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During the past few decades, interest in phenolic substances in aquatic environments has increased due to their wide uses in numerous industries despite their high toxicity. This study aimed to investigate removing phenol from contaminated wastewater using synthesized nanoscale-activated carbon (AC) as a sorbent. The AC was synthesized from reed stalks as a local bio-based material using a chemical activation approach. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive X-ray (EDX) in addition to the Fourier transform-infrared spectroscopy (FTIR) were applied to characterize the synthesizedAC. The study tested four different factors using the experimental statistical design, data analysis with Design Expert Software, and a central composite design (CCD) using response surface methodology (RSM) to maximize phenol elimination. These factors involved initial phenol concentration (ranging from 30 to 120 ppm), pH levels (ranging from 2 to 11), concentration of adsorbent range from 50 to 600 ppm, and reaction time range from 30 to 120 minutes. These variables were used as input data for the prediction model to determine the removal efficiency (%) of phenol. The analysis of the ANOVA was conducted to examine the model performance. The analysis results suggested that the most effective model in explaining the process of phenol elimination was the second-order quadratic model, and the predicted data strongly matched the experimental values. The findings revealed that the optimal adsorption conditions obtained from the experimental work were initial phenol concentration of 30 mg·L-1 , adsorbent dose of 600 mg·L-1, pH equal to 2, reaction time of 120 minutes, and the capacity of the adsorption was 30.0825 mg·g-1. As a consequence, the nanoactivated carbon extracted from reed stalks effectively adsorbs phenol from wastewater. [ABSTRACT FROM AUTHOR]

The spectral‐luminescence properties and photochemical conversions of phenol were analyzed for an isolated molecule as well as in water solvents in a continuum implicit model and explicit atomistic surroundings. This involved employing cut‐edge hybrid quantum‐classical methodologies to generate static optical spectra and the excited dissipative crossing potential energy curves. A combination of electronic excitations, gradient calculations, and embedding electrostatic potential fitting charges on quantum‐classical molecular dynamic propagation trajectories provided statistically averaged absorption spectra. The mixed‐reference spin‐flip multiconfigurational linear response method based on reference triplet preprocessed in the time‐dependent density‐functional theory was utilized to determine conical intersections between the lowest excited and ground states, as well as two‐stage transitions from the second excitation to the ground state. Non‐adiabatic quantum‐classical molecular dynamics defined photodissipative trajectories of excited states, their lifetimes, and crossing points through trajectory surface hopping together with the mixed‐reference spin‐flip and embedding electrostatic potential fitting approaches. Dyson orbitals of the extended Koopmans' theorem were applied to reveal the nature of molecular states at conical intersections and key points on photodynamic trajectories. Potential hydroxyl group cleavage predicted with conical intersections searching turns to "swift" OH deprotonation through |π→σOH*$$ {\upsigma}_{\mathrm{OH}}^{\ast } $$⟩ transition along photodynamic propagations in contrast with "long" processes leading to benzene ring deformation with stable OH bond. [ABSTRACT FROM AUTHOR]

Substantial amounts of phenolic compounds are present in medium‐low temperature coal tar (MLCT), of which dimethylphenol (DMP) is not as valuable to be utilized as the more abundant cresol due to its complex composition and difficulty in isolation. In this study, the disproportionation and transalkylation reactions of MLCT‐related model compound, i.e., 2,6‐DMP, in phenol over zeolite catalysts are investigated using a fixed‐bed reactor for sustainable new option to utilize MLCT‐derived phenolic mixtures. Reactivity is promoted at high temperatures and associated with zeolite acidity and pore structure. Since disproportionation and transalkylation reactions have certain spatial requirements, the micropores of MFI‐type zeolite may cause spatial barriers that make it difficult to carry out the reactions. MCM‐22, characterized by MWW‐type zeolite, maximized the conversion of 2,6‐DMP due to its strong Bronsted acidity and large mesopore volume. FAU‐type zeolite HY with a 3D large 12‐ring through‐channel shows relatively small spatial confinement and certain molecular sieving ability, which enables bimolecular reactions while allowing cresols to flow out of the pores efficiently to obtain the highest cresol selectivity. The addition of phenol significantly inhibits the spontaneous disproportionation of 2,6‐DMP to tricresol. Besides, o‐cresol dominate the cresol products, suggesting that the selectivity of o‐cresol is kinetically controlled. [ABSTRACT FROM AUTHOR]

The Kingdom of Saudi Arabia (KSA) has millions of date palm trees for commercial scale date-fruit production. The respective industry also generates agricultural waste including date palm tree branches. This rich bio-resource can be used for several beneficial applications. The present study therefore investigated the application of granular activated carbon (GAC) produced using date palm tree branches to successfully remove phenol, p-cresol, and copper from synthetic wastewater. The respective adsorption equilibrium results fitted well to the Langmuir-type adsorption isotherm. Furthermore, the pH-dependent adsorption results both for phenol and p-cresol appeared to follow an anionic-type adsorption behavior (i.e., decreasing adsorption with an increase in aqueous phase equilibrium pH). However, the pH-dependent adsorption finding for copper showed a cationic-type adsorption behavior. These adsorption trends were explained employing the pH-dependent speciation of the respective pollutants. In general, findings from the present work indicate that a high-specific-surface-area (SSABET) GAC material from the date palm tree branches can be successfully employed for aqueous phase pollution control. [ABSTRACT FROM AUTHOR]

In this study, anthocyanin and phenolic compounds were extracted from pomegranate peel powder with supercritical CO2 and Lepidium perfoliatum seed gum and maltodextrin were used as the nanoencapsulation wall. The nanoencapsulation extract was dried with a freeze dryer. Color stability and antioxidant activity of nanoencapsulation extract were evaluated. The levels of anthocyanin and phenolic compounds were evaluated by differential pH and FolinCiocalteu method, respectively. Particle size, nanoencapsulation efficiency of anthocyanin, nanoencapsulation phenol, color stability at different temperatures and pH as well as antioxidant activity were evaluated by DPPH. The amount of anthocyanin and phenol extracted in this method was 3.943±0.133 mg/g of pomegranate peel powder and 504.521±2.537 mg/g of gallic acid per 100 g, respectively. Nanoencapsulation efficiency was higher for anthocyanin than phenols. The release of anthocyanin at different pHs was different, so that anthocyanin behaved differently at different pHs. Polymerization and color increased with increasing temperature. The antioxidant activity of the fine-grained extract by DPPH method increased with increasing concentration and its IC50 was equivalent to 1.092± 0.024 m /ml. [ABSTRACT FROM AUTHOR]

This paper aimed to enhance the particle properties of refuse-derived fuel by means of ultrasonic pretreatment and discussed the effect of pretreatment on the pyrolysis products. Firstly, the ultrasonic pretreatment improved the physical properties of refuse-derived fuel. Molding experiments demonstrated that the natural binder component of refuse-derived fuel extruded from the cells after ultrasonic pretreatment, forming a vitreous layer, mechanical interlocking bonds, and fixed bridges between the particles. The impact resistance index could be increased from 0 to 185.71 at most, the extending rate could be reduced by up to 18.38%, and the particle density could be increased by 4.40%. The results of pyrolysis tests showed that ultrasonic pretreatment promoted the formation of phenol with a maximum increase of 14.94%. Besides, the acoustic physical effect and microjets generated by ultrasonic formed multiple porous and multilayer structures on the surface of the pyrolysis char. Overall, ultrasonic pretreatment could improve the pellet characteristics of refuse-derived fuel without adding binders and convert its pyrolysis products into valuable chemicals. [ABSTRACT FROM AUTHOR]

Triclosan, like many other aromatic halides, plays an important role industrially and inevitably ends up in the environment. Chemical treatments have effectively mitigated the presence of such chemicals, through using harsh oxidizing treatments, which are not without issues. A milder and greener alternative, such as an electrochemical method, is needed for the mitigation of compounds, such as triclosan. Herein, we evaluated triclosan treatment via electrochemical cycling and compared it to a traditional chemical oxidative process. Cyclic voltammetry was carried out using a three-electrode cell containing glassy carbon, silver wire, and platinum wire in organic solvent. Electrochemical cycling revealed 6 × greater triclosan conversion compared to traditional chemical oxidation reaction, as monitored by UV–Vis spectroscopy. In terms of reaction product selectivity, the chemical and electrochemical reactions yielded the oxidized triclosan and an ether cleavage product, dichlorophenol, as determined by gas chromatography–mass spectrometry. Of note, the chemical oxidation yielded the chlorinated re-dimerization side product, which was not observed during electrochemical cycling, which is beneficial, as such products have to be degraded again. Overall, our findings indicate that electrochemical methods offer significant advantages over traditional organic methods, such as product selectivity, relative conversion, and greener operation. In addition, electrochemical approaches offer tunability, such as electrode material, electrolyte, solvent, potential, or current applied, all of which may be integrated into a more efficient environmental application. [ABSTRACT FROM AUTHOR]

The experimental results of the present study show that phenol had a certain inhibitory effect on its utilization by phenol-acclimatized activated sludge (PAAS), which was the inoculum for the microbial fuel cell (MFC) inoculation. In co-metabolic study, utilization of para-nitrophenol (PNP) at low concentrations (< 20 mg L−1) when used with phenol at a fixed concentration (250 mg L−1) favorably proceeded. The behavior was interpreted in terms of carbon catabolite repression (CCR), indicating phenol (250 mg L−1) positively affected consumption of PNP (< 20 mg L−1). The calculated values of degradation rate show the necessity of phenol presence in the system where phenol acted on the inoculum's ability to withstand the inhibitory effect of PNP. The MFC functionality in electricity generation is also definable by considering CCR applicability and the results show that the negative effect of PNP was repressed by the presence of phenol. For instance, 20 mg L−1 PNP + 250 mg L−1 phenol yielded the highest power density (66.2 mW m−2) and the lowest internal resistance (189 Ω). The PAAS performance was characterized to evaluate cells' capacity in utilizing inhibitory substrates, and several different models were used. The relevant kinetic parameters are described in terms of PAAS affinity toward the substrate (ks) and the microbe's sensitivity in responding to the toxic substrate (ki). Luong and Aiba equations were chosen to describe MFC behavior when the PAAS utilized phenol as the sole substrate. While Haldane model was more capable of addressing co-metabolic degradation of PNP. [ABSTRACT FROM AUTHOR]

Exploring effective transition metal single-atom catalysts for selective oxidation of benzene to phenol is still a great challenge due to the lack of a comprehensive mechanism and mechanism-driven approach. Here, robust 4N-coordinated transition metal single atom catalysts embedded within graphene (TM1-N4/C) are systematically screened by density functional theory and microkinetic modeling approach to assess their selectivity and activity in benzene oxidation reaction. Our findings indicate that the single metal atom triggers the dissociation of H2O2 to form an active oxygen species (O*). The lone-electronic pair character of O* activates the benzene C-H bond by constructing C-O bond with C atom of benzene, promoting the formation of phenol products. In addition, after benzene captures O* to form phenol, the positively charged bare single metal atom activates the phenol O-H bond by electron interaction with the O atom in the phenol, inducing the generation of benzoquinone by-products. The activation process of O-H bond is accompanied by H atom falling onto the carrier. On this basis, it can be inferred that adsorption energy of the C atom on the O* atom (EC) and the H atom on the TM1-N4/C (EH), which respectively represent activation ability of benzene C-H bond and phenol O-H bond, could be labeled as descriptors describing catalytic activity and selectivity. Moreover, based on the as-obtained volcano map, appropriate EC (−8 to −7 eV) and weakened EH (−1.5 to 0 eV) contribute to the optimization of catalytic performance for benzene oxidation to phenol. This study offers profound opinions on the rational design of metal single-atom catalysts that exhibit favorable catalytic behaviors in hydrocarbon oxidation. [ABSTRACT FROM AUTHOR]

The Folin-Ciocalteu method is a well-established and widely used assay for measuring total (poly)phenol content in food/plant products. In recent years, there has been growing interest in applying this method to human samples due to its simplicity and efficacy. However, biological matrices such as blood and urine contain several interference substances that must be eliminated beforehand. This mini-review summarizes the current state of knowledge regarding the use of the Folin-Ciocalteu assay to measure total phenolic content in human urine and blood samples, as well as the preceding cleaning methods to remove interferences. Higher total (poly)phenol levels measured by the Folin-Ciocalteu method have been associated with a decrease in mortality and several risk variables. We focus on the application of this sustainable assay as a biomarker of poly(phenol) intake and its potential use as an anti-inflammatory biomarker in clinical laboratories. The Folin-Ciocalteu method, with a clean-up extraction step, is a reliable tool for determining total (poly)phenol consumption. Here, we also recommend using the Folin-Ciocalteu assay as means to measure anti-inflammatory activity. [ABSTRACT FROM AUTHOR]

Direct aromatization of cyclohexanones to synthesize substituted phenols represents a significant challenge in modern synthetic chemistry. Herein, we describe a novel ene‐reductase (TsER) catalytic system that converts substituted cyclohexanones into the corresponding phenols. This process involves the successive dehydrogenation of two saturated carbon‐carbon bonds within the six‐membered ring of cyclohexanones and utilizes molecular oxygen to drive the reaction cycle. It demonstrates a versatile and efficient approach for the synthesis of substituted phenols, providing a valuable complement to existing chemical methodologies. [ABSTRACT FROM AUTHOR]

Direct aromatization of cyclohexanones to synthesize substituted phenols represents a significant challenge in modern synthetic chemistry. Herein, we describe a novel ene‐reductase (TsER) catalytic system that converts substituted cyclohexanones into the corresponding phenols. This process involves the successive dehydrogenation of two saturated carbon‐carbon bonds within the six‐membered ring of cyclohexanones and utilizes molecular oxygen to drive the reaction cycle. It demonstrates a versatile and efficient approach for the synthesis of substituted phenols, providing a valuable complement to existing chemical methodologies. [ABSTRACT FROM AUTHOR]

Aim: In recent years, the paradigm for the treatment of sacrococcygeal pilonidal sinus disease (SPSD) has shifted from surgical excision toward more minimally invasive techniques. Although extensive research has been conducted on the minimal invasive phenolization technique for primary SPSD, literature in recurrent SPSD is lacking. The purpose of this study was to report the long-term outcomes of the phenolization technique for recurrent SPSD. Method: This study included all 57 patients who were initially prospectively included in this study for short-term follow-up after phenolization for recurrent SPSD. A questionnaire was sent out to all patients to obtain long-term outcome. The primary endpoint was recurrence. Secondary endpoints included quality of life and symptoms related to SPSD. Results: A total of 47 patients (82.5%) were available for long-term follow-up. Recurrence needing further surgery developed in 7 patients (14.9%) after a mean follow-up of 76 (SD 21.7) months. At follow-up, there was improvement in the quality of life compared to preoperative levels (82.0, IQR 75.0–90.0 versus 74.0 IQR 52.5–80.0, p = 0.024). Additionally, symptoms associated with SPSD, including pain, fluid discharge, and itching sensation, also showed significant improvement. A total of 42 patients (89.4%) would undergo the same treatment again. No significant association was found between known risk factors and recurrence. Conclusion: Phenolization for recurrent SPSD showed a recurrence rate of 14.9% with significant improvement of natal cleft symptoms and quality of life at long-term follow-up. Therefore, phenolization should be considered as a feasible option for patients with recurrent SPSD. [ABSTRACT FROM AUTHOR]

Activated carbons were prepared from kenaf (Hibiscus cannabinus L.). Carbonization was carried out at 600 °C for 2 h, and activation was performed using air at 600 °C and using CO2 at 750 °C. The activated carbons obtained were treated with HNO3 and H2SO4. The samples were characterized by their chemical and physical structure. The activated carbons obtained were mainly macroporous, and their structure underwent major changes with the activation method and acid treatment. Activated carbons were alkaline and acid-treated carbons were neutral. They were used for phenol adsorption and a kinetic and mechanistic study of adsorption was carried out. The fit to the pseudo-second order and Elovich models was predominant. The rate-limiting step of the process was determined to be diffusion within the pores, as the experimental data fit the Bangham model. DFT simulation showed that the preferred adsorption position involves π-π stacking and that oxidation enhances this interaction. Furthermore, the simulation showed that the interaction of phenol with oxygenated functional groups depends on the type of functional group. [ABSTRACT FROM AUTHOR]

Hierarchically structured materials are considered to be one of the important options to enhance the mass transportation efficiency in microporous zeolites. Herein, we reported a highly efficient steam-assisted crystallization strategy for the synthesis of a hierarchical TS-1 zeolite with a tunable macropore size. The amorphous SiO2–TiO2 precursor dissolved gradually and acted as both a nutrient supplier and macropore template in situ. The framework Ti content of the synthesized TS-1 zeolites could be tuned over a wide range (Ti wt% = 0.70–1.39) by varying the Ti content of the SiO2–TiO2 precursor. Moreover, the pore size of the macropores could be modulated according to the particle size of the precursor based on the investigation of the formation mechanism of the macropores in the hierarchical TS-1 zeolite. The hierarchical TS-1 zeolite exhibited better catalytic activity in the epoxidation reaction of 1-hexene and hydroxylation of phenol compared to the typical microporous zeolites. The improved performance of the hierarchical TS-1 zeolite was probably caused by the improved diffusion performance of the hierarchical structure. [ABSTRACT FROM AUTHOR]

Herein we report a new, practical and efficient preparation of benzofuran-3-carboxylates and naphthofuran-3-carboxylates starting from β-nitroacrylates and phenols. The reaction is promoted by indium trichloride and leads to the target compounds in good to very good yields under microwave irradiation. [ABSTRACT FROM AUTHOR]

In this work, silyl ethers of phenols and alcohols have been successfully prepared and tested as neutral carbon (silicon) centered radical precursors. The organophotocatalyzed oxidation (by the Fukuzumi catalyst) of these ethers caused the cleavage of a C−Si (or a Si−Si) bond for the release of the desired radical to be used for the forging of C(sp3) −C(sp3) (or C(sp3) −Si) bonds via a Giese reaction. [ABSTRACT FROM AUTHOR]

A field experiment was carried out to assess the susceptibility of 14 different cauliflower genotypes against infestation by cabbage butterfly. Throughout the growing season of the crop, observations on larval infestation were made by assessing the presence of larvae on randomly selected and tagged plants. The total concentrations of glucosinolates and phenols in the leaves of different varieties were determined. Glucosinolate concentration was estimated by processing samples in triplicates and measuring content by spectrophotometry method utilising a Na2PdCl4 assay, with sinigrin standards for calibration. The estimation of total phenols from field collected samples on the other hand, was carried out using an 80% ethanol extraction method. Following the grinding of samples and ethanol extraction, samples were processed using Folin-Ciocalteau reagent and sodium carbonate. This was followed by spectrophotometric measurement at 650 nm, performed to estimate the phenol content via a pyrogallol standard curve. Statistical analysis demonstrated a significant negative correlation (r = -0.985) between cabbage butterfly infestation and total glucosinolate content. Conversely, a significant positive correlation (r = 0.901) was observed between total phenols and cabbage butterfly infestation. It was found that the Pusa Snowball-1 genotype had the lowest mean larval population at 21.66 and the lowest total glucosinolate content (9.35 µmoles/g). In contrast, the Olympus genotype, which had the highest total phenol concentration of 931.42 mg/100 g, exhibited the highest mean larvae per plant at 30.86. This study underscores the crucial role of host-plant resistance in pest management, highlighting that variations in glucosinolate and phenol content among different cauliflower genotypes significantly influence susceptibility to cabbage butterfly infestation. [ABSTRACT FROM AUTHOR]

The present study evaluates the effect of Eryngium billardieri alcoholic extract (EBAE) at weight/volume levels of 0.5% and 1% on some physicochemical, sensory, and microbial properties of cow milk. Results showed that adding EBAE reduced the samples' pH, lightness index (L*), and whitening index (WI). Besides, it increased the levels of acidity, dry matter, viscosity, color indices a* and b*, total phenol content (TPC), total flavonoid content (TFC), antioxidant activity (AA), and enzyme inhibitory activity (EIA) of the fortified milk samples than the control sample (p <.05). During the storage period, a decrease in TPC, TFC, AA, and EIA was observed in all samples (p <.05). There was a positive direct relationship between the health activity of EBAE and its concentration. Moreover, EBAE was able to reduce the total microbial count (TMC) in the milk samples (p <.05). The sample containing 1% w/v of EBAE had the highest TPC, TFC, AA, and EIA but the lowest TMC, and it was highly acceptable in terms of sensory evaluation. Therefore, this sample was selected as the best treatment in this study. The results of this study confirm that EBAE may be used to improve antioxidant activity and beneficial effects in milk. [ABSTRACT FROM AUTHOR]

Herein, we report an efficient method to access difluoromethyl ethers of thiols and phenols using ethyl bromodifluoroacetate and K2 CO3. This method demonstrates chemoselective difluoromethylation of thiols and phenols in the presence of amines. The current method also discloses the synthesis of bis(aryloxy)fluoromethane compounds which are least reported in the literature. Mechanistic investigations revealed that the reaction proceeds through a nucleophilic substitution pathway. We strongly believe this protocol would offer an efficient alternative to earlier photocatalyzed or radical-mediated difluoromethylation methods and it has a great potential in the scale-up of pharmaceutical and agrochemical intermediates that possess difluoromethyl group. [ABSTRACT FROM AUTHOR]

It has been established that the maximum synergistic effect (more than 100%) is characteristic of the binary mixtures of pentadigalloyl glucose mixed with protocatechuic and vanillic acids in a ratio of 90 : 10 vol % in the reaction with the 2,2'-diphenyl-1-picrylhydrazyl radical in benzene. With an increase in the polarity of the solvent (dimethyl sulfoxide), an increase in the maximum synergistic effect by 15–20% on the average is observed. Using the methods of quantum chemical calculations and difference UV spectroscopy, it is shown that the resulting effect of the compositions of pentadigalloyl glucose with monomeric phenols depends on the following two mechanisms of synergistic action: the first mechanism is related to the formation of the intermolecular H-complex between reagents, which exhibits higher antiradical activity than that of the initial compounds; the second one is associated with the reduction of oxidized forms of the weaker antioxidant (monomeric phenol) by the stronger antioxidant (pentadigalloyl glucose). The mixture of pentadigalloyl glucose with methoxylated forms of plant phenols is a promising synergistic composition with high antiradical activity. [ABSTRACT FROM AUTHOR]

The development of new catalytic systems based on cobalt and iron compounds for the production of oxygen-containing compounds is an urgent task of chemical technology. The purpose of this work is the synthesis of CoFe2O4 stabilized with polyvinylpyrrolidone (PVP), the study of the catalyst by physico-chemical research methods, and the determination of the effectiveness of the CoFe2O4/PVP catalyst in the phenol oxidation reaction. In this work, magnetic composites CoFe2O4 and CoFe2O4 stabilized with polyvinylpyrrolidone were synthesized by co-deposition. A comparison of the characteristics of the properties of the synthesized cobalt (II) ferrite (CoFe2O4) and the composite material CoFe2O4/PVP based on it is carried out. The obtained samples were examined using X-ray phase analysis (XRD), the Debye–Scherrer method, scanning electron microscopy (SEM), Mossbauer and IR Fourier spectroscopy, as well as thermogravimetric analysis (TGA). The textural properties were determined based on the analysis of nitrogen isotherms. The catalytic properties of the synthesized materials in the process of phenol oxidation in the presence of hydrogen peroxide are considered. The analysis of the reaction mixtures by HPLC obtained by the oxidation of phenol in the presence of a CoFe2O4/PVP catalyst showed a decrease in the concentration of phenol in the first 15 min of the process (by 55–60%), and then within 30 min, the concentration of phenol decreased to 21.83%. After 2 h of the process, the conversion of phenol was already more than 95%. The final sample after the reaction contained 28% hydroquinone and 50% benzoquinone. It was found that the synthesized magnetic composites exhibit catalytic activity in this process. [ABSTRACT FROM AUTHOR]

Phenolic pollutants are widespread in aquatic environments and are major contributors to groundwater pollution. In the present study, a new strain of Bacillus cereus, STV1713, isolated from petroleum-contaminated soil, was found to utilize phenol and 2,4-dichlorophenol (2,4-DCP) as sole carbon and energy sources. Response surface methodology analysis revealed that the optimal temperature and pH combination for this bacterium to degrade phenol and 2,4-DCP is 32.5 °C and 7.0, respectively. Under optimized conditions, it could tolerate higher phenol and 2,4-DCP concentrations up to 1400 ppm and 1200 ppm, respectively, while maximum phenol and 2,4-DCP degradation capabilities were observed until 1200 ppm and 1000 ppm, respectively. Metabolic pathway analysis by enzyme assay revealed that the bacterium uses the meta-cleavage pathway to utilize both pollutants. GC/MS analysis showed a significant reduction in the phenol concentration up to 99.51% and 2,4-DCP up to 99.13% after 72 h of degradation. The degradation ability and pollutant tolerance of B. cereus STV1713 were significantly increased after cell immobilization with sodium alginate beads. The bacterium survived up to 1800 ppm phenol and 1600 ppm 2,4-DCP after immobilization, significantly higher than the tolerance of the free cells. Among the 1023 genes identified by transcriptome analysis during phenol degradation, 40 genes were significantly differentially expressed in B. cereus STV1713 compared to the control. Phenol hydroxylase and catechol 2,3-dioxygenase were recognized as the key enzymes of phenol degradation in B. cereus STV1713. [ABSTRACT FROM AUTHOR]

A sensitive analytical procedure for simultaneous extraction and determination of bisphenol A and alkyl phenols, namely, 4‐sec‐butylphenol, 4‐tert‐butylphenol, and 4‐tert‐amylphenol from aqueous samples with metal–organic framework (MOF)‐based dispersive micro‐solid‐phase extraction (D‐µSPE) and high‐performance liquid chromatography (HPLC) technique is developed. Sample contaminants were preconcentrated with amino‐functionalized aluminum MOF and later eluted with acetonitrile. The reconstituted sample was subjected to HPLC analysis. Various procedural parameters related to D‐µSPE were optimized. Under optimized preconcentration and chromatographic conditions, calibration curves with excellent linearity (R2 > 0.9986) in the working range of 0.25–100 ng mL−1 were prepared. Limit of detection (S/N = 3) for every analyte within the range of 0.020–0.022 ng mL−1 was obtained. Analyte's recovery 91.16%–97.01% (RSD = 1.02–3.01) for intraday and 89.86%–95.83% (RSD = 1.15–3.13) for inter‐day analysis was obtained from real water samples. [ABSTRACT FROM AUTHOR]

Poly(p-dioxanone) (PPDO) is crystallized with amorphous poly(p-vinyl phenol) (PVPh) and tannic acid (TA) as co-diluents to regulate and induce dendritic-ringed PPDO spherulites, with spoke- or sector-bands, aiming for convenience of analyses on interior lamellar assembly. Morphologies and interior lamellar arrangement leading to the peculiar rings on individual dendrites are evaluated by using polarized-light microscopy (PLM) and scanning electron microscope (SEM). Combinatory microbeam small-/wide-angle X-ray scattering (SAXS/WAXS) analyses further confirm the unique assembly patterns in periodic cycles. Alternate gratings are packed with periodic ridges composed of feather-like branches and the valley is featured with some embossed textures. The periodic gratings in the ringed spokes resemble those in nature's structured coloration and are proven to display light-interference iridescence. [ABSTRACT FROM AUTHOR]

This study examined the phenol degradation capabilities and oxidative stress responses of Candida tropicalis SHC-03, demonstrating its metabolic superiority and resilience compared to Saccharomyces cerevisiae BY4742 in a culture medium with phenol as the sole carbon source. Through comparative growth, transcriptomic, and metabolomic analyses under different phenol concentrations, this study revealed C. tropicalis SHC-03's specialized adaptations for thriving in phenol as the sole carbon source environments. These include a strategic shift from carbohydrate metabolism to enhanced phenol degradation pathways, highlighted by the significant upregulation of genes for Phenol 2-monoxygenase and Catechol 1,2-dioxygenase. Despite phenol levels reaching 1.8 g/L, C. tropicalis exhibits a robust oxidative stress response, efficiently managing ROS through antioxidative pathways and the upregulation of genes for peroxisomal proteins like PEX2, PEX13, and PMP34. Concurrently, there was significant upregulation of genes associated with membrane components and transmembrane transporters, enhancing the cell's capacity for substance exchange and signal transduction. Especially, when the phenol concentration was 1.6 g/L and 1.8 g/L, the degradation rates of C. tropicalis towards it were 99.47 and 95.91%, respectively. Conversely, S. cerevisiae BY4742 shows limited metabolic response, with pronounced growth inhibition and lack of phenol degradation. Therefore, our study not only sheds light on the molecular mechanisms underpinning phenol tolerance and degradation in C. tropicalis but also positions this yeast as a promising candidate for environmental and industrial processes aimed at mitigating phenol pollution. [ABSTRACT FROM AUTHOR]

The rate constants for the reaction of hydroperoxyl (or perhydroxyl) radical HOO˙ with fifteen phenols and ascorbyl palmitate were measured in acetonitrile at 37 °C by evaluating the effect that the antioxidants had on the rate of autoxidation of γ-terpinene. The HOO˙ radical represents an important reactive species that can be formed by protonation of superoxide anions (O2˙−) or by fragmentation of alkylperoxyl radicals (ROO˙) formed during the autoxidation of pro-aromatic derivatives like γ-terpinene. The phenols investigated in this study include natural compounds like phenolic acids (protocatechuic, caffeic and dihydrocaffeic acids), flavonoids (3-hydroxyflavone, pinobanksin, galangin, catechin, luteolin, quercetin, 6-methoxyluteolin), 4-methylcatechol and antioxidant additives ascorbyl palmitate and the a-tocopherol analogue 2,2,5,7,8-pentamethyl-6-chromanol. The rate constants for the reaction of HOO˙ with the above compounds (kinh) spanned from 1 × 103 M−1 s−1 for the unsubstituted phenol, to 7 × 104 and 9 × 104 M−1 s−1 for 4-methylcatechol and ascorbyl palmitate, respectively. As in a typical Evans–Polanyi plot, the log(kinh) was found to be inversely proportional to the bond dissociation enthalpy of the reactive OH. The comparison of the results with the data reported in the literature shows an unusual kinetic solvent effect that enlightens the unique behavior of HOO˙ and provides a rationale for the superior radical trapping ability of catechols and ascorbyl palmitate. [ABSTRACT FROM AUTHOR]

The electrochemical oxidative phenol coupling reaction is a sustainable method for accessing biphenolic compounds. Using the dimerization of sesamol as a model reaction, insights into the reaction mechanism were gained via operando Raman spectroscopy. By varying the solvent and electrodes, different reaction mechanisms were identified and correlated with the respective product yields. [ABSTRACT FROM AUTHOR]

Hydroesterification of alkynes is a crucial synthetic transformation, enabling the formation of esters directly with high atom economy. Recent advancements have centered on improving the reaction's selectivity, efficiency, and environmental sustainability, particularly through the innovation of ligands and catalysts, making the process more practical for industrial applications. Herein, we report a highly selective and efficient hydroesterification of alkynes using a novel recyclable ligand, accommodating a wide range of alkyne substrates as well as various alcohols and phenols. The reaction proceeds under mild conditions, affording the desired esters in high yields with excellent regioselectivities. A notable feature of this method is the recyclability of the ligand, which can be recovered and reused multiple times without significant loss of activity or selectivity. Mechanistic studies revealed that palladium was well dispersed on the nanoscale and was essential for this sustainable hydroesterification process. [ABSTRACT FROM AUTHOR]

Background: Exposure to phenols has been linked in animal models and human populations to cardiac function alterations and cardiovascular diseases, although their effects on cardiac electrical properties in humans remains to be established. This study aimed to identify changes in electrocardiographic (ECG) parameters associated with environmental phenol exposure in adults of a midwestern large cohort known as the Fernald Community Cohort (FCC). Methods: During the day of the first comprehensive medical examination, urine samples were obtained, and electrocardiograms were recorded. Cross-sectional linear regression analyses were performed. Results: Bisphenol A (BPA) and bisphenol F (BPF) were both associated with a longer PR interval, an indication of delayed atrial-to-ventricle conduction, in females (p < 0.05) but not males. BPA combined with BPF was associated with an increase QRS duration, an indication of delayed ventricular activation, in females (P < 0.05) but not males. Higher triclocarban (TCC) level was associated with longer QTc interval, an indication of delayed ventricular repolarization, in males (P < 0.01) but not females. Body mass index (BMI) was associated with a significant increase in PR and QTc intervals and ventricular rate in females and in ventricular rate in males. In females, the combined effect of being in the top tertile for both BPA urinary concentration and BMI was an estimate of a 10% increase in PR interval. No associations were found with the other phenols. Conclusion: Higher exposure to some phenols was associated with alterations of cardiac electrical properties in a sex specific manner in the Fernald cohort. Our population-based findings correlate directly with clinically relevant parameters that are associated with known pathophysiologic cardiac conditions in humans. [ABSTRACT FROM AUTHOR]

A ternary iron–cobalt–nickel hydroxide nanoarray catalyst was fabricated, which achieves enhanced performance towards electro-oxidative depolymerization of lignin models to produce benzoic acid and phenol. [ABSTRACT FROM AUTHOR]

Many cell culture experiments are performed under light to evaluate the photodynamic or photosensitizing efficacy of various agents. In this study, the modulation of photosensitizing responses and phototoxicity under cell culture conditions by different medium components was investigated. The significant levels of reactive oxygen species (ROS) generated from DMEM, RPMI 1640, and MEM were observed under the irradiation of fluorescent light (FL) and white and blue LEDs, indicating that these media have their own photosensitizing properties; DMEM showed the most potent property. Phenol red-free DMEM (Pf-D) exhibited a stronger photosensitizing property than normal DMEM by 1.31 and 1.25 times under FL and blue LEDs, respectively; phenol red and riboflavin-free DMEM (PRbf-D) did not show any photosensitizing properties. The inhibitory effect on light transmission was more pronounced in DMEM than in RPMI, and the interference effect on green LED light was greatest at 57.8 and 27.4%, respectively; the effect disappeared in Pf-D. The media containing riboflavin induced strong phototoxicity in HaCaT keratinocytes by generating H2O2 under light irradiation, which was quenched by sodium pyruvate in the media. The presence of serum in the media was also reduced the phototoxicity; H2O2 levels in the media decreased serum content dependently. The phototoxicity of erythrosine B and protoporphyrin IX under FL was more sensitively pronounced in PRbf-D than in DMEM. The present results indicate that several medium components, including riboflavin, phenol red, sodium pyruvate, and serum, could modulate photosensitizing responses in a cell culture system by inducing photosensitizing activation and by interfering with irradiation efficacy and ROS generation. [ABSTRACT FROM AUTHOR]

This review examines the technological bottlenecks, potential solutions, and future development directions in the treatment and resource utilization of semi-coking wastewater (SCOW) in China. By comprehensively investigating the semi-coking industry and analyzing wastewater treatment research hotspots and existing projects, this study systematically explores the current status and challenges of each treatment unit, emphasizing the necessity for innovative wastewater treatment technologies that offer high efficiency, engineering feasibility, environmental friendliness, and effective resource recovery. This review highlights prospects and recommendations, including the development of novel extractants for phenol and ammonia recovery, a deeper understanding of biological enhancement mechanisms, exogenous bio-enhancement materials, and the creation of cost-effective advanced oxidation process (AOP)-based combined processes. Additionally, it underscores the potential for repurposing SCOW as a valuable resource through appropriate treatment, whether recycling for production or other applications. [ABSTRACT FROM AUTHOR]

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Phenol is a volatile organic compound, and conventional treatment processes prove to be ineffective for its degradation. The designable electron transfer structures of Fenton-based catalysts show great potential for wastewater treatment. However, attaining a balance between recycling and degradation efficiency remains a challenge. Herein, we prepared a photocatalyst with improved visible-light excitation characteristics. Magnetic N-TiO2/Fe3O4@MXene was prepared by loading N-TiO2 nanoparticles and Fe3O4 onto multilayered MXenes. N-TiO2/Fe3O4@MXene exhibited stable magnetic characteristics (27.1 emu/g) and a high degradation capacity for phenol. The catalyst also showed better performance for phenol removal under simulated solar-light (200–800 nm) irradiation compared with those of other catalysts. The phenol removal rate of the catalyst in the concentration range of 20–60 ppm reached 98% after 30 min of solar-light irradiation. The degradation curves of phenol were kinetically fitted. After four cycles of testing, the material maintained a high efficiency for the degradation of phenol. A total organic carbon removal rate of 61% was achieved in 10 min. The intermediates of phenol degradation were determined via liquid chromatography–mass spectrometry to gain insights into the degradation pathways of phenol. This study paves the way for the development of efficient photo-Fenton-based catalytic systems with good magnetic separation capabilities, which can promote their application in wastewater treatment. [ABSTRACT FROM AUTHOR]

Bio‐oil formaldehyde resole (BFR) can be used as adhesive in plywood industry. However, the BFR has a lower thermal stability, and the reason is still unclear. Herein, the reactivities of four representative phenolic compounds in bio‐oil, including two ortho phenols (2‐methylphenol, 2‐methoxyphenol) and two para phenols (4‐methylphenol and 4‐methoxyphenol), as well as the thermal stabilities of the prepared resoles are investigated. The results show that the reactivity of an ortho phenol is higher than that of a para phenol. The resole prepared from a para phenol has a higher thermal stability than that of an ortho phenol. The resole of an ortho phenol decomposes even when heated at the low temperature of 100 °C. The resole of a methylphenol generally has a higher thermal stability than that of a methoxyphenol. Based on the results, the reason for the low reactivity of bio‐oil and the low thermal stability of BFR are speculated. [ABSTRACT FROM AUTHOR]

Background: To determine the relationship between mixed exposure to three types of endocrine-disrupting chemicals (EDCs), namely phenyl hydroxides, polycyclic aromatic hydrocarbons (PAHs), and phthalates (PAEs), and risk of arthritis. Methods: Participants were selected from National Health and Nutrition Examination Survey (NHANES). The relationships between the urinary concentrations of phenyl hydroxides, PAHs, and PAEs and the risk of arthritis were analyzed by generalized linear regression model. The mixed exposure to these EDCs and the risk of arthritis was analyzed by weighted quantile sums (WQSs) and Bayesian kernel machine regression (BKMR) model. Results: Our analysis showed that participants with urinary benzophenone-3 and methylparaben concentrations in the highest quartile (Q4) had an increased risk of arthritis compared with those in Q1. For each one-unit increase in the natural logarithm-converted urinary concentrations of 1-hydroxynapthalene and 2-hydroxynapthalene, the risk of arthritis increased by 5% and 8%, respectively. Chemical mixing index coefficients were significantly associated with risk of arthritis in both WQS positive- and negative-constraint models. In the BKMR model, there was a significant positive correlation between mixed exposure and the risk of arthritis. Conclusion: Mixed exposure to phenyl hydroxides, PAHs, and PAEs increased the risk of arthritis, with exposure to PAHs being the key factor. [ABSTRACT FROM AUTHOR]

A novel class of chain-like multidentate oxalamide ligands with additional coordinating groups was developed for the coupling of (hetero)aryl bromides with both alcohols and phenols under mild conditions. Introduction of oxygen atoms in N-alkyl chains is pivotal for the high catalytic efficiency and broad substrate versatility. [ABSTRACT FROM AUTHOR]

Background: Chlorophenoxy compounds represent a group of selective herbicides widely used around the world. Chlorophenoxy herbicides are toxic, chemically stable, and can migrate into groundwater through soil leaching, posing a significant threat to drinking water safety and human health. Chlorophenoxy herbicides in groundwater aquifers are subject to anaerobic processes; however, the pathway and microbiology involved in the attenuation of chlorophenoxy herbicides under anaerobic condition are largely unknown. Here, the anaerobic degradation process of 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), a typical chlorophenoxy herbicide, was investigated. Results: The initial 52.5 ± 2.3 μM 2,4,5-T was completely degraded by a sediment-derived microbial consortium, with 3,4-dichlorophenol, 2,5-dichlorophenol, 3-chlorophenol (3-CP) and phenol being identified as the intermediate products. Reductive dechlorination of 3-CP to phenol and the subsequent elimination of phenol were the key transformation steps in the overall degradation process of 2,4,5-T. Amplicon sequencing suggested that Dehalobacter, Sulfuricurvum, Bacteroides, Acetobacterium, and Clostridium sensu stricto 7 might contribute to the transformation of 2,4,5-T to phenol, and Smithella, Syntrophorhabdus, Methanofollis and Methanosaeta likely cooperated to accomplish the complete mineralization of phenol. Conclusions: This study reported the anaerobic degradation of 2,4,5-T via reductive dechlorination and the subsequent syntrophic metabolization of phenol, an intermediate product transformed from 2,4,5-T. Dehalobacter was identified as the organohalide-respiring population catalyzing the reductive dechlorination reaction. Syntrophorhabdus and methanogenic populations were likely involved in anaerobic phenol oxidation and facilitated the complete mineralization of 2,4,5-T. [ABSTRACT FROM AUTHOR]

A general Pd-catalyzed approach for the conversion of phenols into benzonitriles via aryl imidazolylsulfonates with a non-toxic cyanide source, potassium ferrocyanide, has been developed. Salient features of this method include low palladium precatalyst loadings (as low as 1.0 mol% total Pd), mild reaction conditions, and environmentally benign by-products compared to other (pseudo)halide aryl electrophiles. The initial scope of the reaction on a range of phenolic precursors is demonstrated including a one-pot, two-step approach to convert phenols directly into benzonitriles. [ABSTRACT FROM AUTHOR]

A straightforward and efficient electrochemical method for the anodic oxidative selenenylation of 2-(2-arylallyl)phenols and a 2-(3-arylbut-3-en-1-yl)phenol with diselenides under ambient air conditions has been outlined. This method allows for the synthesis of selenyl-dihydrobenzofurans and a chromane featuring a sterically hindered tetrasubstituted carbon center, demonstrated through 25 examples with yields reaching up to 98%. Initial mechanistic investigations suggest the likely participation of pivotal seleniranium cation species in regulating the reactivity. [ABSTRACT FROM AUTHOR]

Phenol soluble modulins (PSMs) are small amphipathic peptides involved in a series of biological functions governing staphylococcal pathogenesis, primarily by facilitating the formation of an extracellular fibril structure with amyloid-like properties. This fibrillar architecture stabilizes the staphylococcal biofilm making it resilient to antibiotic treatment. Our study aims to abrogate the amyloid fibrillation of PSM α1 with novel insights on the amyloid modulatory potential of a prenylated chalcone, Isobavachalcone (IBC). A combination of biophysical and computational assays to address the amyloid modulatory effect of IBC has been undertaken to arrive at a model for the inhibition of PSM α1 fibrillation. ThT kinetics studies indicated that IBC must be stably interacting with the amyloidogenic core of PSM α1 monomers or it may be inhibiting the pre-fibrillar aggregates populated at the early stages of amyloid transformation kinetics. This heteromolecular association further inhibits the amyloid transformation corroborated by a ∼ 94% and ∼ 91% reduction in the ThT maxima, even at sub-stoichiometric concentrations. Transmission electron microscopy (TEM) of end-stage aggregates (∼ 55 h) depict mature, inter-twined, laterally stacked amyloid fibrils in untreated PSM α1 samples while this fibrillar load is remarkably reduced in the presence of IBC. The inhibitory effect of IBC on the β-sheet transitions of PSM α1 were also validated using far-UV CD spectra. Molecular dynamics simulation studies with PSM aggregates (PSM-A) have also suggested that IBC disrupts the hydrogen bonding interactions and corroborates the inhibition of alpha to beta transitions of PSM-A. Collectively, our data proposes a novel structural motif for the rational discovery of non-toxic therapeutic agents targeting the functional amyloids which have slowly emerged as potent factors, consolidating the antibiotic resistant staphylococcal biofilm assembly. [ABSTRACT FROM AUTHOR]

In this study, the potential of using 3,5-bis(5-mercapto-4-R-4H-1,2,4-triazol-3-yl)phenol as a critical component for the synthesis of new compounds is considered, which may be of significant importance in various fields of science and technology. The relevance of the research is due to the fact that studying the properties of new synthetic derivatives of 1,2,4-triazole is a promising direction in modern chemistry. This study opens new opportunities for creating biologically active substances with antioxidant activity and the prospect of their further use as individual and combined drugs for correcting pathological processes associated with oxidative stress. The aim of the study. The main objective of the research is to find new, low-toxic, and highly effective antioxidant compounds based on derivatives of 3,5-bis(5-mercapto-4-R-4H-1,2,4-triazol-3-yl)phenol, as well as to confirm the individuality, structure, and establish their physicochemical constants. Materials and methods. The article investigates the synthesis and establishes the structure of a series of compounds, in particular, diacetic acids and dibenzoic acids, derivatives of 3,5-bis(5-mercapto-4-R-4H-1,2,4-triazol-3-yl)phenol, which were chosen as the material for the search for highly effective antioxidants. The methods used in this work are as follows: organic synthesis, physicochemical methods for determining the structure of synthesized substances (elemental analysis, UV spectrophotometry, 1H NMR spectroscopy, mass- and chromato-mass spectrometry), and a biological method for determining antioxidant activity using the free radical method with DPPH. Results of the study. The results .showed that some of the synthesized compounds have significant potential as antioxidants, which may be important in the context of their application in various fields, particularly in medicine and the food industry. Among the obtained results, it is especially worth noting ethyl 3,3'-((((5-hydroxy-1,3-phenyl- ene)bis(4-R-4-phenyl-1,2,4-triazol-5,3-diyl))bis(sulfandiyl))bis(methylene))dibenzoate (compound 7c) and propyl 3,3'-((((5-hydroxy-1,3-phenylene)bis(4-R-4-methyl-1,2,4-triazol-5,3-diyl))bis(sulfandiyl))bis(methylene))dibenzo- ate (compound 7d), which showed the highest level of antioxidant activity among all the studied compounds. Conclusions. The obtained results indicate the possible application of the studied compounds as potential antioxidants in the production ofmaterials and products, which may be of great significance for further research in this area [ABSTRACT FROM AUTHOR]

Adducts of levoglucosenone with p-cresol, 3,4-dimethylphenol, and 2,3,6-trimethylphenol were synthesized in one step. The antioxidant, anticoagulation, and antiaggregation activities of the obtained levoglucosenone derivatives were studied. All adducts exhibited anticoagulation and antiaggregation activities at the level of aspirin. The antioxidant activity of the synthesized compounds was assessed from the rate of their reaction with the peroxyl radical of 1,4-dioxane. As a result, all levoglucosenone derivatives examined in the present study were found to reduce the radical-chain oxidation rate. The highest inhibitory activity was found for (1S,2R,5R)-2-(4-hydroxy-2,3,5-trimethylphenyl)-6,8-dioxabicyclo[3.2.1]octan-4-one. The effective inhibition rate constant of this addition product of 2,3,6-trimethylphenol with levoglucosenone was double that of ionol. The obtained results opened up the prospect of synthesizing optically active phenols for further development of drugs with desired pharmacological properties. [ABSTRACT FROM AUTHOR]

The development of efficient and environmentally friendly photocatalysts is crucial for addressing global energy and environmental challenges. Perylene diimide, an organic supramolecular material, holds great potential for applications in mineralized phenol. In this study, through the integration of different mass ratios of unmodified perylenimide (PDI-NH) into the self-assembly of amino acid-substituted perylenimide (PDI-COOH), a novel supramolecular organic heterojunction (PDICOOH/PDINH) was fabricated. The ensuing investigation focuses on its visible-light mineralized phenol properties. The results show that the optimal performance is observed with a composite mass fraction of 10%, leading to complete mineralization of 5 mg/L phenol within 5 h. The reaction exhibits one-stage kinetics with rate constants 13.80 and 1.30 times higher than those of PDI-NH and PDI-COOH, respectively. SEM and TEM reveal a heterogeneous interface between PDI-NH and PDI-COOH. Photoelectrochemical and Kelvin probe characterization confirm the generation of a built-in electric field at the interface, which is 1.73 times stronger than that of PDI-COOH. The introduction of PDI-NH promotes π-π stacking of PDI-COOH, while the built-in electric field facilitates efficient charge transfer at the interface, thereby enhancing phenol decomposition. The finding demonstrates that supramolecular heterojunctions have great potential as highly effective photocatalysts for environmental remediation applications. [ABSTRACT FROM AUTHOR]

We recently introduced calix[n]naphth[m]arenes as a novel class of deep-cavity hybrid macrocycles constituted by phenol (n) and naphthalene (m) units. In this study, we report the synthesis, conformational analysis, spectroscopic properties, and solid-state structures of calix[4]naphth[4]arene (C4N4) and its permethylated analog (C4N4-Me), thereby expanding the calix[n]naphth[m]arene family. C4N4 was synthesized through a 2 + 2 fragment coupling macrocyclization under acidic conditions, where the solvent played a crucial role in selectively forming the C4N4 derivative. The X-ray structure of C4N4 reveals a chair-like 1,2,3,4-alternate conformation characterized by two opposing 3/4-cone moieties stabilized by intramolecular hydrogen bonds. In contrast, the X-ray structure of C4N4-Me exhibits a 1,3,5,7-alternate conformation. [ABSTRACT FROM AUTHOR]

Zeolites (Hβ, HZSM-5 and HM), TiO2 and ZrO2 supported NiCo alloy catalysts were tested for the hydrodeoxygenation of phenol in aqueous phase. It has been found that the catalyst acidity remarkably influences the catalyst activity and the product distribution. Zeolites supported catalysts give much higher yield of the deoxygenated products (mainly benzene and cyclohexane) than NiCo/TiO2 and NiCo/ZrO2, where cyclohexanol and cyclohexanone are dominating. Associated with NH3-TPD, we suggest that the catalyst acidity promotes the hydrodeoxygenation. Hβ zeolite supported NiCo alloy is more active than others, attributed to its higher metal dispersion and more acid sites. Therein, the Hβ zeolite calcined at 750 oC has moderate acidity, and its supported NiCo alloy catalyst (NiCo/HB-750) shows the best performance. Under a suitable reaction condition, the phenol conversion and the total yield of deoxygenated products reaches 96.8% and 94.5% on NiCo/HB-750, respectively. [ABSTRACT FROM AUTHOR]

The current research was conducted to compare the growth, yield, and phytochemical composition of basil (Ocimum basilicum) in the open field and the soil and hydroponic cultivation in a greenhouse. Furthermore, the effect of foliar spraying of micronutrients on this crop was also evaluated. In each of the cultivation systems, foliar spraying of one micronutrient, either iron sulfate (Fe), zinc sulfate (Zn), copper sulfate (Cu), manganese sulfate (Mn), or boric acid (B), at a concentration of 0.1% was applied in a randomized complete block design. Plants grown in the hydroponic system had higher yield and biomass. The concentration of the elements K, Ca, Mg, N, P, Mn, Fe, B, and Zn in the leaves of hydroponic plants was higher. Contrarily, plants cultivated in the field showed higher stem dry weight, essential oil content, phenolic and flavonoid content, and antioxidant activity. The level of methyl chavicol was higher in the hydroponic culture, but the level of 1,8-cineole was much lower in this cropping system. Foliar spraying of Cu, Mn, Zn, Fe, or B significantly increased leaf dry weight and anthocyanin content. In field conditions, the highest levels of phenolics, flavonoids, and antioxidant capacity were observed with Zn or Mn application. In the hydroponic system, foliar spraying of Zn or B led to the highest antioxidant capacity, and total phenolic and flavonoid contents. Overall, the basil plants cultivated in the field showed higher bioactive ingredients. However, the essential oil of plants cultivated in the hydroponic system had a higher economic value due to its higher percentage of methyl chavicol. [ABSTRACT FROM AUTHOR]

Artemisia absinthium is a wild edible species presence in Iraqi Kurdistan region the local people has used the plants as a part of their traditional medicine and their daily life. Nowadays, these plants become more attractive and interested due to their phytochemicals and antioxidant activities. Therefore, This study sought to evaluate various phytochemicals of this plant's aerial section generated by micropropagation in-vitro at tissue culture Laboratory of College of Agricultural Engineering science/University of Duhok, and with identical plants harvested from the field from Gali Ali Bak (invivo), including the difference in total phenolic compound and flavonoid content and antioxidant activity using DPPH test. The results showed that A. absinthium plants were rich with the high concentration of phenolic components in the Invivo plant extract was high (1.65 mg gallic acid equivalents/g of dry extract, eq.100g-1 ), while it was lowest in the in-vitro plant extract (0.56 mg gallic acid). and (5.2 and 2.9 g of quercetin equivalents/g of dry extract, eq.100g-1 ) for the Invivo and in-vitro plants, respectively, were the determined amounts of flavonoids extracted in the Invivo plant extract compared to the in-vitro plant extract. The anti-oxidative activity was tested by measuring their ability to scavenge stable 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical, the results displayed that the different quantities of plant extract of Invivo and in-vitro ranged between (150- 300 g/ml) concentrations had radical-scavenging activity as comparative with the positive control (ascorbic acid),however the best value was at 200 g/ml for Invivo(118) as compared with positive control (ascorbic acid) (80.8). Thus, the evidence of this study shown that Artemisia can enhance natural medicines for human being. [ABSTRACT FROM AUTHOR]

To protect skin from harmful ultraviolet (UV) radiation, there has been a resurgence in the use of natural dyes with metal mordants to reduce contamination by advanced chemicals. This study achieved natural dyeing in violet and yellow colors from Gromwell red roots and Cape jasmine seeds for UV-protective materials. The dyed fabrics were subjected to zinc oxide (ZnO) and polyphenol treatments, as well as copper post-mordanting. The SEM, TEM, and XRD tests showed that the ZnO nanoparticles, with hexagonal crystal structures, stuck to the fiber surfaces, and twisted strands resulted in the K/S reduction. First, this study found that the untreated cotton in violet, despite the highest K/S, faded the most intensely when exposed to UV. The color variation of untreated polyester was narrow, with little change in L, a*, and K/S. The color change of yellow-dyed samples treated with ZnO/polyphenol was not considerable in yellowness (b*: 28.838), while the violet fabrics displayed a significant decrease in K/S and an increase in b*. The combination of ZnO and polyphenol treatment improved UV absorption at 350 to 250 nm. Among the Cu-mordanted fabrics after ZnO/phenols treatment, the violet cotton turned reddish from blueish (negative to positive b*), with a hue change of 316° to 59° and the highest ΔE (25.90 ± 4.34) after UV exposure. In this study, the combination of ZnO/polyphenol with Cu-mordants allowed the Cape jasmine-dyed polyester to achieve a minimum ΔE as well as to keep its chroma and hue after UV exposure. [ABSTRACT FROM AUTHOR]