Harmless Compounds Research Articles

Demographic toxicology of insect growth regulators on the nontarget ectolarval parasitoid Habrobracon hebetor

Habrobracon hebetor Say (Hymenoptera: Braconidae) is one of the most important parasitoids of many pyralid moths, including the olive leaf moth, Palpita unionalis Hubner (Lepidoptera: Pyralidae). The widespread use of insecticides threatens natural enemies. Assessing the side effects of insecticides on nontarget organisms supports the rational use of insecticides during field application. The present study evaluates the lethal and sublethal effects of three insect growth regulators (IGRs), novaluron, methoxyfenozide, and pyriproxyfen, on P. unionalis and the demographic toxicology of these IGRs on its parasitoid H. hebetor. The LC50 values of these IGRs on P. unionalis were 0.97, 0.176, and 0.00009 ppm, respectively, indicating that pyriproxyfen was the most toxic. When H. hebetor adults were exposed to these LC50 levels under laboratory conditions to determine possible side effects. The IGRs did not affect the paralysis and parasitism rates of the parasitoid nor the sex ratio of its offspring. IGR treatments slightly reduced hatching rates and immature survival by 15–25%, indicating moderate effects on the early developmental stages of H. hebetor. The longevity and fecundity of treated females were each reduced to < 50% of their respective values in untreated females. Additionally, some demographic parameters of the parasitoid were significantly affected by the IGRs. Nevertheless, despite these observed effects, the positive net reproductive rate (R0 > 0) and intrinsic rate of increase (rm > 1) of H. hebetor indicated an exponential population increase that reflects the compatibility of the IGRs with the parasitoid. Our results demonstrated that the tested IGRs could be categorized as relatively harmless compounds to the parasitoid. Following these laboratory assessments, field studies will be required to confirm the effects of the tested IGRs on H. hebetor as well as other nontarget organisms.

Enhanced synergistic catalysis of bisphenol A in river water using an anti-aging photocatalytic membrane

Bisphenol A (BPA), as an endocrine disruptor, poses a potential threat to ecosystems and human health in aquatic environments. Membrane catalytic systems can accelerate the degradation of BPA and facilitate its conversion into harmless compounds. Nevertheless, the complex nature of the water environments and the limited stability of catalysts often result in challenges such as catalyst aging and deactivation. Herein, an anti-aging multifunctional AgFeO2 catalytic material with electron transfer membrane support was prepared for synergistic catalysis of low-energy LED light (12 W) excitation and peroxydisulfate (PDS) activation. The anti-aging photocatalytic membrane completely degraded 10 ppm of BPA within 30 min, and did not show significant aging after the long-term synergistic catalytic process. In addition, actual river water was employed to assess the aging process and catalytic efficiency in a practical environment. A 60.79 cm2 photocatalytic membrane completely purified 10 L of BPA polluted river water, while the total organic carbon content decreased by 50 %. This was mainly due to the synergistic catalytic effect of the membrane, which boosted photoelectron transfer through electron transfer shortcuts, thereby enhancing persulfate activation. Overall, the multifunctional membrane provides an effective strategy for achieving a long-lasting catalytic effect and controlling photocatalyst aging in practice.

Sustainable Approaches used in Pesticides contaminated Agricultural Waste Water Remediation

With the growing population of our global community and thereby increasing the demand for food has led the farmers to use more and more pesticides. Pesticides are chemical compounds used to kill pests. It is commonly used to control various agricultural pests that destroy crops and ultimately affect our agricultural productivity. Although the use of pesticides is a beneficial approach, but unfortunately it also has some drawbacks in terms of harming the environment and human health. Some pesticides pose significant hazards that ultimately affect human health systems. Contamination of agricultural land and agricultural wastewater by pesticides is a serious environmental problem and has a negative impact on biodiversity. Most synthetic pesticides are not readily biodegradable, they accumulate in the environment and cause soil contamination. To overcome the environmental burden of pesticide-contaminated sites, various sustainable approaches can be effectively used to detoxify contaminants or transform them into harmless secondary compounds. The current review focuses on the role of microorganisms and lignocellulosic biomass and plants in the degradation of agricultural pesticides under sustainable approaches.

Immobilization of silver-loaded graphene oxide (Ag-GO) on canvas fabric support for catalytic conversion of 4 nitrophenol.

Due to the rising human population and industrialization, harmful chemical compounds such as 4-nitrophenol (4-NP) and various dyes are increasingly released into the environment, resulting in water pollution. It is essential to convert these harmful chemicals into harmless compounds to mitigate this pollution. This research focuses on synthesizing a novel heterogeneous catalyst using modified canvas fabric (CF) decorated with silver metal nanoparticles on graphene oxide nanosheets (Ag-GO/CF). The process involves coating the fabrics (CF) with graphene oxide (GO) nanosheets through sonication. Subsequently, silver nanoparticles are deposited in situ and reduced on the GO surface, resulting in the formation of the Ag-GO/CF composite. Various physicochemical characterizations were conducted to examine the interfacial interactions between CF, GO, and Ag nanoparticles. The catalytic activity of the nanocomposite was assessed by hydrogenating 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) in the presence of sodium borohydride (NaBH4). The results showed that the 10%Ag-5%GO/CF with a surface of 6 cm2 (3 × 2 cm) exhibited the highest catalytic activity, achieving a reduction efficiency of over 96% in 5 min. The 4-NP reduction reaction rate was well-fitted with a pseudo-first-order kinetics model with an apparent reaction rate constant (Kapp) of 0.676min-1. Furthermore, the Ag-GO/CF composite demonstrated remarkable stability over successive cycles, with no noticeable decrease in its catalytic activity, suggesting its promising application for long-term chemical catalytic processes. This synthesized composite can be easily added to and removed from the reaction solution while maintaining high catalytic performance in the reduction of 4-NP, and it could be beneficial in avoiding problems related to powder separation.

Multiple Stabilization Effects of Benzylhydrazine on Scalable Perovskite Precursor Inks for Improved Perovskite Solar Cell Production

AbstractPerovskite precursor inks suffer various forms of degradation, such as iodide anion oxidation and organic cation breakdown, hindering reliable perovskite solar cell manufacturing. Here we report that benzylhydrazine hydrochloride (BHC) not only retards the buildup of iodine as previously reported but also prevents the breakdown of organic cations. Through investigating BHC and iodine chemical reactions, we elucidate protonation and dehydration mechanisms, converting BHC to harmless volatile compounds, thus preserving perovskite film crystallization and solar cell performance. This inhibition effect lasts nearly a month with minimal BHC, contrasting control inks without BHC where organic cations fully react in less than a week. This enhanced understanding, from additive stabilization to end products, promises improved perovskite solar cell production reliability.

Multiple Stabilization Effects of Benzylhydrazine on Scalable Perovskite Precursor Inks for Improved Perovskite Solar Cell Production.

Perovskite precursor inks suffer various forms of degradation, such as iodide anion oxidation and organic cation breakdown, hindering reliable perovskite solar cell manufacturing. Here we report that benzylhydrazine hydrochloride (BHC) not only retards the buildup of iodine as previously reported but also prevents the breakdown of organic cations. Through investigating BHC and iodine chemical reactions, we elucidate protonation and dehydration mechanisms, converting BHC to harmless volatile compounds, thus preserving perovskite film crystallization and solar cell performance. This inhibition effect lasts nearly a month with minimal BHC, contrasting control inks without BHC where organic cations fully react in less than a week. This enhanced understanding, from additive stabilization to end products, promises improved perovskite solar cell production reliability.

Enhanced photocatalytic reduction of p-nitrophenol by polyvinylpyrrolidone-modified MOF/porous MgO composite heterostructures

Catalysts derived from Metal-Organic Frameworks (MOF) present a compelling blend of cost-effectiveness and superior performance in reduction reactions. In this study, polymer-decorated MOF-Cobalt (MOF-Co) was deposited onto porous magnesium oxide (MgO) layers, acquired through surface modification of AZ31 Mg alloy via plasma-assisted oxidation, with the aim of fabricating novel catalysts for reduction reactions. Herein, this synthesis involved the utilization of Cobalt-benzene dicarboxylic acid (Co-BDC), where cobalt ions served as metal nodes and 1,4-benzene dicarboxylic acid (H2BDC) functioned as an organic linker, with and without the presence of polyvinylpyrrolidone (PVP) as an active site enhancer. The morphology of the prepared catalysts was affected by several factors such as pH, hydrothermal treatment duration, PVP content, and the presence of a MgO layer. The optimal catalyst, designated as metal-organic frameworks-cobalt at 80 °C temperature and 1 h of hydrothermal treatment at pH 4 (MOF-Co 1.4), was synthesized on the MgO layer using a solution containing 1.7 g of PVP, H2BDC, and Co(NO₃)₂.6H₂O. The paper-like morphology of the MOF-Co 1.4 catalyst facilitated exceptional performance, efficiently degrading p-nitrophenol (p-NP) under visible light irradiation with an impressive 99.74 % efficiency within just 5 min of exposure, while also demonstrating stability over five successive cycles. ·O2− species was found to drive the reduction reaction to p-aminophenol, with harmless compounds as byproducts, while GC-MS analysis identified intermediates in the reduction of p-NP. Density functional theory (DFT) calculations suggested that H2BDC and PVP jointly provided multi-active sites, enabling effective contact with reactants and rapid electron transfer, thus playing a synergistic role in the catalytic reduction process. This study pioneers a novel method for designing efficient bulk catalysts, achieving high efficiency and stability in pollutant degradation with fast, low-energy fabrication.

Kajian Penggunaan Bakteri Bacillus subtilis dalam Penanganan Tumpahan Minyak Mentah

The global demand for energy is driving increased exploration, production and processing of crude oil, increasing the risk of oil spills during these processes and contaminating marine habitats and biota. As hazardous and toxic substances, oil spills require effective and comprehensive management. Bioremediation uses the metabolism of microbes to break down hydrocarbons and convert contaminants into harmless compounds. One species of hydrocarbon-degrading bacteria suitable for bioremediation is Bacillus subtilis. Its adaptability to changes in temperature, salinity, and oxygen levels, as well as its resistance to environmental stress, make it an ideal choice for bioremediation as a sustainable and efficient solution to oil pollution in marine ecosystems. This study aims to explore the potential use of Bacillus subtilis as an alternative for managing crude oil spills, particularly in Indonesian waters.

Boosting the photocatalytic activity of bismuth vanadate (BiVO4) via optimization of the internal polarization

Photocatalytic performance can be improved by optimizing the morphology and surface texture of the photocatalyst or forming different p-n and/or n-n heterojunctions. Although the heterojunction system enhances photocatalytic property; however, an internal spontaneous polarization electric field may be much more effective due to the separation of electron-hole pairs when the polarization field forces them to move in different directions. The present study demonstrated this insight where the BiVO4 synthesis condition and polarization field forces were controlled via homogeneous precipitation in the presence of polyvinylpyrrolidone (PVP). The as-synthesized BiVO4 photocatalysts' structure and morphology were investigated using XRD, SEM, Raman, DRS, and PL. The result revealed that the increase of PVP concentration reformed the shaping to the truncated bipyramid-like shape and creates a spontaneous internal polarization that enhanced BiVO4 photocatalytic performance. The photocatalytic activity of BiVO4 was evaluated by monitoring the photocurrent enhancement using chronoamperometry, electrochemical impedance spectra and the photodegrading of methylene blue (MB) aqueous solution to harmless compounds in the presence of light. The spontaneous polarization between the different facets of BiVO4 crystal enhances the e−/h+ separation during internal facets homojunction and leads to four times photocurrent enhancement and the MB photocatalytic degradation rate increased from 0.43 to 1.92 min−1.

Anti-Leishmanial Effects of a Novel Biocompatible Non-Invasive Nanofibers Containing Royal Jelly and Propolis against Iranian Strain of Leishmania major (MRHO/IR/75/ER): an In-Vitro Study.

Current medications especially the pentavalent antimonial compounds have been used as the first line treatment of cutaneous leishmaniasis (CL), but they have limitations due to serious side effects such as drug resistance, cardio and nephrotoxicity, and high costs. Hence, the demand to find more usable drugs is evident. Synthesis and development of natural, effective, biocompatible, and harmless compounds against Leishmania major is the principal priority of this study. By electrospinning method, a new type of nanofiber were synthesized from royal jelly and propolis with different ratios. Nanofibers were characterized by Scanning Electron Microscope (SEM), Transmission Electron Microscopy (TEM), Thermogravimetric Analysis (TGA), Contact angle, and Fourier-transform infrared spectroscopy (FTIR). The Half-maximal inhibitory concentration (IC50), Half-maximal effective concentration (EC50) and the 50% cytotoxic concentration (CC50) for different concentrations of nanofibers were determined using quantitative calorimetric methods. Inductively coupled plasma-optical emission spectrometry (ICP-OES) and flow cytometry were performed as complementary tests. The results showed that the proposed formulas provide a new achievement that, despite the significant killing activity on L. major, has negligible cytotoxicity on the host cells. Royal jelly nanofibers have significantly shown the best 72 hours results (IC50= 35 μg/ml and EC50=16.4 μg/ml) and the least cytotoxicity. This study presents a great challenge to introduce a new low-cost treatment method for CL, accelerate wound healing, and reduce scarring with minimal side effects and biocompatible materials. Royal jelly and propolis nanofibers significantly inhibit the growth of L. major in-vitro.

Isotherm and Kinetic Studies on Adsorption of Yellow Azo Dyes (Sunset Yellow, Tartrazine) using &lt;i&gt;Kigelia africana&lt;/i&gt; (Lam.) Benth., Leaf Extract Mediated Iron Nanoparticles

Sunset yellow and tartrazine are commonly used azo dyes extensively employed in beverages and food products such as soda, fruit juices, confectionery, and cakes. These dyes hold the distinction of being the second and third most frequently utilized colour additives in a wide array of beverage products. The discharge of these synthetic food dyes into industrial wastewater can lead to significant environmental and health issues. Due to its aromatic structure, this dye is resistant to breaking down into harmless compounds, and its removal through effective adsorption presents an economical and efficient solution. The use of renewable bioresources for the eco-friendly production of metallic nanoparticles represents a recent and growing trend in nanotechnology research, offering enhanced environmental safety. In this current research, we achieved the green and cost-effective synthesis of monodispersed Iron Nanoparticles (FeNPs) with exceptional stability by utilizing an aqueous extract of Kigelia africana (Lam.) Benth is the primary bioresource for this synthesis. The FeNPs were noticed to be uniformly distributed spherical-shaped particles having smooth surfaces with a 26-34 nm size range and an average particle size of 28 ± 0.86 nm. The XRD results confirm that the FeNPs were rhombohedral phase structures with 71.43% of elemental iron. These synthesized nanoparticles were applied for the removal of sunset yellow and tartrazine dyes were investigated and more than 90% were removed. The adsorption isotherm study was best fitted with the Langmuir model, and the maximal adsorption capacity was found to be 76.29 and 47.22 mg/g for sunset yellow and tartrazine respectively. The adsorption reaction follows pseudo-first-order kinetics with a high correlation coefficient. Repeated cycles of regeneration, reuse and stability showed very high removal efficiency and stability. In conclusion, the biosynthesis of metal nanoparticles demonstrates substantial promise for applications in environmental protection.

Study on The Ability of H2O2 and The Effective Concentration of CuSO4 in Degrading Cyanide

PT. Aneka Tambang conducts gold processing using NaCN reagents, then from the gold processing process produces waste containing cyanide which can cause damage to the environment. One method used to reduce cyanide concentrations is the Degussa method. The Degussa method is a method to degrade free cyanide in waste by using H2O2 and Cu2+ ions as a catalyst source so that it becomes a harmless cyanide compound (cyanate ion). The purpose of the study was to determine the ability of hydrogen peroxide and determine the effective concentration of copper sulfate in degrading cyanide in the Degussa process and determine the level of stability of hydrogen peroxide oxidizers in the open air. Sample testing was carried out by varying the H2O2 retrieval time, variations in H2O2 dilution factor and copper sulfate concentration variations, then the sample was stirred with a jartes stirrer for 15 minutes. Cyanide is determined by spectrophotometer, the absorbance obtained is fed into the linear regression equation so that the final free cyanide concentration is obtained. From the experiment, it can be concluded that the concentration of cyanide degradation is effectively obtained when hydrogen peroxide and copper sulfate that have been mixed in the mixing tank are right out of use.

Isolation and Morphological Characterization of Bacteria Degrading on Soil Contaminated by Wasted Cooking Oil

Oil is used as an important component in human life as an energy source. The fried oil gives a delicious taste for consumption. However, the remaining cooking oil that has been cooked is discarded in the surrounding environment which is the cause of soil contamination by the oil. Thus, bioremediation is carried out to degrade contaminants with the ability of microorganisms or macroorganisms to become harmless compounds. The purpose of this research was to isolate and characterize the morphology of bacteria hydrocarbon-degrading from the environment or soil that had used cooking oil spills. The research method used was purposive sampling and descriptive qualitative. Purposive sampling is by determining where the sample to be taken has soil contaminated with used cooking oil and qualitative description is by describing the morphological characterization of the bacterial degrading isolates from the sample. The results of the research obtained that two bacterial isolates had a round shape, optically opaque, and flat edges. BCO-1 isolate has a brown color with a flat elevation and BCO-2 is white with a convex elevation. The bacteria degrading in BCO-1 isolates had a significant ability to degrade used cooking oil that was contaminated in the soil compared to BCO-2 isolates based on changes in the level of oil fluid.

Facile preparation of dual functions zeolite‐carbon composite for zinc ion removal from aqueous solutions

AbstractThe cost‐effective dual functions zeolite‐carbon composite (DFZCC) was prepared using an eco‐friendly substrate prepared from bio‐waste and an organic adhesive at intermediate conditions. The green synthesis method used in this study ensures that chemically harmless compounds are used to obtain a homogeneous distribution of zeolite over porous carbon. The greenly prepared dual‐function composite was extensively characterized using Fourier transform infrared, X‐ray diffraction, thermogravimetric analysis, N2 adsorption/desorption isotherms, field emission scanning electron microscope, dispersive analysis by X‐ray, and point of zero charges. DFZCC had a surface area of 248.84 m2/g and a pore volume of 0.141 cm3/g. DFZCC was used in the sorption process of Zn2+ ions from aqueous solutions, and it achieved higher removal (98%) at normal pH of 6.4 and temperature of 40°C. The Langmuir model was the best model for representing equilibrium data with a maximum sorption capacity of 6.711 mg/g. The kinetic studies showed that the pseudo‐second‐order model was the most appropriate model for representing experimental data. The intra‐particle diffusion kinetics demonstrated that the boundary film is the rate‐determining step in the sorption process. The sorption process of Zn2+ ions by DFZCC was spontaneous and endothermic. Moreover, solidification of the spent DFZCC by kaolin successfully reduced the leaching ions to the solution after 12 weeks from exposure to a salty solution.

Effect of Rhodopseudomonas palustris as a Bioremediation on Reducing Ammonia and Nitrite Levels of Catfish Nursery Pond Water in District Kebakkramat Regency Karanganyar

Catfish nursery pond water generally contains ammonia and nitrites. Ammonia and nitrite in this fish farming system start with uneaten catfish feed residue, feces, and metabolic products that enter the waters. Utilization of catfish feed which contains high protein can absorbed by fish as much as 20-30% of nutrients. The rest will be excreted in the form of feces. Feces and food scraps that settle in this water contain ammonia and nitrites, which affect the quality of the water. Efforts to maintain water quality are by reducing and disposing of pond water in the river. This is categorized as water pollution. Efforts to control this water pollution are the technique of bioremediation. The aim of bioremediation techniques is to restore the ecological balance in waters by utilizing microorganisms so that a process of degradation of harmful and complex compounds occurs into harmless compounds. The microorganisms used in this study were bacteria Rhodopseudomonas palustris which can to oxidize and decompose organic matter effectively reducing water quality. This research was conducted to examine the effect of bacterial efficiency Rhodopseudomonas palustris as a bioremediator for catfish pond water waste based on reducing levels of ammonia and nitrite. Testing the ammonia and nitrite levels using a spectrophotometric method with different wavelengths. Observations in this test were carried out for three days under anaerobic conditions and light at a temperature of 33°C. Observations showed that bacteria Rhodopseudomonas palustris had an effect on reducing nitrite levels 12.65% greater than the control. While the addition of bacteria to the observation of ammonia levels did not have a decreasing effect as indicated by the value F &lt;F crit.

Encapsulation of Allergens into Core–Shell Chitosan Microparticles for Allergen-Specific Subcutaneous Immunotherapy

IgE-mediated allergic reaction occurs in response to harmless environmental compounds, such as tree and grass pollen, fragments of household microorganisms, etc. To date, the only way to treat IgE-mediated allergy is allergen-specific immunotherapy (ASIT), which consists of a prolonged subcutaneous administration of allergen extracts or recombinant proteins. The long duration of the treatment, the cost and the risk of life-threatening adverse reactions are the main limiting factors for ASIT. The aim of this work was to develop allergen proteins encapsulated in chitosan-based microparticles that can be safely administered at high doses and in a rash protocol. The egg white allergen, Gal d 1 protein, was used as a model antigen. The protein was packed into core–shell type microparticles (MPs), in which the core was formed with succinyl chitosan conjugated to Gal d 1, subsequently coated with a shell formed by quaternized chitosan. The obtained core–shell MPs containing Gal d 1 in the core (Gal-MPs) were non-toxic to macrophage and fibroblast cell lines. At the same time, Gal-MPs were quickly engulfed by bone marrow-derived dendritic cells or RAW264.7 macrophage cells, as was visualized using flow cytometry and confocal microscopy. Encapsulated Gal d 1 was not recognized by Gal d 1-specific IgE in ELISA. Female BALB/c mice were immunized with Gal-MPs subcutaneously three times a week for 2 weeks. Immunization of mice resulted in IgG titers 1250 ± 200 without IgE production. Allergy in control and vaccinated mice was induced by low-dose Gal d 1 injections in the withers of mice. IgE was induced in control-sensitized but not in the vaccinated mice. Thus, preventive vaccination with the encapsulated allergens is safe and rapid; it significantly reduces the risk of IgE production induced by respiratory and oral allergens.

Green synthesis of porous carbon cross-linked Y zeolite nanocrystals material and its performance for adsorptive removal of a methyl violet dye from water

The cost-effective carbon cross-linked Y zeolite nanocrystals composite (NYC) was prepared using an eco-friendly substrate prepared from bio-waste and organic adhesive at intermediate conditions. The green synthesis method dependent in this study assures using chemically harmless compounds to ensure homogeneous distribution of zeolite over porous carbon. The greenly prepared cross-linked composite was extensively characterized using Fourier transform infrared, nitrogen adsorption/desorption, Field emission scanning electron microscope, Dispersive analysis by X-ray, Thermogravimetric analysis, and X-ray diffraction. NYC had a surface area of 176.44 m2/g, and a pore volume of 0.0573 cm3/g. NYC had a multi-function nature, sustained at a long-exposure time during the adsorption process of methyl violet dye (MV) from aqueous solutions and achieved higher removal at normal temperature and pH. The Halsey and the Langmuir models were the most appropriate models for representing the equilibrium data with a maximum adsorption capacity of 108.7 mg/g. The kinetic studies showed that the pseudo-second-order kinetics model and Elovich model were the most suitable models to describe the experimental data which indicated the MV adsorption by NYC has a chemical nature. Also, the interpretation of data by the Boyd model demonstrated that the adsorption process of MV was determined by both film diffusion and intra-particle diffusion. The adsorption process of MV by NYC is spontaneous, feasible, and exothermic. The regeneration performance showed that the NYC can be easily regenerated and reused with keeping an acceptable performance until the fourth cycle. Eventually, this study confirmed that the greenly prepared composite can serve as an adorable adsorbent for the removal of cationic dyes such as methyl violet under mild conditions.

An Updated Overview of the Role of CYP450 during Xenobiotic Metabolization in Regulating the Acute Myeloid Leukemia Microenvironment.

Oxidative stress is associated with several acute and chronic disorders, including hematological malignancies such as acute myeloid leukemia, the most prevalent acute leukemia in adults. Xenobiotics are usually harmless compounds that may be detrimental, such as pharmaceuticals, environmental pollutants, cosmetics, and even food additives. The storage of xenobiotics can serve as a defense mechanism or a means of bioaccumulation, leading to adverse effects. During the absorption, metabolism, and cellular excretion of xenobiotics, three steps may be distinguished: (i) inflow by transporter enzymes, (ii) phases I and II, and (iii) phase III. Phase I enzymes, such as those in the cytochrome P450 superfamily, catalyze the conversion of xenobiotics into more polar compounds, contributing to an elevated acute myeloid leukemia risk. Furthermore, genetic polymorphism influences the variability and susceptibility of related myeloid neoplasms, infant leukemias associated with mixed-lineage leukemia (MLL) gene rearrangements, and a subset of de novo acute myeloid leukemia. Recent research has shown a sustained interest in determining the regulators of cytochrome P450, family 2, subfamily E, member 1 (CYP2E1) expression and activity as an emerging field that requires further investigation in acute myeloid leukemia evolution. Therefore, this review suggests that CYP2E1 and its mutations can be a therapeutic or diagnostic target in acute myeloid leukemia.

Recent advances in Fenton-like treatment of radioactive ion exchange resins

Ion exchange resins (IERs) are widely used to remove radioactive contaminants from various commercial nuclear power plant systems. After the completion of their useful life cycle, IERs are removed from the nuclear facility and are known as spent resins. In the past few decades, the development of Fenton/Fenton-like treatments for the management of spent resins has received considerable attention because of their potential to completely break down the IER structure into harmless compounds (e.g., carbon dioxide, water, and inorganic salts). In addition, after Fenton-like treatments, the resulting solutions containing radionuclides can be easily immobilized to stable waste. In this review, we critically discuss the key developments in Fenton/Fenton-like dissolution, degradation, and mineralization of spent resins. We describe the important reaction parameters (initial pH, resin dosage, catalyst type and dosage, hydrogen peroxide dosage, flow rates of the catalyst and oxidant, reaction temperature, treatment time, and other specific parameters) for various Fenton/Fenton-like treatments of spent resins. Moreover, this review focuses heavily on the major reaction intermediates generated in Fenton-like treatments. In the final section of this review (conclusions and perspectives), we discuss the major challenges and suggest future research directions need to be addressed to improve the efficiency of Fenton-like treatments of spent resins.

Implementation of a green chemistry practice for the teaching of spectrophotometry

In the laboratory of Instrumental Analysis the topics of quantification of analytes by colorimetry are addressed, this practice was initially performed using potassium dichromate as a chemical reagent that is toxic and causes damage to the environment. Based on the objective of the practice (to facilitate the teaching of colorimetry) and to reduce the negative impact on the environment and the health of students, an alternative practice was designed that uses a red plant dye to replace the potassium dichromate; the dye is a low-cost and relatively harmless compound for both health and the environment. The practice was carried out with ten student volunteers, who worked individually, from the powder dye prepared a solution and then a series of dilutions to determine the concentration of a test sample. The experience could be carried out individually in work teams and the concentration of a problem sample provided could be determined. The implemented practice is a green alternative for teaching colorimetry in university students.