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Eaton and Kmiec dissipation study
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A paper from the 57th International Wire & Cable Symposium by R. F. Eaton and C. J. Kmiec of Dow Chemical, kept in the Transmission Lines chapter 3 preliminaries folder. It covers foamed polyethylene insulation and gas injection, HDPE/LDPE materials, and the decibel loss definition. It fits power laws to RG-58, RG-8 and hardline loss data, showing loss varies roughly as the square root of frequency from the skin effect, and gives loss formulas in terms of Dk, Df and cable diameters.
AI-written summary; may contain errors.
Extracted text (machine-read; may contain errors)
Electrical Losses in Coaxial Cable
R. F. Eaton and C. J. Kmiec
The Dow Chemical Company, Wire and Cable R&D
171 River Road, Piscataway, NJ 08854
+1-732-563-5056 / [email protected] +1-732-563-5129 / [email protected]
Abstract
As coaxial cables are used at ever higher frequencies in the
Gigahertz range, cable losses become extremely important. Losses are functions of both Dk, dielectric constant, Df, tangent delta, of the polymer and the geometry of the cable construction. Control of the polymer archit ecture and additive package can
reduce electrical losses in the cables fabricated from the polymer resulting in lower cable losses.
Dk of a polymer is related a variety of chemical properties of the
polymer: polarity, Tg, Tm etc. Df of a polymer is related to molecular motions of polar groups either along the polymer chain or the motion of polar molecules within the polymer matrix. We will discuss the Df contributions of the alpha, beta and gamma transition in polyethylene. Dk and Df are also functions of frequency and temperature.
Keywords: Coax; Dielectric Constant; Dissipation Factor;
Polyethylene; Power Loss; Tan Delta.
1. Introduction and Coaxial Cable
Background
Coaxial cables are is an important growing segment for the W&C
industry. This report is a review and summary of the key parameters that control signal loss in COAX cable. We will show
that chemistry fundamentals can be used to reduce losses in the resins to fabricate the coaxial cables.
Intuitively one would expect electrical losses to be related to the
dielectric tangent delta at the frequency of interest. If the polyethylene contained no polar groups, the various polymer molecular motions, the alpha, beta and gamma transitions in polyethylene and related polyolefins, would have little or no dielectric loss. Literature data shows the electrical tangent delta of a polyethylene is related to level of polar impurities in the case of polyethylene
1.
2. Coax Cables by Gas Injection Process
For over many years Coaxial cables have been used in the transmission of Community An tenna Television (CATV) and
radio frequency cables. Both solid and foamed dielectrics are used for coax insulation. Foamed cable has lower electrical losses but is more susceptible to envir onmental degradation especially
moisture pickup. The current foam process that is utilized requires a specialized process wherein typically nitrogen gas is injected via sonic technology into the polymer melt. Incorporation of the gas leads to creation of a foam with expansion levels reaching 70-80%. Coaxial cable is used to tr ansmit a signal (voice, video or
data) received from head end/antenna to a final destination. Coaxial cables are used in a number of high frequency applications including:
Traditional 75 ohm impedance cables include: CATV applications including aluminum jacketed CATV
‘hard line’ Drop: US MIL spec RG59, RG6, RG7, RG11 Distribution
Trunk
Video cables including compone nt video and SPDIF cables
50 ohm RF cable for mobile telephony
LAN/Computer cable Two way communication cable
A typical COAX cable design is shown in Figure 1.
Figure 1: COAX Cable
The key principle of sonic gas injection for COAX cables is to
have consistent flow of nitr ogen gas through the gas control
system in order to obtain the uniform critical cable performance. The gas control system allows gas which flows through a constricting nozzle to reach critical pressure (Pc) wherein the gas flow rate becomes independent of melt pressure.
Calculation for the critical pressure for nitrogen is Pc = 0.53 * Pa
The volumetric gas flow rate required to achieve a given
expansion level can be determined for any given set of production
requirements. Using the values for Extrusion line speed (LS), Insulation cross-sectional thic kness (XSA) and Base and foam
resin density (BD, FD) and then incorporating these values into
the basic equation for SONIC gas injection:
Where c1 = constant Inner conductor : Cu, Cu clad steel, or
tinned Cu clad steel
Insulation : Foamed PE Dielectric
(foam rate depends on Vpneeded)
Outer conductor : Foil/braid
combination utilizing Cu and/or Al;
Solid Al or Cu
Jacket : PVC for indoor or LDPE to HDPE
for outdoor applications Inner Skin : Solid LDPE, LLDPE, or
blend of PE with EAA, EEA,
ionomer , or other copolymers
Pa PbPc
Pa PbPc
Pa PbPc
) 1( 12
BDFDXSA LScPD −∗∗∗=
International Wire & Cable Symposium 515 Proceedings of the 57th IWCS
One can then determine the gas pressure (P) and orifice size (D)
needed to achieve desired foaming
3. Materials Used in Coax Insulation
Coaxial Cable Insulation Materials
Coaxial cable insulation is generally a mixture of High Density
Polyethylene (HDPE), High Pressu re Low Density Polyethylene
(LDPE) and a nucleating masterbatc h. In general the ratio of
HDPE to LDPE is 70-80% HDPE/30-20% LDPE. The nucleating masterbatch is typically added at about 1-3% and is generally also
based on a LDPE resin.
The HDPE Polyethylene products known as High density
polyethylene (HDPE) are manufactured primarily by a low pressure catalyst polymerization process. The low pressure technology was first developed in the late 1970’s and is widely
utilized by man polyethylene manufacturers. The following Figure 2 illustrates a schematic of a typical low pressure manufacturing process.
Figure 2: Low Pressure Polyethylene Process
HDPE is produced in a polymerization process at pressures
typically about 300 psi and temperature of about 100°C.
The LDPE Polyethylene products known as low density
polyethylene (LDPE) are manufactured exclusively by high pressure free radical polymerization. The high pressure technology was first introduced in the late 1930’s and is the oldest of the polyethylene manufacturing technologies.
LDPE is produced in a bulk polymerization process at pressures
typically at 35,000 psi and a temperature of around 300°C. The following Figure 3 illustrates a schematic of a typical low pressure manufacturing process.
Figure 3: High Pressure Polyethylene Process 4. Definition of Electrical Power Loss
In this study we will use simple equations to evaluate the
influence of DC and DF on the decibels/100 ft of electrical loss of a commercial coaxial cable. The decibel or db is simply the 10 times log of the ratio of power input to the cable at one end to the
power available at the other end of the coax:
Db = 10 log10 [(Power output)/Power input)] For example:
-3 db = 1/2 of the input power is available at the output of the
cable
-10 db = 1/10 of the power is available at the output of the cable -30 db = 1/1000 of the power is available at the output of the
cable
5. Loss Data
Data was obtained from published sources2. We fit various
functions to evaluate the functional dependence of the dielectric loss on input frequency. Data Poin ts were taken from Reference 2
and fit in Excel. The fit to a power law equation was excellent as shown in Figure 4.
50 ohm Coaxial cables
y = 0.061x0.5615
R2 = 0.9985y = 0.3937x0.574
R2 = 0.9797
y = 0.196x0.5601
R2 = 0.9923
y = 0.1508x0.5169
R2 = 0.9999
0.1110100
1 10 100 1000
m HzDb/100 ftDb/100 ft 0.5"
Hardline
Db/100 ft 8
Db/100 ft 8 foam
Db/100 ft 58 foam
Db/100 ft 58
Power (Db/100 ft 0.5"
Hardline)
Power (Db/100 ft 58)
Power (Db/100 ft 8)
Power (Db/100 ft 8foam)
Figure 4, Power Law Fit to Cable Loss Data:
Table 1 Summary of Power Law Fit of Coaxial Cable
Data from Figure 4.
Cable Type Pre Exponential
Factor Exponent
RG-58 0.394 0.574
RG-58 Foam 0.331 0.587 RG 8 0.196 0.56 RG-8 Foam 0.151 0.517 Hardline 0.061 0.562
As illustrated in Figure 4 and Table 1, losses appear to vary with
the 0.5 power of frequency. The basis of this dependence will be described next.
International Wire & Cable Symposium 516 Proceedings of the 57th IWCS
In general the equations below describe the calculated coaxial
cable loss as a function of both frequency and cable geometry. The losses in decibel, db, per 100 feet depend on several
geometric factors and both the diel ectric constant and tan delta for
the polymer
3.
Coaxial Cable
Db/100 ft = Fk1+( k2* F) (1)
[( ]() ]bd s F kdD D Z k +⎢⎣⎡∗∗⎟⎟
⎠⎞∗ = / / 4343.00 1 (2)
() Vpdf k / 78.22∗= (3)
F = frequency mega Hz
Zo = nominal impedance = (60/(Sqrt(DC)))*(ln[D/(d*ks)]) for air
dielectric Z0 = 60*ln(b/a)
a = od of inner conductor; b = id of outer conductor
D = dielectric diameter (id of outer conductor, shield) d = center conductor diameter ks = 1.0 for solid center conductor Fbd = braid factor (= 1.0 for solid ‘tube’ braid) DF = dielectric loss (electrical tan delta) Vp = velocity of propagation = 1/Sqrt(DC) DC = Dielectric Constant Db =decibel = 10*{log10 [Power(out)/Power(in)]}
Larger diameter cables like RG-8 and ‘Hardline’ have lower
losses than smaller diameter cables like RG-58. Foamed polyethylene dielectric has a lower loss, RG-8 foam, than solid polyethylene dielectric RG-8.
A -3 db loss means 50% of the input power is dissipated in the
coaxial cable. Losses > 3 db/100 ft are quite significant. Low loss conserves transmitter or amplifier power. For a given geometry, one term for db/100 ft el ectrical losses varies with the
square root of frequency. This k1 term in equation 1 above is due
to the ‘skin effect’, the property of electromagnetic waves to travel near the surface of the c onductor, usually copper or silver.
The skin effect varies with th e square root of the applied
frequency. The depth of penetra tion of the electromagnetic wave
is frequency dependent as shown in the Figure 5 plot below: Skin Effect Depth versus Applied Frequency Hz
y = 66.277x-0.5001
R2 = 1
0.00010.0010.010.1110
1.E+
001.E+
011.E+
021.E+
031.E+
041.E+
051.E+
061.E+
071.E+
081.E+
091.E+
10
HzSkin Depth mm
Figure 5: Skin Effect Depth versus Frequency
We now see that the electrical loss dependence on the square root
of frequency is due to the skin effect. The k1 term in Equation 1 depends on the dielectric constant of the dielectric polymer through the impedance term Zo, the nominal impedance By
inspection we see that: larger DC implies larger k1 which larger slope of the plot of log (db/ 100 ft) versus log frequency. The
larger slope results in higher diel ectric loss at higher frequencies.
Coax diameter impacts the pre-e xponential factor of the log-log
plot of db/100 ft versus frequency. This again is due to the skin effect: larger diameter inner conductor and larger outer shield ‘pipe’ have a larger surface = lower ‘surface resistance’ to dissipate electromagnetic energy.
The raw data in Figure 4 and th e derived equations from Figure 5
can now be understood, much of the loss in coax is due to the skin effect.
Although Equation 1 does not speci fically account for ‘ohmic’
type direct current losses, that loss can be calculated directly from specifications for ohmic resistance of the cable: 0.148 ohms/100 ft. If we assume the source produces 1000 watts of power, only 2.98 watts is lost due to I^2 *r (ohmic) losses. This is
a loss of only 0.0129 db/100 ft. The loss is actually about 2 db/100 ft. Ohmic losses are only a small component of the total db/100 ft loss.
Intuitively we expect losses in coax to also vary with the
electrical tan delta since tan delta represents electrical dissipative mechanisms within the polymer often caused by molecular motions of polar groups either attached to or dissolved in the polymer chain. Usually both electrical and mechanical tangent delta peaks can be observed for a given molecular motion; if the polymer does not contain polar groups the electrical loss of the motion may not be observed. The influence of polar groups on electrical losses in polyethylene’s has been published by Sato in Reference 1. That worked focused on the dependence of tan delta on the presence of polar groups within the polyethylene. Next we will model the quantitative dependence of cable loss on tan delta. For mathematical simplicity we will only model a ‘solid tube’ coax, not the braded outer conductor type.
International Wire & Cable Symposium 517 Proceedings of the 57th IWCS
5.1 Simulations of the Impact of Polymer DF
Parameter on Cable Losses versus Frequency
db/100 ft versus Frequency and tan delta
0.010.1110100100010000100000
0.1 1 10 100 1000 10000
Megahertzdb/100 ft. df 0.0001
df 0.001
df 0.01
df 0.1
Power ( df 0.0001)
Figure 6: Influence of polymer tan delta on Cable
Losses
Clearly tan delta (Figure 6) plays a larger role in electrical loss as
frequencies approach the gigahe rtz region (1000 megahertz). In
Figure 7 we expand the resolution of Figure 6 in the Gigahertz region. We see that tan delta values as low as 0.0001 have a
significant impact on losses:
db/100 ft versus Frequency and tan delta
012345678910
0 2000 4000 6000 8000 10000
Megahertzdb/100 ft. df 0.0001
df 0.001
df 0.01
df 0.1
Power ( df 0.0001)
Poly. (df 0.001)
Poly. ( df 0.01)
Figure 7: Cable Losses in the Gigahertz region,
Influence of tan delta
If there were no polar groups like peroxide residue, antioxidants
and thermal oxidation products present in the polyethylene tan delta would likely be in the ~ 0.00001 range.
The above work fundamentally assumes DF is frequency
independent. This is not the case. At a given temperature the alpha, beta and gamma transitions
in polyethylene are functions of
measurement frequency. The gamma or ‘crankshaft’ transition4,5
occurs at ~ -120 °C at 1 Hz. The using an Arrhenius relationship with an activation energy of ~ 13 kcal/mole, the gamma transition will be near the GHz range at 25 °C. Polar groups in the vicinity of the gamma transition can move and cause electrical losses.
6
The challenge is to minimize polar impurities in the polyolefin insulation material.
6. Polyethylene Characterization
The two critical properties of the polyethylene resins for coaxial
insulation are low dielectric cons tant and low dissipation factor .
DC is a function of crystallinity or density and increases as
density increases. Dissipation Factor (DF) represents a signal loss due to dissipation through the insu lation. Dipolar impurities, end
groups, chain folds and branch points increase the DF, as does increasing the measurement frequency. With the increased need for data and signal transmissi on in today’s environment the
frequency testing can reach upwards of 5-7GHz. The following Figures 8 & 9 represents the DC and DF values of HDPE
materials which are utilized in the application today.
Figure 8
Dieletric Constant of HDPE @2.47 GHz, 23°C
2.262.282.302.322.342.362.38
ABCDE
SampleDielectric Constant
Figure 8: Dieletric Constant of HDPE @2.47 GHz, 23°C
Figure 9
Dissipation Factor of HDPE @ 2.47 GHz, 23°C
0.0000000.0000500.0001000.000150
ABCDE
SampleDissipation Factor
Figure 9: Dissipation Factor of HDPE @2.47 GHz, 23°C
Figures 10 and 11 represent the DC and DF values of HDPE
materials which are utilized in the application today
Figure 10
Dielectric Constant of LDPE @ 2.47 GHZ, 23°C
2.242.252.262.272.282.292.3
ABCDE
SampleDielectic Constant
Figure 10: Dielectric Constant of LDPE @ 2.47 GHz,
23°C
International Wire & Cable Symposium 518 Proceedings of the 57th IWCS
Figure 11
Dissipation Factor of LDPE @ 2.47 GHz, 23°C
0.000000.000100.000200.000300.00040
ABCDE
SampleDissipation Factor
Figure 11: Dissipation Factor of LDPE @ 2.47 GHz,
23°C
COAX insulation as noted previously is a mixture of HDPE and
LDPE. Thus looking at the varying data in Figures 8-11, one can ascertain that the selection of the proper polymers can have an significant effect on the overall cable signal loss.
7. Optimization of LDPE Resins
Initial studies were centered on the improvement in the LDPE
component of the system was an ar ea of focus. Effort in this area
showed that LDPE electrical performance can be influenced by the type and efficiency of a specific LDPE reactor. Samples of similar LDPE were secured form different types of reactors and DC and DF at 2.47 GHz measurem ents were again obtained. The
resulting data is illustrated in Figures 12 and 13.
Reactor operation is affected by the typical reaction parameters
one normally sees in reaction chemistry. These include but are not limited to time, temperature and pressure. Thus as shown in
Figure 13, one can see that not all reactors produce the same type of electrical performance when ma king similar LDPE products. In
addition the LDPE being primarily a non polar aliphatic hydrocarbon, which during polymerization can also incorporate polar functional groups from various sources. Exampl es of these
sources include can include organic peroxides types and chain transfer agents which are known to also influence electrical
performance.
Figure 12
Dielectric Constant of LDPE from Varying Reactors
2.232.2352.242.2452.252.2552.262.265
ABCDE
ReactorDielectric
Consatant @ 2.47
GHZ, 23°C
Figure 12: Dielectric Constant of LDPE from Varying
Reactors
Figure 13
Dissipation Factor of LDPE from Varying Reactors
00.000050.00010.000150.00020.000250.00030.00035
AB CDE
ReactorDissipation Factor
@2.47 GHZ, 23°C
Figure 13: Dissipation Factor of LDPE from Varying
Reactors
In focusing on reactor optimization a study was performed
wherein we adjusted conditions on a single reactor to further illustrate that electrical performance can be influenced or improved by the reaction kinetics. We established an internal
analytical test method to track the performance of the reactor which we define as the Product Performance Factor wherein the lower the number the better the performance. Thus in product
optimization studies we followed the reaction by securing samples and tracking the Product Performance Factor. 2.47 GHz DC and DF data was generated on these samples and is illustrated
in Figure 14.
Figure 14
LDPE Dissipation Factor Optimization
0.000000.000100.000200.000300.00040
0.00 0.10 0.20 0.30 0.40
Product Perfromance F actorDissipation factor @
2.47 GHz , 23°C
Figure 14: LDPE Dissipation Factor Optimization
As observed he dissipation factor can be significantly influenced
by the high pressure reaction, t hus indicating that optimization
control of the reaction is required to obtain the lowest electrical loss of the LDPE.
8. Conclusions
• We have shown that for a given coax diameter and skin
effect losses, an increase in polymer tan delta will negatively impact coax loss especially in the gigahertz region where tan delta losses can overpower skin effect losses.
• Optimization of a polyethylene reactor train can
significantly decrease the electrical loss of the polyethylene in the GHz frequency range.
• We have developed a direct relation between 2.47 GHz
tan delta and a chemical product performance factor which can be used to optimize, minimize, dielectric losses in the product LDPE.
International Wire & Cable Symposium 519 Proceedings of the 57th IWCS
9. Acknowledgments
The authors would like to acknowledge Alex Zamanskiy for his
efforts in conducting the analyti cal testing, Nick Cimato for
helping in the laboratory with sample preparations and Jack Chang for the electrical testing.
10. References
1 Y Sato et al, J. Appl. Polym. Sci., V-22, pp 2141-2153, (1978)
2 The American Radio Relay League Handbook 2001, C.
Hutchinson Ed. Newington CT, 2001
3 P. Smith, Transmission Line Calculator, Electronics, Jan. 1939
4 N.G. McCrum et al, Anelastic and Dielectric Effects in
Polymeric Solids, Wiley, 1967, pp 180-182
5 T.F. Schatzki, J. Polym. Sci. 57, 496 (1962)
6 N.G. McCrum et al, p 364
11. Pictures of Authors
Robert F. Eaton, 171 River Rd.,
Piscataway, NJ 08854
\
Bob Eaton is a Research Leader in Dow’s
Wire and Cable Research Group. He has a Ph.D. in Polymer Chemistry from Princeton University and did post doctoral research in Polymer Physics at UC Berkeley. His research interests include polymer structure property relations,
electrical properties of polymers and ‘green’ chemistry. He is an
active Amateur Radio enthusiast.
Chester J. Kmiec, 171 River Rd., Piscataway, NJ 08854
Chester Kmiec. is a Development Leader for the Wire and Cable Compounds group of The Dow Chemical Company. Chet has 34 years experience in Polymer Applications Research and Development, the last 19 years at The Dow Chemical Company. He holds a B.S in Plastics
Technology from Lowell Technological Institute and an M.B.A.
from the State University of New York at Buffalo. . In his current position as the Telecommunication Cable Materials Application
Technology Leader, Chet is responsible for leading the development and commercializa tion of new product technology
for Telecommunication cable applications. He is holds 17 patents.
International Wire & Cable Symposium 520 Proceedings of the 57th IWCS