Impact of arteriovenous fistula cannulation on the quality of dialysis

Introduction: Adequate hemodialysis directly improves health. Puncturing an arteriovenous fistula (AVF) and the amount of blood recirculation greatly affect the quality of dialysis. Few studies have assessed the method to cannulate a fistula and its influence on efficiency of hemodialysis. Methods: This prospective pilot study included 14 patients with end‐stage renal failure receiving regular intermittent hemodialysis. Patients received three consecutive treatments with both needles directed upstream then three consecutive treatments with the venous needle directed upstream and the arterial needle directed downstream. With both techniques, the distance between the needles was kept constant at 2.5 cm. Recirculation rate and Kt/V ratio were measured during each treatment using thermodilution and a diascan Fresenius generator. Findings: The 14 patients received 84 hemodialysis sessions: i.e., 8 (57.1%) males and 6 (42.8%) females, mean age 62.3 ± 15.57 years. Results showed that mean recirculation rates and Kt/V did not significantly differ between the two techniques. Discussion: Because no significant difference was found between the two techniques, the direction of insertion of needles should be decided upon on a case‐by‐case basis depending on the anatomy of the AVF and the feasibility of the puncture.     

Contribution of Solutes to Density Stratification in a Meromictic Lake (Waldsee/Germany)

Density differences are the key parameter for stratification stability. We used data from the iron-meromictic Waldsee, Germany, a lignite mine pit lake, to quantify the contribution of single solutes to water density and analyzed the density gradient. Iron meromictic lakes maintain their density gradient through chemical reactions. Hence, quantifying the contributions of separate solutes is essential for understanding the entire process. Based on solute concentrations and literature values of partial molal volumes, substance specific density contributions were quantitatively evaluated. Then, by direct measurements of the density of IHSS Waskish peat fulvic acid, we quantified the density contribution of dissolved organic carbon (DOC). While several solutes contributed to the density throughout the water column, only those substances that occurred at higher concentrations in the anoxic monimolimnion than in the oxic mixolimnion were crucial to sustaining the density difference between the two layers. In Waldsee, the density difference between monimolimnion and mixolimnion was attributed to dissolved Fe²⁺ (0.23?g/L, resulting in a 45?% of the density difference due to solutes) and to the carbonate system (HCO₃ ^?, about 0.16?g/L and CO₂, 0.03?g/L) while Ca²⁺ and DOC delivered only a small contribution. In summer, total density differences were dominated by temperature differences; during winter, solutes sustained meromixis. Finally, we present a complete list of specific density fractions for basically all of the density-relevant substances in fresh waters.     

Statistical search space reduction and two-dimensional data display approaches for UPLC-MS in biomarker discovery and pathway analysis

A new analytical strategy for biomarker recovery from directly coupled ultra-performance liquid chromatography time-of-flight mass spectrometry (UPLC Tof MS) data on biofluids is presented and exemplified using a study on hydrazine-induced liver toxicity. A key step in the strategy involves a novel procedure for reducing the spectroscopic search space by differential analysis of cohorts of normal and pathological samples using an orthogonal projection to latent structures discriminant analysis (O-PLS-DA). This efficiently sorts principal discriminators of toxicity from the background of thousands of metabolic features commonly observed in data sets generated by UPLC-MS analysis of biological fluids and is thus a powerful tool for biomarker discovery.     

Stabilization of Ethanol-Based Alumina Suspensions

Al₂O₃ powders have been successfully dispersed in ethanol by varying the suspension acidity. An operational pH (O.pH) was defined to measure the acidity of these ethanol-based suspensions. The isoelectric point of Al₂O₃ in ethanol was at an O.pH of 8. According to Derjaguin–Landau–Verwey–Overbeek (DLVO) theory, suspensions between an O.pH of 3.5–10.5 possessed only attractive inter-particle potential. Suspensions below 3.5 had high ζ potential, fine particle size, and were Newtonian. However, suspensions at high pH were shear thinning and consisted of agglomerates, despite their high ζ potential. The use of citric acid as a dispersant has also been investigated. At an O.pH of 3, optimum additions of citric acid between 0.6 and 1.0 wt% decreased the particle size, resulted in repulsive inter-particle potentials and increased the solid loading capacity to 15 vol% from 2 vol% while maintaining Newtonian behavior and similar viscosity to suspensions at O.pH 2. Addition of citric acid created agglomerated suspensions that were negatively charged at O.pH 10.5 (obtained by adding NH₄OH), but positively charged suspensions at O.pH 13.6 (obtained by adding tetramethylammonium hydroxide).     

State-of-the-Art in the Measurement of Volatile Organic Compounds Emitted from Building Products: Results of European Interlaboratory Comparison

Abstract Eighteen laboratories from 10 European countries participated in a comparison organized as part of the VOCEM project, a 2.5-year research collaboration among 4 research institutes and 4 industrial companies. The scope of the project was to improve the procedure used to measure volatile organic compounds (VOC) emitted from building materials and products in small test chambers. The interlaboratory comparison included the GC-MS determination of 5 target compounds from carpet, 8 from polyvinyl chloride (PVC) cushion vinyl and 2 from paint; for the first time, chamber recovery (sinks), homogeneity of solid materials and possible contamination during transport were tested. The results show that the intralaboratory variance (random errors) is much smaller than the interlaboratory variance (systematic errors). Causes of the largest interlaboratory discrepancies were: (i) analytical errors; (ii) losses of the heaviest compounds due to sorption on the chamber walls; and (iii) non homogeneity of the materials. The output of this work concerns both the objective of labelling materials with regard to their VOC emissions and the pre-standard drafted by the European Commitee for Standardization (CEN) for this type of determination.     

Modelling of the operation of Polymer Exchange Membrane Fuel Cells in the presence of electrodes flooding

This paper presents a simple pseudo-2D model of Polymer Exchange Membrane Fuel Cell including mass transport limitation due to flooding. The gas channels are assumed parallel to the membrane and the changes in gas composition due to the electro-chemical reactions are taken into account. The overpotentials at anode and cathode are evaluated by a Tafel law while a simple reasoning about heat transfer shows that at the highest intensities, liquid water appears at the cathode-backing layers interface. It is assumed that the appearance of liquid defines the local value of the limiting current density. The results of this model differ from those obtained with a conventional 1D approach when there is a high difference in water inlet concentration between hydrogen and air channels. Furthermore, the pseudo-2D model proposes a credible representation of the high-intensity range of the polarization curve, and allows to determine the limiting current in the whole cell, as a function of gases hydration.     

Sintering process optimization for multi-layer CGO membranes by in situ techniques

The sintering of asymmetric CGO bi-layers (thin dense membrane on a porous support; Ce_0.9Gd_0.1O_1.95?δ = CGO) with Co₃O₄ as sintering additive has been optimized by combination of two in situ techniques. Optical dilatometry revealed that bi-layer shape and microstructure are dramatically changing in a narrow temperature range of less than 100 °C. Below 1030 °C, a higher densification rate in the dense membrane layer than in the porous support leads to concave shape, whereas the densification rate of the support is dominant above 1030 °C, leading to convex shape. A flat bi-layer could be prepared at 1030 °C, when shrinkage rates were similar. In situ van der Pauw measurements on tape cast layers during sintering allowed following the conductivity during sintering. A strong increase in conductivity and in activation energy E_a for conduction was observed between 900 and 1030 °C indicating an activation of the reactive sintering process and phase transformation of cobalt oxide.     

Transient air cooling thermal modeling of a PEM fuel cell

Fuel cell utilization for automobile and residential applications is a promising option in order to help reduce environmental concerns such as pollution. However, fuel cell development requires addressing their dynamic behavior to improve their performances and their life cycle. Since the temperature distribution in the cell is known to be an important factor to the fuel cell's efficiency, a cooling device is often added to homogenize the temperature in the cell and to ensure temperature control.     

Formation of pyridone derivates from maltose and lactose. XII. Investigations on the Maillard-reaction (authors transl)]

Effect of sodium nitrite on cultured FM3A cells, a C3H mouse mammary carcinoma cell line, was examined. The chromosomal preparations demonstrated that severe aberrations were induced in more than 80% of the mitotic plates at 10(-2) M and in nearly 40% at 10(-25) M after 24 and 48 h treatment. According to the results of alkaline sucrose gradient analysis sedimentation profiles of cell DNA treated at as high as 10(-1) M for 24 h scarcely changed from that of control cell DNA. Induction of 8-azaguanine-resistant mutation was demonstrated above 10(-3) M sodium nitrite.     

Planar Metal‐Supported SOFC with Novel Cermet Anode

Metal‐supported solid oxide fuel cells are expected to offer several potential advantages over conventional anode (Ni‐YSZ) supported cells. For example, increased resistance against mechanical and thermal stresses and a reduction in material costs. When Ni‐YSZ based anodes are used in metal supported SOFC, elements from the active anode layer may inter‐diffuse with the metallic support during sintering. This work illustrates how the inter‐diffusion problem can be circumvented by using an alternative anode design based on porous and electronically conducting layers, into which electrocatalytically active materials are infiltrated after sintering. The paper presents the electrochemical performance and durability of the novel planar metal‐supported SOFC design. The electrode performance on symmetrical cells has also been evaluated. The novel cell and anode design shows a promising performance and durability at a broad range of temperatures and is especially suitable for intermediate temperature operation at around 650 °C.