Blood Flow,Negative Pressure,and Hemolysis During Hemodialysis

Blood flow, measured by an ultrasound flowmeter, and the extent of hemolysis were assessed during a single, routine dialysis in 100 patients. Before and after the hemodialysis session, blood was drawn for measurements of haptoglobin (HPT), hemoglobin (HGB), albumin (ALB), and lactate dehydrogenase (LDH). The average values were as follows: pump speed 510 mL/ min, real blood flow 422 mL/min, arterial chamber pressure -350 mm Hg, and venous chamber pressure 279 mm Hg. Haptoglobin concentrations were higher in patients with central vein catheters compared to patients with arteriovenous access. The meaning of this finding is unclear. Mean HPT concentrations increased significantly less during hemodialysis (2.37%) than concentrations of ALB (11.3%), HGB (9.17%), and LDH (18.2%), indicating that some hemolysis is present in all dialyses. In dialyses with arterial chamber pressures more negative than -350 the median concentration of ALB (8.70%) increased significantly more than the median concentration of HGB (7.99%). This indicates significantly more hemolysis in dialyses with more negative pressures compared to those with less negative arterial chamber pressures. Median LDH increased more in dialyses with more negative prepump chamber pressures (16.19% vs 13.78%), but not significantly; however, LDH increases were significantly higher than either HGB or ALB, thus indicating significantly more hemolysis in dialyses with more negative pressures compared to those with less negative arterial chamber pressures. Erythropoietin dose was not significantly different in patients dialyzed with more or less negative arterial chamber pressures (17 645 ± 1226 U/week vs 16 308 ± 1506 U/week). We conclude that dialyses with negative arterial chamber pressures greater than -350 mm Hg cause slightly higher hemolysis than dialyses with less negative arterial chamber pressures, but this increased hemolysis is not associated with an increased requirement of erythropoietin dose. Whether this increased hemolysis is of clinical significance is uncertain.     

Grain Size and Wettability of TiO_2/SiO_2 Photocatalytic Composite Thin Filing

1 IntroductionTransparent super-hydrophilic self-cleaningTiO, thin films on glass substrates have highpotentialities for practical aPPlications such asmirrors, window glasses, windshields of automobiles, etc. The super-hydrophilic property ofthe surface allows water to spread completelyacross the surface rather than to remain asdroplets, Which malles the surface anti-foggingand easily washing. Recently, there are some research papers abollt the super-hydrOPhilic prOPerty of TiO, coating fi…     

Living anionic polymerization

For about 40 years living anionic polymerization has been the premier technique for the synthesis of model polymers of controlled architecture and narrow molecular weight distribution (MWD). Nowadays, despite the continuing development of new strategies for the synthesis of well-defined polymers and copolymers (e.g. group transfer polymerization, living radical polymerization, etc.), anionic polymerization continues to be the most reliable and versatile method for the synthesis of a wide variety of model polymers. The main reason for the broad utility of living anionic polymerization is that the conditions necessary for the efficient generation of polyanions that do not undergo termination or chain transfer reactions are well established for many monomers [Hsieh HL, Quirk RP. Anionic polymerization: principles and practical applications, New York: Marcel Dekker, 1996]. Despite these successes, significant challenges remain in the field of anionic polymerization. These challenges include extension of the strategies for anionic synthesis of polymers with controlled architectures (such as star and graft copolymers), further development of strategies for chain end functionalization, and mastering control over polymerization of (meth)acrylates. Recent advances in these areas are summarized in this article.     

NEW TECHNIQUES AND METHODS FOR THE STUDY OF AGGREGATION, ADSORPTION, AND SOLUBILITY OF ASPHALTENES. IMPACT OF THESE PROPERTIES ON COLLOIDAL STRUCTURE AND FLOCCULATION

The solubility of Furrial asphaltene in toluene was 57g L^-1. However, using a new technique, based on the precipitation of this sample by the phenol PNP, we found that a fraction [2], comprising 47% of the asphaltene, is of low solubility. This suggested that this material constitutes the colloidal phase, and the rest acts as the dispersing fraction. This technique allowed the fractionation of asphaltenes in fractions A₁, A₂, and A₃ according to solubility, going from practically insoluble (A₁) to low (A₂, 1 g L^-1) to high (A₃, around 57 g L^-1). The adsorption isotherms of asphaltenes on glass and silica in toluene consist of a sequence of steps or step-wise adsorption. The first layer or first step is formed by the adsorption of free asphaltene molecules and by small aggregates (aggregation number between 3 and 6) which saturate the glass or silica surface in the usual manner (L-type or H-type isotherms). However, we suggest that the second, third, and other asphaltene layers adsorb sequentially according to the above differences in solubility. The very slow changes with time and the negligible desorption from the surface measured for the above isotherms were interpreted as the effect of packing or the building up of a well packed layer. This would be achieved by the slow formation and rupture of bonds between neighboring molecules at the surface. Thus, molecules with difficulties to pack, adsorbed by a kinetically controlled process, are either rejected or relocated in a thermodynamic controlled process. The above results and ideas were used to improve the models for asphaltene and petroleum colloids and to underscore the importance of surfaces and colloid dispersants in asphaltene precipitation during the production of crude oils. For instance, the results described below suggest that colloids are constituted by a well packed and insoluble asphaltene core, impervious to the solvent, and by a loose packed periphery which, by allowing solvent penetration, keep the colloid in solution. According to this model, desorption of compounds in the above loosely packed periphery, such as the one promoted by a surface, would be the main cause of asphaltene precipitation from crude oils. In this case, solubility reductions caused by pressure drops during oil production would have a minor effect. Also, preliminary number average molecular weights M_n for four asphaltenes, obtained using a new procedure, are presented here. The M_n values obtained ranged from 780 to 1150 g/mol.     

超重力法制备纳米硫化锌

以硝酸锌和硫化氢为原料,在超重力旋转床(RPB,Rotating Packed Bed)中首次制备了球形、粒径分布较窄、分散性较好的闪锌矿纳米硫化锌粒子,平均粒径为30nm,转化率97.5％;研究了陈化时间对粒子形貌和大小的影响.并采用TEM、紫外可见光分光光度计、XRD等手段对产品的形貌、紫外吸收性能及晶相进行了表征.     

Tensile Creep Behavior of a Vitreous-Bonded Aluminum Oxide under Static and Cyclic Loading

Creep deformation and rupture behavior of a vitreousbonded aluminum oxide was investigated under uniaxial static and cyclic tensile loadings at 1000°, 1100°, and 1175°C. The material was more creep resistant, i.e., having lower creep strain rates, under cyclic loading compared to that under static loading. For the same maximum applied stress, the ratio of steady-state creep rate under static loading to that under cyclic loading at 1100°C was approximately 100. However, the value of this ratio decreased to about 10 when the testing temperature was raised to 1175°C or lowered to 1000°C. Under static loading the material had more propensity to develop creep damage in the form of micro- and macrocracks, leading to early failure, whereas under cyclic loading the creep damage was more uniformly distributed in the form of cavities confined to the multigrain junctions. Viscous bridging by the grain boundary second phase may be the primary contributor to the lower creep deformation rate and improved lifetime under cyclic loading.     

Conformation of oligo(ethylene glycol) grafted polystyrene in dilute aqueous solutions

Temperature induced conformational changes of poly(p-oligo(ethylene glycol) styrene) (POEGS) in aqueous solutions were investigated by small angle neutron scattering (SANS), neutron transmission and dynamic light scattering (DLS). The molecular weight of the polymer studied was 9400 g/mol with a polydispersity index of 1.18 and each repeat unit of the polymer had four ethylene glycol monomer segments. The polymer was water soluble due to the hydrophilicity of the OEG side chains and these solutions showed lower critical solution temperature (LCST) depending on the concentration of the polymer. Measurements of solution behavior were made as a function of temperature in the range of 25-55 °C for three polymer concentrations (0.1 wt%, 0.3 wt%, and 1.8 wt%). Neutron transmission measurements were used to monitor the amount of polymer which precipitated or remained in solution above the cloud point temperature (T_CP). DLS revealed the presence of large clusters in all solutions both below and above T_CP while SANS provided information on the structure and interactions between individual chains. It was found that in the homogeneous region below T_CP the shape of individual polymers in solution was close to ellipsoidal with the dimensions R_a = 37 Å and R_b = 14 Å and was virtually independent of temperature. The SANS data taken for the most concentrated solution studied (1.8 wt%) were fit to the ellipsoidal model with attractive interactions which were approximated by the Ornstein-Zernike function with a temperature-dependent correlation length in the range of 24-49 Å. The collapse of individual polymers to spherical globules with the radius of 15 Å above T_CP was observed.     

Ag／TiO2光催化氧化还原反应脱除水体中无机氮

采用光催化还原法制备了高活性的载银二氧化钛光催化剂，并用XRF、TEM、XRD及XPS、UV-Vis方法对催化剂进行了表征．考察了负载舨的含量、催化剂制备时间、搅拌气体的种类以及Fe^2＋的添加等条件对该催化剂光催化水体脱氮活性的影响．结果表明：载银量1．0％时去除效果最佳；制备催化剂时光照时间不充分会使催化剂失去还原效力；氮气保护下催化剂反应活性更高；Fe^2＋的加入利于光催化反应；2h光催化含氨氮和亚硝基氮的水样。总脱氮率达到了63．9％．     

Effect of Solvent Quality on Pure and Mixed Brushes

We investigate, theoretically and experimentally, the effect of solvent quality on pure, one-component, and two-component brushes. Both mean-field and self-consistent field models are developed, and their predictions compared to surface forces experiments on polystyrene and mixed polystyrene–polybutadiene brushes. We find that in pure brushes the structure and interactions between surfaces are highly sensitive to solvent quality. In a good solvent, the brush is extended and the interactions are repulsive, while in a poor solvent the brush is “collapsed” and the interactions are strongly attractive. Mixing two incompatible chains significantly reduces the sensitivity of the brush to solvent properties. While one of the chains collapses in a selective solvent, the other chain remains solvated, thus providing long-range repulsive interactions between surfaces. Our experiments show that the interactions between surfaces carrying a 1:1 mixed brush of styrene–butadiene are repulsive even in hexane, a poor solvent for polystyrene. Theoretically, we calculate that incorporating only 10% of an equi-molecular-weight chain into a collapsed brush can eliminate attractive interactions between surfaces.