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
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
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.