Effect of fortification with asparagus powder on the qualitative properties of processed cheese

The qualitative properties of processed cheese (PC) fortified with different levels of asparagus powder (AP) (0.5%, 1% and 1.5% wt/wt) were evaluated during storage. AP decreased the pH and lipolysis indexes and increased the phenolic content, antioxidant activity and proteolysis of the processed cheeses. AP made the structure of the cheese more elastic, increased the rigidity and decreased the spreadability compared with the control sample, which corresponded to the results obtained using dynamic oscillatory rheometry. The results showed that AP as a rich source of bioactive components could be used for the fortification of processed cheeses.     

Catalytic Conversion of NO and C3H6 in Exhaust Gases Over Silver Catalysts Under Stoichiometric or Excess Oxygen

The role of Ag in simultaneously catalyzing NO reduction and C₃H₆ oxidation was shown to be strongly dependent on the redox properties of its local environment. Under an atmosphere of 1,000 ppm NO, 3,000 ppm C₃H₆, and 1% O₂ and a GHSV of 30,000 h⁻¹, a perovskite La_0.88Ag_0.12FeO₃ prepared by reactive grinding is active giving a complete NO conversion and 92% C₃H₆ conversion at 500 °C. These values are much higher than the NO conversion of 55% and C₃H₆ conversion of 45% obtained over a 3 wt.% Ag/Al₂O₃ catalyst under the same conditions. Under an excess of oxygen (10% O₂) a good SCR performance with a plateau of N₂ yield above 97% over a wide temperature window of 350–500 °C along with C₃H₆ conversion of 90% at 500 °C was observed over Ag/Al₂O₃, while minor N₂ yields (∼10% at 250–350 °C) and high C₃H₆ conversions (reaching ∼100% at 450 °C) were obtained over La_0.88Ag_0.12FeO₃. Abundant molecular oxygen is desorbed from Ag substituted perovskite after 10% O₂ adsorption as verified by O₂- temperature programmed desorption (TPD). This reflects the strongly oxidative properties of La_0.88Ag_0.12FeO₃, which lead to a satisfactory NO reduction at 1% O₂ due to the ease of nitrate formation but to a significant C₃H₆ combustion above that value. The formation of nitrate species over the less oxidizing Ag/Al₂O₃ was accelerated under an excess of oxygen resulting in an excellent lean NO reduction behavior. The redox properties of silver catalysts could be adjusted via mixing perovskite with alumina for an optimal elimination of both NO and C₃H₆ over the whole range of oxygen concentration between 0 to 10%.     

A comparative study of two approaches for supporting optimal network location queries

Given a set S of sites and a set O of weighted objects, an optimal location query finds the location(s) where introducing a new site maximizes the total weight of the objects that are closer to the new site than to any other site. With such a query, for instance, a franchise corporation (e.g., McDonald’s) can find a location to open a new store such that the number of potential store customers (i.e., people living close to the store) is maximized. Optimal location queries are computationally complex to compute and require efficient solutions that scale with large datasets. Previously, two specific approaches have been proposed for efficient computation of optimal location queries. However, they both assume p-norm distance (namely, L₁ and L₂/Euclidean); hence, they are not applicable where sites and objects are located on spatial networks. In this article, we focus on optimal network location (ONL) queries, i.e., optimal location queries in which objects and sites reside on a spatial network. We introduce two complementary approaches, namely EONL (short for Expansion-based ONL) and BONL (short for Bound-based ONL), which enable efficient computation of ONL queries with datasets of uniform and skewed distributions, respectively. Moreover, with an extensive experimental study we verify and compare the efficiency of our proposed approaches with real world datasets, and we demonstrate the importance of considering network distance (rather than p-norm distance) with ONL queries.     

An Approach to Synthesize Thick α- and γ-Al2O3 Coatings by High-Speed Physical Vapor Deposition

Crystalline α- and γ-Al₂O₃ exhibit in many applications high wear resistance, chemical resistance, and hot hardness, making them interesting materials for production engineering. To synthesize α-Al₂O₃ with high coating thickness of s ≥ 10 μm, chemical vapor deposition at temperatures T > 1000 °C is well established. However, there are almost no studies dealing with the synthesis of thick α-Al₂O₃ by physical vapor deposition (PVD) at high temperatures T > 700 °C. High-temperature deposition of thick coatings can be realized by means of the dense hollow cathode plasma, combined with the transport function of the plasma gas in high-speed (HS) PVD. Herein, crystalline α- and γ-Al₂O₃ films are deposited on cemented carbides at substrate temperatures T _s ≈ 570 °C and T _s ≈ 780 °C by HS-PVD. These coatings exhibit a thickness up to s = 20 μm. Moreover, phase analysis presents α-phases in coatings synthesized at substrate temperature of T _s ≈ 780 °C with significant higher hardness than films by T _s ≈ 570 °C. These release the potential of HS-PVD to synthesize α-Al₂O₃ coatings with high thickness. Thereby, a higher thickness of these coatings is beneficial for the wear protection of turning and die casting tools.     

Preparation and study of a thermo-responsive membrane using binary liquid crystal mixtures of cholesteryl cetyl ether and cholesteryl oleyl carbonate

A facile method for the synthesis of thermotropic liquid crystalline cholesteryl cetyl ether (CCE) was carried out from cholesterol and cetyl alcohol using montmorillonite K-10 as an acid catalyst. The aim of this study was to investigate the use of liquid crystalline blends of CCE and cholesteryl oleyl carbonate (COC) with appropriate crystal to smectic phase temperature (T _c?Cs) just above body temperature as a temperature-modulated drug permeation system. Using 30/70?mol ratio of COC/CCE, a mixture of desirable phase transition temperature was obtained. The phase transition behavior of COC/CCE binary liquid crystalline mixture was established by differential scanning calorimetry and polarizing optical microsopy. The COC/CCE-embedded cellulose nitrate membrane was used by an in vitro drug penetration studies. Paracetamol and mesalazine were chosen as hydrophobic and hydrophilic drug models, respectively. Paracetamol permeability through the membrane was higher at temperatures above the phase transition of liquid crystal (LC) blends (39?°C) than its permeability below the phase transition temperature of liquid crystal blends (30?°C). The drug penetration through LC-embedded cellulose membrane was influenced by the pore size of the membrane and therefore the adsorbed amount of LC. There was no penetration of mesalazine through that membrane presumably, due to the differences in hydrophilicity of LC-embedded membrane and permeated drug.     

Behavior of Boron in Molten Aluminum and its Grain Refinement Mechanism

The mechanism of heterogeneous grain refining of aluminum by ultrafine elemental boron particles was investigated. In order to facilitate the observation of the boron-aluminum interface, a boron filament was introduced in a melt at 1013 K (740 °C) containing different levels of Ti. The Al/B interface was studied using transmission electron microscopy and different phases were identified using the electron diffraction method. The experimental results showed that boron is dissolved in pure aluminum while its dissolution is inhibited in presence of titanium solute. A thin layer of TiB₂ formed at the surface of boron thickens with residence time in the melt. The mechanisms by which aluminum is crystallized on boron are discussed.