scholarly journals Silica-Based Composites with Enhanced Rheological Properties Thanks to a Nanosized Graphite Functionalized with Serinol Pyrrole

2021 ◽  
Vol 11 (23) ◽  
pp. 11410
Author(s):  
Gea Prioglio ◽  
Silvia Agnelli ◽  
Stefano Pandini ◽  
Maurizio Galimberti
Keyword(s):  
Rheological Properties ◽  
High Surface ◽  
High Surface Area ◽  
Minor Amount ◽  
Carbon Filler ◽  
Hybrid Filler ◽  
Carbon Efficiency ◽  
Dynamic Rigidity ◽  
A Minor ◽  
New Generation

Silica-based rubber composites have tremendous importance, as they allow the reduction in hysteresis in demanding dynamic-mechanical applications such as tire compounds and hence have a lower environmental impact. However, they also present drawbacks such as poor rheological behavior. In this work, an innovative silica-based hybrid filler system was developed, obtaining a rubber composite with an improved set of properties. A nanosized high surface area graphite (HSAG) was functionalized with 2-(2,5-dimethyl-1H-pyrrol-1-yl)propane-1,3-diol, serinol pyrrole (SP), through a simple process characterized by a high carbon efficiency. The HSAG-SP adduct, with about nine parts of SP per hundred parts of carbon filler, was used to form a hybrid filler system with silica. An elastomeric composite, with poly(styrene-co-butadiene) from anionic polymerization and poly(1,4-cis-isoprene) from Hevea brasiliensis was prepared with 50 parts of silica, which was replaced in a minor amount (15%) by either pristine HSAG or HSAG-SP. The best set of composite properties was obtained with HSAG-SP: the same dynamic rigidity and hysteresis and tensile properties of the silica-based material and appreciably better rheological properties, particularly in terms of flowability. This work paves the way for a new generation of silica-based composites, with improved properties, based on a hybrid filler system with a nanosized edge functionalized graphite.

Selectivity of high surface area Ce0.68Zr0.32O2 for the new generation of TWC under environments with different redox character

2001 ◽  
Vol 33 (4) ◽  
pp. 303-314 ◽  
Author(s):  
Juan R González-Velasco ◽  
Miguel A Gutiérrez-Ortiz ◽  
Jean-Louis Marc ◽  
M.Pilar González-Marcos ◽  
Gilbert Blanchard
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
New Generation

scholarly journals Development of a Novel Adsorbent Prepared from Dredging Sediment for Effective Removal of Dye in Aqueous Solutions

2021 ◽  
Vol 11 (22) ◽  
pp. 10722
Author(s):  
Abdelkader Ouakouak ◽  
Messameh Abdelhamid ◽  
Barhoumi Thouraya ◽  
Hadj-Otmane Chahinez ◽  
Grabi Hocine ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Adsorption Process ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Dye Adsorption ◽  
Isotherm Models ◽  
Effective Removal ◽  
Water Media ◽  
A Minor

This study proposed a novel and low-cost adsorbent prepared from dredging sediment (DSD) for effective removal of dye in aqueous solutions. The adsorption efficiency and behavior of the DSD adsorbent toward the crystal violet (CV), a cationic dye, were investigated via batch experiments. The results showed that DSD samples contain mainly clay minerals (illite and kaolinite) and other mineral phases. In addition, DSD is a mesoporous material (Vmesopore = 94.4%), and it exhibits a relatively high surface area (~39.1 m2/g). Adsorption experiments showed that the solution’s pH slightly affects the adsorption process, and a pH of 11 gave a maximum capacity of 27.2 mg/g. The kinetic data of CV dye adsorption is well described by the pseudo–second-order and the Avrami models. The Langmuir and Liu isotherm models provide the best fit for the adsorption equilibrium data. The monolayer adsorption capacity of Langmuir reached 183.6, 198.0, and 243.6 mg/g at 293, 308, and 323 K, respectively. It was also found that the adsorption process was spontaneous (−ΔG°), exothermic (−∆H°), and increased the randomness (+∆S°) during the adsorption operation. The primary mechanisms in CV dye adsorption were ion exchange and pore filling, whereas electrostatic attraction was a minor contribution. In addition, three steps involving intraparticle diffusion occur at the same time to control the adsorption process. The results of this study highlight the excellent efficiency of DSD material as an ecofriendly sorbent for toxic dyes from water media.

FILLER NETWORKING OF A NANOGRAPHITE WITH A HIGH SHAPE ANISOTROPY AND SYNERGISM WITH CARBON BLACK IN POLY(1,4-CIS-ISOPRENE)–BASED NANOCOMPOSITES

2014 ◽  
Vol 87 (2) ◽  
pp. 197-218 ◽  
Author(s):  
Maurizio Galimberti ◽  
Vineet Kumar ◽  
Michele Coombs ◽  
Valeria Cipolletti ◽  
Silvia Agnelli ◽  
...  
Keyword(s):  
Carbon Black ◽  
High Surface ◽  
High Surface Area ◽  
Shape Anisotropy ◽  
Hybrid Filler ◽  
Neat Polymer ◽  
Simple Addition ◽  
Mechanical Measurements ◽  
Initial Modulus ◽  
Filler Network

ABSTRACT A nanoGraphite (nanoG) having a high surface area and a high shape anisotropy, defined as the ratio between the crystallite dimensions in a direction orthogonal and parallel to structural layers, was used to prepare nanocomposites based on poly(1,4-cis-isoprene) (IR), in the neat polymer matrix and in the presence of carbon black (CB). Tensile and dynamic-mechanical measurements showed that nanoG forms a filler network at a relatively low concentration in neat IR and a hybrid filler network at a lower nanoG concentration in the presence of CB. A synergistic effect between the two carbon allotropes was found: composites containing both fillers present initial modulus values much higher than those calculated through the simple addition of the initial moduli of the composites containing only CB or nanoG.

In Situ microscopy of the anodic etching of silicon

1995 ◽  
Vol 53 ◽  
pp. 232-233
Author(s):  
Frances M. Ross ◽  
Peter C. Searson
Keyword(s):  
Composite Structures ◽  
High Surface ◽  
High Surface Area ◽  
Chemical Properties ◽  
Selective Etching ◽  
Silicon On Insulator ◽  
Second Phase ◽  
Porous Layers ◽  
New Class ◽  
Porous Semiconductors

Porous semiconductors represent a relatively new class of materials formed by the selective etching of a single or polycrystalline substrate. Although porous silicon has received considerable attention due to its novel optical properties1, porous layers can be formed in other semiconductors such as GaAs and GaP. These materials are characterised by very high surface area and by electrical, optical and chemical properties that may differ considerably from bulk. The properties depend on the pore morphology, which can be controlled by adjusting the processing conditions and the dopant concentration. A number of novel structures can be fabricated using selective etching. For example, self-supporting membranes can be made by growing pores through a wafer, films with modulated pore structure can be fabricated by varying the applied potential during growth, composite structures can be prepared by depositing a second phase into the pores and silicon-on-insulator structures can be formed by oxidising a buried porous layer. In all these applications the ability to grow nanostructures controllably is critical.

Electron holography of catalysts

1995 ◽  
Vol 53 ◽  
pp. 416-417
Author(s):  
A. K. Datye ◽  
D. S. Kalakkad ◽  
L. F. Allard ◽  
E. Völkl
Keyword(s):  
Heterogeneous Catalysts ◽  
High Surface ◽  
High Surface Area ◽  
Atomic Scale ◽  
Nano Particles ◽  
Phase Image ◽  
Electron Holography ◽  
Specimen Thickness ◽  
Phase Information ◽  
Particle Structure

The active phase in heterogeneous catalysts consists of nanometer-sized metal or oxide particles dispersed within the tortuous pore structure of a high surface area matrix. Such catalysts are extensively used for controlling emissions from automobile exhausts or in industrial processes such as the refining of crude oil to produce gasoline. The morphology of these nano-particles is of great interest to catalytic chemists since it affects the activity and selectivity for a class of reactions known as structure-sensitive reactions. In this paper, we describe some of the challenges in the study of heterogeneous catalysts, and provide examples of how electron holography can help in extracting details of particle structure and morphology on an atomic scale.Conventional high-resolution TEM imaging methods permit the image intensity to be recorded, but the phase information in the complex image wave is lost. However, it is the phase information which is sensitive at the atomic scale to changes in specimen thickness and composition, and thus analysis of the phase image can yield important information on morphological details at the nanometer level.

Structure and composition of metal particles in Pt-Sn/Al2O3 bimetallic catalysts

1990 ◽  
Vol 48 (4) ◽  
pp. 278-279
Author(s):  
A. Sachdev ◽  
J. Schwank
Keyword(s):  
Bimetallic Catalysts ◽  
Bimetallic Catalyst ◽  
Size Structure ◽  
High Surface ◽  
High Surface Area ◽  
Metal Particles ◽  
Alloy Formation ◽  
Particle Size Range ◽  
Oxide Supports ◽  
Petroleum Fractions

Platinum - tin bimetallic catalysts have been primarily utilized in the chemical industry in the catalytic reforming of petroleum fractions. In this process the naphtha feedstock is converted to hydrocarbons with higher octane numbers and high anti-knock qualities. Most of these catalysts contain small metal particles or crystallites supported on high surface area insulating oxide supports. The determination of the structure and composition of these particles is crucial to the understanding of the catalytic behavior. In a bimetallic catalyst it is important to know how the two metals are distributed within the particle size range and in what way the addition of a second metal affects the size, structure and composition of the metal particles. An added complication in the Pt-Sn system is the possibility of alloy formation between the two elements for all atomic ratios.

Intercalation of First Row Transition Metals inside Covalent-Organic Frameworks (COF): a Strategy to Fine Tune the Electronic Properties of Porous Crystalline Materials

2018 ◽  
Author(s):  
Srimanta Pakhira ◽  
Jose Mendoza-Cortes
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Electronic Properties ◽  
High Surface ◽  
Electronic Devices ◽  
High Surface Area ◽  
Main Role ◽  
Covalent Organic Frameworks ◽  
Porous Network ◽  
Crystalline Materials

<div>Covalent organic frameworks (COFs) have emerged as an important class of nano-porous crystalline materials with many potential applications. They are intriguing platforms for the design of porous skeletons with special functionality at the molecular level. However, despite their extraordinary properties, it is difficult to control their electronic properties, thus hindering the potential implementation in electronic devices. A new form of nanoporous material, COFs intercalated with first row transition metal is proposed to address this fundamental drawback - the lack of electronic tunability. Using first-principles calculations, we have designed 31 new COF materials <i>in-silico</i> by intercalating all of the first row transition metals (TMs) with boroxine-linked and triazine-linked COFs: COF-TM-x (where TM=Sc-Zn and x=3-5). This is a significant addition considering that only 187 experimentally COFs structures has been reported and characterized so far. We have investigated their structure and electronic properties. Specifically, we predict that COF's band gap and density of states (DOSs) can be controlled by intercalating first row transition metal atoms (TM: Sc - Zn) and fine tuned by the concentration of TMs. We also found that the $d$-subshell electron density of the TMs plays the main role in determining the electronic properties of the COFs. Thus intercalated-COFs provide a new strategy to control the electronic properties of materials within a porous network. This work opens up new avenues for the design of TM-intercalated materials with promising future applications in nanoporous electronic devices, where a high surface area coupled with fine-tuned electronic properties are desired.</div>

Tenacious Mass Transfer Limitations Drive Catalytic Selectivity during Electrochemical Carbon Dioxide Reduction

2019 ◽  
Author(s):  
Kailun Yang ◽  
Recep Kas ◽  
Wilson A. Smith
Keyword(s):  
Surface Area ◽  
High Surface ◽  
High Surface Area ◽  
Catalyst Layer ◽  
Active Surface ◽  
Active Surface Area ◽  
High Concentration ◽  
Copper Electrodes ◽  
Surface Enhanced ◽  
Local Current

<p>This study evaluated the performance of the commonly used strong buffer electrolytes, i.e. phosphate buffers, during CO<sub>2</sub> electroreduction in neutral pH conditions by using in-situ surface enhanced infrared absorption spectroscopy (SEIRAS). Unfortunately, the buffers break down a lot faster than anticipated which has serious implications on many studies in the literature such as selectivity and kinetic analysis of the electrocatalysts. Increasing electrolyte concentration, surprisingly, did not extend the potential window of the phosphate buffers due to dramatic increase in hydrogen evolution reaction. Even high concentration phosphate buffers (1 M) break down within the potentials (-1 V vs RHE) where hydrocarbons are formed on copper electrodes. We have extended the discussion to high surface area electrodes by evaluating electrodes composed of copper nanowires. We would like highlight that it is not possible to cope with high local current densities on these high surface area electrodes by using high buffer capacity solutions and the CO<sub>2</sub> electrocatalysts are needed to be evaluated by casting thin nanoparticle films onto inert substrates as commonly employed in fuel cell reactions and up to now scarcely employed in CO<sub>2</sub> electroreduction. In addition, we underscore that normalization of the electrocatalytic activity to the electrochemical active surface area is not the ultimate solution due to concentration gradient along the catalyst layer.This will “underestimate” the activity of high surface electrocatalyst and the degree of underestimation will depend on the thickness, porosity and morphology of the catalyst layer. </p> <p> </p>

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