Effects Of Chemical Aging Research Articles

Impact of chemical aging on pyrogenic carbon colloid facilitated transport and transformation of Cr (VI) in anoxic environments

Frequent wildfires have accumulated the pyrogenic carbon (PyC) colloids in the environment, where they undergo environmental aging processes. The altered properties of aged PyC colloids may affect their ability to facilitate transformation and transport of contaminants in post-fire environments, posing unknown threats to ecological security. This study investigated the effect of chemical aging on the PyC colloid-facilitated transformation and transport of chromium (Cr) using batch experiments, column experiments, and transport model simulations. Results showed that aged PyC colloids exhibited weaker electron-donating capacity, and the reduction of Cr (VI) to Cr (III) decreased from 37.6 % to 13.5 % with the increasing aging time. Although PyC colloid transport increased with aging time, the PyC colloid-facilitated Cr (III) transport decreased because of the weakened reduction of Cr (VI). The transport of PyC colloid-facilitated Cr (III) was weaker at low pH. The reactive solute transport model well simulated the aged PyC colloid-facilitated transformation and transport of Cr (VI). Our findings highlight the significance of aging processes and environmentally relevant conditions in influencing the PyC colloid-facilitated transformation and transport of Cr, which is crucial for assessing risks of wildfire-driven Cr pollution and the potential of PyC for in-situ pollution control.

Ozonolysis of Terpene Flavor Additives in Vaping Emissions: Elevated Production of Reactive Oxygen Species and Oxidative Stress.

The production of e-cigarette aerosols through vaping processes is known to cause the formation of various free radicals and reactive oxygen species (ROS). Despite the well-known oxidative potential and cytotoxicity of fresh vaping emissions, the effects of chemical aging on exhaled vaping aerosols by indoor atmospheric oxidants are yet to be elucidated. Terpenes are commonly found in e-liquids as flavor additives. In the presence of indoor ozone (O3), e-cigarette aerosols that contain terpene flavorings can undergo chemical transformations, further producing ROS and reactive carbonyl species. Here, we simulated the aging process of the e-cigarette emissions in a 2 m3 FEP film chamber with 100 ppbv of O3 exposure for an hour. The aged vaping aerosols, along with fresh aerosols, were collected to detect the presence of ROS. The aged particles exhibited 2- to 11-fold greater oxidative potential, and further analysis showed that these particles formed a greater number of radicals in aqueous conditions. The aging process induced the formation of various alkyl hydroperoxides (ROOH), and through iodometric quantification, we saw that our aged vaping particles contained significantly greater amounts of these hydroperoxides than their fresh counterparts. Bronchial epithelial cells exposed to aged vaping aerosols exhibited an upregulation of the oxidative stress genes, HMOX-1 and GSTP1, indicating the potential for inhalation toxicity. This work highlights the indirect danger of vaping in environments with high ground-level O3, which can chemically transform e-cigarette aerosols into new particles that can induce greater oxidative damage than fresh e-cigarette aerosols. Given that the toxicological characteristics of e-cigarettes are mainly associated with the inhalation of fresh aerosols in current studies, our work may provide a perspective that characterizes vaping exposure under secondhand or thirdhand conditions as a significant health risk.

A constitutive model of solid propellants considering aging and confinement pressure

AbstractAging during storage and confinement pressure during launch are the two major loading conditions that affect the integrity of solid rocket motors. In comparison to other component materials, solid propellants, as highly filled composites, have a low modulus and fracture toughness and are therefore common sources of failure. The key to improving the integrity of the solid rocket motor is in assessing the health of the solid propellants during storage or launch. To address this issue, we revised the previous model for the progressive damage viscoelasticity of solid propellants to include the effect of chemical aging during storage and the influence of confinement pressure during launch. Specifically, the increase in relaxation time due to aging and the nonequilibrium volume dilatation characteristics under triaxial tension and compression of solid propellants have been considered. To validate the developed model, standard relaxation tests and uniaxial tensile tests on solid propellants without aging were used to calibrate the model parameters. Furthermore, the model was validated by comparison with uniaxial tensile tests under confined pressure after aging and well predicts the aging temperature/time‐dependent mechanical responses of solid propellants. After validation, the developed model was used to study the influence of confinement pressure on microscopic damage evolution and macroscopic volume expansion. Overall, the developed model can be used for the analysis of the integrity of the solid rocket motor after the aging process.

Effect of chemical aging on phosphate adsorption and ecotoxicological properties of magnesium-modified biochar

Using magnesium-biochar composites (Mg-BC) in adsorption allows for the efficient and economically relevant removal of phosphate (PO43−) from water and wastewater. Applying Mg-BC for pollutant removal requires evaluating the adsorption capacity of composites and their ecotoxicological properties. Investigating the composite aging during the application of these composites into the soil is also essential. In the present study, nonaged and aged (at 60 or 90 °C) Mg-BC composites were investigated in the context of pyrolysis temperature (500 or 700 °C). All analyzed biochars were examined by Fourier transform infrared spectroscopy, X-ray powder diffraction, X-ray photoelectron spectroscopy, Raman spectroscopy and surface area. The content of polycyclic aromatic hydrocarbons (PAHs) (bioavailable Cfree and organic solvent-extractable Ctot), heavy metals (HMs), and environmentally persistent free radicals (EPFRs) were determined. Ecotoxicity was evaluated using tests with Folsomia candida and Allivibrio fischeri. The dependence of adsorption on pyrolysis temperature and composite aging time was observed. Changes in physicochemical properties occurring as a result of aging reduced the adsorption of PO43− on Mg-BC composites. It was found that nonaged Mg-BC700 was more effective (9.55 mg g −1) in the adsorption of PO43− than Mg-BC500 (5.75 mg g−1). The adsorption capacities of aged composites were from 21 to 61% lower than those of the nonaged composites. Due to aging, the content of Cfree PAHs increased by 3–5 times depending on the pyrolysis temperature. However, aging reduced the Ctot PAHs in all composites from 24 to 35% depending on the pyrolysis temperature. Ecotoxicological evaluation of Mg-BC composites showed increased toxicity after aging to both organisms. The use of aged BC potentially increases the contaminant content and toxicity of Mg-BC composites.

Effects of chemical aging on carbonaceous materials: Stability of water-dispersible colloids and their influence on the aggregation of natural-soil colloid

Although hydrochar and biochar have been used as soil conditioners, there is not a clear understanding of how their properties changes due to aging impacts their colloidal particles behavior on the soil system. From this premise, we produced hydrochar and biochar from the same feedstock (cashew bagasse) and aged with different chemical methods: (i) using hydrogen peroxide, (ii) a mixture of nitric and sulfuric acids, and (iii) hot water. It was analyzed the effects of aging on the stability of the carbonaceous materials (CMs) colloids in aqueous medium with different ionic strength (single systems), as well as the stability of the natural-soil colloid when interacting with biochar and hydrochar colloids (binary systems). A chemical composition (C, H, N, and O content) change in CMs due to the chemically induced aging was observed along with minor structural modifications. Chemical aging could increase the amount of oxygen functional groups for both biochar and hydrochar, though in a different level depending on the methodology applied. In this sense, hydrochar was more susceptive to chemical oxidation than biochar. The effectiveness of chemical aging treatments for biochar increased in the order of water < acid < hydrogen peroxide, whereas for hydrochar the order was water < hydrogen peroxide < acid. While the increase in surface oxidation improved the biochar colloidal stability in water medium at different ionic strengths (single systems), the stability and critical coagulation concentration (CCC) slightly changed for hydrochar. Natural-soil clay (NSC) interactions with oxidized carbonaceous material colloids (binary systems) enhanced NSC stability, which is less likely to aggregate. Therefore, the aging of carbonaceous materials modifies the interaction and dynamics of soil small particles, requiring far more attention to the environmental risks due to their application over time.

Water in polyurethane networks: physical and chemical ageing effects and mechanical parameters

The chemical structure, polymer mobility and mechanical properties are studied for a cross-linked amorphous poly(ether urethane) (PU) from glass transition to rubber elasticity for juvenile dry samples and for water-saturated states after exposure to humid air (r.h. = 29, 67, 95, 100%) at 60∘C\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$60~^\\circ \\hbox {C}$$\\end{document} during 1 y of ageing. For saturated samples, network chain cleavage is the chemical ageing mechanism, but it is too weak and slow to affect on the physical properties significantly within 1 y. Water acts primarily in a physical manner. Within 1 d, H2O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {H}_{{2}}\\hbox {O}$$\\end{document} molecules replace part of the weak urethane H-bonds by H2O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {H}_{{2}}\\hbox {O}$$\\end{document}–urethane H-bonds and reduce all other physical interactions between network chains by solvating hydrophilic segments. Thus, the cooperative polymer mobility strongly amplifies: The gain of specific conformational entropy doubles across the caloric glass transition, which shifts by −17 K. A H2O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {H}_{{2}}\\hbox {O}$$\\end{document} concentration of only cH2O≈(0.4…0.5)cH2O,max\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {c}_{{\\mathrm{H}_2\\mathrm{O}}}~\\approx ~(0.4~\\ldots ~0.5)~\\hbox {c}_{\\mathrm{\\mathrm{H}_2\\mathrm{O},max}}$$\\end{document} suffices for the major part of these fast rearrangements. Some part of the water slowly forms (during 3–4 months) a finely dispersed water-rich mixed phase with the PU chains. Except the new phase, these molecular processes of physical ageing strongly affect the mechanical properties at damage-free deformation. For dry PU in the glass transition, the shear modulus, μrelaxed\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\mu _{\\mathrm{relaxed}}$$\\end{document}(T), after viscoelastic stress relaxation only depends on the deformation-induced entropy change—like in the rubber elastic state. Within one month, water drastically decreases the viscoelastic response, as expected for plasticisation. However, μrelaxed\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\mu _{\\mathrm{relaxed}}$$\\end{document}(T) slightly grows in wet PU. H2O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {H}_{{2}}\\hbox {O}$$\\end{document} molecules cause these opposite trends by boosting the cooperative mobility (i.e. extension of the accessible conformational space and entropy by reduction in energy barriers) and by occupation of free volume compartments. Water quickly reduces the fracture parameters by about 50%. We explain that embrittlement by the H2O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {H}_{{2}}\\hbox {O}$$\\end{document}-induced facilitation of cooperative network chain motions, which let fracture proceed with less energy. In summary, our findings provide a detailed conception of the molecular effects the H2O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\hbox {H}_{2}\\hbox {O}$$\\end{document} molecules have on the PU network, and they explain the consequences for the mechanical properties.

Cannabis Consumption in Dispensaries: Public Health Implications of an Emerging Practice.

Cannabis Consumption in Dispensaries: Public Health Implications of an Emerging Practice.

Effect of chemical aging of monoterpene products on biogenic secondary organic aerosol concentrations

Capturing the effects of the complex processes of chemical aging of biogenic secondary organic aerosol (SOA) in chemical transport models (CTMs) has been challenging. Recent laboratory results from atmospheric simulation chambers are used in this study to develop a parameterization for biogenic SOA formation as a result of aging for use in CTMs using the Volatility Basis Set framework. This parameterization was implemented in PMCAMx which was then applied over the eastern United States to simulate summertime conditions. Using the base case parameterization of monoterpene SOA chemical aging resulted in modest increases (17–21%) in predicted domain average biogenic SOA. An alternative parameterization was developed fitting the same laboratory results, but assuming higher volatility products of chemical aging reactions. Use of this parameterization resulted in small increases (1–4%) of the predicted biogenic SOA. The PMCAMx predictions in sites where most of the SOA was biogenic were evaluated against measurements from the EPA IMPROVE network in July 2001 and during the Southern Oxidant and Aerosol Study in June 2013. The differences in the model performance were modest and mixed, a result consistent with the relatively small effect of the proposed parameterization on total organic aerosol levels.

Effect of chemical aging on color stability and surface properties of stained all-ceramic restorations.

To study the effect of artificial aging on color stability, translucency, and surface roughness of stained all-ceramic restorations. Disc-shaped specimens were fabricated from six different all-ceramic materials: two glass ceramics (Vita Mark II and Empress CAD), two lithium disilicate based ceramics (e.max and Suprinity), and two zirconia-based materials (ZirCAD LT and ZirCAD MT Multi). The discs were stained using two universal stains; IPS Ivocolor stain or Vita Akzent stain. Color change (ΔE) and the translucency parameter (TP) were measured before and after artificial aging. The surface roughness (Ra) was evaluated using atomic force microscopy, while the surface microstructure was evaluated using scanning electron microscopy (SEM). Quantitative elemental analysis was performed using the energy dispersive X-ray (EDX). Leached ions were analyzed by inductively coupled plasma (ICP) (n=12, α=0.05). Artificial aging had significantly changed the color (ΔE) and decreased the translucency (TP) of all stained ceramics. The mean surface roughness (Ra) was significantly increased in all specimens, which was also confirmed in the SEM scans. EDX analysis revealed a decrease in the elemental composition of the stained surface as a result of ceramic degradation, except for Ca and Zn in IPS Ivocolor stain. Furthermore, the ICP analysis revealed that most compositional elements of stain and glaze were detected in the aging solution. Chemical aging had significantly affected the optical parameters and surface texture of stained monolithic ceramics. Stained ceramics are liable to color degradation. Each type of stain should be used with its corresponding type of ceramic. Stained all-ceramic restorations are liable to color change and surface degradation during function.

Characterization of the Evolution of Noble Metal Particles in a Commercial Three-Way Catalyst: Correlation between Real and Simulated Ageing

Ageing of automotive catalysts is associated to a loss of their functionality and ultimately to a waste of precious resources. For this reason, understanding catalyst ageing phenomena is necessary for the design of long lasting efficient catalysts. The present work has the purpose of studying in depth all the phenomena that occur during ageing, in terms of morphological modification and deactivation of the active materials: precious metal particles and oxidic support. The topic was deeply investigated using specific methodologies (FT-IR, CO chemisorption, FE-SEM) in order to understand the behavior of metals and support, in terms of their surface properties, morphology and dispersion in the washcoat material. A series of commercial catalysts, aged in different conditions, have been analyzed, in order to find correlations between real and simulated ageing conditions. The characterization highlights a series of phenomena linked to the deactivation of the catalysts. Pd nanoparticles undergo a rapid agglomeration, exhibiting a quick loss of dispersion and of active sites with an increase of particles size. The evolution of the support allows highlighting also the contribution of chemical ageing effects. These results were also correlated with performance tests executed on synthetic gas bench, underlining a good correspondence between vehicle and laboratory aged samples and the contribution of chemical poisoning to vehicle aged ones. The collected data are crucial for the development of accelerated laboratory ageing protocols, which are instrumental for the development and testing of long lasting abatement systems.

Chemical ageing effects on the ply and laminate strength of a filament wound cross-ply GFRP

This work presents a numerical approach to multi-routines based on experiments, and, with a target to analyse strength of a cross-ply glass fibre reinforced plastics (GFRP) composite after immersion in sulphuric acid solution under pressure (5% H2SO4 solution, 95 °C, 15 bar). Two alternative vinyl ester resins (bisphenol A diglycidyl ether and epoxy phenol novolac) were investigated. After 0.5, 1, 1.5 and 2 years of conditioning, the specimens were mechanically tested. The multi-scale definition of the material system and its virtual conditioning were performed in a finite element (FE) model. The Hashin 3D failure criterion was implemented by coding the UMAT subroutine when using the Abaqus software. The experimental results demonstrated better performance of the bisphenol A vinyl ester resin-based GFRP when a thin barrier layer is used. The numerical results indicated that the shear strength property was the most susceptible at weak zones to present a tendency for degradation after one year of conditioning.

EFFECT OF CHEMICAL AGING ON THE COLOR STABILITY OF TWO CERAMIC MATERIALS; ZIRCONIA REINFORCED LITHIUM SILICATE AND LITHIUM DISILICATS CERAMICS

Objectives: The presence of fine-grained crystals of lithium silicate, which contains a high amount of glass provides the material it’s optical and mechanical characteristics. This unique microstructure allows this material to be processed in a dental lab quickly and efficiently in its crystalline state and the exact tooth shade. This study aims to evaluate the color stability of zirconia reinforced lithium silicate ceramic and lithium disilicates ceramic restorations. Materials and Methods: In this in vitro study, 40 discs of 2mm thickness and 10mm in diameter would be fabricated, all samples were divided into two groups (n=20) according to ceramic material used: group Z zirconia reinforced lithium silicates ceramic(ZLS) and group L lithium disilicate ceramic(LS) discs. Each group was subdivided into two subgroups according to the aging process (n=10) (before and after aging). CIELAB color parameters of all samples were calculated from spectral reflectance measurements on a spectrophotometer to evaluate the effect of chemical aging on the color stability. Statistical Analysis: One-way ANOVA analysis was used to compare measurements among groups. Results: ZLS showed lower color stability than LS, and there was a statistical difference between them. Aging affected the color stability of the two ceramics but within an acceptable range with lithium disilicates. Conclusion: ZLS gave lower color stability than LS and aging affected the color stability of both types of ceramic. The postulated hypothecs of this study were ZLS will be higher color stability than LS and chemical aging will have a huge effect.

Influence of part dimension on ageing of injection moulded thermoplastic materials: exemplary studies on amorphous polycarbonate

Injection moulding of polymer micro parts often affects the inner structure due to process conditions with reduced part dimensions. Consequently, ageing effects can increase with reduced part dimensions. This paper investigates the ageing effects in different scaled tensile bars, exemplarily injection moulded of polycarbonate. The results reveal during the here applied artificial ageing conditions the chemical ageing effects have less influence and primary physical ageing effects take place. A reduction of part dimensions leads to increasing impact of ageing effects for the here investigated polycarbonate.

The effect of chemical aging on water permeability of white cement mortars in the context of sol–gel science

In the sol–gel science, the influence of chemical aging on the fundamental water permeability remains open regarding to the durability performance of cement-based material. To reveal the pure effect of chemical aging, the water permeability and related micro-structural characteristics are measured on water-saturated mature mortars, whose aging is accelerated through heat treatment under water. It is found that, the chemical aging increases the volumetric porosity and coarsens the pore structure to a notable extent, which enlarge water permeability by 2.6–4.9 times. Based on the pore structure obtained through the low-field proton NMR technique, the water permeability is predicted by the Katz–Thompson theory with satisfactory accuracy, quantitatively confirming the direct effects of chemical aging on water permeability. Physically, because of the polymerization and rearrangement of C–S–H gel, cement mortars undergo substantial changes with enlarging radii for both interlayer and gel pores, slightly decreasing interlayer space but remarkably enlarging gel pore space.

Effect of chemical aging of aqueous organic aerosols on the rate of their steady-state nucleation.

We present the steady-state solution of the kinetic equation for the size and composition distribution of an ensemble of aqueous organic droplets, evolving via nucleation and concomitant chemical aging. The partial differential equation of second order for the temporal evolution of this distribution can be reduced to the canonical form of the multidimensional Fokker-Planck equation, which can be solved analytically by using the method of complete separation of variables. Its solution for the steady-state process provides the stationary distribution of droplets in the vicinity of the saddle point of the free-energy surface as well as the stationary nucleation rate in the form of the product "kinetic (Zeldovich) factor × normalization factor × exp(-free energy of nucleus formation)". Our numerical evaluations for the formation of aqueous organic aerosols in the air containing the vapors of water, 2-methylglyceric acid, and 3-methyl-4 -hydroxy-benzoic acid, as well as typical atmospheric gaseous species, indicate that the steady-state nucleation rate of such aerosols can be significantly enhanced by their concomitant chemical aging. Thus, one can expect that the application of our approach to the formation and evolution of atmospheric aqueous organic aerosols (via concurrent nucleation and chemical aging) will make aerosol models more adequate and may, once implemented in climate models, improve their forecasting accuracy.

AMB2018-04: Benchmark Physical Property Measurements for Powder Bed Fusion Additive Manufacturing of Polyamide 12.

Laser sintering (LS) of polyamide 12 (PA12) is increasingly being adopted for industrial production of end-use parts, yet the complexity of this process coupled with the lack of organized, rigorous, publicly available process-structure-physical property datasets exposes manufacturers and customers to risks of unacceptably poor part quality and high costs. Although an extensive scientific literature has been developed to address some of these concerns, results are distributed among numerous reports based on different machines, materials, process parameters, and users. In this study, a single commercially important LS PA12 feedstock has been processed along four build dimensions of a modern production LS machine, characterized by a wide range of physical techniques, and compared to the same material formed by conventional melt processing. Results are discussed in the context of the literature, offering novel insights including distributions of particle size and shape, localization of semicrystalline phase changes due to LS processing, effect of chemical aging on melt viscosity, porosity orientation relative to LS build axes, and microstructural effects on tensile properties and failure mechanisms. The resulting datasets will be made publicly available to modelers and practitioners for the purpose of improving certifiability and repeatability of end-use parts manufactured by LS.

Effect of chemical aging of Alternanthera philoxeroides-derived biochar on the adsorption of Pb(II).

In this study, biochar was prepared from Alternanthera philoxeroides (AP) under O2-limited condition at 350 °C (LB) and 650 °C (HB) and treated with aging by HNO3/H2SO4 oxidation. Structural changes of the biochar after aging treatment and the treatment's effect on Pb(II) absorption were explored. The results showed that oxygen-containing functional groups, aromatic structure and surface area of the biochar increased after the aging treatment. However, the integrity of the tubular structure was broken into fragments. The adsorption process of Pb(II) was in accordance with the pseudo-second-order kinetic model and fitted by the Langmuir model. With the increase of pH, the adsorption capacities of Pb(II) increased gradually, and the adsorption effect was best at pH 5. The aged HB presented a decrease of the carboxyl group, which caused less adsorption capacity of Pb(II) than that of aged LB. The maximum adsorption capacities of Pb(II) on fresh biochar at 350 °C and 650 °C were 279.85 and 286.07 mg·g-1 and on aged biochar were 242.57 and 159.82 mg·g-1, respectively. The adsorption capacity of HB for Pb(II) was higher than that of LB, and the adsorption capacity of aged biochar for Pb(II) decreased obviously, which might be attributable to changes in physicochemical properties of biochar after the aging treatment.

Probing nano-heterogeneity and aging effects in lateral 2D heterostructures using tip-enhanced photoluminescence

Interest in two-dimensional (2D) transition metal dichalcogenide materials has recently grown due to their tunable band gap, large exciton binding energy, and flexibility in designing a wide range of optoelectronic devices. However, the presence of adsorbates, strain, and aging-induced heterogeneities can severely influence their excitonic photoluminescence (PL). Therefore, precise nanoscale correlation between the optical and structural heterogeneities is of paramount importance and needs further investigation. In this report, we used tip-enhanced photoluminescence (TEPL) imaging of the nanoscale exciton emission of air-aged monolayer MoSe2-WSe2 multijunction lateral heterostructures with subwavelength spatial resolution of 40 nm. Distinct regions corresponding to monolayer MoSe2 and WSe2 were identified. Near-field excitation was used for the quantitative evaluation of the optical transition width: 40 nm sharp transition (WSe2→MoSe2), and 230 nm smooth interface (MoSe2→WSe2). Nanoscale composition of the alloying properties of the junction was estimated using TEPL. Furthermore, localized optical fluctuations and the role of the aging-induced nanoparticles in the excitonic PL suppression were investigated. The observed linear dependence of the PL suppression as a function of the nanoparticle size indicates the contribution of the chemical aging effects. The correlation between the nanoscale optical and structural characteristics will be useful for controlling and manipulating excitons in the next-generation atomically thin devices.

Chemical ageing effects on the mechanical behaviour of ethylene-propylene diene monomer

Ethylene-propylene diene monomer (EPDM) elastomer diaphragm failures due to material degradation pose a major risk in the biopharmaceutical industry, as they can result in long periods of production downtime. It is suspected that a key cause of this EPDM degradation is due to the chemical solutions used in equipment cleaning processes. However this has never been empirically investigated in the public domain. Twenty four virgin samples were utilised for testing, twelve of which were subject to common chemical cleaning solutions used in the biopharmaceutical sector. The chemical solutions under investigation were aqueous solutions of NaOH, NaClO, H3PO4, and the interaction between 100 °C H2O and NaClO. The characterisation of the degradation process was conducted by mechanical testing. The results show that degradation of the polymer bulk proceeds predominantly via crosslinking for all exposure types. NaOH and H3PO4 exposure results in an accelerated rate of crosslinking compared to NaClO in the early stages of exposure.

Impacts of sodium hydroxide and sodium hypochlorite aging on polyvinylidene fluoride membranes fabricated with different methods

This study compared the effects of chemical aging on the polyvinylidene fluoride (PVDF) membranes fabricated with the methods of non-solvent induced phase separation (NIPS) (named NIPS-PVDF) and thermally induced phase separation (TIPS) (named TIPS-PVDF). The chemical solutions of sodium hypochlorite (NaClO) and sodium hydroxide (NaOH) were chosen at the concentration of 5000mg/L. The equivalence of 5 and 10years was respectively selected as the time of aging. The physicochemical evolutions of membrane aging are characterized on the base of morphology analysis, chemical components, permeation ability and mechanical properties. The aging of NIPS-PVDF membrane led to the elimination of surface hydrophilic additives, while NaOH focused on the dehydrofluorination process resulting in the formation of conjugated chains of polyene on the skeleton structure. The chemical components of the surface of TIPS-PVDF membrane were removed continuously during the aging processes of both NaClO and NaOH, which was caused by the saponification of surface additives and the chain scissions of skeleton structure, but without producing any obvious conjugated chains of polyene. All the aging processes led to the increase of contact angle and the decrease of mechanical properties, and the permeability was reduced first and increased later due to the enlargement of surface membrane pores and membrane block. With the influence of membrane aging, selectivity of membrane was decreased (except coliform bacteria). At the beginning of filtration, the turbidity and particle count were at relatively high levels and declined with the filtration process.