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The morphological structure is of particular importance to the energy storage properties of metal organic framework (MOF) electrode materials. Herein, a series of Co/Cu bimetallic MOFs were achieved by the facile hydrothermal method of cobalt nitrate and copper nitrate with phthalic acid (PA), terephthalic acid (TPA) and isophthalic acid (IPA). Co/Cu–IPA MOF, prepared by the reaction between cobalt nitrate, copper nitrate and IPA ligand, exhibits a loose lamellar structure while Co/Cu–PA MOF and Co/Cu–TPA MOF display a thin-strip structure. Co/Cu–IPA MOF displays a high specific area of 375.8 m2 g−1 compared with Co/Cu–PA MOF (44.09 m2 g−1) and Co/Cu–TPA MOF (9.64 m2 g−1). Besides, Co/Cu–IPA MOF possesses more Cu+ content. Therefore, Co/Cu–IPA MOF shows a high specific capacitance of 369.1 F g−1 at 1 A g−1. A Co/Cu–IPA MOF//AC asymmetric device was constructed successfully. This device shows an energy density of 6.81 W h kg−1 at a power density of 500 W kg−1. [ABSTRACT FROM AUTHOR]

The preparation of amorphous solid dispersions (ASDs) represents a promising strategy for addressing the solubility limitations of poorly soluble drugs, facilitating enhanced oral absorption. Acidic polymers such as cellulose acetate phthalate (CAP) and hydroxypropyl methylcellulose phthalate (HPMCP) have emerged as effective carriers for ASDs. Although the hydrolytic degradation of these polymers has been documented, its impact on the stability of ASDs has not been systematically investigated. This research aimed to explore the potential hydrolysis of CAP and HPMCP and how it influences the stability of ASDs containing ketoconazole (KTZ), at drug loadings of 10 % and 50 %. Our study utilized thermal analysis, infrared spectroscopy, and evaluations of physical and chemical stability. The results revealed that although KTZ remained physically stable in all ASDs over 60 days under various stability conditions, the emergence of crystalline phthalic acid (PA), a byproduct of polymer hydrolysis, was observed at elevated temperatures and relative humidity levels. The acidic microenvironment fostered by the release of PA further catalyzed drug chemical degradation. This study underscores the susceptibility of CAP and HPMCP to hydrolytic degradation, highlighting the inherent risk of PA-induced drug degradation, particularly for acid-labile compounds. These insights into the understanding of polymer hydrolysis in ASDs pave the way for the development of targeted approaches to safeguard drug stability and optimize pharmaceutical formulations for enhanced bioavailability, efficacy, and safety. [Display omitted] [ABSTRACT FROM AUTHOR]

In this study, a potent nitroreductase enzyme was successfully identified and engineered, which was then employed in an efficient and environmentally friendly chemo-bio nitroreduction process to synthesize 3-amino phthalic acid from 3-nitro phthalic acid. The wild-type nitroreductase from Azorhizobium caulinodans ORS 571 (Ac NTR) demonstrated robust catalytic activity. Through error-prone PCR mutagenesis, a mutant variant (Q40R/K267R) was generated, which exhibited a 3.1-fold increase in catalytic efficiency. Molecular docking analysis revealed that the mutations at positions R40 and R267 altered the electrostatic properties of the enzyme's surface, modifying the conformation of the active pocket entrance and thereby enhancing catalytic performance. Additionally, when the mutant Q40R/K267R was combined with divanadium pentaoxide (V 2 O 5), the accumulation of 3-hydroxyamino phthalic acid during the biotransformation process was effectively prevented. Under optimized reaction conditions, a 90.0 % conversion rate was achieved, transforming 100 g/L of 3-nitro phthalic acid into 3-amino phthalic acid in just 12 h. These findings highlight the significant potential of biocatalytic processes for large-scale synthesis applications. [Display omitted] • A nitroreductase from Azorhizobium caulinodans ORS 571 was selected after screening. • Mutant Q40R/K267R with 3.1-fold of activity was identified using epPCR mutagenesis. • Structural modeling and molecular docking unveil structural properties of Q40R/K267R. • Q40R/K267R-V 2 O 5 reduces 100 g/L 3-nitro phthalic acid to 3-amino phthalic acid. [ABSTRACT FROM AUTHOR]

The dicyandiamide/phthalic acid (DCDA/PA) precursor with molecular assembly strategy was prepared by hydrothermal treatment the mixture of dicyandiamine and phthalic acid, in which some of the amines were bound by phthalic acid through hydrogen bonding interactions, and the carbon nitride (CN) photocatalyst was further prepared by thermal polymerization. The results showed that the new chemical structure formed by the interaction of melamine cyanurate and phthalic acid through hydrogen bonding could hinder the intermolecular collision chances during the calcination process of DCDA/PA precursor, which made the polymerization reaction difficult to be carried out, and the CN photocatalysts with irregular layered stacking structure were formed. In addition, the presence of more amino groups in the CN-0.3 structure can effectively improve the separation efficiency of its photogenerated charge carriers, and after simulated visible light irradiation for 60 min, the photocatalytic activity presented by CN-0.3 for MB was 2.72 times higher than that of pristine g-C3N4. [ABSTRACT FROM AUTHOR]

Phthalates are the emerging environmental toxicants derived from phthalic acid and its constituents, which are moderately present in plastics and many personal care products. Phthalate exposure occurs through various environmental factors, including air, water, and soil, with absorption facilitated via ingestion, inhalation, and dermal contact. Upon exposure, phthalates become bioavailable within the biological systems and undergo biotransformation and detoxification processes in the liver. The physicochemical properties of phthalates indicate their lipophilicity, environmental persistence, and bioaccumulation potential, influencing their absorption, distribution, and hepatic biotransformation. The prolonged exposure to phthalates adversely influences the biological redox system by altering the levels of the enzymatic and non-enzymatic antioxidants, molecular signaling pathways, and causing hepatic pathogenesis. The strategies to combat phthalate-induced toxicity include avoiding exposure to these compounds and using plant-based bioactive molecules such as polyphenols, which possess therapeutic potential as antioxidants, suppress inflammatory cascades, prevent oxidative damage, and stabilize cellular integrity. This review presents a comprehensive and updated account of the chemical, biochemical, immunological, and toxicological properties of phthalates, along with novel plant-based therapeutic strategies to mitigate the phthalate-induced adverse effects on living systems. [ABSTRACT FROM AUTHOR]

Introducing organic ligands into metal-organic frameworks (MOFs) is an effective method for preparing defective MOFs. This approach enables the fabrication of cost-effective, efficient, highly conductive, and richly active-site electrocatalysts. Herein, the defective NiMOF is synthesized via a straightforward one-pot solvothermal method by partially substituting phthalic acid (PTA) ligands with acetic acid (HOAc), which effectively regulates the micro-morphology and electronic structure of the NiMOF nanoflowers, thus creating abundant electrochemical active sites, significantly improving electronic conductivity and promoting rapid charge transfer. The resulting DE-NiMOF-0.5 nanoflowers, prepared with HOAc substitution, demonstrate excellent electrochemical performance at a current density of 10 mA cm−2, the hydrogen evolution reaction (HER) overpotential is 188 mV (Tafel slope of 175 mV dec−1), while the oxygen evolution reaction (OER) overpotential is 205 mV (Tafel slope of 37 mV dec−1). The introduction of acetic acid ligands in DE-NiMOF-0.5 not only constructs the ligand defects within the catalyst, but also increases the abundant active sites, enhancing the hydrophilicity of the catalyst and facilitating electronic transfer between the catalyst surface and the electrolyte. This study explores a strategy for preparing defective MOF catalysts through introducing modulators, providing an economically viable material pathway for electrocatalysis and opening new possibilities for designing and synthesizing efficient electrocatalysts in future research endeavors. This study introduces DE-NiMOF-0.5, a defect-rich nickel-based metal-organic framework modified with acetic acid, enhancing its electrocatalytic performance. DE-NiMOF-0.5 achieves low overpotentials of 188 mV for the hydrogen evolution reaction (HER) and 205 mV for the oxygen evolution reaction (OER) at a current density of 10 mA cm⁻2. It also demonstrates significant electrochemical stability and sustained performance during long-term cycling, making it suitable for prolonged use in alkaline water electrolysis systems. This research highlights the potential of defect engineering in MOFs for achieving cost-effective and superior hydrogen production. [Display omitted] • Ligand defects can be produced by introducing acetic acid ligand. • DE-NiMOF shows overpotentials of 188 mV (HER) and 205 mV (OER) at 10 mA cm⁻2. • The catalyst showed remarkable electrochemical stability and sustained performance. [ABSTRACT FROM AUTHOR]

Clematis ispahanica Boiss. is a rare species belonging to the Ranunculaceae family. Clematis ispahanica is highly valued for its ornamental and medicinal properties. The specific traditional uses of Clematis ispahanica in traditional medicine may include curing neurological disorders, syphilis, malaria, rheumatism, gout, diarrhea, and asthma. In this study, leaves of C. ispahanica were collected from collected from Boanat, Kerman Province, Iran. Essential oil isolated from the leaves of C. ispahanica was evaluated for its chemical composition for the first time. GC/MS analyzed the essential oil obtained by hydrodistillation. The chemical analysis of the oil from Clematis ispahanica Boiss. revealed the identification of 50 compounds, accounting for 92.5% of the total oil composition. In the leaves oil, the main components detected were phthalic acid, heptacosane, pentadecanoic acid, methyl ester, and apinene with amounts of 51.1 %, 5.8 %, 3.9 %, and 2.9 %, respectively. The analysis of various extracts from Clematis ispahanica Boiss. revealed a significant difference among all of them in Antioxidant activity (AA), Total phenol content (TPC) and Total flavonoid content (TFC) (p≤0.01, p≤0.05). For the antioxidant activity, the results obtained showed that the highest radical scavenging activity was observed in the extract of hexane with IC50 122 μg/ml, and the lowest activity was found in acetone extraction with IC50 170 μg/ml. The highest TPC value was 15.0 mg GAE/g DW in the extract of hexane. The highest TFC belongs to the extract of hexane and methanol with 7.3 mg QE/g and 7.2 mg QE/g. The analysis between TPC (r= 0.708, p≤0.01) and TFC (r= 0.786, p≤0.01) of C. ispahanica and its antioxidant properties were found to have a strong correlation. C. ispahanica exhibits a relatively high level of antioxidant potency and contains a significant amount of total phenolic compounds when extracted with a hexane solvent. [ABSTRACT FROM AUTHOR]

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Flubendiamide, a phthalic acid diamide insecticide, has been implicated in potential teratogenic effects on non‐target organisms, especially during embryonic development. This study examines the impact of flubendiamide on eye development in chick embryos, a well‐established model for vertebrate development. Exposure to 0.5 µg/µL of flubendiamide significantly impaired early ocular morphogenesis, resulting in severe defects such as underdeveloped optic cups and the absence of lens and corneal structures. Histopathological analysis demonstrated disrupted optic cup differentiation, while in silico docking studies revealed strong interactions between flubendiamide and key oculogenic proteins, including OTX2, PAX6, and SOX2. These interactions were associated with altered expression patterns of these critical regulators, alongside overexpression of SHH and downregulation of BMP4, BMP7, and FGF8, which are essential for optic vesicle formation and lens differentiation. Additionally, increased CASPASE‐3 expression indicated enhanced apoptosis, contributing to the observed ocular anomalies. These findings suggest that flubendiamide disrupts key signaling pathways necessary for proper eye development, potentially leading to congenital eye defects. The study highlights the need for a thorough evaluation of the molecular mechanisms driving flubendiamide‐induced teratogenicity to ensure safer pesticide use and protect environmental and human health. [ABSTRACT FROM AUTHOR]

Clematis ispahanica Boiss. is a rare species belonging to the Ranunculaceae family. Clematis ispahanica is highly valued for its ornamental and medicinal properties. The specific traditional uses of Clematis ispahanica in traditional medicine may include curing neurological disorders, syphilis, malaria, rheumatism, gout, diarrhea, and asthma. In this study, leaves of C. ispahanica were collected from collected from Boanat, Kerman Province, Iran. Essential oil isolated from the leaves of C. ispahanica was evaluated for its chemical composition for the first time. GC/MS analyzed the essential oil obtained by hydrodistillation. The chemical analysis of the oil from Clematis ispahanica Boiss. revealed the identification of 50 compounds, accounting for 92.5% of the total oil composition. In the leaves oil, the main components detected were phthalic acid, heptacosane, pentadecanoic acid, methyl ester, and a-pinene with amounts of 51.1 %, 5.8 %, 3.9 %, and 2.9 %, respectively. The analysis of various extracts from Clematis ispahanica Boiss. revealed a significant difference among all of them in Antioxidant activity (AA), Total phenol content (TPC) and Total flavonoid content (TFC) (p≤0.01, p≤0.05). For the antioxidant activity, the results obtained showed that the highest radical scavenging activity was observed in the extract of hexane with IC50 122 μg/ml, and the lowest activity was found in acetone extraction with IC50 170 μg/ml. The highest TPC value was 15.0 mg GAE/g DW in the extract of hexane. The highest TFC belongs to the extract of hexane and methanol with 7.3 mg QE/g and 7.2 mg QE/g. The analysis between TPC (r= 0.708, p≤0.01) and TFC (r= 0.786, p≤0.01) of C. ispahanica and its antioxidant properties were found to have a strong correlation. C. ispahanica exhibits a relatively high level of antioxidant potency and contains a significant amount of total phenolic compounds when extracted with a hexane solvent.

The presented work presents the results of a study on the effect of small amounts of phthalic acid additives on dendrite formation in low-density polyethene (LDPE). Based on the results obtained, it is shown that the dendrite resistance of LDPE, as expected, increases with the introduction of 0.05 wt% phthalic acid. The established increase in dendrite resistance of LDPE with the introduction of phthalic acid can primarily be explained based on a decrease in inhomogeneities in the form of air pores as a result of accelerated structure formation and the emergence of a more homogeneous supramolecular structure. It was revealed that an increase in dendrite resistance correlates with an improvement in the dielectric characteristics of the composition. The influence of mechanical load on the development of dendrites in polymer dielectrics has been studied. As a result of studying the growth of dendrites in LDPE samples and its optimal composition subjected to unilateral stretching, it was found that under the influence of mechanical tensile stresses, the shape of the surface delimiting tree-like shoots changes, this surface is flattened in the direction of stretching. It has been shown that the rate of dendrite growth increases as mechanical tensile forces increase.

The treatment of cancer represents one of the most significant challenges currently facing modern medicine. The search for new drugs that are effective in the treatment of patients is an ongoing endeavor. It is frequently the case that the molecular target of anticancer drugs is a DNA molecule. The therapeutic effect of a drug is achieved by influencing the structure of a macromolecule or by inhibiting its function. Among the synthetic substances with potential anticancer effects, particular attention should be paid to phthalic acid imide derivatives. Three phthalimide derivatives are employed in the treatment of multiple myeloma: thalidomide, pomalidomide, and lenalidomide. Nevertheless, the search for new derivatives with a diverse range of biological activities is ongoing. In light of the above, the subject of our investigation is four non-toxic phthalic acid imide derivatives. The objective was to analyze the interaction of these compounds with DNA. The use of spectroscopic and in silico methods has enabled us to demonstrate that all of the tested analogs can act as ligands for deoxyribonucleic acid, forming non-covalent bonds with it. All four compounds tested interact with the ctDNA molecule, binding in its minor groove. The most stable complex is formed here between deoxyribonucleic acid and the C derivative, in which the -CF3 group is attached to the benzene ring. What is interesting and important, the described mechanism of action is analogous to that observed between ctDNA and thalidomide, pomalidomide, and lenalidomide. [ABSTRACT FROM AUTHOR]

In this research, the Pistia stratiotes leaf (PSL) extract was evaluated as a green corrosion inhibitor for the corrosion of mild steel in 1 M HCl using electrochemical measurements and surface characterization. Electrochemical impedance spectroscopy (EIS) spectra showed that the inhibitory activity of the phytochemical compounds enhanced with increasing concentration up to 400 ppm, which was reflected in the increase in the charge transfer resistance and double-layer capacitance. Regarding the effect of immersion time, EIS results indicated that the persistence of the PSL extract was between 4 h and 8 h of exposure time. From polarization curve (PCC) results, the best performance of the corrosion inhibitor was achieved at 400 ppm with an inhibition efficiency of 93.7%. The PSL extract acted as a mixed-type corrosion inhibitor. The adsorption of the phytomolecules on the metal surface obeyed the Langmuir isotherm through a mixed mechanism (physical and chemical interactions) dominated by physisorption. Scanning electron microscopy (SEM) examinations and energy-dispersive X-ray spectroscopy (EDS) elemental analysis of the corroded samples confirmed the anticorrosive protection of the PSL extract. Chemical characterization of the PSL extract by GC-MS revealed the presence of phytol, steroids, and aromatic and long-chain unsaturated fatty acid esters, in order of abundance. Chemical quantum calculations by DFT allowed for determining that the phthalic acid, di(2-propylpentyl) ester compound has the most significant potential to act as the main active component in corrosion inhibition activity. [ABSTRACT FROM AUTHOR]

The resistance of pests to common insecticides is a global issue that threatens food production worldwide. Diamide insecticides target insect ryanodine receptors (RyRs), causing uncontrolled calcium release from the sarcoplasmic and endoplasmic reticulum. Despite their high potency and species selectivity, several resistance mutations have emerged. Using a chimeric RyR (chiRyR) approach and cryo-electron microscopy (cryo-EM), we investigate how insect RyRs engage two different diamide insecticides from separate families: flubendiamide, a phthalic acid derivative, and tetraniliprole, an anthranilic compound. Both compounds target the same site in the transmembrane region of the RyR, albeit with different poses, and promote channel opening through coupling with the pore-forming domain. To explore the resistance mechanisms, we also solve two cryo-EM structures of chiRyR carrying the two most common resistance mutations, I4790M and G4946E, both alone and in complex with the diamide insecticide chlorantraniliprole. The resistance mutations perturb the local structure, directly reducing the binding affinity and altering the binding pose. Our findings elucidate the mode of action of different diamide insecticides, reveal the molecular mechanism of resistance mutations, and provide important clues for the development of novel pesticides that can bypass the resistance mutations. Pesticide resistance poses a serious threat to global food security. In this study, the authors show the mode of action of various diamide insecticides and elucidate the molecular mechanisms underlying resistance mutations. [ABSTRACT FROM AUTHOR]

This study assessed the impacts of wheat straw as a cosubstrate on coal biocoverion into methane and the associated mechanism within methane metabolic pathways. Co-digestion of coal with varying wheat straw concentrations resulted in a remarkable (1246.05%) increase in methane yield compared to that of the control (CK). Moreover, microbial analysis revealed a uniform distribution of Methanosarcinaceae (51.14%) and Methanobacteriaceae (39.90%) in the co-digestion of coal and wheat straw (CWS1) at a ratio of 3:1 (w/w) compared to other treatments such as coal and wheat straw (CWS2) at a ratio of 3:0.5. In addition, Hungatieclostridiaceae and Rhodobacteriaceae were abundant in both co-digesters, whereas the bacterial communities in the CK group were significantly different and more abundant than those in the Peptostreptococcaceae and Enterobacteriaceae groups. The key enzymes related to methanogenic metabolic pathways, including EC: 1.2.99.5 and EC: 2.1.1.86 (facilitating the conversion of CO2 into methane), and EC:1.12.98.1 exhibited significant abundance within CWS1. Aromatic compounds such as 4-(2-chloroanilino)-4-oxobutanoic acid and phthalic acid were substantially more abundant in CWS1 and CWS2 than in CK, indicating the increased bioavailability of coal to microbial activities. This novel approach demonstrates that wheat straw co-digestion with coal during anaerobic digestion modulates microbial communities and their metabolic pathways to enhance methane production from complex substrates such as coal. [ABSTRACT FROM AUTHOR]

The most valuable prokaryotes, both biotechnologically and monetarily, are actinomycetes. S. variabilis H2 demonstrated a broad spectrum of antagonistic effects against all tested Gram-negative and Gram-positive bacteria, exhibiting inhibition zones of 18mm against Escherichia coli, 16mm against Bacillus subtilis, 16mm against Staphylococcus aureus, 14mm against Pseudomonas aeruginosa, 14mm against Enterococcus faecalis, and 12mm against Klebsiella pneumoniae. Using Plackett-Burman design and one variable at a time approach and testing against the six different bacterial pathogens, one sought a maximal synthesis of the bioactive chemical. The highest antagonistic activity of S. variabilis H2 metabolites was observed against E. coli, where productivity increased by up to 1.3-fold when the strain was grown in an optimized medium composed of: starch (30g/ L), KNO3 (1.5g/ L), K2HPO4 (0.75g/ L), MgSO4·7H2O (0.25g/ L), FeSO4 (0.015g/ L), NaCl (5.0g/ L), and an inoculum size of 2mL (10³ colony-forming units/mL) for 7 days at 37°C and pH 8. Moreover, the anticancer activity of S. variabilis H2 crude extract was tested against three different cell lines: Lung carcinoma cells, Hepatocellular carcinoma cells and breast carcinoma cells. The inhibition activities were 61.57 and 44.51% for lung and Hepatocellular cells, respectively. In addition, the S. variabilis H2 crude extract acted as antifungal and anti-biofouling agent, but it failed to act as antiviral agent. The primary components of the crude extract of S. variabilis H2 were identified using gas-liquid chromatography-mass spectrometry (GC-MS). The identified compounds included phthalic acid, di(2-propylpentyl) ester, octadecanoic acid methyl ester, and hexadecenoic acid methyl ester. [ABSTRACT FROM AUTHOR]

The composition and concentration of a low-molecular organic additive, leading to a significant improvement in the electrical properties of low-density polyethylene of high pressure grade 10,803-020, were experimentally determined. Phthalic anhydride and phthalic acid were used as modifying organic additives. The content of additives in the polyethylene of high pressure composition varied in the range of 0.01–0.1 wt%. It has been shown that the content of 0.05 wt% phthalic anhydride and phthalic acid in the composition polyethylene of high pressure (PEHP + 0.05 wt% PhAn + 0.05 wt% PhAc) is the optimal composition, since the electrical strength of the film has increased significantly. The dependences of the dielectric loss tangent and specific volumetric electrical resistance on temperature, as well as the kinetics of physicochemical changes in them under the influence of electrical discharges in air and UV irradiation, have been studied. It was established that the dielectric characteristics of the polymer composition PEHP + 0.05 wt% PhAn (storage life 40 years) changed slightly. [ABSTRACT FROM AUTHOR]

Living organisms produce reactive oxygen species (ROS) during the oxygen processing. ROS damage biomolecules and causes oxidative stress. Antioxidants prevent cellular damage against these harmful effects of ROS by neutralizing free radicals. Medicinal plants provide a rich source of antioxidants to reduce oxidative stress and play an important role in the treatment of diseases. Bioactive compounds, especially polyphenols and flavonoids, protect cells against oxidative damage by neutralizing free radicals. Bryophytes, especially mosses, are one of the plant groups that attract attention in this area. Mosses show biologically active properties with secondary metabolites such as terpenes and flavonoids they contain. In this study, extraction of Homalothecium philippeanum moss with ethanol, methanol, and nhexane solvents was carried out and the biochemical content analysis of the extracts was investigated. 1,2- Benzenedicarboxylic acid, bis(2-methylpropyl) ester was detected as the major component in the ethanol and methanol extracts of the H. philippeanum. Biologically active alkanes such as Tetradecane and Hexadecane were found in the nhexane extract. The antioxidant activity of moss ethanol extract was investigated using the DPPH method and the EC50 value was determined as 7.084 mg/ml. [ABSTRACT FROM AUTHOR]

Single crystals of (benzene-1,2-dicarboxylic acid-κO)(2-carboxybenzoato-κO) caesium(I), also known as caesium trihydrodiphthalate (CsADP), were successfully synthesized through a controlled hydrothermal reaction between caesium sulfate and phthalic acid in a 1:2 molar ratio. The resulting crystals, grown over 26–28 days, were analyzed using various techniques. FT-IR spectroscopy revealed characteristic vibrational bands, while powder XRD and single-crystal XRD confirmed phase purity and structural properties. CsADP crystallizes in the orthorhombic system with a centrosymmetric space group (Pbcn). The caesium ion is coordinated by ten oxygen atoms, with Cs···O bond lengths ranging from 3.085 to 3.610 Å, forming a distorted bicapped square antiprism geometry. Thermal analysis indicated stability up to 240 °C, while UV–Vis spectroscopy demonstrated transparency, with a bandgap of 4.17 eV. Nonlinear optical (NLO) properties were investigated using Z-scan techniques, revealing reverse saturation absorption and a strong third-order susceptibility, highlighting CsADP as a promising candidate for NLO applications. Hirshfeld surface analysis identified dominant O···H/H···O interactions, contributing to its NLO behaviour. Additionally, molecular electrostatic potential and Mulliken population analysis provided insights into the charge distribution within the structure. [ABSTRACT FROM AUTHOR]

A hard anodic oxide coating's characteristic porous structure allows for its modification by the incorporation of nanoparticles. However, achieving an appropriate microstructure requires an optimal pore arrangement and shape, which is influenced by the electrolyte composition, current densities, temperature, and processing time. To achieve pores with a diameter of about 50 nm and the most regular structure, a range of these parameters were tested. Using a two-stage manufacturing process had a beneficial effect on increasing the microporosity of the coating. The addition of phthalic acid at 0 °C did not increase the pore diameter, but allowed for the process to be carried out at higher temperatures. However, the coating produced at 20 °C had a larger pore diameter, but numerous defects. The coating obtained from the three-component solution had the most regular structure, but the smallest pore diameter. [ABSTRACT FROM AUTHOR]

Arthospira platensis and Spirulina platensis microalgae are a rich source of pro-health metabolites (% d.m.): proteins (50.0–71.3/46.0–63.0), carbohydrates (16.0–20.0/12.0–17.0), fats (0.9–14.2/6.4–14.3), polyphenolic compounds and phenols (7.3–33.2/7.8–44.5 and 4.2/0.3 mg GAE/g), and flavonoids (1.9/0.2 QUE/g) used in pharmaceutical and cosmetic formulations. This review summarises the research on the chemical profile, therapeutic effects in dermatological problems, application of Arthrospira and Spirulina microalgae, and contraindications to their use. The pro-health properties of these microalgae were analysed based on the relevant literature from 2019 to 2024. The antiviral mechanism of microalgal activity involves the inhibition of viral replication and enhancement of immunity. The anti-acne activity is attributed to alkaloids, alkanes, phenols, alkenes, phycocyanins, phthalates, tannins, carboxylic and phthalic acids, saponins, and steroids. The antibacterial activity generally depends on the components and structure of the bacterial cell wall. Their healing effect results from the inhibition of inflammatory and apoptotic processes, reduction of pro-inflammatory cytokines, stimulation of angiogenesis, and proliferation of fibroblasts and keratinocytes. The photoprotective action is regulated by amino acids, phlorotannins, carotenoids, mycosporins, and polyphenols inhibiting the production of tyrosinase, pro-inflammatory cytokines, and free oxygen radicals in fibroblasts and the stimulation of collagen production. Microalgae are promising molecular ingredients in innovative formulations of parapharmaceuticals and cosmetics used in the prophylaxis and therapy of dermatological problems. This review shows the application of spirulina-based commercial skin-care products as well as the safety and contraindications of spirulina use. Furthermore, the main directions for future studies of the pro-health suitability of microalgae exerting multidirectional effects on human skin are presented. [ABSTRACT FROM AUTHOR]

In the present study, attention has been paid to the development of economically feasible strategies for enhanced remediation of anthracene and its conversion into biofuels. The strategies developed (B1, B2, B3, and B4) include bagasse and lipid-producing strain Rhodotorula mucilagenosa IIPL32 synthesizing surface active metabolites. The results indicate the highest production of surface-active metabolites in strategies B2, B3, and B4 along with a maximum biodegradation rate. GC–MS analysis affirmed the conversion of anthracene into phthalic acid in all the strategies. Biofuel quality of the lipid produced by the strain showed higher cetane number and improved cold flow property indicating the efficiency of the developed strategies for the production of commercial grade biodiesel. Furthermore, the phytotoxicity study of the spent wash revealed that 50% and 75% diluted spent wash were non-toxic and can be employed for ferti-irrigation. Thus, the study signifies the development of an economically feasible process that can be commercially employed in biofuel industries. [ABSTRACT FROM AUTHOR]

Increasing chemical pollution is a threat to sustainable water resources worldwide. Plastics and harmful additives released from plastics add to this burden and might pose a risk to aquatic organisms, and human health. Phthalates, which are common plasticizers and endocrine-disrupting chemicals, are released from polyvinyl chloride (PVC) microplastics and are a cause of concern. Therefore, the leaching kinetics of additives, including the influence of environmental weathering, are key to assessing exposure concentrations but remain largely unknown. We show that photoaging strongly enhances the leaching rates of di(2-ethylhexyl) phthalate (DEHP) by a factor of 1.5, and newly-formed harmful transformation products, such as mono(2-ethylhexyl) phthalate (MEHP), phthalic acid, and phthalic anhydride from PVC microplastics into the aquatic environment. Leaching half-lives of DEHP reduced from 449 years for pristine PVC to 121 years for photoaged PVC. Aqueous boundary layer diffusion (ABLD) is the limiting mass transfer process for the release of DEHP from pristine and photoaged PVC microplastics. The leaching of transformation products is limited by intraparticle diffusion (IPD). The calculated mass transfer rates can be used to predict exposure concentrations of harmful additives in the aquatic environment. The environmental weathering of plastics and the leaching kinetics of additives are key to assessing exposure concentrations. Here, the authors show that photoaging enhances the leaching rate of the common additive di(2-ethylhexyl) phthalate (DEHP) by a factor of 1.5, and newly-formed harmful transformation products, such as mono(2-ethylhexyl) phthalate (MEHP), phthalic acid, and phthalic anhydride, are released from PVC microplastics into the aquatic environment. [ABSTRACT FROM AUTHOR]

Background/Objectives: Endocrine disruptors are ubiquitous agents in the environment and are present in everyday consumer products. These agents can interfere with the endocrine system, and subsequently the reproductive system, especially in pregnancy. An increasing number of studies have been conducted to discover and describe the health effects of these agents on humans, including pregnant women, their fetuses, and the placenta. This review discusses prenatal exposure to various endocrine disruptors, focusing on bisphenols, phthalates, organophosphates, and perfluoroalkyl substances, and their effects on pregnancy and fetal development. Methods: We reviewed the literature via the PubMed and EBSCO databases and included the most relevant studies. Results: Our findings revealed that several negative health outcomes were linked to endocrine disruptors. However, despite the seriousness of this topic and the abundance of research on these agents, it remains challenging to draw strong conclusions about their effects from the available studies. This does not allow for strong, universal guidelines and might result in poor patient counseling and heterogeneous approaches to regulating endocrine disruptors. Conclusions: The seriousness of this matter calls for urgent efforts, and more studies are needed in this realm, to protect pregnant patients, and ultimately, in the long term, society. [ABSTRACT FROM AUTHOR]

STUDY QUESTION What is the longitudinal association between gestational phthalate exposure and in vivo placental outcomes? SUMMARY ANSWER Phthalates were adversely associated with placental microvasculature, stiffness, and presence of calcification, with different metabolites associated with different outcomes. WHAT IS KNOWN ALREADY Phthalate exposure is ubiquitous and implicated as a contributor to adverse pregnancy outcomes, possibly through impacts on the placenta. STUDY DESIGN, SIZE, DURATION A total of 303 women were recruited in early pregnancy and prospectively followed for up to eight visits across gestation in the Human Placenta and Phthalates study. PARTICIPANTS/MATERIALS, SETTING, METHODS At each visit, women provided urine samples and underwent placental ultrasounds. Urine was analyzed for 18 metabolites of phthalates and replacements. We took the geometric mean of repeated measurements to reflect pregnancy-averaged phthalate or replacement exposure for each participant (n = 303). Placental microvasculature, stiffness, and microcalcification presence were quantified from ultrasounds at each visit. Higher scores reflected worse placental function for all measures. Generalized linear mixed models were created to estimate the association between pregnancy-averaged exposure biomarker concentrations and repeated outcome measurements for microvasculature and stiffness. Gestational age at the time of calcification detection was modeled using Cox proportional hazards models. MAIN RESULTS AND THE ROLE OF CHANCE Monocarboxyisononyl phthalate and summed di(2-ethylhexyl) phthalate metabolites were associated with impaired microvasculature development, such that an interquartile range increase in concentration was associated with 0.11 standard deviation increase in the microvasculature ratio, indicating poorer vascularization (95% CI: 0.00, 0.22); 0.11 [95% CI: −0.01, 0.22], respectively. Monoethyl phthalate was associated with increased placental stiffness (0.09 [95% CI: −0.01, 0.19]) while summed di-iso-butyl phthalate metabolites and monobenzyl phthalate were associated with increased hazard of calcification detection (hazard ratios: 1.18 [95% CI: 0.98, 1.42]; 1.13 [95% CI: 0.96, 1.34]). LIMITATIONS, REASONS FOR CAUTION Outcomes used in this study are novel and further investigation is needed to provide clinical context and relevance. WIDER IMPLICATIONS OF THE FINDINGS We found evidence of associations between select phthalate biomarkers and various aspects of in vivo placental health, although we did not observe consistency across placental outcomes. These findings could illustrate heterogeneous effects of phthalate exposure on placental function. STUDY FUNDING/COMPETING INTEREST(S) This research was supported in part by the Intramural Research Program of the NIH, National Institute of Environmental Health Sciences (ZIA ES103344), and NIEHS T32ES007018. The authors declare that they have no competing interests to disclose. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention. Use of trade names is for identification only and does not imply endorsement by the CDC, the Public Health Service, or the US Department of Health and Human Services. TRIAL REGISTRATION NUMBER N/A. [ABSTRACT FROM AUTHOR]

In this study, the appropriate polymer solutions were prepared to create chitosan/PVA blends. By altering the ratio of the ingredients, several chitosan/PVA mixtures were produced, as follows: 12% chitosan and 88% PVA, 40% chitosan and 60% PVA, and 15% chitosan and 85% PVA. To generate physically crosslinked hydrogels for the drug delivery of atenolol, several acid cross-linkers, such as fumaric acid and phthalic acid, were applied to the chitosan/PVA blends. The formulations included 15% chitosan and 85% PVA with 0.02% (0.0024, 0.0041, 0.02) mol of fumaric acid, as well as 15% chitosan and 85% PVA with 0.002, 0.003, and 0.0064 mol of phthalic acid. Using an ultraviolet-visible spectrophotometer, the chemical structures of the modified and unmodified chitosan (Chitosan/PVA) hydrogels were examined. Results regarding the formation of ionic cross-links between the protonated hydroxyl groups of the chitosan and the anionic functional groups of the cross-linking agent were established. The swelling ratio was determined for each hydrogel structure as a function of time in three distinct fluids with pH values of 2, 4, and 7.5, and at three distinct temperatures of 42°C and 44°C. The samples with the greatest swelling ratios were identified as PVA.PA0.002 (chitosan) and PVA.FA0.0024. [ABSTRACT FROM AUTHOR]

Abstract A new DES (MTPPBr-PHTH-DES) was prepared from a mixture of methyltriphenyl-phosphonium bromide (MTPPBr) and phthalic acid (PHTH). The eutectic point phase diagram showed that a one-to-one molar ratio of MTPPBr to PHTH is the optimal molar ratio for the synthesis of new DES. Then, it was characterized with various techniques such as FT-IR, TGA/DTA, densitometer, eutectic point, and NMR and used as a novel acid catalyst in the synthesis of pyrimido[4,5-d]pyrimidines and pyrano[3,2-c]chromes in solvent-free condition. Short reaction time, low temperature, high efficiency, green condition, and easy recycling and separation of the DES catalyst are among the most important features of the presented method.

Polyethylene is a plastic pollutant impacting marine life, calling for advanced remediation methods such as biodegradation. However, there is actually limited information on polyethylene-degrading bacteria in the marine environment. Here, we studied bacterial degradation of polyethylene and associated phthalates additives using scanning electron microscopy, Fourier transform infrared, gel permeation chromatography and genomic and transcriptomic techniques. Results show that a deep-sea bacteria, Acinetobacter venetianus F1, can degrade 12.2% of polyethylene after 56 days, following the alkane metabolic pathway. Phthalates were also degraded via the metabolic pathways of benzoic acid and phthalic acid. This is first report of polyethylene-degrading bacteria from deep-sea environments. [ABSTRACT FROM AUTHOR]

This work presents the studies of a very strong hydrogen bond (VSHB) in biologically active phthalic acids. Research on VSHB comes topical due to its participation in many biological processes. The studies cover the modelling of intermolecular interactions and phthalic acids with 2,4,6-collidine and N,N-dimethyl-4-pyridinamine complexes with aim to obtain a VSHB. The four synthesized complexes were studied by experimental X-ray, IR, and Raman methods, as well as theoretical Car–Parrinello Molecular Dynamics (CP-MD) and Density Functional Theory (DFT) simulations. By variation of the steric repulsion and basicity of the complex' components, a very short intramolecular hydrogen bond was achieved. The potential energy curves calculated by the DFT method were characterized by a low barrier (0.7 and 0.9 kcal/mol) on proton transfer in the OHN intermolecular hydrogen bond for 3-nitrophthalic acid with either 2,4,6-collidine or N,N-dimethyl-4-pyridinamine cocrystals. Moreover, the CP-MD simulations exposed very strong bridging proton dynamics in the intermolecular hydrogen bonds. The accomplished crystallographic and spectroscopic studies indicate that the OHO intramolecular hydrogen bond in 4-nitrophthalic cocrystals is VSHB. The influence of a strong steric effect on the geometry of the studied cocrystals and the stretching vibration bands of the carboxyl and carboxylate groups was elaborated. [ABSTRACT FROM AUTHOR]

The document is a contents list for the journal Chemical Communications. It provides a list of articles and their authors that are featured in the journal's latest issue. The articles cover a range of topics in the field of chemistry, including electrocatalytic water-to-oxygen conversion, catalyst development for oxidative dehydrogenation, and photomechanical properties in metal-organic crystals. The journal aims to connect the global chemistry community and invest its profits back into the field. [Extracted from the article]

An assembly between 1,4-dicarboxylbenzene-2,3-dithiol (H2dcbdt) and different transition metal ions successfully produced 2D metal–organic frameworks (M-dcbdt, M = Ni, Co or Fe) composed of unprecedented butterfly-shaped metal-bis(dithiolene) (MS4) linkers in one-pot fashion. Such strategy provides easier access to the [MS4]-rich network and lowers the prerequisite to explore their applications. [ABSTRACT FROM AUTHOR]

Lanthanide metal–organic frameworks (Ln-MOFs) have unique advantages in sensing due to their excellent optical properties. In this study, we synthesized a dicarboxylic acid ligand with amide groups and successfully synthesized a novel two-dimensional (2D) MOF with the molecular formula C42H31EuN4O10 (Eu-MOF) by a solvothermal method. Single-crystal X-ray diffraction showed that amide groups are exposed on the outside of the two-dimensional coordination layer, with the possibility of recognizing specific molecules through hydrogen bonding interactions. The ligand's "antenna effect" enables Eu-MOF to emit a strong luminescence characterized by the "f–f" transition. Further studies have revealed that Eu-MOF could be used as a bifunctional fluorescent probe for the selective detection of benzaldehyde and Fe3+. The sensing mechanism has been analyzed in detail through powder X-ray diffraction (PXRD) analysis, UV-vis spectroscopy, fluorescence lifetime measurement, and density functional (DFT) theory calculation. This design and research can provide a reference for subsequent related work. [ABSTRACT FROM AUTHOR]

Lanthanide metal–organic frameworks (Ln-MOFs) have unique advantages in sensing due to their excellent optical properties. In this study, we synthesized a dicarboxylic acid ligand with amide groups and successfully synthesized a novel two-dimensional (2D) MOF with the molecular formula C42H31EuN4O10 (Eu-MOF) by a solvothermal method. Single-crystal X-ray diffraction showed that amide groups are exposed on the outside of the two-dimensional coordination layer, with the possibility of recognizing specific molecules through hydrogen bonding interactions. The ligand's "antenna effect" enables Eu-MOF to emit a strong luminescence characterized by the "f–f" transition. Further studies have revealed that Eu-MOF could be used as a bifunctional fluorescent probe for the selective detection of benzaldehyde and Fe3+. The sensing mechanism has been analyzed in detail through powder X-ray diffraction (PXRD) analysis, UV-vis spectroscopy, fluorescence lifetime measurement, and density functional (DFT) theory calculation. This design and research can provide a reference for subsequent related work. [ABSTRACT FROM AUTHOR]

Two new heteroleptic cobalt(III)dialkyldithiophosphate complex cations with a 1,2-bis(diphenylphosphino)ethane (dppe) ancillary ligand having formula [Co{S2P(OR)2}2(dppe)](B(C6H5)4) (R = –C2H5 (Co–Et); –CH(CH3)2 (Co–Pr)) have been synthesized and characterized spectroscopically as well as via single crystal X-ray diffraction analysis. The single crystal X-ray diffraction analyses reveal that the immediate geometries around Co(III) in both complexes are distorted octahedral, which are satisfied by four sulfur atoms of two dialkyldithiophosphate ligands and two phosphorus centers of the dppe ligand. These complex cations are neutralized by tetraphenyl borate B(C6H5)4 anions. The solid-state framework of both complexes are stabilized by C–H⋯π and C–H⋯C interactions. The nature of these interactions have been addressed with the help of Hirshfeld surface analysis, and percent contributions of pertinent interactions in the crystal structure of these complexes have been addressed using fingerprint plots. Both complexes have been used as heterogeneous electrocatalysts for the oxygen evolution reaction (OER). Results suggest that Co–Et is a better electrocatalyst for the OER, displaying an onset potential of 1.68 V and Tafel slope of 114 mV dec−1. Furthermore, in the homogeneous electrocatalysis of the hydrogen evolution reaction (HER) using trifluoroacetic acid, the overpotential for Co–Et and Co–Pr have been 1.05 V and 0.92 V, respectively, with turnover frequencies of 1518 s−1 and 287.5 s−1, respectively. Overall, heterogeneous OER and homogenous HER results suggest that Co–Et can be used as an efficient molecular electrocatalyst for oxygen/hydrogen evolution reactions. [ABSTRACT FROM AUTHOR]

Heavy metal pollution and toxicity from water resources have remained a great concern for the entire population. This research demonstrates the capability of carbon quantum dots (CQDs) for fluorescence-based heavy metal detection in different water resources using a fibre-optic spectrometer device. Two different types of CQDs phthalic acid and triethylenediamine (PT CQDs) and Folic acid (FCQDs) were synthesized using microwave irradiation and hydrothermal method, respectively. CQDs were characterized using several techniques such as TEM, EDX, XPS and FTIR. PTCQD and FCQDs both were tested for sensing capability in water reservoirs like household and river water. The results indicate that both CQDs were able to detect all six heavy metal ions (Pb2+, Co2+, Mn3+, Hg2+, Ni2+, Cr3+) tested in the study in the range of 0–100 µM. It was found that FCQDs show a three-fold higher sensitivity and greater resolution than PTCQDs for all the heavy metals samples. The CQDs' sensing capability shows that they can achieve a limit of detection in the range of 0.15–3 µM along with 100% accuracy in terms of recovery with minimal error, these results indicate that both CQDs have a tremendous potential to be used as a sensor for the detection of heavy metals even in complex water matrices. FCQDs show more sensitivity for all metals compared to PTCQDs and used in future as a sensing tool for heavy metal detection with better sensitivity and accuracy with less response time. [ABSTRACT FROM AUTHOR]

Cystinuria is a genetic disorder, and in severe cases, it might lead to kidney failure. As an important biomarker for cystinuria, the level of arginine (Arg) in urine is a vital indicator for cystinuria screening. Therefore, it is urgently needed to detect Arg with high selectivity and sensitivity. In this work, a boric acid functionalized Zr-based metal–organic framework UiO-PhbA is prepared by grafting phenylboronic acid on UiO-66-NH2 through a Schiff base reaction using a covalent post-synthesis modification (CPSM) strategy. The prepared UiO-PhbA exhibits a sensitive and specific fluorescence "turn-on" response to Arg and can be exploited to detect Arg in human serum and urine samples with a broad linear range of 0.6–350 µM and low limit of detection (LOD) of 18.45 nM. This study provides a new and reliable rapid screening protocol for sulfite oxidase deficiency-related diseases. [ABSTRACT FROM AUTHOR]

The current study investigated the impact of Saccharomyces cerevisiae fermentation on apricot kernel oil extraction and the resulting quality characteristics of the oil. The seed kernels underwent physicochemical and antioxidant studies after being separated, gelatinized, and fermented. The results revealed 43.6 % of oil yield by fermentation. The extracted oil had a lower acid value (3.74 mg KOH/g), and peroxide value (4.25 meq/kg). The investigation of additional oil properties was included, like iodine value (100.26 mg KOH/g), saponification value (190.5 mg KOH/g), specific gravity (0.919), viscosity (4.62), moisture content (0.592 %), and refractive index (1.4836), which signifies optimum physicochemical parameters of oil. As per the FTIR data, some distinct functional groups like C-H stretch and C O, C C, CH3, OH, and R-O-R esters were found in the extracted oil. The oil's fatty acid composition, with 50.47 % saturated, 22.23 % mono-unsaturated, and 35.13 % polyunsaturated fatty acids, enhances stability, oxidative resistance, and nutritional value, justifying its favorable physicochemical properties. The DPPH radical scavenging activity of the oil showed to have good antioxidant activity. Metabolic modeling of S. cerevisiae provided information about compounds received after fermentation. Hence, it can be concluded that fermentation is a suitable approach to extract apricot seed kernel oil with beneficial properties. [Display omitted] • Apricot seed kernel is a good source of oil, we can use it for multiple purposes. • Saccharomyces cerevisiae -based fermentation, we can get 43.6 % of oil. • Different beneficial fatty acids were obtained from this oil: Caprylic, Lauric, Margaric, Paullinic, Phthalic acid, etc. [ABSTRACT FROM AUTHOR]

In the present study, we report the room temperature synthesis of a novel two-dimensional (2D) coordination polymer (CP) having the formula {[Cd(H-PCA)2(H2O)]·0.5(H2O)·0.5(CH3OH)}n (CP1), where H-PCA represents 4-pyrazolecarboxylate. The synthesis of CP1 was achieved through a one-pot reaction, involving the self-assembly of Cd(OAc)2·2H2O and the multitopic mixed N- and O-donor ligand, 4-pyrazolecarboxylic acid (H2-PCA), in methanol. This method demonstrated high yield and purity, enabling the facile production of multigram quantities of CP1 within a short timeframe. Notably, the synthetic procedure selectively deprotonates the carboxylic acid group while retaining the pyrazole moiety in its protonated form. CP1 has been thoroughly characterized using various analytical techniques, including single-crystal X-ray diffraction, FTIR spectroscopy, elemental analysis, scanning electron microscopy, thermogravimetric analysis, and powder X-ray diffraction. The structural analysis revealed that CP1 features a 3, 5-connected binodal net with the point symbol {4.5.6}{4.55.63.7}, leading to a unique -ths net topology. Through hydrogen bonding connections between adjacent 2D sheets, CP1 further extends into a three-dimensional (3D) supramolecular network due to the presence of coordinated water molecules and the protonated pyrazole group. Additionally, a 3D Hirshfeld Surface analysis accompanied by quantitative 2D fingerprint plots was also investigated to explore the intermolecular interactions. [ABSTRACT FROM AUTHOR]

The crystal structure of 2,3,5,6-tetraiodo-1,4-benzenedicarboxylic acid dihydrate is described and the following structural features are established by XRD: C8H6I4O6, M 705.73; monoclinic crystal system, P21/n space group; unit cell parameters: a = 5.78160(10) Å, b = 15.0976(2) Å, c = 17.3437(3) Å; α = 90°, β = 94.602(2)°, γ = 90°; V = 1509.02(4) Å3, Z = 4, ρcalc = 3.106 g/cm3. Some features of the thermolysis of terephthalic acid and its iodine derivatives are described. Diiodoterephthalic acid is the least thermally stable, tetraiodoterephthalic acid is the most stable. The iodinated terephthalic acids have similar heats of fusion. The largest amount of carbon residue is formed during the decomposition of 2,3,5,6-tetraiodo-1,4-benzenedicarboxylic acid. [ABSTRACT FROM AUTHOR]

A simple and rapid method using an energy dispersive X-ray fluorescence (EDXRF) spectrometer is developed for facilitating the analysis of aqueous as well as organic process stream solutions from a zirconium extraction facility for the quantification of zirconium oxide (ZrO2) and hafnium oxide (HfO2). Except for dilution, not much sample preparation is involved in the analysis and accordingly the experimental parameters are optimized. Calibrations are performed separately using a set of synthetic standard solutions of zirconium and hafnium prepared in nitric acid medium for aqueous samples and in TBP + kerosene medium for organic samples. Studies are carried out to examine the effect of free acidity, sample matrix, and sample volume on determination of Zr and Hf and optimization of these parameters has been carried out accordingly for regular analysis. Zirconium oxide (ZrO2) and hafnium oxide (HfO2) are calculated from the results for reporting purposes. The results from the EDXRF method are compared with those of a gravimetric (phthalic acid precipitation) method with respect to zirconium and ICP-AES method with respect to Hf. On comparison, the results are found to be in good agreement. Detection limits for the developed method are found to be 0.06 g L−1 for ZrO2 and 0.03 g L−1 for HfO2. The developed method is employed for the determination of ZrO2 up to 200 g L−1 and HfO2 up to 5 g L−1 in various process stream solutions from a zirconium extraction facility. A RSD of less than 3% has been achieved for ZrO2 and less than 5% has been achieved for HfO2 in this method. [ABSTRACT FROM AUTHOR]

The presented work presents the results of a study on the effect of small amounts of phthalic acid additives on dendrite formation in low-density polyethene (LDPE). Based on the results obtained, it is shown that the dendrite resistance of LDPE, as expected, increases with the introduction of 0.05 wt% phthalic acid. The established increase in dendrite resistance of LDPE with the introduction of phthalic acid can primarily be explained based on a decrease in inhomogeneities in the form of air pores as a result of accelerated structure formation and the emergence of a more homogeneous supramolecular structure. It was revealed that an increase in dendrite resistance correlates with an improvement in the dielectric characteristics of the composition. The influence of mechanical load on the development of dendrites in polymer dielectrics has been studied. As a result of studying the growth of dendrites in LDPE samples and its optimal composition subjected to unilateral stretching, it was found that under the influence of mechanical tensile stresses, the shape of the surface delimiting tree-like shoots changes, this surface is flattened in the direction of stretching. It has been shown that the rate of dendrite growth increases as mechanical tensile forces increase. [ABSTRACT FROM AUTHOR]

A new DES (MTPPBr-PHTH-DES) was prepared from a mixture of methyltriphenyl-phosphonium bromide (MTPPBr) and phthalic acid (PHTH). The eutectic point phase diagram showed that a one-to-one molar ratio of MTPPBr to PHTH is the optimal molar ratio for the synthesis of new DES. Then, it was characterized with various techniques such as FT-IR, TGA/DTA, densitometer, eutectic point, and NMR and used as a novel acid catalyst in the synthesis of pyrimido[4,5-d]pyrimidines and pyrano[3,2-c]chromes in solvent-free condition. Short reaction time, low temperature, high efficiency, green condition, and easy recycling and separation of the DES catalyst are among the most important features of the presented method. [ABSTRACT FROM AUTHOR]

Di-(2-ethylhexyl) phthalic acid (DEHP) pollutes the environment, and posing a significant risk to human and animal health. Consequently, a successful preventative strategy against DEHP-induced liver toxicity needs to be investigated. Morin hydrate (MH), a flavanol compound, possesses toxic preventive attributes against various environmental pollutants. However, the effects of MH have not been investigated against DEHP-induced liver toxicity. Female Swiss albino mice were divided into four groups: control, DEHP (orally administered with 500 mg/kg, DEHP plus MH 10 mg/kg, and DEHP plus MH 100 mg/kg for 14 days. The results showed that the MH treatment ameliorated the DEHP-induced liver dysfunctions by decreasing the alanine transaminase (ALT), aspartate aminotransferase (AST), total bilirubin, liver histoarchitecture, fibrosis, and markers of oxidative stress. Furthermore, DEHP increased apoptosis, increased active caspase 3 and decreased B cell lymphoma-2 (Bcl-2) expression. However, the MH treatment showed a differential effect on these proteins; a lower dose increased, and a higher dose decreased the expression. Thus, a lower dose of MH could be involved in the disposal of damaged hepatocytes. Expression of Estrogen receptors alpha (ERα) also showed a similar trend with active caspase 3. Furthermore, the expression of Tumor necrosis factor alpha (TNF-α) and Nuclear factor-κβ (NF-κβ) were up-regulated by DEHP treatment, and MH treatment down-regulated the expression of these two inflammatory markers. Since this down-regulation of TNF-α and NF-κβ coincides with improved liver functions against DEHP-induced toxicity, it can be concluded that MH-mediated liver function involves the singling of TNF-α and NF-κβ. [ABSTRACT FROM AUTHOR]

Phthalic acid esters (PAEs) are human made chemicals widely used as plasticizers to enhance the flexibility of plastic products. Due to the lack of chemical bonding between phthalates and plastics, these materials can easily enter the environment. Deleterious effects caused by this chemo-pollutant have drawn the attention of the scientific community to remediate them from different ecosystem. In this context, many bacterial strains have been reported across different habitats and Sphingobium yanoikuyae strain P4 is among the few psychrotolerant bacterial species reported to biodegrade simple and complex phthalates. In the present study, biodegradation of three structurally different PAEs viz., diethyl phthalate (DEP), di-isobutyl phthalate (DIBP), and butyl benzyl phthalate (BBP) have been investigated by the strain P4. Quantitative analyses through High-performance liquid chromatography (HPLC) revealed that the bacterium completely degraded 1 g/L of DEP, DIBP, and BBP supplemented individually in minimal media pH 7.0 within 72, 54, and 120 h of incubation, respectively, at 28 °C and under shake culture condition (180 rpm). In addition, the strain could grow in minimal media supplemented individually with up to 3 g/L of DEP and 10.0 g/L of DIBP and BBP at 28 °C and pH 7.0. The strain also could grow in metabolites resulting from biodegradation of DEP, DIBP, and BBP, viz. n-butanol, isobutanol, butyric acid, ethanol, benzyl alcohol, benzoic acid, phthalic acid, and protocatechuic acid. Furthermore, phthalic acid and protocatechuic acid were also detected as degradation pathway metabolites of DEP and DIBP by HPLC, which gave an initial idea about the biodegradation pathway(s) of these phthalates. [ABSTRACT FROM AUTHOR]

Dendrimers are potent nanocarriers in drug delivery systems because their structure can be precisely controlled. We previously reported that polyamidoamine (PAMAM) dendrimers that were modified with 1,2-cyclohexanedicarboxylic acid (CHex) and phenylalanine (Phe), PAMAM-CHex-Phe, exhibited an effective association with various immune cells, including T-cells. In this study, we synthesized various carboxy-terminal Phe-modified dendrimers with different linkers using phthalic acid and linear dicarboxylic acids to determine the association of these dendrimers with Jurkat cells, a T-cell model. PAMAM-n-hexyl-Phe demonstrated the highest association with Jurkat T-cells. In addition, dendri-graft polylysine (DGL) with CHex and Phe, DGL-CHex-Phe, was synthesized, and its association with Jurkat cells was investigated. The association of DGL-CHex-Phe with T-cells was higher than that of PAMAM-CHex-Phe. However, it was insoluble in water and thus it is unsuitable as a drug carrier. Model drugs, such as protoporphyrin IX and paclitaxel, were loaded onto these dendrimers, and the most model drug molecules could be loaded into PAMAM-CHex-Phe. PTX-loaded PAMAM-CHex-Phe exhibited cytotoxicity against Jurkat cells at a similar level to free PTX. These results suggest that PAMAM-CHex-Phe exhibited both efficient T-cell association and drug loading properties. [ABSTRACT FROM AUTHOR]