Microstructural and porosimetry analysis of Ag-TiO2intercalated kaolin and diatomite as nanocomposite ceramic materials

Clay Minerals ◽  
2018 ◽  
Vol 53 (4) ◽  
pp. 665-674 ◽  
Author(s):  
Emmanuel Ajenifuja ◽  
Abimbola P.I. Popoola ◽  
Kabir O. Oyedotun ◽  
Olawale Popoola
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Ceramic Materials ◽  
Mineral Particle ◽  
Scanning Calorimetry ◽  
Sintered Ceramic ◽  
Morphological Studies ◽  
Bet Specific Surface Area ◽  
Bet Analysis

ABSTRACTKaolin and diatomite are abundant and widely available geological materials that may immobilize or stabilize functional chemical species on their surfaces for various applications. Acid-treated kaolin and diatomite were intercalated with photocatalyst Ag-TiO2nanoparticles using the sol–gel technique to prepare nanocomposite ceramic materials. The nanocomposites were sintered between 900°C and 1000°C to induce thermal reactions and to enhance nanoparticle–substrate attachment. Chemical and thermal characterizations of the acid-treated materials and intercalated nanocomposites were performed with energy-dispersive X-ray (EDX) analysis and differential scanning calorimetry (DSC), respectively. The Brunauer–Emmett–Teller (BET)-specific surface area and scanning electron microscopy (SEM) were employed for physical and microstructural characterization of the nanocomposites, respectively. Morphological studies revealed a uniform distribution of Ag-TiO2nanocrystallites in pores and on mineral particle surfaces. The BET analysis showed remarkable surface and grain modification by sintering. Decreases in the BET-specific surface area were observed for the sintered ceramic nanocomposite, Ag-TiO2-kaolin (20.244 to 5.446 m2/g) and Ag-TiO2-diatomite (19.582 to 10.148 m2/g).

scholarly journals Modificação das propriedades da poliamida 12 pela incorporação de carbonato de cálcio nanoparticulado

2020 ◽  
Author(s):  
◽  
R. M. S. Teotonio
Keyword(s):  
Impact Strength ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Flexural Modulus ◽  
Mechanical And Thermal Properties ◽  
Scanning Calorimetry ◽  
Crystallinity Degree ◽  
Bet Analysis ◽  
The Matrix

Polyamide 12 (PA12) was modified by incorporating calcium carbonate nanoparticles (NPCC) to analyze the effect of the filler content on the mechanical and thermal properties of the final nanocomposites. Compositions containing 0.1, 0.2, 0.5, 1, 5 and 10 wt% of Socal 312 and 10 wt% of Socal U1S2 were analyzed. Furthermore, extruded and non-extruded PA12 were compared. NPCC was characterized through BET analysis (Brunauer, Emmett and Teller), which confirmed that Socal 312 had a specific surface area superior to Socal U1S2. Scanning electron microscopy revealed a tendency of the particles to agglomerate at 1 wt% NPCC and higher. However, all samples showed good distribution of the filler throughout the matrix. Differential Scanning Calorimetry (DSC) analyses did not show differences in the melting temperature of the compositions. Crystallization temperature tends to increase as the amount of filler in the matrix increases. Crystallinity degree showed differences only when comparing extruded and non-extruded PA12, the same occurs with Socal 312 in relation to Socal U1S2 containing 10 wt% of filler. Thermogravimetric analysis (TGA) showed that for contents from 0.5 wt% NPCC, increasing NPCC content reduces the thermal stability of the material. Muffle calcination tests confirmed the residues content obtained with TGA at 5 wt% NPCC higher, and evidenced good distribution of the filler along the specimen. Tensile and flexural strength and tensile and flexural modulus started increasing at 1 wt% NPCC and HDT started increasing at 0.2 wt% NPCC, showing the reinforcing effect of nanofiller and the increase in stiffness of the materials. Impact strength at 23 °C decreased at 0.5 wt% NPCC. Impact strength at -40 °C reduced only with addition of 10 wt% NPCC. Strain at break, toughness and impact strength at 23 °C showed reduction in extruded PA12 when compared to non-extruded PA12, possibly because extrusion favors the increase in crystallinity, as verified in the DSC analysis. Socal U1S2 also showed differences in relation to Socal 312 in strain at break, flexural modulus and HDT, probably due to its lower specific surface area in relation to Socal 312. Therefore, the incorporation of 1 wt% NPCC in PA12, already allows to obtain a nanocomposite with greater mechanical strength compared to neat PA12, which can be a feasible alternative for applications where an increase in mechanical properties is desired

scholarly journals Chemical Structure and Microstructure Characterization of Ladder-Like Silsesquioxanes Derived Porous Silicon Oxycarbide Materials

Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1340
Author(s):  
Jakub Marchewka ◽  
Piotr Jeleń ◽  
Izabela Rutkowska ◽  
Patryk Bezkosty ◽  
Maciej Sitarz
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Porous Ceramic ◽  
Sol Gel ◽  
Ceramic Materials ◽  
Porous Ceramics ◽  
Silicon Oxycarbide ◽  
Bet Analysis ◽  
Structure And Microstructure

The aim of this work was to synthesize porous ceramic materials from the SiOC system by the sol-gel method and the subsequent pyrolysis. The usage of two types of precursors (siloxanes) was determined by Si/C ratio in starting materials. It allows us to control the size of the pores and specific surface area, which are crucial for the potential applications of the final product after thermal processing. Methyltrimethoxysilane and dimethyldiethoxysilane were mixed in three different molar ratios: 4:1, 2:1, and 1:1 to emphasize Si/C ratio impact on silicon oxycarbide glasses properties. Structure and microstructure were examined both for xerogels and obtained silicon oxycarbide materials. Brunauer-Emmett-Teller (BET) analysis was performed to confirm that obtained materials are porous and Si/C ratio in siloxanes precursors affects porosity and specific surface area. This kind of porous ceramics could be potentially applied as gas sensors in high temperatures, catalyst supports, filters, adsorbents, or advanced drug delivery systems.

scholarly journals Effect of Glycero-(9,10-trioxolane)-trialeate on the Physicochemical Properties of Non-Woven Polylactic Acid Fiber Materials

Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2517
Author(s):  
Anatoliy Olkhov ◽  
Olga Alexeeva ◽  
Marina Konstantinova ◽  
Vyacheslav Podmasterev ◽  
Polina Tyubaeva ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Polylactic Acid ◽  
Specific Surface Area ◽  
Water Sorption ◽  
Fiber Surface ◽  
High Water ◽  
Scanning Calorimetry ◽  
Fiber Mats ◽  
Fiber Materials

Biocompatible glycero (9,10-trioxolane) trioleate (ozonide of oleic acid triglyceride, OTOA) was incorporated into polylactic acid (PLA) fibers by electrospinning and nonwoven PLA mats with 1%, 3% and 5% OTOA content. The morphological, mechanical, thermal and water sorption properties of electrospun PLA mats after the addition of OTOA were studied. A morphological analysis showed that the addition of OTOA increased the average fiber diameter and induced the formation of pores on the fiber surface, leading to an increase in the specific surface area for OTOA-modified PLA fibrous mats. PLA fiber mats with 3% OTOA content were characterized by a highly porous surface morphology, an increased specific surface area and high-water sorption. Differential scanning calorimetry (DSC) was used to analyze the thermal properties of the fibrous PLA mats. The glass transition temperatures of the fibers from the PLA–OTOA composites decreased as the OTOA content increased, which was attributed to the plasticizing effect of OTOA. DSC results showed that OTOA aided the PLA amorphization process, thus reducing the crystallinity of the obtained nonwoven PLA–OTOA materials. An analysis of the mechanical properties showed that the tensile strength of electrospun PLA mats was improved by the addition of OTOA. Additionally, fibrous PLA mats with 3% OTOA content showed increased elasticity compared to the pristine PLA material. The obtained porous PLA electrospun fibers with the optimal 3% OTOA content have the potential for various biomedical applications such as drug delivery and in tissue engineering.

scholarly journals Tuning the Morphological Properties of Cellulose Aerogels: An Investigation of Salt-Mediated Preparation

2021 ◽  
Author(s):  
Prakash Parajuli ◽  
Sanjit Acharya ◽  
Julia Shamshina ◽  
Noureddine Abidi
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Earth Metal ◽  
Morphological Properties ◽  
Cellulose Solution ◽  
Bet Analysis ◽  
Sol Gel Transition ◽  
Gel Transition

Abstract In this study, alkali and alkaline earth metal chlorides with different cationic radii (LiCl, NaCl, and KCl, MgCl2, and CaCl2) were used to gain insight into the behavior of cellulose solutions in the presence of salts. The specific focus of the study was evaluation of the effect of salts’ addition on the sol-gel transition of the cellulose solutions and on their ability to form monoliths, as well as evaluation of the morphology (e.g., specific surface area, pore characteristics, and microstructure) of aerocelluloses prepared from these solutions. The effect of the salt addition on the sol-gel transition of cellulose solutions was studied using rheology, and morphology of resultant aerogels was evaluated by Scanning Electron Microscopy (SEM) and Brunauer-Emmett-Teller (BET) analysis, while the salt influence on the aerocelluloses’ crystalline structure and thermal stability was evaluated using powder X-Ray Diffraction (pXRD) and Thermogravimetric Analysis (TGA), respectively. The study revealed that the effect of salts’ addition was dependent on the component ions and their concentration. The addition of salts in the amount below certain concentration limit significantly improved the ability of the cellulose solutions to form monoliths and reduced the sol-gel transition time. Salts of lower cationic radii had a greater effect on gelation. However, excessive amount of salts resulted in the formation of fragile monoliths or no formation of gels at all. Analysis of surface morphology demonstrated that the addition of salts resulted in a significant increase in porosity and specific surface area, with salts of lower cationic radii leading to aerogels with much larger (~1.5 and 1.6-fold for LiCl and MgCl2, respectively) specific surface area compared to aerocelluloses prepared with no added salt. Thus, by adding the appropriate salt into the cellulose solution prior to gelation, the properties of aerocelluloses that control material’s performance (specific surface area, density, and porosity) could be tailored for a specific application.

scholarly journals The Effects of Silica-Based Fillers on the Properties of Epoxy Molding Compounds

Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1811 ◽  
Author(s):  
Mitja Linec ◽  
Branka Mušič
Keyword(s):  
Mechanical Properties ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Fused Silica ◽  
Spiral Flow ◽  
Scanning Calorimetry ◽  
Molding Compounds ◽  
Material Development ◽  
The Impact

Global design and manufacturing of the materials with superb properties remain one of the greatest challenges on the market. The future progress is orientated towards researches into the material development for the production of composites of better mechanical properties to the existing materials. In the field of advanced composites, epoxy molding compounds (EMCs) have attained dominance among the common materials due to their excellent properties that can be altered by adding different fillers. One of the main fillers is often based on silicon dioxide (SiO2). The concept of this study was to evaluate the effects of the selected silica-based fillers on the thermal, rheological, and mechanical properties of EMCs. Various types of fillers with SiO2, including crystalline silica and fused silica, were experimentally studied to clarify the impact of filler on final product. Fillers with different shape (scanning electron microscope, SEM), along with different specific surface area (specific surface area analyzer, BET method) and different chemical structure, were tested to explore their modifications on the EMCs. The influence of the fillers on the compound materials was determined with the spiral flow length (spiral flow test, EMMI), glass transition temperature (differential scanning calorimetry, DSC), and the viscosity (Torque Rheometer) of the composites.

N2-BET specific surface area of bentonites

2010 ◽  
Vol 349 (1) ◽  
pp. 275-282 ◽  
Author(s):  
S. Kaufhold ◽  
R. Dohrmann ◽  
M. Klinkenberg ◽  
S. Siegesmund ◽  
K. Ufer
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Bet Specific Surface Area
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