{"id":5112,"date":"2024-08-09T19:41:41","date_gmt":"2024-08-09T19:41:41","guid":{"rendered":"http:\/\/121.199.166.88\/?post_type=resources&#038;p=5112"},"modified":"2024-09-11T15:24:39","modified_gmt":"2024-09-11T15:24:39","slug":"acid-site-characterization-of-h-s-sio2-al2o375-1-a-pulse-chemisorption-and-tpd-application-for-the-autochem","status":"publish","type":"resources","link":"https:\/\/micromeritics.com.cn\/en\/resources\/acid-site-characterization-of-h-s-sio2-al2o375-1-a-pulse-chemisorption-and-tpd-application-for-the-autochem\/","title":{"rendered":"Acid Site Characterization of H+ \u00df (SiO2\/Al2O3:75\/1): A Pulse Chemisorption and TPD Application for the AutoChem"},"content":{"rendered":"\n<p>The Br\u00f8nstead acidity of zeolites and other catalysts is of keen interest, as this affects the kinetics of reactions. Characterization of these sites is consequently very important and is often performed according to the ASTM D 4824 ammonia chemisorption method. An alternative, but comparable, characterization method involves pulse chemisorption of propylamines followed by a temperature-programmed desorption (TPD) combined with a mass spectrometry analysis of propylene (see <strong>Figure 1<\/strong>). A complete characterization analysis can be performed using the AutoChem analyzer with the mass spectrometer and vapor generator accessories.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img fetchpriority=\"high\" decoding=\"async\" width=\"895\" height=\"625\" src=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Amine-reacts-FIG.-1.png\" alt=\"\" class=\"wp-image-5644\" style=\"width:750px\" srcset=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Amine-reacts-FIG.-1.png 895w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Amine-reacts-FIG.-1-300x209.png 300w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Amine-reacts-FIG.-1-768x536.png 768w\" sizes=\"(max-width: 895px) 100vw, 895px\" \/><figcaption class=\"wp-element-caption\">Figure 1. The amine reacts with acid sites to decompose into propylene\nand ammonia via a mechanism analogous to Hofmann Elimination.<\/figcaption><\/figure>\n<\/div>\n\n\n<h3 class=\"wp-block-heading\">Materials<\/h3>\n\n\n\n<p>The zeolite used in this application contained hydrogen cations and had a silica-to-alumina ratio of 75:1. Isopropylamine (&gt;99.5% GC) and propylamine (&gt;99.0% GC) were used, separately, as reagents. Propylene (&gt;99%) was also used for calibration purposes.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Preparation<\/h3>\n\n\n\n<p>A Beta zeolite sample can contain various cations, including ammonium and hydrogen. Cations in these compounds can be converted into hydrogen cations by means of a temperature ramp. The sample was activated first by heating to 500 \u00b0C at 10 \u00b0C\/min in an inert helium environment, then cooling to 200 \u00b0C, the analysis temperature.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Analysis<\/h3>\n\n\n\n<p>The activation of the Beta zeolite was followed by pulse chemisorption. During this step, ten injections of propylamine vapor were dosed onto the sample (to ensure the sample was saturated) by means of an inert gas, helium, flowing through a 5-cm3 loop. The last part of the analysis involved a temperature-programmed desorption (TPD). At this step in the analysis, the mass spectrometer began scanning for propylene, the product of interest. Data were collected during a temperature ramp from 200 \u00b0C to 500 \u00b0C.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Data<\/h3>\n\n\n\n<p>To obtain quantitative data, the mass spectrometer must be calibrated by injecting a known volume of the gas to be detected (propylene), Vcal, through the septum with a highprecision syringe. The peak area of the mass spectrometer signal can be obtained using the AutoChem peak-editing software. To increase the accuracy of the calibration, injections may be made until peaks are similar in area. The areas can then be averaged to give a general conversion factor between mass spectrometer peak area and actual gas volume, allowing for the acidity of zeolites to be calculated. <strong>Figure 2<\/strong> gives an example of this procedure.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img decoding=\"async\" width=\"923\" height=\"1020\" src=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG.-2.png\" alt=\"\" class=\"wp-image-5646\" style=\"width:750px\" srcset=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG.-2.png 923w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG.-2-271x300.png 271w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG.-2-768x849.png 768w\" sizes=\"(max-width: 923px) 100vw, 923px\" \/><figcaption class=\"wp-element-caption\">Figure 2. Example of mass spectrometer signal during an area-volume calibration.<\/figcaption><\/figure>\n<\/div>\n\n\n<p>Additionally, <strong>Figures 3<\/strong> <strong>and 4 <\/strong>show that a thermal conductivity detection method includes residual amine and ammonia from the chemisorption, whereas mass spectrometer detection isolates the propylene signal, allowing the concentration of acid sites to be calculated.<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img decoding=\"async\" width=\"846\" height=\"592\" src=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Thermal-Contivity-FIG.3-3.png\" alt=\"\" class=\"wp-image-5656\" style=\"width:750px\" srcset=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Thermal-Contivity-FIG.3-3.png 846w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Thermal-Contivity-FIG.3-3-300x210.png 300w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Thermal-Contivity-FIG.3-3-768x537.png 768w\" sizes=\"(max-width: 846px) 100vw, 846px\" \/><figcaption class=\"wp-element-caption\">Figure 3. Thermal conductivity data from the AutoChem.<\/figcaption><\/figure>\n<\/div>\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"846\" height=\"592\" src=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG-4-1.png\" alt=\"\" class=\"wp-image-5657\" style=\"width:750px\" srcset=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG-4-1.png 846w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG-4-1-300x210.png 300w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/Mass-Spect.-FIG-4-1-768x537.png 768w\" sizes=\"(max-width: 846px) 100vw, 846px\" \/><figcaption class=\"wp-element-caption\">Figure 4. Mass spectrometer peak results.<\/figcaption><\/figure>\n<\/div>\n\n\n<p>After obtaining the peak area by integration of the propylene signal from Figure 4, A<sub>pms<\/sub>, the acid site concentration, N<sub>as<\/sub>, can be calculated as follows:<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"363\" src=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/acid-cite-equation_1-1024x363.png\" alt=\"\" class=\"wp-image-5659\" style=\"width:750px\" srcset=\"https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/acid-cite-equation_1-1024x363.png 1024w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/acid-cite-equation_1-300x106.png 300w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/acid-cite-equation_1-768x272.png 768w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/acid-cite-equation_1-1536x545.png 1536w, https:\/\/micromeritics.com.cn\/wp-content\/uploads\/2024\/08\/acid-cite-equation_1-2048x726.png 2048w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>The Br\u00f8nstead acidity of zeolites and other catalysts is of keen interest, as this affects the kinetics of reactions. Characterization of these sites is consequently very important and is often performed according to the ASTM D 4824 ammonia chemisorption method. An alternative, but comparable, characterization method involves pulse chemisorption of propylamines followed by a temperature-programmed [&hellip;]<\/p>\n","protected":false},"featured_media":0,"parent":0,"template":"","meta":{"_acf_changed":false},"methods":[25],"resource_type":[8],"class_list":["post-5112","resources","type-resources","status-publish","hentry","methods-chemisorption","resource_type-application-notes"],"acf":[],"_links":{"self":[{"href":"https:\/\/micromeritics.com.cn\/en\/wp-json\/wp\/v2\/resources\/5112","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/micromeritics.com.cn\/en\/wp-json\/wp\/v2\/resources"}],"about":[{"href":"https:\/\/micromeritics.com.cn\/en\/wp-json\/wp\/v2\/types\/resources"}],"wp:attachment":[{"href":"https:\/\/micromeritics.com.cn\/en\/wp-json\/wp\/v2\/media?parent=5112"}],"wp:term":[{"taxonomy":"methods","embeddable":true,"href":"https:\/\/micromeritics.com.cn\/en\/wp-json\/wp\/v2\/methods?post=5112"},{"taxonomy":"resource_type","embeddable":true,"href":"https:\/\/micromeritics.com.cn\/en\/wp-json\/wp\/v2\/resource_type?post=5112"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}