Clay Dispersion (clay + dispersion)

Distribution by Scientific Domains


Selected Abstracts


Elongational Rheology of Polymer/Clay Dispersions: Determination of Orientational Extent in Elongational Flow Processes,

MACROMOLECULAR MATERIALS & ENGINEERING, Issue 4 2008
Eduard A. Stefanescu
Abstract The purpose of the present contribution is to provide an efficient method that would help to quantify the orientational levels occurring in polymer/clay dispersions subjected to elongational flow. The extent of internal orientation developed in salt containing montmorillonite/poly(ethylene oxide) gels is investigated, combining shear and elongational rheology methods. Entropic changes indicate that the strength of the transient network present in each gel affects the orientational ability of clay particles and polymer chains. We found that an increased Hencky strain of the hyperbolic die leads to a higher variation of the calculated entropy of the material. [source]


Elementary processes of soil,water interaction and thresholds in soil surface dynamics: a review

EARTH SURFACE PROCESSES AND LANDFORMS, Issue 9 2004
Richard S. B. Greene
Abstract Elementary processes of soil,water interaction and the thresholds to these processes are important to understand as they control a range of phenomena that occur at the soil surface. In particular processes involved with wetting by rainfall that lead to particle breakdown are critical. This breakdown causes soil detachment and crust formation, which are both key elements in erosion. This paper reviews the range of approaches that have been taken in describing the processes associated with the wetting of a soil surface by rainfall. It assembles the studies that emphasize soil physics, soil chemistry, and erosion mechanics in a framework to enable a balanced consideration of important processes and management strategies to control erosion for a particular situation. In particular it discusses the factors associated with the two basic processes of soil structural breakdown, i.e. slaking and dispersion, and how these processes are critical in particle detachment, transport and surface crust formation. Besides the balance between the exchangeable cation composition and electrolyte concentration (measured as the sodium adsorption ratio (SAR) and total cation concentration (TCC) respectively) of the soil, the importance of energy input and soil organic matter content in controlling clay dispersion is emphasized. Based on the balance between these factors, the soil can be in one of three different regions, i.e. a dispersed region, a ,occulated region and one where the resilience of the soil is variable. The implications of each of these regions to soil erosion management are brie,y outlined, as are the critical roles that soil cover levels and organic matter have in controlling erosion. Finally, the relationship between various laboratory measures of aggregate stability, and corresponding ,eld erosion characteristics, is discussed. Copyright © 2004 John Wiley & Sons, Ltd. [source]


Some factors influencing exfoliation and physical property enhancement in nanoclay epoxy resins based on diglycidyl ethers of bisphenol A and F

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007
S. Ingram
Abstract An investigation of the factors influencing the degree of exfoliation of an organically modified clay in a series of epoxy resins is reported. The use of sonication, choice of curing agent, effect of the moisture content of the clay, and the cure temperature were examined. The dispersion was characterized using a combination of rheological measurements, X-ray diffraction, and dynamic mechanical thermal analysis. Rheological analysis of the clay dispersion in the epoxy monomer indicated that at high clay loads Herschel,Bulkley type behavior is followed. Higher cure temperatures and higher levels of clay moisture were found to influence the extent of exfoliation. Improvements in physical properties were observed through the addition of nanocomposites. The DGEBA/DDM and DEGEBA/DDS exhibited 2 and 4°C increase, respectively, in Tg per wt % of added clay. DGEBF showed virtually no enhancement. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source]


On the mechanisms of oligopeptide reactions in solution and clay dispersion

JOURNAL OF PEPTIDE SCIENCE, Issue 12 2004
Dr Juraj Bujdák
Abstract Mechanisms of the reactions of representative dipeptides (Gly2, Gly-Ala), oligopeptides (Gly3, Gly4) and the polypeptide (poly-Gly)n) in solution and clay suspensions at 85 °C were investigated. The reaction products and their yields were analysed and determined by means of HPLC. Interestingly, hydrolysis, where water molecules act as the reactant, was not the main reaction, even for oligopeptides. Formation of cyclic dipeptides prevailed in the reactions of dimers as well as oligopeptides. The breakdown of oligopeptide molecules proceeded via an intramolecular cyclization reaction. For example, the reaction of Gly3 led to the formation of equal amounts of cyclic dipeptide, c(Gly)2 and Gly. The presence of clay (montmorillonite) significantly increased yields in the reactions of dipeptides but it did not have much effect on the reactions of oligopeptides. However, an opposite effect of clay, protection of poly(Gly)n against decomposition, was proven. Copyright © 2004 European Peptide Society and John Wiley & Sons, Ltd. [source]


Long-lived layered silicates-immobilized 2,6-bis(imino)pyridyl iron (II) catalysts for hybrid polyethylene nanocomposites by in situ polymerization: Effect of aryl ligand and silicate modification

JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 2 2009
Giuseppe Leone
Abstract Heterogeneous-layered silicate-immobilized 2,6-bis(imino)pyridyl iron (II) dichloride/MMAO catalysts, in which the active polymerization species are intercalated within sodium- and organomodified-layered silicate galleries, were prepared for producing hybrid exfoliated polyethylene (PE) nanocomposites by means of in situ polymerization. The inorganic filler was first treated with modified-methylaluminoxane (MMAO) to produce a supported cocatalyst: MMAO reacts with silicates replacing most of the organic surfactant, thus modifying the original crystallographic clay order. MMAO anchored to the nanoclay was able to activate polymerization iron complexes initiating the polymer growth directly from the filler lamellae interlayer. The polymerization mechanism taking place in between the montmorillonite lamellae separates the layers, thus promoting deagglomeration and effective clay dispersion. Transmission electron microscopy revealed that in situ polymerization by catalytically active iron complexes intercalated within the lower organomodified clay led to fine dispersion and high exfoliation extent. The intercalated clay catalysts displayed a longer polymerization life-time and brought about ethylene polymerization more efficiently than analogous homogeneous systems. PEs having higher molecular masses were obtained. These benefits resulted to be dependent more on the filler nature than on the ligand environment around the iron metal center and the experimental synthetic route. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 548,564, 2009 [source]


The Effect of Nanofiller on the Thermomechanical Properties of Polyimide/Clay Nanocomposites

MACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 6 2008
Khine Yi Mya
Abstract The interaction between PI and partially exfoliated clay nanofillers is investigated by studying the thermomechanical properties of the resulting nanocomposites by NMR, XPS, XRD, TEM, TGA, TMA, and DMA. XRD and TEM showed more exfoliated structure at ,2.5 wt.-% clay and a macrophase separation above 2.5 wt.-% clay. Td and the storage modulus increased with increasing clay content. A decrease in CTE was observed for clay content ,2.5 wt.-% because of the good dispersion of the clay in the polymer and the reduced segmental motion of polymer matrix. NMR confirmed the quality of clay dispersion, and XPS exhibited that the interaction in PI/2.5 wt.-% clay is much stronger than that in PI/5 wt.-% clay. [source]


Dynamic mechanical study of clay dispersion in maleated polypropylene/organoclay nanocomposites

POLYMER COMPOSITES, Issue 9 2009
Yeh Wang
Morphological characteristics and the dynamic mechanical properties of maleic anhydride grafted polypropylene (PPgMA) and its clay-filled nanocomposites with different degrees of clay exfoliation have been investigated. Fully and partially exfoliated samples were prepared through powered sonication and melt blending, respectively. Our results indicated that both mechanical , and , relaxations can be identified. The glass (,) transition of the nanocomposites shifted to slightly lower temperatures for nearly all formulations because of reduced chain cooperative motion. However, the broad , transition became more distinct with increasing clay loading for sonicated nanocomposites, and shifted to higher temperatures due to chain confinement of amorphous polymer chains in the crystalline region. The reinforcement in the glassy storage modulus E, of PPgMA was examined by the Halpin,Tsai theory. The high aspect ratio of clay stacks in the fully exfoliated nanocomposites resulted in a significant increase in reinforcing efficiency. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source]


Functionalization of nanoclays with ionic liquids for polypropylene composites,

POLYMER COMPOSITES, Issue 5 2009
Jin Uk Ha
Cationic nanoclays were treated by ion exchange with various ionic liquids (ILs) containing cations and anions of different structure and/or molecular weight in order to investigate the effects of the IL structure and cation chain length on extent of clay dispersion, intercalation, and thermal stability. The modified clays containing imidazolium-, pyridinium-, and phosphonium-based cations were characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, and X-ray diffraction. Although the thermal stability of pure ILs was mostly controlled by the type of the anion present, high temperature thermal stability of the modified clays, at the IL cation loadings achieved in this work, was not significantly dependent on type, structure, or size of the cation. The latter parameters, however, were of significant importance in controlling degree of dispersion of the nanoclays during melt compounding with polypropylene (PP). Basal spacing increased proportionally to the size and type of the intercalated cations and showed little change in the PP composites. Although commercial organoclays were shown to be less thermally stable than IL modified clays, they exhibited larger basal spacing and better dispersion characteristics in the polyolefin matrix; however, they increased to the same extent the thermal stability of the PP matrix as the phosphonium modified clays. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers [source]


Morphology and properties of SAN-clay nanocomposites prepared principally by water-assisted extrusion

POLYMER ENGINEERING & SCIENCE, Issue 1 2010
Michaël Mainil
An efficient extrusion process involving the injection of water while processing was used to prepare poly (styrene- co -acrylonitrile) (SAN)/clay nanocomposites with a high degree of nanoclay delamination. The usefulness of water-assisted extrusion is highlighted here, in comparison with classical extrusion and roll mill processes. Cloisite® 30B (C30B), a montmorillonite clay organomodified with alkylammonium cations bearing 2-hydroxyethyl chains, and pristine montmorillonite were melt blended with SAN (25 wt% AN) in a semi-industrial scale extruder specially designed to allow water injection. XRD analysis, visual and TEM observations were used to evaluate the quality of clay dispersion. The relationship between the nanocomposite morphology and its mechanical and thermal properties was then investigated. The superiority of the SAN/C30B nanocomposite extruded with water has been evidenced by cone calorimetry tests and thermogravimetric measurements (TGA). These analyses showed a substantial improvement of the fire behavior and the thermal properties, while a 20% increase of the Young modulus was recorded. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers [source]


Effect of intercalating agents on clay dispersion and thermal properties in polyethylene/montmorillonite nanocomposites

POLYMER ENGINEERING & SCIENCE, Issue 8 2008
Karen Stoeffler
Alkyl pyridinium, 1-vinyl alkyl imidazolium, 1,3-dialkyl imidazolium, and tetraalkyl phosphonium bromides were successfully used as intercalants for the preparation of highly thermally stable organophilic montmorillonites. Nanocomposites of linear low density polyethylene (LLDPE) and linear low density polyethylene grafted with maleic anhydride (LLDPE/LLDPE- g -MAH) were prepared from those organoclays. The micro- and nano-dispersions were analyzed through X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM): intercalation and/or partial exfoliation were found to occur only for formulations based on organoclays having an initial basal distance higher than 20 Å, suggesting the existence of a critical interfoliar distance for the delamination of silicate layers in a noninteracting polymer matrix. The properties of the nanocomposites were analyzed through differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and oscillatory rheometry. The dynamic crystallization of LLDPE was not significantly affected by the presence of clay. TGA in oxidative atmosphere proved to be very sensitive to the dispersion state of the organoclay: the thermal stability was drastically enhanced for intercalated and partially exfoliated formulations. However, the inherent thermal stability of the organoclay did not appear to influence significantly the overall thermal stability of the composite in the range of temperatures investigated (160,230°C). POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers. [source]


Effect of rotational speed of twin screw extruder on the microstructure and rheological and mechanical properties of nanoclay-reinforced polypropylene nanocomposites

POLYMER ENGINEERING & SCIENCE, Issue 8 2006
Piia Peltola
The morphology and rheological and mechanical properties of nanoclay-reinforced polypropylene nanocomposites were investigated with aid of transmission electron microscopy (TEM), thermo gravimetric analysis, rheometry, and mechanical tests. The organically modified silicate (montmorillonite) was used as a reinforcing material and maleic anhydride-grafted polypropylene oligomer as a compatibilizer to improve the clay dispersion and adhesion. The object of the study was to examine the effect of screw speed of the co-rotating twin-screw extruder on the clay exfoliation and nanocomposite properties. Also, the effect of compatibilizing agent was taken into account. The main result of the study was that nanocomposites showed both intercalated and exfoliated structures depending on the screw speeds of extruder. TEM images revealed that the dispersion of silicate layers was greatly influenced by the screw speed. However, even when the silicate layers were highly exfoliated, there was no remarkable effect on mechanical properties of the nanocomposite. POLYM. ENG. SCI. 46:995,1000, 2006. © 2006 Society of Plastics Engineers. [source]


Elongational Rheology of Polymer/Clay Dispersions: Determination of Orientational Extent in Elongational Flow Processes,

MACROMOLECULAR MATERIALS & ENGINEERING, Issue 4 2008
Eduard A. Stefanescu
Abstract The purpose of the present contribution is to provide an efficient method that would help to quantify the orientational levels occurring in polymer/clay dispersions subjected to elongational flow. The extent of internal orientation developed in salt containing montmorillonite/poly(ethylene oxide) gels is investigated, combining shear and elongational rheology methods. Entropic changes indicate that the strength of the transient network present in each gel affects the orientational ability of clay particles and polymer chains. We found that an increased Hencky strain of the hyperbolic die leads to a higher variation of the calculated entropy of the material. [source]


Intercalation and exfoliation behaviour of clay layers in branched polyol and polyurethane/clay nanocomposites

POLYMER INTERNATIONAL, Issue 2 2006
Hesheng Xia
Abstract The exfoliation of clay layers was realized in a tri-hydroxyl branched polyether polyol by direct mixing and the corresponding exfoliated polyurethane/clay nanocomposite was prepared by further in situ curing. The effects of various surface-modified organoclays and various polyol types on the intercalation and exfoliation behaviour of clay layers were investigated. The interaction between the polyol and clay and the mixing temperature plays an important role in the occurrence of exfoliation and intercalation. The relationship between rheological data of polyol/clay dispersion and the intercalation or exfoliation state of the clay was established. This provides a convenient and efficient way to evaluate the dispersion state of the clay. Based on the experimental results, a possible layer-by-layer exfoliation mechanism is proposed. Copyright © 2006 Society of Chemical Industry [source]