scholarly journals New Separation Material Obtained from Waste Rapeseed Cake for Copper(II) and Zinc(II) Removal from the Industrial Wastewater

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2566
Author(s):  
Krzysztof Mazurek ◽  
Sebastian Drużyński ◽  
Urszula Kiełkowska ◽  
Edward Szłyk

Rapeseed cake biochar was produced by pyrolysis at 973.15 K for 2 h, in anoxic conditions. Porous structure, specific surface area and die composition of waste rapeseed cake were studied. The specific surface area of rapeseed cake biochar was 166.99 m2·g−1, which exceeded most other biochars reported, which made it an attractive material during wastewater treatment. The SEM study of the material demonstrated a large number of pores formed on the cell wall, with a pore volume Vp = 0.08 cm3·g−1. The results indicate lower aromaticity and increased polarity of the tested material. The observed H/C ratio of 0.29 is similar for activated carbons. Furthermore, sorption properties of the obtained carbon material in relation to copper(II), zinc(II) and arsenic(III) ions were also studied. Moreover, the impact of parameters such as: sorption time, temperature, adsorbate concentration, sorbent mass and solution pH on the efficiency of the adsorption process of the studied cations was also examined. Sorption studies revealed that the sorbent can be successfully used for the separation of Cu(II) and Zn(II) from technological wastewaters. Rapeseed cake biochar exhibits superior Cu(II) adsorption capacity (52.2 mg·g−1) with a short equilibrium time (6 h). The experimental data collected show a high selectivity of the obtained carbon material relative to copper(II) and zinc(II) ions in the presence of arsenic(III) ions.

2021 ◽  
Vol 319 ◽  
pp. 111063
Author(s):  
Yury M. Volfkovich ◽  
Valentin E. Sosenkin ◽  
Alexei Y. Rychagov ◽  
Alexandr V. Melezhik ◽  
Alexei G. Tkachev ◽  
...  

Materials ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4169
Author(s):  
Marcel Zambrzycki ◽  
Krystian Sokolowski ◽  
Maciej Gubernat ◽  
Aneta Fraczek-Szczypta

In this work, we present a comparative study of the impact of secondary carbon nanofillers on the electrical and thermal conductivity, thermal stability, and mechanical properties of hybrid conductive polymer composites (CPC) based on high loadings of synthetic graphite and epoxy resin. Two different carbon nanofillers were chosen for the investigation—low-cost multi-layered graphene nanoplatelets (GN) and carbon black (CB), which were aimed at improving the overall performance of composites. The samples were obtained by a simple, inexpensive, and effective compression molding technique, and were investigated by the means of, i.a., scanning electron microscopy, Raman spectroscopy, electrical conductivity measurements, laser flash analysis, and thermogravimetry. The tests performed revealed that, due to the exceptional electronic transport properties of GN, its relatively low specific surface area, good aspect ratio, and nanometric sizes of particles, a notable improvement in the overall characteristics of the composites (best results for 4 wt % of GN; σ = 266.7 S cm−1; λ = 40.6 W mK−1; fl. strength = 40.1 MPa). In turn, the addition of CB resulted in a limited improvement in mechanical properties, and a deterioration in electrical and thermal properties, mainly due to the too high specific surface area of this nanofiller. The results obtained were compared with US Department of Energy recommendations regarding properties of materials for bipolar plates in fuel cells. As shown, the materials developed significantly exceed the recommended values of the majority of the most important parameters, indicating high potential application of the composites obtained.


2021 ◽  
Author(s):  
Imane Guetni ◽  
Claire Marlière ◽  
David Rousseau

Abstract Application of chemical enhanced oil recovery (C-EOR) processes to low-permeability sandstone reservoirs (in the 10-100 mD range) can be very challenging as strong retention and difficult in-depth propagation of polymer and surfactant can occur. Transport properties of C-EOR chemicals are particularly related to porous media mineralogy (clay content). The present experimental study aimed at identifying base mechanisms and providing general recommendations to design economically viable C-EOR injection strategies in low permeability clayey reservoirs. Polymer and surfactant injection corefloods were conducted using granular packs (quartz and clay mixtures) with similar petrophysical characteristics (permeability 70-130 mD) but having various mineralogical compositions (pure quartz sand, sand with 8 wt-% kaolinite and sand with 8 wt-% smectite). The granular packs were carefully characterized in terms of structure (SEM) and specific surface area (BET). The main observables from the coreflood tests were the resistance and residual resistance factors generated during the chemical injections, the irreversible polymer retention and the surfactant retention in various injection scenarios (polymer alone, surfactant alone, polymer and surfactant). A first, the impact of the clay contents on the retention of polymer and surfactant considered independently was examined. Coreflood results have shown that retention per unit mass of rock strongly increased in presence of both kaolinite and smectite, but not in the same way for both chemicals. For polymer, retention was about twice higher with kaolinite than with smectite, despite the fact that the measured specific surface area of the kaolinite was about 5 times less than that of the smectite. Conversely, for surfactant, retention was much higher with smectite than with kaolinite. Secondly, the impact of the presence of surfactant on the polymer in-depth propagation and retention was investigated in pure quartz and kaolinite-bearing porous media. In both mineralogies, the resistance factor quickly stabilized when polymer was injected alone whereas injection of larger solution volumes was required to reach stabilization when surfactant was present. In pure quartz, polymer retention was shown, surprisingly, to be one order of magnitude higher in presence of surfactant whereas with kaolinite, surfactant did not impact polymer retention. The results can be interpreted by considering adsorption-governed retention. The mechanistic pictures being that (a) large polymer macromolecules are not able to penetrate the porosity of smectite aggregates, whereas surfactant molecules can, and (b) that surfactant and polymer mixed adsorbed layers can be formed on surfaces with limited affinity for polymer. Overall, this study shows that C-EOR can be applied in low permeability reservoirs but that successful injection strategies will strongly depend on mineralogy.


Biochar ◽  
2020 ◽  
Author(s):  
Marlene C. Ndoun ◽  
Herschel A. Elliott ◽  
Heather E. Preisendanz ◽  
Clinton F. Williams ◽  
Allan Knopf ◽  
...  

Abstract Biochars produced from cotton gin waste (CG) and guayule bagasse (GB) were characterized and explored as potential adsorbents for the removal of pharmaceuticals (sulfapyridine-SPY, docusate-DCT and erythromycin-ETM) from aqueous solution. An increase in biochar pyrolysis temperature from 350 οC to 700 οC led to an increase in pH, specific surface area, and surface hydrophobicity. The electronegative surface of all tested biochars indicated that non-Coulombic mechanisms were involved in adsorption of the anionic or uncharged pharmaceuticals under experimental conditions. The adsorption capacities of Sulfapyridine (SPY), Docusate (DCT) and Erythromycin (ETM) on biochar were influenced by the contact time and solution pH, as well as biochar specific surface area and functional groups. Adsorption of these pharmaceutical compounds was dominated by a complex interplay of three mechanisms: hydrophobic partitioning, hydrogen bonding and π–π electron donor–acceptor (EDA) interactions. Despite weaker π–π EDA interactions, reduced hydrophobicity of SPY− and increased electrostatic repulsion between anionic SPY− and the electronegative CG biochar surface at higher pH, the adsorption of SPY unexpectedly increased from 40% to 70% with an increase in pH from 7 to 10. Under alkaline conditions, adsorption was dominated by the formation of strong negative charge-assisted H-bonding between the sulfonamide moiety of SPY and surface carboxylic groups. There seemed to be no appreciable and consistent differences in the extent of DCT and ETM adsorption as the pH changed. Results suggest the CG and GB biochars could act as effective adsorbents for the removal of pharmaceuticals from reclaimed water prior to irrigation. High surface area biochars with physico-chemical properties (e.g., presence of functional groups, high cation and anion exchange capacities) conducive to strong interactions with polar-nonpolar functionality of pharmaceuticals could be used to achieve significant contaminant removal from water. Graphic Abstract


Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1811 ◽  
Author(s):  
Mitja Linec ◽  
Branka Mušič

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.


Nanomaterials ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 896 ◽  
Author(s):  
Hye-Min Lee ◽  
Kwan-Woo Kim ◽  
Young-Kwon Park ◽  
Kay-Hyeok An ◽  
Soo-Jin Park ◽  
...  

In this study, low-density polyethylene (LDPE)-derived activated carbons (PE-AC) were prepared as electrode materials for an electric double-layer capacitor (EDLC) by techniques of cross-linking, carbonization, and subsequent activation under various conditions. The surface morphologies and structural characteristics of the PE-AC were observed by field-emission scanning electron microscope, Cs-corrected field-emission transmission electron microscope, and X-ray diffraction analysis, respectively. The nitrogen adsorption isotherm-desorption characteristics were confirmed by Brunauer–Emmett–Teller, nonlocal density functional theory, and Barrett–Joyner–Halenda equations at 77 K. The results showed that the specific surface area and total pore volume of the activated samples increased with increasing the activation time. The specific surface area, the total pore volume, and mesopore volume of the PE-AC were found to be increased finally to 1600 m2/g, 0.86 cm3/g, and 0.3 cm3/g, respectively. The PE-AC also exhibited a high mesopore volume ratio of 35%. This mesopore-rich characteristic of the activated carbon from the LDPE is considered to be originated from the cross-linking density and crystallinity of precursor polymer. The high specific surface area and mesopore volume of the PE-AC led to their excellent performance as EDLC electrodes, including a specific capacitance of 112 F/g.


2014 ◽  
Vol 604 ◽  
pp. 93-101
Author(s):  
Maris Kodols ◽  
Sabine Didrihsone ◽  
Janis Grabis

The influence of glycine, glycerine, ethylene glycol and citric acid fuel and their ratio to NO3- on formation and dispersity of Bi2WO6 nanoparticles prepared by combustion synthesis has been studied. The pure crystalline Bi2WO6 with specific surface area 24,8 m2/g and crystallite size of 28 nm was obtained by using glycerine as fuel at its ratio to NO3- of 0,67. The photocatalytic activity of the prepared Bi2WO6 in degradation of methylene blue depended on its specific surface area of samples and solution pH.


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