Name: surface properties of synthesized nanoporous carbon and silica matrices
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Description: Watch this Scientific Journal Video about Surface Properties of Synthesized Nanoporous Carbon and Silica Matrices at JoVE.com

The authors would like to thank the National Center of Science for providing financial support with grant no. DEC-2013/09/B/ST4/03711 and UMO-2016/22/ST4/00092. The authors are also grateful for the partial support from the Poland Operational Program Human Capital PO KL 4.1.1, as well as from the National Centre for Research and Development, under research grant no. PBS1/A9/13/2012. The authors are especially grateful for Prof. L. Ho&#322;ysz from Interfacial Phenomena Division, Faculty of Chemistry, Maria Curie-Sk&#322;odowska University, Lublin, Poland, for her kindness and enabling the measurements of the wettability in the SBA-15 nanopores.

1. Preparation of the OMC Materials
<ol>
	<li>Synthesis of a silica matrix as OMC precursor
	<ol>
		<li>Prepare 360 mL of 1.6 M HCl by adding 50 mL of HCl (36% - 38%) in a 500 mL round-bottom flask and, then, adding 310 mL of ultrapure water (resistivity of 18.2 M&#937;&#183;cm).</li>
		<li>To that, add 10 g of PE 10500 polymer (6.500 g/mol).</li>
		<li>Place the flask in an ultrasonic bath. Heat the solution to 35 &#176;C and stir it until the solid polymer is completely dissolved, making a homogeneou...

<ol>
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The critical steps during the preparation of the ordered mesoporous carbon material include the preparation of the ordered mesoporous silica materials as the template with well-defined structural properties that affect the properties of the final materials and a tempering/carbonization step under a nitrogen atmosphere. The modification of the typical method of preparation of the mesoporous ordered silicates with cylindrical pores28 concerns the application of an untypical structure-directing agent...

In 1992, ordered nanoporous silica materials were obtained for the first time, using an organic template; since then, a large number of publications related to different aspects of these structures, synthetic methods, the investigation of their properties, their modifications, and different applications have appeared in the literature1,2,3. The interest in SBA-15 nanoporous silica matrix4 is due to their unique quality: a high surface area, wide pores with a uniform pore size distribution, and good chemical and mechanical properties. Nanoporous silica materials with cylindrical pores, such as SBA-155, are often used as a porous matrix for catalysts as they are efficient catalysts in organic reactions6,7. The material can be synthesized with a wide range of methods that can influence their characteristics8,9,10. Therefore, it is crucial to optimize these methods for potential applications in many fields: electrochemical devices, nanotechnology, biology and medicine, drug delivery systems, or in adhesion and tribology. In the present study, two different types of nanoporous structures are presented, namely silica and carbon porous matrices. To compare their properties, the SBA-15 matrix is synthesized using the sol-gel method, and the ordered nanoporous carbon material is prepared by the impregnation of the resulting silica matrix with a carbon precursor.
Porous carbon materials are important in many appliances due to their high surface area and their unique and well-defined physicochemical properties6,11,12. Typical preparation results in materials with randomly distributed porosity and a disordered structure; there is also a limited possibility for the change of the general pore parameters, and thus, structures with relatively broad pore size distributions are obtained13. This possibility is broadened for nanoporous carbon materials with high surface areas and ordered systems of nanopores. More predicted geometry and more control of the physicochemical processes inside the pore space are important in many applications: as catalysts, separation media systems, advanced electronic materials, and nanoreactors in many scientific fields14,15.
To obtain the porous carbon replicas, the ordered silicates can act as a solid matrix to which carbon precursors are directly introduced. The method can be divided into several stages: the selection of ordered silica material; the deposition of a carbon precursor in a silica matrix; carbonization; then, the removal of the silica matrix. Many different types of carbonaceous materials can be obtained by this method, but not all nonporous materials have an ordered structure. An important element of the process is the selection of a suitable matrix whose nanopores must form a stable, three-dimensional structure16.
In this work, the influence of the type of pore walls on the surface properties of synthesized nanoporous matrices is investigated. The surface properties of OMC material are reflected by the surface properties of silica analog (SBA-15) of OMC. The textural and structural properties of both types of materials (OMC and SBA-15) are characterized by low-temperature N2 adsorption/desorption measurements (at 77 K), transmission electron microscopy (TEM), and energy dispersive X-ray analysis (EDX).
Low-temperature gas adsorption/desorption measurement is one of the most important techniques during the characterization of porous materials. Nitrogen gas is used as an adsorbate due to its high purity and the possibility to create a strong interaction with solid adsorbents. Important advantages of this technique are the user-friendly commercial equipment and relatively easy data-processing procedures. The determination of nitrogen adsorption/desorption isotherms is based on the accumulation of the adsorbate molecules on the surface of solid adsorbent at 77 K in a wide range of pressure (P/P0). The Barrett, Joyner, and Halenda (BJH) procedure for calculating the pore size distribution from experimental adsorption or desorption isotherms is applied. The most important assumptions of the BJH method include a planar surface and an even distribution of the adsorbate on the investigated surface. However, this theory is based on the Kelvin equation and it remains the most widely used manner for calculating the pore size distribution in the mesoporous range.
To evaluate the electrochemical character of the samples, a potentiometric titration method is applied. The surface chemistry of the material depends on the surface charge related to the presence of heteroatoms or functional groups on the surface. The surface properties are also investigated by contact angle analysis. The wettability inside the pores provides information about the adsorbate-adsorbent interactions. The influence of the wall roughness on the melting temperature of the water confined in both samples is studied with the dielectric relaxation spectroscopy (DRS) technique. Measurements of the dielectric constant allow the investigation of melting phenomena as the polarizability of the liquid and solid phases are different from each other. A change in the slope of the temperature dependence of the capacitance shows that melting occurs in the system.

<table>
	<tbody>
		<tr>
			<td>1,3,5-trimethylbenzene</td>
			<td>Sigma-Aldrich, Poland</td>
			<td>M7200 Sigma-Aldrich</td>
			<td>Mesitylene, also known as 1,3,5-trimethylbenzene, reagent grade, assay: 98%.</td>
		</tr>
		<tr>
			<td>anhydrous ethanol</td>
			<td>POCH, Avantor Performance Materials Poland S.A.</td>
			<td>396480111</td>
			<td>Assay, min. 99.8 %, analysis-pur (a.p.)</td>
		</tr>
		<tr>
			<td>ASAP 2020. Accelerated Surface Area and Porosimetry System</td>
			<td>Micromeritics Instrument Corporation, Norcross, GA, USA</td>
			<td></td>
			<td>Samples were outgassed before analysis at 120 oC for 24 hours in degas port of analyzer. The dead space volume was measured for calibration on experimental measurement using helium as a adsorbate.</td>
		</tr>
		<tr>
			<td>Automatic burette Dosimat 665</td>
			<td>Metrohm, Switzerland</td>
			<td></td>
			<td>The surface charge properties were experimentally determined by potentiometric titration of the suspension at constant temperature 20&#176;C maintained by the thermostatic device. Prior to potentiometric titration measurements, the solid samples were dried by 24 hours at 120 oC. The initial pH was established by addition of 0.3 cm3 of 0.2 mol/L HCl. T The 0.1 mol/L NaOH solution was used as a titrant, added gradually by using automatic burette.</td>
		</tr>
		<tr>
			<td>Digital pH-meter pHm-240</td>
			<td>Radiometer, Copenhagen</td>
			<td></td>
			<td>Device coupled with automatic burette</td>
		</tr>
		<tr>
			<td>ethyl alcohol</td>
			<td>POCH, Avantor Performance Materials Poland S.A.</td>
			<td>396420420</td>
			<td>Assay, min. 96 %.analysis-pur (a.p.)</td>
		</tr>
		<tr>
			<td>glucose</td>
			<td>POCH, Avantor Performance Materials Poland S.A.</td>
			<td>459560448</td>
			<td>assay 99.5%</td>
		</tr>
		<tr>
			<td>Hydrochloric acid</td>
			<td>POCH, Avantor Performance Materials Poland S.A.</td>
			<td>575283115</td>
			<td>Hydrochloric acid, 35 - 38% analysis-pur (a.p.)</td>
		</tr>
		<tr>
			<td>HOPG graphite substrate</td>
			<td>Spi Supplies</td>
			<td>LOT#1170906</td>
			<td>HOPG SPI-2 Grade, 20x20x1 mm</td>
		</tr>
		<tr>
			<td>Impedance analyzer Solartron 1260</td>
			<td>Solartron</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Pluronic PE 6400 polymer</td>
			<td>BASF (Polska)</td>
			<td></td>
			<td>(EO13PO70EO13)</td>
		</tr>
		<tr>
			<td>Pluronic PE10500</td>
			<td>BASF Canada Inc.</td>
			<td></td>
			<td>Molar mass 6500 g/mol</td>
		</tr>
		<tr>
			<td>potassium hydroxide</td>
			<td>Sigma-Aldrich, Poland</td>
			<td>P5958 Sigma-Aldrich</td>
			<td>BioXtra, &#8805;85% KOH basis</td>
		</tr>
		<tr>
			<td>SEM microscope</td>
			<td>JEOL JSM-7001F</td>
			<td></td>
			<td>Scanning Electron Microscope with EDS detector</td>
		</tr>
		<tr>
			<td>Sigma Force Tensiometer 701</td>
			<td>KSV, Sigma701, Biolin Scientific</td>
			<td></td>
			<td>force tensiometer</td>
		</tr>
		<tr>
			<td>Sulfuric acid (VI)</td>
			<td>POCH, Avantor Performance Materials Poland S.A.</td>
			<td>575000115</td>
			<td></td>
		</tr>
		<tr>
			<td>surface glass type KS 324 Kavalier</td>
			<td>Megan Poland</td>
			<td></td>
			<td>80 % of SiO2 , 11% of Na2O and 9% of CaO</td>
		</tr>
		<tr>
			<td>Tecnai G2 T20 X-TWIN</td>
			<td>FEI, USA</td>
			<td></td>
			<td>Transmission Electron Microscope with EDX detector.</td>
		</tr>
		<tr>
			<td>TEM microscope</td>
			<td>JEOL JEM-1400</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>temperature controller ITC503</td>
			<td>Oxford Instruments</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Tetraethylorthosilicate</td>
			<td>Sigma-Aldrich, Poland</td>
			<td>131903</td>
			<td>Tetraethyl silicate, TEOS, reagent grade, assay 98%</td>
		</tr>
		<tr>
			<td>Ultrapure water</td>
			<td>Millipore, Merck KGaA, Darmstadt, Germany</td>
			<td>SIMSV0001</td>
			<td>Simplicity Water Purification SystemUltrapure Water: 18.2 MegOhm&#183;cm, TOC: &#60;5 ppb</td>
		</tr>
	</tbody>
</table>

surface properties of synthesized nanoporous carbon and silica matrices

In this work, we report the synthesis and characterization of ordered nanoporous carbon material (also called ordered mesoporous carbon material [OMC]) with a 4.6 nm pore size, and ordered silica porous matrix, SBA-15, with a 5.3 nm pore size. This work describes the surface properties of nanoporous molecular sieves, their wettability, and the melting behavior of D2O confined in the differently ordered porous materials with similar pore sizes. For this purpose, OMC and SBA-15 with highly ordered nanoporous structures are synthesized via impregnation of the silica matrix by applying a carbon precursor and by the sol-gel method, respectively. The porous structure of investigated systems is characterized by an N2 adsorption-desorption analysis at 77 K. To determine the electrochemical character of the surface of synthesized materials, potentiometric titration measurements are conducted; the obtained results for OMC shows a significant pHpzc shift toward the higher values of pH, relative to SBA-15. This suggests that investigated OMC has surface properties related to oxygen-based functional groups. To describe the surface properties of the materials, the contact angles of liquids penetrating the studied porous beds are also determined. The capillary rise method has confirmed the increased wettability of the silica walls relative to the carbon walls and an influence of the pore roughness on the fluid/wall interactions, which is much more pronounced for silica than for carbon mesopores. We have also studied the melting behavior of D2O confined in OMC and SBA-15 by applying the dielectric method. The results show that the depression of the melting temperature of D2O in the pores of OMC is about 15 K higher relative to the depression of the melting temperature in SBA-15 pores with a comparable 5 nm size. This is caused by the influence of adsorbate/adsorbent interactions of the studied matrices.

To characterize the porous structure of the investigated samples of OMC and SBA-15, the N2 adsorption-desorption isotherms were recorded at 77 K. The experimental N2 gas adsorption-desorption isotherms characterizing the investigated systems, as well as the pore size distributions (PSD) obtained from the adsorption and desorption data, are presented in Figure 1A-D. The position of the inflection points on the sorption is...

Watch this Scientific Journal Video about Surface Properties of Synthesized Nanoporous Carbon and Silica Matrices at JoVE.com

Surface Properties of Synthesized Nanoporous Carbon and Silica Matrices

Here we report the synthesis and characterization of ordered nanoporous carbon (with a 4.6 nm pore size) and SBA-15 (with a 5.3 nm pore size). The work describes the surface and textural properties of nanoporous molecular sieves, their wettability, and the melting behavior of D2O confined in the materials.

In this work, we report the synthesis and characterization of ordered nanoporous carbon material (also called ordered mesoporous carbon material [OMC]) ...

Research

JoVE Journal

Chemistry

Preparation of Silica Nanoparticles Through Microwave-assisted Acid-catalysis

Microwave-assisted synthetic techniques were used to quickly and reproducibly produce silica nanoparticle sols using an acid catalyst with nanoparticle ...

Exploring the Radical Nature of a Carbon Surface by Electron Paramagnetic Resonance and a Calibrated Gas Flow

While the first Electron Paramagnetic Resonance (EPR) studies regarding the effects of oxidation on the structure and stability of carbon radicals date ...

Synthesis and Catalytic Performance of Gold Intercalated in the Walls of Mesoporous Silica

As a promising catalytically active nano reactor, gold nanoparticles intercalated in mesoporous silica (GMS) were successfully synthesized and properties ...

Transport of Surface-modified Carbon Nanotubes through a Soil Column

Carbon nanotubes (CNTs) are widely manufactured nanoparticles, which are being utilized in a number of consumer products, such as sporting goods, ...

Preparation of Carbon Nanosheets at Room Temperature

Amphiphilic molecules equipped with a reactive, carbon-rich "oligoyne" segment consisting of conjugated carbon-carbon triple bonds self-assemble into ...

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions

Palladium N-Heterocyclic Carbene Complexes: Synthesis from Benzimidazolium Salts and Catalytic Activity in Carbon-carbon Bond-forming Reactions

Detailed and generalized protocols are presented for the synthesis and subsequent purification of four palladium N-heterocyclic carbene complexes from ...

TiO2-coated Hollow Glass Microspheres with Superhydrophobic and High IR-reflective Properties Synthesized by a Soft-chemistry Method

TiO2-coated Hollow Glass Microspheres with Superhydrophobic and High IR-reflective Properties Synthesized by a Soft-chemistry Method

This manuscript proposes a soft-chemistry method to develop superhydrophobic and highly IR-reflective hollow glass microspheres (HGM). The anatase TiO2 ...

Time-resolved Photophysical Characterization of Triplet-harvesting Organic Compounds at an Oxygen-free Environment Using an iCCD Camera

Here, we present a sensible method of the acquisition and analysis of time-resolved photoluminescence using an ultrafast iCCD camera. This system enables ...

Raman and IR Spectroelectrochemical Methods as Tools to Analyze Conjugated Organic Compounds

In the presented work, two spectroelectrochemical techniques are discussed as tools for the analysis of the structural changes occurring in the molecule ...

Preparation of Functional Silica Using a Bioinspired Method

The goal of the protocols described herein is to synthesize bioinspired silica materials, perform enzyme encapsulation therein, and partially or totally ...