The sol–gel transition temperature of skim milk concentrated by microfiltration as affected by pH and protein content

This study aimed at determining sol–gel transition temperatures of microfiltered skim milk retentates for different protein levels (6, 8 and 10% (w/w)) and a wide pH range (native pH to 4.6) by means of small‐amplitude oscillatory shear rheology. For a pH of 5.4 to 5.0, the sol–gel transition temperatures decreased significantly with increasing protein content, which did not differ for pH 4.8 and 4.6. The sol–gel transition temperatures of retentates with 10% (w/w) protein at pH 5.4 and 4.6 were 58.4 °C and 10.9 °C, respectively.     

Single stage hydrogen production from cellulose through photo-fermentation by a co-culture of Cellulomonas fimi and Rhodopseudomonas palustris

Biohydrogen production from cellulose by a bacterial co-culture is a potentially promising approach for producing bioenergy from a low cost substrate. The use of a cellulolytic bacterium, Cellulomonas fimi, permits cellulose conversion and the in situ production of substrate for growth and hydrogen production by the photosynthetic bacterium Rhodopseudomonas palustris. Response surface methodology (RSM) with a Box-Behnken design (BBD) was used to examine variations in the key parameters: substrate (cellulose) concentration, yeast extract concentration and the microorganism ratio (Rps. palustris/C. fimi). For the co-culture of R. palustris and C. fimi the highest hydrogen production (44 mmol H₂/L) was achieved at the highest substrate concentration (5 g/L); however, the highest hydrogen yield (3.84 mol H₂/mol glucose equivalent) was observed at the lowest cellulose concentration and highest microorganism ratio. High COD removal efficiencies, over 70%, were achieved over a wide range of conditions and were positively affected by the concentration of yeast extract.     

An experimental and modeling study of the low- and high-temperature oxidation of cyclohexane

The experimental study of the oxidation of cyclohexane has been performed in a jet-stirred reactor at temperatures ranging from 500 to 1100 K (low- and intermediate temperature zones including the negative temperature-coefficient area), at a residence time of 2 s and for dilute mixtures with equivalence ratios of 0.5, 1, and 2. Experiments were carried out at quasi-atmospheric pressure (1.07 bar). The fuel and reaction product mole fractions were measured using online gas chromatography. A total of 34 reaction products have been detected and quantified in this study. Typical reaction products formed in the low-temperature oxidation of cyclohexane include cyclic ethers (1,2-epoxycyclohexane and 1,4-epoxycyclohexane), 5-hexenal (formed from the rapid decomposition of 1,3-epoxycyclohexane), cyclohexanone, and cyclohexene, as well as benzene and phenol. Cyclohexane displays high low-temperature reactivity with well-marked negative temperature-coefficient (NTC) behavior at equivalence ratios 0.5 and 1. The fuel-rich system (? = 2) is much less reactive in the same region and exhibits no NTC. To the best of our knowledge, this is the first jet-stirred reactor study to report NTC in cyclohexane oxidation. Laminar burning velocities were also measured by the heated burner method at initial gas temperatures of 298, 358, and 398 K and at 1 atm. The laminar burning velocity values peak at ? = 1.1 and are measured as 40 and 63.1 cm/s for T_i = 298 and 398 K, respectively. An updated detailed chemical kinetic model including low-temperature pathways was used to simulate the present (jet-stirred reactor and laminar burning velocity) and literature experimental (laminar burning velocity, rapid compression machine, and shock tube ignition delay times) data. Reasonable agreement is observed with most of the products observed in our reactor, as well as the literature experimental data considered in this paper.     

The effects of heat treatment temperatures on photocatalytic activity of cobalt ferrite nanoparticles synthesised by microwave-assisted combustion method

In this study, the effects on the photocatalytic activities of particles after heat treatment has been applied to cobalt ferrite nanoparticles produced by microwave-assisted combustion method were observed. The heat treatment applied to the samples was produced with only the microwave effect, at temperatures ranging from 300 to 1000°C. Thermogravimetric analysis was performed on the precursor sample in air atmosphere. During this analysis, the gases released up to 1200°C were identified with a Fourier-transform infrared (FTIR) spectrometer integrated into a thermogravimetric analysis system. Then, the cobalt ferrite nanoparticles produced with heat treatments applied at various temperatures were used as a photocatalyst to remove the dyestuff content in synthetic wastewaters prepared by using Astrazon Red GTL textile dye by photocatalytic oxidation, and their photocatalytic activities were compared. In these experiments, the operational parameters for photocatalysis processes were applied as 400 rpm for stirring speed, 50 mg/L for initial contaminant concentration, 0.5 g/L for catalyst dosage, 25°C for temperature, and 4400 μW/cm² for light intensity. As a result of the experiments, it was observed that the crystal structure of the cobalt ferrite nanoparticles produced with the increase of the applied heat treatment temperature improved significantly. The obtained data show a strong relationship between the structural properties of materials and their photocatalytic activities. In addition, it was determined that the dyestuff in the solution was completely degraded in the experiments, and it was determined that all processes were compatible with the pseudo-first-order kinetic model.     

Au/Pt Bimetallic Nanoparticle Decorated Microparticle Hybrid Catalyst System for Heterogeneous Hydrogenation of Styrene

Catalysis Letters - Poly(methacryloyloxy quinoline) microparticles were synthesized and used as reducing and stabilizing agents to prepare Au/Pt bimetallic nanoparticle (NP) decorated microparticle...     

Fenton and Fenton‐like oxidation of CI Basic Yellow 51: a comparative study

When ferric ions are substituted for ferrous ions in Fenton’s reagent, the reactions which occur are called Fenton‐like reactions. This study describes the relative efficiency of Fenton (with ferrous ions) and Fenton‐like (with ferric ions) reactions for the degradation of a basic dyestuff, CI Basic Yellow 51, in aqueous solution. Comparisons were made on the basis of the observed reductions in chemical oxygen demand and visible absorption of the dye solutions at optimum reaction conditions. It was found that the Fenton process with 2.63 mm ferrous ion and 39.96 mm hydrogen peroxide at the optimum pH (3.0) eliminated 92.2% of chemical oxygen demand and 98.9% of colour in 22 min, whereas 43.2% of chemical oxygen demand and 64.6% of colour was eliminated by the Fenton‐like process within the same time period, but at pH 4. The efficiency of the latter was significantly improved (to 96.6% removal of colour and 99.7% removal of chemical oxygen demand) by an increase in temperature of 35 °C (from 15 to 50 °C), while no improvements were observed in the efficiency of the Fenton process by temperature elevations.