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Sample records for high colloidal stability

  1. Stabilized super-thermite colloids: A new generation of advanced highly energetic materials

    Science.gov (United States)

    Elbasuney, Sherif; Gaber Zaky, M.; Radwan, Mostafa; Mostafa, Sherif F.

    2017-10-01

    One of the great impetus of nanotechnology on energetic materials is the achievement of nanothermites (metal-oxide/metal) which are characterized by massive heat output. Yet, full exploitation of super-thermites in highly energetic systems has not been achieved. This manuscript reports on the sustainable fabrication of colloidal Fe2O3 and CuO nanoparticles for thermite applications. TEM micrographs demonstrated mono-dispersed Fe2O3 and CuO with an average particle size of 3 and 15 nm respectively. XRD diffractograms demonstrated highly crystalline materials. SEM micrographs demonstrated a great tendency of the developed oxides to aggregate over drying process. The effective integration and dispersion of mono-dispersed colloidal thermite particles into energetic systems are vital for enhanced performance. Aluminum is of interest as highly energetic metal fuel. In this paper, synthesized Fe2O3 and CuO nanoparticles were re-dispersed in isopropyl alcohol (IPA) with aluminum nanoparticles using ultrasonic prope homogenizer. The colloidal thermite peraticles can be intgegrated into highly energetic system for subsequent nanocomposite development. Thanks to stabilization of colloidal CuO nanoparticles in IPA which could offer intimate mixing between oxidizer and metal fuel. The stabilization mechanism of CuO in IPA was correlated to steric stabilization with solvent molecules. This approach eliminated nanoparticle drying and the re-dispersion of dry aggregates into energetic materials. This manuscript shaded the light on the real development of colloidal thermite mixtures and their integration into highly energetic systems.

  2. Increasing entropy for colloidal stabilization

    Science.gov (United States)

    Mo, Songping; Shao, Xuefeng; Chen, Ying; Cheng, Zhengdong

    2016-11-01

    Stability is of paramount importance in colloidal applications. Attraction between colloidal particles is believed to lead to particle aggregation and phase separation; hence, stability improvement can be achieved through either increasing repulsion or reducing attraction by modifying the fluid medium or by using additives. Two traditional mechanisms for colloidal stability are electrostatic stabilization and steric stabilization. However, stability improvement by mixing attractive and unstable particles has rarely been considered. Here, we emphasize the function of mixing entropy in colloidal stabilization. Dispersion stability improvement is demonstrated by mixing suspensions of attractive nanosized titania spheres and platelets. A three-dimensional phase diagram is proposed to illustrate the collaborative effects of particle mixing and particle attraction on colloidal stability. This discovery provides a novel method for enhancing colloidal stability and opens a novel opportunity for engineering applications.

  3. Proteolytic stability in colloidal systems.

    NARCIS (Netherlands)

    Maste, M.C.L.

    1996-01-01

    Proteolytic enzymes in liquid detergents suffer from lack of stability in the sense that activity diminishes with time. Although the phenomenon could be attributed to several factors, the influence of colloidal surfaces on the enzymatic stability was investigated. Besides the types of surfaces that

  4. Enhanced colloidal stability of hydroxyapatite

    Science.gov (United States)

    Borum, La Rhonda Terese

    Hydroxyapatite, Ca10(PO4)6(OH) 2 is the most thermodynamically stable calcium phosphate in physiological environments. Hence, it is the main inorganic mineral found in bone and teeth. Its colloidal stability, however, is poor because hydroxyapatite (HAp) particles exhibit sediment formation upon standing at short time periods, where agglomerates form and lead to non-homogeneous suspensions. Surface modification is a promising method to tailor the colloidal stability of hydroxyapatite for biomaterial applications. Three techniques to modify the HAp surface and enhance the colloidal stability of HAp were investigated. Modified particles were characterized by methods sensitive to surface chemistry changes, such as sedimentation studies, diffuse reflectance Fourier transform infrared spectroscopy (DRIFT), Brunauer-Emmett-Teller (BET) surface area, and electrophoresis. Sedimentation studies demonstrated how effective each technique was in improving the colloidal stability of hydroxyapatite particles. Electrophoresis provided information on electrostatic interactions within each system. The first technique entailed an esterification reaction of the HAp surface with dodecyl alcohol at elevated temperatures. DRIFT results showed that dodecyl groups from the alcohol replaced acidic hydroxyl and phosphate sites on the HAp surface, giving rise to enhanced colloidal stability through steric interactions in ethanol suspensions. TGA curves gave insight to the degree of esterification for the esterified particles. Higher reaction temperatures give rise to a higher degree of esterification resulting in better colloidal stability. The second technique applied a silica coating on the HAp surface by the hydrolysis of tetraethyl orthosilicate in ethanol. Silica was coated onto the HAp surface at 5--75 wt% loading amounts. A combination of acid dissolution and x-ray diffraction (XRD), along with BET showed that the silica coating is complete at 50 wt% silica loading. The silica coating

  5. Stabilization of Colloidal Silica Using Small Polyols

    Energy Technology Data Exchange (ETDEWEB)

    GULLEY, GERALD L.; MARTIN, JAMES E.

    1999-09-07

    We have discovered that small polyols are reasonably effective at stabilizing colloidal silica against aggregation, even under the conditions of high pH and salt concentration. Both quasielastic and elastic light scattering were used to show that these polyols dramatically decrease the aggregation rate of the suspension, changing the growth kinetics from diffusion-limited cluster-cluster aggregation to reaction-limited cluster-cluster aggregation. These polyols maybe useful in the treatment of tank wastes at the Hanford site.

  6. Sodium meta-autunite colloids: Synthesis, characterization,stability

    Energy Technology Data Exchange (ETDEWEB)

    zzuoping@lbl.gov

    2004-04-10

    Waste forms of U such as those in the United States Department of Energy's Hanford Site often contain high concentrations of Na and P. Low solubility sodium uranyl phosphates such as sodium meta-autunite have the potential to form mobile colloids that can facilitate transport of this radionuclide. In order to understand the geochemical behavior of uranyl phosphate colloids, we synthesized sodiummeta-autunite colloids, and characterized their morphology, chemical composition, structure, dehydration, and surface charge. The stability of these synthetic plate-shaped colloids was tested with respect to time and pH. The highest aggregation rate was observed at pH 3, and the rate decreases as pH increases, indicating that higher stability of colloid dispersion under neutral and alkaline pH conditions. The synthetic colloids are all negatively charged and no isoelectric points were found over a pH range of 3 to 9. The zeta-potentials of the colloids in the phosphate solution show a strong pH-dependence in the more acidic range over time, but are relatively constant in the neutral and alkaline pH range. The geochemical behavior of the synthetic colloids can be interpreted using DLVO theory. The results suggest that formation of mobile sodium meta-autunite colloids can enhance the transport of U in some contaminated sediments.

  7. Electrostatic Stabilized InP Colloidal Quantum Dots with High Photoluminescence Efficiency.

    Science.gov (United States)

    Mnoyan, Anush N; Kirakosyan, Artavazd Gh; Kim, Hyunki; Jang, Ho Seong; Jeon, Duk Young

    2015-06-30

    Electrostatically stabilized InP quantum dots (QDs) showing a high luminescence yield of 16% without any long alkyl chain coordinating ligands on their surface are demonstrated. This is achieved by UV-etching the QDs in the presence of fluoric and sulfuric acids. Fluoric acid plays a critical role in selectively etching nonradiative sites during the ligand-exchange process and in relieving the acidity of the solution to prevent destruction of the QDs. Given that the InP QDs show high luminescence without any electrical barriers, such as long alkyl ligands or inorganic shells, this method can be applied for QD treatment for application to highly efficient QD-based optoelectronic devices.

  8. Biocompatible gold nanorods: one-step surface functionalization, highly colloidal stability, and low cytotoxicity.

    Science.gov (United States)

    Liu, Kang; Zheng, Yuanhui; Lu, Xun; Thai, Thibaut; Lee, Nanju Alice; Bach, Udo; Gooding, J Justin

    2015-05-05

    The conjugation of gold nanorods (AuNRs) with polyethylene glycol (PEG) is one of the most effective ways to reduce their cytotoxicity arising from the cetyltrimethylammonium bromide (CTAB) and silver ions used in their synthesis. However, typical PEGylation occurs only at the tips of the AuNRs, producing partially modified AuNRs. To address this issue, we have developed a novel, facile, one-step surface functionalization method that involves the use of Tween 20 to stabilize AuNRs, bis(p-sulfonatophenyl)phenylphosphine (BSPP) to activate the AuNR surface for the subsequent PEGylation, and NaCl to etch silver from the AuNRs. This method allows for the complete removal of the surface-bound CTAB and the most active surface silver from the AuNRs. The produced AuNRs showed far lower toxicity than other methods to PEGylate AuNRs, with no apparent toxicity when their concentration is lower than 5 μg/mL. Even at a high concentration of 80 μg/mL, their cell viability is still four times higher than that of the tip-modified AuNRs.

  9. Assessing colloidal stability of long term MWCNT based nanofluids.

    Science.gov (United States)

    Lamas, Bruno; Abreu, Bruno; Fonseca, Alexandra; Martins, Nelson; Oliveira, Mónica

    2012-09-01

    This report presents an assessment on colloidal stability of functionalized multiwalled carbon nanotubes based nanofluids. To this end, an innovative technique that allows for measurement of settling velocity during centrifugation is applied. This method also enables measurements without dilution, inferring further accuracy to the experimental study. The results suggest that functionalization techniques enable the production of highly stable nanofluids. It is also found, that the colloidal stabilities of these nanofluids are characterized by hindered settling. The settling velocity decreases when the nanoparticles volume fraction rises from 0.25% to 1.50% due to the increase of interparticle interaction. Furthermore, a high aspect ratio of nanoparticles directly contributed to an increase in colloidal stability. It is expected that these results may significantly contribute to proper tailor of nanofluids engineering, ensuring a long term stable dispersion enhancing industrial application suitability.

  10. Formation and stability of aluminosilicate colloids by coprecipitation

    Energy Technology Data Exchange (ETDEWEB)

    Putri, Kirana Yuniati

    2011-02-15

    Colloids are ubiquitous in natural waters. Colloid-facilitated migration is of importance in safety assessment of a nuclear waste disposal. Aluminosilicate colloids are considered to be the kernel of aquatic colloids. Their stability is affected by a number of geochemical parameters. This work aims to study qualitatively and quantitatively the stability of aluminosilicate colloids formed by coprecipitation under various geochemical conditions, i.e. pH, concentration of Al and Si metal ions, ionic strength, and omnipresent cations (Na{sup +}, Ca{sup 2+}, and Mg{sup 2+}). The work is performed by colorimetric method and laser-induced breakdown detection (LIBD). Two consecutive phase separations at 450 nm and 1 kDa are applied to separate the precipitates and colloids from the ionic species. By means of colorimetry, Si and Al can be detected down to 5.8 x10{sup -8} M and 7.4x10{sup -7} M, respectively. On the other hand, LIBD is able to quantify the colloidal size and its number density down to several ppt. Depending on the concentration of Al and Si metal ions, the formation trend of aluminosilicate colloid changes following its solubility curve. The lower the concentration, the higher the pH range in which the colloids start to emerge. Furthermore, the colloids are stable at higher Al and Si concentration and at low ionic strength. In the low pH range, cations provide different effects at low and high ionic strengths. At high ionic strength, the colloids are stable in the presence of a larger cation, while all cations exhibit similar effects at low ionic strength. However, in the high pH range, valence seems to have a stronger effect than ionic radius; colloids are more stable in the presence of monovalent cations than divalent ones. Meanwhile, XRD shows non- and/or poor crystalline structure of the aluminosilicate species. Nevertheless, results from XPS may suggest that the chemical composition (Si/Al ∼ 0.6) of the aluminosilicate precipitates is sillimanite or

  11. Manipulating semiconductor colloidal stability through doping.

    Science.gov (United States)

    Fleharty, Mark E; van Swol, Frank; Petsev, Dimiter N

    2014-10-10

    The interface between a doped semiconductor material and electrolyte solution is of considerable fundamental interest, and is relevant to systems of practical importance. Both adjacent domains contain mobile charges, which respond to potential variations. This is exploited to design electronic and optoelectronic sensors, and other enabling semiconductor colloidal materials. We show that the charge mobility in both phases leads to a new type of interaction between semiconductor colloids suspended in aqueous electrolyte solutions. This interaction is due to the electrostatic response of the semiconductor interior to disturbances in the external field upon the approach of two particles. The electrostatic repulsion between two charged colloids is reduced from the one governed by the charged groups present at the particles surfaces. This type of interaction is unique to semiconductor particles and may have a substantial effect on the suspension dynamics and stability.

  12. Noncovalent Surface Locking of Mesoporous Silica Nanoparticles for Exceptionally High Hydrophobic Drug Loading and Enhanced Colloidal Stability.

    Science.gov (United States)

    Palanikumar, L; Kim, Ho Young; Oh, Joon Yong; Thomas, Ajesh P; Choi, Eun Seong; Jeena, M T; Joo, Sang Hoon; Ryu, Ja-Hyoung

    2015-09-14

    Advances in water-insoluble drug delivery systems are limited by selective delivery, loading capacity, and colloidal and encapsulation stability. We have developed a simple and robust hydrophobic-drug delivery platform with different types of hydrophobic chemotherapeutic agents using a noncovalent gatekeeper's technique with mesoporous silica nanoparticles (MSNs). The unmodified pores offer a large volume of drug loading capacity, and the loaded drug is stably encapsulated until it enters the cancer cells owing to the noncovalently bound polymer gatekeeper. In the presence of polymer gatekeepers, the drug-loaded mesoporous silica nanoparticles showed enhanced colloidal stability. The simplicity of drug encapsulation allows any combination of small chemotherapeutics to be coencapsulated and thus produce synergetic therapeutic effects. The disulfide moiety facilitates decoration of the nanoparticles with cysteine containing ligands through thiol-disulfide chemistry under mild conditions. To show the versatility of drug targeting to cancer cells, we decorated the surface of the shell-cross-linked nanoparticles with two types of peptide ligands, SP94 and RGD. The nanocarriers reported here can release encapsulated drugs inside the reducing microenvironment of cancer cells via degradation of the polymer shell, leading to cell death.

  13. Stabilization and Control of Rheological Properties of Fe2O3/Al(OH)(3)-rich Colloidal Slurries Under High Ionic Strength and pH

    Energy Technology Data Exchange (ETDEWEB)

    Chun, Jaehun; Poloski, Adam P.; Hansen, E. K.

    2010-08-01

    Controlling the stability and rheological properties of colloidal slurries has been an important but challenging issue for various applications such as cosmetics, ceramic processing, and nuclear waste treatment. For example, at the Department of Energy (DOE) Hanford and Savannah River sites, operation of the waste treatment facilities with increased solids loading affects waste processing rates but impacts the rheological properties. We investigated various rheological modifiers on a Fe2O3-rich nuclear waste simulant, characterized by high ionic strength and pH, in order to reduce rheological properties of the colloidal slurry. Rheological modifiers change particle interactions in colloidal slurries; they mainly alter the electrostatic and steric interactions between particles, leading to a change in rheological properties. Weak acid type rheological modifiers strengthen electrostatic repulsion whereas nonionic/polymer surfactant type rheological modifiers introduce a steric repulsion. Using rheological analysis, it was found that citric acid and polyacrylic acid are good rheological modifiers for the simulant tested, effectively reducing yield stresses by as much as 70%. Further analysis supports that addition of such rheological modifiers increases the stability of the slurry. Binding cations in bulk solution and adsorption on the surface of the particles are identified as a reasonable working mechanism for citric acid and polyacrylic acid.

  14. Sustainable steric stabilization of colloidal titania nanoparticles

    Science.gov (United States)

    Elbasuney, Sherif

    2017-07-01

    A route to produce a stable colloidal suspension is essential if mono-dispersed particles are to be successfully synthesized, isolated, and used in subsequent nanocomposite manufacture. Dispersing nanoparticles in fluids was found to be an important approach for avoiding poor dispersion characteristics. However, there is still a great tendency for colloidal nanoparticles to flocculate over time. Steric stabilization can prevent coagulation by introducing a thick adsorbed organic layer which constitutes a significant steric barrier that can prevent the particle surfaces from coming into direct contact. One of the main features of hydrothermal synthesis technique is that it offers novel approaches for sustainable nanoparticle surface modification. This manuscript reports on the sustainable steric stabilization of titanium dioxide nanoparticles. Nanoparticle surface modification was performed via two main approaches including post-synthesis and in situ surface modification. The tuneable hydrothermal conditions (i.e. temperature, pressure, flow rates, and surfactant addition) were optimized to enable controlled steric stabilization in a continuous fashion. Effective post synthesis surface modification with organic ligand (dodecenyl succinic anhydride (DDSA)) was achieved; the optimum surface coating temperature was reported to be 180-240 °C to ensure DDSA ring opening and binding to titania nanoparticles. Organic-modified titania demonstrated complete change in surface properties from hydrophilic to hydrophobic and exhibited phase transfer from the aqueous phase to the organic phase. Exclusive surface modification in the reactor was found to be an effective approach; it demonstrated surfactant loading level 2.2 times that of post synthesis surface modification. Titania was also stabilized in aqueous media using poly acrylic acid (PAA) as polar polymeric dispersant. PAA-titania nanoparticles demonstrated a durable amorphous polymeric layer of 2 nm thickness. This

  15. Effect of temperature on high shear-induced gelation of charge-stabilized colloids without adding electrolytes.

    Science.gov (United States)

    Wu, Hua; Tsoutsoura, Aikaterini; Lattuada, Marco; Zaccone, Alessio; Morbidelli, Massimo

    2010-02-16

    We demonstrated previously (Wu, H.; Zaccone, A.; Tsoutsoura, A.; Lattuada, M.; Morbidelli, M. Langmuir 2009, 25, 4715) that, for a colloid stabilized by charges from both polymer chain-end groups and adsorbed sulfonate surfactants, when the surfactant surface density reaches a certain critical value, the shear-induced gelation becomes unachievable at room temperature, even at an extremely large Peclet number, Pe = 4.6 x 10(4). This is due to the presence of the short-range, repulsive hydration force generated by the adsorbed surfactant. In this work, we investigate how such hydration force affects the shear-induced gelation at higher temperatures, in the range between 303 and 338 K. It is found that a colloidal system, which does not gel at room temperature in a microchannel at a fixed Pe = 3.7 x 10(4), does gel when temperature increases to a certain value. The critical initial particle volume fraction for the gelation to occur decreases as temperature increases. These results indicate that the effect of the hydration force on the gelation decreases as temperature increases. Moreover, we have observed that at the criticality only part of the primary particles is converted to the gel network and the effective particle volume fraction forming the gel network does not change significantly with temperature. The effective particle volume fraction is also independent of the surfactant surface coverage. Since the effective particle volume fraction corresponds to space filling requirement of a standing gel network, which is mainly related to the clusters structure, this result indicates that at a given shear rate the cluster structure does not change significantly with the surfactant surface coverage. On the other hand, since the cluster morphology is a strong function of the shear rate, we have observed that when the Peclet number is lowered from Pe = 3.7 x 10(4) to 1.7 x 10(4), the effective particle volume fraction reduces from 0.19 to 0.12 at 313 K.

  16. Rheology of stabilized cerium-gadolinium oxide (CGO) colloidal system

    DEFF Research Database (Denmark)

    Marani, Debora; Hjelm, Johan; Wandel, Marie

    Achievement of stable dispersion with high solid loadings and low viscosity is crucial issue in ceramic films processing. In this work, systematic analysis of the rheological properties of CGO colloidal suspension was performed. The study aimed to define methods for evaluating fully stabilized...... conditions and critical parameters. The influences of dispersant and inorganic contents on suspensions properties were investigated. The optimization of dispersant content was achieved by studying flow behaviour of suspensions at different amounts of dispersant. Rotational and oscillatory tests were...

  17. Sterically Stabilized Poly(3,4-ethylenedioxythiophene) Colloidal Dispersions Doped with Different Sulfonic Acids

    Institute of Scientific and Technical Information of China (English)

    Tie Jun WANG; Ping CHEN; Xiu Jie HU; Shu Yun ZHOU

    2006-01-01

    The preparation of sterically stabilized poly(3, 4-ethylenedioxythiophene)(PEDOT)colloidal dispersions doped with different sulfonic acids is described. Three different sulfonic acids, i.e., p-toluenesulfonic acid, β-naphthalenesuffonic acid and D-camphor-10-sulfonic acid are used, facilitating the preparation of sterically stable PEDOT colloidal particles. The influences of the dopants and concentration of polymeric stabilizer on the yields, morphologies and electrical properties of the resultant colloidal particles were investigated. The colloidal particles with the size ranging from 172 to 334 nm have been obtained in good yields. The compressed pellet conductivity was as high as 4.5 Scm-1.

  18. Dispersion stability and electrokinetic properties of intrinsic plutonium colloids: implications for subsurface transport.

    Science.gov (United States)

    Abdel-Fattah, Amr I; Zhou, Dongxu; Boukhalfa, Hakim; Tarimala, Sowmitri; Ware, S Doug; Keller, Arturo A

    2013-06-04

    Subsurface transport of plutonium (Pu) may be facilitated by the formation of intrinsic Pu colloids. While this colloid-facilitated transport is largely governed by the electrokinetic properties and dispersion stability (resistance to aggregation) of the colloids, reported experimental data is scarce. Here, we quantify the dependence of ζ-potential of intrinsic Pu(IV) colloids on pH and their aggregation rate on ionic strength. Results indicate an isoelectric point of pH 8.6 and a critical coagulation concentration of 0.1 M of 1:1 electrolyte at pH 11.4. The ζ-potential/pH dependence of the Pu(IV) colloids is similar to that of goethite and hematite colloids. Colloid interaction energy calculations using these values reveal an effective Hamaker constant of the intrinsic Pu(IV) colloids in water of 1.85 × 10(-19) J, corresponding to a relative permittivity of 6.21 and refractive index of 2.33, in agreement with first principles calculations. This relatively high Hamaker constant combined with the positive charge of Pu(IV) colloids under typical groundwater aquifer conditions led to two contradicting hypotheses: (a) the Pu(IV) colloids will exhibit significant aggregation and deposition, leading to a negligible subsurface transport or (b) the Pu(IV) colloids will associate with the relatively stable native groundwater colloids, leading to a considerable subsurface transport. Packed column transport experiments supported the second hypothesis.

  19. Bonding assembled colloids without loss of colloidal stability

    NARCIS (Netherlands)

    Vutukuri, H.R.; Stiefelhagen, J.C.P.; Vissers, T; Imhof, A.; van Blaaderen, A.

    2012-01-01

    In recent years the diversity of self-assembled colloidal structures has strongly increased, as it is fueled by a wide range of applications in materials science and also in soft condensed-matter physics.[1–4] Some potential applications include photonic bandgap (PBG) crystals, materials for plasmon

  20. Preparation of colloidal Sb2O5 and its stability

    Institute of Scientific and Technical Information of China (English)

    陈文汩; 张利; 龚竹青

    2004-01-01

    Colloidal antimony pentoxide was prepared by oxidation of antimony trioxide with hydrogen peroxide as oxidant and phosphoric acid as stabilizer. Effects of stabilizer, oxidant amount and reaction temperature on the diameter of colloidal particles and their size distribution were discussed. And static electricity effects on colloidal stability were studied by measurement of Zeta potential. Results show that Zeta potential of colloidal Sb2 O5 moves from -30mV to -56.8 mV with the addition of H3 PO4 as the stabilizer, zero point of charge of colloidal H3 PO4-Sb2 O5 moves from pH= 1.85 to more acidic regions, and colloidal H3 PO4-Sb2 O5 is stable in wider pH range. The stable time of colloidal H3 PO4-Sb2 O5 particles without coagulation is more than six months. The size of colloidal particles is smaller and their distribution is narrower by adding H3 PO4 as the stabilizer and decreasing reaction temperature, and the average diameter of H3 PO4-Sb2 O5 particles prepared is 30 nm.

  1. The Colloidal Stability of Magnetic Nanoparticles in Ionic Liquids

    Science.gov (United States)

    2015-08-03

    Final 3. DATES COVERED (From - To) 14 May 2014 – 13 May 2015 4. TITLE AND SUBTITLE The Colloidal Stability of Magnetic Nanoparticles in...Rev. 8-98) Prescribed by ANSI Std Z39-18 Final Report for AOARD Grant 144062 “The Colloidal Stability of Magnetic Nanoparticles in Ionic Liquids...sterically stabilized magnetic nanoparticles : Magnetic nanoparticles with an average core diameter of 25 nm used in this work were obtained from

  2. Addressing Colloidal Stability for Unambiguous Electroanalysis of Single Nanoparticle Impacts.

    Science.gov (United States)

    Robinson, Donald A; Kondajji, Aditya M; Castañeda, Alma D; Dasari, Radhika; Crooks, Richard M; Stevenson, Keith J

    2016-07-01

    Herein the problem of colloidal instability on electrochemically detected nanoparticle (NP) collisions with a Hg ultramicroelectrode (UME) by electrocatalytic amplification is addressed. NP tracking analysis (NTA) shows that rapid aggregation occurs in solution after diluting citrate-stabilized Pt NPs with hydrazine/phosphate buffers of net ionic strength greater than 70 mM. Colloidal stability improves by lowering the ionic strength, indicating that aggregation processes were strongly affected by charge screening of the NP double layer interactions at high cation concentrations. For the system of lowest ionic strength, the overwhelming majority of observed electrocatalytic current signals represent single NP/electrode impacts, as confirmed by NTA kinetic monitoring. NP diffusion coefficients determined by NTA and NP impact electroanalysis are in excellent agreement for the stable colloids, which signifies that the sticking probability of Pt NPs interacting with Hg is unity and that the observed NP impact rate agrees with the expected steady-state diffusive flux expression for the spherical cap Hg UME.

  3. Aqueous Colloidal Stability of Graphene Oxide and Chemically Converted Graphene

    Directory of Open Access Journals (Sweden)

    Swarnima Kashyap

    2014-01-01

    Full Text Available Graphene oxide (GO was prepared by modified Hummer’s method, and chemically converted graphene (CCG was prepared by further reduction of the aqueous GO colloid. The effect of pH on particle size, particle charge, and light absorption of the aqueous colloids of GO and CCG was studied with titration against HCl or NaOH, to find the ideal characteristics for a stable dispersion. The GO colloid was stable in the pH range of 4–11, whereas the CCG colloid gained stability at a relatively narrower pH range of 7–10. Poor stability of the colloids was observed for both GO and CCG colloids at both extremes of the pH scale. Both of the colloids exhibited average size of ~1 micron in the low pH range, whereas for higher pH the size ranged between 300 and 500 nm. The UV-Vis spectra showed absorption peak at 230 nm for GO colloids that shifted to 260 nm for the CCG colloid. Such shift can be ascribed to restoring of electronic conjugation of the C=C bonds in CCG.

  4. Maximizing exosome colloidal stability following electroporation.

    Science.gov (United States)

    Hood, Joshua L; Scott, Michael J; Wickline, Samuel A

    2014-03-01

    Development of exosome-based semisynthetic nanovesicles for diagnostic and therapeutic purposes requires novel approaches to load exosomes with cargo. Electroporation has previously been used to load exosomes with RNA. However, investigations into exosome colloidal stability following electroporation have not been considered. Herein, we report the development of a unique trehalose pulse media (TPM) that minimizes exosome aggregation following electroporation. Dynamic light scattering (DLS) and RNA absorbance were employed to determine the extent of exosome aggregation and electroextraction post electroporation in TPM compared to common PBS pulse media or sucrose pulse media (SPM). Use of TPM to disaggregate melanoma exosomes post electroporation was dependent on both exosome concentration and electric field strength. TPM maximized exosome dispersal post electroporation for both homogenous B16 melanoma and heterogeneous human serum-derived populations of exosomes. Moreover, TPM enabled heavy cargo loading of melanoma exosomes with 5nm superparamagnetic iron oxide nanoparticles (SPION5) while maintaining original exosome size and minimizing exosome aggregation as evidenced by transmission electron microscopy. Loading exosomes with SPION5 increased exosome density on sucrose gradients. This provides a simple, label-free means of enriching exogenously modified exosomes and introduces the potential for MRI-driven theranostic exosome investigations in vivo.

  5. Colloidal stability of polymeric nanoparticles in biological fluids

    Energy Technology Data Exchange (ETDEWEB)

    Lazzari, Stefano [ETH Zurich, Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering (Switzerland); Moscatelli, Davide, E-mail: davide.moscatelli@polimi.it [Materiali e Ingegneria Chimica ' Giulio Natta' , Politecnico di Milano, Dipartimento di Chimica (Italy); Codari, Fabio [ETH Zurich, Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering (Switzerland); Salmona, Mario [Istituto di Ricerche Farmacologiche ' Mario Negri' , Department of Molecular Biochemistry and Pharmacology (Italy); Morbidelli, Massimo [ETH Zurich, Department of Chemistry and Applied Biosciences, Institute for Chemical and Bioengineering (Switzerland); Diomede, Luisa [Istituto di Ricerche Farmacologiche ' Mario Negri' , Department of Molecular Biochemistry and Pharmacology (Italy)

    2012-06-15

    Estimating the colloidal stability of polymeric nanoparticles (NPs) in biological environments is critical for designing optimal preparations and to clarify the fate of these devices after administration. To characterize and quantify the physical stability of nanodevices suitable for biomedical applications, spherical NPs composed of poly-lactic acid (PLA) and poly-methyl-methacrylate (PMMA), in the range 100-200 nm, were prepared. Their stability in salt solutions, biological fluids, serum and tissue homogenates was analyzed by dynamic light scattering (DLS). The PMMA NPs remained stable in all fluids, while PLA NPs aggregated in gastric juice and spleen homogenate. The proposed stability test is therefore useful to see in advance whether NPs might aggregate when administered in vivo. To assess colloidal stability ex vivo as well, spectrophotofluorimetric analysis was employed, giving comparable results to DLS.

  6. Formation of gold colloids using thioether derivatives as stabilizing ligands

    NARCIS (Netherlands)

    Li, X.; de Jong, M.R.; Inoue, K.; Huskens, Jurriaan; Shinkai, Seiji; Reinhoudt, David

    2001-01-01

    Thioethers were used as adsorbates for preparing gold nanoparticles. Different thioether derivatives having from 1 to 4 thioether functionalities were synthesized. Colloids were prepared in a two-phase system, and characterized by 1H NMR and transmission electron microscopy (TEM). The stability of

  7. Using state diagrams for predicting colloidal stability of whey protein beverages.

    Science.gov (United States)

    Wagoner, Ty B; Ward, Loren; Foegeding, E Allen

    2015-05-06

    A method for evaluating aspects of colloidal stability of whey protein beverages after thermal treatment was established. Three state diagrams for beverages (pH 3-7) were developed representing protein solubility, turbidity, and macroscopic state after two ultrahigh-temperature (UHT) treatments. Key transitions of stability in the state diagrams were explored using electrophoresis and chromatography to determine aggregation propensities of β-lactoglobulin, α-lactalbumin, bovine serum albumin, and glycomacropeptide. The state diagrams present an overlapping view of high colloidal stability at pH 3 accompanied by high solubility of individual whey proteins. At pH 5, beverages were characterized by poor solubility, high turbidity, and aggregation/gelation of whey proteins with the exception of glycomacropeptide. Stability increased at pH 6, due to increased solubility of α-lactalbumin. The results indicate that combinations of state diagrams can be used to identify key regions of stability for whey protein containing beverages.

  8. Influence of lysolecithin and Tween 80 on the colloidal stability of branched chain amino acids in a nanosuspension system.

    Science.gov (United States)

    Hong, Chi Rac; Lee, Gyu Whan; Paik, Hyun-Dong; Chang, Pahn-Shick; Choi, Seung Jun

    2017-04-15

    This study examined the influence of stabilizers on the solubility and colloidal stability of branched chain amino acids (BCAAs) nanosuspended through high pressure homogenization at 70°C. Although homogenization increased the initial BCAA solubility, irrespective of pH (pH 3 or 6), homogenization alone was not sufficient to increase their long-term solubility. The incorporation of stabilizers into nanosuspensions increased the saturation concentration of BCAAs but the effect of stabilizers on the increase in the saturation concentration of BCAAs was more pronounced at pH 6.0. At pH 6, Tween 80 dramatically increased the colloidal stability of the BCAA nanosuspensions, independent of the BCAA:stabilizer ratio but not at pH 3. However, the effect of lysolecithin on the colloidal stability of nanosuspended BCAAs varied depending on pH and BCAA:lysolecithin ratio. In lysolecithin-related nanosuspensions, there was no clear relationship between the colloidal stability and nanosuspension conditions including pH and BCAA:lysolecithin ratio. This study could provide a useful information on stabilizer selection for the development of liquid or colloidal products with improved solubility and colloidal stability of nanosuspended BCAAs.

  9. Designing Whey Protein-Polysaccharide Particles for Colloidal Stability.

    Science.gov (United States)

    Wagoner, Ty; Vardhanabhuti, Bongkosh; Foegeding, E Allen

    2016-01-01

    Interactions between whey proteins and polysaccharides, in particular the formation of food-grade soluble complexes, are of interest because of potential functional and health benefits. A specific application that has not received much attention is the use of complexes for enhanced colloidal stability of protein sols, such as protein-containing beverages. In beverages, the primary goal is the formation of complexes that remain dispersed after thermal processing and extended storage. This review highlights recent progress in the area of forming whey protein-polysaccharide soluble complexes that would be appropriate for beverage applications. Research in this area indicates that soluble complexes can be formed and stabilized that are reasonably small in size and possess a large surface charge that would predict colloidal stability. Selection of specific proteins and polysaccharides can be tailored to desired conditions. The principal challenges involve overcoming restrictions on protein concentration and ensuring that protein remains bioavailable.

  10. Colloids with high-definition surface structures

    Science.gov (United States)

    Chen, Hsien-Yeh; Rouillard, Jean-Marie; Gulari, Erdogan; Lahann, Joerg

    2007-01-01

    Compared with the well equipped arsenal of surface modification methods for flat surfaces, techniques that are applicable to curved, colloidal surfaces are still in their infancy. This technological gap exists because spin-coating techniques used in traditional photolithographic processes are not applicable to the curved surfaces of spherical objects. By replacing spin-coated photoresist with a vapor-deposited, photodefinable polymer coating, we have now fabricated microstructured colloids with a wide range of surface patterns, including asymmetric and chiral surface structures, that so far were typically reserved for flat substrates. This high-throughput method can yield surface-structured colloidal particles at a rate of ≈107 to 108 particles per operator per day. Equipped with spatially defined binding pockets, microstructured colloids can engage in programmable interactions, which can lead to directed self-assembly. The ability to create a wide range of colloids with both simple and complex surface patterns may contribute to the genesis of previously unknown colloidal structures and may have important technological implications in a range of different applications, including photonic and phononic materials or chemical sensors. PMID:17592149

  11. Colloids with high-definition surface structures.

    Science.gov (United States)

    Chen, Hsien-Yeh; Rouillard, Jean-Marie; Gulari, Erdogan; Lahann, Joerg

    2007-07-03

    Compared with the well equipped arsenal of surface modification methods for flat surfaces, techniques that are applicable to curved, colloidal surfaces are still in their infancy. This technological gap exists because spin-coating techniques used in traditional photolithographic processes are not applicable to the curved surfaces of spherical objects. By replacing spin-coated photoresist with a vapor-deposited, photodefinable polymer coating, we have now fabricated microstructured colloids with a wide range of surface patterns, including asymmetric and chiral surface structures, that so far were typically reserved for flat substrates. This high-throughput method can yield surface-structured colloidal particles at a rate of approximately 10(7) to 10(8) particles per operator per day. Equipped with spatially defined binding pockets, microstructured colloids can engage in programmable interactions, which can lead to directed self-assembly. The ability to create a wide range of colloids with both simple and complex surface patterns may contribute to the genesis of previously unknown colloidal structures and may have important technological implications in a range of different applications, including photonic and phononic materials or chemical sensors.

  12. A colloidal singularity reveals the crucial role of colloidal stability for nanomaterials in-vitro toxicity testing: nZVI-microalgae colloidal system as a case study.

    Directory of Open Access Journals (Sweden)

    Soledad Gonzalo

    Full Text Available Aggregation raises attention in Nanotoxicology due to its methodological implications. Aggregation is a physical symptom of a more general physicochemical condition of colloidal particles, namely, colloidal stability. Colloidal stability is a global indicator of the tendency of a system to reduce its net surface energy, which may be achieved by homo-aggregation or hetero-aggregation, including location at bio-interfaces. However, the role of colloidal stability as a driver of ENM bioactivity has received little consideration thus far. In the present work, which focuses on the toxicity of nanoscaled Fe° nanoparticles (nZVI towards a model microalga, we demonstrate that colloidal stability is a fundamental driver of ENM bioactivity, comprehensively accounting for otherwise inexplicable differential biological effects. The present work throws light on basic aspects of Nanotoxicology, and reveals a key factor which may reconcile contradictory results on the influence of aggregation in bioactivity of ENMs.

  13. The prepatation and stability of homodisperse colloidal haematite (alpha-Fe2-O3)

    NARCIS (Netherlands)

    Penners, N.H.G.

    1985-01-01

    Since the foundation of colloid chemistry as a branch of science, much attention has been paid to the subject of colloid stability, i.e. the stability of colloid systems against aggregation. Gradually, our knowledge of the mechanisms involved has improved and models were developed, comprised in the

  14. Colloidal stability and chemical reactivity of complex colloids containing Fe³⁺.

    Science.gov (United States)

    van Leeuwen, Y M; Velikov, K P; Kegel, W K

    2014-07-15

    The reactivity of iron contained within insoluble colloidal metal-pyrophosphate salts was determined and compared to the reactivity of a soluble iron salt (FeCl3). As a model system for the reactivity of iron in food products, the formation of an iron-polyphenol complex was followed with spectrophotometry. Three types of systems were prepared and their colloidal stability and reactivity studied: Fe(3+) pyrophosphate, protein-coated Fe(3+) pyrophosphate and mixed-metal pyrophosphates containing Fe(3+) and a second cation M. The additional cation used was either monovalent (sodium) or divalent (M(2+)). It was found that: (i) incorporating iron in a colloidal salt reduced its reactivity compared to free Fe(3+) ions; (ii) coating the particles with a layer of hydrophobic protein (zein) increased stability and further decreased the reactivity. Finally, the most surprising result was that (iii) a mixed system containing more Fe(3+) than M actually increased the reactivity of the contained iron, while the reverse, a system containing excess M, inhibited the reactivity completely.

  15. Stability of orientationally disordered crystal structures of colloidal hard dumbbells.

    Science.gov (United States)

    Marechal, Matthieu; Dijkstra, Marjolein

    2008-06-01

    We study the stability of orientationally disordered crystal phases in a suspension of colloidal hard dumbbells using Monte Carlo simulations. For dumbbell bond length L/sigmafcc structure for a large part of the stable plastic crystal regime. In addition, we study the stability of an orientationally disordered aperiodic crystal structure in which the spheres of the dumbbells are on a random-hexagonal-close-packed lattice, and the dumbbells are formed by taking random pairs of neighboring spheres. Using free-energy calculations, we determine the fluid-aperiodic crystal and periodic-aperiodic crystal coexistence regions for L/sigma>0.88 .

  16. Effect of Gd3+ on the colloidal stability of liposomes.

    Science.gov (United States)

    Sabín, Juan; Prieto, Gerardo; Sennato, Simona; Ruso, Juan M; Angelini, Roberta; Bordi, Federico; Sarmiento, Félix

    2006-09-01

    Lanthanide ions such as La3+ and Gd3+ are well known to have large effects on the structure of phospholipid membranes. Unilamellar vesicles of dipalmitoylphosphatidylcholine (DPPC) were prepared by sonication method and confirmed by transmission electron microscopy. The effects of concentration of gadolinium ions Gd3+ on DPPC unilamellar vesicles in aqueous media were studied by different techniques. As physical techniques, photon correlation spectroscopy, electrophoretic mobility, and differential scanning calorimetry were used. The theoretical predictions of the colloidal stability of liposomes were followed using the Derjaguin-Landau-Verwey-Overbeek theory. Changes in the size of liposomes and high polydispersities values were observed as Gd3+ concentration increases, suggesting that this cation induces the aggregation of vesicles. Electrophoretic mobility measurements on unilamellar vesicles as a function of Gd3+ ion concentration show that the vesicles adsorb Gd3+ ions. Above Gd3+ concentrations of 0.1 mol dm-3, the zeta potential and light scattering measurements indicate the beginning of aggregation process. For comparison with similar phospholipids, the zeta potential of phosphatidylcholine interacting with Gd3+ was measured, showing an analogous behavior. Differential scanning calorimetry has been used to determine the effect of Gd3+ on the transition temperature (Tc) and on the enthalpy (DeltaHc) associated with the process.

  17. Domain and droplet sizes in emulsions stabilized by colloidal particles

    Science.gov (United States)

    Frijters, Stefan; Günther, Florian; Harting, Jens

    2014-10-01

    Particle-stabilized emulsions are commonly used in various industrial applications. These emulsions can present in different forms, such as Pickering emulsions or bijels, which can be distinguished by their different topologies and rheology. We numerically investigate the effect of the volume fraction and the uniform wettability of the stabilizing spherical particles in mixtures of two fluids. For this, we use the well-established three-dimensional lattice Boltzmann method, extended to allow for the added colloidal particles with non-neutral wetting properties. We obtain data on the domain sizes in the emulsions by using both structure functions and the Hoshen-Kopelman (HK) algorithm, and we demonstrate that both methods have their own (dis)advantages. We confirm an inverse dependence between the concentration of particles and the average radius of the stabilized droplets. Furthermore, we demonstrate the effect of particles detaching from interfaces on the emulsion properties and domain-size measurements.

  18. Stability studies of colloidal silica dispersions in binary solvent mixtures

    CERN Document Server

    Bean, K H

    1997-01-01

    A series of monodispersed colloidal silica dispersions, of varying radii, has been prepared. These particles are hydrophilic in nature due to the presence of surface silanol groups. Some of the particles have been rendered hydrophobic by terminally grafting n-alkyl (C sub 1 sub 8) chains to the surface. The stability of dispersions of these various particles has been studied in binary mixtures of liquids, namely (i) ethanol and cyclohexane, and (ii) benzene and n-heptane. The ethanol - cyclohexane systems have been studied using a variety of techniques. Adsorption excess isotherms have been established and electrophoretic mobility measurements have been made. The predicted stability of the dispersions from D.V.L.O. calculations is compared to the observed stability. The hydrophilic silica particles behave as predicted by the calculations, with the zeta potential decreasing and the van der Waals attraction increasing with increasing cyclohexane concentration. The hydrophobic particles behave differently than e...

  19. Pickering emulsions stabilized by oppositely charged colloids: Stability and pattern formation

    Science.gov (United States)

    Christdoss Pushpam, Sam David; Basavaraj, Madivala G.; Mani, Ethayaraja

    2015-11-01

    A binary mixture of oppositely charged colloids can be used to stabilize water-in-oil or oil-in-water emulsions. A Monte Carlo simulation study to address the effect of charge ratio of colloids on the stability of Pickering emulsions is presented. The colloidal particles at the interface are modeled as aligned dipolar hard spheres, with attractive interaction between unlike-charged and repulsive interaction between like-charged particles. The optimum composition (fraction of positively charged particles) required for the stabilization corresponds to a minimum in the interaction energy per particle. In addition, for each charge ratio, there is a range of compositions where emulsions can be stabilized. The structural arrangement of particles or the pattern formation at the emulsion interface is strongly influenced by the charge ratio. We find well-mixed isotropic, square, and hexagonal arrangements of particles on the emulsion surface for different compositions at a given charge ratio. The distribution of coordination numbers is calculated to characterize structural features. The simulation study is useful for the rational design of Pickering emulsifications wherein oppositely charged colloids are used, and for the control of pattern formation that can be useful for the synthesis of colloidosomes and porous shells derived thereof.

  20. Coadsorption of IgG and BSA onto sulfonated polystyrene latex: II. Colloidal stability and immunoreactivity.

    Science.gov (United States)

    Peula, J M; Hidalgo-Alvarez, R; de las Nieves, F J

    1995-01-01

    The present work deals with the study of the colloidal stability and immunoreactivity of sulfonated polystyrene latex particles covered by different amounts of m-BSA and IgG/a-CRP. These proteins have been previously adsorbed onto a sulfonated latex by sequential and competitive coadsorption experiments and it was possible to obtain latex-protein particles with different degrees of coverage by each protein. The latex particles, fully or partially covered by each protein (termed latex-protein complexes), were resuspended under several conditions (different pH and ionic strength values) and their colloidal stability, vs the addition of the electrolyte was studied using turbidity measurements. This stability appeared at a high degree of coverage by BSA and at a pH in which the BSA was negatively charged. At a high degree of coverage by IgG, the latex particles were unstable at all pHs. As a final part of this work, the immunoreactivity of several complexes was studied following the changes in the turbidity after the addition of CRP antigen. Only the complexes which were colloidally stable gave detectable reactivity. However, the complexes with a relatively low degree of coverage by IgG/a-CRP gave good immunoreactivity. Therefore, the latex-protein complex properties depended on the percentage of BSA or IgG adsorbed and on the electric state of the proteins at the redispersion pH. Under specific incubation conditions, sulfonated latex covered by significant IgG/BSA percentages was obtained, which showed a high colloidal stability and good immunoreactivity.

  1. High colloidal stability of gold nanorods coated with a peptide-ethylene glycol: Analysis by cyanide-mediated etching and nanoparticle tracking analysis.

    Science.gov (United States)

    Free, Paul; Conger, Gao; Siji, Wu; Zhang, Jing Bo; Fernig, David G

    2016-10-01

    The stability of gold nanorods was assessed following coating with various charged or uncharged ligands, mostly peptides. Highly stable monodispersed gold nanorods were obtained by coating CTAB-stabilized gold nanorods with a pentapeptide with C-terminal ethylene glycol units (peptide-EG). UV-vis spectroscopy of these nanorods suspended in saline solutions indicated no signs of aggregation, and they were easily purified using size-exclusion chromatography. A more stringent measure of nanorod stability involved observing changes in the UV-vis absorbance of gold nanorods subjected to etching with cyanide. The λmax absorbance of peptide-EG coated nanorods red-shifted in etchant solution. The hypothesis that changes in the nanorod aspect ratio led to this red-shift was confirmed by TEM analysis, which showed pit formation along the transverse axis. The etching process was followed in solution using nanoparticle tracking analysis. The red-shift was shown to occur while the particles remained mono-dispersed, and so was not due to aggregation. Adding both etchant solution and peptide-EG to the nanorods was further shown to allow modulation of the Δλmax red-shift and increase the etchant resistance of peptide-EG nanorods. Thus, very stable gold nanorods can be produced using the peptide-EG coating approach and their optical properties modulated with etchant.

  2. Colloid suspension stability and transport through unsaturated porous media

    Energy Technology Data Exchange (ETDEWEB)

    McGraw, M.A.; Kaplan, D.I.

    1997-04-01

    Contaminant transport is traditionally modeled in a two-phase system: a mobile aqueous phase and an immobile solid phase. Over the last 15 years, there has been an increasing awareness of a third, mobile solid phase. This mobile solid phase, or mobile colloids, are organic or inorganic submicron-sized particles that move with groundwater flow. When colloids are present, the net effect on radionuclide transport is that radionuclides can move faster through the system. It is not known whether mobile colloids exist in the subsurface environment of the Hanford Site. Furthermore, it is not known if mobile colloids would likely exist in a plume emanating from a Low Level Waste (LLW) disposal site. No attempt was made in this study to ascertain whether colloids would form. Instead, experiments and calculations were conducted to evaluate the likelihood that colloids, if formed, would remain in suspension and move through saturated and unsaturated sediments. The objectives of this study were to evaluate three aspects of colloid-facilitated transport of radionuclides as they specifically relate to the LLW Performance Assessment. These objectives were: (1) determine if the chemical conditions likely to exist in the near and far field of the proposed disposal site are prone to induce flocculation (settling of colloids from suspension) or dispersion of naturally occurring Hanford colloids, (2) identify the important mechanisms likely involved in the removal of colloids from a Hanford sediment, and (3) determine if colloids can move through unsaturated porous media.

  3. Surface functionalized LSMO nanoparticles with improved colloidal stability for hyperthermia applications

    Science.gov (United States)

    Thorat, N. D.; Khot, V. M.; Salunkhe, A. B.; Prasad, A. I.; Ningthoujam, R. S.; Pawar, S. H.

    2013-03-01

    LSMO (La0.7Sr0.3MnO3) magnetic nanoparticles (MNPs) coated with double layer oleic acid (OA) surfactant are prepared to make a water based magnetic nanofluid for hyperthermia application. Various experimental techniques are used for bilayer coating analysis. The effect of the bilayer coating on magnetic properties is studied by superconducting quantum interface device (SQUID). Colloidal behaviour of coated MNPs in aqueous medium is studied by the zeta potential and dynamic light scattering. The effects of pH and ionic strength on the colloidal stability of the MNPs are studied in detail. For the bilayer-coated LSMO MNPs aggregation is not observed even in high ionic strength and at physiological pH (7.4). For making the nanofluid of the bilayer-coated MNPs the colloidal stability is studied in physiological media like phosphate buffer solution. Under induction heating experiment, hyperthermia temperature (42-43 °C) could be achieved by the bilayer-coated sample at a magnetic field of 168-335 Oe and frequency of 267 kHz. The bilayer OA coating can hinder the agglomeration of MNPs significantly and produce stable suspension with improved hyperthermia properties. The bilayer OA coating also improves the specific absorption rate (SAR) of LSMO MNPs from 25 to 40 W g-1.

  4. Stability of colloidal silver nanoparticles trapped in lipid bilayer: effect of lecithin concentration and applied temperature

    NARCIS (Netherlands)

    Barani, H.; Montazer, M.; Braun, H.G.; Dutschk, Victoria

    2014-01-01

    The use of silver nanoparticle on various substrates has been widespread because of its good antibacterial properties that directly depend on the stability of the silver nanoparticles in a colloidal suspension. In this study, the colloidal solutions of the silver nanoparticles were synthesised by a

  5. Stability of colloidal silver nanoparticles trapped in lipid bilayer: effect of lecithin concentration and applied temperature

    NARCIS (Netherlands)

    Barani, H.; Montazer, M.; Braun, H.G.; Dutschk, V.

    2014-01-01

    The use of silver nanoparticle on various substrates has been widespread because of its good antibacterial properties that directly depend on the stability of the silver nanoparticles in a colloidal suspension. In this study, the colloidal solutions of the silver nanoparticles were synthesised by a

  6. Colloidal Stability of Graphene Oxide Nanosheets in Aqueous Solutions

    Science.gov (United States)

    Guikema, Janice; Wang, Yung-Li; Chen, Kai

    2013-03-01

    Carbon-based nanomaterials are increasingly used in commercial products as well as in research and industrial applications. Due to its extraordinary properties, graphene has attracted intense research interest and has been demonstrated in many potential applications including solar cells, conductive ink, and transistors. Graphene oxide has also been studied extensively and has been used to produce biocompatible antibacterial paper. Chemical reduction of graphene oxide is commonly used to produce inexpensive graphene in large quantities. With the increasing use of graphene and graphene oxide in consumer products, these nanomaterials may inevitably be released to aqueous systems, resulting in potential risk to environmental ecosystems and human health. The fate and mobility of graphene and its oxides in aquatic systems is dependent on their colloidal stability. We will discuss our study of the early-stage aggregation kinetics of graphene oxide in aqueous solutions. We prepared a suspension of single-layer graphene oxide nanosheets in water and used time-resolved dynamic light scattering to study the influence of electrolytes and pH on the aggregation kinetics of the nanosheets. Atomic force microscopy was employed to further examine the graphene oxide nanosheets.

  7. PEGylation of SPIONs by polycondensation reactions: a new strategy to improve colloidal stability in biological media

    Energy Technology Data Exchange (ETDEWEB)

    Viali, Wesley Renato; Silva Nunes, Eloiza da; Santos, Caio Carvalho dos [Universidade Estadual Paulista, Laboratorio de Materiais Magneticos e Coloides, Departamento de Fisico-quimica, Instituto de Quimica (Brazil); Silva, Sebastiao William da; Aragon, Fermin Herrera; Coaquira, Jose Antonio Huamani; Morais, Paulo Cesar [Universidade de Brasilia, Instituto de Fisica, Nucleo de Fisica Aplicada (Brazil); Jafelicci, Miguel, E-mail: jafeli@iq.unesp.br [Universidade Estadual Paulista, Laboratorio de Materiais Magneticos e Coloides, Departamento de Fisico-quimica, Instituto de Quimica (Brazil)

    2013-08-15

    In this study, we report on a new route of PEGylation of superparamagnetic iron oxide nanoparticles (SPIONs) by polycondensation reaction with carboxylate groups. Structural and magnetic characterizations were performed by X-ray diffractometry (XRD), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and vibrating sample magnetometry (VSM). The XRD confirmed the spinel structure with a crystallite average diameter in the range of 3.5-4.1 nm in good agreement with the average diameter obtained by TEM (4.60-4.97 nm). The TGA data indicate the presence of PEG attached onto the SPIONs' surface. The SPIONs were superparamagnetic at room temperature with saturation magnetization (M{sub S}) from 36.7 to 54.1 emu/g. The colloidal stability of citrate- and PEG-coated SPIONs was evaluated by means of dynamic light scattering measurements as a function of pH, ionic strength, and nature of dispersion media (phosphate buffer and cell culture media). Our findings demonstrated that the PEG polymer chain length plays a key role in the coagulation behavior of the Mag-PEG suspensions. The excellent colloidal stability under the extreme conditions we evaluated, such as high ionic strength, pH near the isoelectric point, and cell culture media, revealed that suspensions comprising PEG-coated SPION, with PEG of molecular weight 600 and above, present steric stabilization attributed to the polymer chains attached onto the surface of SPIONs.

  8. Protein-silver nanoparticle interactions to colloidal stability in acidic environments.

    Science.gov (United States)

    Tai, Jui-Ting; Lai, Chao-Shun; Ho, Hsin-Chia; Yeh, Yu-Shan; Wang, Hsiao-Fang; Ho, Rong-Ming; Tsai, De-Hao

    2014-11-04

    We report a kinetic study of Ag nanoparticles (AgNPs) under acidic environments (i.e., pH 2.3 to pH ≈7) and systematically investigate the impact of protein interactions [i.e., bovine serum albumin (BSA) as representative] to the colloidal stability of AgNPs. Electrospray-differential mobility analysis (ES-DMA) was used to characterize the particle size distributions and the number concentrations of AgNPs. Transmission electron microscopy was employed orthogonally to provide visualization of AgNPs. For unconjugated AgNPs, the extent of aggregation, or the average particle size, was shown to be increased significantly with an increase of acidity, where a partial coalescence was found between the primary particles of unconjugated AgNP clusters. Aggregation rate constant, kD, was also shown to be proportional to acidity, following a correlation of log(kD) = -1.627(pH)-9.3715. Using ES-DMA, we observe BSA had a strong binding affinity (equilibrium binding constant, ≈ 1.1 × 10(6) L/mol) to the surface of AgNPs, with an estimated maximum molecular surface density of ≈0.012 nm(-2). BSA-functionalized AgNPs exhibited highly-improved colloidal stability compared to the unconjugated AgNPs under acidic environments, where both the acid-induced interfacial dissolution and the particle aggregation became negligible. Results confirm a complex mechanism of colloidal stability of AgNPs: the aggregation process was shown to be dominant, and the formation of BSA corona on AgNPs suppressed both particle aggregation and interfacial dissolution of AgNP samples under acidic environments.

  9. Long term stability and reproducibility of magnetic colloids are key issues for steady values of Specific Power Absorption through time

    CERN Document Server

    Sanz, B; Cassinelli, N; Ibarra, M R; Goya, G F

    2016-01-01

    Virtually all clinical applications of magnetic nanoparticles (MNPs) require the formulation of biocompatible, water-based magnetic colloids. For magnetic hyperthermia, the requirements also include a high colloidal stability against precipitation and agglomeration of the constituent MNPs, in order to keep the heating efficiency of the ferrofluid in the long term. The specific power absorption (SPA) of single-domain MNPs depends critically on the average particle size and size distribution width, therefore first-rate reproducibility among different batches regarding these parameters are also needed. We have studied the evolution of the SPA of highly reproducible and stable water-based colloid composed of polymer coated $Fe_{3}O_{4}$ magnetic nanoparticles. By measuring the specific power absorption (SPA) values along one year as a function of field amplitude and frequencies ($H \\leq 24 kA/m$; $260 \\leq f \\leq 830 kHz$), we demonstrated that SPA in these samples can be made reproducible between successive synt...

  10. Facile synthesis and catalytic properties of silver colloidal nanoparticles stabilized by SDBS

    Indian Academy of Sciences (India)

    Wen Wang; Yinmin Song; Quansheng Liu; Keli Yang

    2014-06-01

    A facile method was explored to prepare stable silver colloidal nanoparticles (AgCNPs) in water. Sodium dodecyl benzene sulfonate (SDBS) was used as the stabilizing agent, without addition of any co-surfactant. The reaction was rapid and the product prepared at different conditions was measured by transmission electron microscopy (TEM) and UV-Vis spectroscopy. The results showed that AgCNPs stabilized by SDBS was stable in water with narrow size distribution (1-5 nm). The amount of surfactant has great influence on the products. When the molar ratio of Ag+ to SDBS increased to 1 : 4, AgCNPs can be obtained with high dispersion (2-3 nm), which has high catalytic activity on reduction of 4-nitrobenzoic acid to 4-aminobenzoic acid.

  11. Silver nanoparticle colloids with γ-cyclodextrin: enhanced stability and Gibbs–Marangoni flow

    Energy Technology Data Exchange (ETDEWEB)

    Amiri, Setareh; Duroux, Laurent; Larsen, Kim Lambertsen, E-mail: kll@bio.aau.dk [Aalborg University, Department of Chemistry and Bioscience (Denmark)

    2015-01-15

    Although cyclodextrins (CD) are effective stabilizers for metal nanoparticle colloids, differences between α-, β- and γ-CD in stabilizing such colloids have not been previously reported. In this study, silver nanoparticles (AgNP) were synthesized using NaBH{sub 4} as reducing agent and cyclodextrins as stabilizers. Long-term stability of AgNP colloids in equilibrium conditions showed no marked differences between CD types. Transmission electron microscopy and quantitative image analysis revealed only marginal differences in particle sizes for CD-AgNP, although statistically significant. CD-AgNP colloids showed dispersed particles with average diameters of 7.3 ± 2.2, 6.3 ± 2.9 and 4.9 ± 1.9 nm for α-, β- and γ-CD, respectively, and with similar ζ-potentials about −25 to −30 mV. AgNP without CD showed bigger and aggregated particles of 15.0 ± 2.0 nm with lower ζ-potentials of about −40 mV. When subjected to centrifugal forces, i.e. non-equilibrium conditions, γ-CD was markedly more efficient than α- and β-CD in stabilizing the colloids. Drying patterns of colloid droplets showed a typical self-pinned coffee ring for all but the colloid stabilized by γ-CD, which showed a pattern resulting from a dominant Gibbs–Marangoni flow inside the drying droplet. Calculations using the Derjaguin, Landau, Verwey and Overbeek (DLVO) theory supported the stabilizing effect of CD in equilibrium conditions; it however did not provide clues for the superior stabilization by γ-CD in conditions of hydrodynamic stress.

  12. Highly stable layered double hydroxide colloids: a direct aqueous synthesis route from hybrid polyion complex micelles.

    Science.gov (United States)

    Layrac, Géraldine; Destarac, Mathias; Gérardin, Corine; Tichit, Didier

    2014-08-19

    Aqueous suspensions of highly stable Mg/Al layered double hydroxide (LDH) nanoparticles were obtained via a direct and fully colloidal route using asymmetric poly(acrylic acid)-b-poly(acrylamide) (PAA-b-PAM) double hydrophilic block copolymers (DHBCs) as growth and stabilizing agents. We showed that hybrid polyion complex (HPIC) micelles constituted of almost only Al(3+) were first formed when mixing solutions of Mg(2+) and Al(3+) cations and PAA3000-b-PAM10000 due to the preferential complexation of the trivalent cations. Then mineralization performed by progressive hydroxylation with NaOH transformed the simple DHBC/Al(3+) HPIC micelles into DHBC/aluminum hydroxide colloids, in which Mg(2+) ions were progressively introduced upon further hydroxylation leading to the Mg-Al LDH phase. The whole process of LDH formation occurred then within the confined environment of the aqueous complex colloids. The hydrodynamic diameter of the DHBC/LDH colloids could be controlled: it decreased from 530 nm down to 60 nm when the metal complexing ratio R (R = AA/(Mg + Al)) increased from 0.27 to 1. This was accompanied by a decrease of the average size of individual LDH particles as R increased (for example from 35 nm at R = 0.27 down to 17 nm at R = 0.33), together with a progressive favored intercalation of polyacrylate rather than chloride ions in the interlayer space of the LDH phase. The DHBC/LDH colloids have interesting properties for biomedical applications, that is, high colloidal stability as a function of time, stability in phosphate buffered saline solution, as well as the required size distribution for sterilization by filtration. Therefore, they could be used as colloidal drug delivery systems, especially for hydrosoluble negatively charged drugs.

  13. Colloidal stability and chemical reactivity of complex colloids containing Fe3+

    NARCIS (Netherlands)

    van Leeuwen, Y.M.|info:eu-repo/dai/nl/314850139; Velikov, K. P.; Kegel, W.K.|info:eu-repo/dai/nl/113729464

    2014-01-01

    The reactivity of iron contained within insoluble colloidal metal-pyrophosphate salts was determined and compared to the reactivity of a soluble iron salt (FeCl3). As a model system for the reactivity of iron in food products, the formation of an iron–polyphenol complex was followed with

  14. SYNTHESIS OF POLYMER-STABILIZED RUTHENIUM COLLOIDS BY LOW BOILING POINT ALCOHOL REDUCTION

    Institute of Scientific and Technical Information of China (English)

    Ya-li Su; Xiu-ru Li; Yue-jin Tong; Yue-sheng Li

    2003-01-01

    Stable and well-dispersed poly(N-vinyl-2-pyrrolidone) (PVP)-stabilized ruthenium colloidal clusters were prepared via the reduction of ruthenium(Ⅲ) chloride by refluxing with low boiling point alcohols. Investigation of the size of Ru colloids by transmission electron microscopy (TEM) indicated that the average diameters could be controlled in the range of 1.2-1.6 nm with relative standard deviations of less than 0.33 by changing the molar ratio of PVP to Ru. The X-ray photoelectron spectroscopy (XPS) characterization verified the formation of elemental ruthenium colloids.

  15. Evaluation of effects of pH and ionic strength on colloidal stability of IgG solutions by PEG-induced liquid-liquid phase separation

    Science.gov (United States)

    Thompson, Ronald W.; Latypov, Ramil F.; Wang, Ying; Lomakin, Aleksey; Meyer, Julie A.; Vunnum, Suresh; Benedek, George B.

    2016-11-01

    Colloidal stability of IgG antibody solutions is important for pharmaceutical and medicinal applications. Solution pH and ionic strength are two key factors that affect the colloidal stability of protein solutions. In this work, we use a method based on the PEG-induced liquid-liquid phase separation to examine the effects of pH and ionic strength on the colloidal stability of IgG solutions. We found that at high ionic strength (≥0.25M), the colloidal stability of most of our IgGs is insensitive to pH, and at low ionic strength (≤0.15M), all IgG solutions are much more stable at pH 5 than at pH 7. In addition, the PEG-induced depletion force is less efficient in causing phase separation at pH 5 than at pH 7. In contrast to the native inter-protein interaction of IgGs, the effect of depletion force on phase separation of the antibody solutions is insensitive to ionic strength. Our results suggest that the long-range electrostatic inter-protein repulsion at low ionic strength stabilizes the IgG solutions at low pH. At high ionic strength, the short-range electrostatic interactions do not make a significant contribution to the colloidal stability for most IgGs with a few exceptions. The weaker effect of depletion force at lower pH indicates a reduction of protein concentration in the condensed phase. This work advances our basic understanding of the colloidal stability of IgG solutions and also introduces a practical approach to measuring protein colloidal stability under various solution conditions.

  16. Evaluation of effects of pH and ionic strength on colloidal stability of IgG solutions by PEG-induced liquid-liquid phase separation.

    Science.gov (United States)

    Thompson, Ronald W; Latypov, Ramil F; Wang, Ying; Lomakin, Aleksey; Meyer, Julie A; Vunnum, Suresh; Benedek, George B

    2016-11-14

    Colloidal stability of IgG antibody solutions is important for pharmaceutical and medicinal applications. Solution pH and ionic strength are two key factors that affect the colloidal stability of protein solutions. In this work, we use a method based on the PEG-induced liquid-liquid phase separation to examine the effects of pH and ionic strength on the colloidal stability of IgG solutions. We found that at high ionic strength (≥0.25M), the colloidal stability of most of our IgGs is insensitive to pH, and at low ionic strength (≤0.15M), all IgG solutions are much more stable at pH 5 than at pH 7. In addition, the PEG-induced depletion force is less efficient in causing phase separation at pH 5 than at pH 7. In contrast to the native inter-protein interaction of IgGs, the effect of depletion force on phase separation of the antibody solutions is insensitive to ionic strength. Our results suggest that the long-range electrostatic inter-protein repulsion at low ionic strength stabilizes the IgG solutions at low pH. At high ionic strength, the short-range electrostatic interactions do not make a significant contribution to the colloidal stability for most IgGs with a few exceptions. The weaker effect of depletion force at lower pH indicates a reduction of protein concentration in the condensed phase. This work advances our basic understanding of the colloidal stability of IgG solutions and also introduces a practical approach to measuring protein colloidal stability under various solution conditions.

  17. Charge inversion and colloidal stability of carbon black in battery electrolyte solutions

    NARCIS (Netherlands)

    Zhang, Y.; Narayanan, A.; Mugele, F.; Cohen Stuart, M.A.; Duits, M.H.G.

    2016-01-01

    Colloids and Surfaces A: Physicochemical and Engineering Aspects is an international journal devoted to the science of the fundamentals, engineering fundamentals, and applications of colloidal and interfacial phenomena and processes. The journal aims at publishing research papers of high quality and

  18. On the effect of Ca2+ and La3+ on the colloidal stability of liposomes.

    Science.gov (United States)

    Sabín, Juan; Prieto, Gerardo; Messina, Paula V; Ruso, Juan M; Hidalgo-Alvarez, Roque; Sarmiento, Félix

    2005-11-22

    This work deals with the effect of Ca2+ and La3+ on the colloidal stability of phosphatidylcholine (PC) liposomes in aqueous media. As physical techniques, nephelometry, photon correlation spectroscopy, electrophoretic mobility, and surface tension were used. The theoretical predictions of the colloidal stability of liposomes were followed using the Derjaguin-Landau-Verwey-Overbeek theory. Changes in the size of liposomes and high polydispersity values were observed as La3+ concentration increases, suggesting that this cation induces the aggregation of liposomes. However, changes in polydispersity were not observed with Ca2+, suggesting a coalescence mechanism or fusion of liposomes. The stability factor (W), calculated from the nephelometry measurements indicated that aggregation/fusion occurs at a critical concentration (c.c.) of 0.3 and 0.7 M for La3+ and Ca2+, respectively. To gain a better insight into the interaction mechanism between the liposomes and the studied ions, the interaction between PC monolayers and Ca2+ and La3+ was studied. Changes in the surface area per lipid molecule (A0) in the monolayer at the c.c. values were found for both ions, with a more pronounced effect in the case of Ca2+. This corresponds with a larger reduction of the steric repulsive interaction between the headgroups at the phospholipid membrane (pi(head)). The experimental result validates the hypothesis made on the liposome fusion in the presence of Ca2+ and liposome aggregation in the presence of La3+. These aggregation mechanisms have also been confirmed by transmission electron microscopy.

  19. Superparamagnetic iron oxide/chitosan core/shells for hyperthermia application: Improved colloidal stability and biocompatibility

    Energy Technology Data Exchange (ETDEWEB)

    Patil, R.M.; Shete, P.B.; Thorat, N.D.; Otari, S.V. [Center for Interdisciplinary Research, D.Y. Patil University, Kolhapur 416006, MS (India); Barick, K.C.; Prasad, A.; Ningthoujam, R.S. [Chemistry Division, Bhabha Atomic Research Centre, Mumbai 400085, MS (India); Tiwale, B.M. [Center for Interdisciplinary Research, D.Y. Patil University, Kolhapur 416006, MS (India); Pawar, S.H., E-mail: pawar_s_h@yahoo.com [Center for Interdisciplinary Research, D.Y. Patil University, Kolhapur 416006, MS (India)

    2014-04-15

    Superparamagnetic magnetite nanoparticles are of great interest due to their potential biomedical applications. In the present investigation, Fe{sub 3}O{sub 4} magnetic nanoparticles were prepared by alkaline precipitation using ferrous chloride as the sole source. An amphiphilic polyelectrolyte with the property of biocompatibility and functional carboxyl groups was used as a stabilizer to prepare a well-dispersed suspension of superparamagnetic Fe{sub 3}O{sub 4} nanoparticles. The final material composed of Fe{sub 3}O{sub 4} core and chitosan (CH) shell was produced. The amino groups of CH coated on Fe{sub 3}O{sub 4} nanoparticles were further cross linked using glutaraldehyde (GLD) for stable coating. FTIR spectra, XPS and TGA confirmed the coating of CH/GLD on the surface of Fe{sub 3}O{sub 4} nanoparticles. XRD patterns indicate the pure phase Fe{sub 3}O{sub 4} with a spinel structure. The nanoparticles were superparamagnetic at room temperature with saturation magnetization values for bare and coated nanoparticles which were 51.68 emu/g and 48.60 emu/g, respectively. Zeta potential values showed higher colloidal stability of coated nanoparticles than the bare one. Cytotoxicity study up to 2 mg mL{sup −1} concentration showed no drastic change in cell viability of nanoparticles after coating. Also, coated nanoparticles showed increased SAR value, making them suitable for hyperthermia therapy application. - Highlights: • Fe{sub 3}O{sub 4} nanoparticles were synthesized from FeCl{sub 2} as the sole source by alkaline precipitation. • Coating of Fe{sub 3}O{sub 4} nanoparticles was done with chitosan by simple ultrasonication. • Chitosan cross-linked with glutaraldehyde. • High colloidal stability was observed. • Increased SAR value and least cytotoxicity were observed.

  20. The Colloidal Stabilization of Quantum Dots: Towards Manufacturable, Efficient Solution-Processed Solar Cells

    Science.gov (United States)

    Rollny, Lisa

    Understanding colloidal stabilization can influence the design of optoelectronic devices and enable improvements to their performance and stability. For photovoltaics, important characteristics of the active layer material are high conductivity along with a minimum of recombination centers. In order to capitalize on the benefits of solution-processed materials, it is important to minimize the number of processing steps: ideally, to achieve a low-cost solution, materials would be deposited using a single process step compatible with roll-to-roll manufacturing. Prior to this work, the highest-performing colloidal quantum dots (CQD) solar cells have relied on several deposition steps that are repeated in a layer-by-layer (LBL) fashion. The purpose of these process steps has been to remove the long insulating ligands used in synthesis and replace them with short ligands that allow electrical conduction. The large number of steps combined, typically implemented via spin coating, leads to inefficient materials utilization and fails to show a path to a manufacturable solution. In this work, the first CQD solar cells were designed, built, and characterized combining state-of-art performance with scalable manufacture. Firstly, I report the first automated CQD synthesis to result in CQDs that form high-performance CQD solar cells. I analyze the CQD synthesis and by separating it into two phases---nucleation and growth phase---my insights are used to create higher-quality CQDs exhibiting enhanced monodispersity. I then proceed to develop a CQD ink: a CQD solution ready for direct deposition to form a semiconducting film exhibiting low trap state density. In early trials the CQD ink showed only limited power conversion efficiencies of 2%. I designed a new ink strategy, which I term cleavable hemiketal ligands. This novel two-component ligand strategy enables the combination of colloidal stabilization (via this longer two-component ligand) and cleavability (enabling excellent

  1. Experimental and theoretical studies of the colloidal stability of nanoparticles-a general interpretation based on stability maps.

    Science.gov (United States)

    Segets, Doris; Marczak, Renata; Schäfer, Stefan; Paula, Carolin; Gnichwitz, Jan-Frederik; Hirsch, Andreas; Peukert, Wolfgang

    2011-06-28

    The current work addresses the understanding of the stabilization of nanoparticles in suspension. Specifically, we study ZnO in ethanol for which the influence of particle size and reactant ratio as well as surface coverage on colloidal stability in dependence of the purification progress was investigated. The results revealed that the well-known ζ-potential determines not only the colloidal stability but also the surface coverage of acetate groups bound to the particle surface. The acetate groups act as molecular spacers between the nanoparticles and prevent agglomeration. Next to DLVO calculations based on the theory of Derjaguin, Landau, Verwey and Overbeek using a core-shell model we find that the stability is better understood in terms of dimensionless numbers which represent attractive forces as well as electrostatic repulsion, steric effects, transport properties, and particle concentration. Evaluating the colloidal stability in dependence of time by means of UV-vis absorption measurements a stability map for ZnO is derived. From this map it becomes clear that the dimensionless steric contribution to colloidal stability scales with a stability parameter including dimensionless repulsion and attraction as well as particle concentration and diffusivity of the particles according to a power law with an exponent of -0.5. Finally, we show that our approach is valid for other stabilizing molecules like cationic dendrons and is generally applicable for a wide range of other material systems within the limitations of vanishing van der Waals forces in refractive index matched situations, vanishing ζ-potential and systems without a stabilizing shell around the particle surface.

  2. Solitary waves and their stability in colloidal media: semi-analytical solutions

    CERN Document Server

    Marchant, T R

    2012-01-01

    Spatial solitary waves in colloidal suspensions of spherical dielectric nanoparticles are considered. The interaction of the nanoparticles is modelled as a hard-sphere gas, with the Carnahan-Starling formula used for the gas compressibility. Semi-analytical solutions, for both one and two spatial dimensions, are derived using an averaged Lagrangian and suitable trial functions for the solitary waves. Power versus propagation constant curves and neutral stability curves are obtained for both cases, which illustrate that multiple solution branches occur for both the one and two dimensional geometries. For the one-dimensional case it is found that three solution branches (with a bistable regime) occur, while for the two-dimensional case two solution branches (with a single stable branch) occur in the limit of low background packing fractions. For high background packing fractions the power versus propagation constant curves are monotonic and the solitary waves stable for all parameter values. Comparisons are mad...

  3. Cobalt ferrite nanoparticles with improved aqueous colloidal stability and electrophoretic mobility

    Energy Technology Data Exchange (ETDEWEB)

    Munjal, Sandeep, E-mail: drsandeepmunjal@gmail.com; Khare, Neeraj, E-mail: nkhare@physics.iitd.ernet.in [Department of Physics, Indian Institute of Technology Delhi, Hauz Khas, New Delhi-110016 (India)

    2016-04-13

    We have synthesized CoFe{sub 2}O{sub 4} (CFO) nanoparticles of size ∼ 12.2 nm by hydrothermal synthesis method. To control the size of these CFO nanoparticles, oleic acid was used as a surfactant. The inverse spinel phase of the synthesized nanoparticles was confirmed by X-ray diffraction method. As synthesized oleic acid coated CFO (OA@CFO) nanoparticles has very less electrophoretic mobility in the water and are not water dispersible. These OA@CFO nanoparticles were successfully turned into water soluble phase with a better colloidal aqueous stability, through a chemical treatment using citric acid. The modified citric acid coated CFO (CA@CFO) nanoparticles were dispersible in water and form a stable aqueous solution with high electrophoretic mobility.

  4. Preparation of poly(N-vinylpyrrolidone-stabilized ZnO colloid nanoparticles

    Directory of Open Access Journals (Sweden)

    Tatyana Gutul

    2014-04-01

    Full Text Available We propose a method for the synthesis of a colloidal ZnO solution with poly(N-vinylpyrrolidone (PVP as stabilizer. Stable colloidal solutions with good luminescence properties are obtained by using PVP as stabilizer in the synthesis of ZnO nanoparticles by a sol–gel method assisted by ultrasound. Nanoparticles with sizes of 30–40 nm in a PVP matrix are produced as a solid product. The colloidal ZnO/PVP/methanol solution, apart from the most intense PL band at 356 nm coming from the PVP, exhibits a strong PL band at 376 nm (3.30 eV which corresponds to the emission of the free exciton recombination in ZnO nanoparticles.

  5. High Efficiency Colloidal Quantum Dot Phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Kahen, Keith

    2013-12-31

    The project showed that non-Cd containing, InP-based nanocrystals (semiconductor materials with dimensions of ~6 nm) have high potential for enabling next-generation, nanocrystal-based, on chip phosphors for solid state lighting. Typical nanocrystals fall short of the requirements for on chip phosphors due to their loss of quantum efficiency under the operating conditions of LEDs, such as, high temperature (up to 150 °C) and high optical flux (up to 200 W/cm2). The InP-based nanocrystals invented during this project maintain high quantum efficiency (>80%) in polymer-based films under these operating conditions for emission wavelengths ranging from ~530 to 620 nm. These nanocrystals also show other desirable attributes, such as, lack of blinking (a common problem with nanocrystals which limits their performance) and no increase in the emission spectral width from room to 150 °C (emitters with narrower spectral widths enable higher efficiency LEDs). Prior to these nanocrystals, no nanocrystal system (regardless of nanocrystal type) showed this collection of properties; in fact, other nanocrystal systems are typically limited to showing only one desirable trait (such as high temperature stability) but being deficient in other properties (such as high flux stability). The project showed that one can reproducibly obtain these properties by generating a novel compositional structure inside of the nanomaterials; in addition, the project formulated an initial theoretical framework linking the compositional structure to the list of high performance optical properties. Over the course of the project, the synthetic methodology for producing the novel composition was evolved to enable the synthesis of these nanomaterials at a cost approximately equal to that required for forming typical conventional nanocrystals. Given the above results, the last major remaining step prior to scale up of the nanomaterials is to limit the oxidation of these materials during the tens of

  6. Adsorption of polyelectrolytes and charged block copolymers on oxides consequences for colloidal stability

    NARCIS (Netherlands)

    Hoogeveen, N.G.

    1996-01-01


    The aim of the study described in this thesis was to examine the adsorption properties of polyelectrolytes and charged block copolymers on oxides, and the effect of these polymers on the colloidal stability of oxidic dispersions. For this purpose the interaction of some well-characterised

  7. Spontaneous oil-in-water emulsification induced by charge-stabilized dispersions of various inorganic colloids

    NARCIS (Netherlands)

    Sacanna, S.|info:eu-repo/dai/nl/311471676; Kegel, W.K.|info:eu-repo/dai/nl/113729464; Philipse, A.P.|info:eu-repo/dai/nl/073532894

    2007-01-01

    Charge-stabilized dispersions of inorganic colloids are shown to induce spontaneous emulsification of hydrophobic (TPM) molecules to stable oil-in-water emulsions, with monodisperse, mesoscopic oil droplet diameters in the range of 30-150 nm, irrespective of the polydispersity of the starting

  8. Adsorption of polyelectrolytes and charged block copolymers on oxides. Consequences for colloidal stability.

    NARCIS (Netherlands)

    Hoogeveen, N.G.

    1996-01-01

    The aim of the study described in this thesis was to examine the adsorption properties of polyelectrolytes and charged block copolymers on oxides, and the effect of these polymers on the colloidal stability of oxidic dispersions. For this purpose the interaction of some well-characterised polyelectr

  9. Pickering emulsions: Wetting and colloidal stability of hairy particles - A self-consistent field theory

    NARCIS (Netherlands)

    Salari, J.W.O.; Leermakers, F.A.M.; Klumperman, B.

    2011-01-01

    The assembly of sterically stabilized colloids at liquid–liquid interfaces is studied with the self-consistent field (SCF) theory using the discretization scheme that was developed by Scheutjens, Fleer, and co-workers. The model is based on a poly(methyl methacrylate) (pMMA) particle with poly(isobu

  10. In vitro hyperthermia with improved colloidal stability and enhanced SAR of magnetic core/shell nanostructures.

    Science.gov (United States)

    Patil, R M; Thorat, N D; Shete, P B; Otari, S V; Tiwale, B M; Pawar, S H

    2016-02-01

    Magnetic core/shell nanostructures of Fe3O4 nanoparticles coated with oleic acid and betaine-HCl were studied for their possible use in magnetic fluid hyperthermia (MFH). Their colloidal stability and heat induction ability were studied in different media viz. phosphate buffer solution (PBS), saline solution and glucose solution with different physiological conditions and in human serum. The results showed enhanced colloidal stability in these media owing to their high zeta potential values. Heat induction studies showed that specific absorption rates (SAR) of core/shells were 82-94W/g at different pH of PBS and concentrations of NaCl and glucose. Interestingly, core/shells showed 78.45±3.90W/g SAR in human serum. The cytotoxicity of core/shells done on L929 and HeLa cell lines using 3-(4,5-dimethylthiazol-2-yl)2,5-diphenyl tetrazolium bromide and trypan blue dye exclusion assays showed >89% and >80% cell viability for 24 and 48h respectively. Core/shell structures were also found to be very efficient for in vitro MFH on cancer cell line. About 95% cell death was occurred in 90min after hyperthermia treatment. The mechanism of cell death was found to be elevated ROS generation in cells after exposure to core/shells in external magnetic field. This study showed that these core/shells have a great potential to be used in in vivo MFH. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Colloidal stability of tannins: astringency, wine tasting and beyond

    Science.gov (United States)

    Zanchi, D.; Poulain, C.; Konarev, P.; Tribet, C.; Svergun, D. I.

    2008-12-01

    Tannin-tannin and tannin-protein interactions in water-ethanol solvent mixtures are studied in the context of red wine tasting. While tannin self-aggregation is relevant for the visual aspect of wine tasting (limpidity and related colloidal phenomena), tannin affinities for salivary proline-rich proteins is fundamental for a wide spectrum of organoleptic properties related to astringency. Tannin-tannin interactions are analyzed in water-ethanol wine-like solvents and the precipitation map is constructed for a typical grape tannin. The interaction between tannins and human salivary proline-rich proteins (PRP) are investigated in the framework of the shell model for micellization, known for describing tannin-induced aggregation of β-casein. Tannin-assisted micellization and compaction of proteins observed by SAXS are described quantitatively and discussed in the case of astringency.

  12. Colloidal stability of tannins: astringency, wine tasting and beyond

    Energy Technology Data Exchange (ETDEWEB)

    Zanchi, D; Poulain, C [Laboratoire de Physique Theorique et Hautes Energies, 4 Place Jussieu, BP 126, F-75252 Paris Cedex 05 (France); Konarev, P; Svergun, D I [European Molecular Biology Laboratory, Hamburg Outstation, Notkestrasse 85, D-22603 Hamburg (Germany); Tribet, C [Physico-Chimie des Polymeres et Milieux Disperses, CNRS UMR 7615, ESPCI, 10 rue Vauquelin, F-75231 Paris Cedex 05 (France)], E-mail: drazen@lpthe.jussieu.fr

    2008-12-10

    Tannin-tannin and tannin-protein interactions in water-ethanol solvent mixtures are studied in the context of red wine tasting. While tannin self-aggregation is relevant for the visual aspect of wine tasting (limpidity and related colloidal phenomena), tannin affinities for salivary proline-rich proteins is fundamental for a wide spectrum of organoleptic properties related to astringency. Tannin-tannin interactions are analyzed in water-ethanol wine-like solvents and the precipitation map is constructed for a typical grape tannin. The interaction between tannins and human salivary proline-rich proteins (PRP) are investigated in the framework of the shell model for micellization, known for describing tannin-induced aggregation of {beta}-casein. Tannin-assisted micellization and compaction of proteins observed by SAXS are described quantitatively and discussed in the case of astringency.

  13. PREPARATION OF POLYMER MICROSPHERES WITH PYRIDYL GROUP AND THEIR STABILIZED GOLD METALLIC COLLOIDS

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Narrow disperse poly(ethyleneglycol dimethacrylate-co-4-vinylpyridine) (poly(EGDMA-co-4-VPy)) microspheres were prepared by distillation-precipitation copolymerization of ethyleneglycol dimethacrylate (EGDMA) and 4-vinylpyridine (4-VPy) with 2,2'-azobisisobutyronitrile (AIBN) as initiator in neat acetonitrile. The polymer microspheres containing pyridyl group were then utilized as stabilizer for gold metallic colloids with the diameter around 7 nm, which were prepared by the in situ reduction of gold chloride trihydrate with sodium borohydride through the coordination of the pyridyl group on the gel layer and surface of the microsphere with the gold metallic nano-particles. The catalytic properties of the pyridyl-functionalized microsphere-stabilized gold metallic colloids and the behavior of the stabilized-catalyst for the recycling were investigated with reduction of 4-nitrophenol to 4-aminophenol as a model reaction.

  14. UV and visible light active aqueous titanium dioxide colloids stabilized by surfactants.

    Science.gov (United States)

    Pacia, Michał; Warszyński, Piotr; Macyk, Wojciech

    2014-09-07

    Attempts to increase the stability of photocatalytically active nanodispersions of titanium dioxide over a wide range of pH (3-10) were undertaken. Polyethylene glycols (PEGs) with different molecular weights and polyoxyethylenesorbitan monooleate (Tween® 80) were tested as stabilizing agents of TiO2 nanoparticles. The results of DLS measurements proved the stabilizing effect of Tween® 80 while the systems involving PEGs, independently of the polymer concentration, showed a tendency to form aggregates in neutral solutions. The colloids stabilized with Tween® 80 were photosensitized with 2,3-naphthalenediol (nd) or 2-hydroxy-3-naphthoic acid (hn) or catechol (cat). The photocatalytic activity of such colloids has been assessed in an azure B degradation reaction using both UV and visible light. The nd@TiO2 + Tween colloid appeared particularly photoactive upon visible light irradiation. Moreover, the comparison of activities of nd@TiO2 + Tween and TiO2 + Tween revealed a significantly better performance of the former nanodispersion, independently of the irradiation conditions (UV or visible light). This effect has been explained by different structures of micelles formed in the case of TiO2 and nd@TiO2 stabilized with Tween® 80.

  15. Colloidal stability of iron oxide nanocrystals coated with a PEG-based tetra-catechol surfactant

    Science.gov (United States)

    Mondini, Sara; Drago, Carmelo; Ferretti, Anna M.; Puglisi, Alessandra; Ponti, Alessandro

    2013-03-01

    Long-term colloidal stability of magnetic iron oxide nanoparticles (NPs) is an important goal that has not yet been fully achieved. To make an advance in our understanding of the colloidal stability of iron oxide NPs in aqueous media, we prepared NPs comprising a monodisperse (13 nm) iron oxide core coated with a PEG-based (PEG: polyethyleneglycol) surfactant. This consists of a methoxy-terminated PEG chain (MW = 5000 Da) bearing four catechol groups via a diethylenetriamine linker. The surfactant was grafted onto the nanocrystals by ligand exchange monitored by infrared spectroscopy. The colloidal stability of these nanoparticles was probed by monitoring the time evolution of the Z-average intensity-weighted radius Rh and volume-weighted size distribution Pv obtained from analysis of dynamic light scattering data. The nanoparticles showed no sign of aggregation for four months in deionized water at room temperature and also when subjected to thermal cycling between 25 and 75 °C. In 0.01 M PBS (phosphate buffered saline), aggregation (if any) is slow and partial; after 66 h, about 50% of NPs have not aggregated. Aggregation is more effective in 0.15 M NH4AcO buffer, where isolated particles are not observed after 66 h, and especially in acidic NH4AcO/AcOH buffer, where aggregation is complete within 1 h and precipitation is observed. The differing stability of the NPs in the above aqueous media is closely related to their ζ potential.

  16. Quantitative characterization of the colloidal stability of metallic nanoparticles using UV-vis absorbance spectroscopy.

    Science.gov (United States)

    Ray, Tyler R; Lettiere, Bethany; de Rutte, Joseph; Pennathur, Sumita

    2015-03-31

    Plasmonic nanoparticles are used in a wide variety of applications over a broad array of fields including medicine, energy, and environmental chemistry. The continued successful development of this material class requires the accurate characterization of nanoparticle stability for a variety of solution-based conditions. Although many characterization methods exists, there is an absence of a unified, quantitative means for assessing the colloidal stability of plasmonic nanoparticles. We present the particle instability parameter (PIP) as a robust, quantitative, and generalizable characterization technique based on UV-vis absorbance spectroscopy to characterize colloidal instability. We validate PIP performance with both traditional and alternative characterization methods by measuring gold nanorod instability in response to different salt (NaCl) concentrations. We further measure gold nanorod stability as a function of solution pH, salt, and buffer (type and concentration), nanoparticle concentration, and concentration of free surfactant. Finally, these results are contextualized within the literature on gold nanorod stability to establish a standardized methodology for colloidal instability assessment.

  17. Colloidal stability influenced by inhomogeneous surfactant assemblies in confined spaces

    NARCIS (Netherlands)

    Jodar-Reyes, A.B.; Leermakers, F.A.M.

    2009-01-01

    Recently, a molecular-level self-consistent field approach was used to show that some surfactants assemblies (with local cylindrical structure) can bridge between two surfaces that in turn are covered by surfactant bilayers. The stability of such a connection is related to a higher end-cap (free) en

  18. Copolymer adsorption and the effect on colloidal stability.

    NARCIS (Netherlands)

    Bijsterbosch, H.D.

    1998-01-01

    The main aim of the work described in this thesis is to study the effect of different types of copolymers on the stability of aqueous oxide dispersions. Such dispersions are a major component in water-borne paints. In order to obtain a better insight in steric stabilisation we first investigated the

  19. Algorithm-driven high-throughput screening of colloidal nanoparticles under simulated physiological and therapeutic conditions.

    Science.gov (United States)

    Bhirde, Ashwinkumar A; Sindiri, Sivasish; Calco, Gina N; Aronova, Maria A; Beaucage, Serge L

    2017-02-09

    Colloidal nanoparticles have shown tremendous potential as cancer drug carriers and as phototherapeutics. However, the stability of nanoparticles under physiological and phototherapeutic conditions is a daunting issue, which needs to be addressed in order to ensure a successful clinical translation. The design, development and implementation of unique algorithms are described herein for high-throughput hydrodynamic size measurements of colloidal nanoparticles. The data obtained from such measurements provide clinically-relevant particle size distribution assessments that are directly related to the stability and aggregation profiles of the nanoparticles under putative physiological and phototherapeutic conditions; those profiles are not only dependent on the size and surface coating of the nanoparticles, but also on their composition. Uncoated nanoparticles showed varying degrees of association with bovine serum albumin, whereas PEGylated nanoparticles did not exhibit significant association with the protein. The algorithm-driven, high-throughput size screening method described in this report provides highly meaningful size measurement patterns stemming from the association of colloidal particles with bovine serum albumin used as a protein model. Noteworthy is that this algorithm-based high-throughput method can accomplish sophisticated hydrodynamic size measurement protocols within days instead of years it would take conventional hydrodynamic size measurement techniques to achieve a similar task.

  20. Interactions between laponite and microbial biofilms in porous media: implications for colloid transport and biofilm stability.

    Science.gov (United States)

    Leon-Morales, C Felipe; Leis, Andrew P; Strathmann, Martin; Flemming, Hans-Curt

    2004-09-01

    Quartz sand columns and sand-filled microscope flow cells were used to investigate the transport characteristics of the clay colloid laponite, and a biofilm-forming bacterium, Pseudomonas aeruginosa SG81. Separate experiments were performed with each particle to determine their individual transport characteristics in clean sand columns. In a second set of experiments, bacterial biofilms were formed prior to introduction of the clay colloids. In the independent transport experiments, bacteria and laponite each conformed to known physicochemical principles. A sodium chloride concentration of 7 x 10(-2) M caused complete retention of the laponite within the sand columns. P. aeruginosa SG81 was generally less influenced by ionic strength effects; it showed relatively low mobility at all ionic strengths tested and some (albeit reduced) mobility when introduced to the columns in 1M NaCl, the highest concentration tested, but nevertheless showed reproducible trends. Under conditions favourable to laponite retention and biofilm stability (7 x 10(-2) MNaCl), laponite suspensions were able to remobilise a portion of the attached bacterial biomass. At low ionic strength, the profile of laponite elution was also altered in the presence of a P. aeruginosa biofilm. These observations suggest that while a reduction in ionic strength has a dominant influence on the mobilisation of biological and inorganic colloids, the presence of laponite and biomass can have a distinct influence on the mobility of both types of colloids. Since these events are likely to occur in subsurface environments, our results suggest that colloid-biofilm interactions will have implications for colloid-bound contaminant transport and the remobilisation of pathogens.

  1. The study of the antimicrobial activity of colloidal solutions of silver nanoparticles prepared using food stabilizers.

    Science.gov (United States)

    Balandin, G V; Suvorov, O A; Shaburova, L N; Podkopaev, D O; Frolova, Yu V; Ermolaeva, G A

    2015-06-01

    The bactericidal effect of colloidal solutions of silver nanoparticles based on food stabilizers, gum arabic and chitosan, against bacterial cultures of microorganisms in food production is described. The antibacterial activity of nanotechnology products containing different amounts of stabilizing additives when applied to solid pH-neutral substrates is studied. For its evaluation a method making it possible to take into account the capability of nanoparticles to diffuse in solid media was applied. Minimal inhibitory concentrations of nanoparticles used against Erwinia herbicola, Pseudomonas fluorescens, Bacillus subtilis, Sarcina flava were found. A suggestion was made concerning the influence of the spatial structure of bacteria on the antibacterial activity of colloidal solutions of silver nanoparticles. The data concerning the antibacterial activity and minimal inhibiting concentrations of nanoparticles may be used for development of products suppressing activity of microorganisms hazardous for food production.

  2. Phase equilibria in stratified thin liquid films stabilized by colloidal particles

    OpenAIRE

    Blawzdziewicz, J.; Wajnryb, E.

    2005-01-01

    Phase equilibria between regions of different thickness in thin liquid films stabilized by colloidal particles are investigated using a quasi-two-dimensional thermodynamic formalism. Appropriate equilibrium conditions for the film tension, normal pressure, and chemical potential of the particles in the film are formulated, and it is shown that the relaxation of these parameters occurs consecutively on three distinct time scales. Film stratification is described quantitatively for a hard-spher...

  3. SYNTHESIS OF POLYMER-STABILIZED PLATINUM/RUTHENIUM BIMETALLIC COLLOIDS AND THEIR CATALYTIC PROPERTIES FOR SELECTIVE HYDROGENATION OF CROTONALDEHYDE

    Institute of Scientific and Technical Information of China (English)

    Wei-xia Tu; Han-fan Liu

    2005-01-01

    Polymer-stabilized platinum/ruthenium bimetallic colloids (Pt/Ru) were synthesized by polyol reduction with microwave irradiation and characterized by TEM and XPS. The colloidal nanoparticles have small and narrow size distributions. Catalytic performance of the Pt/Ru colloidal catalysts was investigated on the selective hydrogenation of crontonaldehyde (CRAL). A suitable amount of the added metal ions and base can improve the selectivity of CRAL to crotylalcohol (CROL) remarkably. The catalytic activity and the selectivity are dependent on the compositions of bimetallic colloids. Thereinto, PVP-stabilized 9Pt/1Ru colloid with a molar ratio of metals Pt:Ru = 9:1 shows the highest catalytic selectivity 77.3% to CROL at 333 K under 4.0 MPa of hydrogen.

  4. Electrophoresis in charge-stabilized colloidal cluster phases.

    Science.gov (United States)

    Groenewold, Jan; Zhang, Tianhui; Kegel, Willem K

    2011-06-09

    The reversible properties of cluster phases have been described by theories that invoke Coulomb interactions as a stabilizing mechanism. What is lacking so far is direct measurement of these charges. This contribution aims at predicting what to expect if electrophoresis measurements were to be performed on these systems. As a result, we get a picture that exhibits several interesting features: (1) The existence of monomers and clusters lead to distinctly different mobilities (zeta potentials) in a single sample. (2) Strong dependence of the mobilities on particle volume fraction. It is our aim that the theory outlined in this paper may serve as a guideline to interpret the expectedly "messy" electrophoretic measurements.

  5. Effect of Grape Seed Proanthocyanidin-Gelatin Colloidal Complexes on Stability and in Vitro Digestion of Fish Oil Emulsions.

    Science.gov (United States)

    Su, Yu-Ru; Tsai, Yi-Chin; Hsu, Chun-Hua; Chao, An-Chong; Lin, Cheng-Wei; Tsai, Min-Lang; Mi, Fwu-Long

    2015-11-25

    The colloidal complexes composed of grape seed proanthocyanidin (GSP) and gelatin (GLT), as natural antioxidants to improve stability and inhibit lipid oxidation in menhaden fish oil emulsions, were evaluated. The interactions between GSP and GLT, and the chemical structures of GSP/GLT self-assembled colloidal complexes, were characterized by isothermal titration calorimetry (ITC), circular dichroism (CD), and Fourier transform infrared spectroscopic (FTIR) studies. Fish oil was emulsified with GLT to obtain an oil-in-water (o/w) emulsion. After formation of the emulsion, GLT was fixed by GSP to obtain the GSP/GLT colloidal complexes stabilized fish oil emulsion. Menhaden oil emulsified by GSP/GLT(0.4 wt %) colloidal complexes yielded an emulsion with smaller particles and higher emulsion stability as compared to its GLT emulsified counterpart. The GSP/GLT colloidal complexes inhibited the lipid oxidation in fish oil emulsions more effectively than free GLT because the emulsified fish oil was surrounded by the antioxidant GSP/GLT colloidal complexes. The digestion rate of the fish oil emulsified with the GSP/GLT colloidal complexes was reduced as compared to that emulsified with free GLT. The extent of free fatty acids released from the GSP/GLT complexes stabilized fish oil emulsions was 63.3% under simulated digestion condition, indicating that the fish oil emulsion was considerably hydrolyzed with lipase.

  6. Effect of Extracellular Polymeric Substances on CuO Nanoparticle Dissolution and Colloidal Stability

    Science.gov (United States)

    Adeleye, A. S.; Keller, A. A.

    2013-12-01

    Extracellular polymeric substances (EPS) are high molecular weight polymers produced by microorganisms growing in natural as well as artificial environments. EPS may interact with engineered nanomaterials (ENMs) in aquatic systems via electrostatic and/or hydrophobic associations, therefore, influencing the fate and transport of ENMs. In this study the effect of soluble EPS isolated from Isochrysis galbana, a marine phytoplankton, on the dissolution kinetics and colloidal stability of CuO nanoparticles was investigated. EPS was characterized by measuring hydrodynamic diameter, total organic carbon, carbohydrate, and protein concentrations. CuO nanoparticles were more stable in the presence of EPS in aqueous media as indicated by hydrodynamic size and average count rate measurements. The effect of pH and ionic strength on dissolution was also studied. [Cu2+] and [Cu]total detected after a week were 5.70 mg L-1 and 7.08 mg L-1 respectively when 10 mg L-1 CuO nanoparticles was kept in 10 mM NaCl at pH 4. In the presence of 5 mg-C EPS L-1, [Cu2+] and [Cu]total were slightly lower at 5.0 mg L-1 and 5.53 mg L-1 respectively. Although observed [Cu2+] and [Cu]total were significantly lower at neutral and alkaline pH conditions, a similar pattern was observed.

  7. Investigation on the Stability of Aluminosilicate Colloids by Various Analytical Tools

    Energy Technology Data Exchange (ETDEWEB)

    Putri, Kirana Y.; Lee, D. H.; Yun, J. I. [Korea Advanced Institute of Science and Technology, Daejeon (Korea, Republic of)

    2010-05-15

    Colloids are ubiquitous in natural aquatic systems. Aquatic colloids may play a significant carrier role for radionuclide migration in aquifer systems. Being omnipresent in natural aquatic systems, aluminosilicate colloids are considered as a kernel for various aquatic colloids. Characterization of aluminosilicate colloids formed under various geochemical conditions is of importance to understand their chemical behavior in natural aquatic systems. In this work, a preliminary study on the formation of aluminosilicate colloids with a help of colorimetry and other colloid detection techniques is presented

  8. Stabilization through precipitation in a system of colloidal iron(III) pyrophosphate salts.

    Science.gov (United States)

    van Leeuwen, Y Mikal; Velikov, Krassimir P; Kegel, Willem K

    2012-09-01

    The ionic strength of a solution decreases during the precipitation of an insoluble salt, which can cause an initially unstable colloidal system to stabilize during its formation. We show this effect in the precipitation and aging of colloidal iron(III) pyrophosphate, where we observe two distinct stages in the aggregation process. The first stage is the formation of nanoparticles that immediately aggregate into clusters with sizes on the order of 200 nm. In the second stage these clusters slowly grow in size but remain in dispersion for days, even months for dialyzed systems. Eventually these clusters become macroscopically large and sediment out of dispersion. Noting the clear instability of the nanoparticles, it is interesting to find two stages in their aggregation even without the use of additives such as surface active molecules. This is explained by accounting for the rapid decrease of ionic strength during precipitation, rendering the nanoparticles relatively stable when precipitation is complete. Calculating the interaction potentials for this scenario we find good agreement with the experimental observations. These results indicate that coupling of ionic strength to aggregation state can be significant and should be taken into account when considering colloidal stability of insoluble salts.

  9. Colloidal processing of Fe-based metal ceramic composites with high content of ceramic reinforcement

    Energy Technology Data Exchange (ETDEWEB)

    Escribano, J. A.; Ferrari, B.; Alvaredo, P.; Gordo, E.; Sanchez-Herencia, A. J.

    2013-07-01

    Major difficulties of processing metal-matrix composites by means of conventional powder metallurgy techniques are the lack of dispersion of the phases within the final microstructure. In this work, processing through colloidal techniques of the Fe-based metal-matrix composites, with a high content of a ceramic reinforcement (Ti(C,N) ), is presented for the first time in the literature. The colloidal approach allows a higher control of the powders packing and a better homogenization of phases since powders are mixed in a liquid medium. The chemical stability of Fe in aqueous medium determines the dispersion conditions of the mixture. The Fe slurries were formulated by optimising their zeta potential and their rheology, in order to shape bulk pieces by slip-casting. Preliminary results demonstrate the viability of this procedure, also opening new paths to the microstructural design of fully sintered Fe-based hard metal, with 50 vol. % of Ti(C,N) in its composition. (Author)

  10. PEG-stabilized core-shell nanoparticles: impact of linear versus dendritic polymer shell architecture on colloidal properties and the reversibility of temperature-induced aggregation.

    Science.gov (United States)

    Gillich, Torben; Acikgöz, Canet; Isa, Lucio; Schlüter, A Dieter; Spencer, Nicholas D; Textor, Marcus

    2013-01-22

    Superparamagnetic iron oxide nanoparticles (SPIONs) have been widely used experimentally and also clinically tested in diverse areas of biology and medicine. Applications include magnetic resonance imaging, cell sorting, drug delivery, and hyperthermia. Physicochemical surface properties are particularly relevant in the context of achieving high colloidal nanoparticle (NP) stability and preventing agglomeration (particularly challenging in biological fluids), increasing blood circulation time, and possibly targeting specific cells or tissues through the presentation of bioligands. Traditionally, NP surfaces are sterically stabilized with hydrophilic polymeric matrices, such as dextran or linear poly(ethylene glycol) brushes. While dendrimers have found applications as drug carriers, dispersants with dendritic ("dendrons") or hyperbranched structures have been comparatively neglected despite their unique properties, such as a precisely defined molecular structure and the ability to present biofunctionalities at high density at the NP periphery. This work covers the synthesis of SPIONs and their stabilization based on poly(ethylene glycol) (PEG) and oligo(ethylene glycol) (OEG) chemistry and compares the physicochemical properties of NPs stabilized with linear and dendritic macromolecules of comparable molecular weight. The results highlight the impact of the polymeric interface architecture on solubility, colloidal stability, hydrodynamic radius, and thermoresponsive behavior. Dendron-stabilized NPs were found to provide excellent colloidal stability, despite a smaller hydrodynamic radius and lower degree of soft shell hydration compared to linear PEG analogues. Moreover, for the same grafting density and molecular weight of the stabilizers, OEG dendron-stabilized NPs show a reversible temperature-induced aggregation behavior, in contrast to the essentially irreversible aggregation and sedimentation observed for the linear PEG analogues. This new class of

  11. Stability of colloidal silver nanoparticles trapped in lipid bilayer: effect of lecithin concentration and applied temperature.

    Science.gov (United States)

    Barani, Hossein; Montazer, Majid; Braun, Hans-Georg; Dutschk, Victoria

    2014-12-01

    The use of silver nanoparticle on various substrates has been widespread because of its good antibacterial properties that directly depend on the stability of the silver nanoparticles in a colloidal suspension. In this study, the colloidal solutions of the silver nanoparticles were synthesised by a simple and safe method by using lecithin as a stabilising agent and their stability was examined at various temperatures. The effect of the lecithin concentrations on the stability of the synthesised silver nanoparticles was examined from 25 to 80°C at 5°C intervals, by recording the changes in the UV-vis absorption spectra, the hydrodynamic diameter and the light scattering intensity of the silver nanoparticles. In addition, the morphology of the synthesised silver nanoparticles was investigated with the low-voltage scanning electron microscopy and transmission electron microscopy. The results indicated that increasing temperature caused different changes in the size of the stabilised and the unstabilised silver nanoparticles. The size of the stabilised silver nanoparticles reduced from 38 to 36 nm during increasing temperature, which confirmed good stability.

  12. Highly Elastic and Self-Healing Composite Colloidal Gels.

    Science.gov (United States)

    Diba, Mani; Wang, Huanan; Kodger, Thomas E; Parsa, Shima; Leeuwenburgh, Sander C G

    2017-03-01

    Composite colloidal gels are formed by the pH-induced electrostatic assembly of silica and gelatin nanoparticles. These injectable and moldable colloidal gels are able to withstand substantial compressive and tensile loads, and exhibit a remarkable self-healing efficiency. This study provides new, critical insight into the structural and mechanical properties of composite colloidal gels and opens up new avenues for practical application of colloidal gels.

  13. Amphiphilic comblike polymers enhance the colloidal stability of Fe(3)O(4) nanoparticles.

    Science.gov (United States)

    Kim, Myeongjin; Jung, Jaeyeon; Lee, Jonghwan; Na, Kyunga; Park, Subeom; Hyun, Jinho

    2010-03-01

    Stable colloidal dispersions of magnetite (Fe(3)O(4)) nanoparticles (MNPs) were obtained with the inclusion of an amphiphilic comblike polyethylene glycol derivative (CL-PEG) as an amphiphilic polymeric surfactant. Both the size and morphology of the resulting CL-PEG-modified MNPs could be controlled and were characterized by transmission electron microscopy (TEM). The interaction between MNPs and CL-PEG was confirmed by the presence of characteristic infrared absorption peaks, and the colloidal stability of the nanoparticle dispersion in water was evaluated by long-term observation of the dispersion using UV-visible spectroscopy. SQUID measurements confirmed the magnetization of CL-PEG-modified MNPs. The zeta potential of the CL-PEG-modified MNPs showed a dramatic conversion from positive to negative in response to the pH of the surrounding aqueous medium due to the presence of carboxyl groups at the surface. These carboxyl groups can be used to functionalize the MNPs with biomolecules for biotechnological applications. However, regardless of surface electrostatics, the flexible, hydrophilic side chains of CL-PEG-modified MNPs prevented the approach of adjacent nanoparticles, thereby resisting aggregation and resulting in a stable aqueous colloid. The cytotoxicity of MNPs and CL-PEG-modified MNPs was evaluated by a MTT assay.

  14. Effect of electrolytes on colloidal stability and swelling of hydroxypropyl cellulose microgels

    Science.gov (United States)

    Mithra, K.; Khandai, Santripti; Jena, Sidhartha S.

    2016-05-01

    Hydroxypropyl Cellulose (HPC) microgels were prepared by emulsion polymerization method. The volume phase transition temperature (VPTT) and swelling properties were investigated using Dynamic Light Scattering (DLS). The VPTT for the HPC microgels was found to be˜44°C. Microgel particles swelled˜'3' times of their original size on decreasing temperature from 50°C to 25 °C. In addition we have also studied the effect of salts, sodium nitrate and sodium bromide in the Hofmeister series on deswelling and colloidal stability of HPC microgels using DLS and turbidity measurements respectively. M icrogel particles swelled in presence of NaN03 when its concentration was increased from 10-4 to 0.5 M and deswelled beyond it. As oppose to this, swelling of microgels in presence of NaBr was seen only upto 10-3 M and beyond which deswelling of microgels was observed. The results obtained are consistent with Hofmeister series of anions. Turbidity results showed that the colloidal stability of HPC microgel dispersion was dependent on ionic strength and type of added salt. For both salts, stability of microgels was found to decrease with rise in salt concentration.

  15. Influence of the initial state of carbon nanotubes on their colloidal stability under natural conditions

    Energy Technology Data Exchange (ETDEWEB)

    Schwyzer, Irene [Empa - Swiss Federal Laboratories for Materials Science and Technology, CH-9014 St. Gallen (Switzerland); Eawag - Swiss Federal Institute of Aquatic Science and Technology, CH-8600 Duebendorf (Switzerland); Kaegi, Ralf; Sigg, Laura [Eawag - Swiss Federal Institute of Aquatic Science and Technology, CH-8600 Duebendorf (Switzerland); Magrez, Arnaud [EPFL - Ecole Polytechnique Federale de Lausanne, CH-1015 Lausanne (Switzerland); Nowack, Bernd, E-mail: nowack@empa.ch [Empa - Swiss Federal Laboratories for Materials Science and Technology, CH-9014 St. Gallen (Switzerland)

    2011-06-15

    The colloidal stability of dry and suspended carbon nanotubes (CNTs) in the presence of amphiphilic compounds (i.e. natural organic matter or surfactants) at environmentally realistic concentrations was investigated over several days. The suspensions were analyzed for CNT concentration (UV-vis spectroscopy), particle size (nanoparticle tracking analysis), and CNT length and dispersion quality (TEM). When added in dry form, around 1% of the added CNTs remained suspended. Pre-dispersion in organic solvent or anionic detergent stabilized up to 65% of the added CNTs after 20 days of mild shaking and 5 days of settling. The initial state of the CNTs (dry vs. suspended) and the medium composition hence are critical determinants for the partitioning of CNTs between sediment and the water column. TEM analysis revealed that single suspended CNTs were present in all suspensions and that shaking and settling resulted in a fractionation of the CNTs with shorter CNTs remaining predominantly in suspension. - Highlights: > Individually suspended CNTs are present under environment relevant conditions. > The number of suspended CNTs varies depending on the medium composition. > Surfactants at environmental concentrations have no suspending effect on dry CNTs. > Pre-dispersed CNTs are more stable in suspension than dry CNTs. - The colloidal stability of CNTs varies a lot depending on the initial state of the CNTs (dry vs. pre-dispersed), the applied dispersant for pre-suspension, and the composition of the medium.

  16. Colloidal particles as liquid dispersion stabilizer: Pickering emulsions and materials thereof

    Science.gov (United States)

    Schmitt, Véronique; Destribats, Mathieu; Backov, Rénal

    2014-10-01

    Solid stabilized emulsions, also referred to as Pickering emulsions, are very diverse owing to the large variety of available colloidal particles from naturally occurring to synthesized ones, from hard to very deformable ones and from spheres to more complex shaped particles. Here we illustrate this variety and, despite this huge diversity, we aim at highlighting the common features. We discuss next the remaining open questions that, in our point of view, should sustain special efforts in the future and we illustrate elaboration of original materials based on Pickering emulsions. xml:lang="fr"

  17. CATALYTIC PROPERTIES OF POLYMER-STABILIZED COLLOIDAL METAL NANOPARTICLES SYNTHESIZED BY MICROWAVE IRRADIATION

    Institute of Scientific and Technical Information of China (English)

    Wei-xia Tu; Bao-lin He; Han-fan Liu; Xue-lan Luo; Xun Liang

    2005-01-01

    Catalytic properties of polymer-stabilized colloidal metal nanoparticles synthesized by microwave irradiation were studied in the selective hydrogenation of unsaturated aldehydes, o-chloronitrobenzene and the hydrogenation of alkenes. The results show that nanosized metal particles synthesized by microwave irradiation have similar catalytic performance in selective hydrogenation of unsaturated aldehydes, better selectivity to o-chloroaniline in hydrogenation of o-chloronitrobenzene and higher catalytic activities in hydrogenation of alkenes, compared with metal clusters prepared by conventional heating. The same apparent activation energy (Ea = 29 kJ mol-1) for hydrogenation of 1-heptene catalyzed with platinum nanoparticles prepared by both heating modes implied that the reaction followed the same mechanism.

  18. Stable colloids in molten inorganic salts.

    Science.gov (United States)

    Zhang, Hao; Dasbiswas, Kinjal; Ludwig, Nicholas B; Han, Gang; Lee, Byeongdu; Vaikuntanathan, Suri; Talapin, Dmitri V

    2017-02-15

    A colloidal solution is a homogeneous dispersion of particles or droplets of one phase (solute) in a second, typically liquid, phase (solvent). Colloids are ubiquitous in biological, chemical and technological processes, homogenizing highly dissimilar constituents. To stabilize a colloidal system against coalescence and aggregation, the surface of each solute particle is engineered to impose repulsive forces strong enough to overpower van der Waals attraction and keep the particles separated from each other. Electrostatic stabilization of charged solutes works well in solvents with high dielectric constants, such as water (dielectric constant of 80). In contrast, colloidal stabilization in solvents with low polarity, such as hexane (dielectric constant of about 2), can be achieved by decorating the surface of each particle of the solute with molecules (surfactants) containing flexible, brush-like chains. Here we report a class of colloidal systems in which solute particles (including metals, semiconductors and magnetic materials) form stable colloids in various molten inorganic salts. The stability of such colloids cannot be explained by traditional electrostatic and steric mechanisms. Screening of many solute-solvent combinations shows that colloidal stability can be traced to the strength of chemical bonding at the solute-solvent interface. Theoretical analysis and molecular dynamics modelling suggest that a layer of surface-bound solvent ions produces long-ranged charge-density oscillations in the molten salt around solute particles, preventing their aggregation. Colloids composed of inorganic particles in inorganic melts offer opportunities for introducing colloidal techniques to solid-state science and engineering applications.

  19. Stable colloids in molten inorganic salts

    Science.gov (United States)

    Zhang, Hao; Dasbiswas, Kinjal; Ludwig, Nicholas B.; Han, Gang; Lee, Byeongdu; Vaikuntanathan, Suri; Talapin, Dmitri V.

    2017-02-01

    A colloidal solution is a homogeneous dispersion of particles or droplets of one phase (solute) in a second, typically liquid, phase (solvent). Colloids are ubiquitous in biological, chemical and technological processes, homogenizing highly dissimilar constituents. To stabilize a colloidal system against coalescence and aggregation, the surface of each solute particle is engineered to impose repulsive forces strong enough to overpower van der Waals attraction and keep the particles separated from each other. Electrostatic stabilization of charged solutes works well in solvents with high dielectric constants, such as water (dielectric constant of 80). In contrast, colloidal stabilization in solvents with low polarity, such as hexane (dielectric constant of about 2), can be achieved by decorating the surface of each particle of the solute with molecules (surfactants) containing flexible, brush-like chains. Here we report a class of colloidal systems in which solute particles (including metals, semiconductors and magnetic materials) form stable colloids in various molten inorganic salts. The stability of such colloids cannot be explained by traditional electrostatic and steric mechanisms. Screening of many solute–solvent combinations shows that colloidal stability can be traced to the strength of chemical bonding at the solute–solvent interface. Theoretical analysis and molecular dynamics modelling suggest that a layer of surface-bound solvent ions produces long-ranged charge-density oscillations in the molten salt around solute particles, preventing their aggregation. Colloids composed of inorganic particles in inorganic melts offer opportunities for introducing colloidal techniques to solid-state science and engineering applications.

  20. Studies on the antimicrobial properties of colloidal silver nanoparticles stabilized by bovine serum albumin.

    Science.gov (United States)

    Mathew, Thomas V; Kuriakose, Sunny

    2013-01-01

    Colloidal silver nanoparticles were synthesised using sol-gel method and these nanoparticles were stabilised by encapsulated into the scaffolds of bovine serum albumin. Silver nanoparticles and encapsulated products were characterised by FTIR, NMR, XRD, TG, SEM and TEM analyses. Silver nanoparticle encapsulated bovine serum albumin showed highly potent antibacterial activity towards the bacterial strains such as Staphylococcus aureus, Serratia marcescens, Pseudomonas aeruginosa, Escherichia coli and Klebsiella pneumoniae.

  1. Depletion induced encapsulation by dumbbell-shaped patchy colloids stabilize microspheres against aggregation.

    Science.gov (United States)

    Wolters, Joost Robert; Verweij, Joanne E; Avvisati, Guido; Dijkstra, Marjolein; Kegel, Willem K

    2017-03-08

    In this paper, we demonstrate the stabilization of polystyrene microspheres by encapsulating them with dumbbell-shaped colloids with a sticky and a non-sticky lobe. Upon adding a depletant, an effective short ranged attraction is induced between the microspheres and the smaller, smooth lobes of the dumbbells, making those specifically sticky, whereas the interaction with the larger lobes of the dumbbells is considerably less attractive due to their rough surface, which reduces the overlap volume and leaves them non-sticky. The encapsulation of the microspheres by these rough-smooth patchy dumbbells is investigated using a combination of experiments and computer simulations, both resulting in partial coverage of the template particles. For larger microspheres, the depletion attraction is stronger, resulting in a larger fraction of dumbbells that are attached with both lobes to the surface of microspheres. We thus find a template curvature dependent orientation of the dumbbells. In the Monte Carlo simulations, the introduction of such a small, curvature dependent attraction between the rough lobes of the dumbbells resulted in an increased coverage. However, kinetic constraints imposed by the dumbbell geometry seem to prevent optimal packing of the dumbbells on the template particles under all investigated conditions in experiments and simulations. Despite the incomplete coverage, the encapsulation by dumbbell particles does prevent aggregation of the microspheres, thus acting as a colloid-sized steric stabilizer.

  2. Highly Tunable Colloidal Perovskite Nanoplatelets through Variable Cation, Metal, and Halide Composition.

    Science.gov (United States)

    Weidman, Mark C; Seitz, Michael; Stranks, Samuel D; Tisdale, William A

    2016-08-23

    Colloidal perovskite nanoplatelets are a promising class of semiconductor nanomaterials-exhibiting bright luminescence, tunable and spectrally narrow absorption and emission features, strongly confined excitonic states, and facile colloidal synthesis. Here, we demonstrate the high degree of spectral tunability achievable through variation of the cation, metal, and halide composition as well as nanoplatelet thickness. We synthesize nanoplatelets of the form L2[ABX3]n-1BX4, where L is an organic ligand (octylammonium, butylammonium), A is a monovalent metal or organic molecular cation (cesium, methylammonium, formamidinium), B is a divalent metal cation (lead, tin), X is a halide anion (chloride, bromide, iodide), and n-1 is the number of unit cells in thickness. We show that variation of n, B, and X leads to large changes in the absorption and emission energy, while variation of the A cation leads to only subtle changes but can significantly impact the nanoplatelet stability and photoluminescence quantum yield (with values over 20%). Furthermore, mixed halide nanoplatelets exhibit continuous spectral tunability over a 1.5 eV spectral range, from 2.2 to 3.7 eV. The nanoplatelets have relatively large lateral dimensions (100 nm to 1 μm), which promote self-assembly into stacked superlattice structures-the periodicity of which can be adjusted based on the nanoplatelet surface ligand length. These results demonstrate the versatility of colloidal perovskite nanoplatelets as a material platform, with tunability extending from the deep-UV, across the visible, into the near-IR. In particular, the tin-containing nanoplatelets represent a significant addition to the small but increasingly important family of lead- and cadmium-free colloidal semiconductors.

  3. Realistic calculation of the low- and high-density liquid phase separation in a charged colloidal dispersion

    Science.gov (United States)

    Lai, S. K.; Peng, W. P.; Wang, G. F.

    2001-04-01

    A realistic statistical-mechanics model is applied to describe the repulsive interaction between charged colloids. The latter, in combination with the long-range van der Waals attraction simulated under excess salt environment, gives rise to a total intercolloidal particle potential showing a clear second potential minimum. Differing from the usual Derjaguin-Landau-Verwey-Overbeek (DLVO) model, the present model is valid at any finite concentration of colloids and is thus an appropriate model for investigating the low- and high-density liquid phase transition. Employing this two-body colloid-colloid potential and in conjunction with the Weeks-Chandler-Andersen [J. D. Weeks, D. Chandler, and H. C. Andersen, J. Chem. Phys. 54, 5237 (1971)] thermodynamic perturbation theory, we derive analytical expressions for the pressure, chemical potential, and related thermodynamic functions. These thermodynamic quantities were used to calculate the phase diagrams of charged colloidal dispersions in terms of the critical parameters: temperature, volume fraction, and electrolyte concentration parameter kD. Compared with the DLVO model, we find the areas enclosed within the spinodal decomposition and also the liquid-liquid coexistence curves broader in the present model for an excess salt condition κ=kDσ0300, the disparities between the two models reduce. The same thermodynamic perturbation theory has been employed to study also the weak reversible coagulation whose physical origin is attributed to the presence of the second potential minimum. We examine various colloidal parameters that affect the structure of the latter and deduce from our analysis the conditions of colloidal stability. In comparison with the measured flocculation data for a binary mixture of polystyrene lattices and water, we find that our calculated results are generally reasonable, thus lending great credence to the presently used model.

  4. Stabilization of sputtered gold and silver nanoparticles in PEG colloid solutions

    Energy Technology Data Exchange (ETDEWEB)

    Slepička, P., E-mail: petr.slepicka@vscht.cz; Elashnikov, R. [University of Chemistry and Technology Prague, Department of Solid State Engineering (Czech Republic); Ulbrich, P. [University of Chemistry and Technology Prague, Department of Biochemistry and Microbiology (Czech Republic); Staszek, M. [University of Chemistry and Technology Prague, Department of Solid State Engineering (Czech Republic); Kolská, Z. [University of J. E. Purkyně, Faculty of Science (Czech Republic); Švorčík, V. [University of Chemistry and Technology Prague, Department of Solid State Engineering (Czech Republic)

    2015-01-15

    In this study, a simple technique for preparation of colloid solution of metal nanoparticles in polyethylene glycol (PEG)/H{sub 2}O is described. By this technique, stable colloidal metal solutions can be prepared ready for use without application of chemical reactions, stabilizers, or reducing agents. The nanoparticles are created by direct sputtering of metal into PEG. The influence of sputter conditions and the concentration of PEG/H{sub 2}O on the properties of nanoparticles was studied. The nanoparticles were characterized by transmission electron microscopy, atomic absorption spectrometry, dynamic light scattering, and UV–Vis spectroscopy. UV–Vis spectra of gold nanoparticle solution exhibit localized surface plasmon resonance characteristic peaks located in the region 513–560 nm (PEG/H{sub 2}O—1/1), 509–535 nm (PEG/H{sub 2}O—1/9), and for silver nanoparticles in the region from 401 to 421 nm. Silver nanoparticles have a broader size distribution compared with gold ones. An appropriate choice of concentration, mixing, and deposition conditions allows preparing the stable solution of gold or silver nanoparticles.

  5. Improved magnetic induction heating of nanoferrites for hyperthermia applications: Correlation with colloidal stability and magneto-structural properties

    Energy Technology Data Exchange (ETDEWEB)

    Khot, V.M., E-mail: wish_khot@yahoo.co.in [Center for Interdisciplinary Research, D. Y. Patil University, Kolhapur 416006 (India); Salunkhe, A.B. [Advanced Materials Laboratory, Department of Physics, Savitribai Phule University of Pune (India); Ruso, J.M. [Soft Matter and Molecular Biophysics Group, Applied Physics Department, University of Santiago de Compostela, Santiago de Compostela (Spain); Pawar, S.H. [Center for Interdisciplinary Research, D. Y. Patil University, Kolhapur 416006 (India)

    2015-06-15

    Nanoferrites with compositions Mn{sub 0.4}Zn{sub 0.6}Fe{sub 2}O{sub 4}, Co{sub 0.4}Zn{sub 0.6}Fe{sub 2}O{sub 4}, Ni{sub 0.4}Zn{sub 0.6}Fe{sub 2}O{sub 4} (MZF, CZF and NZF respectively) coated with polyethylene glycol (PEG) were prepared in a single step. These nanoparticles are highly water dispersible with zeta potential values between 14 and 21 mV. Magnetic induction heating characteristics of these NPs have been studied as a function of magnetic field amplitude from 6.7 to 26.7 kA m{sup −1} (at fixed frequency 265 kHz) and concentration of nanoparticles. Notable enhancement in specific absorption rate (334.5 W g{sup −1}) by CZF nanoparticles has been observed. This enhanced induction heating properties have been studied and correlated with colloidal stability and magnetostructural properties such as tuned magnetic anisotropy arising from zinc substitution. Cytotoxicity of synthesized mixed ferrites has been evaluated in vitro on HeLa cell lines using MTT assay to explore their use as heating agents in magnetic hyperthermia. - Highlights: • Magnetic nanoferrites (sizes 8–12 nm) with improved specific absorption rate (334.5 W g{sup −1}) at lowest particle concentration have been prepared • The results have been explained by correlating colloidal stability and magnetostructural properties such as magnetocrystalline anisotropy. • It has been shown that substitution of zinc tunes anisotropy of cobalt iron oxide within the value optimized previously in achieving high throughput in magnetic induction heating. • In vitro cytotoxicity proves nanoparticles are non-toxic suggesting their use as a potential heating agent in hyperthermia therapy.

  6. Highly Elastic and Self-Healing Composite Colloidal Gels.

    NARCIS (Netherlands)

    Diba, M.; Wang, H.; Kodger, T.E.; Parsa, S.; Leeuwenburgh, S.C.G.

    2017-01-01

    Composite colloidal gels are formed by the pH-induced electrostatic assembly of silica and gelatin nanoparticles. These injectable and moldable colloidal gels are able to withstand substantial compressive and tensile loads, and exhibit a remarkable self-healing efficiency. This study provides new,

  7. Colloidal polypyrrole

    Science.gov (United States)

    Armes, Steven P.; Aldissi, Mahmoud

    1990-01-01

    Processable electrically conductive latex polymer compositions including colloidal particles of an oxidized, polymerized aromatic heterocyclic monomer, a stabilizing effective amount of a vinyl pyridine-containing polymer and dopant anions and a method of preparing such polymer compositions are disclosed.

  8. Role of electrostatic repulsion on colloidal stability of Bacillus halmapalus alpha-amylase

    DEFF Research Database (Denmark)

    Olsen, Søren Nymand; Andersen, Kim Bruno; Randolf, Theodor

    2009-01-01

    The colloidal stability of charged particles in suspension is often controlled by electrostatic repulsion, which can be rationalized in a semi-quantitative way by the DLVO theory. In the current study, we investigate this approach towards understanding irreversible protein aggregation, using Baci...

  9. Harnessing the advantages of hard and soft colloids by the use of core-shell particles as interfacial stabilizers

    NARCIS (Netherlands)

    Buchcic, C.; Tromp, R.H.; Meinders, M.B.J.; Cohen Stuart, M.A.

    2017-01-01

    The ability of colloidal particles to penetrate fluid interfaces is a crucial factor in the preparation of particle stabilized disperse systems such as foams and emulsions. For hard micron-sized particles the insertion into fluid interfaces requires substantial energy input, but soft particles

  10. Kinetics and cluster morphology evolution of shear-driven aggregation of well-stabilized colloids.

    Science.gov (United States)

    Meng, Xia; Wu, Hua; Morbidelli, Massimo

    2015-01-27

    We investigate the shear-driven aggregation of polystyrene colloids that are stabilized by both fixed and surfactant charges, using a microchannel device, in various particle volume fractions. The objective is to understand how the primary particles evolve to clusters with shearing time, how the cluster morphology develops along the aggregation with the effect of breakage and restructuring, and whether non-Derjaguin-Landau-Verwey-Overbeek (DLVO) interactions are present, affecting the kinetics. The time evolution of the primary particle conversion to big clusters is characterized by an induction time, followed by an explosive increase when the cluster size reaches a certain critical value, which confirms the self-acceleration kinetics developed in the literature. The size of the critical clusters has been quantified for the first time, and its scaling with the shear rate follows the literature prediction well. Moreover, analysis of the shear-driven kinetics confirms the presence of substantial non-DLVO interactions in the given system.

  11. Poly(acrylic acid)-stabilized colloidal gold nanoparticles: synthesis and properties.

    Science.gov (United States)

    Jans, Hilde; Jans, Karolien; Lagae, Liesbet; Borghs, Gustaaf; Maes, Guido; Huo, Qun

    2010-11-12

    Combining the intriguing optical properties of gold nanoparticles with the inherent physical and dynamic properties of polymers can give rise to interesting hybrid nanomaterials. In this study, we report the synthesis of poly(acrylic acid) (PAA)-capped gold nanoparticles. The polyelectrolyte-wrapped gold nanoparticles were fully characterized and studied via a combination of techniques, i.e. UV-vis and infrared spectroscopy, dark field optical microscopy, SEM imaging, dynamic light scattering and zeta potential measurements. Although PAA-capped nanoparticles have been previously reported, this study revealed some interesting aspects of the colloidal stability and morphological change of the polymer coating on the nanoparticle surface in an electrolytic environment, at various pH values and at different temperatures.

  12. Silver nanoparticles in complex biological media: assessment of colloidal stability and protein corona formation

    Science.gov (United States)

    Argentiere, Simona; Cella, Claudia; Cesaria, Maura; Milani, Paolo; Lenardi, Cristina

    2016-08-01

    Engineered silver nanoparticles (AgNPs) are among the most used nanomaterials in consumer products, therefore concerns are raised about their potential for adverse effects in humans and environment. Although an increasing number of studies in vitro and in vivo are being reported on the toxicity of AgNPs, most of them suffer from incomplete characterization of AgNPs in the tested biological media. As a consequence, the comparison of toxicological data is troublesome and the toxicity evaluation still remains an open critical issue. The development of a reliable protocol to evaluate interactions of AgNPs with surrounding proteins as well as to assess their colloidal stability is therefore required. In this regard, it is of importance not only to use multiple, easy-to-access and simple techniques but also to understand limitations of each characterization methods. In this work, the morphological and structural behaviour of AgNPs has been studied in two relevant biological media, namely 10 % FBS and MP. Three different techniques (Dynamic Light Scattering, Transmission Electron Microscopy, UV-Vis spectroscopy) were tested for their suitability in detecting AgNPs of three different sizes (10, 40 and 100 nm) coated with either citrate or polyvinylpyrrolidone. Results showed that UV-Vis spectroscopy is the most versatile and informative technique to gain information about interaction between AgNPs and surrounding proteins and to determine their colloidal stability in the tested biological media. These findings are expected to provide useful insights in characterizing AgNPs before performing any further in vitro/in vivo experiment.

  13. Effect of laundry surfactants on surface charge and colloidal stability of silver nanoparticles.

    Science.gov (United States)

    Skoglund, Sara; Lowe, Troy A; Hedberg, Jonas; Blomberg, Eva; Wallinder, Inger Odnevall; Wold, Susanna; Lundin, Maria

    2013-07-16

    The stability of silver nanoparticles (Ag NPs) potentially released from clothing during a laundry cycle and their interactions with laundry-relevant surfactants [anionic (LAS), cationic (DTAC), and nonionic (Berol)] have been investigated. Surface interactions between Ag NPs and surfactants influence their speciation and stability. In the absence of surfactants as well as in the presence of LAS, the negatively charged Ag NPs were stable in solution for more than 1 day. At low DTAC concentrations (≤1 mM), DTAC-Ag NP interactions resulted in charge neutralization and formation of agglomerates. The surface charge of the particles became positive at higher concentrations due to a bilayer type formation of DTAC that prevents from agglomeration due to repulsive electrostatic forces between the positively charged colloids. The adsorption of Berol was enhanced when above its critical micelle concentration (cmc). This resulted in a surface charge close to zero and subsequent agglomeration. Extended DLVO theory calculations were in compliance with observed findings. The stability of the Ag NPs was shown to depend on the charge and concentration of the adsorbed surfactants. Such knowledge is important as it may influence the subsequent transport of Ag NPs through different chemical transients and thus their potential bioavailability and toxicity.

  14. THE LIME PURIFICATION OF SUGAR –CONTAINING SOLUTION USING HIGH VISCOSITY COLLOIDAL SOLUTIONS

    Directory of Open Access Journals (Sweden)

    K. V.

    2015-12-01

    Full Text Available Aim of the work was to determine the efficiency of combined application of lime and high-viscous suspensions, containing the aluminium nanoparticles as a precursor in treatment of sugar-containing solutions. At the first stage the aluminium nanopowder, encapsulated into a salt matrix, was produced by the combined precipitation from a gas phase of metal and halogenide of alkali metal (NaCl. For the long-term stabilization of aluminum nanoparticles the method, developed by the authors, for dispersing these powders in the composition of polyethylene glycols was used, providing the colloidal solution of high viscosity (gel. At the second stage, as an object of investigation a juice of sugar beet, produced in the laboratory conditions by water extracting from the beet chips, was applied. In the produced juice the main characteristics of its quality were determined: the content of solids, sucrose, its purity was calculated (ratio of sucrose to solids content, in%. The content of protein and pectin components was also determined (as the main components of the colloidal fraction of the diffusion juice. Conventionally, as a basic reagent for the process of a lime pretreatment a lime milk of 1.18 g/cm3 density, prepared by liming the burned lime using hot water, was used. During the experiments the effectiveness of reagents, containing aluminum in nanoform, on the degree of removal of the colloidal dispersion substances in the process of juice purification in sugar beet production and improvement of its quality, is shown. However, the obtained results show that, depending on the method of producing, the additional reagents with aluminium nanoparticles have different effect on change of diffusion juice purity in the process of its treatment by the lime milk.

  15. MODIFICATION OF TRANSITION METAL CATIONS TO POLYMER- STABILIZED PLATINUM COLLOIDAL CLUSTERS IN ENANTIOSELECTIVE HYDROGENATION OF METHYL PYRUVATE

    Institute of Scientific and Technical Information of China (English)

    Xiao-ping Yan; Bao-lin He; Jie Zhang; Han-fan Liu

    2005-01-01

    Modification of transition metal cations to polymer-stabilized Pt colloidal clusters modified with cinchonidine was studied in enantioselective hydrogenation of methyl pyruvate. Compared to the enantiomeric excess (e.e.) value (71.4%)obtained without the presence of metal cations, obvious e.e. enhancement (up to 82.5%) was resulted from the addition of Zn2+ but with a certain decrease in activity. The reaction parameters in the presence of Zn2+ were also studied. It was found that the Pt colloidal catalysts in the presence of metal cations performed very differently from that in the absence of metal cations.

  16. Stability and structure of protein-lipoamino acid colloidal particles: toward nasal delivery of pharmaceutically active proteins.

    Science.gov (United States)

    Bijani, Christian; Arnarez, Clément; Brasselet, Sabrina; Degert, Corinne; Broussaud, Olivier; Elezgaray, Juan; Dufourc, Erick J

    2012-04-03

    To circumvent the painful intravenous injection of proteins in the treatment of children with growth deficiency, anemia, and calcium insufficiency, we investigated the stability and structure of protein-lipoamino acid complexes that could be nasally sprayed. Preparations that ensure a colloidal and structural stability of recombinant human growth hormone (rhGH), recombinant human erythropoietin (rhEPO), and salmon calcitonin (sCT) mixed with lauroyl proline (LP) were established. Protein structure was controlled by circular dichroism, and very small sizes of ca. 5 nm were determined by dynamic light scattering. The colloidal preparations could be sprayed with a droplet size of 20-30 μm. The molecular structure of aggregates was investigated by all-atom molecular dynamics. Whereas a lauroyl proline capping of globular proteins rhGH and rhEPO with preservation of their active structure was observed, a mixed micelle of sCT and lipoamino acids was formed. In the latter, aggregated LP constitutes the inner core and the surface is covered with calcitonins that acquire a marked α-helix character. Hydrophobic/philic interaction balance between proteins and LP drives the particles' stability. Passage through nasal cells grown at confluence was markedly increased by the colloidal preparations and could reach a 20 times increase in the case of EPO. Biological implications of such colloidal preparations are discussed in terms of furtiveness.

  17. The role of a microscopic colloidally stabilized phase in solubilizing oligoamine-condensed DNA complexes.

    Science.gov (United States)

    Trubetskoy, Vladimir S; Wolff, Jon A; Budker, Vladimir G

    2003-02-01

    DNA complexes of spermine and spermidine become resolubilized at very high concentrations of the oligoamine. It has been postulated that high oligoamine concentrations shift the DNA from the globule back to the coil phase. The present study indicates that DNA resolubilization at high concentrations of spermine and spermidine is explained by formation of small particles of condensed DNA that cannot be precipitated by centrifugation. The fact that DNA stays condensed during resolubilization was confirmed using a relatively new condensation assay and three independent microscopic techniques. A considerable portion of DNA was found to be in particles with diameter <100 nm. Formation of such small particles is likely to be caused by colloidal forces. The ability to form small, condensed DNA particles in solutions that contain high concentrations of oligocation should aid in the design of synthetic DNA vectors for gene transfer and gene therapy and in the handling of DNA for diagnostic studies.

  18. Superparamagnetic iron oxide/chitosan core/shells for hyperthermia application: Improved colloidal stability and biocompatibility

    Science.gov (United States)

    Patil, R. M.; Shete, P. B.; Thorat, N. D.; Otari, S. V.; Barick, K. C.; Prasad, A.; Ningthoujam, R. S.; Tiwale, B. M.; Pawar, S. H.

    2014-04-01

    Superparamagnetic magnetite nanoparticles are of great interest due to their potential biomedical applications. In the present investigation, Fe3O4 magnetic nanoparticles were prepared by alkaline precipitation using ferrous chloride as the sole source. An amphiphilic polyelectrolyte with the property of biocompatibility and functional carboxyl groups was used as a stabilizer to prepare a well-dispersed suspension of superparamagnetic Fe3O4 nanoparticles. The final material composed of Fe3O4 core and chitosan (CH) shell was produced. The amino groups of CH coated on Fe3O4 nanoparticles were further cross linked using glutaraldehyde (GLD) for stable coating. FTIR spectra, XPS and TGA confirmed the coating of CH/GLD on the surface of Fe3O4 nanoparticles. XRD patterns indicate the pure phase Fe3O4 with a spinel structure. The nanoparticles were superparamagnetic at room temperature with saturation magnetization values for bare and coated nanoparticles which were 51.68 emu/g and 48.60 emu/g, respectively. Zeta potential values showed higher colloidal stability of coated nanoparticles than the bare one. Cytotoxicity study up to 2 mg mL-1 concentration showed no drastic change in cell viability of nanoparticles after coating. Also, coated nanoparticles showed increased SAR value, making them suitable for hyperthermia therapy application.

  19. Silver colloidal nanoparticle stability: influence on Candida biofilms formed on denture acrylic.

    Science.gov (United States)

    Monteiro, Douglas Roberto; Takamiya, Aline Satie; Feresin, Leonardo Perina; Gorup, Luiz Fernando; de Camargo, Emerson Rodrigues; Delbem, Alberto Carlos Botazzo; Henriques, Mariana; Barbosa, Debora Barros

    2014-08-01

    Our aim in this study was to evaluate how the chemical stability of silver nanoparticles (SNs) influences their efficacy against Candida albicans and C. glabrata biofilms. Several parameters of SN stability were tested, namely, temperature (50ºC, 70ºC, and 100ºC), pH (5.0 and 9.0), and time of contact (5 h and 24 h) with biofilms. The control was defined as SNs without temperature treatment, pH 7, and 24 h of contact. These colloidal suspensions at 54 mg/L were used to treat mature Candida biofilms (48 h) formed on acrylic. Their efficacy was determined by total biomass and colony-forming unit quantification. Data were analyzed using analysis of variance and the Bonferroni post hoc test (α = 0.05). The temperature and pH variations of SNs did not affect their efficacy against the viable cells of Candida biofilms (P > 0.05). Moreover, the treatment periods were not decisive in terms of the susceptibility of Candida biofilms to SNs. These findings provide an important advantage of SNs that may be useful in the treatment of Candida-associated denture stomatitis.

  20. Colloidal Stability & Conformational Changes in β-Lactoglobulin: Unfolding to Self-Assembly

    Directory of Open Access Journals (Sweden)

    Steven Blake

    2015-08-01

    Full Text Available A detailed understanding of the mechanism of unfolding, aggregation, and associated rheological changes is developed in this study for β-Lactoglobulin at different pH values through concomitant measurements utilizing dynamic light scattering (DLS, optical microrheology, Raman spectroscopy, and differential scanning calorimetry (DSC. The diffusion interaction parameter kD emerges as an accurate predictor of colloidal stability for this protein consistent with observed aggregation trends and rheology. Drastic aggregation and gelation were observed at pH 5.5. Under this condition, the protein’s secondary and tertiary structures changed simultaneously. At higher pH (7.0 and 8.5, oligomerizaton with no gel formation occurred. For these solutions, tertiary structure and secondary structure transitions were sequential. The low frequency Raman data, which is a good indicator of hydrogen bonding and structuring in water, has been shown to exhibit a strong correlation with the rheological evolution with temperature. This study has, for the first time, demonstrated that this low frequency Raman data, in conjunction with the DSC endotherm, can be been utilized to deconvolve protein unfolding and aggregation/gelation. These findings can have important implications for the development of protein-based biotherapeutics, where the formulation viscosity, aggregation, and stability strongly affects efficacy or in foods where protein structuring is critical for functional and sensory performance.

  1. Quantification of Heteroaggregation between Citrate-Stabilized Gold Nanoparticles and Hematite Colloids.

    Science.gov (United States)

    Smith, Brian M; Pike, Daniel J; Kelly, Michael O; Nason, Jeffrey A

    2015-11-03

    Collisions with and attachment to natural colloids (heteroaggregation) is likely to influence significantly the fate, transport, and toxicity of engineered nanoparticles (ENPs). This study investigated heteroaggregation between hematite (α-Fe2O3) colloids and citrate-capped gold nanoparticles (Cit-AuNPs) using a novel approach involving time-resolved dynamic light scattering and parallel experiments designed to quantify nanoparticle attachment and heteroaggregate surface charge. Experiments were performed in low ionic strength synthetic water at environmentally relevant pH in the presence and absence of Suwannee River Natural Organic Matter (SRNOM). In the absence of SRNOM at pH values where Cit-AuNPs and hematite are oppositely charged, attachment efficiencies are high and Cit-AuNPs are capable of destabilizing hematite following an "electrostatic patch" mechanism. Furthermore, maximum observed surface coverages were far below those predicted by geometry alone, a fact predicted by the random sequential adsorption (RSA) model that has significant implications for the estimation of heteroaggregate attachment efficiencies. At pH values where both particles are negative or in the presence of small amounts of SRNOM, attachment was minimal. Calculated attachment efficiencies using the measured surface coverages corroborate these findings. The calculation of attachment efficiencies and the identification of mechanisms governing heteroaggregation represents an important step toward predicting the transport, fate, and toxicity of ENPs in the environment.

  2. Adsorption of polyelectrolyte on the surface of ZnO nanoparticles and the stability of colloidal dispersions

    Institute of Scientific and Technical Information of China (English)

    LIUFU Shengcong; XIAO Hanning; LI Yuping

    2005-01-01

    The present study focuses on the adsorption of a polyelectrolyte, the component of which is a polymer of maleic anhydride sodium salt, on the surface of nanometric zinc oxide particles and the colloidal stability of aqueous dispersions. FTIR spectroscopic data provided evidence in support of hydrogen bonding and chemical interaction in the case of the polyelectrolyte-ZnO system. The adsorption isotherms showed the influences of polyelectrolyte concentration, pH and ionic strength on the adsorption. With the increase of pH the saturated adsorbed amount decreased, while the thickness of adsorption layer increased. The saturated adsorbed amount increased with increasing salt concentration, and decreased with further increasing salt concentration. It should be noted that in the presence of a CaCl2 solution the adsorbed amount and the adsorption layer thickness were greater than those in the NaCl solution of the same concentration. The change of the absorbance of zinc oxide dispersions showed that the absorbance decreased slowly at high pH. There was a maximum point for the absorbance of the zinc oxide dispersions in the presence of various polyelectrolyte concentrations. The change of dispersion stability resulted from the change of macromolecular chains conformation at the interface.

  3. Colloidal photonic glass for electro-optic display stabilized with potassium persulfate (KPS) in polar solvent

    Science.gov (United States)

    Lee, Hye-Young; Kim, Young-Seok; Yi, Gi-Ra

    2016-04-01

    We introduced carbon-shell with potassium persulfate structure to modify the repulsive force between particles and minimize scattered light. The reflected structural color varied from blue to red and showed high color purity with high cycle stability.

  4. Aggregation and stability of anisotropic charged clay colloids in aqueous medium in the presence of salt.

    Science.gov (United States)

    Ali, Samim; Bandyopadhyay, Ranjini

    2016-01-01

    Na-montmorillonite nanoclay is a colloid of layered mineral silicate. When dispersed in water, this mineral swells on absorption of water and exfoliates into platelets with electric double layers on their surfaces. Even at low particle concentration, the aqueous dispersion can exhibit a spontaneous ergodicity breaking phase transition from a free flowing liquid to nonequilibrium, kinetically arrested and disordered states such as gels and glasses. In an earlier publication [Applied Clay Science, 2015, 114, 8592], we showed that the stability of clay gels can be enhanced by adding a salt later to the clay dispersion prepared in deionized water, rather than by adding the clay mineral to a previously mixed salt solution. Here, we directly track the collapsing interface of sedimenting clay gels using an optical method and show that adding salt after dispersing the clay mineral does indeed result in more stable gels even in very dilute dispersions. These weak gels are seen to exhibit a transient collapse after a finite delay time, a phenomenon observed previously in depletion gels. The velocity of the collapse oscillates with the age of the sample. However, the average velocity of collapse increases with sample age up to a peak value before decreasing at higher ages. With increasing salt concentration, the delay time for transient collapse decreases, while the peak value of the collapsing velocity increases. Using ultrasound attenuation spectroscopy, rheometry and cryogenic scanning electron microscopy, we confirm that morphological changes of the gel network assembly, facilitated by thermal fluctuations, lead to the observed collapse phenomenon. Since clay minerals are used extensively in polymer nanocomposites, as rheological modifiers, stabilizers and gas absorbents, we believe that the results reported in this work are extremely useful for several practical applications and also for understanding geophysical phenomena such as the formation and stability of quicksand

  5. Thermal Stability and Anisotropic Sublimation of Two-Dimensional Colloidal Bi2Te3 and Bi2Se3 Nanocrystals

    CERN Document Server

    Buha, Joka; Castillo, Antonio Esau Del Rio; Bonaccorso, Francesco; Manna, Liberato

    2016-01-01

    The structural and compositional stabilities of two dimensional 2D Bi2Te3 and Bi2Se3 nanocrystals, produced by both colloidal synthesis and by liquid phase exfoliation, were studied by in situ transmission electron microscopy TEM during annealing at temperatures between 350 and 500 C. The sublimation process induced by annealing is structurally and chemically anisotropic and takes place through the preferential dismantling of the prismatic 011-0 type planes, and through the preferential sublimation of Te or Se.

  6. Impacts of select organic ligands on the colloidal stability, dissolution dynamics, and toxicity of silver nanoparticles.

    Science.gov (United States)

    Pokhrel, Lok R; Dubey, Brajesh; Scheuerman, Phillip R

    2013-11-19

    Key understanding of potential transformations that may occur on silver nanoparticle (AgNP) surface upon interaction with naturally ubiquitous organic ligands (e.g., -SH (thoil), humic acid, or -COO (carboxylate)) is limited. Herein we investigated how dissolved organic carbon (DOC), -SH (in cysteine, a well-known Ag(+) chelating agent), and -COO (in trolox, a well-known antioxidant) could alter the colloidal stability, dissolution rate, and toxicity of citrate-functionalized AgNPs (citrate-AgNPs) against a keystone crustacean Daphnia magna. Cysteine, DOC, or trolox amendment of citrate-AgNPs differentially modified particle size, surface properties (charge, plasmonic spectra), and ion release dynamics, thereby attenuating (with cysteine or trolox) or promoting (with DOC) AgNP toxicity. Except with DOC amendment, the combined toxicity of AgNPs and released Ag under cysteine or trolox amendment was lower than of AgNO3 alone. The results of this study show that citrate-AgNP toxicity can be associated with oxidative stress, ion release, and the organism biology. Our evidence suggests that specific organic ligands available in the receiving waters can differentially surface modify AgNPs and alter their environmental persistence (changing dissolution dynamics) and subsequently the toxicity; hence, we caveat to generalize that surface modified nanoparticles upon environmental release may not be toxic to receptor organisms.

  7. The role of effective charges in the electrophoresis of highly charged colloids.

    Science.gov (United States)

    Chatterji, Apratim; Horbach, Jürgen

    2010-12-15

    We study the variation of electrophoretic mobility μ of highly charged spherical colloidal macroions for varying surface charge density σ on the colloid using computer simulations of the primitive model for charged colloids. Hydrodynamic interactions between ions are incorporated by coupling the primitive model of charged colloids to the lattice Boltzmann model (LB) of the fluid. In the highly charged regime, the mobility μ of the colloid is known to decrease with the increase of bare charge Q of the colloid; the aim of this paper is to investigate the cause of this. We have identified that the two main factors contributing to the decrease of μ are counterion charge condensation on the highly charged colloid and an increase in effective friction of the macroion-counterion complex due to the condensed counterions. Thus the established O'Brien and White theory, which identified the dipolar force originating from distortion of the electric double layer as the cause of decreasing μ, seems to break down for the case of highly charged colloids with σ in the range of 30-400 µC cm (- 2). To arrive at our conclusions, we counted the number of counterions q0 moving along with the spherical macroion. We observe in our simulations that q0 increases with the increase of bare charge Q, such that the effective charge Qeff = Q - q0 remains approximately constant. Interestingly for our nanometer-sized charged colloid, we observe that, if surface charge density σ of the colloid is increased by decreasing the radius RM of the colloid but fixed bare charge Q, the effective charge Q - q0 decreases with the increase of σ. This behavior is qualitatively different when σ is increased by increasing Q keeping RM fixed. Our observations address a controversy about the effective charge of a strongly charged macroion: some studies claim that effective charge is independent of the bare charge (Alexander et al 1984 J. Chem. Phys. 80 5776; Trizac et al 2003 Langmuir 19 4027) whereas

  8. Formation of aquatic Th(IV) colloids and stabilization by interaction with Cm(III)/Eu(III).

    Science.gov (United States)

    Yun, Jong-Il; Kim, Maria-Anna; Panak, Petra J; Kim, Jae-Il; Fanghänel, Thomas

    2006-03-23

    The present investigation is to ascertain under what conditions actinide ions undergo aggregation via oxo-bridging to form stable colloidal species. Eu and Th are taken for this purpose as trivalent and tetravalent actinide homologue ions, respectively. For verification of the effects of impurities in chemicals on the actinide colloid generation, pH is adjusted either by a conventional acid-base titration or by coulometry without addition of NaOH. The colloid generation is monitored by highly sensitive laser-induced breakdown detection in varying pH from 3 to 7, first in dilute Eu and Th solutions separately and then in a mixture of both, all in 0.5 M HCl/NaCl. The formation of stable colloids is observed particularly in a mixed solution of Eu and Th, suggesting that aggregation via mutual oxo-bridging of trivalent and tetravalent metal ions results in surface polarization, leading to stable hydrophilic particles of 20-30 nm in diameter. When Eu is replaced by Cm in the mixed solution in favor of the high fluorescence intensity of the latter, the chemical speciation is determined on colloid-borne Cm by time-resolved laser fluorescence spectroscopy. Two different colloid-borne Cm species, oxo-bridged with Th, are identified: a minor amount at 598.0 nm (denoted as Cm-Th(1)) and a major amount at 604.8 nm (Cm-Th(2)). The former is found as a transitional state, which converts to the latter with increasing pH and prevails at pH > 5.5. Both colloid-borne species (Cm-Th) are distinctively different from hydrolyzed Cm or its carbonate complexes with respect to their fluorescence peak positions and lifetimes. In conclusion, a mixed oxo-bridging of trivalent and tetravalent actinides elicits the generation of stable colloids, whereas individual ions in their pure state form colloids under oversaturation at near neutral pH only as a transitional state for precipitation.

  9. Evaluation of Colloidal Stability and Ecotoxicity of Metal-based Nanoparticles in the Aquatic and Terrestrial Systems

    Science.gov (United States)

    Pokhrel, Lok Raj

    Intrinsic to the many nano-enabled products are atomic-size multifunctional engineered nanomaterials, which upon release contaminate the environments, raising considerable health and safety concerns. This Ph.D. dissertation is designed to investigate (i) whether metals or oxide nanoparticles are more toxic than ions, and if MetPLATE(TM) bioassay is applicable as a rapid nanotoxicity screening tool; (ii) how variable water chemistry (dissolved organic carbon (DOC), pH, and hardness) and organic compounds (cysteine, humic acid, and trolox) modulate colloidal stability, ion release, and aquatic toxicity of silver nanoparticles (AgNP); and (iii) the developmental responses of crop plants exposed to Ag- or ZnO- (zinc oxide) nanoparticles. Results suggest that the MetPLATE can be considered a high-throughput screening tool for rapid nanotoxicity evaluation. Detectable changes in the colloidal diameter, surface charge, and plasmonic resonance revealed modulating effects of variable water chemistry and organic ligands on the particle stability, dissolution, and toxicity of AgNPs against Escherichia coli or Daphnia magna. Silver dissolution increased as a function of DOC concentrations but decreased with increasing hardness, pH, cysteine, or trolox levels. Notably, the dissociated Ag+ was inadequate to explain AgNP toxicity, and that the combined effect of AgNPs and dissolved Ag+ under each ligand treatment was lower than of AgNO 3. Significant attenuation by trolox signifies an oxidative stress-mediated AgNP toxicity; its inability to attenuate AgNO3 toxicity, however, negates oxidative stress as Ag+ toxicity mechanism, and that cysteine could effectively quench free Ag+ to alleviate AgNO 3 toxicity in D. magna. Surprisingly, DOC-AgNPs complex that apparently formed at higher DOC levels might have led daphnids filter-feed on aggregates, potentially elevating internal dose, and thus higher mortality. Maize root anatomy showed differential alterations upon exposure to Ag

  10. The colloid investigations conducted at the Aespoe Hard Rock Laboratory during 2000-2004

    Energy Technology Data Exchange (ETDEWEB)

    Laaksoharju, Marcus [Geopoint AB, Stockholm (Sweden); Wold, Susanna [Royal Inst. of Tech., Stockholm (Sweden). School of Chemical Science and Engineering, Nuclear Chemistry] (eds.)

    2005-12-15

    In 2000, SKB decided to initiate an international colloid project at the Aespoe Hard Rock Laboratory in Sweden. The objectives of the colloid project are to: (i) study the role of bentonite as a colloid source, (ii) verify the background colloid concentration at Aespoe HRL and, (iii) investigate the potential for colloid formation/transport in natural groundwater concentrations. The experimental concepts for the colloid project are: laboratory experiments with bentonite, background field measurements of natural colloids, borehole specific bentonite colloid stability experiments and a fracture specific transport experiment. The activities concerning the laboratory experiments and background field measurements are described in this work; the other activities are ongoing or planned. The following conclusions were made: The bentonite colloid stability is strongly dependent on the groundwater ionic strength. Natural colloids are organic degradation products such as humic and fulvic acids, inorganic colloids (clay, calcite, iron hydroxide) and microbes. Microbes form few but large particles and their concentration increase with increasing organic carbon concentrations. The small organic colloids are present in very low concentrations in deep granitic groundwater. The concentrations can be rather high in shallow waters. The colloid concentration decreases with depth and salinity, since colloids are less stable in saline waters. The colloid content at Aespoe is less than 300 ppb. The colloid content at repository level is less than 50 ppb. The groundwater variability obtained in the boreholes reflects well the natural groundwater variability along the whole HRL tunnel.

  11. Synthesis of Monodispersed Gold Nanoparticles with Exceptional Colloidal Stability with Grafted Polyethylene Glycol-g-polyvinyl Alcohol

    Directory of Open Access Journals (Sweden)

    Alaaldin M. Alkilany

    2015-01-01

    Full Text Available Herein, we report the synthesis of spherical gold nanoparticles with tunable core size (23–79 nm in the presence of polyethylene glycol-g-polyvinyl alcohol (PEG-g-PVA grafted copolymer as a reducing, capping, and stabilizing agent in a one-step protocol. The resulted PEG-g-PVA-capped gold nanoparticles are monodispersed with an exceptional colloidal stability against salt addition, repeated centrifugation, and extensive dialysis. The effect of various synthesis parameters and the kinetic/mechanism of the nanoparticle formation are discussed.

  12. Functional PEG-PAMAM-tetraphosphonate capped NaLnF₄ nanoparticles and their colloidal stability in phosphate buffer.

    Science.gov (United States)

    Zhao, Guangyao; Tong, Lemuel; Cao, Pengpeng; Nitz, Mark; Winnik, Mitchell A

    2014-06-17

    Developing surface coatings for NaLnF4 nanoparticles (NPs) that provide long-term stability in solutions containing competitive ions such as phosphate remains challenging. An amine-functional polyamidoamine tetraphosphonate (NH2-PAMAM-4P) as a multidentate ligand for these NPs has been synthesized and characterized as a ligand for the surface of NaGdF4 and NaTbF4 nanoparticles. A two-step ligand exchange protocol was developed for introduction of the NH2-PAMAM-4P ligand on oleate-capped NaLnF4 NPs. The NPs were first treated with methoxy-poly(ethylene glycol)-monophosphoric acid (M(n) = 750) in tetrahydrofuran. The mPEG750-OPO3-capped NPs were stable colloidal solutions in water, where they could be ligand-exchanged with NH2-PAMAM-4P. The surface amine groups on the NPs were available for derivatization to attach methoxy-PEG (M(n) = 2000) and biotin-terminated PEG (M(n) = 2000) chains. The surface coverage of ligands on the NPs was examined by thermal gravimetric analysis, and by a HABA analysis for biotin-containing NPs. Colloidal stability of the NPs was examined by dynamic light scattering. NaGdF4 and NaTbF4 NPs capped with mPEG2000-PAMAM-4P showed colloidal stability in DI water and in phosphate buffer (10 mM, pH 7.4). A direct comparison with NaTbF4 NPs capped with a mPEG2000-lysine-based tetradentate ligand that we reported previously (Langmuir 2012, 28, 12861-12870) showed that both ligands provided long-term stability in phosphate buffer, but that the lysine-based ligand provided better stability in phosphate-buffered saline.

  13. Protocol optimization for the mild detemplation of mesoporous silica nanoparticles resulting in enhanced texture and colloidal stability

    NARCIS (Netherlands)

    Zhang, Zheng; Mayoral, Alvaro; Melian-Cabrera, Ignacio

    2016-01-01

    Porosity development of mesostructured colloidal silica nanoparticles is related to the removal of the organic templates and co-templates which is often carried out by calcination at high temperatures, 500 -600 degrees C. In this study a mild detemplation method based on the oxidative Fenton chemist

  14. Superparamagnetic iron oxide nanoparticles incorporated into silica nanoparticles by inelastic collision via ultrasonic field: Role of colloidal stability

    Energy Technology Data Exchange (ETDEWEB)

    Sodipo, Bashiru Kayode; Azlan, Abdul Aziz [Nano-Optoelectronics Research and Technology (NOR) Lab, School of Physics, Universiti Sains Malaysia, 11800 Pulau Pinang, Malaysia Nano-Biotechnology Research (Malaysia); Innovation (NanoBRI), Institute for Research in Molecular Medicine (INFORMM), Universiti Sains Malaysia, 11800, Pulau Pinang (Malaysia)

    2015-04-24

    Superparamagnetic iron oxide nanoparticles (SPION)/Silica composite nanoparticles were prepared by ultrasonically irradiating colloidal suspension of silica and SPION mixture. Both silica and SPION were synthesized independently via co-precipitation and sol-gel method, respectively. Their mixtures were sonicated at different pH between 3 and 5. Electrophoresis measurement and other physicochemical analyses of the products demonstrate that at lower pH SPION was found incorporated into the silica. However, at pH greater than 4, SPION was unstable and unable to withstand the turbulence flow and shock wave from the ultrasonic field. Results suggest that the formation of the SPION/silica composite nanoparticles is strongly related to the inelastic collision induced by ultrasonic irradiation. More so, the formation the composite nanoparticles via the ultrasonic field are dependent on the zeta potential and colloidal stability of the particles.

  15. Stable colloids in molten inorganic salts

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Hao; Dasbiswas, Kinjal; Ludwig, Nicholas B.; Han, Gang; Lee, Byeongdu; Vaikuntanathan, Suri; Talapin, Dimitri V.

    2017-02-16

    A colloidal solution is a homogeneous dispersion of particles or droplets of one phase (solute) in a second, typically liquid, phase (solvent). Colloids are ubiquitous in biological, chemical and technological processes1, 2, homogenizing highly dissimilar constituents. To stabilize a colloidal system against coalescence and aggregation, the surface of each solute particle is engineered to impose repulsive forces strong enough to overpower van der Waals attraction and keep the particles separated from each other2. Electrostatic stabilization3, 4 of charged solutes works well in solvents with high dielectric constants, such as water (dielectric constant of 80). In contrast, colloidal stabilization in solvents with low polarity, such as hexane (dielectric constant of about 2), can be achieved by decorating the surface of each particle of the solute with molecules (surfactants) containing flexible, brush-like chains2, 5. Here we report a class of colloidal systems in which solute particles (including metals, semiconductors and magnetic materials) form stable colloids in various molten inorganic salts. The stability of such colloids cannot be explained by traditional electrostatic and steric mechanisms. Screening of many solute–solvent combinations shows that colloidal stability can be traced to the strength of chemical bonding at the solute–solvent interface. Theoretical analysis and molecular dynamics modelling suggest that a layer of surface-bound solvent ions produces long-ranged charge-density oscillations in the molten salt around solute particles, preventing their aggregation. Colloids composed of inorganic particles in inorganic melts offer opportunities for introducing colloidal techniques to solid-state science and engineering applications.

  16. Stability and minimum size of colloidal clusters on a liquid-air interface.

    Science.gov (United States)

    Pergamenshchik, V M

    2012-02-01

    A vertical force applied to each of two colloids, trapped at a liquid-air interface, induces their logarithmic pairwise attraction. I recently showed [Phys. Rev. E 79, 011407 (2009)] that in clusters of size R much larger than the capillary length λ, the attraction changes to that of a power law and is much stronger due to a many-body effect, and I derived two equations that describe the equilibrium coarse-grained meniscus profile and colloid density in such clusters. In this paper, this theory is shown also to describe small clusters with R≪ λ provided the number N of colloids therein is sufficiently large. An analytical solution for a small circular cluster with an arbitrary short-range power-law pairwise repulsion is found. The energy of a cluster is obtained as a function of its radius R and colloid number N. As in large clusters, the attraction force and energy universally scale with the distance L between colloids as L(-3) and L(-2), respectively, for any repulsion forces. The states of an equilibrium cluster, predicted by the theory, are shown to be stable with respect to small perturbations of the meniscus profile and colloid density. The minimum number of colloids in a circular cluster, which sustains the thermal motion, is estimated. For standard parameters, it can be very modest, e.g., in the range 20-200, which is in line with experimental findings on reversible clusterization on a liquid-air interface. © 2012 American Physical Society

  17. Photo-stability and time-resolved photoluminescence study of colloidal CdSe/ZnS quantum dots passivated in Al2O3 using atomic layer deposition

    Science.gov (United States)

    Cheng, Chih-Yi; Mao, Ming-Hua

    2016-08-01

    We report photo-stability enhancement of colloidal CdSe/ZnS quantum dots (QDs) passivated in Al2O3 thin film using the atomic layer deposition (ALD) technique. 62% of the original peak photoluminescence (PL) intensity remained after ALD. The photo-oxidation and photo-induced fluorescence enhancement effects of both the unpassivated and passivated QDs were studied under various conditions, including different excitation sources, power densities, and environment. The unpassivated QDs showed rapid PL degradation under high excitation due to strong photo-oxidation in air while the PL intensity of Al2O3 passivated QDs was found to remain stable. Furthermore, recombination dynamics of the unpassivated and passivated QDs were investigated by time-resolved measurements. The average lifetime of the unpassivated QDs decreases with laser irradiation time due to photo-oxidation. Photo-oxidation creates surface defects which reduces the QD emission intensity and enhances the non-radiative recombination rate. From the comparison of PL decay profiles of the unpassivated and passivated QDs, photo-oxidation-induced surface defects unexpectedly also reduce the radiative recombination rate. The ALD passivation of Al2O3 protects QDs from photo-oxidation and therefore avoids the reduction of radiative recombination rate. Our experimental results demonstrated that passivation of colloidal QDs by ALD is a promising method to well encapsulate QDs to prevent gas permeation and to enhance photo-stability, including the PL intensity and carrier lifetime in air. This is essential for the applications of colloidal QDs in light-emitting devices.

  18. Stabilization of plutonium nano-colloids by epitaxial distortion on mineral surfaces.

    Science.gov (United States)

    Powell, Brian A; Dai, Zurong; Zavarin, Mavrik; Zhao, Pihong; Kersting, Annie B

    2011-04-01

    The subsurface migration of Pu may be enhanced by the presence of colloidal forms of Pu. Therefore, complete evaluation of the risk posed by subsurface Pu contamination needs to include a detailed physical/chemical understanding of Pu colloid formation and interactions of Pu colloids with environmentally relevant solid phases. Transmission electron microscopy (TEM) was used to characterize Pu nanocolloids and interactions of Pu nanocolloids with goethite and quartz. We report that intrinsic Pu nanocolloids generated in the absence of goethite or quartz were 2-5 nm in diameter, and both electron diffraction analysis and HRTEM confirm the expected Fm3m space group with the fcc, PuO2 structure. Plutonium nanocolloids formed on goethite have undergone a lattice distortion relative to the ideal fluorite-type structure, fcc, PuO2, resulting in the formation of a bcc, Pu4O7 structure. This structural distortion results from an epitaxial growth of the plutonium colloid on goethite, leading to stronger binding of plutonium to goethite compared with other minerals such as quartz, where the distortion was not observed. This finding provides new insight for understanding how molecular-scale behavior at the mineral-water interface may facilitate transport of plutonium at the field scale.

  19. Spectral properties of zinc sulfide sols stabilized by high-molecular polyvinylpyrrolidone

    Science.gov (United States)

    Evstrop'ev, S. K.; Gatchin, Yu. A.; Evstrop'ev, K. S.; Dukel'skii, K. V.; Kislyakov, I. M.

    2015-12-01

    Spectral properties of zinc sulfide sols stabilized by high-molecular polyvinylpyrrolidone have been studied. It is shown that the absorption spectra of colloidal solutions in the UV spectral range are determined by the quantum-confinement effect, exhibiting a dependence of the absorption edge on the size of zinc sulfide nanocrystals.

  20. SCREENING OF HIGH-Z GRAINS AND RELATED PHENOMENA IN COLLOIDAL PLASMAS

    Directory of Open Access Journals (Sweden)

    O.Bystrenko

    2003-01-01

    Full Text Available Recent important results are briefly presented concerning the screening of high-Z impurities in colloidal plasmas. The review focuses on the phenomenon of nonlinear screening and its effects on the structure of colloidal plasmas, the role of trapped ions in grain screening, and the effects of strong collisions in the plasma background. It is shown that the above effects may strongly modify the properties of the grain screening giving rise to considerable deviations from the conventional Debye-Huckel theory as dependent on the physical processes in the plasma background.

  1. Enhanced Colloidal Stability of CeO2 Nanoparticles by Ferrous Ions: Adsorption, Redox Reaction, and Surface Precipitation.

    Science.gov (United States)

    Liu, Xuyang; Ray, Jessica R; Neil, Chelsea W; Li, Qingyun; Jun, Young-Shin

    2015-05-05

    Due to the toxicity of cerium oxide (CeO2) nanoparticles (NPs), a better understanding of the redox reaction-induced surface property changes of CeO2 NPs and their transport in natural and engineered aqueous systems is needed. This study investigates the impact of redox reactions with ferrous ions (Fe2+) on the colloidal stability of CeO2 NPs. We demonstrated that under anaerobic conditions, suspended CeO2 NPs in a 3 mM FeCl2 solution at pH 4.8 were much more stable against sedimentation than those in the absence of Fe2+. Redox reactions between CeO2 NPs and Fe2+ lead to the formation of 6-line ferrihydrite on the CeO2 surfaces, which enhanced the colloidal stability by increasing the zeta potential and hydrophilicity of CeO2 NPs. These redox reactions can affect the toxicity of CeO2 NPs by increasing cerium dissolution, and by creating new Fe(III) (hydr)oxide reactive surface layers. Thus, these findings have significant implications for elucidating the phase transformation and transport of redox reactive NPs in the environment.

  2. Poly(ethylene imine)-modified graphene oxide with improved colloidal stability and its adsorption of methyl orange.

    Science.gov (United States)

    Liu, Hongxi; Wu, Ting; Wu, Zhimin; Zhang, Yong; Xuan, Keqin; Zhang, Jinglin; Tan, Shaozao

    2014-01-01

    Graphene oxide (GO) was chemically modified with poly(ethylene imine) (PEI) to improve its colloidal stability and was investigated as a potential adsorbent for the removal of methyl orange (MO). The synthesis of PEI-GO was verified with a Fourier transform infrared spectrometer and thermogravimetric analysis. A series of adsorption experiments were carried out to investigate the adsorption capacity of PEI-GO. Adsorption kinetics and thermodynamics studies were performed, and the thermodynamic parameters were calculated. The results showed that PEI could improve the colloidal stability of GO in aqueous solution, and the obtained PEI-GO showed a macroscopically homogeneous dispersion after more than three months. After standing for 90 days, the Brunauer-Emmett-Teller specific surface area of GO decreased from 353 to 214 m2·g(-1), while that of PEI-GO remained almost unchanged (from 432 to 413 m2·g(-1)). The PEI-GO exhibited significantly faster kinetic and higher adsorption capacity for MO than GO. Moreover, PEI-GO had a good adsorption capacity in the acidic range, and the highest adsorption of MO occurred at pH=6.0. The adsorption of MO on PEI-GO was an endothermic, spontaneous and physisorption process.

  3. Maceration enzymes and mannoproteins: a possible strategy to increase colloidal stability and color extraction in red wines.

    Science.gov (United States)

    Guadalupe, Zenaida; Palacios, Antonio; Ayestaran, Belén

    2007-06-13

    Different strategies were adopted to achieve increases in color stability in Tempranillo wines: (i) addition of maceration enzymes directly to the must, (ii) addition of commercial mannoproteins to the must, and (iii) inoculation of must with yeast overexpressed of mannoproteins. The addition of enzymes favored color extraction, and the wines obtained presented higher values of wine color, color intensity, bisulfite-stable color, and visually enhanced color intensity. The enzyme hydrolytic activity produced an increase in the acid polysaccharide content and polyphenol index and yielded to wines with more astringency, tannin, and length. Added mannoproteins had clearer effects on the analyzed parameters than yeast. Contrary to what may be thought, mannoproteins did not maintain the extracted polyphenols in colloidal dispersion and neither ensured color stability. These compounds clearly modified the gustative structure of the wines, enhancing the sweetness and roundness.

  4. High-Resolution Transmission Electron Microscopy Observation of Colloidal Nanocrystal Growth Mechanisms using Graphene Liquid Cells

    Energy Technology Data Exchange (ETDEWEB)

    Yuk, Jong Min; Park, Jungwon; Ercius, Peter; Kim, Kwanpyo; Hellebusch, Danny J.; Crommie, Michael F.; Lee, Jeong Yong; Zettl, A.; Alivisatos, A. Paul

    2011-12-12

    We introduce a new type of liquid cell for in-situ electron microscopy based upon entrapment of a liquid film between layers of graphene. We employ this cell to achieve high-resolution imaging of colloidal platinum nanocrystal growth. The ability to directly image and resolve critical steps at atomic resolution provides new insights into nanocrystal coalescence and reshaping during growth.

  5. Highly luminescent CdTe/CdSe colloidal heteronanocrystals with temperature-dependent emission color

    NARCIS (Netherlands)

    Chin, P.T.K.; de Mello Donega, C.; van Bavel, S.S.; Meskers, S.C.J.; Sommerdijk, N.A.J.M.; Jansen, R.A.J.

    2007-01-01

    In this work we present the preparation of highly luminescent anisotropic CdTe/CdSe colloidal heteronanocrystals. The reaction conditions used (low temperature, slow precursor addition, and surfactant composition) resulted in a tunable shape from prolate to branched CdTe/CdSe nanocrystals. Upon CdSe

  6. Pu Sorption, Desorption and Intrinsic Colloid Stability under Granitic Chemical Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Pihong [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Zavarin, Mavrik [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Dai, Zurong [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kersting, Annie B. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2014-09-04

    This progress report (M4FT-14LL0807031) describes research conducted at LLNL as part of the Crystalline Repository effort within the UFD program. Part I describes the dissolution kinetics of intrinsic Pu colloids synthesized in an alkaline solution. Part II describes the morphology and dissolution characteristics of various forms of Pu oxides prepared over a range of solution and temperature conditions. Proposed FY15 activities are identified.

  7. High reduction of interfacial charge recombination in colloidal quantum dot solar cells by metal oxide surface passivation.

    Science.gov (United States)

    Chang, Jin; Kuga, Yuki; Mora-Seró, Iván; Toyoda, Taro; Ogomi, Yuhei; Hayase, Shuzi; Bisquert, Juan; Shen, Qing

    2015-03-12

    Bulk heterojunction (BHJ) solar cells based on colloidal QDs and metal oxide nanowires (NWs) possess unique and outstanding advantages in enhancing light harvesting and charge collection in comparison to planar architectures. However, the high surface area of the NW structure often brings about a large amount of recombination (especially interfacial recombination) and limits the open-circuit voltage in BHJ solar cells. This problem is solved here by passivating the surface of the metal oxide component in PbS colloidal quantum dot solar cells (CQDSCs). By coating thin TiO2 layers onto ZnO-NW surfaces, the open-circuit voltage and power conversion efficiency have been improved by over 40% in PbS CQDSCs. Characterization by transient photovoltage decay and impedance spectroscopy indicated that the interfacial recombination was significantly reduced by the surface passivation strategy. An efficiency as high as 6.13% was achieved through the passivation approach and optimization for the length of the ZnO-NW arrays (device active area: 16 mm2). All solar cells were tested in air, and exhibited excellent air storage stability (without any performance decline over more than 130 days). This work highlights the significance of metal oxide passivation in achieving high performance BHJ solar cells. The charge recombination mechanism uncovered in this work could shed light on the further improvement of PbS CQDSCs and/or other types of solar cells.

  8. 生物法制备纳米银溶胶的稳定性%Stability of Colloidal Silver Nanoparticles Prepared by Bioreduction

    Institute of Scientific and Technical Information of China (English)

    孙道华; 李清彪; 何宁; 黄加乐; 王惠璇

    2011-01-01

    利用生物还原法制备纳米银溶胶,借助于UV-Vis表征技术对其热稳定性和化学稳定性进行考察.结果表明:生物法制备的纳米银溶胶在100℃下加热6 h,UV-Vis谱图未发生明显变化;H+和具有高价阳离子的电解质对其稳定性的影响明显;OH-对银溶胶的稳定性影响相对较弱.生物法制备的纳米银溶胶在热稳定性、化学稳定性方面均略优于柠檬酸三钠法制得的银溶胶.%The thermal and chemical statoilities of the colloid silver nanoparticles prepared by bioreduction were investigated in virtue of UV-Vis spectrometer.The results indicate that UV-Vis spectra of silver colloid prepared by bioreduction have not significant change after heat treatment at 100 ℃ for 6 h.Hydrogen ion and the electrolyte with multivalent cation markedly influence stabilities of the silver colloid, while hydroxide anion has a weak influence on its stability.Thermal and chemical stabilities of the silver colloid prepared by bioreduction are superior to that of the silver colloid prepared by the sodium citrate reduction method.

  9. Pure colloidal metal and ceramic nanoparticles from high-power picosecond laser ablation in water and acetone.

    Science.gov (United States)

    Bärsch, Niko; Jakobi, Jurij; Weiler, Sascha; Barcikowski, Stephan

    2009-11-04

    The generation of colloids by laser ablation of solids in a liquid offers a nearly unlimited material variety and a high purity as no chemical precursors are required. The use of novel high-power ultra-short-pulsed laser systems significantly increases the production rates even in inflammable organic solvents. By applying an average laser power of 50 W and pulse durations below 10 ps, up to 5 mg min(-1) of nanoparticles have been generated directly in acetone, marking a breakthrough in productivity of ultra-short-pulsed laser ablation in liquids. The produced colloids remain stable for more than six months. In the case of yttria-stabilized zirconia ceramic, the nanoparticles retain the tetragonal crystal structure of the ablated target. Laser beam self-focusing plays an important role, as a beam radius change of 2% on the liquid surface can lead to a decrease of nanoparticle production rates of 90% if the target position is not re-adjusted.

  10. Improvement of kinetics, yield, and colloidal stability of biogenic gold nanoparticles using living cells of Euglena gracilis microalga

    Science.gov (United States)

    Dahoumane, Si Amar; Yéprémian, Claude; Djédiat, Chakib; Couté, Alain; Fiévet, Fernand; Coradin, Thibaud; Brayner, Roberta

    2016-03-01

    Recent years have witnessed a boom in the biosynthesis of a large variety of nanomaterials using different biological resources among which algae-based entities have been gaining much more attention within the community of material scientists worldwide. In our previously published findings, we explored some factors that governed the biofabrication of gold nanoparticles using living cultures of microalgae, such as the utilized microalgal genera, the phylum they belong to, and the impact of tetrachloroauric acid concentrations on the ability of these strains to perform the biosynthesis of gold nanoparticles once in contact with these cations. As a follow-up, we present in this paper an improvement of the features of bioproduced gold colloids using living cells of Euglena gracilis microalga when this species is grown under either mixotrophic or autotrophic conditions, i.e., exposed to light and grown in an organic carbon-enriched culture medium versus under autotrophic conditions. As an outcome to this alteration, the growth rate of this photosynthetic microorganism is multiplied 7-8 times when grown under mixotrophic conditions compared to autotrophic ones. Therefore, the yield, the kinetics, and the colloidal stability of the biosynthesized gold nanoparticles are dramatically enhanced. Moreover, the shape and the size of the as-produced nano-objects via this biological method are affected. In addition to round-shaped gold nanoparticles, particular shapes, such as triangles and hexagons, appear. These findings add up to the amassed knowledge toward the design of photobioreactors for the scalable and sustainable production of interesting nanomaterials.

  11. Efficient One-Pot Synthesis of Colloidal Zirconium Oxide Nanoparticles for High-Refractive-Index Nanocomposites.

    Science.gov (United States)

    Liu, Chao; Hajagos, Tibor Jacob; Chen, Dustin; Chen, Yi; Kishpaugh, David; Pei, Qibing

    2016-02-01

    Zirconium oxide nanoparticles are promising candidates for optical engineering, photocatalysis, and high-κ dielectrics. However, reported synthetic methods for the colloidal zirconium oxide nanoparticles use unstable alkoxide precursors and have various other drawbacks, limiting their wide application. Here, we report a facile one-pot method for the synthesis of colloidally stable zirconium oxide nanoparticles. Using a simple solution of zirconium trifluoroacetate in oleylamine, highly stable zirconium oxide nanoparticles have been synthesized with high yield, following a proposed amidization-assisted sol-gel mechanism. The nanoparticles can be readily dispersed in nonpolar solvents, forming a long-term stable transparent solution, which can be further used to fabricate high-refractive-index nanocomposites in both monolith and thin-film forms. In addition, the same method has also been extended to the synthesis of titanium oxide nanoparticles, demonstrating its general applicability to all group IVB metal oxide nanoparticles.

  12. Synthesis and characterization of colloidal fluorescent silver nanoclusters.

    Science.gov (United States)

    Huang, Sherry; Pfeiffer, Christian; Hollmann, Jana; Friede, Sebastian; Chen, Justin Jin-Ching; Beyer, Andreas; Haas, Benedikt; Volz, Kerstin; Heimbrodt, Wolfram; Montenegro Martos, Jose Maria; Chang, Walter; Parak, Wolfgang J

    2012-06-19

    Ultrasmall water-soluble silver nanoclusters are synthesized, and their properties are investigated. The silver nanoclusters have high colloidal stability and show fluorescence in the red. This demonstrates that like gold nanoclusters also silver nanoclusters can be fluorescent.

  13. Dynamic Colloidal Molecules Maneuvered by Light-Controlled Janus Micromotors.

    Science.gov (United States)

    Gao, Yirong; Mou, Fangzhi; Feng, Yizheng; Che, Shengping; Li, Wei; Xu, Leilei; Guan, Jianguo

    2017-07-12

    In this work, we propose and demonstrate a dynamic colloidal molecule that is capable of moving autonomously and performing swift, reversible, and in-place assembly dissociation in a high accuracy by manipulating a TiO2/Pt Janus micromotor with light irradiation. Due to the efficient motion of the TiO2/Pt Janus motor and the light-switchable electrostatic interactions between the micromotor and colloidal particles, the colloidal particles can be captured and assembled one by one on the fly, subsequently forming into swimming colloidal molecules by mimicking space-filling models of simple molecules with central atoms. The as-demonstrated dynamic colloidal molecules have a configuration accurately controlled and stabilized by regulating the time-dependent intensity of UV light, which controls the stop-and-go motion of the colloidal molecules. The dynamic colloidal molecules are dissociated when the light irradiation is turned off due to the disappearance of light-switchable electrostatic interaction between the motor and the colloidal particles. The strategy for the assembly of dynamic colloidal molecules is applicable to various charged colloidal particles. The simulated optical properties of a dynamic colloidal molecule imply that the results here may provide a novel approach for in-place building functional microdevices, such as microlens arrays, in a swift and reversible manner.

  14. Silver coated aluminium microrods as highly colloidal stable SERS platforms.

    Science.gov (United States)

    Pazos-Perez, Nicolas; Borke, Tina; Andreeva, Daria V; Alvarez-Puebla, Ramon A

    2011-08-01

    We report on the fabrication of a novel material with the ability to remain in solution even under the very demanding conditions required for structural and dynamic characterization of biomacromolecule assays. This stability is provided by the increase in surface area of a low density material (aluminium) natively coated with a very hydrophilic surface composed of aluminium oxide (Al(2)O(3)) and metallic silver nanoparticles. Additionally, due to the dense collection of active hot spots on their surface, this material offers higher levels of SERS intensity as compared with the same free and aggregated silver nanoparticles.

  15. Control of the PEO chain conformation on nanoparticles by adsorption of PEO-block-poly(L-lysine) copolymers and its significance on colloidal stability and protein repellency.

    Science.gov (United States)

    Louguet, Stéphanie; Kumar, Anitha C; Guidolin, Nicolas; Sigaud, Gilles; Duguet, Etienne; Lecommandoux, Sébastien; Schatz, Christophe

    2011-11-01

    The physical adsorption of PEO(n)-b-PLL(m) copolymers onto silica nanoparticles and the related properties of poly(ethylene oxide) (PEO)-coated particles were studied as a function of the block copolymer composition. Copolymers adopt an anchor-buoy conformation at the particle surface owing to a preferential affinity of poly(L-lysine) (PLL) blocks with the silica surface over PEO blocks when a large excess of copolymer is used. The interdistance between PEO chains at particle surface is highly dependent on the size of PLL segments; a dense brush of PEO is obtained for short PLL blocks (DP = 10), whereas PEO chains adopt a so-called interacting "mushroom" conformation for large PLL blocks (DP = 270). The size of the PEO blocks does not really influence the copolymer surface density, but it has a strong effect on the PEO layer thickness as expected. Salt and protein stability studies led to similar conclusions about the effectiveness of a PEO layer with a dense brush conformation to prevent colloidal aggregation and protein adsorption. Besides, a minimal PEO length is required to get full stabilization properties; as a matter of fact, both PEO(45)-b-PLL(10) and PEO(113)-b-PLL(10) give rise to a PEO brush conformation but only the latter copolymer efficiently stabilizes the particles in the presence of salt or proteins.

  16. Effect of polyethylene glycol conjugation on conformational and colloidal stability of a monoclonal antibody antigen-binding fragment (Fab').

    Science.gov (United States)

    Roque, Cristopher; Sheung, Anthony; Rahman, Nausheen; Ausar, S Fernando

    2015-02-01

    We have investigated the effects of site specific "hinge" polyethylene glycol conjugation (PEGylation) on thermal, pH, and colloidal stability of a monoclonal antibody antigen-binding fragment (Fab') using a variety of biophysical techniques. The results obtained by circular dichroism (CD), ultraviolet (UV) absorbance, and fluorescence spectroscopy suggested that the physical stability of the Fab' is maximized at pH 6-7 with no apparent differences due to PEGylation. Temperature-induced aggregation experiments revealed that PEGylation was able to increase the transition temperature, as well as prevent the formation of visible and subvisible aggregates. Statistical comparison of the three-index empirical phase diagram (EPD) revealed significant differences in thermal and pH stability signatures between Fab' and PEG-Fab'. Upon mechanical stress, micro-flow imaging (MFI) and measurement of the optical density at 360 nm showed that the PEG-Fab' had significantly higher resistance to surface-induced aggregation compared to the Fab'. Analysis of the interaction parameter, kD, indicated repulsive intermolecular forces for PEG-Fab' and attractive forces for Fab'. In conclusion, PEGylation appears to protect Fab' against thermal and mechanical stress-induced aggregation, likely due to a steric hindrance mechanism.

  17. Two-substrate vertical deposition for stable colloidal crystal chips

    Institute of Scientific and Technical Information of China (English)

    CHEN Xin; SUN Zhiqiang; CHEN Zhimin; ZHANG Kai; YANG Bai

    2005-01-01

    By combining vertical deposition with micromolding in capillaries method, we have demonstrated the two-substrate vertical deposition, an alternative and versatile procedure for fabricating high-quality stable colloidal crystal chips. Apparent bright colors, special UV-vis spectra, scanning electron microscopy (SEM) and atomic force microscopy (AFM) images all prove that high-quality colloidal crystal structures are formed in between the two substrates. During the two-substrate vertical deposition for colloidal crystal chips, capillary force and evaporation of the medium are critical to the formation of the colloidal crystals; while the confinement in between two close substrates makes the resulting colloidal crystal chips more stable. Due to the excellent stability, these colloidal crystal chips can be used to construct some composite optical devices via a simpler and more flexible process. Meanwhile, they can also be further used as the templates for ordered multiporous materials.

  18. EDITORIAL: Colloidal suspensions Colloidal suspensions

    Science.gov (United States)

    Petukhov, Andrei; Kegel, Willem; van Duijneveldt, Jeroen

    2011-05-01

    fluid-fluid interface [2]. Together with Remco Tuinier, Henk has recently completed a book in this area which is to appear later this year. A major theme in Henk's research is that of phase transitions in lyotropic liquid crystals. Henk, together with Daan Frenkel and Alain Stroobants, realized in the 1980s that a smectic phase in dispersions of rod-like particles can be stable without the presence of attractive interactions, similar to nematic ordering as predicted earlier by Onsager [3]. Together with Gert-Jan Vroege he wrote a seminal review in this area [4]. Henk once said that 'one can only truly develop one colloidal model system in one's career' and in his case this must be that of gibbsite platelets. Initially Henk's group pursued another polymorph of aluminium hydroxide, boehmite, which forms rod-like particles [5], which already displayed nematic liquid crystal phases. The real breakthrough came when the same precursors treated the produced gibbsite platelets slightly differently. These reliably form a discotic nematic phase [6] and, despite the polydispersity in their diameter, a columnar phase [7]. A theme encompassing a wide range of soft matter systems is that of colloidal dynamics and phase transition kinetics. Many colloidal systems have a tendency to get stuck in metastable states, such as gels or glasses. This is a nuisance if one wishes to study phase transitions, but it is of great practical significance. Such issues feature in many of Henk's publications, and with Valerie Anderson he wrote a highly cited review in this area [8]. Henk Lekkerkerker has also invested significant effort into the promotion of synchrotron radiation studies of colloidal suspensions. He was one of the great supporters of the Dutch-Belgian beamline 'DUBBLE' project at the ESRF [9]. He attended one of the very first experiments in Grenoble in 1999, which led to a Nature publication [7]. He was strongly involved in many other experiments which followed and also has been a

  19. Electrophoresis and stability of nano-colloids: history, theory and experimental examples.

    Science.gov (United States)

    Felix, C; Yaroshchuk, A; Pasupathi, S; Pollet, B G; Bondarenko, M P; Kovalchuk, V I; Zholkovskiy, E K

    2014-09-01

    The paper contains an extended historical overview of research activities focused on determining interfacial potential and charge of dispersed particles from electrophoretic and coagulation dynamic measurements. Particular attention is paid to nano-suspensions for which application of Standard Electrokinetic Model (SEM) to analysis of experimental data encounters difficulties, especially, when the solutions contain more than two ions, the particle charge depends on the solution composition and zeta-potentials are high. Detailed statements of Standard Electrokinetic and DLVO Models are given in the forms that are capable of addressing electrophoresis and interaction of particles for arbitrary ratios of the particle to Debye radius, interfacial potentials and electrolyte compositions. The experimental part of the study consists of two groups of measurements conducted for Pt/C nano-suspensions, namely, the electrophoretic and coagulation dynamic studies, with various electrolyte compositions. The obtained experimental data are processed by using numerical algorithms based on the formulated models for obtaining interfacial potential and charge. While analyzing the dependencies of interfacial potential and charge on the electrolyte compositions, conclusions are made regarding the mechanisms of charge formation. It is established that the behavior of system stability is in a qualitative agreement with the results computed from the electrophoretic data. The verification of quantitative applicability of the employed models is conducted by calculating the Hamaker constant from experimental data. It is proposed how to explain the observed variations of predicted Hamaker constant and its unusually high value.

  20. Green synthesis of highly concentrated aqueous colloidal solutions of large starch-stabilised silver nanoplatelets.

    Science.gov (United States)

    Cheng, Fei; Betts, Jonathan W; Kelly, Stephen M; Hector, Andrew L

    2015-01-01

    A simple, environmentally friendly and cost-effective method has been developed to prepare a range of aqueous silver colloidal solutions, using ascorbic acid as a reducing agent, water-soluble starch as a combined crystallising, stabilising and solubilising agent, and water as the solvent. The diameter of silver nanoplatelets increases with higher concentrations of AgNO3 and starch. The silver nanoparticles are also more uniform in shape the greater the diameter of the nanoparticles. Colloidal solutions with a very high concentration of large, flat, hexagonal silver nanoplatelets (~230 nm in breadth) have been used to deposit and fix an antibacterial coating of these large starch-stabilised silver nanoplates on commercial cotton fibres, using a simple dip-coating process using water as the solvent, in order to study the dependence of the antibacterial properties of these nanoplatelets on their size.

  1. Reproducible, high-throughput synthesis of colloidal nanocrystals for optimization in multidimensional parameter space.

    Science.gov (United States)

    Chan, Emory M; Xu, Chenxu; Mao, Alvin W; Han, Gang; Owen, Jonathan S; Cohen, Bruce E; Milliron, Delia J

    2010-05-12

    While colloidal nanocrystals hold tremendous potential for both enhancing fundamental understanding of materials scaling and enabling advanced technologies, progress in both realms can be inhibited by the limited reproducibility of traditional synthetic methods and by the difficulty of optimizing syntheses over a large number of synthetic parameters. Here, we describe an automated platform for the reproducible synthesis of colloidal nanocrystals and for the high-throughput optimization of physical properties relevant to emerging applications of nanomaterials. This robotic platform enables precise control over reaction conditions while performing workflows analogous to those of traditional flask syntheses. We demonstrate control over the size, size distribution, kinetics, and concentration of reactions by synthesizing CdSe nanocrystals with 0.2% coefficient of variation in the mean diameters across an array of batch reactors and over multiple runs. Leveraging this precise control along with high-throughput optical and diffraction characterization, we effectively map multidimensional parameter space to tune the size and polydispersity of CdSe nanocrystals, to maximize the photoluminescence efficiency of CdTe nanocrystals, and to control the crystal phase and maximize the upconverted luminescence of lanthanide-doped NaYF(4) nanocrystals. On the basis of these demonstrative examples, we conclude that this automated synthesis approach will be of great utility for the development of diverse colloidal nanomaterials for electronic assemblies, luminescent biological labels, electroluminescent devices, and other emerging applications.

  2. Colloidal stability of carbonate-coated silver nanoparticles in synthetic and natural freshwater.

    Science.gov (United States)

    Piccapietra, Flavio; Sigg, Laura; Behra, Renata

    2012-01-17

    To gain important information on fate, mobility, and bioavailability of silver nanoparticles (AgNP) in aquatic systems, the influence of pH, ionic strength, and humic substances on the stability of carbonate-coated AgNP (average diameter 29 nm) was systematically investigated in 10 mM carbonate and 10 mM MOPS buffer, and in filtered natural freshwater. Changes in the physicochemical properties of AgNP were measured using nanoparticle tracking analysis, dynamic light scattering, and ultraviolet-visible spectroscopy. According to the pH-dependent carbonate speciation, below pH 4 the negatively charged surface of AgNP became positive and increased agglomeration was observed. Electrolyte concentrations above 2 mM Ca(2+) and 100 mM Na(+) enhanced AgNP agglomeration in the synthetic media. In the considered concentration range of humic substances, no relevant changes in the AgNP agglomeration state were measured. Agglomeration of AgNP exposed in filtered natural freshwater was observed to be primarily controlled by the electrolyte type and concentration. Moreover, agglomerated AgNP were still detected after 7 days of exposure. Consequently, slow sedimentation and high mobility of agglomerated AgNP could be expected under the considered natural conditions. A critical evaluation of the different methods used is presented as well.

  3. Colloid Release from Soil Aggregates

    DEFF Research Database (Denmark)

    Vendelboe, Anders Lindblad; Møldrup, Per; Schjønning, Per;

    2012-01-01

    The content of water-dispersible colloids (WDC) has a major impact on soil functions and structural stability. In addition, the presence of mobile colloids may increase the risk of colloid-facilitated transport of strongly sorbing environmental contaminants. The WDC content was measured in 39 soils......, using laser diffraction, by agitating the samples using a wet-dispersion unit. This approach eliminated the need for long sedimentation times required by the more classical end-over-end shaking approach and provided information about the time-dependent release of WDC. The total clay content of the soils...... ranged from 0.1 to 0.44 kg kg−1. The WDC content was measured on air-dry and moist 1- to 2-mm aggregates. The WDC content at a reference time was highly correlated to the total clay content (r > 0.91, P soils. Only for two sites was the WDC content correlated to the content of clay...

  4. Life at ultralow interfacial tension: Wetting, waves and droplets in demixed colloid-polymer mixtures

    NARCIS (Netherlands)

    Lekkerkerker, H.N.W.; de Villeneuve, V.W.A.; de Folter, J.W.J.; Schmidt, M.; Hennequin, Y.; Bonn, D.; Indekeu, J.O.; Aarts, D.G.A.L.

    2008-01-01

    Mixtures of colloids and polymers display a rich phase behavior, involving colloidal gas (rich in polymer, poor in colloid), colloidal liquid (poor in polymer, rich in colloid) and colloidal crystal phases (poor in polymer, highly ordered colloids). Recently, the colloidal gas-colloidal liquid inter

  5. Life at ultralow interfacial tension: wetting, waves and droplets in demixed colloid-polymer mixtures

    NARCIS (Netherlands)

    Lekkerkerker, H.N.W.; de Villeneuve, V.W.A.; de Folter, J.W.J.; Schmidt, M.; Hennequin, Y.; Bonn, D.; Indekeu, J.O.; Aarts, D.G.A.L.

    2008-01-01

    Mixtures of colloids and polymers display a rich phase behavior, involving colloidal gas (rich in polymer, poor in colloid), colloidal liquid (poor in polymer, rich in colloid) and colloidal crystal phases (poor in polymer, highly ordered colloids). Recently, the colloidal gas-colloidal liquid inter

  6. In situ growth of hollow gold-silver nanoshells within porous silica offers tunable plasmonic extinctions and enhanced colloidal stability.

    Science.gov (United States)

    Li, Chien-Hung; Jamison, Andrew C; Rittikulsittichai, Supparesk; Lee, Tai-Chou; Lee, T Randall

    2014-11-26

    Porous silica-coated hollow gold-silver nanoshells were successfully synthesized utilizing a procedure where the porous silica shell was produced prior to the transformation of the metallic core, providing enhanced control over the structure/composition of the bimetallic hollow core. By varying the reaction time and the precise amount of gold salt solution added to a porous silica-coated silver-core template solution, composite nanoparticles were tailored to reveal a readily tunable surface plasmon resonance that could be centered across the visible and near-IR spectral regions (∼445-800 nm). Characterization by X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy, scanning electron microscopy, and transmission electron microscopy revealed that the synthetic methodology afforded particles having uniform composition, size, and shape. The optical properties were evaluated by absorption/extinction spectroscopy. The stability of colloidal solutions of our composite nanoparticles as a function of pH was also investigated, revealing that the nanoshells remain intact over a wide range of conditions (i.e., pH 2-10). The facile tunability, enhanced stability, and relatively small diameter of these composite particles (∼110 nm) makes them promising candidates for use in tumor ablation or as photothermal drug-delivery agents.

  7. The Structure-Function Relationship of Polymeric Sorbents for Colloid Stabilization of Beer

    OpenAIRE

    Basarova, Gabriela

    1990-01-01

    This review considers the research relating to the formation of non-biological haze in beer. The basic information regarding mutual interactions of haze-causing substances with precipitating, enzymatic, and adsorptive stabilizers of beer is discu ssed. The main haze-causing compounds in beer are polypeptides and polyphenols. To reduce the levels of these compounds in beer, adsorptive stabilizing agents are usually used during filt ration. Electron microscopy and methods measuring the surface ...

  8. High reduction of interfacial charge recombination in colloidal quantum dot solar cells by metal oxide surface passivation

    Science.gov (United States)

    Chang, Jin; Kuga, Yuki; Mora-Seró, Iván; Toyoda, Taro; Ogomi, Yuhei; Hayase, Shuzi; Bisquert, Juan; Shen, Qing

    2015-03-01

    Bulk heterojunction (BHJ) solar cells based on colloidal QDs and metal oxide nanowires (NWs) possess unique and outstanding advantages in enhancing light harvesting and charge collection in comparison to planar architectures. However, the high surface area of the NW structure often brings about a large amount of recombination (especially interfacial recombination) and limits the open-circuit voltage in BHJ solar cells. This problem is solved here by passivating the surface of the metal oxide component in PbS colloidal quantum dot solar cells (CQDSCs). By coating thin TiO2 layers onto ZnO-NW surfaces, the open-circuit voltage and power conversion efficiency have been improved by over 40% in PbS CQDSCs. Characterization by transient photovoltage decay and impedance spectroscopy indicated that the interfacial recombination was significantly reduced by the surface passivation strategy. An efficiency as high as 6.13% was achieved through the passivation approach and optimization for the length of the ZnO-NW arrays (device active area: 16 mm2). All solar cells were tested in air, and exhibited excellent air storage stability (without any performance decline over more than 130 days). This work highlights the significance of metal oxide passivation in achieving high performance BHJ solar cells. The charge recombination mechanism uncovered in this work could shed light on the further improvement of PbS CQDSCs and/or other types of solar cells.Bulk heterojunction (BHJ) solar cells based on colloidal QDs and metal oxide nanowires (NWs) possess unique and outstanding advantages in enhancing light harvesting and charge collection in comparison to planar architectures. However, the high surface area of the NW structure often brings about a large amount of recombination (especially interfacial recombination) and limits the open-circuit voltage in BHJ solar cells. This problem is solved here by passivating the surface of the metal oxide component in PbS colloidal quantum dot solar

  9. Structure, stability, and formation pathways of colloidal gels in systems with short-range attraction and long-range repulsion.

    Science.gov (United States)

    van Schooneveld, Matti M; de Villeneuve, Volkert W A; Dullens, Roel P A; Aarts, Dirk G A L; Leunissen, Mirjam E; Kegel, Willem K

    2009-04-09

    We study colloidal gels formed upon centrifugation of dilute suspensions of spherical colloids (radius 446 nm) that interact through a long-range electrostatic repulsion (Debye length approximately 850 nm) and a short-range depletion attraction (approximately 12.5 nm), by means of confocal scanning laser microscopy (CSLM). In these systems, at low colloid densities, colloidal clusters are stable. Upon increasing the density by centrifugation, at different stages of cluster formation, we show that colloidal gels are formed that significantly differ in structure. While significant single-particle displacements do not occur on the hour time scale, the different gels slowly evolve within several weeks to a similar structure that is at least stable for over a year. Furthermore, while reference systems without long-range repulsion collapse into dense glassy states, the repulsive colloidal gels are able to support external stress in the form of a centrifugal field of at least 9g.

  10. Lysozyme adsorption on the colloidal chromium(III) oxide surface: Its impact on the system stability

    Energy Technology Data Exchange (ETDEWEB)

    Szewczuk-Karpisz, Katarzyna, E-mail: k.szewczuk-karpisz@wp.pl; Wiśniewska, Małgorzata; Myśliwiec, Dawid

    2015-08-30

    Highlights: • Lysozyme adsorption mechanism on the chromium(III) oxide surface was determined. • Surface charge density as well as zeta potential of Cr{sub 2}O{sub 3} particles were measured. • Turbidimetric method was used to estimate the suspension stability. • Depending on the pH value, lysozyme increases or decreases the system stability. - Abstract: This paper describes the lysozyme (LSZ) presence effect on the chromium(III) oxide (Cr{sub 2}O{sub 3}) suspension stability. First, the electrokinetic properties of the examined system, i.e. surface charge density and zeta potential of solid particles in the absence and presence of LSZ, were determined. The lysozyme addition reduces the metal oxide surface charge, which may be related to the interaction of the LSZ protonated amino groups with the adsorbent surface moieties. The LSZ macromolecules undergo adsorption on the Cr{sub 2}O{sub 3} surface only under electrostatic attraction. At the LSZ concentrations above 50 ppm the macromolecules cover completely the particle surface, which is evidenced by the observed zeta potential values. The LSZ influence on the Cr{sub 2}O{sub 3} suspension stability depends on the solution pH value. At pH 3, 4.6 and 7.6, the LSZ addition improves the system stability. In turn, at pH 9 it is associated with the slight suspension destabilization.

  11. Enhancing the stability of colloidal silver nanoparticles using polyhydroxyalkanoates (PHA) from Bacillus circulans (MTCC 8167) isolated from crude oil contaminated soil.

    Science.gov (United States)

    Phukon, Pinkee; Saikia, Jyoti Prasad; Konwar, Bolin Kumar

    2011-09-01

    Polyhydroxyalkanoate (PHA) was produced by growing Bacillus circulans (MTCC 8167) in the specific detection medium. The identification of the polymer as PHA was confirmed by fluorescence microscopy. The PHA was purified and characterized using FT-IR. The silver nanoparticles (SNP) were synthesized from AgNO3 in the dispersed colloids of PHA (0.085%) using NaBH4 (sodium borohydrate as reducing agent). The stability was tested using wave length scanning with a UV-Vis spectrophotometer and finally with transmission electron microscopy. The PHA stabilized solution was found to be stable for 30 days as against the low stability of silver nanoparticles (SNP) solution alone.

  12. LABORATORY STUDIES ON THE STABILITY AND TRANSPORT OF INORGANIC COLLOIDS THROUGH NATURAL AQUIFER MATERIAL

    Science.gov (United States)

    The stability and transport of radio-labeled Fe2O3 particles were studied using laboratory batch and column techniques. Core material collected from shallow sand and gravel aquifer was used as the immobile column matrix material. Variables in the study included flow rate, pH, i...

  13. Colloidal Properties and Stability of Graphene Oxide Nanomaterials in the Aquatic Environment

    Science.gov (United States)

    While graphene oxide (GO) has been found to be the most toxic graphene-based nanomaterial, its environmental fate is still unexplored. In this study, the aggregation kinetics and stability of GO were investigated using time-resolved dynamic light scattering over a wide range of a...

  14. Influence of Temperature on the Colloidal Stability of Polymer-Coated Gold Nanoparticles in Cell Culture Media.

    Science.gov (United States)

    Zyuzin, Mikhail V; Honold, Tobias; Carregal-Romero, Susana; Kantner, Karsten; Karg, Matthias; Parak, Wolfgang J

    2016-04-06

    The temperature-dependence of the hydrodynamic diameter and colloidal stability of gold-polymer core-shell particles with temperature-sensitive (poly(N-isopropylacrylamide)) and temperature-insensitive shells (polyallylaminine hydrochloride/polystyrensulfonate, poly(isobutylene-alt-maleic anhydride)-graft-dodecyl) are investigated in various aqueous media. The data demonstrate that for all nanoparticle agglomeration, i.e., increase in effective nanoparticle size, the presence of salts or proteins in the dispersion media has to be taken into account. Poly(N-isopropylacrylamide) coated nanoparticles show a reversible temperature-dependent increase in size above the volume phase transition of the polymer shell when they are dispersed in phosphate buffered saline or in media containing protein. In contrast, the nanoparticles coated with temperature-insensitive polymers show a time-dependent increase in size in phosphate buffered saline or in medium containing protein. This is due to time-dependent agglomeration, which is particularly strong in phosphate buffered saline, and induces a time-dependent, irreversible increase in the hydrodynamic diameter of the nanoparticles. This demonstrates that one has to distinguish between temperature- and time-induced agglomerations. Since the size of nanoparticles regulates their uptake by cells, temperature-dependent uptake of thermosensitive and non-thermosensitive nanoparticles by cells lines is compared. No temperature-specific difference between both types of nanoparticles could be observed.

  15. A Highly Efficient Hybrid GaAs Solar Cell Based on Colloidal-Quantum-Dot-Sensitization

    Science.gov (United States)

    Han, Hau-Vei; Lin, Chien-Chung; Tsai, Yu-Lin; Chen, Hsin-Chu; Chen, Kuo-Ju; Yeh, Yun-Ling; Lin, Wen-Yi; Kuo, Hao-Chung; Yu, Peichen

    2014-07-01

    This paper presents a hybrid design, featuring a traditional GaAs-based solar cell combined with various colloidal quantum dots. This hybrid design effectively boosts photon harvesting at long wavelengths while enhancing the collection of photogenerated carriers in the ultraviolet region. The merits of using highly efficient semiconductor solar cells and colloidal quantum dots were seamlessly combined to increase overall power conversion efficiency. Several photovoltaic parameters, including short-circuit current density, open circuit voltage, and external quantum efficiency, were measured and analyzed to investigate the performance of this hybrid device. Offering antireflective features at long wavelengths and luminescent downshifting for high-energy photons, the quantum dots effectively enhanced overall power conversion efficiency by as high as 24.65% compared with traditional GaAs-based devices. The evolution of weighted reflectance as a function of the dilution factor of QDs was investigated. Further analysis of the quantum efficiency response showed that the luminescent downshifting effect can be as much as 6.6% of the entire enhancement of photogenerated current.

  16. Colloidal Covalent Organic Frameworks

    Science.gov (United States)

    2017-01-01

    Covalent organic frameworks (COFs) are two- or three-dimensional (2D or 3D) polymer networks with designed topology and chemical functionality, permanent porosity, and high surface areas. These features are potentially useful for a broad range of applications, including catalysis, optoelectronics, and energy storage devices. But current COF syntheses offer poor control over the material’s morphology and final form, generally providing insoluble and unprocessable microcrystalline powder aggregates. COF polymerizations are often performed under conditions in which the monomers are only partially soluble in the reaction solvent, and this heterogeneity has hindered understanding of their polymerization or crystallization processes. Here we report homogeneous polymerization conditions for boronate ester-linked, 2D COFs that inhibit crystallite precipitation, resulting in stable colloidal suspensions of 2D COF nanoparticles. The hexagonal, layered structures of the colloids are confirmed by small-angle and wide-angle X-ray scattering, and kinetic characterization provides insight into the growth process. The colloid size is modulated by solvent conditions, and the technique is demonstrated for four 2D boronate ester-linked COFs. The diameter of individual COF nanoparticles in solution is monitored and quantified during COF growth and stabilization at elevated temperature using in situ variable-temperature liquid cell transmission electron microscopy imaging, a new characterization technique that complements conventional bulk scattering techniques. Solution casting of the colloids yields a free-standing transparent COF film with retained crystallinity and porosity, as well as preferential crystallite orientation. Collectively this structural control provides new opportunities for understanding COF formation and designing morphologies for device applications. PMID:28149954

  17. Colloidal Covalent Organic Frameworks.

    Science.gov (United States)

    Smith, Brian J; Parent, Lucas R; Overholts, Anna C; Beaucage, Peter A; Bisbey, Ryan P; Chavez, Anton D; Hwang, Nicky; Park, Chiwoo; Evans, Austin M; Gianneschi, Nathan C; Dichtel, William R

    2017-01-25

    Covalent organic frameworks (COFs) are two- or three-dimensional (2D or 3D) polymer networks with designed topology and chemical functionality, permanent porosity, and high surface areas. These features are potentially useful for a broad range of applications, including catalysis, optoelectronics, and energy storage devices. But current COF syntheses offer poor control over the material's morphology and final form, generally providing insoluble and unprocessable microcrystalline powder aggregates. COF polymerizations are often performed under conditions in which the monomers are only partially soluble in the reaction solvent, and this heterogeneity has hindered understanding of their polymerization or crystallization processes. Here we report homogeneous polymerization conditions for boronate ester-linked, 2D COFs that inhibit crystallite precipitation, resulting in stable colloidal suspensions of 2D COF nanoparticles. The hexagonal, layered structures of the colloids are confirmed by small-angle and wide-angle X-ray scattering, and kinetic characterization provides insight into the growth process. The colloid size is modulated by solvent conditions, and the technique is demonstrated for four 2D boronate ester-linked COFs. The diameter of individual COF nanoparticles in solution is monitored and quantified during COF growth and stabilization at elevated temperature using in situ variable-temperature liquid cell transmission electron microscopy imaging, a new characterization technique that complements conventional bulk scattering techniques. Solution casting of the colloids yields a free-standing transparent COF film with retained crystallinity and porosity, as well as preferential crystallite orientation. Collectively this structural control provides new opportunities for understanding COF formation and designing morphologies for device applications.

  18. Surface speciation of myo-inositol hexakisphosphate adsorbed on TiO{sub 2} nanoparticles and its impact on their colloidal stability in aqueous suspension: A comparative study with orthophosphate

    Energy Technology Data Exchange (ETDEWEB)

    Wan, Biao; Yan, Yupeng; Liu, Fan; Tan, Wenfeng; He, Jiajie; Feng, Xionghan, E-mail: fxh73@mail.hzau.edu.cn

    2016-02-15

    Despite extensive research demonstrating the influence of organic matter and inorganic phosphate on the stability of TiO{sub 2} nanoparticles (NPs), far less research has assessed the impact of myo-inositol hexakisphosphate (IHP), a common organic phosphate widely present in the environment. In this study, the adsorption of IHP on TiO{sub 2} NPs and its impact on their colloidal stability were investigated using batch experiments, dynamic light scattering (DLS) techniques, in situ attenuated total reflectance Fourier transform infrared (ATR-FTIR) and solid-state {sup 31}P nuclear magnetic resonance (NMR) spectroscopy. Inorganic orthophosphate (P{sub i}) adsorption was run for comparison. The ratio of the P{sub i}/IHP adsorption density (1.528: 0.453) at pH 5.0 suggested that IHP may complex on the TiO{sub 2} surface through three of its six phosphate groups. Zeta potential measurements, ATR-FTIR and NMR spectra indicated that IHP/P{sub i} adsorbed onto TiO{sub 2} NPs by forming inner-sphere complexes and modified the surface charge of these NPs, which exerted a great impact on their colloidal stability. Interactions between NPs measured by sedimentation and aggregation size highly depended on the pH, surface phosphorus coverage, and surface phosphorus species. The impact of IHP on the aggregation and dispersion of TiO{sub 2} NPs was significantly larger than that of P{sub i}, in agreement with the calculation from the DLVO theory. This study highlighted the impact of IHP relative to P{sub i} on the colloidal stability of TiO{sub 2} NPs in phosphorus-enriched environments. - Highlights: • IHP/P{sub i} plays a significant role in the colloidal stability of TiO{sub 2} NPs. • The effect of IHP is much greater than P{sub i}. • TiO{sub 2} surface charge is modified by the formed inner-sphere P complexes. • IHP binds on TiO{sub 2} by 3 of its 6 P groups leaving the other 3 dissociated and ionized. • Interaction between NPs depends on pH, surface P coverage, and

  19. Colloidal Thermal Fluids

    Science.gov (United States)

    Lotzadeh, Saba

    In this dissertation, a reversible system with a well controlled degree of particle aggregation was developed. By surface modification of colloidal silica with aminosilanes, interactions among the particles were tuned in a controlled way to produce stable sized clusters at different pH values ranges from well-disposed to a colloidal gel. N-[3-(trimethoxysilyl)propyl]ethylenediamine (TMPE) monolayer on particle surface not only removes all the reactive sites to prevent chemical aggregation, also provides steric stabilization in the absence of any repulsion. After surface modification, electrokinetic behavior of silica particles were changed to that of amino groups, positive in acidic pH and neutral at basic pH values. By tuning the pH, the balance between electrostatic repulsion and hydrophobic interactions was reversibly controlled. As a result, clusters with different sizes were developed. The effect of clustering on the thermal conductivity of colloidal dispersions was quantified using silane-treated silica, a system engineered to exhibit reversible clustering under well-controlled conditions. Thermal conductivity of this system was measured by transient hot wire, the standard method of thermal conductivity measurements in liquids. We show that the thermal conductivity increases monotonically with cluster size and spans the entire range between the two limits of Maxwell's theory. The results, corroborated by numerical simulation, demonstrate that large increases of the thermal conductivity of colloidal dispersions are possible, yet fully within the predictions of classical theory. Numerical calculations were performed to evaluate the importance of structural properties of particles/aggregates on thermal conduction in colloidal particles. Thermal conductivity of non-spherical particles including hollow particles, cubic particles and rods was studied using a Monte Carlo algorithm. We show that anisotropic shapes, increase conductivity above that of isotropic

  20. Synthesis of nanosized silver colloids by microwave dielectric heating

    Indian Academy of Sciences (India)

    Kirti Patel; Sudhir Kapoor; D P Dave; Tulsi Mukherjee

    2005-01-01

    Silver nanosized crystallites have been synthesized in aqueous and polyols viz., ethylene glycol and glycerol, using a microwave technique. Dispersions of colloidal silver have been prepared by the reduction of silver nitrate both in the presence and absence of stabilizer poly(vinylpyrolidone) (PVP). It was observed that PVP is capable of complexing and stabilizing Ag nanoparticles formed through the reduction of Ag+ ions in water and ethylene glycol. In the case of ethylene glycol, it has been shown that the use of PVP leads to particles with a high degree of stability. The colloids are stable in glycerol for months even in the absence of stabilizer.

  1. Dendronization-induced phase-transfer, stabilization and self-assembly of large colloidal Au nanoparticles

    Science.gov (United States)

    Malassis, Ludivine; Jishkariani, Davit; Murray, Christopher B.; Donnio, Bertrand

    2016-07-01

    The phase-transfer of CTAB-coated aqueous, spherical gold nanoparticles, with metallic core diameters ranging from ca. 27 to 54 nm, into organic solvents by exchanging the primitive polar bilayer with lipophilic, disulfide dendritic ligands is reported. The presence of such a thick nonpolar organic shell around these large nanoparticles enhances their stabilization against aggregation, in addition to enabling their transfer into a variety of solvents such as chloroform, toluene or tetrahydrofuran. Upon the slow evaporation of a chloroform suspension deposited on a solid support, the dendronized hybrids were found to self-assemble into ring structures of various diameters. Moreover, their self-assembly at the liquid-air interface affords the formation of fairly long-range ordered monolayers, over large areas, that can then be entirely transferred onto solid substrates.The phase-transfer of CTAB-coated aqueous, spherical gold nanoparticles, with metallic core diameters ranging from ca. 27 to 54 nm, into organic solvents by exchanging the primitive polar bilayer with lipophilic, disulfide dendritic ligands is reported. The presence of such a thick nonpolar organic shell around these large nanoparticles enhances their stabilization against aggregation, in addition to enabling their transfer into a variety of solvents such as chloroform, toluene or tetrahydrofuran. Upon the slow evaporation of a chloroform suspension deposited on a solid support, the dendronized hybrids were found to self-assemble into ring structures of various diameters. Moreover, their self-assembly at the liquid-air interface affords the formation of fairly long-range ordered monolayers, over large areas, that can then be entirely transferred onto solid substrates. Electronic supplementary information (ESI) available: TEM microscope images. See DOI: 10.1039/c6nr03404g

  2. Colloidal organization

    CERN Document Server

    Okubo, Tsuneo

    2015-01-01

    Colloidal Organization presents a chemical and physical study on colloidal organization phenomena including equilibrium systems such as colloidal crystallization, drying patterns as an example of a dissipative system and similar sized aggregation. This book outlines the fundamental science behind colloid and surface chemistry and the findings from the author's own laboratory. The text goes on to discuss in-depth colloidal crystallization, gel crystallization, drying dissipative structures of solutions, suspensions and gels, and similar-sized aggregates from nanosized particles. Special emphas

  3. Crosslinking to enhance colloidal stability and redispersity of layered double hydroxide nanoparticles.

    Science.gov (United States)

    Zuo, Huali; Gu, Zi; Cooper, Helen; Xu, Zhi Ping

    2015-12-01

    This article introduces a strategy for stabilizing and redispersing layered double hydroxide (LDH) nanoparticles by crosslinking bovine serum albumin (BSA) coated onto the surface. The strategy involves optimization of the amount of the crosslinking agent glutaraldehyde (GTA) to achieve minimal aggregation and ready redispersion. LDH nanoparticles were prepared by co-precipitation and hydrothermal treatment, with subsequent BSA coating at the BSA/LDH mass ratio of 5:2. BSA coated onto LDH nanoparticles was crosslinked with different amounts of GTA. Aggregation studies using dilution assays, dynamic light scattering, and zeta potential analysis indicated that severe aggregation at lower LDH nanoparticle concentrations can be prevented by proper crosslinking of BSA with GTA. The GTA-crosslinked BSA-coated nanoparticles showed excellent redispersity compared to the non-crosslinked nanoparticles. In vitro cytotoxicity and cell uptake were found to be minimally affected by GTA-crosslinking. The new strategy therefore provides a much more effective method for the prevention of LDH nanoparticle aggregation and improved LDH nanoparticle redispersion for use in a wide variety of bio-applications in vitro and in vivo.

  4. Influence of Nanoscale Surface Roughness on Colloidal Force Measurements.

    Science.gov (United States)

    Zou, Yi; Jayasuriya, Sunil; Manke, Charles W; Mao, Guangzhao

    2015-09-29

    Forces between colloidal particles determine the performances of many industrial processes and products. Colloidal force measurements conducted between a colloidal particle AFM probe and particles immobilized on a flat substrate are valuable in selecting appropriate surfactants for colloidal stabilization. One of the features of inorganic fillers and extenders is the prevalence of rough surfaces-even the polymer latex particles, often used as model colloidal systems including the current study, have rough surfaces albeit at a much smaller scale. Surface roughness is frequently cited as the reason for disparity between experimental observations and theoretical treatment but seldom verified by direct evidence. This work reports the effect of nanoscale surface roughness on colloidal force measurements carried out in the presence of surfactants. We applied a heating method to reduce the mean surface roughness of commercial latex particles from 30 to 1 nm. We conducted force measurements using the two types of particles at various salt and surfactant concentrations. The surfactants used were pentaethylene glycol monododecyl ether, Pluronic F108, and a styrene/acrylic copolymer, Joncryl 60. In the absence of the surfactant, nanometer surface roughness affects colloidal forces only in high salt conditions when the Debye length becomes smaller than the surface roughness. The adhesion is stronger between colloids with higher surface roughness and requires a higher surfactant concentration to be eliminated. The effect of surface roughness on colloidal forces was also investigated as a function of the adsorbed surfactant layer structure characterized by AFM indentation and dynamic light scattering. We found that when the layer thickness exceeds the surface roughness, the colloidal adhesion is less influenced by surfactant concentration variation. This study demonstrates that surface roughness at the nanoscale can influence colloidal forces significantly and should be taken

  5. [Toxicological evaluation of colloidal nano-sized silver stabilized polyvinylpyrrolidone. III. Enzymological, biochemical markers, state of antioxidant defense system].

    Science.gov (United States)

    Gmoshinsky, I V; Shipelin, V A; Vorozhko, I V; Sentsova, T B; Soto, S Kh; Avren'eva, L I; Guseva, G V; Kravchenko, L V; Khotimchenko, S A; Tutelyan, V A

    2016-01-01

    Nanosized colloidal silver (NCS) with primary nanoparticles (NPs) size in the range of 10-80 nm in aqueous suspension was administered to rats with initial weight 80±10 gfor the first 30 day intragastrically and for lasting 62 days with the diet consumed in doses of 0.1; 1.0 and 10 mg/kg of body weight b.w) per day based on silver (Ag). The control animals received deionized water and carrier of NPs - aqueous solution of stabilizer polyvinylpyrrolidone. Activity (Vmax) was determined in liver of microsomal mixed function monooxygenase isoforms CYP 1A1, 1A2 and 2B1 against their specific substrates, the activity of liver conjugating enzymes (glutathione-S-transferase and UDP-glucuronosyltransferase) in the microsomal fraction and a cytosol, and the overall and non-sedimentable activities of lysosomal hydrolases. In blood plasma there were evaluated malonic dialdehyde, PUFA diene conjugates, in erythrocytes - the activity of antioxidant enzymes. A set of standard biochemical indicators of blood serum was also determined. The studies revealed changes in a number of molecular markers of toxic action. Among them - the increase in the activity of key enzymes I and II stages of detoxification of xenobiotics, indicating its functional overvoltage; reducing the activity of glutathione peroxidase (GP), the total arylsulfatase A and B, β-galactosidase (in the absence of changes in their non-sedimentable activity), levels of uric acid, increased alkaline phosphatase activity. These changes occurred mainly at the dose Ag of 10 mg/kg b.w., except for the GP to which the threshold dose was 1 mg/kg b.w. No significant changes in the studied markers in a dose Ag 0,1 mg/kg b.w. were identified. Possible mechanisms of the toxic action of silver NPs are discussed.

  6. Thermal Stability and Anisotropic Sublimation of Two-Dimensional Colloidal Bi2Te3 and Bi2Se3 Nanocrystals.

    Science.gov (United States)

    Buha, Joka; Gaspari, Roberto; Del Rio Castillo, Antonio Esau; Bonaccorso, Francesco; Manna, Liberato

    2016-07-13

    The structural and compositional stabilities of two-dimensional (2D) Bi2Te3 and Bi2Se3 nanocrystals, produced by both colloidal synthesis and by liquid phase exfoliation, were studied by in situ transmission electron microscopy (TEM) during annealing at temperatures between 350 and 500 °C. The sublimation process induced by annealing is structurally and chemically anisotropic and takes place through the preferential dismantling of the prismatic {011̅0} type planes, and through the preferential sublimation of Te (or Se). The observed anisotropic sublimation is independent of the method of nanocrystal's synthesis, their morphology, or the presence of surfactant molecules on the nanocrystals surface. A thickness-dependent depression in the sublimation point has been observed with nanocrystals thinner than about 15 nm. The Bi2Se3 nanocrystals were found to sublimate below 280 °C, while the Bi2Te3 ones sublimated at temperatures between 350 and 450 °C, depending on their thickness, under the vacuum conditions in the TEM column. Density functional theory calculations confirm that the sublimation of the prismatic {011̅0} facets is more energetically favorable. Within the level of modeling employed, the sublimation occurs at a rate about 700 times faster than the sublimation of the {0001} planes at the annealing temperatures used in this work. This supports the distinctly anisotropic mechanisms of both sublimation and growth of Bi2Te3 and Bi2Se3 nanocrystals, known to preferentially adopt a 2D morphology. The anisotropic sublimation behavior is in agreement with the intrinsic anisotropy in the surface free energy brought about by the crystal structure of Bi2Te3 or Bi2Se3.

  7. Hybrid halide perovskite solar cell precursors: colloidal chemistry and coordination engineering behind device processing for high efficiency.

    Science.gov (United States)

    Yan, Keyou; Long, Mingzhu; Zhang, Tiankai; Wei, Zhanhua; Chen, Haining; Yang, Shihe; Xu, Jianbin

    2015-04-01

    The precursor of solution-processed perovskite thin films is one of the most central components for high-efficiency perovskite solar cells. We first present the crucial colloidal chemistry visualization of the perovskite precursor solution based on analytical spectra and reveal that perovskite precursor solutions for solar cells are generally colloidal dispersions in a mother solution, with a colloidal size up to the mesoscale, rather than real solutions. The colloid is made of a soft coordination complex in the form of a lead polyhalide framework between organic and inorganic components and can be structurally tuned by the coordination degree, thereby primarily determining the basic film coverage and morphology of deposited thin films. By utilizing coordination engineering, particularly through employing additional methylammonium halide over the stoichiometric ratio for tuning the coordination degree and mode in the initial colloidal solution, along with a thermal leaching for the selective release of excess methylammonium halides, we achieved full and even coverage, the preferential orientation, and high purity of planar perovskite thin films. We have also identified that excess organic component can reduce the colloidal size of and tune the morphology of the coordination framework in relation to final perovskite grains and partial chlorine substitution can accelerate the crystalline nucleation process of perovskite. This work demonstrates the important fundamental chemistry of perovskite precursors and provides genuine guidelines for accurately controlling the high quality of hybrid perovskite thin films without any impurity, thereby delivering efficient planar perovskite solar cells with a power conversion efficiency as high as 17% without distinct hysteresis owing to the high quality of perovskite thin films.

  8. Preparation of high dispersion and high performance PtRu/CNTs catalyst by an organic colloid method

    Institute of Scientific and Technical Information of China (English)

    王宁卡特; 刘军民; 廖世军; V.Birss

    2006-01-01

    A high dispersion and high performance PtRu catalyst supported on carbon nanotubes was prepared by an organic colloid method. The particle size of the active components could be as small as 1.0 nm,the active surface area was about 466 m2/g(Pt). The catalytic activity toward anodic oxidation of methanol was about 3 ~ 4 times higher than that of Johnson Matthey PtRu/XC-72R catalyst. The single testing showed that the performance of the prepared catalyst was higher than that of the commercial one.

  9. Nanoporous silica membranes with high hydrothermal stability

    DEFF Research Database (Denmark)

    Boffa, Vittorio; Magnacca, Giualiana; Yue, Yuanzheng

    Despite the use of sol-gel derived nanoporous silica membranes in substitution of traditional separation processes is expected leading to vast energy savings, their intrinsic poor steam-stability hampers their application at an industrial level. Transition metal ions can be used as dopant...... to improve the stability of nanoporous silica structure. This work is a quantitative study on the impact of type and concentration of transition metal ions on the microporous structure and stability of amorphous silica-based membranes, which provides information on how to design chemical compositions...... and synthetic paths for the fabrication of silica-based membranes with a well accessible and highly stabile nanoporous structure...

  10. Adsorption of water-soluble polymers onto barium titanate and its effects on colloidal stability

    NARCIS (Netherlands)

    Laat, de A.W.M.

    1995-01-01

    Ceramic products are usually made from powders which are processed into a green body, with a shape dictated by the final product. Organic binders are used to give the green product sufficient mechanical strength. A sintering process at high temperature converts the green body into the final ceramic

  11. Adsorption of water-soluble polymers onto barium titanate and its effect on colloidal stability.

    NARCIS (Netherlands)

    Laat, de A.W.M.

    1995-01-01

    Ceramic products are usually made from powders which are processed into a green body, with a shape dictated by the final product. Organic binders are used to give the green product sufficient mechanical strength. A sintering process at high temperature converts the green body into the final ceramic

  12. High efficiency silicon nanodisk laser based on colloidal CdSe/ZnS QDs

    Directory of Open Access Journals (Sweden)

    Min-Hsiung Shih

    2011-07-01

    Full Text Available Using colloidal CdSe/ZnS quantum dots in the submicron-sized silicon disk cavity, we have developed a visible wavelength nanodisk laser that operates under extremely low threshold power at room temperature. Time-resolved photoluminescence (PL of QDs; nanodisk by e-beam lithography. Observation of lasing action at 594 nm wavelength for quantum dots on a nanodisk (750 nm in diameter cavity and an ultra-low threshold of 2.8 µW. From QD concentration dependence studies we achieved nearly sevenfold increase in spontaneous emission (SE rate. We have achieved high efficient and high SE coupling rate in such a QD nanodisk laser.

  13. Colloidal Stability in Asymmetric Electrolytes: Modifications of the Schulze-Hardy Rule.

    Science.gov (United States)

    Trefalt, Gregor; Szilagyi, Istvan; Téllez, Gabriel; Borkovec, Michal

    2017-02-21

    The Schulze-Hardy rule suggests a strong dependence of the critical coagulation concentration (CCC) on the ionic valence. This rule is addressed theoretically and confronted with recent experimental results. The commonly presented derivation of this rule assumes symmetric electrolytes and highly charged particles. Both assumptions are incorrect. Symmetric electrolytes containing multivalent ions are hardly soluble, and experiments are normally carried out with the well-soluble salts of asymmetric electrolytes containing monovalent and multivalent ions. In this situation, however, the behavior is completely different whether the multivalent ions represent the counterions or co-ions. When these ions represent the counterions, meaning that the multivalent ions have the opposite sign than the charge of the particle, they adsorb strongly to the particles. Thereby, they progressively reduce the magnitude of the surface charge with increasing valence. In fact, this dependence of the charge density on the counterion valence is mainly responsible for the decrease of the CCC with the valence. In the co-ion case, where the multivalent ions have the same sign as the charge of the particle, the multivalent ions are repelled from the particles, and the surfaces remain highly charged. In this case, the inverse Schulze-Hardy rule normally applies, whereby the CCC varies inversely proportional to the co-ion valence.

  14. Water dispersible CoFe{sub 2}O{sub 4} nanoparticles with improved colloidal stability for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Munjal, Sandeep [Department of Physics, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016 (India); Khare, Neeraj, E-mail: nkhare@physics.iitd.ernet.in [Department of Physics, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016 (India); Nehate, Chetan; Koul, Veena [Centre for Biomedical Engineering, Indian Institute of Technology Delhi, Hauz Khas, New Delhi 110016 (India)

    2016-04-15

    Single phase cobalt ferrite (CoFe{sub 2}O{sub 4}, CFO) nanoparticles of a controlled size (∼6 nm) exhibiting superparamagnetic properties have been synthesized by hydrothermal technique using oleic acid (OA) as surfactant. The oleic acid coated CFO nanoparticles are stable in non-polar organic media, such as hexane but are not well dispersible in water. The surface of these nanoparticles has been further modified by citric acid using ligand exchange process, which makes CFO nanoparticles more stable colloidal solution in water. Citric acid coated CFO nanoparticles exhibits high dispersibility in water, high zeta potential, very low coercivity and moderate saturation magnetization. Biocompatibility of these CFO nanoparticles is demonstrated through cytotoxicity test in L929 cell line. - Highlights: • Synthesis of uniform size (~6nm) CoFe{sub 2}O{sub 4} (CFO) magnetic nano-particles, with a narrow size distribution using hydrothermal techniques with oleic acid as surfactant and convert the CFO nano-particles highly dispersible in water by modifying the surface of nanoparticles through ligand exchange process. • The bio-compatibility of these highly water dispersal citric acid coated CoFe{sub 2}O{sub 4} nanoparticles was demonstrated with mouse fibroblast L929 cells lines, using a MTT cytotoxicity assay. • The surface of these oleic acid coated nanoparticles was modified with citric acid using ligand exchange method, that makes these nanoparticles water highly dispersible. • The biocompatibility of citric acid coated CoFe{sub 2}O{sub 4} nanoparticles was demonstrated with mouse fibroblast L929 cells lines, using a MTT cytotoxicity assay.

  15. Silica encapsulation of fluorescent nanodiamonds for colloidal stability and facile surface functionalization.

    Science.gov (United States)

    Bumb, Ambika; Sarkar, Susanta K; Billington, Neil; Brechbiel, Martin W; Neuman, Keir C

    2013-05-29

    Fluorescent nanodiamonds (FNDs) emit in the near-IR and do not photobleach or photoblink. These properties make FNDs better suited for numerous imaging applications compared with commonly used fluorescence agents such as organic dyes and quantum dots. However, nanodiamonds do not form stable suspensions in aqueous buffer, are prone to aggregation, and are difficult to functionalize. Here we present a method for encapsulating nanodiamonds with silica using an innovative liposome-based encapsulation process that renders the particle surface biocompatible, stable, and readily functionalized through routine linking chemistries. Furthermore, the method selects for a desired particle size and produces a monodisperse agent. We attached biotin to the silica-coated FNDs and tracked the three-dimensional motion of a biotinylated FND tethered by a single DNA molecule with high spatial and temporal resolution.

  16. Old relief printing applied to the current preparation of multi-color and high resolution colloidal photonic crystal patterns.

    Science.gov (United States)

    Yang, Dongpeng; Ye, Siyun; Ge, Jianping

    2015-12-11

    Monodisperse SiO2 colloids are assembled into colloidal crystals in the mixture of monomer and solvent, which is transformed into a mechanochromic photonic crystal paper by polymerization. Following the relief printing strategy, the printing plates are pressed onto the paper to generate letters or images due to the contrast of structural color between the deformed and the undeformed paper, and the images can be permanently retained through UV curing. The wide tunable range of structural color for the current paper under deformation helps to realize multi-color printing. The localized deformation among or even inside the colloidal microcrystals renders the paper with a precise mechanochromic response to the printing plates and leads to the production of high resolution photonic crystal patterns.

  17. Nearly Blinking-Free, High-Purity Single-Photon Emission by Colloidal InP/ZnSe Quantum Dots.

    Science.gov (United States)

    Chandrasekaran, Vigneshwaran; Tessier, Mickaël D; Dupont, Dorian; Geiregat, Pieter; Hens, Zeger; Brainis, Edouard

    2017-10-11

    Colloidal core/shell InP/ZnSe quantum dots (QDs), recently produced using an improved synthesis method, have a great potential in life-science applications as well as in integrated quantum photonics and quantum information processing as single-photon emitters. Single-particle spectroscopy of 10 nm QDs with 3.2 nm cores reveals strong photon antibunching attributed to fast (70 ps) Auger recombination of multiple excitons. The QDs exhibit very good photostability under strong optical excitation. We demonstrate that the antibunching is preserved when the QDs are excited above the saturation intensity of the fundamental-exciton transition. This result paves the way toward their usage as high-purity on-demand single-photon emitters at room temperature. Unconventionally, despite the strong Auger blockade mechanism, InP/ZnSe QDs also display very little luminescence intermittency ("blinking"), with a simple on/off blinking pattern. The analysis of single-particle luminescence statistics places these InP/ZnSe QDs in the class of nearly blinking-free QDs, with emission stability comparable to state-of-the-art thick-shell and alloyed-interface CdSe/CdS, but with improved single-photon purity.

  18. Photo-stability and time-resolved photoluminescence study of colloidal CdSe/ZnS quantum dots passivated in Al{sub 2}O{sub 3} using atomic layer deposition

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Chih-Yi [Graduate Institute of Photonics and Optoelectronics, National Taiwan University, Taipei 10617, Taiwan (China); Mao, Ming-Hua, E-mail: mhmao@ntu.edu.tw [Graduate Institute of Photonics and Optoelectronics, National Taiwan University, Taipei 10617, Taiwan (China); Graduate Institute of Electronics Engineering, National Taiwan University, Taipei 10617, Taiwan (China); Department of Electrical Engineering, National Taiwan University, Taipei 10617, Taiwan (China)

    2016-08-28

    We report photo-stability enhancement of colloidal CdSe/ZnS quantum dots (QDs) passivated in Al{sub 2}O{sub 3} thin film using the atomic layer deposition (ALD) technique. 62% of the original peak photoluminescence (PL) intensity remained after ALD. The photo-oxidation and photo-induced fluorescence enhancement effects of both the unpassivated and passivated QDs were studied under various conditions, including different excitation sources, power densities, and environment. The unpassivated QDs showed rapid PL degradation under high excitation due to strong photo-oxidation in air while the PL intensity of Al{sub 2}O{sub 3} passivated QDs was found to remain stable. Furthermore, recombination dynamics of the unpassivated and passivated QDs were investigated by time-resolved measurements. The average lifetime of the unpassivated QDs decreases with laser irradiation time due to photo-oxidation. Photo-oxidation creates surface defects which reduces the QD emission intensity and enhances the non-radiative recombination rate. From the comparison of PL decay profiles of the unpassivated and passivated QDs, photo-oxidation-induced surface defects unexpectedly also reduce the radiative recombination rate. The ALD passivation of Al{sub 2}O{sub 3} protects QDs from photo-oxidation and therefore avoids the reduction of radiative recombination rate. Our experimental results demonstrated that passivation of colloidal QDs by ALD is a promising method to well encapsulate QDs to prevent gas permeation and to enhance photo-stability, including the PL intensity and carrier lifetime in air. This is essential for the applications of colloidal QDs in light-emitting devices.

  19. Experimental Studies to Evaluate the Role of Colloids on the Radionuclide Migration in a Crystalline Medium

    Energy Technology Data Exchange (ETDEWEB)

    Albarran, Nairoby; Missana, Tiziana; Alonso, Ursula; Garcia-Gutierrez, Miguel; Mingarro, Manuel; Lopez, Trinidad [CIEMAT, Departamento de Medioambiente, Avenida Complutense, 22 28040 Madrid (Spain)

    2008-07-01

    In a deep geological repository (DGR) of high level radioactive waste, all the possible phenomena affecting radionuclide migration have to be studied to assess its security over time. Colloids can play an important role for contaminant transport if the following conditions are fulfilled: colloids exist in a non negligible concentration, they are mobile and stable in the environment of interest, and they are able to adsorb radionuclides irreversibly. In this study, different transport experiments where performed to improve the knowledge on the main mechanisms affecting the radionuclide migration in the presence of colloids in a crystalline medium. Firstly, colloid stability was analysed and then transport experiments in an artificial granite longitudinal fracture were carried out. Synthetic colloids of different size and bentonite clay colloids were used to evaluate the effects of colloid size, charge, and water flow rate on their mobility. Results showed that both major importance of the water flow rate on the mobility of colloids and their recovery and a higher interaction of smaller particles with the surface. Finally, the migration behaviour of Sr, and Sr adsorbed onto bentonite colloids was compared. The elution curves of Sr adsorbed onto colloid were significantly different from the ones of Sr alone, pointing out that sorption/desorption mechanisms must be taken into account to understand the radionuclide migration in the fracture in the presence of colloids. (authors)

  20. Manipulation of colloidal crystallization

    NARCIS (Netherlands)

    Vermolen, E.C.M.

    2008-01-01

    Colloidal particles (approximately a micrometer in diameter) that are dispersed in a fluid, behave thermodynamically similar to atoms and molecules: at low concentrations they form a fluid, while at high concentrations they can crystallize into a colloidal crystal to gain entropy. The analogy with m

  1. A High Power, Frequency Tunable Colloidal Quantum Dot (CdSe/ZnS) Laser

    Science.gov (United States)

    Prasad, Saradh; Saleh AlHesseny, Hanan; AlSalhi, Mohamad S.; Devaraj, Durairaj; Masilamai, Vadivel

    2017-01-01

    Tunable lasers are essential for medical, engineering and basic science research studies. Most conventional solid-state lasers are capable of producing a few million laser shots, but limited to specific wavelengths, which are bulky and very expensive. Dye lasers are continuously tunable, but exhibit very poor chemical stability. As new tunable, efficient lasers are always in demand, one such laser is designed with various sized CdSe/ZnS quantum dots. They were used as a colloid in tetrahydrofuran to produce a fluorescent broadband emission from 520 nm to 630 nm. The second (532 nm) and/or third harmonic (355 nm) of the Nd:YAG laser (10 ns, 10 Hz) were used together as the pump source. In this study, different sized quantum dots were independently optically pumped to produce amplified spontaneous emission (ASE) with 4 nm to 7 nm of full width at half-maximum (FWHM), when the pump power and focusing were carefully optimized. The beam was directional with a 7 mrad divergence. Subsequently, these quantum dots were combined together, and the solution was placed in a resonator cavity to obtain a laser with a spectral width of 1 nm and tunable from 510 to 630 nm, with a conversion efficiency of about 0.1%.

  2. Sustainable and scalable production of monodisperse and highly uniform colloidal carbonaceous spheres using sodium polyacrylate as the dispersant.

    Science.gov (United States)

    Gong, Yutong; Xie, Lei; Li, Haoran; Wang, Yong

    2014-10-28

    Monodisperse, uniform colloidal carbonaceous spheres were fabricated by the hydrothermal treatment of glucose with the help of a tiny amount of sodium polyacrylate (PAANa). This synthetic strategy is effective at high glucose concentration and for scale-up experiments. The sphere size can be easily tuned by the reaction time, temperature and glucose concentration.

  3. [Toxicological evaluation of nanosized colloidal silver, stabilized with polyvinylpyrrolidone, in 92-day experiment on rats. II. Internal organs morphology].

    Science.gov (United States)

    Zaytseva, N V; Zemlyanova, M A; Zvezdin, V N; Dovbysh, A A; Gmoshinsky, I V; Khotimchenko, S A; Akafieva, T I

    2016-01-01

    The aim of the study was to evaluate the safe doses of commercially available nanosized colloidal silver (NCS), stabilized with polyvinilpirrolidone (PVP, food additive E1201) when administered in gastrointestinal tract of rats in the 92-day experiment in terms of the morphological changes in the internals of animals. The sample studied contained non-aggregated nanoparticles (NPs) of silver belonging to size fractions with a diameter of less than 5 nm, 10-20 nm or 50-80 nm. 80% of NPs were inside the range of hydrodynamic diameters 10.6-61.8 nm. The preparation of NCS was administered to growing male Wistar rats. (initial body weight 80 ± 10 g) for 1 month by intragastric gavage and then consumed with food at doses of 0.1, 1.0 and 10 mg/kg of body weight based on silver. The control animals received water or vehicle of nanomaterial--water solution of PVP. After withdrawal of animals from the experiment by exsanguination under ether anesthesia organs (liver, spleen, kidney, ileum) were isolated and their slides were prepared by standard methods following 'by staining with hematoxylin-eosin. Analysis was performed in light optical microscope equipped with a digital camera at a magnification from 1 x 100 to 1 x 1000. It was shown that the experimental animals treated with the NCS developed series of morphological changes in the tissues of the internal organs (liver, spleen and kidney) with the elevation of the range and severity of structural changes with increasing doses of silver. The most sensitive target of NCS action was apparently liver, which has already shown at a dose of 0.1 mg of silver NP/kg of body weight marked eosinophilic infiltration of portal tracts, which was accompanied at doses of 1.0 and 10.0 mg/kg by the emergence of medium and large-drop fat vacuoles in the cytoplasm of hepatocytes, swelling and lympho-macrophage. infiltration of the portal tracts. Detectable changes can be regarded as symptoms of inflammation of hepatocytes, at least, at a

  4. Thermodynamic stabilization of colloids

    NARCIS (Netherlands)

    Stol, R.J.; Bruyn, P.L. de

    1980-01-01

    An analysis is given of the conditions necessary for obtaining a thermodynamically stable dispersion (TSD) of solid particles in a continuous aqueous solution phase. The role of the adsorption of potential-determining ions at the planar interface in lowering the interfacial free energy (γ) to promot

  5. Crystallization and colloidal stabilization of Ca(OH)2 in the presence of nopal juice (Opuntia ficus indica): Implications in architectural heritage conservation.

    Science.gov (United States)

    Rodriguez-Navarro, Carlos; Ruiz-Agudo, Encarnacion; Burgos-Cara, Alejandro; Elert, Kerstin; Hansen, Eric F

    2017-09-20

    Hydrated lime (Ca(OH)2) is a vernacular art and building material produced following slaking of CaO in water. If excess water is used, a slurry, called lime putty forms, which has been the preferred craftsman selection for formulating lime mortars since Roman times. A variety of natural additives were traditionally added to the lime putty to improve its quality. The mucilaginous juice extracted from nopal cladodes has been and still is used as additive incorporated in the slaking water for formulation of lime mortars and plasters both in ancient Mesoamerica as well as in the USA Southwest. Little is known on the ultimate effects of this additive on the crystallization and microstructure of hydrated lime. Here, we show that significant changes in habit and size of portlandite crystals occur following slaking in the presence of nopal juice as well as compositionally-similar citrus pectin. Both additives contain polysaccharides made up of galacturonic acid and neutral sugar residues. The carboxyl (and hydroxyl) functional groups present in these residues and in their alkaline degradation by-products, which are deprotonated at the high pH (12.4) produced during lime slaking, strongly interact with newly formed Ca(OH)2 crystals acting in two ways: a) as nucleation inhibitors, promoting the formation of nanosized crystals, and b) as habit modifiers, favoring the development of planar habit following their adsorption onto positively charged (0001)Ca(OH)2 faces. Adsorption of polysaccharides on Ca(OH)2 crystals prevents the development of large particles, resulting in a very reactive, nanosized portlandite slurry. It also promotes steric stabilization, which limits aggregation, thus enhancing the colloidal nature of the lime putty. Overall, these effects are very favorable for the preparation of highly plastic lime mortars with enhanced properties.

  6. Stability parameters of high moisture pet foods

    OpenAIRE

    Fernández-Salguero Carretero, J.; Gómez Díaz, R.; Sánchez Sánchez, E.; Vioque Amor, M.

    1996-01-01

    In the present work were analyzed the stability conditions of a group of high moisture petfoods. The samples considered complete preserves forming part of a widest study which are included lowmoisture animal feed. It was confirmed that in base to the individual water activity values (aw), pH and moisture contents of 20 analyzed samples, is not assured its stability in relation to microorganism spoilage, only exclusively with a sterilization process. It is discussed the utilization of Hurdle ...

  7. Gold nanostar-polymer hybrids for siRNA delivery: Polymer design towards colloidal stability and in vitro studies on breast cancer cells.

    Science.gov (United States)

    Sardo, Carla; Bassi, Barbara; Craparo, Emanuela F; Scialabba, Cinzia; Cabrini, Elisa; Dacarro, Giacomo; D'Agostino, Agnese; Taglietti, Angelo; Giammona, Gaetano; Pallavicini, Piersandro; Cavallaro, Gennara

    2017-03-15

    To overcome the low bioavailability of siRNA (small interfering RNA) and to improve their transfection efficiency, the use of non-viral delivery carriers is today a feasible approach to transform the discovery of these incredibly potent and versatile drugs into clinical practice. Polymer-modified gold nanoconstructs (AuNCs) are currently viewed as efficient and safe intracellular delivery carriers for siRNA, as they have the possibility to conjugate the ability to stably entrap and deliver siRNAs inside cells with the advantages of gold nanoparticles, which can act as theranostic agents and radiotherapy enhancers through laser-induced hyperthermia. In this study, AuNCs were prepared by coating Gold Nano Stars (GNS) with suitable functionalised polymers, to give new insight on the choice of the coating in order to obtain colloidal stability, satisfying in vitro transfection behaviour and reliability in terms of homogeneous results upon GNS type changing. For this goal, GNS synthesized with three different sizes and shapes were coated with two different polymers: i) α-mercapto-ω-amino polyethylene glycol 3000Da (SH-PEG3000-NH2), a hydrophilic linear polymer; ii) PHEA-PEG2000-EDA-LA (PPE-LA), an amphiphilic hydroxyethylaspartamide copolymer containing a PEG moiety. Both polymers contain SH or SS groups for anchoring on gold surface and NH2 groups, which can be protonated in order to obtain a positive surface for successive siRNA layering. The effect of the features of the coating polymers on siRNA layering, and the extent of intracellular uptake and luciferase gene silencing effect were evaluated for each of the obtained coated GNS. The results highlight that amphiphilic biocompatible polymers with multi-grafting function are more suitable for ensuring the colloidal stability and the effectiveness of these colloidal systems, compared to the coating with linear PEG. Copyright © 2017 Elsevier B.V. All rights reserved.

  8. Low-temperature approach to high-yield and reproducible syntheses of high-quality small-sized PbSe colloidal nanocrystals for photovoltaic applications.

    Science.gov (United States)

    Ouyang, Jianying; Schuurmans, Carl; Zhang, Yanguang; Nagelkerke, Robbert; Wu, Xiaohua; Kingston, David; Wang, Zhi Yuan; Wilkinson, Diana; Li, Chunsheng; Leek, Donald M; Tao, Ye; Yu, Kui

    2011-02-01

    Small-sized PbSe nanocrystals (NCs) were synthesized at low temperature such as 50-80 °C with high reaction yield (up to 100%), high quality, and high synthetic reproducibility, via a noninjection-based one-pot approach. These small-sized PbSe NCs with their first excitonic absorption in wavelength shorter than 1200 nm (corresponding to size colloidal PbSe NCs, also called quantum dots, are high-quality, in terms of narrow size distribution with a typical standard deviation of ∼7-9%, excellent optical properties with high quantum yield of ∼50-90% and small full width at half-maximum of ∼130-150 nm of their band-gap photoemission peaks, and high storage stability. Our synthetic design aimed at promotion of the formation of PbSe monomers for fast and sizable nucleation with the presence of a large number of nuclei at low temperature. For formation of the PbSe monomer, our low-temperature approach suggests the existence of two pathways of Pb-Se (route a) and Pb-P (route b) complexes. Either pathway may dominate, depending on the method used and its experimental conditions. Experimentally, a reducing/nucleation agent, diphenylphosphine, was added to enhance route b. The present study addresses two challenging issues in the NC community, the monomer formation mechanism and the reproducible syntheses of small-sized NCs with high yield and high quality and large-scale capability, bringing insight to the fundamental understanding of optimization of the NC yield and quality via control of the precursor complex reactivity and thus nucleation/growth. Such advances in colloidal science should, in turn, promote the development of next-generation low-cost and high-efficiency solar cells. Schottky-type solar cells using our PbSe NCs as the active material have achieved the highest power conversion efficiency of 2.82%, in comparison with the same type of solar cells using other PbSe NCs, under Air Mass 1.5 global (AM 1.5G) irradiation of 100 mW/cm(2).

  9. High-Efficiency Colloidal Quantum Dot Photovoltaics via Robust Self-Assembled Monolayers.

    Science.gov (United States)

    Kim, Gi-Hwan; García de Arquer, F Pelayo; Yoon, Yung Jin; Lan, Xinzheng; Liu, Mengxia; Voznyy, Oleksandr; Jagadamma, Lethy Krishnan; Abbas, Abdullah Saud; Yang, Zhenyu; Fan, Fengjia; Ip, Alexander H; Kanjanaboos, Pongsakorn; Hoogland, Sjoerd; Kim, Jin Young; Sargent, Edward H

    2015-11-11

    The optoelectronic tunability offered by colloidal quantum dots (CQDs) is attractive for photovoltaic applications but demands proper band alignment at electrodes for efficient charge extraction at minimal cost to voltage. With this goal in mind, self-assembled monolayers (SAMs) can be used to modify interface energy levels locally. However, to be effective SAMs must be made robust to treatment using the various solvents and ligands required for to fabricate high quality CQD solids. We report robust self-assembled monolayers (R-SAMs) that enable us to increase the efficiency of CQD photovoltaics. Only by developing a process for secure anchoring of aromatic SAMs, aided by deposition of the SAMs in a water-free deposition environment, were we able to provide an interface modification that was robust against the ensuing chemical treatments needed in the fabrication of CQD solids. The energy alignment at the rectifying interface was tailored by tuning the R-SAM for optimal alignment relative to the CQD quantum-confined electron energy levels. This resulted in a CQD PV record power conversion efficiency (PCE) of 10.7% with enhanced reproducibility relative to controls.

  10. Slow cooling and highly efficient extraction of hot carriers in colloidal perovskite nanocrystals

    Science.gov (United States)

    Li, Mingjie; Bhaumik, Saikat; Goh, Teck Wee; Kumar, Muduli Subas; Yantara, Natalia; Grätzel, Michael; Mhaisalkar, Subodh; Mathews, Nripan; Sum, Tze Chien

    2017-02-01

    Hot-carrier solar cells can overcome the Schottky-Queisser limit by harvesting excess energy from hot carriers. Inorganic semiconductor nanocrystals are considered prime candidates. However, hot-carrier harvesting is compromised by competitive relaxation pathways (for example, intraband Auger process and defects) that overwhelm their phonon bottlenecks. Here we show colloidal halide perovskite nanocrystals transcend these limitations and exhibit around two orders slower hot-carrier cooling times and around four times larger hot-carrier temperatures than their bulk-film counterparts. Under low pump excitation, hot-carrier cooling mediated by a phonon bottleneck is surprisingly slower in smaller nanocrystals (contrasting with conventional nanocrystals). At high pump fluence, Auger heating dominates hot-carrier cooling, which is slower in larger nanocrystals (hitherto unobserved in conventional nanocrystals). Importantly, we demonstrate efficient room temperature hot-electrons extraction (up to ~83%) by an energy-selective electron acceptor layer within 1 ps from surface-treated perovskite NCs thin films. These insights enable fresh approaches for extremely thin absorber and concentrator-type hot-carrier solar cells.

  11. High Quantum Yield Blue Emission from Lead-Free Inorganic Antimony Halide Perovskite Colloidal Quantum Dots.

    Science.gov (United States)

    Zhang, Jian; Yang, Ying; Deng, Hui; Farooq, Umar; Yang, Xiaokun; Khan, Jahangeer; Tang, Jiang; Song, Haisheng

    2017-09-26

    Colloidal quantum dots (QDs) of lead halide perovskite have recently received great attention owing to their remarkable performances in optoelectronic applications. However, their wide applications are hindered from toxic lead element, which is not environment- and consumer-friendly. Herein, we utilized heterovalent substitution of divalent lead (Pb(2+)) with trivalent antimony (Sb(3+)) to synthesize stable and brightly luminescent Cs3Sb2Br9 QDs. The lead-free, full-inorganic QDs were fabricated by a modified ligand-assisted reprecipitation strategy. A photoluminescence quantum yield (PLQY) was determined to be 46% at 410 nm, which was superior to that of other reported halide perovskite QDs. The PL enhancement mechanism was unraveled by surface composition derived quantum-well band structure and their large exciton binding energy. The Br-rich surface and the observed 530 meV exciton binding energy were proposed to guarantee the efficient radiative recombination. In addition, we can also tune the inorganic perovskite QD (Cs3Sb2X9) emission wavelength from 370 to 560 nm via anion exchange reactions. The developed full-inorganic lead-free Sb-perovskite QDs with high PLQY and stable emission promise great potential for efficient emission candidates.

  12. High-Efficiency Colloidal Quantum Dot Photovoltaics via Robust Self-Assembled Monolayers

    KAUST Repository

    Kim, Gi-Hwan

    2015-11-11

    © 2015 American Chemical Society. The optoelectronic tunability offered by colloidal quantum dots (CQDs) is attractive for photovoltaic applications but demands proper band alignment at electrodes for efficient charge extraction at minimal cost to voltage. With this goal in mind, self-assembled monolayers (SAMs) can be used to modify interface energy levels locally. However, to be effective SAMs must be made robust to treatment using the various solvents and ligands required for to fabricate high quality CQD solids. We report robust self-assembled monolayers (R-SAMs) that enable us to increase the efficiency of CQD photovoltaics. Only by developing a process for secure anchoring of aromatic SAMs, aided by deposition of the SAMs in a water-free deposition environment, were we able to provide an interface modification that was robust against the ensuing chemical treatments needed in the fabrication of CQD solids. The energy alignment at the rectifying interface was tailored by tuning the R-SAM for optimal alignment relative to the CQD quantum-confined electron energy levels. This resulted in a CQD PV record power conversion efficiency (PCE) of 10.7% with enhanced reproducibility relative to controls.

  13. Influence of α-amylase template concentration on systematic entrapment of highly stable and monodispersed colloidal gold nanoparticles

    Science.gov (United States)

    Ananth, A. Nitthin; Ananth, A. Nimrodh; Jose, Sujin P.; Umapathy, S.; Mathavan, T.

    2016-01-01

    Nano gold / α-amylase colloidal dispersions of profound stability were made using simple procedure with a conventional reducing agent. The surface plasmon resonance of the gold nanocrystals was used to quantify the extent of the dispersion stability and functionalization. It is found that the reduced gold nanoparticles were trapped into the protein network without denaturation the structure of α-amylase protein. This kind of entrapment of particles into the protein network prevents clustering of individual gold nanoparticles (6.42 nm ± 0.92 nm) by acting as a natural spacer. Systematic entrapment was facilitated by the affinity of gold to the sulfur moieties (Au-S) in the protein structure.

  14. Preparation of colloidal gold immunochromatography strip for detection of methamidophos residue

    Institute of Scientific and Technical Information of China (English)

    SHI Chenggang; ZHAO Suqing; ZHANG Kun; HONG Guobao; ZHU Zhenyu

    2008-01-01

    Methamidophos (Met) is a broad spectrum organophosphorus insecticide and acaricide. Even a trace of its residue is harmful to humans and many animals. In this study, the synthesis and identification of colloidal gold particles and antibody-colloidal gold conjugates were performed, and the preparation of colloidal gold immunochromatography strip was conducted for detection of Met residue. The size of colloidal gold particles was checked using a transmission electron microscope (TEM). The formation of antibody-colloidal gold conjugates was monitored by UV/Vis spectroscopy. The preparation of colloidal gold immunochromatography strips,analysis of Met standard solutions, and other four pesticides and vegetable samples were operated with common methods and principals.The TEM images showed the average diameter of colloidal gold particles was almost the same size: approximately 40.0 nm in diameter.For the conjugation of colloidal gold and monoclonal antibody (MAb), 0.03 mg/ml of MAb was confirmed to be the minimum amount for stabilization of colloidal gold. With the prepared colloidal gold immunochromatography test strip to determine the standard Met solution, the results demonstrated a detection limit of approximately 1.0 μg/ml. Cross-reaction indicated that the strip had a high specificity to Met. The results of 10 green vegetable sample tests confirmed that one sample was positive by HPLC analysis. There was evidence to suggest that colloidal gold particles and antibody-colloidal gold conjugates were synthesized successfully. The prepared colloidal gold immunochromatography strip was applicable for preliminary screening of Met residue.

  15. Influence of colloidal particle transfer on the quality of self-assembling colloidal photonic crystal under confined condition

    Institute of Scientific and Technical Information of China (English)

    赵永强; 李娟; 刘秋艳; 董文钧; 陈本永; 李超荣

    2015-01-01

    The relationship between colloidal particle transfer and quality of colloidal photonic crystal (CPC) is investigated by comparing colloidal particle self-assembling under the vertical channel (VC) and horizontal channel (HC) conditions. Both the theoretical analyses and the experimental measurements indicate that crystal quality depends on the stability of mass transfer. For the VC, colloidal particle transfer takes place in a stable laminar flow, which is conducive to forming high-quality crystal. In contrast, it happens in an unstable turbulent flow for the HC. Crystals with cracks and uneven surface formed under the HC condition can be seen from the images of field emission scanning electron microscope (SEM) and three-dimensional (3D) laser scanning microscope (LSM), respectively.

  16. The influence of ionic strength and mixing ratio on the colloidal stability of PDAC/PSS polyelectrolyte complexes.

    Science.gov (United States)

    Zhang, Yanpu; Yildirim, Erol; Antila, Hanne S; Valenzuela, Luis D; Sammalkorpi, Maria; Lutkenhaus, Jodie L

    2015-10-01

    Polyelectrolyte complexes (PECs) form by mixing polycation and polyanion solutions together, and have been explored for a variety of applications. One challenge for PEC processing and application is that under certain conditions the as-formed PECs aggregate and precipitate out of suspension over the course of minutes to days. This aggregation is governed by several factors such as electrostatic repulsion, van der Waals attractions, and hydrophobic interactions. In this work, we explore the boundary between colloidally stable and unstable complexes as it is influenced by polycation/polyanion mixing ratio and ionic strength. The polymers examined are poly(diallyldimethylammonium chloride) (PDAC) and poly(sodium 4-styrenesulfonate) (PSS). Physical properties such as turbidity, hydrodynamic size, and zeta potential are investigated upon complex formation. We also perform detailed molecular dynamics simulations to examine the structure and effective charge distribution of the PECs at varying mixing ratios and salt concentrations to support the experimental findings. The results suggest that the colloidally stable/unstable boundary possibly marks the screening effects from added salt, resulting in weakly charged complexes that aggregate. At higher salt concentrations, the complexes initially form and then gradually dissolve into solution.

  17. Understanding the stabilization of liquid-phase-exfoliated graphene in polar solvents: molecular dynamics simulations and kinetic theory of colloid aggregation.

    Science.gov (United States)

    Shih, Chih-Jen; Lin, Shangchao; Strano, Michael S; Blankschtein, Daniel

    2010-10-20

    Understanding the solution-phase dispersion of pristine, unfunctionalized graphene is important for the production of conducting inks and top-down approaches to electronics. This process can also be used as a higher-quality alternative to chemical vapor deposition. We have developed a theoretical framework that utilizes molecular dynamics simulations and the kinetic theory of colloid aggregation to elucidate the mechanism of stabilization of liquid-phase-exfoliated graphene sheets in N-methylpyrrolidone (NMP), N,N'-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), γ-butyrolactone (GBL), and water. By calculating the potential of mean force between two solvated graphene sheets using molecular dynamics (MD) simulations, we have found that the dominant barrier hindering the aggregation of graphene is the last layer of confined solvent molecules between the graphene sheets, which results from the strong affinity of the solvent molecules for graphene. The origin of the energy barrier responsible for repelling the sheets is the steric repulsions between solvent molecules and graphene before the desorption of the confined single layer of solvent. We have formulated a kinetic theory of colloid aggregation to model the aggregation of graphene sheets in the liquid phase in order to predict the stability using the potential of mean force. With only one adjustable parameter, the average collision area, which can be estimated from experimental data, our theory can describe the experimentally observed degradation of the single-layer graphene fraction in NMP. We have used these results to rank the potential solvents according to their ability to disperse pristine, unfunctionalized graphene as follows: NMP ≈ DMSO > DMF > GBL > H(2)O. This is consistent with the widespread use of the first three solvents for this purpose.

  18. Flexible amorphous metal films with high stability

    Science.gov (United States)

    Liu, M.; Cao, C. R.; Lu, Y. M.; Wang, W. H.; Bai, H. Y.

    2017-01-01

    We report the formation of amorphous Cu50Zr50 films with a large-area of more than 100 cm2. The films were fabricated by ion beam assisted deposition with a slow deposition rate at moderate temperature. The amorphous films have markedly enhanced thermal stability, excellent flexibility, and high reflectivity with atomic level smoothness. The multifunctional properties of the amorphous films are favorites in the promising applications of smart skin or wearable devices. The method of preparing highly stable amorphous metal films by tuning the deposition rate instead of deposition temperature could pave a way for exploring amorphous metal films with unique properties.

  19. Colloidal stability of CeO2 nanoparticles coated with either natural organic matter or organic polymers under various hydrochemical conditions

    Science.gov (United States)

    Dippon, Urs; Pabst, Silke; Klitzke, Sondra

    2016-04-01

    The worldwide marked for engineered nanoparticles (ENPs) is growing and concerns on the environmental fate- and toxicity of ENPs are rising. Understanding the transport of ENPs within and between environmental compartments such as surface water and groundwater is crucial for exposition modeling, risk assessment and ultimately the protection of drinking water resources. The transport of ENPs is strongly influenced by the surface properties and aggregation behavior of the particles, which is strongly controlled by synthetic and natural organic coatings. Both, surface properties and aggregation characteristics are also key properties for the industrial application of ENPs, which leads to the development and commercialization of an increasing number of surface-functionalized ENPs. These include metals and oxides such as Cerium dioxide (CeO2) with various organic coatings. Therefore, we investigate CeO2 ENPs with different surface coatings such as weakly anionic polyvinyl alcohol (PVA) or strongly anionic poly acrylic acid (PAA) with respect to their colloidal stability in aqueous matrix under various hydrochemical conditions (pH, ionic strength) and their transport behavior in sand filter columns. Furthermore, we investigate the interaction of naturally occurring organic matter (NOM) with CeO2 ENPs and its effect on surface charge (zeta potential), colloidal stability and transport. While uncoated CeO2 ENPs aggregate at pH > 4 in aqueous matrix, our results show that PAA and PVA surface coatings as well as NOM sorbed to CeO2-NP surfaces can stabilize CeO2 ENPs under neutral and alkaline pH conditions in 1 mM KCl solution. Under slightly acidic conditions, differences between the three particle types were observed. PVA can stabilize particle suspensions in presence of 1 mM KCl at pH > 4.3, PAA at pH >4.0 and NOM at >3.2. While the presence of KCl did not influence particle size of NOM-CeO2 ENPs, CaCl2 at >2 mM lead to aggregation. Further results on the influence of KCl

  20. Mechanical Failure in Colloidal Gels

    Science.gov (United States)

    Kodger, Thomas Edward

    When colloidal particles in a dispersion are made attractive, they aggregate into fractal clusters which grow to form a space-spanning network, or gel, even at low volume fractions. These gels are crucial to the rheological behavior of many personal care, food products and dispersion-based paints. The mechanical stability of these products relies on the stability of the colloidal gel network which acts as a scaffold to provide these products with desired mechanical properties and to prevent gravitational sedimentation of the dispersed components. Understanding the mechanical stability of such colloidal gels is thus of crucial importance to predict and control the properties of many soft solids. Once a colloidal gel forms, the heterogeneous structure bonded through weak physical interactions, is immediately subject to body forces, such as gravity, surface forces, such as adhesion to a container walls and shear forces; the interplay of these forces acting on the gel determines its stability. Even in the absence of external stresses, colloidal gels undergo internal rearrangements within the network that may cause the network structure to evolve gradually, in processes known as aging or coarsening or fail catastrophically, in a mechanical instability known as syneresis. Studying gel stability in the laboratory requires model colloidal system which may be tuned to eliminate these body or endogenous forces systematically. Using existing chemistry, I developed several systems to study delayed yielding by eliminating gravitational stresses through density matching and cyclic heating to induce attraction; and to study syneresis by eliminating adhesion to the container walls, altering the contact forces between colloids, and again, inducing gelation through heating. These results elucidate the varied yet concomitant mechanisms by which colloidal gels may locally or globally yield, but then reform due to the nature of the physical, or non-covalent, interactions which form

  1. High stability of few layer graphene nanoplatelets in various solvents

    KAUST Repository

    Xu, X

    2017-04-25

    Dispersion of few-layer graphene nanoplatelets (GNPs) in liquid media is a crucial step for various applications. Here, we highlight a simple, nondestructive method for preparing stable aqueous colloidal solutions with GNP powder quickly dispersed in 5 wt.% sodium–hypochlorite- (NaClO) and sodium-bromide- (NaBr) salted solvent by bath sonication. This method makes it possible to easily prepare a highly concentrated colloidal solution (1 mgcenterdotml−1) of GNPs that can easily be re-dispersed in water (treated GNPs). The aqueous suspension we prepared remained stable for longer than a few weeks. We made similar tests with various solvents and dispersibility appeared to decrease with decreasing polarity. High-concentration suspensions using our facile dispersion method could be of particular interest to the large community using graphene for a diversity of applications.

  2. Double-Sided Junctions Enable High-Performance Colloidal-Quantum-Dot Photovoltaics.

    Science.gov (United States)

    Liu, Mengxia; de Arquer, F Pelayo García; Li, Yiying; Lan, Xinzheng; Kim, Gi-Hwan; Voznyy, Oleksandr; Jagadamma, Lethy Krishnan; Abbas, Abdullah Saud; Hoogland, Sjoerd; Lu, Zhenghong; Kim, Jin Young; Amassian, Aram; Sargent, Edward H

    2016-06-01

    The latest advances in colloidal-quantum-dot material processing are combined with a double-sided junction architecture, which is done by efficiently incorporating indium ions in the ZnO eletrode. This platform allows the collection of all photogenerated carriers even at the maximum power point. The increased depletion width in the device facilitates full carrier collection, leading to a record 10.8% power conversion efficiency.

  3. Magnetic Assisted Colloidal Pattern Formation

    Science.gov (United States)

    Yang, Ye

    phase transitions in condensed matter systems that can be tracked with single particle resolution. Compared with other research on colloidal crystal formation, my research has focused on multi-component colloidal systems of magnetic and non-magnetic colloids immersed in a ferrofluid. Initially, I studied the types of patterns that form as a function of the concentrations of the different particles and ferrofluid, and I discovered a wide variety of chains, rings and crystals forming in bi-component and tri-component systems. Based on these results, I narrowed my focus to one specific crystal structure (checkerboard lattice) as a model of phase transformations in alloy. Liquid/solid phase transitions were studied by slowly adjusting the magnetic field strength, which serves to control particle-particle interactions in a manner similar to controlling the physical temperature of the fluid. These studies were used to determine the optimal conditions for forming large single crystal structures, and paved the way for my later work on solid/solid phase transitions when the angle of the external field was shifted away from the normal direction. The magnetostriction coefficient of these crystals was measured in low tilt angle of the applied field. At high tilt angles, I observed a variety of martensitic transformations, which followed different pathways depending on the crystal direction relative to the in-plane field. In the last part of my doctoral studies, I investigated colloidal patterns formed in a superimposed acoustic and magnetic field. In this approach, the magnetic field mimics "temperature", while the acoustic field mimics "pressure". The ability to simultaneously tune both temperature and pressure allows for more efficient exploration of phase space. With this technique I demonstrated a large class of particle structures ranging from discrete molecule-like clusters to well ordered crystal phases. Additionally, I demonstrated a crosslinking strategy based on

  4. Enhanced hydrogen evolution rates at high pH with a colloidal cadmium sulphide–platinum hybrid system

    Energy Technology Data Exchange (ETDEWEB)

    Schneider, Julian; Vaneski, Aleksandar; Susha, Andrei S.; Rogach, Andrey L., E-mail: andrey.rogach@cityu.edu.hk [Department of Physics and Materials Science and Centre for Functional Photonics (CFP), City University of Hong Kong, 83 Tat Chee Avenue, Kowloon (Hong Kong); Pesch, Georg R.; Yang Teoh, Wey [Clean Energy and Nanotechnology (CLEAN) Laboratory, School of Energy and Environment, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon (Hong Kong)

    2014-12-01

    We demonstrate enhanced hydrogen generation rates at high pH using colloidal cadmium sulphide nanorods decorated with Pt nanoparticles. We introduce a simplified procedure for the decoration and subsequent hydrogen generation, reducing both the number of working steps and the materials costs. Different Pt precursor concentrations were tested to reveal the optimal conditions for the efficient hydrogen evolution. A sharp increase in hydrogen evolution rates was measured at pH 13 and above, a condition at which the surface charge transfer was efficiently mediated by the formation of hydroxyl radicals and further consumption by the sacrificial triethanolamine hole scavenger.

  5. Enhanced hydrogen evolution rates at high pH with a colloidal cadmium sulphide–platinum hybrid system

    Directory of Open Access Journals (Sweden)

    Julian Schneider

    2014-12-01

    Full Text Available We demonstrate enhanced hydrogen generation rates at high pH using colloidal cadmium sulphide nanorods decorated with Pt nanoparticles. We introduce a simplified procedure for the decoration and subsequent hydrogen generation, reducing both the number of working steps and the materials costs. Different Pt precursor concentrations were tested to reveal the optimal conditions for the efficient hydrogen evolution. A sharp increase in hydrogen evolution rates was measured at pH 13 and above, a condition at which the surface charge transfer was efficiently mediated by the formation of hydroxyl radicals and further consumption by the sacrificial triethanolamine hole scavenger.

  6. Oil-in-water Pickering emulsions stabilized by colloidal particles from the water-insoluble protein zein

    OpenAIRE

    de Folter, J.W.J.; van Ruijven, M.W.M.; Velikov, K.

    2012-01-01

    Few fully natural and biocompatible materials are available for the effective particle-stabilization of emulsions since strict requirements, such as insolubility in both fluid phases and intermediate wettability, need to be met. In this paper, we demonstrate the first use of water-insoluble proteins, employing the corn protein zein as a representative of this family, as effective particle-stabilizers of oil-in-water emulsions of natural oils and water. For this purpose, we synthesized zein co...

  7. Clay Effect in the Electrochemical Stabilization of Colloidal CoO(OH Applied as a Modified Electrode

    Directory of Open Access Journals (Sweden)

    Lucéli Roloff

    2016-12-01

    Full Text Available In this work, a mixed material was prepared using a montmorillonite clay (denominated imported sodic, IS modified with colloidal cobalt (Co. The obtained mixed material (ISCo was characterized by X-ray diffractometry and simultaneous thermal analysis and used to modify the surface of a platinum electrode for electrochemical determination of oxalic acid. The electrochemical behavior of the ISCo material was evaluated by cyclic voltammetry and the performance as a sensor for oxalic acid was assessed by square wave voltammetry. The platinum electrode showed no response to peak current when the oxalic acid concentration was increased in the range of 4.99 x 10-4 to 4.95 x 10-3 mol L-1. On the other hand, the platinum electrode modified with the mixed material presented a linear response in the studied range with a detection limit of 2.55 × 10-4 mol L-1. DOI: http://dx.doi.org/10.17807/orbital.v0i0.876

  8. Preparation of colloidal graphene in quantity by electrochemical exfoliation.

    Science.gov (United States)

    Chen, Kunfeng; Xue, Dongfeng

    2014-12-15

    We reported the preparation of colloidal graphene in quantity via the anodic exfoliation of graphite in (NH4)2SO4 aqueous solution. In the currently designed electrochemical exfoliation route, mass high-quality graphene was produced within short reaction time, around 1h. The proposed electrochemical exfoliation mechanism showed that SO4(2-) and H2O can be intercalated into those graphite sheets, monolayer and few-layer graphene were obtained by the formation of gaseous SO2 and O2 within graphite sheets. Stability evaluation showed that our exfoliated colloidal graphene can be perfectly stabilized in DMF solvent more than 1 week. The colloidal graphene can be used to construct various simple and complex patterns by writing it on A4 paper, which can be applied to flexible printed electronic devices. Furthermore, colloidal graphene can show promising applications in the fabrication of binder- and additive-free electrodes for supercapacitors and lithium-ion batteries. Our present method shows huge potential for industrial-scale synthesis of high-quality graphene and further commercialization of graphene colloid for numerous advanced applications in flexible printed electronics and energy storage devices.

  9. Colloidal stability of Ni(OH){sub 2} in water and its dispersion into a ceramic matrix from the reaction media to obtain Ni/Al{sub 2}O{sub 3} materials

    Energy Technology Data Exchange (ETDEWEB)

    Cabanas-Polo, S.; Ferrari, B.; Sanchez-Herencia, A. J.

    2014-07-01

    Ni/Al{sub 2}O{sub 3} composites have been fabricated by slip casting of concentrated Ni(OH){sub 2}/Al{sub 2}O{sub 3} suspensions and subsequent in situ reduction to metallic nickel during sintering. For that, the synthesis assisted by ultrasound of both α- and β-Ni(OH){sub 2} polymorphs, as well as their colloidal stability, have been studied. The structural differences between both polymorphs have been thoroughly studied by means of XRD, FTIR, DTA-TG, SSA, SEM and TEM, in order to optimize the starting suspensions. This way, the IEP of both polymorphs have been established (9.7 y 12 for β- and α-Ni(OH){sub 2}, respectively), as well as the optimal content of an anionic dispersant (PAA) to stabilize the particles (0.8 wt. % for beta phase and 3.0 wt. % for alpha phase). Three different Ni/Al{sub 2}O{sub 3} composites, with a high dispersion degree of the metallic phase, have been obtained considering the potential vs. particles distance curve of the Ni(OH){sub 2}, and their structure has been discussed in terms of the strength of the agglomerates and/or aggregates of the Ni(OH){sub 2}. (Author)

  10. Effects of hydrophilic colloids on the stability of orange juice%亲水性胶体对橙汁饮料稳定性的影响

    Institute of Scientific and Technical Information of China (English)

    姚森; 王亮; 童彦

    2016-01-01

    Objective To study the effects of hydrophilic colloids such as gellan gum, xanthan gum and sodium alginate andetc. on the stability of 30% orange juice.MethodsThe significant factors that affected the stability of orange juice were screened by the U8(88) uniform design, and then the L9(34) orthogonal design was used to further optimize the best colloids compound.ResultsThe colloids of sodium alginate, gellan gum, pectin and xanthan gum had the most significant influence on orange juice precipitation, while guar gum, Arabic gum and carboxymethyl cellulose sodium (CMC) had no significant effect. Meanwhile, gellan gum and xanthan gum were conducive to turbid stability of orange juice, and xanthan gum and CMC could accelerate the flocculation of orange juice. The most important factors that affected the stability of orange juice were sodium alginate and gellen gum, which could inhibit precipitation and maintain turbid stability effectively when properly used. The main factor that accelerated flocculation was xanthan gum, however, suitable pectin and sodium alginate could prevent the formation of flocculation.ConclusionThe orange juices had the best stability with minimum precipitation or flocculation, and maximum turbid stability when adding 1.2‰ sodium alginate, 0.32‰ gellan gum and 0.8‰ pectin, respectively. The experiments conformed that under the best conditions, orange juice had good stability and no evident flocculation with the precipitation stability of 98.52% and the turbid stability of 94.89%.%目的:以30%橙汁饮料为对象,研究结冷胶、黄原胶、海藻酸钠等亲水性胶体对橙汁稳定性的影响。方法采用U8(88)均匀设计筛选出对橙汁稳定性影响最为显著的因素,再通过L9(34)正交设计进一步验证优化橙汁饮料中的胶体最佳复配方案。结果对橙汁沉淀影响最为显著的胶体是海藻酸钠、结冷胶、果胶、黄原胶,而瓜尔胶、阿拉伯胶和羧甲基纤维素钠(CMC)的

  11. Effects of hydrophilic colloids on the stability of orange juice%亲水性胶体对橙汁饮料稳定性的影响

    Institute of Scientific and Technical Information of China (English)

    姚森; 王亮; 童彦

    2016-01-01

    Objective To study the effects of hydrophilic colloids such as gellan gum, xanthan gum and sodium alginate and etc. on the stability of 30%orange juice. Methods The significant factors that affected the stability of orange juice were screened by the U8(88) uniform design, and then the L9(34) orthogonal design was used to further optimize the best colloids compound. Results The colloids of sodium alginate, gellan gum, pectin and xanthan gum had the most significant influence on orange juice precipitation, while guar gum, Arabic gum and carboxymethyl cellulose sodium (CMC) had no significant effect. Meanwhile, gellan gum and xanthan gum were conducive to turbid stability of orange juice, and xanthan gum and CMC could accelerate the flocculation of orange juice. The most important factors that affected the stability of orange juice were sodium alginate and gellen gum, which could inhibit precipitation and maintain turbid stability effectively when properly used. The main factor that accelerated flocculation was xanthan gum, however, suitable pectin and sodium alginate could prevent the formation of flocculation. Conclusion The orange juices had the best stability with minimum precipitation or flocculation, and maximum turbid stability when adding 1.2‰sodium alginate, 0.32‰gellan gum and 0.8‰pectin, respectively. The experiments conformed that under the best conditions, orange juice had good stability and no evident flocculation with the precipitation stability of 98.52%and the turbid stability of 94.89%.%目的:以30%橙汁饮料为对象,研究结冷胶、黄原胶、海藻酸钠等亲水性胶体对橙汁稳定性的影响。方法采用U8(88)均匀设计筛选出对橙汁稳定性影响最为显著的因素,再通过L9(34)正交设计进一步验证优化橙汁饮料中的胶体最佳复配方案。结果对橙汁沉淀影响最为显著的胶体是海藻酸钠、结冷胶、果胶、黄原胶,而瓜尔胶、阿拉伯胶和羧甲基纤维素钠(CMC)

  12. Complexation of Statins with β-Cyclodextrin in Solutions of Small Molecular Additives and Macromolecular Colloids

    Science.gov (United States)

    Süle, András; Csempesz, Ferenc

    The solubility of lovastatin and simvastatin (inevitable drugs in the management of cardiovascular diseases) was studied by phase-solubility measurements in multicomponent colloidal and non-colloidal media. Complexation in aqueous solutions of the highly lipophilic statins with β-cyclodextrin (β-CD) in the absence and the presence of dissolved polyvinyl pyrrolidone, its monomeric compound, tartaric acid and urea, respectively, were investigated. For the characterization of the CD-statin inclusion complexes, stability constants for the associates have been calculated.

  13. Stability and Occurrence of the Molecule-Containing SiO2 Clathrate Melanophlogite: Metastable Crystallization from a Colloid or Gel?

    Science.gov (United States)

    Geiger, C. A.; Dachs, E.

    2008-12-01

    The mineral melanophlogite is the only known natural SiO2 clathrate. It has been found in a number of localities worldwide in different low-temperature geologic environments. Melanophlogite's thermodynamic stability is not known. Low-temperature hydrothermal laboratory experiments indicate that structure-directing agents and colloid formation are needed for crystallization. The formation of silica-rich colloids/gels and following crystal growth can be observed in glass-ampoule synthesis experiments. In order to better address these issues, the heat capacities of two different molecule-containing melanophlogites of approximate composition 46SiO2·1.80CH4·3.54N2·1.02CO2 from Mt. Hamilton, CA and 46SiO2·3.59CH4·3.10N2·1.31CO2 from Racalmuto, Sicily, along with a heated (molecule-free) sample of composition SiO2, were studied between 5 and 300 K using heat- pulse microcalorimetry. The molecule-free sample was obtained by heating a natural Racalmuto sample at 1173 K for 24 hr. It has a slightly larger low-temperature heat capacity and standard third-law entropy compared to other low-density SiO2 polymorphs such as various zeosils. The standard third-law entropy of the molecule-free sample is S° = 2216.3 J/(mol·K) for 46SiO2 and the natural Mt. Hamilton and Racalmuto samples give S° = 2805.7 J/(mol·K) and S° = 2956.8 J/(mol· K), respectively. The entropy and Gibbs free energy for molecule-free melanophlogite relative to quartz at 298 K are Δ Strans = 6.7 J/(mol·K) and Δ Gtrans = 7.5 kJ/mol, respectively and, thus, it does not have a thermodynamic field of stability in the SiO2 system. The difference in Cp values between molecule-containing and molecule-free melanophlogite is characterized by an increase in Cp from 0 K to approximately 70 K and then reaches a roughly constant value at 70 K cristobalite and chalcedony, suggest that melanophlogite crystallizes metastabily from gels. The occurrence of melanophlogite, and the lack of other SiO2clathrates

  14. Thermal Lens Phenomenon Studied by the Z-Scan Technique: Measurement of the Thermal Conductivity of Highly Absorbing Colloidal Solutions

    Science.gov (United States)

    Sehnem, A. L.; Espinosa, D.; Gonçalves, E. S.; Figueiredo Neto, A. M.

    2016-10-01

    We discuss the thermal lens phenomenon in high-absorbing colloidal systems, studied by using the Z-scan technique. The characteristics of the experimental setup to avoid undesirable effects are presented, in particular when pulsed laser beam is used. We show that a cumulative effect may appear in the experiment with chopped laser beams and compromise the results obtained with this technique. This artefact is more significative when colloidal suspensions are investigated. These materials have different characteristic times of heat and mass diffusion, which must be carefully considered to choose the appropriate time interval for the laser pulse and the time between pulses. Two experimental cases with a chopped laser beam, with and without a shutter, are discussed. The sample employed is a magnetic colloidal suspension (a ferrofluid). This sample has magnetic nanoparticles electrically charged in an aqueous solution with free ions and counter ions. Besides the thermal lens effect, charge and mass diffusion may take place when the sample is illuminated by the Gaussian beam, which imposes a thermal gradient on it. The results show that, with the experimental setup without a shutter, the sample does not achieve a complete relaxation between two laser pulses. This generates a measurable cumulative effect after the sample is illuminated during a relatively long period of time. A time modulation with longer time interval between chopped pulses allows the complete relaxation of the sample. This procedure is important for the correct analysis of the thermal lens effect. Reliable values of the thermal conductivity of the sample in different temperatures are obtained and discussed.

  15. Effect of the Polymeric Stabilizer in the Aqueous Phase Fischer-Tropsch Synthesis Catalyzed by Colloidal Cobalt Nanocatalysts

    Directory of Open Access Journals (Sweden)

    Jorge A. Delgado

    2017-03-01

    Full Text Available A series of small and well defined cobalt nanoparticles were synthesized by the chemical reduction of cobalt salts in water using NaBH4 as a reducing agent and using various polymeric stabilizers. The obtained nanocatalysts of similar mean diameters (ca. 2.6 nm were fully characterized and tested in the aqueous phase Fischer-Tropsch Synthesis (AFTS. Interestingly, the nature and structure of the stabilizers used during the synthesis of the CoNPs affected the reduction degree of cobalt and the B-doping of these NPs and consequently, influenced the performance of these nanocatalysts in AFTS.

  16. Effect of the Polymeric Stabilizer in the Aqueous Phase Fischer-Tropsch Synthesis Catalyzed by Colloidal Cobalt Nanocatalysts

    Science.gov (United States)

    Delgado, Jorge A.; Claver, Carmen; Castillón, Sergio; Curulla-Ferré, Daniel; Godard, Cyril

    2017-01-01

    A series of small and well defined cobalt nanoparticles were synthesized by the chemical reduction of cobalt salts in water using NaBH4 as a reducing agent and using various polymeric stabilizers. The obtained nanocatalysts of similar mean diameters (ca. 2.6 nm) were fully characterized and tested in the aqueous phase Fischer-Tropsch Synthesis (AFTS). Interestingly, the nature and structure of the stabilizers used during the synthesis of the CoNPs affected the reduction degree of cobalt and the B-doping of these NPs and consequently, influenced the performance of these nanocatalysts in AFTS. PMID:28336892

  17. Raspberry Extract as Both a Stabilizer and a Reducing Agent in Environmentally Friendly Process of Receiving Colloidal Silver

    Directory of Open Access Journals (Sweden)

    Jolanta Pulit

    2013-01-01

    Full Text Available An ecofriendly method of nanosilver obtaining has been studied. The process involves the chemical reduction method carried out in aqueous environment. Silver nitrate (V was applied as a silver ions source. Raspberry extract was used as a natural source of both reducing and stabilizing agents. The total amount of phenolic compounds was determined by the Folin-Ciocalteu method. Obtained nanoparticles were analyzed by the dynamic light scattering technique so as to determine the particles size and suspension stability which was characterized by an electrokinetic potential. The results confirmed that the size of some nanoparticles was under 100 nm.

  18. Chemical stability of high-temperature superconductors

    Science.gov (United States)

    Bansal, Narottam P.

    1992-01-01

    A review of the available studies on the chemical stability of the high temperature superconductors (HTS) in various environments was made. The La(1.8)Ba(0.2)CuO4 HTS is unstable in the presence of H2O, CO2, and CO. The YBa2Cu3O(7-x) superconductor is highly susceptible to degradation in different environments, especially water. The La(2-x)Ba(x)CuO4 and Bi-Sr-Ca-Cu-O HTS are relatively less reactive than the YBa2Cu3O(7-x). Processing of YBa2Cu3O(7-x) HTS in purified oxygen, rather than in air, using high purity noncarbon containing starting materials is recommended. Exposure of this HTS to the ambient atmosphere should also be avoided at all stages during processing and storage. Devices and components made out of these oxide superconductors would have to be protected with an impermeable coating of a polymer, glass, or metal to avoid deterioration during use.

  19. Anisotropic Model Colloids

    Science.gov (United States)

    van Kats, C. M.

    2008-10-01

    The driving forces for fundamental research in colloid science are the ability to manage the material properties of colloids and to unravel the forces that play a role between colloids to be able to control and understand the processes where colloids play an important role. Therefore we are searching for colloidal materials with specific physical properties to better understand our surrounding world.Until recently research in colloid science was mainly focused on spherical (isotropic) particles. Monodisperse spherical colloids serve as a model system as they exhibit similar phase behaviour as molecular and atomic systems. Nevertheless, in many cases the spherical shape is not sufficient to reach the desired research goals. Recently the more complex synthesis methods of anisotropic model colloids has strongly developed. This thesis should be regarded as a contribution to this research area. Anisotropic colloids can be used as a building block for complex structures and are expected not only to lead to the construction of full photonic band gap materials. They will also serve as new, more realistic, models systems for their molecular analogues. Therefore the term ‘molecular colloids” is sometimes used to qualify these anisotropic colloidal particles. In the introduction of this thesis, we give an overview of the main synthesis techniques for anisotropic colloids. Chapter 2 describes the method of etching silicon wafers to construct monodisperse silicon rods. They subsequently were oxidized and labeled (coated) with a fluorescent silica layer. The first explorative phase behaviour of these silica rods was studied. The particles showed a nematic ordering in charge stabilized suspensions. Chapter 3 describes the synthesis of colloidal gold rods and the (mesoporous) silica coating of gold rods. Chapter 4 describes the physical and optical properties of these particles when thermal energy is added. This is compared to the case where the particles are irradiated with

  20. Oil-in-water Pickering emulsions stabilized by colloidal particles from the water-insoluble protein zein

    NARCIS (Netherlands)

    de Folter, J.W.J.; van Ruijven, M.W.M.; Velikov, K.

    2012-01-01

    Few fully natural and biocompatible materials are available for the effective particle-stabilization of emulsions since strict requirements, such as insolubility in both fluid phases and intermediate wettability, need to be met. In this paper, we demonstrate the first use of water-insoluble proteins

  1. Synthesis and stabilization of oxide-based colloidal suspensions in organic media: application in the preparation of hybrids organic-inorganic materials for very high laser damage threshold coatings; Synthese et stabilisation de suspensions colloidales d'oxydes en milieu organique: application a la preparation de materiaux hybrides organiques-inorganiques pour des revetements a tres haute tenue au flux laser

    Energy Technology Data Exchange (ETDEWEB)

    Marchet, N.

    2008-02-15

    Multilayer coatings are widely used in optic and particular in the field of high power laser on the components of laser chains. The development of a highly reflective coating with a laser damage resistance requires the fine-tuning of a multilayer stack constituted by a succession alternated by materials with low and high refractive index. In order to limit the number of layers in the stack, refractive indexes must be optimized. To do it, an original approach consists in synthesizing new organic-inorganic hybrid materials satisfying the criteria of laser damage resistance and optimized refractive index. These hybrid materials are constituted by nano-particles of metal oxides synthesized by sol-gel process and dispersed in an organic polymer with high laser damage threshold. Nevertheless, this composite system requires returning both compatible phases between them by chemical grafting of alc-oxy-silanes or carboxylic acids. We showed that it was so possible to disperse in a homogeneous way these functionalized nano-particles in non-polar, aprotic solvent containing solubilized organic polymers, to obtain time-stable nano-composite solutions. From these organic-inorganic hybrid solutions, thin films with optical quality and high laser damage threshold were obtained. These promising results have permitted to realize highly reflective stacks, constituted by 7 pairs with optical properties in agreement with the theoretical models and high laser damage threshold. (author)

  2. Colloidal nematostatics

    Directory of Open Access Journals (Sweden)

    V.M. Pergamenshchik

    2010-01-01

    Full Text Available We give a review of the theory of large distance colloidal interaction via the nematic director field. The new area of nematic colloidal systems (or nematic emulsions has been guided by the analogy between the colloidal nematostatics and electrostatics. The elastic charge density representation of the colloidal nematostatics [V.M. Pergamenshchik, V.O. Uzunova, Eur. Phys. J. E, 2007, 23, 161; Phys. Rev. E, 2007, 76, 011707] develops this analogy at the level of charge density and Coulomb interaction. The analogy is shown to lie in common mathematics based on the solutions of Laplace equation. However, the 3d colloidal nematostatics substantially differs from electrostatics both in its mathematical structure and physical implications. The elastic charge is a vector fully determined by the torque exerted upon colloid, the role of Gauss' theorem is played by conservation of the torque components. Elastic multipoles consist of two tensors (dyads. Formulas for the elastic multipoles, the Coulomb-like, dipole-dipole, and quadrupole-quadrupole pair interaction potentials are derived and illustrated by particular examples. Based on the tensorial structure, we list possible types of elastic dipoles and quadrupoles. An elastic dipole is characterized by its isotropic strength, anisotropy, chirality, and its longitudinal component. An elastic quadrupole can be uniaxial and biaxial. Relation between the multipole type and its symmetry is discussed, sketches of some types of multipoles are given. Using the mirror image method of electrostatics as a guiding idea, we develop the mirror image method in nematostatics for arbitrary director tilt at the wall. The method is applied to the charge-wall and dipole-wall interaction.

  3. Synthesis of Colloidal Nanocrystal Heterostructures for High-Efficiency Light Emission

    Science.gov (United States)

    Lu, Yifei

    Group II-VI semiconductor nanocrystals, particularly those based on ZnCdS(Se), can be synthesized using well established chemical colloidal processes, and have been a subject of extensive research over the past decade. Their optical properties can be easily tuned through size and composition variations, making them very attractive for many optoelectronic applications including light-emitting diodes (LEDs) and solar cells. Incorporation of diverse internal heterostructures provides an additional means for tuning the optical and electronic properties of conventional ZnCdS(Se) nanocrystals. Extensive bandgap and strain engineering may be applied to the resultant nanocrystal heterostructures to achieve desirable properties and enhanced performance. Despite the high scientific and practical interests of this unique class of nanomaterials, limited efforts have been made to explore their synthesis and potential device applications. This thesis focuses on the synthesis, engineering, characterization, and device demonstration of two types of CdSe-based nanocrystal heterostructures: core/multishell quantum dots (QDs) and QD quantum wells (QDQWs). Their optical properties have been tuned by bandgap and strain engineering to achieve efficient photoluminescence (PL) and electroluminescence (EL).Firstly, yellow light-emitting CdSe QDs with a strain-compensated ZnS/ZnCdS bilayer shell were synthesized using the successive ion layer adsorption and reaction technique and the effects of the shell on the luminescent properties were investigated. The core/shell/shell QDs enjoyed the benefits of excellent exciton confinement by the ZnS intermediate shell and strain compensation by the ZnCdS outer shell, and exhibited 40% stronger PL and a smaller peak redshift upon shell growth compared to conventional CdSe/ZnCdS/ZnS core/shell/shell QDs with an intermediate lattice adaptor. CdSe/ZnS/ZnCdS QD-LEDs had a luminance of 558 cd/m2 at 20 mA/cm 2, 28% higher than that of CdSe/ZnCdS/ZnS QD

  4. Freezing of Charge-stabilized Colloidal Dispersions%电荷稳定的胶体分散体的凝固

    Institute of Scientific and Technical Information of China (English)

    周世琦

    2003-01-01

    Rogers-Young approximation for Ornstein-Zernike integral equation is com-bined with Hansen-Verlet one phase criterion for freezing to predict freezing of hard core re-pulsive Yukawa model ( HCRYM ) fluid. Comparison of theoretical predictions with corre-sponding computer simulation data uncloses the superiority of the Rogers-Young approxima-tion over Hypemetted chain approximation and rescaled mean spherical approximation forfreezing. Then, the Rogers-Young approximation combined with the Hansen-Verlet one phasecriterion is employed for the freezing of many-component charge-stabilized colloidal disper-sions, which consist of colloidal macro-ions, electrolyte small ions and solvent molecules, andare modeled as a single-component charged hard core macro-ion interacting through ascreened Coulomb potential. The theoretically predicted freezing line with the macro-ion sur-face charge number being assumed as an adjustable parameter is in very good agreement withthe corresponding experimental data. The reason why by the empirical Hansen-Verlet struc-ture function approach,the single-component coarse-grained effective potential is valid for thefreezing description of the many-component charge-stabilized colloidal solutions, but not validfor the case of asymmetric binary hard sphere mixtures, is discussed.%Rogers-Young近似结合ornstein-Zernike积分方程与Hansen-Verlet单相凝固标准预言硬核排斥汤川模型流体的凝固.理论预言与相应的计算机模拟数据的比较揭示了Rogers-Young近似比超网链近似与重标度平均球形近似精度高.在此基础上,Rogers-Young近似结合Hansen-Verlet单相凝固标准预言多组分电荷稳定的胶体分散体的凝固,胶体分散体由胶体大离子、电解质小离子和溶剂分子组成,用单组分荷电硬核大离子(由屏蔽库伦相互作用势描述)来模拟.当荷电硬核大离子的表面电荷被当作可调参数时,所预言的凝固线与相应的实验数据符合很好.讨

  5. Colloidal microcapsules: Surface engineering of nanoparticles for interfacial assembly

    Science.gov (United States)

    Patra, Debabrata

    2011-12-01

    Colloidal Microcapsules (MCs), i.e. capsules stabilized by nano-/microparticle shells are highly modular inherently multi-scale constructs with applications in many areas of material and biological sciences e.g. drug delivery, encapsulation and microreactors. These MCs are fabricated by stabilizing emulsions via self-assembly of colloidal micro/nanoparticles at liquid-liquid interface. In these systems, colloidal particles serve as modular building blocks, allowing incorporation of the particle properties into the functional capabilities of the MCs. As an example, nanoparticles (NPs) can serve as appropriate antennae to induce response by external triggers (e.g. magnetic fields or laser) for controlled release of encapsulated materials. Additionally, the dynamic nature of the colloidal assembly at liquid-liquid interfaces result defects free organized nanostructures with unique electronic, magnetic and optical properties which can be tuned by their dimension and cooperative interactions. The physical properties of colloidal microcapsules such as permeability, mechanical strength, and biocompatibility can be precisely controlled through the proper choice of colloids and preparation conditions for their. This thesis illustrates the fabrication of stable and robust MCs through via chemical crosslinking of the surface engineered NPs at oil-water interface. The chemical crosslinking assists NPs to form a stable 2-D network structure at the emulsion interface, imparting robustness to the emulsions. In brief, we developed the strategies for altering the nature of chemical interaction between NPs at the emulsion interface and investigated their role during the self-assembly process. Recently, we have fabricated stable colloidal microcapsule (MCs) using covalent, dative as well as non-covalent interactions and demonstrated their potential applications including encapsulation, size selective release, functional devices and biocatalysts.

  6. Colloidal superballs

    NARCIS (Netherlands)

    Rossi, L.

    2012-01-01

    This thesis is organized in four parts as follows. Part 1 focuses on the synthetic aspects of the colloidal model systems that will be used throughout the work described in this thesis. In Chapter 2 we describe synthetic procedures for the preparation of polycrystalline hematite superballs and super

  7. Preparation of highly permeable BPPO microfiltration membrane with binary porous structures on a colloidal crystal substrate by the breath figure method.

    Science.gov (United States)

    Yuan, Hua; Yu, Bing; Cong, Hailin; Peng, Qiaohong; Yang, Zhen; Luo, Yongli; Chi, Ming

    2016-01-01

    A highly permeable brominated poly(phenylene oxide) (BPPO) microfiltration membrane with binary porous structures was fabricated by combination of the breath figure and colloidal crystal template methods. The pore size in the bottom layer of the membrane was adjusted by the diameter of SiO2 microspheres in the colloidal crystal template, while the pore size in the top layer of the membrane was adjusted by varying the BPPO concentration in the casting solution. The permeability of the membrane cast on the colloidal crystal substrate was much higher than that of the membrane cast on a bare silicon wafer. The binary porous BPPO membrane with high permeability and antifouling property was used for microfiltration applications.

  8. The influence of cilica gel on wheat beer colloidal stabilization%硅胶处理对小麦啤酒胶体稳定性的影响

    Institute of Scientific and Technical Information of China (English)

    王海明; 余功德; 朱景林

    2001-01-01

    The aim was to discover the influence of cilica gel on wheat beercolloidal stabilization. In comparison with normal beer, wheat beer has poor colloidal stabilization, especially when stored in refrigerator, it tends to generate chill haze due to the higher concentration of protein from wheat malt which used as main brewing material. Shelf-life can been predicted by SASPL test and hot/cold cycle forcing test. We found that treatment with silica gel in the cold conditioning process could effectively prolong shelf-life of wheat beer .%表明硅胶处理对小麦啤酒胶体稳定性的影响。小麦啤酒与正常的啤酒相比,小麦啤酒的抗冷能力较差,尤其是啤酒在冰箱内保藏温度接近0℃时,啤酒容易出现冷混浊,这是由于用于酿造小麦啤酒的主要原料小麦麦芽含有较高的蛋白质。我们通过在贮酒后期添加硅胶,将成品啤酒经饱和硫酸铵极限试验和冷热试验测定啤酒的SASPL值和保质期,发现使用硅胶可以有效地延长小麦啤酒的保质期。

  9. Ultrasonic wave interactions with magnetic colloids

    CERN Document Server

    Chapman, J R

    2001-01-01

    fluids have been performed in an effort to determine the relative stability of the fluids. The experimental results have been compared with a combined scattering and hydrodynamic model (Allegra and Hawley 1972) and the ultrasonic anisotropy theory of Skumiel (1997). An on-line quality assurance process is proposed. Originally invented as a method for moving spacecraft fuel in weightless conditions, magnetic colloids or ferrofluids are now used in applications as diverse as the dissipation of heat in the voice coils of a loudspeaker, and for the separation of scrap metal. It has been found that aqueous ferrofluids become unstable after a period of time and with dilution. Therefore, there is a need to characterize the colloidal fluid to study the effects of degradation. Additionally, due to the high cost of ferrofluids and the large volumes required for some applications, the fluid is recycled. It is therefore necessary to develop a system for quality assurance for the fluid reclamation process. Ultrasonic meth...

  10. Colloidal pen lithography.

    Science.gov (United States)

    Xue, Mianqi; Cai, Xiaojing; Chen, Ghenfu

    2015-02-04

    Colloidal pen lithography, a low-cost, high-throughput scanning probe contact printing method, has been developed, which is based on self-assembled colloidal arrays embedded in a soft elastomeric stamp. Patterned protein arrays are demonstrated using this method, with a feature size ranging from 100 nm to several micrometers. A brief study into the specificity reorganization of protein gives evidence for the feasibility of this method for writing protein chips. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. MOLECULAR DESIGN OF COLLOIDS IN SUPERCRITICAL FLUIDS

    Energy Technology Data Exchange (ETDEWEB)

    Keith P. Johnston

    2009-04-06

    The environmentally benign, non-toxic, non-flammable fluids water and carbon dioxide (CO2) are the two most abundant and inexpensive solvents on earth. Emulsions of these fluids are of interest in many industrial processes, as well as CO2 sequestration and enhanced oil recovery. Until recently, formation of these emulsions required stabilization with fluorinated surfactants, which are expensive and often not environmentally friendly. In this work we overcame this severe limitation by developing a fundamental understanding of the properties of surfactants the CO2-water interface and using this knowledge to design and characterize emulsions stabilized with either hydrocarbon-based surfactants or nanoparticle stabilizers. We also discovered a new concept of electrostatic stabilization for CO2-based emulsions and colloids. Finally, we were able to translate our earlier work on the synthesis of silicon and germanium nanocrystals and nanowires from high temperatures and pressures to lower temperatures and ambient pressure to make the chemistry much more accessible.

  12. Laser Synthesis and Processing of Colloids: Fundamentals and Applications.

    Science.gov (United States)

    Zhang, Dongshi; Gökce, Bilal; Barcikowski, Stephan

    2017-03-08

    Driven by functionality and purity demand for applications of inorganic nanoparticle colloids in optics, biology, and energy, their surface chemistry has become a topic of intensive research interest. Consequently, ligand-free colloids are ideal reference materials for evaluating the effects of surface adsorbates from the initial state for application-oriented nanointegration purposes. After two decades of development, laser synthesis and processing of colloids (LSPC) has emerged as a convenient and scalable technique for the synthesis of ligand-free nanomaterials in sealed environments. In addition to the high-purity surface of LSPC-generated nanoparticles, other strengths of LSPC include its high throughput, convenience for preparing alloys or series of doped nanomaterials, and its continuous operation mode, suitable for downstream processing. Unscreened surface charge of LSPC-synthesized colloids is the key to achieving colloidal stability and high affinity to biomolecules as well as support materials, thereby enabling the fabrication of bioconjugates and heterogeneous catalysts. Accurate size control of LSPC-synthesized materials ranging from quantum dots to submicrometer spheres and recent upscaling advancement toward the multiple-gram scale are helpful for extending the applicability of LSPC-synthesized nanomaterials to various fields. By discussing key reports on both the fundamentals and the applications related to laser ablation, fragmentation, and melting in liquids, this Article presents a timely and critical review of this emerging topic.

  13. Influence of high-pressure treatment on charge carrier transport in PbS colloidal quantum dot solids.

    Science.gov (United States)

    Heo, Seung Jin; Yoon, Seokhyun; Oh, Sang Hoon; Yoon, Doo Hyun; Kim, Hyun Jae

    2014-01-21

    We investigated the effects of high-pressure treatment on charge carrier transport in PbS colloidal quantum dot (CQD) solids. We applied high pressure to PbS CQD solids using nitrogen gas to reduce the inter-dot distance. Using this simple process, we obtained conductive PbS CQD solids. Terahertz time-domain spectroscopy was used to study charge carrier transport as a function of pressure. We found that the minimum pressure needed to increase the dielectric constant, conductivity, and carrier mobility was 4 MPa. All properties dramatically improved at 5 MPa; for example, the mobility increased from 0.13 cm(2) V(-1) s(-1) at 0.1 MPa to 0.91 cm(2) V(-1) s(-1) at 5 MPa. We propose this simple process as a nondestructive approach for making conductive PbS CQD solids that are free of chemical and physical defects.

  14. Solution processable colloidal nanoplates as building blocks for high-performance electronic thin films on flexible substrates.

    Science.gov (United States)

    Lin, Zhaoyang; Chen, Yu; Yin, Anxiang; He, Qiyuan; Huang, Xiaoqing; Xu, Yuxi; Liu, Yuan; Zhong, Xing; Huang, Yu; Duan, Xiangfeng

    2014-11-12

    Low-temperature solution-processed electronic materials on plastic substrates are of considerable interest for flexible electronics. Solution dispersible inorganic nanostructures (e.g., zero-dimensional (0D) quantum dots or one-dimensional (1D) nanowires) have emerged as interesting ink materials for low-temperature solution processing of electronic thin films on flexible substrates, but usually with limited performance due to the large number of grain boundaries (0D) or incomplete surface coverage (1D). Here, we report two-dimensional (2D) colloidal nanoplates of layered materials as a new ink material for solution assembly of high-performance electronic thin films. The 2D colloidal nanoplates exhibit few dangling bonds and represent an ideal geometry for the assembly of highly uniform continuous thin films with greatly reduced grain boundaries dictated by large-area conformal plane-plane contact with atomically flat/clean interfaces. It can therefore promise efficient charge transport across neighboring nanoplates and throughout the entire thin film to enable unprecedented electronic performance. We show that Bi2Se3 and Bi2Te3 nanoplates can be synthesized with well-controlled thickness (6-15 nm) and lateral dimension (0.5-3 μm) and can be used for the assembly of highly uniform continuous thin films with a full surface coverage and an excellent room temperature carrier mobility >100 cm(2)·V(-1)·s(-1), approaching that of chemical vapor deposition grown materials. Our study demonstrates a general strategy to using 2D nanoplates as a unique building block for the construction of high-performance electronic thin films on plastic substrates for future flexible electronics and optoelectronics.

  15. Dismantling the "Red Wall" of Colloidal Perovskites: Highly Luminescent Formamidinium and Formamidinium-Cesium Lead Iodide Nanocrystals.

    Science.gov (United States)

    Protesescu, Loredana; Yakunin, Sergii; Kumar, Sudhir; Bär, Janine; Bertolotti, Federica; Masciocchi, Norberto; Guagliardi, Antonietta; Grotevent, Matthias; Shorubalko, Ivan; Bodnarchuk, Maryna I; Shih, Chih-Jen; Kovalenko, Maksym V

    2017-03-28

    Colloidal nanocrystals (NCs) of APbX3-type lead halide perovskites [A = Cs(+), CH3NH3(+) (methylammonium or MA(+)) or CH(NH2)2(+) (formamidinium or FA(+)); X = Cl(-), Br(-), I(-)] have recently emerged as highly versatile photonic sources for applications ranging from simple photoluminescence down-conversion (e.g., for display backlighting) to light-emitting diodes. From the perspective of spectral coverage, a formidable challenge facing the use of these materials is how to obtain stable emissions in the red and infrared spectral regions covered by the iodide-based compositions. So far, red-emissive CsPbI3 NCs have been shown to suffer from a delayed phase transformation into a nonluminescent, wide-band-gap 1D polymorph, and MAPbI3 exhibits very limited chemical durability. In this work, we report a facile colloidal synthesis method for obtaining FAPbI3 and FA-doped CsPbI3 NCs that are uniform in size (10-15 nm) and nearly cubic in shape and exhibit drastically higher robustness than their MA- or Cs-only cousins with similar sizes and morphologies. Detailed structural analysis indicated that the FAPbI3 NCs had a cubic crystal structure, while the FA0.1Cs0.9PbI3 NCs had a 3D orthorhombic structure that was isostructural to the structure of CsPbBr3 NCs. Bright photoluminescence (PL) with high quantum yield (QY > 70%) spanning red (690 nm, FA0.1Cs0.9PbI3 NCs) and near-infrared (near-IR, ca. 780 nm, FAPbI3 NCs) regions was sustained for several months or more in both the colloidal state and in films. The peak PL wavelengths can be fine-tuned by using postsynthetic cation- and anion-exchange reactions. Amplified spontaneous emissions with low thresholds of 28 and 7.5 μJ cm(-2) were obtained from the films deposited from FA0.1Cs0.9PbI3 and FAPbI3 NCs, respectively. Furthermore, light-emitting diodes with a high external quantum efficiency of 2.3% were obtained by using FAPbI3 NCs.

  16. Development and comparison of immunochromatographic strips with three nanomaterial labels: Colloidal gold, nanogold-polyaniline-nanogold microspheres (GPGs) and colloidal carbon for visual detection of salbutamol.

    Science.gov (United States)

    Liu, Bing; Wang, Lingling; Tong, Bei; Zhang, Yan; Sheng, Wei; Pan, Mingfei; Wang, Shuo

    2016-11-15

    In this study, the three nanomaterials: colloidal gold, nanogold-polyaniline-nanogold microspheres (GPGs) and colloidal carbon were respectively labeled with the antibody against salbutamol (SAL). We aimed to develop immunochromatographic strips with these nanomaterial labels and determine their performance in visual detection of SAL. For the colloidal gold-based strip, the detection limit of SAL was 1.0µgL(-1) in standard solution and 5.0µgkg(-1) in meat samples. For the GPG- and colloidal carbon-based strips, the limit of detection was 2.0µgL(-1) in standard solution and 10µgkg(-1) in meat samples. The results obtained using the test strips were found to be highly consistent with those obtained using a commercial kit, indicating the high accuracy of these strips. The three strips were also found to be stable up to 18 weeks under laboratory conditions. In terms of sensitivity, the colloidal gold-based strip was slightly better than the other two. For the GPG- and colloidal carbon-based strips, the difference between the results obtained for different batches was small (high consistency), and the stability was much better than that of the colloidal gold-based one. Our results indicate that colloidal carbon can be used as a label in immunochromatographic tests; it can also help reduce the cost involved and scale-up the production. The use of immunochromatographic test strips labeled with colloidal carbon can be a rapid and inexpensive method for SAL assays in on-site applications.

  17. Interplay between Colloids and Interfaces : Emulsions, Foams and Microtubes

    NARCIS (Netherlands)

    de Folter, J.W.J.

    2013-01-01

    The central theme of this thesis is the interplay between colloids and interfaces. The adsorption of colloids at fluid-fluid interfaces is the main topic and covers Chapters 2-6. Pickering emulsions where colloidal particles act as emulsion stabilizers in the absence of surfactants are studied in a

  18. What happens when pharmaceuticals meet colloids.

    Science.gov (United States)

    Xing, Yingna; Chen, Xijuan; Zhuang, Jie; Chen, Xin

    2015-12-01

    Pharmaceuticals (PCs) have been widely detected in natural environment due to agricultural application of reclaimed water, sludge and animal wastes. Their potential risks to various ecosystems and even to human health have caused great concern; however, little was known about their environmental behaviors. Colloids (such as clays, metal oxides, and particulate organics) are kind of substances that are active and widespread in the environment. When PCs meet colloids, their interaction may influence the fate, transport, and toxicity of PCs. This review summarizes the progress of studies on the role of colloids in mediating the environmental behaviors of PCs. Synthesized results showed that colloids can adsorb PCs mainly through ion exchange, complexation and non-electrostatic interactions. During this process the structure of colloids and the stability of PCs may be changed. The adsorbed PCs may have higher risks to induce antibiotic resistance; besides, their transport may also be altered considering they have great chance to move with colloids. Solution conditions (such as pH, ionic strength, and cations) could influence these interactions between PCs and colloids, as they can change the forms of PCs and alter the primary forces between PCs and colloids in the solution. It could be concluded that PCs in natural soils could bind with colloids and then co-transport during the processes of irrigation, leaching, and erosion. Therefore, colloid-PC interactions need to be understood for risk assessment of PCs and the best management practices of various ecosystems (such as agricultural and wetland systems).

  19. Synthesis of colloidal Mn2+:ZnO quantum dots and high-TC ferromagnetic nanocrystalline thin films.

    Science.gov (United States)

    Norberg, Nick S; Kittilstved, Kevin R; Amonette, James E; Kukkadapu, Ravi K; Schwartz, Dana A; Gamelin, Daniel R

    2004-08-04

    We report the synthesis of colloidal Mn(2+)-doped ZnO (Mn(2+):ZnO) quantum dots and the preparation of room-temperature ferromagnetic nanocrystalline thin films. Mn(2+):ZnO nanocrystals were prepared by a hydrolysis and condensation reaction in DMSO under atmospheric conditions. Synthesis was monitored by electronic absorption and electron paramagnetic resonance (EPR) spectroscopies. Zn(OAc)(2) was found to strongly inhibit oxidation of Mn(2+) by O(2), allowing the synthesis of Mn(2+):ZnO to be performed aerobically. Mn(2+) ions were removed from the surfaces of as-prepared nanocrystals using dodecylamine to yield high-quality internally doped Mn(2+):ZnO colloids of nearly spherical shape and uniform diameter (6.1 +/- 0.7 nm). Simulations of the highly resolved X- and Q-band nanocrystal EPR spectra, combined with quantitative analysis of magnetic susceptibilities, confirmed that the manganese is substitutionally incorporated into the ZnO nanocrystals as Mn(2+) with very homogeneous speciation, differing from bulk Mn(2+):ZnO only in the magnitude of D-strain. Robust ferromagnetism was observed in spin-coated thin films of the nanocrystals, with 300 K saturation moments as large as 1.35 micro(B)/Mn(2+) and T(C) > 350 K. A distinct ferromagnetic resonance signal was observed in the EPR spectra of the ferromagnetic films. The occurrence of ferromagnetism in Mn(2+):ZnO and its dependence on synthetic variables are discussed in the context of these and previous theoretical and experimental results.

  20. TiO/sub 2/ and CdS colloids stabilized by. beta. -cyclodextrins: tailored semiconductor-receptor systems as a means to control interfacial electron-transfer processes

    Energy Technology Data Exchange (ETDEWEB)

    Willner, I.; Eichen, Y.

    1987-10-28

    The photocatalytic activity of semiconductor particles is of substantial interest in synthesis as well as a means of solar energy conversion and storage. Electron-transfer reactions such as charge ejection or charge injection at semiconductor - solution interfaces are important factors that control the photocatalytic activity of the semiconductors. Electrostatic attraction of solute to the semiconductor surface has improved charge ejection from the excited semiconductor to solute relays. Adsorption of dyes to the semiconductor surface, i.e., by hydrophobic interactions, resulted in effective charge injection to the semiconductor and consequently the photocatalytic activity of semiconductors operative in the UV region could be shifted to the visible absorption spectrum. Substantial efforts have also been directed in recent years toward the preparation of semiconductor particles in colloidal forms to improve their light harvesting and interfacial electron-transfer properties. Stabilization of semiconductor colloids by polymers, microemulsions, and vesicle encapsulation has been reported. Here they report on a novel method for stabilizing semiconductor colloids by ..beta..-cyclodextrin (..beta..-CD).

  1. High internal phase emulsions stabilized solely by whey protein isolate-low methoxyl pectin complexes: effect of pH and polymer concentration.

    Science.gov (United States)

    Wijaya, Wahyu; Van der Meeren, Paul; Wijaya, Christofora Hanny; Patel, Ashok R

    2017-02-22

    In recent years, there has been significant progress in edible emulsion technology especially with respect to creating and stabilizing surfactant-free emulsion systems for food applications. In this paper, we demonstrate the fabrication of high internal phase emulsions (HIPE) (φoil = 0.82) stabilized using colloidal complexes of non-gelling biopolymers (at concentrations as low as 0.3 wt%). The colloidal complexes were pre-formed by combining whey protein isolate (WPI) and low-methoxyl pectin (LMP) at three different pH values (i.e. pH 3.5, 4.5, 5.5) and used further for fabricating stable HIPEs. In addition to the effect of pH, the influence of total biopolymer concentration on the formation and properties of HIPEs was also evaluated. Depending on the total concentration of biopolymers used, the WPI-LMP complexes (formed at pH 4.5) showed a Z-average diameter in the range of 250-350 nm. It was found that the formation of HIPEs was strongly influenced by the pH of the colloidal complexes. At a pH close to the isoelectric point of WPI (≈pH 4.8) and WPI-LMP complexes (≈pH 3.4), severe aggregation of colloidal particles occurred, resulting in poor formation and stability of HIPEs. On comparing the stabilization behaviour of the complexes with the uncomplexed protein, it was noticed that the former provided comparatively better stabilization to the HIPEs against coalescence at pH 4.5 and 5.5. Based on the rheological data (low amplitude oscillatory shear rheology and flow measurements), all HIPE samples showed viscoelastic and shear-thinning behaviour. We believe that such viscoelastic gel-like systems could find potential commercial applications in the development of label-friendly novel food products with interesting textures.

  2. Biocompatible and colloidally stabilized mPEG-PE/calcium phosphate hybrid nanoparticles loaded with siRNAs targeting tumors.

    Science.gov (United States)

    Gao, Pei; Zhang, Xiangyu; Wang, Hongzhi; Zhang, Qinghong; Li, He; Li, Yaogang; Duan, Yourong

    2016-01-19

    Calcium phosphate nanoparticles are safe and effective delivery vehicles for small interfering RNA (siRNA), as a result of their excellent biocompatibility. In this work, mPEG-PE (polyethylene glycol-L-α-phosphatidylethanolamine) was synthesized and used to prepare nanoparticles composed of mPEG-PE and calcium phosphate for siRNA delivery. Calcium phosphate and mPEG-PE formed the stable hybrid nanoparticles through self-assembly resulting from electrostatic interaction in water. The average size of the hybrid nanoparticles was approximately 53.2 nm with a negative charge of approximately -16.7 mV, which was confirmed by dynamic light scattering (DLS) measurements. The nanoparticles exhibited excellent stability in serum and could protect siRNA from ribonuclease (RNase) degradation. The cellular internalization of siRNA-loaded nanoparticles was evaluated in SMMC-7721 cells using a laser scanning confocal microscope (CLSM) and flow cytometry. The hybrid nanoparticles could efficiently deliver siRNA to cells compared with free siRNA. Moreover, the in vivo distribution of Cy5-siRNA-loaded hybrid nanoparticles was observed after being injected into tumor-bearing nude mice. The nanoparticles concentrated in the tumor regions through an enhanced permeability and retention (EPR) effect based on the fluorescence intensities of tissue distribution. A safety evaluation of the nanoparticles was performed both in vitro and in vivo demonstrating that the hybrid nanoparticle delivery system had almost no toxicity. These results indicated that the mPEG-PE/CaP hybrid nanoparticles could be a stable, safe and promising siRNA nanocarrier for anticancer therapy.

  3. Colloid-Facilitated Transport of Low-Solubility Radionuclides: A Field, Experimental, and Modeling Investigation

    Energy Technology Data Exchange (ETDEWEB)

    Kersting, A B; Reimus, P W; Abdel-Fattah, A; Allen, P G; Anghel, I; Benedict, F C; Esser, B K; Lu, N; Kung, K S; Nelson, J; Neu, M P; Reilly, S D; Smith, D K; Sylwester, E R; Wang, L; Ware, S D; Warren, RG; Williams, R W; Zavarin, M; Zhao, P

    2003-02-01

    rate of Pu transport. Currently, the role of colloids in facilitating the transport of low-solubility radionuclides is not understood well enough to effectively model contaminant transport. A fundamental understanding of the role that colloids may or may not play in the transport of low-solubility radionuclides is needed in order to predict contaminant transport, design remediation strategies and provide risk assessments. Ryan and Elimelech (1996) have argued that in order to evaluate the potential for colloids to transport radionuclides, several criteria must be met: (1) colloids must exist and be stable, (2) radionuclides must have a high sorption affinity for the colloids, and (3) colloids must be transported. Only then can we understand the conditions where colloids can and will facilitate transport of radionuclides. In this report we compile the results from a series of field, laboratory and modeling studies funded by the UGTA program in order to evaluate the potential for colloids to transport low-solubility radionuclides at the NTS. The studies presented in this report fall under three general areas of investigation: Characterization of natural colloids in groundwater at NTS, Pu sorption/desorption experiments on colloid minerals identified in NTS groundwater, and Transport of Pu-doped colloids through fractured rock core. Chapter 1 is a background review of our current understanding of colloids and their role in facilitating contaminant transport. Chapters 2, and 3 are field studies that focused on characterizing natural colloids at different hydrologic environments at the NTS and address Ryan and Elimelech's (1996) first criteria regarding the existence and stability of colloids. Chapters 4, 5 and 6 are laboratory experimental studies that investigate the sorption/desorption behavior of Pu and other low-solubility radionuclides on colloid minerals observed in NTS groundwater. These studies evaluate Ryan and Elimelech's (1996) second criteria that the

  4. Soil colloidal behavior

    Science.gov (United States)

    Recent understanding that organic and inorganic contaminants are often transported via colloidal particles has increased interest in colloid science. The primary importance of colloids in soil science stems from their surface reactivity and charge characteristics. Characterizations of size, shape,...

  5. Colloidal gold and silica in mesothermal vein systems

    Science.gov (United States)

    Herrington, R. J.; Wilkinson, J. J.

    1993-06-01

    Some of the textural features of mesothermal gold-quartz veins may be best explained by the initial precipitation of amorphous silica gel (colloid), which subsequently crystallizes to quartz. This can occur in brittle-ductile shear zones where a significant fluid-pressure drop occurs during stick-slip failure. Such a process rapidly supersaturates the hydrothermal fluid with respect to amorphous silica, which precipitates instead of quartz, owing to favorable kinetics. Depressurization also commonly leads to fluid unmixing and destabilization of soluble gold complexes. However, the presence of colloidal silica can stabilize gold colloid, allowing further transport of particulate gold in suspension in the hydrothermal fluid. Silica gel would be highly unstable under mesothermal conditions and would undergo rapid syneresis and crystallization to form quartz; solid impurities would tend to be expelled toward grain boundaries. This model can account for the primary anhedral aggregate textures typical of mesothermal quartz veins, the concentration of gold along grain boundaries and the formation of discrete gold nuggets, and the rare occurrence of low-order silica polymorphs and relict spheroidal structures. The transport of gold in colloidal form may be one reason for the frequently consistent bulk grade distribution in gold-quartz vein systems over many hundreds of metres (in some cases kilometres) of depth. In addition, the formation of charged colloidal particles may help to explain the attraction of gold grains to specific mineral surfaces.

  6. One-pot synthesis of stable colloidal solutions of MFe{sub 2}O{sub 4} nanoparticles using oleylamine as solvent and stabilizer

    Energy Technology Data Exchange (ETDEWEB)

    Pérez-Mirabet, Leonardo [Departament de Química, Universitat Autònoma de Barcelona, Campus de la UAB, 08193 Bellaterra (Spain); Solano, Eduardo, E-mail: eduardo.solano@uab.cat [Departament de Química, Universitat Autònoma de Barcelona, Campus de la UAB, 08193 Bellaterra (Spain); Martínez-Julián, Fernando; Guzmán, Roger [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain); Arbiol, Jordi [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain); Institució Catalana de Recerca i Estudis Avançats (ICREA), 08019 Barcelona (Spain); Puig, Teresa; Obradors, Xavier; Pomar, Alberto [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain); Yáñez, Ramón; Ros, Josep [Departament de Química, Universitat Autònoma de Barcelona, Campus de la UAB, 08193 Bellaterra (Spain); Ricart, Susagna [Institut de Ciència de Materials de Barcelona, ICMAB-CSIC, Campus de la UAB, 08193 Bellaterra (Spain)

    2013-03-15

    Highlights: ► One-pot synthesis of ferrite magnetic nanoparticles (<10 nm) in non-polar media. ► Nanoparticles present high monocrystal quality and monodispersion. ► Superparamagnetic behavior at room temperature. ► Nanoparticles transfer to polar media via ligand exchange. - Abstract: An easy, efficient, reproducible and scalable one-pot synthetic methodology to obtain magnetic spinel ferrite nanoparticles has been developed. This approach is based on one-pot thermal decomposition of Fe(acac){sub 3} and M(acac){sub 2} (M = Co, Mn, Cu and Zn) in oleylamine, which also acts as a capping ligand, by producing stable colloidal dispersions of nanoparticles in non-polar solvents. The properties of the nanoparticles have been studied via different techniques, such as transmission electron microscopy, which shows that nanoparticles are monocrystallines and a narrow dispersion in size; magnetic analyses have demonstrated that the resulting ferrite nanoparticles show high saturation values and superparamagnetic behavior at room temperature; X-ray diffraction has also been performed, and it confirms that the synthesized nanoparticles have a spinel structure. Complementarily, ligand exchange has been also carried out in order to produce dispersions of the synthesized nanoparticles in polar media.

  7. Specific detection of cysteine and homocysteine in biological fluids by tuning the pH values of fluorosurfactant-stabilized gold colloidal solution.

    Science.gov (United States)

    Xiao, Qunyan; Shang, Fei; Xu, Xuechen; Li, Qianqian; Lu, Chao; Lin, Jin-Ming

    2011-12-15

    This study describes the use of 14 nm nonionic fluorosurfactant-capped gold nanoparticles (FSN-capped AuNPs) for the simultaneous detection of cysteine (Cys) and homocysteine (Hcy) using colorimetric method, requiring no use of separation techniques. It was found that the kinetics of Cys/Hcy-induced aggregation of the 14 nm FSN-capped AuNPs strongly depends on the pH value of gold colloidal solution. At a pH of 6.5, the Cys-induced aggregation kinetics of the FSN-capped AuNPs was almost identical to that induced by Hcy, facilitating simultaneous detection of total Cys and Hcy up to a concentration as low as 0.15 μM; while at pH 12.0, the kinetics of Cys-induced aggregation was much faster than that inducted by Hcy, leading to selective detection of Cys at concentration as low as 1.0 μM in the presence of Hcy. The applicability of the method was validated by spiking known amount of Cys and Hcy in human urine and plasma samples, obtaining a recovery of 95.4-105.5%. The present approach is simple, high selective and provides high reproducibility, and has a great potentiality in disease diagnosis.

  8. Reliability Analysis of High Rockfill Dam Stability

    Directory of Open Access Journals (Sweden)

    Ping Yi

    2015-01-01

    Full Text Available A program 3DSTAB combining slope stability analysis and reliability analysis is developed and validated. In this program, the limit equilibrium method is utilized to calculate safety factors of critical slip surfaces. The first-order reliability method is used to compute reliability indexes corresponding to critical probabilistic surfaces. When derivatives of the performance function are calculated by finite difference method, the previous iteration’s critical slip surface is saved and used. This sequential approximation strategy notably improves efficiency. Using this program, the stability reliability analyses of concrete faced rockfill dams and earth core rockfill dams with different heights and different slope ratios are performed. The results show that both safety factors and reliability indexes decrease as the dam’s slope increases at a constant height and as the dam’s height increases at a constant slope. They decrease dramatically as the dam height increases from 100 m to 200 m while they decrease slowly once the dam height exceeds 250 m, which deserves attention. Additionally, both safety factors and reliability indexes of the upstream slope of earth core rockfill dams are higher than that of the downstream slope. Thus, the downstream slope stability is the key failure mode for earth core rockfill dams.

  9. Stability and energy confinement of highly elongated plasmas in TCV

    Energy Technology Data Exchange (ETDEWEB)

    Hofmann, F.; Behn, R.; Dutch, M.J.; Martin, Y.; Moret, J.M.; Nieswand, C.; Pietrzyk, Z.A.; Reimerdes, H.; Ward, D.J. [Ecole Polytechnique Federale, Lausanne (Switzerland). Centre de Recherche en Physique des Plasma (CRPP)

    1997-06-01

    One of the principal aims of TCV is the creation and active stabilization of highly elongated plasmas, {kappa}{>=}3. This implies high growth rates of axisymmetric modes and a very low stability margin. To stabilize such modes, TCV is equipped with a vertical position control system using a combination of slow coils outside the vacuum vessel (response time {approx_equal}1 ms) and a fast coil inside the vessel (response time {approx_equal}0.2 ms). The fast coil became operational in August 1996 and this paper describes the first experiments using both fast and slow coils for vertical stabilization. (author) 4 figs., 8 refs.

  10. Mesquite Gum as a Novel Reducing and Stabilizing Agent for Modified Tollens Synthesis of Highly Concentrated Ag Nanoparticles

    Directory of Open Access Journals (Sweden)

    Maira Berenice Moreno‐Trejo

    2016-10-01

    Full Text Available The synthesis that is described in this study is for the preparation of silver nanoparticles of sizes ranging from 10 nm to 30 nm with a defined shape (globular, confirmed by UV-vis, SEM, STEM and DLS analysis. This simple and favorable one-step modified Tollens reaction does not require any special equipment or other stabilizing or reducing agent except for a solution of purified mesquite gum, and it produces aqueous colloidal dispersions of silver nanoparticles with a stability thatexceeds three months, a relatively narrow size distribution, a low tendency to aggregate and a yield of at least 95% for all cases. Reaction times are between 15 min and 60 min to obtain silver nanoparticles in concentrations ranging from 0.1 g to 3 g of Ag per 100 g of reaction mixture. The proposed synthetic method presents a high potential for scale-up, since its production capacity is rather high and the methodology is simple.The synthesis that is described in this study is for the preparation of silver nanoparticles of sizes ranging from 10 nm to 30 nm with a defined shape (globular, confirmed by UV-vis, SEM, STEM and DLS analysis. This simple and favorable one-step modified Tollens reaction does not require any special equipment or other stabilizing or reducing agent except for a solution of purified mesquite gum, and it produces aqueous colloidal dispersions of silver nanoparticles with a stability thatexceeds three months, a relatively narrow size distribution, a low tendency to aggregate and a yield of at least 95% for all cases. Reaction times are between 15 min and 60 min to obtain silver nanoparticles in concentrations ranging from 0.1 g to 3 g of Ag per 100 g of reaction mixture. The proposed synthetic method presents a high potential for scale-up, since its production capacity is rather high and the methodology is simple.

  11. Colloidal Stability and Magnetic Field-Induced Ordering of Magnetorheological Fluids Studied with a Quartz Crystal Microbalance

    Directory of Open Access Journals (Sweden)

    Jaime Rodriguez-López

    2015-12-01

    Full Text Available This work proposes the use of quartz crystal microbalances (QCMs as a method to analyze and characterize magnetorheological (MR fluids. QCM devices are sensitive to changes in mass, surface interactions, and viscoelastic properties of the medium contacting its surface. These features make the QCM suitable to study MR fluids and their response to variable environmental conditions. MR fluids change their structure and viscoelastic properties under the action of an external magnetic field, this change being determined by the particle volume fraction, the magnetic field strength, and the presence of thixotropic agents among other factors. In this work, the measurement of the resonance parameters (resonance frequency and dissipation factor of a QCM are used to analyze the behavior of MR fluids in static conditions (that is, in the absence of external mechanical stresses. The influence of sedimentation under gravity and the application of magnetic fields on the shifts of resonance frequency and dissipation factor were measured and discussed in the frame of the coupled resonance produced by particles touching the QCM surface. Furthermore, the MR-fluid/QCM system has a great potential for the study of high-frequency contact mechanics because the translational and rotational stiffness of the link between the surface and the particles can be tuned by the magnetic field.

  12. Are All Colloids Same? How to Select the Right Colloid?

    Directory of Open Access Journals (Sweden)

    Sukanya Mitra

    2009-01-01

    Full Text Available The administration of intravenous fluids is one of the most common and universal interventions in medicine. Colloids are an alternative to the frequently used crystalloids, with highly variable use depending on a myriad of clinical variables. A colloid is defined as a high molecular weight (MW substance that largely remains in the intravas-eular compartment, thereby generating an oncotic pressure. Colloids are considered to have a greater intravaseular persistence when compared to crystalloids. All colloids, however, are clearly not the same. Differences in the physi-cochemical properties, pharmacokinetics and safety profile exist amongst various colloids. This review explores the different types of colloids, with their properties and usefulness as well as adverse effects. While all the available colloids are reviewed briefly (e.g., albumin, gelatin, dextran with respect to their pharmacology, indications, advan-tages and disadvantages, particular emphasis is laid on the hydroxyethyl starches (HES because of their rising prominence. It is shown that HES differ widely in their physicochemical and pharmacokinetic properties, composition, usefulness, and especially in their adverse effect profiles. The third generation HES (tetrastarches, in particular, seem to offer a unique combination of safety and efficacy. Several issues related to this are discussed in detail. This review of the available clinical data demonstrates that HES should not be regarded as one homogenous group, and data for one product should not be automatically extrapolated to another. Thus, among the synthetic colloids, the tetrastarches appear to offer the best currently available compromise between efficacy, safety profile, and cost. They also appear to be the best suited for use in the intensive care setting. Finally, balanced (rather than saline-based HES solutions appear promising as a plasma-adapted volume replacement strategy and may further refine the ongoing quest of

  13. Application of modern time series analysis to high stability oscillators

    Science.gov (United States)

    Farrell, B. F.; Mattison, W. M.; Vessot, R. F. C.

    1980-01-01

    Techniques of modern time series analysis useful for investigating the characteristics of high-stability oscillators and identifying systematic perturbations are discussed with reference to an experiment in which the frequencies of superconducting cavity-stabilized oscillators and hydrogen masers were compared. The techniques examined include transformation to stationarity, autocorrelation and cross-correlation, superresolution, and transfer function determination.

  14. Colloidal CuFeS2 Nanocrystals: Intermediate Fe d-Band Leads to High Photothermal Conversion Efficiency

    CERN Document Server

    Ghosh, S; Petrelli, A; Kriegel, I; Gaspari, R; Almeida, G; Bertoni, G; Cavalli, A; Scotognella, F; Pellegrino, T; Manna, L

    2016-01-01

    We describe the colloidal hot-injection synthesis of phase-pure nanocrystals (NCs) of a highly abundant mineral, chalcopyrite (CuFeS2). Absorption bands centered at around 480 and 950 nm, spanning almost the entire visible and near infrared regions, encompass their optical extinction characteristics. These peaks are ascribable to electronic transitions from the valence band (VB) to the empty intermediate band (IB), located in the fundamental gap and mainly composed of Fe 3d orbitals. Laser-irradiation (at 808 nm) of an aqueous suspension of CuFeS2 NCs exhibited significant heating, with a photothermal conversion efficiency of 49%. Such efficient heating is ascribable to the carrier relaxation within the broad IB band (owing to the indirect VB-IB gap), as corroborated by transient absorption measurements. The intense absorption and high photothermal transduction efficiency (PTE) of these NCs in the so-called biological window (650-900 nm) makes them suitable for photothermal therapy as demonstrated by tumor ce...

  15. Fabrication of high-quality colloidal photonic crystals with sharp band edges for ultrafast all-optical switching

    Institute of Scientific and Technical Information of China (English)

    Feng Tian-Hua; Dai Qiao-Feng; Wu Li-Jun; Guo Qi; Hu Wei; Lan Sheng

    2008-01-01

    Application of the pressure controlled isothermal heating vertical deposition method to the fabrication of colloidal photonic crystals is systematically investigated in this paper. The fabricated samples are characterized by scanning electron microscope and transmission spectrum. High-quality samples with large transmissions in the pass bands and the sharp band edges are obtained and the optimum growth condition is determined. For the best sample, the transmission in the pass bands approaches 0.9 while that in the band gap reaches 0.1. More importantly, the maximum differential transmission as high as 0.1/nm is achieved. In addition, it is found that the number of stacking layers does not increase linearly with concentration of PS spheres in a solution, and a gradual saturation occurs when the concentration of PS spheres exceeds 1.5 wt.%. The uniformity of the fabricated samples is examined by transmission measurements on areas with different sizes. Finally, the tolerance of the fabricated samples to baking was studied.

  16. Towards Directional Colloidal Interactions

    NARCIS (Netherlands)

    Kamp, M.

    2015-01-01

    Colloids are particles with a size on the scale of microns in at least one dimension. The central theme of this thesis is the synthesis of model colloids with anisotropic interactions - often called `patchy' colloids, as well as the search for new ways to assemble such colloids. Methods to build

  17. Chancellor Water Colloids: Characterization and Radionuclide Association

    Energy Technology Data Exchange (ETDEWEB)

    Abdel-Fattah, Amr I. [Los Alamos National Laboratory

    2012-06-18

    Concluding remarks about this paper are: (1) Gravitational settling, zeta potential, and ultrafiltration data indicate the existence of a colloidal phase of both the alpha and beta emitters in the Chancellor water; (2) The low activity combined with high dispersion homogeneity of the Chancellor water indicate that both alpha and beta emitters are not intrinsic colloids; (3) Radionuclides in the Chancellor water, particularly Pu, coexist as dissolved aqueous and sorbed phases - in other words the radionuclides are partitioned between the aqueous phase and the colloidal phase; (4) The presence of Pu as a dissolved species in the aqueous phase, suggests the possibility of Pu in the (V) oxidation state - this conclusion is supported by the similarity of the k{sub d} value of Pu determined in the current study to that determined for Pu(V) sorbed onto smectite colloids, and the similar electrokinetic behavior of the Chancellor water colloids to smectite colloids; (5) About 50% of the Pu(V) is in the aqueous phase and 50% is sorbed on colloids (mass concentration of colloids in the Chancellor water is 0.12 g/L); (6) The k{sub d} of the Pu and the beta emitters (fission products) between aqueous and colloidal phases in the Chancellor water is {approx}8.0 x 10{sup 3} mL/g using two different activity measurement techniques (LSC and alpha spectroscopy); (7) The gravitational settling and size distributions of the association colloids indicate that the properties (at least the physical ones) of the colloids to which the alpha emitters are associated with seem to be different that the properties of the colloids to which the beta emitters are associated with - the beta emitters are associated with very small particles ({approx}50 - 120 nm), while the alpha emitters are associated with relatively larger particles; and (8) The Chancellor water colloids are extremely stable under the natural pH and ionic strength conditions, indicating high potential for transport in the

  18. Effect of highly dispersed yttria addition on thermal stability of hydroxyapatite

    Energy Technology Data Exchange (ETDEWEB)

    Parente, P., E-mail: pparente@icv.csic.es [Instituto de Ceramica y Vidrio, CSIC, C/Kelsen 5, Madrid 28049 (Spain); Savoini, B. [Departamento de Fisica, Universidad Carlos III de Madrid, Avda. Universidad 30, Leganes 28911 (Spain); Ferrari, B. [Instituto de Ceramica y Vidrio, CSIC, C/Kelsen 5, Madrid 28049 (Spain); Monge, M.A.; Pareja, R. [Departamento de Fisica, Universidad Carlos III de Madrid, Avda. Universidad 30, Leganes 28911 (Spain); Sanchez-Herencia, A.J. [Instituto de Ceramica y Vidrio, CSIC, C/Kelsen 5, Madrid 28049 (Spain)

    2013-03-01

    The capability of the colloidal method to produce yttria (Y{sub 2}O{sub 3}) dispersed hydroxyapatite (HA) has been investigated as an alternative method to the conventional method of mechanical mixing and sintering for developing HA-based materials that could exhibit controllable and enhanced functional properties. A water based colloidal route to produce HA materials with highly dispersed Y{sub 2}O{sub 3} has been applied, and the effect of 10 wt.% Y{sub 2}O{sub 3} addition to HA investigated by thermal analysis, X-ray diffraction and Fourier transform infrared spectroscopy. These measurements evidence a remarkable effect of this Y{sub 2}O{sub 3} addition on decomposition mechanisms of synthetic HA. Results show that incorporation of Y{sub 2}O{sub 3} as dispersed second phase is beneficial because it hinders the decomposition mechanisms of HA into calcium phosphates. This retardation will allow the control of the sintering conditions for developing HA implants with improved properties. Besides, substitution of Ca{sup 2+} with Y{sup 3+} ions appears to promote the formation of OH{sup -} vacancies, which could improve the conductive properties of HA favorable to osseointegration. - Highlights: Black-Right-Pointing-Pointer We reveal the influence of Y{sub 2}O{sub 3} on thermal stability of hydroxyapatite. Black-Right-Pointing-Pointer Incorporation of Y{sub 2}O{sub 3} delays decomposition of hydroxyapatite to calcium phosphates. Black-Right-Pointing-Pointer Addition of Y{sub 2}O{sub 3} enables sintering conditions more favorable to the densification.

  19. Highly Luminescent Water-Dispersible NIR-Emitting Wurtzite CuInS2/ZnS Core/Shell Colloidal Quantum Dots

    Science.gov (United States)

    2017-01-01

    Copper indium sulfide (CIS) quantum dots (QDs) are attractive as labels for biomedical imaging, since they have large absorption coefficients across a broad spectral range, size- and composition-tunable photoluminescence from the visible to the near-infrared, and low toxicity. However, the application of NIR-emitting CIS QDs is still hindered by large size and shape dispersions and low photoluminescence quantum yields (PLQYs). In this work, we develop an efficient pathway to synthesize highly luminescent NIR-emitting wurtzite CIS/ZnS QDs, starting from template Cu2-xS nanocrystals (NCs), which are converted by topotactic partial Cu+ for In3+ exchange into CIS NCs. These NCs are subsequently used as cores for the overgrowth of ZnS shells (≤1 nm thick). The CIS/ZnS core/shell QDs exhibit PL tunability from the first to the second NIR window (750–1100 nm), with PLQYs ranging from 75% (at 820 nm) to 25% (at 1050 nm), and can be readily transferred to water upon exchange of the native ligands for mercaptoundecanoic acid. The resulting water-dispersible CIS/ZnS QDs possess good colloidal stability over at least 6 months and PLQYs ranging from 39% (at 820 nm) to 6% (at 1050 nm). These PLQYs are superior to those of commonly available water-soluble NIR-fluorophores (dyes and QDs), making the hydrophilic CIS/ZnS QDs developed in this work promising candidates for further application as NIR emitters in bioimaging. The hydrophobic CIS/ZnS QDs obtained immediately after the ZnS shelling are also attractive as fluorophores in luminescent solar concentrators. PMID:28638177

  20. A High Reliability Frequency Stabilized Semiconductor Laser Source Project

    Data.gov (United States)

    National Aeronautics and Space Administration — NASA needs high stability laser source of 1W output power for Lidar applications. Princeton Optronics has developed ultra-stable, narrow linewidth diode pumped solid...

  1. Highly efficient large-area colourless luminescent solar concentrators using heavy-metal-free colloidal quantum dots.

    Science.gov (United States)

    Meinardi, Francesco; McDaniel, Hunter; Carulli, Francesco; Colombo, Annalisa; Velizhanin, Kirill A; Makarov, Nikolay S; Simonutti, Roberto; Klimov, Victor I; Brovelli, Sergio

    2015-10-01

    Luminescent solar concentrators serving as semitransparent photovoltaic windows could become an important element in net zero energy consumption buildings of the future. Colloidal quantum dots are promising materials for luminescent solar concentrators as they can be engineered to provide the large Stokes shift necessary for suppressing reabsorption losses in large-area devices. Existing Stokes-shift-engineered quantum dots allow for only partial coverage of the solar spectrum, which limits their light-harvesting ability and leads to colouring of the luminescent solar concentrators, complicating their use in architecture. Here, we use quantum dots of ternary I-III-VI2 semiconductors to realize the first large-area quantum dot-luminescent solar concentrators free of toxic elements, with reduced reabsorption and extended coverage of the solar spectrum. By incorporating CuInSexS2-x quantum dots into photo-polymerized poly(lauryl methacrylate), we obtain freestanding, colourless slabs that introduce no distortion to perceived colours and are thus well suited for the realization of photovoltaic windows. Thanks to the suppressed reabsorption and high emission efficiencies of the quantum dots, we achieve an optical power efficiency of 3.2%. Ultrafast spectroscopy studies suggest that the Stokes-shifted emission involves a conduction-band electron and a hole residing in an intragap state associated with a native defect.

  2. Highly efficient large-area colourless luminescent solar concentrators using heavy-metal-free colloidal quantum dots

    Energy Technology Data Exchange (ETDEWEB)

    Meinardi, Francesco; McDaniel, Hunter; Carulli, Francesco; Colombo, Annalisa; Velizhanin, Kirill A.; Makarov, Nikolay S.; Simonutti, Roberto; Klimov, Victor I.; Brovelli, Sergio

    2015-08-24

    Luminescent solar concentrators serving as semitransparent photovoltaic windows could become an important element in net zero energy consumption buildings of the future. Colloidal quantum dots are promising materials for luminescent solar concentrators as they can be engineered to provide the large Stokes shift necessary for suppressing reabsorption losses in large-area devices. Existing Stokes-shift-engineered quantum dots allow for only partial coverage of the solar spectrum, which limits their light-harvesting ability and leads to colouring of the luminescent solar concentrators, complicating their use in architecture. Here, we use quantum dots of ternary I–III–VI2 semiconductors to realize the first large-area quantum dot–luminescent solar concentrators free of toxic elements, with reduced reabsorption and extended coverage of the solar spectrum. By incorporating CuInSexS2–x quantum dots into photo-polymerized poly(lauryl methacrylate), we obtain freestanding, colourless slabs that introduce no distortion to perceived colours and are thus well suited for the realization of photovoltaic windows. Thanks to the suppressed reabsorption and high emission efficiencies of the quantum dots, we achieve an optical power efficiency of 3.2%. Ultrafast spectroscopy studies suggest that the Stokes-shifted emission involves a conduction-band electron and a hole residing in an intragap state associated with a native defect.

  3. Colloidal quantum dots: synthesis, properties and applications

    Science.gov (United States)

    Brichkin, S. B.; Razumov, V. F.

    2016-12-01

    Key recent results obtained in studies of a new class of luminophores, colloidal quantum dots, are analyzed. Modern methods for the synthesis and post-synthetic treatment of colloidal quantum dots that make it possible to achieve record high quantum yield of luminescence and to modify their characteristics for specific applications are considered. Currently important avenues of research on colloidal quantum dots and the problems in and prospects for their practical applications in various fields are discussed. The bibliography includes 272 references.

  4. Characterization of Whey Protein Oil-In-Water Emulsions with Different Oil Concentrations Stabilized by Ultra-High Pressure Homogenization

    Directory of Open Access Journals (Sweden)

    Essam Hebishy

    2017-02-01

    Full Text Available In this study, the effect of ultra-high-pressure homogenization (UHPH: 100 or 200 MPa at 25 °C, in comparison to colloid mill (CM: 5000 rpm at 20 °C and conventional homogenization (CH: 15 MPa at 60 °C, on the stability of oil-in-water emulsions with different oil concentrations (10, 30 or 50 g/100 g emulsified by whey protein isolate (4 g/100 g was investigated. Emulsions were characterized for their microstructure, rheological properties, surface protein concentration (SPC, stability to creaming and oxidative stability under light (2000 lux/m2. UHPH produced emulsions containing lipid droplets in the sub-micron range (100–200 nm and with low protein concentrations on droplet surfaces. Droplet size (d3.2, µm was increased in CH and UHPH emulsions by increasing the oil concentration. CM emulsions exhibited Newtonian flow behaviour at all oil concentrations studied; however, the rheological behaviour of CH and UHPH emulsions varied from Newtonian flow (n ≈ 1 to shear-thinning (n ˂ 1 and thixotropic behaviour in emulsions containing 50% oil. This was confirmed by the non-significant differences in the d4.3 (µm value between the top and bottom of emulsions in tubes left at room temperature for nine days and also by a low migration velocity measured with a Turbiscan LAB instrument. UHPH emulsions showed significantly lower oxidation rates during 10 days storage in comparison to CM and CH emulsions as confirmed by hydroperoxides and thiobarbituric acid-reactive substances (TBARS. UHPH emulsions treated at 100 MPa were less oxidized than those treated at 200 MPa. The results from this study suggest that UHPH treatment generates emulsions that have a higher stability to creaming and lipid oxidation compared to colloid mill and conventional treatments.

  5. Review of Power System Stability with High Wind Power Penetration

    DEFF Research Database (Denmark)

    Hu, Rui; Hu, Weihao; Chen, Zhe

    2015-01-01

    analyzing methods and stability improvement approaches. With increasing wind power penetration, system balancing and the reduced inertia may cause a big threaten for stable operation of power systems. To mitigate or eliminate the wind impacts for high wind penetration systems, although the practical......This paper presents an overview of researches on power system stability with high wind power penetration including analyzing methods and improvement approaches. Power system stability issues can be classified diversely according to different considerations. Each classified issue has special...... and reliable choices currently are the strong outside connections or sufficient reserve capacity constructions, many novel theories and approaches are invented to investigate the stability issues, looking forward to an extra-high penetration or totally renewable resource based power systems. These analyzing...

  6. High-efficiency CdTe/CdS core/shell nanocrystals in water enabled by photo-induced colloidal hetero-epitaxy of CdS shelling at room temperature

    Institute of Scientific and Technical Information of China (English)

    Hakimeh Zare[1; Maziar Marandi[2; Somayeh Fardindoost[1; Vijay Kumar Sharma[3,4; Aydan Yeltik[3; Omid Akhavan[1,5; Hilmi Volkan Demir[3,4; Nima Taghavinia[1,5

    2015-01-01

    We report high-efficiency CdTe/CdS core/shell nanocrystals synthesized in water by epitaxially growing CdS shells on aqueous CdTe cores at room temperature, enabled by the controlled release of S species under low-intensity ultraviolet (UV) light illumination. The resulting photo-induced dissociation of S2O2- ions conveniently triggers the formation of critical two-dimensional CdS epitaxy on the CdTe surface at room temperature, as opposed to initiating the growth of individual CdS core-only nanocrystals. This controlled colloidal hetero-epitaxy leads to a substantial increase in the photoluminescence (PL) quantum yield (QY) of the shelled nanocrystals in water (reaching 64%). With a systematic set of studies, the maximum PL QY is found to be almost independent of the illuminating UV intensity, while the shell formation kinetics required for reaching the maximum QY linearly depends on the illuminating UV intensity. A stability study of the QD films in air at various temperatures shows highly improved thermal stability of the shelled QDs (up to 120 ℃ in ambient air). These results indicate that the proposed aqueous CdTe/CdS core/shell nanocrystals hold great promise for applications requiring efficiency and stability.

  7. Multiple Colors Output on Voile through 3D Colloidal Crystals with Robust Mechanical Properties.

    Science.gov (United States)

    Meng, Yao; Tang, Bingtao; Ju, Benzhi; Wu, Suli; Zhang, Shufen

    2017-01-25

    Distinguished from the chromatic mechanism of dyes and pigments, structural color is derived from physical interactions of visible light with structures that are periodic at the scale of the wavelength of light. Using colloidal crystals with coloring functions for fabrics has resulted in significant improvements compared with chemical colors because the structural color from colloidal crystals bears many unique and fascinating optical properties, such as vivid iridescence and nonphotobleaching. However, the poor mechanical performance of the structural color films cannot meet actual requirements because of the weak point contact of colloidal crystal particles. Herein, we demonstrate in this study the patterning on voile fabrics with high mechanical strength on account of the periodic array lock effect of polymers, and multiple structural color output was simultaneously achieved by a simple two-phase self-assembly method for printing voile fabrics with 3D colloidal crystals. The colored voile fabrics exhibit high color saturation, good mechanical stability, and multiple-color patterns printable. In addition, colloidal crystals are promising potential substitutes for organic dyes and pigments because colloidal crystals are environmentally friendly.

  8. Etched colloidal LiFePO4 nanoplatelets toward high-rate capable Li-ion battery electrodes.

    Science.gov (United States)

    Paolella, Andrea; Bertoni, Giovanni; Marras, Sergio; Dilena, Enrico; Colombo, Massimo; Prato, Mirko; Riedinger, Andreas; Povia, Mauro; Ansaldo, Alberto; Zaghib, Karim; Manna, Liberato; George, Chandramohan

    2014-12-10

    LiFePO4 has been intensively investigated as a cathode material in Li-ion batteries, as it can in principle enable the development of high power electrodes. LiFePO4, on the other hand, is inherently "plagued" by poor electronic and ionic conductivity. While the problems with low electron conductivity are partially solved by carbon coating and further by doping or by downsizing the active particles to nanoscale dimensions, poor ionic conductivity is still an issue. To develop colloidally synthesized LiFePO4 nanocrystals (NCs) optimized for high rate applications, we propose here a surface treatment of the NCs. The particles as delivered from the synthesis have a surface passivated with long chain organic surfactants, and therefore can be dispersed only in aprotic solvents such as chloroform or toluene. Glucose that is commonly used as carbon source for carbon-coating procedure is not soluble in these solvents, but it can be dissolved in water. In order to make the NCs hydrophilic, we treated them with lithium hexafluorophosphate (LiPF6), which removes the surfactant ligand shell while preserving the structural and morphological properties of the NCs. Only a roughening of the edges of NCs was observed due to a partial etching of their surface. Electrodes prepared from these platelet NCs (after carbon coating) delivered a capacity of ∼ 155 mAh/g, ∼ 135 mAh/g, and ∼ 125 mAh/g, at 1 C, 5 C, and 10 C, respectively, with significant capacity retention and remarkable rate capability. For example, at 61 C (10.3 A/g), a capacity of ∼ 70 mAh/g was obtained, and at 122 C (20.7 A/g), the capacity was ∼ 30 mAh/g. The rate capability and the ease of scalability in the preparation of these surface-treated nanoplatelets make them highly suitable as electrodes in Li-ion batteries.

  9. Crystallization of DNA-coated colloids.

    Science.gov (United States)

    Wang, Yu; Wang, Yufeng; Zheng, Xiaolong; Ducrot, Étienne; Yodh, Jeremy S; Weck, Marcus; Pine, David J

    2015-06-16

    DNA-coated colloids hold great promise for self-assembly of programmed heterogeneous microstructures, provided they not only bind when cooled below their melting temperature, but also rearrange so that aggregated particles can anneal into the structure that minimizes the free energy. Unfortunately, DNA-coated colloids generally collide and stick forming kinetically arrested random aggregates when the thickness of the DNA coating is much smaller than the particles. Here we report DNA-coated colloids that can rearrange and anneal, thus enabling the growth of large colloidal crystals from a wide range of micrometre-sized DNA-coated colloids for the first time. The kinetics of aggregation, crystallization and defect formation are followed in real time. The crystallization rate exhibits the familiar maximum for intermediate temperature quenches observed in metallic alloys, but over a temperature range smaller by two orders of magnitude, owing to the highly temperature-sensitive diffusion between aggregated DNA-coated colloids.

  10. Manipulating colloids with charges and electric fields

    Science.gov (United States)

    Leunissen, M. E.

    2007-02-01

    This thesis presents the results of experimental investigations on a variety of colloidal suspensions. Colloidal particles are at least a hundred times larger than atoms or molecules, but suspended in a liquid they display the same phase behavior, including fluid and crystalline phases. Due to their relatively large size, colloids are much easier to investigate and manipulate, though. This makes them excellent condensed matter model systems. With this in mind, we studied micrometer-sized perspex (‘PMMA’) spheres, labeled with a fluorescent dye for high-resolution confocal microscopy imaging, and suspended in a low-polar mixture of the organic solvents cyclohexyl bromide and cis-decalin. This system offered us the flexibility to change the interactions between the particles from ‘hard-sphere-like’ to long-ranged repulsive (between like-charged particles), long-ranged attractive (between oppositely charged particles) and dipolar (in an electric field). We investigated the phase behavior of our suspensions as a function of the particle concentration, the ionic strength of the solvent and the particles’ charges. In this way, we obtained new insight in the freezing and melting behavior of like-charged and oppositely charged colloids. Interestingly, we found that the latter can readily form large crystals, thus defying the common belief that plus-minus interactions inevitably lead to aggregation. Moreover, we demonstrated that these systems can serve as a reliable model system for classical ionic matter (‘salts’), and that opposite-charge interactions can greatly facilitate the self-assembly of new structures with special properties for applications. On a slightly different note, we also studied electrostatic effects in mixtures of the cyclohexyl bromide solvent and water, both with and without colloidal particles present. This provided new insight in the stabilization mechanisms of oil-water emulsions and gave us control over the self-assembly of various

  11. High Power Test for Klystron Stability

    Energy Technology Data Exchange (ETDEWEB)

    Seol, Kyung-Tae; Kim, Seong-Gu; Kwon, Hyeok-Jung; Kim, Han-Sung; Cho, Yong-Sub [Korea Atomic Energy Research Institute, Gyeongju (Korea, Republic of)

    2015-10-15

    The 100-MeV linac consists of a 50-keV proton injector based on a microwave ion source, a 3-MeV RFQ with a four-vane structure, and a 100-MeV DTL. Nine sets of 1MW klystrons have been operated for the 100-MeV proton linac. The klystron filament heating time was approximately 5700 hours in 2014. During the high power operation of the klystron, unstable RF waveforms appeared at the klystron output, and we have checked and performed cavity frequency adjustments, magnet and heater current, reflection from a circulator, klystron test without a circulator, and the frequency spectrum measurement. The problems may be from harmonic power stay between the klystron and the circulator. A harmonic filter of waveguide type is designed to eliminate the harmonic power. Nine sets of the klystrons have been operated for the KOMAC 100-MeV proton linac. Some klystrons have unstable RF waveforms at specific power level. We have checked and tested the cavity frequency adjustment, reflection from a circulator, high power test without a circulator, and frequency spectrum at the unstable RF. The unstable RF may be from harmonic power stay between the klystron and the circulator. To eliminate the harmonic power, a harmonic filter of waveguide type is designed.

  12. Transfection Studies with Colloidal Systems Containing Highly Purified Bipolar Tetraether Lipids from Sulfolobus acidocaldarius

    Science.gov (United States)

    Pinnapireddy, Shashank Reddy; Baghdan, Elias; Jedelská, Jarmila

    2017-01-01

    Lipid vectors are commonly used to facilitate the transfer of nucleic acids into mammalian cells. In this study, two fractions of tetraether lipids from the archaea Sulfolobus acidocaldarius were extracted and purified using different methods. The purified lipid fractions polar lipid fraction E (PLFE) and hydrolysed glycerol-dialkyl-nonitol tetraether (hGDNT) differ in their structures, charge, size, and miscibility from conventional lipids. Liposomes were prepared by mixing tetraether lipids with cholesterol (CH) and 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) resulting in stable vectors for gene delivery. Lipoplexes were prepared by complexation of liposomes with a luciferase expressing plasmid (pCMV-luc) at certain nitrogen-to-phosphorus (N/P) ratios and optimised for the transient transfection of ovarian adenocarcinoma cells (SK-OV-3). Complexation efficacy was investigated by gel-red fluorescence assay. Biophysical properties, like size, surface charge, and morphology, were investigated by differential light scattering (DLS), atomic force microscopy (AFM), and scanning electron microscopy (Cryo-SEM), respectively, revealing structural differences between liposomes and lipoplexes. A range of stable transfecting agents containing tetraether lipids were obtained by incorporating 5 mol% of tetraether lipids. Lipoplexes showed a decrease in free gel-red with increasing N/P ratios indicating efficient incorporation of plasmid DNA (pDNA) and remarkable stability. Transfection experiments of the lipoplexes revealed successful and superior transfection of SK-OV-3 cell line compared to the commercially available DOTAP and branched polyethyleneimine (25 kDa bPEI).

  13. Transfection Studies with Colloidal Systems Containing Highly Purified Bipolar Tetraether Lipids from Sulfolobus acidocaldarius.

    Science.gov (United States)

    Engelhardt, Konrad H; Pinnapireddy, Shashank Reddy; Baghdan, Elias; Jedelská, Jarmila; Bakowsky, Udo

    2017-01-01

    Lipid vectors are commonly used to facilitate the transfer of nucleic acids into mammalian cells. In this study, two fractions of tetraether lipids from the archaea Sulfolobus acidocaldarius were extracted and purified using different methods. The purified lipid fractions polar lipid fraction E (PLFE) and hydrolysed glycerol-dialkyl-nonitol tetraether (hGDNT) differ in their structures, charge, size, and miscibility from conventional lipids. Liposomes were prepared by mixing tetraether lipids with cholesterol (CH) and 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) resulting in stable vectors for gene delivery. Lipoplexes were prepared by complexation of liposomes with a luciferase expressing plasmid (pCMV-luc) at certain nitrogen-to-phosphorus (N/P) ratios and optimised for the transient transfection of ovarian adenocarcinoma cells (SK-OV-3). Complexation efficacy was investigated by gel-red fluorescence assay. Biophysical properties, like size, surface charge, and morphology, were investigated by differential light scattering (DLS), atomic force microscopy (AFM), and scanning electron microscopy (Cryo-SEM), respectively, revealing structural differences between liposomes and lipoplexes. A range of stable transfecting agents containing tetraether lipids were obtained by incorporating 5 mol% of tetraether lipids. Lipoplexes showed a decrease in free gel-red with increasing N/P ratios indicating efficient incorporation of plasmid DNA (pDNA) and remarkable stability. Transfection experiments of the lipoplexes revealed successful and superior transfection of SK-OV-3 cell line compared to the commercially available DOTAP and branched polyethyleneimine (25 kDa bPEI).

  14. Transfection Studies with Colloidal Systems Containing Highly Purified Bipolar Tetraether Lipids from Sulfolobus acidocaldarius

    Directory of Open Access Journals (Sweden)

    Konrad H. Engelhardt

    2017-01-01

    Full Text Available Lipid vectors are commonly used to facilitate the transfer of nucleic acids into mammalian cells. In this study, two fractions of tetraether lipids from the archaea Sulfolobus acidocaldarius were extracted and purified using different methods. The purified lipid fractions polar lipid fraction E (PLFE and hydrolysed glycerol-dialkyl-nonitol tetraether (hGDNT differ in their structures, charge, size, and miscibility from conventional lipids. Liposomes were prepared by mixing tetraether lipids with cholesterol (CH and 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP resulting in stable vectors for gene delivery. Lipoplexes were prepared by complexation of liposomes with a luciferase expressing plasmid (pCMV-luc at certain nitrogen-to-phosphorus (N/P ratios and optimised for the transient transfection of ovarian adenocarcinoma cells (SK-OV-3. Complexation efficacy was investigated by gel-red fluorescence assay. Biophysical properties, like size, surface charge, and morphology, were investigated by differential light scattering (DLS, atomic force microscopy (AFM, and scanning electron microscopy (Cryo-SEM, respectively, revealing structural differences between liposomes and lipoplexes. A range of stable transfecting agents containing tetraether lipids were obtained by incorporating 5 mol% of tetraether lipids. Lipoplexes showed a decrease in free gel-red with increasing N/P ratios indicating efficient incorporation of plasmid DNA (pDNA and remarkable stability. Transfection experiments of the lipoplexes revealed successful and superior transfection of SK-OV-3 cell line compared to the commercially available DOTAP and branched polyethyleneimine (25 kDa bPEI.

  15. Synthesis of pure colloidal silver nanoparticles with high electroconductivity for printed electronic circuits: the effect of amines on their formation in aqueous media.

    Science.gov (United States)

    Natsuki, Jun; Abe, Takao

    2011-07-01

    This paper describes a practical and convenient method to prepare stable colloidal silver nanoparticles for use in printed electronic circuits. The method uses a dispersant and two kinds of reducing agents including 2-(dimethylamino) ethanol (DMAE), which play important roles in the reduction of silver ions in an aqueous medium. The effect of DMAE and dispersant, as well as the factors affecting particle size and morphology are investigated. In the formation of the silver nanoparticles, reduction occurs rapidly at room temperature and the silver particles can be separated easily from the mixture in a short time. In addition, organic solvents are not used. Pure, small and relatively uniform particles with a diameter less than 10 nm can be obtained that exhibit high electroconductivity. The silver nanoparticles are stable, and can be isolated as a dried powder that can be fully redispersed in deionized water. This method of producing colloidal silver nanoparticles will find practical use in electronics applications.

  16. Temperature Stabilized Characterization of High Voltage Power Supplies

    CERN Document Server

    Krarup, Ole

    2017-01-01

    High precision measurements of the masses of nuclear ions in the ISOLTRAP experiment relies on an MR-ToF. A major source of noise and drift is the instability of the high voltage power supplies employed. Electrical noise and temperature changes can broaden peaks in time-of-flight spectra and shift the position of peaks between runs. In this report we investigate how the noise and drift of high-voltage power supplies can be characterized. Results indicate that analog power supplies generally have better relative stability than digitally controlled ones, and that the high temperature coefficients of all power supplies merit efforts to stabilize them.

  17. Colloidal superlattices for unnaturally high-index metamaterials at broadband optical frequencies

    CERN Document Server

    Lee, Seungwoo

    2015-01-01

    The recent advance in the assembly of metallic nanoparticles (NPs) has enabled sophisticated engineering of unprecedented light-matter interaction at the optical domain. In this work, I expand the design flexibility of NP optical metamaterial to push the upper limit of accessible refractive index to the unnaturally high regime. The precise control over the geometrical parameters of NP superlattice monolayer conferred the dramatic increase in electric resonance and related effective permittivity far beyond the naturally accessible regime. Simultaneously, effective permeability, another key factor to achieving high refractive index, was effectively suppressed by reducing the thickness of NPs. By establishing this design rule, I have achieved unnaturally high refractive index (15.7 at the electric resonance and 7.3 at the quasi-static limit) at broadband optical frequencies (100 THz ~ 300 THz). I also combined this NP metamaterial with graphene to electrically control the high refractive index over the broad opt...

  18. Colloidal superlattices for unnaturally high-index metamaterials at broadband optical frequencies.

    Science.gov (United States)

    Lee, Seungwoo

    2015-11-02

    The recent advance in the assembly of metallic nanoparticles (NPs) has enabled sophisticated engineering of unprecedented light-matter interaction at the optical domain. In this work, I expand the design flexibility of NP optical metamaterial to push the upper limit of accessible refractive index to the unnaturally high regime. The precise control over the geometrical parameters of NP superlattice monolayer conferred the dramatic increase in electric resonance and related effective permittivity far beyond the naturally accessible regime. Simultaneously, effective permeability change, another key factor to achieving high refractive index, was effectively suppressed by reducing the thickness of NPs. By establishing this design rule, I have achieved unnaturally high refractive index (15.7 at the electric resonance and 7.3 at the quasi-static limit) at broadband optical frequencies (100 THz ~300 THz). I also combined this NP metamaterial with graphene to electrically control the high refractive index over the broad optical frequencies.

  19. Stability Analysis for Stochastic Delayed High-order Neural Networks

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    In this paper, the global asymptotic stability analysis problem is considered for a class of stochastic high-order neural networks with time-delays. Based on a Lyapunov-Krasovskii functional and the stochastic stability analysis theory, several sufficient conditions are derived in order to guarantee the global asymptotic convergence of the equilibrium point in the mean square. Investigation shows that the addressed stochastic highorder delayed neural networks are globally asymptotically stable in the mean square if there are solutions to some linear matrix inequalities (LMIs). Hence, the global asymptotic stability of the studied stochastic high-order delayed neural networks can be easily checked by the Matlab LMI toolbox. A numerical example is given to demonstrate the usefulness of the proposed global stability criteria.

  20. Atomistic Model of Fluorescence Intermittency of Colloidal Quantum Dots

    KAUST Repository

    Voznyy, O.

    2014-04-16

    Optoelectronic applications of colloidal quantum dots demand a high emission efficiency, stability in time, and narrow spectral bandwidth. Electronic trap states interfere with the above properties but understanding of their origin remains lacking, inhibiting the development of robust passivation techniques. Here we show that surface vacancies improve the fluorescence yield compared to vacancy-free surfaces, while dynamic vacancy aggregation can temporarily turn fluorescence off. We find that infilling with foreign cations can stabilize the vacancies, inhibiting intermittency and improving quantum yield, providing an explanation of recent experimental observations. © 2014 American Physical Society.

  1. Formation of colloidal silver nanoparticles stabilized by Na+-poly(gamma-glutamic acid)-silver nitrate complex via chemical reduction process.

    Science.gov (United States)

    Yu, Da-Guang

    2007-10-01

    Macromolecular and polyanionic Na(+)-poly(gamma-glutamic acid) (PGA) silver nitrate complex acted as both a metal ion provider and a particle protector to fabricate nanosized silver colloids under chemical reduction by dextrose. The formation and size of particles have been characterized from transmission electron microscopy (TEM), dynamic light scattering analysis and UV-vis spectrophotometer. The results showed that the average particle size was 17.2+/-3.4 to 37.3+/-5.5 nm, apparently depending on the complex concentration. It was found that the rate constant and conversion of silver nanoparticles were proportional to the concentration of PGA. The growth mechanism of nanosized silver colloid was fully discussed. In addition, the in vitro cytotoxicity evaluated by L929 fibroblasts proliferation and antibacterial activity against Gram-positive strain (methicillin-resistant S. aureus (MRSA)) and Gram-negative strain (P. aeruginosa) bacteria have been assessed.

  2. Aggregation kinetics of inorganic colloids in eutrophic shallow lakes: Influence of cyanobacterial extracellular polymeric substances and electrolyte cations.

    Science.gov (United States)

    Xu, Huacheng; Yang, Changming; Jiang, Helong

    2016-12-01

    The stability/aggregation propensity of inorganic colloids in eutrophic shallow lakes is of great essence in governing the water transparency and contaminant behavior. In this study, time-resolved dynamic light scattering was employed to investigate the aggregation kinetics of Al2O3 inorganic colloids over a wide range of cyanobacterial extracellular polymeric substance (EPS) concentrations in the absence and presence of electrolyte cations. The results showed that EPS adsorption alone greatly decreased the hydrodynamic diameters of colloidal particles, whose stability behavior followed closely the predictions of the classical DLVO theory. Electrolyte cations, however, can induce the aggregation of colloidal particles, and divalent Ca(2+) were found to be more efficient in destabilizing the colloids than monovalent Na(+), as indicated by the considerably lower critical coagulation concentrations (2.5 mM for Ca(2+) vs. 170 mM for Na(+)). Further addition of Ca(2+), i.e., >2.5 mM, caused an extremely high aggregation degree and rate. High resolution transmission electron microscopy revealed that this enhanced aggregation should be attributed to the gel-like bridging between colloidal particles, which were verified to be the amorphous EPS-Ca(2+) complexes. Field-emission scanning electron microscopy coupled with elemental mapping provided additional evidence that the bridging interaction of EPS with Ca(2+) was the predominant mechanism for the aggregation enhancement. Copyright © 2016 Elsevier Ltd. All rights reserved.

  3. Polar-solvent-free colloidal synthesis of highly luminescent alkylammonium lead halide perovskite nanocrystals

    Science.gov (United States)

    Vybornyi, Oleh; Yakunin, Sergii; Kovalenko, Maksym V.

    2016-03-01

    A novel synthesis of hybrid organic-inorganic lead halide perovskite nanocrystals (CH3NH3PbX3, X = Br or I) that does not involve the use of dimethylformamide or other polar solvents is presented. The reaction between methylamine and PbX2 salts is conducted in a high-boiling nonpolar solvent (1-octadecene) in the presence of oleylamine and oleic acid as coordinating ligands. The resulting nanocrystals are characterized by high photoluminescence quantum efficiencies of 15-50%, outstanding phase purity and tunable shapes (nanocubes, nanowires, and nanoplatelets). Nanoplatelets spontaneously assemble into micrometer-length wires by face-to-face stacking. In addition, we demonstrate amplified spontaneous emission from thin films of green-emitting CH3NH3PbBr3 nanowires with low pumping thresholds of 3 μJ cm-2.A novel synthesis of hybrid organic-inorganic lead halide perovskite nanocrystals (CH3NH3PbX3, X = Br or I) that does not involve the use of dimethylformamide or other polar solvents is presented. The reaction between methylamine and PbX2 salts is conducted in a high-boiling nonpolar solvent (1-octadecene) in the presence of oleylamine and oleic acid as coordinating ligands. The resulting nanocrystals are characterized by high photoluminescence quantum efficiencies of 15-50%, outstanding phase purity and tunable shapes (nanocubes, nanowires, and nanoplatelets). Nanoplatelets spontaneously assemble into micrometer-length wires by face-to-face stacking. In addition, we demonstrate amplified spontaneous emission from thin films of green-emitting CH3NH3PbBr3 nanowires with low pumping thresholds of 3 μJ cm-2. Electronic supplementary information (ESI) available: Materials and methods, additional figures. See DOI: 10.1039/c5nr06890h

  4. Probing deviations from traditional colloid filtration theory by atomic forces microscopy.

    Energy Technology Data Exchange (ETDEWEB)

    Reno, Marissa Devan

    2005-12-01

    Colloid transport through saturated media is an integral component of predicting the fate and transport of groundwater contaminants. Developing sound predictive capabilities and establishing effective methodologies for remediation relies heavily on our ability to understand the pertinent physical and chemical mechanisms. Traditionally, colloid transport through saturated media has been described by classical colloid filtration theory (CFT), which predicts an exponential decrease in colloid concentration with travel distance. Furthermore, colloid stability as determined by Derjaguin-Landau-Veney-Overbeek (DLVO) theory predicts permanent attachment of unstable particles in a primary energy minimum. However, recent studies show significant deviations from these traditional theories. Deposition in the secondary energy minimum has been suggested as a mechanism by which observed deviations can occur. This work investigates the existence of the secondary energy minimum as predicted by DLVO theory using direct force measurements obtained by Atomic Forces Microscopy. Interaction energy as a function of separation distance between a colloid and a quartz surface in electrolyte solutions of varying ionic strength are obtained. Preliminary force measurements show promise and necessary modifications to the current experimental methodology have been identified. Stringent surface cleaning procedures and the use of high-purity water for all injectant solutions is necessary for the most accurate and precise measurements. Comparisons between direct physical measurements by Atomic Forces Microscopy with theoretical calculations and existing experimental findings will allow the evaluation of the existence or absence of a secondary energy minimum.

  5. Stability of Materials in High Temperature Water Vapor: SOFC Applications

    Science.gov (United States)

    Opila, E. J.; Jacobson, N. S.

    2010-01-01

    Solid oxide fuel cell material systems require long term stability in environments containing high-temperature water vapor. Many materials in fuel cell systems react with high-temperature water vapor to form volatile hydroxides which can degrade cell performance. In this paper, experimental methods to characterize these volatility reactions including the transpiration technique, thermogravimetric analysis, and high pressure mass spectrometry are reviewed. Experimentally determined data for chromia, silica, and alumina volatility are presented. In addition, data from the literature for the stability of other materials important in fuel cell systems are reviewed. Finally, methods for predicting material recession due to volatilization reactions are described.

  6. Simulation analysis of construction process of high rock slope's stabilization

    Institute of Scientific and Technical Information of China (English)

    ZHU Zhan-yuan; LING Xian-zhang; WANG Xuan-qing; ZOU Zu-yin

    2008-01-01

    A self-developed elasto-plastic finite element program was used to analyze the construction sequence of high rock slope' s stabilization in a coal-coking plant, and the result was compared with that employing the ultimate equilibrium method. Based on the results of finite element analysis, the stress contour graphs and dis-placement vector graphs at different construction steps were obtained, and the behavior of the slope during stabi-lization construction process was analyzed quantitatively. Based on the analysis of safety factors of three different schemes of stabilization and two different construction schemes, the assessment of stability and bracing design of the construction process were performed. The results show that the original reinforcement design is improper;the stability of the rock slope is controlled by a developed structural plane, the stability factor after excavation is less than 1, and the free surface should be braced in time ; for stability, the construction sequence should adopt that bracing follows excavation step by step up to down; the local slide occurred during the construction process agrees with the dangerous slide determined by the numerical analysis, which proves the validity and rationality of the adopted method.

  7. Highly Emissive Divalent-Ion-Doped Colloidal CsPb1-xMxBr3 Perovskite Nanocrystals through Cation Exchange.

    Science.gov (United States)

    van der Stam, Ward; Geuchies, Jaco J; Altantzis, Thomas; van den Bos, Karel H W; Meeldijk, Johannes D; Van Aert, Sandra; Bals, Sara; Vanmaekelbergh, Daniel; de Mello Donega, Celso

    2017-03-22

    Colloidal CsPbX3 (X = Br, Cl, and I) perovskite nanocrystals (NCs) have emerged as promising phosphors and solar cell materials due to their remarkable optoelectronic properties. These properties can be tailored by not only controlling the size and shape of the NCs but also postsynthetic composition tuning through topotactic anion exchange. In contrast, property control by cation exchange is still underdeveloped for colloidal CsPbX3 NCs. Here, we present a method that allows partial cation exchange in colloidal CsPbBr3 NCs, whereby Pb(2+) is exchanged for several isovalent cations, resulting in doped CsPb1-xMxBr3 NCs (M= Sn(2+), Cd(2+), and Zn(2+); 0 cells upon incorporation of the guest cations. The partial Pb(2+) for M(2+) exchange leads to a blue-shift of the optical spectra, while maintaining the high photoluminescence quantum yields (>50%), sharp absorption features, and narrow emission of the parent CsPbBr3 NCs. The blue-shift in the optical spectra is attributed to the lattice contraction that accompanies the Pb(2+) for M(2+) cation exchange and is observed to scale linearly with the lattice contraction. This work opens up new possibilities to engineer the properties of halide perovskite NCs, which to date are demonstrated to be the only known system where cation and anion exchange reactions can be sequentially combined while preserving the original NC shape, resulting in compositionally diverse perovskite NCs.

  8. Colloid-Associated Radionuclide Concentration Limits: ANL

    Energy Technology Data Exchange (ETDEWEB)

    C. Mertz

    2000-12-21

    The purpose and scope of this report is to describe the analysis of available colloidal data from waste form corrosion tests at Argonne National Laboratory (ANL) to extract characteristics of these colloids that can be used in modeling their contribution to the source term for sparingly soluble radioelements (e.g., Pu). Specifically, the focus is on developing a useful description of the following waste form colloid characteristics: (1) composition, (2) size distribution, and (3) quantification of the rate of waste form colloid generation. The composition and size distribution information are intended to support analysis of the potential transport of the sparingly soluble radionuclides associated with the waste form colloids. The rate of colloid generation is intended to support analysis of the waste form colloid-associated radionuclide concentrations. In addressing the above characteristics, available data are interpreted to address mechanisms controlling colloid formation and stability. This report was developed in accordance with the ''Technical Work Plan for Waste Form Degradation Process Model Report for SR'' (CRWMS M&O 2000). Because the end objective is to support the source term modeling we have organized the conclusions into two categories: (1) data analysis conclusions and (2) recommendations for colloid source term modeling. The second category is included to facilitate use of the conclusions from the data analysis in the abstraction of a colloid source term model. The data analyses and conclusions that are presented in this report are based on small-scale laboratory tests conducted on a limited number of waste glass compositions and spent fuel types.

  9. Piezo-based miniature high resolution stabilized gimbal

    Science.gov (United States)

    Karasikov, Nir; Peled, Gal; Yasinov, Roman; Yetkariov, Rita

    2016-05-01

    Piezo motors are characterized by higher mechanical power density, fast response and direct drive. These features are beneficial for miniature gimbals. A gimbal based on such motors was developed. Diameter is 58 mm, weight is 190 grams. The gimbal carries two cameras: a Flir Quark and an HD day camera. The dynamic performance is as high as 3 rad/sec velocity and 100 rad/secΛ2 acceleration. A two axes stabilization algorithm was developed, yielding 80 micro radian stabilization. Further, a panoramic image capture, at a rate of six stabilized field of views per second, was developed. The manuscript reviews the gimbal structure and open architecture, allowing adaptation to other cameras (SWIR etc.), the control algorithm and presents experimental results of stabilization and of panoramic views taken on a vibration platform and on a UAV.

  10. Colloid Transport and Retention

    DEFF Research Database (Denmark)

    Yuan, Hao; Shapiro, Alexander

    2012-01-01

    Book Description: Colloidal science and technology is one of the fastest growing research and technology areas. This book explores the cutting edge research in colloidal science and technology that will be usefull in almost every aspect of modern society. This book has a depth of information...... related to historical prospective, synthesis, characterization, theoretical modeling and application of unique class of colloidal materials starting from colloidal gold to coated silica colloid and platinum, titania colloids. This book is unique in its design, content, providing depth of science about...... different colloidal materials and their applications in chemistry, physics, biological, medical sciences and environment. Graduate students, academic and industrial researchers and medical professionals will discover recently developed colloidal materials and their applications in many areas of human...

  11. Governing metal-organic frameworks towards high stability.

    Science.gov (United States)

    Li, Na; Xu, Jian; Feng, Rui; Hu, Tong-Liang; Bu, Xian-He

    2016-06-30

    Metal-organic frameworks (MOFs) constructed with metal ions/clusters and organic ligands have emerged as an important family of porous materials for various applications. However, the stability of this class of materials is crucial for their practical applications, which might be improved by varying their chemical composition and/or structurally tuning them. To fabricate MOFs with high stability, several strategies for enhancing the stability of MOFs have been developed, in which the strength of metal-ligand bonds is especially considered: the use of highly charged cations and higher pKa ligands, and varying the chemical functionality of linkers. On the other hand, the regulation of their structural architectures is also investigated: interpenetrated frameworks, multi-walled frameworks, and self-strengthening of the frameworks. In addition, the surface modification can also improve the stability of the materials. In this review, we introduce and summarize these strategies from the viewpoint of structural tuning and component choosing, providing useful instructions for the further design and synthesis of MOFs with high-level stability.

  12. High pressure organic colloid method for the preparation of high performance carbon nanotube-supported Pt and PtRu catalysts for fuel cell applications

    Institute of Scientific and Technical Information of China (English)

    WANG; KateNing; Viola; BIRSS

    2010-01-01

    Highly dispersed,high performance Pt and PtRu catalysts,supported on multiwalled carbon nanotubes(CNTs),were prepared by a high pressure organic colloid method.The particle sizes of the active components were as small as 1.2 nm for Pt and 1.1 nm for PtRu,and the active Pt surface areas were 295 and 395 m2/g,respectively.The catalysts showed very high activities toward the anodic oxidation of methanol,evaluated by cyclic voltammetry,being up to 4 times higher than that of commercial Johnson Matthey Hispec 2000 Pt/XC-72R and 5 times better than Hispec 5000 PtRu/XC-72R catalysts.In a full air/hydrogen fuel cell,a membrane-electrode assembly prepared using our Pt/CNT and PtRu/CNT catalysts showed 50% and 100% higher performances than those prepared with commercial Johnson Matthey Pt/XC-72R and PtRu/XC-72R catalysts for the same Pt loading and operating conditions.

  13. Formation of uranium(IV)-silica colloids at near-neutral pH

    Science.gov (United States)

    Dreissig, Isabell; Weiss, Stephan; Hennig, Christoph; Bernhard, Gert; Zänker, Harald

    2011-01-01

    Evidence is provided by photon correlation spectroscopy, ultrafiltration and ultracentrifugation that uranium(IV) can form silicate-containing colloids of a size of ⩽20 nm. A concentration of up to 10 -3 M of colloid-borne U(IV) was observed. The particles are generated in near-neutral to slightly alkaline solutions containing background chemicals of geogenic nature (carbonate, silicate, sodium ions). They remain stable in aqueous suspension over years. Electrostatic repulsion due to a negative zeta potential in the near-neutral to alkaline pH range caused by the silicate stabilizes the U(IV) colloids. The isoelectric point of the nanoparticles is shifted toward lower pH values by the silicate. The mechanism of the colloidal stabilization can be regarded as "sequestration" by silicate, a phenomenon well known from heavy metal ions of high ion potential such as iron(III) or manganese(III,IV), but never reported for uranium(IV) so far. Extended X-ray absorption fine structure (EXAFS) spectroscopy showed that U-O-Si bonds, which increasingly replace the U-O-U bonds of the amorphous uranium(IV) oxyhydroxide with increasing silicate concentrations, make up the internal structure of the colloids. The next-neighbor coordination of U(IV) in the U(IV)-silica colloids is comparable with that of coffinite, USiO 4. The assessment of uranium behavior in the aquatic environment should take the possible existence of U(IV)-silica colloids into consideration. Their occurrence might influence uranium migration in anoxic waters.

  14. Colloidal Plasmas : Basic physics of colloidal plasmas

    Indian Academy of Sciences (India)

    C B Dwivedi

    2000-11-01

    Colloidal plasma is a distinct class of the impure plasmas with multispecies ionic composition. The distinction lies in the phase distribution of the impurity-ion species. The ability to tailor the electrostatic interactions between these colloidal particles provides a fertile ground for scientists to investigate the fundamental aspects of the Coulomb phase transition behavior. The present contribution will review the basic physics of the charging mechanism of the colloidal particles as well as the physics of the collective normal mode behavior of the general multi-ion species plasmas. Emphasis will be laid on the clarification of the prevailing confusing ideas about distinct qualities of the various acoustic modes, which are likely to exist in colloidal plasmas as well as in normal multi-ion species plasmas. Introductory ideas about the proposed physical models for the Coulomb phase transition in colloidal plasma will also be discussed.

  15. 纳米片状ZnO的室温制备及其胶状前体的稳定性分析%Synthesis of ZnO Nano Flake at Room Temperature and the Stability of Colloidal Precursors

    Institute of Scientific and Technical Information of China (English)

    许泳吉; 张利; 赵雪萍

    2012-01-01

    Colloidal precursors were synthesized by precipitation method using zinc acetate ( ZnAc2 ) and sodium hydroxide(NaOH) aqueous solution at room temperature. The products of Zns (OH)8 ( Ac)2 ·2H2O and ZnO were prepared by controlling the pH values of the reaction system. The composition, structure, and morphology of the resultant soild were characterized by using X-ray diffraction, scanning electron microscopy and energy dispersive spectrometer. We found that when the pH value of the precursor solution was 7, a steady colloid could be synthesized by the precipitation method, and the composition of the product was Zn5 ( OH)8 ( Ac ) 2 · 2 H2 O after dried at room temperature. If the pH value was 14, the coagulation phenomenon occurred with the ageing of colloidal precursor, and the coagulation product was hexagonal flake ZnO. In addition, the growth mechanism of ZnO nanomaterials was discussed, and it was also considered from the effects of pH value on the stability of colloidal precursor.%以醋酸锌和氢氧化钠为原料,采用室温直接沉淀法得到了ZnO的前体胶状醋酸锌碱式盐,通过控制pH值,在室温下分别制备了碱式盐Zn5(OH)8(Ac)2·2H2O和六方晶系纤锌矿ZnO,并利用X射线衍射、扫描电子显微镜和能谱(EDS)等测试技术对产物进行表征.结果表明,采用直接沉淀法在pH值为7的环境下得到了具有{n{[Zn5(OH)8(H2O)2]2+}·(2n-x)Ac-}x+·xAc-胶团结构的稳定胶体体系,室温下干燥后的产物的成分为碱式盐Zn5(OH)8(Ac)2 ·2H2O;而在pH值为14时,胶状前体发生聚沉生成白色沉淀,室温干燥后得到纳米片状ZnO.还考察了pH值对胶状前体稳定性的影响,并探讨了ZnO的生成机理.

  16. Quantum dot–induced phase stabilization of α-CsPbI3 perovskite for high-efficiency photovoltaics

    Science.gov (United States)

    Swarnkar, Abhishek; Marshall, Ashley R.; Sanehira, Erin M.; Chernomordik, Boris D.; Moore, David T.; Christians, Jeffrey A.; Chakrabarti, Tamoghna; Luther, Joseph M.

    2016-10-01

    We show nanoscale phase stabilization of CsPbI3 quantum dots (QDs) to low temperatures that can be used as the active component of efficient optoelectronic devices. CsPbI3 is an all-inorganic analog to the hybrid organic cation halide perovskites, but the cubic phase of bulk CsPbI3 (α-CsPbI3)—the variant with desirable band gap—is only stable at high temperatures. We describe the formation of α-CsPbI3 QD films that are phase-stable for months in ambient air. The films exhibit long-range electronic transport and were used to fabricate colloidal perovskite QD photovoltaic cells with an open-circuit voltage of 1.23 volts and efficiency of 10.77%. These devices also function as light-emitting diodes with low turn-on voltage and tunable emission.

  17. Quantum dot-induced phase stabilization of α-CsPbI3 perovskite for high-efficiency photovoltaics.

    Science.gov (United States)

    Swarnkar, Abhishek; Marshall, Ashley R; Sanehira, Erin M; Chernomordik, Boris D; Moore, David T; Christians, Jeffrey A; Chakrabarti, Tamoghna; Luther, Joseph M

    2016-10-07

    We show nanoscale phase stabilization of CsPbI3 quantum dots (QDs) to low temperatures that can be used as the active component of efficient optoelectronic devices. CsPbI3 is an all-inorganic analog to the hybrid organic cation halide perovskites, but the cubic phase of bulk CsPbI3 (α-CsPbI3)-the variant with desirable band gap-is only stable at high temperatures. We describe the formation of α-CsPbI3 QD films that are phase-stable for months in ambient air. The films exhibit long-range electronic transport and were used to fabricate colloidal perovskite QD photovoltaic cells with an open-circuit voltage of 1.23 volts and efficiency of 10.77%. These devices also function as light-emitting diodes with low turn-on voltage and tunable emission.

  18. Quantum Dot-Induced Phase Stabilization of ..alpha..-CsPbI3 Perovskite for High-Efficiency Photovoltaics

    Energy Technology Data Exchange (ETDEWEB)

    Swarnkar, Abhishek; Marshall, Ashley R.; Sanehira, Erin M.; Chernomordik, Boris D.; Moore, David T.; Christians, Jeffrey A.; Chakrabarti, Tamoghna; Luther, Joseph M.

    2016-10-07

    We show nanoscale phase stabilization of CsPbI3 quantum dots (QDs) to low temperatures that can be used as the active component of efficient optoelectronic devices. CsPbI3 is an all-inorganic analog to the hybrid organic cation halide perovskites, but the cubic phase of bulk CsPbI3 (..alpha..-CsPbI3) -- the variant with desirable band gap -- is only stable at high temperatures. We describe the formation of ..alpha..-CsPbI3 QD films that are phase-stable for months in ambient air. The films exhibit long-range electronic transport and were used to fabricate colloidal perovskite QD photovoltaic cells with an open-circuit voltage of 1.23 volts and efficiency of 10.77%. These devices also function as light-emitting diodes with low turn-on voltage and tunable emission.

  19. Ideal MHD stability of very high beta tokamaks

    Energy Technology Data Exchange (ETDEWEB)

    Chance, M.S.; Jardin, S.C.; Kessel, C.; Manickam, J.; Monticello, D. (Princeton Univ., NJ (USA). Plasma Physics Lab.); Peng, Y.K.M.; Holmes, J.A.; Strickler, D.J.; Whitson, J.C. (Oak Ridge National Lab., TN (USA)); Glasser, A.H. (Los Alamos National Lab., NM (USA)); Sykes, A. (UKAEA Culham Lab., Abingdon (UK)); Ramos, J.J. (Massachusetts Inst. of Tech., Cambridge, MA (USA). Plasma Fusion Center)

    1990-12-01

    Achieving very high {beta} and high {beta}{sub p} simultaneously in tokamaks generally implies that the second stability region against ballooning modes must be accessed. We describe several approaches for doing this, which are characterized by the choice of constraints imposed on the equilibrium profiles and the cross-sectional shape of the plasma. The combination of high toroidal beta, restricting the current density to vanish at the edge of the plasma and maintaining a monotonic q profile, proves to be the most stringent. Consideration of equilibria with high {epsilon}{beta}{sub p} but low {beta} facilitates accessibility with peaked pressure profiles and high values of q{sub 0}. Allowing the pressure gradient and, hence, the current density to be finite at the plasma edge allows all surfaces to lie within the second stability regime. For free boundary plasmas with divertors, the divertor stabilized edge region remains in the first stability regime while the plasma core reaches into the second regime. Careful tailoring of the profiles must be used to traverse the unstable barrier commonly seen near the edge of these plasmas. The CAMINO code allows us to compute s-{alpha} curves for general tokamak geometry. These diagrams enable us to construct equilibria whose profiles are only constrained, at worst, to be marginally stable everywhere, but do not necessarily satisfy the constraints on the current or {beta}. There are theoretical indications that under certain conditions the external kinks possess a second region of stability at high q{sub 0} that is analogous to that of the ballooning modes. It is found that extremely accurate numerical means must be developed and applied to confidently establish the validity of these results. 14 refs., 5 figs., 1 tab.

  20. Triaxial fluxgate gradiometer of high stability and linearity

    DEFF Research Database (Denmark)

    Merayo, José M.G.; Brauer, Peter; Primdahl, Fritz

    2005-01-01

    . The transducers are of the ringcore type with very low noise and high thermal stability. They use amorphous metal magnetic core (Vitrovac 6025). The cores have been annealed in two different processes with different temperatures and stress. With this instrument, three components of the gradient tensor can...

  1. Triaxial fluxgate gradiometer of high stability and linearity

    DEFF Research Database (Denmark)

    Merayo, José M.G.; Brauer, Peter; Primdahl, Fritz

    2005-01-01

    . The transducers are of the ringcore type with very low noise and high thermal stability. They use amorphous metal magnetic core (Vitrovac 6025). The cores have been annealed in two different processes with different temperatures and stress. With this instrument, three components of the gradient tensor can...

  2. Microfluidic colloid filtration

    Science.gov (United States)

    Linkhorst, John; Beckmann, Torsten; Go, Dennis; Kuehne, Alexander J. C.; Wessling, Matthias

    2016-03-01

    Filtration of natural and colloidal matter is an essential process in today’s water treatment processes. The colloidal matter is retained with the help of micro- and nanoporous synthetic membranes. Colloids are retained in a “cake layer” – often coined fouling layer. Membrane fouling is the most substantial problem in membrane filtration: colloidal and natural matter build-up leads to an increasing resistance and thus decreasing water transport rate through the membrane. Theoretical models exist to describe macroscopically the hydrodynamic resistance of such transport and rejection phenomena; however, visualization of the various phenomena occurring during colloid retention is extremely demanding. Here we present a microfluidics based methodology to follow filter cake build up as well as transport phenomena occuring inside of the fouling layer. The microfluidic colloidal filtration methodology enables the study of complex colloidal jamming, crystallization and melting processes as well as translocation at the single particle level.

  3. Design guidelines for high dimensional stability of CFRP optical bench

    Science.gov (United States)

    Desnoyers, Nichola; Boucher, Marc-André; Goyette, Philippe

    2013-09-01

    In carbon fiber reinforced plastic (CFRP) optomechanical structures, particularly when embodying reflective optics, angular stability is critical. Angular stability or warping stability is greatly affected by moisture absorption and thermal gradients. Unfortunately, it is impossible to achieve the perfect laminate and there will always be manufacturing errors in trying to reach a quasi-iso laminate. Some errors, such as those related to the angular position of each ply and the facesheet parallelism (for a bench) can be easily monitored in order to control the stability more adequately. This paper presents warping experiments and finite-element analyses (FEA) obtained from typical optomechanical sandwich structures. Experiments were done using a thermal vacuum chamber to cycle the structures from -40°C to 50°C. Moisture desorption tests were also performed for a number of specific configurations. The selected composite material for the study is the unidirectional prepreg from Tencate M55J/TC410. M55J is a high modulus fiber and TC410 is a new-generation cyanate ester designed for dimensionally stable optical benches. In the studied cases, the main contributors were found to be: the ply angular errors, laminate in-plane parallelism (between 0° ply direction of both facesheets), fiber volume fraction tolerance and joints. Final results show that some tested configurations demonstrated good warping stability. FEA and measurements are in good agreement despite the fact that some defects or fabrication errors remain unpredictable. Design guidelines to maximize the warping stability by taking into account the main dimensional stability contributors, the bench geometry and the optical mount interface are then proposed.

  4. Stabilization of high mercury contaminated brine purification sludge.

    Science.gov (United States)

    Zhuang, J Ming; Lo, Tony; Walsh, Tony; Lam, Tak

    2004-09-10

    The highly leachable mercury contaminants of brine purification sludge (BPS) generated from the Hg-cell electrolysis process in chlorine production can be stabilized in the treatment procedure employing ferric-lignin derivatives (FLD) (Ligmet binder) and Portland cement (PC). The stabilization effectiveness has been examined by time-based multiple toxicity characteristic leaching procedure (TCLP) tests and sequential TCLP tests. In a period of 50 days, the multiple TCLP tests showed a variation of less than 90 microg l(-1) for the leachable mercury level, and the sequential TCLP tests for the same sample displayed a declining TCLP mercury level. Based on this study, the stabilization of approximately 2000 t of brine purification sludge has been successfully processed with the ferric-lignin derivatives treatment.

  5. High Stability Optical Mount for Space Laser Applications

    Science.gov (United States)

    Mosciarello, P.; Di Carmine, E.

    2014-06-01

    In the frame of Atmospheric Lidar (ATLID) project, one of the active instruments foreseen to be boarded on the EarthCARE satellite, a high stability optical mount has been designed, developed and tested in order to fulfil the tight program requirements.A description of the design solution developed, manufactured and qualified for the most critical optical mount inside the PLH, located on the Laser Master Oscillator Plate (the laser resonance cavity), is presented. In order to minimize optical mount mass and envelope, the developed solution foresees a glued interface (I/F) between the mechanical support and the mirror.A collection of stability results obtained on the optical mount breadboards is also presented, including a description of environmental tests performed and the way to assess the mirror stability after each environmental test, as well as the acceptance criteria derived in order to establish the flight worthiness of the manufactured and assembled hardware.

  6. A HIGH STABILITY, LOW NOISE RF DISTRIBUTION SYSTEM

    Energy Technology Data Exchange (ETDEWEB)

    Bernstein, Dorel

    2002-08-20

    Next generation linear colliders require high stability, low noise distribution of RF phase and timing signals. We describe a fiber-optics system that transmits phase at 357MHz, at a 1500nm wavelength, over a distance of 15 kilometers. Phase length errors in the transmission fiber are measured using the phase of the signal reflected from the fiber end. Corrections are performed by controlling the temperature of a 6-kilometer fiber spool placed in series with the main transmission fiber. This system has demonstrated a phase stability better than 10 femtoseconds per degree C, per kilometer, an improvement of a factor of >2000 relative to un-stabilized fiber. This system uses standard low cost telecom fiber and components.

  7. Transport and Deposition of Variably Charged Soil Colloids in Saturated Porous Media

    DEFF Research Database (Denmark)

    Sharma, Anu; Kawamoto, Ken; Møldrup, Per

    2011-01-01

    A series of column experiments was conducted to investigate the transport and deposition of variably charged colloids in saturated porous media. Soil colloids with diameters colloids) and a red-yellow soil from...... Okinawa (RYS colloids) in Japan. The VAS colloids exhibited a negative surface charge with a high pH dependency, whereas the RYS colloids exhibited a negative surface charge with less pH dependency. The soil colloids were applied as colloidal suspensions to 10-cm-long saturated sand columns packed....... Breakthrough curves and deposition profiles for soil colloids were strong functions of the hydrodynamics, solution pH, and surface charge of the colloids and sand grains. Greater deposition was typical for lower flow rates and lower pH. The deposition of VAS colloids in both sands under low-pH conditions...

  8. Measurement of H!gh Power Current-Stabilized Power Supply with High Stability

    Institute of Scientific and Technical Information of China (English)

    YanHuaihai; FengXiuming; BaiZhen; ZhouZhongzu

    2003-01-01

    The DC power supply system of HIRFL has been upgraded since 1999, these new power supplies are used mainly as high frequency ZVS soft-switching converters or thyristor phase-controlled rectifiers. Each power supply is strictly tested before being put into operation, especially for long-term current stability, current ripple, efficiency, repeatability, EMI and so on. The tested results indicated that performances of power supplies satisfy requirement of HIRFL.

  9. Colloidal quantum dot solar cells

    Science.gov (United States)

    Sargent, Edward H.

    2012-03-01

    Solar cells based on solution-processed semiconductor nanoparticles -- colloidal quantum dots -- have seen rapid advances in recent years. By offering full-spectrum solar harvesting, these cells are poised to address the urgent need for low-cost, high-efficiency photovoltaics.

  10. Colloidal suspensions of functionalized mesoporous silica nanoparticles.

    Science.gov (United States)

    Kobler, Johannes; Möller, Karin; Bein, Thomas

    2008-04-01

    The synthesis and characterization of colloidal mesoporous silica (CMS) functionalized with vinyl-, benzyl-, phenyl-, cyano-, mercapto-, aminopropyl- or dihydroimidazole moieties is reported. Uniform mesoporous particles ranging in size from 40 to 150 nm are generated in a co-condensation process of tetraethylorthosilicate (TEOS) and organotriethoxysilanes (RTES) in alkaline aqueous media containing triethanolamine (TEA) in combination with cetyltrimethylammonium chloride (CTACl) serving as a structure-directing agent. The materials are obtained as colloidal suspensions featuring long-term stability after template removal by ion exchange with an ethanolic solution of ammonium nitrate or HCl. The spherical particles exhibit a wormlike pore system with defined pore sizes and high surface areas. Samples are analyzed by a number of techniques including TEM, SEM, DLS, TGA, Raman, and cross-polarized (29)Si-MAS NMR spectroscopy, as well as nitrogen sorption measurements. We demonstrate that co-condensation and grafting methods result in similar changes in the nitrogen adsorption behavior, indicating a successful internal lining of the pores with functional groups through both procedures.

  11. Synthesis and performance of colloidal silica nano-abrasives with controllable size for chemical mechanical planarization.

    Science.gov (United States)

    Zhang, K L; Song, Z T; Wang, F; Wang, L Y; Feng, S L

    2009-02-01

    Under the analysis of particle growth mechanism, the monodisperse colloidal silica abrasives for chemical mechanical planarization (CMP) slurry were synthesized by the modified ion-exchanged and hydrothermal step-polymerization process. After the colloidal silica with controllable size was synthesized, its microstructure, stability and CMP performance was characterized and tested by SEM, HRTEM, Zeta potential Analyzer and CMP tester. Results show that the spherical, high stable (Zeta potential: -52.8 mV) colloidal silica with controllable size was achieved. About its CMP performance, the polishing rate for silicon double-side CMP is increased to be 317 nm/min and the polished surface roughness (RMS) was reduced to 0.32 nm.

  12. Interaction forces between colloidal particles in a solution of like-charged, adsorbing nanoparticles.

    Science.gov (United States)

    McKee, Clayton T; Walz, John Y

    2012-01-01

    We have measured the force between a weakly charged micron-sized colloidal particle and flat substrate in the presence of highly charged nanoparticles of the same sign under solution conditions such that the nanoparticles physically adsorb to the colloidal particle and substrate. The objective was to investigate the net effect on the force profile between the microparticle and flat substrate arising from both nanoparticle adsorption and nanoparticles in solution. The experiments used colloidal probe atomic force microscopy (CP-AFM) to measure the force profile between a relatively large (5 μm) colloidal probe glass particle and a planar glass substrate in aqueous solutions at varying concentrations of spherical nanoparticles. At very low nanoparticle concentrations, the primary effect was an increase in the electrostatic repulsion between the surfaces due to adsorption of the more highly charged nanoparticles. As the nanoparticle concentration is increased, a depletion attraction formed, followed by longer-range structural forces at the highest nanoparticle concentrations studied. These results suggest that, depending on their concentration, such nanoparticles can either stabilize a dispersion of weakly-charged colloidal particles or induce flocculation. This behavior is qualitatively different from that in nonadsorbing systems, where the initial effect is the development of an attractive depletion force. Copyright © 2011. Published by Elsevier Inc.

  13. Facile and highly efficient removal of trace Gd(III) by adsorption of colloidal graphene oxide suspensions sealed in dialysis bag

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Weifan, E-mail: dragon0791@sohu.com [School of Materials Science and Engineering, Nanchang University, Nanchang 330031 (China); Research Center of Rare Earths and Micro/Nano Functional Materials, Nanchang University, Nanchang 330031 (China); Wang, Linlin; Zhuo, Mingpeng; Liu, Yue; Wang, Yiping [School of Materials Science and Engineering, Nanchang University, Nanchang 330031 (China); Li, Yongxiu [Research Center of Rare Earths and Micro/Nano Functional Materials, Nanchang University, Nanchang 330031 (China)

    2014-08-30

    Graphical abstract: Schematic diagram of Gd(III) adsorption and desorption on GO nanosheets in colloidal suspensions sealed by dialysis membrane. - Highlights: • Loading GO suspensions into dialysis bag for sorption of Gd(III) avoids re-pollution. • GO shows higher adsorption capacity for Gd(III) than any other currently reported. • Effects of pH, ionic strength and temperature on GO sorption for Gd(III) were studied. • Gd(III)-saturated GO has high desorption rate in nitric acid aqueous solution. • The thermodynamics and kinetics models of Gd(III) sorption on GO were studied. - Abstract: A facile, highly efficient and second-pollution-free strategy to remove trace Gd(III) from aqueous solutions by adsorption of colloidal graphene oxide (GO) suspensions in dialysis bag has been developed. The effects of pH, ionic strength and temperature on Gd(III) adsorption, and the pH-dependent desorption were investigated. The maximum adsorption capacity of Gd(III)on GO at pH = 5.9 ± 0.1 and T = 303 K was 286.86 mg g{sup −1}, higher than any other currently reported. The Gd(III)-saturated GO suspension could resume colloidal state in 0.1 M HNO{sub 3} with desorption rate of 85.00% in the fifth adsorption–desorption cycle. Gd(III) adsorption rate on GO was dependent more on pH and ionic strength than on temperature. The abundant oxygen-containing functional groups such as carboxyl and hydroxyl played a vital role on adsorption. The thermodynamics and kinetics investigations revealed that the adsorption of Gd(III) on GO was an endothermic, spontaneous and monolayer absorption process, which well fitted the pseudo-second-order model. GO could be a promising adsorbent applied in the enrichment and removal of lanthanides from aqueous solutions. More significantly, the combination of colloidal GO suspension with dialysis membrane facilely solves the re-pollution of the treated solutions due to the great difficulties in separation and recovery of GO.

  14. Standard versus high-flexion posterior stabilized total knee prostheses.

    Science.gov (United States)

    Li, Ning; Li, Junwei; Li, Peng; Wang, Dan; Liu, Ming; Xia, Lei

    2015-03-01

    This meta-analysis compared clinical outcomes between standard and high-flexion posterior-stabilized total knee prostheses to evaluate which type of total knee prosthesis was superior. Randomized, controlled trials published until October 2013 comparing standard and high-flexion posterior-stabilized total knee prostheses were reviewed. Methodologic quality was assessed with the Physiotherapy Evidence Database scale. After data extraction, the authors compared results with fixed effects or random effects models, depending on the heterogeneity of the included studies. Eight randomized, controlled trials involving 660 patients met the predetermined inclusion criteria. No statistically significant differences between patients undergoing standard and high-flexion posterior-stabilized total knee prostheses were noted in postoperative range of motion (ROM) (weighted mean difference, -1.43; 95% confidence interval [CI], -4.52 to 1.67; P=.37); flexion angle (weighted mean difference, 0.54; 95% CI, -3.75 to 4.84; P=.80); Knee Society Score (weighted mean difference, 0.92; 95% CI, -0.64 to 2.48; P=.25); Hospital for Special Surgery knee score (weighted mean difference, 0.57; 95% CI, -0.42 to 1.55; P=.26); or Knee Society function score (weighted mean difference, 1.00; 95% CI, -1.49 to 3.49; P=.43). No statistical difference was found between the 2 prosthesis types in complications, involving 21 cases in the standard group and 14 cases in the high-flexion group. The current findings confirm that high-flexion posterior-stabilized total knee prostheses are not superior to standard prostheses in terms of ROM, flexion angle, knee scores, or complications with 5 years or less of follow-up.

  15. Synthesis of biolubricants with high viscosity and high oxidation stability

    Directory of Open Access Journals (Sweden)

    Bondioli Paolo

    2003-03-01

    Full Text Available The synthetic procedure as well as the main properties of obtained products of a group of complex esters are reported here. Complex esters were prepared using low molecular weight saturated fatty acids, trimethylolpropane and a dicarboxylic acid as a feedstock. By means of this procedure it is possible to obtain products having high viscosity and very good lubricating, thermal and cold properties. Thanks to the absence of unsaturations into the ester also the oxidation property is good, opening several application perspective for these products which are partly prepared from renewable source.

  16. Gel trapping of dense colloids.

    Science.gov (United States)

    Laxton, Peter B; Berg, John C

    2005-05-01

    Phase density differences in sols, foams, or emulsions often lead to sedimentation or creaming, causing problems for materials where spatial uniformity over extended periods of time is essential. The problem may be addressed through the use of rheology modifiers in the continuous phase. Weak polymer gels have found use for this purpose in the food industry where they appear to be capable of trapping dispersoid particles in a three-dimensional matrix while displaying water-like viscosities at low shear. Attempts to predict sedimentation stability in terms of particle properties (size, shape, density difference) and gel yield stress have led to qualitative success for suspensions of large particles. The effect of particle size, however, in particular the case in which colloidal dimensions are approached, has not been investigated. The present work seeks to determine useful stability criteria for colloidal dispersions in terms of readily accessible viscoelastic descriptors. Results are reported for systems consisting of 12 microm poly(methyl methacrylate) (PMMA) spheres dispersed in aqueous gellan gum. Monovalent salt concentration is varied to control rheological properties, and sedimentation/centrifugation experiments are performed to determine dispersion stability. Necessary conditions for stability consist of a minimum yield stress together with a value of tan delta less than unity.

  17. Rheological properties of highly concentrated protein-stabilized emulsions.

    Science.gov (United States)

    Dimitrova, Tatiana D; Leal-Calderon, Fernando

    2004-05-20

    We prepared concentrated quasi monodisperse hexadecane-in-water emulsions stabilized by various proteins and investigated their rheological properties. Some protein-stabilized emulsions possess remarkably high elasticity and at the same time they are considerably fragile--they exhibit coalescence at yield strain and practically do not flow. The elastic storage modulus G' and the loss modulus G" of the emulsions were determined for different oil volume fractions above the random close packing. Surprisingly, the dimensionless elastic moduli G'/(sigma/a), sigma being the interfacial tension, and a being the mean drop radius, obtained for emulsions stabilized by different proteins do not collapse on a single master curve. They are almost always substantially higher than the corresponding values obtained for equivalent Sodium Dodecyl Sulfate (SDS)-stabilized emulsions. The unusually high elasticity cannot be attributed to a specificity of the continuous phase, because the osmotic equation of state of our emulsions is found identical to the one obtained for samples stabilized by classical surfactants. In parallel, we mimicked the thin films that separate the droplets in the concentrated emulsion and found that the protein adsorption layers contain a substantial number of sticky surface aggregates. These severely obstruct local rearrangements of individual drops in respect to their neighbors which leads to coalescence at yield strain. Furthermore, we found that G'/(sigma/a) is correlated (for a given oil volume fraction) to the dilatational elastic modulus, of the protein layer adsorbed on the droplets. The intrinsic elasticity of the protein layers, together with the blocked local rearrangements are considered as the main factors determining the unusual bulk elasticity of the studied emulsions.

  18. A high stability and repeatability electrochemical scanning tunneling microscope

    Energy Technology Data Exchange (ETDEWEB)

    Xia, Zhigang; Wang, Jihao; Lu, Qingyou, E-mail: qxl@ustc.edu.cn [High Magnetic Field Laboratory, Chinese Academy of Sciences and University of Science and Technology of China, Hefei, Anhui 230026 (China); Hefei National Laboratory for Physical Sciences at Microscale, University of Science and Technology of China, Hefei, Anhui 230026 (China); Hou, Yubin [High Magnetic Field Laboratory, Chinese Academy of Sciences and University of Science and Technology of China, Hefei, Anhui 230026 (China)

    2014-12-15

    We present a home built electrochemical scanning tunneling microscope (ECSTM) with very high stability and repeatability. Its coarse approach is driven by a closely stacked piezo motor of GeckoDrive type with four rigid clamping points, which enhances the rigidity, compactness, and stability greatly. It can give high clarity atomic resolution images without sound and vibration isolations. Its drifting rates in XY and Z directions in solution are as low as 84 pm/min and 59 pm/min, respectively. In addition, repeatable coarse approaches in solution within 2 mm travel distance show a lateral deviation less than 50 nm. The gas environment can be well controlled to lower the evaporation rate of the cell, thus reducing the contamination and elongating the measurement time. Atomically resolved SO{sub 4}{sup 2−} image on Au (111) work electrode is demonstrated to show the performance of the ECSTM.

  19. The Benefit of Currency Substitution during High Inflation and Stabilization The Benefit of Currency Substitution during High Inflation and Stabilization

    Directory of Open Access Journals (Sweden)

    Jacek Rostowski

    1992-03-01

    Full Text Available Allowing currency substitution in a very high inflation helps to maintain the level of output, as, the distortion of the information carried by prices is mitigated. The total (primary plus secondary money supply may increase if currency substitution is permitted. Currency substitution does not even necessarily reduce the real primary money stock. Moreover, the demand for the primary money fragments at very high rates of inflation, which means that the authorities may loose little when they give up the attempt to obtain inflation tax revenue. Currency substitution need be no more expensive, in term of the real resources it consumes, than is indexation. Finally the availability of a second stable currency may reduce the severity of post-stabilization recessions. The Benefit of Currency Substitution during High Inflation and Stabilization

  20. A High-Stability Capacitance Sensor System and Its Evaluation

    Science.gov (United States)

    2008-12-01

    15:45 from IEEE Xplore . Restrictions apply. Report Documentation Page Form ApprovedOMB No. 0704-0188 Public reporting burden for the collection of...45 from IEEE Xplore . Restrictions apply. AVRAMOV-ZAMUROVIC AND LEE: HIGH-STABILITY CAPACITANCE SENSOR SYSTEM AND ITS EVALUATION 957 Fig. 4...Authorized licensed use limited to: US Naval Academy. Downloaded on May 13, 2009 at 15:45 from IEEE Xplore . Restrictions apply. 958 IEEE TRANSACTIONS

  1. Stability of discoidal high-density lipoprotein particles

    Science.gov (United States)

    Maleki, Mohsen; Fried, Eliot

    Motivated by experimental and numerical studies revealing that discoidal high-density lipoprotein (HDL) particles may adopt flat elliptical and nonplanar saddle-like configurations, it is hypothesized that these might represent stabilized configurations of initially unstable flat circular particles. A variational description is developed to explore the stability of a flat circular discoidal HDL particle. While the lipid bilayer is modeled as two-dimensional fluid film endowed with surface tension and bending elasticity, the apoA-I belt is modeled as one-dimensional inextensible twist-free chain endowed with bending elasticity. Stability is investigated using the second variation of the underlying energy functional. Various planar and nonplanar instability modes are predicted and corresponding nondimensional critical values of salient dimensionless parameters are obtained. The results predict that the first planar and nonplanar unstable modes occur due to in-plane elliptical and transverse saddle-like perturbations. Based on available data, detailed stability diagrams indicate the range of input parameters for which a flat circular discoidal HDL particle is linearly stable or unstable.

  2. kT-scale colloidal interactions in high-frequency inhomogeneous AC electric fields. II. Concentrated ensembles.

    Science.gov (United States)

    Juárez, Jaime J; Liu, Brian G; Cui, Jing-Qin; Bevan, Michael A

    2011-08-02

    We report nonintrusive optical microscopy measurements of ensembles of polystyrene colloids in inhomogeneous AC electric fields as a function of field frequency and particle size. By using an inverse Monte Carlo (MC) simulation analysis of time-averaged particle microstructures, we sensitively measure induced dipole-dipole interactions on the kT energy scale. Measurements are reported for frequencies when the particle polarizability is greater and less than the medium, as well as the crossover between these conditions when dipole-dipole interactions vanish. By using measured single dipole-field interactions and associated parameters from Part I as input in the inverse analysis, the dipole-dipole interactions in this work are accurately modeled with no adjustable parameters for conditions away from the crossover frequency (i.e., |f(CM)| > 0). As dipolar interactions vanish at the crossover, a single frequency-dependent parameter is introduced to account for microstructures that appear to result from weak AC electro-osmotic flow induced interactions. By connecting quantitative measures of equilibrium microstructures and kT-scale dipole-field and dipole-dipole interactions, our findings provide a basis to understand colloidal assembly in inhomogeneous AC electric fields.

  3. Complex coacervation between colloidal silica and polyacrylamide

    Energy Technology Data Exchange (ETDEWEB)

    Kawase, Kaoru; Sakami, Hiroshi; Hayakawa, Kiyoshi

    1989-03-01

    Complex coacervation introduced by gamma-ray induced polymerization of acrylamide in colloidal silica was studied. The complex coaservate was formed by polymerization of acrylamide dissolved in a colloidal silica and methanol mixture. Complex coacervation (two-phase separation of the mixture) was observed only when the concentration of methanol was between 33 and 41 percent by volume, and the concentration of colloidal silica did not affect it. Although two phase separation was not influenced by pH change, the content of polyacrylamide was bigger in the equilibrated solution in acidic regions. It was, however, bigger in the complex coacervate at neutral and in alkaline regions. The content of polyacrylamide was also calculated from the particle diameter of complex coacervate measured by small angle X-ray scattering, and the result was well coincided with the analytical result. The stability of the complex coacervate against the addition of salts was better than that of the untreated colloidal silica. The rate of electrophoretic transport of the complex coacervate was also lower than that of the colloidal silica. From these observation it was concluded that the hydrophobic colloidal silica particles were protected by the surrounding hydrophilic polyacrylamide. (author).

  4. Process Design Concepts for Stabilization of High Level Waste Calcine

    Energy Technology Data Exchange (ETDEWEB)

    T. R. Thomas; A. K. Herbst

    2005-06-01

    The current baseline assumption is that packaging ¡§as is¡¨ and direct disposal of high level waste (HLW) calcine in a Monitored Geologic Repository will be allowed. The fall back position is to develop a stabilized waste form for the HLW calcine, that will meet repository waste acceptance criteria currently in place, in case regulatory initiatives are unsuccessful. A decision between direct disposal or a stabilization alternative is anticipated by June 2006. The purposes of this Engineering Design File (EDF) are to provide a pre-conceptual design on three low temperature processes under development for stabilization of high level waste calcine (i.e., the grout, hydroceramic grout, and iron phosphate ceramic processes) and to support a down selection among the three candidates. The key assumptions for the pre-conceptual design assessment are that a) a waste treatment plant would operate over eight years for 200 days a year, b) a design processing rate of 3.67 m3/day or 4670 kg/day of HLW calcine would be needed, and c) the performance of waste form would remove the HLW calcine from the hazardous waste category, and d) the waste form loadings would range from about 21-25 wt% calcine. The conclusions of this EDF study are that: (a) To date, the grout formulation appears to be the best candidate stabilizer among the three being tested for HLW calcine and appears to be the easiest to mix, pour, and cure. (b) Only minor differences would exist between the process steps of the grout and hydroceramic grout stabilization processes. If temperature control of the mixer at about 80„aC is required, it would add a major level of complexity to the iron phosphate stabilization process. (c) It is too early in the development program to determine which stabilizer will produce the minimum amount of stabilized waste form for the entire HLW inventory, but the volume is assumed to be within the range of 12,250 to 14,470 m3. (d) The stacked vessel height of the hot process vessels

  5. Novel active stabilization technology in highly crosslinked UHMWPEs for superior stability

    Science.gov (United States)

    Oral, Ebru; Neils, Andrew L.; Wannomae, Keith K.; Muratoglu, Orhun K.

    2014-12-01

    Radiation cross-linked ultrahigh molecular weight polyethylene (UHMWPE) is the bearing of choice in joint arthroplasty. The demands on the longevity of this polymer are likely to increase with the recently advancing deterioration of the performance of alternative metal-on-metal implants. Vitamin E-stabilized, cross-linked UHMWPEs are considered the next generation of improved UHMWPE bearing surfaces for improving the oxidation resistance of the polymer. It was recently discovered that in the absence of radiation-induced free radicals, lipids absorbed into UHMWPE from the synovial fluid can initiate oxidation and result in new free radical-mediated oxidation mechanisms. In the presence of radiation-induced free radicals, it is possible for the polymer to oxidize through both existing free radicals at the time of implantation and through newly formed free radicals in vivo. Thus, we showed that reducing the radiation-induced free radicals in vitamin E-stabilized UHMWPE would increase its oxidative stability and presumably lead to improved longevity. We describe mechanical annealing and warm irradiation of irradiated vitamin E blends as novel methods to eliminate 99% of radiation-induced free radicals without sacrificing crystallinity. These are significant improvements in the processing of highly cross-linked UHMWPE for joint implants with improved longevity.

  6. Preparation of (non-)aqueous dispersins of colloidal boehmite needles

    NARCIS (Netherlands)

    Buining, P.A.; Pathmamanoharan, C.; Philipse, A.P.; Lekkerkerker, H.N.W.

    1993-01-01

    A novel hydrothermal alkoxide method is presented for the preparation of stable, aqueousdispersions of fairly monodisperse, charged colloidal boehmite needles. A polymer coating procedure for the needles is described which leads to sterically stabilized dispersions in organic solvents.

  7. Lyotropic hexagonal columnar liquid crystals of large colloidal gibbsite platelets

    NARCIS (Netherlands)

    Mourad, M.C.D.; Petukhov, A.V.; Vroege, G.J.; Lekkerkerker, H.N.W.

    2010-01-01

    We report the formation of hexagonal columnar liquid crystal phases in suspensions of large (570 nm diameter), sterically stabilized, colloidal gibbsite platelets in organic solvent. In thin cells these systems display strong iridescence originating from hexagonally arranged columns that are

  8. Accelerated purification of colloidal silica sols

    Science.gov (United States)

    Bahnsen, E. B.; Garofalini, S.; Pechman, A.

    1979-01-01

    Accelerated purification process for colloidal sols using heat/deionization scheme, sharply reduces waiting time between deionization cycles from several months to a few days. Process produces same high purity silica sols as conventional methods.

  9. UZ Colloid Transport Model

    Energy Technology Data Exchange (ETDEWEB)

    M. McGraw

    2000-04-13

    The UZ Colloid Transport model development plan states that the objective of this Analysis/Model Report (AMR) is to document the development of a model for simulating unsaturated colloid transport. This objective includes the following: (1) use of a process level model to evaluate the potential mechanisms for colloid transport at Yucca Mountain; (2) Provide ranges of parameters for significant colloid transport processes to Performance Assessment (PA) for the unsaturated zone (UZ); (3) Provide a basis for development of an abstracted model for use in PA calculations.

  10. Colloid process engineering

    CERN Document Server

    Peukert, Wolfgang; Rehage, Heinz; Schuchmann, Heike

    2015-01-01

    This book deals with colloidal systems in technical processes and the influence of colloidal systems by technical processes. It explores how new measurement capabilities can offer the potential for a dynamic development of scientific and engineering, and examines the origin of colloidal systems and its use for new products. The future challenges to colloidal process engineering are the development of appropriate equipment and processes for the production and obtainment of multi-phase structures and energetic interactions in market-relevant quantities. The book explores the relevant processes and for controlled production and how they can be used across all scales.

  11. Colloid Transport and Retention

    DEFF Research Database (Denmark)

    Yuan, Hao; Shapiro, Alexander

    2012-01-01

    different colloidal materials and their applications in chemistry, physics, biological, medical sciences and environment. Graduate students, academic and industrial researchers and medical professionals will discover recently developed colloidal materials and their applications in many areas of human......Book Description: Colloidal science and technology is one of the fastest growing research and technology areas. This book explores the cutting edge research in colloidal science and technology that will be usefull in almost every aspect of modern society. This book has a depth of information...

  12. Fabrication of a composite colloidal particle with unusual Janus structure as a high-performance solid emulsifier.

    Science.gov (United States)

    Meng, Xiaohui; Guan, Yinyan; Zhang, Zhengdong; Qiu, Dong

    2012-08-28

    Core-shell particles with cross-linked core and shell were used as seed particles to produce composite Janus particles. It was found that when the shell has distinctly higher cross-linking degree than the core, Janus particles with very unusual structures can be obtained. These particles have two parts, with one part embraced partially or entirely by the other part, adjustable by parameters such as phase ratio or cross-linking degree. On the basis of experimental observations, a possible mechanism for the formation of such unusual Janus particles has been proposed. Janus particles with arms are used to emulsify water-toluene mixtures, forming oil-in-water (O/W) emulsions at very high internal phase content with rather low concentration of particles. Nonspherical emulsion droplets were observed, indicating that these Janus particles are likely to jam at the interface, forming a strong protecting layer to stabilize emulsions.

  13. Cementitious Stabilization of Mixed Wastes with High Salt Loadings

    Energy Technology Data Exchange (ETDEWEB)

    Spence, R.D.; Burgess, M.W.; Fedorov, V.V.; Downing, D.J.

    1999-04-01

    Salt loadings approaching 50 wt % were tolerated in cementitious waste forms that still met leach and strength criteria, addressing a Technology Deficiency of low salt loadings previously identified by the Mixed Waste Focus Area. A statistical design quantified the effect of different stabilizing ingredients and salt loading on performance at lower loadings, allowing selection of the more effective ingredients for studying the higher salt loadings. In general, the final waste form needed to consist of 25 wt % of the dry stabilizing ingredients to meet the criteria used and 25 wt % water to form a workable paste, leaving 50 wt % for waste solids. The salt loading depends on the salt content of the waste solids but could be as high as 50 wt % if all the waste solids are salt.

  14. Phase stability of high manganese austenitic steels for cryogenic applications

    CERN Document Server

    Couturier, K

    2000-01-01

    The aim of this work is to study the austenitic stability against a' martensitic transformation of three non-magnetic austenitic steels : a new stainless steel X2CrMnNiMoN 19-12-11-1 grade, a traditional X8CrMnNiN 19-11-6 grade and a high manganese X8MnCrNi 28-7-1 grade. Measurements of relative magnetic susceptibility at room temperature are performed on strained tensile specimens at 4.2 K. A special extensometer for high precision strain measurements at low temperature has been developed at CERN to test specimens up to various levels of plastic strain. Moreover, the high precision strain recording of the extensometer enables a detailed study of the serrated yield phenomena associated with 4.2 K tensile testing and their influence on the evolution of magnetic susceptibility. The results show that high Mn contents increase the stability of the austenitic structure against a' martensitic transformation, while keeping high strength at cryogenic temperature. Moreover, proper elaboration through primary and possi...

  15. Stability of high cell density brewery fermentations during serial repitching.

    Science.gov (United States)

    Verbelen, Pieter J; Dekoninck, Tinne M L; Van Mulders, Sebastiaan E; Saerens, Sofie M G; Delvaux, Filip; Delvaux, Freddy R

    2009-11-01

    The volumetric productivity of the beer fermentation process can be increased by using a higher pitching rate (i.e. higher inoculum size). However, the decreased yeast net growth observed in these high cell density brewery fermentations can adversely affect the physiological stability throughout subsequent yeast generations. Therefore, different O(2) conditions (wort aeration and yeast preoxygenation) were applied to high cell density fermentation and eight generations of fermentations were evaluated together with conventional fermentations. Freshly propagated high cell density populations adapted faster to the fermentative conditions than normal cell density populations. Preoxygenating the yeast was essential for the yeast physiological and beer flavor compound stability of high cell density fermentations during serial repitching. In contrast, the use of non-preoxygenated yeast resulted in inadequate growth which caused (1) insufficient yield of biomass to repitch all eight generations, (2) a 10% decrease in viability, (3) a moderate increase of yeast age, (4) and a dramatic increase of the unwanted flavor compounds acetaldehyde and total diacetyl during the sequence of fermentations. Therefore, to achieve sustainable high cell density fermentations throughout the economical valuable process of serial repitching, adequate yeast growth is essential.

  16. Colloid-Facilitated Transport of Low-Solubility Radionuclides: A Field, Experimental, and Modeling Investigation

    Energy Technology Data Exchange (ETDEWEB)

    Kersting, A B; Reimus, P W; Abdel-Fattah, A; Allen, P G; Anghel, I; Benedict, F C; Esser, B K; Lu, N; Kung, K S; Nelson, J; Neu, M P; Reilly, S D; Smith, D K; Sylwester, E R; Wang, L; Ware, S D; Warren, RG; Williams, R W; Zavarin, M; Zhao, P

    2003-02-01

    rate of Pu transport. Currently, the role of colloids in facilitating the transport of low-solubility radionuclides is not understood well enough to effectively model contaminant transport. A fundamental understanding of the role that colloids may or may not play in the transport of low-solubility radionuclides is needed in order to predict contaminant transport, design remediation strategies and provide risk assessments. Ryan and Elimelech (1996) have argued that in order to evaluate the potential for colloids to transport radionuclides, several criteria must be met: (1) colloids must exist and be stable, (2) radionuclides must have a high sorption affinity for the colloids, and (3) colloids must be transported. Only then can we understand the conditions where colloids can and will facilitate transport of radionuclides. In this report we compile the results from a series of field, laboratory and modeling studies funded by the UGTA program in order to evaluate the potential for colloids to transport low-solubility radionuclides at the NTS. The studies presented in this report fall under three general areas of investigation: Characterization of natural colloids in groundwater at NTS, Pu sorption/desorption experiments on colloid minerals identified in NTS groundwater, and Transport of Pu-doped colloids through fractured rock core. Chapter 1 is a background review of our current understanding of colloids and their role in facilitating contaminant transport. Chapters 2, and 3 are field studies that focused on characterizing natural colloids at different hydrologic environments at the NTS and address Ryan and Elimelech's (1996) first criteria regarding the existence and stability of colloids. Chapters 4, 5 and 6 are laboratory experimental studies that investigate the sorption/desorption behavior of Pu and other low-solubility radionuclides on colloid minerals observed in NTS groundwater. These studies evaluate Ryan and Elimelech's (1996) second criteria that the

  17. Phase Stability Diagrams for High Temperature Corrosion Processes

    Directory of Open Access Journals (Sweden)

    J. J. Ramos-Hernandez

    2013-01-01

    Full Text Available Corrosion phenomena of metals by fused salts depend on chemical composition of the melt and environmental conditions of the system. Detail knowledge of chemistry and thermodynamic of aggressive species formed during the corrosion process is essential for a better understanding of materials degradation exposed to high temperature. When there is a lack of kinetic data for the corrosion processes, an alternative to understand the thermodynamic behavior of chemical species is to utilize phase stability diagrams. Nowadays, there are several specialized software programs to calculate phase stability diagrams. These programs are based on thermodynamics of chemical reactions. Using a thermodynamic data base allows the calculation of different types of phase diagrams. However, sometimes it is difficult to have access to such data bases. In this work, an alternative way to calculate phase stability diagrams is presented. The work is exemplified in the Na-V-S-O and Al-Na-V-S-O systems. This system was chosen because vanadium salts is one of the more aggressive system for all engineering alloys, especially in those processes where fossil fuels are used.

  18. High temperature SMES for improving power system stabilities

    Institute of Scientific and Technical Information of China (English)

    CHENG ShiJie; TANG YueJin

    2007-01-01

    Superconducting magnetic energy storage (SMES) system has been proven very effective to improve power system stabilities. It is realized with superconductivity technology, power electronics and control theory. In order to promote the application of such kind control device and to further investigate the properties of the controller, a detail mathematic model of such control device is developed. Based on the developed model, extensive analysis including time domain simulation is carried out to investigate the characteristic of the SMES to compensate the unba- lanced dynamic active and reactive power of AC power system. The capability of SMES to increase power system transient and small signal perturbation stabilities are analyzed. A prototype SMES is developed, in which the conduction cooling and the high temperature superconductive techniques are used. The performance of the prototype is experimentally investigated in a laboratory environment. Very encouraging results are obtained. After a brief introduction of the SMES control system and the principle of its capability to improve power system stabilities, the details of the mathematic model, the theoretical analysis, the developed device and the experiment test results are all given in this paper.

  19. High temperature SMES for improving power system stabilities

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Superconducting magnetic energy storage (SMES) system has been proven very effective to improve power system stabilities. It is realized with superconductivity technology, power electronics and control theory. In order to promote the applica-tion of such kind control device and to further investigate the properties of the controller, a detail mathematic model of such control device is developed. Based on the developed model, extensive analysis including time domain simulation is carried out to investigate the characteristic of the SMES to compensate the unba- lanced dynamic active and reactive power of AC power system. The capability of SMES to increase power system transient and small signal perturbation stabilities are analyzed. A prototype SMES is developed, in which the conduction cooling and the high temperature superconductive techniques are used. The performance of the prototype is experimentally investigated in a laboratory environment. Very en-couraging results are obtained. After a brief introduction of the SMES control sys-tem and the principle of its capability to improve power system stabilities, the de-tails of the mathematic model, the theoretical analysis, the developed device and the experiment test results are all given in this paper.

  20. Stability of vocational interests among high school students.

    Science.gov (United States)

    Mullis, R L; Mullis, A K; Gerwels, D

    1998-01-01

    The purpose of this study was to examine the stability of adolescents' career interests using the Strong-Campbell Interest Inventory (SCII). Students at a Midwestern high school were administered the SCII twice over a three-year period, and comparisons were made on Occupational Themes and Basic Interests. Significant differences in mean scores were found by gender and parental occupation, and these differences were relatively stable. The findings are discussed in relation to previous research and Holland's theory, and the implications are addressed.

  1. Comparision of {sup 188}Rhenuim-tin colloid and {sup 188}Rhenium-sulfur colloid as a radiation synovectomy agent

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Y. J.; Jung, J. M.; Kim, Y. J.; Jang, Y. S.; Lee, D. S.; Jung, J. K.; Song, Y. W.; Lee, M. C. [KAERI, Taejon (Korea, Republic of)

    1999-10-01

    Beta-emitting radiocolloids have been used for the treatment of rheumatoid arthritis. As a generator produced beta-emitting radionuclide, the importance of Re-188 for radionuclide therapy is increasing rapidly. We compared the radiochemistry of two {sup 188}Re labeled radiocolloids: {sup 188}Re-tin colloid and {sup 188}Re-sulfur colloid. {sup 188}Re-tin colloid was obtained by reacting 10 mg SnCl{sub 2}{center_dot}H{sub 2}O and {sup 188}Re perrhenate. {sup 188}Re-sulfur colloid was labeled by boiling 40 mg sodium thiosulfate, 0.8 mg Na{sub 2}{center_dot}EDTA, and 0.8 mg potassium perrhenate with {sup 188}Re perrhenate. Radiochemical purity was checked by ITLC-SG/ saline. Labeling efficiencies reached >98% for tin colloid at 2 hr and 89{approx}94% for sulfur colloid at 3 hr. All the preparations were stable for 72 hr in water, serum, and synovial fluid. If labeled at higher temperature, particle size of tin colloid increased. Remained radioactivity of {sup 188}Re-sulfur colloid in disposable polypropylene syringe after injecting to mice was high (62.0{+-}7.0%) due to its hydrophobic nature, although, tin colloid did not show high remained radioactivity (2.9{+-}1.6%). Biodistribution in Antigen induced arthratitis model rabbit after synovial space injection showed that {sup 188}Re-tin colloid was well retained in synovial space for 48 hr. Although, both {sup 188}Re-tin colloid and {sup 188}Re-sulfur colloid might be useful for radionuclide therapy, we concluded that {sup 188}Re-tin colloid is more adventageous over {sup 188}Re-sulfur colloid, due to higher labeling efficency, size-controllable property, and lower residual activity in syringe.

  2. Dynamic Stability Analysis Using High-Order Interpolation

    Directory of Open Access Journals (Sweden)

    Juarez-Toledo C.

    2012-10-01

    Full Text Available A non-linear model with robust precision for transient stability analysis in multimachine power systems is proposed. The proposed formulation uses the interpolation of Lagrange and Newton's Divided Difference. The High-Order Interpolation technique developed can be used for evaluation of the critical conditions of the dynamic system.The technique is applied to a 5-area 45-machine model of the Mexican interconnected system. As a particular case, this paper shows the application of the High-Order procedure for identifying the slow-frequency mode for a critical contingency. Numerical examples illustrate the method and demonstrate the ability of the High-Order technique to isolate and extract temporal modal behavior.

  3. High Volume Manufacturing and Field Stability of MEMS Products

    Science.gov (United States)

    Martin, Jack

    Low volume MEMS/NEMS production is practical when an attractive concept is implemented with business, manufacturing, packaging, and test support. Moving beyond this to high volume production adds requirements on design, process control, quality, product stability, market size, market maturity, capital investment, and business systems. In a broad sense, this chapter uses a case study approach: It describes and compares the silicon-based MEMS accelerometers, pressure sensors, image projection systems, and gyroscopes that are in high volume production. Although they serve several markets, these businesses have common characteristics. For example, the manufacturing lines use automated semiconductor equipment and standard material sets to make consistent products in large quantities. Standard, well controlled processes are sometimes modified for a MEMS product. However, novel processes that cannot run with standard equipment and material sets are avoided when possible. This reliance on semiconductor tools, as well as the organizational practices required to manufacture clean, particle-free products partially explains why the MEMS market leaders are integrated circuit manufacturers. There are other factors. MEMS and NEMS are enabling technologies, so it can take several years for high volume applications to develop. Indeed, market size is usually a strong function of price. This becomes a vicious circle, because low price requires low cost - a result that is normally achieved only after a product is in high volume production. During the early years, IC companies reduced cost and financial risk by using existing facilities for low volume MEMS production. As a result, product architectures are partially determined by capabilities developed for previous products. This chapter includes a discussion of MEMS product architecture with particular attention to the impact of electronic integration, packaging, and surfaces. Packaging and testing are critical, because they are

  4. Polymer adsorption and its effect on colloidal stability : a theoretical and experimental study on the polyvinyl alcohol-silver iodide system

    NARCIS (Netherlands)

    Fleer, G.J.

    1971-01-01

    The purpose of this study was to gain insight in the factors determining the stability of hydrophobic sols in the presence of polymers, with the emphasis on the destabilisation of sols by polymers and the role played by salts therein.In chapter 1. the practical importance of polymer stabilisation an

  5. Self-Assembling of Colloidal Particles Dispersed in Mixture of Ethanol and Water at the Air-Liquid Interface of Colloidal Suspension at Room Temperature

    Institute of Scientific and Technical Information of China (English)

    WANG Ai-Jun; CHEN Sheng-Li; DONG Peng; ZHOU Qian; YUAN Gui-Mei; SU Gu-Cong

    2009-01-01

    Self-assembling of colloidal particles dispersed in a mixture of ethanol and water at the air-liquid interface of the colloidal suspension at room temperature is investigated,and a method of rapidly assembling colloidal particles is proposed.By this method,a uniform colloidal crystal thin 61m over ten square centimeters in area can be fabricated in 10 min without special facilities and heating the suspension.SEM images and a normal incidence transmission spectrum of the sample show that the colloidal crystal film fabricated by this method is of high quality.In addition,this method is very suitable for fabricating colloidal crystal heterostructures.

  6. In-situ characterization of colloidal soft solution processes.

    Energy Technology Data Exchange (ETDEWEB)

    Tallant, David Robert; Rodriguez, Mark Andrew; Bell, Nelson Simmons

    2003-11-01

    The purpose of this program was to investigate methods to characterize the colloidal stability of nanoparticles during the synthesis reaction, and to characterize their organization related to interparticle forces. Studies were attempted using Raman spectroscopy and ultrasonic attenuation to observe the nucleation and growth process with characterization of stability parameters such as the zeta potential. The application of the techniques available showed that the instrumentation requires high sensitivity to the concentration of the system. Optical routes can be complicated by the scattering effects of colloidal suspensions, but dilution can cause a lowering of signal that prevents collection of data. Acoustic methods require a significant particle concentration, preventing the observation of nucleation events. Studies on the dispersion of nanoparticles show that electrostatic routes are unsuccessful with molecular surfactants at high particle concentration due to electrostatic interaction collapse by counterions. The study of molecular surfactants show that steric lengths on the order of 2 nm are successful for dispersion of nanoparticle systems at high particle concentration, similar to dispersion with commercial polyelectrolyte surfactants.

  7. Saturated Zone Colloid Transport

    Energy Technology Data Exchange (ETDEWEB)

    H. S. Viswanathan

    2004-10-07

    This scientific analysis provides retardation factors for colloids transporting in the saturated zone (SZ) and the unsaturated zone (UZ). These retardation factors represent the reversible chemical and physical filtration of colloids in the SZ. The value of the colloid retardation factor, R{sub col} is dependent on several factors, such as colloid size, colloid type, and geochemical conditions (e.g., pH, Eh, and ionic strength). These factors are folded into the distributions of R{sub col} that have been developed from field and experimental data collected under varying geochemical conditions with different colloid types and sizes. Attachment rate constants, k{sub att}, and detachment rate constants, k{sub det}, of colloids to the fracture surface have been measured for the fractured volcanics, and separate R{sub col} uncertainty distributions have been developed for attachment and detachment to clastic material and mineral grains in the alluvium. Radionuclides such as plutonium and americium sorb mostly (90 to 99 percent) irreversibly to colloids (BSC 2004 [DIRS 170025], Section 6.3.3.2). The colloid retardation factors developed in this analysis are needed to simulate the transport of radionuclides that are irreversibly sorbed onto colloids; this transport is discussed in the model report ''Site-Scale Saturated Zone Transport'' (BSC 2004 [DIRS 170036]). Although it is not exclusive to any particular radionuclide release scenario, this scientific analysis especially addresses those scenarios pertaining to evidence from waste-degradation experiments, which indicate that plutonium and americium may be irreversibly attached to colloids for the time scales of interest. A section of this report will also discuss the validity of using microspheres as analogs to colloids in some of the lab and field experiments used to obtain the colloid retardation factors. In addition, a small fraction of colloids travels with the groundwater without any significant

  8. In situ visualisation and characterisation of the capacity of highly reactive minerals to preserve soil organic matter (SOM) in colloids at submicron scale.

    Science.gov (United States)

    Xiao, Jian; Wen, Yongli; Li, Huan; Hao, Jialong; Shen, Qirong; Ran, Wei; Mei, Xinlan; He, Xinhua; Yu, Guanghui

    2015-11-01

    Mineral-organo associations (MOAs) are a mixture of identifiable biopolymers associated with highly reactive minerals and microorganisms. However, the in situ characterization and correlation between soil organic matter (SOM) and highly reactive Al and Fe minerals are still unclear for the lack of technologies, particularly in the long-term agricultural soil colloids at submicron scale. We combined several novel techniques, including nano-scale secondary ion mass spectrometry (NanoSIMS), X-ray absorption near edge structure (XANES) and confocal laser scanning microscopy (CLSM) to characterise the capacity of highly reactive Al and Fe minerals to preserve SOM in Ferralic Cambisol in south China. Our results demonstrated that: (1) highly reactive minerals were strongly related to SOM preservation, while SOM had a more significant line correlation with the highly reactive Al minerals than the highly reactive Fe minerals, according to the regions of interest correlation analyses using NanoSIMS; (2) allophane and ferrihydrite were the potential mineral species to determine the SOM preservation capability, which was evaluated by the X-ray photoelectron spectroscopy (XPS) and Fe K-edge XANES spectroscopy techniques; and (3) soil organic biopolymers with dominant compounds, such as proteins, polysaccharides and lipids, were distributed at the rough and clustered surface of MOAs with high chemical and spatial heterogeneity according to the CLSM observation. Our results also promoted the understanding of the roles played by the highly reactive Al and Fe minerals in the spatial distribution of soil organic biopolymers and SOM sequestration.

  9. Shape recognition of microbial cells by colloidal cell imprints

    Science.gov (United States)

    Borovička, Josef; Stoyanov, Simeon D.; Paunov, Vesselin N.

    2013-08-01

    We have engineered a class of colloids which can recognize the shape and size of targeted microbial cells and selectively bind to their surfaces. These imprinted colloid particles, which we called ``colloid antibodies'', were fabricated by partial fragmentation of silica shells obtained by templating the targeted microbial cells. We successfully demonstrated the shape and size recognition between such colloidal imprints and matching microbial cells. High percentage of binding events of colloidal imprints with the size matching target particles was achieved. We demonstrated selective binding of colloidal imprints to target microbial cells in a binary mixture of cells of different shapes and sizes, which also resulted in high binding selectivity. We explored the role of the electrostatic interactions between the target cells and their colloid imprints by pre-coating both of them with polyelectrolytes. Selective binding occurred predominantly in the case of opposite surface charges of the colloid cell imprint and the targeted cells. The mechanism of the recognition is based on the amplification of the surface adhesion in the case of shape and size match due to the increased contact area between the target cell and the colloidal imprint. We also tested the selective binding for colloid imprints of particles of fixed shape and varying sizes. The concept of cell recognition by colloid imprints could be used for development of colloid antibodies for shape-selective binding of microbes. Such colloid antibodies could be additionally functionalized with surface groups to enhance their binding efficiency to cells of specific shape and deliver a drug payload directly to their surface or allow them to be manipulated using external fields. They could benefit the pharmaceutical industry in developing selective antimicrobial therapies and formulations.

  10. Electrosteric stabilization of colloidal TiO2 nanoparticles with DNA and polyethylene glycol for selective enhancement of UV detection sensitivity in capillary electrophoresis analysis.

    Science.gov (United States)

    Alsudir, Samar; Lai, Edward P C

    2017-03-01

    A new approach to selectively enhance the ultraviolet (UV) detection sensitivity of titania (TiO2), albeit in the presence of silica (SiO2), alumina (Al2O3), and zinc oxide (ZnO), nanoparticles in capillary electrophoresis (CE) analysis was developed. Interactions of Triton X-100 (TX-100), polyethylene glycol (PEG), and deoxyribonucleic acid (DNA) with TiO2 nanoparticles produced larger CE-UV peaks at various enhancement factors. Single-stranded DNA (ssDNA) was a more effective adsorbate than double-stranded DNA (dsDNA) due to its flexible molecular structure that participated in a stronger interaction with TiO2 nanoparticles via its sugar-phosphate backbone. Disaggregation of TiO2 nanoparticles upon DNA binding due to electrosteric stabilization was validated using dynamic light scattering. PEG coating of TiO2-DNA nanoparticles further enhanced the UV detection sensitivity in CE analysis by providing extra electrosteric stabilization. This analytical technique, which involves binding of TiO2 nanoparticles with DNA followed by coating with PEG, has allowed us to achieve progressively an enhancement factor up to 13.0 ± 3.0 - fold in analytical sensitivity for the accurate determination of disaggregated TiO2 nanoparticles. Graphical Abstract Selective enhancement of UV detection sensitivity for TiO2 nanoparticles via electrosteric stabilization using ssDNA and PEG.

  11. Hybrid passivated colloidal quantum dot solids

    Science.gov (United States)

    Ip, Alexander H.; Thon, Susanna M.; Hoogland, Sjoerd; Voznyy, Oleksandr; Zhitomirsky, David; Debnath, Ratan; Levina, Larissa; Rollny, Lisa R.; Carey, Graham H.; Fischer, Armin; Kemp, Kyle W.; Kramer, Illan J.; Ning, Zhijun; Labelle, André J.; Chou, Kang Wei; Amassian, Aram; Sargent, Edward H.

    2012-09-01

    Colloidal quantum dot (CQD) films allow large-area solution processing and bandgap tuning through the quantum size effect. However, the high ratio of surface area to volume makes CQD films prone to high trap state densities if surfaces are imperfectly passivated, promoting recombination of charge carriers that is detrimental to device performance. Recent advances have replaced the long insulating ligands that enable colloidal stability following synthesis with shorter organic linkers or halide anions, leading to improved passivation and higher packing densities. Although this substitution has been performed using solid-state ligand exchange, a solution-based approach is preferable because it enables increased control over the balance of charges on the surface of the quantum dot, which is essential for eliminating midgap trap states. Furthermore, the solution-based approach leverages recent progress in metal:chalcogen chemistry in the liquid phase. Here, we quantify the density of midgap trap states in CQD solids and show that the performance of CQD-based photovoltaics is now limited by electron-hole recombination due to these states. Next, using density functional theory and optoelectronic device modelling, we show that to improve this performance it is essential to bind a suitable ligand to each potential trap site on the surface of the quantum dot. We then develop a robust hybrid passivation scheme that involves introducing halide anions during the end stages of the synthesis process, which can passivate trap sites that are inaccessible to much larger organic ligands. An organic crosslinking strategy is then used to form the film. Finally, we use our hybrid passivated CQD solid to fabricate a solar cell with a certified efficiency of 7.0%, which is a record for a CQD photovoltaic device.

  12. Hybrid passivated colloidal quantum dot solids

    KAUST Repository

    Ip, Alex

    2012-07-29

    Colloidal quantum dot (CQD) films allow large-area solution processing and bandgap tuning through the quantum size effect. However, the high ratio of surface area to volume makes CQD films prone to high trap state densities if surfaces are imperfectly passivated, promoting recombination of charge carriers that is detrimental to device performance. Recent advances have replaced the long insulating ligands that enable colloidal stability following synthesis with shorter organic linkers or halide anions, leading to improved passivation and higher packing densities. Although this substitution has been performed using solid-state ligand exchange, a solution-based approach is preferable because it enables increased control over the balance of charges on the surface of the quantum dot, which is essential for eliminating midgap trap states. Furthermore, the solution-based approach leverages recent progress in metal:chalcogen chemistry in the liquid phase. Here, we quantify the density of midgap trap states in CQD solids and show that the performance of CQD-based photovoltaics is now limited by electrong-"hole recombination due to these states. Next, using density functional theory and optoelectronic device modelling, we show that to improve this performance it is essential to bind a suitable ligand to each potential trap site on the surface of the quantum dot. We then develop a robust hybrid passivation scheme that involves introducing halide anions during the end stages of the synthesis process, which can passivate trap sites that are inaccessible to much larger organic ligands. An organic crosslinking strategy is then used to form the film. Finally, we use our hybrid passivated CQD solid to fabricate a solar cell with a certified efficiency of 7.0%, which is a record for a CQD photovoltaic device. © 2012 Macmillan Publishers Limited. All rights reserved.

  13. Colloids with continuously tunable surface charge.

    Science.gov (United States)

    van Ravensteijn, Bas G P; Kegel, Willem K

    2014-09-09

    In this paper, we present a robust way to tune the surface potential of polystyrene colloids without changing the pH, ionic strength, etc. The colloids are composed of a cross-linked polystyrene core and a cross-linked vinylbenzyl chloride layer. Besides the chlorine groups, the particle surface contains sulfate/sulfonate groups (arising from the polymerization initiators) that provide a negative surface potential. Performing a Menschutkin reaction on the surface chlorine groups with tertiary amines allows us to introduce quaternary, positively charged amines. The overall charge on the particles is then determined by the ratio between the sulfate/sulfonate moieties and the quaternary amines. Using this process, we were able to invert the charge in a continuous manner without losing colloidal stability upon passing the isoelectric point. The straightforward reaction mechanism together with the fact that the reaction could be quenched rapidly resulted in a colloidal system in which the ζ potential can be tuned between -80 and 45 mV. As proof of principle, the positively charged particles were used in heterocoagulation experiments with nanometer- and micrometer-sized negatively charged silica particles to create geometrically well-defined colloidal (nano) clusters.

  14. Stability boundaries for wrinkling in highly stretched elastic sheets

    Science.gov (United States)

    Li, Qingdu; Healey, Timothy J.

    2016-12-01

    We determine stability boundaries for the wrinkling of highly unidirectionally stretched, finely thin, rectangular elastic sheets. For a given fine thickness and length, a stability boundary here is a curve in the parameter plane, aspect ratio vs. the macroscopic strain; the values on one side of the boundary are associated with stable unwrinkled (flat) states, while stable wrinkled configurations correspond to all values on the other. In our recent work we demonstrated the importance of finite elasticity in the membrane part of such a model in order to capture the correct phenomena. Here we present and compare results for four distinct models: (i) the popular Föppl-von Kármán plate model (FvK), (ii) a correction of the latter, used in our earlier work, in which the approximate 2D Föppl strain tensor is replaced by the exact Green strain tensor, (iii) and (iv): effective 2D finite-elasticity membrane models based on 3D incompressible neo-Hookean and Mooney-Rivlin materials, respectively. In particular, (iii) and (iv) are superior models for elastomers. The 2D nonlinear, hyperelastic models (ii)-(iv) all incorporate the same quadratic bending energy used in FvK. Our results illuminate serious shortcomings of the latter in this problem, while also pointing to inaccuracies of model (ii) - in spite of yielding the correct qualitative phenomena in our earlier work. In each of these, the shortcoming is a due to a deficiency of the membrane part of the model.

  15. Colloids in Biotechnology

    CERN Document Server

    Fanun, Monzer

    2010-01-01

    Colloids have come a long way from when Thomas Graham coined the term colloid to describe 'pseudo solutions'. This book enables scientists to close the gap between extensive research and translation into commercial options in biomedicine and biotechnology. It covers biosurfactants and surface properties, phase behavior, and orientational change of surfactant mixtures with peptides at the interface. It also covers adsorption of polymers and biopolymers on the surface and interface, discusses colloidal nanoparticles and their use in biotechnology, and delves into bioadhesion and microencapsulati

  16. High energy density Z-pinch plasmas using flow stabilization

    Energy Technology Data Exchange (ETDEWEB)

    Shumlak, U., E-mail: shumlak@uw.edu; Golingo, R. P., E-mail: shumlak@uw.edu; Nelson, B. A., E-mail: shumlak@uw.edu; Bowers, C. A., E-mail: shumlak@uw.edu; Doty, S. A., E-mail: shumlak@uw.edu; Forbes, E. G., E-mail: shumlak@uw.edu; Hughes, M. C., E-mail: shumlak@uw.edu; Kim, B., E-mail: shumlak@uw.edu; Knecht, S. D., E-mail: shumlak@uw.edu; Lambert, K. K., E-mail: shumlak@uw.edu; Lowrie, W., E-mail: shumlak@uw.edu; Ross, M. P., E-mail: shumlak@uw.edu; Weed, J. R., E-mail: shumlak@uw.edu [Aerospace and Energetics Research Program, University of Washington, Seattle, Washington, 98195-2250 (United States)

    2014-12-15

    The ZaP Flow Z-Pinch research project[1] at the University of Washington investigates the effect of sheared flows on MHD instabilities. Axially flowing Z-pinch plasmas are produced that are 100 cm long with a 1 cm radius. The plasma remains quiescent for many radial Alfvén times and axial flow times. The quiescent periods are characterized by low magnetic mode activity measured at several locations along the plasma column and by stationary visible plasma emission. Plasma evolution is modeled with high-resolution simulation codes – Mach2, WARPX, NIMROD, and HiFi. Plasma flow profiles are experimentally measured with a multi-chord ion Doppler spectrometer. A sheared flow profile is observed to be coincident with the quiescent period, and is consistent with classical plasma viscosity. Equilibrium is determined by diagnostic measurements: interferometry for density; spectroscopy for ion temperature, plasma flow, and density[2]; Thomson scattering for electron temperature; Zeeman splitting for internal magnetic field measurements[3]; and fast framing photography for global structure. Wall stabilization has been investigated computationally and experimentally by removing 70% of the surrounding conducting wall to demonstrate no change in stability behavior.[4] Experimental evidence suggests that the plasma lifetime is only limited by plasma supply and current waveform. The flow Z-pinch concept provides an approach to achieve high energy density plasmas,[5] which are large, easy to diagnose, and persist for extended durations. A new experiment, ZaP-HD, has been built to investigate this approach by separating the flow Z-pinch formation from the radial compression using a triaxial-electrode configuration. This innovation allows more detailed investigations of the sheared flow stabilizing effect, and it allows compression to much higher densities than previously achieved on ZaP by reducing the linear density and increasing the pinch current. Experimental results and

  17. Studies of colloids and their importance for repository performance assessment

    Energy Technology Data Exchange (ETDEWEB)

    Laaksoharju, M.; Skaarman, C. [GeoPoint AB, Sollentuna (Sweden); Degueldre, C. [Geneva Univ. (Switzerland)

    1995-12-01

    The processes, parameters and data used to evaluate the potential of nuclide transport by a colloid facilitated mechanism are reviewed and discussed in this report. Both steady-state (present situation) and possible future non-steady-state hydrogeochemistry in the geosphere are covered. In the steady-state scenario, the colloid (clay, silica, iron(III)hydroxide) concentration is around 20-45 micrograms/l which is considered to be a low value. The low colloid concentration is justified by the large attachment factor to the rock which reduces the stability of the colloids in the aquifer. Both reversible and irreversible sorption processes are reviewed. In the non-steady-state scenario, changes of hydrogeochemical properties may induce larger colloid concentrations. The increase of concentration is however limited and relaxation is always observed after any change. Emphasis is placed on the glaciation-deglaciation scenario. 53 refs, 12 figs, 3 tabs.

  18. STRUCTURAL STABILITY OF HIGH NITROGEN AUSTENITIC STAINLESS STEELS

    Directory of Open Access Journals (Sweden)

    Jana Bakajová

    2011-05-01

    Full Text Available This paper deals with the structural stability of an austenitic stainless steel with high nitrogen content. The investigated steel was heat treated at 800°C using different annealing times. Investigation was carried out using light microscopy, transmission electron microscopy and thermodynamic calculations. Three phases were identified by electron diffraction: Cr2N, sigma – phase and M23C6. The thermodynamic prediction is in good agreement with the experimental result. The only is the M23C6 carbide phase which is not thermodynamically predicted. Cr2N is the majority secondary phase and occurs in the form of discrete particles or cells (lamellas of Cr2N and austenite.

  19. High stability piezomotor driven mirror mounts for LINC-NIRVANA

    Science.gov (United States)

    Bramigk, A.; Marth, H.; Rohloff, R.-R.

    2012-09-01

    For the LINC-NIRVANA (LN) project, MPIA requested an appropriate motorized mount for initial alignment of two dichroic beam splitters in the instrument. These dichroic mirrors which reflect the visible light and transmit the NIR are located close to the pupil plane are therefore very sensitive to tilt and flexure errors which could be introduced to the wave-front sensor. Considering this the following high level specifications were requested in a very tight operating envelope: range of adjustment tip and tilt +/-2° around the major axis of the elliptical mirror, resolution of adjustment <0.5 arcsec , position repeatability <1 arcsec, static position stability within an elevation 0° up to 90° <20 arc seconds and a minimum eigenfrequency <110Hz.

  20. Implant materials modified by colloids

    Directory of Open Access Journals (Sweden)

    Zboromirska-Wnukiewicz Beata

    2016-03-01

    Full Text Available Recent advances in general medicine led to the development of biomaterials. Implant material should be characterized by a high biocompatibility to the tissue and appropriate functionality, i.e. to have high mechanical and electrical strength and be stable in an electrolyte environment – these are the most important properties of bioceramic materials. Considerations of biomaterials design embrace also electrical properties occurring on the implant-body fluid interface and consequently the electrokinetic potential, which can be altered by modifying the surface of the implant. In this work, the surface of the implants was modified to decrease the risk of infection by using metal colloids. Nanocolloids were obtained using different chemical and electrical methods. It was found that the colloids obtained by physical and electrical methods are more stable than colloids obtained by chemical route. In this work the surface of modified corundum implants was investigated. The implant modified by nanosilver, obtained by electrical method was selected. The in vivo research on animals was carried out. Clinical observations showed that the implants with modified surface could be applied to wounds caused by atherosclerotic skeleton, for curing the chronic and bacterial inflammations as well as for skeletal reconstruction surgery.

  1. Transport of barrel and spherical shaped colloids in unsaturated porous media.

    Science.gov (United States)

    Knappenberger, Thorsten; Aramrak, Surachet; Flury, Markus

    2015-09-01

    Model colloids are usually spherical, but natural colloids have irregular geometries. Transport experiments of spherical colloids may not reflect the transport characteristics of natural colloids in porous media. We investigated saturated and unsaturated transport of colloids with spherical and angular shapes under steady-state, flow conditions. A pulse of negatively-charged colloids was introduced into a silica sand column at three different effective water saturations (Se = 0.31, 0.45, and 1.0). Colloids were introduced under high ionic strength of [106]mM to cause attachment to the secondary energy minimum and later released by changing the pore water to low ionic strength. After the experiment, sand was sampled from different depths (0, -4, and -11 cm) for scanning electron microscopy (SEM) analysis and colloid extraction. Water saturation affected colloid transport with more retention under low than under high saturation. Colloids were retained and released from a secondary energy minimum with more angular-shaped colloids being retained and released. Colloids extracted from the sand revealed highest colloid deposition in the top layer and decreasing deposition with depth. Pore straining and grain-grain wedging dominated colloid retention. Copyright © 2015 Elsevier B.V. All rights reserved.

  2. Formation of stable uranium(VI) colloidal nanoparticles in conditions relevant to radioactive waste disposal.

    Science.gov (United States)

    Bots, Pieter; Morris, Katherine; Hibberd, Rosemary; Law, Gareth T W; Mosselmans, J Frederick W; Brown, Andy P; Doutch, James; Smith, Andrew J; Shaw, Samuel

    2014-12-09

    The favored pathway for disposal of higher activity radioactive wastes is via deep geological disposal. Many geological disposal facility designs include cement in their engineering design. Over the long term, interaction of groundwater with the cement and waste will form a plume of a hyperalkaline leachate (pH 10-13), and the behavior of radionuclides needs to be constrained under these extreme conditions to minimize the environmental hazard from the wastes. For uranium, a key component of many radioactive wastes, thermodynamic modeling predicts that, at high pH, U(VI) solubility will be very low (nM or lower) and controlled by equilibrium with solid phase alkali and alkaline-earth uranates. However, the formation of U(VI) colloids could potentially enhance the mobility of U(VI) under these conditions, and characterizing the potential for formation and medium-term stability of U(VI) colloids is important in underpinning our understanding of U behavior in waste disposal. Reflecting this, we applied conventional geochemical and microscopy techniques combined with synchrotron based in situ and ex situ X-ray techniques (small-angle X-ray scattering and X-ray adsorption spectroscopy (XAS)) to characterize colloidal U(VI) nanoparticles in a synthetic cement leachate (pH > 13) containing 4.2-252 μM U(VI). The results show that in cement leachates with 42 μM U(VI), colloids formed within hours and remained stable for several years. The colloids consisted of 1.5-1.8 nm nanoparticles with a proportion forming 20-60 nm aggregates. Using XAS and electron microscopy, we were able to determine that the colloidal nanoparticles had a clarkeite (sodium-uranate)-type crystallographic structure. The presented results have clear and hitherto unrecognized implications for the mobility of U(VI) in cementitious environments, in particular those associated with the geological disposal of nuclear waste.

  3. Liquid crystal colloids

    CERN Document Server

    Muševič, Igor

    2017-01-01

    This book brings together the many concepts and discoveries in liquid crystal colloids contributed over the last twenty years and scattered across numerous articles and book chapters. It provides both a historical overview of the development of the field and a clear perspective on the future applications in photonics. The book covers all phenomena observed in liquid crystal colloids with an emphasis on experimental tools and applications of topology in condensed matter, as well as practical micro-photonics applications. It includes a number of spectacular manifestations of new topological phenomena not found or difficult to observe in other systems. Starting from the early works on nematic colloids, it explains the basics of topological defects in ordered media, charge and winding, and the elastic forces between colloidal particles in nematics. Following a detailed description of experimental methods, such as optical tweezing and particle tracking, the book eases the reader into the theoretical part, which de...

  4. Confocal microscopy of colloids

    Energy Technology Data Exchange (ETDEWEB)

    Prasad, V; Semwogerere, D; Weeks, Eric R [Department of Physics, Emory University, Atlanta, GA 30322 (United States)

    2007-03-21

    Colloids have increasingly been used to characterize or mimic many aspects of atomic and molecular systems. With confocal microscopy these colloidal particles can be tracked spatially in three dimensions with great precision over large time scales. This review discusses equilibrium phases such as crystals and liquids, and non-equilibrium phases such as glasses and gels. The phases that form depend strongly on the type of particle interaction that dominates. Hard-sphere-like colloids are the simplest, and interactions such as the attractive depletion force and electrostatic repulsion result in more non-trivial phases which can better model molecular materials. Furthermore, shearing or otherwise externally forcing these colloids while under microscopic observation helps connect the microscopic particle dynamics to the macroscopic flow behaviour. Finally, directions of future research in this field are discussed. (topical review)

  5. Colloidal oatmeal: history, chemistry and clinical properties.

    Science.gov (United States)

    Kurtz, Ellen S; Wallo, Warren

    2007-02-01

    Oatmeal has been used for centuries as a soothing agent to relieve itch and irritation associated with various xerotic dermatoses. In 1945, a ready to use colloidal oatmeal, produced by finely grinding the oat and boiling it to extract the colloidal material, became available. Today, colloidal oatmeal is available in various dosage forms from powders for the bath to shampoos, shaving gels, and moisturizing creams. Currently, the use of colloidal oatmeal as a skin protectant is regulated by the U.S. Food and Drug Administration (FDA) according to the Over-The-Counter Final Monograph for Skin Protectant Drug Products issued in June 2003. Its preparation is also standardized by the United States Pharmacopeia. The many clinical properties of colloidal oatmeal derive from its chemical polymorphism. The high concentration in starches and beta-glucan is responsible for the protective and water-holding functions of oat. The presence of different types of phenols confers antioxidant and anti-inflammatory activity. Some of the oat phenols are also strong ultraviolet absorbers. The cleansing activity of oat is mostly due to saponins. Its many functional properties make colloidal oatmeal a cleanser, moisturizer, buffer, as well as a soothing and protective anti-inflammatory agent.

  6. Aggregation kinetics of coalescing polymer colloids.

    Science.gov (United States)

    Gauer, Cornelius; Jia, Zichen; Wu, Hua; Morbidelli, Massimo

    2009-09-01

    The aggregation behavior of a soft, rubbery colloidal system with a relatively low glass transition temperature, T(g) approximately -20 degrees C, has been investigated. It is found that the average gyration and hydrodynamic radii, R(g) and R(h), measured by light scattering techniques, evolve in time in parallel, without exhibiting the crossover typical of rigid particle aggregation. Cryogenic scanning electron microscopy (cryo-SEM) images reveal sphere-like clusters, indicating that complete coalescence between particles occurs during aggregation. Since coalescence leads to a reduction in the total colloidal surface area, the surfactant adsorption equilibrium, and thus the colloidal stability, change in the course of aggregation. It is found that to simulate the observed kinetic behavior based on the population balance equations, it is necessary to assume that all the clusters are spherical and to account for variations in the colloidal stability of each aggregating particle pair with time. This indicates that, for the given system, the coalescence is very fast, i.e., its time scale is much smaller than that of the aggregation.

  7. Structural stability of high entropy alloys under pressure and temperature

    DEFF Research Database (Denmark)

    Ahmad, Azkar S.; Su, Y.; Liu, S. Y.

    2017-01-01

    The stability of high-entropy alloys (HEAs) is a key issue before their selection for industrial applications. In this study, in-situ high-pressure and high-temperature synchrotron radiation X-ray diffraction experiments have been performed on three typical HEAs Ni20Co20Fe20Mn20Cr20, Hf25Nb25Zr25Ti......25, and Re25Ru25Co25Fe25 (at. %), having face-centered cubic (fcc), body-centered cubic (bcc), and hexagonal close-packed (hcp) crystal structures, respectively, up to the pressure of ∼80 GPa and temperature of ∼1262 K. Under the extreme conditions of the pressure and temperature, all three studied...... HEAs remain stable up to the maximum pressure and temperatures achieved. For these three types of studied HEAs, the pressure-dependence of the volume can be well described with the third order Birch-Murnaghan equation of state. The bulk modulus and its pressure derivative are found to be 88.3 GPa and 4...

  8. Stabilization of actinides and lanthanides in unusually high oxidation states

    Energy Technology Data Exchange (ETDEWEB)

    Eller, P.G.; Penneman, R.A.

    1986-01-01

    Chemical environments can be chosen which stabilize actinides and lanthanides in unusually high or low oxidation states and in unusual coordination. In many cases, one can rationalize the observed species as resulting from strong charge/size influences provided by specific sites in host lattices (e.g., Tb(IV) in BaTbO/sub 3/ or Am(IV) in polytungstate anions). In other cases, the unusual species can be considered from an acid-base viewpoint (e.g., U(III) in AsF/sub 5//HF solution or Pu(VII) in Li/sub 5/PuO/sub 6/). In still other cases, an interplay of steric and redox effects can lead to interesting comparisons (e.g., instability of double fluoride salts of Pu(V) and Pu(VI) relative to U, Np, and Am analogues). Generalized ways to rationalize compounds containing actinides and lanthanides in unusual valences (particularly high valences), including the above and numerous other examples, will form the focus of this paper. Recently developed methods for synthesizing high valent f-element fluorides using superoxidizers and superacids at low temperatures will also be described. 65 refs., 8 figs., 9 tabs.

  9. High mobility and high stability glassy metal-oxynitride materials and devices

    Science.gov (United States)

    Lee, Eunha; Kim, Taeho; Benayad, Anass; Hur, Jihyun; Park, Gyeong-Su; Jeon, Sanghun

    2016-04-01

    In thin film technology, future semiconductor and display products with high performance, high density, large area, and ultra high definition with three-dimensional functionalities require high performance thin film transistors (TFTs) with high stability. Zinc oxynitride, a composite of zinc oxide and zinc nitride, has been conceded as a strong substitute to conventional semiconductor film such as silicon and indium gallium zinc oxide due to high mobility value. However, zinc oxynitride has been suffered from poor reproducibility due to relatively low binding energy of nitrogen with zinc, resulting in the instability of composition and its device performance. Here we performed post argon plasma process on zinc oxynitride film, forming nano-crystalline structure in stable amorphous matrix which hampers the reaction of oxygen with zinc. Therefore, material properties and device performance of zinc oxynitride are greatly enhanced, exhibiting robust compositional stability even exposure to air, uniform phase, high electron mobility, negligible fast transient charging and low noise characteristics. Furthermore, We expect high mobility and high stability zinc oxynitride customized by plasma process to be applicable to a broad range of semiconductor and display devices.

  10. Charge-Controlled Colloids on Liquid-Liquid Interfaces

    Science.gov (United States)

    Kunz, Daniel A.; Reck, Bernd; Manoharan, Vinothan N.

    2014-03-01

    The tendency of colloidal particles to stabilize interfaces has been exploited for many years to generate Pickering emulsions with a variety of industrial applications. However, the exact stabilization mechanism and its dependence on the surface properties of the colloidal particles are not yet fully understood. We provide new interfacial studies on the nonequilibrium dynamics of a colloidal system with tunable surface charge density. We push individual sub-micron colloidal particles towards an oil-water interface and track their motion in three-dimensions using holographic microscopy to examine the influence of zeta potential on the dynamics of the system. This project was funded by the BASF Advanced Research Initiative, BASF SE, Germany.

  11. High solid and high stability waterborne polyurethanes via ionic groups in soft segments and chain termini.

    Science.gov (United States)

    Lee, S K; Kim, B K

    2009-08-01

    High solid and high stability waterborne polyurethanes were molecularly designed and synthesized. The positions and concentrations of the anionic groups were varied, along with the molecular weights of the polyol. It was found that the dispersions containing ionic groups at the chain termini (called terminal ions) gave the smallest dispersion size, and the highest dispersion stability and viscosity, whereas the hard ions, containing ionic groups in the hard segments, resulted in the greatest swelling in water. However, the mechanical and dynamic mechanical properties of the dispersion cast films were similar. It was demonstrated that highly stable dispersions with a high solid content (45%) can be obtained at a low ionic content (2%) by simply incorporating the ionic groups at the flexible chain ends. The results were interpreted in terms of the high mobility and low free energy of the chain ends.

  12. Equilibrium crystal phases of triblock Janus colloids

    Science.gov (United States)

    Reinhart, Wesley F.; Panagiotopoulos, Athanassios Z.

    2016-09-01

    Triblock Janus colloids, which are colloidal spheres decorated with attractive patches at each pole, have recently generated significant interest as potential building blocks for functional materials. Their inherent anisotropy is known to induce self-assembly into open structures at moderate temperatures and pressures, where they are stabilized over close-packed crystals by entropic effects. We present a numerical investigation of the equilibrium phases of triblock Janus particles with many different patch geometries in three dimensions, using Monte Carlo simulations combined with free energy calculations. In all cases, we find that the free energy difference between crystal polymorphs is less than 0.2 kBT per particle. By varying the patch fraction and interaction range, we show that large patches stabilize the formation of structures with four bonds per patch over those with three. This transition occurs abruptly above a patch fraction of 0.30 and has a strong dependence on the interaction range. Furthermore, we find that a short interaction range favors four bonds per patch, with longer range increasingly stabilizing structures with only three bonds per patch. By quantifying the effect of patch geometry on the stability of the equilibrium crystal structures, we provide insights into the fundamental design rules for constructing complex colloidal crystals.

  13. Carbocation Stability in H-ZSM5 at High Temperature

    Energy Technology Data Exchange (ETDEWEB)

    Ferguson, Glen A. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Cheng, Lei [Argonne National Lab. (ANL), Argonne, IL (United States); Bu, Lintao [National Renewable Energy Lab. (NREL), Golden, CO (United States); Kim, Seonah [National Renewable Energy Lab. (NREL), Golden, CO (United States); Robichaud, David J. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Nimlos, Mark R. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Curtiss, Larry A. [Argonne National Lab. (ANL), Argonne, IL (United States); Beckham, Gregg T. [National Renewable Energy Lab. (NREL), Golden, CO (United States)

    2015-10-26

    Zeolites are common catalysts for multiple industrial applications, including alcohol dehydration to produce olefins, and given their commercial importance, reaction mechanisms in zeolites have long been proposed and studied. Some proposed reaction mechanisms for alcohol dehydration exhibit noncyclic carbocation intermediates or transition states that resemble carbocations, and several previous studies suggest that the tert-butyl cation is the only noncyclic cation more stable than the corresponding chemisorbed species with the hydrocarbon bound to the framework oxygen (i.e., an alkoxide). To determine if carbocations can exist at high temperatures in zeolites, where these catalysts are finding new applications for biomass vapor-phase upgrading (~500 °C), the stability of carbocations and the corresponding alkoxides were calculated with two ONIOM embedding methods (M06-2X/6-311G(d,p):M06-2X/3-21G) and (PBE-D3/6-311G(d,p):PBE-D3/3-21G) and plane-wave density functional theory (DFT) using the PBE functional corrected with entropic and Tkatchenko–Scheffler van der Waals corrections. Additionally, the embedding methods tested are unreliable at finding minima for primary carbocations, and only secondary or higher carbocations can be described with embedding methods consistent with the periodic DFT results. The relative energy between the carbocations and alkoxides differs significantly between the embedding and the periodic DFT methods. The difference is between ~0.23 and 14.30 kcal/mol depending on the molecule, the model, and the functional chosen for the embedding method. At high temperatures, the pw-DFT calculations predict that the allyl, isopropyl, and sec-butyl cations exhibit negligible populations while acetyl and tert-butyl cations exhibit significant populations (>10%). Furthermore, the periodic DFT results indicate that mechanisms including secondary and tertiary carbocations intermediates or carbocations stabilized by adjacent oxygen or double bonds are

  14. Tuning Colloid-Interface Interactions by Salt Partitioning

    Science.gov (United States)

    Everts, J. C.; Samin, S.; van Roij, R.

    2016-08-01

    We show that the interaction of an oil-dispersed colloidal particle with an oil-water interface is highly tunable from attractive to repulsive, either by varying the sign of the colloidal charge via charge regulation or by varying the difference in hydrophilicity between the dissolved cations and anions. In addition, we investigate the yet unexplored interplay between the self-regulated colloidal surface charge distribution with the planar double layer across the oil-water interface and the spherical one around the colloid. Our findings explain recent experiments and have direct relevance for tunable Pickering emulsions.

  15. Asymptotic Stability of High-dimensional Zakharov-Kuznetsov Solitons

    Science.gov (United States)

    Côte, Raphaël; Muñoz, Claudio; Pilod, Didier; Simpson, Gideon

    2016-05-01

    We prove that solitons (or solitary waves) of the Zakharov-Kuznetsov (ZK) equation, a physically relevant high dimensional generalization of the Korteweg-de Vries (KdV) equation appearing in Plasma Physics, and having mixed KdV and nonlinear Schrödinger (NLS) dynamics, are strongly asymptotically stable in the energy space. We also prove that the sum of well-arranged solitons is stable in the same space. Orbital stability of ZK solitons is well-known since the work of de Bouard [Proc R Soc Edinburgh 126:89-112, 1996]. Our proofs follow the ideas of Martel [SIAM J Math Anal 157:759-781, 2006] and Martel and Merle [Math Ann 341:391-427, 2008], applied for generalized KdV equations in one dimension. In particular, we extend to the high dimensional case several monotonicity properties for suitable half-portions of mass and energy; we also prove a new Liouville type property that characterizes ZK solitons, and a key Virial identity for the linear and nonlinear part of the ZK dynamics, obtained independently of the mixed KdV-NLS dynamics. This last Virial identity relies on a simple sign condition which is numerically tested for the two and three dimensional cases with no additional spectral assumptions required. Possible extensions to higher dimensions and different nonlinearities could be obtained after a suitable local well-posedness theory in the energy space, and the verification of a corresponding sign condition.

  16. Bio-inactivation of human malignant cells through highly responsive diluted colloidal suspension of functionalized magnetic iron oxide nanoparticles

    Science.gov (United States)

    Ferreira, Roberta V.; Silva-Caldeira, Priscila P.; Pereira-Maia, Elene C.; Fabris, José D.; Cavalcante, Luis Carlos D.; Ardisson, José D.; Domingues, Rosana Z.

    2016-04-01

    Magnetic fluids, more specifically aqueous colloidal suspensions containing certain magnetic nanoparticles (MNPs), have recently been gaining special interest due to their potential use in clinical treatments of cancerous formations in mammalians. The technological application arises mainly from their hyperthermic behavior, which means that the nanoparticles dissipate heat upon being exposed to an alternating magnetic field (AMF). If the temperature is raised to slightly above 43 °C, cancer cells are functionally inactivated or killed; however, normal cells tend to survive under those same conditions, entirely maintaining their bioactivity. Recent in vitro studies have revealed that under simultaneous exposure to an AMF and magnetic nanoparticles, certain lines of cancer cells are bio-inactivated even without experiencing a significant temperature increase. This non-thermal effect is cell specific, indicating that MNPs, under alternating magnetic fields, may effectively kill cancer cells under conditions that were previously thought to be implausible, considering that the temperature does not increase more than 5 °C, which is also true in cases for which the concentration of MNPs is too low. To experimentally test for this effect, this study focused on the feasibility of inducing K562 cell death using an AMF and aqueous suspensions containing very low concentrations of MNPs. The assay was designed for a ferrofluid containing magnetite nanoparticles, which were obtained through the co-precipitation method and were functionalized with citric acid; the particles had an average diameter of 10 ± 2 nm and a mean hydrodynamic diameter of approximately 40 nm. Experiments were first performed to test for the ability of the ferrofluid to release heat under an AMF. The results show that for concentrations ranging from 2.5 to 1.0 × 103 mg L-1, the maximum temperature increase was actually less than 2 °C. However, the in vitro test results from K562 cells and suspensions

  17. Molecular Recognition in the Colloidal World.

    Science.gov (United States)

    Elacqua, Elizabeth; Zheng, Xiaolong; Shillingford, Cicely; Liu, Mingzhu; Weck, Marcus

    2017-10-06

    Colloidal self-assembly is a bottom-up technique to fabricate functional nanomaterials, with paramount interest stemming from programmable assembly of smaller building blocks into dynamic crystalline domains and photonic materials. Multiple established colloidal platforms feature diverse shapes and bonding interactions, while achieving specific orientations along with short- and long-range order. A major impediment to their universal use as building blocks for predesigned architectures is the inability to precisely dictate and control particle functionalization and concomitant reversible self-assembly. Progress in colloidal self-assembly necessitates the development of strategies that endow bonding specificity and directionality within assemblies. Methodologies that emulate molecular and polymeric three-dimensional (3D) architectures feature elements of covalent bonding, while high-fidelity molecular recognition events have been installed to realize responsive reconfigurable assemblies. The emergence of anisotropic 'colloidal molecules', coupled with the ability to site-specifically decorate particle surfaces with supramolecular recognition motifs, has facilitated the formation of superstructures via directional interactions and shape recognition. In this Account, we describe supramolecular assembly routes to drive colloidal particles into precisely assembled architectures or crystalline lattices via directional noncovalent molecular interactions. The design principles are based upon the fabrication of colloidal particles bearing surface-exposed functional groups that can undergo programmable conjugation to install recognition motifs with high fidelity. Modular and versatile by design, our strategy allows for the introduction and integration of molecular recognition principles into the colloidal world. We define noncovalent molecular interactions as site-specific forces that are predictable (i.e., feature selective and controllable complementary bonding partners

  18. Spherical colloidal photonic crystals.

    Science.gov (United States)

    Zhao, Yuanjin; Shang, Luoran; Cheng, Yao; Gu, Zhongze

    2014-12-16

    CONSPECTUS: Colloidal photonic crystals (PhCs), periodically arranged monodisperse nanoparticles, have emerged as one of the most promising materials for light manipulation because of their photonic band gaps (PBGs), which affect photons in a manner similar to the effect of semiconductor energy band gaps on electrons. The PBGs arise due to the periodic modulation of the refractive index between the building nanoparticles and the surrounding medium in space with subwavelength period. This leads to light with certain wavelengths or frequencies located in the PBG being prohibited from propagating. Because of this special property, the fabrication and application of colloidal PhCs have attracted increasing interest from researchers. The most simple and economical method for fabrication of colloidal PhCs is the bottom-up approach of nanoparticle self-assembly. Common colloidal PhCs from this approach in nature are gem opals, which are made from the ordered assembly and deposition of spherical silica nanoparticles after years of siliceous sedimentation and compression. Besides naturally occurring opals, a variety of manmade colloidal PhCs with thin film or bulk morphology have also been developed. In principle, because of the effect of Bragg diffraction, these PhC materials show different structural colors when observed from different angles, resulting in brilliant colors and important applications. However, this angle dependence is disadvantageous for the construction of some optical materials and devices in which wide viewing angles are desired. Recently, a series of colloidal PhC materials with spherical macroscopic morphology have been created. Because of their spherical symmetry, the PBGs of spherical colloidal PhCs are independent of rotation under illumination of the surface at a fixed incident angle of the light, broadening the perspective of their applications. Based on droplet templates containing colloidal nanoparticles, these spherical colloidal PhCs can be

  19. Stability Of Rubble Mound Breakwaters Using High Density Rock

    DEFF Research Database (Denmark)

    Burcharth, H. F.; Beck, J. B.

    2000-01-01

    The present paper discusses the effect of mass density on stability of rubble mound breakwaters. A short literature review of existing knowledge is give to establish a background for the ongoing research. Furthermore, several model tests are described in which the stability of rubble mound breakw...

  20. Stability of monoclonal antibodies at high-concentration

    DEFF Research Database (Denmark)

    Neergaard, Martin S; Nielsen, Anders D; Parshad, Henrik;

    2014-01-01

    Few studies have so far directly compared the impact of antibody subclass on protein stability. This case study investigates two mAbs (one IgG1 and one IgG4 ) with identical variable region. Investigations of mAbs that recognize similar epitopes are necessary to identify possible differences....... The stability of our mAb molecules is clearly affected by the IgG framework, and this study suggests that subclass switching may alter aggregation propensity and aggregation pathway and thus potentially improve the overall formulation stability while retaining antigen specificity....... between the IgG subclasses. Both physical and chemical stability were evaluated by applying a range of methods to measure formation of protein aggregates [size-exclusion chromatography (SEC)-HPLC and UV340 nm], structural integrity (circular dichroism and FTIR), thermodynamic stability (differential...

  1. Dynamics of the colloidal suspensions

    Institute of Scientific and Technical Information of China (English)

    ZHANG Hai-yan; MA Hong-ru

    2006-01-01

    This article offers a survey on our current knowledge of the dynamics of the colloidal suspension,where each particle experiences the friction force with solvent,hydrodynamic interaction,and potential force from surrounding particles and thermodynamic force.It further contains a summary of the basic concepts about microstructures and equilibrium properties,and of analytical and numerical methods,which are relevant for the theoretical description of the suspensions.The description of the dynamics of colloidal particles,based on the generalized Smoluchowski equation,is justified for the time scale accessible in DLS experiments.The combined influence of hard sphere or electrostatic potential and solvent-mediated hydrodynamic interaction on the short-time dynamics of monodisperse suspensions is investigated in detail.A thorough study of tracer-diffusion in hard sphere and charge-stabilized suspensions is presented.Mean-square displacements and long-time tracer-diffusion coefficients are calculated with two alternative approximations,i.e.,a mode-coupling scheme and a single relaxation time ansatz.

  2. High current density stability of ohmic contacts to silicon carbide

    Science.gov (United States)

    Downey, Brian P.

    The materials properties of SiC, such as wide bandgap, high breakdown electric field, and good thermal conductivity, make it an appealing option for high temperature and high power applications. The replacement of Si devices with SiC components could lead to a reduction in device size, weight, complexity, and cooling requirements along with an increase in device efficiency. One area of concern under high temperature or high current operation is the stability of the ohmic contacts. Ohmic contact degradation can cause an increase in parasitic resistance, which can diminish device performance. While contact studies have primarily focused on the high temperature stability of ohmic contacts to SiC, different failure mechanisms may arise under high current density stressing due to the influence of electromigration. In addition, preferential degradation may occur at the anode or cathode due to the directionality of current flow, known as a polarity effect. The failure mechanisms of ohmic contacts to p-type SiC under high current density stressing are explored. Complementary materials characterization techniques were used to analyze contact degradation, particularly the use of cross-sections prepared by focused ion beam for imaging using field emission scanning electron microscopy and elemental analysis using Auger electron spectroscopy. Initially the degradation of commonly studied Ni and Al-based contacts was investigated under continuous DC current. The contact metallization included a bond pad consisting of a TiW diffusion barrier and thick Au overlayer. The Ni contacts were found to degrade due to the growth of voids within the ohmic contact layer, which were initially produced during the high temperature Ni/SiC ohmic contact anneal. The Al-based contacts degraded due to the movement of Al from the ohmic contact layer to the surface of the Au bond pad, and the movement of Au into the ohmic contact layer from the bond pad. The inequality of Al and Au fluxes generated

  3. Development of high-sensitive, reproducible colloidal surface-enhanced Raman spectroscopy active substrate using silver nanocubes for potential biosensing applications

    Science.gov (United States)

    Hasna, Kudilatt; Lakshmi, Kiran; Ezhuthachan Jayaraj, Madambi Kunjukuttan; Kumar, Kumaran Rajeev; Matham, Murukeshan Vadakke

    2016-04-01

    Surface-enhanced Raman spectroscopy (SERS) has emerged as one of the thrust research areas that could find potential applications in bio and chemical sensing. We developed colloidal SERS active substrate with excellent sensitivity and high reproducibility using silver nanocube (AgNC) synthesized via the solvothermal method. Finite-difference time-domain simulation was carried out in detail to visualize dipole generation in the nanocube during localized surface plasmon resonance and to locate the respective hot spots in AgNC responsible for the huge Raman enhancement. The prediction is verified by the SERS analysis of the synthesized nanocubes using Rhodamine 6G molecule. An excellent sensitivity with a detection limit of 10-17 M and a very high enhancement factor of 1.2×108 confirms the "hot spots" in the nanocube. SERS activity is also carried out for crystal violet and for food adulterant Sudan I molecule. Finally, label-free DNA detection is performed to demonstrate the versatility of SERS as a potential biosensor.

  4. Fast and highly-efficient removal of methylene blue from aqueous solution by poly(styrenesulfonic acid-co-maleic acid)-sodium-modified magnetic colloidal nanocrystal clusters

    Science.gov (United States)

    Song, Yu-Bei; Lv, Shao-Nan; Cheng, Chang-Jing; Ni, Guo-Li; Xie, Xiao-Wa; Huang, Wei; Zhao, Zhi-Gang

    2015-01-01

    Magnetic colloidal nanocrystal clusters (MCNCs) modified with different amounts of poly(4-styrenesulfonic acid-co-maleic acid) sodium (PSSMA) have been prepared through simple one-step solvothermal method for removal of methylene blue (MB) from aqueous solution. The prepared MCNCs are characterized by Fourier transform infrared (FT-IR) spectra, scanning electron microscope (SEM), transmission electron microscope (TEM), thermogravimetric analysis (TGA), vibrating sample magnetometer (VSM), X-ray diffraction (XRD), nitrogen adsorption-desorption technique and dynamic light scattering (DLS). Moreover, effects of the solution pH, contact time, adsorbent dosage, ionic strength and initial dye concentration on MB adsorption onto the MCNCs are systematically investigated. The PSSMA-modified MCNCs show fast and highly-efficient MB removal capacity, which dramatically depends on the immobilization amounts of PSSMA, solution pH and adsorbent dosage. Their adsorption kinetics and isotherms exhibit that the kinetics and equilibrium adsorptions can be well-described by pseudo-second-order kinetic and Langmuir model, respectively. These magnetic nanocomposites, with high separation efficiency, low production cost and recyclable property, are promising as functional adsorbents for efficient removal of cationic organic pollutants from aqueous solution.

  5. Stabilization

    Directory of Open Access Journals (Sweden)

    Muhammad H. Al-Malack

    2016-07-01

    Full Text Available Fuel oil flyash (FFA produced in power and water desalination plants firing crude oils in the Kingdom of Saudi Arabia is being disposed in landfills, which increases the burden on the environment, therefore, FFA utilization must be encouraged. In the current research, the effect of adding FFA on the engineering properties of two indigenous soils, namely sand and marl, was investigated. FFA was added at concentrations of 5%, 10% and 15% to both soils with and without the addition of Portland cement. Mixtures of the stabilized soils were thoroughly evaluated using compaction, California Bearing Ratio (CBR, unconfined compressive strength (USC and durability tests. Results of these tests indicated that stabilized sand mixtures could not attain the ACI strength requirements. However, marl was found to satisfy the ACI strength requirement when only 5% of FFA was added together with 5% of cement. When the FFA was increased to 10% and 15%, the mixture’s strength was found to decrease to values below the ACI requirements. Results of the Toxicity Characteristics Leaching Procedure (TCLP, which was performed on samples that passed the ACI requirements, indicated that FFA must be cautiously used in soil stabilization.

  6. Aerosol printing of colloidal nanocrystals by aerodynamic focusing

    Science.gov (United States)

    Qi, Lejun

    Colloidal semiconductor nanocrystals, or quantum dots, have shown promise as the active material in electronic and optoelectronic applications, because of their high quantum yield, narrow spectral emission band, size-tunable bandgap, chemical stability, and easy processibility. Meanwhile, it is still challenging to print patterns of nanocrystal films with desired linewidth and thickness, which is a critical step in fabrication of nanocrystal-based devices. In this thesis, a direct-write method of colloidal semiconductor nanocrystals has been developed. Like other direct-write techniques, this aerosol based method simplifies printing process and reduces the manufacturing cost, as it avoids mask screening, lithography, and pre-patterning of the substrate. Moreover, the aerosol printing with aerodynamic lenses needs neither microscale nozzles nor sheath gases, and is able to incorporate into the vacuum systems currently used in microelectronic fabrication. This thesis research presents systematic efforts to develop an aerosol-based method to directly write patterns of semiconductor nanocrystals from colloidal dispersions by aerodynamic focusing. First, the synthesized colloidal nanocrystals in hexane were nebulized into compact and spherical agglomerates suspending in the carrier gas. The details about the impact dynamics of individual aerosolized nanocrystal agglomerates were investigated. As building blocks of printed nanocrystal films, the agglomerate exhibited cohesive and granular behaviors during impact deformation on the substrate. The strength of cohesion between nanocrystals in the agglomerates could be adjusted by tuning the number concentration of colloidal nanocrystal dispersion. Second, ultrathin films of nanocrystals were obtained by printing monodisperse nanocrystal agglomerates. As the result of the granular property of nanocrystal agglomerates, it was found that the thickness of deposited agglomerates strongly depended on the size of agglomerates. A

  7. On monolithic stability and reinforcement analysis of high arch dams

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Monolithic stability safety and reinforcement based on monolithic stability are very important for arch dam design.In this paper,the issue is addressed based on deformation reinforcement theory.In this approach,plastic complementary energy norm can be taken as safety Index for monolithic stability.According to deformation reinforcement theory,the areas where unbalanced force exists require reinforcement,and the required reinforcement forces are just the unbalanced forces with opposite direction.Results show that areas with unbalanced force mainly concentrate in dam-toes,dam-heels and faults.

  8. Development of high-stability magnet power supply

    Science.gov (United States)

    Choi, W. S.; Kim, M. J.; Jeong, I. W.; Kim, D. E.; Park, H. C.; Park, K. H.

    2016-06-01

    A very stable (≤10 ppm) magnet power supply (MPS) is required in an accelerator to achieve acceptable beam dynamics. Many factors affect the stability of an MPS, so design of the MPS requires much attention to noise-reduction schemes and to good processing of the signals from the feedback stage. This paper describes some design considerations for an MPS installed and operated in the Pohang Accelerator Laboratory: (1) control method, (2) oversampling technology, (3) ground isolation between hardware modules and (4) low-pass filter design to reduce the switching noise and rectifier ripple components, and shows the stability of three designed devices. The MPS design considerations were verified and validated in simulations and experiments. This paper also shows the relationship between stability and measurement aperture time of digital voltage meter 3458 A to measure stability of a current.

  9. Development of high-stability magnet power supply

    Energy Technology Data Exchange (ETDEWEB)

    Choi, W.S.; Kim, M.J.; Jeong, I.W. [Graduate School of Wind Energy, Pohang University of Science and Technology, 77 Cheongam-ro, Nam-gu, Pohang, Gyeongbuk 37673 (Korea, Republic of); Kim, D.E. [Pohang Accelerator Laboratory, Pohang University of Science and Technology, 80 Jigokro-127-beongil, Nam-gu, Pohang, Gyeongbuk 37673 (Korea, Republic of); Park, H.C. [Graduate School of Wind Energy, Pohang University of Science and Technology, 77 Cheongam-ro, Nam-gu, Pohang, Gyeongbuk 37673 (Korea, Republic of); Park, K.H. [Pohang Accelerator Laboratory, Pohang University of Science and Technology, 80 Jigokro-127-beongil, Nam-gu, Pohang, Gyeongbuk 37673 (Korea, Republic of)

    2016-06-21

    A very stable (≤10 ppm) magnet power supply (MPS) is required in an accelerator to achieve acceptable beam dynamics. Many factors affect the stability of an MPS, so design of the MPS requires much attention to noise-reduction schemes and to good processing of the signals from the feedback stage. This paper describes some design considerations for an MPS installed and operated in the Pohang Accelerator Laboratory: (1) control method, (2) oversampling technology, (3) ground isolation between hardware modules and (4) low-pass filter design to reduce the switching noise and rectifier ripple components, and shows the stability of three designed devices. The MPS design considerations were verified and validated in simulations and experiments. This paper also shows the relationship between stability and measurement aperture time of digital voltage meter 3458 A to measure stability of a current.

  10. Iron-rich colloids as carriers of phosphorus in streams

    NARCIS (Netherlands)

    Baken, Stijn; Regelink, Inge C.; Comans, Rob N.J.; Smolders, Erik; Koopmans, Gerwin F.

    2016-01-01

    Colloidal phosphorus (P) may represent an important fraction of the P in natural waters, but these colloids remain poorly characterized. In this work, we demonstrate the applicability of asymmetric flow field-flow fractionation (AF4) coupled to high resolution ICP-MS for the characterization of

  11. Tuning colloid-interface interactions by salt partitioning

    NARCIS (Netherlands)

    Everts, Jeffrey; Samin, Sela; Roij, René van

    2016-01-01

    We show that the interaction of an oil-dispersed colloidal particle with an oil-water interface is highly tunable from attractive to repulsive, either by varying the sign of the colloidal charge via charge regulation, or by varying the difference in hydrophilicity between the dissolved cations and a

  12. The Immobilization of a Transfer Hydrogenation Catalyst on Colloidal Particles

    NARCIS (Netherlands)

    van Ravensteijn, Bas G P; Schild, Dirk Jan; Kegel, Willem K.; Klein Gebbink, Robertus J M

    2017-01-01

    In this paper, we report a new synthetic procedure to immobilize a transfer hydrogenation catalyst on the surface of colloidal polystyrene particles. Using supports of colloidal dimensions allows for combining a relatively high surface area for catalyst binding, mobility of the catalyst, and facile

  13. Fluorine-Doped Tin Oxide Nanocrystal/Reduced Graphene Oxide Composites as Lithium Ion Battery Anode Material with High Capacity and Cycling Stability.

    Science.gov (United States)

    Xu, Haiping; Shi, Liyi; Wang, Zhuyi; Liu, Jia; Zhu, Jiefang; Zhao, Yin; Zhang, Meihong; Yuan, Shuai

    2015-12-16

    Tin oxide (SnO2) is a kind of anode material with high theoretical capacity. However, the volume expansion and fast capability fading during cycling have prevented its practical application in lithium ion batteries. Herein, we report that the nanocomposite of fluorine-doped tin oxide (FTO) and reduced graphene oxide (RGO) is an ideal anode material with high capacity, high rate capability, and high stability. The FTO conductive nanocrystals were successfully anchored on RGO nanosheets from an FTO nanocrystals colloid and RGO suspension by hydrothermal treatment. As the anode material, the FTO/RGO composite showed high structural stability during the lithiation and delithiation processes. The conductive FTO nanocrystals favor the formation of stable and thin solid electrolyte interface films. Significantly, the FTO/RGO composite retains a discharge capacity as high as 1439 mAhg(-1) after 200 cycles at a current density of 100 mAg(-1). Moreover, its rate capacity displays 1148 mAhg(-1) at a current density of 1000 mAg(-1).

  14. Dynamics of colloidal particles in ice

    KAUST Repository

    Spannuth, Melissa

    2011-01-01

    We use x-ray photon correlation spectroscopy (XPCS) to probe the dynamics of colloidal particles in polycrystalline ice. During freezing, the dendritic ice morphology and rejection of particles from the ice created regions of high particle density, where some of the colloids were forced into contact and formed disordered aggregates. The particles in these high density regions underwent ballistic motion, with a characteristic velocity that increased with temperature. This ballistic motion is coupled with both stretched and compressed exponential decays of the intensity autocorrelation function. We suggest that this behavior could result from ice grain boundary migration. © 2011 American Institute of Physics.

  15. Colloidal quantum dot light-emitting devices

    Directory of Open Access Journals (Sweden)

    Vanessa Wood

    2010-07-01

    Full Text Available Colloidal quantum dot light-emitting devices (QD-LEDs have generated considerable interest for applications such as thin film displays with improved color saturation and white lighting with a high color rendering index (CRI. We review the key advantages of using quantum dots (QDs in display and lighting applications, including their color purity, solution processability, and stability. After highlighting the main developments in QD-LED technology in the past 15 years, we describe the three mechanisms for exciting QDs – optical excitation, Förster energy transfer, and direct charge injection – that have been leveraged to create QD-LEDs. We outline the challenges facing QD-LED development, such as QD charging and QD luminescence quenching in QD thin films. We describe how optical downconversion schemes have enabled researchers to overcome these challenges and develop commercial lighting products that incorporate QDs to achieve desirable color temperature and a high CRI while maintaining efficiencies comparable to inorganic white LEDs (>65 lumens per Watt. We conclude by discussing some current directions in QD research that focus on achieving higher efficiency and air-stable QD-LEDs using electrical excitation of the luminescent QDs.

  16. Fast microbial reduction of ferrihydrite colloids from a soil effluent

    Science.gov (United States)

    Fritzsche, Andreas; Bosch, Julian; Rennert, Thilo; Heister, Katja; Braunschweig, Juliane; Meckenstock, Rainer U.; Totsche, Kai U.

    2012-01-01

    Recent studies on the microbial reduction of synthetic iron oxide colloids showed their superior electron accepting property in comparison to bulk iron oxides. However, natural colloidal iron oxides differ in composition from their synthetic counterparts. Besides a potential effect of colloid size, microbial iron reduction may be accelerated by electron-shuttling dissolved organic matter (DOM) as well as slowed down by inhibitors such as arsenic. We examined the microbial reduction of OM- and arsenic-containing ferrihydrite colloids. Four effluent fractions were collected from a soil column experiment run under water-saturated conditions. Ferrihydrite colloids precipitated from the soil effluent and exhibited stable hydrodynamic diameters ranging from 281 (±146) nm in the effluent fraction that was collected first and 100 (±43) nm in a subsequently obtained effluent fraction. Aliquots of these oxic effluent fractions were added to anoxic low salt medium containing diluted suspensions of Geobacter sulfurreducens. Independent of the initial colloid size, the soil effluent ferrihydrite colloids were quickly and completely reduced. The rates of Fe2+ formation ranged between 1.9 and 3.3 fmol h-1 cell-1, and are in the range of or slightly exceeding previously reported rates of synthetic ferrihydrite colloids (1.3 fmol h-1 cell-1), but greatly exceeding previously known rates of macroaggregate-ferrihydrite reduction (0.07 fmol h-1 cell-1). The inhibition of microbial Fe(III) reduction by arsenic is unlikely or overridden by the concurrent enhancement induced by soil effluent DOM. These organic species may have increased the already high intrinsic reducibility of colloidal ferrihydrite owing to quinone-mediated electron shuttling. Additionally, OM, which is structurally associated with the soil effluent ferrihydrite colloids, may also contribute to the higher reactivity due to increasing solubility and specific surface area of ferrihydrite. In conclusion, ferrihydrite

  17. Structural Stability and Optical Properties of Nanomaterials with Reconstructed Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Puzder, A; Williamson, A; Reboredo, F; Galli, G

    2003-10-24

    The authors present density functional and quantum Monte Carlo calculations of the stability and optical properties of semiconductor nanomaterials with reconstructed surfaces. they predict the relative stability of silicon nanostructures with reconstructed and unreconstructed surfaces, and show that surface step geometries unique to highly curved surfaces dramatically reduce the optical gaps and decrease excitonic lifetimes. These predictions provide an explanation of both the variations in the photoluminescence spectra of colloidally synthesized nanoparticles and observed deep gap levels in porous silicon.

  18. Physical factors affecting the transport and fate of colloids in saturated porous media

    Science.gov (United States)

    Bradford, Scott A.; Yates, Scott R.; Bettahar, Mehdi; Simunek, Jirka

    2002-12-01

    Saturated soil column experiments were conducted to explore the influence of colloid size and soil grain size distribution characteristics on the transport and fate of colloid particles in saturated porous media. Stable monodispersed colloids and porous media that are negatively charged were employed in these studies. Effluent colloid concentration curves and the final spatial distribution of retained colloids by the porous media were found to be highly dependent on the colloid size and soil grain size distribution. Relative peak effluent concentrations decreased and surface mass removal by the soil increased when the colloid size increased and the soil median grain size decreased. These observations were attributed to increased straining of the colloids; i.e., blocked pores act as dead ends for the colloids. When the colloid size is small relative to the soil pore sizes, straining becomes a less significant mechanism of colloid removal and attachment becomes more important. Mathematical modeling of the colloid transport experiments using traditional colloid attachment theory was conducted to highlight differences in colloid attachment and straining behavior and to identify parameter ranges that are applicable for attachment models. Simulated colloid effluent curves using fitted first-order attachment and detachment parameters were able to describe much of the effluent concentration data. The model was, however, less adequate at describing systems which exhibited a gradual approach to the peak effluent concentration and the spatial distribution of colloids when significant mass was retained in the soil. Current colloid filtration theory did not adequately predict the fitted first-order attachment coefficients, presumably due to straining in these systems.

  19. Electrocatalytic Oxidation of NADH Based on Self-assembled Colloidal Gold and Nafion Matrixes and Co Complex Mediator

    Institute of Scientific and Technical Information of China (English)

    Na WANG; Ruo YUAN; Ya Qin CHAI; Dian Ping TANG; Qiang ZHU; Xue Lian LI

    2006-01-01

    A novel approach based on self-assembled colloidal gold and Nafion matrixes and Co complex mediator to construct Co(bpy)33+/nano-Au/Co(bpy)33+/nafion/GC electrode, on which formed stable redox-active films. This electrode can decrease the overpotential about 330 mV for the oxidation of NADH with high stability, wide linear range and low detection limit.

  20. Medical applications of colloids

    CERN Document Server

    Matijevic, Egon

    2008-01-01

    The first book of its type on the medical and biomedical applications of colloids, although there are some related titles on different topicsDiscusses the effects of uniform particles in drug formulations and releaseEvaluates particle transport and deposition in the human body.

  1. Liquid crystal colloids

    Directory of Open Access Journals (Sweden)

    2010-01-01

    Full Text Available This special issue of "Condensed Matter Physics" focuses on the most recent developments in the study of a fascinating soft matter system, representing colloidal particles in a liquid crystalline environment. Furthermore, some articles address pioneering steps in the discovery of liquid crystals going back to 1861 paper by Julius Planer.

  2. Nucleation in food colloids

    Science.gov (United States)

    Povey, Malcolm J. W.

    2016-12-01

    Nucleation in food colloids has been studied in detail using ultrasound spectroscopy. Our data show that classical nucleation theory (CNT) remains a sound basis from which to understand nucleation in food colloids and analogous model systems using n-alkanes. Various interpretations and modifications of CNT are discussed with regard to their relevance to food colloids. Much of the evidence presented is based on the ultrasound velocity spectrometry measurements which has many advantages for the study of nucleating systems compared to light scattering and NMR due to its sensitivity at low solid contents and its ability to measure true solid contents in the nucleation and early crystal growth stages. Ultrasound attenuation spectroscopy also responds to critical fluctuations in the induction region. We show, however, that a periodic pressure fluctuation such as a quasi-continuous (as opposed to a pulse comprising only a few pressure cycles) ultrasound field can alter the nucleation process, even at very low acoustic intensity. Thus care must be taken when using ultrasound techniques that the measurements do not alter the studied processes. Quasi-continuous ultrasound fields may enhance or suppress nucleation and the criteria to determine such effects are derived. The conclusions of this paper are relevant to colloidal systems in foods, pharmaceuticals, agro-chemicals, cosmetics, and personal products.

  3. Binary colloidal crystals

    NARCIS (Netherlands)

    Christova-Zdravkova, C.G.

    2005-01-01

    Binary crystals are crystals composed of two types of particles having different properties like size, mass density, charge etc. In this thesis several new approaches to make binary crystals of colloidal particles that differ in size, material and charge are reported We found a variety of crystal st

  4. Electrodynamics of colloids.

    NARCIS (Netherlands)

    Minor, M.

    1998-01-01

    The goal of the present study is to deepen the insight into the non-equilibrium properties of the electric double layer of colloidal systems. Of basic interest are the ionic mobilities in the different regions of the electric double layer as well as the potential at the plane of shear, i.e., the ele

  5. Viscosity of colloidal suspensions

    Energy Technology Data Exchange (ETDEWEB)

    Cohen, E.G.D. [Rockefeller Univ., New York, NY (United States); Schepper, I.M. de [Delft Univ. of Technology (Netherlands)

    1995-12-31

    Simple expressions are given for the effective Newtonian viscosity as a function of concentration as well as for the effective visco-elastic response as a function of concentration and imposed frequency, of monodisperse neutral colloidal suspensions over the entire fluid range. The basic physical mechanisms underlying these formulae are discussed. The agreement with existing experiments is very good.

  6. Doped Colloidal ZnO Nanocrystals

    Directory of Open Access Journals (Sweden)

    Yizheng Jin

    2012-01-01

    Full Text Available Colloidal ZnO nanocrystals are promising for a wide range of applications due to the combination of unique multifunctional nature and remarkable solution processability. Doping is an effective approach of enhancing the properties of colloidal ZnO nanocrystals in well-controlled manners. In this paper, we analyzed two synthetic strategies for the doped colloidal ZnO nanocrystals, emphasizing our understanding on the critical factors associated with the high temperature and nonaqueous approach. Latest advances of three topics, bandgap engineering, n-type doping, and dilute magnetic semiconductors related to doped ZnO nanocrystals were discussed to reveal the effects of dopants on the properties of the nanocrystalline materials.

  7. Plasmonic films based on colloidal lithography.

    Science.gov (United States)

    Ai, Bin; Yu, Ye; Möhwald, Helmuth; Zhang, Gang; Yang, Bai

    2014-04-01

    This paper reviews recent advances in the field of plasmonic films fabricated by colloidal lithography. Compared with conventional lithography techniques such as electron beam lithography and focused ion beam lithography, the unconventional colloidal lithography technique with advantages of low-cost and high-throughput has made the fabrication process more efficient, and moreover brought out novel films that show remarkable surface plasmon features. These plasmonic films include those with nanohole arrays, nanovoid arrays and nanoshell arrays with precisely controlled shapes, sizes, and spacing. Based on these novel nanostructures, optical and sensing performances can be greatly enhanced. The introduction of colloidal lithography provides not only efficient fabrication processes but also plasmonic films with unique nanostructures, which are difficult to be fabricated by conventional lithography techniques.

  8. Separation of Organic Dyes from Water by Colloidal Gas Aphrons

    Institute of Scientific and Technical Information of China (English)

    黄颖怡; 王运东; 戴猷元

    2002-01-01

    Colloidal gas aphrons (CGAs) are micron-sized gas bubbles produced by stirring surfactant solutions at high speed. A single CGA dispersed in water is composed of a gaseous inner core, surrounded by a double water-soapy layer. CGAs have large interfacial area per unit volume and exhibit relatively high stability. These characteristics make CGAs very suitable in flotation systems. This paper studied the flotation of organic dyes from water using CGAs. The experimental results show that the flotation process may follow four mechanisms, i.e., ion coupling of the oppositely charged species of the surfactant forming the CGA and the organic dye, reactions between CGA and the organic dye, ion-dye complex adsorbed on the surface of CGAs, and hydrophilic or hydrophobic characteristics of the organic dyes.

  9. Conditions for equilibrium solid-stabilized emulsions.

    Science.gov (United States)

    Kraft, Daniela J; de Folter, Julius W J; Luigjes, Bob; Castillo, Sonja I R; Sacanna, Stefano; Philipse, Albert P; Kegel, Willem K

    2010-08-19

    Particular types of solid-stabilized emulsions can be thermodynamically stable as evidenced by their spontaneous formation and monodisperse droplet size, which only depends on system parameters. Here, we investigate the generality of these equilibrium solid-stabilized emulsions with respect to the basic constituents: aqueous phase with ions, oil, and stabilizing particles. From systematic variations of these constituents, we identify general conditions for the spontaneous formation of monodisperse solid-stabilized emulsions droplets. We conclude that emulsion stability is achieved by a combination of solid particles as well as amphiphilic ions adsorbed at the droplet surface, and low interfacial tensions of the bare oil-water interface of order 10 mN/m or below. Furthermore, preferential wetting of the colloidal particles by the oil phase is necessary for thermodynamic stability. We demonstrate the sufficiency of these basic requirements by extending the observed thermodynamic stability to emulsions of different compositions. Our findings point to a new class of colloid-stabilized meso-emulsions with a potentially high impact on industrial emulsification processes due to the associated large energy savings.

  10. Third-order nonlinear optical response of colloidal gold nanoparticles prepared by sputtering deposition

    Energy Technology Data Exchange (ETDEWEB)

    Castro, Hemerson P. S.; Alencar, Márcio A. R. C.; Hickmann, Jandir M. [Optics and Materials Group–OPTMA, Universidade Federal de Alagoas, CAIXA POSTAL 2051, 57061-970 Maceió (Brazil); Wender, Heberton [Brazilian Synchrotron National Laboratory (LNLS), CNPEM, Rua Giuseppe Máximo Scolfaro 10.000, 13083-970 Campinas (Brazil); Department of Physics, Universidade Federal do Mato Grosso do Sul, 79070-900, Campo Grande (Brazil); Teixeira, Sergio R. [Institute of Physics, Universidade Federal do Rio Grande do Sul, 91501-970, Porto Alegre (Brazil); Dupont, Jairton [Laboratory of Molecular Catalysis, Institute of Chemistry, Universidade Federal do Rio Grande do Sul, 91501-970, Porto Alegre (Brazil)

    2013-11-14

    The nonlinear optical responses of gold nanoparticles dispersed in castor oil produced by sputtering deposition were investigated, using the thermally managed Z-scan technique. Particles with spherical shape and 2.6 nm of average diameter were obtained and characterized by transmission electron microscopy and small angle X-ray scattering. This colloid was highly stable, without the presence of chemical impurities, neither stabilizers. It was observed that this system presents a large refractive third-order nonlinear response and a negligible nonlinear absorption. Moreover, the evaluation of the all-optical switching figures of merit demonstrated that the colloidal nanoparticles prepared by sputtering deposition have a good potential for the development of ultrafast photonic devices.

  11. Dynamics of non-spherical colloidal particles near and at oil-water interfaces

    Science.gov (United States)

    Wang, Anna; Dimiduk, Thomas G.; Fung, Jerome; Chaudhary, Kundan; Lewis, Jennifer A.; Razavi, Sepideh; Kretzschmar, Ilona; Manoharan, Vinothan N.

    2014-03-01

    Whereas much is known about how spherical colloidal particles interact with and at oil-water interfaces, not much is known about their non-spherical counterparts. The rotation of non-spherically symmetric particles adds extra degrees of freedom to how such particles interact with each other and the interface, so to study their three-dimensional dynamics we must first be able to image the rotation which has so far only been possible in viscous fluids or for particles with large aspect ratios. Here we track both the three-dimensional translation and the rotation of non-spherical colloidal particles at high speeds using the discrete dipole approximation in conjunction with digital holographic microscopy. We study the dynamics of such particles at an oil-water interface to determine interactions and dynamics prior to or after attachment. We aim to connect these measurements to the formation and stability of Pickering emulsions.

  12. Finite particle size drives defect-mediated domain structures in strongly confined colloidal liquid crystals

    Science.gov (United States)

    Gârlea, Ioana C.; Mulder, Pieter; Alvarado, José; Dammone, Oliver; Aarts, Dirk G. A. L.; Lettinga, M. Pavlik; Koenderink, Gijsje H.; Mulder, Bela M.

    2016-06-01

    When liquid crystals are confined to finite volumes, the competition between the surface anchoring imposed by the boundaries and the intrinsic orientational symmetry-breaking of these materials gives rise to a host of intriguing phenomena involving topological defect structures. For synthetic molecular mesogens, like the ones used in liquid-crystal displays, these defect structures are independent of the size of the molecules and well described by continuum theories. In contrast, colloidal systems such as carbon nanotubes and biopolymers have micron-sized lengths, so continuum descriptions are expected to break down under strong confinement conditions. Here, we show, by a combination of computer simulations and experiments with virus particles in tailor-made disk- and annulus-shaped microchambers, that strong confinement of colloidal liquid crystals leads to novel defect-stabilized symmetrical domain structures. These finite-size effects point to a potential for designing optically active microstructures, exploiting the as yet unexplored regime of highly confined liquid crystals.

  13. Morphological instability of a non-equilibrium ice-colloid interface

    KAUST Repository

    Peppin, S. S. L.

    2009-10-02

    We assess the morphological stability of a non-equilibrium ice-colloidal suspension interface, and apply the theory to bentonite clay. An experimentally convenient scaling is employed that takes advantage of the vanishing segregation coefficient at low freezing velocities, and when anisotropic kinetic effects are included, the interface is shown to be unstable to travelling waves. The potential for travelling-wave modes reveals a possible mechanism for the polygonal and spiral ice lenses observed in frozen clays. A weakly nonlinear analysis yields a long-wave evolution equation for the interface shape containing a new parameter related to the highly nonlinear liquidus curve in colloidal systems. We discuss the implications of these results for the frost susceptibility of soils and the fabrication of microtailored porous materials. © 2009 The Royal Society.

  14. Stability

    Directory of Open Access Journals (Sweden)

    Nada S. Abdelwahab

    2017-05-01

    Full Text Available The present work concerns with the development of stability indicating the RP-HPLC method for simultaneous determination of guaifenesin (GUF and pseudoephedrine hydrochloride (PSH in the presence of guaifenesin related substance (Guaiacol. GUC, and in the presence of syrup excepients with minimum sample pre-treatment. In the developed RP-HPLC method efficient chromatographic separation was achieved for GUF, PSH, GUC and syrup excepients using ODS column as a stationary phase and methanol: water (50:50, v/v, pH = 4 with orthophosphoric acid as a mobile phase with a flow rate of 1 mL min−1 and UV detection at 210 nm. The chromatographic run time was approximately 10 min. Calibration curves were drawn relating the integrated area under peak to the corresponding concentrations of PSH, GUF and GUC in the range of 1–8, 1–20, 0.4–8 μg mL−1, respectively. The developed method has been validated and met the requirements delineated by ICH guidelines with respect to linearity, accuracy, precision, specificity and robustness. The validated method was successfully applied for determination of the studied drugs in triaminic chest congestion® syrup; moreover its results were statistically compared with those obtained by the official method and no significant difference was found between them.

  15. Armoring confined bubbles in concentrated colloidal suspensions

    Science.gov (United States)

    Yu, Yingxian; Khodaparast, Sepideh; Stone, Howard

    2016-11-01

    Encapsulation of a bubble with microparticles is known to significantly improve the stability of the bubble. This phenomenon has recently gained increasing attention due to its application in a variety of technologies such as foam stabilization, drug encapsulation and colloidosomes. Nevertheless, the production of such colloidal armored bubble with controlled size and particle coverage ratio is still a great challenge industrially. We study the coating process of a long air bubble by microparticles in a circular tube filled with a concentrated microparticles colloidal suspension. As the bubble proceeds in the suspension of particles, a monolayer of micro-particles forms on the interface of the bubble, which eventually results in a fully armored bubble. We investigate the phenomenon that triggers and controls the evolution of the particle accumulation on the bubble interface. Moreover, we examine the effects of the mean flow velocity, the size of the colloids and concentration of the suspension on the dynamics of the armored bubble. The results of this study can potentially be applied to production of particle-encapsulated bubbles, surface-cleaning techniques, and gas-assisted injection molding.

  16. Colloidal silver solutions with antimicrobial properties

    Energy Technology Data Exchange (ETDEWEB)

    Petica, A. [INCDIE ICPE-Advanced Research, Bucharest (Romania)], E-mail: petica@icpe-ca.ro; Gavriliu, S.; Lungu, M.; Buruntea, N. [INCDIE ICPE-Advanced Research, Bucharest (Romania); Panzaru, C. [Institute of Medicine and Pharmacy, Iassy (Romania)

    2008-08-25

    Some colloidal silver solutions involving the electrochemical technique with 'sacrificial anode method and different stabilizers and co-stabilizers' have been prepared. A constant current pulse generator with stirrer at different working times has been used. To achieve stable colloidal silver solutions, a mix of different tensioactive agents namely [poly (N-vinylpyrrolidone)], Na-naphthalene sulphonate, Na-lauryl sulfate and Na-dodecyl sulphonate were tested. The effects of these various mixes of polymer and ionic surfactants upon the Ag concentration and UV-vis spectra of silver nanoparticles were determined by spectrophotometer techniques. The nanoparticles sizes have been analyzed through dynamic light scattering technique and the silver nanoparticle morphology has been evidenced by transmission electron microscopy (TEM). Micobiological analysis has been made by determining minimal inhibitorial concentration upon the following germs: Staphylococcus aureus (ATCC) (Gram-positive cocci), Pseudomonas aeruginosa (ATTC), Escherichia coli (ATCC) and Acinetobacter spp. (Gram-negative coccobacillus). To evaluate the antifungal effect, the antibiogram method involving various tests using a fungi mix of Aspergillus, Penicillium and Trichoderma species has been used. The presented method allows obtaining of some stable colloidal solutions containing up to 35 ppm of Ag with very good antimicrobial and antifungal properties.

  17. The hydrodynamics of colloidal gelation.

    Science.gov (United States)

    Varga, Zsigmond; Wang, Gang; Swan, James

    2015-12-14

    Colloidal gels are formed during arrested phase separation. Sub-micron, mutually attractive particles aggregate to form a system spanning network with high interfacial area, far from equilibrium. Models for microstructural evolution during colloidal gelation have often struggled to match experimental results with long standing questions regarding the role of hydrodynamic interactions. In nearly all models, these interactions are neglected entirely. In the present work, we report simulations of gelation with and without hydrodynamic interactions between the suspended particles executed in HOOMD-blue. The disparities between these simulations are striking and mirror the experimental-theoretical mismatch in the literature. The hydrodynamic simulations agree with experimental observations, however. We explore a simple model of the competing transport processes in gelation that anticipates these disparities, and conclude that hydrodynamic forces are essential. Near the gel boundary, there exists a competition between compaction of individual aggregates which suppresses gelation and coagulation of aggregates which enhances it. The time scale for compaction is mildly slowed by hydrodynamic interactions, while the time scale for coagulation is greatly accelerated. This enhancement to coagulation leads to a shift in the gel boundary to lower strengths of attraction and lower particle concentrations when compared to models that neglect hydrodynamic interactions. Away from the gel boundary, differences in the nearest neighbor distribution and fractal dimension persist within gels produced by both simulation methods. This result necessitates a fundamental rethinking of how dynamic, discrete element models for gelation kinetics are developed as well as how collective hydrodynamic interactions influence the arrest of attractive colloidal dispersions.

  18. High thermal stability and sluggish crystallization kinetics of high-entropy bulk metallic glasses

    Science.gov (United States)

    Yang, M.; Liu, X. J.; Ruan, H. H.; Wu, Y.; Wang, H.; Lu, Z. P.

    2016-06-01

    Metallic glasses are metastable and their thermal stability is critical for practical applications, particularly at elevated temperatures. The conventional bulk metallic glasses (BMGs), though exhibiting high glass-forming ability (GFA), crystallize quickly when being heated to a temperature higher than their glass transition temperature. This problem may potentially be alleviated due to the recent developments of high-entropy (or multi-principle-element) bulk metallic glasses (HE-BMGs). In this work, we demonstrate that typical HE-BMGs, i.e., ZrTiHfCuNiBe and ZrTiCuNiBe, have higher kinetic stability, as compared with the benchmark glass Vitreoy1 (Zr41.2Ti13.8Cu12.5Ni10Be22.5) with a similar chemical composition. The measured activation energy for glass transition and crystallization of the HE-BMGs is nearly twice that of Vitreloy 1. Moreover, the sluggish crystallization region ΔTpl-pf, defined as the temperature span between the last exothermic crystallization peak temperature Tpl and the first crystallization exothermic peak temperature Tpf, of all the HE-BMGs is much wider than that of Vitreloy 1. In addition, high-resolution transmission electron microscopy characterization of the crystallized products at different temperatures and the continuous heating transformation diagram which is proposed to estimate the lifetime at any temperature below the melting point further confirm high thermal stability of the HE-BMGs. Surprisingly, all the HE-BMGs show a small fragility value, which contradicts with their low GFA, suggesting that the underlying diffusion mechanism in the liquid and the solid of HE-BMGs is different.

  19. Snapshotted glass and gel transitions of stable colloidal dispersions after shear-driven aggregation in a microchannel.

    Science.gov (United States)

    Meng, Xia; Wu, Hua; Morbidelli, Massimo

    2015-02-07

    Intense shear can lead to aggregation of colloids that are highly stable at rest. The aggregation process typically has an induction time, and then becomes explosive, leading to rapid phase transitions. We study the phase evolution during shear-driven aggregation in a short microchannel (MC) under intense shear for a colloid with a high interaction energy barrier that ensures high stability of particles and clusters before and after intense shear. The short residence time allows us to snapshot the phase evolution by repeatedly cycling the colloid in the MC. It is found that, depending on the particle concentration, in addition to a fluid of clusters and a solid-like gel, there is another solid-like state between them: Wigner glass of clusters. Their transitions occur over a large range of particle concentrations. We have proposed a phase diagram that describes how the transitions of the three phases evolve in the aggregation steady state in the colloidal interaction vs. particle concentration plane.

  20. Composition and cycling of colloids in marine environments

    Science.gov (United States)

    Guo, Laodong; Santschi, Peter H.

    1997-02-01

    Colloidal (COM) or macromolecular organic matter makes up a significant portion of the bulk dissolved organic matter (DOM) pool in aquatic environments. Because of their high specific surface areas and complexation capacities, marine colloids are of great importance not only in the global carbon cycle but also in the biogeochemical cycling of many particle-reactive nuclides and trace elements in the ocean. However, the colloidal pool as a whole is still poorly understood and largely uncharacterized. Recently, cross-flow ultrafiltration and other separation techniques, which have been successfully used to isolate marine colloids, combined with a multitracer approach, have greatly advanced our understanding of the cycling of COM and its associated trace elements in marine environments. In this paper we focus on recent developments on isotopic and elemental composition of colloids which allow organic matter cycling in marine environments to be constrained. Major sections review sampling techniques for aquatic colloids, concentrations and distribution of COM, biochemical and elemental (organic and inorganic) characterization, and stable isotopic (13C and 15N) and radioisotopic (14C and 234Th) characterization of marine colloids. We discuss sources and turnover rates of organic matter in the ocean, importance of benthic boundary layer processes in the cycling of DOM, changes in the paradigms of marine organic matter cycling, and research needs for a better understanding of the biogeochemistry of marine colloids.

  1. Multifunctional self-assembled composite colloids and their application to SERS detection

    Science.gov (United States)

    La Porta, Andrea; Sánchez-Iglesias, Ana; Altantzis, Thomas; Bals, Sara; Grzelczak, Marek; Liz-Marzán, Luis M.

    2015-06-01

    We present a simple method for the co-encapsulation of gold nanostars and iron-oxide nanoparticles into hybrid colloidal composites that are highly responsive to both light and external magnetic fields. Self-assembly was driven by hydrophobic interactions between polystyrene capped gold nanostars and iron oxide nanocrystals stabilized with oleic acid, upon addition of water. A block copolymer was then used to encapsulate the resulting spherical colloidal particle clusters, which thereby became hydrophilic. Electron microscopy analysis unequivocally shows that each composite particle comprises a single Au nanostar surrounded by a few hundreds of iron oxide nanocrystals. We demonstrate that this hybrid colloidal system can be used as an efficient substrate for surface enhanced Raman scattering, using common dyes as model molecular probes. The co-encapsulation of iron oxide nanoparticles renders the system magnetically responsive, so that application of an external magnetic field leads to particle accumulation and limits of detection are in the nM range.We present a simple method for the co-encapsulation of gold nanostars and iron-oxide nanoparticles into hybrid colloidal composites that are highly responsive to both light and external magnetic fields. Self-assembly was driven by hydrophobic interactions between polystyrene capped gold nanostars and iron oxide nanocrystals stabilized with oleic acid, upon addition of water. A block copolymer was then used to encapsulate the resulting spherical colloidal particle clusters, which thereby became hydrophilic. Electron microscopy analysis unequivocally shows that each composite particle comprises a single Au nanostar surrounded by a few hundreds of iron oxide nanocrystals. We demonstrate that this hybrid colloidal system can be used as an efficient substrate for surface enhanced Raman scattering, using common dyes as model molecular probes. The co-encapsulation of iron oxide nanoparticles renders the system magnetically

  2. The origin of virgin argan oil's high oxidative stability unraveled.

    Science.gov (United States)

    Gharby, Saïd; Harhar, Hicham; Guillaume, Dominique; Haddad, Aziza; Charrouf, Zoubida

    2012-05-01

    To prepare either virgin edible or beauty argan oil, roasted or unroasted argan kernels are cold-pressed, respectively. Comparing the physicochemical parameters of edible and beauty argan oil immediately after preparation and after a two-year delay has led to the suggestion that phospholipids are a new and essential type of oil component participating in the excellent oxidative stability of edible argan oil, in addition to the already suggested Maillard-reaction products, phenols, and tocopherols.

  3. Visual detection of 2,4,6-trinitrotolune by molecularly imprinted colloidal array photonic crystal

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Wei [School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing, 100081 (China); Asher, Sanford A., E-mail: asher@pitt.edu [Department of Chemistry, University of Pittsburgh, Pittsburgh, PA 15260 (United States); Meng, Zihui, E-mail: m_zihui@yahoo.com [School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing, 100081 (China); Yan, Zequn [School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing, 100081 (China); Xue, Min, E-mail: minxue@bit.edu.cn [School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing, 100081 (China); Qiu, Lili, E-mail: qiulili@bit.edu.cn [School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing, 100081 (China); Yi, Da [School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing, 100081 (China)

    2016-10-05

    Graphical abstract: Molecularly imprinted colloidal array (MICA) was explored for the selective visual detection of TNT with color changing from green to red. And molecularly imprinted colloidal particles (MICs) were evaluated for the adsorption capacity and the imprinting efficiency. The MICA had excellent flexibility, reversibility and stability. It promised high potential for the visual semi-quantitative detection of other explosives. - Highlights: • Molecularly imprinted colloidal array (MICA) was used to visually detect TNT. • The relationship of particle size, diffracted wavelength and color was discussed. • The adsorption capacity and imprinting efficiency of MICs were calculated. • MICA had short response time, high selectivity, good reversibility and stability. • MICA had high potential to be used in other customed visual explosive detection. - Abstract: We developed a photonic crystal (PhC) sensor for the quantification of 2,4,6-trinitrotoluene (TNT) in solution. Monodisperse (210 nm in diameter) molecularly imprinted colloidal particles (MICs) for TNT were prepared by the emulsion polymerization of methyl methacrylate and acrylamide in the presence of TNT as a template. The MICs were then self-assembled into close-packed opal PhC films. The adsorption capacity of the MICs for TNT was 64 mg TNT/g. The diffraction from the PhC depended on the TNT concentration in a methanol/water (3/2, v/v) potassium dihydrogen phosphate buffer solution (pH = 7.0, 30 mM). The limit of detection (LOD) of the sensor was 1.03 μg. The color of the molecularly imprinted colloidal array (MICA) changed from green to red with an 84 nm diffraction red shift when the TNT concentration increased to 20 mM. The sensor response time was 3 min. The PhC sensor was selective for TNT compared to similar compounds such as 2,4,6-trinitrophenol, 2,4-dinitrotoluene, 2,6-dinitrotoluene, 2-nitromesitylene, 4-nitrotoluene, 2-nitrotoluene, 1,3-dinitrobenzene, methylbenzene, 4-nitrophenol

  4. Geochemistry of colloid systems. For earth scientists

    NARCIS (Netherlands)

    Nickel, E.

    1979-01-01

    The second part of the title of this book gives an indication for whom it has been written. It is a real 'synthesizer'. Throughout ten chapters the reader is introduced into the highly complex matter of colloid chemistry and its role in geochemistry, pedology, oceanography, and geology.

  5. Infrared Colloidal Quantum Dots for Photovoltaics: Fundamentals and Recent Progress

    KAUST Repository

    Tang, Jiang

    2010-09-14

    Colloidal quantum dots (CQDs) are solution-processed semiconductors of interest in low-cost photovoltaics. Tuning of the bandgap of CQD films via the quantum size effect enables customization of solar cells\\' absorption profile to match the sun\\'s broad visible- and infrared-containing spectrum reaching the earth. Here we review recent progress in the realization of low-cost, efficient solar cells based on CQDs. We focus in particular on CQD materials and approaches that provide both infrared and visible-wavelength solar power conversion CQD photovoltaics now exceed 5% solar power conversion efficiency, achieved by the introduction of a new architecture, the depleted-heterojunction CQD solar cell, that jointly maximizes current, voltage, and fill factor. CQD solar cells have also seen major progress in materials processing for stability, recently achieving extended operating lifetimes in an air ambient. We summarize progress both in device operation and also in gaining new insights into materials properties and processing - including new electrical contact materials and deposition techniques, as well as CQD synthesis, surface treatments, film-forming technologies - that underpin these rapid advances. Infrared colloidal quantum dots that absorb most of the solar radiation enable potential efficient and low-cost photovoltaic devices. Careful optimization of quantum dot passivation and device configuration leads to solar cells with AM1.5G efficiency as high as 5.1% Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. A combined crystalloid and colloid pd solution as a glucose-sparing strategy for volume control in high-transport apd patients: a prospective multicenter study.

    Science.gov (United States)

    Freida, Philippe; Issad, Belkacem; Dratwa, Max; Lobbedez, Thierry; Wu, Lieling; Leypoldt, John K; Divino-Filho, Jose Carolino

    2009-01-01

    Evidence is accumulating that the continuous exposure to high glucose concentrations during peritoneal dialysis (PD) is an important cause of ultrafiltration (UF) failure. The cornerstone of prevention and treatment of UF failure is reduction of glucose exposure, which will also alleviate the systemic impact of significant free glucose absorption. The challenge for the future is to discover new therapeutic strategies to enhance fluid and sodium removal while diminishing glucose load and exposure using combinations of available osmotic agents. To investigate in patients on automated PD (APD) with a fast transport pattern whether there is a glucose-sparing advantage to replacing 7.5% icodextrin (ICO) during the long dwell with a mixed crystalloid and colloid PD fluid (bimodal UF) in an attempt to promote daytime UF and sodium removal while diminishing the glucose strength of the dialysate at night. A 2 parallel arm, 4 month, prospective nonrandomized study. PD units or university hospitals in 4 French and Belgian districts. During the 4-month intervention period, net UF and peritoneal sodium removal during the long dwell when treated by bimodal UF was about 2-fold higher than baseline (with ICO). The estimated percent change (95% confidence interval) from baseline in net daytime UF for the bimodal solution was 150% (106% - 193%), versus 18% (-7% - 43%) for ICO (p ICO (p ICO. Prescription of bimodal UF during the day in APD patients offers the opportunity to optimize the long dwell exchange in a complete 24-hour APD cycle. The current study demonstrated that a bimodal solution based on the mixing of glucose (2.6%) and icodextrin (6.8%) achieved the double target of significantly improving UF and peritoneal sodium removal by exploring a new concept of glucose-sparing PD therapy.

  7. Electromagnetic stabilization of tokamak microturbulence in a high-$\\beta$ regime

    CERN Document Server

    Citrin, J; Goerler, T; Jenko, F; Mantica, P; Told, D; Bourdelle, C; Hatch, D R; Hogeweij, G M D; Johnson, T; Pueschel, M J; Schneider, M

    2014-01-01

    The impact of electromagnetic stabilization and flow shear stabilization on ITG turbulence is investigated. Analysis of a low-$\\beta$ JET L-mode discharge illustrates the relation between ITG stabilization, and proximity to the electromagnetic instability threshold. This threshold is reduced by suprathermal pressure gradients, highlighting the effectiveness of fast ions in ITG stabilization. Extensive linear and nonlinear gyrokinetic simulations are then carried out for the high-$\\beta$ JET hybrid discharge 75225, at two separate locations at inner and outer radii. It is found that at the inner radius, nonlinear electromagnetic stabilization is dominant, and is critical for achieving simulated heat fluxes in agreement with the experiment. The enhancement of this effect by suprathermal pressure also remains significant. It is also found that flow shear stabilization is not effective at the inner radii. However, at outer radii the situation is reversed. Electromagnetic stabilization is negligible while the flow...

  8. Colloidal Double Quantum Dots.

    Science.gov (United States)

    Teitelboim, Ayelet; Meir, Noga; Kazes, Miri; Oron, Dan

    2016-05-17

    Pairs of coupled quantum dots with controlled coupling between the two potential wells serve as an extremely rich system, exhibiting a plethora of optical phenomena that do not exist in each of the isolated constituent dots. Over the past decade, coupled quantum systems have been under extensive study in the context of epitaxially grown quantum dots (QDs), but only a handful of examples have been reported with colloidal QDs. This is mostly due to the difficulties in controllably growing nanoparticles that encapsulate within them two dots separated by an energetic barrier via colloidal synthesis methods. Recent advances in colloidal synthesis methods have enabled the first clear demonstrations of colloidal double quantum dots and allowed for the first exploratory studies into their optical properties. Nevertheless, colloidal double QDs can offer an extended level of structural manipulation that allows not only for a broader range of materials to be used as compared with epitaxially grown counterparts but also for more complex control over the coupling mechanisms and coupling strength between two spatially separated quantum dots. The photophysics of these nanostructures is governed by the balance between two coupling mechanisms. The first is via dipole-dipole interactions between the two constituent components, leading to energy transfer between them. The second is associated with overlap of excited carrier wave functions, leading to charge transfer and multicarrier interactions between the two components. The magnitude of the coupling between the two subcomponents is determined by the detailed potential landscape within the nanocrystals (NCs). One of the hallmarks of double QDs is the observation of dual-color emission from a single nanoparticle, which allows for detailed spectroscopy of their properties down to the single particle level. Furthermore, rational design of the two coupled subsystems enables one to tune the emission statistics from single photon

  9. Design of a high-resolution high-stability positioning mechanism for crystal optics

    Energy Technology Data Exchange (ETDEWEB)

    Shu, D.; Toellner, T. S.; Alp, E. E.

    1999-10-11

    The authors present a novel miniature multi-axis driving structure that will allow positioning of two crystals with better than 50-nrad angular resolution and nanometer linear driving sensitivity.The precision and stability of this structure allow the user to align or adjust an assembly of crystals to achieve the same performance as does a single channel-cut crystal, so they call it an artificial channel-cut crystal. In this paper, the particular designs and specifications, as well as the test results,for a two-axis driving structure for a high-energy-resolution artificial channel-cut crystal monochromator are presented

  10. Influence of particle size on the low and high strain rate behavior of dense colloidal dispersions of nanosilica

    Science.gov (United States)

    Asija, Neelanchali; Chouhan, Hemant; Gebremeskel, Shishay Amare; Bhatnagar, Naresh

    2017-01-01

    Shear thickening is a non-Newtonian flow behavior characterized by the increase in apparent viscosity with the increase in applied shear rate, particularly when the shear rate exceeds a critical value termed as the critical shear rate (CSR). Due to this remarkable property of shear-thickening fluids (STFs), they are extensively used in hip protection pads, protective gear for athletes, and more recently in body armor. The use of STFs in body armor has led to the development of the concept of liquid body armor. In this study, the effect of particle size is explored on the low and high strain rate behavior of nanosilica dispersions, so as to predict the efficacy of STF-aided personal protection systems (PPS), specifically for ballistic applications. The low strain rate study was conducted on cone and plate rheometer, whereas the high strain rate characterization of STF was conducted on in-house fabricated split Hopkinson pressure bar (SHPB) system. Spherical nanosilica particles of three different sizes (100, 300, and 500 nm) as well as fumed silica particles of four different specific surface areas (Aerosil A-90, A-130, A-150, and A-200), respectively, were used in this study. The test samples were prepared by dispersing nanosilica particles in polypropylene glycol (PPG) using ultrasonic homogenization method. The low strain rate studies aided in determining the CSR of the synthesized STF dispersions, whereas the high strain rate studies explored the impact-resisting ability of STFs in terms of the impact toughness and the peak stress attained during the impact loading of STF in SHPB testing.

  11. Generalized colloidal synthesis of high-quality, two-dimensional cesium lead halide perovskite nanosheets and their applications in photodetectors

    Science.gov (United States)

    Lv, Longfei; Xu, Yibing; Fang, Hehai; Luo, Wenjin; Xu, Fangjie; Liu, Limin; Wang, Biwei; Zhang, Xianfeng; Yang, Dong; Hu, Weida; Dong, Angang

    2016-07-01

    All-inorganic cesium lead halide perovskite (CsPbX3, X = Cl, Br, and I) nanocrystals (NCs) are emerging as an important class of semiconductor materials with superior photophysical properties and wide potential applications in optoelectronic devices. So far, only a few studies have been conducted to control the shape and geometry of CsPbX3 NCs. Here we report a general approach to directly synthesize two-dimensional (2D) CsPbX3 perovskite and mixed perovskite nanosheets with uniform and ultrathin thicknesses down to a few monolayers. The key to the high-yield synthesis of perovskite nanosheets is the development of a new Cs-oleate precursor. The as-synthesized CsPbX3 nanosheets exhibit bright photoluminescence with broad wavelength tunability by composition modulation. The excellent optoelectronic properties of CsPbX3 nanosheets combined with their unique 2D geometry and large lateral dimensions make them ideal building blocks for building functional devices. To demonstrate their potential applications in optoelectronics, photodetectors based on CsPbBr3 nanosheets are fabricated, which exhibit high on/off ratios with a fast response time.All-inorganic cesium lead halide perovskite (CsPbX3, X = Cl, Br, and I) nanocrystals (NCs) are emerging as an important class of semiconductor materials with superior photophysical properties and wide potential applications in optoelectronic devices. So far, only a few studies have been conducted to control the shape and geometry of CsPbX3 NCs. Here we report a general approach to directly synthesize two-dimensional (2D) CsPbX3 perovskite and mixed perovskite nanosheets with uniform and ultrathin thicknesses down to a few monolayers. The key to the high-yield synthesis of perovskite nanosheets is the development of a new Cs-oleate precursor. The as-synthesized CsPbX3 nanosheets exhibit bright photoluminescence with broad wavelength tunability by composition modulation. The excellent optoelectronic properties of CsPbX3 nanosheets

  12. Colloidal metal oxide nanocrystals as charge transporting layers for solution-processed light-emitting diodes and solar cells.

    Science.gov (United States)

    Liang, Xiaoyong; Bai, Sai; Wang, Xin; Dai, Xingliang; Gao, Feng; Sun, Baoquan; Ning, Zhijun; Ye, Zhizhen; Jin, Yizheng

    2017-02-28

    Colloidal metal oxide nanocrystals offer a unique combination of excellent low-temperature solution processability, rich and tuneable optoelectronic properties and intrinsic stability, which makes them an ideal class of materials as charge transporting layers in solution-processed light-emitting diodes and solar cells. Developing new material chemistry and custom-tailoring processing and properties of charge transporting layers based on oxide nanocrystals hold the key to boosting the efficiency and lifetime of all-solution-processed light-emitting diodes and solar cells, and thereby realizing an unprecedented generation of high-performance, low-cost, large-area and flexible optoelectronic devices. This review aims to bridge two research fields, chemistry of colloidal oxide nanocrystals and interfacial engineering of optoelectronic devices, focusing on the relationship between chemistry of colloidal oxide nanocrystals, processing and properties of charge transporting layers and device performance. Synthetic chemistry of colloidal oxide nanocrystals, ligand chemistry that may be applied to colloidal oxide nanocrystals and chemistry associated with post-deposition treatments are discussed to highlight the ability of optimizing processing and optoelectronic properties of charge transporting layers. Selected examples of solution-processed solar cells and light-emitting diodes with oxide-nanocrystal charge transporting layers are examined. The emphasis is placed on the correlation between the properties of oxide-nanocrystal charge transporting layers and device performance. Finally, three major challenges that need to be addressed in the future are outlined. We anticipate that this review will spur new material design and simulate new chemistry for colloidal oxide nanocrystals, leading to charge transporting layers and solution-processed optoelectronic devices beyond the state-of-the-art.

  13. High-precision, high-throughput stability determinations facilitated by robotics and a semiautomated titrating fluorometer.

    Science.gov (United States)

    Edgell, Marshall Hall; Sims, Dorothy A; Pielak, Gary J; Yi, Fang

    2003-06-24

    The use of statistical modeling to test hypotheses concerning the determinants of protein structure requires stability data (e.g., the free energy of denaturation in H(2)O, DeltaG(HOH)) from hundreds of protein mutants. Fluorescence-monitored chemical denaturation provides a convenient method for high-precision, high-throughput DeltaG(HOH) determination. For eglin c we find that a throughput of about 20 min per protein can be attained in a two-channel semiautomated titrating fluorometer. We find also that the use of robotics for protein purification and preparation of the solutions for chemical denaturation gives highly precise DeltaG(HOH) values in which the standard deviation of values from multiple preparations (+/-0.051 kcal/mol) differs very little from multiple measurements from a single preparation (+/-0.040 kcal/mol). Since the variance introduced into model fitting by DeltaG(HOH) increases as the square of measurement error, there is a premium on precision. In fact, the fraction of stability behavior explicable by otherwise perfect models goes from 98% to only 50% over the error range commonly reported for chemical denaturation measurements (0.1-0.6 kcal/mol). We have found that the precision of chemical denaturation DeltaG(HOH) measurements depends most heavily on the precision of the instrument used, followed by protein purity and the capacity to precisely prepare the solutions used for titrations.

  14. Stabilized high-power laser system for the gravitational wave detector advanced LIGO.

    Science.gov (United States)

    Kwee, P; Bogan, C; Danzmann, K; Frede, M; Kim, H; King, P; Pöld, J; Puncken, O; Savage, R L; Seifert, F; Wessels, P; Winkelmann, L; Willke, B

    2012-05-07

    An ultra-stable, high-power cw Nd:YAG laser system, developed for the ground-based gravitational wave detector Advanced LIGO (Laser Interferometer Gravitational-Wave Observatory), was comprehensively characterized. Laser power, frequency, beam pointing and beam quality were simultaneously stabilized using different active and passive schemes. The output beam, the performance of the stabilization, and the cross-coupling between different stabilization feedback control loops were characterized and found to fulfill most design requirements. The employed stabilization schemes and the achieved performance are of relevance to many high-precision optical experiments.

  15. Colloidal Organolead Halide Perovskite with a High Mn Solubility Limit: A Step Toward Pb-Free Luminescent Quantum Dots.

    Science.gov (United States)

    Arunkumar, Paulraj; Gil, Kyeong Hun; Won, Seob; Unithrattil, Sanjith; Kim, Yoon Hwa; Kim, Ha Jun; Im, Won Bin

    2017-09-07

    Organolead halide perovskites have emerged as a promising optoelectronic material for lighting due to its high quantum yield, color-tunable, and narrow emission. Despite their unique properties, toxicity has intensified the search for ecofriendly alternatives through partial or complete replacement of lead. Herein, we report a room-temperature synthesized Mn(2+)-substituted 3D-organolead perovskite displacing ∼90% of lead, simultaneously retaining its unique excitonic emission, with an additional orange emission of Mn(2+) via energy transfer. A high Mn solubility limit of 90% was attained for the first time in lead halide perovskites, facilitated by the flexible organic cation (CH3NH3)(+) network, preserving the perovskite structure. The emission intensities of the exciton and Mn were influenced by the halide identity that regulates the energy transfer to Mn. Homogeneous emission and electron spin resonance characteristics of Mn(2+) indicate a uniform distribution of Mn. These results suggest that low-toxicity 3D-CH3NH3Pb1-xMnxBr3-(2x+1)Cl2x+1 nanocrystals may be exploited as magnetically doped quantum dots with unique optoelectronic properties.

  16. Theory and methods of global stability analysis for high arch dam

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    The global stability of high arch dam is one of the key problems in the safety study of arch dams,but no feasible method with theoretical basis is available.In this paper,based on the stability theory of mechanical system,it is demonstrated that the global failure of high arch dams belongs to a physical instability starting from local strength failure,which is the extreme point instability according to the characteristics of load-displacement curve obtained from the failure process of dam-foundation system. So the global failure of dam-foundation system should be studied with the stability theory of mechanical system.It is also pointed out that the current stability analysis methods used in engineering are consistent with the stability theory,but not established according to the mechanical system stability theory directly.A perfect method can be obtained through the study of physical disturbance equations.

  17. Quantification and Composition Analysis of Small Mobile Colloids from Different Aquatic Ecosystem

    Science.gov (United States)

    Yan, Jing; Lazouskaya, Volha; Jin, Yan

    2014-05-01

    Natural colloids, often defined as entities with sizes stream water and groundwater samples. Colloids of various size fractions are separated using centrifugation or membrane filters and quantified gravimetrically and characterized using SEM or TEM with XEDs to analyze the morphology and compositions of colloidal organo-mineral associations. Preliminary results based on stream water at base flow, during storm event and wetland soil water showed that, in general, small natural colloids (0.1 - 0.45 µm or 0.2 - 0.4 µm) contribute significantly to the whole colloidal pools (stream order, precipitation time and intensity, and redox conditions. In this presentation, we will present results on quantification and characterization of mobile colloids from field samples and factors that control their mobilization and stabilization, and their role in carbon and phosphorus fate and transport.

  18. Fabrication of anisotropic multifunctional colloidal carriers

    Science.gov (United States)

    Jerri, Huda A.

    The field of colloidal assembly has grown tremendously in recent years, although the direct or template-assisted methods used to fabricate complex colloidal constructions from monodisperse micro- and nanoparticles have been generally demonstrated on model materials. In this work, novel core particle syntheses, particle functionalizations and bottom-up assembly techniques are presented to create functional colloidal devices. Using particle lithography, high-information colloidal vectors have been developed and modified with imaging and targeting agents. Localized nanoscale patches have been reliably positioned on microparticles to serve as foundations for further chemical or physical modifications. Site-specific placement of RGD targeting ligands has been achieved in these lithographed patches. Preferential uptake of these targeted vectors by RGD-specific 3T3 fibroblasts was verified using confocal laser scanning microscopy. A transition was made from the functionalization of model imaging core particles to the lithography of colloidal cartridges, in an effort to construct colloidal syringes with specialized, programmable release profiles. A variety of functional, pH-sensitive fluorescent cores were engineered to respond to solution conditions. When triggered, the diverse composite core microparticles and reservoir microcapsules released embedded fluorescent moieties such as dye molecules, and fluorophore-conjugated nanoparticles. The microcapsules, created using layer-by-layer polyelectrolyte deposition on sacrificial templates, were selectively modified with a robust coating. The pH-responsive anisotropic reservoir microcapsules were extremely stable in solution, and exhibited a "Lazarus" functionality of rehydrating to their original state following desiccation. A snapshot of focused-release of core constituents through the lone opening in colloidal monotremes has been obtained by anisotropically-functionalizing degradable cores with barrier shells. Additionally

  19. Fractal nematic colloids

    Science.gov (United States)

    Hashemi, S. M.; Jagodič, U.; Mozaffari, M. R.; Ejtehadi, M. R.; Muševič, I.; Ravnik, M.

    2017-01-01

    Fractals are remarkable examples of self-similarity where a structure or dynamic pattern is repeated over multiple spatial or time scales. However, little is known about how fractal stimuli such as fractal surfaces interact with their local environment if it exhibits order. Here we show geometry-induced formation of fractal defect states in Koch nematic colloids, exhibiting fractal self-similarity better than 90% over three orders of magnitude in the length scales, from micrometers to nanometres. We produce polymer Koch-shaped hollow colloidal prisms of three successive fractal iterations by direct laser writing, and characterize their coupling with the nematic by polarization microscopy and numerical modelling. Explicit generation of topological defect pairs is found, with the number of defects following exponential-law dependence and reaching few 100 already at fractal iteration four. This work demonstrates a route for generation of fractal topological defect states in responsive soft matter. PMID:28117325

  20. Fractal nematic colloids

    Science.gov (United States)

    Hashemi, S. M.; Jagodič, U.; Mozaffari, M. R.; Ejtehadi, M. R.; Muševič, I.; Ravnik, M.

    2017-01-01

    Fractals are remarkable examples of self-similarity where a structure or dynamic pattern is repeated over multiple spatial or time scales. However, little is known about how fractal stimuli such as fractal surfaces interact with their local environment if it exhibits order. Here we show geometry-induced formation of fractal defect states in Koch nematic colloids, exhibiting fractal self-similarity better than 90% over three orders of magnitude in the length scales, from micrometers to nanometres. We produce polymer Koch-shaped hollow colloidal prisms of three successive fractal iterations by direct laser writing, and characterize their coupling with the nematic by polarization microscopy and numerical modelling. Explicit generation of topological defect pairs is found, with the number of defects following exponential-law dependence and reaching few 100 already at fractal iteration four. This work demonstrates a route for generation of fractal topological defect states in responsive soft matter.

  1. Oxygen-Deficient TiO2 - x/Methylene Blue Colloids: Highly Efficient Photoreversible Intelligent Ink.

    Science.gov (United States)

    Imran, M; Yousaf, Ammar B; Zhou, Xiao; Liang, Kuang; Jiang, Yi-Fan; Xu, An-Wu

    2016-09-06

    Oxygen-sensitive photoreversible intelligent ink capable of assessment with the human eye is an ongoing demand in the modern era. In the food industry, redox-dye-based oxygen indicator films have been proposed, but the leaching of dyes from the film that contaminates the food is one unsolved issue. On the other hand, it is also highly desirable to develop rewritable paper that significantly reduces the pressure on modern society for the production and consumption of paper. Herein, we have developed an oxygen-deficient TiO2 - x/methylene blue (MB) sol without relying on external sacrificial electron donors (SEDs) for photoreversible color switching. Oxygen vacancies in TiO2 - x can work as electron donor to favor the adsorption of the substrate and improve the charge separation that is required for the redox-based color-switching system. The problems of rewriteable paper and food packaging are addressed as two sides of a single coin in this article. We have used hydroxyethyl cellulose (HEC) for rewritable paper that can significantly delay the oxidation of leuco-MB (LMB) through hydrogen bonding and retain the printed information for a long time. The dye leaching from oxygen indicator films is also significantly reduced (only 1.54%) by using furcelleran as the coating polymer that is extracted from edible red seaweed.

  2. Colloid and Phosphorus Leaching From Undisturbed Soil Cores Sampled Along a Natural Clay Gradient

    DEFF Research Database (Denmark)

    Vendelboe, Anders Lindblad; Møldrup, Per; Heckrath, Goswin Johann;

    2011-01-01

    The presence of strongly sorbing compounds in groundwater and tile drains can be a result of colloid-facilitated transport. Colloid and phosphorus leaching from macropores in undisturbed soil cores sampled across a natural clay gradient at Aarup, Denmark, were studied. The aim of the study...... was to correlate easily measurable soil properties, such as clay content and water-dispersible colloids, to colloid and phosphorus leaching. The clay contents across the gradient ranged from 0.11 to 0.23 kg kgj1. Irrigating with artificial rainwater, all samples showed a high first flush of colloids and phosphorus...

  3. Colloid and phosphorus leaching from undisturbed soil cores sampled along a natural clay gradient

    DEFF Research Database (Denmark)

    Vendelboe, Anders Lindblad; Møldrup, Per; Heckrath, Goswin Johann

    2011-01-01

    was to correlate easily measurable soil properties, such as clay content and water-dispersible colloids, to colloid and phosphorus leaching. The clay contents across the gradient ranged from 0.11 to 0.23 kg kgj1. Irrigating with artificial rainwater, all samples showed a high first flush of colloids and phosphorus...... and the so-called degree of P saturation (oxalate-extractable P on iron and aluminum minerals). Because higher colloidal P concentration was countered by a lower colloidal leaching, the total amount of leached P stayed remarkably constant along the natural clay gradient....

  4. Stability condition of FAST TCP in high speed network Oil the basis of control theory

    Institute of Scientific and Technical Information of China (English)

    Zhao Fuzhe; Zhou Jianzhong; Luo Zhimeng; Xiao Yang

    2008-01-01

    Considering the instability of data transferred existing in high speed network.a near method is proposed for improving the stability using control theory.Under this method,the mathematical model of such a network is established.Stability condition is derived from the mathematical model.Several sivaulation experiments are performed.The results show that the method can increase the stability of data transferred in terms of the congestion window,queue size,and sending rate of the source.

  5. A silica long base tiltmeter with high stability and resolution.

    Science.gov (United States)

    Boudin, F; Bernard, P; Longuevergne, L; Florsch, N; Larmat, C; Courteille, C; Blum, P-A; Vincent, T; Kammentaler, M

    2008-03-01

    In order to be able to provide valuable data in multiparameter measurement field operations, tiltmeters need to have a noise level better or equal than 10(-9) rad for a period range from a few minutes to a few years and a long term stability ranging from 10(-7) to 10(-8) rad/yr. Tiltmeter measurements should also be as much as possible insensitive to thermal disturbances, by taking great care of the horizontality of the base line tube first. Secondly, thermal responses have been assessed. We also took great care of the coupling of our tiltmeters with the bedrock. We've designed a long base tiltmeter with sensors in silica which has a low dilatation coefficient. The linear variable displacement transducer is based on coil coupling (powered by an alternative voltage). Finally we show the results of two 100 m silica water tube tiltmeters which were installed in a mine in the French Vosges massif in the framework of a hydrology research project. These instruments show a remarkably good stability (6.5x10(-9) rad/month) and a low noise level (of the order of 10(-11) rad). Toroidal and spheroidal free modes of the Earth were observed after the two last major earthquakes on Sumatra.

  6. Structural stability of methane hydrate at high pressures

    Science.gov (United States)

    Shu, J.; Chen, X.; Chou, I.-Ming; Yang, W.; Hu, Jiawen; Hemley, R.J.; Mao, Ho-kwang

    2011-01-01

    The structural stability of methane hydrate under pressure at room temperature was examined by both in-situ single-crystal and powder X-ray diffraction techniques on samples with structure types I, II, and H in diamond-anvil cells. The diffraction data for types II (sII) and H (sH) were refined to the known structures with space groups Fd3m and P63/mmc, respectively. Upon compression, sI methane hydrate transforms to the sII phase at 120 MPa, and then to the sH phase at 600 MPa. The sII methane hydrate was found to coexist locally with sI phase up to 500 MPa and with sH phase up to 600 MPa. The pure sH structure was found to be stable between 600 and 900 MPa. Methane hydrate decomposes at pressures above 3 GPa to form methane with the orientationally disordered Fm3m structure and ice VII (Pn3m). The results highlight the role of guest (CH4)-host (H2O) interactions in the stabilization of the hydrate structures under pressure. ?? 2011, China University of Geosciences (Beijing) and Peking University. Production and hosting by Elsevier B.V. All rights reserved.

  7. Flocking ferromagnetic colloids

    Science.gov (United States)

    Kaiser, Andreas; Snezhko, Alexey; Aranson, Igor S.

    2017-01-01

    Assemblages of microscopic colloidal particles exhibit fascinating collective motion when energized by electric or magnetic fields. The behaviors range from coherent vortical motion to phase separation and dynamic self-assembly. Although colloidal systems are relatively simple, understanding their collective response, especially under out-of-equilibrium conditions, remains elusive. We report on the emergence of flocking and global rotation in the system of rolling ferromagnetic microparticles energized by a vertical alternating magnetic field. By combing experiments and discrete particle simulations, we have identified primary physical mechanisms, leading to the emergence of large-scale collective motion: spontaneous symmetry breaking of the clockwise/counterclockwise particle rotation, collisional alignment of particle velocities, and random particle reorientations due to shape imperfections. We have also shown that hydrodynamic interactions between the particles do not have a qualitative effect on the collective dynamics. Our findings shed light on the onset of spatial and temporal coherence in a large class of active systems, both synthetic (colloids, swarms of robots, and biopolymers) and living (suspensions of bacteria, cell colonies, and bird flocks). PMID:28246633

  8. Differentiation of colloidal and dissolved silica: Analytical separation using spectrophotometry and inductively coupled plasma atomic emission spectrometry

    Science.gov (United States)

    Lewis-Russ, A.; Ranville, J.; Kashuba, A.T.

    1991-01-01

    A method is described that differentiates between solutions containing silica-dominated colloids and solutions that are essentially free of colloids. Suspensions of tuff particles were treated to remove colloids by centrifugation, filtration or both. Agreement of silica concentrations determined by inductively coupled plasma atomic emission spectrometry and by a spectrophotometric method was taken as an indication of colloid-free solutions. For two tuffs, centrifugation was effective for removing colloids. For the third, highly altered tuff, filtration was more effective for removing colloids.

  9. Patchy particles made by colloidal fusion.

    Science.gov (United States)

    Gong, Zhe; Hueckel, Theodore; Yi, Gi-Ra; Sacanna, Stefano

    2017-09-18

    Patches on the surfaces of colloidal particles provide directional information that enables the self-assembly of the particles into higher-order structures. Although computational tools can make quantitative predictions and can generate design rules that link the patch motif of a particle to its internal microstructure and to the emergent properties of the self-assembled materials, the experimental realization of model systems of particles with surface patches (or 'patchy' particles) remains a challenge. Synthetic patchy colloidal particles are often poor geometric approximations of the digital building blocks used in simulations and can only rarely be manufactured in sufficiently high yields to be routinely used as experimental model systems. Here we introduce a method, which we refer to as colloidal fusion, for fabricating functional patchy particles in a tunable and scalable manner. Using coordination dynamics and wetting forces, we engineer hybrid liquid-solid clusters that evolve into particles with a range of patchy surface morphologies on addition of a plasticizer. We are able to predict and control the evolutionary pathway by considering surface-energy minimization, leading to two main branches of product: first, spherical particles with liquid surface patches, capable of forming curable bonds with neighbouring particles to assemble robust supracolloidal structures; and second, particles with a faceted liquid compartment, which can be cured and purified to yield colloidal polyhedra. These findings outline a scalable strategy for the synthesis of patchy particles, first by designing their surface patterns by computer simulation, and then by recreating them in the laboratory with high fidelity.

  10. DNA- and AC electric field-assisted assembly of two-dimensional colloidal photonic crystals and their controlled defect insertion

    Science.gov (United States)

    Kim, Sejong

    Photonic crystals (PC) are structures in which the refractive index is a periodic function in space. The ability of photonic crystals to localize and manipulate electromagnetic waves has attracted considerable attention from the scientific community. The self-assembly of monodisperse micrometer scale colloidal spheres into hexagonal closed-packed colloidal crystals provides a simple, fast, and cheap materials chemistry approach to PCs. Employing DNA supramolecular recognition, 2-dimensional (2D) photonic crystal monolayer was fabricated with monodisperse polystyrene colloidal microspheres. Amine-terminated DNA oligomers were covalently attached onto carboxy-decorated microspheres and enabled their DNA-functionalization while preserving their colloidal stability and organization properties. Following a capillary-force-assisted organization of DNA-decorated microspheres into close-packed 2D opaline arrays, the first monolayer was immobilized by DNA hybridization. Insertion of vacancies at predetermined sites within the lattice of colloidal crystals is a prerequisite in order to realize high-quality, opaline-based photonic devices. The previously obtained DNA-hybridization type binding of 2D-opaline arrays provides a heat-sensitive "adhesive" between substrate and microspheres within a surrounding aqueous medium that enables tuning the hybridization strength of DNA linker as well as a mechanism to facilitate the removal of unbound microspheres. Focusing a laser beam onto a single microsphere of the opaline array induces localized heating that enables the microsphere to detach, leaving behind vacancies. By repeating this process, line vacancies were successfully obtained. The effects of salt concentration, laser power, light-absorbing dyes, DNA length and refractive index mismatch were investigated and found to correlate with heat-induced DNA dehybridization. In addition, AC (alternating current) electrokinetic force was also utilized to obtain assembly of colloidal

  11. A High Reliability Frequency Stabilized Semiconductor Laser Source Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Ultrastable, narrow linewidth, high reliability MOPA sources are needed for high performance LIDARs in NASA for, wind speed measurement, surface topography and earth...

  12. On the Potential Origins of the High Stability of Reconstructed Ancestral Proteins.

    Science.gov (United States)

    Trudeau, Devin L; Kaltenbach, Miriam; Tawfik, Dan S

    2016-10-01

    Ancestral reconstruction provides instrumental insights regarding the biochemical and biophysical characteristics of past proteins. A striking observation relates to the remarkably high thermostability of reconstructed ancestors. The latter has been linked to high environmental temperatures in the Precambrian era, the era relating to most reconstructed proteins. We found that inferred ancestors of the serum paraoxonase (PON) enzyme family, including the mammalian ancestor, exhibit dramatically increased thermostabilities compared with the extant, human enzyme (up to 30 °C higher melting temperature). However, the environmental temperature at the time of emergence of mammals is presumed to be similar to the present one. Additionally, the mammalian PON ancestor has superior folding properties (kinetic stability)-unlike the extant mammalian PONs, it expresses in E. coli in a soluble and functional form, and at a high yield. We discuss two potential origins of this unexpectedly high stability. First, ancestral stability may be overestimated by a "consensus effect," whereby replacing amino acids that are rare in contemporary sequences with the amino acid most common in the family increases protein stability. Comparison to other reconstructed ancestors indicates that the consensus effect may bias some but not all reconstructions. Second, we note that high stability may relate to factors other than high environmental temperature such as oxidative stress or high radiation levels. Foremost, intrinsic factors such as high rates of genetic mutations and/or of transcriptional and translational errors, and less efficient protein quality control systems, may underlie the high kinetic and thermodynamic stability of past proteins.

  13. Assembly of Colloidal Materials Using Bioadhesive Interactions

    Science.gov (United States)

    Hammer, Daniel A.; Hiddessen, Amy L.; Tohver, Valeria; Crocker, John C.; Weitz, David A.

    2002-01-01

    We have pursued the use of biological crosslinking molecules of several types to make colloidal materials at relatively low volume fraction of colloidal particles. The objective is to make binary alloys of colloidal particles, made of two different colloidal particles coated with complementary biological lock-and-key binding molecules, which assemble due to the biological specificity. The long-term goal is to use low affinity lock-and-key biological interactions, so that the can anneal to form crystalline states. We have used a variety of different surface chemistries in order to make colloidal materials. Our first system involved using selectin-carbohydrate (sialyl-Lewis) interactions; this chemistry is derived from immune system. This chemical interaction is of relatively low affinity, with timescales for dissociation of several seconds. Furthermore, the adhesion mediated by these molecules can be reversed by the chelation of calcium atoms; thus assembled structures can be disassembled reversibly. Our second system employed avidin-biotin chemistry. This well-studied system is of high affinity, and is generally irreversible on a laboratory time-scale. Thus, we would expect selectin-carbohydrate interactions at high molecular density and avidin-biotin interactions to give kinetically-trapped structures; however, at low densities, we would expect significant differences in the structure and dynamics of the two materials, owing to their very different release rates. We have also begun to use a third chemistry - DNA hybridization. By attaching single stranded DNA oligonucleotide chains to beads, we can drive the assembly of colloidal materials by hybridization of complementary DNA chains. It is well known that DNA adenosine-thymine (A-T) and guanine-cytosine (G-C) bases hybridize pairwise with a Gibbs free energy change of 1.7 kcal/mol per base; thus, the energy of the assembly can be modulated by altering the number of complementary bases in the DNA chains. Using

  14. Formation of Negatively Charged AgI Colloid Nanoparticles by Condensation

    OpenAIRE

    Kalniņa, D; Gross, K; Medvids, A.; Onufrijevs, P.

    2015-01-01

    The stability of silver halide colloids is reported to be important for the toxicological outcome. This study shows a well-suited and cheap condensation reaction to obtain negatively charged silver iodide (AgI) nanoparticles without additional stabilization agents. Charged AgI colloids were synthesized from silver nitrate and potassium iodide solutions. An excess of potassium iodide not only imparted a negative charge, but provided a narrow particle size distribution (50 ± 10 n...

  15. Designing Zirconium Coated Polystyrene Colloids and Application

    Directory of Open Access Journals (Sweden)

    Diana Chira

    2009-01-01

    Full Text Available A simple technique has been developed to prepare core colloids that are modified using zirconium oxychloride, based on heating a solution of core colloid composites, consisting of poly (ethylenimine (PEI and zirconium oxychloride. The interaction of zirconium oxychloride with the polystyrene (PS core colloids has been investigated using Fourier transform-infrared spectroscopy (FT-IR, energy dispersive X-ray spectroscopy (EDX, and scanning electron microscopy (SEM data. FT-IR studies confirm the occurrence of amine groups present in PEI which are oxidized to carboxyl groups after the reaction. The EDX data and the SEM images confirm the presence of zirconium particles immobilized on the polystyrene surfaces. Demeton, a highly toxic nerve agent, was used due to its ability to easily bind through its organophosphate group illustrating a practical application of the PS-PEI-Zr particles. Attenuated Total Reflection (ATR Spectroscopy was used to assess the interactions between the toxic nerve agent demeton-S and the PS-PEI-Zr particles. The results show that the presented technique for coating polystyrene core colloids with zirconium was successfully accomplished, and the newly formed particles easily bond with demeton agents through the P=O functional group.

  16. Highly Emissive Divalent-Ion-Doped Colloidal CsPb1–xMxBr3 Perovskite Nanocrystals through Cation Exchange

    Science.gov (United States)

    2017-01-01

    Colloidal CsPbX3 (X = Br, Cl, and I) perovskite nanocrystals (NCs) have emerged as promising phosphors and solar cell materials due to their remarkable optoelectronic properties. These properties can be tailored by not only controlling the size and shape of the NCs but also postsynthetic composition tuning through topotactic anion exchange. In contrast, property control by cation exchange is still underdeveloped for colloidal CsPbX3 NCs. Here, we present a method that allows partial cation exchange in colloidal CsPbBr3 NCs, whereby Pb2+ is exchanged for several isovalent cations, resulting in doped CsPb1–xMxBr3 NCs (M= Sn2+, Cd2+, and Zn2+; 0 50%), sharp absorption features, and narrow emission of the parent CsPbBr3 NCs. The blue-shift in the optical spectra is attributed to the lattice contraction that accompanies the Pb2+ for M2+ cation exchange and is observed to scale linearly with the lattice contraction. This work opens up new possibilities to engineer the properties of halide perovskite NCs, which to date are demonstrated to be the only known system where cation and anion exchange reactions can be sequentially combined while preserving the original NC shape, resulting in compositionally diverse perovskite NCs. PMID:28260380

  17. Highly bioactive nano-hydroxyapatite/partially stabilized zirconia ceramics

    Institute of Scientific and Technical Information of China (English)

    WANG Qing-liang; GE Shi-rong; ZHANG De-kun

    2004-01-01

    Nanocrystalline hydroxyapatite (HA) powders have been synthesized by precipitation using Ca(NO3)2.4H2O and (NH4)2 HPO4 at room temperature and atmospheric pressure. Nanocomposites of HA and partially stabilized zirconia (HA/PSZ) were sintered at atmospheric pressure and 1300℃ for 2h in air. The preparation techniques, structure and mechanical properties of these materials were characterized. The addition of nanosized PSZ reinforcing phase to HA may lead to an improvement of the macro and micro mechanical properties and not affect its biocompatibility and bioactivity. The bending strength, fracture toughness and nano-hardness were near to or greater than those for human cortical bone and human tooth (dentine and enamel). The composite was incubated in a fresh human plasma which confirmed the bioactivity of nanosized HA/PSZ materials. The bonding reaction between HA/PSZ ceramic and the plasma proteins was found, and hematopoietic cell phosphatase (HCP) layers formed on surface of each composite incubated in human plasma for two weeks.The diameter of a single HCP globule was less than 100 nm. Furthermore, the precipitating mechanism investigation was carried out through a comparative experiment in this paper.

  18. High-precision temperature control and stabilization using a cryocooler.

    Science.gov (United States)

    Hasegawa, Yasuhiro; Nakamura, Daiki; Murata, Masayuki; Yamamoto, Hiroya; Komine, Takashi

    2010-09-01

    We describe a method for precisely controlling temperature using a Gifford-McMahon (GM) cryocooler that involves inserting fiber-reinforced-plastic dampers into a conventional cryosystem. Temperature fluctuations in a GM cryocooler without a large heat bath or a stainless-steel damper at 4.2 K are typically of the order of 200 mK. It is particularly difficult to control the temperature of a GM cryocooler at low temperatures. The fiber-reinforced-plastic dampers enabled us to dramatically reduce temperature fluctuations at low temperatures. A standard deviation of the temperature fluctuations of 0.21 mK could be achieved when the temperature was controlled at 4.200 0 K using a feedback temperature control system with two heaters. Adding the dampers increased the minimum achievable temperature from 3.2 to 3.3 K. Precise temperature control between 4.200 0 and 300.000 K was attained using the GM cryocooler, and the standard deviation of the temperature fluctuations was less than 1.2 mK even at 300 K. This technique makes it possible to control and stabilize the temperature using a GM cryocooler.

  19. Gas Electron Multiplier detectors with high reliability and stability

    CERN Document Server

    Ovchinnikov, B M; Ovchinnikov, Yu B

    2010-01-01

    The Gas Electron Multiplier detectors with wire and metallic electrodes, with a gas filling in the gap between them were proposed and tested. The main advantage of these Gas Electron Multipliers compared to standard ones consists in their increased stability and reliability. The experimental results on testing of such detectors with gaps between the electrodes of 1 and 3 mm are reported. It is demonstrated, that the best gas filling for the gas electron multipliers is neon with small admixture of quenching gases (for example, (N2+H2O) at ~100ppm). This filling offers the greatest coefficient of proportional multiplication as compared with other gases, at small electric potential difference between the GEM electrodes, in absence of streamer discharges in the proportional region. The results on operation of the multi-channel gas electron multiplier with wire cathode and continuous anode filled with Ne, Ar, Ar+CH4 and Ar+1%Xe are presented also. Based on the experimental observations, the explanation of the mech...

  20. Stability of numerous novel potassium chlorides at high pressure

    Science.gov (United States)

    Zhang, Weiwei; Oganov, Artem R.; Zhu, Qiang; Lobanov, Sergey S.; Stavrou, Elissaios; Goncharov, Alexander F.

    2016-05-01

    K-Cl is a simple system displaying all four main types of bonding, as it contains (i) metallic potassium, (ii) elemental chlorine made of covalently bonded Cl2 molecules held together by van der Waals forces, and (iii) an archetypal ionic compound KCl. The charge balance rule, assigning classical charges of “+1” to K and “‑1” to Cl, predicts that no compounds other than KCl are possible. However, our quantum-mechanical variable-composition evolutionary simulations predict an extremely complex phase diagram, with new thermodynamically stable compounds K3Cl, K2Cl, K3Cl2, K4Cl3, K5Cl4, K3Cl5, KCl3 and KCl7. Of particular interest are 2D-metallic homologs Kn+1Cln, the presence of positively charged Cl atoms in KCl7, and the predicted stability of KCl3 already at nearly ambient pressures at zero Kelvin. We have synthesized cubic -KCl3 at 40–70 GPa and trigonal -KCl3 at 20–40 GPa in a laser-heated diamond anvil cell (DAC) at temperature exceeding 2000 K from KCl and Cl2. These phases were identified using in situ synchrotron X-ray diffraction and Raman spectroscopy. Upon unloading to 10 GPa, -KCl3 transforms to a yet unknown structure before final decomposition to KCl and Cl2 at near-ambient conditions.

  1. Stability of Dy{sub 6}UO{sub 12} under high pressure and high temperature

    Energy Technology Data Exchange (ETDEWEB)

    Shukla, Balmukund; Sanjay Kumar, N.R.; Sekar, M. [Condensed Matter Physics Division, Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102 Tamil Nadu (India); Chandra Shekar, N.V., E-mail: chandru@igcar.gov.in [Condensed Matter Physics Division, Materials Science Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102 Tamil Nadu (India); Jena, H.; Asuvathraman, R. [Materials Chemistry Division, Chemistry Group, Indira Gandhi Centre for Atomic Research, Kalpakkam, 603102 Tamil Nadu (India)

    2016-07-05

    In this paper, results obtained from high pressure-high temperature X-ray diffraction study of Dy{sub 6}UO{sub 12} are reported. X-ray diffraction (XRD) studies at ambient temperature on Dy{sub 6}UO{sub 12} reveals that the rhombohedral structure is stable up to 21.6 GPa. Beyond 21.6 GPa the peaks broaden out substantially indicating emergence of disorder in the system. Bulk modulus and its pressure derivative is 144 GPa and 7.0 respectively. High Pressure and High Temperature (HP-HT) XRD studies up to ∼ 11 GPa and ∼673 K was carried out using novel combination of membrane cell DAC coupled to a high flux micro-focus X-ray generator. At ambient pressure, thermal expansion coefficient comes out to be 14.5 × 10{sup −6} K{sup −1} at 400 K. Further, at 1 GPa and 2.6 GPa the thermal expansion coefficients are 21.4 × 10{sup −6} K{sup −1} and 32 × 10{sup −6} K{sup −1} respectively, in the temperature range ∼293–673 K. The thermal expansion coefficient shows an increasing trend with pressure. - Highlights: • First report on high pressure-high temperature (HP-HT) structural study of Dy{sub 6}UO{sub 12}. • HP studies show structural stability up to 21 GPa in rhombohedral structure. • Pressure induced structural disorder seen above 21 GPa. • HP-HT studies show that Dy{sub 6}UO{sub 12} remains stable up to 11.3 GPa and ∼673 K. • The thermal expansion coefficients increase with pressure.

  2. On the observation of the need for an unusually high concentration of cysteine and homocysteine to induce aggregation of polymer-stabilized gold nano particles

    Energy Technology Data Exchange (ETDEWEB)

    Radhakumary, C.; Sreenivasan, K., E-mail: sreeni@sctimst.ac.in [Sree Chitra Tirunal Institute for Medical Sciences and Technology, Laboratory for Polymer Analysis, Biomedical Technology Wing (India)

    2013-02-15

    This study reports the interaction of chitosan-stabilized gold nanoparticles (CH-AuNPs) with cysteine (Cys) and homocysteine (Hcys) in aqueous media at pH 1.4. Since the polymer precipitates at higher pH, and the amino acids Cys and HCys are soluble at acidic pH, we kept the pH around 1.4 for stabilizing the particles. Zeta potential of CH-AuNPs was found to be positive and it is reasonable to assume that +ve Cys or Hcys at pH 1.4 will experience repulsive force. However, TEM images and absorption spectra indicated formation of aggregates including rod-like assembly. An interesting observation was the need for unusually high concentration of analytes (Cys and Hcys) to induce the assembly of CH-AuNPs. We also found time bound variation of the optical properties probably indicating the interaction is kinetically controlled and only a fraction of the analyte molecules having sufficient energy can bind onto the particles. We observed that at elevated temperature, the reaction was faster with a lower concentration of Cys or Hcys. These observations were supported by the classical Derjaguin-Landau-Verwey-Overbeek (DLVO) theory which describes the interparticle interaction and the colloidal stability in solution. Only molecules possessing enough energy to cross this force barrier can cause the aggregation. We also noted a time lag between Cys and Hcys to influence optical properties reflecting the possibility of using this simple approach to discriminate these two clinically relevant molecules. Our observation shows that simple sensing as well as generation of novel nanostructures could be manipulated by a judicious choice of conditions such as stabilizing agents, pH, etc.Graphical AbstractMore energetic ones cross the barrier to induce aggregation.

  3. Space-Qualifiable High Reliability Frequency-Stabilized CW Laser Source Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose the development and space qualification of a high reliability frequency-stabilized CW laser source at 1064 nm wavelength region to satisfy the...

  4. Space-Qualifiable High Reliability Frequency-Stabilized CW Laser Source Project

    Data.gov (United States)

    National Aeronautics and Space Administration — We propose the SBIR Phase II effort to develop and space-qualify a 1.06 micron high reliability frequency-stabilized CW laser source that fully satisfies the...

  5. Twin stability in highly nanotwinned Cu under compression, torsion and tension

    DEFF Research Database (Denmark)

    Hodge, A.M.; Furnish, T.A.; Shute, C.J.;

    2012-01-01

    Twin stability under four distinct mechanical loading states has been investigated for highly nanotwinned Cu containing parallel nanotwins 40 nm thick. Observed deformation-induced microstructural changes under tension, compression, tension–tension fatigue and torsion are qualitatively compared...

  6. Marine phages as excellent tracers for reactive colloidal transport in porous media

    Science.gov (United States)

    Ghanem, Nawras; Chatzinotas, Antonis; Harms, Hauke; Wick, Lukas Y.

    2016-04-01

    Question: Here we evaluate marine phages as specific markers of hydrological flow and reactive transport of colloidal particles in the Earth's critical zone (CZ). Marine phages and their bacterial hosts are naturally absent in the CZ, and can be detected with extremely high sensitivity. In the framework of the DFG Collaborative Research Center AquaDiva, we asked the following questions: (1) Are marine phages useful specific markers of hydrological flow and reactive transport in porous media? and (2) Which phage properties are relevant drivers for the transport of marine phages in porous media? Methods: Seven marine phages from different families (as well two commonly used terrestrial phages) were selected based on their morphology, size and physico-chemical surface properties (surface charge and hydrophobicity). Phage properties were assessed by electron microscopy, dynamic light scattering and water contact angle analysis (CA). Sand-filled laboratory percolation columns were used to study transport. The breakthrough curves of the phages were analyzed using the clean bed filtration theory and the XDLVO theory of colloid stability, respectively. Phages were quantified by a modified high- throughput plaque assay and a culture-independent particle counting method approach. Results: Our data show that most marine tested phages exhibited highly variable transport rates and deposition efficiency, yet generally high colloidal stability and viability. We find that size, morphology and hydrophobicity are key factors shaping the transport efficiency of phages. Differing deposition efficiencies of the phages were also supported by calculated XDLVO interaction energy profile. Conclusion: Marine phages have a high potential for the use as sensitive tracers in terrestrial habitats with their surface properties playing a crucial role for their transport. Marine phages however, exhibit differences in their deposition efficiency depending on their morphology, hydrophobicity and

  7. Colloidal QDs-polymer nanocomposites

    Science.gov (United States)

    Gordillo, H.; Suárez, I.; Rodríguez-Cantó, P.; Abargues, R.; García-Calzada, R.; Chyrvony, V.; Albert, S.; Martínez-Pastor, J.

    2012-04-01

    Nanometer-size colloidal semiconductor nanocrystals, or Quantum Dots (NQD), are very prospective active centers because their light emission is highly efficient and temperature-independent. Nanocomposites based on the incorporation of QDs inside a polymer matrix are very promising materials for application in future photonic devices because they combine the properties of QDs with the technological feasibility of polymers. In the present work some basic applications of these new materials have been studied. Firstly, the fabrication of planar and linear waveguides based on the incorporation of CdS, CdSe and CdTe in PMMA and SU-8 are demonstrated. As a result, photoluminescence (PL) of the QDs are coupled to a waveguide mode, being it able to obtain multicolor waveguiding. Secondly, nanocomposite films have been evaluated as photon energy down-shifting converters to improve the efficiency of solar cells.

  8. Adaptive Finite-Time Stabilization of High-Order Nonlinear Systems with Dynamic and Parametric Uncertainties

    Directory of Open Access Journals (Sweden)

    Meng-Meng Jiang

    2016-01-01

    Full Text Available Under the weaker assumption on nonlinear functions, the adaptive finite-time stabilization of more general high-order nonlinear systems with dynamic and parametric uncertainties is solved in this paper. To solve this problem, finite-time input-to-state stability (FTISS is used to characterize the unmeasured dynamic uncertainty. By skillfully combining Lyapunov function, sign function, backstepping, and finite-time input-to-state stability approaches, an adaptive state feedback controller is designed to guarantee high-order nonlinear systems are globally finite-time stable.

  9. Polymers and colloids

    Energy Technology Data Exchange (ETDEWEB)

    Schurtenberger, P. [ETH Zurich, Inst. fuer Polymere, Zurich (Switzerland)

    1996-11-01

    A wealth of structural information from colloid and polymer solutions on a large range of length scales can be obtained using small angle neutron scattering (SANS) experiments. After a general introduction to the field of soft condensed matter, I shall give a few selected examples on how SANS combined with suitable contrast variation schemes can be used to extract information on the size and conformation of polymer coils in solution and in the melt, and on the local structure and flexibility of polymerlike micelles and microemulsions. (author) 8 figs., tabs., 44 refs.

  10. Nanocomposites Based on Luminescent Colloidal Nanocrystals and Polymeric Ionic Liquids towards Optoelectronic Applications

    Directory of Open Access Journals (Sweden)

    Annamaria Panniello

    2014-01-01

    Full Text Available Polymeric ionic liquids (PILs are an interesting class of polyelectrolytes, merging peculiar physical-chemical features of ionic liquids with the flexibility, mechanical stability and processability typical of polymers. The combination of PILs with colloidal semiconducting nanocrystals leads to novel nanocomposite materials with high potential for batteries and solar cells. We report the synthesis and properties of a hybrid nanocomposite made of colloidal luminescent CdSe nanocrystals incorporated in a novel ex situ synthesized imidazolium-based PIL, namely, either a poly(N-vinyl-3-butylimidazolium hexafluorophosphate or a homologous PIL functionalized with a thiol end-group exhibiting a chemical affinity with the nanocrystal surface. A capping exchange procedure has been implemented for replacing the pristine organic capping molecules of the colloidal CdSe nanocrystals with inorganic chalcogenide ions, aiming to disperse the nano-objects in the PILs, by using a common polar solvent. The as-prepared nanocomposites have been studied by TEM investigation, UV-Vis, steady-state and time resolved photoluminescence spectroscopy for elucidating the effects of the PIL functionalization on the morphological and optical properties of the nanocomposites.

  11. Nanomedicine: Interaction of biomimetic apatite colloidal nanoparticles with human blood components.

    Science.gov (United States)

    Choimet, Maëla; Hyoung-Mi, Kim; Jae-Min, Oh; Tourrette, Audrey; Drouet, Christophe

    2016-09-01

    This contribution investigates the interaction of two types of biomimetic-apatite colloidal nanoparticles (negatively-charged 47nm, and positively-charged 190nm NPs) with blood components, namely red blood cells (RBC) and plasma proteins, with the view to inspect their hemocompatibility. The NPs, preliminarily characterized by XRD, FTIR and DLS, showed low hemolysis ratio (typically lower than 5%) illustrating the high compatibility of such NPs with respect to RBC, even at high concentration (up to 10mg/ml). The presence of glucose as water-soluble matrix for freeze-dried and re-dispersed colloids led to slightly increased hemolysis as compared to glucose-free formulations. NPs/plasma protein interaction was then followed, via non-specific protein fluorescence quenching assays, by contact with whole human blood plasma. The amount of plasma proteins in interaction with the NPs was evaluated experimentally, and the data were fitted with the Hill plot and Stern-Volmer models. In all cases, binding constants of the order of 10(1)-10(2) were found. These values, significantly lower than those reported for other types of nanoparticles or molecular interactions, illustrate the fairly inert character of these colloidal NPs with respect to plasma proteins, which is desirable for circulating injectable suspensions. Results were discussed in relation with particle surface charge and mean particle hydrodynamic diameter (HD). On the basis of these hemocompatibility data, this study significantly complements previous results relative to the development and nontoxicity of biomimetic-apatite-based colloids stabilized by non-drug biocompatible organic molecules, intended for use in nanomedicine.

  12. Formation and Stability of High-Spin Alkali Clusters

    Science.gov (United States)

    Schulz, C. P.; Claas, P.; Schumacher, D.; Stienkemeier, F.

    2004-01-01

    Helium nanodroplet isolation has been applied to agglomerate alkali clusters at temperatures of 380mK. The very weak binding to the surface of the droplets allows a selection of only weakly bound, high-spin states. Here we show that larger clusters of alkali atoms in high-spin states can be formed. The lack of strong bonds from pairing electrons makes these systems nonmetallic, vanderWaals like complexes of metal atoms. We find that sodium and potassium readily form such clusters containing up to 25atoms. In contrast, this process is suppressed for rubidium and cesium. Apparently, for these heavy alkalis, larger high-spin aggregates are not stable and depolarize spontaneously upon cluster formation.

  13. Bulk synthesis of polymer-inorganic colloidal clusters.

    Science.gov (United States)

    Perro, Adeline; Manoharan, Vinothan N

    2010-12-21

    We describe a procedure to synthesize colloidal clusters with polyhedral morphologies in high yield (liter quantities at up to 70% purity) using a combination of emulsion polymerization and inorganic surface chemistry. We show that the synthesis initially used for silica-polystyrene hybrid clusters can be generalized to create clusters from other inorganic and polymer particles. We also show that high yields of particular morphologies can be obtained by precise control of the inorganic seed particle size, a finding that can be explained using a hard-sphere packing model. These clusters can be further chemically modified for a variety of applications. Introducing a cross-linker leads to colloidal clusters that can be index matched in an appropriate solvent, allowing them to be used for particle tracking or optical studies of colloidal self-assembly. Also, depositing a thin silica layer on these colloids allows the surface properties to be controlled using silane chemistry.

  14. Size- and concentration-dependent deposition of fluorescent silica colloids in saturated sand columns: transport experiments and modeling.

    Science.gov (United States)

    Vitorge, Elsa; Szenknect, Stéphanie; Martins, Jean M F; Gaudet, Jean-Paul

    2013-08-01

    This study investigates the size and concentration effects on the transport of silica colloids in columns of sandy aquifer material. Colloid transport experiments were performed with specifically developed fluorescent labeled silica colloids in columns of a repacked natural porous medium under hydro-geochemical conditions representative of sandy aquifers. Breakthrough curves and vertical deposition profiles of colloids were measured for various colloid concentrations and sizes. The results showed that for a given colloid concentration injected, deposition increased when increasing the size of the colloids. For a given colloid size, retention was also shown to be highly concentration-dependent with a non-monotonous pattern presenting low and high concentration specificities. Deposition increases when increasing both size and injected concentration, until a threshold concentration is reached, above which retention decreases, thus increasing colloid mobility. Results observed above the threshold concentration agree with a classical blocking mechanism typical of a high concentration regime. Results observed at lower colloid concentrations were not modeled with a classical blocking model and a depth- and time-dependent model with a second order kinetic law was necessary to correctly fit the experimental data in the entire range of colloid concentrations with a single set of parameters for each colloidal size. The colloid deposition mechanisms occuring at low concentrations were investigated through a pore structure analysis carried out with Mercury Intrusion Porosimetry and image analysis. The determined pore size distribution permitted estimation of the maximal retention capacity of the natural sand as well as some low flow zones. Altogether, these results stress the key role of the pore space geometry of the sand in controlling silica colloids deposition under hydro-geochemical conditions typical of sandy aquifers. Our results also showed originally that colloid

  15. Strong collective attraction in colloidal clusters on a liquid-air interface.

    Science.gov (United States)

    Pergamenshchik, V M

    2009-01-01

    It is shown that in a cluster of many colloids, trapped at a liquid-air interface, the well-known vertical-force-induced pairwise logarithmic attraction changes to a strongly enhanced power-law attraction. In large two-dimensional clusters, the attraction energy scales as the inverse square of the distance between colloids. The enhancement is given by the ratio eta = (square of the capillary length) / (interface surface area per colloid) and can be as large as 10;{5} . This explains why a very small vertical force on colloids, which is too weak to bring two of them together, can stabilize many-body structures on a liquid-air interface. The profile of a cluster is shown to consist of a large slow collective envelope modulated by a fast low-amplitude perturbation due to individual colloids. A closed equation for the slow envelope, which incorporates an arbitrary power-law repulsion between colloids, is derived. For example, this equation is solved for a large circular cluster with the hard-core colloid repulsion. It is suggested that the predicted effect is responsible for mysterious stabilization of colloidal structures observed in experiments on a surface of isotropic liquid and nematic liquid crystal.

  16. Colloidal nanocrystal synthesis and the organic-inorganicinterface

    Energy Technology Data Exchange (ETDEWEB)

    Yin, Yadong; Alivisatos, A. Paul

    2005-05-12

    Colloidal nanocrystals are nanometer-sized, solution-grown inorganic particles stabilized by a layer of surfactants attached to their surface. The inorganic cores exhibit useful properties controlled by composition as well as size and shape, while the surfactant coating ensures that these structures are easy to fabricate and process. It is this combination of features that makes colloidal nanocrystals attractive and promising building blocks for advanced materials and devices. But their full potential can only be exploited if we achieve exquisite control over their composition, size, shape, crystal structure and surface properties. Here we review what is known about nanocrystal growth and outline strategies for controlling it.

  17. Colloids in the mortar backfill of a cementitious repository for radioactive waste.

    Science.gov (United States)

    Wieland, E; Spieler, P

    2001-01-01

    Colloids are present in groundwater aquifers and water-permeable engineered barrier systems and may facilitate the migration of radionuclides. A highly