黄瓜保绿的Mg^(++)盐方法研究(英文)

研究了用Mg+ + 盐使黄瓜保绿保鲜的一种方法。先用Mg+ + 盐冰预冷黄瓜 ,然后将其贮存于 10～ 12℃。在贮存的 12d中测定了 3种生理生化指标 :(1)水份 ;(2 )呼吸强度 ;(3)叶绿素含量。结果显示 ,用Mg+ + 盐冰预冷使黄瓜保绿保鲜是一种有效的方法。

Electrochemical mechanism of electrolysis codeposition of Mg-Sr alloy in molten salt

The electrochemical process of Mg-Sr codeposition was studied in MgCl2-SrCl2-KCl melts containing different MgCl2 concentrations at 700 ℃ by cyclic voltammetry, chronopotentiometry and chronoamperometry. The results show that the actual precipitation potential of Sr reduces by nearly 0.5 V because of the depolarization effects of Sr activity reduced by forming Mg-Sr alloy. The codeposition potential condition of Mg and Sr to form Mg-Sr alloy is as follows： When electrode potential is more negative than -1.5 V, the magnesium will precipitate; when electrode potential is more negative than -2.0 V, the magnesium and strontium will both deposit. The control step of codeposition process of Mg and Sr is not diffusion control step. The codeposition current condition of Mg and Sr to form Mg-Sr alloy by chronoptentiometry is as follows： cathode current densities are higher than 0.71, 1.57 and 2.83 A/cm^2 in MgCl2-SrCl2-KCl melts with MgCl2 concentrations of 2%, 5% and 10% （mass fraction）, respectively. Key words：

Effect of oxide and fluoride addition on electrolytic preparation of Mg-La alloy in chloride molten salt

Mg-La alloys were prepared by constant voltage electrolysis in the molten salt system of MgC12-LaC13-KC1 at 750℃, with a graphite crucible as the anode and a tungsten rod as the cathode. The effect of oxide and fluoride addition on the electrolysis was investigated comprehensively. X-ray diffraction （XRD） was used to characterize some of the Mg-La alloy products and the sludges. As the content of MgO or La203 in the electrolyte increased, both the current efficiency and the mass of alloy product decreased, indicating that both MgO and La203 may take part in the reactions in the electrolyte. When the same mass of the oxide was added, compared with La203, MgO had a more pronounced effect on both the current efficiency and the mass of alloy product. XRD studies confirmed the formation of LaOC1 when MgO or LazO3 was added into the electrolyte. The formation of LaOCl sludge would be the main reason for the negative effect of the oxide addition on both the current efficiency and the mass of alloy. In the electrolytic system, the addition of CaF2 was not helpful to suppress the negative effect of MgO on the electrolysis, probably due to the complex reactions of the La compounds in the electrolyte.

Electrochemical codeposition of Mg-Li-Gd alloys from LiCl-KCl-MgCl_2-Gd_2O_3 melts

Mg-Li-Gd alloys were prepared by electrochemical codeposition from LiCl-KCl-MgCl 2 -Gd 2 O 3 melts on molybdenum electrode with constant current density at 823 and 973 K. The microstructure of the Mg-Li-Gd alloys was analyzed by X-ray diffraction （XRD）, optical microscopy （OM） and scanning electron microscopy （SEM）. The results show that magnesium and gadolinium deposit mainly in the first 30 min, and the alloy obtained contains 96.53% Mg, 0.27% Li and 3.20% Gd （mass fraction）. Then, the reduction of lithium ions occurs quickly. The composition of alloy can be adjusted by controlling electrolysis time or Gd 2 O 3 concentration in LiCl-KCl melts. With the addition of Gd into Mg-Li alloys, the corrosion resistance of the alloys is enhanced. XRD results suggest that Mg 3 Gd and Mg 2 Gd can be formed in Mg-Li-Gd alloys. The distribution of Gd element in Mg-Li-Gd alloys indicates that Gd element mainly distributes at the grain boundaries of Mg-Li-Gd alloys.

Boron isotope geochemistry of Zigetang Co saline lake sediments,Tibetan Plateau

The origin of boron in boron-rich salt lakes in the Tibetan Plateau is highly controversial.In this study,we carried out a detailed study on boron geochemistry and isotope composition of lake sediments collected in Zigetang Co,central Tibet.Evaporites had high boron concentrations of 172.3–418.6 lg/g and δ^(11)B values of-8.2%to-3.3%,suggesting a non-marine origin for the saline lake.The boron isotopic fractionation factor,a,between evaporite and brackish water(a_(evaporite–brackish))decreased systematically with depth,from 0.9942 at the top of the drill core to 0.9893 at the bottom;the linear variation between α_(evaporite–brackish)and depth reflects boron isotopic fractionation associated with progressive crystallization.The positive correlation between δ^(11)B versus[B]and δ^(11)B versus depth in the evaporite phase reflects pH and boron speciation in the solution control on the adsorption of boron,and B(OH)_3 species incorporated preferentially into Mg(OH)_2 precipitation at high pH.

Study the Effect of Boron and Titanium to Resist Corrosion in the Salt Solution for the Alloy （Al-Cu-Mg）

The alloy （AI-Cu-Mg） alloy important one dating back to the series （2xxx） where copper foundries basic element which represents the number （2）, the study relied on foundries add elements boron （B） and titanium （Ti） and then use a heat treatment （homogenizing process） to improve the corrosion resistance in saline （NaC1 3.5%） of the base alloy （A1-Cu-Mg）, was prepared four types of alloys （A, B, C, D） depending on the chemical composition. The results showed that the corrosion resistance in saline solution was the best resistance in the alloy （D） （A1-2% Cu-2% Mg-0.1% B-1.0% Ti） compared with the rest of bullion when an examination of corrosion of the alloy prepared after homogenizing. But by examining the surface roughness of the alloy ingot turned out that （D） is softer than the rest of the surface alloys and this is due to the addition of boron and titanium together increases surface smoothness in alloys because it works to reduce the grain size.

Carbon Dioxide Mineralisation and Integration with Flue Gas Desulphurisation Applied to a Modern Coal-Fired Power Plant

For Finland, carbon dioxide mineralisation was identified as the only option for CCS （carbon capture and storage） application. Unfortunately it has not been embraced by the power sector. One interesting source-sink combination, however, is formed by magnesium silicate resources at Vammala, located -85 km east of the 565 MWe coal-fired Meri-Pori Power Plant on the country＇s southwest coast. This paper assesses mineral sequestration of Meri-Pori power plant CO2, using Vammala mineral resources and the mineralisation process under development at Abo Akademi University. That process implies Mg（OH）E production from magnesium silicate-based rock, followed by gas/solid carbonation of the Mg（OH）2 in a pressurised fluidised bed. Reported are results on experimental work, i.e., Mg（OH）2 production, with rock from locations close to Meri-Pori. Results suggest a total CO2 fixation capacity -50 Mt CO2 for the Vammala site, although production of Mg（OH）2 from rock from the site is challenging. Finally, as mineralisation could be directly applied to flue gases without CO2 pre-capture, we report from experimental work on carbonation of Mg（OH）2 with CO2 and CO2-SO2-O2 gas mixtures. Results show that SO2 readily reacts with Mg（OH）2, providing an opportunity to simultaneously capture SO2 and CO2, which could make separate flue gas desulphurisation redundant.