Amol V. Pansare

A novel spray‐on elemental barcode technology is reported for the secure, permanent, and tamper‐proof identification of polymeric and fiber‐reinforced composite materials. This system utilizes the in situ reduction of metal salts to nanoparticles embedded within a polymer matrix, creating a unique barcode that is detectable through X‐ray fluorescence (XRF). The barcode's composition is based on the metallic nanoparticle mixture and offers a semi‐quantitative, non‐destructive, and thermally stable method for material authentication. The process is straightforward, involving the manual application of metal salt solutions followed by mild heating, ensuring no significant alteration to the material's properties. The barcodes can be read through protective coatings or paints and are robust even under extreme conditions, such as high temperatures. This low‐cost method does not introduce additional manufacturing steps and demonstrates significant potential for anti‐counterfeiting and lifecycle tracking in various industries. Moreover, with an information density of up to 12 bits mm⁻¹, this elemental barcode significantly surpasses the data storage capabilities of traditional optical barcodes. This approach holds promise for broad substrate applicability and can be expanded to other metals and reduction protocols, making it versatile for diverse material applications.

This study examines the intrinsic optical enhancements of carbon fiber-reinforced polymers (CFRPs) achieved through the integration of magnesium oxide (MgO) nanoparticles, as well as Mg/MgO and titanium dioxide (TiO₂) thin films onto carbon fibers. Integration was performed by quasi-continuous electrophoretic deposition (EPD) and physical vapor deposition (PVD), respectively. Employing a customized electrophoretic cell, EPD facilitated uniform MgO nanoparticle deposition onto unsized carbon fibers, ensuring stable nanoparticle dispersion and precise fiber coating. As a result, the fibers exhibited increased ultraviolet (UV) reflectance, largely attributed to the optical properties of the protective MgO layer. In parallel, PVD enabled the deposition of Mg/MgO and TiO₂ thin films with tailored thicknesses, providing precise control over key optical parameters such as reflectivity and interference effects. Mg/MgO coatings demonstrated high UV reflectivity, while TiO₂ layers, with their varying refractive indices, generated vibrant colors in the visible (Vis) range through thickness-dependent light interference. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) assessed the quality, thickness, and uniformity of these thin films, and UV/Vis spectroscopy confirmed the influence of deposition parameters on the resulting optical performance. Post-lamination analyses revealed that both EPD and PVD modifications significantly enhanced UV reflectivity and allowed for customizable color effects. This dual strategy underscores the potential of combining EPD and PVD to develop advanced CFRPs with superior UV resistance, decorative optical features, and improved environmental stability.

Thermosetting materials with differing properties bond without adhesives via dynamic covalent exchange forming interfacial zone. This enables hydrophobic polymers to bond polar materials and fabricate layered composites with distinct failure modes.

In this manuscript, we have demonstrated an efficient and rapid synthetic strategy for preparation of new fluorene–dendron-hybridized blue light-emitting polymers P1–P7 by the reaction of 9,9 long-chain dialkylated fluorenes M2–M8 with dendronized monomer (M1) under microwave-assisted reaction condition. These fluorene–dendron-hybridized polymers P1–P7 were characterized using different spectroscopic techniques. Furthermore, the optophysical properties of these polymers P1–P7 were studied which revealed that these synthesized polymers P1–P7 have potential to emerge as capable materials in the development of diodes, particularly for blue light emission. In the future, similar approaches would be utilized for preparation of light-emitting polymer composite.

We report the controlled growth of biologically active compounds: gold nanoparticles (AuNPs) in various shapes, including their green synthesis, characterization, and studies of their applications towards biological, degradation and recycling. Using spectroscopic methods, studies on responsive binding mechanisms of AuNPs with biopolymers herring sperm deoxyribonucleic acid (hsDNA), bovine serum albumin (BSA), dyes degradation study, and exquisitely gold separation studies/recovery from nanowaste, COVID-19 testing kits, and pregnancy testing kits are discussed. The sensing ability of the AuNPs with biopolymers was investigated via various analytical techniques. The rate of degradation of various dyes in the presence and absence of AuNPs was studied by deploying stirring, IR, solar, and UV-Vis methods. AuNPs were found to be the most active cytotoxic agent against human breast cancer cell lines such as MCF-7 and MDAMB-468. Furthermore, an economical process for the recovery of gold traces from nanowaste, COVID-19 detection kits, and pregnancy testing kits was developed using inexpensive and eco-friendly α-cyclodextrin sugar. This method was found to be easy and safest in comparison with the universally accepted cyanidation process. In the future, small gold jewelry makers and related industries would benefit from the proposed gold-recycling process and it might contribute to their socio-economic growth. The methodologies proposed are also beneficial for trace-level forensic investigation.

We developed a cost-effective and eco-friendly click biosynthesis of small molecule quercetin–gold quantum dots (QRT–AuQDs) involving quick conjugation using an ultrasonication method at ambient temperature by utilizing QRT and gold ions in the proportion of 0.1 : 1 (molar ratio). A comparatively very short amount of time (60 seconds) was required as compared to conventional procedures. The present biomimetics research relates to the isolation of bioactive QRT by the circularly spread silica gel layer technique (CSSGLT) and characterization (UV-Vis, FTIR, NMR and DSC analysis). Characterization of the synthesized QRT–AuQDs conjugated complex was carried out by UV-Vis, HR-TEM, DLS, zeta potential and X-ray diffraction. The main objective of the present work was to study the comparative anticancer activity of QRT and QRT–AuQDs on human lung cancer HOP-62 and leukemia K-562 cell lines. The results suggested that QRT–AuQDs showed potential for applications in anticancer treatment and were found to be a more cytotoxic agent in comparison to QRT, causing > 50% inhibition of cancer cells at the concentration < 10⁻⁷ M. Hence, small molecule conjugated QRT–AuQDs can be used as a promising material for biomedical, bioengineering and anti-infectives applications.

In this study, we focus on the biomimetic development of small molecules and their biological sensing with DNA. The binding of herring sperm deoxyribonucleic acid (hs-DNA) with naturally occurring bioactive small molecule α-amyrin acetate (α-AA), a biomimetic – isolated from the leaves of Ficus (F.) arnottiana is investigated. Collective information from various imaging, spectroscopic and biophysical experiments provides evidence that α-AA is a minor groove sensor of hs-DNA and preferentially binds to the A–T-rich regions. Interactions of different concentrations of small molecule α-AA with hsDNA were evaluated via various analytical techniques such as UV-Vis, circular dichroism (CD) and fluorescence emission spectroscopy. Fluorescence emission spectroscopy results suggest that α-AA decreases the emission level of hsDNA. DNA minor groove sensor Hoechst 33258 and intercalative sensor EB, melting transition analysis (T_M) and viscosity analysis clarified that α-AA binds to hs-DNA via a groove site. Biophysical chemistry and molecular docking studies show that hydrophobic interactions play a major role in this binding. The present research deals with a natural product biosynthesis-linked chemical–biology interface sensor as a biological probe for α-AA: hs-DNA.

Chitosan biological macromolecule is a versatile polymer; chemical modification has been carried out that lead to the formation of chitosan grafted polymers composites (Chito-g-PC). We proposed synthesis of six various Chito-g-PC as sorbents for toxic dyes. A novel graft copolymerization method based on radical polymerization with vinyl monomer like acrylic acid, acrylamide, N-isopropylacrylamide, methacrylic acid and polyacrylonitrile were utilized in order to address the large amount of swelling at four different pH buffers solution. The effect of initiator and monomer concentration, time and temperature on % grafting and % grafting efficiency were performed. Comparative characterization of Chito and Chito-g-PC were evaluated by SEM, XRD and FTIR, as well as solubility characteristics of the composites were determined by various pH buffer solution. Cationic toxic dyes Malachite green (MG) and Methylene blue (MB) were selected as the sorbet, and Chito-g-PC were used as biosorbents. Thermodynamic analysis showed that the sorption process was spontaneous and endothermic with an increased randomness. The sorption experiments were realized with six different Chito-g-PC for MG and MB at various pH.

Bioinorganic chemistry has achieved great importance by considering environmental and health issues. Here we present anticancer, antioxidant, good protein quencher single pot biosynthesized one dimensional palladium Nanoneedles (PdNNs) as a negative catalyst, where water plays a role of safer solvent. Needle-shaped one-dimensional PdNNs was synthesized using filamentous fungal stain of Aspergillus oryzae (biomass) was successively applied as a suppressant for the growth of human breast, colon and leukemia cancer Cell Lines. Quenching process of bovine serum albumin by PdNNs was spontaneous with hydrogen bonding and hydrophilic interaction. Interaction of protein and PdNNs showed binding constant in the range of 10⁴ M^-1 and one binding site. Forster's resonance energy transfer (FRET) theory applied to find out distance between the interaction of PdNNs and protein, where critical distance and energy transfer distance varies with change in concentrations of PdNNs 4.84 x 10⁻⁶ M to 9.69 x 10^-7 M from 2.9 to 3.7 nm and 3.2 to 5.4 nm respectively. Radical scavenging method was applied to find out an antioxidant activity which of nanoneedles. Needle-shaped palladium nanoparticles and particle size found to be ̴ 3.0 nm using high-resolution transmission electron microscopes.