Absorption Spectroscopy Techniques Research Articles

Shell thickness influence on the carrier dynamics of InP/ZnS QDs

InP/ZnS core/shell quantum dots (QDs) have been widely applied in many fields due to their excellent luminescence performance. In this study, the correlation between the ZnS shell thickness and the ultrafast carrier dynamics in InP/ZnS QDs was investigated by using femtosecond time-resolved transient absorption spectroscopy and time-resolved photoluminescence techniques. We found that a thicker ZnS shell could confine more carriers to the InP core, thus effectively weakening the interactions between the carriers in the core and the interfacial defect states; this further enhanced the quantum yields and photoluminescence properties in InP/ZnS QDs.

Ultrafast Dynamics, Optical Nonlinearities, and Chemical Sensing Application of Free-Standing Porous Silicon-Based Optical Microcavities.

The present work demonstrates the ultrafast carrier dynamics and third-order nonlinear optical properties of electrochemically fabricated free-standing porous silicon (FS-PSi)-based optical microcavities via femtosecond transient absorption spectroscopy (TAS) and single-beam Z-scan techniques, respectively. The TAS (pump: 400 nm, probe: 430-780 nm, ∼70 fs, 1 kHz) decay dynamics are dominated by the photoinduced absorption (PIA, lifetime range: 4.7-156 ps) as well as photoinduced bleaching (PIB, 4.3-324 ps) for the cavity mode (λc) and the band edges. A fascinating switching behavior from the PIB (-ve) to the PIA (+ve) has been observed in the cavity mode, which shows the potential in ultrafast switching applications. The third-order optical nonlinearities revealed an enhanced two-photon absorption coefficient (β) in the order of 10-10 mW-1 along with the nonlinear refractive index (n2) in the range of 10-17 m2 W-1. Furthermore, a real-time sensing application of such FS-PSi microcavities has been demonstrated for detecting organic solvents by simultaneously monitoring the kinetics in reflection and transmission mode.

Study transport of hesperidin based on the DPPC lipid model and the BSA transport model

Hesperidin (HE), a significant flavonoid polyphenolic compound present in citrus plants, exhibits diverse pharmacological effects. Considering the crucial involvement of biological membranes and transporter proteins in the transportation and biological processes of HE, it becomes essential to comprehend the potential mechanisms through which HE interacts with membranes and transporter proteins. In order to simulate the process of active molecule transport, a cell membrane model consisting of 1,2-dipalmitoyl-n-glycero-3-phosphatidylcholine (DPPC) and a transporter protein model of bovine serum albumin (BSA) were employed for investigation. The present study aimed to investigate the mechanism of action of hesperidin (HE) in DPPC and BSA using fluorescence quenching, Fourier transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC). The localization and interaction of HE within liposomes were also elucidated. Furthermore, the binding of BSA and HE was analyzed through UV/Vis absorption spectroscopy, fluorescence spectroscopy, infrared spectroscopy, and computational biology techniques. Computational biology analysis revealed that the binding between HE and BSA primarily occurred via hydrogen bonding and hydrophobic interactions. This study aimed to investigate the role and mechanism of HE in the DPPC cell membrane model and the BSA transporter protein model, thereby offering novel insights into the action of HE in DPPC and BSA.

Correlation of electronic structure and magnetic properties of [formula omitted] nanostructure using synchrotron soft XAS

The present study reports crystalline structure, electronic structure and magnetic properties for nanoparticles undoped CeO2 and Ce1-xSmxO2 (x = 0.02 to 0.10, @ 0.02). The nanoparticle samples are synthesized by the co-precipitation method. XRD data shows the successful incorporation of Sm3+ ions at Ce4+ sites in the face-centered cubic (fcc) lattice. The soft X-ray absorption spectroscopy technique is utilized to get an insightful overview of electronic structural properties due to structural defects, chemical states and the development of oxygen vacancies in Ce1-xSmxO2 nanoparticles. The soft XAS spectra show a significant Ce and Sm peak in the M4,5 domain, along with the well-defined O K-edge peak. Analysis of Ce M4,5-edges indicates that Ce-ions have both 3 + and 4 + oxidation states. With the incorporation of Sm+3 ions, there is a reduction of Ce4+ states and oxidation of Ce3+ states, as well as a substantial increase in oxygen vacancy concentration. The room-temperature magnetic properties of Ce1-xSmxO2 nanoparticles reveal ferromagnetic behavior. The origin of ferromagnetism is explained by F-center exchange (FCE) coupling mechanisms mediated via development of oxygen vacancy and defects.

Pyridine appended pyrimidine bis hydrazone: Zn2+/ATP detection, bioimaging and functional properties of its dinuclear Zn(II) complex

A pyridine functionalized pyrimidine-based system, H2P was successfully synthesized, characterized, and evaluated for its remarkable selective characteristics towards Zn2+ and ATP ions. The chemical sensing capabilities of H2P were demonstrated through absorption, fluorescence, and NMR spectroscopic techniques. The probe exhibited outstanding sensitivity when interacting with the ions, demonstrating relatively strong association constants and impressively low detection limits. The comprehensive binding mechanism of H2P with respect to Zn2+ and ATP ions was investigated using a combination of analytical methods, including Job's plot, NMR spectroscopy, mass spectrometry, and density functional theory (DFT) experiments. The interesting sensing ability of H2P for Zn2+/ATP ions was harnessed for live cell bioimaging and other diverse on-site detection purposes, including paper strips, cotton swabs, and applications involving mung bean sprouts. Further, the fluorescent probe demonstrated its effectiveness in detecting Zn2+ and ATP within live cells, indicating its significant potential in the realm of biological imaging applications. Moreover, the molecular configuration of the zinc complex (H2P–Zn2Cl4), derived from H2P, was elucidated using X-ray crystallography. This complex exhibited intriguing multifunctional attributes, encompassing its capability for detecting picric acid and for reversible acid/base sensing responses. The enhanced conducting behavior of the complex as well as its resistance properties were investigated by performing I–V characteristics and electrochemical impedance spectroscopic (EIS) experiments respectively.

Nutritional Composition and Antinutritional Factors of Five Wild Edible Fruits Grown in the Mekdela District, South of Wollo, Ethiopia.

This study was carried out to determine the mineral content and nutritional properties of five wild fruits Rhus vulgaris, Rosa abyssinica, Rhus natalensis, Euclea racemosa, and Ficus sur. The proximate composition parameters (moisture, ash, crude fiber, crude fat, and crude protein) and antinutritional factors were evaluated using methods of the Association of Official Analytical Chemists and elemental analysis using the atomic absorption spectroscopy technique. Among the five wild edible fruit species, Rhus vulgaris had the highest carbohydrate content (83.3 ± 0.28 g/100 g) and a high total energy (344.5 ± 2.21 kcal/100 g). Euclea racemosa was found to have the maximum ash content (12.8 ± 0.37 g/100 g), protein content (3.22 ± 0.01 g/100 g), and moisture (16.24 ± 0.003 g/100 g), respectively. Rhus natalensis showed the highest fiber content (9.54 ± 0.003 g/100 g). Mineral analysis showed that local wild fruits contained a considerable amount of minerals. The calcium concentration ranged from 99.51 mg/100 g in Euclea racemosa to 160.12 mg/100 g in Ficus sur. Potassium concentration varied from 54.34 mg/100 g in Euclea racemosa to 234 mg/100 g in Rhus vulgaris. Iron ranges from 21.4 mg/100 g in Rosa abyssinica to 41 mg/100 g in Rhus natalensis, and zinc ranges from 2.3 mg/100 g in Rhus vulgaris to 4.2 mg/100 g in Ficus sur. A high saponin content (2.12 mg/100 g) and a low tannin content (0.23 mg/100 g) were obtained in Rosa abyssinica. The phytate content (1.52 mg/100 g) and the oxalate content (0.9 mg/100 g) were high in Rhus natalensis. In conclusion, the present study shows that wild fruits can be used as food supplementation in food in a safe area.

In-situ and operando Grazing Incidence XAS: a novel set-up and its application to model Pd electrodes for alcohols oxidation

Abstract In this article, we present an in-situ and operando time-resolved X-ray Absorption Spectroscopy (XAS) technique which exploits a combination of Grazing Incidence XAS (GIXAS) and Fixed Energy X-ray Absorption Voltammetry (FEXRAV), the Grazing Incidence FEXRAV (GI-FEXRAV). A case-study is also outlined. Palladium ultra-low loadings were deposited above Au polycrystalline iso-oriented substrates adopting three different deposition methods: surface-controlled electrochemical methods, direct electrodeposition, and physical vapour deposition (PVD). These catalytical surfaces were prepared for the investigation by GI-FEXRAV of the Pd oxidation/dissolution phenomenon that could occur when the metal is used in the anodic compartment of Direct Alcohol Fuel Cells (DAFCs) or in electrochemical reformers. Moreover, we report a robust, low cost and versatile procedure to obtain wide and flat iso-oriented gold substrates that can mimic monocrystalline gold (1 1 1) in the electrochemical response. The use of GI-FEXRAV for the operando characterization of the catalysts, in conjunction with the designed experimental cell and our flexible Au-based electrochemical substrates show an invaluable potential in the operando study of fundamental phenomena in heterogeneous electrocatalysis model systems and, due to its versatility, paves the way to further studies on a wide selection of electrochemical systems.

Molecular Interactions of Sodium Dodecyl Sulphate with a Sulpha Drug and its Nanoaggregates in Aqueous System

AbstractInteraction study between sulfanilamide (SM) and sodium dodecyl sulfate (SDS) in an aqueous environment has been conducted using electrical conductivity, emission, and absorption spectroscopy techniques. Conductivity measurements were performed over the temperature range of (288.15 to 318.15) K and SM concentrations ranging from (c=0.005 to 0.03) mol ⋅ L−1. Thermodynamic parameters: Gibbs free energy (ΔGom), enthalpy (ΔHom), and entropy (ΔSom) associated with micellization have been calculated. To further investigate the interactions between (SM and SDS), the absorption and emission spectroscopy were employed at premicellar concentrations of SDS. Resulting SM‐SDS conjugate was then utilized to examine its interaction behavior with electrolytes and vitamins commonly found in biofluids namely chlorides and sulfates of sodium, potassium, magnesium, and calcium, along with L‐ascorbic acid (LAA) and nicotinic acid (NA). Moreover, SM drug has been transformed into its nanoaggregates (SMNA). These nanoaggregates have been characterized using dynamic light scattering (DLS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Interactions between SMNA‐SDS conjugates were also studied in the presence of the above‐mentioned electrolytes and vitamins. The findings of this study have been interpreted within the context of the interactions occurring in the solution phase. This research provides valuable insights into the complicated interactions between SM, SDS, electrolytes, and vitamins in aqueous system.

High-precision characterization of quantum-cascade laser frequency response using wavelength modulation spectroscopy.

This paper investigates the impact of the quantum cascade laser's frequency modulation response on its tuning rate and tunability. We show a significant disparity in laser tuning rates and tunability between single and dual-frequency modulation schemes frequently used in typical direct absorption and wavelength modulation spectroscopy (WMS) techniques. We show that the DC-characterized tuning rate of a laser can be reduced significantly under a specific set of modulation frequencies of the laser injection current. We characterize these effects by simultaneous measurements of higher harmonic WMS of methane and nitrous oxide in the 7.8 µm spectral regions. We further show that WMS signal modulation broadening mechanisms and spectral structure, i.e., its zero-crossings and turning points, can be used to quantify such laser-modulation effects and validate laser frequency response under dual modulation schemes.

Temperature-Dependent Kinetics of the Reactions of the Criegee Intermediate CH2OO with Hydroxyketones.

Though there is a growing body of literature on the kinetics of CIs with simple carbonyls, CI reactions with functionalized carbonyls such as hydroxyketones remain unexplored. In this work, the temperature-dependent kinetics of the reactions of CH2OO with two hydroxyketones, hydroxyacetone (AcOH) and 4-hydroxy-2-butanone (4H2B), have been studied using a laser flash photolysis transient absorption spectroscopy technique and complementary quantum chemistry calculations. Bimolecular rate constants were determined from CH2OO loss rates observed under pseudo-first-order conditions across the temperature range 275-335 K. Arrhenius plots were linear and yielded T-dependent bimolecular rate constants: kAcOH(T) = (4.3 ± 1.7) × 10-15 exp[(1630 ± 120)/T] and k4H2B(T) = (3.5 ± 2.6) × 10-15 exp[(1700 ± 200)/T]. Both reactions show negative temperature dependences and overall very similar rate constants. Stationary points on the reaction energy surfaces were characterized using the composite CBS-QB3 method. Transition states were identified for both 1,3-dipolar cycloaddition reactions across the carbonyl and 1,2-insertion/addition at the hydroxyl group. The free-energy barriers for the latter reaction pathways are higher by ∼4-5 kcal mol-1, and their contributions are presumed to be negligible for both AcOH and 4H2B. The cycloaddition reactions are highly exothermic and form cyclic secondary ozonides that are the typical primary products of Criegee intermediate reactions with carbonyl compounds. The reactivity of the hydroxyketones toward CH2OO appears to be similar to that of acetaldehyde, which can be rationalized by consideration of the energies of the frontier molecular orbitals involved in the cycloaddition. The CH2OO + hydroxyketone reactions are likely too slow to be of significance in the atmosphere, except at very low temperatures.

Methylation Induces a Low‐energy Emissive State in N6‐methyladenine Containing Dinucleotides

AbstractMethylation of adenine at the N6 position is a crucial epigenetic modification that profoundly influences gene regulation and expression. Moreover, this modification intricately alters the excited state dynamics of adenine nucleobases. To explore the impact of N6‐methyladenine on the excited state dynamics within oligonucleotides, we conducted a comprehensive investigation of two dinucleotides containing N6‐methyladenosine, in conjunction with adenosine or guanosine. Using steady‐state and time‐resolved absorption and fluorescence spectroscopy techniques, we not only observed the customary monomer‐like and charge transfer emissive states, as reported in previous dinucleotides, but also identified an additional low‐energy emissive state. This unique state exhibits an extraordinary Stokes Shift exceeding 2.3 eV and has a relatively long lifetime of 4–5 ns. We propose that this state corresponds to a bonded exciplex state, governed by ground‐state geometries.

New copper (II) complexes bearing tryptophan‐based Schiff bases and 2,2′‐bipyridine: Crystal structures, DNA/BSA interactions and antiproliferative activities

Abstract[Cu(5‐ClSal‐Trp)(bpy)]·CH3OH (1) and [Cu(3,5‐ClSal‐Trp)(bpy)]·H2O (2) (5‐ClSal‐Trp: Schiff base derived from 5‐chlorosalicylaldehyde and tryptophan, 3,5‐ClSal‐Trp: Schiff base derived from 3,5‐dichlorosalicylaldehyde and tryptophan, bpy: 2,2′‐bipyridine) have been synthesized and analyzed by CHN analysis, FTIR, electronic absorption spectroscopy, ESI‐MS and XRD techniques. Interaction of the complexes with biomolecules {calf thymus DNA (CT‐DNA) and bovine serum albumin (BSA)} has been researched by fluorescence and electronic absorption spectroscopy. The results show that the complexes can bind via a moderate intercalation binding mode. According to the results obtained with both methods, the logKb and logKSV values of the complexes were found to be very close to each other. BSA quenching mechanism was found to be static. The results showed that the interaction between the complexes and BSA is driven by the hydrogen bond and van der Waals interaction. Additionally, the r values of the complexes (the complex 1 = 0.59 nm and the complex 2 = 0.53 nm) calculated from FRET theory suggested that the distance between the complexes (acceptor) and BSA (donor) is quite close. The complexes exhibited free radical scavenging activity compared to the standard antioxidant β‐carotene and catechin. Antiproliferative efficiency of the complexes on both breast cancer cells (MCF‐7 and MDA‐MB‐231) were also researched using the Sulforhodamine B (SRB) viability assay. It was found that the complex 1 (IC50 = 10.99 μM) exhibited higher cytotoxicity than cisplatin (IC50 = 15.6 μM) against MDA‐MB‐231 cell line. Additionally, intracellular reactive oxygen species (ROS) formation was determined by dihydroethidium (DHE) fluorescent staining. N‐acetylcysteine (NAC) was used as an efficient reactive oxygen species (ROS) scavenger. It was observed that newly synthesized Cu (II) complexes exhibited anti‐growth potential in human breast cancer cells. Additionally, it was determined that the complexes induced reactive oxygen species (ROS) formation in cells in a dose‐dependent manner.

Effect of Direct Alkyne Substitution on the Photophysical Properties of Two Novel Octasubstituted Zinc Phthalocyanines.

The synthesis of two novel phthalonitrile derivatives (3-4) bearing ethynylcyclohex-1-ene and ethynylcyclohexane groups and two peripherally octa substituted zinc (II) phthalocyanines (5-6) were prepared. The synthesis of phthalonitrile derivatives was performed with Sonagashira coupling reaction by using palladium-catalyzed. The newly synthesized compounds were characterized by using FT-IR, NMR, mass, and UV-Vis absorption spectroscopy techniques. Aggregation studies of 5 and 6 were performed in various organic solvents and different concentrations in tetrahydrofuran (THF). The photophysical studies of the Pcs were performed in THF to determine the effect of the alkyne groups on the fluorescence of the Pc ring. Substances showing fluorescence properties can be used in practical applications such as to create an image in microscopy. Fluorescence quantum yield (ΦF) and fluorescence lifetime (τF) of 5-6 were calculated. The fluorescence quenching studies of 5-6 were performed by adding the different concentrations of 1,4-benzoquinone (BQ) to a constant concentration of the Pcs in THF and it was found that benzoquinone was an effective quencher. The values of the Stern-Volmer constant (Ksv) and quenching constant (kq) of zinc phthalocyanines (5-6) were examined. All obtained results were compared with each other and with unsubstituted zinc Pc compound used as a reference.

Enhanced sunlight-driven photocatalysis owing to synergetic effect of gold nanoparticles-incorporated ZnO/rGO ternary heterostructures

The combination of gold nanoparticles (Au NPs) incorporated ZnO/rGO heterostructures is unique for sunlight-driven photocatalysis (SPC). Here, hydrothermally synthesized pristine ZnO nanostructures (NSs), ZnO/rGO binary nanocomposites (BNCs) and ZnO/rGO/Au ternary nanocomposites (TNCs) of bandgap (Eg) values 3.56 eV, 3.37 eV and 3.17 eV, respectively are reported. These NSs are analyzed optically, structurally and morphologically via UV–Vis absorption spectroscopy, X-ray diffraction and SEM techniques, respectively. The SPC of methylene blue (MB) organic dye was considered using all three samples. The slow charge transfer over grain boundaries of ZnO results in the prohibition of photogenerated electron-hole pairs, exhibiting low photodegradation efficiency (87%). However, in BNCs the creation of alternative pathway of the carriers due to low work function level of rGO as compared to ZnO enhances the charge separation with an increased photocatalytic efficiency (92%). In contrast, TNCs show rather fast photodegradation efficiency (96%) as the photoexcited electrons on Au NPs surface migrate to the CB of ZnO because of the SPR stimulation of Au. These electrons easily shift to the conductive rGO layers and react with oxygen species (O2) producing superoxide radicals (•O2–). Thus, TNCs sample has appeared to be auspicious candidate for the photodegradation of organic pollutants in untreated water.

Measuring Turbulent Water Vapor Fluxes Using a Tunable Diode Laser-Based Open-Path Gas Analyzer

The reliable observation and accurate estimates of land–atmosphere water vapor (H2O) flux is essential for ecosystem management and the development of Earth system models. Currently, the most direct measurement method for H2O flux is eddy covariance (EC), which depends on the development of fast-response H2O sensors. In this study, we presented a cost-efficient open-path H2O analyzer (model: HT1800) based on the tunable diode laser absorption spectroscopy (TDLAS) technique, and investigated its applicability for measuring atmospheric turbulent flux of H2O using the EC method. We prepared two HT1800 analyzers with lasers that operate at wavelengths of 1392 nm and 1877 nm, respectively. The field performance of the two analyzers was evaluated through inter-comparative experiments with LI-7500RS and IRGASON, two of the most commonly used H2O analyzers in the EC community. Water vapor densities measured by the three types of analyzers had high overall agreement with the reference sensor; however, they all experienced drift. The mean density drifts of HT1800, LI-7500 and IRGASON were 3.7–5.2%, 4.0% and 3.8%, respectively. Even so, the half-hourly H2O fluxes measured by HT1800 were highly consistent with those by LI-7500RS and IRGASON (with a difference of less than 2%), suggesting that HT1800 can obtain H2O fluxes with high confidence. The HT1800 was also proved to be suitable for EC application in terms of data availability, flux detection limit and response to the high-frequency turbulent variation. Furthermore, we investigated how the spectroscopic effect influences the measurements of H2O density and flux. Despite the fact that the 1392 nm laser was much more susceptible to the spectroscopic effect, the fluxes after correcting for this bias showed excellent agreement with the IRGASON fluxes. Considering the cost advantage in laser and photodetector, the HT1800 analyzer using a 1392 nm infrared laser is a promising and economical solution for EC measurement studies of water vapor.

Nocturnal downward transport of NO3 radical from the residual layer to a surface site by the mountain breeze in Seoul, South Korea

Using the long-path differential optical absorption spectroscopy (LP-DOAS) technique, the nocturnal mixing ratios of NO3 radicals were measured at an urban site in Seoul, South Korea, from May 13 to June 12, 2022. The primary objectives of the study were to estimate the NO3 radical concentration in the nighttime boundary layer and to examine the variations in their generation and loss over time, including an evaluation of their sources and sinks. The observed mean NO3 mixing ratios and lifetimes were 16 pptv and 73 s, respectively. NO3 concentrations and lifetimes were closely associated with their production, involving O3 and NO2, as well as the loss processes regulated by NO, VOCs, and aerosol surface area. Applying the steady-state assumption for NO3 and N2O5, the mean N2O5 uptake coefficient on the aerosol surface for the entire period was 0.031. When foggy nights were excluded from the analysis, the uptake coefficient decreased to 0.025. These values are within the higher range of the results reported in other studies. High relative humidity, which averaged 75% at night throughout the collection period, favored high N2O5 uptake coefficients. NO3 concentrations generally peaked shortly after sunset and gradually declined until sunrise. However, we frequently observed distinct increases in NO3 throughout the early morning hours, especially during clear nights, when local circulation with the westerly mountain breeze prevailed at the research site. The mountain breeze transported residual air downward, resulting in 110% and 38% higher NO3 and O3 levels at the sampling locations, respectively, compared to normal conditions. This additional source of nocturnal radicals and O3 has consequences for increased secondary aerosols and O3 production, particularly at urban surface levels where they are readily depleted in the early morning hours. To this end, a more thorough examination is required to measure N2O5 and a larger spectrum of VOCs species, as these parameters are crucial for nighttime radical budgets, secondary aerosols, and O3 generation in cities like Seoul.

Chemical Kinetics for the Oxidation of Californium(III) Ions with Select Radiation-Induced Inorganic Radicals (Cl2•- and SO4•-).

Despite the availability of transuranic elements increasing in recent years, our understanding of their most basic and inherent radiation chemistry is limited and yet essential for the accurate interpretation of their physical and chemical properties. Here, we explore the transient interactions between trivalent californium ions () and select inorganic radicals arising from the radiolytic decomposition of common anions and functional group constituents, specifically the dichlorine (Cl2•-) and sulfate (SO4•-) radical anions. Chemical kinetics, as measured using integrated electron pulse radiolysis and transient absorption spectroscopy techniques, are presented for the reactions of these two oxidizing radicals with ions. The derived and ionic strength-corrected second-order rate coefficients (k) for these radiation-induced processes are k( + Cl2•-) = (8.28 ± 0.61) × 105 M-1 s-1 and k( + SO4•-) = (9.50 ± 0.43) × 108 M-1 s-1 under ambient temperature conditions (22 ± 1 °C).

Recovery of waste cooking palm oil as a crosslinker for inverse vulcanized adsorbent to remove iron (Fe3+) ions

Gas and oil reservoirs around the world leave megatons of unused elemental sulfur as industrial byproducts which has been successfully used in inverse vulcanization. We reported the successful application of inverse vulcanized porous adsorbent from waste cooking palm oil (WCO) to remove ferric (Fe3+) ions. Sodium chloride (NaCl) acted as a porogen to get the porous polysulfide. The removal of Fe3+ was observed through the atomic absorption spectroscopic (AAS) technique. The effects of pH (3,7, and 11) and initial concentration (35, 40, 45 mg/L) of Fe3+ solution, and dosage (10, 15, and 20 g/100 mL) on Fe3+ adsorption were studied to determine the best removal condition. Later, fixing the best parameters (pH 3, 40 mg/L, 20 g/100 mL), Langmuir and Freundlich equations were used to study the adsorption isotherm. Adsorption kinetics were described using linear and nonlinear pseudo-first and second-order reactions. The Freundlich isothermal model and linear pseudo-second-order kinetics fit best for the removal process. The comparison between the pre and post-adsorption analyses using FTIR, SEM-EDX, and the isothermal model confirmed the physisorption of Fe3+. The current study concluded with some further scopes of the adsorbent for diverse removal applications.

Assessment of toxicity of residues of normal/green cracker and their impact on soil

In the present work, laser-induced breakdown spectroscopy (LIBS) is used to examine the hazardous constituents present in the residues of six types of normal and six types of green firecracker samples. The residue of the normal firecracker’s samples contains the spectral lines of toxic chemicals such as Al, Ba, Sr, Mg, and Ti in a similar way as the fresh powder of normal crackers. The residues of the green firecracker’s samples contain toxic elements such as Al and Ba, and the intensities of these toxic elements are so high that these samples also contain the electronic bands of AlO and SrO. The UV-vis spectra of residues of normal and green firecracker samples contain the molecules of KNO3, CaO, Al2O3, and SrO in a similar way as the fresh powder of these firecrackers does. This reflects that the toxicity of the powder of firecracker samples remains similar after the burning of these firecrackers’ samples. Therefore, these toxic residues are mixed in the soil, where they burn and contaminate it. For the assessment of the contamination of the soil, the concentration of micronutrients such as Fe, Cu, Mn, Zn, and P is calculated using atomic absorption spectroscopy (AAS) techniques and found to increase in all the contaminated soil compared to blank soil. This reflects that the soil is contaminated. For the classification of the residues and soil contaminated with residues, the principal component analysis (PCA) and hierarchical clustering analysis (HCA) are applied to the LIBS data set.

Measurement of the absorption cross-sections of sulfur compounds in the 180-270 nm region considering nonlinear effects.

Sulfur compounds (SO2, CS2, H2S and OCS) are common toxic pollutants in the atmospheric environment, and the absorption spectroscopy technique can indeed help to realize online monitoring of their concentrations. However, nonlinear effects that occur during absorption spectroscopy measurements have a serious impact on the measurement of the absorption cross-sections (ACSs) of sulfur compounds, leading to serious deviations in both the substance absorption properties and concentrations obtained based on ACS analysis. In this paper, the maximum effective ACSs of sulfur compounds in the linear region are obtained by considering the influence of nonlinear effects and eliminating interference factors such as oxygen and photolysis. In addition, the nonlinear effects are found to be greatly attenuated in spectra with broad band absorption characteristics by comparing the oscillatory absorption spectra before and after the differential treatment and by comparing the change in the oscillatory ACS with the broad band ACS. The experimental results show that the effective ACSs of SO2, CS2, H2S, and OCS with a resolution of 0.23 nm are 14.15 × 10-18 cm2 per molecule, 5.61 × 10-16 cm2 per molecule, 7.09 × 10-18 cm2 per molecule, and 3.20 × 10-19 cm2 per molecule, respectively. So far, it is the largest ACS obtained at room temperature and atmospheric pressure, which is of great significance for online measurement of sulfur compounds.