Adsorption of phosphorus onto nanoscale zero-valent iron/activated carbon: removal mechanisms, thermodynamics, and interferences

This study investigated removal mechanisms, thermodynamics, and interferences of phosphorus adsorption onto nanoscale zero-valent iron (nZVI)/activated carbon composite. Activated carbon was successfully used as support for nZVI particles to overcome shortcomings of using nZVI include its tendency to aggregate and separation difficulties. A comprehensive characterization was done for the composite particles, which revealed a high specific surface area of 72.66 m2/g and an average particle size of 37 nm. Several adsorption isotherms and kinetic models have been applied to understand the removal mechanisms. Adsorption isotherm is best fitted by Freundlich and Langmuir models, which indicates that the estimated maximum phosphorus adsorption capacity is 53.76 mg/g at pH 4. Adsorption kinetics showed that the chemisorption process behaved according to a pseudo-second-order model. An adsorption mechanism study conducted using the intra-particle diffusion and Boyd kinetic models indicated that the adsorption rate is limited by surface diffusion. A thermodynamic study showed that phosphorus removal efficiency increased as the solution temperature increased from 15 to 37 °C. Finally, the results of an interference study showed that the presence of Ni2+, Cu2+, Ca2+, Na+ cations, nitrate ions (), and sodium acetate improves removal efficiency, while the presence of sulfate ions () and urea reduces removal efficiency.

Examining Impacts of Acidic Bath Temperature on Nano-Synthesized Lead Selenide Thin Films for the Application of Solar Cells

The influence of bath temperature on nano-manufactured PbSe (lead selenide) films was successfully generated by utilizing CBD on the acid solution’s metal surface tool. Pb (NO3)2 was employed as a lead ion source as a precursor, while Na2O4Se was used as a selenide ion source. The XRD characterization revealed that the prepared samples are the property of crystalline structure (111), (101), (100), and (110) Miller indices. The scanning electron microscope indicated that the particles have a rock-like shape. There was a decrement of energy bandgap that is from 2.4 eV to 1.2 eV with increasing temperature 20°C–85°C. Thin films prepared at 85°C revealed the best polycrystal structure as well as homogeneously dispersed on the substrate at superior particle scales. The photoluminescence spectrophotometer witnessed that as the temperature of the solution bath increases from 20°C to 85°C, the average strength of PL emission of the film decreases. The maximum photoluminescence strength predominantly exists at high temperatures because of self-trapped exciton recombination, formed from O2 vacancy and particle size what we call defect centres, for the deposited thin films at 45°C and 85°C. Therefore, the finest solution temperature is 85°C.

PRODUCTIVITY AND QUALITY EVALUATION OF TARRAGON AND THYME GROWN UNDER ARTIFICIAL LIGHT

The research aimed at evaluation of productivity and quality of tarragon and thyme medicinal material was carried out on hydroponic installations during 2019-2020. The objects under study were Monarkh and Gudvin tarragon varieties as well as Medok and Zmeyka thyme varieties. The plants were grown in mineral cotton substratum. Fertikea Hydro complex fertiliser with microelements and calcium nitrate were used. The growing conditions: ambient temperature +22…+25℃, solution temperature +20℃, ambient humidity 55…65%. Experiment regimens: growing under white LEDs (luminous flux 8000 lm, color temperature 4000 K, PPF 165 mkmol/s/m2) and color LEDs (combination of red, blue and white LEDs (32:16:32), luminous flux 6573 lm, PPF 143 mkmol/s/m2), for 16-hour light regimen. We found that thyme grown on a vertical hydroponic system increase its biomass 2.0…3.5 times compared to the conventional growing. The highest productivity of Zmeyka thyme variety is reached under white light, while for both the tarragon varieties and Medok thyme variety it is reached under coloured LEDs. Chlorophyll-a content in green biomass is a little higher under coloured LEDs for Zmeyka thyme variety and Gudvin tarragon variety, while the reverse trend is observed for Monarkh tarragon variety. All the varieties show higher chlorophyll-b content under coloured LEDs. Combined chlorophyll-a and chlorophyll-b content increases under coloured LEDs for the thyme varieties and Gudvin tarragon variety. Monarkh tarragon variety shows the highest combined chlorophyll content under white LEDs. Carotenoid concentration in Medok thyme variety and Monarkh tarragon variety is higher under white LEDs and it is higher under color LEDs for the rest of the varieties. Flavonoids in the studied varieties accumulate statistically better (1.5…3.0 times) under white LEDs

Reversible down-regulation and up-regulation of catalytic activity of poly(N-isopropylacrylamide)-anchored gold nanoparticles

Regulating catalytic activity plays an important role in further optimizing and developing multifunctional catalysts with high selectivity and high activity. Reversible dual regulation of catalytic activity has always been a challenging task. Here, we prepared poly(N-isopropylacrylamide)-anchored gold nanoparticles (AuNP@CDs-Azo-PNIPAM) through host-guest interaction of cyclodextrin capped gold nanoparticles (AuNP@CDs) and azobenzene-terminated poly(N-isopropylacrylamide) (Azo-PNIPAM). Azo-PNIPAM as thermal and light responsive ligand allows reversible dual regulation of catalytic activity. When the temperature is higher than the lowest critical solution temperature (LCST), the PNIPAM chain shrinks rapidly, increasing the steric hindrance around AuNPs and reducing the catalytic activity. Under ultraviolet light irradiation, cis-azobenzene disassembles from cyclodextrin and the number of surface active sites of AuNPs increases, which improves the catalytic activity. The reaction rate of UV irradiation is almost 1.3 times that of visible light irradiation. This work provides a simple and effective strategy for the construction of reversible catalysts.

Low-Cost and Eco-Friendly Hydroxyapatite Nanoparticles Derived from Eggshell Waste for Cephalexin Removal

This work describes the hydroxyapatite nanoparticle (HAP) preparation from eggshell waste and their application as an adsorbent for Cephalexin (Ceph) antibiotic removal from aqueous solutions. Chemical precipitation with phosphoric acid was used to evaluate the feasibility of calcium oxide for HAP preparation. The structural properties of HAP were characterized by X-ray diffraction, which revealed the formation of the hydroxyapatite crystalline phase formation. In addition, transmitting electron spectroscopy showed an irregular shape with a variation in size. The impact of various experimental conditions on the removal efficiency such as the solution’s pH, contact time, HAP mass, solution temperature, and Ceph concentration were studied. Experimental data showed that HAP could remove most Ceph species from aqueous solutions within 1 h at pH = 7 with 70.70% adsorption efficiency utilizing 50 mg of the HAP. The removal process of Ceph species by HAP was kinetically investigated using various kinetic models, and the results showed the suitability of the pseudo-second-order kinetic model for the adsorption process description. Moreover, the removal process was thermodynamically investigated; the results showed that the removal was spontaneous endothermic and related to the randomness increase. The data confirmed that HAP had high efficiency in removing Ceph antibiotics from an aqueous solution.

Removing The Acid Orange 12 Azo Dye from Aqueous Solution Using Sodium Hypochlorite, A Kinetic and Thermodynamic Study

This study investigated the feasibility of using sodium hypochlorite as an advanced oxidation process to remove Acid Orange 12 azo dye from wastewater. For this purpose, batch reactor experiments were done. Several variables to address the efficiency of using this process were considered. These variables are initial pH (5, 7, and 9), the concentration of hypochlorite (50 – 250 mg/l), temperature (20-50) degrees Celsius, and time of electrolysis (1-75) min. also investigate the effects of UV on the process was done. Experimental results showed that the color removal efficiency using NaOCl with UV is more effective than NaOCl alone. The highest removal efficiency was obtained by increasing the concentration of NaOCl from (50-250mg/l) at PH=5. When the solution temperature was increased from (20-50) °C, the removal efficiency increased, and at the same time, the time required was reduced from (20-5) minutes to obtain the highest removal efficiency. The kinetic study also showed that the oxidation process follows a second-order reaction. The thermodynamic functions indicate that the response is spontaneous, endothermic, and increases randomness.

A Rapid and Sensitive Method for the Simultaneous Determination of Multipolar Compounds in Plant Tea by Supercritical Fluid Chromatography Coupled to Ion Mobility Quadrupole Time-of-Flight Mass Spectrometry

In this study, matrix solid phase dispersion (MSPD) microextraction combined with supercritical fluid chromatography-ion mobility quadrupole time-of-flight mass spectrometry (SFC/IM-QTOF-MS) was used to analyze the multipolar compounds in plant tea. The parameters of stationary phase, mobile phase, make-up solution, temperature, and back pressure were optimized. The target analytes were gradient eluted in 8 min by supercritical CO2 on a Zorbax RX-SIL column. Collisional Cross Section (CCS) values for single and multiple fields were measured. A series of validation studies were carried out under the optimal conditions, and the linear relationship and reproducibility were good. The limits of detection were 1.4 (Scoparone (1))~70 (Naringenin (4)) ng/mL, and the limits of quantification were 4.7 (Scoparone (1))~241 (Naringenin (4)) ng/mL. The recoveries of most compounds ranged from 60.7% to 127%. As a consequence, the proposed method was used for the separation and quantitative analysis of active ingredients in caulis dendrobii.

Optimization of a Solution Treatment in the Al-Cu-Mg-Ag Alloy via a Microstructural Investigation

We investigated the effect of solution temperature (Tsol. = 440–530 °C) on the mechanical properties of the Al–3.4Cu–0.34Mg–0.3Mn–0.17Ag alloy, finding that the investigated Al alloy showed the highest mechanical strength of σUTS = ~329 MPa at a Tsol. value of 470 °C. The microstructural investigation demonstrates that the mechanical properties for different Tsol. values stem from grain growth, precipitation hardening, and the formation of large particles at the grain boundaries. On the basis of Tsol. = 470 °C, the effect of each microstructural evolution is significantly different on the mechanical properties. In this study, the relationships between the microstructural evolution and the mechanical properties were investigated with respect to different values of Tsol.

RAFT Emulsion Polymerization of Styrene Using a Poly((N,N-dimethyl acrylamide)-co-(N-isopropyl acrylamide)) mCTA: Synthesis and Thermosensitivity

Thermoresponsive poly((N,N-dimethyl acrylamide)-co-(N-isopropyl acrylamide)) (P(DMA-co-NIPAM)) copolymers were synthesized via reversible addition−fragmentation chain transfer (RAFT) polymerization. The monomer reactivity ratios were determined by the Kelen–Tüdős method to be rNIPAM = 0.83 and rDMA = 1.10. The thermoresponsive properties of these copo-lymers with varying molecular weights were characterized by visual turbidimetry and dynamic light scattering (DLS). The copolymers showed a lower critical solution temperature (LCST) in water with a dependence on the molar fraction of DMA in the copolymer. Chaotropic and kosmotropic salt anions of the Hofmeister series, known to affect the LCST of thermoresponsive polymers, were used as additives in the aqueous copolymer solutions and their influence on the LCST was demonstrated. Further on, in order to investigate the thermoresponsive behavior of P(DMA-co-NIPAM) in a confined state, P(DMA-co-NIPAM)-b-PS diblock copolymers were prepared via polymerization induced self-assembly (PISA) through surfactant-free RAFT mediated emulsion polymerization of styrene using P(DMA-co-NIPAM) as the macromolecular chain transfer agent (mCTA) of the polymerization. As confirmed by cryogenic transmission electron microscopy (cryoTEM), this approach yielded stabilized spherical micelles in aqueous dispersions where the PS block formed the hydrophobic core and the P(DMA-co-NIPAM) block formed the hydrophilic corona of the spherical micelle. The temperature-dependent behavior of the LCST-type diblock copolymers was further studied by examining the collapse of the P(DMA-co-NIPAM) minor block of the P(DMA-co-NIPAM)-b-PS diblock copolymers as a function of temperature in aqueous solution. The nanospheres were found to be thermosensitive by changing their hydrodynamic radii almost linearly as a function of temperature between 25 °C and 45 °C. The addition of kosmotropic salt anions, as a potentially useful tuning feature of micellar assemblies, was found to increase the hydrodynamic radius of the micelles and resulted in a faster collapse of the micelle corona upon heating.