Reduction of aqueous carbonate photocatalysed by treated semiconductors

Heterogeneous photocatalysed reduction of aqueous Na₂CO₃ solution (1 m) was achieved by using phthalocyanine-coated semiconductor powders (1–3% coating) as well as bare semiconductors. The suspensions were irradiated with 254 nm light from a low-pressure mercury lamp in a nitrogen atmosphere. The phthalocyanine dyes (Fe²⁺-Pc or Co²⁺-Pc) absorb > 80% of the 254 nm radiation and thus sensitize the semiconductor. The products of reduction (CH₃OH and HCHO) were determined spectrophotometrically. The CH₃OH yields obtained are much higher than the HCHO yields, due to a photocatalysed reduction of HCHO to CH₃OH. The CH₃OH yields from coated titania increased linearly with irradiation time over the period 6–18 h. However, the straight line does not pass through the origin, and it seems that a slowing-down occurs at times > 6 h. Titania coated with both dyes gave an optimum CH₃OH yield at 2% surface coating. At higher coating percentages, phthalocyanine screens the surface, thus reducing the light reaching the semiconductor. Changing the redox potential of the phthalocyanine dye by changing its central metal from Fe to Co affects the CH₃OH yields. The bare MoS₂ photocatalyst gave a much higher CH₃OH yield due to the characteristic behaviour of the semiconducting layer-type disulphide, distinguished from that of classical semiconducting materials. In the various semiconductors studied, it seems that there is no correlation between the position of the conduction band and the yield of CH₃OH. Such correlation was argued. Generally, a decrease in the yield of CH₃OH was observed as the band gap width of the semiconductor increased. The yields of the photoproduced CH₃OH generally increased with the percentage of light absorbed at 254 nm by the various semiconductors. Irradiation leads to the production of electrons in the conduction band of the semiconductor. It is likely that the photoproduced electrons reduce CO₃²- initially to HCOO- and then to HCHO and CH₃OH.     

Production of Well-Dispersed Aqueous Cross-Linked Chitosan-Based Nanomaterials as Alternative Antimicrobial Approach

In the current study, chitosan was extracted by deacetylation of chitin, which is extracted from shrimp shell. chitosan nanoparticles (CSNPs) were prepared by ionotropic gelation technique. chitosan/tripolyphosphate ratio (CS:TPP) was kept at 3:1 to prepare CSNPs. chitosan/silver nanocomposite (CS/AgNCs) were prepared by incorporating silver nanoparticles into CSNPs. The quality of the prepared nanocomposite was evaluated by infrared spectroscopy, UV–Vis spectroscopy, transmission electron microscopy, and antibacterial activity. Results showed that chitosan/silver nanocomposite in which, both chitosan and silver are in nanoscale was successfully prepared for the first time in a well-dispersed aqueous form. Whereas CSNPs act as a host material to form the nanocomposite unlike the previously prepared forms of chitosan–silver nanocomposites, that used chitosan bulk as host materials and the dispersion medium was slightly acidic. Moreover, results revealed that the antibacterial activity of CSNPs was significantly enhanced after incorporating trace amount of silver nanoparticles (0.535% w/w AgNPs/CSNPs).     

Transient computational fluid dynamics modeling of pervaporation separation of aromatic/aliphatic hydrocarbon mixtures using polymer composite membrane

Pervaporation (PV) separation of toluene/n‐heptane mixtures was studied experimentally and theoretically by means of a molecular surface engineering (MSE) polymer composite membrane. A comprehensive mathematical model was developed to predict unsteady state transport of toluene and n‐heptane (nC₇) through the membrane. Conservation equations including continuity, and heat transfer equations were solved using finite element method (FEM). Computational fluid dynamics (CFD) technique was applied to solve the model equations. The model was then verified with PV experimental data. The simulation results were in good agreement with the experimental data. The simulation results revealed that the proposed model could provide a general simulation of transport in the PV process. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

The Effect of Different Plasticizers on Lactose Crystallization During Spray Drying

Lactose crystallization may occur during spray drying, depending on the operating conditions for drying, and this work reviews previous and new evidence for the effects of different additives or plasticizers on retarding or accelerating the rate of crystallization. The effects of different operating conditions during spray drying are also considered in the experimental work reviewed and performed here, which was mainly carried out with Buchi B-290 laboratory-scale spray dryers (Buchi, Flawil, Switzerland), although some work on pilot-scale equipment is also discussed. The additives used and reviewed in this article include milk proteins, such as casein and whey protein isolate, polyethylene glycol, and ascorbic acid. The key physical properties, such as glass transition temperature and drying characteristics of the material, are discussed, allowing degrees of amorphicity in spray-dried lactose to be controlled over a wide range, from close to 0% to nearly 100%.