The Suizhou meteorite is a heavily shocked and melted vein-containing L6 chondrite.It contains a minor amount of diopside with a(Ca_(0.419)Mg_(0.466)Fe_(0.088))SiO_(3)composition,and a shock-metamorphosed diopside gra...The Suizhou meteorite is a heavily shocked and melted vein-containing L6 chondrite.It contains a minor amount of diopside with a(Ca_(0.419)Mg_(0.466)Fe_(0.088))SiO_(3)composition,and a shock-metamorphosed diopside grain associated with ringwoodite and lingunite was found in a melt vein of this meteorite.Our electron microprobe,transmission electron microscopic and Raman spectroscopic analyses revealed four silicate phases with different compositions and structures inside this shock-metamorphosed diopside grain,termed phase A,B,C and D in this paper.Phase A is identified as orthorhombic(Ca_(0.663)-Mg_(0.314))SiO_(3)-perovskite which is closely associated with phase B,the vitrified(Mg_(0.642)Ca_(0.290)Fe_(0.098))SiO_(3)perovskite.Phase D is assigned to be(Mg_(0.578)Ca_(0.414))SiO_(3)majorite which is associated with phase C,the vetrified Carich Mg-perovskite with a(Mg_(0.853)Ca_(0.167))SiO_(3)composition.Based on high-pressure and high-temperature experiments,the diopside grain in the melt vein of the Suizhou meteorite would have experienced a P–T regime of 20–24GPa and 1800–>2000℃.Such P–T conditions are high enough for the decomposition of the diopside and the formation of four different silicate phases.The orthorhombic(Ca_(0.663)Mg_(0.314))SiO_(3)perovskite found in the Suizhou L6 chondrite might be considered as the third lower-mantle silicate mineral after bridgmanite and davemaoite after the detailed analyses of its crystal structure and physical properties being completed.展开更多
This work looked into the influence of the sealing treatment on the structural feature and electrochemical response of AZ31 Mg alloy coated via plasma electrolytic oxidation(PEO).Here,the inorganic layers produced by ...This work looked into the influence of the sealing treatment on the structural feature and electrochemical response of AZ31 Mg alloy coated via plasma electrolytic oxidation(PEO).Here,the inorganic layers produced by PEO in an alkaline-phosphate electrolyte were subsequently immersed for different periods in cold(60°C)and hot(100°C)aqueous solutions containing either 1 or 3 gr of cobalt nitrate hexahydrate in the presence of hydrogen peroxide as an initiator.The results showed that the sealing treatments in the hot solutions could trigger the hydration reactions of PEO coating which would largely assist the surface incorporation of Co_(3)O_(4)into the coating.In contrast,the sealing in cold solutions led to less compact coatings,which was attributed to the fact the hydration reactions would be restricted at 60°C.A nearly fully sealed coating with a porosity of~0.5%was successfully formed on the sample immersed in the hot solution containing 1 gr of cobalt nitrate hexahydrate.Thus,the electrochemical stability of this fully sealed coating was superior to the other samples as it had the lowest corrosion current density(4.71×10^(-10)A·cm^(-2))and the highest outer layer resistance(3.81×10^(7)Ω·cm^(2)).The composite coatings developed in this study are ideal for applications requiring high electrochemical stability.展开更多
The hydrolysis of MgH_(2) delivers high hydrogen capacity(15.2 wt%),which is very attractive for real-time hydrogen supply.However,the formation of a surface passivation Mg(OH)_(2) layer and the large excess of H_(2)O...The hydrolysis of MgH_(2) delivers high hydrogen capacity(15.2 wt%),which is very attractive for real-time hydrogen supply.However,the formation of a surface passivation Mg(OH)_(2) layer and the large excess of H_(2)O required to ensure complete hydrolysis are two key challenges for the MgH_(2) hydrolysis systems.Now,a low-cost method is reported to synthesize MgH_(2)@Mg(BH_(4))_(2) composite via ball-milling MgH_(2) with cheap and widely available B_(2)O_(3)(or B(OH)_(3)).By adding small amounts of B_(2)O_(3),the in-situ formed Mg(BH_(4))_(2) could significantly promote the hydrolysis of MgH_(2).In particular,the MgH_(2)–10 wt%B_(2)O_(3) composite releases 1330.7 mL·g^(−1) H_(2)(close to 80%theoretical hydrogen generation H_(2))in H_(2)O and 1520.4 mL·g^(−1) H_(2)(about 95%)in 0.5 M MgCl_(2) in 60 min at 26℃ with hydrolysis rate of 736.9 mL·g^(−1)·min^(−1) and 960.9 mL·g^(−1)·min^(−1) H_(2) during the first minute of the hydrolysis,respectively.In addition,the MgCl_(2) solution allows repeated use by filtering and exhibits high cycle stability(20 cycles),therefore leading to much reduced capacity loss caused by the excess H_(2)O.We show that by introducing B_(2)O_(3) and recycling the 0.5 M MgCl_(2) solution,the system hydrogen capacity can approach 5.9 wt%,providing a promising hydrogen generation scheme to supply hydrogen to the fuel cells.展开更多
文摘The Suizhou meteorite is a heavily shocked and melted vein-containing L6 chondrite.It contains a minor amount of diopside with a(Ca_(0.419)Mg_(0.466)Fe_(0.088))SiO_(3)composition,and a shock-metamorphosed diopside grain associated with ringwoodite and lingunite was found in a melt vein of this meteorite.Our electron microprobe,transmission electron microscopic and Raman spectroscopic analyses revealed four silicate phases with different compositions and structures inside this shock-metamorphosed diopside grain,termed phase A,B,C and D in this paper.Phase A is identified as orthorhombic(Ca_(0.663)-Mg_(0.314))SiO_(3)-perovskite which is closely associated with phase B,the vitrified(Mg_(0.642)Ca_(0.290)Fe_(0.098))SiO_(3)perovskite.Phase D is assigned to be(Mg_(0.578)Ca_(0.414))SiO_(3)majorite which is associated with phase C,the vetrified Carich Mg-perovskite with a(Mg_(0.853)Ca_(0.167))SiO_(3)composition.Based on high-pressure and high-temperature experiments,the diopside grain in the melt vein of the Suizhou meteorite would have experienced a P–T regime of 20–24GPa and 1800–>2000℃.Such P–T conditions are high enough for the decomposition of the diopside and the formation of four different silicate phases.The orthorhombic(Ca_(0.663)Mg_(0.314))SiO_(3)perovskite found in the Suizhou L6 chondrite might be considered as the third lower-mantle silicate mineral after bridgmanite and davemaoite after the detailed analyses of its crystal structure and physical properties being completed.
基金supported by the National Research Foundation of Korea(NRF)funded by the Korean government(MSIT)(No.2022R1A2C1006743)
文摘This work looked into the influence of the sealing treatment on the structural feature and electrochemical response of AZ31 Mg alloy coated via plasma electrolytic oxidation(PEO).Here,the inorganic layers produced by PEO in an alkaline-phosphate electrolyte were subsequently immersed for different periods in cold(60°C)and hot(100°C)aqueous solutions containing either 1 or 3 gr of cobalt nitrate hexahydrate in the presence of hydrogen peroxide as an initiator.The results showed that the sealing treatments in the hot solutions could trigger the hydration reactions of PEO coating which would largely assist the surface incorporation of Co_(3)O_(4)into the coating.In contrast,the sealing in cold solutions led to less compact coatings,which was attributed to the fact the hydration reactions would be restricted at 60°C.A nearly fully sealed coating with a porosity of~0.5%was successfully formed on the sample immersed in the hot solution containing 1 gr of cobalt nitrate hexahydrate.Thus,the electrochemical stability of this fully sealed coating was superior to the other samples as it had the lowest corrosion current density(4.71×10^(-10)A·cm^(-2))and the highest outer layer resistance(3.81×10^(7)Ω·cm^(2)).The composite coatings developed in this study are ideal for applications requiring high electrochemical stability.
基金supported by the Basic and Applied Basic Research Foundation of Guangdong Province(No.2022A1515011832 and 2021A1515110676)supported by GDAS’Project of Science and Technology Development(2022GDASZH-2022010104,2022GDASZH-2022030604-04).
文摘The hydrolysis of MgH_(2) delivers high hydrogen capacity(15.2 wt%),which is very attractive for real-time hydrogen supply.However,the formation of a surface passivation Mg(OH)_(2) layer and the large excess of H_(2)O required to ensure complete hydrolysis are two key challenges for the MgH_(2) hydrolysis systems.Now,a low-cost method is reported to synthesize MgH_(2)@Mg(BH_(4))_(2) composite via ball-milling MgH_(2) with cheap and widely available B_(2)O_(3)(or B(OH)_(3)).By adding small amounts of B_(2)O_(3),the in-situ formed Mg(BH_(4))_(2) could significantly promote the hydrolysis of MgH_(2).In particular,the MgH_(2)–10 wt%B_(2)O_(3) composite releases 1330.7 mL·g^(−1) H_(2)(close to 80%theoretical hydrogen generation H_(2))in H_(2)O and 1520.4 mL·g^(−1) H_(2)(about 95%)in 0.5 M MgCl_(2) in 60 min at 26℃ with hydrolysis rate of 736.9 mL·g^(−1)·min^(−1) and 960.9 mL·g^(−1)·min^(−1) H_(2) during the first minute of the hydrolysis,respectively.In addition,the MgCl_(2) solution allows repeated use by filtering and exhibits high cycle stability(20 cycles),therefore leading to much reduced capacity loss caused by the excess H_(2)O.We show that by introducing B_(2)O_(3) and recycling the 0.5 M MgCl_(2) solution,the system hydrogen capacity can approach 5.9 wt%,providing a promising hydrogen generation scheme to supply hydrogen to the fuel cells.
