Large Size Distribution Research Articles

Pseudomorphic synthesis of pore size-tunable mesoporous silica spherical particles and their application for the fraction of low-molecular-weight heparin.

In this study, spherical silica with pore size varied from 30 to 200 Å was synthesized by pseudomorphic transformation at atmospheric pressure. 40-80 Å silica particles with a narrow pore distribution were obtained by using quaternary amine cationic surfactants and different kinds of swelling agents, including polypropylene glycol, 1,3,5-trimethylbenzene, alkanes, and alkanols. Alkyl imidazolium ionic liquid surfactants were used to synthesize large pore size distribution silica spheres with pore sizes in the range of 110-200 Å. All these silica particles can be synthesized under mild conditions within 12h, which provides a facile synthesis method for the preparation of a chromatographic matrix with tunable pore size. The method is reproducible and the relative standard deviation of silica sphere pore structure parameters in scaled-up preparations is less than 6%. The pore size on the fraction of low-molecular-weight heparin (LMWH) was investigated in size exclusion chromatography. Matrixes with different pore size distributions have various size exclusion regions. By using UPS-60-Diol columns in a twin-column recirculation separation process, LMWH with>85% heparin with molecular weight within the range of 3000-8000Da were separated in five-column volumes.

Co-sintering of a ceramic-metal bilayer: Coupled experimental, analytical and numerical approaches

The co-sintering behavior of a ceramic-metal bilayer is carefully investigated. This bilayer is composed of a gold film deposited by screen-printing on a silica-based low-temperature cofired ceramic (LTCC) layer. First, behaviors of both materials in free sintering are finely characterized. LTCC exhibits a viscous flow sintering mechanism, whereas the densification mechanism of gold is controlled by grain boundary diffusion (with an identified apparent activation energy of 101 ± 15 kJ mol−1). Free sintering of gold is also marked by a two-step densification process due to its large bimodal particle size distribution. A methodology is proposed to estimate gold viscosity at high temperatures directly from raw experimental data in free sintering, without performing dedicated mechanical characterizations. Based on the constitutive laws identified for LTCC and gold materials, analytical and numerical models of the bilayer co-sintering process are built. During co-sintering, stresses generated by densification kinetic mismatch between gold and LTCC are progressively relaxed by camber phenomenon. Calculated evolutions of camber in co-sintering are compared to curvature monitoring by ombroscopy. Finite element simulation in 3D fits well with the experimental data, whereas the analytical solution strongly underestimates camber rates. This shows that the simplified numerical approach suggested here leads to a robust numerical model, faithfully describing thermomechanical interactions occurring in co-sintering within the ceramic-metal bilayer.

Effects of a 3D-Printed Atomizer Component on Fuel-Spray and Flame Characteristics of a Jet-Stabilized Compact Gas Turbine Combustor Fed With Liquid Fuels

Abstract In this work, the effects of replacing an atomizer component of a confined jet-stabilized gas turbine combustor with a 3D-printed part have been studied. The part is called airblast, and it serves as a wall that collects and flows liquid droplets for a secondary atomization. Therefore, the liquid-surface interaction on the rough surface of the 3D-printed part was of interest. The combustor was operated under various conditions with either a conventionally machined airblast or the 3D-printed airblast. Flames with two liquid fuels were studied for fuel flexibility, and the position of a primary fuel injection was varied to study the influence of the liquid-surface interaction length. Load flexibility was investigated with air jet velocity settings, and flame equivalence ratios of ϕ = 0.8 and 1.0 were tested. Shadowgraphy-based particle tracking analyses presented a reduced atomization performance with the 3D-printed airblast, showing large droplet size distributions. However, no significant change in the combustor performance was observed from OH* chemiluminescence images and emission data, which confirms the versatility of the combustor and assures the compatibility of 3D-printed components with the combustor of this study.

Comparative insight into crystal evolutions of monodisperse MNb2O6 (M = Ni, Cu, Zn) spheres during electrochemical cycling in Li/Al-ion batteries

Niobates have emerged as advanced anode materials for lithium-ion batteries, owing to their inherently higher voltage and the occurrence of multiple one-electron redox reactions. However, there is a lack of comprehensive comparative analysis regarding their performance in lithium-ion and aluminum-ion battery applications. In this study, a facile solvothermal process is developed to synthesize uniform submicrospheres of three niobates: NiNb2O6, CuNb2O6, and ZnNb2O6 with large specific surface area and narrow size distribution. Their superior textural properties consisting of interconnected nanograins offer numerous active sites, delivering enhanced capacity and rate performance for the constructed half and full cells. Our in-situ XRD analysis reveals that all three niobates exhibit ultralow crystal volume expansion (< 6 %). But they exhibit distinct ion storage mechanisms: CuNb2O6 undergoes a phase transition to LiNb3O8 and NbO2 upon cyclic insertion of Li+ ions; NiNb2O6 mainly involves a classic hybrid-controlled process, facilitating easy ion insertion/extraction into/from the crystal lattices, especially at low sweep rates; while ZnNb2O6 stores charges via a pseudocapacitive-controlled process. Density functional theory (DFT) calculation and ex-situ XRD analysis confirm that CuNb2O6 outperforms the others, displaying the best electrochemical performance and holding promise as a high-energy electrode material thanks to favorable phase conversion, enhanced transport channels, porous structure and spherical morphology.

An analysis of microstructure and property of cerium dioxide incorporated in tungsten-copper composites prepared by activation sintering method

A series of W–Cu–Co-xCeO2 composites were obtained through activation sintering method, and their microstructure and properties were systematically researched. As the amount of CeO2 increased, the size of W particle in composites showed a decreasing trend as a whole. When the CeO2 amount was 0∼0.8 wt%, the W particles in composites exhibited a large size and dense distribution. As the CeO2 amount further increased, the size of W particle began to significantly decrease and the distribution area of Cu phase was uneven. The porosity of W–Cu–Co-xCeO2 composites first decreased and then increased. The density, relative density, and hardness exhibited an opposite trend. When the CeO2 amount was 0.8 wt%, these values reached their maximum values of 14.16 g/cm3, 98.66%, and 223 HV3.0, respectively. In addition, the friction coefficient (COF) and wear rate of W–Cu–Co-xCeO2 composites first decreased and then increased, which reached the lowest values at CeO2 of 0.8 wt%. At this time, the COF and wear rate were about 0.356 and 5.78 × 10−6 mm3/Nm, respectively.

Regulation of tea polyphenols in gluten-glucose Maillard reaction: Evaluation and analysis

Maillard reaction plays an important role in the flavour and color of some food. However, the excessive occurrence of Maillard reaction may affect the quality and safety of food. In this study, a simulated Maillard system composed of gluten and glucose was established to evaluate and analyze the regulatory role of tea polyphenols (TP) in it. The addition of tea polyphenols alleviated excessive browning of the Maillard reaction and significantly inhibited the accumulation of fructosamine and late glycosylation end products in the system. Based on the analysis of laser particle sizer and atomic force microscope, the large particle size distribution and aggregation structure of the Maillard reaction products in the tea polyphenol group disappeared. Further experiments showed that with the addition of tea polyphenols, the free radicals content in the system decreased, while the amount of reaction substrates increased. It was also shown that tea polyphenols effectively inhibited the isomerism of glucose to fructose and affected the content of free sulfhydryl and free amino groups in the system. The results indicated that tea polyphenols can regulate the Maillard reaction between gluten and glucose, which gives it the potential for application in the field of bakery and thermally processed foods.

Supercooled large droplet size distribution effects on airfoil icing: A numerical investigation based on a new coupled Eulerian method

Supercooled large droplets (SLDs) under natural icing conditions have the characteristics of easy deformation in motion and easy splashing on impact, and a bimodal droplet size distribution that has received less attention. The modified form of the Rosin-Rammler function was improved to achieve a more accurate nonlinear fitting of the SLD distribution curve. The droplet size distribution was divided into non-equipartition continuous multiple components. The drag source term of each component was coupled with the overall droplet size distribution, and the Eulerian equations of each component of SLDs were solved simultaneously. A new coupled Eulerian method for non-equipartition continuous multi-size droplets was proposed to simulate the impact characteristics of SLDs, and the SLD collection coefficients were validated. Effects of the ratio between the number of large and small droplet components and the number of all components on the simulation results were investigated to select a better combination based on stable convergence calculation steps and the calculation time. This new method was added to the multi-step icing numerical method, and the accuracy and robustness of the method in icing shape prediction were verified based on the freezing drizzle, median volume diameter &lt; 40 μm (FZDZ, MVD &lt; 40 μm) icing condition. Airfoil icing characteristics based on the bimodal and monomodal distribution were compared, and the icing shapes at the leading edge were similar. Still, the upper and lower limits of the icing shapes with the bimodal distribution were nearer to the trailing edge and the ice layer was thicker there.

Multifunctional CoCe/silica and CoMnCe/silica spinel ferrite nanocomposite: in vitro and in vivo evaluation for cancer therapy

Multifunctional magnetic spinel ferrite based on CoCe and CoMnCe/silica nanocomposites (NCs) were developed for targeted cancer therapeutics. The formation of spinel ferrite and co-existence of spinel ferrite/silica/chemo-drug, surface/pore size distribution, morphological features and magnetic properties were investigated using different characterization techniques. XRD pattern confirmed the pure phase of CoCe and CoMnCe spinel ferrite with estimated crystal size of 27.9 nm. After silica coating and pegylation, the crystal size of CoCe and CoMnCe increases to 36.3 nm and 76.2 nm. Nitrogen adsorption isotherm confirm an effective embedment of both spinel ferrites into silica with large surface area (653 m2/g and 718 m2/g) and uniform pore size distributions (6.1 nm and 6.9 nm). FT-IR spectra confirm the magnetic spinel ferrite/silica interactions (977, 1705 and 3410 cm−1), cisplatin functionalization (1645 cm−1) and PEG (1275–2900 cm−1). Coating SFNPswith Si and/or Cp and/or PEG, tunes the magnetic characteristics of the NCs system. For both CoCe and CoMnCe SFNPs, saturation magnetization (Ms) of 14.96 and 10.91 emu/g, residual magnetization (Mr) of 4.40 and 2.42 emu/g, Hc (coercivity) of 1072.1 and 719.3 Oe gradually diminish upon Si, respectively. The chemical state of CoMnCe SFNPs, CoCe SFNPs, their silica and active cisplatin NCs (Pt0 and Pt2+) were investigated using X-ray Photoelectron Spectroscopy (XPS). The anti-cancer efficacy of pegylated nanoformulations were tested in in vitro cells (HeLa, HCT-116 and HEK-293) and Hemolysis assay. The toxicity of different nanoformulations administered in different concentrations (20–2000 mg/kg) in in vivo was estimated based on LD50 value.

Study of a Copper Oxide Leaching in Alkaline Monosodium Glutamate Solution

Oxide copper minerals are commonly extracted via acidic leaching, using acids such as H2SO4, HCl, or HNO3. These strong acids are the most widely used because of their high dissolution kinetics. However, their main concern is the high acid consumption because copper oxide deposits contain large amounts of acid-consuming gangue. This paper proposes using an alternative aqueous alkaline monosodium glutamate (MSG) system to leach copper oxide minerals. Tenorite (CuO) was used as the copper oxide mineral under study. The influence of process variables (such as temperature and glutamate concentration) and kinetics of this system on copper leaching from tenorite were studied. The results showed that temperature has a significant effect on copper dissolution rates. Increased temperature from 15 °C to 60 °C enhanced the copper extraction from 9.1% to 97.7% after 2 h. Leaching kinetics were analyzed using the shrinking core model (SCM) under various conditions, indicating that the leaching rate presented a mixed control. This method, however, fails to describe leaching for broad particle sizes due to its requirement for single-sized solid grains. This study demonstrated that a large particle size distribution in tenorite supported a successful extension of the SCM for leaching it from mixed glutamate solutions. The activation energy for the 15–60 °C temperature range was calculated to be 102.6 kJ/mol for the chemical control.

The buckwheat-derived hard carbon as an anode material for sodium-ion energy storage system

Biomass-derived hard carbon (HC) has attracted much attention as a promising electrode material for sodium-ion batteries (SIBs) due to its unique properties such as high porosity, large surface area and adjustable pore size distribution. This work presents the results of electrochemical studies of HC derived from buckwheat seeds. The HCs were preoxidized at 300 °C and synthesized using a pyrolysis method in the range 600–1400 °C. It was found that the electrochemical characteristics of the HC anodes are strongly dependent on the morphology and structure. Furthermore, the positive effect of preoxidation on the porosity of HC was confirmed. Although all buckwheat-derived HC-based anodes showed stable cyclability over 100 cycles with CE of approximately 97–98 %, the preoxidized HCs pyrolyzed at 1400 °C achieved the highest reversible capacity of 330.23 mAh g−1 with excellent stability. Additional study using “single particle” measurement of HC1400 and HCox1400 showed that the preoxidation may significantly contribute to the improvement of the mass transfer.

Multiple interaction electron beam powder bed fusion for controlling melt pool dynamics and improving surface quality

Low surface quality of fabricated parts and long processing times are two commonly stated reasons against a more wide-spread adoption of electron beam powder bed fusion (PBF-EB) as a commercially viable manufacturing technique. Aside from the large particle size distribution (45–150 µm) of processed powders, the surface roughness, limited structural resolution and process instabilities are attributed to unwanted dynamics of the melt pool, like spattering, balling, evaporation and melt pool displacement. As a result, a contouring step using slow but stable melting parameters is usually added to the process to improve surface quality, leading to increased processing times.In this study, we demonstrate how the surface quality can be improved by supplying the energy for melt pool formation over multiple, timely separated interactions. To investigate the effect of this multiple interaction processing (MIP), series of single line melt structures with increasing number of interactions were fabricated, characterized and corresponding thermal diffusion simulations performed. The experimental results show how MIP allows to lower surface roughness of melted structures through a reduction of spattering, balling and melt pool displacement during processing, while our simulation model identifies these benefits to be caused by a significant reduction in surface temperature and thus evaporation, with increasing number of interactions for melt pool formation. Our model further demonstrates, how a relatively simple, computationally inexpensive and thus scalable thermal diffusion model is capable of providing valuable information about thermal conditions during melt pool formation. Lastly, we introduce a few simple equations to calculate appropriate MIP parameters for any kind of scan strategy.

Gas CO2 foaming and intermixing in portland cement paste to sequester CO2

In this study, concentrated CO2 gas was used to create foamed cement paste, and concentrated CO2 gas was intermixed in fresh cement paste to produce regular cement paste materials that were not foamed. The potential of both methods to form CaCO3 from calcium ions that would form Ca(OH)2 was investigated. After curing the materials for different ages, the Ca(OH)2 and CaCO3 contents were measured using thermogravimetric analysis; the large void size distributions, dynamic modulus, and compressive strength were tested and compared against Control (no gas added), and N2 foamed and N2 intermixed specimens. A 10% increase in dynamic modulus and compressive strength was measured in CO2 foamed specimens compared to N2 foamed specimens. The increase in mechanical properties was the result of both a narrow void diameter distribution and CaCO3 formation in place of Ca(OH)2. The CO2 foamed cement generation method shows the potential to sequester 0.06 ton of CO2 for every ton of cement which is a CO2 emission reduction of 7.0% of the CO2 production associated with cement production. For the CO2 intermixing method, the void content, compressive strength, and dynamic modulus results were consistent between the Control and CO2 intermixed specimens while the N2 intermixed specimens showed a decrease in compressive strength and dynamic modulus. The CO2 intermixing method showed potential to sequester 0.04 ton of CO2 for every ton of cement or a 4.7% CO2 emission reduction of the total CO2 production associated with cement manufacturing. The reported CO2 emissions are not based on life cycle assessment and do not account for emissions associated with CO2 collection, transportation, and intermixing. The present paper does not investigate the mechanisms of hydration under CO2 intermixing.

INTERSTELLAR EXTINCTION MODELLING BY AGGREGATE DUST

Extinction generally ours whenever electromagnetic radiation propagates through a medium containing small particles. The spectral dependence of extinction, or extinction curve, is a function of the composition, structure and size distribution of the particles. The study of interstellar extinction is important because they provide essential information for understanding the properties of the dust. In this work we have considered the aggregate dust model to interpret the extinction efficiency (Qext) of interstellar dust in the wavelength range 0.11µm to 3.4µm. Using Superposition T-matrix code with Ballistic Cluster-Cluster Aggregate (BCCA) aggregate having 64 number of monomers with graphite, astronomical silicates and amorphous carbon, the normalized extinction efficiency has been calculated for a well designed size distribution within a size range 0.001 to 0.077 micron of extinction near wavelength 0.2175µm. It is seen that for large grain size distribution the well pronounced UV-bump almost disappear. Moreover the nature of variation of extinction curve with increasing size of the grain has also been shown.

Potential Optimization of Industrial Waste as an Alternative Material for Composite Filler in Brake Pad Manufacturing – A Review

This study investigates the sustainable utilization of fly ash, palm slag and Cement By-Pass Dust (CBPD) waste as alternative materials for environmentally friendly brake pad development. These waste materials, with compositions similar to Asbestos, historically used in brake pad composites, present an eco-conscious solution. Integrating industrial waste in brake pad production offers substantial environmental benefits, technological progress, and commercial advantages. The compaction value and particle size distribution significantly impact brake pad mechanical properties. Adjusting these factors is crucial for meeting desired mechanical property requirements. A large particle size distribution enhances material density and hardness poses challenges in maintaining performance stability at high temperatures despite good recovery values. This paper highlights the potential of waste materials for sustainable brake pad development and underscores the need for careful optimization for high-temperature stability.

Liquid dispersion behaviors in a rotating packed bed with different packing arrangements: A comparison study

Wire mesh packing is widely used in the rotating packed bed (RPB). Packing arrangements have been proven to influence the mass transfer of an RPB. However, the liquid dispersion behaviors including dispersion characteristics and mechanisms for packing with different arrangements require further study. In this work, the dispersion behaviors of wire mesh packing with coiled and concentric arrangements were compared. An in-situ Doppler optical probe method was firstly employed to obtain fundamental parameters of liquid dispersion characteristics, such as the Sauter mean diameter, size distribution, and velocity of liquid droplets. The obtained results showed that the coiled arrangement was conducive to generating droplets with large velocity and narrow size distribution owing to the capturing and spreading of liquid inside the packing, while the concentric arrangement was beneficial in decreasing droplet size due to the shearing and carrying actions of the packing. Based on the optimization of liquid dispersion, the max and average reductions of d32 were 34.8% and 19.0% for packing with concentric arrangement than a coiled one. Further comparison results of dispersion characteristics indicated that the optimized concentric arrangement with 3 layers could provide better liquid dispersion than that of a coiled one with around 20 layers.

Trace Silicon Determination in Biological Samples by Inductively Coupled Plasma Mass Spectrometry (ICP-MS): Insight into the Volatility of Silicon Species in Hydrofluoric Acid Digests for Optimal Sample Preparation and Introduction to ICP-MS

A method for the determination of trace levels of silicon from biological materials by inductively coupled plasma mass spectrometry (ICP-MS) has been developed. The volatility of water-soluble silicon species, hexafluorosilicic acid (H2SiF6), and sodium metasilicate (Na2SiO3) was investigated by evaporating respective solutions (50 µg/mL silicon) in HNO3), nitric acid + hydrochloric acid (HNO3 + HCl), and nitric acid + hydrochloric acid + hydrofluoric acid (HNO3 + HCl + HF) at 120 °C on a hot-block to near dryness. The loss of silicon from H2SiF6 solutions was substantial (&gt;99%) regardless of the digestion medium. Losses were also substantial (&gt;98%) for metasilicate solutions heated in HNO3 + HCl + HF, while no significant loss occurred in HNO3 or HNO3 + HCl. These results show that H2SiF6 species were highly volatile and potential losses could confound accuracy at trace level determinations by ICP-MS if digestates prepared in HF are heated to eliminate HF. Among the various matrices comprising major elements, sodium appeared to be effective in reducing silicon loss from H2SiF6 solutions. Excess sodium chloride (NaCl) matrix provided better stability, improving silicon recoveries by up to about 80% in evaporated HF digestates of soil and mine waste samples, but losses could not be fully prevented. To safely remove excess acids and circumvent the adverse effects of excess HF (e.g., risk of high Si background signals), a two-step digestion scheme was adopted for the preparation of biological samples containing trace silicon levels. A closed-vessel digestion was performed either in 4 mL of concentrated HNO3 and 1 mL of concentrated HCl or 4 mL of concentrated HNO3, 1 mL of concentrated HCl and 1 mL of concentrated HClO4 on a hot plate at 140 °C. Digestates were then evaporated to incipient dryness at 120 °C to remove the acids. A second closed-vessel digestion was carried out to dissolve silicates in 0.5 mL of concentrated HNO3 and 0.5 mL of concentrated HF at 130 °C. After digestion, digestates were diluted to 10 mL. The solution containing about 5% HNO3 and 5% HF was directly analyzed by ICP-MS equipped with an HF-inert sample introduction system. The limit of detection was about 110 µg/L for 28Si when using the Kinetic Energy Discrimination (KED) mode. The method was used to determine silicon in various plant and tissue certified reference materials. Data were acquired for 28Si using KED and standard (STD) modes, and 74Ge and 103Rh as internal standard elements. There was not any significant difference between the accuracy and precision of the results obtained with 74Ge and 103Rh within the same measurement mode. Precision, calculated as relative standard deviation for four replicate analyses, varied from 5.3 (tomato leaves) to 21% (peach leaves) for plant and from 2.2 (oyster tissue) to 33% (bovine liver) for tissue SRM/CRMs. Poor precision was attributed to material heterogeneity and the large particle size distribution. An analysis of lung tissue samples from those with occupational exposure to silica dust revealed that tissues possessed substantial levels of water-soluble silicates, but the most silicon was present in the particulate matter fraction.

Effect of Molecular Architecture of Surface-Active Organosilicon Macromers on Their Colloidal Properties in Relation to Heterophasic Radical Polymerization of Styrene and Methyl Methacrylate

The effects of the molecular architecture of water-insoluble organosilicon polymerizable surfactant macromers (SAMs) on their colloidal-chemical characteristics and on their efficiency in heterophase radical polymerization of styrene and methyl methacrylate were studied. It was shown that despite considerable differences in the structure of three synthesized oligomers (linear α,ω-dipropylmethacrylatepolydimethylsiloxane with a number of repeated siloxane units n = 20—l-SAM; branched γ-methacryloxypropyl containing dimethylsiloxane oligomer—b-SAM; and “spherical” oligo-(γ-methacryloxypropyl)silsesquioxane—s-SAM), the colloidal-chemical characteristics (interfacial tension, layer thickness, adsorption, etc.) were rather similar. In particular, they all form “thick” multimolecular adsorption layers on the toluene–water interphase. All three SAMs were shown to act as effective colloidal stabilizers in heterophase radical polymerization of styrene and methyl methacrylate, which resulted in one-step preparation of large (0.5–1.5 µm) polymer particles with narrow particle size distribution. The obtained results are consistent with the published data on the use of water-insoluble polymerizable oligomers of various chemical structures on the heterophase radical polymerization. The use of these colloidal stabilizers may be considered as an effective way to obtain stable suspensions with large particles and narrow particle size distribution.

Mesoporous organosilicas with highly-content tyrosine framework as extractive phases for non-steroidal anti-inflammatory drugs in aquatic media

BackgroundAttentions regarding ordered mesoporous silica materials (OMSs), with large specific surface areas and narrow pore size distribution, which are prepared via self-assembly techniques, have been raised in sorption, separation, and sample preparation. However, in order to extend and improve their applications, a functionalization step is required. Organic units can be anchored on the inner or outer surface as well as in the silica wall framework by co-condensation-, grafting-, and periodic mesoporous organosilica (PMO) preparation approaches. Apparently, by synthesizing PMO with extensive and flexible organic bridging groups within the mesoporous wall, an efficient extractive phase can be achieved. ResultsWe employed tyrosine amino acid to synthesize a PMO-based extractive phase. The FT-IR, 1H NMR, HR-ESI-MS, Low angle-XRD, TEM, FESEM, BET, and EDX-MAP analyses confirmed the successful synthesis of PMO within the salt-assisted templating method. A comprehensive study on sorption behavior of PMO was performed and its efficiency was evaluated against the grafting and co-condensation methods. Then, it was implemented to the pipette tip-micro solid phase extraction (PT-μ-SPE) of widely used non-steroidal anti-inflammatory drugs (NSAIDs) in water/wastewaters. Limits of detection and quantification were obtained in the range of 0.1–1.5 and 0.3–5 μg L−1, respectively. The calibration plots are linear in the 1–1000, 3–1000, 10–750, and 3–750 μg L−1, respectively. The intra-and inter-day precision at 50 and 200 μg L−1 levels are 2.9–7.1 % and 3.5–8%, while recoveries are between 84 and 111 %. SignificanceHigh-capacity tyrosine functionalized PMO with 2D hexagonal symmetry silica mesoporous structures found to be highly efficient extractive media. Despite the bulkiness and flexibility of the bridging group within the mesoporous wall, the synthesis condition was optimized in order to load more organic content in the PMO structure. The PMO performance was superior over organically modified ordered mesoporous silica materials prepared by the grafting and co-condensation methods.

Further study on particle size, stability, and complexation of silver nanoparticles under the composite effect of bovine serum protein and humic acid.

Silver nanoparticles (AgNPs) are widely used due to their unique antibacterial properties and excellent photoelectric properties. Wastewater treatment plants form a pool of AgNPs due to the social cycle of wastewater. During biological treatment processes, the particle size and stability of AgNPs change. We studied the particle size changes and stability of silver nanoparticles in the presence of bovine serum albumin (BSA) and humic acid (HA). The experimental results indicated that silver nanoparticles can complex with the functional groups in BSA. For AgNP-BSA composites, as the BSA concentration increases, the size of the silver nanoparticles first decreases and then increases. AgNPs can combine with the amide, amino, and carboxyl groups in HA. As the concentration of HA increases, the particle size and large particle size distribution of AgNPs increase. This increasing trend is more obvious when the HA concentration is lower than 20 mg L-1. When HA and BSA exist at the same time, HA will occupy the adsorption sites of BSA on the surface of AgNPs, and the AgNP-HA complex will dominate the system. This study aims to provide key operational control strategies for the process operation of wastewater treatment plants containing AgNPs and theoretical support for promoting water environment improvement and economic development such as tourism.

Few-layer graphene as an ‘active’ conductive additive for flexible aqueous supercapacitor electrodes

We demonstrate that few layer graphene (FLG), formed by high-shear exfoliation into an aqueous suspension, can be successfully employed as an ‘active’ conductive additive in flexible activated carbon-based aqueous electric double layer capacitor (supercapacitor) electrodes if introduced by a novel ‘vacuum infiltration’ technique. The effectiveness of the FLG can be optimised by tailoring its size distribution and loading. It is found that best performance is achieved using FLG with the broadest size distribution and, moreover, that the larger size distribution is effective over the broadest range of loading. With optimum size distribution and loading, FLG is shown to outperform a commercial carbon black conductive additive (Timcal C65). Electrodes containing 8 wt% infiltrated FLG have an equivalent series resistance (ESR) of 1.3±0.4Ω, and a specific capacitance of 142.3±0.1 F g−1 over a voltage window of 1.2 V, compared with an ESR of 3±1Ω and a specific capacitance of 96.81±0.02 F g−1 for equivalent electrodes produced with an optimal loading of carbon black additive. As a result, the specific energy density of electric double layer capacitors (EDLCs) produced with a vacuum infused FLG additive is demonstrated to be an average of 47±3% superior to those containing carbon black measured at similar power densities. In contrast to vacuum infiltration, direct mixing of FLG suspension into the electrodes is found to be ineffective, resulting in limited improvement relative to electrodes without conductive additive, the reasons for which are discussed.