Physicochemical Investigations Research Articles

Exploring the Subsistence of Solvation Consequences of l-Asparagine and l-Glutamine Prevailing in Aqueous Ionic Liquid Solutions by Physicochemical and Computational Investigations

Exploring the Subsistence of Solvation Consequences of <scp>l</scp>-Asparagine and <scp>l</scp>-Glutamine Prevailing in Aqueous Ionic Liquid Solutions by Physicochemical and Computational Investigations

Physicochemical investigation and molecular docking analysis of Maha yogaraj Guggulu tablet and virtual screening of its major bioactive compound

Guggulsterone plays a significant role in cholesterol-lowering by inhibiting Farnesoid X Receptor. The present study aims to identify the isomers of Guggulsterone with high binding affinity and good binding interaction with targeted protein and positive control atorvastatin. The pharmacokinetic parameters of Guggulsterone isomers were estimated from P.K.C.S.M. online server, and molecular docking analysis was performed from Autodock V.® 4.2.6 Program. From the computer-aided drug designing, we have confirmed that guggulsterone isomers are inhibitors of the CYP3A4 enzyme and hepatotoxic. Guggulsterone isomer showed a stronger binding affinity when compared with atorvastatin. The docking score for Guggulsterone was −9.28 kcal/mol, E-Guggulsterone −9.56 kcal/mol, Z-Guggulsterone −9.79 kcal/mol, M-Guggulsterone −9.45 kcal/mol, and positive control atorvastatin −8.26 kcal/mol. The present study revealed that the isomers of Guggulsterone have high binding affinity and good binding interaction with targeted proteins.

Gasification of organic solid waste for syngas: Physicochemical and conversion mechanism investigation

The syngas of organic solid waste (OSW) obtained through gasification is of great interest in energy and fuel production owing to its clean and environmentally friendly characteristics. In this study, the physicochemical properties of typical OSW were systematically studied, and the mechanism of the influence of OSW sample structure and composition on gasification behavior was studied by thermogravimetric mass spectrometry and gasification experiments. Scanning electron microscopy was used to observe the surface morphology of the samples, showing that waste wood chips (WWC) and Pennisetum giganteum (PG) have well-developed pore structures. Fourier transform infrared spectroscopy results indicated that polyurethane foam (PF) and polyethylene terephthalate (PET) have more oxygen-containing functional groups than WWC and PG. X-Ray diffraction showed that the order of crystallinity index was WWC > PET > PF > PG. X-ray photoelectron spectroscopy results showed the order of the surface alkali content was PG > PF > WWC. Furthermore, thermogravimetric and mass spectrometry experiments were used to explore the components released from volatiles during heating, demonstrating that WWC and PG produce mainly H2O, while PF and PET produce mainly CO2. Gasification experiments were carried out at different heating rates, and PET had the highest initial and final gasification temperatures. The distributed activation energy model was used to calculate the apparent activation energy, which was in the order WWC (153.7 kJ/mol) > PET (136.9 kJ/mol) > PG (81.2 kJ/mol) > PF (78.9 kJ/mol) and was consistent with the carbon ordering degree result.

Physicochemical investigation of mercury sorption on mesoporous thioacetamide/chitosan from wastewater

Mercury is a toxic environmental element, so it was necessary to prepare a new, highly efficient, cheap sorbent to remove it. A mesoporous thioacetamide/chitosan (MTA/CS) was manufactured via a simplistic strategy; the chitin deacetylation to gain chitosan (CS) and the addition of thioacetamide. The as-prepared MTA/CS was characterized using X-ray diffraction, EDX, SEM, FTIR, and BET surface analysis. According to the findings, the MTA/CS was effectively synthesized. The removal behaviors of Hg2+ onto MTA/CS composite were inspected, which suggested that the MTA/CS composite exhibited great sorption properties for Hg2+ in liquid solutions. The maximal Hg2+ sorption capacity was 195 mg/g. The effects of temperature, Hg2+ concentration, contacting time, and MTA/CS concentration on sorption were analyzed. The 2nd-order model and Langmuir isotherm were suitable for the physicochemical adsorption processes. Thermodynamic analysis showed that the Hg2+ adsorption process onto the MTA/CS composite is exothermic and occurred spontaneously. The desorption condition of Hg2+ from its loaded MTA/CS was also gained. Likewise, the MTA/CS sorbent was undoubtedly regenerated by 0.8 M NaNO3 80 min contacting and 1:50 S:L ratio. The versatility and durability of MTA/CS sorbent were investigated via nine sorption-extraction cycles. The optimum parameters were applied to wastewater. Based on the result, the as-prepared MTA/CS might be a potential sorbent for removing Hg2+ from liquid solutions.

Lessons Using an Electrochemical Method to Produce Lithium Manganese Oxide Cathodes for Lithium-Ion Batteries

Lithium manganese oxide (LMO) has been a well-studied Li-ion battery cathode material for for many years. It offers high thermal stability for high-temperature battery applications and a prolonged cycle life compared to other materials. LMO also has an acceptably high energy density from a naturally abundant, inexpensive, and environmentally benign material, i.e. manganese (Mn). The cathodes for LIBs are conventionally synthesized via solid-state reaction techniques, which require harsh and complex conditions including high temperature (> 700oC) and high pressure. The resulting powders are incorporated into a slurry that is cast onto a current collector using a binder, additives, and solvent. Though this results in high-performing electrodes, it also usually increases the production cost. Another approach that is gaining traction to make LMOs is electrodeposition. Electrodeposition can allow for the direct synthesis of the active material on the current collector without using any binder or additives. Using electrodeposition not only could eliminate the mass and volume of inactive material but also reduce the cost of electrode fabrication. It also can facilitate recycling by depositing the active material from lower purity, material-digested streams.A few reports in the literature have discussed the electrochemical preparation of LMO cathode from the following steps: electrodeposition of manganese oxide (s) (MnxOy) onto a substrate followed by chemical lithiation and heat treatment of MnxOy [1,2]. Although a few reports showed the active materials with reasonable capacity, it is presently unknown what LiMnxOy phase or phases are active and which MnxOy is responsible. However, without sufficient physicochemical investigation, multiple works have postulated that the LMO is created from crystalline MnO2 or Mn3O4. It is also not known what the typical active phase yield is or what physical structures or conditions are responsible for increased capacity. If electrodeposition-to-LMO is to become a viable commercial pathway, a rational understanding of the solid-state chemistry for the LMO formation is needed.This talk will discuss the deposition and lithiation of multiple manganese oxide phases – linking the chemistry and morphology of the surface features to their charge/discharge properties. It will be shown that traditional crystalline phases are not responsible for the formation of LMOs. It will also be shown that the LMOs do not fully delithiate during charging. Lastly, the precise morphology of the active phase – separated out through new processing approaches – will be identified. The composition, structure, and crystallinity of the Mn oxides and LMOs were characterized by X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The resulting LMO electrodes were incorporated into coin cells, cycled – achieving a capacity of 261 mAh g-1, and post-characterized.References J. Rana, M. Stan, R. Kloepsch, J. Li, G. Schumacher, E. Welter, I. Zizak, J. Banhart, and M. Winter, Adv. Energy Mater., 4, 1300998 (2014).Z. Quan, S. Ohguchi, M. Kawase, H. Tanimura, and N. Sonoyama, J. Power Sources, 244, 375 (2013).

Thiadiazine-thiones as inhibitors of leishmania pteridine reductase (PTR1) target: investigations and in silico approach

Leishmaniasis is a widespread parasitic disease and is one of the major public health concerns in developing countries. Many drugs have been identified for leishmania as targets, but the potential toxicity and long-term treatment remain the most significant problems in terms of further development. The present study employed physicochemical investigations, structure-based virtual screening, ADMET analysis, molecular dynamics simulation, and MM-PBSA, to identify potential compounds for Leishmania. We evaluated 30,926 natural products from the NPASS database, and four potentials passed the pharmacokinetic ADMET studies and were verified using the molecular docking approach. Molecular docking results showed good binding interaction of the compounds with the active site of leishmania pteridine reductase enzyme PTR1, with compound TTC1 showing FRED and Autodock binding energies of −10.33 and −10.94, respectively, which were comparable with the antileishmania drugs of Allopurinol, Miltefosine and the original ligand, methotrexate. TTC1 compound was found to be favorable for hydrophobic interaction with PTR1. In addition, the physicochemical properties of the compounds were studied using the SwissADME web server. All compounds followed Lipinski’s rule of five and can be considered as good oral candidates. The analysis of the 100 ns molecular dynamics simulation results based on the best-docked TTC1 with PTR1 receptor demonstrates stable interactions, and the complex undergoes low conformational fluctuations. The average of the calculated binding free energy of the TTC1-1e7w complex is (−68.67 kJ/mol), and the result demonstrated that the TTC1 promoted stability to the Leishmania-PTR1 complex. The potential compounds can be further explored for their antileishmanial activity. Communicated by Ramaswamy H. Sarma

Accelerating Lipid Flip-Flop at Low Concentrations: A General Mechanism for Membrane Binding Peptides.

We report a physicochemical investigation of the lipid transport properties of model lipid membranes in the presence of the antimicrobial peptide indolicidin through comparisons of experimental SANS/SAXS scattering techniques to fully atomistic molecular dynamics simulations. In agreement with the experiment, we show that upon peripheral binding of the peptides, even at low concentrations, lipid flip-flop dynamics is greatly accelerated. Computer modeling elucidates the interplay between structural changes and lipid dynamics induced by peptides and proposes a mechanism for the mode of action of antimicrobial peptides, assessing the major role of entropy for the catalysis of the flipping events. The mechanism introduced here is universal for all peptides with preferential peripheral binding to the membrane as it does not depend on the specific amino acid sequence.

Physicochemical Study of the Molecular Signal Transfer of Ultra-High Diluted Antibodies to Interferon-Gamma.

Physicochemical investigations of (UHD) solutions subjected to certain physical factors (like shaking) are becoming more frequent and increasingly yielding convincing results. A much less studied phenomenon is the transfer of molecular information (UHD signals) from one fluid to another without an intermediate liquid phase. The purpose of this study was to investigate the possibility of such a UHD signal transfer from UHD solutions into the receiver fluid, especially when the molecular source used in solutions was a biologically active molecule of antibodies to interferon-gamma. We used physicochemical measurements and UV spectroscopy for this purpose. The results of this large pilot study confirm the possibility of such a transfer and a rough similarity to the original UHD signal donors, the weaker signal detection relative to the original donor fluids, and that exposure time improves the effect.

A Microfluidic Approach for Synthesis of Silver Nanoparticles as a Potential Antimicrobial Agent in Alginate-Hyaluronic Acid-Based Wound Dressings.

The recognized antimicrobial activity of silver nanoparticles is a well-studied property, especially when designing and developing biomaterials with medical applications. As biological activity is closely related to the physicochemical characteristics of a material, aspects such as particle morphology and dimension should be considered. Microfluidic systems in continuous flow represent a promising method to control the size, shape, and size distribution of synthesized nanoparticles. Moreover, using microfluidics widens the synthesis options by creating and controlling parameters that are otherwise difficult to maintain in conventional batch procedures. This study used a microfluidic platform with a cross-shape design as an innovative method for synthesizing silver nanoparticles and varied the precursor concentration and the purging speed as experimental parameters. The compositional and microstructural characterization of the obtained samples was carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and dynamic light scattering (DLS). Four formulations of alginate-based hydrogels with the addition of hyaluronic acid and silver nanoparticles were obtained to highlight the antimicrobial activity of silver nanoparticles and the efficiency of such a composite in wound treatment. The porous structure, swelling capacity, and biological properties were evaluated through physicochemical analysis (FT-IR and SEM) and through contact with prokaryotic and eukaryotic cells. The results of the physicochemical and biological investigations revealed desirable characteristics for performant wound dressings (i.e., biocompatibility, appropriate porous structure, swelling rate, and degradation rate, ability to inhibit biofilm formation, and cell growth stimulation capacity), and the obtained materials are thus recommended for treating chronic and infected wounds.

Examining the microbial composition of natural springs in Bhaderwah, Jammu and Kashmir, India.

Natural springs are the main source of water supply for domestic and agricultural use for humans living in the mountainous regions of Asia. Increasing anthropogenic activities with associated waste load, coupled with inadequate sanitation, and contamination of natural water resources and the environment are emerging as important public health issues. We performed a prospective microbiological and physicochemical investigation of water samples from seven distinct natural springs situated at an altitude of 1615m in the Bhaderwah region of Jammu and Kashmir, India. Bacterial groups belonging to opportunistic pathogens such as members of Moraxellaceae (Acinetobacter), Arcobacteraceae (Pseudoarcobacter), Pseudomonadaceae (Pseudomonas), Oxalobacteraceae (Massilia), and Flavobacteriaceae (Flavobacterium) were observed. The total coliform test indicated an intermediate level of risk of fecal contamination of the springs, except for one site. Through a questionnaire-based survey of the local population, we discovered that around 40% of participants had suffered from waterborne diseases including typhoid (~14%) and diarrhea (~11%). Our data suggests that increased surveillance of fecal contamination and heterotrophic opportunistic pathogens is needed to enhance water quality and reduce health risks for people living in mountainous regions.

Synthesis, characterization, and nonlinear optical properties of copper (II) ligand Schiff base complexes derived from 3-Nitrobenzohydrazide and benzyl

A new series of Cu (II) complexes were prepared using Schiff base ligand of N–N′-(1,2-diphenyl ethane-1,2-diylidene)bis(3-Nitrobenzohydrazide). The prepared ligand and Cu (II) complex were characterized using various physicochemical investigations such as X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), and Energy dispersive X-ray analysis (EDX), Fourier Transform Infrared (FT-IR), {}^{13}C Nuclear Magnetic Resonance (NMR), {}^{1}H NMR, Diffuse Reflectance Spectroscopy (DRS), Vibrating Sample Magnetometer (VSM), and Z-Scan technique (Nonlinear optical (NLO) properties). In addition, the prepared samples have been examined for their NLO characteristics with the help of the Density Functional Theory calculations which proved that the Cu (II) Complex is more polarized than Ligand. According to XRD and FESEM results, the nanocrystalline nature of the samples is confirmed. The metal-oxide bond assigned in the functional studies by FTIR. Magnetic studies demonstrate weak ferromagnetic and paramagnetic nature for Cu (II) complex and diamagnetic nature for the ligand, respectively. DRS spectrum exhibited higher reflectance for Cu (II) than the ligand. The band gap energies of the synthesized samples were estimated by employing the Tauc relation and Kubelka–Munk theory on reflectance data and found to be 2.89 eV and 2.67 eV for Cu (II) complex and ligand, respectively. Extinction coefficient and refractive index values were calculated using the Kramers–Kronig method. The z-scan technique was applied to estimate the NLO properties by a 532 nm Nd:YAG laser.

Physicochemical properties of waxy rice varieties with contrasting hardening rates

ABSTRACT In the present study, four waxy rice varieties (two japonica and two indica) with contrasting hardening rates were used for physicochemical properties investigation. The results showed that the hardness of cooked rice grains from zhenzhunuo and zhennuo29 increased slowly after cool storage, whereas those from zaonuo5 and yj98 raised rapidly. The peak gelatinisation temperatures for yj98, zaonuo5, zhennuo29, and zhenzhunuo flours were 78.60°C, 73.55°C, 69.00°C, and 67.25°C, respectively. The retrogradation enthalpies of stored flours (4°C, 48 h) followed the order: yj98 (3.876 J/g) > zaonuo5 (2.202 J/g) > zhennuo29 (1.684 J/g) > zhenzhunuo (1.370 J/g). Scanning electron microscopy (SEM) results exhibited that after cool storage, the cooked rice grains of zhenzhunuo and zhennuo29 had no obvious changes in morphology, whereas zaonuo5 presented increased cavities and yj98 occurred new fissures. Among intra-subspecies varieties, the rapid hardening rice accessions had a lower ratio of A chains (DP 6–12) but larger proportion of B3 chains (DP ≥ 37) than that of the corresponding genotypes with slow hardening. The physicochemical characteristics disclosed here will facilitate the application of the four cultivars in food processing industry.

Compendium of P. Scrobiculatum: Phytochemical, Physicochemical, Antioxidant, Antiulcer, and Spectroscopic Analysis

Background: Paspalum Scrobiculatum (Kodomillet) plant is found in various regions of India and possesses several pharmacological activities such as nutritive, anti-fungal, anti-diabetic, etc. The researchers are more focused these days on exploring other potential activities of this plant and the constituents present. Methods: Present study emphasized preliminary analysis such as macroscopic study, phytochemical analysis, Physicochemical investigation, determination of ash content, (Total flavonoid content), antioxidant property and characterization of extracted components with different spectral techniques and antiulcer potential. later, this study will be helpful in the determination of its medicinal importance in Pharmacy. Results: In macroscopic analysis, it was studied that paspalum scrobiculatum seeds are light brown to dark brown colored, round to oval shaped grain having a size approximately 4mm. Further, the seeds were analyzed for determination of the extractive values and found to be 2.82 % w/w, 0.79 %w/w, 4.26 % w/w 2.40 % w/w in pet. ether, chloroform, ethanol, and water extracts respectively, and extractive value was found highest in ethanol extract. Furthermore, phytochemical analysis of all the different extracts revealed the presence of phenolic components, flavonoids amino acids, protein, and carbohydrates in ethanolic extract, whereas in aqueous extract there was the presence of saponins and carbohydrates. Then, spectral characterization analysis was done with Infrared spectroscopy, Nuclear magnetic resonance, and Mass spectroscopy techniques and revealed the presence of different active metabolites in the ethanolic extract which may be considered for numerous pharmacological properties, thus further processed for anti-ulcer potential. The ethanolic extract has given promising results as an antiulcer agent against the standard drug omeprazole. The present research concluded from various parameters such as macroscopic evaluation, successive extraction, physicochemical investigation, phytochemical investigation, and spectral analysis that ethanolic extract of plant P. Scrobiculatum contains the maximum amount of secondary metabolites and was further investigated for anti-ulcer potential at a dose of 250 mg/kg and 500 mg/kg and the % Ulcer protection was found to be 26.81% and 49.24 % respectively against the standard drug omeprazole.

Monitoring of soil contamination from olive mill wastewater (OMW) using physico-chemical, geotechnical analysis and electrical resistivity tomography (ERT) investigation

Monitoring of soil contamination from olive mill wastewater (OMW) using physico-chemical, geotechnical analysis and electrical resistivity tomography (ERT) investigation

Long-Term and Stable Dental Therapies via an In Situ Spontaneous Medicine Delivery System.

Chronic oral diseases are boring, long-term, and discomfort intense diseases, which endanger the physical and mental health of patients constantly. Traditional therapeutic methods based on medicines (including swallowing drugs, applying ointment, or injection in situ) bring much inconvenience and discomfort. A new method possessing accurate, long-term, stable, convenient, and comfortable features is in great need. In this study, we demonstrated a development of one spontaneous administration for the prevention and therapy on a series of oral diseases. By uniting dental resin and medicine-loaded mesoporous molecular sieve, nanoporous medical composite resin (NMCR) was synthesized by a simple physical mixing and light curing method. Physicochemical investigations of XRD, SEM, TEM, UV-vis, N2 adsorption, and biochemical experiments of antibacterial and pharmacodynamic evaluation on periodontitis treatment of SD rats were carried on to characterize an NMCR spontaneous medicine delivery system. Compared to existing pharmacotherapy and in situ treatments, NMCR can keep a quite long time of stable in situ medicine release during the whole therapeutic period. Taking the periodontitis treatment as an instance, the probing pocket depth value in a half-treatment time of 0.69 from NMCR@MINO was much lower than that of 1.34 from the present commercial Periocline ointment, showing an over two times effect.

Physicochemical Investigation of Convective Solar Drying for Post-Harvest Conservation of Hot Peppers in Adrar, Algeria

In this study, the impact of convective solar drying on the physiochemical characteristics of hot peppers harvested in Algeria was investigated. The freshly harvested peppers underwent convective drying until they reached a desired stable weight. Various parameters including moisture content, water activity (Aw), pH, crude protein, crude fat, total sugars, and polyphenol content were measured. The drying process, using an optimal method, took approximately 2 to 3 days and resulted in moisture content levels of (32.41 %), Aw of (0.26%), pH of (4.1), acidity of (2.8), ash content of (73.38%), dry matter of (67,59 %), total protein content of (0.83%), sugar content of (2.9%), polyphenol content of (89%), and crude fat content of (0.23%). In comparison, the values for the freshly harvested hot peppers were (89%), (0.92%), (5.34%), (3.6%), (8%), (11%), (1.64%), (1.64%), (125%), and (0.36%) respectively. These findings confirm that solar drying effectively preserved the nutritional quality of the hot peppers, with minimal losses in some properties compared to the values of the freshly harvested peppers

Physicochemical investigations of clouding development and physicochemical properties of Triton X-100 and levofloxacin hemihydrate mixture: influence of sodium salts composition

Physicochemical investigations of clouding development and physicochemical properties of Triton X-100 and levofloxacin hemihydrate mixture: influence of sodium salts composition

Hydrothermal carbonization of waste furniture for clean blast furnace fuel production: Physicochemical, gasification characteristics and conversion mechanism investigation

This study aimed to investigate the physical and chemical characteristics of hydrochar derived from waste furniture through hydrothermal carbonization (HTC) and evaluate its suitability as a fuel for blast furnace injection, the formation mechanism of biomass conversion to hydrochar was also systematically investigated. The optimal HTC conditions were determined as 260 °C, liquid–solid mass ratio of 2:1. The resulting hydrochar exhibited a high calorific value of 27.78 MJ/kg, a specific surface area (St) of 3.01 m2/g, and K and Na concentrations of 203 mg/kg and 416 mg/kg, respectively. The apparent activation energy (E) for gasification was measured as 154.54 kJ/mol, indicating its potential as a clean injection fuel for blast furnaces. During HTC, cellulose, hemicellulose, and lignin underwent hydrolysis, decarboxylation, polymerization, and aromatization processes, resulting in the transformation of water-soluble small molecules into polymerized hydrochar and water-insoluble large molecules into polyaromatic hydrochar. This study provides insights into the possibility of replacing fossil fuels in the blast furnace iron-making process.

Synthesis of doped and porous CuO with boosted light-harvesting features for the photocatalytic mineralization of azo dyes

Porous Ni-doped copper oxide (NCO) photocatalyst has been produced using chemical activation and metal doping techniques. Structural, optical, morphological, and electrical analyses were performed on copper oxide (CO) and porous NCO photocatalysts. The monoclinic-phased, UV/Vis light-triggered, electrically conductive, and porous-surfaced NCO photocatalyst was successfully synthesized, according to a detailed physicochemical investigation. The photo-decomposition abilities of synthetic porous NCO and counterpart CO photocatalysts were investigated and compared using Allura red (AR). According to the photocatalytic study, the porous NCO photocatalyst outperformed its counterpart (CuO) and eliminated 91.4% (adsorption: 18%; decomposition: 79%) of the AR dye in 48 min. Over the porous NCO photocatalyst, the AR dye disintegrated at a rate of 0.024 min−1, which is more than 1.84 times quicker than the rate of disintegration over the CO photocatalyst. The porous NCO photocatalyst, as synthesized, preserved 88% of its photocatalytic activity after five recyclability tests and had remarkable electron-hole separation activity, according to reusability tests and transient-photocurrent measurements. Also, the radical capture experiment suggested that superoxide and hydroxyl are important for porous NCO's photocatalytic activity. According to the findings of this research, the synthesis of ferromagnetic metal-doped and porous semiconductive materials has a great potential for azo dye breakdown, which makes it an efficient, cost-effective, and environmentally acceptable solution for the clean-up of polluted water.

Physicochemical Assessment of the Road Vehicle Traffic Pollution Impact on the Urban Environment

Vehicle traffic pollution requires complex physicochemical analysis besides emission level measuring. The current study is focused on two campaigns of emissions measurements held in May and September 2019 in Alba Iulia City, Romania. There was found a significant excess of PM2.5 for all measuring points and PM10 for the most circulated points during May, along with significant VOC and CO2 emissions. September measurements reveal threshold excess for all PM along with increased values for VOC and CO2 emissions. These are the consequences of the complex environmental interaction of the traffic. Street dust and air-suspended particle samples were collected and analyzed to evidence the PM2.5 and PM10 sources. Physicochemical investigation reveals highly mineralized particulate matter: PM2.5 fractions within air-suspended particle samples predominantly contain Muscovite, Kaolinite, and traces of Quartz and Calcite, while PM10 fractions within air-suspended particle samples predominantly contain Quartz and Calcite. These mineral fractions originate in street dust and are suspended in the atmosphere due to the vehicles’ circulation. A significant amount of soot was found as small micro-sized clusters in PM2.5 and fine micro-spots attached over PM10 particles, as observed by Mineralogical Optical Microscopy (MOM) and Fourier Transformed Infrared Spectroscopy (FTIR). GC-MS analysis found over 53 volatile compounds on the investigated floating particles that are related to the combustion gases, such as saturated alkanes, cycloalkanes, esters, and aromatic hydrocarbons. It proves a VOC contamination of the measured particulate matters that make them more hazardous for the health. Viable strategies for vehicle traffic-related pollutants mitigation would be reducing the street dust occurrence and usage of modern catalyst filters of the combustion gas exhausting system.