The sodium silicate, ferric chloride, ferrous sulfate, sodium chlorate and other common inorganic materials were used to synthesize two new poly silicate iron coagulants: Polysilicate Ferric Chloride (PFSiC) and Po...The sodium silicate, ferric chloride, ferrous sulfate, sodium chlorate and other common inorganic materials were used to synthesize two new poly silicate iron coagulants: Polysilicate Ferric Chloride (PFSiC) and Polymeric Ferric Silicate Sulfate (PFSiS). Their coagulation effect on micro-polluted water was compared with the poly ferric choride (PFC) saled in the market. The results showed that turbidity, organic matter, total phosphorus, total nitrogen removal rate ofPFSiC, PFSiS coagulant were better than PFC on micro-polluted water treatment at the same dosage. The coagulation effect of PFSiC was the best. The surface morphology of three coagulants was observed by scanning electron microscopy (SEM), and the coagulation mechanism was discussed preliminarily.展开更多
Coupled with a petrographical study, I carried out an ion probe study of rare earth element microdistributions in mineral phases of silicate inclusions from the Colomera ⅡE iron meteorite. Most mineral grains have ho...Coupled with a petrographical study, I carried out an ion probe study of rare earth element microdistributions in mineral phases of silicate inclusions from the Colomera ⅡE iron meteorite. Most mineral grains have homogeneous REEs, but show considerable inter-grain variations by a factor of 2 to 100. The whole rock REE abundances for Colomera, estimated by combining REE data with modal abundances, are relatively LREE-enriched with REEs of -10'CI, which suggest that Colomera silicates were highly differentiated and might represent a low degree partial melt (-10%) of a chondritic source. REE geochemistry of Colomera silicate inclusions points to an origin that involves differentiation, dynamic mixing, remelting, reduction, recrystallization, and subsequent rapid cooling near the surface of a planetary body.展开更多
Low grade siliceous manganese ores from the iron ore group of the Bonai-Keonjhar belt, Orissa, India are found mostly in shear zones. The ore characteristics of siliceous manganese ore samples from three differ- ent m...Low grade siliceous manganese ores from the iron ore group of the Bonai-Keonjhar belt, Orissa, India are found mostly in shear zones. The ore characteristics of siliceous manganese ore samples from three differ- ent mines, viz. the Shankar (Barbil OMC lease hold area), the Sone-Patuli (Patmunda, OMM lease hold area), and the Musaghar (Roida, OMDC lease hold area), were studied. These siliceous manganese ores are of three types, respectively: (i) spongy-granular; (ii) massive-mosaic; and (iii) hard-mylonitized. The spongy-gran- ular type contains granular, saccharoidal quartz and the major manganese mineral present is pyrolusite. The second type contains well crystallized quartz and cryptomelane, while the third has cherty, fine grained quartz (mylonite) along with romanechite. All three ores were subjected to physical beneficiation under similar conditions. Both gravity and magnetic separation techniques were employed. The mineral-fabric of the ores has been correlated to the extent of their beneficiation using these physical techniques. Of these three ores only the spongy-granular type responded well to upgrading. The feed with 22% Mn content could be upgraded to 44% with a 28% yield and a 49% recovery. The good response to beneficiation of the spongy- granular sample could be due to the large euhedral crystals of pyrolusite and the friable nature of the sac- charoidal quartz. This study reveals the influence of mineral-fabric on beneficiation of low grade ore, siliceous Mn ore in particular.展开更多
Lithium iron silicate (Li2FeSiO4) is capable of affording a much higher capacity than conventional cathodes, and thus, it shows great promise for high-energy battery applications. However, its capacity has often bee...Lithium iron silicate (Li2FeSiO4) is capable of affording a much higher capacity than conventional cathodes, and thus, it shows great promise for high-energy battery applications. However, its capacity has often been adversely affected by poor reaction activity due to the extremely low electronic and ionic conductivity of silicates. Here, we for the first time report on a rational engineering strategy towards a highly active Li2FeSiO4 by designing a carbon nanotube (CNT) directed three-dimensional (3D) porous Li2FeSiO4 composite. As the CNT framework enables rapid electron transport, and the rich pores allow efficient electrolyte penetration, this unique 3D Li2FeSiO4-CNT composite exhibits a high capacity of 214 mAh·g^-1 and retains 96% of this value over 40 cycles, thus, outstripping many previously reported Li2FeSiO4-based materials. Kinetic analysis reveals a high Li+ diffusivity due to coupling of the migration of electrons and ions. This research highlights the potential for engineering 3D porous structure to construct highly efficient electrodes for battery applications.展开更多
Three synthetic Fe3+ bearing λ-Fe2SiO4 were analyzed using electron probe method, and the M?ssbauer spectra of the samples at 298 K, 150 K, and 95 K were measured. Each spectrum at three temperatures is composed of t...Three synthetic Fe3+ bearing λ-Fe2SiO4 were analyzed using electron probe method, and the M?ssbauer spectra of the samples at 298 K, 150 K, and 95 K were measured. Each spectrum at three temperatures is composed of two doublets. These two doublets are assigned to Fe2+ in the octahedral sites and Fe3+ in the tetrahedral sites, respectively. Site occupancies were determined. The results show that Fe3+ and a small amount of Si4+ are in the tetrahedral and octahedral sites, respectively. The average bond lengths of the octahedral and tetrahedral sites were calculated according to the equations primarily given by Hill et al., O’Neill and Navrotsky and modified by the authors. Furthermore, the octahedral and tetrahedral bond lengths were used to calculate cell parameters and oxygen parameters. In addition, Fe3+ line broadening in the M?ssbauer spectra of Fe3+ bearing λ-Fe2SiO4 were interpreted by using the next nearest neighbor effects展开更多
文摘The sodium silicate, ferric chloride, ferrous sulfate, sodium chlorate and other common inorganic materials were used to synthesize two new poly silicate iron coagulants: Polysilicate Ferric Chloride (PFSiC) and Polymeric Ferric Silicate Sulfate (PFSiS). Their coagulation effect on micro-polluted water was compared with the poly ferric choride (PFC) saled in the market. The results showed that turbidity, organic matter, total phosphorus, total nitrogen removal rate ofPFSiC, PFSiS coagulant were better than PFC on micro-polluted water treatment at the same dosage. The coagulation effect of PFSiC was the best. The surface morphology of three coagulants was observed by scanning electron microscopy (SEM), and the coagulation mechanism was discussed preliminarily.
基金This work was partly supported by National Natural Science Foundation of China(Grant No.40325009)by“One-hundred Talent Program”of the Chinese Academy of Sciences.
文摘Coupled with a petrographical study, I carried out an ion probe study of rare earth element microdistributions in mineral phases of silicate inclusions from the Colomera ⅡE iron meteorite. Most mineral grains have homogeneous REEs, but show considerable inter-grain variations by a factor of 2 to 100. The whole rock REE abundances for Colomera, estimated by combining REE data with modal abundances, are relatively LREE-enriched with REEs of -10'CI, which suggest that Colomera silicates were highly differentiated and might represent a low degree partial melt (-10%) of a chondritic source. REE geochemistry of Colomera silicate inclusions points to an origin that involves differentiation, dynamic mixing, remelting, reduction, recrystallization, and subsequent rapid cooling near the surface of a planetary body.
文摘Low grade siliceous manganese ores from the iron ore group of the Bonai-Keonjhar belt, Orissa, India are found mostly in shear zones. The ore characteristics of siliceous manganese ore samples from three differ- ent mines, viz. the Shankar (Barbil OMC lease hold area), the Sone-Patuli (Patmunda, OMM lease hold area), and the Musaghar (Roida, OMDC lease hold area), were studied. These siliceous manganese ores are of three types, respectively: (i) spongy-granular; (ii) massive-mosaic; and (iii) hard-mylonitized. The spongy-gran- ular type contains granular, saccharoidal quartz and the major manganese mineral present is pyrolusite. The second type contains well crystallized quartz and cryptomelane, while the third has cherty, fine grained quartz (mylonite) along with romanechite. All three ores were subjected to physical beneficiation under similar conditions. Both gravity and magnetic separation techniques were employed. The mineral-fabric of the ores has been correlated to the extent of their beneficiation using these physical techniques. Of these three ores only the spongy-granular type responded well to upgrading. The feed with 22% Mn content could be upgraded to 44% with a 28% yield and a 49% recovery. The good response to beneficiation of the spongy- granular sample could be due to the large euhedral crystals of pyrolusite and the friable nature of the sac- charoidal quartz. This study reveals the influence of mineral-fabric on beneficiation of low grade ore, siliceous Mn ore in particular.
基金Acknowledgements We acknowledge the financial support of the National Natural Science Foundation of China (Nos. 51302181, 51372159, 51422206, and 51672182), the Thousand Youth Talents Plan, the Jiangsu Shuangchuang Plan, the Natural Science Foundation of Jiangsu Province (Nos. BK20151219 and BK20140009), the Jiangsu Undergraduate Student Innovation and Entrepreneurship Project, the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), and Russian Scientific Fund (No. 14-43-00072).
文摘Lithium iron silicate (Li2FeSiO4) is capable of affording a much higher capacity than conventional cathodes, and thus, it shows great promise for high-energy battery applications. However, its capacity has often been adversely affected by poor reaction activity due to the extremely low electronic and ionic conductivity of silicates. Here, we for the first time report on a rational engineering strategy towards a highly active Li2FeSiO4 by designing a carbon nanotube (CNT) directed three-dimensional (3D) porous Li2FeSiO4 composite. As the CNT framework enables rapid electron transport, and the rich pores allow efficient electrolyte penetration, this unique 3D Li2FeSiO4-CNT composite exhibits a high capacity of 214 mAh·g^-1 and retains 96% of this value over 40 cycles, thus, outstripping many previously reported Li2FeSiO4-based materials. Kinetic analysis reveals a high Li+ diffusivity due to coupling of the migration of electrons and ions. This research highlights the potential for engineering 3D porous structure to construct highly efficient electrodes for battery applications.
基金the National Natural Science Foundation of China(Grant No.40072019)the Japan Society for the Promotion of Science(JSPA)
文摘Three synthetic Fe3+ bearing λ-Fe2SiO4 were analyzed using electron probe method, and the M?ssbauer spectra of the samples at 298 K, 150 K, and 95 K were measured. Each spectrum at three temperatures is composed of two doublets. These two doublets are assigned to Fe2+ in the octahedral sites and Fe3+ in the tetrahedral sites, respectively. Site occupancies were determined. The results show that Fe3+ and a small amount of Si4+ are in the tetrahedral and octahedral sites, respectively. The average bond lengths of the octahedral and tetrahedral sites were calculated according to the equations primarily given by Hill et al., O’Neill and Navrotsky and modified by the authors. Furthermore, the octahedral and tetrahedral bond lengths were used to calculate cell parameters and oxygen parameters. In addition, Fe3+ line broadening in the M?ssbauer spectra of Fe3+ bearing λ-Fe2SiO4 were interpreted by using the next nearest neighbor effects