TWI303715B - Method for continuously evaluating an amount of gas adsorbed on materials - Google Patents

Method for continuously evaluating an amount of gas adsorbed on materials Download PDF

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TWI303715B
TWI303715B TW94128815A TW94128815A TWI303715B TW I303715 B TWI303715 B TW I303715B TW 94128815 A TW94128815 A TW 94128815A TW 94128815 A TW94128815 A TW 94128815A TW I303715 B TWI303715 B TW I303715B
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sample
adsorption
weight
tested
desorption
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TW94128815A
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TW200708738A (en
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Chaochun Perng
Pohsiung Huang
Derhuah Wu
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Taiwan Textile Res Inst
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l3〇37l5 九、發明說明: 【發明所屬之技術領域】 本發明係有關於一種辞^ 的評估系統與方法,㈣是=料對氣體分子之吸附性能 評估系統與方法。 _於連續式氣體吸附性能的 【先前技術】 淨化工具有吸附性能的材料來進行如化學廢氣 ^ 1心慮或軋體混合物分離等程序。而具有氣體吸 的材料種類極多,如多孔性材料(如活性碳:分子 二:石)、織物與過濾、材質(如口罩、濾網)。因此,必須 屮、在不同的吸附氣體種類與各種環境條件下材料所表 見出來的吸附與脫附性能,才能選出最適合的材料。 測定吸附性材料之吸附性能的方法大 D3467測試標準。此測試標㈣在規定條件下,使氣體(如 揮發性有機溶劑、水氣、含粉塵之氣體)流經已知== 之待測樣品,並於吸附過程中多次測定待測樣品之重旦, 直到樣品重量不再增加為止。 里 在傳統方法中,先將一空管柱進行秤重來得至 重。隨後在空柱中填充待測樣品並測量其重量來得到^品 柱重。並將已填充待測樣品的管柱與欲吸附之氣體來源2 通,使得氣體進入管柱並流經待測樣品以進行吸附反應、。 每隔-段時間後(如每隔5、10、15或3〇分鐘),需阻斷氣 體並取下含有待測樣品的管柱。將管柱擦拭乾淨以去除 面的水氣或其他附著物後進行秤重。所秤得的重量為管柱 1303715 加上已吸附氣體分子之待測樣品的重量(吸附後樣品柱 重)。再將秤重後的管柱與氣體來源連通,再度使氣體流經 待測樣品。重複取下管柱進行秤重與安裝的動作,直到吸 附後樣品柱重不再變化為止。利用下列公式來將所得數據 轉換成待測樣品對此氣體的吸附性。 l〇〇x(吸附後樣品柱重—樣品柱重)/(樣品柱重一空柱 重)=吸附百分率 然而傳統裝置與方法具有一些缺點。其一是在吸附過 転中需反覆地取下含有待測樣品的管柱進行秤重後再安裝 的動作極為不便。其二在於樣品之吸附重量變化極微小, 同時將管柱移出裝置後的環境因素變化(如溫度)均會使測 仵之數據具有極大的人為誤差。其三在於對於實驗操作者 需全程監控實驗過程是一種人力浪費,同時操作人員可能 接觸到如揮發性有機氣體或粉塵等有害物質,進而影響健 康。其四在於傳統方法之步驟麻煩,故無法在短時間内獲 取多時間點之吸附數據而不能反應出待測樣品真實的吸附 性。其五在於傳統裝置與方法不易進行脫附反應,因此不 適合用來評估待測樣品的脫附性能。 因此,目前需要一種簡便且快速的評估系統與方法。 其能降低因傳統方法中需要操作者反覆取出待測吸附材並 測畺其重昼之步驟所造成的人為誤差,而正確地評估出吸 附材之吸附與脫附性能。 6 1303715 【發明内容】 因此,本發明之方向在於提供一種簡易、快速又精確 的氣體吸附性評估系統與方法。 本發月之另-方向在於提供一種能連續且即時監控吸 寸材之吸附狀况’在吸附過程中能獲得更多有效資訊的評 估系統’以求反應出待測樣品的真實吸附與脫附性能。 根據上述觀點,本發明提供一種連續式氣體分子吸附 〖生:砰估系統’其至少包含一重量測定裝置、一樣品座、 一%境產生裝置、一反應室與一記錄與運算裝置。其中樣 口π座位於反應室中,用來放置待測樣品,例如多孔性材質 (如活性碳、分子篩、沸石)、織物、過渡材質(口罩、濾網 等氣體吸附過濾材質)。重量測定裝置需與樣品座連接,用 來偵測待測樣品之重量變化。重量測定裝置可以是電子天 秤或任何可用來測定重量並將數據傳遞至記錄與運算裝置 的儀器。環境產生裝置需與反應室連接,以將吸附或脫附 環境導入反應室中。反應室則在該樣品座周圍形成一反應 空間以進行吸附或脫附試驗。記錄與運算裝置需與重量測 疋裝置連接,並記錄由重量測定裝置傳遞至記錄與運算裝 置的數據來進行數據處理與分析。 根據上述觀點,本發明提供一種連續式氣體吸附性評 估方法。此方法將一待測樣品安置於一樣品座上,並將含 有待測樣品之樣品座置於一反應室中。利用一重量測定裝 置偵測待測樣品之初始重量。利用一環境產生裝置產生一 吸附環境,並將此吸附環境導入反應室中使待測樣品進行 吸附反應。利用重量測定裝置在吸附反應過程中測定任意 7 1303715 犄間點上待測樣品的吸附後重量。將測得的重量數據由重 1測定裝置傳輸至一記錄與運算裝置。利用記錄與運算裝 置執行一軟體來處理接收到的數據以產生待測樣品之吸附 結=。利用重量測定裝置偵測完成吸附反應之待測樣品的 重里。利用環境產生裝置產生一脫附環境,並將此脫附環 境導入反應室中,使待測樣品進行脫附反應。利用重量測 定裝置在脫附過程中測定任意時間點上待測樣品的脫附後 重里。脫附過程中,重量測定裝置收集到的重量數據傳輸 至記錄與運算裝置。利用記錄與運算裝置來處理接收到的 數據以產生待測樣品之脫附結果。將脫附結果建立在資料 庫中作為樣品篩選與比較之用。 本發明之優點在於吸附與脫附過程中,藉著使用一個 可連續即時制樣品重量變化的重量測定裝置,來免除 傳,方法中需由操作人員將待測樣品自評估系統中取出並 測量重量之動作所造成的人為誤差。 本發明之另一優點在於利用記錄與運算裝置來控制系 統並記錄結果,操作人M不需全程監控試驗過程,故能大 幅減少人力與時間。 本I明之又一優點在於操作人員不需人為測量待測樣 之重1、史化,可減少操作人員受到化學品的污染與傷害。 Λ本發明之再一優點在於可於短時間内獲取大量資訊而 能顯示出各種待測樣品的真實吸附性。 本發明之又再一優點在於將多種待測物在各種環境條 件與:同吸附氣體種類下所表現出來的吸附與脫附性能建 立成貝料庫。並可輸入指定的條件後,利用此資料庫進行 8 Ϊ303715 =材料的吸附性能比對㈣選來選出符合使用者需求的 樣α口。 本發明更有-優點在於提供一種能應用於廣泛領域, 如材料吸濕、材料乾燥速度、氣體分離、化學品純化以及 吸附劑之吸附力測試等具有氣體重量變化之反應的評估方 法與系統。 【實施方式】 本發明係揭露-種連續式氣體吸附性評估系統與方 法,用來簡便、快速且正確地評估出具吸附性材料的吸附 性能。請參考第1 ® ’其顯示根據本發明之—系統較佳實 施例。此系統具有樣品座刚,用來放置不同種類的待測樣 品114’如活性碳不織布、分子篩、口罩、遽網或沸石。 樣品座100位於反應室1〇2中,並與反應室1〇2上方 之重里測定裝置104連接,此連接方法可以是鉤掛、卡榫、 螺絲釘或其他固定方式。又重量測定裝置1〇4亦可安置於 反應室102下方,並將樣品座1〇〇改置放在重量測定裝置 104上方。在反應室1〇2外圍可加裝反應條件控制器116 用來控制如溫度專反應條件。 環境產生裝置108會透過輸入口 11〇來與反應室1〇2 連通’得以將產生的吸附或脫附環境導入反應室1〇2中, 使待測樣品114進行吸附或脫附反應。並透過輸出口 U2 來將吸附或脫附環境解除或導出,例如解除真空狀態或導 出吸附氣體。記錄與運算裝置106則可透過如數據傳輸線 等線路,分別與重量測定裝置1〇4、環境產生裝置1〇8以及 9L3〇37l5 IX. DESCRIPTION OF THE INVENTION: TECHNICAL FIELD OF THE INVENTION The present invention relates to an evaluation system and method for a word, and (d) is a system and method for evaluating adsorption performance of a gas molecule. _In the continuous gas adsorption performance [Prior Art] The purification tool has an adsorption property for a process such as chemical exhaust gas or separation of the rolling body mixture. There are many types of materials with gas absorption, such as porous materials (such as activated carbon: molecular two: stone), fabrics and filtration, materials (such as masks, filters). Therefore, it is necessary to select the most suitable materials for the adsorption and desorption properties exhibited by the materials under different adsorbed gas types and various environmental conditions. The method for determining the adsorption performance of an adsorbent material is large D3467 test standard. This test standard (4) allows gas (such as volatile organic solvents, water vapor, dust-containing gas) to flow through the sample to be tested with known == under the specified conditions, and determine the weight of the sample to be tested multiple times during the adsorption process. Once, until the sample weight no longer increases. In the traditional method, an empty column is first weighed to the weight. The sample to be tested is then filled in an empty column and its weight is measured to obtain a column weight. The column that has filled the sample to be tested is connected to the gas source to be adsorbed, so that the gas enters the column and flows through the sample to be tested for adsorption reaction. After every other period of time (eg every 5, 10, 15 or 3 minutes), block the gas and remove the column containing the sample to be tested. Wipe the column to remove moisture or other deposits on the surface and weigh it. The weight weighed is the weight of the sample to be tested, 1303715 plus the adsorbed gas molecules (the weight of the sample after adsorption). The weighted column is then connected to the gas source, and the gas is again passed through the sample to be tested. Repeat the removal of the column for weighing and installation until the sample weight is no longer changed after absorbing. The resulting data was converted to the adsorptivity of the sample to be tested using the following formula. L〇〇x (sample weight after adsorption - sample column weight) / (sample column weight - empty column weight) = percent adsorption However, conventional devices and methods have some disadvantages. One of them is that it is extremely inconvenient to remove the column containing the sample to be tested and to perform the weighing after the adsorption is carried out. The second is that the adsorption weight of the sample changes very little, and the environmental factors (such as temperature) after the column is removed from the device will cause great error in the data of the measurement. The third is that it is a waste of manpower for the experimental operator to monitor the entire process, and the operator may be exposed to harmful substances such as volatile organic gases or dust, which may affect health. The fourth is that the steps of the conventional method are troublesome, so it is impossible to obtain the adsorption data at multiple time points in a short time and cannot reflect the true adsorption property of the sample to be tested. The fifth is that the conventional apparatus and method are not easy to carry out the desorption reaction, and therefore are not suitable for evaluating the desorption performance of the sample to be tested. Therefore, there is a need for a simple and fast evaluation system and method. It can reduce the human error caused by the steps of the conventional method that requires the operator to repeatedly take out the adsorbent material to be tested and measure its heavy weight, and correctly evaluate the adsorption and desorption performance of the adsorbent. 6 1303715 SUMMARY OF THE INVENTION Accordingly, the present invention is directed to providing a simple, fast, and accurate gas adsorption evaluation system and method. The other direction of this month is to provide an evaluation system that continuously and instantly monitors the adsorption state of the suction material, which can obtain more effective information during the adsorption process, in order to reflect the true adsorption and desorption of the sample to be tested. performance. In view of the above, the present invention provides a continuous gas molecular adsorption system comprising at least one weight measuring device, a sample holder, a % environment generating device, a reaction chamber and a recording and computing device. The sample π is located in the reaction chamber and is used to place samples to be tested, such as porous materials (such as activated carbon, molecular sieves, zeolites), fabrics, transition materials (masks, filters, etc.). The weight measuring device is connected to the sample holder to detect the change in weight of the sample to be tested. The weight measuring device can be an electronic scale or any instrument that can be used to measure weight and transfer data to a recording and computing device. The environment generating device is connected to the reaction chamber to introduce the adsorption or desorption environment into the reaction chamber. The reaction chamber forms a reaction space around the sample holder for adsorption or desorption experiments. The recording and computing device is connected to the weight measuring device, and the data transmitted from the weight measuring device to the recording and computing device is recorded for data processing and analysis. In view of the above, the present invention provides a continuous gas adsorption evaluation method. In this method, a sample to be tested is placed on a sample holder, and a sample holder containing the sample to be tested is placed in a reaction chamber. The initial weight of the sample to be tested is detected by a weight measuring device. An environment-generating device is used to generate an adsorption environment, and the adsorption environment is introduced into the reaction chamber to cause the sample to be tested to undergo an adsorption reaction. The post-adsorption weight of the sample to be tested at any 7 1303715 intercalation point was measured during the adsorption reaction using a weight measuring device. The measured weight data is transmitted from the weight 1 measuring device to a recording and computing device. A software is executed by the recording and computing device to process the received data to produce an adsorption junction of the sample to be tested. The weight measuring device is used to detect the weight of the sample to be tested which has completed the adsorption reaction. A desorption environment is generated by the environment generating device, and the desorption environment is introduced into the reaction chamber to cause the sample to be tested to undergo desorption reaction. The desorption after the desorption of the sample to be tested at any time point is measured by the weight measuring device during the desorption process. During the desorption process, the weight data collected by the weight measuring device is transmitted to the recording and computing device. The received data is processed using a recording and computing device to produce a desorption result of the sample to be tested. Desorption results were established in the database for sample screening and comparison. The invention has the advantages that during the adsorption and desorption process, the weight is measured by using a weight measuring device which can continuously change the weight of the sample, and the operator needs to take the sample to be tested from the evaluation system and measure the weight. Human error caused by the action. Another advantage of the present invention is that the recording and computing device is used to control the system and record the results. The operator M does not need to monitor the test process throughout, so the manpower and time can be greatly reduced. Another advantage of the present invention is that the operator does not need to manually measure the weight of the sample to be tested, and can reduce the contamination and damage of the operator by chemicals. Still another advantage of the present invention is that a large amount of information can be acquired in a short time to display the true adsorptivity of various samples to be tested. Still another advantage of the present invention is that a plurality of analytes are constructed in a variety of environmental conditions and adsorption and desorption properties exhibited by the same adsorbed gas species. After entering the specified conditions, use this database to select 8 Ϊ 303715 = material adsorption performance comparison (4) to select the sample α port that meets the user's needs. Moreover, the present invention has an advantage in that it provides an evaluation method and system that can be applied to a wide range of fields, such as moisture absorption of materials, material drying speed, gas separation, chemical purification, and adsorption test of adsorbents. [Embodiment] The present invention discloses a continuous gas adsorption evaluation system and method for evaluating the adsorption performance of an adsorbent material simply, quickly and correctly. Please refer to Section 1 '', which shows a preferred embodiment of the system in accordance with the present invention. This system has a sample holder for placing different types of sample 114's to be tested, such as activated carbon nonwovens, molecular sieves, masks, mesh or zeolite. The sample holder 100 is located in the reaction chamber 1〇2 and is connected to the gravity measuring device 104 above the reaction chamber 1〇2, which may be hooked, snapped, screwed or otherwise fixed. Further, the weight measuring device 1〇4 may be placed under the reaction chamber 102, and the sample holder 1 is placed on top of the weight measuring device 104. A reaction condition controller 116 may be added to the periphery of the reaction chamber 1 to control conditions such as temperature specific reaction conditions. The environment generating device 108 is connected to the reaction chamber 1〇2 through the input port 11〇 to introduce the generated adsorption or desorption environment into the reaction chamber 1〇2 to cause the sample 114 to be tested to undergo adsorption or desorption reaction. The adsorption or desorption environment is released or exported through the output port U2, for example, to release the vacuum state or to introduce the adsorbed gas. The recording and computing device 106 can pass through a line such as a data transmission line, and the weight measuring device 1 and 4, and the environment generating devices 1 and 8 respectively.

1303715 反應條件控制器116連接。 其中重量測定裝置104可以是電子天秤或任何能測定 重量變化並將數據傳輸給記錄與運算裝置1〇6的儀器。反 應條件控制器116則可以是丨亙溫水浴槽、電子控溫裝置或 蒸汽加熱管等設備。記錄與運算裝置1〇6可以是電腦或其 他具有數據處理與運算功能的裝置。並且記錄與運算裝置 106中更可包含參數設定裝置或/與資料儲存系統。參數設 定裝置可用來控制環境產生裝置或/與反應條件控制器。而 資料儲存系統則儲存吸附或脫附結果以建立成資料庫,並 利用該資料庫進行樣品吸附結果的比較與篩選。環境產生 裝置10 8則用來產生各種吸附與脫附環境,例如揮發性有 機溶劑氣體、氣體與粉成混合物、水蒸氣、熱氣體(如熱氣 氣)或真空狀態。 並根據第1圖所顯示之系統較佳實施例,來敘述一方 法較佳實施例以說明本發明之評估方法。此方法較佳實施 例先將待測樣品114置於樣品座1 〇 〇上/中。再將含有待測 樣品114之樣品座100置入反應室1〇2中並固定在重量測 定裝置104上。隨後重量測定裝置1〇4會偵測待測樣品U4 之初始重:g: ’並將收集到的重量數據傳遞至記錄與運算裝 置 106。 利用記錄與運算裝置106中的參數設定裝置來控制環 境產生裝置以決定產生何種吸附環境,或/與控制反應條件 控制器來決定反應進行的條件。因此,在記錄與運算裝置 106的控制下,藉著反應條件控制器來決定反應條件,如溫 度’並利用環境產生裝置108產生吸附環境,例如揮發性 13037151303715 Reaction condition controller 116 is connected. The weight measuring device 104 may be an electronic scale or any instrument capable of measuring the weight change and transmitting the data to the recording and computing device 1〇6. The reaction condition controller 116 may be a device such as a warm water bath, an electronic temperature control device, or a steam heating tube. The recording and computing device 1 6 can be a computer or other device having data processing and computing functions. Further, the recording and computing device 106 may further include a parameter setting device or/and a data storage system. The parameter setting device can be used to control the environmental generation device or/and the reaction condition controller. The data storage system stores the adsorption or desorption results to create a database, and uses the database to compare and screen the sample adsorption results. The environmental generation device 108 is used to create various adsorption and desorption environments, such as volatile organic solvent gases, gas to powder mixtures, water vapor, hot gases (e.g., hot gases) or vacuum conditions. In accordance with a preferred embodiment of the system shown in Figure 1, a preferred embodiment of the method is described to illustrate the evaluation method of the present invention. The preferred embodiment of the method first places the sample to be tested 114 on/in the sample holder 1 〇 。. The sample holder 100 containing the sample to be tested 114 is placed in the reaction chamber 1〇2 and fixed to the weight measuring device 104. The weight measuring device 1〇4 then detects the initial weight of the sample U4 to be tested: g: ' and transfers the collected weight data to the recording and computing device 106. The parameter setting means in the recording and arithmetic unit 106 is used to control the environment generating means to determine which adsorption environment is generated, or to control the reaction condition controller to determine the conditions under which the reaction proceeds. Therefore, under the control of the recording and computing device 106, the reaction conditions are determined by the reaction condition controller, such as temperature, and the environment generating device 108 is used to generate an adsorption environment, such as volatility 1303715.

有機氣體(如四氣化碳cci4)、濕氣(如水蒸氣)或氣體與粉 塵混合物。隨後通過輸入口 U0將吸附環境導入反應室1〇2 中使待測樣品114進行吸附反應。重量測定裝置1 〇4會在 吸附反應過程中測定任意時間點上待測樣品丨14的重量, 並將測得的重量數據傳輸至記錄與運算裝置1〇6,直到待測 樣品114的重量不再變化為止。利用記錄與運算裝置1〇6 來處理數據以產生待測樣品的吸附結果。吸附結果可以是 吸附重量百分比對時間變化之吸附曲線圖。利用記錄與運 算裝置106中的資料儲存系統來儲存吸附結果以建立成資 料庫。 得到吸附結果後,更可以同一系統進行脫附性能評 估。同樣重量測定裝置104偵測完成吸附反應後的待測樣 品重量。利用環境產生裝置108產生脫附環境,例如真空 狀態或熱氣體(如熱氮氣),並將此脫附環境導入反應室中使 待測樣品進行脫附反應。重量測定裝置1〇4會在脫附反應 過程中測定任意時間點上待測樣品114的重量,並將脫附 後的重量數據傳輸至記錄與運算裝置1〇6。隨後可利用記錄 與運算裝置106執行計算公式A=(c_B)/Bxl〇〇以處理收集 到的數據,以產生待測樣品114的脫附結果。在公式中,A 為吸附重量百分比,B為初始重量,c為任一時間點之樣品 重量。脫附結果可以是吸附重量百分比對時間變化之脫附 曲線圖。再度利用記錄與運算裝置1〇6中的資料儲存系統 來將脫附結果建立在資料庫中。 完成待測樣品114的吸附與脫附反應後,更可再藉著 記錄與運算裝置106來改變環境產生裝置1〇8與反應條件 1303715 控制器116所提供的吸附與脫附環境以及反應條件(如溫 度)’來對同一種測試樣品進行不同吸附與脫附環境下的吸 附丨生此„平估。或是在相同的吸附或脫附環境下,藉著更換 待測樣品114來測試不同吸附材料的吸附性能。最後,可 利用記錄與運算裝f⑽來將各種樣品在不同環境下的吸 附與/或脫附結果建立成資料庫。作為比較各種樣品或同一 樣πα不同環境下的吸附與脫附性能。並可在記錄與運算裝 置1〇6中輸入吸附環境的條件後,利用資料庫中吸附性能 來進行樣品篩選與比較。 以下為數個利用上述系統較佳實施例與方法較佳實施 例來進行待測樣品之吸附與脫附性能評估的較佳實施例。 用來說明本發明之評估系統與方法的優點與效果。 I·二Α隹實施例 山在此較佳實施例中,係利用上述方法與系統來進行活 性碳不織布對四氯化碳的吸附性能評估1料吸附環境 為相對濕度5%的四氯化碳氣體。並洲反應條件裝置將吸 附反應的溫度控制在25t。以上述較佳實施例所提供之方 法來進行評估試驗,所得結果請參考第2圖。 第2圖係為記錄與運算裝置顯示吸附結果的較佳示範 晝面。圖中可具有數個欄位用來標示樣品的材料、吸附反 應條件與吸附氣體種類。並且請參考右下角之圖形棚位, 絲顯示樣品的吸㈣果,此處為活性碳錢布對四氣化 碳之吸附重量百分率對時間作圖所緣出的吸附曲線,用來 表達活性碳錢布的㈣性[結果顯㈣性碳不織布會 12 1303715 在反應進行的前數分鐘内(3〜4分鐘内)即達到餘和吸附量。 第二較佳f施例 在此較佳實施例中,係利用上述之方法與系統來進行 數種市售商品對四氯化碳的吸附性能評估。所使用的樣品 分別為活性碳不織布丨、待測樣品i、活性碳不織布2、待 測樣品2、活性碳口罩丨、活性碳口罩2、活性韻布、待 J樣σσ 3 A J·生兔口罩3與待測樣品4。使用的吸附環境為 相對濕度5%的四氯化碳氣體。並利用反應條件裝置將吸附 反應的溫度控制在25°C。同上述方法較佳實施例所述之步 驟進订評估試驗,並將各樣品之吸附性能結果進行比較。 所得結果請參考第3圖。 第3圖係為記錄與運算裝置顯示比較數種樣品之吸附 結果的較佳示範晝面。圖中,將上述各種樣品在相同吸附 環境下的吸附曲線顯示在同一個座標格上作為比較之用。 1三較佳f施你丨 在此較佳實施例中,係利用上述之方法較佳實施例與 系統較佳實施例來進行活性碳纖維(Active ca]rb〇n fiber; ACF)與顆粒活性碳(Granuiar Active Carbon; GAC)對四氯化 碳的吸附與脫附性能評估。使用的吸附環境為相對濕度5〇/〇 的四氯化碳氣體。並利用反應條件裝置將吸附反應的溫度 控制在34°C,脫附反應溫度控制在u〇°c。並依照上述方 法較佳實施例所述之步驟反覆進行數次的吸附與脫附性能 評估試驗。所得結果請參考第4圖。 13Organic gases (such as four gasified carbon cci4), moisture (such as water vapor) or a mixture of gas and dust. Then, the adsorption environment is introduced into the reaction chamber 1〇2 through the input port U0 to cause the sample 114 to be tested to undergo an adsorption reaction. The weight measuring device 1 〇4 measures the weight of the sample 丨 14 to be tested at any time point during the adsorption reaction, and transmits the measured weight data to the recording and computing device 1〇6 until the weight of the sample 114 to be tested is not Change again. The data is processed by the recording and computing device 1〇6 to produce an adsorption result of the sample to be tested. The adsorption result can be an adsorption curve of the adsorption weight percentage versus time. The data storage system in the recording and computing device 106 is utilized to store the adsorption results to create a repository. After the adsorption results are obtained, the desorption performance evaluation can be performed in the same system. Similarly, the weight measuring device 104 detects the weight of the sample to be tested after the completion of the adsorption reaction. The desorption environment is generated by the environment generating device 108, such as a vacuum state or a hot gas (e.g., hot nitrogen gas), and the desorption environment is introduced into the reaction chamber to cause the sample to be tested to undergo a desorption reaction. The weight measuring device 1〇4 measures the weight of the sample 114 to be tested at any time point during the desorption reaction, and transmits the desorbed weight data to the recording and computing device 1〇6. The calculation formula A = (c_B) / Bxl 随后 can then be performed by the recording and computing device 106 to process the collected data to produce a desorption result of the sample 114 to be tested. In the formula, A is the weight percent of adsorption, B is the initial weight, and c is the weight of the sample at any point in time. The desorption result can be a desorption curve of the adsorption weight percentage versus time. The data storage system in the recording and computing device 1 6 is again utilized to establish the desorption result in the database. After the adsorption and desorption reaction of the sample 114 to be tested is completed, the recording and computing device 106 can be further used to change the adsorption and desorption environment and reaction conditions provided by the environment generating device 1〇8 and the reaction condition 1303715 controller 116 ( If the temperature is 'to evaluate the adsorption of the same test sample in different adsorption and desorption environments, or to measure different adsorptions by replacing the sample to be tested 114 in the same adsorption or desorption environment. The adsorption performance of the material. Finally, the recording and calculation equipment f(10) can be used to establish the data of adsorption and/or desorption of various samples in different environments. As a comparison of various samples or adsorption and desorption in different environments of πα With the performance of the conditions of the adsorption environment in the recording and computing device 1〇6, the sample performance and comparison are performed using the adsorption performance in the database. The following are a few preferred embodiments using the above system preferred embodiment and method. A preferred embodiment for evaluating the adsorption and desorption properties of a sample to be tested is used to illustrate the advantages and effects of the evaluation system and method of the present invention. I. II. Example Mountain In the preferred embodiment, the adsorption performance of activated carbon non-woven fabric for carbon tetrachloride is evaluated by the above method and system. The adsorption environment is carbon tetrachloride with a relative humidity of 5%. The gas and the reaction condition device control the temperature of the adsorption reaction at 25t. The evaluation test is carried out by the method provided in the above preferred embodiment, and the obtained result is referred to the second figure. Fig. 2 shows the recording and calculation device showing adsorption A better example of the results. There are several fields in the figure to indicate the material of the sample, the adsorption reaction conditions and the type of adsorbed gas. Please refer to the graphic shed in the lower right corner, and the silk shows the sample (four) of the sample. The adsorption curve of the weight fraction of activated carbon on the adsorption of carbon monoxide on time is used to express the (four) nature of the activated carbon money cloth [results of (four) carbon non-woven fabrics 12 1303715 in the reaction In the first few minutes (within 3 to 4 minutes), the amount of adsorption and adsorption is reached. Second preferred embodiment In this preferred embodiment, several commercially available products are used in the above-described method and system. Evaluation of the adsorption performance of carbon. The samples used were activated carbon non-woven fabric, sample to be tested i, activated carbon non-woven fabric 2, sample to be tested 2, activated carbon mask, activated carbon mask 2, active rhyme cloth, to be sampled Σσ 3 AJ·raw rabbit mask 3 and sample to be tested 4. The adsorption environment used is carbon tetrachloride gas with a relative humidity of 5%, and the temperature of the adsorption reaction is controlled at 25 ° C by using a reaction condition device. The steps described in the preferred embodiment were evaluated and the results of the adsorption performance of each sample were compared. For the results obtained, please refer to Figure 3. Figure 3 is a comparison of the adsorption results of several samples compared with the recording and computing devices. In the figure, the adsorption curves of the above various samples in the same adsorption environment are displayed on the same coordinate grid for comparison. The preferred embodiment of the above method and the preferred embodiment of the system for the adsorption and desorption of carbon tetrachloride by activated carbon fiber (ACF) and granular activated carbon (GAC) To assess. The adsorption environment used was carbon tetrachloride gas having a relative humidity of 5 〇/〇. The temperature of the adsorption reaction was controlled at 34 ° C by means of a reaction condition device, and the desorption reaction temperature was controlled at u 〇 °c. The adsorption and desorption performance evaluation tests were repeated several times in accordance with the procedure described in the preferred embodiment of the above method. Please refer to Figure 4 for the results obtained. 13

1303715 第4圖中係顯示活性碳纖維與顆粒活性碳在相同條件 下對四氯化碳的吸附與脫附性能進行比較結果。 由上述本發明較佳實施例可知,藉著使用一個可連續 且即時偵測樣品重量變化的重量測定裝置,來免除傳統方 法中為由操作人員將待測樣品自評估系統中取出並測量重 里之動作所造成的人為誤差。且操作人員僅需藉著記錄與 運#裝置來控制所有反應進行的條件,大幅減少人力與時 間的浪費。 此外,根據上述較佳實施例之結果可發現,樣品會在 短時間内即達到吸附飽和狀態。例如第一較佳實施例中, 活性碳不織布在4分鐘以内即達到飽和吸附狀態。相較於 傳統方法與系統無法對前數分鐘内的吸附變化做即時測量 的問題,本發明之系統與方法可於短時間内獲取大量資訊 而顯示出各種樣品的真實吸附性能,如吸附速率、飽和時 間點專吸附特性。 ' 同時,本發明系統能將多種待測物在各種環境條件與 不同吸附氣體種類下所表現出來的吸附與脫附性能建立成 資料庫。並可輸入指定的條件後,利用此資料庫進行各種 材料的吸附性能比對與篩選來選出符合使用者需求的樣 品。更可應用於廣泛領域,如材料吸濕、材料乾燥逮度、 氣體分離、化學品純化以及吸附劑之吸附力測試等具有氣 體重量變化之反應的評估方法與系統。 雖然本發明已以數個較佳實施例揭露如上,然其並非 用以限定本發明,任何熟習此技藝者,在不脫離本發明之 精神和範圍内,當可作各種更動與潤飾,因此本發明之保 優點與實施例1303715 Figure 4 shows the comparison of the adsorption and desorption properties of activated carbon fiber and granular activated carbon for carbon tetrachloride under the same conditions. It can be seen from the above preferred embodiment of the present invention that by using a weight measuring device capable of continuously and instantly detecting the change in the weight of the sample, the conventional method is omitted for the operator to take the sample to be tested from the evaluation system and measure the weight. Human error caused by the action. Moreover, the operator only needs to control the conditions of all reactions by recording and transporting the device, thereby greatly reducing manpower and time waste. Further, according to the results of the above preferred embodiment, it was found that the sample reached the adsorption saturation state in a short time. For example, in the first preferred embodiment, the activated carbon non-woven fabric reaches a saturated adsorption state within 4 minutes. Compared with the conventional method and system, it is impossible to make an instantaneous measurement of the adsorption change in the first few minutes, and the system and method of the present invention can obtain a large amount of information in a short time and display the true adsorption performance of various samples, such as adsorption rate, Special adsorption characteristics at the saturation time point. At the same time, the system of the present invention can establish a data base for the adsorption and desorption properties of various analytes under various environmental conditions and different adsorbed gas species. After inputting the specified conditions, this database can be used to select and match the adsorption performance of various materials to select samples that meet the user's needs. It can be applied to a wide range of fields, such as moisture absorption of materials, material drying arrest, gas separation, chemical purification, and adsorption test of adsorbents, etc., and methods and systems for evaluating the reaction of gas weight changes. While the present invention has been described above in terms of several preferred embodiments, it is not intended to limit the invention, and the invention may be modified and modified without departing from the spirit and scope of the invention. Advantages and embodiments of the invention

1303715 護範圍當視後附之申請專利範圍所界定者為準。 【圖式簡單說明】 為讓本發明之上述和其他目的、特徵、 能更明顯易懂,所附圖式之詳細說明如下: ^第1圖係顯示根據本發明一系統較佳實施例之連續式 氣體吸附性評估系統。 只工 第2圖係顯示根據本發明糸統較佳實施例與方法較佳 實施例所進行活性碳不織布對四氯化碳之吸附性能評估結 果。 第3圖根據本發明系統較佳實施例與方法較佳實施例 所進行數種樣品在相同條件下對四氣化碳的吸附性能評估 結果。 第4圖根據本發明系統較佳實施例與方法較佳實施例 所進行活性碳纖維與顆粒活性碳在相同條件下對四氣化碳 的吸附與脫附性能評估與比較結果。 【主要元件符號說明】 wo :樣品座 104 :重量測定裝置 108 :環境產生裝置 112 :輸出口 116 :反應條件控制器 102 :反應室 106 :記錄與運算裝置 110 :輸入口 114 :待測樣品 151303715 The scope of protection is subject to the definition of the scope of the patent application. BRIEF DESCRIPTION OF THE DRAWINGS In order to make the above and other objects and features of the present invention more apparent, the detailed description of the drawings is as follows: Figure 1 shows a continuation of a preferred embodiment of a system in accordance with the present invention. Gas adsorption evaluation system. Fig. 2 is a view showing the evaluation results of the adsorption performance of activated carbon non-woven fabric on carbon tetrachloride according to a preferred embodiment of the present invention and a preferred embodiment of the method. Figure 3 is a graph showing the results of evaluating the adsorption performance of four gasified carbons under the same conditions for several samples according to a preferred embodiment of the system of the present invention and a preferred embodiment of the method. Fig. 4 is a graph showing the evaluation and comparison of the adsorption and desorption properties of activated carbon fibers and activated carbon on four carbonized carbons under the same conditions according to a preferred embodiment of the system and a preferred embodiment of the method. [Main component symbol description] wo : Sample holder 104 : Weight measuring device 108 : Environment generating device 112 : Output port 116 : Reaction condition controller 102 : Reaction chamber 106 : Recording and arithmetic device 110 : Input port 114 : Sample to be tested 15

Claims (1)

申請專利範圍:Patent application scope: 1·一連續式氣體吸附性評估方法,該方法至少包括: ⑷將-待測樣品安置於—樣品座中,並將含有該待測 樣口口之該樣品座置於一反應室中; ⑻利用-重量測定裝置偵測該待測樣品之初始重量; ⑷利用-環境產生裝置產生一吸附環境,並將該吸附 環境導人該反應室中使該待測樣品進行—吸附反應; ⑷利用該重里測定裝置測定該吸附反應中任意時間點 上該待測樣品的樣品重量; ⑷將初始重量與樣品重量的數據由該重量測定裝置傳 輸至一記錄與運算裝置; /、f)利用該記錄與運算裝置來處理接收到的數據以產生 該待測樣品隨時間變化之_ 口双 Μ 及附結果,並利用該記錄與運 鼻裝置執行含有一公式Μ 飞Α-(C-B)/Bxl〇〇來處理數據,其中 A為吸附重量百分比,b為揭π 马樣π口初始重罝,c為任一時間點 之樣品重量;以及 (g)將該吸附結果建立在一資料庫中。 估古2.如申料利範圍帛1賴述之連續式氣體吸附性 牛驟ΐ =中於⑻步驟後更至少包含—脫附步驟,該联 步驟至少包括: ()利重里測&袭置债測完成該吸附反 樣品的樣品重量; 1 16 1303715 a (1)利_環境產生裝置產生—脫附環境,並將該脫附 衣兄v入該反應至中,使該待測樣品進行—脫附反應; /⑴利用該重量測定裝置測定脫附反應中任意時間點上 該待測樣品的樣品重量; (k) 將測仔的吸附後重量數據由該重量$則定裝置傳輸至 一記錄與運算裝置; (l) 利用該記錄與運算裝置來處理數據以產生該待測樣 品隨時間變化之—脫㈣果,並利觀錄與運算裝置執 打:有-公式A=(C-B)/Bx1⑼來處理數據,其中A為吸附 重量百分比,B為樣品初始重量,c為任一時間點之樣品重 量;以及 (m) 將該脫附結果建立在該資料庫中。 3.如申請專利範圍第1項所述之連續式氣體吸附性評 :方法’請吸附環境為一氣體、—濕氣或一氣體與粉 塵混合物。 4·如申請專利範圍第2 ϋ挪、七 ^ * 項所述之連績式氣體吸附性評 估方法,其中該脫附環垮Α 衣兄马熱氣體或一真空狀態。 5·如申請專利範圍第1 ^ t 項或苐2項所述之連續式氣體 吸附性評估方法,其中()步 ^ ^ fc、 驟與(m)步驟更至少包括利用該 έ己錄與運算裝置在該資料庫 L ^ , 早甲進仃樣品的吸附或脫附結果 比較與篩選。 17A continuous gas adsorption evaluation method, the method comprising at least: (4) placing a sample to be tested in a sample holder, and placing the sample holder containing the mouth of the sample to be tested in a reaction chamber; (8) Detecting the initial weight of the sample to be tested by using a weight measuring device; (4) generating an adsorption environment by using the environment generating device, and guiding the adsorption environment to the reaction sample to perform an adsorption reaction; (4) using the The weight measuring device measures the sample weight of the sample to be tested at any time point in the adsorption reaction; (4) transmitting the data of the initial weight and the sample weight from the weight measuring device to a recording and computing device; /, f) using the recording and The arithmetic device processes the received data to generate a sample of the sample to be tested as a function of time, and attaches the result, and uses the record and the nasal device to perform a formula containing a formula - (CB) / Bxl Processing data, where A is the weight percent of adsorption, b is the initial weight of π horse sample π, c is the weight of the sample at any time point; and (g) the adsorption result is established In the library. Estimated ancient 2. If the continuous gas adsorption bovine ΐ 赖 赖 赖 赖 赖 赖 赖 赖 ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ ΐ The weight of the sample of the adsorption counter sample is completed by the debt test; 1 16 1303715 a (1) The environment-generating device generates a desorption environment, and the desorption chamber is brought into the reaction to make the sample to be tested - desorption reaction; / (1) using the weight measuring device to determine the sample weight of the sample to be tested at any time point in the desorption reaction; (k) transferring the post-adsorption weight data of the measuring piece to the record by the weighting device And the computing device; (1) using the recording and computing device to process the data to generate the sample to be tested over time - (four) fruit, and the viewing and computing device is executed: yes - formula A = (CB) / Bx1 (9) to process the data, where A is the weight percent of adsorption, B is the initial weight of the sample, c is the weight of the sample at any point in time; and (m) the desorption result is established in the database. 3. Continuous gas adsorption evaluation as described in item 1 of the patent application: Method 'Please adsorb the environment as a gas, moisture or a mixture of gas and dust. 4. The method of assessing the gas adsorption of the performance as described in the second paragraph of the patent application, No. 7, VII, wherein the desorption ring is a hot gas or a vacuum state. 5. If the continuous gas adsorption evaluation method described in the Patent Application No. 1 ^ t or 苐 2, wherein the steps ( ), ^ ^ fc, and (m) further include at least the use of the recording and calculation The device was compared and screened in the data library L ^ , the adsorption or desorption results of the early A. 17
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