An extended graphical targeting technique for direct reuse/recycle in concentration and property-based resource conservation networks

Minimum flowrate targeting methods for resource conservation networks (RCNs) have been developed over the last decades. The existing methodologies still have certain drawbacks. Their design insights could be deepened and some steps should be more convenient for the users. A targeting tool called the material surplus composite curve (MSCC), which is an improvement of the surplus diagram for water and hydrogen networks is introduced. The approach is illustrated on several cases selected from the literature. Using this technique, it is possible to determine rigorous flowrate targets for different variants of the RCN problem.     

The precursor compound of two types of ZnSe magic-sized clusters

Precursor compounds(PCs)link quantum dots(QDs)and magic-sized clusters(MSCs),which is pivotal in the conversion between QDs and MSCs.Here,for the first time,we report the transformation,synthesis,and composition of a type of ZnSe PCs.ZnSe PCs can be directly transformed to two different MSCs with the assistance of octylamine and acetic acid at room temperature.The two types of MSCs exhibit sharp absorption peaks at 299 and 328 nm which are denoted as MSC-299 and MSC-328.In the preparation of ZnSe PCs,diphenylphosphine(DPP)as an additive plays a key role which not only inhibits the thermal decomposition of Zn precursor,but also acts as a reducing agent to reduce the by-products produced in the reaction.The composition was explored by X-ray photoelectron spectroscopy,energy dispersive spectrometer,matrix-assisted laser desorption/ionization time-of-flight mass spectra with ZnSe PC powder appeared as white powder after purifying by toluene(Tol)and methanol(MeOH).The results indicate that the molar ratio of Zn/Se is 2:1 with a molecular of?3,350 Da.Therefore,we propose that the molecular formula of ZnSe PCs is Zn₃₂Se₁₆.In addition,at the molecular level,the covalent bond of Zn-Se is formed in ZnSe PCs.This study offers a deeper understanding of the transformation from PCs to MSCs and for the first time proposes the composition of PCs.Meanwhile,this research provides us with a new understanding of the role of DPP in the synthesis of colloidal semiconductor nanoparticles.     

Unfreezable Water in Apple Treated by Pulsed Electric Fields: Impact of Osmotic Impregnation in Glycerol Solutions

The effects of pulsed electric fields (PEF) and osmotic impregnation in glycerol solution on the amount of unfreezable water in apple were determined by means of low-temperature differential scanning calorimetry (DSC). The obtained data were compared with behaviour of pure water–glycerol solutions (sample WG). PEF treatment was applied using a near-rectangular monopolar generator with pulse duration of 100 μs at electric field strength of 800 V/cm. The osmotic impregnation of PEF-treated apple discs was done using water–glycerol (sample AWG) and apple juice–glycerol (sample AJG) osmotic solutions at different concentration of water or juice in glycerol, W = 30–100 wt%. The data evidenced that for the PEF-treated samples the glycerol was able to penetrate successfully inside apple tissue. The state diagrams for WG, AWG and AJG samples were rather similar. It was observed that free water existed only for moisture content above some minimum value. The unfreezable water content was the largest in AJG, followed by WG and AWG. The juice concentration in glycerol W ≈ 80 wt% was found to be optimal for preservation of the texture of PEF-treated samples.     

Identification of New Coloured Anthocyanin–Flavanol Adducts in Pressure-Extracted Pomegranate (<Emphasis Type=BoldItalic>Punica granatum</Emphasis> L.) Juice by High-Performance Liquid Chromatography/Electrospray Ionization Mass Spectrometry

Pomegranate (Punica granatum L.) juice, obtained by pressure extraction of the whole fruit, contains coloured flavanol–anthocyanin adducts (the flavanol occupies the upper part of the dimmer) from the direct condensation between anthocyanidins delphinidin, cyanidin and pelargonidin and flavan-3-ols (epi)gallocatechin, (epi)catechin and (epi)afzelechin. The presence of adducts between these same flavanols and anthocyanidins, but belonging to the coloured anthocyanin–flavanol adduct type (anthocyanin occupies the upper part of the dimmer) has been revealed by reversed-phase liquid chromatography coupled to tandem mass spectrometry (ion trap), with positive electrospray ionization (LC–ESI/MS ⁿ ). These new adducts are isotopic with their corresponding counterparts (flavanol–anthocyanin adducts) and indistinguishable from them by comparison of the mass spectra from the MS² of the isotopic parent ions. However, they can be distinguished by comparison of the mass spectra from the MS³ of their corresponding isotopic aglycons. Hence, the MS³ of the aglycon from a given flavanol–anthocyanin adduct always yields a mass spectrum containing five characteristic ions, the three with smaller m/z being only dependent on the anthocyanidin and the other two on both the anthocyanidin and the flavanol. In contrast, the mass spectrum from the MS³ of the aglycon of its counterpart anthocyanin–flavanol adduct gives only two of the above five characteristic ions, where the ion with smaller m/z only depends on the anthocyanidin and the other on both the anthocyanidin and the flavanol. Ten 3-hexoside derivatives of coloured anthocyanin–flavanol adducts were detected in pomegranate juice being reported for the first time this type of adducts from a natural source.     

Inhibition of biofilm formation of Pseudomonas aeruginosa by an acylated homoserine lactones-containing culture extract

The objective of this study was to examine the effect of an acylated homoserine lactones-containing culture extract (AHL-CCE) on bacterial growth, enzyme activity and biofilm formation of Pseudomonas aeruginosa. Chicken breast muscle broth in which P. aeruginosa had been grown for 24 h at 20 °C was extracted with acidified ethyl acetate, the solvent was evaporated and the residue was dissolved in water and heated at 100 °C for 15 min. Thin-layer chromatography combined with Agrobacterium tumefaciens KYC55-based bioassays indicated the presence of C₄-, C₆-, C₈- and C₁₂-homoserine lactones in the extract. The addition of AHL-CCE to a culture of P. aeruginosa caused the bacteria to reach their highest count after 36 h whereas cultures without the extract required 72 h to reach their peak counts, but the maximum cell count was higher for the extract-free culture. No biofilm was detected when P. aeruginosa was cultured in chicken broth at 10 °C when the extract was present. Addition of extract reduced proteolysis of actin, troponin-T and tropomyosin by P. aeruginosa, but had no effect on lipase activity. Therefore, AHL-CCE can be used to reduce the bacterial growth time and inhibit biofilm formation; thus, benefiting food safety and quality.     

Degradation Kinetics of Anthocyanin of Traditional and Low-Sugar Blackberry Jam

The objective of this study was to monitor the stability of anthocyanin and phenolic compounds contained in two formulations of blackberry jam (traditional and low-sugar) during storage. For that purpose, jams were prepared with varying amounts of hydrocolloids and investigated as to pH, total soluble solids, water activity, total acidity, total anthocyanins and total polyphenols. In order to accompany and assess the levels of phenolic compounds and colour (L*, a* and b*) changes, the samples were stored for 180 days at two different temperatures (10 and 25 °C). The Arrhenius model was used to determine the relationship between the reaction rate (k) at the different storage temperatures, yielding activation energy values of 19 and 12 kcal/mol and Q ₁₀ values of 3.0 and 2.0 for traditional and low-sugar jams, respectively. The results show that by the end of the storage time investigated, the anthocyanin compounds had been partially degraded, with the greatest loss being observed in traditional jam stored at 25 °C. Colour stability was also lower in traditional jam as compared to the low-sugar product.     

Effect of High Hydrostatic Pressure on Physicochemical and Structural Properties of Rice Starch

Rice starch–water suspension (20%) were subjected to high hydrostatic pressure (HHP) treatment at 120, 240, 360, 480, and 600 MPa for 30 min. Polarizing light microscope, scanning electron microscopy (SEM), rapid visco analyzer (RVA), differential scanning calorimeter (DSC), and X-ray diffraction were used to investigate the physicochemical and structural changes of starch. Microscopy studies showed that the treatment of starch with HHP under 600 MPa for 30 min resulted in a complete loss of birefringence and a gel-like appearance. The treatment of starch suspension with HHP at 600 MPa resulted in a significant increase in swelling power and solubility at low temperature (50–60 °C), but opposite trends were found at high temperature (70–90 °C). The DSC analysis showed a decrease in gelatinization temperatures and gelatinization enthalpy with increase of pressure levels. RVA viscograms of starches exhibited an increase in peak, trough, and final viscosities, peak time, and pasting temperature but decrease of breakdown, setback viscosities, and pasting temperature when pressure was increased. X-ray diffraction studies showed that the HHP treatment converted rice starch that displayed the A-type X-ray patterns to the B-type-like pattern. These results showed that the treatment of rice starch in 20% starch/water suspension at a pressure of 600 MPa for 30 min led to a complete gelatinization of starch granules.     

Relating dietary diversity and food variety scores to vegetable production and socio-economic status of women in rural Tanzania

The objective of the present study was to measure diversity in nutrition with dietary scores, and to assess their relationship to vegetable production and the socio-economic status of women in rural Tanzania. A dietary diversity score (DDS) and a food variety score (FVS) were created from data gathered with three semi-quantitative 24-h recalls performed during three non-consecutive seasons during 2006/2007. Data on vegetable production, selling and buying and socio-economic data was gathered with a semi-quantitative questionnaire. A total of 252 randomly selected women from three districts of north-eastern and central Tanzania participated. The median DDS of 6 and the mean FVS of 8.3 were low, suggesting an overall poor dietary quality, with about one third of participants having an alarmingly low DDS of only two to four food groups per day. These women consumed a very basic diet consisting mainly of cereals and vegetables. Differences among districts were pronounced while those among seasons were less distinct. The DDS and FVS were both significantly associated with ethnicity, occupation and status within the household of participants. As a more varied diet is not necessarily healthier, integration of both quantity and quality in the scores is proposed for future studies. This can be achieved, for example, by weighing food types according to their importance in the diet. As both scores are linked to the production, selling and buying of vegetables, the promotion of homestead food production may be a good way to improve dietary diversity.     

Micelle-Mediated Extraction and Flame Atomic Absorption Spectrometric Method for Determination of Trace Cobalt Ions in Beverage Samples

A new method has been developed for preconcentration of cobalt at trace levels in beverage samples using calcon carboxylic acid as chelating agent and cetyl pyridinium chloride as an auxiliary ligand and entrapped into Triton X-114 prior to its determination by flame atomic absorption spectrometry (FAAS). The main parameters affecting cloud point extraction (CPE) efficiency such as pH, concentration of the complexing agent, cationic and nonionic surfactant concentration, salt effect, the equilibrium time, and temperature were investigated and optimized. After optimization of the CPE conditions, a preconcentration factor of 60, an enhancement factor of 106, and a detection limit of 0.20 μg L⁻¹ by (R ² = 0.9978) were obtained from a calibration curve constructed in the range of 0.7–100 μg L⁻¹. The proposed preconcentration procedure was successfully applied to the determination of cobalt ions in some real samples including natural drinking water, tap water, and beer and wine samples. The accuracy and validity of the proposed CPE/FAAS method was tested by means of five repeated analysis of reference standard materials (TM-253, a low level fortified water standard for trace elements). A good agreement between analytical results (28.8 and 28.5 μg L⁻¹ with calibration curve and standard addition curve method, respectively) and certified value (27.9 μg L⁻¹) for Co (p < 0.05) were obtained and verified by means of calibration curve and standard addition curve method using CPE procedure.