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NOVEL INSULATION MATERIALS
FOR HIGH VOLTAGE CABLE
SYSTEMS
OUTLINE
• Introduction
• Limitations of XLPE
• Thermoplastics
 Polyethylene
 Polypropylene
• Conclusion
• References
INTRODUCTION
• Most common polymeric insulation material.
• Produced with high throughput and well-controlled extrusion
technology .
• Base for this insulation is polyethylene (PE).
• Crosslinked either with peroxide cure , or by grafting silane
onto the polymer chains, and the use of moisture-based cure .
PEROXIDE CURE
• Organic peroxide is added to polyethylene
• Dicumyl Peroxide(DCP) is the most commonly used cross
linking agent.
• Cross linking occurs at 150-200 °C
• Cropensity for premature crosslinking (scorch) .
• peroxide mediated crosslinking generates byproducts
(acetophenone, cumyl alcohol, methylstyrene, and methane).
MOISTURE CURE
• Silane is added to the polyethylene in the polymerization
process
• Simpler curing process
• Cross linking occurs at 90 °C in water bath
• Increased risk of water tree formation
BENEFITS OF XLPE
• Improved thermal stability
• High melting point
• Cost effective
LIMITATIONS OF XLPE
• Thermal expansion
• Cause damage to the sheath and joints
• If the insulation system is subjected to mechanical forces
between 90 to 100°C, mechanical damage can result
POLYETHYLENE
• Produced by the
polymerization of monomer
ethylene
 Branched LDPE
 Linear HDPE
LOW DENSITY POLYETHYLENE
• Obtained by polymerization of
ethene under high pressure.
• Chemically inert and tough but
flexible
• Poor conductor of electricity
• having density between 0.91 and
0.923 g/cm3
• much lower crystalline content
compared to HDPE
HIGH DENSITY POLYETHYLENE
• Obtained by polymerization of
ethylene under low pressure
• Density between 0.94 and 0.98 g
/cm3
• Higher crystalline content
BLENDING OF HDPE AND LDPE
Fig: Differential scanning calorimetry trace of the melting behavior of samples
isothermally crystallized at 124°C for different high-density polyethylene
(HDPE)/low-density polyethylene blend compositions
NANOSCALE INCLUSION OF LDPE
Figure 4. Scanning electron microscopy graph showing the crystalline high-
density polyethylene “skeleton” structure, which is embedded in the
noncrystalline majority component low-density polyethylene
• Rise to an increase in breakdown strength of 24% compared
with a material of the same molecular composition
• Tree growth rates being significantly reduced in PE blends
compared to XLPE
• Nanoscale inclusion of the LDPE provide low temperature
flexibility
• HDPE crystals gives good high temperature mechanical
integrity
• This integrity is retained to some 30°C above the melting
temperature of XLPE
POLYPROPYLENE
• Polypropylene, a synthetic resin built up by the
polymerization of propylene.
PROPYLENE BASED SYSTEMS
• Difference between polyethylene and polypropylene:
 The melting temperature of isotactic polypropylene (iPP) is much higher
than that of HDPE.
 iPP tends to form particularly large spherulites. The benefit is that the
material is intrinsically clean.
 The synthesis method of PP does not produce branched molecular
structures akin to LDPE
 Manipulating the structure and properties of PP is much more difficult
than in PE
• propylene-based systems in cable applications is driven by two factors:
 high melting temperature of PP (above 160°C) provides the potential for
much higher cable current ratings.
 Apparent cleanliness of PP exhibits excellent electrical properties for
correctly designed systems.
• A widely accepted strategy for the design of propylene-based systems for
use in cable applications is to blend iPP with a more flexible, lower
crystallinity copolymer.
Scanning electron microscopy graph showing (a) isotactic polypropylene after
isothermal crystallization at 120°C, showing clear interspherulitic boundaries; (b)
polypropylene blend with 12% ethylene, showing clear phase separation, resulting in
electrically weak regions
Fig: (Left) Electric breakdown strength of polypropylene and high-density polyethylene
samples of different thickness as function of spherulite mean diameter size . (Right)
Illustration of the breakdown path along the weak boundaries
Scanning electron microscopy graph showing (a) isotactic polypropylene blend system with
ethylene/propylene copolymer, virtual elimination of weak boundaries; (b) example of
successful polypropylene blend without phase separation.
CONCLUSIONS
• It is now possible to formulate thermoplastic polymer blends
that are able to overcome the limitations of XLPE.
• These new materials promise more sustainable systems , both
economically and environmentally and provide greater design
freedom for HV and extra high voltage AC and DC cable
developments.
REFRENCES
• Thomas Andritsch , Alun Vaughan ,and Gary C. Stevens , “Novel Insulation
Materials for High Voltage Cable Systems” ,IEEE Electrical Insulation Magazine, Vol.
33, No. 4 , 2017.
• C. D. Green, A. S. Vaughan, G. C. Stevens, A. Pye, S. J. Sutton, T. Geussens, and M.
J. Fairhurst, “Thermoplastic cable insulation comprising a blend of isotactic
polypropylene and a propylene-ethylene copolymer,” IEEE Trans. Dielectr. Electr.
Insul., vol. 33, no. 3, pp. 639–648, 2015.
• P. J. Caronia, J. M. Cogen, and P. Dluzneski, “Novel polymer crosslinking chemistries
for cable insulation,” in Electr. Insul. Conf., 2014, pp. 392– 396.
THANK YOU !

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Xlpe cables

  • 1. NOVEL INSULATION MATERIALS FOR HIGH VOLTAGE CABLE SYSTEMS
  • 2. OUTLINE • Introduction • Limitations of XLPE • Thermoplastics  Polyethylene  Polypropylene • Conclusion • References
  • 3. INTRODUCTION • Most common polymeric insulation material. • Produced with high throughput and well-controlled extrusion technology . • Base for this insulation is polyethylene (PE). • Crosslinked either with peroxide cure , or by grafting silane onto the polymer chains, and the use of moisture-based cure .
  • 4. PEROXIDE CURE • Organic peroxide is added to polyethylene • Dicumyl Peroxide(DCP) is the most commonly used cross linking agent. • Cross linking occurs at 150-200 °C • Cropensity for premature crosslinking (scorch) . • peroxide mediated crosslinking generates byproducts (acetophenone, cumyl alcohol, methylstyrene, and methane).
  • 5. MOISTURE CURE • Silane is added to the polyethylene in the polymerization process • Simpler curing process • Cross linking occurs at 90 °C in water bath • Increased risk of water tree formation
  • 6. BENEFITS OF XLPE • Improved thermal stability • High melting point • Cost effective
  • 7. LIMITATIONS OF XLPE • Thermal expansion • Cause damage to the sheath and joints • If the insulation system is subjected to mechanical forces between 90 to 100°C, mechanical damage can result
  • 8. POLYETHYLENE • Produced by the polymerization of monomer ethylene  Branched LDPE  Linear HDPE
  • 9. LOW DENSITY POLYETHYLENE • Obtained by polymerization of ethene under high pressure. • Chemically inert and tough but flexible • Poor conductor of electricity • having density between 0.91 and 0.923 g/cm3 • much lower crystalline content compared to HDPE
  • 10. HIGH DENSITY POLYETHYLENE • Obtained by polymerization of ethylene under low pressure • Density between 0.94 and 0.98 g /cm3 • Higher crystalline content
  • 11. BLENDING OF HDPE AND LDPE Fig: Differential scanning calorimetry trace of the melting behavior of samples isothermally crystallized at 124°C for different high-density polyethylene (HDPE)/low-density polyethylene blend compositions
  • 12. NANOSCALE INCLUSION OF LDPE Figure 4. Scanning electron microscopy graph showing the crystalline high- density polyethylene “skeleton” structure, which is embedded in the noncrystalline majority component low-density polyethylene
  • 13. • Rise to an increase in breakdown strength of 24% compared with a material of the same molecular composition • Tree growth rates being significantly reduced in PE blends compared to XLPE • Nanoscale inclusion of the LDPE provide low temperature flexibility • HDPE crystals gives good high temperature mechanical integrity • This integrity is retained to some 30°C above the melting temperature of XLPE
  • 14. POLYPROPYLENE • Polypropylene, a synthetic resin built up by the polymerization of propylene.
  • 15. PROPYLENE BASED SYSTEMS • Difference between polyethylene and polypropylene:  The melting temperature of isotactic polypropylene (iPP) is much higher than that of HDPE.  iPP tends to form particularly large spherulites. The benefit is that the material is intrinsically clean.  The synthesis method of PP does not produce branched molecular structures akin to LDPE  Manipulating the structure and properties of PP is much more difficult than in PE
  • 16. • propylene-based systems in cable applications is driven by two factors:  high melting temperature of PP (above 160°C) provides the potential for much higher cable current ratings.  Apparent cleanliness of PP exhibits excellent electrical properties for correctly designed systems. • A widely accepted strategy for the design of propylene-based systems for use in cable applications is to blend iPP with a more flexible, lower crystallinity copolymer.
  • 17. Scanning electron microscopy graph showing (a) isotactic polypropylene after isothermal crystallization at 120°C, showing clear interspherulitic boundaries; (b) polypropylene blend with 12% ethylene, showing clear phase separation, resulting in electrically weak regions
  • 18. Fig: (Left) Electric breakdown strength of polypropylene and high-density polyethylene samples of different thickness as function of spherulite mean diameter size . (Right) Illustration of the breakdown path along the weak boundaries
  • 19. Scanning electron microscopy graph showing (a) isotactic polypropylene blend system with ethylene/propylene copolymer, virtual elimination of weak boundaries; (b) example of successful polypropylene blend without phase separation.
  • 20.
  • 21. CONCLUSIONS • It is now possible to formulate thermoplastic polymer blends that are able to overcome the limitations of XLPE. • These new materials promise more sustainable systems , both economically and environmentally and provide greater design freedom for HV and extra high voltage AC and DC cable developments.
  • 22. REFRENCES • Thomas Andritsch , Alun Vaughan ,and Gary C. Stevens , “Novel Insulation Materials for High Voltage Cable Systems” ,IEEE Electrical Insulation Magazine, Vol. 33, No. 4 , 2017. • C. D. Green, A. S. Vaughan, G. C. Stevens, A. Pye, S. J. Sutton, T. Geussens, and M. J. Fairhurst, “Thermoplastic cable insulation comprising a blend of isotactic polypropylene and a propylene-ethylene copolymer,” IEEE Trans. Dielectr. Electr. Insul., vol. 33, no. 3, pp. 639–648, 2015. • P. J. Caronia, J. M. Cogen, and P. Dluzneski, “Novel polymer crosslinking chemistries for cable insulation,” in Electr. Insul. Conf., 2014, pp. 392– 396.