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.

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).

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.

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.

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.

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.

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.

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.

Experimental Study on the Chloride Ion Concentration of Cement Pastes Prepared with Limestone Powder

To investigate the impact of limestone powder on the chloride ion concentration coefficient of cement pastes,various techniques such as scanning electron microscopy(SEM),X-ray diffraction(XRD),thermogravimetric analysis(TGA),and mercury-porosimetry(MIP)were employed in this paper.The findings demonstrate that the creation of Friedel's salt is inversely associated with the addition of limestone powder,that is,Friedel's salt production is lessened by adding more limestone powder,however,the coefficient of chloride ion concentration initially decreased and then increased again,as does the porosity,and most likely the pore size as well.The specific surface area of limestone powder has increased,and the content of Friedel’s salt increased first and then decreased.However,the shifting trend of Friedel's salt and chloride ion concentration coefficient is in direct opposition,and the pore structure was therefore significantly enhanced.The results of this study offer robust theoretical backing for the inclusion of limestone powder in concrete and provide a positive assessment of its potential applications.

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.

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.

Surface Chemical Properties of Colloids in Main Soils of China

Surface chemical properties of soil colloids are the important factor affecting soil fertility and genesis. To provide scientific basis for soil genetic classification, promotion of soil fertility and reasonable fertilization, the specific surface area and electric charge of soil colloids in relation to clay minerals and organic matter are further discussed on the basis of the results obtained from the studies on surface chemical properties of soil colloids in five main soils of China. Results from the studies show that the effect of clay minerals and organic matter on the surface chemical properties of soil colloids is very complicated because the siloxane surface, hydrated oxide surface and organic matter surface do not exist separately, but they are always mixed together and influenced each other. The understanding of the relationship among clay minerals, organic matter and surface chemical properties of soil colloids depends upon further study of the relevant disciplines of soil science, especially the study on the mechanisms of organo-mineral complexes.

Development of a drill energy utilization index for aiding selection of drill machines in surface mines

Drill machines used in surface mines, particularly in coal, is characterized by a very poor utilization （around 40%） and low availability （around 60%）. The main purpose of this study is to develop a drill selec- tion methodology and simultaneously a performance evaluation technique based on drill cuttings produced and drilling rate achieved. In all 28 blast drilled through were investigated. The drilling was accomplished by 5 different drill machines of Ingersoll-Rand and Revathi working in coal mines of Sonepur Bazari （SECL） and Block-II （BCCL）. The drills are Rotary and Rotary Percussive type using tri- cone rock roller bits. Drill cuttings were collected and sieve analysis was done in the laboratory. Using Rosin Ramler Diagram, coarseness index （CI）, mean chip size （d）, specific-st trace area （SSA） and charac- teristic particle size distribution curves for all the holes drilled were plotted. The predictor equation for drill penetration rate established through multiple regressions was found to have a very good correlation with an index of determination of 0.85. A comparative analysis of particle size distribution curves was used to evaluate the drill efficiency. The suggested approach utilises the area under the curve, after the point of trend reversal and brittleness ratio of the respective bench to arrive at drill energy utilization index （DEUI）, for mapping of drill machine to bench, The developed DEU1 can aid in selecting or mapping a right machine to right bench for achieving higher penetration rate and utilizations.

Study on Physicochemical Properties and Surface Properties of Biochar from Different Materials

[Objectives]This study was conducted to explore the differences in physicochemical properties and surface properties of biochar from different sources.[Methods]Four kinds of materials including rice husk and corn straw were prepared at 450℃by the limited-oxygen program temperature control method into biochar,and the differences in physicochemical properties and surface properties of the biochar from different sources were studied.[Results]All four kinds of biochar were alkaline(pH=8.7-10.0).Corn straw biochar had the highest organic carbon content(653.6 g/kg),while rice husk biochar had the lowest organic carbon content(486.1 g/kg).Corn straw biochar had the highest nitrogen content(2.7%),while rice husk biochar had the lowest nitrogen content(0.75%).Corn straw biochar had the highest total phosphorus content(5.64 g/kg),while rice husk biochar had the lowest total phosphorus content(1.1 g/kg).Rice straw biochar had the highest total potassium content(53.1 g/kg),while rice husk biochar had the lowest total potassium content(10.6 g/kg).The four types of biochar were all porous,but their pore structure sizes and shapes were different to certain degrees.The order of the specific surface areas of the four types of biochar was rice stalk biochar>corn stalk biochar>wheat stalk biochar>rice husk biochar;the order of the pore volumes was rice stalk biochar>corn stalk biochar>wheat stalk biochar Charcoal>rice husk biochar;and the pore sizes ranked as wheat stalk biochar>corn stalk biochar>rice husk biochar>rice stalk biochar.The biochar from different sources ranked according to the comprehensive evaluation of all indicators as corn straw biochar>wheat straw biochar>rice straw biochar>rice husk biochar.[Conclusions]This study provides reference data for the preparation process of biochar from industrial and agricultural wastes and its application and promotion.

A comparative study of the specific surface area and pore structure of different shales and their kerogens

The pore structures and controlling factors of several different Paleozoic shales from Southern China and their kerogens were studied using nitrogen adsorption and scanning electron microscopy methods. The results indicate that： 1） The specific surface area is 2.22-3.52 m2/g and has no correlation with the TOC content of the Permian Dalong Formation shales, nanopores are extremely undeveloped in the Dalong Formation kerogens, which have specific surface areas of 20.35-27.49 me/g; 2） the specific surface area of the Silurian Longmaxi Formation shales is in the range of 17.83-29.49 m2/g and is positively correlated with TOC content, the kerogens from the Longmaxi Formation have well-developed nanopores, with round or elliptical shapes, and the specific surface areas of these kerogens are as high as 279.84-300.3 m2/g; 3） for the Niutitang Formation shales, the specific surface area is 20.12-29.49 m2/grock and increases significantly with increasing TOC and smectite content. The Niuti- tang Formation kerogens develop a certain amount of nanopores with a specific surface area of 161.2 m2/g. Oil shale was also examined for comparison, and was found to have a specific surface area of 19.99 m2/g. Nanopores are rare in the Youganwo Formation kerogen, which has a specific surface area of only 5.54 m2/g, suggesting that the specific surface area of oil shale is due mainly to the presence of smectite and other clay minerals. The specific surface area and the number of pores present in shales are closely related to TOC, kerogen type and maturity, smectite content, and other factors. Low-maturity kerogen has very few nanopores and therefore has a very low specific surface area, whereas nanopores are abundant in mature to over- mature kerogen, leading to high specific surface areas. The Longmaxi Formation kerogen has more developed nanopores and a higher specific surface area than the Niutitang Formation kerogen, which may be due to differences in the kerogen type and maceral components. A high content of smectite may also contribute to shale surface area. The pore volume and specific sur- face area of low-maturity kerogens are mainly attributable to pores with diameters above 10 nm. By contrast, the pore volume of mature kerogens consists predominantly of pores with diameters above 10 nm with some contribution from about 4 nm diameter pores, while the specific surface area is due mainly to pores with diameters of less than 4 nm. Through a comparative study of the specific surface area and pore structure characteristics of different shales and their kerogens, we conclude that the Longmaxi Formation shales and Niutitang Formation shales have greater sorption capacities than the Dalong Formation shales.

Well-dispersed NiCoS_(2) nanoparticles/rGO composite with a large specific surface area as an oxygen evolution reaction electrocatalyst

Developing efficient oxygen evolution reaction(OER) electrocatalysts such as transition metal sulfides(TMSs) is of great importance to advance renewable hydrogen fuel toward further practical applications.Herein,NiCoS_(2) nanoparticles well decorated on double-sided N-doped reduced graphene oxide sheets(NiCoS_(2)/rGO) are prepared from an Al-containing ternary NiCoAl-layered double hydroxide precursor(NiCoAl-LDH) grown on GO support as an OER electrocatalyst.The Al-confinementassisted sulfurization,followed by selective acid treatment,endows the resulting NiCoS_(2)/rGO composite with the advantages:well-dispersed NiCoS_(2) nanoparticles,dualsided rGO support,as well as a large specific surface area of 119.4 m^(2)·g^(-1) and meso-/macroporous size distribution.The NiCoS_(2)/rGO electrocatalyst exhibits an overpotential of 273 mV at 10 mA·cm^(-2) and a good stability of 24 h,which outperform those of the counterparts of NiS_(2)/rGO and CoS_(2)/rGO.The results of electrochemical active surface area and electrochemical impedance spectra experimentally provide convincing rationales of the information of active sites and good conductivity,both underpin the enhanced electrocatalytic performances.