Effect in variation of the cationic precursor temperature on the electrical and crystalline properties of MnS growth by SILAR.

The crystallographic, optical, and electrical properties of manganese sulfide thin films depend on the control of the temperature precursors in the synthesis process, as shown by the results of this work. MnS thin films were deposited on glass substrates using the SILAR method and over an additional layer of CdS synthesized by chemical bath deposition (CBD) to acquire a p-n heterojunction. SILAR is an inexpensive method performed with a homemade robot in this case. Temperature in the solution precursors varied from 20 to 80 °C in four experiments. The morphology and structure of MnS and FTO/CdS/MnS thin films were studied through scanning electron microscopy (SEM) and grazing-incidence X-ray diffraction (GIXRD); the results indicate that materials showed a polycrystalline behavior, a diffraction peak of α- MnS cubic phase was observed with lattice constants values, ranging from 4.74 to 4.75 Å. Additionally, Raman spectroscopy showed a signal corresponding to the transversal optical phonons of MnS at a wavenumber near 300 cm-1. UV-vis spectroscopy showed optical bandgap values of 3.94, 4.0, 4.09, and 4.26 eV for thin films obtained at 20°, 40°, 60°, and 80 °C. respectively. Results indicated 80 °C as an optimal cationic precursor process temperature, achieving optical transmittance T% and good film quality according to SEM and GIXRD for the synthetization of MnS. The current-voltage (I-V) characterization in the heterojunction showed a characteristic diode curve with an open circuit voltage (VOC) of 300 mV under illumination, which indicated that the manganese sulfide behaves as p-type material contributing with positive charge carriers, while CdS behaves as n-type material.

Biodiesel production using microbial lipids derived from food waste discarded by catering services.

Biodiesel production using microbial oil derived from food waste discarded by the hospilatity sector could provide a sustainable replacement for diesel fuel. Discarded potato peels were used in solid-state fermentations of Aspergillus awamori for the production of glucoamylase (30 U/g) and protease (50 U/g). Hospitality food waste hydrolysis led to 98% (w/w) starch to glucose conversion yields. Crude hydrolyzates were used in shake flask fermentations with the oleaginous yeast Rhodosporidium toruloides Y-27012 leading to 32.9 g/L total dry weight (TDW) with 36.4% (w/w) intracellular lipid content. Fed-bath bioreactor cultures resulted in TDW of 53.9 g/L and lipid concentration of 26.7 g/L. Principal component analysis showed a fatty acid profile similar to soybean oil and solid food waste oil. Microbial oil was transesterified into biodiesel with satisfactory performance considering the European standard EN 14214. This work demonstrated that valorization of food waste for biodiesel production is feasible.

Food waste from restaurant sector - Characterization for biorefinery approach.

The aim of this study is the analysis of food waste (FW) composition from local catering services to assess potential biorefinery development. Moisture content of different FW samples showed that 27-47% (w/w) was organic material. Main components were lipids (25.7-33.2, w/w), starch (16.2-29.4%, w/w) and proteins (23.5-18.3%, w/w) on a dry basis. A metal profile with Na and Mg as main components, followed by trace elements, i.e. Zn or Fe, was also found in food waste samples. Statistical tests in combination with principal component analysis provides an efficient methodology to establish specific composition variations between FW from different catering services, while relating them to FW typology. The combination of chemical characterization with statistical study constitutes a promising decision-making tool for FW processing and valorization. The innovative methodology presented in this study provides systematic evaluation of FW composition and variability to allow selection of the most appropriate valorization paths.

Biorefining of by-product streams from sunflower-based biodiesel production plants for integrated synthesis of microbial oil and value-added co-products.

This study focuses on the valorisation of crude glycerol and sunflower meal (SFM) from conventional biodiesel production plants for the separation of value-added co-products (antioxidant-rich extracts and protein isolate) and for enhancing biodiesel production through microbial oil synthesis. Microbial oil production was evaluated using three oleaginous yeast strains (Rhodosporidium toruloides, Lipomyces starkeyi and Cryptococcus curvatus) cultivated on crude glycerol and nutrient-rich hydrolysates derived from either whole SFM or SFM fractions that remained after separation of value-added co-products. Fed-batch bioreactor cultures with R. toruloides led to the production of 37.4gL(-1) of total dry weight with a microbial oil content of 51.3% (ww(-1)) when a biorefinery concept based on SFM fractionation was employed. The estimated biodiesel properties conformed with the limits set by the EN 14214 and ASTM D 6751 standards. The estimated cold filter plugging point (7.3-8.6°C) of the lipids produced by R. toruloides is closer to that of biodiesel derived from palm oil.

Evaluation of by-products from the biodiesel industry as fermentation feedstock for poly(3-hydroxybutyrate-co-3-hydroxyvalerate) production by Cupriavidus necator.

Utilization of by-products from oilseed-based biodiesel production (crude glycerol, rapeseed meal hydrolysates) for microbial polyhydroxyalkanoate (PHA) production could lead to the replacement of expensive carbon sources, nutrient supplements and precursors for co-polymer production. Batch fermentations in shake flasks with varying amounts of free amino nitrogen led to the production of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (P(3HB-co-3HV)) with a 2.8-8% 3HV content. Fed-batch fermentations in shake flasks led to the production of 10.9g/L P(3HB-co-3HV) and a 55.6% P(3HB-co-3HV) content. NaCl concentrations between 2 and 6g/L gradually became inhibitory to bacterial growth and PHA formation, whereas in the case of K(2)SO(4), the inhibitory effect was observed only at concentrations higher than 20g/L. Differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and nuclear magnetic resonance ((13)C NMR) demonstrated that the incorporation of 3HV into the obtained P(3HB-co-3HV) lowered glass transition temperature, crystallinity and melting point as compared to polyhydroxybutyrate. Integrating PHA production in existing oilseed-based biodiesel plants could enhance the viability and sustainability of this first generation biorefinery.

Extending the dynamic range of flame atomic absorption spectrometry: a comparison of procedures for the determination of several elements in milk and mineral waters using on-line dilution.

Three approaches based on continuous flow methodology are assessed for the purpose of extending the dynamic range of flame atomic absorption spectrometry. The determination of several elements in infant liquid and powdered milk and water samples is used to check the performances of the manifolds. Two of the systems are fully computer-controlled and permit a calibration graph to be obtained by using a single standard solution. The results confirm that continuous flow methodology is a reliable alternative to the time-consuming common dilution procedures based on glassware. Since the systems are versatile and permit a wide range of degrees of dilution to be obtained, they can be easily adapted for the automated or semi-automated analysis of other liquid samples which are too concentrated to be aspirated directly into the atomic absorption spectrometer.

Indirect flame atomic absorption detection for the liquid chromatographic separation of alkaline metals.

Alkaline metals and ammonium ion are separated by cationic exchange liquid chromatography using a 60 microg ml(-1) aqueous copper solution as the mobile phase at 1.5 ml min(-1). Detection is carried out by measuring copper with an atomic absorption spectrometer directly interfaced to the chromatograph. A simple T-piece is used to compensate the difference between the nebulizer uptake rate and the chromatographic flow-rate with air. The method is applicable to the analysis of alkaline metals and ammonium in waters. Average recovery ( n = 16) was 100.3 +/- 4.0%.

Flow injection flame atomic absorption spectrometry for slurry atomization. Determination of iron, calcium and magnesium in samples with high silica content.

A study on the use of slurries in flame atomic absorption spectrometry is reported. Samples with a very high silica content are ground and then slurried in a solution containing 2% hydrochloric and 3% v/v hydrofluoric acids. The suspensions are prepared in the 0.01-1% m/v range and introduced into the flame by means of a simple flow injection manifold. Relative standard deviations for the measurements of iron, calcium and magnesium in diatomaceous earth samples are in the 1.5-2.8, 2.2-5.3 and 2.8-5.0% ranges, respectively. To avoid the use of suspensions prepared with a very low percentage of solid sample and to improve the reproducibility, an on-line dilution manifold is tried. The use of an easy-to-construct variable volume dilution chamber allows the on-line dilution of the slurries, thus permitting the determination of calcium and magnesium over a wide range of concentrations. Calibration is performed using aqueous standards. The experimental conditions, optimized for the determination of iron, calcium and magnesium in diatomaceous earth samples, can also be applied to other silica-based materials, as is shown by the analysis of several standard reference materials.

Vaccine against group B Neisseria meningitidis: protection trial and mass vaccination results in Cuba.

The Cuban vaccine, first in the world with proven efficacy against group B-caused disease, is based on outer membrane proteins from B meningococci capable of inducing long-lasting and high-titered bactericidal antibodies in humans. This bactericidal activity has a wide spectrum against all pathogenic group B Neisseria meningitidis tested. A randomized, double-blind controlled trial of the vaccine efficacy was performed during 1987-1989 with 106,000 10-14 years old students from 197 boarding schools in seven provinces. The efficacy obtained was 83% (chi 2, p less than 0.002; Fischer exact, p less than 0.001). In a second field trial including 133,600 persons from 5 months to 24 years of age in Ciego de Avila province (30 cases/10(5) inhabitants, the highest incidence rate in Cuba) by comparing vaccinated and non-vaccinated population after 2.5 years of observation and careful follow-up, the efficacy and safety was confirmed. Because of these results and because of the very low reactogenicity of the vaccine, the Ministry of Public Health took the advice of the Scientific Council to vaccinate all children between 3 months and 6 years of age in the most affected provinces. No severe or long lasting reactions to the vaccine were observed after the millions of doses administered. The efficacy of vaccination varied in the provinces between 83% and 94%, among age groups ranging from 3 months and 20 years. After 3 years of massive application no severe reactions occurred and one of the most severe epidemics has been practically eradicated.

A fast method for the determination of lead in paprika by electrothermal atomic-absorption spectrometry with slurry sample introduction.

A rapid procedure for the determination of lead in commercial paprika samples is described. The samples are first calcined at 350 degrees , then suspensions are prepared in water containing 0.1% v/v Triton X-100 and 0.1% w/v ammonium phosphate and injected into the electrothermal atomiser. The use of platform atomisation with a preatomisation cooling step allows for simple calibration with aqueous standards. When using 0.4% suspensions the detection limit is 0.2 ug/g. The results for seven paprika samples agree with those obtained by an alternative method involving calcination and dissolution in acid.

Manual and fia methods for the determination of cadmium with malachite green and iodide.

A sensitive and rapid spectrophotometric method for the determination of cadmium is described, based on the formation of a blue complex at pH 4 between the anionic iodide complex of cadmium(II) and Malachite Green; the colour is stabilized with poly(vinyl alcohol). The calibration graph for measurement at 685 nm is linear over the range 1-50 mug of cadmium per 25 ml of final solution, with a relative standard deviation of +/-1.7% for 1 mug/ml cadmium. The molar absorptivity is 6.1 x 10(4) 1.mole(-1).cm(-1). The method can be successfully adapted for FIA, the peak height being proportional to the cadmium concentration over the range 0.1-3 mug/ml; a two-channel manifold is used and an improvement in selectivity is obtained. The use of a gradient tube is demonstrated to give a good calibration for Cd(II) over the range 2 x 10(-2) -2 x 10(-6)M.

Determination of palladium with thiocyanate and rhodamine b by a solvent-extraction method.

Sensitive spectrophotometric and spectrofluorimetric procedures for the determination of palladium have been developed, based on solvent-extraction of the ion-pair formed between Rhodamine B and the anionic complex of Pd(II) with thiocyanate. With an organic to aqueous phase-volume ratio of 1:5, the molar absorptivity is 9.0 x 10(4) l.mole(-1).cm(-1) and the absorbance of the reagent blank is 0.026. Spectrophotometrically, palladium can be determined in the range 0.1-8.8 mug. Spectrofluorimetrically, it can be determined over the range 0.04-1.5 mug. The spectrophotometric procedure has been applied to the determination of palladium in dental alloys, organopalladium compounds and hydrogenation catalysts.

Spectrophotometric determination of saccharin in different materials by a solvent extraction method using Nile Blue as reagent.

In a slightly acidic medium (sodium acetate-acetic acid buffer, pH 4) saccharin and Nile Blue form an ion-association compound which is extractable into methyl isobutyl ketone and allows the spectrophotometric determination of saccharin. At 630 nm Beer's law is obeyed over the saccharin concentration range 0.1-3.5 microg/ml in the aqueous phase and the apparent molar absorptivity is 5.8 x 10(4) l.mole(-1).cm(-1). The method shows good selectivity and can be applied to the determination of saccharin in artificial sweeteners, soft drinks and toothpastes.