Influence of hydrodynamic instability on the heat transfer coefficient during condensation of R134a and R404A refrigerants in pipe mini-channels

This paper presents the results of an investigation of the influence of hydrodynamic instabilities on heat transfer intensity during the condensation of R134a and R404A refrigerants in pipe mini-channels. The heat transfer coefficient h is a measure of the effectiveness of the condensation process. It is particularly important to determine the value of the coefficient in the two-phase condensation area in a compact condenser. In other condenser areas (i.e., precooling of superheated vapor and subcooling of condensate), the heat efficiency is substantially smaller. Hydrodynamic instabilities of a periodic nature have an influence on size changes in these areas. A decrease in the heat transfer coefficient h in the two-phase area results in decreased intensity of the heat removal process in the whole condenser.The experimental investigations were based on the condensation of R134a and R404A refrigerants in horizontal pipe mini-channels with internal diameters of d = 0.64; 0.90; 1.40; 1.44; 1.92; 2.30 and 3.30 mm. Disturbances of the condensation process were induced with a periodic stop and a repetition of the flow of the refrigerant.In the range of frequencies, f = 0.25–5 Hz, of the periodically generated disturbances, an unfavorable influence on the intensity of the heat transfer during the condensation process in pipe mini-channels was identified. The reduction in the intensity of the heat transfer during the condensation process, which was induced with hydrodynamic instabilities, was presented in the form of the dependence of the heat transfer coefficient h on the vapor quality x and the frequencies f of the disturbances.The influence of the refrigerant, the diameter of the mini-channels and the frequency f on the damping phenomenon of the periodical disturbances in the pipe mini-channels was identified.     

Late psychosocial improvement in a case of severe head injury with bilateral fronto-orbital lesions.

Describes the results of a 19-yr follow-up study of a head-injured female patient. At age 17 yrs, the S sustained a blunt head trauma with bilateral fronto-orbital lesions verified by late regional cerebral blood flow. The S presented an extreme state of regression for many months after injury. During the first posttraumatic years no behavioral disorders were reported, but after the 5th yr lack of control, including sexual disinhibition, and lack of motivation became severe problems. More than 10 yrs after the accident, a partner applied a simple program of behavioral modification to the S. After 2 yrs of rigid training, an unexpected improvement in psychosocial adaptation took place. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

A Bench‐Scale Study of Conditioning Behaviour in Oil Sands Slurries

Proper conditioning of an oil sand/water slurry is essential for the efficient extraction of bitumen. The conditioning process depends on such variables as ore grade, temperature, mixing intensity, mixing time, and water composition. A technique has been developed in which a microscope and video cameras are used to observe a slurry stirred in a glass cell to evaluate, on a comparative basis, the effect of conditioning parameters on bitumen recovery. Several ores and their blends were studied and found to exhibit large differences in their conditioning behaviour. The method offers the capability of diagnosing ore processability problems and optimizing slurry conditioning.     

BioCatNet: A Database System for the Integration of Enzyme Sequences and Biocatalytic Experiments

The development of novel enzymes for biocatalytic processes requires knowledge on substrate profile and selectivity; this can be derived from databases and from publications. Often, these sources lack time‐course data for the substrate or product, and an unambiguous link between experiment and enzyme sequence. The lack of integrated, original data hampers the comprehensive analysis of enzyme kinetics and the evaluation of sequence–function relationships. In order to accelerate enzyme engineering, BioCatNet integrates protein sequence, protein structure, and experimental data for a given enzyme family. BioCatNet explicitly assigns the enzyme sequence to the experimental data, which consists of information on reaction conditions and time‐course data. BioCatNet facilitates the consistent documentation of reaction conditions, the archiving of time‐course data, and the efficient exchange of experimental data among collaborators. Data integration is demonstrated for three case studies by using the TEED (Thiamine diphosphate‐dependent Enzymes Engineering Database).     

A property‐based approach to the synthesis of material conservation networks with economic and environmental objectives

This article presents a multiobjective optimization model for the recycle and reuse networks based on properties while accounting for the environmental implications of the discharged wastes using life‐cycle assessment. The economic objective function considers fresh sources and treatment costs, whereas the environmental objective function is measured through the eco‐indicator 99. The model considers constraints in the process sinks as well as in the environment based on stream properties such as pH, chemical oxygen demand, toxicity, density, and color, in addition to the composition of the waste streams. A global optimization procedure is developed by indirectly tackling properties through property operators and by segregating the process streams before treatment. Three examples are included, and the results show that it is possible to consider simultaneously the trade‐offs between the total annual costs and the overall environmental impact using the proposed methodology. © 2010 American Institute of Chemical Engineers AIChE J, 2011     

Destruction of polyunsaturated alkyl/acyl and alkenyl/acyl glycerophosphocholine of plasma lipoproteins during incubation with group V and X secretory phospholipase A2s

Plasma lipoproteins are carriers of various glycerophospholipids including diacyl, alkenyl/acyl, and alkyl/acyl glycerophosphocholines (GPCs), which become distributed among cells and tissues during metabolism. For metabolic function, these phospholipids require hydrolysis by phospholipases, but the responsible enzymes have not been identified. We had previously shown that after complete digestion of lipoprotein diacyl- and oxo-diacyl-GPCs, degradation of residual alkyl/acyl and alkenyl/acyl GPCs continues, despite the fact that ether lipids are resistant to hydrolysis by Ca²⁺-activated secretory PLA₂s and require the presence of the Ca²⁺-independent PLA₂. In the course of further investigation, we came across a report by Khaselev and Murphy in which the autoxidative degradation of plasmalogens in the presence of 2,2′-azobis(2-amidinopropane) dihydrochloride (AAPH) proceeded beyond the formation of dihydroperoxides, hydroxides and epoxides, and led to an attack on the enyl bond of the plasmalogen, resulting in formation of 1-OH/2-20:4-GPC and 1-formyl/2-20:4-GPC. Our preliminary investigation indicated that lipoprotein 16:0p/20:4ω6-GPC yielded the same autoxidation products as those reported for synthetic 16:0p/20:4ω6-GPC in the presence of AAPH. Such autoxidative degradation of lipoprotein plasmalogens had not been previously reported with or without AAPH. Subsequent study led to the conclusion that this reaction was not limited to arachidonates, but extended to other polyunsaturated eicosanoids, docosanoids, and tetracosanoids, as well as oligounsaturated octadecanoids. These observations led to a hypothesis that the autoxidative cleavage of the lipoprotein plasmalogens proceeded under the influence of apo-protein-derived free radicals as intermediates of oxidative processes.     

The Effect of ZnAl2O4 on the Performance of Cu/ZnxAlyOx+1.5y Supported Catalysts in Steam Reforming of Methanol

This paper demonstrates the benefit of using spinel (ZnAl₂O₄) as a support for copper catalysts in hydrogen generation. We have investigated the influence of catalyst pre-treatment, support composition and copper content on the physicochemical and catalytic properties of copper catalysts supported on Zn_xAl_yO_x+1.5y in the methanol steam reforming. The physicochemical properties of the catalysts were examined by X-ray diffraction, temperature-programmed reduction, specific surface area and porosity, X-ray photoelectron spectroscopy, FTIR and chemisorption methods. The reduced copper catalysts showed higher conversion of methanol and higher hydrogen production. We also found that the presence of Cu⁺ and Cu⁰ species on the catalyst surface strongly influences the reaction yield and hydrogen production. FTIR measurements performed for copper catalysts confirmed that increasing of aluminium content in the case of catalytic systems caused the growth of adsorbed species on the catalyst surface.     

Solvent-Induced Formation of Novel Ni(II) Complexes Derived from Bis-Thiosemicarbazone Ligand: An Insight from Experimental and Theoretical Investigations

In this work, we report solvent-induced complexation properties of a new N₂S₂ tetradentate bis-thiosemicarbazone ligand (H₂L^I), prepared by the condensation of 4-phenylthiosemicarbazide with bis-aldehyde, namely 2,2’-(ethane-1,2-diylbis(oxy)dibenzaldehyde, towards nickel(II). Using ethanol as a reaction medium allowed the isolation of a discrete mononuclear homoleptic complex [NiL^I] (1), for which its crystal structure contains three independent molecules, namely 1-I, 1-II, and 1-III, in the asymmetric unit. The doubly deprotonated ligand L^I in the structure of 1 is coordinated in a cis-manner through the azomethine nitrogen atoms and the thiocarbonyl sulfur atoms. The coordination geometry around metal centers in all the three crystallographically independent molecules of 1 is best described as the seesaw structure. Interestingly, using methanol as a reaction medium in the same synthesis allowed for the isolation of a discrete mononuclear homoleptic complex [Ni(L^II)₂] (2), where L^II is a monodeprotonated ligand 2-(2-(2-(2-(dimethoxymethyl)phenoxy)ethoxy)benzylidene)-N-phenylhydrazine-1-carbothioamide (HL^II). The ligand L^II was formed in situ from the reaction of L^I with methanol upon coordination to the metal center under synthetic conditions. In the structure of 2, two ligands L^II are coordinated in a trans-manner through the azomethine nitrogen atom and the thiocarbonyl sulfur atom, also yielding a seesaw coordination geometry around the metal center. The charge and energy decomposition scheme ETS-NOCV allows for the conclusion that both structures are stabilized by a bunch of London dispersion-driven intermolecular interactions, including predominantly N–H∙∙∙S and N–H∙∙∙O hydrogen bonds in 1 and 2, respectively; they are further augmented by less typical C–H∙∙∙X (where X = S, N, O, π), CH∙∙∙HC, π∙∙∙π stacking and the most striking, attractive long-range intermolecular C–H∙∙∙Ni preagostic interactions. The latter are found to be determined by both stabilizing Coulomb forces and an exchange-correlation contribution as revealed by the IQA energy decomposition scheme. Interestingly, the analogous long-range C–H∙∙∙S interactions are characterized by a repulsive Coulomb contribution and the prevailing attractive exchange-correlation constituent. The electron density of the delocalized bonds (EDDB) method shows that the nickel(II) atom shares only ~0.8|e| due to the σ-conjugation with the adjacent in-plane atoms, demonstrating a very weak σ-metalloaromatic character.