Correction to: Embrittlement Analysis of Σ5[210]/(-1-20) FeAl Grain Boundary in Presence of Defects: An Ab Initio Study

Metallurgical and Materials Transactions A -     

Cellulose/acrylic acid copolymer blends for films and coating applications

Enzymatically treated cellulose was dissolved in a NaOH/ZnO solvent system and mixed together with poly(ethylene‐co‐acrylic acid) (PE‐co‐AA) or poly(acrylamide‐co‐acrylic acid) (PAA‐co‐AA) polymers, in order to improve the properties of dissolved cellulose and to prepare homogeneous cellulose‐based blends for films and coatings. The solution stage properties of the blends were evaluated by rheological methods and the precipitated dry blends were characterized by dynamic mechanical analysis, differential scanning calorimetry, and scanning electron microscopy. Paperboard coating tests done at laboratory scale showed dissolved cellulose/acrylic acid copolymer‐based blends function well as coating materials. All of the tested blends showed a good resistance against grease in the coating trials, having grease resistance from 60 to 69 days despite a very thin (～2 µm) coating layer. In addition, cellulose/PE‐co‐AA coating showed improved water vapor and oxygen barrier properties when compared with neat dissolved cellulose‐coated paperboard. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40286.     

Functionalized polypropylene prepared by melt free radical grafting of low volatile oxazoline and its potential in compatibilization of PP/PBT blends

This article concerns the functionalization of polypropylene (PP) with oxazoline functionality by melt free radical grafting along with a low degree of degradation of PP in a batch mixer. A low volatile oxazoline, ricinoloxazoline maleinate (OXA), was used as the monomer. The grafting yield of OXA ranged from about 0.5 phr up to 1.5 phr (grams per 100 grams of PP) when its initial concentration and that of the peroxide ranged from 1.5 to 6.0 phr and 0.1 to 0.7 phr, respectively. The corresponding conversion of OXA to grafted OXA ranged from about 15 to 50%. Addition of styrene (St) as the comonomer did not enhance the grafting yield of OXA but markedly reduced the PP degradation. Also, little homo-and/or copolymers of OXA and/or St were found in the grafting system. This agrees with our finding that OXA and St did not copolymerize easily. The potential of using an OXA modified PP (PP-g-OXA) as the compatibilizer precursor in PP/PBT blends was examined as well. The presence of PP-g-OXA reduced the particle size of the dispersed phase (PBT) along with improved cohesion between the PP and PBT phases. This is consistent with a model kinetic study, which showed that the reaction between oxazoline and carboxylic functionalities was very fast. © 1996 John Wiley & Sons, Inc.     

Silage fermentation of fish or fish waste products with lactic acid bacteria

Silage fermentation of minced fish and fish offal after inoculation with cereals prefermented with Pediococcus acidilactici and Lactobacillus plantarum initiates a rapid fall in pH to below 4.5 within 30 h, and the content of competing gram-negative fermenters and fish pathogens, such as Vibrio anguillarum and Aeromonas salmonicida, is eliminated. The addition of 0.1% sorbic acid inhibits the growth of yeasts during the initial fermentation period and during storage but does not affect the lactic acid fermentation. Degradation of nitrogen components proceeds during storage and is manifested as an increase in volatile basic nitrogen compounds, amino acids and peptides. These substances increase the pH and/or force the bacteria to produce more acid. The rate of production of these basic substances is mainly temperature-dependent and cannot be attributed to microbial activity. The proteolytic activity is mainly caused by tissue proteases (e.g., cathepsins) and, to a lower degree, by gut proteases. It is doubtful whether fish fermentation can be utilised on an industrial scale without improving the technique. Such improvements consist of the selection and use of psychotrophic lactic acid fermenters and commercially acceptable inhibitors of proteolytic activity and yeast growth.     

A hybrid lithium‐ion battery model for system‐level analyses

We describe an advanced lithium‐ion battery model for system‐level analyses such as electric vehicle fleet simulation or distributed energy storage applications. The model combines an empirical multi‐parameter model and an artificial neural network with particular emphasis on thermal effects such as battery internal heating. The model is fast and can accurately describe constant current charging and discharging of a battery cell at a variety of ambient temperatures. Comparison to a commonly used linear kilowatt‐hour counter battery model indicates that a linear model overestimates the usable capacity of a battery at low temperatures. We highlight the importance of including internal heating in a battery model at low temperatures, as more capacity is available when internal heating is taken into account. Copyright © 2016 John Wiley & Sons, Ltd.     

Water hydraulic manipulator for fail safe and fault tolerant remote handling operations at ITER

Department of Intelligent Hydraulics and Automation (IHA) of Tampere University of Technology has been involved in the European Fusion program since 1994 within the ITER reactor maintenance activities. In this paper we discuss the design and development of a six degrees of freedom water hydraulic manipulator with a force feedback for teleoperation tasks. The manipulator is planned to be delivered to Divertor Test Platform 2 (DTP2) during year 2008. The paper also discusses the possibility to improve the fail safe and redundant operation of the manipulator. During the design of the water hydraulic manipulator, special provisions have been made in order to meet the safety requirements such as servo valve block for redundant operation and safety vane brakes for fail safe operation.     

Experimental Novel Silane System in Adhesion Promotion Between Dental Resin and Pretreated Titanium

Five silane blends were evaluated as experimental adhesion-promoter primers. First, five organosilane monomers (silicon esters), 3-acryloxypropyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, tetrakis-(2-ethyloxyethoxy)silane and bis-[3-(triethoxysilyl)propyl]tetrasulfide, were diluted to 1% (v/v) and blended with a non-functional cross-linking silane, 1,2-bis-(triethoxysilyl)ethane (1%), in 95% ethanol. After activation, each blend was applied to silica-coated Ti coupons. A resin based on bis-phenol-A-diglycidyldimethacrylate was then bonded and photo-polymerized as stubs to the pretreated Ti coupons. Half of the specimens were stored in dry conditions and half were artificially aged by thermo-cycling. The primers containing 3-acryloxypropyltrimethoxysilane and 3-methacryloxypropyltrimethoxysilane produced significantly higher shear bond strength values than the control silane, a standard pre-activated product used in clinical dentistry.     

Germanium-68 as a tracer for silicon fluxes in freshwater sediment

The sorption of Si may decisively influence the P dynamics in surface sediment through competitive ligand exchange mechanisms. Many aspects of the process, such as the impact of Si dissolving from diatoms, are both insufficiently known and difficult to monitor by quantitative analyses due to the ubiquitousness of Si in sediment. Since the radioactive isotopes of Si have impractical half-times, the applicability of 68Ge as a tracer for Si additions in both inorganic and biogenic form to freshwater sediment (Lake Vesij?rvi, Southern Finland) was studied in a 24-h laboratory experiment. The 68Ge-label was added to the sediment with either inorganic Si (940mg l(-1)) or diatoms (3.2 x 10(6) cellsl(-1)), and the distributions of the 68Ge-label and the different forms of added Si between the interstitial water and sequentially extracted, solid-phase sediment pools were critically examined. The inorganic Si addition significantly increased the amount of Si in the interstitial water and in the reversibly bound fraction, while the diatom addition had no discernible effects. The relative distribution of Si and 68Ge between the various sediment pools indicated that the first sorption phase of the added inorganic Si was similar to that reported for P. The high concentration of diatom-derived 68Ge-labelled Si in the interstitial water and in the easily soluble, reversibly bound pool indicated rapid dissolution of the added diatoms. The comparable distributions of the diatom-derived and inorganic Si-derived 68Ge-label within the studied pools indicated that the sorption of Si dissolving from diatoms in surface sediment closely resembles that of an inorganic addition of Si. Caution about the chemical speciation of the 68Ge-label is, however, advisable in sediment environments. Fractionation procedures designed for e.g. P may also be of limited use when applied to a different element, such as Si.