Synthesis under pressure of potential precursors of CNx materials based on melamine and phenolic resins

Journal of Macromolecular Science, Part B: Physics

Volumn 49, Issue 2, 2010, Pages 371-382

  Dante, Roberto C ^a   Gil, Jesús Martín ^b   Pallavidino, Luca ^c   Geobaldo, Francesco ^c  

^a ITT Italia Srl   (Italy)

^b UNIVERSITY OF VALLADOLID   (Spain)

^c POLITECNICO DI TORINO   (Italy)

Author keywords

Carbon nitrides; Cross linking; Melamine resin; Phenolic resin; Synthesis; Thermosets

Indexed keywords

HIGHEST TEMPERATURE; MELAMINE RESIN; NOVOLAK; PRESSURE AND TEMPERATURE; PRESSURE LEVEL; REACTION VESSEL; STRUCTURING EFFECTS; THERMAL STABILITY; WEIGHT RATIOS; XRD;

CARBON NITRIDE; MELAMINE FORMALDEHYDE RESINS; PHENOLIC RESINS; PLASTICS; SYNTHESIS (CHEMICAL); SYNTHETIC RESINS; THERMOGRAVIMETRIC ANALYSIS; X RAY DIFFRACTION;

PHENOLS;

EID: 77951096892     PISSN: 00222348     EISSN: 1525609X     Source Type: Journal    
DOI: 10.1080/00222340903355859     Document Type: Article

References (19)

1. Cohen, M.L. Calculation of bulk moduli of diamond and zinc-blende solids. Phys. Rev. B 1985, 32, 7988.
2. 4. Phys. Rev. B 1990, 41, 10727.
3. Li, X.; Zhang, J.; Shen, L.; Ma, Y.; Lei, W.; Cui, Q.; Zou, G. Preparation and characterization of graphitic carbon nitride through pyrolisis of melamine. Appl. Phys. A 2009, 94, 387.
4. Zhao, Y.; Zheng, L.; Chu, W.; Song, L.; Zhang, Z.; Yu, D.; Tian, Y.; Xie, S.; Sun, L. Largescale synthesis of nitrogen-rich carbon nitride microfibers by using graphitic carbon nitride as precursor. Adv. Mater. 2008, 9999, 1.
5. Vinu, A.; Ariga, K.; Mori, T.; Nakanishi, T.; Hishita, S.; Goldberg, D.; Bando, Y. Preparation and chracterization of well-ordered hexagonal mesoporous carbon nitride. Adv. Mater. 2005, 17, 1648.
6. Zhao, H.Z.; Lei, M.; Yang, X.; Jian, J.K.; Chen, X.L. Route to GaN and VN assisted by carbothermal reduction process. J. Am. Chem. Soc. 2005, 127, 15722.
7. Zimmerman, J.L.;Williams, R.; Khabashesku,V.N.;Margrave, J.L. Synthesis of spherical carbon nitride nanostructures. Nano Lett. 2001, 1, 731.
8. Cao, C.B.; Huang, F.L.; Cao, C.T.; Li, J.; Zhu, H.S. Synthesis of carbon nitride nanotubes via a catalytic-assembly solvothermal route. Chem. Mater. 2004, 16, 5213.
9. Yacaḿan, M.J.; Martin-Gil, J.; Martin-Gil, F.J.; Sarikaya, M.; Qian, M.X. New carbon-nitrogen materials. A likely alternative to diamond. Mater. Chem. and Phys. 1997, 47, 109.
10. Martin-Gil, J.; Martin-Gil, F.J.; Sarikaya, M.; Qian, M.; Yacaḿan, M.J.; Rubio, A. Evidence of low compressibility carbon nitride with defect-zincblende structure. J. Appl. Phys. 1997, 81(6), 2555.
11. Cutiongco, E.C.; Li, D.; Chung, Y.W.; Bhatia, C.S. Tribological behavior of amorphous carbon nitirde overcoats for magnetic thin-film rigid disks. J. Tribol. 1996, 118, 543.
12. Khurshudov, A.G.; Kato, K. Tribological properties of carbon nitride overcoat for thin-film magnetic rigid disks. Surf. Coat. Technol. 1996, 86/87, 664.
13. Ming, L.C.; Zinin, P.; Meng, X.R.; Liu, X.R.; Hong, S.M. Xie, Y. A cubic phase of C3N4 sythesized in the diamond-anvill cell. J. Appl. Phys. 2006, 99, 033520.
14. Hultman, L.; Neidhardt, J.; Hellgren, N.; Sjöström, H.; Sundgren, J.E. Theme article-Fullerenelike carbon nitride: A resilient coating material. MRS Bull. 2003, 28(3), 194.
15. Donnet, C.; Erdemir,A.Historical developments and newtrends in tribological and solid lubricant coatings. Surf. Coat. Technol. 2004, 180-181, 76.
16. Ozao, R.; Nishimoto, Y.; Pan, W.P.; Okabe, T. Theromoanlytical characterization of carbon/ carbon hybrid material, apple woodceramics. Thermochim. Acta 2006, 440, 75.
17. Ko, T.H.; Chen, P.C. Study of pyrolysis of phenolic resin reinforced with two-dimensional plain woven carbon fabric-I. J. Mater. Sci. Lett. 1991, 10, 301.
18. Zhao, Y.C.; Yu, D.L.; Yanagisawa, O.; Matsugi, K.; Tian, Y.J. Structural evolution of turbostratic carbon nitride after being treated with a pulse discharge. Diamond Relat. Mater. 2005, 14, 1700.
19. Subrayan, R.P.; Jones, F.N. Condensation of substituted phenols with hexakis(methoxymethyl) melamine: Synthesis, characterization, and properties of substituted 2,4,6-tris[3,4-dihydro-1,3- (2H)-benzoxazin-3yl]-s-triazine derivatives. Chem. Mater. 1998, 10, 3506.