Steric effects in adsorption of ions from mixed electrolytes into microporous carbon

With the goal to improve the capacitance in electrochemical double-layer capacitors (EDLCs) many studies on pore size/ion size relationship have been undertaken to achieve a better understanding of the charge storage mechanism in the electrochemical double-layer in confinement. A significant capacitance increase was achieved by using carbon electrodes with micropores (b1 nm), when the carbon pore size was close to the ion size. In this paper, the accessibility of narrow pores is investigated by selecting a carbon with a small pore size (b0.7 nm) and electrolyte mixtures with different ion sizes. It has been shown that the adsorption capacitance limitation observed for large cations and anions could be overcome by adding ions with a smaller effective size. This result demonstrates that the pores are accessible when their size matches the effective ion size and contradicts the surface saturation assumption; effective ion size which exceeds the pore size leads to current limitation. This work confirms that the steric effect is involved when ions are adsorbed into pores and highlights the importance of controlling ion size/pore size relationship for optimisation of the capacitive performance of EDLC devices

Multi-scale simulation of capillary pores and gel pores in Portland cement paste

The microstructures of Portland cement paste (water to cement ratio is 0.4, curing time is from 1 day to 28 days) are simulated based on the numerical cement hydration model, HUMOSTRUC3D (van Breugel, 1991; Koenders, 1997; Ye, 2003). The nanostructures of inner and outer C-S-H are simulated by the packing of monosized (5 nm) spheres. The pore structures (capillary pores and gel pores) of Portland cement paste are established by upgrading the simulated nanostructures of C-S-H to the simulated microstructures of Portland cement paste. The pore size distribution of Portland cement paste is simulated by using the image segmentation method (Shapiro and Stockman, 2001) to analyse the simulated pore structures of Portland cement paste. The simulation results indicate that the pore size distribution of the simulated capillary pores of Portland cement paste at the age of 1 day to 28 days is in a good agreement with the pore size distribution determined by scanning electron microscopy (SEM). The pore size distribution of the simulated gel pores of Portland cement paste (interlayer gel pores of outer C-S-H and gel pores of inner C-S-H are not included) is validated by the pore size distribution obtained by mercury intrusion porosimetry (MIP). The pores with pore size of 20 nm to 100 nm occupy very small volume fraction in the simulated Portland cement paste at each curing time (0.69% to 1.38%). This is consistent with the experimental results obtained by nuclear magnetic resonance (NMR)

Quantitative characterization of pore structure of several biochars with 3D imaging

Pore space characteristics of biochars may vary depending on the used raw material and processing technology. Pore structure has significant effects on the water retention properties of biochar amended soils. In this work, several biochars were characterized with three-dimensional imaging and image analysis. X-ray computed microtomography was used to image biochars at resolution of 1.14 $\mu$m and the obtained images were analysed for porosity, pore-size distribution, specific surface area and structural anisotropy. In addition, random walk simulations were used to relate structural anisotropy to diffusive transport. Image analysis showed that considerable part of the biochar volume consist of pores in size range relevant to hydrological processes and storage of plant available water. Porosity and pore-size distribution were found to depend on the biochar type and the structural anisotopy analysis showed that used raw material considerably affects the pore characteristics at micrometre scale. Therefore attention should be paid to raw material selection and quality in applications requiring optimized pore structure.Comment: 16 pages, 4 figures. The final publication is available at Springer via http://dx.doi.org/10.1007/s11356-017-8823-

A new method for the determination of thin film porosity

Internal reflection spectroscopy may be used to determine presence of water in thin film pores. Presence of water in such pores is function of relative humidity and pore size. Thus, one can determine pore size by controlling humidity. Fluids with surface tension different from that of water can be used to detect pores

Computer program calculates and plots surface area and pore size distribution data

Computer program calculates surface area and pore size distribution of powders, metals, ceramics, and catalysts, and prints and plots the desired data directly. Surface area calculations are based on the gas adsorption technique of Brunauer, Emmett, and Teller, and pore size distribution calculations are based on the gas adsorption technique of Pierce

Polymer Translocation Through a Long Nanopore

Polymer translocation through a nanopore in a membrane investigated theoretically. Recent experiments on voltage-driven DNA and RNA translocations through a nanopore indicate that the size and geometry of the pore are important factors in polymer dynamics. A theoretical approach is presented which explicitly takes into account the effect of the nanopore length and diameter for polymer motion across the membrane. It is shown that the length of the pore is crucial for polymer translocation dynamics. The present model predicts that for realistic conditions (long nanopores and large external fields) there are two regimes of translocation depending on polymer size: for polymer chains larger than the pore length, the velocity of translocation is nearly constant, while for polymer chains smaller than the pore length the velocity increases with decreasing polymer size. These results agree with experimental data.Comment: 14 pages, 5 figure