Nitrite is a common nitrogen-containing compound that possesses high biological toxicity, thereby posing a serious threat to aquatic organisms. Therefore, it is imperative to develop a rapid and quantitative determination approach for nitrite. In this study, the aim was to prepare a novel electrochemical sensor to determine nitrite. This was achieved by synthesizing Au/Zn dendritic complexes on a carbon cloth self-supported electrode after plasma treated by a stepwise strategy of electrodeposition and in-situ corrosion. In accordance with the optimal experimental conditions, the electrode exhibited remarkable catalytic activity for the electrooxidation of nitrite ions (pH = 8.0), accompanied by a considerable enhancement in peak anodic current in comparison to the unmodified electrode. The sensor exhibited a wide linear range (1-833 μM, 833-8330 μM), high sensitivity (3506 μA mM-1 cm-2, 538 μA mM-1 cm-2), a low detection limit (0.43 μM), and excellent selectivity, reproducibility, and stability for the determination of nitrite. Furthermore, the prepared sensor was successfully applied to the detection of nitrite in tap water, fish holding pond water and duck pond water, demonstrating good recovery and no significant difference from the spectrophotometric results. The results suggest that the electrochemical sensor developed in this study represents a straightforward yet efficacious approach to the development of advanced portable sensors for aquaculture applications.

Precise monitoring of nitrite from real samples has gained significant attention due to its detrimental impact on human health. Herein, we have fabricated poly(3,4-ethylenedioxythiophene) functionalized carbon matrix suspended Cu nanoparticles (PEDOT-C@Cu-NPs) through a facile green synthesis approach. Additionally, we have used machine learning (ML) to optimize experimental parameters such as pH, drying time, and concentrations to predict current of the designed electrochemical sensor. The ML optimized concentration of fabricated C@Cu-NPs was further functionalized by PEDOT (π-electron mediator). The designed PEDOT functionalized C@Cu-NPs (PEDOT-C@Cu-NPs) electrode has shown excellent electro-oxidation capability towards NO2- ions due to highly exposed Cu facets, defects rich graphitic C and high π-electron density. Additionally, the designed material has shown low detection limit (3.91 μM), high sensitivity (0.6372 μA/μM/cm2), and wide linear range (5-580 μM). Additionally, the designed electrode has shown higher electrochemical sensing efficacy against real time monitoring from pickled vegetables extract.

Nitrite ions (NO2-), as one of the leading type-A inorganic-anion, showing significant-effects in the aquatic environment and also to humans health. Whereas, the higher uptake causes detrimental threat to human health leading to various chronic diseases, thus demanding efficient, reliable and convenient method for its monitoring. For this purpose, in the present research study we have fabricated the mimetic nonozyme like catalyst based colorimetric nitrite sensor. The acetic acid capped Zinc Oxide (ZnO) nanosheets (NSs) were introduce as per-oxidase mimetic like catalyst which shows high efficiency towards the oxidative catalysis of colorless tetramethylbenzidine (TMB) to oxidized-TMB (blue color) in the presence of Hydrogen-peroxide (H2O2). The present nitrite ions will stimulate the as formed oxidized-TMB (TMBox), and will caused diazotization reaction (diazotized-TMBox), which will not only decreases the peak intensity of UV-visible peak of TMBox at 652 nm but will also produces another peak at 446 nm called as diazotized-TMBox peak, proving the catalytic reaction between the nitrite ions and TMBox. Further, the prepared colorimetric sensor exhibits better sensitivity with a wider range of concentration (1 × 10-3-4.50 × 10-1 µM), lowest limit of detection (LOD) of 0.22 ± 0.05 nM and small limit of quantification (LOQ) 0.78 ± 0.05 nM having R2 value of 0.998. Further, the colorimetric sensor also manifest strong selectivity towards NO2- as compared to other interference in drinking water system. Resultantly, the prepared sensor with outstanding repeatability, stability, reproducibility, re-usability and its practicability in real water samples also exploit its diverse applications in food safety supervision and environmental monitoring.

In this work, condensation temperature, H2O vapor, SO2, SO3 and NH3 were studied to explore the formation mechanism of nitrate ions (NO3-) and nitrite ions (NO2-) in condensable particulate matter (CPM) discharged by ultra-low emission coal-fired power plants. Some important results were obtained: (i) The concentration of NO3- and NO2- increased with the decrease of condensation temperature, and H2O vapor could also promote the formation of NO3- and NO2-. (ii) The effects of SO2 and SO3 varied at different saturated states of flue gas, which was caused by the redox reaction of SO2 and NOX or the formation of H2SO4. (iii) NH3 could promote the nucleation of NO3- and NO2-, and the promotion effect also existed in the existence of SO2 or SO3. It is worth mentioning that SO3 and SO2 might synergistically inhibit the formation of NO3- and NO2-, regardless of the presence of NH3. The research results would enrich peoples understanding of the chemical and physical characteristics of NO3- and NO2- in CPM and provide a basic reference for the control of CPM emitted from coal-fired power plants.

Through a solvothermal reaction between the corresponding lanthanide(III) nitrate, 1,10 o-phenanthroline and pyridine 3,5-dicarboxylic acid ligands, a novel two-dimensional terbium-based metal-organic framework (Tb-MOF), named {Tb2O0.5(C12H8N2)2(C7H3NO4)3(H2O)2.75}n (1) with strong fluorescence was synthesized by hydrothermal method. The single crystal structure and phase purity of the as-synthesized Tb-MOF were verified by single crystal X-ray diffraction. Subsequently, some studies on the morphology, structure, and optical properties of the compound were carried out. The results show that the synthesized Tb-MOF (1) can be used for the fluorescence sensing of nitrite and ferric ions. Simultaneously, the as-synthesized crystal structure offers good chemical stability in different environments, such as common organic solvents, solutions with a wide pH range, and aqueous solutions of metal ions. Besides, it has good chemical stability in a certain temperature range. In addition, a detection method for nitrite and iron ions was established based on the principle of fluorescence quenching of Tb-MOF by the analytical target, showing good recovery and precision. The proposed method provides a reliable new method for detecting nitrite and ferric ions concentrations in actual water samples.

Developing photoelectrochemical (PEC) sensors based on photocatalytic materials has recently attracted great interest as an emerging technology for environmental monitoring. TiO2 P25 is a well-known highly active photocatalyst, cheap, and produced commercially on a large scale. In the current work, a practical and durable TiO2-based PEC sensor has been fabricated by immobilizing TiO2 P25 nanoparticles at disposable screen-printed carbon substrates using drop-casting method. The fabricated PEC sensor has been applied for the anodic-detection and determination of nitrite (NO2-) ions under UV(A) light (LED, 365 nm) using chronoamperometry (CA) and differential pulse voltammetry (DPV). Linear calibration curves were obtained between the photocurrent responses and the concentrations of NO2- ions in the ranges of 0.1-5.0 and 0.5-10 mg L-1 for CA and DPV, respectively. Surprisingly, the detection limits (sensitivities) of the fabricated sensor towards NO2- ions under light were enhanced by a factor of 4.75 (4.1) and 8.3 (37.4) for CA and DPV, respectively, in comparsion with those measured in the dark. It is found that the photo-excitation of TiO2 facilitates the photooxidation of NO2- ions via the photo-generated holes whereas the photogenerated electrons contribute to the enhanced photocurrent and consequently the enhanced detection limit and sensitivity. The fabricated TiO2-based PEC sensor exhibits a good stability, durability, and satisfying selectivity for NO2- ions determination. These results indicate that the TiO2-based PEC sensor fabricated by utilizing cheap and commercially available components has great potential for being transferred from lab-to-factory.

Halloysite nanotubes loaded with 4-aminothiophenol capped silver nanoparticles (mHNTs-AgNPs4-ATP) composite was synthesized as a sensitive surface-enhanced Raman scattering (SERS) probe for the determination of nitrite ions in sausage and pork luncheon meat. The as-prepared composite was characterized by transmission electron microscope, X-ray diffraction spectroscopy and Fourier transform infrared spectroscopy. The as-synthesized mHNTs-AgNPs4-ATP composite with evenly distribution of AgNPs can provide in-situ derivatization site for sensitive and selective SERS detection of nitrite ions. Under acid condition, the 4-ATP capped on the AgNPs can be transformed into p,p\'-dimercaptoazobenzene (DMAB) through nitrite-triggered diazo reaction. This efficient nitrite-triggered reaction can be used to detect nitrite via the characteristic peaks of DMAB at 1143 cm-1, 1392 cm-1, and 1434 cm-1. This SERS method has a wide logarithmic range of 0.0069-6.9 mg L-1, with detection limit of 0.78, 3.4, 0.51 μg L-1 at the peak of 1143 cm-1, 1392 cm-1, and 1434 cm-1, respectively. Besides, this method can be applied to detect nitrite ions in sausage and pork luncheon meat with relative standard deviation less than 10.3%, and the results were consistent with that analyzed by UV-Vis method. This method has good potential in efficient detection of meat product in food safety.

The method for assessing the level of nitric oxide (II) (NO) by voltammetric monitoring of nitrite ions was carried out on models M1 and M2 of polarized macrophages induced from monocytes of human peripheral blood with the addition of lipopolysaccharide (LPS) and interleukin-4 (IL-4), respectively. The model of induction of M1 and M2 macrophages was used in the work to achieve the corresponding shifts in the functional status of studied cells. Ethyl nitrite (EtONO) was used as a standard compound of nitrite ions for electrochemical measurements. Electrochemical determination of nitrite ions was performed by anodic linear sweep voltammetry in the first-order derivative mode (ALSV FOD) in Britton-Robinson (BR) buffer with pH 4.02 on carbon ink modified graphite electrode. EtONO calibrations were linear over a concentration range from 2 to 9 μmol L-1 with corresponding regression equation y = 0.768c - 0.048. Limit of detection (LOD) (S/N = 3) was 0.38 μmol L-1. The results of the study showed the fundamental possibility of using voltammetry to assess indirectly the production of nitric oxide by cells in supernatants of the monocytic macrophage lineage. The level of nitric oxide metabolites (nitrite ions) in supernatants was associated with the functional state of macrophages.

Tris-(hydroxymethyl)-aminomethane and urea were used as low-cost precursor compounds to synthesize highly fluorescent N-doped carbon nanodots (CNDs), in an environmentally-friendly, inexpensive process. The as-prepared CNDs exhibit blue fluorescence, excellent photostability under various conditions, water dispersibility and stability over several parameters, such as a wide range of pH. The N-doped CNDs were applied as a multi-probe fluorescence quenching system to the sensitive detection of nitrite (NO2-), nitrate (NO3-) and ferric (Fe3+) ions in food matrices. The recoveries from spiked food samples were fairly acceptable without significant interferences despite the complexity of the tested matrices. The decrease in fluorescence intensity is in linear relationship with the concentrations of NO2-, NO3- and Fe3+, in the ranges of 0.015-1.11 mM, 0.072-0.60 mM and 2.9-176 μΜ, respectively. The as-synthesized carbon dots were used for the detection of NO2-, NO3- and Fe3+ in food matrices after proper pretreatment, concluding that the multi-probe fluorescence system may potentially be implemented in food control. The FRET mechanism is able to describe the quenching of the CNDs-NO2- system, while the proportional temperature-dependent relationship with the slopes of calibration plots hint at a dynamic quenching mechanism. In the case of the CNDs-Fe3+ system, the slopes exhibit an inverse temperature dependence, indicating a static mechanism while there is no indication of a FRET mechanism.

A novel fluorescence sensor of NR-β-CD@AuNPs was prepared for the trace detection of nitrite in quantities as low as 4.25 × 10-3 μg∙mL-1 in an aqueous medium. The fluorescence was due to the host-guest inclusion complexes between neutral red (NR) molecules and gold nanoparticles (AuNPs), which were modified by per-6-mercapto-beta-cyclodextrins (SH-β-CDs) as both a reducing agent and a stabilizer under microwave radiation. The color of the NR-β-CD@AuNPs changed in the presence of nitrite ions. A sensor was applied to the determination of trace nitrites in environmental water samples with satisfactory results.