scholarly journals Study on the synthesis of β-SiC nanoparticles from diamond-wire silicon cutting waste

RSC Advances ◽  
2019 ◽  
Vol 9 (41) ◽  
pp. 23785-23790 ◽  
Author(s):  
Shengnan Jiang ◽  
Shuaibo Gao ◽  
Jian Kong ◽  
Xing Jin ◽  
Donghui Wei ◽  
...  

β-SiC nanoparticles was synthesized using silicon cutting waste (SCW) as silicon source and sucrose as carbon source.

Author(s):  
Zhao Wang ◽  
Shu-lin Wang ◽  
Jia-you Ji ◽  
Man Xu
Keyword(s):  

2008 ◽  
Vol 403 ◽  
pp. 211-214
Author(s):  
Yoshiki Yoshioka ◽  
Hidehiko Tanaka ◽  
Mikio Konishi ◽  
Toshiyuki Nishimura

Nano sized SiC powder was successfully synthesized by the carbothermal reduction in SiO2. Precursor for SiC was prepared by using phenolic resin as a carbon source and ethylsilicate as a silicon source. After mixing, hydrolysis, drying and pyrolysis at 1000°C, SiC precursor consisted of C and SiO2 was obtained. The precursor was heat treated at 1500-1800°C in Ar to synthesize SiC by the carbothermal reduction. The carbothermal redction reaction was almost completed at 1700°C and then SiC particle with suitable size was obtained at this temperature. Nano-sized SiC particles could be achieved at 1600 °C, and unreacted SiO2 and C remained in the sample. Pure SiC particles were obtained by oxidation and acid treatment. Nano-sized SiC powder had the diameter of 10-20 nm and BET surface area of 156 m²/g.


2015 ◽  
Vol 3 (19) ◽  
pp. 4876-4882 ◽  
Author(s):  
Tengfei Cao ◽  
Yan Cheng ◽  
Haibao Zhang ◽  
Binhang Yan ◽  
Yi Cheng

SiC nanocrystals with room temperature red region photoluminescence are fabricated at a high rate in atmospheric pressure thermal plasma using SiCl4 and C2H2 as the silicon source and carbon source, respectively.


2013 ◽  
Vol 785-786 ◽  
pp. 488-492
Author(s):  
Kang Li He ◽  
Ning Liu ◽  
Rui Yuan Zheng ◽  
Wang Yi Liu ◽  
Bing Li ◽  
...  

A simple and cost effective method was reported for the synthesis of β-SiC nanoparticles with differernt morphologies using Taixi coal as carbon source and Fe (NO3)3·9H2O, Co (NO3)2·6H2O and NiCO3·2Ni (OH)2·4H2O as additives, respectively. The structures and morphologies were characterized by XRD, FTIR, BET and SEM. The results show that SiC nanoparticles with lamellar structures were successfully synthesized at 1450 °C with NiCO3·2Ni (OH)2·4H2O as an additive which are very scarce to our knowledge. whats more, the formation mechanism of lamellar structures SiC nanoparticles were also discussed.


Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


2018 ◽  
Author(s):  
Zhanyu Li ◽  
Mengru Zhang ◽  
Yu Zhang ◽  
Shuang Liu ◽  
Jinbo Zhao ◽  
...  

Deployment of organoboron in lieu of the strongly basic <br>organometallic reagents as carbon source in Cu-catalyzed <br>cyclopropene carbometallation opens unprecedented three-<br>component reactivity for stereoselective synthesis of poly-substituted cyclopropanes. A proof-of-principle demonstration of this novel carbometallation strategy is presented herein for a highly convergent access to poly-substituted aminocyclopropane framework via <br>carboamination. Preliminary results on asymmetric desymmetrization with commercial bisphosphine ligands attained high levels of enantioselection, offering a straightforward access to enantioenriched aminocyclopropanes bearing all-three chiral centers, including an all-carbon quaternary center. This strategy may underpin a host of novel synthetic protocols for poly-substituted cyclopropanes. <br>


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