Electrodialysis for bleach effluent recycling in kraft pulp production: Simultaneous control of chloride and other non-process elements

In the United States, more than 50 million tons of kraft pulp are produced per year. A strong effort by kraft pulp producers has been under way for several years to reduce water use. The in-process recycling of the acidic bleach effluent carrying metals, transition metals, calcium, and often large amounts of chloride is still a significant challenge. The simultaneous selective removal of chloride, and detrimental cations from the acidic bleach effluent of bleached kraft pulp mills by electrodialysis was investigated. The laboratory results with actual effluents show that very good removal levels can be achieved in an economical process. The chloride removal from acidic bleach effluent will aid significantly in keeping chloride levels acceptable in the recovery cycle.     

Strain Rate Dependency of Simulated Welding Residual Stresses

In the present work, the influence of taking into consideration the strain rate-dependent nature of steel S355 during a calculation of the welding residual stresses through a finite element simulation is investigated. The Perzyna material model is calibrated using experimental values found in the literature and is introduced to a validated weld simulation model, where the strain rate dependency had not been taken into consideration before this study. The calculated profiles of the welding residual stresses, for strain rate-dependent and independent behavior, are then compared with experimentally measured profiles. The results of this first-step analysis show that taking into consideration strain rate dependency during a welding simulation of the investigated S355 has non-negligible influence on the calculated welding residual stresses.     

Experimental validation of a 1-D continuous thickening model using a pilot column

Predictive modelling of solid–liquid separation can greatly assist the design and operation of thickening and filtration equipment, improving water recovery and reducing costs. A phenomenological model describing continuous thickening has been previously developed with primary inputs being the material properties, (compressive yield stress and hindered settling function) derived from routine laboratory batch settling and filtration tests. This work aimed to validate the model by operating a pilot column continuously and measuring the underflow solids. The column was operated at two different solid fluxes and several bed heights. Additionally, the influence of flocculation conditions (polymer dosage and residence time) on thickening performance were studied. The model predicted the experimental underflow solids concentration at a given flux. For the observed underflow solids concentration, the ratio of the actual to predicted flux was observed to be between a factor of 1 (accurate) and 10. The model was most accurate for the lowest bed heights. This work confirmed the model was able to correctly predict trends for the case where minimal bed height and shear forces are present. Deviation from the model is postulated to be due to changes in the dewatering properties of flocculated aggregates over time that are not adequately captured using conventional batch sedimentation tests. The data from these tests are traditionally used as a key input to thickening models.     

Poly[(N‐isopropylacrylamide)‐co‐(itaconic acid)] hydrogels with poly(ethylene glycol)

The aim of the work reported here was to investigate temperature‐ and pH‐sensitive hydrogels of N‐isopropylacrylamide (NIPAM) and itaconic acid (IA) and their semi‐interpenetrating polymer networks (semi‐IPNs) with varying contents of poly(ethylene glycol) (PEG). The stimuli responsiveness, swelling behaviour and mechanical properties of the hydrogels and semi‐IPNs were studied in order to investigate the effect of various amounts of PEG. Pulsed‐gradient spin‐echo NMR experiments were carried out to investigate the diffusion process. The pH sensitivity increased with an increasing amount of PEG in the semi‐IPNs, while the overall rate of water uptake was diffusion‐controlled (n < 0.5). For certain PEG contents (5 and 10 wt%), the semi‐IPNs exhibited better mechanical properties than the poly(NIPAM‐co‐IA) copolymer. The calculated values of the self‐diffusion coefficients of water indicated facilitated diffusion of water through the system with increased amounts of PEG, while the self‐diffusion coefficients of a model compound, metoprolol tartrate, showed no significant dependence on the amount of PEG. According to the results obtained and compared to results reported in the literature, the investigated semi‐IPNs may have potential applications in the controlled release of macromolecular active agents such as proteins and peptides. Copyright © 2009 Society of Chemical Industry     

Improved mechanical properties of poly(ethylene terephthalate) nanocomposite fibers

Improvements in Young's modulus and strength (tenacity) of poly(ethylene terephthalate) (PET) fibers were obtained by drawing unoriented nanocomposite filaments containing low concentrations (<3 wt%) of various organically modified montmorillonites (MMTs) in a second step at temperatures above the glass transition. Prior to melt spinning, solid‐state polymerization was used to rebuild lost molecular weight, due to MMT‐induced degradation, to a level suitable for producing high strength fibers. Greater improvements in mechanical properties occurred when the MMT stacks were intercalated with PET. A nominal 1 wt% loading of dimethyl‐dehydrogenated tallow quaternary ammonium surface modified MMT in drawn PET fiber showed a 28% and 63% increase in Young's modulus and strength, respectively. Relative to an unfilled PET fiber, these results surpassed the upper bound of the rule of mixtures estimate and suggested that both the type of surface modification and concentration of MMT affect the degree of PET orientation and crystallinity. Furthermore, drawability above T_g and elongation at break increased upon the addition of organically modified MMT to unoriented PET fibers, which was a key distinction of this work from others examining similar systems. POLYM. ENG. SCI., 2010. © 2010 Society of Plastics Engineers     

An ideal point method for the design of compromise experiments to simultaneously estimate the parameters of rival mathematical models

When several rival mathematical models are proposed for one and the same process, experimental design techniques are available to design optimal discriminatory experiments. Because these techniques are model-based, it is important that the model predictions are not too uncertain. Therefore, model discrimination may become more efficient and effective if this uncertainty is reduced first. This can be achieved by performing experiments designed to increase the accuracy of the parameter estimates and, thus, the model predictions. However, performing such an additional experiment for each rival model may undermine the overall goal of optimal experimental design, which is to minimize the experimental effort. This paper deals with the design of a so-called compromise experiment, which is an experiment that is not optimal for each of the rival models, but sufficiently informative to improve the overall accuracy of the parameters of all rival models. For this purpose, the problem is approached as a multi-objective optimization problem and the ideal point method is proposed to design the compromise experiment. This method searches for the experiment that is as close as possible to the optimal experiments of the individual rival models. The method is applied to a case study where nine rival models are competing to describe the kinetics of an enzymatic reaction, and the obtained results show that the ideal method is capable of designing a compromise experiment.     

NanoSIMS: Insights into the Organization of the Proteinaceous Scaffold within Hexactinellid Sponge Spicules

The giant basal spicules (GBS) from Monorhaphis chuni (Porifera [sponges], Hexactinellida) represent the largest biosilica structures on Earth and can reach lengths of 300 cm (diameter of 1.1 cm). The amorphous silica of the inorganic matrix is formed enzymatically by silicatein. During this process, the enzyme remains trapped inside the lamellar‐organized spicules. In order to localize the organic silicatein scaffold, the inside of a lamella has been analyzed by nano‐secondary ion mass spectrometry (NanoSIMS). It is shown that the GBSs are composed of around 245 concentrically arranged individual siliceous lamellae. These surround an internal siliceous axial cylinder. The lamellae adjacent to the cylinder are thicker (10–30 μm) than the more peripheral lamellae (2–10 μm). One lamella of a thickness of 18 μm has been selected for further analysis. This lamella itself is composed of three sublamellae with an individual thickness of 2–6 μm each, which are then further organized into three cylindrical slats (thickness: 1.6–1.8 μm). Other than the main lamellae, the sublamellae are not separated from each other by gaps. The element analysis of the sublamellae by NanoSIMS revealed that the siliceous matrix is embedded in an organic matrix that consists of up to 6–10 wt/% of C. The pattern of C distribution reflects a distinct zonation of the organic material within the solid intralamellar biosiliceous material. A growth model for the lamella starting from nanosized silica particles is proposed: During formation of a lamella nanosized silica particles fuse, through biosintering processes, to slats that build the individual sublamellae, which then finally form the lamellae. In turn, those lamellae may form the higher structural entity, the axial cylinder.     

Membrane‐Surface Anchoring of Charged Diacylglycerol‐Lactones Correlates with Biological Activities

Synthetic diacylglycerol‐lactones (DAG‐lactones) are effective modulators of critical cellular signaling pathways, downstream of the lipophilic second messenger diacylglycerol, that activate a host of protein kinase C (PKC) isozymes and other nonkinase proteins that share similar C1 membrane‐targeting domains with PKC. A fundamental determinant of the biological activity of these amphiphilic molecules is the nature of their interactions with cellular membranes. This study examines the biological properties of charged DAG‐lactones exhibiting different alkyl groups attached to the heterocyclic nitrogen of an α‐pyridylalkylidene chain, and particularly the relationship between membrane interactions of the substituted DAG‐lactones and their respective biological activities. Our results suggest that bilayer interface localization of the N‐alkyl chain in the R² position of the DAG‐lactones inhibits translocation of PKC isoenzymes onto the cellular membrane. However, the orientation of a branched alkyl chain at the bilayer surface facilitates PKC binding and translocation. This investigation emphasizes that bilayer localization of the aromatic side residues of positively charged DAG‐lactone derivatives play a central role in determining biological activity, and that this factor contributes to the diversity of biological actions of these synthetic biomimetic ligands.     

Copper Transfer from Cu–Aβ to Human Serum Albumin Inhibits Aggregation,Radical Production and Reduces Aβ Toxicity

Amyloid‐β peptides (Aβ) and the protein human serum albumin (HSA) interact in vivo. They are both localised in the blood plasma and in the cerebrospinal fluid. Among other functions, HSA is involved in the transport of the essential metal copper. Complexes between Aβ and copper ions have been proposed to be an aberrant interaction implicated in the development of Alzheimer's disease, where Cu is involved in Aβ aggregation and production of reactive oxygen species (ROS). In the present work, we studied copper‐exchange reaction between Aβ and HSA or the tetrapeptide DAHK (N‐terminal Cu‐binding domain of HSA) and the consequence of this exchange on Aβ‐induced ROS production and cell toxicity. The following results were obtained: 1) HSA and DAHK removed Cu^II from Aβ rapidly and stoichiometrically, 2) HSA and DAHK were able to decrease Cu‐induced aggregation of Aβ, 3) HSA and DAHK suppressed the catalytic HO^. production in vitro and ROS production in neuroblastoma cells generated by Cu–Aβ and ascorbate, 4) HSA and DAHK were able to rescue these cells from the toxicity of Cu–Aβ with ascorbate, 5) DAHK was more potent in ROS suppression and restoration of neuroblastoma cell viability than HSA, in correlation with an easier reduction of Cu^II–HSA than Cu–DAHK by ascorbate, in vitro. Our data suggest that HSA is able to decrease aberrant Cu^II–Aβ interaction. The repercussion of the competition between HSA and Aβ to bind Cu in the blood and brain and its relation to Alzheimer's disease are discussed.