y del 3-nitro- 1,2,4-triazol- 5-ona (NTO) han sido te\u00f3ricamente caracterizados con respecto a su desempe\u00f1o como explosivos y propulsantes. La velocidad y presi\u00f3n de detonaci\u00f3n de los derivados, calculadas con el software EXPLO5, estaban al mismo nivel o ligeramente por encima del rendimiento del 1,3,5- trinitroperhidro-1,3,5- triazina (RDX). Los resultados mostraron que composiciones de 1,3,4-trinitro- 1,2,4-triazol- 5-ona y GAP pueden dar impulsos espec\u00edficos por encima de 2600 m\/s en propulsores de cohete.<!--more--><\/p>\n<div id=\"pageContainer1\" class=\"page\" data-page-number=\"1\"><\/div>\n<div id=\"pageContainer2\" class=\"page\" data-page-number=\"2\"><\/div>\n<div id=\"pageContainer3\" class=\"page\" data-page-number=\"3\"><\/div>\n<div id=\"pageContainer4\" class=\"page\" data-page-number=\"4\"><\/div>\n<div id=\"pageContainer5\" class=\"page\" data-page-number=\"5\"><\/div>\n<div id=\"pageContainer6\" class=\"page\" data-page-number=\"6\"><\/div>\n<div id=\"pageContainer7\" class=\"page\" data-page-number=\"7\"><\/div>\n<div id=\"pageContainer8\" class=\"page\" data-page-number=\"8\"><\/div>\n<div id=\"pageContainer9\" class=\"page\" data-page-number=\"9\"><\/div>\n<div id=\"pageContainer10\" class=\"page\" data-page-number=\"10\"><\/div>\n<div id=\"pageContainer11\" class=\"page\" data-loaded=\"true\" data-page-number=\"11\"><\/div>\n<div id=\"pageContainer12\" class=\"page\" data-page-number=\"12\"><\/div>\n<div id=\"pageContainer13\" class=\"page\" data-loaded=\"true\" data-page-number=\"13\"><\/div>\n<div id=\"pageContainer14\" class=\"page\" data-page-number=\"14\"><\/div>\n<div id=\"pageContainer15\" class=\"page\" data-loaded=\"true\" data-page-number=\"15\"><\/div>\n<div id=\"pageContainer16\" class=\"page\" data-loaded=\"true\" data-page-number=\"16\"><\/div>\n<div id=\"pageContainer17\" class=\"page\" data-page-number=\"17\"><\/div>\n<div id=\"pageContainer18\" class=\"page\" data-page-number=\"18\"><\/div>\n<div id=\"pageContainer19\" class=\"page\" data-loaded=\"true\" data-page-number=\"19\"><\/div>\n<div data-canvas-width=\"27.499999999999996\">463<\/div>\n<div data-canvas-width=\"474.36\">A Study of the Detonation Properties, Propellant Impulses, Impact Sensitivities&#8230;<\/div>\n<div data-canvas-width=\"576.3816666666664\">5-nitrimino-3-nitro-1,2,4-triazole, 1,3-dinitro-1,2,4-triazol-5-one and 3,4-dinitro-<\/div>\n<div data-canvas-width=\"494.4206666666667\">1,2,4-triazol-5-one were suggested. When NTO was dissolved in a<\/div>\n<div data-canvas-width=\"81.96833333333332\">mixture of<\/div>\n<div data-canvas-width=\"580.2939999999999\">nitric acid and acetic anhydride the compound decomposed. NTO did not seem<\/div>\n<div data-canvas-width=\"582.0265000000002\">to decompose if chloride-assisted nitration was used and the temperature was<\/div>\n<div data-canvas-width=\"105.16\">kept below 15<\/div>\n<div data-canvas-width=\"12.558333333333332\">\u00b0<\/div>\n<div data-canvas-width=\"206.67716666666666\">C. The FTIR spectrum of a<\/div>\n<div data-canvas-width=\"252.0191666666666\">derivative obtained indicated that<\/div>\n<div data-canvas-width=\"71.13516666666666\">an N\u2212NO<\/div>\n<div>2<\/div>\n<div data-canvas-width=\"503.4993333333334\">bond had been formed in the molecule. However, the derivative was<\/div>\n<div data-canvas-width=\"198.07333333333335\">not stable for more than 24<\/div>\n<div data-canvas-width=\"171.58166666666668\">h at room temperature.<\/div>\n<div data-canvas-width=\"16.25\">5<\/div>\n<div data-canvas-width=\"199.19249999999997\">Experimental Section<\/div>\n<div data-canvas-width=\"583.6416666666668\">NTO was used as received from Chemring Nobel. Sigma-Aldrich supplied<\/div>\n<div data-canvas-width=\"580.6350000000001\">acetic anhydride and concentrated nitric acid. The FTIR spectra were recorded<\/div>\n<div data-canvas-width=\"33.56833333333333\">on a<\/div>\n<div data-canvas-width=\"540.419\">Nicolet FTIR (iS10) with diamond ATR. The absorbance bands were<\/div>\n<div data-canvas-width=\"478.0416666666665\">characterized as broad (b), strong (s), medium (m) and weak (w).<\/div>\n<div data-canvas-width=\"29.999999999999996\">5.1<\/div>\n<div data-canvas-width=\"421.99800000000005\">Nitration of NTO in the presence of zinc chloride<\/div>\n<div data-canvas-width=\"170.59716666666662\">Acetic anhydride (1.86<\/div>\n<div data-canvas-width=\"315.843\">g) was added dropwise to nitric acid (0.69<\/div>\n<div data-canvas-width=\"48.92433333333332\">g) at 0<\/div>\n<div data-canvas-width=\"12.961666666666666\">\u00b0<\/div>\n<div data-canvas-width=\"16.811666666666664\">C.<\/div>\n<div data-canvas-width=\"224.3981666666666\">The solution was stirred for 30<\/div>\n<div data-canvas-width=\"221.5326666666667\">min before zinc chloride (0.15<\/div>\n<div data-canvas-width=\"126.0783333333333\">g) was dissolved<\/div>\n<div data-canvas-width=\"515.0419999999999\">in the mixture. After stirring for 30 min, small portions of NTO (0.30<\/div>\n<div data-canvas-width=\"61.34333333333333\">g) were<\/div>\n<div data-canvas-width=\"265.353\">added. This mixture was stirred for 1<\/div>\n<div data-canvas-width=\"127.88233333333332\">h, heated to 15-18<\/div>\n<div data-canvas-width=\"10.706666666666667\">\u00b0<\/div>\n<div data-canvas-width=\"172.7275\">C and stirred overnight.<\/div>\n<div data-canvas-width=\"208.52516666666665\">Finally, it was heated to 40<\/div>\n<div data-canvas-width=\"14.153333333333334\">\u00b0<\/div>\n<div data-canvas-width=\"143.32266666666666\">C and stirred for 2<\/div>\n<div data-canvas-width=\"210.40983333333332\">h. During the reaction the<\/div>\n<div data-canvas-width=\"581.1519999999999\">colour of the slurry-like mixture changed from yellow to weak-red and then to<\/div>\n<div data-canvas-width=\"269.577\">white. The slurry was poured into a<\/div>\n<div data-canvas-width=\"306.7991666666666\">beaker containing ice-cold water and the<\/div>\n<div data-canvas-width=\"580.9649999999999\">precipitate was filtered off and washed with water. The precipitate dissolved<\/div>\n<div data-canvas-width=\"580.8531666666668\">rapidly and decomposed during the washing step. The procedure was repeated<\/div>\n<div data-canvas-width=\"579.5478333333332\">using chloroform instead of water. The precipitate was more stable in this solvent<\/div>\n<div data-canvas-width=\"401.97299999999996\">and was therefore filtered off and dried under vacuum.<\/div>\n<div data-canvas-width=\"79.30816666666666\">IR (ATR):<\/div>\n<div>\u1fe6<\/div>\n<div data-canvas-width=\"90.7775\">= 3363 (b),<\/div>\n<div data-canvas-width=\"560.0961666666666\">2215 (w), 1542 (s), 1455(s), 1408 (s), 1301(s), 1028 (m), 957 (w), 809 (w) cm<\/div>\n<div data-canvas-width=\"11.703999999999999\">\u22121<\/div>\n<div>.<\/div>\n<div data-canvas-width=\"172.51666666666665\">Acetic anhydride (1.57<\/div>\n<div data-canvas-width=\"368.80250000000007\">g) was added dropwise to nitric acid (0.57 g) at<\/div>\n<div>0<\/div>\n<div data-canvas-width=\"11.401666666666667\">\u00b0<\/div>\n<div data-canvas-width=\"84.99516666666665\">C. After 30<\/div>\n<div data-canvas-width=\"231.0935\">min stirring, zinc chloride (0.27<\/div>\n<div data-canvas-width=\"235.69883333333334\">g) was dissolved in the mixture,<\/div>\n<div data-canvas-width=\"187.48583333333332\">followed by stirring for 30<\/div>\n<div data-canvas-width=\"239.32883333333334\">min. After addition of NTO (0.59<\/div>\n<div data-canvas-width=\"145.816\">g) in small portions,<\/div>\n<div data-canvas-width=\"220.23833333333326\">the mixture was stirred for 1<\/div>\n<div data-canvas-width=\"153.63333333333333\">h, then heated to 15<\/div>\n<div data-canvas-width=\"14.226666666666668\">\u00b0<\/div>\n<div data-canvas-width=\"188.3383333333333\">C and stirred overnight.<\/div>\n<div data-canvas-width=\"580.9613333333334\">Thereafter, the white slurry was poured into cold chloroform and filtered off.<\/div>\n<div data-canvas-width=\"580.5323333333332\">The precipitate was dried under vacuum, washed with acetone, filtered and dried.<\/div>\n<div data-canvas-width=\"101.39066666666666\">FTIR (ATR):<\/div>\n<div>\u1fe6<\/div>\n<div data-canvas-width=\"470.50116666666656\">= 3207 (b), 1717 (m), 1639 (w), 1546 (s), 1456 (m), 1411 (m),<\/div>\n<div data-canvas-width=\"450.9615000000001\">1369 (m), 1290 (s), 1108 (w), 1022 (m), 977 (m), 861 (w) cm<\/div>\n<div data-canvas-width=\"11.703999999999999\">\u22121<\/div>\n<div>.<\/div>\n<div data-canvas-width=\"126.31116666666668\">Nitric acid (0.36<\/div>\n<div data-canvas-width=\"136.5631666666667\">g) was cooled to 0<\/div>\n<div data-canvas-width=\"12.448333333333334\">\u00b0<\/div>\n<div data-canvas-width=\"213.4201666666667\">C and acetic anhydride (2.06<\/div>\n<div data-canvas-width=\"54.00999999999999\">g) was<\/div>\n<div data-canvas-width=\"391.03716666666656\">then added dropwise. The mixture was stirred for 20<\/div>\n<div data-canvas-width=\"185.361\">min before zinc chloride<\/div>\n<div class=\"canvasWrapper\"><\/div>\n<div data-canvas-width=\"27.499999999999996\">464<\/div>\n<div data-canvas-width=\"320.76450000000006\">T.L. Jensen, J.F. Moxnes, E.F. Kj\u00f8nstad, E. Unneberg<\/div>\n<div data-canvas-width=\"38.18833333333334\">(0.20<\/div>\n<div data-canvas-width=\"290.56133333333327\">g) was added followed by stirring for 30<\/div>\n<div data-canvas-width=\"58.58416666666666\">min at 0<\/div>\n<div data-canvas-width=\"11.165\">\u00b0<\/div>\n<div data-canvas-width=\"174.05299999999997\">C. Subsequently, small<\/div>\n<div data-canvas-width=\"158.51733333333328\">portions of NTO (0.38<\/div>\n<div data-canvas-width=\"331.3841666666666\">g) were added and the mixture was stirred for 5<\/div>\n<div data-canvas-width=\"52.69\">h at 0-5<\/div>\n<div data-canvas-width=\"10.651666666666666\">\u00b0<\/div>\n<div data-canvas-width=\"21.266666666666666\">C,<\/div>\n<div data-canvas-width=\"233.31366666666665\">poured into cold chloroform (5.0<\/div>\n<div data-canvas-width=\"321.442\">g), filtered off, washed with chloroform (10.0<\/div>\n<div data-canvas-width=\"19.76333333333333\">g)<\/div>\n<div data-canvas-width=\"580.9155\">and dried under vacuum. The product consisted of small white crystals. FTIR<\/div>\n<div data-canvas-width=\"56.415333333333336\">(ATR):<\/div>\n<div>\u1fe6<\/div>\n<div data-canvas-width=\"515.4966666666666\">= 3257 (b), 1716 (s), 1634 (w), 1545 (s), 1463 (w), 1412 (w), 1369 (m),<\/div>\n<div data-canvas-width=\"453.3466666666667\">1305 (s), 1282 (s), 1199 (m), 1128 (w), 1003 (m), 978 (m) cm<\/div>\n<div data-canvas-width=\"11.703999999999999\">\u22121<\/div>\n<div data-canvas-width=\"9.166666666666666\">.<\/div>\n<div data-canvas-width=\"29.999999999999996\">5.2<\/div>\n<div data-canvas-width=\"480.36000000000007\">Nitration of NTO in the presence of ammonium chloride<\/div>\n<div data-canvas-width=\"359.4066666666667\">Acetic anhydride was dripped into nitric acid at 0<\/div>\n<div data-canvas-width=\"11.531666666666666\">\u00b0<\/div>\n<div data-canvas-width=\"168.1478333333333\">C. After stirring for 30<\/div>\n<div data-canvas-width=\"37.69333333333333\">min,<\/div>\n<div data-canvas-width=\"465.27616666666665\">ammonium chloride was added. The mixture was stirred for 30<\/div>\n<div data-canvas-width=\"111.11833333333334\">min before the<\/div>\n<div data-canvas-width=\"455.1323333333334\">addition of small portions of NTO, followed by stirring for 1<\/div>\n<div data-canvas-width=\"121.25849999999998\">h. The mixture<\/div>\n<div data-canvas-width=\"431.4419999999999\">was then heated, first to room temperature and stirred for 4<\/div>\n<div data-canvas-width=\"116.16549999999998\">h, then to 35-40<\/div>\n<div data-canvas-width=\"11.935\">\u00b0<\/div>\n<div data-canvas-width=\"16.811666666666664\">C<\/div>\n<div data-canvas-width=\"119.85233333333332\">and stirred for 1<\/div>\n<div data-canvas-width=\"453.1303333333333\">h. The white slurry was poured onto crushed ice, filtered off<\/div>\n<div data-canvas-width=\"182.95566666666664\">and dried. FTIR (ATR):<\/div>\n<div>\u1fe6<\/div>\n<div data-canvas-width=\"388.92333333333335\">= 3194 (m), 1690 (s), 1539 (m), 1471 (m), 1338 (s),<\/div>\n<div data-canvas-width=\"322.98750000000007\">1279 (m), 1186 (m), 1108 (w), 1005 (m) cm<\/div>\n<div data-canvas-width=\"11.703999999999999\">\u22121<\/div>\n<div data-canvas-width=\"9.166666666666666\">.<\/div>\n<div data-canvas-width=\"228.87700000000004\">FTIR spectrum of NTO (ATR):<\/div>\n<div>\u1fe6<\/div>\n<div data-canvas-width=\"309.95616666666666\">= 3194 (m), 1690 (s), 1541 (m), 1471 (m),<\/div>\n<div data-canvas-width=\"392.74766666666665\">1338 (s), 1280 (m), 1187 (m), 1109 (w), 1006 (m) cm<\/div>\n<div data-canvas-width=\"11.703999999999999\">\u22121<\/div>\n<div><\/div>\n<p><strong>Fuente:<\/strong> <em><a href=\"http:\/\/www.wydawnictwa.ipo.waw.pl\/cejem\/Vol-13- Number-2- 2016\/Jensen.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">http:\/\/www.wydawnictwa.ipo.waw.pl<\/a><\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Los derivados nitrados del 5-amino- 3-nitro- 1,2,4-triazol (ANTA) y del 3-nitro- 1,2,4-triazol- 5-ona (NTO) han sido te\u00f3ricamente caracterizados con respecto a su desempe\u00f1o como explosivos&hellip; <\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[29,24],"tags":[],"_links":{"self":[{"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=\/wp\/v2\/posts\/1127"}],"collection":[{"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1127"}],"version-history":[{"count":0,"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=\/wp\/v2\/posts\/1127\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1127"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1127"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.fie.undef.edu.ar\/ceptm\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1127"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}