一种高效节能降耗的碳碱法制造硼砂新工艺

通过对现行的碳碱法制硼砂的工艺过程进行分析,提出碳解过程可分为反应初期、主反应期和反应末期3个阶段。反应初期和末期吸收速率大于反应速率;主反应期开始吸收速率大于反应速率,后期二者相当。针对反应过程的特点,提出了改进碳解反应的核心是提高碳解的二氧化碳压力和适当提高温度,并对现行工艺进行了改进。改进后的工艺技术指标为:硼矿碳解率90%、碳解时间9 h、二氧化碳利用率大于96%、蒸汽消耗(以1 t硼砂计)1 292 kg。改进后的碳碱法工艺与原工艺比,反应时间缩短了1/2,能耗显著减少,二氧化碳减排效果明显,有助于提高环境质量。

凤城—宽甸硼镁矿焙烧的研究

研究几种不同产地的硼镁矿石焙烧的温度与碳解率的关系,结果表明;矿石品位、焙烧温度对碳解率的影响很大。生产中要根据实际情况,在600—700℃范围内,选择最佳焙烧温度,可达到90％以上的碳解率。

Supercritical Carbon Dioxide Extraction of Andrographolide from Andrographis paniculata： Effect of the Solvent Flow Rate, Pressure, and Temperature

Andrographis paniculata Nees has been extensively used for traditional medicine and help against fever dysentery, diarrhoea, inflammation, and sore throat. In this study, andrographolide, the main component of this plant was extracted from the leaves of A. paniculata using supercritical carbon dioxide. The operating pressures were varied from 7.50 to 20MPa, the temperatures were varied from 30℃ to 60℃, and the flow rates were varied from 0.5 to 4ml.min^-1. The best extraction condition occurred at 10MPa, 40℃, and a flow rate of 2ml.min^-1 for a 3g sample of A. paniculata ground-dried leaves. The measured extraction rate was found to be about 0.0174g of andrographolide per gram of andrographolide present in the leaves per hour of operation. The future studies must focus on the interaction between the various operating parameters such as temperature, pressure, and flow rate of supercritical carbon dioxide.

An investigation on dissolution kinetics of single sodium carbonate particle with image analysis method

Dissolution kinetics of sodium carbonate is investigated with the image analysis method at the approach of single particle.The dissolution experiments are carried out in an aqueous solution under a series of controlled temperature and p H.The selected sodium carbonate particles are all spherical with the same mass and diameter.The dissolution process is quantified with the measurement of particle diameter from dissolution images.The concentration of dissolved sodium carbonate in solvent is calculated with the measured diameter of particle.Both surface reaction model and mass transport model are implemented to determine the dissolution mechanism and quantify the dissolution rate constant at each experimental condition.According to the fitting results with both two models,it is clarified that the dissolution process at the increasing temperature is controlled by the mass transport of dissolved sodium carbonate travelling from particle surface into solvent.The dissolution process at the increasing pH is controlled by the chemical reaction on particle surface.Furthermore,the dissolution rate constant for each single spherical sodium carbonate particle is quantified and the results show that the dissolution rate constant of single spherical sodium carbonate increases significantly with the rising of temperature,but decreases with the increasing of pH conversely.

Non-isothermal decomposition kinetics of hydrogarnet in sodium carbonate solution

Carbonation decomposition of hydrogarnet is a significant reaction of the calcification-carbonation new method for alumina production by using low-grade bauxite.In this work,non-isothermal decomposition kinetics of hydrogarnet in sodium carbonate solution was studied by high-pressure differential scanning calorimetry(HPDSC) at different heating rates of 2,5,8,10,15 and 20 K·min^(-1),respectively.The activation energy(E_α) was calculated with the help of isoconversional method(model-free),and the reaction mechanism was determined by the differential equation method.The calculated activation energy of this reaction was 115.66 kJ·mol^(-1).Furthermore,the mechanism for decomposition reaction is Avrami-Erofeev(n=1.5),and the decomposition process is diffusion-controlled.

Reaction heat-driven CO2 desorption during CO oxidation on Au(997) at low temperatures

Adsorption and reaction of CO and CO2 were studied on oxygen-covered Au（997） surfaces by means of temperature- programmed desorption/reaction spectroscopy. Oxygen atoms （O（a）） on Au（997） enhances the CO2 adsorption and stabilizes the adsorbed COe（a）, and the stabilization effect also depends on the CO2（a） coverage and involved Au sites. CO2（a） desorp- tion is the rate-limiting step for the CO＋O（a） reaction to produce CO2 on Au（997） at 105 K and exhibits complex behaviors, including the desorption of CO2（a） upon CO exposures at 105 K and the desorption of O（a）-stabilized CO2（a） at elevated temperatures. The desorption of CO2（a） from the surface upon CO exposures at 105 K to produce gaseous CO2 depends on the surface reaction extent and involves the reaction heat-driven CO2（a） desorption channel. CO＋O（a） reaction proceeds more easily with weakly-bound oxygen adatoms at the （111） terraces than strongly-bound oxygen adatoms at the （111） steps. These re- sults reveal complex rate-limiting COe（a） desorption behaviors during CO＋O（a） reaction on Au surfaces at low temperatures which provide novel information on the fundamental understanding of Au catalysis.

Ash-free coal as fuel for direct carbon fuel cell

This work describes the performance of the direct carbon fuel cell(DCFC)fuelled by ash-free coal.Employing coal in the DCFC might be problematic,mainly because of the ash deposition after the cell reactions.In the study,the carbonaceous ash-free component of coal is obtained,which is then evaluated as the DCFC fuel and compared with raw coal,active carbon,carbon black,and graphite.The electrolyte-supported SOFC structure is adapted to build the DCFC.The DCFC based on the ash-free coal fuel exhibits good performance with regard to the maximum power density,day-by-day measurements,and durability at continuous run.When the carbon fuels are internally gasified to H2 and CO,the power density is generally much improved,compared to N2 pyrolysis environment.The power generation is most likely related to the concentration of pyrolyzed gases as well as the electrochemical reactivity of the solid carbon.

Investigation of interfacial processes in graphite thin film anodes of lithium-ion batteries by both in situ and ex situ infrared spectroscopy

Graphite thin film anodes with a high IR reflectivity have been prepared by a spin coating method. Both ex situ and in situ mi- croscope FTIR spectroscopy （MFFIRS） in a reflection configuration were employed to investigate interfacial processes of the graphite thin film anodes in lithium-ion batteries. A solid electrolyte interphase layer （SEI layer） was formed on the cycled graphite thin film anode. Ex situ MFTIRS revealed that the main components of the SEI layer on cycled graphite film anodes in 1 tool L 1 LiPF6/ethylene carbonate ＋ dimethyl carbonate （1：1） are alkyl lithium carbonates （ROCOzLi）. The desolvation process on graphite anodes during the initial intercalation of lithium ion with graphite was also observed and analyzed by in situ MFTIRS.