Effects of Citric Acid Concentration and Activation Temperature on the Synthesis of Carbon Nanotubes

A series of Ni-La-Mg catalyst samples were prepared by citric acid complex method, and carbon nanotubes were synthesized by catalytic decomposition of CH4 on these catalysts. The effects of the citric acid concentration and the activation temperature on catalytic activity were investigated by CO adsorption, TEM and XRD techniques. The experimental results showed that the particle size of the catalysts prepared through gel auto-combustion varied with the concentration of citric acid. Therefore carbon nanotubes with different diameters were obtained correspondingly. The effect of activation temperature on the activity of catalyst was negligible from 500 to 700 ℃, but it became pronounced at lower or higher temperatures.

Effect of activation temperature on the properties of double layer capacitance of diatomite-templated carbon

1 Introduction In recent years porous carbons have been widely used in many fields such as energy storage(Mc Creery,2008;Liu et al,2009;Ho et al,2014;Yang et al,2015),adsorption,wastewater treatment,air purification

Characteristics of the dynamic changes in active accumulated temperature in Sichuan,China in the last 51 years against the background of climate change

It is of utmost necessity to understand the dynamics of regional active accumulated temperature(AAT)to cope with the negative impacts of global warming on agroforestry development and food security and to provide a real-time and effective reference basis for regional agroforestry planning.The daily temperature data from 30 meteorological stations in Sichuan Province from 1970 to 2020,and sea surface temperature(SST)index data from the Atlantic Multiphase Oscillation(AMO)and Pacific Decadal Oscillation(PDO)were used for the study.Sichuan Province was divided into the western region(WS)and the eastern region(ES),considering 1000 m above sea level as the boundary.The spatiotemporal characteristics of≥0℃ and≥10℃ active accumulated temperature(AAT0,AAT10)in WS and ES were analyzed comprehensively using 5-day average sliding,empirical orthogonal function(EOF),ensemble empirical mode decomposition(EEMD),and multiple mutation tests.The results show that(1)AAT0 and AAT10 of WS ranged from 3034℃ to 3586℃ and 1971℃ to 2636℃,respectively,while the AAT0 and AAT10 of ES ranged from 5863℃ to 6513℃ and 4847℃ to 5875℃,respectively.The period around 1997 was a significant abrupt change,and the AAT in the province generally increased during the subsequent time period(2)AAT in the study area is mainly driven by the fluctuations of AMO,as reflected by the low-to-high variation of AAT coinciding with the jump of the cold-to-warm phase of AMO.Considering different time scale fluctuations in the past 51 years,the major cycle for both AAT0 and AAT10 in WS is 3.40 a,while the major cycles in ES are 3.64 a and 3.19 a,respectively with a sub-cycle of 7.29 a.AAT fluctuation has an insignificant periodic characteristic of 25.50 a on the interdecadal scale(3)The spatial heterogeneity of AAT in WS is prominent and is mainly reflected by the significantly warm conditions in the south of the WS region and relatively slight warm conditions in the north,as well as by the isolated cooling area in the form of"freezing point",i.e.,Xiaojin county.In contrast,the spatial variability of AAT in ES is more or less consistent,with the warming areas concentrated in the foothills of the western edge of the basin and a slight increase in AAT observed in the central part of the basin.

Activation and pumping characteristics of Ti-Zr-V films deposited on narrow tubes

Non-evaporable getter(NEG)films are an integral part of many particle accelerators.These films provide conductance-free evenly distributed pumping,a low thermal outgassing rate,and a low photon-and electron-stimulated desorption.These characteristics make it an ideal solution for resolving the non-uniform pressure distribution in conductance-limited narrow vacuum tubes.In this study,ternary Ti-Zr-V films were deposited on Si substrates and Ag-Cu(Ag 0.085 wt%)tubes with an inner diameter of 22 mm.All Ti-Zr-V films were prepared from an alloy target using the same DC magnetron sputtering parameters.The compositions and corresponding chemical bonding states were analyzed by X-ray photoelectron spectroscopy after activation at different temperatures.The test particle Monte Carlo(TPMC)method was used to measure the sticking probability of the Ti-Zr-V film based on pressure readings during gas injection.The results indicate that activation commences at temperatures as low as 150℃and Ti~0,Zr~0,and V~0 exist on the surface after annealing at 180℃for 1 h.Ti-Zr-V films can be fully activated at 180℃for 24 h.The CO sticking probability reaches 0.15,with a pumping capacity of 1 monolayer.

Compositions,Proportions,and Equilibrium Temperature of Coexisting Two-feldspar in Crystalline Rocks

Compositions, proportions, and equilibrium temperature of coexisting two-feldspar in crystalline rocks are of great importance to classification in petrography and interpretation of petrogenesis. Crystalline rocks are usually composed of 4-6 minerals （phases）, depending on their independent chemical components and the equilibrium temperature of crystallizations. In general, number of mineral phases can be determined by the ＂Phase Rule＂. According to the mass balance principle, bulk composition of coexisting two-feldspar could be evaluated from the bulk chemistry of a rock, provided that the compositions of the coexisting mafic mineral phases containing calcium, sodium, and potassium oxides are determined, e.g., by microprobe analysis. The compositions, proportions, and temperature of two-feldspar in equilibrium can thus be simultaneously resolved numerically from bulk composition of the rock, by incorporating the activity/composition relations of the ternary feldspars with the mass balance constraints. Upon the numerical approximation method presented in this paper, better-quality, internally consistent data on feldspar group could usually be obtained, which would be expected more realistic and accurate in consideration of thermodynamic equilibria in the system of crystalline rocks, as well as bulk chemistry of a rock and the composing minerals.

Research on Diamond Enhanced Tungsten Carbide Composite Button

At the present, the cutters used in button bits and rock bits are mainly cobalt tungsten carbide in our country. Because of its low abrasive resistance, the bit service life and drilling efficiency was very low when the hard and extremely hard formations were being drilled. Owing to its high abrasive resistance, the diamond composite material is widely used in drilling operations. However, its toughness against impact is too low to be used in percussion drilling, only can it be used in rotary drilling. In order to solve the problems encountered by DTH hammer in hard rock drilling, make bit life longer, increase rate of penetration and decrease drilling cost, a new type diamond enhanced tungsten carbide composite button with high abrasive resistance and high toughness against impact, which may be used in percussion drilling, has been developed. The key problems to make the button are to improve the thermal stability of diamond, to increase the welding strength between diamond and cemented tungsten carbide, and to lower the sintering temperature of tungsten carbide. All these problems have been solved effectively by pretreatment of diamond, low temperature activation hot-press sintering and high sintering pressure. (1) To plate tungsten on the surface of diamond. Diamond suffers easily from erosion in the environment of high temperature containing oxygen and iron family elements. There is very high energy between the interface of diamond and bonding metal and so the metallurgical bond can’t form at the interface between diamond and bond metal. This will lower greatly the bending strength and the toughness against impact of diamond enhanced tungsten carbide composite button. In order to improve thermal stability of diamond and increase the bonding strength of the interface between diamond and bond metal, to plate tungsten on the surface of diamond by vacuum vapor deposit is adopted. (2) To lower the sintering temperature by adding nickel, phosphorus and boron etc into conventional mixed powder. In general, the sintering temperature of cemented tungsten carbide is more than 1 350 ℃ in which diamond will suffer from serious heat erosion, so the sintering temperature must be lowered. To add nickel, phosphorus and boron etc into cobalt-base bond whose melting point is more than 1 350 ℃ will lower the sintering temperature to about 1 050 ℃. To add phosphorus can lower the temperature of liquid phase occurring and promote the densification of matrix alloy in advance because the co-crystallization temperature of Ni-P and Co-P is 880 ℃ and 1 020 ℃ respectively. The proper adding amount of nickel, phosphorus and boron etc is a key problem. To substitute nickel for partial cobalt can improve the toughness against impact of diamond enhanced tungsten carbide composite button and lower the sintering temperature. To add boron is helpful for sintering and improving the toughness against impact of diamond enhanced tungsten carbide composite button. (3) To increase the sintering press. Under the same sintering temperature, to improve the sintering press can improve the density and strength of sintering products. In this study to increase the sintering press 35 MPa in the usual conditions to 50～60 MPa in sintering diamond enhanced tungsten carbide button by adopting ceramic material as pressing rod has improved the sintering quality effectively. The properties of the button have been measured under lab conditions. The testing results show that its hardness is more than HRA86 and that its abrasiveness resistance is 100 times more than conventional cemented tungsten carbide, and its toughness against impact is more than 100J. All these data theoretically show that the button has very good mechanical properties that can meet the need of percussion drilling, and can solve the problems encountered with button bit of conventional cemented tungsten carbide.

Activity Enhancement of Vanadium Catalysts with Ultrasonic Preparation Process for the Oxidation of Sulfur Dioxide

The effect of ultrasonic cavitations on the activity of vanadium catalysts atlow temperatures for the oxidation of sulfur dioxide, in which refined carbonized mother liquor hadbeen added, was investigated. Twenty minutes were needed to produce obvious cavitations when thecatalyst raw material was treated in the 50 W ultrasonic generator. However, only 10 minutes wouldbe needed in a 150 W ultrasonic generator. The higher the temperature of the wet material, the lesstime was needed to produce cavitations, and the optimal temperature was 60℃. The water content inthe wet material mainly affected the quantity of cavitations. Ls-8 catalyst was prepared usingultrasonic. Its activity for conversion of SO_2 reached to 52.5% at 410℃ and 4.2% at 350℃. Thedifferential thermal analyses indicate that both endothermic peaks and exothermic peaks noticeablyshifted forward compared with Ls catalyst prepared without ultrasonic, and SEM results show auniform pore size distribution for Ls-8 catalyst.

Preparation of Cs-Rb-V series sulphuric acid catalyst

Cs Rb V series low temperature sulphuric acid catalyst was prepared for the first time by using carbonized mother liquor containing alkali metal salts. The results show that the conversion of SO 2 on catalyst prepared directly with carbonized mother liquor could reach to 24.8% at 410?℃. If n (Na)/ n (V) was adjusted properly, the conversion of SO 2 could be increased to 35.6% at 410?℃. Refined carbonized mother liquor could make the catalytic activity even higher at low temperature, the conversion of SO 2 could be increased to 36.65% at 410?℃. The catalyst was examined with differential thermal analysis. It was found that both endothermic peaks and exothermic peaks of catalyst shifted forward obviously and the catalyst possessed higher activity at low temperature.

Dielectric Properties of Bi_4Ti_3O_(12) Ceramics by Impedance Spectroscopic Method

Various lead-free ceramics have been investigated in search for new high-temperature dielectrics. In particular, Bi_4Ti_3O_（12） is a type of ferroelectric ceramics, which is supposed to replace leadcontaining ceramics for its outstanding dielectric properties in the near future. Ferroelectric ceramics of Bi_4Ti_3O_（12） made by conventional mixed oxide route have been studied by impedance spectroscopy in a wide range of temperature. X-ray diffraction patterns show that Bi_4Ti_3O_（12） ceramics are a single-phase of ferroelectric Bi-layered perovskite structure whether it is calcined at 800 ℃ or after sintering production. This study focused on the effect of the grain size on the electric properties of BIT ceramics. The BIT ceramics with different grain sizes were prepared at different sintering temperatures. Grain becomes coarser with the sintering temperature increasing by 50 ℃, relative permittivity and dielectric loss also change a lot. When sintered at 1 100 ℃, r values peak can reach 205.40 at a frequency of 100 k Hz, the minimum dielectric losses of four different frequencies make no difference, all close to 0.027. The values of Ea range from 0.52 to 0.68 e V. The dielectric properties of the sample sintered at 1 100 ℃ are relatively better than those of the other samples by analyzing the relationship of the grain, the internal stresses, the homogeneity and the dielectric properties. SEM can better explain the results of the dielectric spectrum at different sintering temperatures. The results show that Bi_4Ti_3O_（12） ceramics are a kind of dielectrics. Thus, Bi_4Ti_3O_（12） can be used in high-temperature capacitors and microwave ceramics.

GaN-based violet laser diodes grown on free-standing GaN substrate

A violet laser diode （LD） structure is grown on a free-standing c-plane GaN substrate and 4 μm×800μm ridge waveguide LDs are fabricated. The electrical and the optical characteristics of LDs under different facet-coating and chip-mounting conditions are investigated under pulse mode operation. The active region temperatures of p-side up and p-side down mounted LDs are calculated with different injection currents. The calculated thermal resistances of p-side up and p-side down mounted LDs are 4.6 K/W and 3 K/W, respectively. The threshold current of the p-side down mounted LD is much lower than that of the p-side up mounted LD. The blue shift of the emission wavelength with increasing injection current is observed only for the LD with p-side down mounting configuration, due to the more efficient heat dissipation.

Screening Psychrophilic Fungi of Cellulose Degradation and Characteristic of Enzyme Production

A fungus（WR-C1） decomposed cellulose was isolated from a hypothermal litter layer using Congo red medium as the preliminary screening culture medium and then using a filter as the secondary screening medium at low temperature. The experiment showed that the weight loss rate of filter paper on the 15 th days could reach 30.69%. A morphologic and ITS gene sequence analysis suggested that CF-C1 was Cladosporium. We mainly studied the effects of culture time, inoculation amount, initial p H and different sources of carbon, nitrogen and inorganic salt on the cellulase production of strain WR-C1. Under optimum cultural condition, the highest value of WR-C1 enzyme production and filter paper enzyme were 3.27 U · m L～（-1） and 0.51 U · m L～（-1）.

Effects of SO2 on the low temperature selective catalytic reduction of NO by NH3 over CeO2-V2O5-WO3/TiO2 catalysts

The CeO2-V2O5-WO3/TiO2 （CeO2-VWT） catalysts were prepared by one-step and two-step impregnation methods. The effects of different loading of CeO2 and different preparation methods on De-NOx activity of catalysts had been investigated. CeO2 helped to improve the De-NOx activity and sulfur resistance. The optimal loading of CeO2 was 3% with the De-NOx efficiency reached 89.9% at 140℃. The results showed that the De-NOx activity of 3% CeO2-VWT catalysts by one-step method was the same as two-step method basically and reached the level of industrial applications, the N2 selectivity of catalysts was more than 99.2% between 110℃ and 320℃. In addition, CeO2 promoted the oxidation of NO to NO2, which adsorbed on the Lewis acid site （V5＋-O） to form V5＋-NO3 and inspired the fast SCR reaction. Not only the thermal stability but also the De-NOx activity of catalysts decreased with excess CeO2 competed with V2O5. Characterizations of catalysts were carried out by XRF, BET, XRD, TG and FT-IR. BET showed that the specific surface area of catalysts decreased with the loading of CeO2 increased, the active components content and specific surface area of catalysts decreased slightly after entering SO2. Ammonium sulfate species were formed in poisoned catalyst which had been investigated by XRF, BET, TG and FT-IR. The largest loss rate of weight fraction was 0.024%.℃-1 at 380℃ 390℃, which was in accordance with the decomposition temperature of NH4HSO4 and （NH4）2SO4,

Temperature stability of symmetric activated carbon supercapacitors assembled with in situ electrodeposited poly (vinyl alcohol) potassium borate hydrogel electrolyte

The temperature stability of supercapacitor（SC） is largely determined by the properties of the electrolyte.Hydrogel electrolytes（HGE）, due to their hydrophilic polymer skeleton, show different temperature stability to that of liquid aqueous electrolytes. In this study, symmetric activated carbon（AC） SCs had been assembled with in situ electrodeposited poly（vinyl alcohol） potassium borate（PVAPB） HGE. The electrochemical performance of the SCs was systematically studied at different temperatures. Results show that the conductivity of PVAPB HGE is comparable with that of liquid aqueous electrolytes at different temperatures. The operating temperature range of PVAPB HGE SCs is -5–60°C, while those of the 1 mol/L Na2SO4SCs and the 0.9 mol/L KClSCs are 20–80°C and 20–40°C, respectively. The specific capacitance of PVAPB HGE SC is higher than those of SCs using liquid aqueous electrolytes at any temperature. The excellent temperature stability of PVAPB HGE makes it possible to build stable aqueous SCs in the wider temperature range.

Deposition and characterization of Pd-Ti thin film by sublimation

Introduction Pd/Ti double-layer thin film as non-evaporable getter(NEG)was deposited by sublimation,and its activation temperature was as low as 100℃.The Pd film was deposited in situ after Ti deposition to ensure no oxidization on Ti film.Pumping speed test and characterization method The pumping speed of the coated pipe was measured by a pumping speed test system.The sticking factor was calculated by Molflow.The surface morphology was observed by a scanning electron microscope(SEM).The chemical composition of the film was measured by an energy-dispersive spectrum inbuilt with the SEM.The crystalline structure of the film was measured using grazing incidence X-ray diffraction.Conclusion It was found that the pumping performance of the Pd/Ti film still remained high after 15 times of activation.The maximum pumping speed after heating at 100℃for 24 h was 1.1 L/s cm^(2)and 0.49 L/s cm^(2)for H_(2)and CO,respectively.It can be concluded that the key to reducing the activation temperature of NEG materials is to enhance the oxidation resistance of the surface of NEG.

Shape design of cerium oxide nanoparticles for enhancement of enzyme mimetic activity in therapeutic applications

Cerium oxide nanoparticles （CONPs）, widely used in catalytic applications owing to their robust redox reaction, are now being considered in therapeutic applications based on their enzyme mimetic properties such as catalase and super oxide dismutase （SOD） mimetic activities. In therapeutic applications, the emerging demand for CONPs with low cytotoxicity, high cost efficiency, and high enzyme mimetic capability necessitates the exploration of alternative synthesis and effective material design. This study presents a room temperature aqueous synthesis for low-cost production of shape-selective CONPs without potentially harmful organic substances, and additionally, investigates cell viability and catalase and SOD mimetic activities. This synthesis, at room temperature, produced CONPs with particular planes： {111}/{100} nanopolyhedra, {100} nano/submicron cubes, and {111}/{100} nanorods that grew in [110] longitudinal direction. Enzymatic activity assays indicated that nanopolyhedra with a high concentration of Ce4＋ ions promoted catalase mimetic activity, while nanocubes and nanorods with high Ce3＋ ion concentrations enhanced SOD mimetic activity. This is the first study indicating that shape and facet configuration design of CONPs, coupled with the retention of dominant, specific Ce valence states, potentiates enzyme mimetic activities. These findings may be utilized for CONP design aimed at enhancing enzyme mimetic activities in therapeutic applications.