Selective adsorption of zearalenone by a novel magnetic molecularly imprinted carbon nanomaterial.

In this paper, the objective is to immobilize molecularly imprinted polymers (MIPs) onto the surface of magnetic carbon nanoparticles (Fe3O4@SiO2@C) to develop an effective method for the adsorption of zearalenone (ZEN). The prepared products were characterized by FT-IR, SEM, TEM, XRD, VSM, TGA, and BET. The content of zearalenone in corn samples was monitored by HPLC. The results indicate that the particle size of magnetic molecularly imprinted polymers (MMIPs) is approximately 200 nm. The adsorption mechanism of MMIPs was confirmed by static adsorption and dynamic adsorption experiments. The maximum adsorption capacity was 1.56 mg/g, and the adsorption equilibrium was reached within 50 min. The scatchard model showed that MMIPs had two binding sites, a high-affinity binding site and a low-affinity site. Kinetic second-order fitting indicates that MMIPs are mainly through chemisorption. In the actual sample application, the limit of detection (LOD) and limit of quantitation (LOQ) were 0.3 mg/L and 0.9 mg/L, respectively. The recovery of corn with the standard addition of ZEN was 73.6-88.1%, and the relative standard deviation (RSD) was 2.86-5.63%. The results demonstrated that MMIPs possess the advantages of straightforward operation, high precision, and cost-effectiveness, rendering them suitable for rapid ZEN detection.

Fabrication of OVs enriched BiOCl microflowers doped with Fe3+ for effective destruction of two typical contaminants.

In this study, a one-step solvothermal method was used to fabricate Fe3+ doped BiOCl microflowers with abundant oxygen vacancies (OVs) in the presence of glacial acetic acid. Various analytical techniques were employed to characterize the structural, morphological, and optical properties of the prepared samples. The presence of OVs was confirmed by low temperature electron paramagnetic resonance (EPR) analysis. The photocatalytic results show that Fe3+ doped BiOCl photocatalysts have higher activity than the bare BiOCl, and 10% Fe3+/BiOCl exhibits the highest photocatalytic performance, the photocatalytic efficiency of this sample is 2.3 and 1.1 times higher than that of the blank BiOCl toward photocatalytic degradation of perfluorooctanoic acid (PFOA) and rhodamine B (RhB), respectively. Furthermore, Fe3+ doped BiOCl demonstrates excellent reusability. Based on the experimental observations, an enhancement mechanism for the photocatalytic activity of Fe3+ doped BiOCl was reasonably elucidated.

Preparation of a hydrophilic nanofiber membrane by electrospinning for application in the detection of NO2 by chemiluminescence.

The strong hydrophobicity of the PVDF membrane is prone to contamination that is hard to clean for long-term usage. In this study, hydrophilic and antifouling nanofiber membranes (NMs) were prepared with the hydrophilic polymer PVP and inorganic nanoparticles TiO2NPS. This NM was found to have excellent cleanability and good recyclability. Within 30 minutes, the residual ions could be removed by cleaning with deionized water. In alkaline solutions with the power of hydrogen (PH) ≤10, NM exhibits good alkaline resistance and recycling performance. It was also found, for the first time, that TiO2NPS could enhance the sensitivity of Luminol-NO2 (L-NO2) by 4 times. The detection of NO2 concentration by NM presents an excellent linear relationship with the chemiluminescence reading. This linear relationship would aid quick and convenient detection of NO2 using chemiluminescence.

A Novel SPR Immunosensor Based on Dual Signal Amplification Strategy for Detection of SARS-CoV-2 Nucleocapsid Protein.

Since the global outbreak of coronavirus disease 2019 (COVID-19), it has spread rapidly around the world. The nucleocapsid (N) protein is one of the most abundant SARS-CoV-2 proteins. Therefore, a sensitive and effective detection method for SARS-CoV-2 N protein is the focus of research. Here, we developed a surface plasmon resonance (SPR) biosensor based on the dual signal-amplification strategy of Au@Ag@Au nanoparticles (NPs) and graphene oxide (GO). Additionally, a sandwich immunoassay was utilized to sensitively and efficiently detect SARS-CoV-2 N protein. On the one hand, Au@Ag@Au NPs have a high refractive index and the capability to electromagnetically couple with the plasma waves propagating on the surface of gold film, which are harnessed for amplifying the SPR response signal. On the other hand, GO, which has the large specific surface area and the abundant oxygen-containing functional groups, could provide unique light absorption bands that can enhance plasmonic coupling to further amplify the SPR response signal. The proposed biosensor could efficiently detect SARS-CoV-2 N protein for 15 min and the detection limit for SARS-CoV-2 N protein was 0.083 ng/mL, with a linear range of 0.1 ng/mL~1000 ng/mL. This novel method can meet the analytical requirements of artificial saliva simulated samples, and the developed biosensor had a good anti-interference capability.

Surface Plasmon Resonance Sensor Based on Core-Shell Fe3O4@SiO2@Au Nanoparticles Amplification Effect for Detection of T-2 Toxin.

In this paper, a core-shell based on the Fe3O4@SiO2@Au nanoparticle amplification technique for a surface plasmon resonance (SPR) sensor is proposed. Fe3O4@SiO2@AuNPs were used not only to amplify SPR signals, but also to rapidly separate and enrich T-2 toxin via an external magnetic field. We detected T-2 toxin using the direct competition method in order to evaluate the amplification effect of Fe3O4@SiO2@AuNPs. A T-2 toxin-protein conjugate (T2-OVA) immobilized on the surface of 3-mercaptopropionic acid-modified sensing film competed with T-2 toxin to combine with the T-2 toxin antibody-Fe3O4@SiO2@AuNPs conjugates (mAb-Fe3O4@SiO2@AuNPs) as signal amplification elements. With the decrease in T-2 toxin concentration, the SPR signal gradually increased. In other words, the SPR response was inversely proportional to T-2 toxin. The results showed that there was a good linear relationship in the range of 1 ng/mL~100 ng/mL, and the limit of detection was 0.57 ng/mL. This work also provides a new possibility to improve the sensitivity of SPR biosensors in the detection of small molecules and in disease diagnosis.

Research on the on-line determination of formaldehyde gas by the gas-liquid phase chemiluminescence method.

Based on the gas-liquid phase chemiluminescence tester independently developed by our laboratory, a highly sensitive, fast and accurate on-line detection method of formaldehyde gas in ambient atmosphere is established. The chemiluminescence system and the trace formaldehyde gas in the air directly undergo an interface heterogeneous chemiluminescence reaction to obtain a strong chemiluminescence signal. Through the measurement of the chemiluminescence signal intensity, a highly sensitive, real-time and on-line method for the determination of formaldehyde in the air was established. Factors influencing the experimental results such as gallic acid, potassium dichromate, reaction medium concentration, surfactant type and concentration, pump speed, tube length, and interfering gas were discussed based on the single factor and orthogonal analysis results. Finally, the optimal detection conditions were collected, and the detection results were compared with the national standard phenol reagent method. The results show that when the concentration of the standard formaldehyde gas is in the range of 0-0.582 µg L-1, the linear equation of this method is y = 208x + 29.667, the linear coefficient is R 2 = 0.997, and the minimum detection concentration of formaldehyde is 2.327 × 10-3 µg L-1. Under the same external conditions, the comparison and analysis using the national standard phenol reagent method proved that this method has the advantages of fast detection speed, low detection limit, good sensitivity, and accurate results, which can be used for real-time and online determination of trace formaldehyde in ambient air.

Rapid and sensitive online determination of ozone via gas-liquid chemiluminescence synergistically enhanced by graphene quantum dots and Triton X-100.

The determination of the ozone concentration in the atmosphere is an urgent need but most current methods are limited by large-scale equipment or complex procedures. Herein, a gas-liquid chemiluminescence (GL-CL) assay based on a portable GL-CL detector platform was reported for the fast and sensitive online determination of ozone. Graphene quantum dots (GQDs) and Triton X-100 were employed to synergistically enhance the CL intensity of chromotropic acid (CA)-ozone. The increase was about seven-fold upon the addition of GQDs and Triton X-100. The potential enhancement mechanism was also investigated. The speculated CL enhancement mechanism was that GQDs could catalyze dissolved oxygen in the CA solution to produce more free radicals in the presence of UV-light, and these radicals converted CA into more active compounds that could react with ozone and emit photons. The free radicals, active compounds and luminophores were protected from water quenching by micelles produced by dissolving Triton X-100 in water and as a result, CL was markedly enhanced. Most importantly, the response time of the GL-CL detector platform towards ozone was less than 0.5 s. Based on this outcome, a GL-CL assay for detecting atmospheric ozone was successfully developed with a linear range from 0.1 to 150 ppbv and a detection limit of 0.02 ppbv. This work provides a rapid and sensitive method for the online measurement of ozone, and has great potential in environmental applications; the potential applications of GQDs and Triton X-100 in the field of GL-CL have also been highlighted.

[Surface properties of ZuMgAl hydrotalcite-like compounds by inverse gas chromatography].

The structure of ZnMgAl hydrotalcite-like compounds (ZnMgAl-HTLC) prepared by hydrothermal synthesis was studied by X-ray diffraction (XRD). With a series of polar and nonpolar molecules as probes, inverse gas chromatography (IGC) was used to measure the surface properties of ZnMgAl-HTLC. It was found that the XRD pattern of ZnMgAl-HTLC was narrow, sharp and high. The results showed that ZnMgAl-HTLC with a higher purity was obtained by hydrothermal synthesis. The surface adsorption free energy was less than zero. The surface dispersive free energy was 6.02 mJ/m2. The acid-base interaction free energy was 5.33 kJ/mol. The adsorption enthalpy was 43.6 kJ/mol, and the adsorption entropy was 0.15 kJ/mol. The IGC method is significant in the study of the surface properties of ZnMgAl-HTLC.