超临界流体技术在微孔发泡聚合物制备中的应用

介绍了超临界流体技术和微孔聚合物的概念及优点。着重介绍了超临界流体技术在微孔聚合物制备中的应用及发展状况，并简单介绍了制备微孔聚合物的影响因素，最后阐述了对超临界流体技术的展望和建议。     

N.m.r. studies on the effect of water on the glass transition of polystyrene

These investigations are concerned with water-polymer interactions in polymer latices. It is known that water can act as a plasticizer for many solid polymers and cause a reduction in the glass transition temperature, T_g, of the amorphous regions. Experiments were carried out to determine whether pulsed n.m.r. techniques could be used to study the T_g of a polymer suspension and hence the influence of water and electrolyte on it. From T₁ and T₂ proton relaxation measurements as a function of temperature on polystyrene latex systems it was shown that the presence of water lowers the T_g of the polymer particles (by about 10°C), the effect being slightly greater in the presence of concentrated electrolyte. The extent of electrolyte penetration into the particles was deduced by studying relaxation as a function of particle diameter in latices containing paramagnetic Mn²⁺ ions. Using simple theories of relaxation and spin diffusion it was concluded that for all but the smallest particles electrolyte penetration is restricted to a very thin shell of the order of 1 nm. These conclusions were supported by the results of similar measurements on PTFE particles.     

Mirror Constant for Tyranno® Silicon-Titanium-Carbon-Oxygen Fibers Measured in Situ in a Three-Dimensional Woven Silicon Carbide/Silicon Carbide Composite

The strength, S , of ceramic and glass fibers often can be estimated from fractographic investigation using the fracture mirror radius, r _m, and the relationship S = A _m/( r _m)^1/2, where A _mis the "mirror constant." The present work estimates the value of A _mfor Tyranno^® Si-Ti-C-O fibers in situ in a three-dimensional woven SiC/SiC-based composite to be 2.50 ± 0.09 MPa·m^1/2. This value is within the range of 2–2.51 MPa·m^1/2 previously obtained for nominally similar Nicalon^® Si-C-O fibers.     

Role of semiochemicals in mate location by parasitic sea louse,Lepeophtheirus salmonis

The role of olfaction and diffusible pheromones in mate location behavior of sea lice, Lepeophtheirus salmonis, was assessed with Y-tube behavioral bioassays. The pheromone emitting animals were located in a chamber in one arm of a Y-tube arena, with artificial seawater flowing through both arms. Adult male sea lice displayed both activation and directional responses to seawater conditioned with preadult II virgin females, but were only activated by mated adult female conditioned water. Further, when males were given the choice of preadult II virgin females or mated adult females, a significant number of males chose the arm with the preadult II virgin females. Adult males showed activation responses when presented with water conditioned with adult males but were not attracted to them. When presented with adult males, preadult II virgin females showed only directional responses, but not activation responses. Preadult II virgin female conditioned water was extracted using solid-phase extraction (SPE) protocols pioneered for semiochemical isolation. Adult male sea lice showed significant directional responses to the preadult II virgin female SPE extract. Distillation under vacuum was performed on the extract to give a distillate comprising components with a molecular weight range and physical properties comparable to those of compounds utilized as volatile semiochemicals by terrestrial organisms and a residue comprising components with higher molecular weight range comparable to those utilized as involatile semiochemicals. Adult males were found to be both significantly activated and attracted to the distillate, but not to the residue. This research provides evidence that small, lipophilic organic molecules are used by sea lice as sex pheromone signals to locate a member of the opposite sex.     

Bioremediation of polycyclic aromatic hydrocarbons: current knowledge and future directions

Polycyclic aromatic hydrocarbons (PAHs) are a class of organic compounds that have accumulated in the natural environment mainly as a result of anthropogenic activities such as the combustion of fossil fuels. Interest has surrounded the occurrence and distribution of PAHs for many decades due to their potentially harmful effects to human health. This concern has prompted researchers to address ways to detoxify/remove these organic compounds from the natural environment. Bioremediation is one approach that has been used to remediate contaminated land and waters, and promotes the natural attenuation of the contaminants using the in situ microbial community of the site. This review discusses the variety of fungi and bacteria that are capable of these transformations, describes the major aerobic and anaerobic breakdown pathways, and highlights some of the bioremediation technologies that are currently available. Copyright © 2005 Society of Chemical Industry     

<Emphasis Type="Italic">In situ</Emphasis> monitoring of solid fat content by means of pulsed nuclear magnetic resonance spectrometry and ultrasonics

An ultrasonic technique was developed to study the crystallization process of edible fats on-line. A chirp wave was used instead of the conventional pulser signal, thus achieving a higher signal-to-noise ratio. This enabled measurements to be made in concentrated systems [≈20% solid fat content (SFC)] through a 8.11-cm thick sample without significant signal loss. Fat samples were crystallized at 20, 25, and 30°C at a constant agitation rate of 400 rpm for 90 min. The crystallization process was followed by ultrasonic spectroscopy and a low-resolution pulsed nuclear magnetic resonance spectrometer. Specific relationships were found between ultrasonic parameters [integrated response, time of flight (TF), and full width half maximum] and SFC. TF, which is an indirect measurement of the ultrasonic velocity (v), was highly correlated to SFC (r ²>0.9) in a linear fashion (v=2.601 SFC+1433.0).     

The Instabilisation of Dye-Fibre Bonds by Peroxide Treatments

The results are presented of an investigation into the instability induced in dye-fibre bonds by peroxide treatments. The nature of the reactions involved are discussed.     

The mechanism of photoprotection of wool by UV absorbers of the 2-hydroxybenzophenone class

The mechanism by which sulfonated 2-hydroxybenzophenone ultraviolet (UV) absorbers protect wool fabric against photoyellowing has been studied. The absorption and luminescence properties of two 2-hydroxybenzophenone-5-sulfonates and four 2-hydroxybenzophenone-2′hyphen;sulfonates are compared. The 2-hydroxy-benzophenones are nonfluorescent in wool, but they all show phosphorescence at room temperature. The phosphorescence is attributed to the phenolate anion produced by ionization of the hydroxyl group. The nature of substituents in the 3-position and 4-position of the phenolic ring is important in controlling the formation of luminescent species which may initiate unwanted photochemical reactions in wool. The protective screening effect of each absorber in wool fabric has been determined theoretically, using a method of analysis based on diffuse reflectance spectroscopy; the results are compared with the values determined experimentally by measuring the changes in yellowness that result when treated and untreated fabrics are exposed to fluorescent sunlamps (maximum energy at 310 nm). In all cases, UV screening was shown to be the important mode of photostabilization. The levels of photoprotection were much higher than those reported previously for treated fabrics that were exposed for long periods to simulated sunlight, behind glass. Possible reasons for the poor long-term performance of the 2-hydroxybenzophenones in wool are discussed.     

Relative roles of chemical and mass transfer rate control in fluidized-bed combustion of coal chars

The relative roles of mass transfer and chemical reaction in controlling combustion rates in fluidized beds are examined in the light of measurements of char-particle combustion kinetics and correlated data on gas—particle mass transfer in fluidized beds. It is concluded that at 1200 K mass transfer is the main rate-control influence for materials having reactivities the same as, or higher than, a char from a swelling bituminous coal. Mass transfer has little effect on the combustion rate of materials whose reactivity to oxygen is one-tenth that of the bituminous coal char. At 800 K, chemical reaction control is dominant for all reactivities considered. The main uncertainty in the present calculations arises from the lack of a suitable analysis of mass-transfer rates in conditions appropriate to fluidized-bed combustion.