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Extraction Experiments (extraction + experiment)
Selected AbstractsComparison of conventional and ultrasound-assisted extraction of carvone and limonene from caraway seedsFLAVOUR AND FRAGRANCE JOURNAL, Issue 3 2004Smain Chemat Abstract Extraction experiments with hexane were carried out at atmospheric pressure in Soxhlet, conventional and ultrasound extractions of ,aked caraway seeds, and detailed results are given for two major plant extract components, carvone and limonene. The results indicate that carvone yield and plant extract quality are better in ultrasound extraction compared to those given by conventional methodology. Extraction rates of carvone and limonene reported that ultrasound-assisted extraction was 1.3,2 times more rapid, depending on temperature, than a conventional system, according to the rate constant obtained during the initial 10 minutes of extraction. Moreover, the SEM micrographs provided more evidence for the mechanical effects of ultrasound, mainly appearing on cell walls and shown by the destruction of cells, faulitating the release of their contents, in contrast to conventional maceration or extraction, which involve diffusion of plant extracts across glandular walls and causing cell rupture over longer time periods. Copyright © 2004 John Wiley & Sons, Ltd. [source] Improved compatibility of EVOH/LDPE blends by ,-ray irradiationADVANCES IN POLYMER TECHNOLOGY, Issue 3 2009Haihong Li Abstract The change of compatibility of poly(ethylene- co -vinyl alcohol) (EVOH)/LDPE blends induced by,-ray radiation was studied. Gel extraction experiment results show that the gel fraction of blends increases linearly with the content of LDPE and reaches a maximum at 100 kGy, because neat EVOH is difficult to cross-link by irradiation. A comparison of theoretical and experimental gel contents indicates that some EVOH molecular chains enter the LDPE gel network. The peak at 3363 cm,1 on the Fourier transform infrared spectrum of pure blend gel is assigned to typical stretching of an OH bond, which indicates that a "graft" reaction occurs in the interface between EVOH and LDPE phases during the irradiation process. Mechanical property measurement results support such a structural change. The tensile strength of cross-linked blends increases with absorbed dose first, reaches a maximum value at 150 kGy, and then decreases with dose. A similar trend can also be observed in bending tests. © 2009 Wiley Periodicals, Inc. Adv Polym Techn 28:192,198, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20160 [source] The unconventional myosin-VIIa associates with lysosomesCYTOSKELETON, Issue 1 2005Lily E. Soni Abstract Mutations in the myosin-VIIa (MYO7a) gene cause human Usher disease, characterized by hearing impairment and progressive retinal degeneration. In the retina, myosin-VIIa is highly expressed in the retinal pigment epithelium, where it plays a role in the positioning of melanosomes and other digestion organelles. Using a human cultured retinal pigmented epithelia cell line, ARPE-19, as a model system, we have found that a population of myosin-VIIa is associated with cathepsin D- and Rab7-positive lysosomes. Association of myosin-VIIa with lysosomes was Rab7 independent, as dominant negative and dominant active versions of Rab7 did not disrupt myosin-VIIa recruitment to lysosomes. Association of myosin-VIIa with lysosomes was also independent of the actin and microtubule cytoskeleton. Myosin-VIIa copurified with lysosomes on density gradients, and fractionation and extraction experiments suggested that it was tightly associated with the lysosome surface. These studies suggest that myosin-VIIa is a lysosome motor. Cell Motil. Cytoskeleton 62:13,26, 2005. © 2005 Wiley-Liss, Inc. [source] A Rb/Sr record of catchment weathering response to Holocene climate change in Inner MongoliaEARTH SURFACE PROCESSES AND LANDFORMS, Issue 3 2006Zhangdong Jin Abstract Variation in the rubidium to strontium (Rb/Sr) ratio of the loess,palaeosol sequences has been proposed to reflect the degree of pedogenesis and weathering in the northwestern region of China. To characterize the Rb/Sr ratio of the dissolved loads of a single catchment, we analysed a 12·08 m sediment core from Daihai Lake in Inner Mongolia, north China. Dating control was provided by 210Pb, 137Cs and AMS- 14C. Sequential extraction experiments were conducted to investigate the concentrations of Rb and Sr on various chemical fractions in the lake sediments. Down-core variation in the Rb/Sr ratios provides a record of Holocene weathering history. From 9 to 3·5 ka bp, accelerated chemical weathering was experienced throughout the Daihai catchment under mainly warm and humid conditions, and this reached a maximum at c. 5 ka bp. However, weathering was reduced between c. 8·25 and 7·90 ka bp, which may reflect the global 8·2 ka cooling event. After c. 2·5 ka bp, increased Rb/Sr ratios with higher frequency of fluctuations indicate reduced weathering within the Daihai catchment. The highest Rb/Sr ratios in the Little Ice Age lake sediments indicate the weakest phase of Holocene chemical weathering, resulting from a marked reduction in Sr flux into the basin. The Rb/Sr record also shows an enhancement of chemical weathering under today's climate, but its intensity is less than that of the Medieval Warm Period. Increased Rb/Sr in lake sediment corresponding to reduced catchment weathering is in striking contrast to Rb/Sr decrease in the glacial loess layers in the loess,palaeosol sequence. Copyright © 2005 John Wiley & Sons, Ltd. [source] Oxidation chemistry of acid-volatile sulfide during analysisENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 5 2002Adrian M. Gonzalez Abstract The susceptibility of some components of sediment acid-volatile sulfide (AVS) to chemical oxidation is a critical factor impacting accurate measurement of AVS in sediment samples. This well-documented susceptibility to oxidation led to the requirement for oxygen-free conditions in the analytical method developed for AVS. In light of this acute potential to oxidize, the serendipitous finding that air can be used in the analysis of sediment AVS is counterintuitive and unexpected. To demonstrate and investigate this interesting observation, extraction experiments were performed using aqueous and solid-phase sulfide species. Experiments using air as the carrier gas showed a mean percentage recovery of sulfide matching that of traditional (nitrogen gas) analysis (i.e., >91%) and a time to completion of less than 30 min for aqueous sulfide and less than 60 min for sediment samples. These results are consistent with those of sulfide oxidation studies reported in the literature. Using air as the analytical carrier gas can provide an interesting alternative for developing an analytical method to determine AVS parameters in the field. [source] Highly Organosoluble Metal-Free Phthalocyanines and Metallophthalocyanines: Synthesis and CharacterizationEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 12 2007Ahmet Bilgin Abstract The syntheses and characterization of metal-free and metal-containing (Zn and Ni) derivatives of a symmetrically octa-substituted phthalocyanine derived from 4,5:12,13-bis(4,- tert -butylbenzo)-8,9-(4,,5,-dicyanobenzo)-6,11-ditosyl-6,11-diaza-2,15-dithiacyclohexadeca-4,8,12-triene and CuPc from 4,5:12,13-bis(4,- tert -butylbenzo)-8,9-(4,,5,-dibromobenzo)-6,11-ditosyl-6,11-diaza-2,15-dithiacyclohexadeca-4,8,12-triene were carried out. Pentanuclear silver(I) and palladium(II) complexes have also been prepared from nickel(II) phthalocyaninate derivatives. The prepared phthalocyanines were semiconducting materials in the range of 10,5 to10,10 S,cm,1 in vacuo and under atmospheric pressure. The extraction abilities of NiPc and detosylated phthalocyanines were evaluated in chloroform/water by using several heavy-metal picrates such as Ag+, Cd2+, Cu2+, Hg2+, Pb2+, Pd2+, and Zn2+. The extraction affinities of NiPc and detosylated phthalocyanines for Ag+ were found to be the highest in solvent extraction experiments. The new compounds were characterized by using elemental analysis, UV/Vis, FTIR, NMR, MS spectroscopic data and DTA/TG. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Covalent-Ionically Cross-linked Poly(Etheretherketone)-Basic Polysulfone Blend Ionomer MembranesFUEL CELLS, Issue 3-4 2006J. Kerres Abstract Sulfinated-sulfonated PEEK was synthesized via partial reduction of sulfochlorinated PEEK with aqueous Na2SO3. From these polymers, covalent-ionically cross-linked ionomer blend membranes were prepared by mixing the sulfinated-sulfonated PEEK with different base-modified polysulfones (PSU-base), followed by cross-linking with 1,4-diiodobutane. These membranes have been compared with covalently cross-linked membranes which were obtained by the cross-linking of sulfinated-sulfonated PEEK and with ionically cross-linked membranes obtained by mixing sulfonated PEEK with different PSU bases. The membranes have been characterized in terms of thermal stability by means of thermogravimetry (TGA) and coupled TGA-FTIR, in terms of cross-linking extent by extraction experiments, in terms of proton conductivity by impedance spectroscopy, and finally, in terms of water uptake by gravimetric analysis. [source] An experimental study of single-screw extrusion of HDPE,wood compositesADVANCES IN POLYMER TECHNOLOGY, Issue 3 2010Karen Xiao Abstract Single-screw extrusion experiments were carried out to study the extrusion characteristics of HDPE,wood composites. Three screw geometries (A, B, and C) were used, and the effects of screw speed on output, melting, and pressure profile were studied. Screw A had a much higher compression ratio than screws B and C, which directly affected the melting behavior of the polymers. Screws B and C had the same compression ratio; however, screw C had the same metering capacity as screw A. Therefore, by comparing screws B and C, the effect of feed depth on the solid conveying capacity was investigated. It was found that while screw B had higher outputs than both screws A and C as expected, screw C had a much lower output than screw A for highly filled resins even though they had the same metering capacity. For HDPE, screws A and C showed the same output as expected. Further examinations of the pressure profiles and melting profiles from screw extraction experiments confirmed that screw C showed a severely starved solids conveying capacity for wood-filled resins, which limited the total outputs. Comparing the outputs and pressure generations between theoretical predictions and actual experimental results, it was evident that due to the inaccurate assumption of fully filled channels common in single screw extrusion, both outputs and pressure generations in the extruders were overpredicted. © 2010 Wiley Periodicals, Inc. Adv Polym Techn 29:197,218, 2010; View this article online at wileyonlinelibrary. DOI 10.1002/adv.20190 [source] Biodegradable poly(D,L -lactide) coating of implants for continuous release of growth factorsJOURNAL OF BIOMEDICAL MATERIALS RESEARCH, Issue 4 2001G. Schmidmaier Abstract Local application of growth factors like insulin like growth factor-I (IGF-I) and transforming growth factor-beta 1 (TGF-,1) from a biodegradable thin layer of poly(D,L -lactide) (PDLLA) coated implants could stimulate fracture healing. A new "cold coating technique" for metallic implants was established to produce a biodegradable coating with a high mechanical stability that provides a continuous release of incorporated growth factors. The properties of this bioactive coating were investigated in vitro and in vivo. Scanning electron microscope analysis revealed a coating thickness of in average 14.8 ,m on titanium and 10.7 ,m on steel wires. Intramedullary implantation and extraction experiments depicted a loss of PDLLA coating from titanium and steel implants of less than 5%. After explantation of the implants, the coating displayed a complete and regular layer without any defects of PDLLA uncovering the metallic surface. Smear tests demonstrate that the coating can be performed under sterile conditions. The PDLLA depicted a reduction of about 8% within 6 weeks in vitro and in vivo. The growth factors were incorporated in a stable form and demonstrated a loss of stability of less than 3% within 42 days and less than 5% within one year. In an elution experiment, 54% IGF-I and 48% TGF-,1 were released within the first 48 h. After 42 days, 76% of IGF-I and 71% of TGF-,1 were detected in the elution fluid by ELISA. Comparable results were obtained in the in vivo experiments after 42 days. © 2001 John Wiley & Sons, Inc. J Biomed Mater Res (Appl Biomater) 58: 449,455, 2001 [source] Ag+ selection by aza-18-crown-6 ethers N -Substituted on heterocyclic aromatics ,,JOURNAL OF HETEROCYCLIC CHEMISTRY, Issue 2 2005Kiyoshi Matsumoto Substitution on the nitrogen atom, where necessary by high-pressure SNAr reactions, of aza-18-crown-6 ethers linked to heterocyclic aromatics has extended the number of potential host compounds for Ag+. The complexation of Ag+ by the new compounds has been evaluated by liquid membrane ion transport and ion extraction experiments. The nature of the binding sites of these new host compounds for Ag+ has been assessed, in DMF/D2O (4/1), by 13C nmr titration experiments with AgClO4. [source] PVC modification through polymerization of a monomer absorbed in porous suspension-type PVC particlesJOURNAL OF VINYL & ADDITIVE TECHNOLOGY, Issue 3 2004M. Narkis In-situ polymerization is the polymerization of one monomer in the presence of another polymer. It can be performed by sequential emulsion polymerization, or by reactions in the melt, in the solid phase, or in solution. The current report describes two methods to obtain poly(vinyl chloride) (PVC) modification through polymerization of a monomer absorbed in commercial porous suspension-type PVC particles. The generated modified PVC products differ significantly in their structure and properties. The first approach includes absorption of a monomer/peroxide solution within porous suspension-type PVC particles, followed by polymerization/crosslinking in the solid state at 80°C in an aqueous stabilizer-free dispersion. The monomer/crosslinker pairs selected are styrene/DVB (divinyl benzene), methylmethacrylate/EGDMA (ethylene glycol dimethacrylate), butyl acrylate/EGDMA, and ethylhexyl acrylate/EGDMA. The influence of composition and nature of the polymerizing/crosslinking constituents on the modified PVC particle structure was studied by microscopy methods, porosity measurements, and dynamic mechanical behavior (DMTA). The level of molecular grafting between PVC and the modifying polymer was determined by solvent extraction experiments. This work shows that the different monomers used represent distinct courses of monomer transport through the PVC particles. The characteristics of the modified PVC particle indicate that the polymerization/crosslinking process occurs in both the PVC bulk, i.e., within the walls constituting a particle, and in the PVC pores. No indication of chemical intermolecular interaction within the modified PVC particles was found. In the second approach, a solution of monomer, initiator, and a crosslinking agent is absorbed in commercial suspension-type porous PVC particles, thus forming a dry blend. This dry blend is subsequently reactively polymerized in a twin-screw extruder at an elevated temperature, 180°C, in the molten state. The properties of the reactively extruded PVC/PMMA blends are compared with those of physical blends at similar compositions. Owing to the high polymerization temperature, short-chain polymers are formed in the reactive polymerization process. Reactively extruded PVC/PMMA blends are transparent, form single-phase morphology, have a single Tg, and show mechanical properties comparable with those of the neat PVC. The resulting reactively extruded PVC/PMMA blends have high compatibility. J. Vinyl Addit. Technol. 10:109,120, 2004. © 2004 Society of Plastics Engineers. [source] Studies on nylon-6/EVOH/clay ternary compositesPOLYMER COMPOSITES, Issue 1 2006N. Artzi Nylon-6 (Ny-6)/EVOH blends are interesting host multiphase systems for incorporation of low clay contents. The Ny-6/EVOH blend is a unique system, which tends to chemically react during melt-mixing, affecting thermal, morphological and mechanical properties of the ternary systems containing clay. The addition of clay seems to interrupt the chemical reaction between the host polymers at certain compositions, leading to lower blending torque levels when clay is added. A competition between Ny-6 and EVOH regarding the intercalation process takes place. Ny-6 seems to lead to exfoliated structure, whereas EVOH forms intercalated structure, as revealed from XRD and TEM analyses, owing to thermodynamic considerations and preferential localization of the clay in Ny-6. Hence, the ternary systems have combined intercalated and delaminated morphology or complete exfoliated morphology depending on blend composition and clay content. Selective extraction experiments (gel content) indicate the formation of chemical reaction between the Ny-6 and EVOH, and give an indirect indication of the polymer content residing in the galleries. The thermal properties of the polymers were found to be affected by the occurrence of chemical reaction, the level of intercalation and exfoliation and plasticizing effect of the low molecular weight onium ions treating the clay. Of special interest is the increased storage modulus attained upon the addition of only 1.5 wt% clay. POLYM. COMPOS. 27:15,23, 2006. © 2005 Society of Plastics Engineers [source] Removal of dyes from water by poly(vinyl pyrrolidone) hydrogel,POLYMERS FOR ADVANCED TECHNOLOGIES, Issue 11-12 2006Bahire Filiz Senkal Abstract The interaction between polymer and dye leading to polymer-dye complex formation exhibits many interesting and important practical features. For this purpose, a hydrogel was prepared by crosslinking copolymerization of vinyl pyrrolidone with tetraallyl ammonium bromide in aqueous solution, using K2S2O8 as a radical initiator. Dye extraction experiments were carried out simply by contacting wetted gel samples with aqueous dye solutions at room temperature. Capacities were determined by colorimetric analysis of the residual dye contents. The hydrogel swelled in water showing that reasonable high dye sorption capacity (0.71,1.13,g per gram of gel) was achieved. This material is also able to remove the anionic dyes completely even from highly diluted aqueous dye solutions. No trace absorbance was detected in the visible range, after processing. Copyright © 2006 John Wiley & Sons, Ltd. [source] Active Transport of Amino Acids by a Guanidiniocarbonyl,Pyrrole ReceptorCHEMISTRY - A EUROPEAN JOURNAL, Issue 31 2010Christian Urban Dr. Abstract Herein we report the synthesis and characterization of a transporter 9 for N-acetylated amino acids. Transporter 9 is a conjugate of a guanidiniocarbonyl pyrrole cation, one of the most efficient carboxylate binding motifs reported so far, and a hydrophobic tris(dodecylbenzyl) group, which ensures solubility in organic solvents. In its protonated form, 9 binds N-acetylated amino acid carboxylates in wet organic solvents with association constants in the range of 104,M,1 as estimated by extraction experiments. Aromatic amino acids are preferred due to additional cation-,-interactions of the amino acid side chain with the guanidiniocarbonyl pyrrole moiety. U-tube experiments established efficient transport across a bulk liquid chloroform phase with fluxes approaching 10,6,mol,m,2,s,1. In experiments with single substrates, the release rate of the amino acid from the receptor,substrate complex at the interface with the receiving phase is rate determining. In contrast to this, in competition experiments with several substrates, the thermodynamic affinity to 9 becomes decisive. As 9 can only transport anions in its protonated form and has a pKa value of approximately 7, pH-driven active transport of amino acids is also possible. Transport occurs as a symport of the amino acid carboxylate and a proton. [source] Calix[4] crowns with Methoxynaphthoylmethyl Pendant GroupsCHINESE JOURNAL OF CHEMISTRY, Issue 11 2003Chuan-Min Jin Abstract The novel calix [4] crowns with two pendant groups were prepared by the alkylation of calix [4] crowns with 6-methoxy-2-bromoacetylnaphthalene. 1H NMR titration and picrate extraction experiments indicated that they exhibit higher complexing efficiency than their parent compounds and possess obvious selectivity for Na+ or K+, respectively, and that the cation is encapsulated inside the preorganized ionophoric cavity defined by carbonyl oxygens, the crown ether and the phenoxy oxygens. From UV and fluorescent spectra it is revealed that calix [4]-crown-4 3a with 6-methoxy-2-naphthoylmethyl pedant groups exhibits remarkable cation-induced photophysical effects and it could be utilized as a selective fluorescent sensor for Ca2+. [source] | ||||||||||||||||