Fractionation of menhaden oil ethyl esters using supercritical fluid CO2

Supercritical fluid CO₂ was used to fractionate menhaden oil fatty acid ethyl esters to obtain concentrates of the esters of allcis-5,8,11,14,17-eicosapentaenoic acid (EPA) and allcis-4,7,10,13,16,19-docosahexaenoic acid (DHA). Separation of the ethyl esters was found to occur primarily by carbon number, thus limiting the degree to which the ethyl esters of EPA and DHA could be concentrated. Urea fractionation of whole esters in order to remove saturates, monoenes and dienes prior to fractionation with supercritical fluid CO₂ resulted in concentrates of EPA and DHA in purities exceeding 90%. Several criteria are given for the selection of crude oils in order to maximize both purity and yield of concentrates.     

Functional finishing of nonwoven fabrics. I. Accessibility of surface modified PET spunbond by atmospheric pressure He/O2 plasma treatment

The surface of a polyethylene terephthalate (PET) spunbond nonwoven was modified by using atmospheric pressure He/O₂ plasma treatment. Accessibility of the modified PET nonwoven has been investigated in terms of crystallinity, surface chemical composition, hydrophilicity, and dye uptake. Differential scanning calorimetry (DSC) for crystallinity measurement and X‐ray photoelectron spectroscopy (XPS) for chemical composition measurement were used. Surface morphology was studied by using scanning electron microscopy (SEM) and atomic force microscopy (AFM). Percentage crystallinity increased due to the depletion of amorphous region by plasma etching. Redeposition of etched particles was observed. Oxygen‐based functional groups on the surface of PET increase from 27 to about 32% after 90 s exposure. Wettability increases by more than 10 times and moisture regain increases by three times, compared with the untreated sample. Dye uptake was not changed significantly. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4306–4310, 2006     

Flow Microcalorimetric Estimation of Energy Changes During Surface Reactions of Glass Powders with Aqueous Media

Flow microcalorimetry was used for an investigation of the surface chemical nature of glass surfaces. A commercially available flow microcalorimeter allowed for the measurement of heat energy changes during surface reactions of two different glass powders with pyridine and water solutions. Pure fused silica glass and a fluorozirconate glass were the materials studied by flow microcalorimetry.     

Hydrogen impurity in natural gem diamond

Five natural gem diamonds which included type I_A, I_B and II_A specimens, have been investigated by ion beam spectrochemical analysis (IBSCA) to determine the total hydrogen impurity concentration in the diamonds. These data were compared with that obtained from other conventional techniques such as infrared and ultraviolet absorption spectroscopy, electron spin resonance and transmission electron microscopy (TEM). IBSCA indicated that all the specimens appeared to contain 1 at. % of hydrogen contrary to the infrared evidence. The highest hydrogen concentration was recorded by a type I_B specimen which contained small ( 3nm) bubbles. The hydrogen concentration did not correlate with any defect within the specimens, for example the {100} planar faults, and appeared to be a general impurity. No evidence was found to suggest that inclusions were responsible for the impurity.     

Effect of chitosan on morphology and conformation of electrospun silk fibroin nanofibers

The electrospinning of silk fibroin(SF)/chitosan(CS) blends with different composition ratios was performed with formic acid as a spinning solvent. The SF/CS blends containing up to the CS content of 30% could be electrospun into the continuous fibrous structure, although pure CS was not able to be electrospun into the fibrous structure. As-spun SF/CS blend nanofibers showed smaller diameter and narrower diameter distribution than pure SF nanofibers, and the diameter gradually decreased from 450 to 130 nm with the addition of CS in blends. However, at the blend compositions with above 40 wt% chitosan, the continuous SF nanofibers containing CS beads were produced. We also investigated the influence of the methanol treatment on the secondary structure of as-spun SF or SF/CS blend nanofibers by means of ATR-IR and solid-state CP-MAS ¹³C-NMR. Comparing with the pure SF nanofibers, the conformational change of the as-spun SF/CS blend nanofibers into β-sheet was faster because the CS with rigid backbone synergistically might promote the conformational transition of SF by an intermolecular interaction.     

Some factors influencing exfoliation and physical property enhancement in nanoclay epoxy resins based on diglycidyl ethers of bisphenol A and F

An investigation of the factors influencing the degree of exfoliation of an organically modified clay in a series of epoxy resins is reported. The use of sonication, choice of curing agent, effect of the moisture content of the clay, and the cure temperature were examined. The dispersion was characterized using a combination of rheological measurements, X‐ray diffraction, and dynamic mechanical thermal analysis. Rheological analysis of the clay dispersion in the epoxy monomer indicated that at high clay loads Herschel–Bulkley type behavior is followed. Higher cure temperatures and higher levels of clay moisture were found to influence the extent of exfoliation. Improvements in physical properties were observed through the addition of nanocomposites. The DGEBA/DDM and DEGEBA/DDS exhibited 2 and 4°C increase, respectively, in T_g per wt % of added clay. DGEBF showed virtually no enhancement. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007