Thermodynamic state of reinforced interpenetrating polymer networks

The free energies of mixing of two networks in the interpenetrating polymer network based on crosslinked polyurethane and poly(ester acrylate) have been determined by the vapour sorption method. It was established that the constituent networks in the IPN are not miscible. The introduction of fillers of different chemical nature increases the compatibility. The thermodynamic affinity of the fillers to the individual networks and IPN was estimated. It was established that when the free energy of interaction of one or both components of the IPN with the filler is negative, reinforcement leads to the formation of a compatible and equilibrium system. For fillers having no affinity to the polymers, compatibilization is observed, which is connected with slowing down of phase separation in the system in the presence of filler.     

Process conditions for separating fatty acid esters by supercritical CO2

The solubilities of ethyl palmitate, ethyl oleate, ethyl eicosapentaenoate (EPA) and ethyl docosahexaenoate (DHA) in supercritical carbon dioxide were determined by a continuous flow method. The solubilities of fatty acid ethyl esters increased with pressure and decreased as the temperature was increased. An empirical equation, similar to Chrastil's equation, was used to describe the relationship between solute solubility and the density of carbon dioxide. The empirical equation was further used to qualitatively estimate the separation efficiency of isolating EPA and DHA ethyl esters from fatty acid esters. The operating conditions yielding high solubility gave fast extraction rate but resulted in low separation efficiency. Experiments were conducted to separate ethyl EPA and ethyl DHA from a model mixture containing four fatty acid ethyl esters and from esterified squid visceral oil. The experimental data compared closely with the calculated values.     

Monoalkyl Esters of Isoalkylphosphonic Acid as Extractants in Rare Earth Separation

Four monoalkyl esters of isoalkylphosphonic acids have been studied for the chromatographic separation ofrare earths (RE).The relationship between distribution ratios and acid concentration of the eluants forsamarium and ytterbium has been explored.The characteristics of these extractants loaded onto macroreticularpoly (methyl methacrylate) resin beads for the separation of lanthanum,cerium,praseodymium and neodymiumhave been compared.Among the extractants studied,mono(1-methylheptyl) ester of isooctylphosphonic acidwas found to be the best for RE separation.The acidity for separation is lower than any known P-containingextractants for the same purpose.For instance,with 1.73 mol·L~(-1) nitric acid as eluent,thulium,ytterbium andlutetium can be separated quantitatively.The extractant-loaded resins possess high column efficiency with goodkinetic characteristics.The extraction mechanism was also explored.     

Perverse Spite: The Possessive Gleam in the Mother's Eye and the Struggle to Own One's Soul: Reply to Stern (2004).

In this response to Jeffrey Stern's (2004) (see record 2004-21113-016) commentary on my article, "Giving the Devil His Due: Spite and the Struggle for Individual Dignity" (P. Shabad, 2000) (see record 2000-00917-004), I suggest that in emphasizing the conscious vindictiveness of explicit spite, Stern minimizes the perverse aspects of "cutting off one's nose to spite one's face" as a means of avenging oneself against powerful others. The underlying impetus of perverse spite is to break free from the prison of subtle developmental contingencies and unconscious seductions surrounding maternal possessiveness. When the child's self-assertive strivings are blocked because of the shame and fear of premature separateness, the inward obsessional churning of resentment becomes a fertile ground for perverse spite. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Complementary modelling of fluid separation processes

Optimal functioning of numerous technological processes depends primarily on relevant process design, properly selected column internals and sufficient understanding of the process behaviour. This can be achieved only with the help of accurate and reliable process models capable of considering process rates in a rigorous way, with respect to both transport phenomena and chemistry. In this article, a new modelling concept called complementary modelling is suggested for a large class of fluid separation processes. Since the conditions and criteria for these processes vary considerably, it is impossible to develop a unified modelling approach. Instead, a reasonable and effective combination of different modelling approaches provides solutions to many present and future tasks. The complementary modelling is discussed in detail and illustrated with several case studies.     

Development of a predictive model for polymer/solvent diffusion coefficient calculations

A new calculation procedure for free‐volume parameters is considered in this work by using viscosity prediction methods and the Levenberg‐Marquardt calculation scheme. All parameters used in the Vrentas–Duda free‐volume theory can be estimated from pure component properties. The prediction results are compared with experimental data for some polymer/solvent systems. The diffusion coefficient calculated by Vrentas–Duda theory can be used in the modeling of membrane separation processes. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Preparation and adsorption behavior of a cellulose‐based,mixed‐mode adsorbent with a benzylamine ligand for expanded bed applications

A novel mixed‐mode expanded bed adsorbent with anion‐exchange properties was explored with benzylamine as the functional ligand. The cellulose composite matrix, densified with stainless steel powder, was prepared with the method of water‐in‐oil suspension thermal regeneration. High activation levels of the cellulose matrix were obtained with allyl bromide because of the relative inertness of the allyl group under the conditions of the activation reaction. After the formation of the bromohydrin with N‐bromosuccinimide and coupling with benzylamine, the activated matrix was derived to function as a mixed‐mode adsorbent containing both hydrophobic and ionic groups. The protein adsorption capacity was investigated with bovine serum albumin as a model protein. The results indicated that the prepared adsorbent could bind bovine serum albumin with a high adsorption capacity, and it showed salt tolerance. Effective desorption was achieved by a pH adjustment across the isoelectric point of the protein. The interactions between the cell and adsorbent were studied, and the bioadhesion was shielded by the adjustment of the salt concentration above 0.1M. Stable fluidization in the expanded bed was obtained even in a 2% (dry weight) yeast suspension. The direct capture of target proteins from a biomass‐containing feedstock without extra dilution steps could be expected with the mixed‐mode adsorbent prepared in this work, and this would be especially appropriate for expanded bed adsorption applications. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

PbS-Sb2S3-FeS三元系在水蒸气气氛下的铅锑分离

在1073K下通过测定三硫化锑和硫化铅的挥发速度,研究了PbS-Sb_2S_3-FeS三元系在水蒸气气氛下的铅锑分离规律。X-射线衍射结果表明,焙砂由PbS、Fe_3O_4、FePb_4Sb_6S_(14)、Pb_5Sb_4S_(11)和FeSb_2O_4组成。当试样中FeS含量在5％～7％时,铅锑分离效果最好。当试样中FeS的含量≥10％时,铅锑分离效果较差,这时过量的FeS会与Sb_2S_3和PbS形成复杂的硫化物(FePb_4Sb_6S_(14)、Pb_5Sb_4S_(11))或被氧化成F4Sb_2O_4,使锑的挥发变得困难,导致残留在焙砂中的锑含量升高。     

某硅线石矿石选别中除铁研究

针对矿石中硅线石微细嵌布，铁矿物嵌布亦较细。且有近二分之一铁在非金属矿物晶格之中，除铁难的特点，通过试验研究对比采用一段磨矿磁选除铁后磁尾浮选富集硅线石．浮选精矿再磨后酸浸再除铁的工艺方法，获得了理想的除铁效果，使硅线石精矿质量达到较高品质。