preparation of the metal&#45;organic framework &#40;mof&#41; sample for nitrogen porosimetry

窒素ポロシメトリーを使用した金属有機フレームワークの特性評価

Relevance of surface area and pore volume 
The accurate characterization of porous materials is imperative to understanding their potential applications. Surface area and pore volume are important quantitative metrics that provide insight into metal-organic framework (MOF) performance in a variety of applications, including gas adsorption, separation, catalysis, and sensing1.
The surface area of a MOF is a parameter that quantifies the amount of surface available for interactions with guest molecules and can affect its performance in various applications2,3. In gas adsorption applications, the surface area of a MOF reflects binding site availability and affinity, which is directly related to its separation performance4. In catalysis applications, MOF surface area can affect the number of active sites and their accessibility to reactant molecules and, thus, their catalytic activity5. The quantity and accessibility of active sites are also relevant in sensing applications, as more guest interactions with active sites lead to improved sensitivity (and potentially selectivity)6. The surface area can also affect the stability of the MOF under extreme conditions, as a larger surface area can indicate a higher number of surface defects7.
The pore volume of a MOF is a parameter that quantifies the amount of void space within the porous structure. It is defined as the total volume of the pores in the MOF, which includes both the open (accessible) and closed (inaccessible) pores. The pore volume of a MOF can affect its performance in various applications, including gas adsorption, separation, and catalysis. Like surface area, the pore volume of a MOF is directly related to its capacity for gas uptake and storage and its ability to allow guest molecules to reach adsorptive or catalytic sites8.
Using nitrogen sorption to determine surface area and pore volume 
Both surface area and pore volume are typically measured using gas adsorption techniques, most commonly nitrogen sorption. Nitrogen is chosen as the adsorbate in Brunauer-Emmett-Teller (BET) analysis due to its quadrupole moment, where the orientation of the nitrogen molecule is dependent on the surface chemistry of the adsorbent, allowing for the formation of a monolayer. The plot of nitrogen uptake as a function of pressure can be used to obtain information about the surface and pore sizes of the MOF. The material surface area and total pore volume can be calculated using the sorption data9. The overall goal of the method detailed here is to obtain nitrogen sorption data and use that data to calculate MOF surface area and pore volume.
The BET method10 is a widely used technique for determining the specific surface area of a porous material, based on the principle that the adsorption of a gas onto a solid surface is a function of the surface area, the properties of the gas molecule, and the system. A known amount of an adsorbate gas (such as nitrogen) is introduced to the sample material over a given pressure range, and the amount of gas adsorbed onto the surface is measured at each pressure increment. The data is used to calculate the specific surface area by relating the adsorbate uptake, pressure, and monolayer capacity, which is represented by the BET equation9:
<img alt="Equation 1" src="/files/ftp_upload/65716/65716eq01.jpg" style="margin: auto;" /> (equation 1; eq. 1)
where: 
p = equilibrium pressure of adsorbate (Pa) 
p0 = adsorbate saturation pressure (Pa) 
n = adsorbate uptake amount (m3/g) 
nm = monolayer capacity (m3/g) 
C = BET constant (unitless)
The monolayer capacity is related to the total surface area by the following equation:
<img alt="Equation 2" src="/files/ftp_upload/65716/65716eq02.jpg" style="margin: auto;" /> (equation 2; eq. 2)
where: 
St = total MOF surface area (m2) 
nm = monolayer capacity (m3/g) 
NAv = Avogadro&#39;s number (molecule/mol) 
scs = cross sectional area of adsorbate molecule (m2/molecule) 
Vmolar = adsorbate molar volume (m3/mol)
The Barrett-Joyner-Halenda (BJH) method11 is a common procedure that utilizes desorption data to calculate the total pore volume. Like the BET method, a known amount of adsorbate gas (often nitrogen) is introduced to the sample. The partial pressure of the adsorbate is then incrementally decreased, and the volume of gas desorbed at each step is measured. Under the assumption that desorption in each pore first occurs in the capillary volume, followed by a reduction in adsorbed layer thickness, the BJH equation relates the volume desorbed to the adsorbed layer thickness, pore radius, and pore volume. This relationship can be represented with a BJH pore size distribution plot, which plots pore radius against pore volume. The distribution is integrated with respect to pore size to determine the total pore volume. The BJH equation12 is written as:
<img alt="Equation 3" src="/files/ftp_upload/65716/65716eq03.jpg" style="margin: auto;" /> (equation 3; eq. 3)
where: 
n = desorption step (unitless) 
vn = volume of pores emptied of capillary condensate (m3) 
&#916;Vn = volume of adsorbate removed from pores (m3) 
&#916;tn = change in adsorbed layer thickness (m) 
A = surface area of pores involved in desorption (m2) 
Rn = BJH constant dependent on average pore size (unitless) 
c = BJH constant, dependent on average adsorbed layer thickness (unitless)

著者スポットライト:吸着挙動を持つ堅牢な金属有機構造体の開発を支援するための多孔質材料の特性評価 

有機金属骨格の表面積と細孔容積の決定

Watch this Scientific Journal Video about Preparation of the Metal-Organic Framework MOF Sample for Nitrogen Porosimetry at JoVE.com

Preparation of the Metal-Organic Framework (MOF) Sample for Nitrogen Porosimetry  

窒素多孔圧測定のための金属有機構造体(MOF)サンプルの調製

まず、空のサンプルチューブの質量を測定します。次に、30〜50ミリグラムの金属有機フレームワークまたはMOF UIO 66をサンプルチューブにロードし、サンプルロードされたチューブの質量を測定します。次に、0.5インチのOリングでシールを固定しながら、サンプルチューブをサンプル前処理システムに取り付けます。チューブを加熱マントルの内側に置きます。温度コントローラーを指定された起動温度である摂氏120度に設定します。次に、システムを真空に接続するバルブを開き、圧力が安定するのを待ってから、指定された活性化時間の24時間サンプルを離れます。その後、チューブを加熱マントルから取り外し、サンプルを室温まで冷却します。サンプルチューブを窒素で埋め戻し、前処理システムから取り出します。最後に、活性化されたサンプルとともにサンプルチューブの質量を測定します。表示された式を使用して、活性化されたサンプルの質量を計算します。

preparation-metal-organic-framework-mof-sample-for-nitrogen

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Chemistry

Preparation of the Metal&#45;Organic Framework &#40;MOF&#41; Sample for Nitrogen Porosimetry

563 ビュー. まず、空のサンプルチューブの質量を測定します。次に、30〜50ミリグラムの金属有機フレームワークまたはMOF UIO 66をサンプルチューブにロードし、サンプルロードされたチューブの質量を測定します。次に、0.5インチのOリングでシールを固定しながら、サンプルチューブをサンプル前処理システムに取り付けます。チューブを加熱マントルの内側に置きます。温?...

ビデオ: Preparation of the Metal-Organic Framework (MOF) Sample for Nitrogen Porosimetry  

Determining Surface Areas and Pore Volumes of Metal-Organic Frameworks

The surface area and pore volume of a metal-organic framework (MOF) can provide insight into its structure and potential applications. Both parameters are commonly determined using the data from nitrogen sorption experiments; commercial instruments to perform these measurements are also widely available. These instruments will calculate structural parameters, but it is essential to understand how to select input data and when calculation methods apply to the sample MOF. This article outlines the use of the Brunauer-Emmett-Teller (BET) method and Barrett-Joyner-Halenda (BJH) method for the calculation of surface area and pore volume, respectively. Example calculations are performed on the representative MOF UiO-66. Although widely applicable to MOFs, sample materials and adsorption data must meet certain criteria for the calculated results to be considered accurate, in addition to proper sample preparation. The assumptions and limitations of these methods are also discussed, along with alternative and complementary techniques for the MOF pore space characterization.

This article describes the use of nitrogen porosimetry to characterize metal-organic frameworks, using UiO-66 as a representative material.

The surface area and pore volume of a metal-organic framework (MOF) can provide insight into its structure and potential applications. Both parameters are ...