N-doped graphene with Curie temperature higher than room temperature is a good candidate for nanomagnetic applications. Here we report a kind of N-doped graphene that exhibits ferromagnetic property with high Curie temperature (>600 K). Four graphene samples were prepared through self-propagating high-temperature synthesis (SHS), and the doped nitrogen contents of in the samples were 0 at.%, 2.53 at.%, 9.21 at.% and 11.17 at.%. It has been found that the saturation magnetization and coercive field increase with the increasing of nitrogen contents in the samples. For the sample with the highest nitrogen content, the saturation magnetizations reach 0.282 emu/g at 10 K and 0.148 emu/g at 300 K; the coercive forces reach 544.2 Oe at 10 K and 168.8 Oe at 300 K. The drop of magnetic susceptibility at ~625 K for N-doped graphene is mainly caused by the decomposition of pyrrolic N and pydinic N. Our results suggest that SHS method is an effective and high-throughput method to produce N-doped graphene with high nitrogen concentration and that N-doped graphene produced by SHS method is promising to be a good candidate for nanomagnetic applications.
Apatites of composition (Ca10−xPbx)(VO4)6F2 with 0 ≤x≤ 9 were synthesized by sintering in air at 800°C the oxides of calcium, lead, and vanadium that were mixed with calcium fluoride. Variations in lattice parameters, grain size, and durability were monitored as a function of composition. The expected dilation in unit cell edges with increasing replacement of calcium (IR = 1.26 Å) by lead (IR = 1.45 Å) was observed. The a cell edge (in angstroms) varied linearly (0.0458 x+ 9.7068) with x, while c followed the binomial function 0.0018x2+ 0.0279x+ 7.0118. Average grain sizes increased from approximately 5 μm (x= 0) to 25 μm (x= 9) as grain growth was enhanced due to incipient melting of the lead‐rich compositions. For x < 5 the materials were biphasic. Overall dissolution, as determined by the toxicity characteristic leaching procedure (TCLP), was faster in calcium‐rich apatites. Etching of well‐crystallized apatite grains occurred preferentially on {1010} faces. These leach losses were augmented through the more rapid removal of cryptocrystalline regions and intergranular thin films.
Graphene with ultrahigh intrinsic strength and excellent thermal physical properties has the potential to be used as the reinforcement of many kinds of composites. Here, we show that very high tensile strength can be obtained in the copper matrix composite reinforced by reduced graphene oxide (RGO) when micro-layered structure is achieved. RGO-Cu powder with micro-layered structure is fabricated from the reduction of the micro-layered graphene oxide (GO) and Cu(OH)2 composite sheets, and RGO-Cu composites are sintered by spark plasma sintering process. The tensile strength of the 5 vol.% RGO-Cu composite is as high as 608 MPa, which is more than three times higher than that of the Cu matrix. The apparent strengthening efficiency of RGO in the 2.5 vol.% RGO-Cu composite is as high as 110, even higher than that of carbon nanotube, multilayer graphene, carbon nano fiber and RGO in the copper matrix composites produced by conventional MLM method. The excellent tensile and compressive strengths, high hardness and good electrical conductivity are obtained simultaneously in the RGO-Cu composites. The results shown in the present study provide an effective method to design graphene based composites with layered structure and high performance.
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