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Particle Size Analysis (particle + size_analysis)
Kinds of Particle Size Analysis Selected AbstractsEnzymatic modification as a tool to improve the functional properties of heat-processed soy flourJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 2 2008Cheruppanpullil Radha Abstract BACKGROUND: There are a number of antinutritional factors present in soybeans that exert a negative impact on the nutritional quality of the protein. Among those factors that are destroyed by heat treatment are protease inhibitors and lectins. Protease inhibitors show antinutritional effect and moreover the digestibility of the protein is limited by the presence of these antinutrients. The aims of the present study are (1) to study the effect of autoclaving on the trypsin inhibitor inactivation, nitrogen solubility and protein digestibility of defatted soy flour and (2) to study the effect of enzymatic modification on the functional properties of autoclaved soy flour. RESULTS: The solubility of the soy flour decreased with increase in autoclaving time. Partial hydrolysis of the autoclaved soy flour increased its acid solubility (pH 4.5) from 17% to 56% over a control value of 24% without affecting its functional properties. Inactivation of trypsin inhibitors improved the protein digestibility of soy flour from 25% to 95%. Particle size analysis of the autoclaved flour indicated the formation of soy protein aggregates, which resulted in poor solubility. The enzymatic modification of autoclaved soy flour resulted in its property as a good emulsifying agent with an emulsion capacity of 118 ± 4 mL. CONCLUSION: Enzymatic modification of the heat-processed soy flour increased its solubility and other functional attributes. The increased acid solubility would be advantageous in the utilization of soy proteins in acidic foods. Thus the autoclaved and partially modified soy flour is a potential source for specific functional foods. Copyright © 2007 Society of Chemical Industry [source] Synthesis and characterization of uniform-sized hollow chitosan microspheresADVANCES IN POLYMER TECHNOLOGY, Issue 1 2009Shan Wang Abstract Hollow chitosan (CS) microspheres were obtained using an inverse-emulsion crosslinking method. The temperature and viscosity of the CS emulsion affected the characteristics of the derived microspheres. The microspheres were characterized by differential scanning calorimetry, Fourier transform infrared (FT-IR) spectroscopy, transmission electron microscopy, optical microscopy, scanning electron microscopy (SEM), and laser particle size analysis. FT-IR indicated the sequence of transformations taking place before, during, and after the crosslinking of CS. Optical microscopy and SEM confirmed the spherical morphology of the gel. The formation of hollow microspheres with a single cavity was identified by SEM. The CS microspheres exhibited a narrow particle size distribution. Furthermore, particle size could be controlled by changing the stirring speed. © 2009 Wiley Periodicals, Inc. Adv Polym Techn 28:40,47, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20145 [source] Crystal structure of cobalt-substituted calcium hydroxyapatite nanopowders prepared by hydrothermal processingJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2 2010Ljiljana Veselinovi A series of cobalt-exchanged hydroxyapatite (CoHAp) powders with different Ca/Co ratios and nominal unit-cell contents Ca10,xCox(PO4)6(OH)2, x = 0, 0.5, 1.0, 1.5 and 2.0, were synthesized by hydrothermal treatment of a precipitate at 473,K for 8,h. Based on ICP (inductively coupled plasma) emission spectroscopy analysis, it was established that the maximum amount of cobalt incorporation saturated at ,12,at.% under these conditions. The effects of cobalt content on the CoHAp powders were investigated using ICP emission spectroscopy, particle size analysis, transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM) analyses as well as X-ray powder diffraction (XRPD) including Rietveld analysis. According to XRPD, all the materials are single-phase HAp and CoHAp of low crystallinity. Rietveld analysis shows that Co enrichment causes the c cell parameter to decrease at a faster rate than the a cell parameter. A microstructural analysis showed anisotropic X-ray line broadening due to crystallite size reduction. In CoHAp there is significant crystal elongation in [001], and the average size decreases with increasing cobalt content. The crystallite morphology transforms from rod-like for the pure HAp to lamellae at the highest degree of Co substitution. The results of Rietveld refinement (symmetry, size and morphology of the crystallites) were confirmed by TEM and HRTEM analysis. [source] Reactivation of spent Pd/AC catalyst by supercritical CO2 fluid extractionAICHE JOURNAL, Issue 9 2009Xiaoxin Zhang Abstract In this article, we reported a nondestructive and environmentally friendly method for the reactivation of a spent Pd/AC catalyst for the hydrogenation of benzoic acid by using supercritical CO2 (scCO2) fluid extraction. The effects of reactivation conditions, such as extraction temperature, pressure, CO2 flow rate, and time, on the activity of the reactivated Pd/AC catalyst, were presented. The catalyst was characterized by N2 physisorption, laser particle size analysis, and transmission electron spectroscopy, and the liquid extract was analyzed by GC-MS. It is found that scCO2 fluid extraction was very efficient in eliminating organic substances blocking the pores of the catalyst, while did not affect noticeably the granule size of the catalyst and the particle size of Pd. The reactivated Pd/AC catalyst regained more than 70% of the activity of the fresh 5.0 wt % Pd/AC catalyst, and has been successfully used in an industrial unit for the hydrogenation of benzoic acid. © 2009 American Institute of Chemical Engineers AIChE J, 2009 [source] Gaining fluid bed process understanding by in-line particle size analysisJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 3 2009Tero Närvänen Abstract Different process phenomena and process failure modes could be monitored using the in-line particle size data measured by spatial filtering technique (SFT). In addition to the real-time granule growth monitoring, other events, such as the blocking of filter bags and the distributor plate, could be observed. SFT was used off-line, at-line and in-line in 14 differently manufactured granulation batches. No significant fouling occurred during the manufacturing due to the appropriate positioning of the probe. The off-line SFT results correlated well (R2,=,0.97) with the sieve analysis results. It was also found that size segregation influenced both the in-line and at-line particle size results during the fluidization: in-line method underestimated and at-line method overestimated the final particle size. © 2008 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 98:1110,1117, 2009 [source] Stabilization of alum-adjuvanted vaccine dry powder formulations: Mechanism and applicationJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 2 2003Yuh-Fun Maa Abstract Studies were performed to elucidate the mechanism of alum gel coagulation upon freezing and drying and its relationship to vaccine potency loss and to develop a novel freeze-drying process for the production of stable alum-adjuvanted vaccine formulations suitable for conventional needle injection and epidermal powder immunization (EPI). The alum hydroxide-adjuvanted hepatitis-B surface antigen (Alum-HBsAg) and the alum phosphate-adjuvanted diphtheria and tetanus toxoids (Alum-DT) were dehydrated by freeze drying (FD), spray drying (SD), air drying (AD), or spray freeze drying (SFD). After drying by FD, SD, or AD, alum gels coagulated when examined by optical microscopy and particle size analysis. In addition, desorption of antigen molecules from the coagulated when examined by optical microscopy and particle size analysis. In addition, desorption of antigen molecules from the coagulated alum gel upon reconstitution appeared to be difficult, as indicated by attenuated band intensity on SDS-PAGE. In contrast, SFD alum gels turned a homogenous suspension upon reconstitution, suggesting minimal alum coagulation. In the mouse model, the in vivo immunogenicity of SFD Alum-HBsAg was preserved, whereas the FD Alum-HBsAg suffered significant immunogenicity loss. Grinding of coagulated FD Alum-HBsAg into smaller particles could partially recover the immunogenicity. In a guinea pig study using EPI, the SD Alum-DT formulation was not immunogenic, but the SFD Alum-DT formulations had a vaccine potency comparable to that of the untreated DT administered by I.M. injection. Overall, the relationship of coagulation of alum gel upon reconstitution and the loss of vaccine potency was established in this study. Alum gels became highly coagulated after dehydration by spray drying and traditional freeze-drying processes. However, freezing rate played a critical role in preserving the adjuvant effect of alum and fast freezing decreased the tendency of alum coagulation. Spraying the alum gel into liquid nitrogen represents the fastest freezing rate achievable and resulted in no discernible alum coagulation. Therefore, SFD presents a novel and effective drying process for alum-adjuvanted vaccine formulations and is particularly valuable for dry powder applications such as EPI. © 2003 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 92:319,332, 2003 [source] Sedimentation field-flow fractionation and granulometric analysis of PLGA microspheresJOURNAL OF SEPARATION SCIENCE, JSS, Issue 15-16 2003Nathalie Faisant Abstract Sedimentation field flow fractionation operated in the steric hyperlayer mode was used to obtain fractions of defined characteristics from crude samples of poly(D,L-lactic-co-glycolic acid) microspheres which were polydisperse in size. In less than ten minutes, Sedimentation Field Flow Fractionation (SdFFF) separation yielded three analytical fractions of very different size and particle size distribution (PSD) characteristics, as determined by granulometric analyses (Coulter Counter® and image analysis of SEM). A crude sample (average size = 45 ,m, 105% size polydispersity index) was separated into fractions of 73 ,m, 56 ,m, 8 ,m average diameters which showed a PSD of 39%, 33%, 30%, respectively. Our results demonstrated that SdFFF used in conjunction with particle size analysis offers a new approach to laboratory scale production of drug vectors of a specified average size and reduced size dispersity. In the future, this could be used to select the most convenient particles for drug loading and release. [source] Barium Holmium Zirconate, A New Perovskite Oxide: II, Synthesis as Nanoparticles through a Modified Combustion ProcessJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2002Rajan Jose Nanoparticles of barium holmium zirconate, a new complex perovskite ceramic oxide, has been synthesized using a modified self-propagating combustion process. The solid combustion products obtained were characterized by X-ray diffraction (XRD), electron diffraction, differential thermal analysis, thermogravimetric analysis, infrared spectroscopy, particle size analysis, surface area determination, and high-resolution transmission electron microscopy. The XRD and electron diffraction studies have shown that the as-prepared powder is phase pure Ba2HoZrO5.5 and has a complex cubic perovskite (A2BB,O6) structure with a lattice constant a= 8.428 Å. The transmission electron microscopic investigation has shown that the particle size of the as-prepared powder was in the range 4,16 nm with a mean grain size of 8.2 nm. The nanoparticles of Ba2HoZrO5.5 obtained by the present method could be sintered to 98% theoretical density at 1500°C. [source] Transmission Fluctuation Spectrometry in Concentrated Suspensions.PARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 1 2005Part Three: Measurements Abstract The theory of transmission fluctuation spectrometry (TFS) was developed for particle size analysis in flowing particle suspensions, whereby the statistical transmission fluctuations are used to extract the particle size distribution (PSD) and particle concentration. In the previous parts of this publication high concentration effects on TFS were investigated theoretically and by simulation. This work presents a study on TFS measurements in concentrated suspensions. By introducing an empirical correction to include the high concentration effects from both the monolayer structure and particle overlapping in the inversion algorithm, it is possible to obtain the particle size distribution and particle concentration over broad ranges of particle sizes and concentrations. [source] Effects of synthesis conditions on crystal morphological structures and thermal degradation behavior of hydrotalcites and flame retardant and mechanical properties of EVA/hydrotalcite blendsPOLYMER COMPOSITES, Issue 2 2007Longchao Du The effects of synthesis methods and reaction conditions on the crystal morphological structures and thermal degradation behavior of hydrotalcites have been studied by X-ray diffraction (XRD), transmission electron microscopy (TEM), particle size analysis (PSA), and differential thermal analysis (DTA). The flame retardant and mechanical properties of ethylene,vinyl acetate (EVA) blends with the corresponding hydrotalcites have been estimated by limiting oxygen index (LOI), UL-94, and mechanical measurements. The results from the XRD, TEM, and PSA demonstrate that the hydrotalcites synthesized by ultrasound method have larger crystal sizes and particle size distribution than those by mechanical stirring method. Higher reaction temperature, longer dripping time, and lower solution concentration can increase the crystal and particle sizes of ultrasound-synthesized hydrotalcites, whereas the longer ultrasound aging time can increase the crystal sizes and decrease the particle sizes of hydrotalcites because of the smashing conglomeration. The DTA data give a positive evidence that the hydrotalcite samples prepared by mechanical stirring method with longer alkaline dripping time have higher thermal degradation temperature than those by ultrasound method, since the ultrasound-synthesized hydrotalcites have more lattice defects than stirring-prepared hydrotalcites. The data from LOI, UL-94, and mechanical tests show that the ultrasonic-synthesized hydrotalcites have better flame retardant properties, whereas the stirring-synthesized hydrotalcites have better tensile strength in the EVA/hydrotalcite blends. POLYM. COMPOS., 28:131,138, 2007. © 2007 Society of Plastics Engineers [source] Effect of fabrication temperature on strain-sensing capacity of polypyrrole-coated conductive fabricsPOLYMER INTERNATIONAL, Issue 7 2007Joanna Tsang Abstract Textile strain sensors were made from polypyrrole-coated stretchable fabrics by a method of screen printing with chemical vapor deposition. The effect of polymerization temperature on the sensing performances was studied. It was found that polymerization at low temperature significantly improved the electrical conductivity, strain sensitivity and environmental stability of the fabric sensors. The conductive fabrics were characterized using X-ray diffraction, thermogravimetry, contact angle measurements, particle size analysis, scanning electron microscopy and scanning probe microscopy. Powders of pure polypyrrole prepared by the same fabrication method were characterized for a better understanding of the polypyrrole coating. Copyright © 2007 Society of Chemical Industry [source] Glass bead grafting with poly(carboxylic acid) polymers and maleic anhydride copolymersPOLYMERS FOR ADVANCED TECHNOLOGIES, Issue 2 2008H. Zengin Abstract Glass beads were etched with acids and bases to increase the surface porosity and the number of silanol groups that could be used for grafting materials to the surfaces. The pretreated glass beads were functionalized using 3-aminopropyltriethoxysilane (APS) coupling agent and then further chemically modified by reacting the carboxyl groups of carboxylic acid polymers with the amino groups of the pregrafted APS. Several carboxylic acid polymers and poly(maleic anhydride) copolymers, such as poly(acrylic acid) (PAA), poly(methacrylic acid) (PMA), poly(styrene-alt-maleic anhydride) (PSMA), and poly(ethylene-alt-maleic anhydride) (PEMA) were grafted onto the bead surface. The chemical modifications were investigated and characterized by FT-IR spectroscopy, particle size analysis, and tensiometry for contact angle and porosity changes. The amount of APS and the different polymer grafted on the surface was determined from thermal gravimetric analysis and elemental analysis data. Spectroscopic studies and elemental analysis data showed that carboxylic acid polymers and maleic anhydride copolymers were chemically attached to the glass bead surface. The improved surface properties of surface modified glass beads were determined by measuring water and hexane penetration rates and contact angle. Contact angles increased and porosity decreased as the molecular weights of the polymer increased. The contact angles increased with the hydrophobicity of the attached polymer. The surface morphology was examined by scanning electron microscopy (SEM) and showed an increase in roughness for etched glass beads. Copyright © 2007 John Wiley & Sons, Ltd. [source] Synthesis and modification of zeolite NaA adsorbents for separation of hydrogen and methaneASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 5 2009Yanna Liu Abstract To improve the adsorption capacity of zeolite A, two kinds of zeolite NaA with submicron and hierarchical structure were prepared. The XRD patterns indicated that both synthesized products were pure zeolite with LTA-type framework. The SEM images and laser particle size analysis showed that the particle size of submicron zeolite NaA was about 240 nm. The TEM and N2 adsorption/desorption isotherms proved the existence of mesopores in the hierarchical zeolite NaA. The adsorption capacities of single component CH4 or H2 on zeolite SrA adsorbents, obtained by Sr2+ ion-exchange of submicron and hierarchical zeolite NaA, and commercial zeolite 5A adsorbent were measured by the static volume method at 25 °C and pressures up to 1 MPa. The results show that both prepared zeolite SrA adsorbents have higher adsorption capacities of CH4 and ideal separation factors of CH4/H2 than commercial zeolite 5A, and the submicron zeolite SrA has the largest adsorption capacity of CH4 and ideal separation factor of CH4/H2. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source] Electrical transport properties of aliovalent cation-doped CeO2ASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 1 2009Mark C. Pearce Abstract We report the comparative electrical properties of monovalent (Na+), divalent (Ca2+, Sr2+), trivalent (In3+, La3+) and coupled substitution of divalent and trivalent (Ca2+ + Sm3+) cation-doped CeO2. The investigated samples were prepared by solid-state reaction (ceramic) using the corresponding metal oxides and salts in the temperature range 1000,1600 °C in air. Powder X-ray diffraction (PXRD), laser particle size analysis (LPSA), scanning electron microscopy (SEM), and ac impedance spectroscopy measurements were employed for structural, morphology, and electrical characterization. PXRD studies reveal the formation of single-phase cubic fluorite-type structures for all investigated samples except those doped with In3+. The variation of lattice parameters is consistent with ionic radii (IR) of the dopant metal ions, with the exception of Na+ -doped CeO2. Our attempt to substitute In3+ for Ce4+ in CeO2 using both ceramic and wet chemical methods was unsuccessful. Furthermore, diffraction peaks attributed to CeO2 and In2O3 were observed up to sintering conditions of 1600 °C. Among the single-phase compounds investigated, Ce0.85Ca0.05Sm0.1O1.9 exhibits the highest bulk conductivity of 1.3 × 10,3 S/cm at 500 °C with activation energy of 0.64 eV in air. The electrical conductivity data obtained for Ce0.85Ca0.05Sm0.1O1.9 in air and Ar were found to be very similar over the investigated temperature range, indicating the absence of p-electronic conduction in the high oxygen partial pressure (pO2) range which is consistent with literature reported on Sm-doped CeO2. Copyright © 2008 Curtin University of Technology and John Wiley & Sons, Ltd. [source] Understanding the key factors for enzymatic conversion of pretreated lignocellulose by partial least square analysisBIOTECHNOLOGY PROGRESS, Issue 2 2010Renliang Huang Abstract The relationship between the physicochemical properties of lignocellulosic substrates and enzyme digestion is still not well known. After different pretreatments, cellulase hydrolysis and measurements of physicochemical characteristics by column solute exclusion, particle size analysis, X-ray diffraction, Fourier transform infrared spectroscopy and solid state 13C nuclear magnetic resonance were performed in this study. Partial least squares was then applied to seek the key factors limiting the rate and extent of cellulose digestion. According to the PLS results, the most important factor for cellulose digestion was accessible interior surface area, followed by delignification and the destruction of the hydrogen bonds. The cellulose digestion at 2 and 24 hr were improved with the increased accessibility of interior surface area to the reporter molecules of 5.1-nm diameter. Removal of lignin and breaking of hydrogen bonds were also found to significantly promote cellulose conversion. Other properties, including the breakdown of intramolecular hydrogen bonds, cellulose crystallinity, and hemicellulose content, had less effect on the efficiency of enzymatic hydrolysis. © 2009 American Institute of Chemical Engineers Biotechnol. Prog., 2010 [source] Ultra scale-down approaches for clarification of mammalian cell culture broths in disc-stack centrifugesBIOTECHNOLOGY PROGRESS, Issue 6 2009Ferhana Zaman Abstract Ultra-scale down (USD) methodology developed by University College London for cell broth clarification with industrial centrifuges was applied to two common cell lines (NS0 and GS-CHO) expressing various therapeutic monoclonal antibodies. A number of centrifuges at various scales were used with shear devices operating either by high speed rotation or flow-through narrow channels. The USD methodology was found effective in accounting for both gravitational and shear effects on clarification performance with three continuous centrifuges at pilot and manufacturing scales. Different shear responses were observed with the two different cell lines and even with the same cell line expressing different products. Separate particle size analysis of the treated broths seems consistent with the shear results. Filterability of the centrifuged solutions was also evaluated to assess the utility of the USD approach for this part of the clarification operation. © 2009 American Institute of Chemical Engineers Biotechnol. Prog., 2009 [source] | |||||||||||||