Ecotoxicological impact of dinotefuran insecticide and its metabolites on non-targets in agroecosystem: Harnessing nanotechnology- and bio-based management strategies to reduce its impact on non-target ecosystems.

The class of insecticides known as neonicotinoid insecticides has gained extensive application worldwide. Two characteristics of neonicotinoid pesticides are excellent insecticidal activity and a wide insecticidal spectrum for problematic insects. Neonicotinoid pesticides can also successfully manage pest insects that have developed resistance to other insecticide classes. Due to its powerful insecticidal properties and rapid plant absorption and translocation, dinotefuran, the most recent generation of neonicotinoid insecticides, has been widely used against biting and sucking insects. Dinotefuran has a wide range of potential applications and is often used globally. However, there is growing evidence that they negatively impact the biodiversity of organisms in agricultural settings as well as non-target organisms. The objective of this review is to present an updated summary of current understanding regarding the non-target effects of dinotefuran; we also enumerated nano- and bio-based mitigation and management strategies to reduce the impact of dinotefuran on non-target organisms and to pinpoint knowledge gaps. Finally, future study directions are suggested based on the limitations of the existing studies, with the goal of providing a scientific basis for risk assessment and the prudent use of these insecticides.

A bibliometric analysis of pre- and post-Stockholm Convention research publications on the Dirty Dozen Chemicals (DDCs) in the African environment.

Persistent organic pollutants (POPs) are toxic chemicals that stay in the environment for a long time. To address the toxicity issues, global nations, including 53 African countries, ratified the Stockholm Convention to minimize or eliminate the production of 12 POPs known as the "Dirty Dozen". However, these Dirty Dozen Chemicals (DDCs) still exist in significant concentration in the African environment, prompting numerous research to investigate the level of their occurrences. Here, we conducted a bibliometric analysis to examine the publication trends in DDCs-related research in Africa using articles published between 1949 and 2021 from the Web of Science and Scopus databases. A total of 884 articles were published within the survey period, with a publication/author and author/publication ratio of 0.36 and 2.76, respectively. South Africa ranked first in terms of number of publications (n = 133, 15.05%), and total citations (n = 3115), followed by Egypt (n = 117), Nigeria (n = 77), USA (n = 40), and Ghana (n = 38). Research collaboration was relatively high (collaboration index = 2.88). The insignificant difference between the theoretical and observed Lotka's distribution indicates Lotka's law does not fit the DDC literature. An annual growth rate of 0.57% implies that a substantial increase of articles in years to come is not expected. More research programs should be established in other African countries to measure up to South Africa's supremacy. This is critical in order to provide a basis for effective compliance to the Stockholm Convention on POPs in Africa.

Experimental and theoretical studies of the influence of alkyl groups on the photovoltaic properties of (E)-6-((2, 3-dihydroxylnaphthalene)diazenyl)-1H-benzoisoquinoline-1,3-dione-based organic solar cell.

The manipulation of the active dye material for application in dye-sensitized solar cell (DSSC) using simple or bulky group substituents is necessary for improved dye performance. Herein, we carried out a combined experimental and theoretical studies of different alkylated novel reactive (E)-6-(2,3-dihydroxyl naphthalene diazinyl)-1H-benzoisoquinoline-1,3-dione azo-based dyes using spectral (FTIR, UV-visible, and NMR) analysis and electronic structure theory method based first principle density functional theory (DFT) calculations to investigate the molecular electronic properties, structural analysis, excitation behavior, and the theoretical potential application in photovoltaic cell. The synthesized azo dye (azoD) was theoretically modeled by varying the number of alkyl chains denoted as AzoD1, AzoD2, AzoD3, and AzoD4 to represent azo dyes having ten (10), twelve (12), fourteen (14), and sixteen (16) alkyl chain length respectively. From the natural bond orbital (NBO) analysis, the higher stabilization energies, 227.80 and 227.77 kcal/mol respectively, recorded for AzoD1 and AzoD4 may be due to extra orbital contribution by π*(N21-N22) to π*C54-C56 31.19 eV for AzoD1 and π*(N21-N22) → π*(C53-C55) 31.43 eV AzoD4 confirming that chain length affected the orbital interaction of the molecules. The driving force (ΔGinject) of electron injection into the TiO2 surface (- 1.92 to - 1.93) shown in this study is indicative that alkylated azo dyes are good for improved DSSCs performance. Again, the open circuit voltage (Voc) of 1.090 (AzoD1), 1.092 (AzoD2), 1.093 (AzoD3), and 1.095 (AzoD4) are also evidence of the suitability of azo dyes as photosensitizers. All the spectroscopic analysis, FTIR, UV-visible, and NMR combined with theoretical calculations, provided accurate data for characterizing the titled azo dye compound and showed that it has good photophysical properties. The presence of alkyl groups and chain length promoted the stability of the dyes thereby making them suitable for application in DSSCs. Increase in chain length as well enhanced the electron injection into the conduction band of the semiconductor.

Trapping Rhodamine B dye using functionalized mango (Mangifera indica) pod.

The use of acid-modified mango pod (AMMP) sorbent for removing Rhodamine B (Rh-B) dye from aqueous media was investigated. Raw mango pod (RMP) and AMMP sorbents were characterized using scanning electron microscopy (SEM), energy dispersive X-ray (EDX), powdered X-ray diffractogram (PXRD), Fourier transform infrared (FTIR), point of zero charge pH (pHpzc ), and Boehm titration (BT) techniques. Batch adsorption was employed to examine the influence of operational factors. Sorption kinetic parameters were calculated using pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion models. The pseudo-second-order model best fitted the adsorption kinetic data most with maximum correlation coefficient (R2 > 0.99). The process of the adsorption was controlled by both boundary layer and intraparticle diffusion mechanisms. Four isotherm models (Langmuir, Freundlich, Dubinin-Radushkevich, and Temkin) were utilized to analyze the equilibrium data at various temperatures. Freundlich model gave the best fit with the maximum regression (0.99), while the Langmuir isotherm model established a maximum monolayer adsorption capacity of 500 mg g-1 . Thermodynamic parameters studied revealed that the interaction is spontaneous and endothermic in nature. The cost analysis of the current study provides convincing proof that AMMP is efficient for removing Rh-B dye from solution by providing a saving of 225.2 USD/kg, which is eight times cheaper than commercial activated carbon. Consequently, the study revealed that AMMP is a viable, effective, and sustainable sorbent for Rhodamine B dye removal. PRACTITIONER POINTS: The powdered X-ray diffractogram (PXRD) showed the formation of new and intense peaks with the presence of highly organized crystalline structures on acid-modified mango pod (AMMP). Surface morphology of AMMP showed well-developed open surface pores required for effective adsorption of Rh B dye molecules. Economic feasibility of the present study showed that AMMP is more affordable than commercial activated carbon that costs USD 259.5/kg, thus translated to a saving cost of USD 225.2/kg and more than 7.5 times cheaper than the commercial activated carbon (CAC).