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Journal articles on the topic 'Colloid and Surface Chemistry'

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1

Amézaga González, María Fernanda, Jazzely Acosta Bezada, Víctor Gómez Flores, et al. "Effect of Physiological Fluid on the Photothermal Properties of Gold Nanostructured." International Journal of Molecular Sciences 24, no. 9 (2023): 8339. http://dx.doi.org/10.3390/ijms24098339.

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Colloidal gold particles have been extensively studied for their potential in hyperthermia treatment due to their ability to become excited in the presence of an external laser. However, their light-to-heat efficiency is affected by the physiologic environment. In this study, we aimed to evaluate the ability of gold sphere, rod, and star-shaped colloids to elevate the temperature of blood plasma and breast cancer-simulated fluid under laser stimulation. Additionally, the dependence of optical properties and colloid stability of gold nanostructures with physiological medium, particle shape, and
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2

Čermáková, Kateřina, Ondřej Šesták, Pavel Matějka, Vladimír Baumruk, and Blanka Vlčková. "Surface-Enhanced Raman Scattering (SERS) Spectroscopy with Borohydride-Reduced Silver Colloids: Controlling Adsorption of the Scattering Species by Surface Potential of Silver Colloid." Collection of Czechoslovak Chemical Communications 58, no. 11 (1993): 2682–94. http://dx.doi.org/10.1135/cccc19932682.

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Formation of Ag colloid/adsorbate SERS-active systems (upon adsorption of the selected adsorbates on the surface of Ag colloidal particles) as a function of (i) NaBH4 to AgNO3 molar ratio in the preparation protocol of Ag colloid, and (ii) aging of the colloid has been investigated by Surface-enhanced Raman scattering (SERS) spectroscopy. Oligomeric synthetic polypeptides, bovine serum albumin, phosphate coadsorbed with CuTMePyP [copper(II) derivative of 5,10,15,20-tetrakis-(N-methylpyridinium-4-yl)porphyrin chloride] and borates in systems with N-containing bases were selected as model adsorb
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3

Pietrowski, Mariusz, Michał Zieliński, and Maria Wojciechowska. "Nanocolloidal Ru/MgF2 Catalyst for Hydrogenation of Chloronitrobenzene and Toluene." Polish Journal of Chemical Technology 16, no. 2 (2014): 63–68. http://dx.doi.org/10.2478/pjct-2014-0031.

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Abstract The use of magnesium fluoride support for ruthenium active phase allowed obtaining new catalysts of high activities in the hydrogenation of toluene and ortho-chloronitrobenzene. Ruthenium colloid catalysts (1 wt.% of Ru) were prepared by impregnation of the support with the earlier produced polyvinylpyrrolidone (PVP)-stabilized ruthenium colloids. The performances of the colloidal catalysts and those obtained by traditional impregnation were tested in the reactions of toluene hydrogenation to methylcyclohexane and selective hydrogenation of ortho-chloronitrobenzene (o-CNB) to ortho-ch
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4

Chrzastowski, Tina. "Information Sources in Surface and Colloid Chemistry." Science & Technology Libraries 9, no. 3 (1989): 75–96. http://dx.doi.org/10.1300/j122v09n03_09.

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5

Kerker, Milton. "Eighteen years of colloid and surface chemistry." Journal of Colloid and Interface Science 150, no. 2 (1992): 599. http://dx.doi.org/10.1016/0021-9797(92)90230-j.

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6

Zuo, Rui, Kexue Han, Rongtao Shi, et al. "Effect of Colloidal Silicate on the Migration Behaviour of Strontium in Groundwater Environment of Geological Disposal Candidate Site." Journal of Chemistry 2019 (September 23, 2019): 1–11. http://dx.doi.org/10.1155/2019/9606121.

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Various colloids are present in the natural groundwater environment, and colloids act on the processes involved when radionuclides leak from a repository in a high-level waste disposal site. This paper investigates the effect of colloidal silicate in natural groundwater environments on the migration behaviour of Sr(II). Three different experimental cases have been designed: (1) effect in the presence of colloidal silicate, (2) effect in the presence of a porous medium, and (3) effect in the presence of both colloidal silicate and porous medium (referred to as CS, PM, and PC, respectively). Bat
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7

Wang, Xiaolu, Martin In, Christophe Blanc, Paolo Malgaretti, Maurizio Nobili, and Antonio Stocco. "Wetting and orientation of catalytic Janus colloids at the surface of water." Faraday Discussions 191 (2016): 305–24. http://dx.doi.org/10.1039/c6fd00025h.

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Janus colloidal particles show remarkable properties in terms of surface activity, self-assembly and wetting. Moreover they can perform autonomous motion if they can chemically react with the liquid in which they are immersed. In order to understand the self-propelled motion of catalytic Janus colloids at the air–water interface, wetting and the orientation of the catalytic surface are important properties to be investigated. Wetting plays a central role in active motion since it determines the contact between the fuel and the catalytic surface as well as the efficiency of the transduction of
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8

Zhang, Xiao Lin, and Qing Han. "Study on the Colloid Chemistry Behavior in Domestic Old Book Paper (DOBP) Deinking System." Advanced Materials Research 236-238 (May 2011): 1463–66. http://dx.doi.org/10.4028/www.scientific.net/amr.236-238.1463.

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In this paper, the domestic old book paper(DOBP) was subjected to deinking process. Surface and colloid characterisitics of DOBP deinking pulp(DIP) system was investigated. The relation between surface and colloid characterisitic changes and efficiency of deinking (brightness and residual ink particles content) was studied. Technical conditions that affect the deinking pulp’s colloid chemical behavior were also analyzed here.The results showed that colloid-chemical behavior of DOBP deinking system could be changed during the deinking process. The colloid-chemical behavior, such as Zeta potenti
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9

Yu, Xiang, and P. Somasundaran. "Colloid Chemistry in Mineral Processing." Colloids and Surfaces A: Physicochemical and Engineering Aspects 83, no. 2 (1994): 183–84. http://dx.doi.org/10.1016/0927-7757(94)80103-7.

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10

Li, Runwei, Changfu Wei, Hefa Cheng, and Gang Chen. "Adhesion of Colloids and Bacteria to Porous Media: A Critical Review." Reviews of Adhesion and Adhesives 7, no. 4 (2019): 417–60. http://dx.doi.org/10.7569/raa.2019.097314.

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Adhesion of colloids and bacteria to various surfaces is important for a variety of environmental phenomena including microbial biofouling and contamination prevention. Under saturated conditions, both colloids and bacteria have the opportunity to attach to porous medium surfaces. Under water unsaturated conditions or in the presence of the air-water interface, besides the porous medium surfaces, colloids and bacteria can also attach to the air-water interface, including the air-water-solid threephase interface. The magnitudes of adhesion of colloids and bacteria are correlated to the interact
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11

Shaw, D. J., and Bernard Costello. "Introduction to colloid and surface chemistry (4th edition)." Tribology International 26, no. 3 (1993): 222. http://dx.doi.org/10.1016/0301-679x(93)90102-7.

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12

Tadros, Th F. "Surface and colloid chemistry in advanced ceramics processing." Advances in Colloid and Interface Science 61 (1995): 192–93. http://dx.doi.org/10.1016/0001-8686(95)90003-9.

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13

Song, Xiao Zong, Yong Zhang, and Fei Hu Zhang. "Study on Removal Mechanism of Nanoparticle Colloid Jet Machining." Advanced Materials Research 53-54 (July 2008): 363–68. http://dx.doi.org/10.4028/www.scientific.net/amr.53-54.363.

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We developed a nanoparticle colloid jet machining to fulfill the requirement for ultrasmooth surface in terms of the studying on micro structure of work surface, the high surface energy and intense adsorption of SiO2 nanoparticle. In this paper, three types impact in nanoparticle colloid jet machining have been analysed and the atom removing model has been founded based on the physical chemistry theory of solid surface and interface. The factors which may influence the nanoparticle colloid jet machining quality (such as the diameter of nanoparticle, colloid jet velocity and dynamical viscidity
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14

Yokoyama, Kazushige, Kieran Brown, Peter Shevlin, et al. "Examination of Adsorption Orientation of Amyloidogenic Peptides Over Nano-Gold Colloidal Particle Surfaces." International Journal of Molecular Sciences 20, no. 21 (2019): 5354. http://dx.doi.org/10.3390/ijms20215354.

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The adsorption of amyloidogenic peptides, amyloid beta 1–40 (Aβ1–40), alpha-synuclein (α-syn), and beta 2 microglobulin (β2m), was attempted over the surface of nano-gold colloidal particles, ranging from d = 10 to 100 nm in diameter (d). The spectroscopic inspection between pH 2 and pH 12 successfully extracted the critical pH point (pHo) at which the color change of the amyloidogenic peptide-coated nano-gold colloids occurred due to aggregation of the nano-gold colloids. The change in surface property caused by the degree of peptide coverage was hypothesized to reflect the ΔpHo, which is the
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15

Schmid, Günter, Andreas Lehnert, Ulrich Kreibig, Zbignew Adamczyk, and Peter Belouschek. "Synthese und elektronenmikroskopische Untersuchung kontrolliert gewachsener, ligandstabilisierter Goldkolloide sowie theoretische Überlegungen zur Oberflächenbelegung durch Kolloide / Synthesis and Electron Microscopic Investigation of Controlled Grown, Ligand Stabilized Gold Colloids and Theoretical Considerations on the Covering of Surfaces by Colloids." Zeitschrift für Naturforschung B 45, no. 7 (1990): 989–94. http://dx.doi.org/10.1515/znb-1990-0713.

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18 nm Gold colloids are used as seeds for a controlled growth of 36 nm colloids which are then stabilized by P(m-C6H4SO3Na)3. These colloids can be isolated as golden leaflets and are readily soluble in water in virtually any concentration. Electron microscopic investigations prove a very small particle size distribution. X-ray powder diffraction and molecular weight determinations support the results of the electron microscopic investigations. The distance between the colloidal particles in two-dimensional layers corresponds to double-layers of phosphane ligands around each colloid, twice 1.2
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16

Ogata, Naoya. "Surface and Colloid Science." Angewandte Chemie International Edition in English 27, no. 11 (1988): 1584–85. http://dx.doi.org/10.1002/anie.198815841.

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17

Goel, Alok, and Johannes Lützenkirchen. "Relevance of Colloid Inherent Salt Estimated by Surface Complexation Modeling of Surface Charge Densities for Different Silica Colloids." Colloids and Interfaces 6, no. 2 (2022): 23. http://dx.doi.org/10.3390/colloids6020023.

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Potentiometric titrations have been routinely used to measure the proton-related surface charge density (SCD) of particles in solution. Here, we quantify the SCD of silica nanoparticles (NPs) that are commercially available as charge-stabilized colloids (by the addition of NaOH) in the presence of known amounts of added NaCl. The experimental results are simulated by surface complexation models (SCMs) of the electrical double layer (EDL). The modeling results suggest that involving only the added NaCl electrolyte yields poor agreement between the experiment and the best achievable fit. An incr
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18

Lozovski, V. Z., A. G. Vasiljev, T. A. Vasyliev, I. S. Petrik, A. M. Eremenko, and N. P. Rybalchenko. "Resonance properties of the solution of quercetin stabilized silver nanoparticles in a nutrient medium." Himia, Fizika ta Tehnologia Poverhni 15, no. 1 (2024): 86–93. http://dx.doi.org/10.15407/hftp15.01.086.

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Changes in the light absorption spectrum when mixing colloids of Ag nanoparticles with a diameter of 7 nm in a quercetin shell with a nutrient medium were studied in the present article. Colloids of silver nanoparticles were prepared by chemical reduction of AgNO3 silver salt with sodium tetrahydroborate (NaBH4) in an aqueous solution. Quercetin is a flavonoid of plant origin. It was chosen to stabilize nanoparticles due to its capability to form complexes with metals. The quercetin shell is capable to preserve the bactericidal effect of silver NPs on bacteria and weaken their toxic effect on
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19

Ahmadi-Sénichault, A., V. Canseco, N. Sefrioui-Chaibainou, A. Omari, and H. Bertin. "Displacement of Colloidal Dispersions in Porous Media: Experimental & Numerical Approaches." Diffusion Foundations 7 (June 2016): 53–68. http://dx.doi.org/10.4028/www.scientific.net/df.7.53.

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The main objective of this paper is to give more insight on colloids deposition and re-entrainment in presence of a rough surface. Experiments on retention and release of colloids in a porous medium are first presented. The influence of physicochemical and hydrodynamic conditions is investigated. The experimental results cannot be qualitatively interpreted using the DLVO theory and knowledges at pore scale are then needed. A 3D numerical simulation approach at the pore scale is therefore proposed where the motion of colloids is solved in presence of collector surfaces bearing various kinds of
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20

Roto, Roto, Hani Prima Rasydta, Adhitasari Suratman, and Nurul Hidayat Aprilita. "Effect of Reducing Agents on Physical and Chemical Properties of Silver Nanoparticles." Indonesian Journal of Chemistry 18, no. 4 (2018): 614. http://dx.doi.org/10.22146/ijc.26907.

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Silver nanoparticles having uniform size and shape, a diameter range of 10–50 nm, excellent stability, and high zeta potential are always desirable for many applications. The silver nanoparticles were synthesized by chemical reduction method using some reducing agents in a polyvinyl alcohol solution. This study aims at determining the effect of reducing agents on the chemical and physical properties of silver nanoparticles. Ascorbic acid, sodium borohydride, hydrazine, sodium citrate, and glucose were used as reducing agents. Surface Plasmon Resonance (SPR) absorbance, morphology, zeta potenti
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21

Krott, Leandro B., and José Rafael Bordin. "How Dimensionality Affects the Structural Anomaly in a Core-Softened Colloid." Colloids and Interfaces 7, no. 2 (2023): 33. http://dx.doi.org/10.3390/colloids7020033.

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The interaction between hard core–soft shell colloids are characterized by having two characteristic distances: one associated with the penetrable, soft corona and another one corresponding to the impenetrable core. Isotropic core-softened potentials with two characteristic length scales have long been applied to understand the properties of such colloids. Those potentials usually show water-like anomalies, and recent findings have indicated the existence of multiple anomalous regions in the 2D limit under compression, while in 3D, only one anomalous region is observed. In this direction, we p
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22

Amadu, Mumuni, and Adango Miadonye. "Determination of the Point of Zero Charge pH of Borosilicate Glass Surface Using Capillary Imbibition Method." International Journal of Chemistry 9, no. 3 (2017): 67. http://dx.doi.org/10.5539/ijc.v9n3p67.

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The point of zero charge pH of an oxide surface is a fundamental surface chemistry property or solids or metal oxides that determine the nature of interaction at the solid-aqueous solution interface. In colloid chemistry this physical parameter controls the evolution of the electric double layer as well as adsorption and desorption processes.In colloid chemistry a number of methods have been used for the determination of the point of zero charge pH of an oxide surface. This ranges from titrimetric to radiation chemistry approach that deals with scanning electron microscopy.In this study, the d
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23

Aveyard, R., B. P. Binks, J. Chen, et al. "Surface and Colloid Chemistry of Systems Containing Pure Sugar Surfactant." Langmuir 14, no. 17 (1998): 4699–709. http://dx.doi.org/10.1021/la980519x.

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24

Thurman, E. M. "Surface and colloid chemistry in natural waters and water treatment." Chemical Geology 95, no. 3-4 (1992): 362–63. http://dx.doi.org/10.1016/0009-2541(92)90023-x.

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25

Biggs, Simon. "Handbook of Applied Surface and Colloid Chemistry. (Ed K. Holmberg)." Australian Journal of Chemistry 55, no. 3 (2002): 237. http://dx.doi.org/10.1071/chv55n3_br.

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26

Ramsey, John D. F. "Extended Summaries— SCI Colloid and Surface Chemistry Group Meeting. Introduction." Journal of Chemical Technology & Biotechnology 65, no. 4 (1996): 385. http://dx.doi.org/10.1002/(sici)1097-4660(199604)65:4<385::aid-jctb419>3.0.co;2-m.

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27

De Corato, Marco, and Ignacio Pagonabarraga. "Onsager reciprocal relations and chemo-mechanical coupling for chemically active colloids." Journal of Chemical Physics 157, no. 8 (2022): 084901. http://dx.doi.org/10.1063/5.0098425.

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Similar to cells, bacteria, and other micro-organisms, synthetic chemically active colloids can harness the energy from their environment through a surface chemical reaction and use the energy to self-propel in fluidic environments. In this paper, we study the chemo-mechanical coupling that leads to the self-propulsion of chemically active colloids. The coupling between chemical reactions and momentum transport is a consequence of Onsager reciprocal relations. They state that the velocity and the surface reaction rate are related to mechanical and chemical affinities through a symmetric matrix
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28

Kerker, Milton. "Surface and colloid science." Journal of Colloid and Interface Science 107, no. 2 (1985): 589. http://dx.doi.org/10.1016/0021-9797(85)90219-x.

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29

Barišić, Antun, Johannes Lützenkirchen, Nikol Bebić, et al. "Experimental Data Contributing to the Elusive Surface Charge of Inert Materials in Contact with Aqueous Media." Colloids and Interfaces 5, no. 1 (2021): 6. http://dx.doi.org/10.3390/colloids5010006.

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We studied the charging of inert surfaces (polytetrafluoroethylene, i.e., PTFE; graphite; graphene; and hydrophobic silica) using classical colloid chemistry approaches. Potentiometric titrations showed that these surfaces acquired less charge from proton-related reactions than oxide minerals. The data from batch-type titrations for PTFE powder did not show an effect of ionic strength, which was also in contrast with results for classical colloids. In agreement with classical colloids, the electrokinetic results for inert surfaces showed the typical salt level dependence. In some cases, the po
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30

Park, Jong-Min, Chan-Woo Lee, Wan-Sul Lee, et al. "MONTMORILLONITE-REINFORCED NATURAL RUBBER NANOCOMPOSITES THROUGH EMULSION STABILIZATION–DESTABILIZATION METHOD." Rubber Chemistry and Technology 85, no. 2 (2012): 165–79. http://dx.doi.org/10.5254/rct.12.88978.

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Abstract A nanoplatelet of montmorillonite (MMT) was incorporated in the natural rubber (NR) matrix at a high loading content using a newly developed stabilization–destabilization process in the colloid states. Examination of the surface charge of the colloid drops by zeta potential measurement led to the identification of the stable and unstable conditions of the colloid mixture as well as each colloid system as a function of pH. The stabilized mixture of the MMT and NR colloids was subsequently destabilized by changing the pH of the mixture to achieve a well-dispersed and intercalated NR/MMT
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31

Moreels, Iwan, Bernd Fritzinger, José C. Martins, and Zeger Hens. "Surface Chemistry of Colloidal PbSe Nanocrystals." Journal of the American Chemical Society 130, no. 45 (2008): 15081–86. http://dx.doi.org/10.1021/ja803994m.

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32

Vargas-Baca, Ignacio, Andrew P. Brown, Mark P. Andrews, et al. "Linear and nonlinear optical responses of a dye anchored to gold nanoparticles dispersed in liquid and polymeric matrixes." Canadian Journal of Chemistry 80, no. 11 (2002): 1625–33. http://dx.doi.org/10.1139/v02-147.

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The compound [4-CH3C6H4-SS-CH2CH2-N(CH3)C6H4C(C6H4N(CH3)2)-4)2]Cl (1a) consists of the triarylmethyl chromophore of crystal violet appended to an organic disulfide, to entail direct attachment of this dye to gold surfaces. Addition of 1a to colloidal dispersions of the metal produced a stable dispersion in methanol–water mixtures. Transmission electron microscopy of Freeze-Fracture sections shadowed with carbon and platinum confirmed that the dispersion remains unaggregated. Local-field effects and coupling to the surface plasmon of gold magnified the interaction of the chromophore with optica
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33

Taylor, Spencer E. "Colloids and Interfaces in Oil Recovery." Colloids and Interfaces 3, no. 2 (2019): 50. http://dx.doi.org/10.3390/colloids3020050.

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34

Fuster, H. A., Xin Wang, Xiaoguang Wang, E. Bukusoglu, S. E. Spagnolie, and N. L. Abbott. "Programming van der Waals interactions with complex symmetries into microparticles using liquid crystallinity." Science Advances 6, no. 25 (2020): eabb1327. http://dx.doi.org/10.1126/sciadv.abb1327.

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Asymmetric interactions such as entropic (e.g., encoded by nonspherical shapes) or surface forces (e.g., encoded by patterned surface chemistry or DNA hybridization) provide access to functional states of colloidal matter, but versatile approaches for engineering asymmetric van der Waals interactions have the potential to expand further the palette of materials that can be assembled through such bottom-up processes. We show that polymerization of liquid crystal (LC) emulsions leads to compositionally homogeneous and spherical microparticles that encode van der Waals interactions with complex s
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35

Valentine, M. T., Z. E. Perlman, M. L. Gardel, et al. "Colloid Surface Chemistry Critically Affects Multiple Particle Tracking Measurements of Biomaterials." Biophysical Journal 86, no. 6 (2004): 4004–14. http://dx.doi.org/10.1529/biophysj.103.037812.

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36

Perry, Reeves B. "Principles of Colloid and Surface Chemistry, Second Edition (Hiemenz, P. C.)." Journal of Chemical Education 64, no. 12 (1987): A328. http://dx.doi.org/10.1021/ed064pa328.3.

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37

Maurice, Patricia A. "Applications of atomic-force microscopy in environmental colloid and surface chemistry." Colloids and Surfaces A: Physicochemical and Engineering Aspects 107 (February 1996): 57–75. http://dx.doi.org/10.1016/0927-7757(95)03372-6.

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38

Andreasson, A., B. J�nsson, and B. Lindman. "Surface and colloid chemistry of peat and peat dewatering. Electrostatic effects." Colloid & Polymer Science 266, no. 2 (1988): 164–72. http://dx.doi.org/10.1007/bf01452814.

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39

Kerker, Milton. "Some historical ruminations on the ACS Colloid and Surface Chemistry Symposium." Journal of Colloid and Interface Science 291, no. 2 (2005): 606–9. http://dx.doi.org/10.1016/j.jcis.2005.08.036.

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40

Valverde-Alva, Miguel A., Jhenry F. Agreda-Delgado, Juan A. Vega-González, et al. "Effect of the magnetic field on the synthesis of colloidal silver and gold nanoparticles by laser ablation in bidestilated water." MOMENTO, no. 63 (July 9, 2021): 1–11. http://dx.doi.org/10.15446/mo.n63.91515.

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The effect of magnetic field of 0.3 T on the concentration, distribution of sizes in suspension and zeta potential of colloidal gold and colloidal silver nanoparticles, obtained by considering the pulsed laser ablation in double distilled water was studied. The magnetic field was transverse to the direction of incidence of the laser radiation and parallel to the surface of a submerged target. An Nd: YAG laser was used (1064 nm in wavelength, 10 ns in duration, repetition rate of 10 Hz and 37 mJ of energy) to ablate targets. The colloids were characterized by inductively coupled plasma optical
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41

Adachi, Kenta, Yukimasa Ura, and Naoya Kanetada. "Stimuli-triggered reversible switching mechanism between H- and J-type supramolecular assemblies of cationic porphyrins adsorbed on tungsten(VI) oxide surface." Journal of Porphyrins and Phthalocyanines 22, no. 08 (2018): 658–69. http://dx.doi.org/10.1142/s1088424618500372.

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Supramolecular organic dye–inorganic semiconductor nanocrystal assemblies are potentially useful in a broad range of technologies and applications, including photovoltaic systems, but the molecular basis of the adsorption of dye molecules onto the semiconductor surfaces remains poorly understood. Herein, we investigated the pH-dependent adsorption and conformational change of two cationic porphyrin stereoisomers [5,10-diphenyl-15,20-di([Formula: see text]-methyl-4-pyridyl)porphyrin (cis-DMPyP) and 5,15-diphenyl-10,20-di([Formula: see text]-methyl-4-pyridyl)porphyrin (trans-DMPyP)] on the tungs
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42

Roto, Roto, Marcelina Marcelina, Nurul Hidayat Aprilita, Mudasir Mudasir, Taufik Abdillah Natsir, and Bella Mellisani. "Investigation on the Effect of Addition of Fe3+ Ion into the Colloidal AgNPs in PVA Solution and Understanding Its Reaction Mechanism." Indonesian Journal of Chemistry 17, no. 3 (2017): 439. http://dx.doi.org/10.22146/ijc.22695.

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Analysis of Fe3+ ion present in aqueous solutions is always of interests. Recently, this ion has been analyzed by colorimetric methods using colloid of silver nanoparticles (AgNPs) in capping agents of polymers. The reaction mechanism between AgNPs and Fe3+ is still subject to the further investigation. In this work, 1,10-phenanthroline was used to probe the reaction mechanism between AgNPs and Fe3+ ion in the solution. The colloids of AgNPs were prepared in the polyvinyl alcohol (PVA) solution and reacted with Fe3+. The colloid surface plasmon absorbance decreases linearly along with the incr
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43

Song, Xiaozong, and Gui Gao. "Removal Mechanism Investigation of Ultraviolet Induced Nanoparticle Colloid Jet Machining." Molecules 26, no. 1 (2020): 68. http://dx.doi.org/10.3390/molecules26010068.

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Ultraviolet induced nanoparticle colloid jet machining is a new ultra-precision machining technology utilizing the reaction between nanoparticles and the surface of the workpiece to achieve sub-nanometer ultra-smooth surface manufacturing without damage. First-principles calculations based on the density functional theory (DFT) were carried out to study the atomic material removal mechanism of nanoparticle colloid jet machining and a series of impacting and polishing experiments were conducted to verify the mechanism. New chemical bonds of Ti-O-Si were generated through the chemical adsorption
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44

Peula-García, J. M., R. Hidalgo-Alvarez, and F. J. de las Nieves. "Colloid stability and electrokinetic characterization of polymer colloids prepared by different methods." Colloids and Surfaces A: Physicochemical and Engineering Aspects 127, no. 1-3 (1997): 19–24. http://dx.doi.org/10.1016/s0927-7757(96)03890-3.

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45

Wolff, Thomas, and Bernhard Klaussner. "Overlap of colloid chemistry and photochemistry in surfactant systems." Advances in Colloid and Interface Science 59 (August 1995): 31–94. http://dx.doi.org/10.1016/0001-8686(95)80004-m.

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46

Li, Ning, Chengzhi Hu, Xiaoning Fu, et al. "Identification of Al13 on the Colloid Surface Using Surface-Enhanced Raman Spectroscopy." Environmental Science & Technology 51, no. 5 (2017): 2899–906. http://dx.doi.org/10.1021/acs.est.6b05721.

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47

Jovanovic, Svetlana, Zoran Markovic, Duska Kleut, et al. "Singlet oxygen generation by higher fullerene-based colloids." Journal of the Serbian Chemical Society 75, no. 7 (2010): 965–73. http://dx.doi.org/10.2298/jsc090617062j.

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In this paper, the results of the synthesis and characterization of higher fullerene-based colloids is presented. The generation of singlet oxygen 1O2 (1?g) by fullerene water-based colloids (nC60, nC70 and nC84) was investigated. It was found by electron paramagnetic resonance spectroscopy that the generation of singlet oxygen was the highest by the nC84 colloid. The amplitude of the electron paramagnetic resonance (EPR) signal was two orders of magnitude higher than the amplitude of the EPR signals which originated from nC60 and nC70. The surface morphology and the structure of the particles
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48

Walsch, J., and S. Dultz. "Effects of pH, Ca- and SO4-concentration on surface charge and colloidal stability of goethite and hematite – consequences for the adsorption of anionic organic substances." Clay Minerals 45, no. 1 (2010): 1–13. http://dx.doi.org/10.1180/claymin.2010.045.1.01.

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AbstractSoil solution chemistry, especially pH and the presence of multivalent ions, affects the surface charge (SC) of Fe oxides and accordingly colloidal stability and sorption properties. The SC of synthetic goethite and hematite was quantified in the presence of different electrolytes (NaCl, CaCl2, Na2SO4and CaSO4) by combining the streaming potential with polyelectrolyte titration. The point of zero charge (PZC) for goethite was observed at pH 8.2 and the stability field around the PZC, where colloids are flocculated, is more extended (±1 pH unit) than that of hematite with a PZC at pH 7.
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Nelson, E. C., and P. V. Braun. "CHEMISTRY: Enhancing Colloids Through the Surface." Science 318, no. 5852 (2007): 924–25. http://dx.doi.org/10.1126/science.1148009.

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50

Mahynski, Nathan A., Bliss Han, Daniel Markiewitz, and Vincent K. Shen. "Derivable genetic programming for two-dimensional colloidal materials." Journal of Chemical Physics 157, no. 11 (2022): 114112. http://dx.doi.org/10.1063/5.0106131.

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We describe a method for deriving surface functionalization patterns for colloidal systems that can induce self-assembly into any chosen periodic symmetry at a planar interface. The result is a sequence of letters, s ∈ {A,T,C,G}, or a gene, that describes the perimeter of the colloidal object and programs its self-assembly. This represents a genome that is finite and can be exhaustively enumerated. These genes derive from symmetry, which may be topologically represented by two-dimensional parabolic orbifolds; since these orbifolds are surfaces that may be derived from first principles, this re
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