Active Functional Groups Research Articles

Photocatalytic properties of ZnO semiconductor nanoparticles green synthesized employing Ipomoea stans leave extracts

One of the biggest problems in the ecosystem is wastewater contaminated with industrial dyes. These pollutants have a very stable chemical structure, which causes complicated removal. However, a possible alternative for wastewater treatment is zinc oxide semiconductor nanoparticles (ZnO NPs). The approach of this study was the implementation of a green synthesis methodology for the obtention of ZnO nanoparticles employing Ipomoea stans (TV) leaves as extracts. The properties of the ZnO nanoparticles synthesized at 1 %, 2 %, and 4 % w/v (weight/volume) concentration of the extract were obtained from the characterization using different techniques. The FTIR analysis determined the presence of the active functional groups attached to the surface, which capped and stabilized the ZnO NPs; a band located in the range of 500-390 cm−1 confirms the presence of the Zn–O bond. The UV absorption spectra of all ZnO NPs samples were determined by executing the ultraviolet–visible spectroscopy technique, with a characteristic signal located at ∼370 nm and energy gap values between 3.036 eV and 3.101 eV. In addition, XRD patterns determined the average crystallite sizes to be 30.78 nm for ZnO-TV 1 %, 18.68 nm ZnO-TV 2 %, and 11.96 nm ZnO-TV 4 %, respectively. Furthermore, the results from transmission electron microscopy (TEM) displayed the following values of mean particle size of 21 nm, 24.4 nm, and 10.16 nm for ZnO-TV 1 %, ZnO-TV 2 % and ZnO-TV 4 % with S.D. 9.10, 12.5 and 3.6. Finally, the photocatalytic activity was evaluated utilizing the industrial dyes Methyl Orange, Methylene Blue, Rhodamine B, Malachite Green, and Congo Red. Obtaining outstanding results in the degradation of all industrial dyes. All syntheses achieved degradation greater than 91 % for methyl orange, methylene blue, and rhodamine B.

Interfacial engineering and defect passivation of SnO2 through agmatine sulfate in carbon-based perovskite solar cells

Electron transport layer has always played a crucial role in the performance of the perovskite solar cells (PSCs). Particularly, SnO2-based PSC has sparked considerable interest due to its superior properties. Even with such remarkable properties, certain challenges persist such as agglomeration of SnO2 particles which can lead to interfacial defects and poor morphology. To solve this problem, Agmatine Sulfate (AGTS) has been introduced as an interfacial modification agent which with the help of its active functional group including amide (-NH2) and hydroxyl (OH) has allowed to facilitate the interaction at the interface between SnO2 and perovskite. The interaction facilitates the growth of perovskite crystals while tuning the energy levels which has boosted the charge transfer capability of the layer. All these improvements in the properties have led to enhanced power conversion efficiency (PCE) from 11.17 % to 15.20 % for the encapsulated device. Furthermore, the modification also improved the long-term stability of the device as the AGTS-modified devices retained 87 % of their performance at 15–25 °C with humidity levels between 10 and 20 % for over a period of 31 days. Finally, the devices prepared with the AGTS also showed repeatability in their performance while boosting the overall performance of carbon-based PSCs (C–PSCs) and indicating a novel approach to not only increase but also accelerate the commercialization of C-PSC.

Determination of five veterinary drug residues in milk by ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap mass spectrometry based on modified chitosan membrane purification

Milk is an important consumer product with high nutritional value. The presence of veterinary drug residues in milk owing to the indiscriminate use of veterinary drugs may affect consumer health. In the mass spectrometric analysis of trace compounds, chromatographic co-eluting components easily interfere with the mass spectral signals obtained, affecting the accuracy of qualitative and quantitative analyses. Matrix purification is a promising method to reduce the matrix effect. Chitosan is a natural biopolymer with numerous active functional groups such as amino, acetyl, and hydroxyl groups; these groups can adsorb lipids through hydrophobic and electrostatic interactions. Chitosan also has the advantages of low production cost, stable chemical properties, and convenient modification. Novel chitosan-based materials are promising candidates for lipid purification. In this study, a chitosan membrane was modified with trimethoxyoctadecylsilane (C18-CSM). C18-CSM was prepared through one-step hydrolysis and used as a dispersive solid phase extraction (DSPE) adsorbent to purify the matrix during milk pretreatment. We combined C18-CSM with ultra-high performance liquid chromatography-quadrupole/electrostatic field orbitrap mass spectrometry (UHPLC-Q/Exactive Orbitrap MS) to develop an effective method for the extraction and determination of ofloxacin, enrofloxacin, ciprofloxacin, diazepam, and metronidazole in milk. C18-CSM was characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, and water contact angle testing. The results indicated that the material has a rough surface and uniformly dense cross-section. The water contact angle of C18-CSM was 104°, indicating its good hydrophobicity. The pretreatment conditions (extraction solvent, dosage of NaCl, extraction frequency, and dosage of C18-CSM) that influenced the recoveries of the five veterinary drugs were investigated in detail. The optimal conditions were established as follows: 5% formic acid in acetonitrile, 1 g NaCl, extraction 1 time, 20 mg C18-CSM. Separation was performed on a Hypersil GOLD VANQUISH column (100 mm×2.1 mm, 1.9 μm). The mobile phase consisted of 0.1% formic acid aqueous solution and 0.1% formic acid in acetonitrile, and was flowed at a rate of 0.3 mL/min. The sample injection volume was 1 μL, and the column temperature was maintained at 25 ℃. Mass spectrometric analysis was performed in positive electrospray ionization mode. To verify the necessity of the purification material, the matrix effect was investigated using the matrix-matched standard curve method. The use of C18-CSM reduced the matrix effects of the five necessity drugs from the range of -22%-8.8% to the range of -13%-3.6%, indicating that C18-CSM is a highly efficient DSPE material. Under optimal conditions, the developed method showed good linearities within the range of 0.5-100 μg/L, with correlation coefficients (r2)≥0.9970. The limits of detection(LODs) and quantification (LOQs) were 0.2 μg/L and 0.5 μg/L, respectively. To assess the accuracy and precision of the method, we prepared milk samples with three spiked levels (low, medium, and high). The recoveries of the five veterinary drugs were ranged from 79.5% to 115%, and the intra-day and inter-day relative standard deviations were 7.0%-13% (n=6) and 1.3%-11% (n=3), respectively. This study provides a simple, accurate, and reliable method for the rapid and simultaneous determination of the five veterinary drug residues in milk.

The Deep Removal of Mercury in Contaminated Acid by Colloidal Agglomeration Materials M201

The high-temperature roasting/smelting process of copper and zinc concentrates will cause the mercury in the concentrate to evaporate into the flue gas, and most of the mercury in the flue gas will eventually enter the waste acid in its ionic form. A highly efficient mercury removal agent M201 with long carbon chains and loaded active functional groups can adsorb and disperse fine particles for mercury removal in the system. Through bridging, the linear structure is woven into a network to achieve large-scale capture and dispersion of fine particles and colloidal substances. The recommended operating conditions for developing mercury deep purification technology are as follows: M201 reagent concentration of 50 g/L, 6 mL/L added acid solution, room temperature, mixing time of 5 min, air flotation time of 10 min, ventilation rate of 0.1 L/min, H2SO4 concentration of 33.67 g/L, and the residual mercury content of 2 mg/L (the mercury content reaches 0.01 mg/L after two-stage mercury removal treatment). Meanwhile, the residual arsenic content is 21.9 mg/L. This study shows a better separation of arsenic and mercury and achieves one-step mercury removal.

Tailoring the Molecular Structure of 6-Gingerol for Targeting the Phase Separation in Human Lysozyme.

Human lysozyme undergoes a phase-separation process to form insoluble amyloid-architects that cause several pathologies including systemic amyloidosis. Here we have tailored 6-gingerol by extending its molecular framework with active functional groups to specifically target lysozyme phase-transition events. Aggregation assay revealed that tailored 6-gingerol with 4-aromatic moieties (MTV4) substantially suppressed the conversion of the lysozyme low-density liquid phase (LDLP) to solid-phase structured amyloids. The data obtained from biophysical, computational, and microscopic imaging tools suggest direct intervention of MTV4 with the liquid-liquid phase separation. The CD data suggest that MTV4 was able to retain the native conformation of lysozyme. Both biomolecular and computational data reveal the interference of MTV4 with the aggregation-prone hydrophobic stretches within the lysozyme, thereby retaining the native structure and reversing the misfolded intermediates to active monomers. Also, MTV4 was able to induce rapid dissolution of preformed-toxic amyloid fibrils. These results reinforce the importance of the aromatic-aromatic interaction in preventing human lysozyme phase separation.

Insights into the co-pyrolysis interaction of cellulose and Zhundong coal via ReaxFF molecular dynamics simulation

Experiments on the co-pyrolysis of coal and cellulose were conducted using a fixed-bed reactor in this paper. The results demonstrated that co-pyrolysis increases gas and char yields while reducing tar yield. The reactive force field molecular dynamics (ReaxFF MD) was then used to simulate co-pyrolysis in order to analyze the mutual reaction between coal and cellulose from the perspective of carbon skeleton, enabling the co-pyrolysis mechanism to be examined precisely. The results demonstrated that co-pyrolysis accelerates the crosslinking of cellulose fragments and coal char. The cellulose-derived component in cross-linked char (char products containing both cellulose and coal fragments) rises from 0.21 wt% at 2000 K to 12.82 wt% at 3000 K, resulting in higher char production. The examination of the yields and distribution of co-pyrolysis products at 2400 K reveals that the volatiles generated by cellulose and coal char undergo mainly crosslinking reaction, resulting in a lower tar yield and a higher inorganic gas yield. Due to the combination of oxygen-containing functional groups in the coal char with cellulose volatiles and free hydroxyl groups, the oxygen-containing active functional groups were consumed, rendering the cross-linked char more stable and inactive, thereby suppressing coal polymerization.

Bond strength of epoxy-based composites at the interface with surface deposited metal layer: A comparative study with different dimensional fillers

With the complexity of the working environment, pure epoxy resin can no longer meet the requirements, and the weak interfacial bonding between metal layer and epoxy-based composites limits its development. In this work, we propose a novel molecular grafting modification technique by using the active functional groups of polymers, which can apply to epoxy-based composites with various fillers to improve the adhesive strength of the interface between the metal film and matrix. 3D surface profile and surface wettability were used to characterize the effect of fillers on the surface of epoxy composites. Scanning electron microscope (SEM) and Raman spectroscopy were utilized to judge the interface failure modes of the composites. Peeling test and surface-enhanced Raman scattering (SERS) were conducted to examine how fillers affected adhesion. The results showed that silane grafting substantially improved the bonding between the epoxy-based composite matrix and the metal layer without the need for alkaline washing and palladium (Pd) activation steps on the substrate. The average adhesive strength can reach a maximum of 17.76 N/cm. The study also revealed the effect of filler size on the interfacial adhesive strength. The interfacial adhesive strength was increased by two dimensional lamellar materials, decreased by one-dimensional tubular materials, and remained unaffected by zero-dimensional spherical materials. This study may have positive implications for improving interfacial bonding between metal and polymer composite surfaces.

Assembly and in vitro cytotoxicity of polylactic acid-phosphoglyceride composite drug loaded microspheres

Electrostatic spraying is recognized as a straightforward technique for the fabrication of polylactic acid (PLA) microspheres. PLA is notable for its biodegradability and versatile mechanical properties. Nonetheless, its limited cell affinity and the absence of active functional groups for drug interaction restrict its usage. In this study, we employed phosphoglyceride (P-P-Gly) coating to enhance the properties of PLA microspheres. The modified PLA microspheres underwent characterization through scanning electron microscopy (SEM), X-ray diffraction (XRD), and differential scanning calorimetry (DSC). The findings confirmed the successful coating of P-P-Gly onto the microspheres. The in vitro cytotoxicity of the modified PLA microspheres was assessed using the CCK-8 assay. The results demonstrated improved cell affinity for both modified and curcumin-loaded PLA microspheres. Notably, when the curcumin loading concentration in PLA microspheres reached 3 mg/mL, the cell viability of L-929 cells surged to 127%. PLA microspheres with lower concentrations of curcumin exhibited a proliferative effect on both L-929 cells and HUVECs. These findings suggest that PLA microspheres, when modified and loaded with curcumin, exhibit commendable biocompatibility, making them suitable for applications in tissue engineering.

Preparation and Properties of Composite Double-Network Gel for Inhibiting Coal Spontaneous Combustion.

In order to improve the inhibition effect of gel on coal spontaneous combustion, a chitosan (CS)/polyacrylamide (PAM)/metal ion (Al3+) composite double-network gel was developed in this study. The optimum formula of the composite double-network gel was determined using orthogonal experimentation. The microstructure, water retention, compressibility, and anti-destruction properties of the composite double-network gel were analyzed. The inhibition effect of the composite double-network gel on coal spontaneous combustion was studied via infrared spectroscopy and a synchronous thermal analyzer from the micro and macro perspectives. The results show that the composite double-network gel has a denser interpenetrating double-network structure and a larger void ratio than the ordinary gel. The water retention rate was 55% after standing at 150 °C for 12 h. The deformation memory ratio of the composite double-network gel was 78%, which was 26.8% higher than that of the ordinary gel, and the compressive strength also increased by 59.96%. In addition, the critical temperature point and the maximum thermal weight-loss rate temperature point decreased by 7.01 °C and 39.62 °C, respectively, and the composite double-network gel effectively reduced active functional groups in the treated coal sample, such as hydroxyl and aliphatic hydrocarbons. In this study, a CS/PAM/Al3+ composite double-network gel was produced, which exhibited good gel performance and inhibition effects, with physical effects such as the covering, wetting, and cementation of coal.

Superior Anodic Lithium Storage in Core–Shell Heterostructures Composed of Carbon Nanotubes and Schiff‐Base Covalent Organic Frameworks

Covalent organic frameworks (COFs) after undergoing the superlithiation process promise high‐capacity anodes while suffering from sluggish reaction kinetics and low electrochemical utilization of redox‐active sites. Herein, integrating carbon nanotubes (CNTs) with imine‐linked covalent organic frameworks (COFs) was rationally executed by in‐situ Schiff‐base condensation between 1,1′‐biphenyl]‐3,3′,5,5′‐tetracarbaldehyde and 1,4‐diaminobenzene in the presence of CNTs to produce core–shell heterostructured composites (CNT@COF). Accordingly, the redox‐active shell of COF nanoparticles around one‐dimensional conductive CNTs synergistically creates robust three‐dimensional hybrid architectures with high specific surface area, thus promoting electron transport and affording abundant active functional groups accessible for electrochemical utilization throughout the whole electrode. Remarkably, upon the full activation with a superlithiation process, the as‐fabricated CNT@COF anode achieves a specific capacity of 2324 mAh g−1, which is the highest specific capacity among organic electrode materials reported so far. Meanwhile, the superior rate capability and excellent cycling stability are also obtained. The redox reaction mechanisms for the COF moiety were further revealed by Fourier‐transform infrared spectroscopy in conjunction with X‐ray photoelectron spectroscopy, involving the reversible redox reactions between lithium ions and C=N groups and gradual electrochemical activation of the unsaturated C=C bonds within COFs.

Zea mays bracts extract as an eco-friendly corrosion inhibitor for steel in HCl pickling solution: Experimental and simulation studies

Active phytochemicals with unique electron structures can adsorb on metal surfaces and effectively mitigate metal corrosion. Recently, plant extracts have garnered significant attention as green and renewable corrosion inhibitors. In this study, the abundant agricultural byproducts, namely Zea mays bracts, were used as the extract raw materials, and Zea mays bracts extract (ZMBE) was served as an eco-friendly corrosion inhibitor for mild steel (MS) in 1 M HCl pickling solution. The organic substances in ZMBE were analyzed via ultra-high performance liquid chromatography- quadrupole time-of-flight mass spectrometry (UPLC-QTFMS). The interaction between the active functional groups and MS was investigated using Fourier transform infrared (FT-IR) and ultraviolet–visible (UV–visible) spectroscopy and X-ray photoelectron spectroscopy (XPS). The corrosion inhibition behavior was scrutinized through potentiodynamic polarization (PDP) curves and electrochemical impedance spectroscopy (EIS). The results show that functional groups such as aromatic rings, double bonds, and hydroxyls successfully adsorb on the MS surface to form the protective films. ZMBE exhibits a mixed-type corrosion inhibition with a “geometric coverage” effect. The corrosion inhibition efficiency (η) increases with ZMBE concentration and solution temperature, the optimum η with 5.0 g·L−1 ZMBE at 318 K is 96.2 %. The adsorption of active ingredients follows the Langmuir and El-Awady isotherms. Density functional theory (DFT) and molecular dynamics (MD) simulations prove the synergistic effect of complex components in ZMBE and the corrosion inhibition mechanism. ZMBE is a promising acid pickling corrosion inhibitor with broad application prospects.

Outstanding interlaminar strength of carbon fiber reinforced epoxy resin via graphene oxide chemical bridge bonding

Carbon fiber reinforced polymers (CFRPs) are susceptible to interlaminar failure under high shear stress, which reduces their service life. Herein, we report a strategy to address the interlaminar damage problem of CFRPs by utilizing graphene oxide (GO) as a bridge to chemically bond carbon fibers and epoxy resin. Amino groups were grafted on the surface of carbon fibers to react with GO, then active amino functional groups were introduced onto GO, enabling crosslink with the epoxy resin. The chemical bonding force and mechanical interlocking effect of GO tightly integrated the carbon fibers with the epoxy resin, greatly reducing relative slip under high shear stress. This flexible and robust connection resulted in a significant improvement in the interfacial adhesion strength of CFRPs. The GO content and type of amino reactants were optimized to fabricate CFRPs, and the interlaminar shear strength and transverse fiber bundle tensile strength were increased to 76.36 MPa and 34.2 MPa, which were 46.2 % and 77.2 % higher than those of pre-modification materials, respectively. This research demonstrates that the chemical bonding provided by grafting graphene oxide significantly enhances interlaminar bond strength, thereby extending the service life of CFRPs and offering a promising path for manufacturing high-strength composites.

Biogenic Bovine Serum Albumin/Zn3(PO4)2/Cr2O3 hybrid electrocatalyst for improved oxygen evolution reaction

The fabrication of nanostructured protein-inorganic hybrid materials is crucial for the development of advanced multifunctional materials. Protein-inorganic mesoporous composites are gaining attention due to their remarkable properties, including large surface areas and active surface functional groups. We have successfully synthesized mesoporous BSA/Zn3(PO4)2/Cr2O3 catalysts to improve the kinetics of the oxygen evolution reaction (OER) in electrocatalytic water splitting for sustainable energy generation. This approach utilizes BSA in the synthesis process and is environmentally friendly. By adjusting the BSA quantity, we could control the yield of BSA/Zn3(PO4)2/Cr2O3 mesoporous. We employed various techniques, including FE-SEM, XRD, and FTIR, to analyze the morphology and structural characteristics of the biogenic BSA/Zn3(PO4)2/Cr2O3 electrocatalyst. Our comprehensive evaluation of the electrocatalytic OER activity of the BSA/Zn3(PO4)2/Cr2O3 hybrid structure demonstrated its remarkable performance. The biologically synthesized catalyst exhibited exceptional OER efficiency, maintaining a high current density of 10 mA cm−2 at very low overpotentials (only 216 mV) under alkaline conditions. The elongated peptide backbone of BSA significantly facilitated ion and electron transport, contributing to improved OER activity. The synergistic interaction between various amino acids from BSA and the metal ions within Zn3(PO4)2/Cr2O3 can be attributed to this enhancement, highlighting the potential of this hybrid structure in electrocatalytic OER applications.

Functionalized sea urchin-like MnO2 with chitosan to load CaCo layered double hydroxides for advanced catalytic oxidation of antibiotics through activation of peroxymonosulfate

Novel composite catalysts based on the functionalization of sea urchin-like MnO2 with chitosan (CS) to load CaCo layered double hydroxides were prepared by a simple hydrothermal method, and the physicochemical properties of the resulting MnO2@CS-CaCo LDHs were analyzed by various characterization methods. Then advanced oxidation processes (AOPs) were constructed based on MnO2@CS-CaCo LDHs through activation of peroxymonosulfate (PMS) to degrade ciprofloxacin (CIP), norfloxacin (NOR) and sulfamethoxazole (SMX) in water. Sea urchin-like MnO2 modified by CS created a unique interface and a variety of active functional groups for the loading of CaCo LDHs where MnO2 particles were uniformly attached to the surface of CaCo LDHs. The results showed that the MnO2@CS-CaCo LDHs composites had excellent catalytic performances compared with monomeric MnO2, MnO2@CS and CaCo LDHs, and the enhanced catalytic performances were mainly due to the synergistic effects between LDHs, CS and MnO2. Under optimal experimental conditions, the removal efficiencies of CIP and NOR reached up to 96.45 % and 96.58 % within 20 min, respectively, and the removal of SMX was 93.12 % within 30 min. Quenching experiments demonstrated that 1O2 was the main active oxygen species for catalytic degradation through a non-radical pathway. In addition, the degradation efficiency of NOR was still as high as 93.78 % after the 10th cycle of degradation experiments, indicating that the composite catalysts had excellent reproducibility and stability. Finally, the activation mechanisms of MnO2@CS-CaCo LDHs/PMS and degradation pathways of SMX were proposed. The catalytic performances of MnO2@CS-CaCo LDHs/PMS for removal of three drugs in actual water bodies were further evaluated their practical application ability.

Optimization of Synthesizing Conditions for MXene (Ti3C2) Photocatalyst: Effect of LiF:Ti3AlC2 Mass Ratio

The analysis of the proposed work, specifically the development of the MXene photocatalyst, will be described in this chapter. The results of the analysis are useful for comparing the pristine precursor and etched structures of the MXene photocatalyst. A minimally intensive layer delamination (MILD) method will be used to create the MXene photocatalyst which uses lower fluorine content solution (HCl-LiF) creating a safer and easier method. The synthesis parameters for the development of highly efficient MXene photocatalysts, such as LiF:Ti3AlC2 mass ratio will be optimized. FTIR, XRD, SAP, FESEM and DR UV-Vis analysis will be used to characterize the as-developed MXene photocatalyst and its precursor, Ti3AlC2. The hypothesis of this study is etching treatment will increase the hydrophilicity and active functional group such as oxygen (O), fluorine (F) and hydroxyl (-OH) on MXene surfaces. The performance of photocatalytic degradation will be tested with an initial dye concentration of 30 ppm, solution pH at pH7 at room temperature (±27 ̊C). Each photocatalytic degradation study was performed in 50 ml of methylene blue solution with 0.1 g photocatalyst. All developed MXenes will undergo photocatalytic degradation performance to identify the optimized synthesizing conditions. The highest MXene photodegradation performance was found to reach 90% removal within 180 min.

Thermodynamic characteristics and mechanism of low-rank coal oxidation in oxygen-poor environment

Aiming at the restricted oxygen environment of coal mine, this paper focus on the whole process from physical adsorption to chemical reaction between coal and oxygen, and quantum chemical calculations investigate the potentiating or inhibiting effects of different active groups on the amount of oxygen adsorbed and thermally released from the main coal structure, and experimentally investigate the effect of oxygen concentration (OC) on the transformation relationship between active functional groups and active sites. The results showed the coal side-chain structure has an effect on the heat release characteristics of the aromatic ring in the process of oxygen adsorption, and the heat of adsorption of the aromatic ring with alkyl and aldehyde side-chains reaches 422.706 kJ/mol. The relationship between carbon oxide release and temperature at different OC all conformed to the exponential function model, and the apparent activation energy was positively correlated with the OC. The increase of OC narrows the gap between the production and consumption rates of active sites, which is helpful for the further understanding of the coal spontaneous combustion (CSC).

Bioinspired green synthesis of ZnO nanoparticles by marine-derived Streptomyces plicatus and its multifaceted biomedicinal properties

The present study explores the bioinspired green synthesis of zinc oxide nanoparticles (ZnONPs) using marine Streptomyces plicatus and its potent antibacterial, antibiofilm activity against dental caries forming Streptococcus mutans MTCC and S. mutans clinical isolate (CI), cytotoxicity against oral KB cancer cells, hemolysis against blood erythrocytes and artemia toxicity. The bioinspired ZnONPs showed a distinctive absorption peak at 375 nm in UV–Vis spectra, the FT-IR spectra divulged the active functional groups, and XRD confirmed the crystalline nature of the nanoparticles with an average grain size of 41.76 nm. SEM analysis evidenced hexagonal morphology, and EDX spectra affirmed the presence of zinc. The ZnONPs exerted higher antagonistic activity against S. mutans MTCC (Inhibitory zone: 19 mm; MIC: 75 μg/ml) than S. mutans CI (Inhibitory zone: 17 mm; MIC: 100 μg/ml). Results of biofilm inhibitory activity showed a concentration-dependent reduction with S. mutans MTCC (15 %–95 %) more sensitive than S. mutans CI (13 %–89 %). The 50 % biofilm inhibitory concentration (BIC50) of ZnONPs against S. mutans MTCC was considerably lower (71.76 μg/ml) than S. mutans CI (78.13 μg/ml). Confocal Laser Scanning Microscopic visuals clearly implied that ZnONPs effectively distorted the biofilm architecture of both S. mutans MTCC and S. mutans CI. This was further bolstered by a remarkable rise in protein leakage (19 %–85 %; 15 %–77 %) and a fall in exopolysaccharide production (34 mg–7 mg; 49 mg–12 mg). MTT cytotoxicity of ZnONPs recorded an IC50 value of 22.06 μg/ml against KB cells. Acridine orange/ethidium bromide staining showed an increasing incidence of apoptosis in KB cells. Brine shrimp cytotoxicity using Artemia salina larvae recorded an LC50 value of 78.41 μg/ml. Hemolysis assay substantiated the biocompatibility of the ZnONPs. This study underscores the multifaceted application of bioinspired ZnONPs in dentistry.

Solid-State Red Carbon Dots Based on Biomass Furan Derivatives.

In the preparation of carbon dots (CDs), precursors are crucial, and abundant precursors endow CDs with various structures and fluorescence characteristics. Furan (FU) and its derivatives are considered excellent carbonization materials due to their π conjugated structures and active functional groups, such as hydroxyl and aldehyde groups. Herein, we prepare FU-derivative-based CDs by a solvothermal method and investigate the influences of the precursor structure on the fluorescence characteristics. Surprisingly, CDs prepared from 5-hydroxymethylfurfural (HMF) with both aldehyde and hydroxyl groups exhibit red-shifted fluorescence characteristics in the solid state. We postulate that this solid-state fluorescence characteristic is due to the enhancement of supramolecular cross-linking fluorescence between CDs. The unique precursor structure leads to carboxyl groups on the surface of HMF-CDs that are conducive to the hydrogen bond formation. As the concentration of CDs increases, the hydrogen bonding effect increases, leading to a red-shift in the fluorescence wavelength. Therefore, basically full-color CDs/poly(vinyl alcohol) (PVA) phosphor-based light-emitting diodes can be achieved by controlling the degree of supramolecular cross-linking of CDs in PVA. This research provides a new approach for the preparation of solid-state luminescent CDs.

Carbon dots functionalized polyaniline as efficient sensing platform for cancer biomarker detection

Implementing simple and rapid detection of cancer biomarker using biosensors has the potential to contribute greatly to basic biological research and early detection of cancer. Tailoring of biosensor matrix based on conducting polymers has gained significant attention in recent years due to its electroactivity, redox property and biocompatibility. Herein, biomass derived carbon dots (CDs) were anchored on polyaniline (PANI) surface to get biocompatible and fluorescent, carbon dots functionalized polyaniline (CDs@PANI) that enable binding of large amount of prostate cancer biomarker, prostate specific antigen (PSA) antibody on its surface via active functional groups. Immobilization efficiency of CDs@PANI was investigated by electrochemical methods which revealed dense immobilization of biomolecules on CDs@PANI as compared to conventional PANI. A sandwich electrochemical biosensor was constructed using CDs@PANI as immobilization matrix for detection of prostate cancer biomarker PSA. The sensor displayed good sensitivity, specificity, stability, reproducibility, wide linear range (0.01–60 ng/ml) and a low detection limit of 20 pg/ml. The importance of CDs in improving the sensor performance was demonstrated by carrying out detailed electrochemical studies using glucose oxidase as a model biomolecule. Biocompatibility of sensing matrix was assessed by performing 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay for cell viability using WI26 cells. The sensing platform demonstrated herein provides great potential for the detection of different cancer biomarkers and metabolites.

A new type of wood bio-adhesives production: Effect of hydrochar from sewage sludge on adhesives's physicochemical properties

This contribution discloses a new method to prepare formaldehyde-free plywood adhesive using hydrochar after hydrothermal carbonization (HTC) of sewage sludge (SS). Proteins and polysaccharides on the surface of hydrochar can react via cross-linking to form bio-adhesives. The bio-adhesives have an excellent wet shear strength value, meeting the Chinese national standard GB/T 9846-2015 (≥0.7 MPa). During HTC, SS will disrupt the extracellular polymer structure and release organic matter as well as hydrolysis, dehydration, and Maillard reaction occur to develop hydrophobicity in hydrochar. Ash in SS also can play a key role in improving the wet shear strength value of bio-adhesives due to its organic-inorganic hybrid structure. HTC temperature can also significantly influence bonding strength as modifier of the active functional groups in hydrochar.