Low temperature solid-phase sintering of sintered metal fibrous media with high specific surface area

A procedure of low temperature solid-phase sintering（LTSS） was carried out to fabricate sintered metal fibrous media（SMFM） with high specific surface area.Stainless steel fibers which were produced by cutting process were first plated with a coarse copper coating layer by electroless plating process.A low-temperature sintering process was then completed at about 800 °C for 1 h under the protection of hydrogen atmosphere.The results show that a novel SMFM with complex surface morphology and high specific surface area（0.2 m2/g） can be obtained in this way.The effect of sintering temperature on the surface morphology and specific surface area of SMFM was studied by means of scanning electron microscopy and Brunauer-Emmett-Teller.The damage of micro-structure during the sintering process mainly contributed to the loss of specific surface area of SMFM and the optimal sintering temperature was 800 °C.

Nickel catalysts supported on MgO with different specific surface area for carbon dioxide reforming of methane

In this paper, three kinds of MgO with different specific surface area were prepared, and their effects on the catalytic performance of nickel catalysts for the carbon dioxide reforming of methane were investigated. The results showed that MgO support with the higher specific surface area led to the higher dispersion of the active metal, which resulted in the higher initial activity. On the other hand, the specific surface area of MgO materials might not be the dominant factor for the basicity of support to chemisorb and activate CO2, which was another important factor for the performance of catalysts. Herein, Ni/MgO(CA) catalyst with proper specific surface area and strong ability to activate CO2exhibited stable catalytic property and the carbon species deposited on the Ni/MgO(CA) catalyst after 10 h of reaction at 650 ?C were mainly activated carbon species.

Study on Preparation of Rice Husk Ash with High Specific Surface Area and Its Chemical Reactivity

Preparation of rice husk ash with high specific surface area and chemical reactivity of the product are reported in this paper. The amorphous rice husk ash with high specific surface area of 311 m2·g-1 was produced by heating acid treated rice husk at 700℃ for 4 h. The isotherms of rice husk ash are similar in shape to type Ⅱof Brunaner's classification with mesopores being predominant. The rice husk ash has a high chemical reactivity,especially that pretreated with acid. This chemical reactivity depends on ashing temperature and pretreatment conditions. There is an exponential relation between the specific surface area of rice husk ash and the change in the conductivity of saturated Ca(OH)2 solution with rice husk ash, from which the specific surface area can be known according to the conductivity change.

Metal-Free C_(3)N_(4) with plentiful nitrogen vacancy and increased specific surface area for electrocatalytic nitrogen reduction

As a substitute for synthetic ammonia under mild condition, electrocatalytic nitrogen reduction reaction(NRR) provides a hopeful approach for the development of ammonia. Nevertheless, the current development of NRR electrocatalysts is far from enough and a systematic research is needed to gain a better improvement. This article presents that 2 D C_(3)N_(4)-NV with a large specific surface area and abundant nitrogen vacancies is prepared by a simple and feasible method, and used as a metal-free catalyst for electrocatalytic NRR. Experiment result and density functional theory(DFT) calculation reveal that nitrogen vacancies in 2 D C_(3)N_(4)-NV can act as an efficient active site for catalytic NRR, which is conducive to capturing and activating N_(2), lowering Gibbs free energy(DG) in reaction and inhibiting hydrogen evolution reaction(HER) at the same time. In addition, the larger specific surface area also makes more active site exposed, which is good for the contact between the electrolyte and the active site, thus enhancing its NRR activity. The electrocatalyst shows an excellent catalytic activity for NRR in 0.1 M HCl, including Faradaic efficiency of 10.96%, NH_(3) yields of 17.85 lg h^(-1) mg_(cat)^(-1)., and good stability(over 20 h).

Relationship between the specific surface area of rust and the electrochemical behavior of rusted steel in a wet–dry acid corrosion environment

The relationship between the specific surface area（SSA） of rust and the electrochemical behavior of rusted steel under wet-dry acid corrosion conditions was investigated. The results showed that the corrosion current density first increased and then decreased with increasing SSA of the rust during the corrosion process. The structure of the rust changed from single-layer to double-layer, and the γ-FeOOH content decreased in the inner layer of the rust with increasing corrosion time; by contrast, the γ-FeOOH content in the outer layer was constant. When the SSA of the rust was lower than the critical SSA corresponding to the relative humidity during the drying period, condensed water in the micropores of the rust could evaporate, which prompted the diffusion of O_2 into the rust and the following formation process of γ-FeOOH, leading to an increase of corrosion current density with increasing corrosion time. However, when the SSA of the rust reached or exceeded the critical SSA, condensate water in the micro-pores of the inner layer of the rust could not evaporate which inhibited the diffusion of O_2 and decreased the γ-FeOOH content in the inner rust, leading to a decrease of corrosion current density with increasing corrosion time.

Effects of Specific Surface Area and Impurities of Reactive Alumina on Properties of Corundum Based Castables

Effects of specific surface area and tiny amount of impurities of reactive alumina on the workability, sinte- ring and high temperature mechanical strength of corun- dum based castables were investigated. The results show that the presence of reactive alumina with high specific surface area leads to accelerating of the hydration of calcium aluminate cement, thus shortening the working time and setting time of the castables, which can be as- cribed that the critical energy barrier for stable nuclei of hydration products of cement can be reduced by the high specific surface area of reactive alumina. The sintering of the corundum based castables can be accelerated by the reactive alumina with high specific surface area and high amount of impurities, however, the reactive alumina with too high specific surface area and impurities can al- so lead to noticeable shrinkage of castables. In addition, high temperature mechanical strength of corundum based castables can be decreased by the higher amount of trace impurities of reactive alumina due to formation of low- melting phase at high temperatures.

Preparation of Zirconia-Ceria Powders with High Specific Surface Area

Zirconia-ceria mixed oxide powders were prepared by high temperature aging method.The effects of the temperature and the time of aging, cerium content and calcination on powder performance were studied.The result shows that high temperature aging is an efficient way of preparation of ZrO2-CeO2 mixed oxide powders with high specific surface area and good thermal stability, and that addition of a small amount of cerium to hydrous zirconia can promote the preparation of high specific surface area powders.

Measurement of Specific Surface Area of Ceramisite Made from River Sediment

Principle and method of measuring Specific Surface Area (SSA) of ceramisite made from dredged river sediment, sewage sludge and adherent materials are discussed. Brunauer-Emmett-Teller Procedure tests SSA of the ceramisite. Influences of sewage sludge content, adherent content and sintering point on the SSA of ceramisite made of river sediment are also analyzed. Results show that with the right sewage sludge content, adherent content and sintering point, the ceramisite can have the highest SSA value and be widely used.

Preparation of activated carbon with low ash content and high specific surface area from coal in the presence of KOH

An activated carbon with ash content less than 10% and specific surface area more than 1 600 m 2 /g was prepared from coal and the effect of K containing compounds in preparation of coal based activated carbon was investigated in detail in this paper. KOH was used in co carbonization with coal, changes in graphitic crystallites in chars derived from carbonization of coal with and without KOH were analyzed by X ray diffraction (XRD) technique, activation rates of chars with different contents of K containing compounds were deduced, and resulting activated carbons were characterized by nitrogen adsorption isotherms at 77 K and iodine numbers. The results showed that the addition of KOH to the coal before carbonization can realize the intensive removal of inorganic matters from chars under mild conditions, especially the efficient removal of dispersive quartz, an extremely difficult separated mineral component in other processes else. Apart from this, KOH demonstrates a favorable effect in control over coal carbonization with the goal to form nongraphitizable isotropic carbon precursor, which is a necessary prerequisite for the formation and development of micro pores. However, the K containing compounds such as K 2 CO 3 and K 2 O remaining in chars after carbonization catalyze the reaction between carbon and steam in activation, which leads to the formation of macro pores. In the end an innovative method, in which KOH is added to coal before carbonization and K containing compounds are removed by acid washing after carbonization, was proposed for the synthesis of quality coal based activated carbon.

A statistical reappraisal of the relationship between liquid limit and specific surface area, cation exchange capacity and activity of clays

More than 500 datasets from the literature have been used to evaluate the relationships of specific surface area (SSA),cation exchange capacity (CEC) and activity versus the liquid limit (LL).The correlations gave R^2 values ranging between 0.71 and 0.92.Independent data were also used to validate the correlations.Estimated SSA values slightly overestimate the measured SSA up to 100 m^2/g.Regarding the estimated CEC values,they overestimated the measured CEC values up to 20 meq/(100 g).A probabilistic approach was performed for the correlations of SSA,CEC and activity versus LL.The analysis shows that the relations of SSA,CEC and activity with LL are robust.Using the LL values,it is possible to assess other basic engineering properties of clays.

Li<SUB>4</SUB>Ti<SUB>5</SUB>O<SUB>12</SUB>Synthesis with High Specific Surface Area and Single Phase

We have investigated a novel Li4Ti5O12 synthesis with high specific surface area, high crystallization and single phase and its mechanism. The method was performed with a solid phase synthesis by using CH3COOLi·2H2O and anatase TiO2 via Li2TiO3 as an intermediate in pre-sintering at 500°C and sintering at 750°C. This result showed specific surface area of 12 m2/g and single phase- Li4Ti5O12 by applying the high specific surface anatase TiO2 as a precursor.

Surface distribution of alkalinity and specific alkalinity and their application to water mass tracing in Kuroshio area of the East China Sea

Surface distribution and seasonal variation of alkalinity and specific alkalinity in Kuroshio area of the East ChinaSea and their application to the water mass tracing are discussed in this paper. Results show a distinct seasonal variation of the alkalinity, which is concerned with the process of vertical mixing. Different specific alkalinity in various water masses has been found. On the basis of the difference of the specific alkalinity and the distribution of alkalinity, two water fronts in summer season, located at 27°-30°N and 124°-1 27°E, (Ⅰ), and at the northern waters about one latitude from the Taiwan Island, (Ⅱ); one in winter season at about one longitude from coast of mainland of China and 26°-30°N were found. In summer season, about 1-2 longitudes eastward shift of front (Ⅰ) is found by comparison of data in May and August. And the high alkalinity of the northern East China Sea in summer season may be caused by the Huanghe River runoff flowing southward along with the Huanghai Sea Coastal Current.

Effects of specific surface area of metallic nickel particles on carbon deposition kinetics

Carbon deposition on nickel powders in methane involves three stages in different reaction temperature ranges. Temperature programing oxidation test and Raman spectrum results indicated the formation of complex and ordered carbon structures at high deposition temperatures. The values of I（D）/I（G） of the deposited carbon reached 1.86, 1.30, and 1.22 in the first, second, and third stages, respectively. The structure of carbon in the second stage was similar to that in the third stage. Carbon deposited in the first stage rarely contained homogeneous pyrolytic deposit layers. A kinetic model was developed to analyze the carbon deposition behavior in the first stage. The rate-determining step of the first stage is supposed to be interfacial reaction. Based on the investigation of carbon deposition kinetics on nickel powders from different resources, carbon deposition rate is suggested to have a linear relation with the square of specific surface area of nickel particles.

New Method for Measurement of Plant Roots Specific Surface

To provide enough space to carry all surface charges responsible for high cation exchange capacity of plant roots, large area of the root specific surface is necessary, however all experimental methods used up to date give too small surface area values. In this paper, we propose to measure the plant roots surface area using water vapor adsorption isotherm. This method gives roots specific surface areas compatible to CEC. Methodical aspects of the measurements are described along with theoretical background for calculating specific surface area on the example of roots of barley grown in nutrient solution.

Nitrogen and sulfur dual-doped high-surface-area hollow carbon nanospheres for efficient CO2 reduction

The electrochemical reduction of CO2(CO2 RR) can substantially contribute to the production of useful chemicals and reduction of global CO2 emissions. Herein, we presented N and S dual-doped high-surface-area carbon materials(SZ-HCN) as CO2 RR catalysts. N and S were doped by one-step pyrolysis of a N-containing polymer and S powder. ZnCl2 was applied as a volatile porogen to prepare porous SZ-HCN. SZ-HCN with a high specific surface area(1510 m2 g–1) exhibited efficient electrocatalytic activity and selectivity for CO2 RR. Electrochemical measurements demonstrated that SZ-HCN showed excellent catalytic performance for CO2-to-CO reduction with a high CO Faradaic efficiency(~93%) at-0.6 V. Furthermore, SZ-HCN offered a stable current density and high CO selectivity over at least 20 h continuous operation, revealing remarkable electrocatalytic durability. The experimental results and density functional theory calculations indicated that N and S dual-doped carbon materials required lower Gibbs free energy to form the COOH* intermediate than that for single-N-doped carbon for CO2-to-CO reduction, thereby enhancing CO2 RR activity.

Preparation of High Surface Area, Large Pore Volume Alumina by Using β-Cyclodextrin as a Non-surfactant Template

A series of alumina samples were prepared using β-cyclodextrin as the non-surfactant template. These samples were characterized by XRD, BET and TEM. The results showed that the alumina samples prepared using β-cyclodextrin template had the higher surface areas （124-484 m^2/g）, larger pore volumes （0.7-1.27 mL/g） and more thermal stability than samples prepared without using β-cyclodextrin.

Construction of the hierarchical porous biochar with an ultrahigh specific surface area for application in high-performance lithium-ion capacitor cathode

Biochar with a highly accessible specific surface area can display a higher performance when it is used as the cathode of lithium-ion capacitors.Facing the complex composition and diversity of biomass precursors,there is a lack of a universally applicable method to construct hierarchical porous biochar controllably.In this work,a multi-stage activation strategy combining the feature of different activation methods is proposed for this target.To confirm the porous characteristic in prepared samples,N_(2) adsorption-desorption and transmission electron microscope were used.As the optimal sample,BC-P3K4S had the highest specific surface area of 3583.3 m^(2) g^(−1).Evaluated as the electrode for a lithium-ion capacitor,BC-P3K4S displayed a capacity of 139.1 mAh g^(−1) at 0.1 A g^(−1).After coupling it with pre-lithiated hard carbon,the full device exhibited a high energy density of 129.3 W h kg^(−1) at 153 W kg^(−1).The work outlined herein offers some insights into the preparation of hierarchical porous biochar from complex biomass by multistep activation method.

Carbon cathode with heteroatom doping and ultrahigh surface area enabling enhanced capacitive behavior for potassium-ion hybrid capacitors

Potassium-ion hybrid capacitors(PIHCs)are widely regarded as highly promising energy storage devices,due to their exceptional energy density,impressive power density,and abundant potassium resources.Unfortunately,restricted by the inherent capacitive storage mechanism,the carbon cathodes possess a much lower specific capacity than battery-type anodes.Therefore,designing high-performance carbon cathodes is extremely urgent for the development of PIHCs.Herein,N,O codoped porous carbon(NOPC)was fabricated through the NaCl hard template method and combined KOH/melamine chemical activation technique,displaying the characteristics of abundant N/O content(4.7 at%/16.9 at%),ultrahigh specific surface area(3092 m^(2)g^(-1))and hierarchical pore network.The designed NOPC cathode delivers a high specific capacity(164.4 mAh.g^(-1)at 0.05 A.g^(-1))and superior cyclability(95.1%retention ratio at 2 A·g^(-1)over 2500 cycles).Notably,the adjustable ratio of micropores to mesopores facilitates the achievement of the optimal bal-ance between capacity and rate capability.Moreover,the pseudocapacitance can be further augmented through the incorporation of N/O functional groups.As expected,the graphite//NOPC based PIHC possesses a high energy density of 113 Wh·kg-at 747 W·kg^(-1)and excellent capacity retention of 84.4% fter 400 cycles at 1.0 A·g^(-1).This work introduces a novel strategy for designing carbon cathodes that enhances the electrochemical performance of PIHCs.

Dominant role of wettability in improving the specific capacitance

Here we report a strategy to enhance the energy density of supercapacitors by increasing the utilization rate of the specific surface area(SSA)via wettability improvement. The nonporous gold(NPG) film is used as the electrodes and the ionic liquid [EMIM]BF4 is the electrolyte. When the electrode is coated by paraffin, an increase of the contact angle leads to a remarkable reduction of the specific capacitance. While when acetonitrile is added into the electrolyte, the contact angle is decreased and the utilization rate of SSA is improved, which results in an increase of the specific capacitance. The addition of isopropyl acetate into the electrolyte leads to a further increase of the specific capacitance. To generalize the role of the wettability in improving the energy density, a carbon-based electrode is evaluated in the solution of potassium hydroxide. An addition of propyl alcohol into the potassium hydroxide solution leads to an increase of the specific capacitance, as well as a long-term stability of the supercapacitor. The role of conductivity in this study is excluded by designing experiments. This paper highlights the significance of wettability in determining the specific capacitance, showing an alternative to improve the energy density of supercapacitors.