Carbonaceous Matrix Research Articles

Potassium and soot interaction in fast biomass pyrolysis at high temperatures

This study aims to investigate the interaction between potassium and carbonaceous matrix of soot produced from wood and herbaceous biomass pyrolysis at high heating rates at 1250°C in a drop tube reactor. The influence of soot carbon chemistry and potassium content in the original biomass on the CO2 reactivity was studied by thermogravimetric analysis. The XPS results showed that potassium incorporation with oxygen-containing surface groups in the soot matrix did not occur during high temperature pyrolysis. The potassium was mostly found as water-soluble salts such as KCl, KOH, KHCO3 and K2CO3 in herbaceous biomass soot. The low ash-containing pinewood soot was less reactive than the potassium rich herbaceous biomass soot, indicating a dominating role of potassium on the soot reactivity. However, the catalytic effect of potassium on the reactivity remained the same after a certain potassium amount was incorporated in the soot matrix during pyrolysis. Raman spectroscopy results showed that the carbon chemistry of biomass soot also affected the CO2 reactivity. The less reactive pinewood soot was more graphitic than herbaceous biomass soot samples with the disordered carbon structure.

Holey nickel-cobalt layered double hydroxide thin sheets with ultrahigh areal capacitance

Strong coupling of electroactive components on conductive carbonaceous matrix to fabricate flexible hybrid electrodes represents a promising approach towards high performance supercapacitors. This work reports the fabrication of holey nickel cobalt layered double hydroxide (NiCo-LDH) nanosheets that are vertically grown on the cotton cloth-derived activated textile carbon (aTC). The abundant nanoholes on the thin-sheet NiCo-LDH not only enhance the electrode efficiency for efficient Faradaic redox reactions but also facilitate access of electrolyte to the electrode surface, thus giving rise to 70% capacitance arising from their outer surface. As a result, the aTC-NiCo hybrid electrode is capable of simultaneously achieving extremely high areal capacitance (6.37 F cm−2), mass capacitance (525 F g−1) and volumetric capacitance (249 F cm−3) at a practical level of mass loading (6.72 mg cm−2). Moreover, a solid-state asymmetric capacitor built with aTC-NiCo as positive electrode and active carbon-coated on aTC as negative electrode can deliver a volumetric energy density of 7.4 mWh cm−3 at a power density of 103 mW cm−3, while preserving a superior power performance, satisfying cycling stability and good mechanical flexibility.

Making Ultrafast High‐Capacity Anodes for Lithium‐Ion Batteries via Antimony Doping of Nanosized Tin Oxide/Graphene Composites

AbstractTin oxide‐based materials attract increasing attention as anodes in lithium‐ion batteries due to their high theoretical capacity, low cost, and high abundance. Composites of such materials with a carbonaceous matrix such as graphene are particularly promising, as they can overcome the limitations of the individual materials. The fabrication of antimony‐doped tin oxide (ATO)/graphene hybrid nanocomposites is described with high reversible capacity and superior rate performance using a microwave assisted in situ synthesis in tert‐butyl alcohol. This reaction enables the growth of ultrasmall ATO nanoparticles with sizes below 3 nm on the surface of graphene, providing a composite anode material with a high electric conductivity and high structural stability. Antimony doping results in greatly increased lithium insertion rates of this conversion‐type anode and an improved cycling stability, presumably due to the increased electrical conductivity. The uniform composites feature gravimetric capacity of 1226 mAh g−1 at the charging rate 1C and still a high capacity of 577 mAh g−1 at very high charging rates of up to 60C, as compared to 93 mAh g−1 at 60C for the undoped composite synthesized in a similar way. At the same time, the antimony‐doped anodes demonstrate excellent stability with a capacity retention of 77% after 1000 cycles.

Metal–Thiobenzoato Complexes: Synthesis, Structure, and Processing as Carbon‐Supported Nanoparticles

Six new compounds of formula [M(TBn)2L] [TBn: thiobenzoato; M: PdII, ZnII, CdII; L: 2,2′‐bipyridine (bpy), 1,10‐phenanthroline (phen), 1,2‐di‐(4‐pyridil)‐ethylene (bpe), neocuproine (neo), adenine (ade)] are obtained by the reaction of M(CH3COO)2·2H2O with thiobenzoic acid and N‐heterocyclic ligands. The use of chelating ligands and adenine leads to monomeric compounds: [Pd(TBn)2(bpy)] (PdBPY), [Pd(TBn)2(phen)] (PdPHEN), [Zn(TBn)2(neo)] (ZnNEO), [Cd(TBn)2(neo)] (CdNEO), and [Cd(TBn)2(ade)(CH3OH)] (CdADE). In these compounds, the metal is bonded to the sulfur atoms of two TBn anions, while the remaining coordination positions are completed by the donor atoms of the ancillary ligands. The bridging capability of the bpe ligand gives rise to the polymeric [Cd(TBn)2(µ‐bpe)]n (CdBPE) compound. The presence of direct sulfur–metal bonds and carbon‐rich coligands enables these complexes to yield, by means of a dry thermolysis process, a set of metallic and metal–sulfide nanoparticles embedded into a carbonaceous support. The process to produce the latter materials consists of aerobic thermolysis using moderate temperatures (300–500 °C) and short exposure times (minute scale). Analysis of the XRD patterns and SEM/TEM images reveals that the carbonaceous matrix hosts well‐dispersed nanocrystallites. The influence of the metal(II) atom, ancillary ligand, and thermal treatment parameters on the crystalline phase, size, and purity of the resulting carbon‐supported nanoparticles is discussed.

Hydrogen-bond supramolecular hydrogels as efficient precursors in the preparation of freestanding 3D carbonaceous architectures containing BCNO nanocrystals and exhibiting a high CO2/CH4 adsorption ratio

Oxygen-enriched boron carbonitrides – known as boron carbon oxinitrides, BCNOs – have exhibited remarkable properties with numerous works reporting on their performance as phosphors and some few ones as H2-adsorbents. However, the study of BCNOs capability for CO2 uptaking has yet to be achieved. Herein, we have designed a simple process for preparation of freestanding three-dimensional (3D) BCNO structures via pyrolysis of supramolecular gels formed by H-bonding of melamine, boric acid and glucose. The 3D porous materials obtained by pyrolysis of supramolecular gels containing glucose exhibited a seaweed-like 3D structure formed by BCNO nanocrystals embedded within a carbonaceous matrix with a certain content of amorphous hydrogenated carbon. The particularly narrow porosities exhibited by these samples proved effective for CO2 adsorption with uptakes of up to ca. 1.8 mmol/g at 25 °C. More interestingly, those samples prepared with high concentration of glucose behaved as molecular sieves and exhibited an excellent performance for CO2–CH4 separation, especially at low pressures with kH values of up to 1.04∙103.

Studies of field emission process influence on changes in CNT films with different CNT superficial density

AbstractField emission from materials at high electric fields can be associated with unfavorable or even destructive effect on the surface of the investigated cathode. The impact of high voltage electric power supply causes locally very strong electric fields focusing on the cathode surface. It causes a number of phenomena, which can adversely affect the morphology and the structure of the cathode material. Such a phenomenon is, for example, peeling of an emissive layer from the substrate or its burnout. It results in tearing of the layer and a decrease or loss of its ability to electrons emission. The cold cathodes in a form of CNT films with various CNTs superficial distribution are obtained by physical vapor deposition followed by chemical vapor deposition. CNTs are catalyzed in pyrolytic process with xylene (CVD), by Ni in a form of nanograins (few nm in size) placed in carbonaceous matrix. These films are built of emissive CNTs - carbonaceous film deposited on different substrates. In this work, the morphology and topography of superficial changes resulting from external electric field in such films were investigated.

An alternative to hydrogenation processes. Electrocatalytic hydrogenation of benzophenone.

The electrocatalytic hydrogenation of benzophenone was performed at room temperature and atmospheric pressure using a polymer electrolyte membrane electrochemical reactor (PEMER). Palladium (Pd) nanoparticles were synthesised and supported on a carbonaceous matrix (Pd/C) with a 28 wt % of Pd with respect to carbon material. Pd/C was characterised by transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). Cathodes were prepared using Pd electrocatalytic loadings (LPd) of 0.2 and 0.02 mg cm−2. The anode consisted of hydrogen gas diffusion for the electrooxidation of hydrogen gas, and a 117 Nafion exchange membrane acted as a cationic polymer electrolyte membrane. Benzophenone solution was electrochemically hydrogenated in EtOH/water (90/10 v/v) plus 0.1 M H2SO4. Current densities of 10, 15 and 20 mA cm−2 were analysed for the preparative electrochemical hydrogenation of benzophenone and such results led to the highest fractional conversion (XR) of around 30% and a selectivity over 90% for the synthesis of diphenylmethanol upon the lowest current density. With regards to an increase by ten times the Pd electrocatalytic loading the electrocatalytic hydrogenation led neither to an increase in fractional conversion nor to a change in selectivity.

Free-standing sulfur-polypyrrole cathode in conjunction with polypyrrole-coated separator for flexible Li-S batteries

A free-standing sulfur-polypyrrole cathode and a polypyrrole coated separator were designed for flexible Li-S batteries. The free-standing sulfur-polypyrrole cathode was prepared by directly pasting a sulfur-coated polypyrrole (S@PPy) nanofiber composite on a flexible and conductive polypyrrole (PPy) film. Compared with carbonaceous matrixes, PPy has a strong interaction with polysulfides to mitigate the dissolution of polysulfides due to its unique chain structure and the lone pair electrons in the nitrogen atoms in PPy. In addition, the as-prepared PPy film not only shows excellent mechanical elasticity, but also possesses a rough surface, which can accommodate volume expansion, enhance the adhesion of active materials, and further trap the dissolved polysulfides. Due to the synergistic effect provided by the PPy film, the free-standing sulfur-polypyrrole cathode shows better electrochemical performance than the traditional cathode with S@PPy composite coated on Al foil. In order to further improve the cycling stability of Li-S batteries, a PPy coated separator was prepared, which acts as a fishing net to capture polysulfides and alleviate the shuttle effect, leading to a stable cycling performance. Moreover, the PPy layer coated on commercial separator is much lighter than many other free-standing interlayers reported previously. Considering the flexibility of the free-standing sulfur cathode and PPy coated separator, a soft-packaged flexible Li-S battery based on them has been designed and fabricated to power a device consisting of 24 light emitting diode (LED) lights. After repeated bending, the flexible Li-S battery can still maintain good performance, indicating the excellent mechanical flexibility of the designed Li-S battery.

Advanced characterization unravels the structure and reactivity of wood-based chars

This study aims at understanding the structural changes occurring in the carbonaceous matrix of wood-based chars during their thermal conversion. Although chars are routinely characterized by porosity measurements or scanning electron microscopy, the composition and structure of the carbonaceous matrix is often not investigated. Here, advanced characterization using X-ray synchrotron microtomography, transmission electron microscopy, Raman spectroscopy and X-ray diffraction provided a precise description of the char properties, allowing for an accurate discussion of their catalytic properties. Two chars were produced by slow pyrolysis of wood waste (400 and 700 °C) and a third one was fabricated by activation under steam at 850 °C of the char obtained at 700 °C. The results show that the pyrolysis temperature and the activation performed did not affect the macrostructure of the chars and that the pores were interconnected at the macroscopic scale. However, at 700 °C, the micro- and nanostructures were modified: short-range organized graphene fringes were observed. The activated char showed a homogeneous microstructure similar to that of its precursor. Besides, the ratio of graphene-like structures, the local organization of graphene sheets, and the imperfections in graphene-like sheets were clearly improved by the post-treatment. To our knowledge, this is the first time that such an approach, combining various tools, is applied for the study of pyrolysis chars.

Effect of Nb/C ratio in the morphological, structural, optical and photocatalytic properties of novel and inexpensive Nb2O5/carbon xerogel composites

This work explores the development of hybrid Nb2O5/carbon xerogel photocatalysts. The precursor materials used, such as tannin and recycled niobium scraps, enhance the economic and environmental aspects of the synthesis. The materials were characterized by diffuse reflectance spectroscopy, scanning electron microscopy, dispersive energy spectroscopy, infrared spectroscopy, Raman spectroscopy and X-ray diffraction. The photocatalytic action of the material was evaluated by methylene blue decomposition as determined by UV–visible spectroscopy. Anhydrous niobium oxide has a hexagonal structure. The X-ray profiles of the materials developed (XC-wNb) are similar to Nb2O5, confirming the presence of inorganic oxide in the matrix of these composites. The chemical elements that compose the samples are homogeneously distributed on the surface of the samples, confirming the dispersion of the oxide in the carbonaceous matrix. The XC-wNb absorbs radiation in a considerably wider range than inorganic oxides, in this case, for the entire wavelength range used in the experiments, thereby suggesting the synergistic effect of xerogel and niobium oxide on the optical properties of the XC-wNb samples. All XC-wNb presented photocatalytic activity under visible radiation, evidencing the beneficial coupling effect on the photocatalytic properties of the material. The XC-24Nb was the most effective photocatalyst at the wavelength used due its composition, morphological and photochemical properties. The methylene blue photodegradation is controlled to a greater extent by reaction with the OH• radical. The XC-24Nb also presents high stability and reusability, which are optimal properties for industrial application.

Comparative study of post-growth annealing of Cu(hfac)2, Co2(CO)8 and Me2Au(acac) metal precursors deposited by FEBID.

Non-noble metals, such as Cu and Co, as well as noble metals, such as Au, can be used in a number modern technological applications, which include advanced scanning-probe systems, magnetic memory and storage, ferroelectric tunnel junction memristors, metal interconnects for high performance integrated circuits in microelectronics and nano-optics applications, especially in the areas of plasmonics and metamaterials. Focused-electron-beam-induced deposition (FEBID) is a maskless direct-write tool capable of defining 3-dimensional metal deposits at nanometre scale for above applications. However, codeposition of organic ligands when using organometallic precursors is a typical problem that limits FEBID of pure metal nanostructures. In this work, we present a comparative study using a post-growth annealing protocol at 100, 200, and 300 °C under high vacuum on deposits obtained from Co2(CO)8, Cu(II)(hfac)2, and Me2Au(acac) to study improvements on composition and electrical conductivity. Although the as-deposited material was similar for all precursors, metal grains embedded in a carbonaceous matrix, the post-growth annealing results differed. Cu-containing deposits showed the formation of pure Cu nanocrystals at the outer surface of the initial deposit for temperatures above 100 °C, due to the migration of Cu atoms from the carbonaceous matrix containing carbon, oxygen, and fluorine atoms. The average size of the Cu crystals doubles between 100 and 300 °C of annealing temperature, while the composition remains constant. In contrast, for Co-containing deposits oxygen release was observed upon annealing, while the carbon content remained approximately constant; the cobalt atoms coalesced to form a metallic film. The as-deposited Au-containing material shows subnanometric grains that coalesce at 100 °C, maintaining the same average size at annealing temperatures up to 300 °C. Raman analysis suggests that the amorphous carbonaceous matrix of the as-written Co, Cu and Au deposits turned into nanocrystalline graphite with comparable crystal sizes of 12–14 nm at 300 °C annealing temperature. However, we observed a more effective formation of graphite clusters in Co- than in Cu- and Au-containing deposits. The graphitisation has a minor influence on the electrical conductivity improvements of Co–C deposits, which is attributed to the high as-deposited Co content and the related metal grain percolation. On the contrary, electrical conductivity improvements by factors of 30 and 12 for, respectively, Cu–C and Au–C deposits with low metal content are mainly attributed to the graphitisation. This relatively simple vacuum-based post-growth annealing protocol may be useful for other precursors as it proved to be efficient in reliably tuning the electrical properties of as-deposited FEBID materials. Finally, a H2-assisted gold purification protocol is demonstrated at temperatures around 300 °C by fully removing the carbon matrix and drastically reducing the electrical resistance of the deposit.

Electron-driven and thermal chemistry during water-assisted purification of platinum nanomaterials generated by electron beam induced deposition.

Focused electron beam induced deposition (FEBID) is a versatile tool for the direct-write fabrication of nanostructures on surfaces. However, FEBID nanostructures are usually highly contaminated by carbon originating from the precursor used in the process. Recently, it was shown that platinum nanostructures produced by FEBID can be efficiently purified by electron irradiation in the presence of water. If such processes can be transferred to FEBID deposits produced from other carbon-containing precursors, a new general approach to the generation of pure metallic nanostructures could be implemented. Therefore this study aims to understand the chemical reactions that are fundamental to the water-assisted purification of platinum FEBID deposits generated from trimethyl(methylcyclopentadienyl)platinum(IV) (MeCpPtMe3). The experiments performed under ultrahigh vacuum conditions apply a combination of different desorption experiments coupled with mass spectrometry to analyse reaction products. Electron-stimulated desorption monitors species that leave the surface during electron exposure while post-irradiation thermal desorption spectrometry reveals products that evolve during subsequent thermal treatment. In addition, desorption of volatile products was also observed when a deposit produced by electron exposure was subsequently brought into contact with water. The results distinguish between contributions of thermal chemistry, direct chemistry between water and the deposit, and electron-induced reactions that all contribute to the purification process. We discuss reaction kinetics for the main volatile products CO and CH4 to obtain mechanistic information. The results provide novel insights into the chemistry that occurs during purification of FEBID nanostructures with implications also for the stability of the carbonaceous matrix of nanogranular FEBID materials under humid conditions.

Petrography of the carbonaceous, diamond-bearing stone “Hypatia” from southwest Egypt: A contribution to the debate on its origin

The stone named “Hypatia” found in the Libyan Desert Glass area of southwest Egypt is carbon-dominated and rich in microdiamonds. Previous noble gas and nitrogen isotope studies suggest an extraterrestrial origin. We report on a reconnaissance study of the carbonaceous matrix of this stone and the phases enclosed in it. This focused on areas not affected by numerous transecting fractures mostly filled with secondary minerals. The work employed scanning electron microscopy (SEM) with energy-dispersive (EDS) and wavelength-dispersive (WDS) electron microprobe (EMPA) analysis, Proton Induced X-ray Emission (PIXE) spectrometry and micro-Raman spectroscopy. We found that carbonaceous matrices of two types occur irregularly intermingled on the 50–500 μm scale: Matrix-1, consisting of almost pure carbonaceous matter, and Matrix-2, containing Fe, Ni, P and S at abundances analyzable by microprobe. Matrix-2 contains the following phases as inclusions: (i) (Fe,Ni) sulphide occurring in cloud-like concentrations of sub-μm grains, in domains of the matrix that are enriched in Fe and S. These domains have (Fe + Ni)/S (atomic) = 1.51 ± 0.24 and Ni/Fe = 0.086 ± 0.061 (both 1SD); (ii) grains up to ∼5 μm in size of moissanite (SiC); (iii) Ni-phosphide compound grains up to 60 μm across that appear cryptocrystalline or amorphous and have (Ni + Fe)/P (atomic) = 5.6. ± 1.7 and Ni/Fe = 74 ± 29 (both 1SD), where both these ratios are much higher than any known Ni-phosphide minerals; (iv) rare grains (observed only once) of graphite, metallic Al, Fe and Ag, and a phase consisting of Ag, P and I. In Matrix-2, Raman spectroscopy shows a prominent narrow diamond band at 1340 cm−1. In Matrix-1 the D and G bands of disordered carbon are dominant, but a minor diamond band is ubiquitous, accounting for the uniform hardness of the material. The D and G bands have average full width at half maximum (FWHM) values of 295 ± 19 and 115 ± 19 cm−1, respectively, and the D/G intensity ratio is 0.75 ± 0.09 (both 1SD). These values are similar to those of the most primitive solar system carbonaceous matter. The diamond phase is considered to be a product of shock. The (Fe, Ni) sulphide phase is probably pyrrhotite and a shock origin is likewise proposed for it. Moissanite is frequently associated with the Ni-phosphide phase, and a presolar origin for both is suggested. The lack of recrystallization of the Ni-phosphide phase suggests that the Hypatia stone did not experience long-lasting thermal metamorphism, in accord with the Raman D-G band characteristics.A lack of silicate matter sets the stone apart from interplanetary dust particles and known cometary material. This, along with the dual intermingled matrices internal to it, could indicate a high degree of heterogeneity in the early solar nebula.

High-performance MoS2-based nanocomposite anode prepared by high-energy mechanical milling: The effect of carbonaceous matrix on MoS2

A MoS2-based nanocomposite for use as an anode in lithium-ion batteries was prepared via a facile and scalable high-energy mechanical milling (HEMM) technique. In this study, we report the effect of the type of carbon matrix (2D graphite (G), 1D carbon nanotube (CNT), and 0D amorphous carbon (C)) as well as that of the HEMM time on the electrochemical performances. Among all nanocomposites studied, MoS2/G exhibited the most excellent cycle life, delivering a gravimetric capacity of 737 mAh g−1 after 210 cycles (84% retention) and outstanding rate performance, resulted from a homogenous mixing between MoS2 and G. In addition, as compared to MoS2/CNT and MoS2/C, the capacity retention of MoS2/G over long-term cycling was markedly steady and stable for various milling times applied. Furthermore, the best weight ratio between MoS2 and G was experimentally determined to be 7:3 based on the electrochemical performances. The superiority of MoS2/G was further investigated by density functional theory calculations, which showed the much higher binding energy of G than CNT toward MoS2, leading to the improved miscibility and the mechanical robustness of MoS2/G. Overall, the MoS2/G nanocomposite synthesized by a simple HEMM process presents a new and promising candidate for high-performance anodes for LIBs.

Decomposition of palladium acetate and C60fullerite during thermal evaporation in PVD process

AbstractThe mechanisms of thermal decomposition of evaporated material during Physical Vapor Deposition (PVD) process depend on the kind of evaporated material. Such parameters of PVD process as deposition rate, source temperature and deposition time should be carefully selected taking into account the properties of material. Deposited films can span the range of chemical compositions based on the source materials. The nanostructural carbon films in form of palladium nanograins embedded in various carbonaceous matrixes were obtained by thermal evaporation during PVD process from two separated sources containing C60fullerite and palladium acetate, both in a form of powder. The evaporation was realized by resistive heating of sources under a dynamic vacuum of 10-3Pa. The influence of decomposition path of evaporated materials on the film structure has been discussed. Prepared C-Pd films were characterized using thermo-gravimetric method, differential thermal analysis, infrared spectroscopy and X-ray diffraction. The influence of decomposition of Pd acetate and fullerite on the final film structure was also shown.

Sub-micrometer refractory carbonaceous particles in the polar stratosphere

Abstract. Eleven particle samples collected in the polar stratosphere during SOLVE (SAGE III Ozone loss and validation experiment) from January until March 2000 were characterized in detail by high-resolution transmission and scanning electron microscopy (TEM/SEM) combined with energy-dispersive X-ray microanalysis. A total of 4202 particles (TEM = 3872; SEM = 330) were analyzed from these samples, which were collected mostly inside the polar vortex in the altitude range between 17.3 and 19.9 km. Particles that were volatile in the microscope beams contained ammonium sulfates and hydrogen sulfates and dominated the samples. Some particles with diameters ranging from 20 to 830 nm were refractory in the electron beams. Carbonaceous particles containing additional elements to C and O comprised from 72 to 100 % of the refractory particles. The rest were internal mixtures of these materials with sulfates. The median number mixing ratio of the refractory particles, expressed in units of particles per milligram of air, was 1.1 (mg air)−1 and varied between 0.65 and 2.3 (mg air)−1. Most of the refractory carbonaceous particles are completely amorphous, a few of the particles are partly ordered with a graphene sheet separation distance of 0.37 ± 0.06 nm (mean value ± standard deviation). Carbon and oxygen are the only detected major elements with an atomic O∕C ratio of 0.11 ± 0.07. Minor elements observed include Si, S, Fe, Cr and Ni with the following atomic ratios relative to C: Si∕C: 0.010 ± 0.011; S∕C: 0.0007 ± 0.0015; Fe∕C: 0.0052 ± 0.0074; Cr∕C: 0.0012 ± 0.0017; Ni∕C: 0.0006 ± 0.0011 (all mean values ± standard deviation).High-resolution element distribution images reveal that the minor elements are distributed within the carbonaceous matrix; i.e., heterogeneous inclusions are not observed. No difference in size, nanostructure and elemental composition was found between particles collected inside and outside the polar vortex. Based on chemistry and nanostructure, aircraft exhaust, volcanic emissions and biomass burning can certainly be excluded as sources. The same is true for the less probable but globally important sources: wood burning, coal burning, diesel engines and ship emissions. Recondensed organic matter and extraterrestrial particles, potentially originating from ablation and fragmentation, remain as possible sources of the refractory carbonaceous particles studied. However, additional work is required in order to identify the sources unequivocally.

Effect of particle size and oxidant concentration in the yield of humic acids from mineral coal using response surface methodology

Los ácidos húmicos se producen por la descomposición de la materia orgánica de los suelos y por la oxidación de carbones minerales. En este estudio se analizó mediante superficies de respuesta el efecto de la oxidación en la extracción de ácidos húmicos de un carbón colombiano. Las variables de oxidación estudiadas fueron las siguientes: tamaño de partícula (0,063, 0,106 y 0,150 mm), concentración del agente oxidante (permanganato de potasio (KMnO4): 0,010, 0,020 y 0,050 M) y tiempo de oxidación (30, 60 and 90 minutos). El grado de oxidación se verificó con espectroscopia infrarroja. La oxidación incrementó los grupos oxigenados en la matriz carbonácea debido, principalmente, a la oxidación de componentes alifáticos. Se obtuvieron porcentajes de extracción superiores a 24 % al usar partículas de 0,063 mm y KMnO4 con 0,020 M. © 2017. Acad. Colomb. Cienc. Ex. Fis. Nat.

Unusual Mesoporous Carbonaceous Matrix Loading with Sulfur as the Cathode of Lithium Sulfur Battery with Exceptionally Stable High Rate Performance.

Unusual three-dimensional mesoporous carbon/reduced graphene oxide (MP-C/rGO) matrix possessing graphene nanolayer pore walls built up by three to five graphene monosheets and some carbon particles with the sizes of about 5 nm located between the graphene nanolayers was prepared by facile freeze-drying and then carbonization of the poly(vinyl alcohol) and graphene oxide mixture. The mesoporous carbonaceous MP-C/rGO sample has a high specific surface area of 661.6 m2 g-1, large specific pore volume of 1.54 m3 g-1, and focused pore size distribution of 2-10 nm. About 64 wt % sulfur could be held in the pores of the MP-C/rGO matrix. As the cathode of a Li-S battery, the MP-C/rGO/S composite showed excellent electrochemical property including a high initial specific capacity of 919 mA h g-1 at 1 C with the capacity retention ratio of 63.3% and the Coulombic efficiency above 90% after 500 cycles. Meanwhile, the initial specific capacity of 602 mA h g-1 at 5 C and remaining capacity of 391 mA h g-1 after 500 cycles with an outstanding Coulombic efficiency of 97% indicate its exceptionally stable rate performance.

Dust particles characterization and innate resistance for Thevetia peruviana in different land-use pattern of urban area

The present work is an attempt to investigate pollution effect on an ornamental tree species Thevetia peruviana (Pers.) K. Schum. The study was conducted in various green spaces of institutional, industrial, residential and near traffic site representing as different status of air pollution concentration depending on land-use type. The resistance index calculated for selected species had mean value of 14.57 ± 0.41 observed at study sites. The dust deposition was found in range of 5.14–7.74 mg cm−2 on foliar surface of 12 cm2. The examination of leaf structure with scanning electron microscope showed presence of airborne dust particles in coarse and fine sizes with higher deposition found in industrial and residential sites. The epicuticular wax layer on upper surface of foliar was found eroded at industrial and traffic regions. The equivalent diameter of particles was observed to range from 0.45 to 12.71 µm in Poisson distributional pattern. The density of number concentration of dust particles was observed 1411 and 3703 in institutional and industrial area deposited on 0.22 mm2 of foliar surface. The elemental distribution on leaves of Thevetia peruviana has revealed a mixture of carbonaceous and soil matrix elements such as C, O, Al, Na, Si, K and Mg observed in proportion of X-rays counts per second. The whole experiment gave a positive indication for plant species as a tolerant bio-indicator of air pollutants in Delhi. The diverse flora present in city provides an opportunity for reducing harmful concentration of PM10 and PM2.5 and improving quality of air for human health.

Functionalized hydrothermal carbon derived from waste pomelo peel as solid-phase extractant for the removal of uranyl from aqueous solution.

To develop a high-performance solid-phase extractant for the separation of uranyl f, pomelo peel, a kind of waste biomass, has been employed as carbon source to prepare carbonaceous matrix through low-temperature hydrothermal carbonization (200°C, 24h). After being oxidized by Hummers method, the prepared hydrothermal carbon matrix was functionalized with carboxyl and phenolic hydroxyl groups (1.75mmolg-1). The relevant characterizations and batch studies had demonstrated that the obtained carbon material possessed excellent affinity toward uranyl (436.4mgg-1) and the sorption process was a spontaneous, endothermic and rapid chemisorption. The selective sorption of U(VI) from the simulated nuclear effluent demonstrated that the sorbent displayed a desirable selectivity (56.14% at pH=4.5) for the U(VI) ions over the other 11 competitive cations from the simulated industrial nuclear effluent. The proposed synthetic strategy in the present work had turned out to be effective and practical, which provides a novel approach to prepare functional materials for the recovery and separation of uranyl or other heavy metals from aqueous environment.