Bound Rubber and Elastomer-Filler Interaction

1995 ◽  
Vol 68 (2) ◽  
pp. 297-310 ◽  
Author(s):  
B. Meissner

Abstract The statistical theory of bound rubber and the polymer-filler gel formation theory are shown to offer a satisfactory quantitative description of a set of experimental bound-rubber data recently obtained by Wolff, Wang, Tan (Rubber Chem. Technol. 66, 163 (1993)) on SBR compounds filled with 17 furnace blacks covering the whole range of rubber grades. The observed decrease of bound-rubber content per unit of interfacial area with increasing loading and/or specific surface area of carbon black is explained by the theory as being due to the statistical nature of the adsorption process. A correlation was found to exist between specific surface activity of filler D (adjustable parameter of the theory, number of active sites per unit surface area) and filler structure, the latter being characterized by the difference between DBP absorption and crushed DBP absorption. Also, D was found to increase with loading of a high-structure black. The two effects are ascribed to filler aggregates breakdown during mixing, which leads to a new active surface formation for polymer bonding.

Author(s):  
Yaqi Yang ◽  
Ziqiang Shao ◽  
Feijun Wang

Abstract Due to the low specific capacitance and small specific surface area of conventional carbon materials used as electrode materials for double-layer capacitors, the search for more ideal materials and ingenious preparation methods remains a major challenge. In this study, fractional porous carbon nanosheets were prepared by co-doping Fe and N with chitosan as nitrogen source. The advantage of this method is that the carbon nanosheets can have a large number of pore structures and produce a large specific surface area. The presence of Fe catalyzes the graphitization of carbon in the carbon layer during carbonization process, and further increases the specific surface area of the electrode material. This structure provides an efficient ion and electron transport pathway, which enables more active sites to participate in the REDOX reaction, thus significantly enhancing the electrochemical performance of SCs. The specific surface area of CS-800 is up to 1587 m2 g−1. When the current density is 0.5 A g−1, the specific capacitance of CS-800 reaches 308.84 F g−1, and remains 84.61 % of the initial value after 10,000 cycles. The Coulomb efficiency of CS-800 is almost 100 % after a long cycle, which indicates that CS-800 has more ideal double-layer capacitance and pseudo capacitance.


2022 ◽  
Author(s):  
Kainan Li ◽  
Ke Zheng ◽  
Zhifang Zhang ◽  
Kuan Li ◽  
Ziyao Bian ◽  
...  

Abstract Construction of metal selenides with a large specific surface area and a hollow structure is one of the effective methods to improve the electrochemical performance of supercapacitors. However, the nano-material easily agglomerates due to the lack of support, resulting in the loss of electrochemical performance. Herein, we successfully design a three-dimensional graphene (3DG) encapsulation-protected hollow nanoboxes (CoSe2-SnSe2) composite aerogel (3DG/CoSe2-SnSe2) via a co-precipitation method coupled with self-assembly route, followed by a high temperature selenidation strategy. The obtained aerogel possesses porous 3DG conductive network, large specific surface area and plenty of reactive active sites. It could be used as a flexible and binder-free electrode after a facile mechanical compression process, which provided a high specific capacitance of 460 F g-1 at 0.5 A g-1, good rate capability of 212.7 F g-1 at 10 A g-1, and excellent cycle stability due to the fast electron/ion transfer and electrolyte diffusion. With the as-prepared 3DG/CoSe2-SnSe2 as positive electrodes and the AC (activated carbon) as negative electrodes, an asymmetric supercapacitor (3DG/CoSe2-SnSe2//AC) was fabricated, which delivered a high specific capacity of 38 F g-1 at 1A g-1 and an energy density of 11.89 W h kg-1 at 749.9 W kg-1, as well as a capacitance retention of 91.1% after 3000 cycles. This work provides a new method for preparing electrode material.


Minerals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1064
Author(s):  
Masanori Kohno

Considering the relevance of clay mineral-bearing geomaterials in landslide/mass movement hazard assessment, various engineering projects for resource development, and stability evaluation of underground space utilization, it is important to understand the permeability of these clay mineral-based geomaterials. However, only a few quantitative data have been reported to date regarding the effects of the clay mineral type and hydraulic gradient on the permeability of clay mineral materials. This study was conducted to investigate the permeability of clay mineral materials based on the clay mineral type, under different hydraulic gradient conditions, through a constant-pressure permeability test. Comparative tests have revealed that the difference in the types of clay mineral influences the swelling pressure and hydraulic conductivity. In addition, it has been found that the difference in water pressure (hydraulic gradient) affects the hydraulic conductivity of clay mineral materials. The hydraulic conductivity has been found to be closely associated with the specific surface area of the clay mineral material. Furthermore, the hydraulic conductivity value measured is almost consistent with the value calculated theoretically using the Kozeny–Carman equation. Moreover, the hydraulic conductivity is also found to be closely associated with the hydrogen energy, calculated from the consistency index of clay. This result suggests that the hydraulic conductivity of clay mineral materials can be estimated based on the specific surface area and void ratio, or consistency index of clay.


2007 ◽  
Vol 7 (3) ◽  
pp. 5941-6036 ◽  
Author(s):  
F. Domine ◽  
M. Albert ◽  
T. Huthwelker ◽  
H.-W. Jacobi ◽  
A. A. Kokhanovsky ◽  
...  

Abstract. Snow on the ground is a complex multiphase photochemical reactor that dramatically modifies the chemical composition of the overlying atmosphere. A quantitative description of the emissions of reactive gases by snow requires the knowledge of snow physical properties. This overview details our current understanding of how those physical properties relevant to snow photochemistry vary during snow metamorphism. Properties discussed are density, specific surface area, optical properties, thermal conductivity, permeability and gas diffusivity. Inasmuch as possible, equations to parameterize these properties as a function of climatic variables are proposed, based on field measurements, laboratory experiments and theory. The potential of remote sensing methods to obtain information on some snow physical variables such as grain size, liquid water content and snow depth are discussed. The possibilities for and difficulties of building a snow photochemistry model by adapting current snow physics models are explored. Elaborate snow physics models already exist, and including variables of particular interest to snow photochemistry such as light fluxes and specific surface area appears possible. On the other hand, understanding the nature and location of reactive molecules in snow seems to be the greatest difficulty modelers will have to face for lack of experimental data, and progress on this aspect will require the detailed study of natural snow samples.


2020 ◽  
Vol 44 (18) ◽  
pp. 7417-7423
Author(s):  
Jiannan Cai ◽  
Xiaofeng Zhang ◽  
Yi Zhang ◽  
Mingxing Yang ◽  
Baohua Huang ◽  
...  

The enhanced electrocatalytic properties of rGO/TiO2NTs for the ORR are a result of increased specific surface area, number of active sites and accelerated electron conductivity.


2016 ◽  
Vol 16 (20) ◽  
pp. 13359-13378 ◽  
Author(s):  
Hassan Beydoun ◽  
Michael Polen ◽  
Ryan C. Sullivan

Abstract. Heterogeneous ice nucleation remains one of the outstanding problems in cloud physics and atmospheric science. Experimental challenges in properly simulating particle-induced freezing processes under atmospherically relevant conditions have largely contributed to the absence of a well-established parameterization of immersion freezing properties. Here, we formulate an ice active, surface-site-based stochastic model of heterogeneous freezing with the unique feature of invoking a continuum assumption on the ice nucleating activity (contact angle) of an aerosol particle's surface that requires no assumptions about the size or number of active sites. The result is a particle-specific property g that defines a distribution of local ice nucleation rates. Upon integration, this yields a full freezing probability function for an ice nucleating particle. Current cold plate droplet freezing measurements provide a valuable and inexpensive resource for studying the freezing properties of many atmospheric aerosol systems. We apply our g framework to explain the observed dependence of the freezing temperature of droplets in a cold plate on the concentration of the particle species investigated. Normalizing to the total particle mass or surface area present to derive the commonly used ice nuclei active surface (INAS) density (ns) often cannot account for the effects of particle concentration, yet concentration is typically varied to span a wider measurable freezing temperature range. A method based on determining what is denoted an ice nucleating species' specific critical surface area is presented and explains the concentration dependence as a result of increasing the variability in ice nucleating active sites between droplets. By applying this method to experimental droplet freezing data from four different systems, we demonstrate its ability to interpret immersion freezing temperature spectra of droplets containing variable particle concentrations. It is shown that general active site density functions, such as the popular ns parameterization, cannot be reliably extrapolated below this critical surface area threshold to describe freezing curves for lower particle surface area concentrations. Freezing curves obtained below this threshold translate to higher ns values, while the ns values are essentially the same from curves obtained above the critical area threshold; ns should remain the same for a system as concentration is varied. However, we can successfully predict the lower concentration freezing curves, which are more atmospherically relevant, through a process of random sampling from g distributions obtained from high particle concentration data. Our analysis is applied to cold plate freezing measurements of droplets containing variable concentrations of particles from NX illite minerals, MCC cellulose, and commercial Snomax bacterial particles. Parameterizations that can predict the temporal evolution of the frozen fraction of cloud droplets in larger atmospheric models are also derived from this new framework.


2014 ◽  
Vol 931-932 ◽  
pp. 421-425 ◽  
Author(s):  
Son Tung Pham ◽  
William Prince

The objective of this work was to examine the microstructural changes caused by the carbonation of normal mortar. Samples were prepared and subjected to accelerated carbonation at 20°C, 65% relative humidity and 20% CO2concentration. The evolutions of the pore size distribution and the specific surface area during carbonation were calculated from the adsorption - desorption isotherms of water vapour and nitrogen. Conflicts observed in the results showed that the porous domains explored by these two methods are not the same due to the difference in molecular sizes of nitrogen and water. These two techniques therefore help to complementarily evaluate the effects of carbonation. The study also helped to explain why results in the literature diverge greatly on the influence of carbonation on specific surface area.


Clay Minerals ◽  
2015 ◽  
Vol 50 (2) ◽  
pp. 211-219 ◽  
Author(s):  
Bo Xue ◽  
Hongmei Guo ◽  
Lujie Liu ◽  
Min Chen

AbstractA new yttrium-zirconium-pillared montmorillonite (Y-Zr-MMT), was synthesized, characterized and used as a Ce catalyst support. The Y-Zr-MMT is a good support for dispersing cerium active sites and it is responsible for the high activity in the total oxidation of acetone, toluene and ethyl acetate. The Y-Zr-MMT shows greater advantages than the conventional alumina/cordierite honeycomb supports such as large specific surface area, lower cost and easier preparation. Catalytic tests demonstrated that Ce/Y-Zr-MMT (Ce loading 8.0%) was the most active, with the total oxidation of acetone, toluene and ethyl acetate being achieved at 220, 300 and 220°C, respectively. The catalyst displayed better activity for the oxidation of acetone and ethyl acetate than a conventional, supported Pd-catalyst under similar conditions. The special structure of the yttrium-doped zirconium-pillared montmorillonite can strengthen the interaction between the CeO2 and Zr-MMT support and improve the dispersion of the Ce particles, which enhances the catalytic activity for the oxidation of VOCs. The new catalyst, 8.0%Ce/Y-Zr-MMT, could be promising for industrial applications due to its high catalytic activity and low cost. The support and the catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET specific surface area measurements.


1993 ◽  
Vol 66 (2) ◽  
pp. 163-177 ◽  
Author(s):  
Siegfried Wolff ◽  
Meng-Jiao Wang ◽  
Ewe-Hong Tan

Abstract SBR compounds were filled with 17 carbon blacks covering the whole range of rubber grades and tested for bound-rubber content. It was found that the bound-rubber content of a polymer at high loadings is higher for large surface-area carbon blacks. On the other hand, the bound-rubber content per unit of interfacial area in the compound (specific bound-rubber content) decreases with increasing specific surface area and filler loading. This observation was interpreted in terms of interaggregate multiple molecular adsorption, filler agglomeration, and change of molecular weight of rubber during mixing. When the comparison was carried out at critical loading of a coherent mass, the specific bound-rubber content was found to be higher for the high-surface-area products which are characterized by high surface energies. The critical loading of coherent mass of bound rubber also shows a strong surface-area dependence, indicating that large particle carbon blacks give high critical loadings. The measurements of bound rubber at high temperatures for carbon-black-filled compounds and in an ammonia atmosphere for silica-filled compounds suggest that bound rubber is caused essentially by physical adsorption.


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