The effect of biochar, compost, peat and wheat straw at 1 and 5% on adsorption isotherm of chlorantraniliprole, dinotefuran, bispyribac-sodium, and metribuzin was studied in clay loam soil and sandy loam soil. Biochar, compost, peat and wheat straw (at a rate of 1 % in soil) improved the adsorption capacity of chlorantraniliprole and metribuzin in sandy loam soil. The sorption coefficients are higher for chlorantraniliprole and metribuzin whereas lower for dinotefuran and bispyribac-sodium in amended soil compared to unamended sandy loam soil. There is not a clear direct correlation between Freundlich parameters as well as Kd or Koc and type of organic amendment. The sorption of all tested pesticides on biochar was increased, whereas on compost was decreased. The order of pesticides sorption in soils and different organic amendments is generally inversely proportional to their aqueous solubilites. Adsorption of chlorantraniliprole increases on the sandy loam soil amendment at the rate of 1% in the following order: peat > compost > biochar > original soil. Also, the magnitude of adsorption on soil A amendment at the rate of 5% can be arranged for dinotefuran in the order; peat > biochar > compost > original soil and for bispyribac-sodium and metribuzin peat = wheat straw > biochar > original soil.

In the present study, we have prepared two phenyl ring substituted sulfanilamide bearing acrylamide linking groups. The four derivatives (C1-C4) were prepared by changing the left n-alkoxy terminal group. The liquid crystalline properties of the synthesized sulfanilamide-based compounds were investigated using POM and DSC studies. All four materials exhibit nematic liquid crystalline properties during both heating and cooling. They also demonstrate a broad temperature range and thermal stability. Further, we have studied the structure-property relationship to gain a better understanding of the effect of the linking group and variable alkoxy tail group on mesomorphic behavior. The results indicate that thermal stability, mesophase temperature range, and liquid crystalline properties depend on the linking group and variable alkyl chain length.

The present study was conducted to evaluate the feasibility of apatitic tricalcium phosphate with a Ca/P ratio of 1.50 for the adsorption of phenol and tyrosine from aqueous solutions. The adsorbent was synthesized at room temperature using an aqueous double decomposition method and characterized through physicochemical methods. Batch adsorption studies were conducted as a function of contact time, initial adsorbate concentration, temperature, and pH. The adsorption kinetics of phenol and tyrosine were well fitted to the pseudo-second-order model. The maximum adsorption capacity was found to be 5.56 mg/g for phenol and 9.65 for tyrosine mg/g at 298 K. The adsorption of phenol and tyrosine was well explained using the Langmuir, Freundlich, Temkin, and Dubinin-Radushkevick models. The Langmuir model is the most suitable, with a maximum monolayer adsorption capacity of 7.32 mg/g for phenol and 11.43 mg/g for tyrosine at 298 K. The thermodynamic parameters indicate that the adsorption process is favorable, spontaneous, exothermic, and controlled by physisorption with electrostatic interactions between compounds containing the phenolic group and apatite. The results of this study have demonstrated the potential utility of apatitic tricalcium phosphate, which could be developed into a viable technology for the adsorption of compounds containing the phenolic group from aqueous solutions.

In this work we report, aluminized polyborate catalyzed facile and efficient one-pot four component Hantzsch synthesis of 1,8-dioxo-decahydroacridines using substituted aromatic aldehydes (1 mmol), dimedone (2 mmol) and ammonium acetate (1.5 mmol) at 95-100oC under solvent-free condition. The prominent advantages of this methodology are good product yields (85-95%), eco-friendliness, mild reaction conditions and use of inexpensive catalyst. The structures of the targeted molecules were examined by FT-IR, 1H-NMR and mass spectral techniques.

Science and technology of nanosized bimetallic oxide nanomaterials records the various properties and applications. Especially biomedical applications are viewed in particular due to its nanosized particle size. The present experimentation is reporting the microwave-assisted synthesis of nanosized bimetallic oxides like copper ferrite (CuFe2O4) and barium titanate (BaTiO3) by solid state combustion route using poly (vinyl alcohol) (PVA) as a fuel. The structural and morphological characterizations of the bimetallic oxide nanomaterials are performed out by X-ray diffraction (XRD) and scanning electron micrograph (SEM) tools respectively. These analyses report the crystalline nature of both samples. EDX spectral study is also undertaken to know the existence of different metals in the above-mentioned samples. Bonding nature of the bimetallic oxide samples were readied by Fourier transfer infrared (FT-IR) instrumentation. The study reviewed the varied vibrational modes confirms the phase formation of the samples. UV-Vis and thermal study of these bimetallic oxide samples are also studied extensively to know the thermal and absorption behavior respectively. TGA of both the samples are traced and are showing decomposition at rapid rate. In addition, the maximum absorption peaks due to π - π* transition confirms the sample formation. Antimicrobial activity of the prepared oxide samples was studied for antibacterial and antifungal behavior. Both samples showing considerable activity against various bacteria and fungi.

An isocratic HPLC technique was exploited and validated for the quick simultaneous separation and measurement of cefotaxime and paracetamol in vials dosage forms, with a total analysis time of 3 minutes. The process of separation was carried out on a Thermo Scientific® Venusil XBPC18 (L) (5µm, 4.6x250 mm) using a mobile phase of ACN: distilled water (70:30, v/v) at the ambient temperature. The flow rate used in the experiment was 1 mL/min, and the highest level of absorption was determined by high-performance liquid chromatography with photodiode array detection (HPLC-PDA) employing a PDA detector set at a wavelength of 255 nm. The established retention times for cefotaxime and paracetamol were 1.79 and 2.97 minutes, respectively, suggesting reduced analysis duration. The observed limits of detection for ceftaxime and paracetamol were 4.2×10-5 and 1.2×10-5 µg/mL, respectively, indicating a significant level of sensitivity in the approach. The approach was subsequently verified in accordance with the requirements set out by the Food and Drug Administration (FDA) for the quantification of medicines in vial dosage form.

In this work, ribonucleoside products have been prepared by employing stannic tetrachloride (SnCl4) and natural phosphate as catalysts. The obtained result suggests that this catalyst facilitates the reactions of ribonucleoside-like products in a stereo-controlled manner, exhibiting β-selectivity when reacting with trimethylsilyl uracil, the ribonucleosides derivatives were obtained in suitable yields. In addition, we have performed the molecular docking analysis, demonstrated that the synthesized compounds have potential for antiviral activity against the omicron variant of coronavirus, and the D3, D4, E and F products have a higher binding energy than the molnupiravir drug, indicating that these products may be a probable drugs for the omicron variant.