Revealing the mechanism of quartz sand seeding in accelerating phosphorus recovery from anaerobic fermentation supernatant through vivianite crystallization.

The recovery of phosphorus (P) through vivianite crystallization offers a promising approach for resource utilization in wastewater treatment plants. However, this process encounters challenges in terms of small product size and low purity. The study aimed to assess the feasibility of using quartz sand as a seed material to enhance P recovery and vivianite crystal characteristics from anaerobic fermentation supernatant. Various factors, including seed dosage, seed size, Fe/P ratio, and pH, were systematically tested in batch experiments to assess their influence. Results demonstrated that the effect of seed enhancement on vivianite crystallization was more pronounced under higher seed dosages, smaller seed sizes, and lower pH or Fe/P ratio. The addition of seeds increased P recovery by 4.43% in the actual anaerobic fermentation supernatant and also augmented the average particle size of the recovered product from 19.57 to 39.28 µm. Moreover, introducing quartz sand as a seed material effectively reduced co-precipitation, leading to a notable 12.5% increase in the purity of the recovered vivianite compared to the non-seeded process. The formation of an ion adsorption layer on the surface of quartz sand facilitated crystal attachment and growth, significantly accelerating the vivianite crystallization rate and enhancing P recovery. The economic analysis focused on chemical costs further affirmed the economic viability of using quartz sand as a seed material for P recovery through vivianite crystallization, which provides valuable insights for future research and engineering applications.

Complementary Operando Electrochemical Quartz Crystal Microbalance and UV/Vis Spectroscopic Studies: Acetate Effects on Zinc-Manganese Batteries.

Zinc-ion batteries, in which zinc ions and protons do intercalation and de-intercalation during battery cycling with various proposed mechanisms under debate, have been studied. Recently, electrolytic zinc-manganese batteries, exhibiting the pure dissolution-deposition behavior with a large charge capacity, have been accomplished through using electrolytes with Lewis acid. However, the complicated chemical environment and mixed products hinder the investigation though it is crucial to understand the detailed mechanism. Here, cyclic voltammetry coupled electrochemical quartz crystal microbalance (EQCM) and ultraviolet-visible spectrophotometry (UV-Vis) are respectively, for the very first time, used to study the transition from zinc-ion batteries to zinc electrolytic batteries by the continuous addition of acetate ions. These complementary techniques operando trace the mass and the composition evolution. The observed formation and dissolution of zinc hydroxide sulfate (ZHS) and manganese oxides evince the effect of acetate ions on zinc-manganese batteries from an alternative perspective. Both the amount of acetate and the pH value have large impacts on the capacity and Coulombic efficiency of the MnO2 electrode, and thus they should be optimized when constructing a full zinc-manganese battery with high rate capability and reversibility.

Biomimetic Nanotechnology Vol. 3.

Biomimetic nanotechnology pertains to the fundamental elements of living systems and the translation of their properties into human applications. The underlying functionalities of biological materials, structures and processes are primarily rooted in the nanoscale domain, serving as a source of inspiration for materials science, medicine, physics, sensor technologies, smart materials science and other interdisciplinary fields. The Biomimetics Special Issues Biomimetic Nanotechnology Vols. 1-3 feature a collection of research and review articles contributed by experts in the field, delving into significant realms of biomimetic nanotechnology. This publication, Vol. 3, comprises four research articles and one review article, which offer valuable insights and inspiration for innovative approaches inspired by Nature's living systems. The spectrum of the articles is wide and deep and ranges from genetics, traditional medicine, origami, fungi and quartz to green synthesis of nanoparticles.

Quartz Crystal Microbalance Technology Coupled with Impedance for the Dynamic Monitoring of the Cardiomyocyte Beating Function and Drug Screening.

The main sensing techniques used to study myocardial pulsation are electrical impedance sensing (EIS) and by quartz crystal microbalance (QCM). While electrical impedance technology is the gold standard for the study of myocardial pulsation, the clinical application of drugs is being followed up in real time additionally, thus, QCM technology needs to be further developed as a very important class of quality sensor technology. Moreover, the application of EIS, in combination with the QCM, for monitoring myocardial pulsation, has been rarely reported. In this paper, a series of cell growth and adhesion conditions were optimized using rat primary cardiomyocytes, and QCM was used in combination with EIS to monitor the adhesion and the myocardial pulsation ability of the cells in real time. Furthermore, cardiomyocytes that adhered to the QCM and EIS were treated with isoprenaline (ISO), a positive inotropic drug, and verapamil (VRP), a negative inotropic drug. Next, the cell index (CI)-time (T) plots, beating amplitude (BA) and beating rate (BR) of the cardiomyocytes were calculated and changes in these parameters, before and after, dosing were evaluated. The results showed that the QCM technique results were not only consistent with the results obtained with EIS, but also that the QCM technique had a certain degree of sensitivity for the calculation of cardiomyocyte beating. Thus, our findings validate the reliability and validity of the QCM technique for measuring cardiomyocyte beating and drug testing. We hope that further studies would evaluate the application of the QCM technology for clinical use.

Smart bio-nano interface derived from zein protein as receptors for biotinyl moiety.

Proteinaceous, tunable nanostructures of zein (prolamine of corn) were developed as biotinyl-specific receptors using a molecular imprinting technique. Sacrificial templates, such as latex beads (LB3) and anodized alumina membrane (AAM), have been used to control nanostructural patterns in biotin-imprinted zein (BMZ). Briefly, a methanolic solution of the zein-biotin complex was drop cast upon a self-organized LB3 and AAM templates on Au/quartz surfaces. Subsequent dissolution of these sacrificial templates affords highly oriented, predetermined, and uniformly grown hyperporous (300 nm) and nanowires (150 nm) motifs of zein (BMZ-LB3 and BMZ-AAM), as shown by scanning electron microscopy (SEM). Selective extraction of biotin molecular template cast-off site-selective biotin imprints within these zein nanostructures complementary to biotinyl moieties. Alternatively, biotin-imprinted zein nanoparticles (BMZ-Np) and thin film (BMZ-MeOH) were prepared by coacervation and drop casting methods, respectively. Density functional theoretical (DFT) studies reveal strong hydrogen-bonded interaction of biotin with serine and glutamine residues of zein. Quartz crystal microbalance (QCM) studies show remarkable sensitivity of the hyperporous-BMZ-LB3 and nanowires of BMZ-AAM towards biotin derivative (biotin methyl ester) by five (24.75 ± 1.34 Hz/mM) and four (18.19 ± 0.75 Hz/mM) times, respectively, higher than the BMZ-MeOH. Enhanced permeability features of the zein nanostructures, when templated with LB3, enable the QCM detection of biotin- or its derivatives down to 12.9 ng mL-1 from dairy products (Kefir). The outcome of this study shall be a key aspect in interfacing biological materials with micro-/nano-sensors and electronic devices for detecting pertinent analytes using sustainably developed biopolymer-based nanostructures.

A highly sensitive method for uranium quantification in water samples at ultra-trace level by total reflection X-ray fluorescence, after its direct pre-concentration on the surface of amidoxime functionalized quartz sample supports.

In this work we have developed a Total reflection X-Ray Fluorescence (TXRF) based methodology for the determination of uranium in natural water samples at ultra-trace concentration level. The methodology involves functionalization of quartz sample supports used for TXRF measurements with (3-Amidoxy) triethoxysilane, which has very high uranium uptake efficiency. (3-Amidoxy) triethoxysilane has been synthesized from (3-Cyanopropyl) triethoxysilane (CPTS). This amidoxime functionalized sample supports, simply needed to be dipped in the uranium solution for 3 h after which, it can be directly taken for TXRF measurements. The developed methodology is very fast, simple with less sample preparation steps involved. The present work utilizes Rayleigh scattered peak to construct the calibration curve for the quantification purpose. The developed methodology has improved accuracy as well as precision for the quantification of uranium at such low concentrations level. The detection limit and accuracy obtained are 0.013 ng/mL (13 ppt) and 1.9%, respectively which are the lowest using any X-Ray Fluorescence based method, to the best of our knowledge. The method was successfully applied for the U determination in natural water samples like ground water, river water and sea water.

Life cycle assessment of waste printed wiring board-derived Ag photocatalyst for sustainable fermentable sugar production.

An exploratory work involving waste printed wiring board (WPWB)-derived inexpensive silver oxide (Ag2O)-grafted silica-alumina composite photocatalyst (SAA) using quartz halogen and UVA irradiations (QHUV) (wavelength: 315 nm-1000 nm) has been revealed. The efficacy of the novel SAA photocatalyst was assessed in the synthesis of fermentable sugar (FS) by photo-hydrolysis of pure crystalline cellulose (PCC) in the QHUV-assisted batch reactor (QHUVBR), and the process parameters (5% AgNO3 doping, 7.5% catalyst concentration, 20 min PH time, and 80 °C PH temperature) were optimized using Taguchi orthogonal array design. The BET analysis of the optimal SAA catalyst possessed high surface area (27.24 m2/g), high pore volume, and pore diameter (0.042 cc/g and 13.1684 nm), respectively, whereas the XRD indicated the presence of significant crystalline phases of Ag2O. EDS mapping displayed the uniform distribution of silver active sites on silica-alumina support of the optimal SAA photocatalyst. The optimized parametric conditions in QHUVBR resulted in a maximum FS yield of 77.53% which was significantly higher compared to that achieved (34.52%) in a conventionally heated batch reactor (CHBR). Besides, the energy consumption was 75% more in CHBR (600 W) in comparison with QHUVBR (150 W), making the process energy-efficient and cost-effective. The environmental sustainability could be ascertained from the life cycle assessment (LCA) study in terms of low climate change, ionizing radiation, metal depletion, human toxicity, and other potential indicator values.

Highly Sensitive and Real-Time Detection of Zinc Oxide Nanoparticles Using Quartz Crystal Microbalance via DNA Induced Conjugation.

With the development of nanotechnology, nanomaterials have been widely used in the development of commercial products. In particular, zinc oxide nanoparticles (ZnONPs) have been of great interest due to their extraordinary properties, such as semiconductive, piezoelectric, and absorbance properties in UVA and UVB (280-400 nm) spectra. However, recent studies have investigated the toxicity of these ZnONPs; therefore, a ZnONP screening tool is required for human health and environmental problems. In this study, we propose a detection method for ZnONPs using quartz crystal microbalance (QCM) and DNA. The detection method was based on the resonance frequency shift of the QCM. In detail, two different complementary DNA strands were used to conjugate ZnONPs, which were subjected to mass amplification. One of these DNA strands was designed to hybridize to a probe DNA immobilized on the QCM electrode. By introducing the ZnONP conjugation, we were able to detect ZnONPs with a detection limit of 100 ng/mL in both distilled water and a real sample of drinking water, which is 3 orders less than the reported critical harmful concentration of ZnONPs. A phosphate terminal group, which selectively interacts with a zinc oxide compound, was also attached at one end of a DNA linker and was attributed to the selective detection of ZnONPs. As a result, better selective detection of ZnONPs was achieved compared to gold and silicon nanoparticles. This work demonstrated the potential of our proposed method as a ZnONP screening tool in real environmental water systems.

Effects of mineral species and petroleum components on thermal desorption behavior of petroleum-contaminated soil.

Thermal desorption (TD) behavior of high-concentration petroleum-contaminated soil (PCS) is affected by soil composition, especially inorganic minerals. In this study, the TD behavior of petroleum-contaminated quartz (original mineral) and kaoline (clay mineral) were compared with those of pure petroleum (Petro-free); their "saturate, aromatic, resin, and asphaltenes" (SARA) fractions were investigated using thermogravimetry and differential thermogravimetry (TG-DTG). The modelling of the petroleum removal kinetics was also analyzed to provide insights into the mechanism. The results revealed that the limiting factor controlling the desorption of petroleum from quartz (Petro-Qtz) and kaoline (Petro-Kln) is the minerals, which increased the effective TD temperature by 200 °C and decreased TD efficiency by 2%. Compared to Petro-Qtz, Petro-Kln showed a lower desorption efficiency of 5% and the process was accomplished at a higher temperature of 100 °C. The investigation on SARA fractions indicated that polar fractions (i.e., aromatics, resins, and asphaltenes) were strongly captured by the minerals. The increment of the TD temperature of petroleum (resins-160 °C > aromatics-20 °C > saturates-5 °C) increased with the polarity of petroleum components. These results could be validated by thermogravimetry-gas chromatography/mass spectroscopy (TG-GC/MS) through the delayed desorption of naphthalene and acenaphthene. Furthermore, the increment of the TD temperature of SARA fractions on kaoline was higher than those on quartz. This makes sense because the kaoline decreased the diffusion of hydrocarbons due to its porosity features and higher specific surface area (kaoline 5.3300 m2 g-1, quartz 0.1153 m2 g-1). In addition, the analysis of the desorption kinetic models showed that the observed hysteresis was related to the diffusion barrier caused by chemisorption (n＜1). In consequence, the Petro-Kln showed a lower desorption efficiency, a slower desorption, and as a result, a higher energy consumption (0.476 kW h) for thermal remediation than Petro-Qtz (0.238 kW h).

Theaflavin and its derivatives exert antibacterial action against Bacillus coagulans through adsorption to cell surface phospholipids.

AIMS: To investigate the antibacterial effects of tea theaflavins and catechins against Bacillus coagulans and the underlying mechanism of antibacterial action. METHODS AND RESULTS: Bactericidal activities of theaflavin and its analogues were evaluated and compared with that of epigallocatechin gallate. Theaflavin derivatives exhibited high bactericidal activity at 50 µmol L-1 , whereas epigallocatechin gallate did not, even at 500 µmol L-1 . Furthermore, we investigated the adsorption of theaflavins to model phospholipid membranes and corresponding effects on membrane fluidity to reveal their effects on the B. coagulans cell surface. Cell membrane fluidity was decreased after treatment with theaflavin derivatives with one or more galloyl moieties. Quartz-crystal microbalance analysis showed a strong affinity of the membrane phosphatidyl glycerol (PG) bilayers for theaflavin derivatives, correlating their bactericidal activity. CONCLUSION: These findings suggest that theaflavins could effectively inhibit B. coagulans by decreasing cell membrane fluidity. SIGNIFICANCE AND IMPACT: Bacillus coagulans is a spore-forming heat-resistant bacterium responsible for spoilage in low-acidic beverages. Natural antimicrobial components in tea-based beverages are central to reducing microbial contamination and product quality deterioration, although mechanisms underlying their antimicrobial action remain obscure. This study highlights the inhibitory action of theaflavins on B. coagulans and their potential application in food and beverage industries.

High throughput onion-like liposome formation with efficient protein encapsulation under flash antisolvent mixing.

Achieving a high encapsulation efficiency and loading capacity of proteins in lecithin-based liposomes has always been a challenge. Here, we use Flash Nano-Precipitation (FNP) to produce liposomes and investigated the encapsulation of model protein (Bovine Serum Albumin, BSA). Through rapid turbulent mixing, we obtained liposomes with small size, low polydispersity, and good batch repeatability at a high production rate. We demonstrated that the bilayer of liposomes prepared solely using lecithin was defective, which led to the fusion, and increased size and polydispersity. When cholesterol was added to reach a lecithin-to-cholesterol molar ratio of 5:3, a compact bilayer formed to effectively inhibit liposome fusion. The encapsulation efficiency and loading capacity of BSA was as high as âˆ¼ 68% and âˆ¼ 6% in lecithin-cholesterol liposome, respectively, far exceeding the values reported in the literature. Further study by Quartz Crystal Microbalance with Dissipation (QCM-D) revealed that the highly effective encapsulation was due to the rapid mutual adsorption between BSA and defective/curved lecithin double layers during the liposome formation. Such rapid mutual adsorption leads to the layer-by-layer assembly and formation of onion-like compact liposome structure as revealed by Cryo-TEM. This simple FNP method provides a scalable manufacturing approach for liposomes with efficient protein encapsulation. The revealed adsorption mechanism between protein and lecithin bilayers could also serve as a guide for similar studies.

E-waste derived silica-alumina for eco-friendly and inexpensive Mg-Al-Ti photocatalyst towards glycerol carbonate (electrolyte) synthesis: Process optimization and LCA.

Valorization ofe-waste, i.e. waste printed circuit board (WPCB) through mechano-chemical activation to obtain silica as the catalyst support and alumina as the catalyst precursor for eco-friendly synthesis of inexpensive highly proficient photocatalyst has been explored. The WPCB derived silica-supported layered double oxide photocatalyst (MATLSW) and its counterpart (MATLSC) involving commercial silica and alumina precursors were synthesized through the wet-impregnation method under energy-efficient solar simulated quartz halogen lamp (SSQHL) irradiations to improve its photocatalytic properties compared to conventional methods. The prepared MATLSWpossessed a significantly low band-gap-energy (1.58 eV) that rendered efficient photocatalysis in the green-synthesis of glycerol carbonate (GC) (an effective electrolyte). The catalytic performance of the optimal MATLSWresulted in a superior yield of GC (98.68%) compared to that rendered by MATLSCcatalyst (GC yield: 96.56%) at optimal process conditions. Detailed life cycle assessment (LCA) of the entire process (deploying Ecoinvent 3.5 database) dictated conducive environmental impacts concerning 1 kg GC synthesis alongside a scale-up study for 1 MT GC synthesis encompassing silica-alumina extraction from WPCB, MATLSW preparation, and employment of SSQHL-radiated batch reactor (SSQHLBR) (56.64% less energy consumption than conventional). The overall process deploying the novel MATLSWin conjunction with the effectual reactor demonstrated superiority over the conventional GC synthesis process through appreciable reductions of environmental impact parameters, namely GWP, FDP, and HTP by 5.78%, 3.60%, and 5.72% respectively. The developed green process for e-waste utilization can procreate an effective waste management protocol towards a cleaner world.

A study of vegetable oil modified QCM sensor to detect ß-pinene in Indian cardamom.

A quartz crystal microbalance (QCM) sensor was developed in this study with the vegetable oil from olive (OLV-QCM) to detect an important volatile organic compound, ß-pinene in Indian cardamom. Hydrophobic vegetable oil from olive, which contains oleic acid and omega-9, a monounsaturated fatty acid was found to be suitable for binding ß-pinene through non-covalent bonds. The fabricated QCM sensor coating was examined with the field emission scanning electron microscope (FESEM) and Fourier-transform infrared spectroscopy (FTIR) to determine its surface morphology and chemical compositions. The sensitivity, reproducibility, repeatability, and reusability were studied for the developed sensor. Notably, the sensor was observed to be highly selective towards ß-pinene as compared to the other volatile components present in cardamom. The limit of detection (LOD) and limit of quantitation (LOQ) parameters were determined as 5.57 mg L-1 and 18.57 mg L-1, respectively. Moreover, the adsorption isotherm models of the sensor were studied to validate the physical adsorption affinity towards ß-pinene applying Langmuir, Freundlich, and Langmuir-Freundlich isotherm models. The sensor showed a correlation factor of 0.99 with the peak area percentage of gas chromatography-mass spectrometry (GC-MS) analysis for ß-pinene in cardamom samples. The sensor was prepared with natural vegetable oil, unlike health hazard chemicals. In addition to this, the low-cost, easy fabrication process ensured the suitability of the sensor for practical deployment.

Episodes of fissure formation in the Alps: connecting quartz fluid inclusion, fissure monazite age, and fissure orientation data.

Fluid assisted Alpine fissure-vein and cleft formation starts at prograde, peak or retrograde metamorphic conditions of 450-550 °C and 0.3-0.6 GPa and below, commonly at conditions of ductile to brittle rock deformation. Early-formed fissures become overprinted by subsequent deformation, locally leading to a reorientation. Deformation that follows fissure formation initiates a cycle of dissolution, dissolution/reprecipitation or new growth of fissure minerals enclosing fluid inclusions. Although fissures in upper greenschist and amphibolite facies rocks predominantly form under retrograde metamorphic conditions, this work confirms that the carbon dioxide fluid zone correlates with regions of highest grade Alpine metamorphism, suggesting carbon dioxide production by prograde devolatilization reactions and rock-buffering of the fissure-filling fluid. For this reason, fluid composition zones systematically change in metamorphosed and exhumed nappe stacks from diagenetic to amphibolite facies metamorphic rocks from saline fluids dominated by higher hydrocarbons, methane, water and carbon dioxide. Open fissures are in most cases oriented roughly perpendicular to the foliation and lineation of the host rock. The type of fluid constrains the habit of the very frequently crystallizing quartz crystals. Open fissures also form in association with more localized strike-slip faults and are oriented perpendicular to the faults. The combination of fissure orientation, fissure quartz fluid inclusion and fissure monazite-(Ce) (hereafter monazite) Th-Pb ages shows that fissure formation occurred episodically (1) during the Cretaceous (eo-Alpine) deformation cycle in association with exhumation of the Austroalpine Koralpe-Saualpe region (~ 90 Ma) and subsequent extensional movements in association with the formation of the Gosau basins (~ 90-70 Ma), (2) during rapid exhumation of high-pressure overprinted Briançonnais and Piemontais units (36-30 Ma), (3) during unroofing of the Tauern and Lepontine metamorphic domes, during emplacement and reverse faulting of the external Massifs (25-12 Ma; except Argentera) and due to local dextral strike-slip faulting in association with the opening of the Ligurian sea, and (4) during the development of a young, widespread network of ductile to brittle strike-slip faults (12-5 Ma). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s00015-021-00391-9.

Determination of nickel in daphne tea extract and lake water samples by flame atomic absorption spectrophotometry with a zirconium-coated T-shaped slotted quartz tube-atom trap and photochemical vapor generation sample introduction.

Nickel determination is important because of its use in many industrial areas and its negative effects on human health. In this study, an ultraviolet-based photochemical vapor generation (UV-PVG) setup was combined with a T-shaped zirconium-coated slotted quartz tube-atom trapping (T-SQT-AT) apparatus to boost the sensitivity of a flame atomic absorption spectrophotometer for nickel determination. Nickel was separated from the sample matrix by converting it into its volatile species prior to online preconcentration by trapping on the zirconium-coated T-SQT inner surface. Analytical performance was maximized by optimizing all variable conditions. The limit of detection (LOD) and limit of quantification (LOQ) were found as 10 and 33 µg/L, respectively. Daphne tea and lake water samples were analyzed under optimum conditions, and there was no detectable nickel in the samples. For this purpose, spiking experiments were carried out for the samples in order to evaluate the applicability and accuracy of the method. The percent recovery values calculated for the two samples spiked at three different concentrations ranged between 90 and 112%. To our best knowledge, this is the first study in literature where UV-PVG was combined with T-SQT-AT for the determination of nickel in daphne tea and lake water samples prior to FAAS determination.

Grain-surface microtextures in deposits affected by periglacial conditions (Abalakh High-Accumulation Plain, Central Yakutia, Russia).

Our paper describes and interprets grain microtexture and microstructure collected from periglacial sediments on the Abalakh High-Accumulation Plain (AHAP) in Central Yakutia. This territory occupies the Lena-Amga Rivers interfluve. In borehole 18/1, five sediment Complexes (I-V) of successive environments were recognized: 1) alluvial in the base of the borehole-Complex I; 2) alluvial-lake-Complex II; 3) lake-complex-Complex III; 4) ice-complex (yedoma)-Complex IV; and finally 5) a Holocene cover-Complex V. Quartz sand-grain and silt-grain microtextural analysis was undertaken in a scanning electron microscope (SEM) and supplemented by mineralogical analyses to reconstruct the sedimentary-accumulation environment, discern the influence of periglacial conditions on the grains, and identify the sediment source(s) for each complex. Based on the results, a conclusion can be reached that the accumulation of Complex I took place as a result of multiple repetitive transportation events recycling the same material and introducing a limited supply of new material into the fluvial environment. Upward in the succession, fluvial-process activities decreased in favour of lake-deposit accumulation. Frozen syngenetic ice-rich silty deposits-yedoma or ice complex-of Complex IV are composed of grains with a precipitated surface, but differ from the underlying deposits in the degree of crusting and mineralogy. Most probably aeolian processes are responsible for their transport. They include a variety of sediments, including older-sourced sediments such as retransported loess and the detritus from mechanical weathering coeval with sediment accumulation. Traces of frost and chemical weathering have been identified on the grain surfaces, the former visible in the form of breakage blocks and conchoidal fracture microtextures and the latter - as surface crusting. However, the frequencies of these microtextures are low, which suggests a relatively high rate of sediment accumulation.

Preservation of Aloe vera and soybean flour fortified Granny Smith apple through optimised quartz-halogen radiated vacuum drying: kinetics and quality evaluation.

BACKGROUND: Granny Smith (GS) apple has low protein content and poor antimicrobial properties; hence it has been blended with Aloe vera (AV; high ascorbic acid, antimicrobial and antioxidant properties) and soybean flour (SF; rich in phenols, flavonoids, ascorbic acid, total antioxidant and protein) in different proportions to obtain fortified GS, i.e. GSAVSF. Moreover, GS being a perishable fruit, its moisture content should be reduced to enhance shelf life. Accordingly, this GSAVSF was osmotically pre-dehydrated and finally dried through energy-efficient quartz-halogen radiation (QHR) assisted vacuum-drying (QHRVD) to produce dried GSAVSF i.e. (DGSAVSF) under optimized conditions. RESULTS: The optimally dehydrated DGSAVSF product resulted in minimum moisture (4.85% w/w) and maximum protein (6.24 g kg-1 ) content. The application of osmotic dehydration and QHRVD afforded acceptable colour of DGSAVSF compared to GSAVSF (ΔEI * = 10.07 ± 0.21). A parametric drying model was formulated that corroborated well with Fick's equation. QHRVD rendered high moisture diffusivity (1.49 × 10-8 m2 s-1 ) and low activation energy (27.64 kJ mol-1  K-1 ). Appreciable quality improvements with respect to fresh GS concerning ascorbic acid (176.05%), total phenolic (579.07%), total flavonoid (333.33%) contents and 2,2'-diphenyl-1-picrylhydrazyl radical scavenging activity (446.71%) could be achieved. The product demonstrated satisfactory shelf life (1 × 104 CFU g-1 : aerobic mesophilic; 1 × 104 CFU g-1 : mould and yeast) and high rehydration ratio (4.25 ± 0.1). CONCLUSION: The enrichment of GS with AV and SF along with optimal drying protocols could provide a quality fortified DGSAVSF through an energy-proficient sustainable process. The highly nutritious product with suitable colour, microbial stability and rehydration ratio also satisfied a 9-point hedonic scale, thus confirming consumer acceptability. © 2020 Society of Chemical Industry.

An accurate determination method for cobalt in sage tea and cobalamin: Slotted quartz tube-flame atomic absorption spectrometry after preconcentration with switchable liquid-liquid microextraction using a Schiff base.

This study reports a stepwise optimization of switchable liquid-liquid microextraction (SLLME) for cobalt determination by flame atomic absorption spectrometry (FAAS) coupled with a slotted quartz tube (SQT). The main purpose of this study was to develop an accurate and sensitive analytical method for cobalt. Extraction method was used to separate and preconcentrate cobalt from sage tea and vitamin B12 samples after complexing with a Schiff base ligand. 107.7 folds enhancement in detection power under the optimum conditions was recorded with respect to direct FAAS. This enhancement correlated to 3.1 µg/L limit of detection and 10 µg/L limit of quantification. The SLLME-SQT-FAAS method was linear over a broad concentration range and low %RSD values established high precision for the method. Appreciable percent recovery results (94-108%) obtained from spiked sage sample and from cobalamin also validated the accuracy of the method.

Changes in IR band areas and band shifts during water adsorption to lecithin and ceramide.

Adsorption of water to a phospholipid (lecithin) and a ceramide were studied by IR microspectroscopy equipped with a humidity control system and quartz crystal microbalance (QCM). The water weight ratios increase up to 12.2 wt% for lecithin and 1.2 wt% for ceramide at RH ~80%, with linear correlations with infrared OH (+NH) band areas. For lecithin, the 1230 cm-1 band (PO2-) and the 1735 cm-1 band (CO) shift to lower wavenumbers, while the 1060 cm-1 band (PO2-, POC) shift to higher wavenumber with RH. Band areas of phosphates (1230 and 1060 cm-1) increase with RH showing positive relations with the band area of bound water. Bound water molecules with shorter H bonds might be bound to these phosphate groups. Band areas of aliphatic CHs are negatively correlated with the increasing adsorption of free water. Free water molecules with longer H bonds might interact loosely with aliphatic chains of lecithin. For ceramide, only the 1045 cm-1 band (CO) shows a small red shift at higher RHs than 60%, indicating adsorption of bound water to CO bonds. Amounts of water molecules adsorbed to ceramide are very limited due to few adsorption of free water.

Accurate and sensitive determination of lead in black tea samples using cobalt magnetic particles based dispersive solid-phase microextraction prior to slotted quartz tube-flame atomic absorption spectrometry.

Newly developed combination of magnetic cobalt particles based dispersive solid-phase microextraction (Co-MP-DSPME) and slotted quartz tube attached flame atomic absorption spectrometry (SQT-FAAS) was utilized to determine lead at trace levels in tea samples. Co-MPs' adsorbent properties were tested and validated for their selectiveness to lead. Only with a few and short extraction steps (i.e. adding MPs, mixing, decanting and eluting) analyte was extracted from sample solution rapidly and efficiently. Limit of detection (LOD) and limit of quantification (LOQ) for the developed method (Co-MP-DSPME-SQT-FAAS) were found to be 7.77 µg/L and 25.9 µg/L, respectively. Matrix matching strategy was performed and outcomes indicated that the developed method is applicable with the high percent recovery values of 110.1 ±â€¯4.5 and %102.9 ±â€¯4.2 for 100 and 300 µg/kg lead standard spiked black tea samples, respectively. The method was also applied to standard reference material to check the accuracy of the method.