Deep-learning based flat-fielding quantitative phase contrast microscopy.

Quantitative phase contrast microscopy (QPCM) can realize high-quality imaging of sub-organelles inside live cells without fluorescence labeling, yet it requires at least three phase-shifted intensity images. Herein, we combine a novel convolutional neural network with QPCM to quantitatively obtain the phase distribution of a sample by only using two phase-shifted intensity images. Furthermore, we upgraded the QPCM setup by using a phase-type spatial light modulator (SLM) to record two phase-shifted intensity images in one shot, allowing for real-time quantitative phase imaging of moving samples or dynamic processes. The proposed technique was demonstrated by imaging the fine structures and fast dynamic behaviors of sub-organelles inside live COS7 cells and 3T3 cells, including mitochondria and lipid droplets, with a lateral spatial resolution of 245 nm and an imaging speed of 250 frames per second (FPS). We imagine that the proposed technique can provide an effective way for the high spatiotemporal resolution, high contrast, and label-free dynamic imaging of living cells.

Zn/Al layered double hydroxide and carboxymethyl cellulose composite beads as support for the catalytic gold nanoparticles and their applications in the reduction of nitroarenes.

Until now, many efficient catalysts have been reported that are used for the reduction of nitroarenes. However, a catalyst reusability is a challenge that is often faced in practical environment. In this report, we designed a hydrogel composite (CMC-LDH), which act as support and making it possible to address this challenge. In this research work, zinc/aluminum based layered double hydroxides (Zn/Al LDH) have been assembled with carboxymethyl cellulose (CMC) to prepare CMC/LDH hydrogel beads. The CMC/LDH hydrogel beads were prepared by the ionotropic gelation method. For CMC/LDH/Au preparation, the already prepared CMC/LDH beads were kept in gold ion (Au3+) solution, and their subsequent reduction with sodium borohydride (NaBH4). For the characterization of the prepared samples different instrumental techniques, such as Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy, and scanning electron microscopy (SEM) were adopted. For the catalytic evaluation of CMC/LDH/Au, it was utilized as a catalyst in 4-NP and 4-NA reduction reactions. The continuity of the reaction was monitored by a UV-visible spectrophotometer. Rate constant (kapp) of 0.48474 min-1 and 0.7486 min-1 were obtained for 4-NP and 4-NA reduction, respectively. The hydrogel beads were recycled and reused for up to five successive cycles without significantly changing their catalytic efficiency.

Biomimetic Electrochemical Sensors Based on Core-Shell Imprinted Polymers for Targeted Sunset Yellow Estimation in Environmental Samples.

Magnetic molecularly imprinted polymers (MMIPs) contain the predesigned specialized recognition capability that can be chosen to build credible functional materials, that are easy to handle and have a good degree of specificity. Hence, the given piece of work is intended to design a novel electrochemical sensor incorporating magnetite-based molecularly imprinted polymers. The building materials consisted of a cross-linker (EGDMA), reaction-initiator (AIBN), monomer (methylene succinic acid-MSA), and template molecule (Sunset Yellow-SY dye). MMIPs exhibited a diameter of 57 nm with an irregular shape due to the presence of cavities based on SEM analysis. XRD patterns exhibited crystallinity, as well as amorphous peaks that are attributed to polymeric and non-polymeric frameworks of MMIPs. The crystallite size of the MMIPs from XRD analysis was found to be 16.28 nm based on the Debye-Scherrer's equation. Meanwhile, the FTIR bands showed the synthesis of MMIPs using monomer and methylene succinic acid. The sorption data at the optimized operating conditions (pH 2, sorbent dosage 3 mg, time 18 min) showed the highest sorption capacity of 40 mg/g. The obtained data best fitted to the Langmuir sorption isotherm and followed the pseudo-second-order kinetics. The magneto-sensors were applied for ultrasensitive, rapid, and simple sensing of SY dye. The electrochemical experiments were run at the operating condition range of (scan rate 10-50 mV/s, tads 0-120 s, pH 5-9, potential range 1-1.5 V for CV and 1-1.3 V for SWAdASV). The linear range of detection was set to 1.51 × 10-6 M to 1.51 × 10-6 M posing LOD and LOQ values of 8.6242 × 10-5 M and 0.0002874 M, respectively. The regression analysis value for the calibration was found to be 0.950. Additionally, high adsorption efficiency, selectivity, reusability, and strong structural stability of the magneto-sensors showed potential use for SY detection in real samples. These characteristics make MMIPs a viable electrochemical substrate for the detection of chemical contaminants in the environment and in health-related products.

Software selection in large-scale software engineering: A model and criteria based on interactive rapid reviews.

Context: Software selection in large-scale software development continues to be ad hoc and ill-structured. Previous proposals for software component selection tend to be technology-specific and/or do not consider business or ecosystem concerns. Objective: Our main aim is to develop an industrially relevant technology-agnostic method that can support practitioners in making informed decisions when selecting software components for use in tools or in products based on a holistic perspective of the overall environment. Method: We used method engineering to iteratively develop a software selection method for Ericsson AB based on a combination of published research and practitioner insights. We used interactive rapid reviews to systematically identify and analyse scientific literature and to support close cooperation and co-design with practitioners from Ericsson. The model has been validated through a focus group and by practical use at the case company. Results: The model consists of a high-level selection process and a wide range of criteria for assessing and for evaluating software to include in business products and tools. Conclusions: We have developed an industrially relevant model for component selection through active engagement from a company. Co-designing the model based on previous knowledge demonstrates a viable approach to industry-academia collaboration and provides a practical solution that can support practitioners in making informed decisions based on a holistic analysis of business, organisation and technical factors.

Engineering of oxygen vacancy defect in CeO2 through Mn doping for toluene catalytic oxidation at low temperature.

Catalytic oxidation is considered a highly effective method for the elimination of volatile organic compounds. Oxygen vacancy defect engineering in a catalyst is considered an effective approach for high-performance catalysts. Herein, a series of doped MnxCe1-xO2 catalysts (x = 0.05-0.2) with oxygen vacancy defects were synthesized by doping low-valent Mn in a CeO2 lattice. Different characterization techniques were utilized to inspect the effect of doping on oxygen vacancy defect generation. The characterization results revealed that the Mn0.15Ce0.85O2 catalyst has the maximum oxygen vacancy concentration, leading to increased active oxygen species and enhanced oxygen mobility. Thus, Mn0.15Ce0.85O2 catalyst showed an excellent toluene oxidation activity with 90% toluene conversion temperature (T90) of 197 °C at a weight hourly space velocity of 40,000 mL g-1 h-1 as compared to undoped CeO2 (T90 = 225 °C) and Ce based oxides in previous reports. In addition, the Mn0.15Ce0.85O2 catalyst displayed strong recyclability, water resistant ability and long-time stability. The in situ DRIFT results showed that the Mn0.15Ce0.85O2 catalyst has a robust oxidation capability as toluene is quickly adsorbed and actuated as compared to CeO2. Thus, the present work lays the foundation for designing a highly active catalyst for toluene elimination from the environment.

Broad Complex Tachycardia, Addison's disease, and Ascending Flacid Paralysis: An Interesting Case on Cardiology Floor.

Broad complex tachycardia is a common presentation in the cardiology emergency room but is not always due to ventricular tachycardia, especially in a young patient who has other important medical illnesses and with no underlying cardiac illness. We present a case of a 40-year male who was admitted with complaints of palpitation associated with rapidly progressive weakness of lower limbs progressing to quadriparesis in about 10 hours. His clinical presentation was due to hyperkalemia and weakness due to Addison's disease. The patient was treated with drugs to lower potassium levels and steroids. His muscle power improved dramatically as potassium levels normalized and he recovered completely. Key Words: Acute flaccid paralysis, Hyperkalemia, Broad complex tachycardia.

Solitary Cystic Mediastinal Lymphangioma: A Rare Incidental Case in an Adult Female.

Introduction: Lymphangiomas are rare, congenital malformations arising from lymphatic hyperplasia. More than 90% of cases are found in children under 2 years of age. Cystic lymphangiomas usually occur in the neck and axillary region and only rarely extend to the mediastinum. Case Description: We present the case of a middle-aged woman who presented with dyspnoea and productive cough. A chest x-ray showed right lower medial lung opacity, and a CT scan of the thorax showed a cystic mediastinal mass, encroaching on the superior vena cava and approaching the trachea and mainstem bronchus. An anterior thoracotomy with tumour resection was performed to relieve compression symptoms. The final pathology report confirmed the diagnosis of mediastinal lymphangioma. Discussion: Lymphangioma should be considered as one of the differential diagnoses when mediastinal widening is found on chest x-ray, and it should be investigated further with a CT scan and biopsy. Infiltration of surrounding structures can cause compression symptoms and can also make surgical resection more challenging. LEARNING POINTS: Lymphangiomas are benign tumours of the paediatric population that can rarely occur in middle-aged adults as an acquired form.It is essential to investigate mediastinal enlargement seen on chest x-ray images even in the absence of any symptoms, as mediastinal lymphangiomas can grow to involve nearby anatomical structures.Although benign, lymphangiomas should be excised at the time of diagnosis to avoid anticipated complications and compression of anatomical structures causing respiratory difficulty, hoarseness and superior vena cava syndrome.Complete surgical resection is the mainstay of treatment and provides an excellent postoperative prognosis.

Design and fabrication of chitosan cross-linked bismuth sulfide nanoparticles for sequestration of mercury in river water samples.

The existence of heavy metals in ecological systems poses great threats to living organisms due to their toxicant and bio-accumulating properties. Mercury is a known toxicant with notable malignant impacts. It has long been known to cause toxic threats to the health of living organisms since the break out of Minamata disease. The turbulent expulsion of mercury-based pollutants from the industrial sector, requires a proper solution. Many attempts have been made to design a greener and more efficient route for a satisfactory removal of mercury. In the current study, bismuth sulfide nanoparticles (BiSNPs) have been synthesized via the co-precipitation method. The BiSNPs were supported with crosslinked chitosan to enhance their sorption capacity and avoid leaching. The average size of the BiSNPs was 42 nm based on SEM micrographs. The SEM analysis of the bismuth sulfide chitosan-crosslinked beads (BiS-CB) showed that the beads possessed a spherical and smooth morphology with a size of 1.02 mm. The FTIR analysis showed that the beads possessed the characteristics bands of imine groups of chitosan, bismuth, sulfur, and glycosidic linkages present in the molecules. The XRD analysis confirmed the phase crystallinity of the BiS-CB with an average crystallite size of 11 nm. The BiS-CB was employed for the sorption of mercury from water samples. The maximum sorption capacity of 65.51 mg/g was achieved at optimized conditions of pH 5, concentration 80 ppm, in 45 min at 30 °C. The mechanism studied for mercury removal showed that sorption followed the complexation mechanism according to the SHAB concept. In conclusion, the results showed that the BiS-CB sorbent exhibited an excellent sorption capacity to remove mercury.

Exploration of solid waste materials for sustainable manufacturing of cementitious composites.

The problem of disposing and managing solid waste materials has become one of the major environmental, economic, and social issues. Utilization of solid wastes in the production of building materials not only solves the problem of their disposal but also helps in the conversion of wastes into useful and cost-effective products. In the present study, solid waste materials of organic and inorganic nature were applied in the production of sustainable cementitious composites (CC) and studied the effect of incorporated wastes on physical and mechanical properties of the resultant CC. The selected solid waste materials were cotton, polyester, PET, carpet, glass, and granulated blast furnace slag (GBFS). These wastes were incorporated in CC in different proportions and form the tuff tiles using moulds (12.5″ × 6″ × 2.5″). The various physical (fineness, setting time, bulk density, and water absorption capacity) and mechanical (flexural strength) properties of all the specimens were determined after curing period of 3, 7, and 28 days. The results show that the incorporation of solid wastes in CC did not much affect their physical characteristics. However, the CC incorporated with the selected solid waste materials have a pronounced effect of their flexural strength and found to be higher (12-875%) compared to the plain CC. Similarly, the incorporation of the selected inorganic wastes (302-715 psi) in CC exhibit much higher flexural strength compared to the organic wastes (136-235 psi). The maximum flexural strength was observed when GBFS was utilized as a solid waste. The present work will provide a reliable step for the solid waste management and conversion of such wastes into useful commercial products for concrete manufacturing.

Designing, characterization, and evaluation of chitosan-zinc selenide nanoparticles for visible-light-induced degradation of tartrazine and sunset yellow dyes.

Employing dyes in different industrial sectors has produced a serious threat to the environment and living organisms of water bodies and land. For the decontamination of such toxic dyes, efforts have been made to develop an efficient, feasible, and low maintenance processes. In this context, chitosan-zinc selenide (CS-ZnSe) nanoparticles were prepared through chemical reduction method as the efficient photocatalysts for the decontamination of toxic dyes through photocatalysis. Photocatalyst's synthesis was confirmed with the help of FTIR spectroscopy. XRD indicated the hexagonal crystal structure of the CS-ZnSe with a crystallite size of 12 nm. SEM micrographs showed the average nano photocatalyst size as 25 nm. EDX analysis was employed to determine the elemental composition of the CS-ZnSe. An excellent photocatalytic degradation efficiency for tartrazine and sunset yellow dyes was obtained using CS-ZnSe. The results showed a 98% and 97% degradation efficiency for tartrazine dye and sunset yellow (SY) dye at optimized conditions of time (3 h), pH (5), dye concentration (30 ppm), catalyst dosage (0.09 g and 0.01 g) , and at a temperature of 35 °C. Findings of the photocatalytic degradation process fitted well with first-order kinetics for both the dyes. Rate constant, 'K' value was found to be 0.001362 min-1 and 0.001257 min-1 for tartrazine and SY dyes, respectively. While value for (correlation coefficient, R2) was 0.99307 and 0.99277 for tartrazine and sunset yellow dyes, respectively. Recyclability of the photocatalyst was confirmed using it for consecutive cycles to degrade organic dyes. Results showed that the CH-ZnS possesses excellent efficiency in decontaminating organic dyes from industrial wastewater.

Core-shell magnetic molecularly imprinted polymer for selective recognition and detection of sunset yellow in aqueous environment and real samples.

Magnetic Molecularly imprinted polymers (MMIPs) have been recently recognized as an exceptional tool for monitoring and decontamination of environmental and biological samples of diverse nature. Based on the potential applications as sorbents and biomimetic sensors, herein, a core-shell magnetic-molecularly imprinted polymer (MMIP) was developed as a selective material for separation and sensing of sunset yellow (SY) dye in an aqueous environment and real samples. The MMIP was synthesized via precipitation polymerization using SY as a template, MAA as a functional monomer (chosen based on simulation studies), EGDMA as a cross-linking agent, and AIBN as an initiator. To elaborate the specificity of MMIP, a comparative agent, magnetic non-imprinted polymer (MNIP) was also synthesized. The XRD results showed that the MMIP showed both crystalline and amorphous structure attributed to the presence and polymeric and non-polymeric groups. The FTIR spectra confirmed synthesis of intermediate and final MMIP product. The SEM results showed spherical morphology and porous structure of the MMIP with an average particle size of 0.636 µm in diameter. The MMIP was first employed as a sorbent for the removal of SY from the aqueous environment. The binding experiments performed at optimized operating conditions (pH 2; time 30 min; sorbent dosage 3 mg; sorbate concentration 80 ppm) showed more selectivity when compared with MNIP. The data fitted best to Langmuir's sorption isotherm (Qo 359.8 mg/g) and followed the pseudo-second-order kinetic model. The synthesized MMIP was also used as an electrochemical sensor for detection of SY dye in the aqueous environment, which exhibited a linear range of detection as (1.51 × 10-6 - 1.5 × 10-3 M). The limit of detection (LOD) and limit of quantification (LOQ) were found to be 0.00413 M and 0.0137 M, respectively. While the R2 value was found to be 0.997 at optimized analytical conditions. These results suggested that the synthesized MMIP can be applied for the selective separation and quantification of SY dye in sample of diverse nature.

Smart and Adaptive Architecture for a Dedicated Internet of Things Network Comprised of Diverse Entities: A Proposal and Evaluation.

Advances in 5G and the Internet of Things (IoT) have to cater to the diverse and varying needs of different stakeholders, devices, sensors, applications, networks, and access technologies that come together for a dedicated IoT network for a synergistic purpose. Therefore, there is a need for a solution that can assimilate the various requirements and policies to dynamically and intelligently orchestrate them in the dedicated IoT network. Thus we identify and describe a representative industry-relevant use case for such a smart and adaptive environment through interviews with experts from a leading telecommunication vendor. We further propose and evaluate candidate architectures to achieve dynamic and intelligent orchestration in such a smart environment using a systematic approach for architecture design and by engaging six senior domain and IoT experts. The candidate architecture with an adaptive and intelligent element ("Smart AAA agent") was found superior for modifiability, scalability, and performance in the assessments. This architecture also explores the enhanced role of authentication, authorization, and accounting (AAA) and makes the base for complete orchestration. The results indicate that the proposed architecture can meet the requirements for a dedicated IoT network, which may be used in further research or as a reference for industry solutions.

Cadmium Phytotoxicity, Tolerance, and Advanced Remediation Approaches in Agricultural Soils; A Comprehensive Review.

Cadmium (Cd) is a major environmental contaminant due to its widespread industrial use. Cd contamination of soil and water is rather classical but has emerged as a recent problem. Cd toxicity causes a range of damages to plants ranging from germination to yield suppression. Plant physiological functions, i.e., water interactions, essential mineral uptake, and photosynthesis, are also harmed by Cd. Plants have also shown metabolic changes because of Cd exposure either as direct impact on enzymes or other metabolites, or because of its propensity to produce reactive oxygen species, which can induce oxidative stress. In recent years, there has been increased interest in the potential of plants with ability to accumulate or stabilize Cd compounds for bioremediation of Cd pollution. Here, we critically review the chemistry of Cd and its dynamics in soil and the rhizosphere, toxic effects on plant growth, and yield formation. To conserve the environment and resources, chemical/biological remediation processes for Cd and their efficacy have been summarized in this review. Modulation of plant growth regulators such as cytokinins, ethylene, gibberellins, auxins, abscisic acid, polyamines, jasmonic acid, brassinosteroids, and nitric oxide has been highlighted. Development of plant genotypes with restricted Cd uptake and reduced accumulation in edible portions by conventional and marker-assisted breeding are also presented. In this regard, use of molecular techniques including identification of QTLs, CRISPR/Cas9, and functional genomics to enhance the adverse impacts of Cd in plants may be quite helpful. The review's results should aid in the development of novel and suitable solutions for limiting Cd bioavailability and toxicity, as well as the long-term management of Cd-polluted soils, therefore reducing environmental and human health hazards.

Synthesis of ternary-based visible light nano-photocatalyst for decontamination of organic dyes-loaded wastewater.

The release of dyes-loaded wastewater from various industries is a major threat to human beings due to their health hazard effects. Ternary ferrites-based visible light photocatalyst Fe2Zn0.5Cu0.5 O4-CM (CZF-CM) was formed via the co-precipitation method. These prepared ternary ferrites nanoparticles Fe2Zn0.5Cu0.5O4 (CZF-NPs) and photocatalyst (CZF-CM) were analyzed using different spectroscopic techniques. The average crystallite size of CZF-NPs was calculated from XRD data using Scherer's equation and found to be 12 nm. The elemental composition of the synthesized ternary ferrites nanoparticles (CZF-NPs) was defined by the EDX images. The morphology of CZF-CM photocatalyst is spherical, having a smooth surface and average microspheres size of 810 µm based on SEM micrographs. The photocatalyst has bandgap of 2.57 eV, which lies in the visible range of the electromagnetic spectrum derived by extrapolating Tauc's plot. Photocatalyst CZF-CM showed 94% degradation efficiency for Rhodamine B (RB) dye at optimized conditions of initial dye concentration, catalyst dosage, pH and sunlight irradiation contact time as 40 ppm, 0.7 g, pH 8 and 125 min, respectively. Maximum degradation (96%) of methyl orange (MO) dye occurred at pH 6, at similar optimized conditions as the RB dye. The binary ferrites photocatalyst Fe2CuO4-CM (CF-CM) and Fe2ZnO4-CM (ZF-CM) of the selected metals showed lesser photocatalytic efficiency than ternary ferrites. An artificial neural network in addition to the response surface methodology was used for the optimization process. The artificial neural network is highly in agreement with the experimental results obtained for the selected dyes. The corresponding predicted response for each data set from ANOVA showed high R2, R2adj, and R2pred values for the proposed model. It also indicates that contributing parameters in the model are significant due to having very high F-values and low p-values. It is concluded that the synthesized photocatalysts are considered an efficient entrant for the decolorization of industrial wastewater.

Catalytic reduction of 4-nitrophenol and methylene blue pollutants in water by copper and nickel nanoparticles decorated polymer sponges.

In the present study, two catalysts based-on copper and nickel nanoparticles anchored on agarose-coated sponge (Cu-AG-sponge and Ni-AG-sponge) were prepared, respectively. Both catalysts were characterized by analytical techniques of thermogravimetric analysis energy dispersive X-ray spectroscopy (EDX) and scanning electron microscopy (SEM). Spherical Cu and Ni nanoparticles on struts of AG-coated sponge were observed by FESEM and the samples' elemental composition was confirmed by EDX technique. After characterization, the Cu-AG-sponge and Ni-AG-sponge catalysts were tested in 4-nitrophenol (4-NP) and methylene blue dye (MB) reduction in an aqueous medium. The reduction of the 4-NP to 4-aminophenol (4-AP) was achieved up to 95% using the NaBH4 reductant and Cu-AG-sponge and Ni-AG-sponge catalysts, respectively. Similarly, the rate of reduction of MB was faster for the Cu-AG-sponge as compared to the Ni-AG-sponge which was discussed based-on the catalyst morphology and other factors. The high rate of reactions for the 4-NP and MB reduction suggests that the Cu-AG-sponge and Ni-AG-sponge catalyst possess high catalytic efficiency, low cost and good reusability having the potential to be used in similar other reactions.

Development and characterization of regenerable chitosan-coated nickel selenide nano-photocatalytic system for decontamination of toxic azo dyes.

In this investigation, chitosan-coated nickel selenide nano-photocatalyst (CS-NiSe) was successfully prepared through the chemical reduction method. FTIR spectroscopy confirmed the synthesis of CS-NiSe nano-photocatalyst. Further, XRD analysis exhibited a monoclinic crystalline phase of photocatalyst with a crystallite size of 32 nm based on Scherer's equation. The SEM micrographs showed that the photocatalyst has an average particle size of 60 nm. The bandgap of CS-NiSe was (2.85 eV) in the visible region of the spectrum. Due to this reason, the CS-NiSe was applied under solar light illumination for the photocatalytic activity of Erythrosine and Allura red dyes. The CS-NiSe presented the highest degradation efficiency of 99.53% for Erythrosine dye in optimized experimental conditions of 100 min at 30 °C, 30 ppm concentration, pH 5.0, and 0.14 g catalyst dose. For Allura red dye, a high degradation of 96.12% was attained in 120 min at pH 4.0, 100 ppm initial dye concentration, 35 °C temperature, and 0.1 g catalyst dose. The CS-NiSe showed excellent degradation efficiency and reduced to (95% for Erythrosine and 91% for Allura red dye) after five consecutive batches. Moreover, the statistical and neural network modelling analysis showed the significant influence of all studied variables on dyes degradation performance. The results demonstrated that CS-NiSe exhibited excellent photocatalytic performances for Erythrosine and Allura red dyes and could be a better photocatalyst for removing these dyes from industrial effluents.

Photocatalytic degradation of crystal violet dye under sunlight by chitosan-encapsulated ternary metal selenide microspheres.

Organic dyes that are extensively released in wastewater from various industries remain the priority concern in the modern world. Therefore, a novel catalyst, bismuth-iron selenide, was prepared through the solvothermal process for photocatalytic degradation of a carcinogenic crystal violet dye. The catalyst was supported with chitosan to form iron-bismuth selenide-chitosan microspheres (BISe-CM). The synthesized catalyst was composed of iron, bismuth, and selenium in a definite proportion based on EDX analysis. FTIR analysis confirmed the synthesis of BISe-CM from characteristic bands of metal selenium bond as well as the typical bands of chitosan. SEM analysis illustrated the average diameter of the barren catalyst to be 54.8 nm, while the average size of the microspheres was 982.5 um. The BISe-CM has the surface of a pore with an average size of 0.5 um. XRD analysis revealed that the synthesized catalyst was composed of Fe3Se4 and Bi2Se3. The prepared catalyst showed better degradation efficiency for crystal violet dye at optimized conditions under solar irradiation. Employing 0.2 g of BISe-CM resulted in complete degradation for 30 ppm of crystal violet dye in 150 min at pH 8.0. The reusability of the catalyst up to four consecutive times makes it a more attractive and practical candidate. Moreover, the catalyst followed pseudo-first-order kinetics in the decontamination of crystal violet. Conclusively, the novel photocatalyst showed the best decolorizing property of crystal violet under sunlight irradiation and could be a suitable alternative for dye decontamination from wastewater.

Chitosan-capped ternary metal selenide nanocatalysts for efficient degradation of Congo red dye in sunlight irradiation.

Wastewater emerging from the industries containing organic pollutants is a severe threat to humans' health and aquatic life. Therefore, the degradation of highly poisonous organic dye pollutants is necessary to ensure public health and environmental protection. To tackle this problem, visible-light-driven ternary metal selenide nanocomposites were synthesized successfully by the solvothermal method and supported by chitosan microspheres (FeNiSe-CHM). The prepared nanoparticles were capped in chitosan microspheres to avoid leaching and facilitate easy recovery of the catalyst. FTIR spectrum confirmed the synthesis of nanocomposite and nanocomposite-chitosan microspheres (FeNiSe-CHM). Based on the SEM images, the nanomaterial and FeNiSe-CHM has an average particle size of 64 nm and 874 µm, respectively. The presence of iron, nickel and selenium elements in the EDX spectrum revealed the synthesis of FeNiSe-NPs. XRD analysis determined the crystallite structure of nanocomposites as 14.2 nm. The photocatalyst has a crystalline structure and narrow bandgap of 2.09 eV. Moreover, the as-synthesized FeNiSe-CHM were employed for the photodegradation of carcinogenic and mutagenic Congo red dye. The catalyst microspheres showed efficient photocatalytic degradation efficiency of up to 99% for Congo red dye under the optimized conditions of 140 min, pH 6.0, dye concentration 60 ppm and catalyst dose of 0.2 g in the presence of sunlight irradiation following the second-order kinetics. After five consecutive cycles, it showed a slight loss in the degradation efficiency. In conclusion, the results demonstrate a high potential of chitosan-based ternary metal selenide nanocomposites for abatement of dye pollutants from the industrial wastewater.

The frequency of radial artery occlusion following cardiac catheterization with the use of transradial pneumatic compression band.

OBJECTIVES: Radial artery occlusion is a silent complication of a transradial approach to cardiac catheterization that may complicate subsequent transradial procedures in patients undergoing cardiac catheterization. A transradial band reduces vascular complications and provides brisk, powerful and effective haemostasis. The purpose of this study was to assess the frequency of radial artery occlusion in 180 patients undergoing transradial coronary catheterization. RESULTS: The median age of the study cohort was 58 years. Radial artery occlusion was found in 14 (7.8%) patients. When stratifying by age group and sex, there was no significant difference in radial artery occlusion between age groups and sex. It was likewise found that comorbidities such as diabetes mellitus, hypertension and smoking, increased the risk of radial artery occlusion however this was observed to be significant only for diabetes mellitus. We therefore conclude that a transradial pneumatic pressure band is an extremely helpful and safe strategy to prevent radial artery occlusion.

Catalytic potential of cobalt oxide and agar nanocomposite hydrogel for the chemical reduction of organic pollutants.

In this study, cobalt oxide nanoparticles (Co3O4 NPs) were synthesized by precipitation method from cobalt sulphate solution with basic pH, followed by calcination. The ex-situ synthesized Co3O4 NPs were mixed with hot agar (AG) aqueous solution. The preparation of AG- Co3O4 nanocomposite hydrogel was carried out by self-association method promoted by thermal denaturation. The quenching of hot suspension from 80 °C to room temperature resulted in the formation of AG-Co3O4 nanocomposite hydrogel. The as-synthesized AG-Co3O4 was characterized by FTIR, XRD and SEM techniques. In order to test the catalytic activity, AG-Co3O4 was used as a heterogeneous catalyst for the reduction of methylene blue (MB), congo red (CR) and 4-nitrophenol (4-NP). The excellent performance of the AG-Co3O4 was shown by the reaction rate constant (kapp) values of 0.3623, 0.2114 and 0.2893 for MB, 4-NP and CR, respectively. All these results were obtained with R2 above 94 and utilization of an AG-Co3O4 catalyst. Furthermore, the catalytic reduction was studied with varying dye concentration and catalyst dose. This study showed that AG-Co3O4 catalyst has high potential for remediation of environmental pollutants in wastewaters.