scholarly journals Preparation of a Photosensitive Composite Carbon Fiber for Spilled Oil Cleaning

2022 ◽  
Vol 6 (1) ◽  
pp. 28
Author(s):  
Yong X. Gan ◽  
Ali Arjan ◽  
Jimmy Yik

This paper deals with preparing a functional composite carbon fiber with a large surface area for spilled oil cleaning. The composite fiber consisted of photosensitive oxide particles and polymer-derived carbon. It was made by co-spinning the polymer and metallic compounds. After heat treatment at high temperatures, an activated carbon fiber containing oxide particles was obtained. The particles were found distributed in the fiber and at the surface of the fiber. The composite fiber was found sensitive to sunlight. Fiber mats made of the composite fiber possessed a high surface area for oil absorption and removal. Cobalt(II) titanate particles were obtained from the reaction of titanium dioxide and cobalt oxide. The reaction happened in situ through the hydrolysis of metallic compounds in the spun fiber. The titanium dioxide and cobalt(II) titanate particle-containing fibers demonstrated the photoactivity in the visible light spectrum. It was concluded that particle-containing composite carbon fiber mats can be prepared successfully by co-electrospinning. Due to the oleophilic property and the high active surface area, the composites are suitable for spilled oil cleaning through fast absorption.

2021 ◽  
Vol 28 (4) ◽  
Author(s):  
Johannes Erben ◽  
Alenica Heußner ◽  
Simon Thiele ◽  
Sven Kerzenmacher

AbstractFirst, we present a fabrication process for electrospun carbon fiber mats with mean fiber diameters between 108 nm and 623 nm. The carbon fiber mats were produced by electrospinning of polyacrylonitrile (PAN) solutions and subsequent carbonization. The fiber mats feature small variations of their properties that are required for parameter studies. Second, we investigate the kinetics of steam and CO2 activation with three different activation temperatures and times. Both activation methods result in a surface area increase depending on activation temperature and time. Detailed analysis of the macroscopic properties burn-off, surface area, and conductivity reveals insights into the microscopic activation kinetics. The different fiber diameters of the carbon fiber mats enable the distinction of surface driven and bulk processes. Our results indicate, that CO2 activation kinetics are mass transport controlled, and that steam activation kinetics are reaction rate controlled. The turbostratic nature of PAN derived carbon and the distinct characteristics of the activation agents could explain the nonlinear behavior of the burn-off and surface area development.


Author(s):  
Kailun Yang ◽  
Recep Kas ◽  
Wilson A. Smith

<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>


Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 256
Author(s):  
Irina V. Pushkareva ◽  
Artem S. Pushkarev ◽  
Valery N. Kalinichenko ◽  
Ratibor G. Chumakov ◽  
Maksim A. Soloviev ◽  
...  

Platinum (Pt)-based electrocatalysts supported by reduced graphene oxide (RGO) were synthesized using two different methods, namely: (i) a conventional two-step polyol process using RGO as the substrate, and (ii) a modified polyol process implicating the simultaneous reduction of a Pt nanoparticle precursor and graphene oxide (GO). The structure, morphology, and electrochemical performances of the obtained Pt/RGO catalysts were studied and compared with a reference Pt/carbon black Vulcan XC-72 (C) sample. It was shown that the Pt/RGO obtained by the optimized simultaneous reduction process had higher Pt utilization and electrochemically active surface area (EASA) values, and a better performance stability. The use of this catalyst at the cathode of a proton exchange membrane fuel cell (PEMFC) led to an increase in its maximum power density of up to 17%, and significantly enhanced its performance especially at high current densities. It is possible to conclude that the optimized synthesis procedure allows for a more uniform distribution of the Pt nanoparticles and ensures better binding of the particles to the surface of the support. The advantages of Pt/RGO synthesized in this way over conventional Pt/C are the high electrical conductivity and specific surface area provided by RGO, as well as a reduction in the percolation limit of the components of the electrocatalytic layer due to the high aspect ratio of RGO.


Polymers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 2517
Author(s):  
Anatoliy Olkhov ◽  
Olga Alexeeva ◽  
Marina Konstantinova ◽  
Vyacheslav Podmasterev ◽  
Polina Tyubaeva ◽  
...  

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.


Author(s):  
Teera Butburee ◽  
Yang Bai ◽  
Lianzhou Wang

Branched nanostructures represent a unique group of nanoarchitectures exhibiting advantageous high surface area and excellent charge transport for energy conversion application compared to their bulk counterparts. Especially, branched titanium dioxide...


2002 ◽  
Vol 76 (3) ◽  
pp. 217-223 ◽  
Author(s):  
Jining Xie ◽  
Pramod K Sharma ◽  
V.V Varadan ◽  
V.K Varadan ◽  
Bhabendra K Pradhan ◽  
...  

2012 ◽  
Vol 12 (6) ◽  
pp. 4919-4927 ◽  
Author(s):  
Nithi Atthi ◽  
Jakrapong Supadech ◽  
Gaetan Dupuy ◽  
On-uma Nimittrakoolchai ◽  
Apirak Pankiew ◽  
...  

2013 ◽  
Vol 747 ◽  
pp. 599-602
Author(s):  
Surachet Toommee ◽  
Nisanart Traiphol

This research investigates using of poly (dimethylsiloxane-b-hydroxy ethyl acrylate) (PDMS-b-PHEA) diblock copolymer to stabilized TiO2nanoparticles in silicone fluid. The polar PHEA segment is expected to anchor on TiO2surface while the non-polar PDMS segment extends into silicone medium. To study effects of polymer structure on its stabilizing efficiency, PDMS-b-PHEA of structures 5-b-0.3, 5-b-1.1 and 8-b-1.0 are used. Results show that suspensions of particle with surface area ~40 and ~200 m2/g can be stabilized for longer than 1 and 7 hrs, respectively. The copolymer with relatively long PHEA and PDMS segments is highly effective as a dispersant. This is due to enhanced adsorption on particle surface and steric stabilization. However, in the system of 40 m2/g-TiO2, excess amounts could lead to polymer entanglement and particle agglomeration. The copolymer dispersant exhibits high efficiency for the 200 m2/g-TiO2suspension as well. In the latter system, higher concentration is required to effectively cover particle surface.


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