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Nagy Thesis 20178
Nagy Thesis 20178
A Thesis
by
MASTER OF SCIENCE
December 2014
Throughout the course of the American Society of Heating Refrigeration and Air
Handbooks. However, this information is not constant, rather varying as each subsequent
handbook edition is released. Thirteen properties (liquid and vapor viscosity, thermal
conductivity, specific heat, enthalpy, surface tension, density and specific volume) from
five widely used refrigerants (R-22, R-134a, R-410a, R-152a, R-600a) are examined at
variables such as effect on Reynolds number are obtained using these properties. Mass
flux rates of 100 and 300 lbm/ft2-s are considered with pipe diameter of 8.52mm. The
resultant values are compared to 2013, the most recent ASHRAE Handbook edition, as
It is seen that physical properties can vary by nearly 30% with respect to edition
2013 and up to 25% between editions with a stabilizing effect appearing near more
equations became a function of more physical properties, percent change became more
erratic. With regards to mass flux rate, percent change was not affected for the selected
single phase design variables as mass flux increased due to a scaling factor response, yet
plus and minus 50 percent through the quality range of 0.2 to 0.8 for condensation and
ii
plus 15 percent to negative 20 percent for qualities of 0.2 and 0.8, respectively. R-22
showed the lowest error with R-152a revealing at times negative 40 percent error for
iii
DEDICATION
This thesis is dedicated to my mom and my dad for their love and support every
iv
ACKNOWLEDGEMENTS
First and foremost I would like to thank Dr. Pate for his guidance and giving me
the opportunity to work on this thesis. I would also like to thank Dr. Alvarado and Dr.
Mukherjee for being on my committee. A big thank you to Jason Korn for assisting me
with the proof reading and helping throughout the entire process, I couldn’t have done it
without you. Also I would like to acknowledge my brother, Phillip Nagy for helping
through the proofing process and putting up with the late nights. Lastly, thank you to
v
NOMENCLATURE
ρ Density, 𝑙𝑏𝑚/𝑓𝑡 3
V Velocity, 𝑓𝑡/𝑠
D Diameter,𝑓𝑡, 𝑚𝑚
Re Reynolds Number
Nu Nusselt Number
vi
Pr Prandtl Number
f Friction Factor
P Pressure, 𝑙𝑏𝑓/𝑖𝑛2
x Quality
Fr Froude Number
Bo Boiling Number
Co Convection Number
vii
TABLE OF CONTENTS
Page
ABSTRACT .......................................................................................................................ii
DEDICATION ..................................................................................................................iv
ACKNOWLEDGEMENTS ............................................................................................... v
NOMENCLATURE ..........................................................................................................vi
1. INTRODUCTION .......................................................................................................... 1
viii
5. SINGLE PHASE FLOW CORRELATIONS .............................................................. 32
7. CONCLUSIONS .......................................................................................................... 86
REFERENCES ................................................................................................................. 87
APPENDIX A .................................................................................................................. 90
APPENDIX B .................................................................................................................. 92
ix
LIST OF FIGURES
Page
Figure 4: Liquid Viscosity Percent Change With Respect to 2013, 40F ......................... 17
x
Figure 21: Liquid Prandtl Number-2013, 100F ............................................................... 43
Figure 25: Liquid Nusselt Number Percent Change with Respect to 2013, 100F ........... 49
Figure 26: Liquid Nusselt Number Percent Change Previous Edition, 100F .................. 49
Figure 27: Vapor Nusselt Number Percent Change 2013, 100F ...................................... 50
Figure 31: Liquid Heat Transfer Coefficient Change Previous, 40F ............................... 56
Figure 32: Liquid Heat Transfer Coefficient Change Previous, 100F ............................. 56
xi
Figure 43: R-152a Condensation, D = 8.52mm ............................................................... 73
Figure 45: R-22 Condensation Percent Change with Respect to 2013 ............................ 75
Figure 46: R-152a Condensation Percent Change With Respect to 2013 ........................ 76
Figure 51: R-22 Evaporation Percent Change With Respect to 2013 .............................. 82
Figure 52: R-152a Evaporation Percent Change With Respect to 2013 .......................... 83
Figure 53: R-600a Evaporation Percent Change With Respect to 2013 .......................... 84
xii
LIST OF TABLES
Page
Table 4: Liquid Viscosity Percent Change With Respect to Previous Edition ................ 15
Table 18: Liquid Heat Transfer Coefficient, G = 100 lbm/ft2s, D = 8.52mm .................. 53
Table 19: Vapor Heat Transfer Coefficient, G = 100 lbm/ft2s, D = 8.52mm .................. 53
xiii
Table 21: Vapor Friction Factor, G = 100 lbm/ft2s, D = 8.52mm .................................... 60
Table 22: Liquid Pressure Drop, G = 100 lbm/ft2s, D = 8.52mm, Δx = 1ft ..................... 65
Table 23: Vapor Pressure Drop, G = 100 lbm/ft2s, D = 8.52mm, Δx = 1ft ..................... 66
xiv
1. INTRODUCTION
values for a material’s physical properties are brought into question with regards to the
level of dependability and precision over time. This paper intends to introduce
discrepancies with the progression of tabulated data concerning a variety of heavily used
properties for the selected refrigerants, correlations will be drawn to commonly used
design variables highlighting areas of the most concern. The selected refrigerants of
five refrigerants are used in different applications; however, all designs for use with one
properties of various refrigerants have been included in the publishing Every four years
the respective editions of these ASHRAE Handbooks are published with up-to-date data,
Because these handbooks are considered one of the most important references for
it is imperative that the data listed is precise. Because new editions are published every
1
four years, there are sometimes significant discrepancies between editions resulting in a
possible large percentage of error for systems designed using a previous compilation of
the data. As a result of this, it is the intent of this paper to explore these incidences and to
derive several important parameters used in refrigeration systems associated with these
properties that may be affected by the variations recorded in the available refrigerant
data.
As stated earlier, due to the non-annual nature of the handbook releases, there are
possibilities for data to become outdated since technology advances quickly and often.
As the tools for measuring physical properties become more advanced and precise, it
creates the problem, how much were the previous measurements off and how do they
affect design parameters of systems already built? The results that will be presented
reveal that there are large changes between some years for a plethora of physical
properties in nearly all the refrigerants analyzed. The result of this research will allow
companies and individuals to see conclusively how far off the design of a system is if
already made, as well as provide a solid set of data to use that is accurate. The
exploration conducted is also expected to draw correlations between the earliest edition
published and the most recent in order to firmly obtain a standard data set.
2
2. BACKGROUND AND HISTORY
Conditioning Engineers can be traced back to 1894 and focuses on refrigeration, energy
efficiency and sustainability to name a few. The organization came into existence due to
a merger of two groups, The American Society of Heating and Air Conditioning
Engineers, or ASHAE that started in 1894 and The American Society of Refrigerating
Engineers, or ASRE which was established in 1904. ASHAE was formed as a result of
the apathetic attitude of Master Steam and Hot Water Fitters Association in regard to the
scientific merits of heating and ventilation which created ASHAE with an expressed
ASRE on the other hand, was organized by members of the American Society of
Mechanical Engineers, or ASME, due to refrigeration only playing a small role in annual
needed due to a growing demand for refrigeration [13]. Thoughts of a merger of the two
societies were not seriously considered until the 1950’s when there was substantial
overlap in the research between them. As a result of these similarities, by June 1958 each
society has approved the Proposed Merger plan. Following a vote, ASRE and ASHAE
dissolved and became known as ASHRAE on January 29, 1959 which it is still known as
3
2.2 ASHRAE Handbook
The ASHRAE Handbooks can be traced back to 1922. The handbooks were
initially known as the Heating and Ventilating Guide published by the American Society
of Heating and Ventilating Engineers, or ASH&VE which was changed to ASHAE. The
new edition of The Guide annually until 1961. It was then that The Guide was
amalgamated with the Refrigerating Data Book produced by ASRE and renamed the
ASHRAE Guide and Data Book with only two separate editions, Applications and
Fundamentals and Equipment. It was not until 1967 that a change occurred with the
Equipment. In 1973 the name of the ASHRAE Guide and Data Book was changed to the
ASHRAE Handbooks and it was not until 1985 that separate editions were introduced
At the moment, there are four versions of the handbooks available; Refrigeration,
Fundamentals, HVAC Systems & Equipment and finally HVAC Applications. These
versions are rotated, each coming out every four years from the last publication. For
Applications in 2011 and then again in 2015 and so on. These handbooks are “the
4
the previous statement, the physical property data included in the handbooks are
typically used by design engineers. The version which will be utilized in this herein is
the Fundamentals Handbook dating back to 1981 to the most revision in 2013,
clarify the uses for each refrigerant as well as acknowledge any shortcomings each
possesses in order to ensure a firm understanding of the data presented later in this
thesis. The fluids to be examined are R-22, R-152a, R-134a, R-410a and lastly R-600a.
2.3.1 R-22
potential. R-22 has been used as a refrigerant for air conditioning units for decades yet,
Agency, or EPA, with a prohibition of new unit manufactures beginning in 2010 and the
end of production of R-22 by 2020 [20]. The usage of this refrigerant will dwindle in the
future in the United States of America and worldwide due to the Montreal Protocol,
signed in 1987 with 197 ratifiers and worldwide usage is expected to be sharply curbed
5
in the near future [29]. Because of this, it remains important to examine the trends of
2.3.2 R-152a
potential of zero, a lower global warming potential (GWP) than R-134a at approximately
120 [21], and as such is a viable replacement for use in automobiles. Not until recently
was R-152a selected by the EPA as the refrigerant of choice for mobile air conditioners
although having physical property data listed in the ASHRAE Handbooks since 1981 as
2.3.3 R-134a
mobile air conditioners such as automobiles and according to the EPA, all vehicles
manufactured with air conditioning worldwide use this refrigerant [19] and as such is
extremely valuable to examine the trends in this fluid. First showing up in early 1990
and listed in the Fundamentals handbook in 1993, 134a was initially developed as a
replacement for R-12 due to its less environmentally harmful nature [24]. However,
recently in the European Union it was announced that all vehicles sold in EU countries
with air conditioning must use refrigerants with a global GWP of less than 150 starting
6
in 2011 for new automobiles and by 2017 for all vehicles[19]. Because of this R-134a
will not qualify as it has a GWP of 1300 although usage worldwide will continue.
2.3.4 R-410a
The fourth refrigerant which will be analyzed is the relatively new R-410a also
known as Puron. Originally invented by Allied Signal in 1991, it first appeared in the
and R-125. This has begun to replace R-22 in commercial and residential air
conditioning systems in the United States due to the EPA phase-out plan as well as other
developed countries due to R-410a possessing a zero ozone depletion potential (ODP).
However, although R-410a has a zero ODP, the GWP is very large akin to that of R-22
at higher pressures and efficiencies than its predecessor R-22, the impact on global
warming due to the use of R-410a will be significantly less than R-22 as a result of lower
energy consumption and coincidentally lower emissions from power plants [23].
2.3.5 R-600a
Contrary to the other four refrigerants, isobutane is not explicitly used in residential or
commercial air conditioning and is not used in automobile air conditioning systems due
to the fluid being highly flammable with a low flash point. Instead, R-600a is used
primarily in residential refrigerators and freezers but due to the insignificant ODP and
7
with a GWP of approximately three, it is foreseeable that isobutane will eventually
become a dominant source for permanent air conditioning systems and refrigeration.
Isobutane was first used in small systems in the 1920’s, but faded when
chlorofluorocarbons (CFC) type refrigerants arrived onto the market in the 1930’s and
did not return to use in Unites States appliances until 2008 [33]. Because of the present
and clear continued use of R-600a for refrigeration into the future, it is important to
8
3. DATA ANALYSIS METHODOLOGY
3.1 Overview
used refrigerants in the Fundamentals Handbook as a way for designers to easily access
reliable data concerning these fluids. It is crucial to note that during the compilation of
the data from the various editions, not all the refrigerants of interest have information
are not recorded, even so, the temperatures of interest of forty and one hundred degrees
Fahrenheit are well documented due to them being more typical operating conditions for
3.2 Method
There are twelve physical properties that are to be considered, these are saturated
vapor and liquid viscosity, saturated vapor and liquid thermal conductivity, surface
tension, saturated liquid and vapor specific heat, liquid enthalpy, vapor enthalpy, liquid
density and vapor specific volume. All of these properties are considered as they play
significant roles in the design of a system. The refrigerant data sheet for each fluid was
total of nine edition and subsequently nine data points per refrigerant. The properties for
R-22, R-152a and R-600a were available dating back to the first edition while R-134a
did not appear until 1993 and R-410a not appearing until 1997. Also, starting at the 1993
9
edition the table format was altered which is when the first appearance of surface
All the refrigerants, with the exception of R-410a, are tabulated in the handbooks
according the value of each property corresponding to a set temperature. For R-410a the
physical properties are listed corresponding to a set pressure with temperatures of the
liquid on the bubble line and vapor on the dew line. In order to obtain values for each of
the twelve properties, standard interpolation was performed on the data using the
Where 𝑥1 and 𝑥3 are the temperatures immediately before and after the desired
temperature on the bubble and dew line and 𝑦1 and 𝑦3 are the corresponding values of
the physical property in liquid or vapor form, respectively. A selected example of this is
10
Table 1: R-410a Interpolation
R-410a 2001
40 Degrees Fahrenheit
Liquid Temp. Vapor Temp. Liquid Enthalpy Vapor Enthalpy
Lower Bound 38.65 38.82 27.02 120.1
Desired 40 40 27.513 120.176
Upper Bound 43 43.18 28.61 120.38
100 Degrees Fahrenheit
Liquid Temp. Vapor Temp. Liquid Enthalpy Vapor Enthalpy
Lower Bound 97.32 97.53 49.95 121.64
Desired 100 100 51.105 121.551
Upper Bound 101.75 101.95 51.86 121.48
As seen in Table 1, interpolation for R-410a was crucial to remain consistent with the
other refrigerants as well as accurate due to a non-uniform upper and lower bound
temperature with regards to the bubble and dew lines. This was implemented for every
After all of the data was interpreted, the data was then placed into a table
showing the trend of the selected physical property for each refrigerant with respect to
the year. As can be seen in Table 2, the progression of data shows a stabilization effect
nearing 2013 as there are several years in a row with identical information obtained from
the handbooks.
11
Table 2: Saturated Liquid Velocity Trend
Saturated Liquid Viscosity (lbm/ft-h)
ASHRAE Edition 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 0.5530 0.5530 0.5530 0.4840 0.4840 0.5030 0.5030 0.5030 0.5030
R-152a 0.5030 0.5030 0.5030 0.4940 0.4940 0.4930 0.5030 0.5030 0.5030
40 ◦F
R-600a 0.4800 0.4800 0.4800 0.4800 0.4580 0.4580 0.4560 0.4570 0.4570
R-134a 0.6580 0.6580 0.6200 0.6200 0.6200 0.6200
R-410a 0.3797 0.3894 0.3894 0.3894
R-22 0.4490 0.4490 0.4490 0.3380 0.3380 0.3460 0.3460 0.3460 0.3460
R-152a 0.3760 0.3760 0.3760 0.3480 0.3480 0.3430 0.3400 0.3400 0.3400
100 ◦F
R-600a 0.3500 0.3500 0.3500 0.3500 0.3190 0.3190 0.3170 0.3200 0.3200
R-134a 0.4430 0.4430 0.4070 0.4070 0.4070 0.4070
R-410a 0.2442 0.2450 0.2450 0.2450
The blanks in the table are indicative of unavailable data in the ASHRAE
Handbook for the respective year and refrigerant and this format is carried through for
all results. It is evident that there are changes from year to year, often coming after
several years of no change. All thirteen selected properties were organized in this same
fashion for ease of access. The remaining twelve property tables can be seen in the
appendix and in addition to this these results are exported into a line plot showing the
trend of the data. This can be visualized on Figure 1 and Figure 2 for saturated liquid
12
Saturated Liquid Viscocity 40 Degrees Fahrenheit
0.70
0.65
Viscosity (lbm/ft-h)
0.60
0.55
0.50
0.45
0.40
0.35
1981 1985 1989 1993 1997 2001 2005 2009 2013
Year
0.45
Viscosity (lbm/ft-h)
0.40
0.35
0.30
0.25
0.20
1981 1985 1989 1993 1997 2001 2005 2009 2013
Year
13
From Figure 1 and Figure 2 as noted earlier, the trend of the data shows
stabilization closer to 2013 for all refrigerants, but very large fluctuations in recorded
data for earlier editions of the ASHRAE handbooks primarily centered from 1989 to
2001. It is apparent that there are numerous large jumps in the data resulting in the
presented property value change from edition to edition being particularly concerning.
To assess these instances the data was arranged into another line plot.
In order to pinpoint problem areas it was imperative to find the percent change of
the data for two separate baselines. Firstly, the change with respect to the previous year
Where Yr is the handbook year and i represents the edition number. This
equation relates the increase or decrease of a data set relative to the immediately
preceding one. The second percent change formula is used to compare years before 2013
For the percent change with respect to 2013 as seen in Equation 3, i represents
the year of interest and generates a value relative to 2013. This enables one to identify
years with the greatest amount of contrast with the most recent handbook edition as a
14
benchmark. Combining Equations 2 and 3 with the information in Table 2, the results
R-600a 5.03 5.03 5.03 5.03 0.22 0.22 -0.22 0.00 0.00
R-134a 6.13 6.13 0.00 0.00 0.00 0.00
R-410a -2.49 0.00 0.00 0.00
R-22 29.77 29.77 29.77 -2.31 -2.31 0.00 0.00 0.00 0.00
R-152a 10.59 10.59 10.59 2.35 2.35 0.88 0.00 0.00 0.00
100 ◦F
R-600a 9.37 9.37 9.37 9.37 -0.31 -0.31 -0.94 0.00 0.00
R-134a 8.85 8.85 0.00 0.00 0.00 0.00
R-410a -0.33 0.00 0.00 0.00
15
Following the results obtained in the percent tables line plots revealing this data
are created to enable ease of visualization for rapid acquisition of concern years and
refrigerants; this is shown in Figure 3 and Figure 4 for percent change with respect to the
0.00
-2.00 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-4.00
-6.00
-8.00
-10.00
-12.00
-14.00
Years
Each data point represented in Figure 3 corresponds to the change between the
years indicated. For example, considering R-22 it is seen that there is no change from
1985 to 1989; however in 1993 the recorded values are altered by nearly -13% from
1989. The change from 2013 is shown in figure 4 below and is more straightforward.
16
Liquid Viscosity Percent Change With Respect to 2013, 40F
12.00
10.00
8.00
Percent Change %
6.00
4.00
2.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
-4.00
-6.00
Year
From Figure 4, due to the nature of the percent change correlation regarding
2013 as the baseline, all refrigerants converge to 2013. This is very important, as it
allows one to instantly recognize years differing greatly than the values accepted for a
certain physical property of a refrigerant at this point in time. When used in conjunction
with percent change between editions, the graphs reveal a very complete picture of the
progression of the data through the years allowing individuals to pinpoint years where
system designs or research were incorrect due to inaccurate information utilized. All
remaining twelve property tables and graphs are obtainable in the appendix. At this
variables.
17
4. PHYSICAL PROPERTIES
4.1 Preface
Upon compiling all data from the ASHRAE handbooks, there are several
instances where the physical properties change considerably through time. Although this
occurs with many of the examined properties, not all experienced notable change and
therefore, only selected occurrences that pose the most impact will be highlighted in this
4.2 Viscosity
Both saturated liquid and saturated vapor viscosity exposed percent changes
relative to 2013 with liquid viscosity containing the largest change. Because viscosity is
used in a wide range of fluid and heat transfer calculations, it is important to understand
which refrigerants show the most concern and at what year range. Viscosity is a fluids
resistance to deformation by shear and tensile stresses [32] and is important when
considering frictional losses in pipe flow. The units used in the ASHRAE handbooks are
𝑙𝑏𝑚/(𝑓𝑡 ∙ ℎ𝑟). Liquid viscosity was briefly touched upon in the previous section for 40
degrees Fahrenheit and at 100 degrees an increased error is realized when viewing the
below figures.
18
Liquid Viscosity Percent Change With Respect to 2013,
100F
35.00
30.00
25.00
Percent Change %
20.00
15.00
10.00
5.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
Year
The results in Figure 5 are very striking as R-22 shows a thirty percent increase
over the most recent handbook edition while all other refrigerants with the exception of
R-410a show values ten percent above 2013 as well. This occurs until 1997 where all
refrigerants begin a declination to values in use today. Such a large discrepancy would
significantly affect systems designed with this data and any calculations involving liquid
viscosity raised to a power will result in an even more severe offset. From Figure 6 and
Figure 7, the change with respect to 2013 for vapor viscosity can be seen.
19
Percent Change From 2013, Vapor Viscosity, 40 Degrees F
5.00
4.00
Percent Change %
3.00
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
Year
5.50
4.50
Percent Change %
3.50
2.50
1.50
0.50
-0.50 1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.50
Year
R-22 as the liquid, and about a third for the remainder of the refrigerants. One instance
for Figure 7 and Figure 8 which differs from Figure 6 is that the data does not reach a
steady state until 2005, a whole edition later than the liquid viscosity. Additionally, at
elevated temperatures the error became greater for both refrigerant states.
important property as it references how well a refrigerant is able to transmit heat with
larger values resulting in a higher amount of possible heat transfer [30]. As with
viscosity, both liquid and vapor forms of the five refrigerants must be analyzed,
21
Liquid Thermal Conductivity Percent Change With Respect
to 2013, 40F
20.00
15.00
Percent Change %
10.00
5.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
Year
20.00
Percent Change %
15.00
10.00
5.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
Year
22
Figure 8 and Figure 9 depict a great deal about the anticipated thermal
conductivity of the five refrigerants through time because of two reasons. Firstly, none
of the recorded values are below the values obtained in the most recent handbook, all
exhibiting a downward trend, reducing the liquid thermal conductivity through time.
Secondly, all refrigerants with the exception of isobutane level off at 2001 with
isobutane maintaining around an 8 percent error until 2005. Because of this, system
designers and researchers could have used this information believing that these
and as a result would have been able to transport much more energy than would be
than its liquid counterpart, however, the vapor portion must be addressed due to an
outlier which appear when comparing the recorded values of 40 and 100 Fahrenheit. In
this case, vapor thermal conductivity does not exhibit the extreme change that liquid
conductivity shows with maximums at negative 8 percent and 4 percent for R-22 and R-
600a at 100 and 40 degrees Fahrenheit, respectively. The outliers shown in Figure 10
and Figure 11 for R-22 and R-600a at 40 degrees expose that instead of steadily nearing
the most recent value, they instead both make jumps at 1993 in the wrong direction.
23
Vapor Thermal Conductivity Percent Change With Respect
to 2013, 40F
3.00
2.00
1.00
Percent Change %
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
-2.00
-3.00
-4.00
Year
4.00
2.00
Percent Change %
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
-4.00
-6.00
-8.00
-10.00
Year
24
Additionally, when looking at these two refrigerants at the temperatures
indicated, at the lower temperature isobutane is below the zero and above the zero at the
higher temperature, this is reversed for R-22 in 1993. This is peculiar as the fluid is
heated the declared property begins at a set percentage above 2013 values and instead of
4.4 Enthalpy
and is provided in the ASHRAE handbooks as specific enthalpy with the units of
𝐻 = 𝑈 + 𝑃𝑉 (4)
system. This property is an extensive property and relies on the size of the system. For
ℎ = 𝑢 + 𝑃𝜈 (5)
Where h is the specific enthalpy, u is the internal energy and v is the specific
volume. In this case enthalpy is regarded as an intensive property due to the per unit
mass. The data obtained via the ASHRAE handbooks show an extremely surprising
result for specific enthalpy, both liquid and vapor exhibit extreme percent changes with
respect to current edition. As can be seen Table 5 and Table 6 below, the tables represent
25
Table 5: Saturated Liquid Enthalpy
Saturated Liquid Enthalpy, h f , (Btu/lb)
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 21.422 21.474 21.474 21.688 21.688 21.662 21.662 21.662 21.662
R-152a 24.700 24.427 24.427 31.628 31.628 31.490 31.490 31.490 31.490
40 ◦F
R-600a -818.40 140.520 140.520 140.520 42.439 42.448 42.259 42.035 42.035
R-134a 24.051 24.694 24.694 24.890 24.890 24.890 24.890
R-410a 27.620 27.513 27.818 27.818 27.818
R-22 39.267 39.233 39.233 39.538 39.538 39.502 39.502 39.502 39.502
R-152a 48.430 48.004 48.004 57.366 57.366 57.124 57.124 57.124 57.124
100 ◦F
R-600a -782.900 175.860 175.860 175.860 77.399 77.418 77.137 76.639 76.639
R-134a 44.230 44.943 44.943 45.155 45.155 45.155 45.155
R-410a 51.266 51.106 51.667 51.667 51.667
R-600a -668.700 291.690 291.690 291.690 193.598 193.609 193.133 192.647 192.647
R-134a 107.389 108.705 108.705 108.856 108.856 108.856 108.856
R-410a 120.662 120.176 120.644 120.644 120.644
R-22 112.105 111.810 111.810 112.081 112.081 112.276 112.276 112.276 112.276
R-152a 163.860 163.490 163.490 170.092 170.092 170.258 170.258 170.258 170.258
100 ◦F
R-600a -649.800 311.020 311.020 311.020 212.830 212.847 212.281 211.820 211.820
R-134a 114.888 116.166 116.166 116.289 116.289 116.289 116.289
R-410a 121.741 121.551 121.971 121.971 121.971
The most evident point in these tables are all entries for R-600a in 1981. The
given values are an anomaly resulting in a -450% change with respect to 2013 for vapor
and up to -2050% change from 2013 for the liquid. This skews the data to the point
where the typical percent change graphs implemented become ineffective due to the
dominance of isobutane. After careful consideration of the tables for R-600a, it was
determined that the reference point for both liquid and vapor was inconsistent until 1997.
26
Therefore, all years prior to 1997 will be omitted from any graphs displayed, however if
Notwithstanding the previous occurrence, there are several points where the
liquid enthalpy, or hf, and the vapor enthalpy, or hg, deviate significantly. Selecting forty
degrees as a point of examination the following two figures reveal other refrigerants of
interest.
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
Percent Change %
-5.00
-10.00
-15.00
-20.00
-25.00
Title
27
Percent Change From 2013, Vapor Enthalpy, 40 Degrees F
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
Percent Change %
-1.00
-2.00
-3.00
-4.00
-5.00
Title
Analyzing Figure 12 and Figure 13, there is still a significant percent change
with R-600a in 1985, coming to within one percent of the accepted values by 1997. In
addition to this, R-152a shows up as only 5 percent under the zero but almost 23 percent
under for vapor and liquid enthalpy, respectively. It should be noted that for single phase
flow, calculations would be grossly incorrect until 1997 where the values stabilized.
Although individually the liquid and vapor enthalpies have issues, ℎ𝑓𝑔 which is the
specific enthalpy change for evaporation, defined as ℎ𝑓𝑔 = ℎ𝑔 − ℎ𝑓 shows a near zero
28
4.5 Summary
Although there was not change in every category, there is still significance in
determining the maximum error for each refrigerant at each property. The maximum
percent change from 2013 is typically centered about two editions, 1981 and 1993, and
deviates occasionally to the previous or later edition. Since some refrigerants only
reported large changes at one edition such as R-134a, there is but one year selected to
represent its maximum. Results were obtained for both forty and one hundred degrees as
well as the maximum error between editions for any year range or temperature. A
snapshot of the maximum inaccuracies are seen below in Table 7 and Table 8.
29
Table 8: Maximum Percent Change-2013,100F
Maximum Percent Change 100F
Refrigerant R-22 R-134a R-152a R-600a R-410a
Year 1981 1993 1993 1981 1993 1981 1993 2001
Liquid Viscosity 29.77 -2.31 8.85 10.59 2.35 9.37 9.37 -0.33
Vapor Viscosity 5.86 5.86 3.99 1.95 4.21 4.21 3.74
Liquid Conductivity 4.67 3.56 0.46 5.61 1.50 20.41 20.41 0.57
Vapor Conductivity -7.73 -7.73 1.37 2.27 2.27 4.47
Surface Tension 2.18 0.25 -8.19
Liquid Specific Heat -1.14 -0.13 0.11 -2.93 0.31 4.17 1.01 -1.24
Vapor Specific Heat -2.88 1.25 -2.12 -8.34 10.43 2.11 1.28 -9.19 (97)
Liquid Enthalpy -.68(85) 0.12 -2.05 -15.97(85) 0.42 .99(97) -1.09
Vapor Enthalpy -.42(85) -0.17 -1.2(89) -3.98(85) 0.10 .48(97) -0.34
h(fg) -.27(85) 0.32 -.67(89) 2.08(85) -0.36 .18(97) .24(97)
Liquid Density 0.25 -0.01 .07(89) -0.04 -0.02 0.09 -0.01 0.34
Specific Volume -.3(85) -0.23 -.5(89) 1.43 -0.35 0.49 -0.08 0.35
The data represented in the Table 7 and Table 8 reveal several insights about the
trend of change for the refrigerants. Typically, at the higher temperature there is more
error realized except for a select few instances. The headings represent the years of
interest with the largest change occurring at the earliest appearance of the refrigerant.
Even so, the year 1993 showed substantial changes across the board with a few
exceptions noted in parentheses next to the value. This is especially true for enthalpy
The next important set of maximum percent changes are from edition to edition.
Since each new handbook effectively replaces the previous version, making the old data
obsolete, there is an interest to examine maximum changes that result from the
information increases the overall error rather than correct and stabilize it and the largest
30
Table 9: Maximum Percent Change Edition to Edition
Maximum Percent Change, Edition to Edition
Refrigerant R-22 R-134a R-152a R-600a R-410a
Liquid Viscosity -24.72 -8.13 -7.45 -8.86 2.55
Vapor Viscosity -5.54 -3.83 -2.17 -4.04 -3.60
Liquid Conductivity -3.71 -1.33 -5.21 -11.69 -0.57
Vapor Conductivity 8.38 -2.27 -0.73 3.90 -4.28
Surface Tension 2.18 0.25 -8.19
Liquid Specific Heat 1.02 0.37 25.04 -3.03 1.25
Vapor Specific Heat 4.29 2.16 20.47 -1.43 12.79
Liquid Enthalpy 1.00 2.67 29.48 -0.65 1.11
Vapor Enthalpy -0.26 1.23 4.69 -0.27 -0.40
h(fg) -0.36 0.81 -2.39 -0.21 -0.20
Liquid Density -0.26 -0.10 0.04 0.21 -0.34
Specific Volume -0.47 0.68 -1.77 -0.57 0.50
The above table illuminates several extremely large changes with a substantial
amount centered about R-152a for specific heat. There are also numerous points of
greater than 5 percent change although there is little deviation surrounding any point in
time for liquid density, specific volume and surface tension. Blanks in the table represent
that there has been zero change since initial documentation with only two instances, both
31
5. SINGLE PHASE FLOW CORRELATIONS
One of the most important variables in fluid mechanics and heat transfer is the
Reynolds number. This is a dimensionless value which is defined as the ratio of inertial
forces to viscous forces [22] and is used to determine turbulent or laminar flow either in
a stream or tube. From this point on, all variables analyzed will be related to pipe flow
As seen in Figure 14, the entrance region of a pipe is shown [18]. For all
considerations herein fluid flow is fully developed, constant properties and steady state
are assumed, unless otherwise noted. Since only the hydrodynamic fully developed flow
32
𝜕𝑣(𝑟, 𝑥) (6)
= 0, 𝑣 = 𝑣(𝑟)
𝜕𝑥
Where v is the flow velocity, x is the pipe length, and r is the pipe inner diameter.
Due to constant velocity for any position inside the pipe as well as constant inner pipe
𝜌𝑉𝐷𝐻 (7)
𝑅𝑒 =
𝜇
From Equation 7 the Reynolds number for pipe flow is obtained where ρ is
density, V is velocity, µ is dynamic viscosity and DH is the hydraulic diameter where for
a pipe 𝐷𝐻 = 𝐷. All calculations involving pipe diameter in this section utilize the same
diameter at 8.52mm.
𝐺 = 𝜌𝑉 (8)
The equation for mass flux is seen above simply as the product of density and
velocity. For Reynolds number analysis as well as all variables yet to be discussed, the
mass flux rates are 100 and 300 𝑙𝑏𝑚⁄𝑓𝑡 2 𝑠. With Equation 8 substituted into Equation 7
and pipe diameter for hydraulic diameter, the working Reynolds number equation is
𝐺𝐷 (9)
𝑅𝑒 =
𝜇
Using Equation 9, the Reynolds number for each mass flux rate can be obtained.
Both saturated liquid viscosity and saturated vapor viscosity are used to find the liquid
Reynolds number, 𝑅𝑒𝑙 , and the vapor Reynolds number, 𝑅𝑒𝑣 respectively. The resultant
tables generated for liquid Reynolds number are seen below in Table 10 and Table 11.
33
Table 10: Liquid Reynolds Number, G = 100 lbm/ft2s, D = 8.52mm
ReL At G=100 lbm/ft2s
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 1.82E+4 1.82E+4 1.82E+4 2.08E+4 2.08E+4 2.00E+4 2.00E+4 2.00E+4 2.00E+4
R-152a 2.00E+4 2.00E+4 2.00E+4 2.04E+4 2.04E+4 2.04E+4 2.00E+4 2.00E+4 2.00E+4
40 ◦F
R-600a 2.10E+4 2.10E+4 2.10E+4 2.10E+4 2.20E+4 2.20E+4 2.21E+4 2.20E+4 2.20E+4
R-134a 1.53E+4 1.53E+4 1.62E+4 1.62E+4 1.62E+4 1.62E+4
R-410a 2.65E+4 2.58E+4 2.58E+4 2.58E+4
R-22 2.24E+4 2.24E+4 2.24E+4 2.98E+4 2.98E+4 2.91E+4 2.91E+4 2.91E+4 2.91E+4
R-152a 2.68E+4 2.68E+4 2.68E+4 2.89E+4 2.89E+4 2.93E+4 2.96E+4 2.96E+4 2.96E+4
100 ◦F
R-600a 2.88E+4 2.88E+4 2.88E+4 2.88E+4 3.15E+4 3.15E+4 3.17E+4 3.14E+4 3.14E+4
R-134a 2.27E+4 2.27E+4 2.47E+4 2.47E+4 2.47E+4 2.47E+4
R-410a 4.12E+4 4.11E+4 4.11E+4 4.11E+4
R-600a 6.29E+4 6.29E+4 6.29E+4 6.29E+4 6.59E+4 6.59E+4 6.62E+4 6.61E+4 6.61E+4
R-134a 4.59E+4 4.59E+4 4.87E+4 4.87E+4 4.87E+4 4.87E+4
R-410a 7.95E+4 7.75E+4 7.75E+4 7.75E+4
R-22 6.72E+4 6.72E+4 6.72E+4 8.93E+4 8.93E+4 8.73E+4 8.73E+4 8.73E+4 8.73E+4
R-152a 8.03E+4 8.03E+4 8.03E+4 8.68E+4 8.68E+4 8.80E+4 8.88E+4 8.88E+4 8.88E+4
100 ◦F
R-600a 8.63E+4 8.63E+4 8.63E+4 8.63E+4 9.46E+4 9.46E+4 9.52E+4 9.43E+4 9.43E+4
R-134a 6.81E+4 6.81E+4 7.42E+4 7.42E+4 7.42E+4 7.42E+4
R-410a 1.24E+5 1.23E+5 1.23E+5 1.23E+5
In order to obtain dimensionally correct Reynolds numbers, the liquid and vapor
0.0279528 ft. Applying Equations 2 and 3 to the data in the above tables the Reynolds
number percent change is obtained. It should be noted that for internal flow from
𝑅𝑒𝐷 < 2000 the flow is laminar, for 𝑅𝑒𝐷 > 3000 the flow is turbulent and between
these two values the flow is transitional [34]. Consequently, it is apparent that all liquid
Reynolds numbers, as well as vapor, fall within turbulent fluid flow parameters.
34
Liquid Reynolds Number Percent Change With Respect to
2013, 40F
6.00
4.00
2.00
Percent Change %
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
-4.00
-6.00
-8.00
-10.00
Year
R-22 R-152a R-600a R-134a R-410a
6.00
4.00
2.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2.00
-4.00
-6.00
Years
R-22 R-152a R-600a R-134a R-410a
considerable discrepancies in the liquid Reynolds number with the greatest occurring for
R-22 from 1981 to 1989 with nearly a ten percent difference from present day. Similar
problems arise with R-600a and R-410a, beginning in the first two years the latter was
introduced. Comparing these issues with the edition to edition change, the graph reveals
a twelve percent differential from 1989 to 1993. When comparing the liquid Reynolds
number percent changes to the vapor Reynolds number percent there are similar
R-600a 5.75E+5 5.75E+5 5.75E+5 5.75E+5 5.85E+5 5.85E+5 5.95E+5 5.95E+5 5.95E+5
R-134a 3.73E+5 3.73E+5 3.81E+5 3.81E+5 3.81E+5 3.81E+5
R-410a 3.33E+5 3.37E+5 3.37E+5 3.37E+5
R-600a 5.08E+5 5.08E+5 5.08E+5 5.08E+5 5.08E+5 5.08E+5 5.30E+5 5.30E+5 5.30E+5
R-134a 3.22E+5 3.22E+5 3.34E+5 3.34E+5 3.34E+5 3.34E+5
R-410a 2.79E+5 2.89E+5 2.89E+5 2.89E+5
36
Table 13: Vapor Reynolds Number, G = 300 lbm/ft2s, D = 8.52mm
Rev for G = 300 lbm/ft2s
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 1.02E+6 1.02E+6 1.02E+6 1.04E+6 1.04E+6 1.07E+6 1.07E+6 1.07E+6 1.07E+6
R-152a 1.31E+6 1.34E+6 1.34E+6 1.34E+6
40 ◦F
R-600a 1.73E+6 1.73E+6 1.73E+6 1.73E+6 1.76E+6 1.76E+6 1.79E+6 1.79E+6 1.79E+6
R-134a 1.12E+6 1.12E+6 1.14E+6 1.14E+6 1.14E+6 1.14E+6
R-410a 1.00E+6 1.01E+6 1.01E+6 1.01E+6
R-600a 1.52E+6 1.52E+6 1.52E+6 1.52E+6 1.52E+6 1.52E+6 1.59E+6 1.59E+6 1.59E+6
R-134a 9.65E+5 9.65E+5 1.00E+6 1.00E+6 1.00E+6 1.00E+6
R-410a 8.36E+5 8.68E+5 8.68E+5 8.68E+5
Examining Table 12 and Table 13, the vapor Reynolds number for both mass
flux rates are well above acceptable values for turbulent flow in all instances.
Additionally, it should be noted that the blanks are indicative of nonexistent data as
some refrigerants were not available, however in the case of R-22 for 100 degrees
information was not published in 1993 or 1997 contrary to the preceding and
aforementioned years. Applying Equations 2 and 3 to the vapor tables the following
37
Vapor Reynolds Number Percent Change With Respect to
2013, 40 F
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
Percent Change %
-1.00
-2.00
-3.00
-4.00
-5.00
Year
2.50
2.00
Percent Change %
1.50
1.00
0.50
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.50
-1.00
Years
situated at negative percent change points on the graph as seen in Figure 17. Also, there
is significantly lower percent change with respect to the liquid values. As for the edition
to edition graph seen above as Figure 18, the results show a peculiar trend with property
changes occurring essentially every other edition until it reaches current values.
Although there are differences between the percent changes for the states, this can be
explained by Equation 9. Because mass flux and pipe diameter are considered constant,
Reynolds numbers for each are only a function of the respective viscosities, which also
explains that although there are two different mass fluxes considered resulting in
different values, it only increases by a factor of 3, thus holding the percent change for
each flux constant. The remaining 100 degree Fahrenheit graphs for each Rev and Rel
can be found in the appendix showing approximately the same trends as the 40 degree
Fahrenheit graphs.
transfer calculations and is defined by the ratio of momentum diffusivity to the thermal
diffusivity [14]. It is very important to calculate the Prandtl number for each entry using
vapor and liquid properties rather than select a predetermined value for future equations
due to the constantly changing Prandtl number. The equation shown below is used for all
𝑣 𝑐𝑝 𝜇 (10)
𝑃𝑟 = =
𝛼 𝑘
39
Where v is the kinematic viscosity, 𝛼 is the thermal diffusivity, 𝑐𝑝 is specific
heat, µ is dynamic viscosity and 𝑘 is the thermal conductivity. Considering three of the
properties provided in the ASHRAE handbooks are specific heat, dynamic viscosity and
its percent change and effects on refrigeration and heat transfer. Applying the 𝑐𝑝 , 𝜇 and 𝑘
property tables referenced in Appendix A, the vapor and liquid Prandtl numbers are
R-600a 4.138 4.138 4.138 4.138 4.210 4.210 4.523 4.500 4.500
R-134a 4.017 4.017 3.850 3.850 3.850 3.850
R-410a 2.127 2.207 2.207 2.207
R-22 2.984 2.984 2.984 2.293 2.293 2.434 2.434 2.434 2.434
R-152a 2.888 2.888 2.888 2.874 2.874 2.861 2.841 2.841 2.841
100 ◦F
R-600a 3.719 3.719 3.719 3.719 3.723 3.723 3.940 3.931 3.931
R-134a 3.587 3.587 3.307 3.307 3.307 3.307
R-410a 2.060 2.105 2.105 2.105
R-600a 0.833 0.833 0.833 0.833 0.835 0.835 0.789 0.782 0.782
R-134a 0.828 0.828 0.842 0.842 0.842 0.842
R-410a 1.158 1.144 1.144 1.144
R-600a 0.851 0.851 0.851 0.851 0.873 0.873 0.829 0.818 0.818
R-134a 0.926 0.926 0.922 0.922 0.922 0.922
R-410a 1.343 1.340 1.340 1.340
40
Scrutinizing Table 14 and Table 15, there are large differences in the Prandtl
number with respect to present day values. The importance of the Prandtl number in
momentum and energy transport by diffusion in the velocity and thermal boundary
layers” [14]. Therefore, large discrepancies will result in a skewed understanding of the
true nature of the fluid. When placing significance on the numbers it should be noted
that for 𝑃𝑟 ≪ 1 the energy diffusion of the material exceeds the momentum diffusion
rate and the converse is true for 𝑃𝑟 ≫ 1 where the momentum diffusion rate is
dominant. From the above tables, it is apparent that for the liquid refrigerants energy
diffusion rate is key staying well above 1. Whereas for the vapor refrigerants the trend is
to rely on a greater momentum diffusion rate, although there are fluctuations in the vapor
Prandtl numbers resulting in a more unstable understanding of the fluid nature due to the
values of all vapor refrigerants hovering at 1. Transferring this data into percent change
graphs, referenced below as Figures 19 and 20, it becomes apparent how large the data is
varied.
41
Liquid Prandtl Number Percent Change With Respect to
2013, 40F
10.00
5.00
0.00
Percent Change %
-10.00
-15.00
-20.00
-25.00
Year
20.00
15.00
Percent Change %
10.00
5.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.00
-10.00
-15.00
Years
very large changes in data with the greatest occurring with R-152a as it differs from
present day values by nearly 20 percent. This also reveals the aforementioned
discrepancies in Figure 20 between 1989 and 1993 with a 20 percent increase in the
calculated Prandtl number between these two editions. All other refrigerants show
concerns with R-600a and R-22 nearing a 10 percent offset in some years, although
much less severe than R-152a. Stabilization of values occurs at the 2005 edition and is
similar to the 100 degree Fahrenheit values. Even though constant values are obtained
around 2005, the variance in earlier years for the higher temperature are even more
20.00
15.00
Percent Change %
10.00
5.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
-10.00
Year
43
Liquid Prandtl Number Previous Percent Change, 100F
10.00
5.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
Percent Change %
-5.00
-10.00
-15.00
-20.00
-25.00
-30.00
-35.00
Years
The most striking instance in these figures occurs with R-22 from 1981-1993 and
present day and negative 30 percent change, respectively. R-152a is much less
represented at the higher temperature although, as stated earlier, the leveling off effect
smaller percent change than liquid. The change is more sensitive for vapor with values
all at approximately one, which allows a slim margin for error on either side.
44
Vapor Prandtl Number Percent Change From 2013, 100F
14.00
12.00
10.00
Percent Change %
8.00
6.00
4.00
2.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
Year
2.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
Percent Change %
-2.00
-4.00
-6.00
-8.00
-10.00
-12.00
-14.00
Years
between the editions with regard to the temperatures of 40 or 100 degrees Fahrenheit.
The former can be viewed in the appendixes. Looking at the above graphs, it is apparent
that R-22 shows the greatest deviation from the norm at nearly 12 percent with isobutene
showing a plus 4 to plus 6 percent change before settling at current values. Editions of
the most interest are the 1997 to 2001 as there is a negative 12 percent change between
Prandtl number calculations using ASHRAE handbook data show some of the
greatest discrepancies out of the selected calculations due to the base equation being a
conductivity and specific heat. In addition to this, the equation is linear which does not
place more emphasis on any certain variable as all 3 properties contribute equally to the
percent change. Nevertheless, when referencing the physical property percent change
tables, the property most affecting Prandtl number in this scenario is dynamic viscosity
due to the high percent changes recorded. The importance of the Prandtl number is seen
The Nusselt number is another dimensionless number that is used in several heat
heat transfer [14]. For forced turbulent flow, Nusselt number is a function of the
Reynolds number and the Prandtl number or, 𝑁𝑢 = 𝑓(𝑅𝑒, 𝑃𝑟). For an internal turbulent
46
flow with a cooling load, we find the Nusselt number via the Dittus-Boelter equation as
seen below.
Examining Equation 11, the dominating number in terms of percent change is the
Reynolds number as opposed to the Prandtl number due to them being raised to the 4/5th
and 1/3rd power, respectively. Similar to section 5.1, Nusselt number is obtained for both
mass fluxes although this will have no effect on the percent change due to the scaling
for hydrodynamically and thermally fully developed turbulent flow in a smooth circular
pipe [14]. These restrictions are experimentally confirmed in the range of conditions
0.6 ≤ 𝑃𝑟 ≤ 16,700
𝑅𝑒𝐷 ≥ 10,000
[ ]
𝐿
≥ 10
𝐷
As is evident from the Reynolds and Prandtl number tables all eligible values fall
within these parameters indicating that Equation 11 is valid for this scenario. The
calculated liquid Nusselt number and vapor Nusselt number, or 𝑁𝑢𝐷,𝐿 and 𝑁𝑢𝐷,𝑉
respectively, can be seen in the Table 16 and Table 17 below for a mass flux of 100𝑙𝑏𝑚/
𝑓𝑡 2 𝑠.
47
Table 16: Liquid Nusselt Number, G = 100 lbm/ft2s, D = 8.52mm
NuD,L at G = 100
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 83.089 82.597 82.597 89.001 89.001 87.806 87.806 87.806 87.806
R-152a 88.248 88.248 88.248 96.267 94.035 95.661 94.820 94.820 94.820
40 ◦F
R-600a 105.808 105.808 105.808 105.808 110.491 110.491 113.560 113.164 113.164
R-134a 81.398 81.398 84.167 84.167 84.167 84.167
R-410a 102.235 101.440 101.440 101.440
R-22 100.085 100.085 100.085 115.064 115.064 115.197 115.197 115.197 115.197
R-152a 114.105 114.105 114.105 121.198 121.198 122.420 123.000 123.000 123.000
100 ◦F
R-600a 131.467 131.467 131.467 131.467 141.633 141.633 145.062 143.863 143.863
R-134a 107.576 107.576 112.044 112.044 112.044 112.044
R-410a 143.992 144.644 144.644 144.644
R-600a 876.998 876.998 876.998 876.998 890.074 890.074 885.737 883.178 883.178
R-134a 0.000 618.729 618.729 633.448 633.448 633.448 633.448
R-410a 632.631 635.171 635.171 635.171
R-600a 684.329 684.329 684.329 684.329 707.559 707.559 684.439 671.728 671.728
R-134a 529.738 529.738 543.661 543.661 543.661 543.661
R-410a 766.557 786.499 786.499 786.499
The above tables reveal an increase in Nusselt number for every liquid
refrigerant from the earliest ASHRAE handbook to the most recent, with the exception
of R-410a where the change is minor. Vapor has a more sporadic trend with some
higher temperatures such as can be seen for isobutane. As discussed earlier, the tables
are transferred into line plots representing the change in Nusselt number as can be seen
48
NuD,L Percent Change with Respect to 2013, 100F
2.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
Percent Change %
-4.00
-6.00
-8.00
-10.00
-12.00
-14.00
Year
Figure 25: Liquid Nusselt Number Percent Change with Respect to 2013, 100F
12.00
10.00
Percent Change %
8.00
6.00
4.00
2.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2.00
Years
Figure 26: Liquid Nusselt Number Percent Change Previous Edition, 100F
49
All refrigerants as stated earlier show an upward trend. This was initially
documented as much as 13 percent different from 2013. With R-152a and R-600a
lingering around negative 8 percent, the largest jumps occurred from 1989 to 1997 for
those three refrigerants. The upward movement is reassuring as it shows uniformity for
all the refrigerant trends allowing comparison to 2013 as a baseline value. The graphs for
forty degrees Fahrenheit show the same upward inclination and can be accessed in the
appendix. When analyzing the resultant graphs for the vapor Nusselt number, there
appears to be a slight disconnect with the refrigerants and consistency plus or minus
from 2013.
10.00
8.00
Percent Change %
6.00
4.00
2.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
-4.00
Year
50
NuD,V Percent Change with Respect to Previous Edition,
100F
4.00
2.00
0.00
Percent Change %
-4.00
-6.00
-8.00
-10.00
-12.00
Year Range
Similar to liquid Nusselt Number, Figure 27 and Figure 28 reveal R-22 having
the largest deviance from the most recent handbook edition at 10 percent; although after
the absence of data from 1993-1997 the values line up with 2013. Remarkably, R-600a
reveals a near constant value of 2 percent above the latest edition extending until 2005.
As a consequence of the gap in R-22 data, it can be concluded that individuals used the
1989 data until new information was published in 2001 which is seen in Figure 27.This
could indicate as much as a negative 10 percent error in Nusselt number values from just
this one instance. It should be noted that the values obtained are for the local Nusselt
number and the local heat transfer coefficient can be easily obtained.
51
5.4 Heat Transfer Coefficient
The heat transfer coefficient can be defined as either being local or average
across the system, in this evaluation the local coefficient will be calculated due to
simplicity as well as following the local Nusselt numbers obtained in section 5.3. This
variable is defined as a proportionality between heat flux and the temperature difference
𝑞̈ (12)
ℎ=
𝑇𝑠 − 𝑇∞
Where 𝑞̈ is heat flux, and Ts and T∞ are temperatures of the surface and bulk fluid
provided in the ASHRAE handbooks and the previously calculated Nusselt numbers as
ℎ𝐷 (13)
𝑁𝑢𝐷 =
𝑘
Where h is the local heat transfer coefficient, D is the pipe diameter, k is the
thermal conductivity and NuD is the local Nusselt number calculated in the previous
section. Rearranging this equation to solve for h obtains the working Equation 14.
𝑁𝑢𝐷 𝑘 (14)
ℎ=
𝐷
Using this equation, the change in heat transfer coefficient is a function of the
Nusselt number and the thermal conductivity, or ℎ = 𝑓(𝑁𝑢𝐷 , 𝑘). Since there are no
exponents in this expression, the percent change affected by ASHRAE provided physical
property data. This has a linear relationship and is influenced only by these two variables
52
and unaffected by pipe diameter. Applying the required variables to Equation 14 the
R-600a 249.827 249.827 249.827 249.827 239.538 239.538 227.503 226.710 226.710
R-134a 153.752 153.752 156.874 156.874 156.874 156.874
R-410a 238.463 236.245 236.245 236.245
R-22 168.642 168.642 168.642 191.823 191.823 185.450 185.450 185.450 185.450
R-152a 230.635 230.635 230.635 235.434 235.434 234.743 235.414 235.414 235.414
100 ◦F
R-600a 277.488 277.488 277.488 277.488 263.983 263.983 253.249 252.186 252.186
R-134a 168.948 168.948 175.164 175.164 175.164 175.164
R-410a 273.017 272.700 272.700 272.700
R-600a 260.406 260.406 260.406 260.406 261.105 261.105 269.972 268.876 268.876
R-134a 155.829 155.829 155.910 155.910 155.910 155.910
R-410a 167.025 167.014 167.014 167.014
R-600a 264.401 264.401 264.401 264.401 264.264 264.264 258.567 253.765 253.765
R-134a 168.665 168.665 170.765 170.765 170.765 170.765
R-410a 313.722 308.097 308.097 308.097
Because of the dual mass fluxes described, it was necessary to calculate the heat
transfer coefficient for both flow rates at liquid and vapor states. Although this was
necessary, the percent change for this variable was not affected by flow rate due to the
53
Nusselt number which is similar to how diameter does not affect the percent change as it
is constant for every entry. Because the thermal conductivity is given in 𝐵𝑡𝑢/ℎ𝑟 ∙ 𝑓𝑡 ∙ 𝐹,
the resulting heat transfer coefficient is maintained in a per hour format. Comparing
Table 18 and Table 19, it is most evident that the liquid values fluctuate considerably
10.00
8.00
Percent Change %
6.00
4.00
2.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
-4.00
Year
54
Liquid HT Coefficient Percent Change With Respect to
2013, 100F
15.00
10.00
Percent Change %
5.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
-10.00
-15.00
Year
From the above two graphs, Figure 29 and Figure 30, representing the liquid heat
transfer coefficient, there are several obvious areas of concern. At both temperatures, R-
600a maintains a positive ten percent difference from present-day values until 1997
where it is slightly corrected to five percent. In addition to this, although R-22 is of little
interest at 40 degrees Fahrenheit, at 100 degrees there is a minus ten percent error which
acceptable level of error until 1993 where the offset increases dramatically. These
variances can be viewed according to their effect on values between editions as seen in
55
Liquid HT Coefficient Percent Change With Respect to
Previous Edition, 40F
8.00
6.00
4.00
Percent Change %
2.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2.00
-4.00
-6.00
Years
6.00
4.00
2.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2.00
-4.00
-6.00
Years
between editions especially concerning R-152a for 40 degrees. While the heat transfer
coefficients obtained until 1989 were identical to present day values, beginning in 1993
until 2005 the values were egregiously wrong. The non-constant values for the heat
conducted using the given data, but because of the changes for some years the results
will be incorrect. This can be seen from the numerous corrections of R-600a and R-22
The results for vapor were less significant than the liquid with a much minor
deviation although isobutane still held as the refrigerant with the largest percent change
57
Vapor HT Coefficient Percent Change With Respect to
2013, 100F
5.00
4.00
3.00
Percent Change %
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
-2.00
Year
Figure 33 shows only minor issues for vapor refrigerants with the greatest being
approximately plus four percent difference for R-600. Because of this, issues resulting
from incorrect vapor heat transfer coefficients are minimal compared their liquid
counterpart. The remaining graphs and data tables can be viewed in the appendix
Fluid flow in a pipe encounters frictional losses along the length of pipe due to
several factors. Reynolds number and pipe roughness are key players in a formulation of
58
1 𝜀 2.51 (15)
= −2𝑙𝑜𝑔10 ( + )
√𝑓 3.7𝐷ℎ 𝑅𝑒√𝑓
Where f is the friction factor and ε is the roughness coefficient. Typically this
equation is solved via iteration, however due to the wide range of pipe roughnesses and
for simplicity in showing how the progression of published physical property data
directly affects design variables, only smooth pipe correlations will be used. However, if
the roughness for a pipe is known Equation 15 can be used to determine the friction
As an alternative to this, the Blasius friction correlations can be used. These are
for smooth pipe, turbulent flow and are valid for Reynolds numbers up to 100,000.
Observing that the cutoff Reynolds number is twenty thousand, Table 10 through
Table 14 must be referenced for calculation parameters. All values for vapor fall within
the range of Equation 17 as well as all the values for liquid at a mass flux of 300.
However, for a mass flux of 100 at the liquid state at 40 degrees, there are a select few
instances where the Reynolds number does fall in the range of Equation 16. Because the
difference of approximately 1,000 is small, it was decided that only Equation 17 will be
used for the data analysis. The resultant friction factors are shown in Table 20 and Table
59
Table 20: Liquid Friction Factor, G = 100 lbm/ft2s, D = 8.52mm
Liquid Friction Factor, G = 100
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 0.02587 0.02587 0.02587 0.02519 0.02519 0.02539 0.02539 0.02539 0.02539
R-152a 0.02539 0.02539 0.02539 0.02529 0.02529 0.02528 0.02539 0.02539 0.02539
40 ◦F
R-600a 0.02515 0.02515 0.02515 0.02515 0.02491 0.02491 0.02489 0.02490 0.02490
R-134a 0.02679 0.02679 0.02647 0.02647 0.02647 0.02647
R-410a 0.02400 0.02412 0.02412 0.02412
R-22 0.02482 0.02482 0.02482 0.02345 0.02345 0.02356 0.02356 0.02356 0.02356
R-152a 0.02395 0.02395 0.02395 0.02358 0.02358 0.02351 0.02347 0.02347 0.02347
100 ◦F
R-600a 0.02361 0.02361 0.02361 0.02361 0.02318 0.02318 0.02315 0.02319 0.02319
R-134a 0.02475 0.02475 0.02433 0.02433 0.02433 0.02433
R-410a 0.02197 0.02198 0.02198 0.02198
R-600a 0.01297 0.01297 0.01297 0.01297 0.01292 0.01292 0.01288 0.01288 0.01288
R-134a 0.01414 0.01414 0.01408 0.01408 0.01408 0.01408
R-410a 0.01446 0.01443 0.01443 0.01443
R-600a 0.01329 0.01329 0.01329 0.01329 0.01329 0.01329 0.01318 0.01318 0.01318
R-134a 0.01457 0.01457 0.01445 0.01445 0.01445 0.01445
R-410a 0.01499 0.01488 0.01488 0.01488
As stated earlier about the decision to use only Equation 17, the percent change
in all scenarios is not affected by flow rate. However, if a small enough mass flux
occurred and reduced the Reynolds number by enough, then both equations would have
different mass flux. Because of this, at the cutoff Reynolds number the correct formula
must be applied to ensure consistency. From the correlation, it is predictable that friction
60
factor does not show a great deal of change with respect to the various ASHRAE
editions.
5.00
4.00
Percent Change %
3.00
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
-2.00
Year
61
Liquid Friction Factor Percent Change With Respect to
Previous Edition,100F
3.00
2.00
1.00
0.00
Percent Change %
Figures 34 and 35 representing the liquid friction factor at 100 degrees, illustrates
the largest offset occurring for R-22 in the earliest editions, with the common percent
change for the other refrigerants lingering at approximately plus 2 percentage points
from the 2013 values. This occurs because of the heavy reliance on Reynolds number in
the equation as in the Blasius equation the friction factor is only a function of Reynolds
number, or 𝑓 = 𝑓(𝑅𝑒). Equation 17 reveals that the only variable of interest is taken to
the negative one fifth power and therefore, even though the liquid Reynolds number
revealed instances of nearly 25 percent difference from the most recent edition, the error
for the friction factor using this correlation is significantly reduced. Viewing the vapor
62
Vapor Friction Factor Percent Change With Respect to
2013, 40F
1.10
0.90
0.70
Percent Change %
0.50
0.30
0.10
-0.10 1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.30
-0.50
Year
0.20
0.10
Percent Change %
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.10
-0.20
-0.30
-0.40
-0.50
-0.60
Years
nearly insignificant with the exception being in extremely long pipes. The friction factor
is necessary to determine the pressure drop in a pipe and using the obtained values
allowing one to determine how far a fluid can travel before it becomes a stagnant flow as
well as allowing a designer to predict power required to overcome the drop in pressure.
This stems directly from the Darcy friction factor that that was calculated in the previous
section. As seen from White Fluid Mechanics [34], the head loss is represented as
𝑃1 𝑃2 ∆𝑃 (18)
ℎ𝑓 = (𝑧1 − 𝑧2 ) + ( − ) = ∆𝑧 +
𝜌𝑔 𝜌𝑔 𝜌𝑔
where x is the pipe elevation change, P is pressure, ρ is density, g is gravity and hf is the
𝐿 𝑉2 (19)
ℎ𝑓 = 𝑓
𝐷 2𝑔
Substituting Equation 19 into Equation 18 and solving for ΔΡ, while taking into
account that pipe length L can be defined as the difference between the two points along
𝑝𝑉 2 (20)
∆𝑃 = 𝑓 (𝑥 − 𝑥1 )
2𝐷 2
64
Equation 20 is referred to as the Darcy-Weisbach equation [15]. With regards to
finding the percent change in pressure drop for refrigerants listed in the ASHRAE
handbooks, the diameter and pipe length are noncontributing factors. Mass flux as
recalled from equation 8 is 𝐺 = 𝜌𝑉, substituting this into Equation 20 a working formula
is produced .
𝐺𝑉 (21)
∆𝑃 = 𝑓 ∙ ∆𝑥
2𝐷
the division of the mass flux by the liquid density and inverse of vapor specific volume
provided in the ASHRAE handbooks. In order to maintain a constant mass flux with
inconsistent densities, the flow velocity must be adjusted to compensate at each scenario
and because of this pressure drop is a function of the Darcy friction factor and density, or
∆𝑃 = 𝑓(𝑓, 𝐺 ⁄𝜌). Using this information, the following tables are obtained showing
pressure drop.
R-600a 0.0270 0.0270 0.0270 0.0270 0.0268 0.0268 0.0268 0.0268 0.0268
R-134a 0.0130 0.0130 0.0128 0.0128 0.0128 0.0128
R-410a 0.0129 0.0129 0.0129 0.0129
R-22 0.0134 0.0135 0.0135 0.0127 0.0127 0.0128 0.0128 0.0128 0.0128
R-152a 0.0171 0.0171 0.0171 0.0168 0.0168 0.0168 0.0168 0.0168 0.0168
100 ◦F
R-600a 0.0273 0.0273 0.0273 0.0273 0.0268 0.0268 0.0269 0.0268 0.0268
R-134a 0.0132 0.0132 0.0130 0.0130 0.0130 0.0130
R-410a 0.0137 0.0138 0.0138 0.0138
65
Table 23: Vapor Pressure Drop, G = 100 lbm/ft2s, D = 8.52mm, Δx = 1ft
Vapor ΔP, G = 100
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 0.3655 0.3644 0.3644 0.3634 0.3634 0.3622 0.3622 0.3622 0.3622
R-152a 0.8719 0.8681 0.8681 0.8681
40 ◦F
R-600a 1.6347 1.6304 1.6304 1.6304 1.6278 1.6279 1.6197 1.6176 1.6176
R-134a 0.5206 0.5206 0.5179 0.5179 0.5179 0.5179
R-410a 0.2544 0.2535 0.2535 0.2535
R-600a 0.6405 0.6368 0.6368 0.6368 0.6387 0.6386 0.6321 0.6321 0.6321
R-134a 0.1918 0.1918 0.1901 0.1901 0.1901 0.1901
R-410a 0.0964 0.0954 0.0954 0.0954
For Table 22 and 23, the same diameter as all previous calculations was used
although Δx was set to 1ft arbitrarily as actual pressure drop is not of interest, rather the
percent change of the refrigerants for identical internal flow conditions. Since the Darcy-
Weisbach equation relies on friction factor and density which does not fluctuate greatly,
66
Liquid ΔP Percent Change With Respect to 2013, 40F
2.50
2.00
1.50
Percent Change %
1.00
0.50
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.50
-1.00
Year
5.00
4.00
Percent Change %
3.00
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
-2.00
Year
67
Figure 38 and Figure 39 indicates some issues that arise with the pressure drop
for single phase flow with R-22 achieving the highest error values of approximately 5
deviation until 1997. This is minor unless the pipe length is very long or flow rate is very
high, in which case could cause readings to be incorrect and display a pressure drop
higher than what would show if properties from 2013 were used. The vapor pressure
drop shows even less of a change as the editions progressed as can be referenced from
0.70
0.50
0.30
0.10
-0.10 1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.30
-0.50
Year
68
Vapor ΔP Percent Change With Respect to 2013, 100F
1.60
1.40
1.20
1.00
Percent Change %
0.80
0.60
0.40
0.20
0.00
-0.20 1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.40
-0.60
Year
As is expected due to the reliance on friction factor and density, the pressure drop
percent change occurring at a vapor state is significantly less than that at a liquid state.
With the highest difference occurring for R-22, R-134a and R-600a at around one
percent until 2001, the effect could be considered negligible unless extremely long
lengths of pipe were used or a system had a very small margin for error. As stated in
section 4.5, due to the Dittus-Boyler equation, the resultant Darcy friction factor has a
very small percent change which was transferred to the pressure drop equation.
For the results provided in section 4 and the appendix, one should be cautious in
applying the results to a specific system. To begin with, the Reynolds number
69
correlations rely on a predetermined, constant internal diameter pipe size. As there are
many possible pipe sizes in refrigeration, heating and cooling, one must take care to
assure this is accurate. In addition to this, only two mass flux rates were examined to
highlight typical flow rates and reveal data trends; for excessively high or low mass flux
rates results will vary due to changes in Reynolds number and ultimately friction factor
as well. Moreover, although there will be fluctuations in data for external flow the data
obtained is only applicable for internal flow. With regards to friction factor, as stated in
section 4.5, there is no roughness coefficient accounted for and thus care must be taken
pipe, helical pipe correlations are not accounted. The results obtained are for the specific
parameters outlined as stated earlier, any alterations for systems not matching the
70
6. TWO PHASE FLOW CORRELATIONS
Two phase flow is approached differently than single phase in the above sections.
For both condensation and evaporation, only three of the five refrigerants were
examined, R-22, R-152a and isobutane. In addition to this, the flow rates were altered to
100 and 300 𝑘𝑔/(𝑚2 𝑠) in order to maintain compatibility with the correlations in the
following sections due to a minimum flow rate limit for the equations being above the
mass flux rates discussed in the previous sections. To complement this change the
diameter was maintained at 8.52mm and the tubes are assumed horizontal with no
change in elevation. Although there were changes in these values, the temperature range
remains the same as 40 and 100 degrees Fahrenheit corresponds well with a typical
condenser and evaporator. In order to maintain simplicity only three years were chosen
to compare, 1981, 2013 and for the third year the data was analyzed from the ASHRAE
handbooks and chosen based on which year contained the greatest number of
discrepancies for each respective refrigerant. In a select few cases where the data for a
physical property was unavailable, the previous year was used as it can be assumed this
6.2 Condensation
cycle. An integral part of this is the condenser which removes the superheated vapor
71
entering from the compressor and converts it to saturated liquid. The focus will be on the
Shah correlation for heat transfer during condensation in plain tubes. This correlation,
0.8
3.8𝑥 0.76 (1 − 𝑥)0.04 (22)
ℎ𝑇𝑃 = ℎ𝐿𝑇 [(1 − 𝑥) +
𝑃𝑟 0.38
From Equation 22, hTP is the two phase heat transfer coefficient, hLT is the heat
transfer coefficient assuming all flow is liquid, Pr is the reduced pressure and x is the
quality of the vapor. This is stated as accurate for the conditions of 𝑅𝑒𝐿𝑇 > 350, 𝑅𝑒𝐺𝑇 >
35,000 and 𝑉𝐺𝑇 > 3 𝑚/𝑠 where ReGT is the vapor Reynolds number and VGT is the
velocity assuming all flow is vapor however it has been noted that these are very
Equation 22 was applied to the three selected refrigerants with the selected year
of interest being 1993 for both R-22 and R-152a and 1997 for R-600a. The local heat
transfer coefficients were plotted from a quality of 0 to 1 for both mass flux rates yet it
should be noted that the selected data range only contains qualities from 0.2 to 0.8 due to
large discontinuities which occur prior and immediately following these limits. The
following three figures reveal the trends of R-22, R-152a and R-600 for condensation.
72
Figure 42: R-22 Condensation, D = 8.52mm
Upon analyzing Figures 42, 43 and 44, there are obvious striking differences
between the flow rates and the years for each instance. With regard to mass flux, the
trends do not stay constant revealing that at these two different flows will not have the
same percent change for each respective entry. It is expected that the each edition will
have discrepancies when compared to a different year but due to the disparities caused
by different mass fluxes, some refrigerants show concerning differences for the same
year.
It is seen that R-22 has a very close fit, with the higher mass flux for each edition
not altered greatly resulting in a predictable percent change distribution for each
74
R-22 Condensation Percent Change With Respect to 2013
1993, G = 100 1993, G = 300 1981, G = 100 1981, G = 300
5
-3.6
4.5
-3.8
1993 Percent Change %
3.5
-4.2
3
-4.4
-4.6 2.5
-4.8 2
-5 1.5
0.16
0.01
0.06
0.11
0.21
0.26
0.31
0.36
0.41
0.46
0.51
0.56
0.61
0.66
0.71
0.76
0.81
0.86
0.91
0.96
Quality
Between the years of 1981 and 1993 for the mass flux of 100, there is
approximately a 0.1 percent difference, however at the higher mass flux this increases to
approximately a 0.5 percent difference and instead of a near constant change through all
qualities, the change shows a slight upward curl at the lower qualities indicating an
75
R-152a Condensation Percent Change With Respect to
2013
1981, G = 100 1993, G = 100 1993, G = 300 1981, G=300
2.5 0
-5
-15
1.5
-20
1
-25
-30
0.5
-35
0 -40
0.06
0.81
0.01
0.11
0.16
0.21
0.26
0.31
0.36
0.41
0.46
0.51
0.56
0.61
0.66
0.71
0.76
0.86
0.91
0.96
Quality
Analyzing Figure 46, the percent change for both flow rates in 1993 line up with
approximately a 0.5 percent difference while remaining fairly constant through all
qualities. This changes when the year 1981 is referenced at the two mass flux rates
where the mass flux of 100 remains constant and close to the subsequent edition.
However, if the next flow rate is examined it is seen that there is a massive change,
revealing a negative non-linear trend as the quality increases while revealing a negative
similar occurrences to both R-22 and R-152a albeit with much higher percent changes.
76
R-600a Condensation Percent Change With Respect to
2013
1981, G = 100 1997, G = 100 1981, G = 300 1997, G = 300
60
50
40
30
Percent Change %
20
10
0
0.36
0.01
0.06
0.11
0.16
0.21
0.26
0.31
0.41
0.46
0.51
0.56
0.61
0.66
0.71
0.76
0.81
0.86
0.91
0.96
-10
-20
-30
-40
-50
Quality
Figure 47 highlights the changes that occur when flow rate is changed. While the
change in 1981 is steady and small between the flows, it is important to note that for 100
and 300 𝑘𝑔/(𝑚2 𝑠) thers is still a 10 and nearly 20 percent difference with respect to the
heat transfer coefficient for 2013 flows. The drastic deviations occur for the year of
1997. As opposed to 1981, the slower flow relates to a plus 50 percent difference and the
higher flow rate relates to a negative 40 percent difference with a downward trend
nearing negative 50 percent at a quality of 0.80. Such large differences are disquieting as
it shows that both years had heat transfer coefficients which differed significantly from
present day data. Additionally, the uncertainty created with the enormous contrast
between the flow rates is something that must be considered for future research and
77
certainly resulted in systems designed with this data to obtain unreasonably high or low
two phase heat transfer coefficients. The other major refrigeration and air conditioning
6.3 Evaporation
the saturated liquid from the condenser is passed into the expansion valve and flashed
into a vapor and liquid mix drastically decreasing the pressure and temperature, from
where it is input into the evaporator and is evaporated by absorbing the heat from the
refrigerated space. Air conditioners are essentially refrigerators cooling a larger space
The correlations for determination of the two phase heat transfer coefficient in
evaporators is presented by S.G Kandlikar in 1990 [27]. These are seen in equation 23
and 24 below:
ℎ𝑇𝑃 (23)
= 𝐶1 𝐶𝑜𝐶2 (25𝐹𝑟𝑙𝑜 )𝐶5 + 𝐶3 𝐵𝑜𝐶4 𝐹𝑓𝑙
ℎ𝑙
From Equation 23 hTP is the two phase heat transfer coefficient, Ffl is defined as
the fluid-dependent parameter, Flo is the Froude number with all liquid flow Bo is the
1 − 𝑥 0.8 𝜌𝑔 0.5
𝐶𝑜 = ( ) ( )
𝑥 𝜌𝑙
And hl defined as the single phase liquid heat transfer coefficient show in Equation 24
78
ℎ𝑙 = 0.023𝑅𝑒𝑙 0.8 𝑃𝑟𝑙 0.4 (𝑘𝑙 ⁄𝐷 ) (24)
And the constants C1-C5 provided in Table 24, however it should be noted that C5 is zero
for horizontal tubes with a liquid Froude number of less than 0.04.
C1 1.1360 0.6683
C2 -0.9 -0.2
C3 667.2 1058.0
C4 0.7 0.7
C5 0.3 0.3
Applying the above correlations to the same years for each refrigerant the
following figures are obtained revealing the two phase evaporative heat transfer
coefficient. Comparable to condensation, only vapor qualities from 0.2 to 0.8 were
79
Figure 48: R-22 Evaporation, D = 8.52mm
Examining Figures 48, 49 and 50, the most significant difference between the
two heat transfer coefficient for evaporation and condensation using these correlations is
that there appears to be no discrepancies between the two flow rates with regard to
percent change. The graphs exhibit uniform increases and decreases for each refrigerant
regardless of year or mass flux for the selected quality range. The invariable percent
change with respect to flow rate can be seen in the below figure.
81
R-22 Evaporation Percent Change With Respect to 2013
1993 1981
2.3 -1.76
2.25 -1.78
1993 Percent Change %
2.15 -1.82
2.1 -1.84
2.05 -1.86
2 -1.88
0.11
0.01
0.06
0.16
0.21
0.26
0.31
0.36
0.41
0.46
0.51
0.56
0.61
0.66
0.71
0.76
0.81
0.86
0.91
0.96
Quality
Figure 51, representing R-22, reveals a small shift from 1981 to 1993, changing
Additionally, it can be seen that both flow rates display identical changes with respect to
present data, enabling only a single curve to be plotted per year as opposed to
condensation. This trend continues for every instance during the examination of
evaporation. R-22 displayed the least change among the three refrigerants selected with
R-152a showing the second most change as seen in the below figure.
82
R-152a Evaporation Percent Change With Respect to
2013
1993 1981
7.24 -1.72
-1.74
7.22
-1.76
1993 Percent Change %
7.18 -1.8
-1.82
7.16
-1.84
7.14
-1.86
7.12 -1.88
0.01
0.06
0.11
0.16
0.21
0.26
0.31
0.36
0.41
0.46
0.51
0.56
0.61
0.66
0.71
0.76
0.81
0.86
0.91
0.96
Quality
percent under 2013 values for dual phase heat transfer coefficient. However, in 1993
there is a much more substantial result at 7 percent difference, slightly decreasing as the
quality nears one. This is the converse of 1981 values for both of the refrigerants
also contains the largest errors among the three selected fluids, similar to condensation.
83
R-600a Evaporation Percent Change With Respect to
2013
1981 1997
15 15
10 10
5 5
1981 Percent Change %
0.41
0.46
0.51
0.56
0.61
0.66
0.71
0.76
0.81
0.86
0.91
0.96
-5 -5
-10 -10
-15 -15
-20 -20
Quality
heat transfer coefficients obtained using the most recent data for isobutane. Like the
previous two refrigerants, mass flux does not affect the percent change, yet, unlike these
two fluids the change for both years is not localized to either the positive or negative
axis. Instead, in the year 1997 there is a crossing of the zero axis at a quality of
approximately 0.45. The error begins at nearly positive 15 percent, and then decreases to
approximately negative 20 percent from qualities of 0.2 to 0.8 respectively. This will
bring up the conclusion, at a specific quality the heat transfer coefficient is equal to
84
the2013 value. 1981 shows a similarity in this regard, nearing zero at higher qualities
85
7. CONCLUSIONS
After careful consideration of the physical properties for R-22, R-152a, R-134a,
R-410a and R-600a published by ASHRAE from 1981 to 2013, it is evident that there is
cause for concern at certain points. For most cases the greater the length of time the
refrigerant has been in the handbooks, the more stable and closer the data came to
present day values, however with the introduction of new refrigerants it was seen that
there is always a correction in the next edition which warrants that care be taken when
Additionally, as seen in the section containing two phase flow, there are large
discontinuities which arise, especially for isobutane. As a result of this, it is not unlikely
that research conducted using past data obtained incorrect results. This would be
86
REFERENCES
10. ASHRAE. (2014). A Brief History of the ASHRAE Handbook. Retrieved from
https://www.ashrae.org/resources--publications/a-brief-history-of-the-ashrae-
handbook
87
11. ASHRAE. (2014). The Merger of ASHVE/ASHAE and ASRE to become
ASHRAE. Retrieved from https://www.ashrae.org/about-ashrae/ashrae-and-
industry-history
12. ASHRAE. (n.d.). American Society of Heating and Ventilating Engineers. 1-15.
Retrieved October 14, 2014, from
https://www.ashrae.org/File%20Library/docLib/Public/20070222_historyofashra
e.pdf
14. Bergman, T. L., & Incropera, F. P. (2011). Fundamentals of heat and mass
transfer. Hoboken, NJ: Wiley.
15. Brown, G. (2000, June 22). The Darcy-Weisbach Equation. Retrieved from
http://biosystems.okstate.edu/darcy/DarcyWeisbach/Darcy-WeisbachEq.htm
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entrance Region of a Pipe [Digital image]. Retrieved October 13, 2014, from
http://commons.wikimedia.org/wiki/File:Development_of_fluid_flow_in_the_ent
rance_region_of_a_pipe.jpg
19. EPA. (2009, May 20). HFC-152a as an Alternative to HFC-134a in Mobile Air
Conditioners. Retrieved from http://www.epa.gov/cpd/mac/152a/
20. EPA. (2014, April 23). Ozone Layer Protection - Regulatory Programs | US EPA.
Retrieved from http://www.epa.gov/ozone/title6/phaseout/22phaseout.html
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Layer Protection | US EPA. Retrieved from
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88
23. Forster, P., V. Ramaswamy, P. Artaxo, T. Berntsen, R. Betts, D.W. Fahey, J.
Haywood, J. Lean, D.C. Lowe, G. Myhre, J. Nganga, R. Prinn, G. Raga, M.
Schulz and R. Van Dorland, 2007: Changes in Atmospheric Constituents and in
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25. Han, J. (2012). Analytical heat transfer. Boca Raton, FL: CRC Press.
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Montreal 1997, Beijing 1999. (2000). Nairobi, Kenya: Ozone Secretariat, United
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30. Muneer, T., Kubie, J., & Grassie, T. (2003). Forced convection. In Heat transfer:
A problem solving approach (pp. 209-211). New York: Taylor & Francis.
31. Shah, M. M. (2009). An Improved and Extended General Correlation for Heat
Transfer During Condensation in Plain Tubes. HVAC&R Research, 15(5), 889-
913. doi: 10.1080/10789669.2009.10390871
34. White, F. M. (2011). Fluid mechanics. New York, NY: McGraw Hill.
89
APPENDIX A
R-600a 0.5690 0.5690 0.5690 0.5690 0.5571 0.5571 0.5555 0.5514 0.5514
R-134a 0.3223 0.3223 0.3235 0.3235 0.3235 0.3235
R-410a 0.3663 0.3652 0.3690 0.3690 0.3690
R-22 0.3130 0.3130 0.3130 0.3162 0.3162 0.3166 0.3166 0.3166 0.3166
R-152a 0.4340 0.4340 0.4340 0.4485 0.4485 0.4471 0.4471 0.4471 0.4471
100 ◦F
R-600a 0.6270 0.6270 0.6270 0.6270 0.6080 0.6080 0.6065 0.6019 0.6019
R-134a 0.3555 0.3555 0.3551 0.3551 0.3551 0.3551
R-410a 0.4480 0.4471 0.4527 0.4527 0.4527
R-600a 0.3950 0.3950 0.3950 0.3950 0.3982 0.3982 0.3978 0.3939 0.3939
R-134a 0.2159 0.2159 0.2194 0.2194 0.2194 0.2194
R-410a 0.2509 0.2830 0.2813 0.2813 0.2813
R-22 0.2260 0.2260 0.2260 0.2356 0.2356 0.2327 0.2327 0.2327 0.2327
R-152a 0.2980 0.2980 0.2980 0.3590 0.3590 0.3251 0.3251 0.3251 0.3251
100 ◦F
R-600a 0.4640 0.4640 0.4640 0.4640 0.4602 0.4602 0.4610 0.4544 0.4544
R-134a 0.2633 0.2633 0.2690 0.2690 0.2690 0.2690
R-410a 0.3829 0.4257 0.4215 0.4215 0.4215
90
h(fg), (Btu/lb)
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 86.720 86.466 86.466 86.503 86.503 86.651 86.651 86.651 86.651
R-152a 129.750 129.813 129.813 129.845 129.845 130.149 130.149 130.149 130.149
40 ◦F
R-600a 149.700 151.170 151.170 151.170 151.159 151.161 150.874 150.612 150.612
R-134a 83.338 84.011 84.011 83.966 83.966 83.966 83.966
R-410a 93.042 92.662 92.826 92.826 92.826
R-22 72.838 72.577 72.577 72.543 72.543 72.774 72.774 72.774 72.774
R-152a 115.430 115.486 115.486 112.726 112.726 113.134 113.134 113.134 113.134
100 ◦F
R-600a 133.100 135.160 135.160 135.160 135.431 135.429 135.144 135.181 135.181
R-134a 70.658 71.223 71.223 71.134 71.134 71.134 71.134
R-410a 70.476 70.445 70.304 70.304 70.304
R-600a 35.930 35.922 35.922 35.922 35.920 35.920 35.910 35.920 35.920
R-134a 79.933 79.850 79.850 79.900 79.900 79.900 79.900
R-410a 71.966 71.978 71.910 71.910 71.910
R-22 71.236 71.061 71.061 71.050 71.050 71.060 71.060 71.060 71.060
R-152a 54.030 54.028 54.028 54.040 54.040 54.050 54.050 54.050 54.050
100 ◦F
R-600a 33.380 33.347 33.347 33.347 33.350 33.350 33.280 33.350 33.350
R-134a 72.219 72.160 72.160 72.170 72.170 72.170 72.170
R-410a 61.872 61.936 61.727 61.727 61.727
R-600a 3.26500 3.25640 3.25640 3.25640 3.26240 3.26270 3.25760 3.25350 3.25350
R-134a 0.94700 0.95340 0.95340 0.95280 0.95280 0.95280 0.95280
R-410a 0.45773 0.45554 0.45489 0.45489 0.45489
R-22 0.25703 0.25582 0.25582 0.25600 0.25600 0.25660 0.25660 0.25660 0.25660
R-152a 0.61090 0.61104 0.61104 0.60020 0.60020 0.60230 0.60230 0.60230 0.60230
100 ◦F
R-600a 1.24800 1.24090 1.24090 1.24090 1.24450 1.24430 1.24190 1.24190 1.24190
R-134a 0.33900 0.34110 0.34110 0.34070 0.34070 0.34070 0.34070
R-410a 0.16574 0.16657 0.16599 0.16599 0.16599
91
APPENDIX B
R-600a 3.55 3.55 3.55 3.55 1.78 1.78 0.00 0.00 0.00
R-134a 2.27 2.27 0.00 0.00 0.00 0.00
R-410a 1.00 0.00 0.00 0.00
R-600a 4.21 4.21 4.21 4.21 4.21 4.21 0.00 0.00 0.00
R-134a 3.99 3.99 0.00 0.00 0.00 0.00
R-410a 3.74 0.00 0.00 0.00
92
Liquid Thermal Conductivity Percent Change From 2013
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 3.54 5.40 5.40 1.49 1.49 0.00 0.00 0.00 0.00
R-152a 6.96 6.96 6.96 5.66 5.66 0.16 0.00 0.00 0.00
40 ◦F
R-600a 17.86 17.86 17.86 17.86 8.21 8.21 0.00 0.00 0.00
R-134a 1.34 1.34 0.00 0.00 0.00 0.00
R-410a 0.15 0.00 0.00 0.00
R-22 4.67 4.67 4.67 3.56 3.56 0.00 0.00 0.00 0.00
R-152a 5.61 5.61 5.61 1.50 1.50 0.19 0.00 0.00 0.00
100 ◦F
R-600a 20.41 20.41 20.41 20.41 6.33 6.33 -0.41 0.00 0.00
R-134a 0.46 0.46 0.00 0.00 0.00 0.00
R-410a 0.57 0.00 0.00 0.00
R-600a -2.47 -2.47 -2.47 -2.47 -3.64 -3.64 0.12 0.00 0.00
R-134a 2.33 2.33 0.00 0.00 0.00 0.00
R-410a 0.41 0.00 0.00 0.00
R-22 -7.73 -7.73 -7.73 -7.73 -7.73 0.00 0.00 0.00 0.00
R-152a 0.74 0.00 0.00 0.00
100 ◦F
R-600a 2.27 2.27 2.27 2.27 -1.14 -1.14 0.00 0.00 0.00
R-134a 1.37 1.37 0.00 0.00 0.00 0.00
R-410a 4.47 0.00 0.00 0.00
93
Vapor Thermal Conductivity Percent Change From Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 0.00 0.00 0.89 0.00 -0.53 0.00 0.00 0.00
R-152a -0.14 0.00 0.00
40 ◦F
94
Surface Tension Percent Change From Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 0.00 0.00 0.00
R-152a 0.00 -0.16 0.00 0.00 0.00
40 ◦F
R-600a 3.19 3.19 3.19 3.19 1.03 1.03 0.74 0.00 0.00
R-134a -0.37 -0.37 0.00 0.00 0.00 0.00
R-410a -0.73 -1.03 0.00 0.00 0.00
R-22 -1.14 -1.14 -1.14 -0.13 -0.13 0.00 0.00 0.00 0.00
R-152a -2.93 -2.93 -2.93 0.31 0.31 0.00 0.00 0.00 0.00
100 ◦F
R-600a 4.17 4.17 4.17 4.17 1.01 1.01 0.76 0.00 0.00
R-134a 0.11 0.11 0.00 0.00 0.00 0.00
R-410a -1.04 -1.24 0.00 0.00 0.00
95
Liquid Specific Heat Percent Change From Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 0.00 0.00 -0.04 0.00 -0.14 0.00 0.00 0.00
R-152a 0.00 0.00 25.04 -6.80 -0.49 0.00 0.00 0.00
40 ◦F
R-600a 0.28 0.28 0.28 0.28 1.09 1.09 0.99 0.00 0.00
R-134a -1.60 -1.60 0.00 0.00 0.00 0.00
R-410a -10.81 0.60 0.00 0.00 0.00
R-22 -2.88 -2.88 -2.88 1.25 1.25 0.00 0.00 0.00 0.00
R-152a -8.34 -8.34 -8.34 10.43 10.43 0.00 0.00 0.00 0.00
100 ◦F
R-600a 2.11 2.11 2.11 2.11 1.28 1.28 1.45 0.00 0.00
R-134a -2.12 -2.12 0.00 0.00 0.00 0.00
R-410a -9.16 1.00 0.00 0.00 0.00
96
Vapor Specific Heat Percent Change From Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 0.00 0.00 4.29 0.00 -0.66 0.00 0.00 0.00
R-152a 0.00 0.00 15.86 0.00 -8.08 0.00 0.00 0.00
40 ◦F
R-22 -0.59 -0.68 -0.68 0.09 0.09 0.00 0.00 0.00 0.00
R-152a -15.22 -15.97 -15.97 0.42 0.42 0.00 0.00 0.00 0.00
100 ◦F
R-22 -0.15 -0.42 -0.42 -0.17 -0.17 0.00 0.00 0.00 0.00
R-152a -3.76 -3.98 -3.98 -0.10 -0.10 0.00 0.00 0.00 0.00
100 ◦F
R-600a -0.61 0.37 0.37 0.37 0.36 0.36 0.17 0.00 0.00
R-134a -0.75 0.05 0.05 0.00 0.00 0.00 0.00
R-410a 0.23 -0.18 0.00 0.00 0.00
R-22 0.09 -0.27 -0.27 -0.32 -0.32 0.00 0.00 0.00 0.00
R-152a 2.03 2.08 2.08 -0.36 -0.36 0.00 0.00 0.00 0.00
100 ◦F
R-600a -1.54 -0.02 -0.02 -0.02 0.18 0.18 -0.03 0.00 0.00
R-134a -0.67 0.13 0.13 0.00 0.00 0.00 0.00
R-410a 0.24 0.20 0.00 0.00 0.00
98
h(fg) Percent Change From Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 -0.29 0.00 0.04 0.00 0.17 0.00 0.00 0.00
R-152a 0.05 0.00 0.02 0.00 0.23 0.00 0.00 0.00
40 ◦F
R-600a 0.03 0.01 0.01 0.01 0.00 0.00 -0.03 0.00 0.00
R-134a 0.04 -0.06 -0.06 0.00 0.00 0.00 0.00
R-410a 0.08 0.09 0.00 0.00 0.00
R-22 0.25 0.00 0.00 -0.01 -0.01 0.00 0.00 0.00 0.00
R-152a -0.04 -0.04 -0.04 -0.02 -0.02 0.00 0.00 0.00 0.00
100 ◦F
R-600a 0.09 -0.01 -0.01 -0.01 0.00 0.00 -0.21 0.00 0.00
R-134a 0.07 -0.01 -0.01 0.00 0.00 0.00 0.00
R-410a 0.24 0.34 0.00 0.00 0.00
99
Liquid Density Percent Change From Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 -0.26 0.00 0.03 0.00 -0.03 0.00 0.00 0.00
R-152a -0.01 0.00 0.04 0.00 0.02 0.00 0.00 0.00
40 ◦F
R-600a 0.35 0.09 0.09 0.09 0.27 0.28 0.13 0.00 0.00
R-134a -0.61 0.06 0.06 0.00 0.00 0.00 0.00
R-410a 0.62 0.14 0.00 0.00 0.00
R-22 0.17 -0.30 -0.30 -0.23 -0.23 0.00 0.00 0.00 0.00
R-152a 1.43 1.45 1.45 -0.35 -0.35 0.00 0.00 0.00 0.00
100 ◦F
R-600a 0.49 -0.08 -0.08 -0.08 0.21 0.19 0.00 0.00 0.00
R-134a -0.50 0.12 0.12 0.00 0.00 0.00 0.00
R-410a -0.15 0.35 0.00 0.00 0.00
100
Vapor Specific Volume Percent Change From Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 -0.28 0.00 0.06 0.00 0.17 0.00 0.00 0.00
R-152a 0.01 0.00 -0.75 0.00 0.25 0.00 0.00 0.00
40 ◦F
R-600a -4.79 -4.79 -4.79 -4.79 -0.22 -0.22 0.22 0.00 0.00
R-134a -5.78 -5.78 0.00 0.00 0.00 0.00
R-410a 2.55 0.00 0.00 0.00
R-22 -22.94 -22.94 -22.94 2.37 2.37 0.00 0.00 0.00 0.00
R-152a -9.57 -9.57 -9.57 -2.30 -2.30 -0.87 0.00 0.00 0.00
100 ◦F
R-600a -8.57 -8.57 -8.57 -8.57 0.31 0.31 0.95 0.00 0.00
R-134a -8.13 -8.13 0.00 0.00 0.00 0.00
R-410a 0.33 0.00 0.00 0.00
R-600a -3.43 -3.43 -3.43 -3.43 -1.74 -1.74 0.00 0.00 0.00
R-134a -2.22 -2.22 0.00 0.00 0.00 0.00
R-410a -0.99 0.00 0.00 0.00
R-600a -4.04 -4.04 -4.04 -4.04 -4.04 -4.04 0.00 0.00 0.00
R-134a -3.83 -3.83 0.00 0.00 0.00 0.00
R-410a -3.60 0.00 0.00 0.00
R-600a -8.04 -8.04 -8.04 -8.04 -6.43 -6.43 0.52 0.00 0.00
R-134a 4.33 4.33 0.00 0.00 0.00 0.00
R-410a -3.64 0.00 0.00 0.00
R-22 22.57 22.57 22.57 -5.79 -5.79 0.00 0.00 0.00 0.00
R-152a 1.65 1.65 1.65 1.16 1.16 0.69 0.00 0.00 0.00
100 ◦F
R-600a -5.38 -5.38 -5.38 -5.38 -5.29 -5.29 0.23 0.00 0.00
R-134a 8.47 8.47 0.00 0.00 0.00 0.00
R-410a -2.12 0.00 0.00 0.00
102
Vapor Prandtl Number Precent Change From 2013
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 0.98 0.98 0.98 2.60 2.60 0.00 0.00 0.00 0.00
R-152a 2.08 0.00 0.00 0.00
40 ◦F
R-600a 6.47 6.47 6.47 6.47 6.78 6.78 0.87 0.00 0.00
R-134a -1.65 -1.65 0.00 0.00 0.00 0.00
R-410a 1.20 0.00 0.00 0.00
R-600a 4.05 4.05 4.05 4.05 6.75 6.75 1.45 0.00 0.00
R-134a 0.41 0.41 0.00 0.00 0.00 0.00
R-410a 0.28 0.00 0.00 0.00
R-600a -6.50 -6.50 -6.50 -6.50 -2.36 -2.36 0.35 0.00 0.00
R-134a -3.29 -3.29 0.00 0.00 0.00 0.00
R-410a 0.78 0.00 0.00 0.00
R-22 -13.12 -13.12 -13.12 -0.12 -0.12 0.00 0.00 0.00 0.00
R-152a -7.23 -7.23 -7.23 -1.47 -1.47 -0.47 0.00 0.00 0.00
100 ◦F
R-600a -8.62 -8.62 -8.62 -8.62 -1.55 -1.55 0.83 0.00 0.00
R-134a -3.99 -3.99 0.00 0.00 0.00 0.00
R-410a -0.45 0.00 0.00 0.00
R-600a -0.70 -0.70 -0.70 -0.70 0.78 0.78 0.29 0.00 0.00
R-134a -2.32 -2.32 0.00 0.00 0.00 0.00
R-410a -0.40 0.00 0.00 0.00
R-600a 1.88 1.88 1.88 1.88 5.33 5.33 1.89 0.00 0.00
R-134a -2.56 -2.56 0.00 0.00 0.00 0.00
R-410a -2.54 0.00 0.00 0.00
104
Vapor Nusselt Number Percent Change With Respect to Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 0.00 0.00 1.88 0.00 1.09 0.00 0.00 0.00
R-152a 1.07 0.00 0.00
40 ◦F
R-600a 10.20 10.20 10.20 10.20 5.66 5.66 0.35 0.00 0.00
R-134a -1.99 -1.99 0.00 0.00 0.00 0.00
R-410a 0.94 0.00 0.00 0.00
R-22 -9.06 -9.06 -9.06 3.44 3.44 0.00 0.00 0.00 0.00
R-152a -2.03 -2.03 -2.03 0.01 0.01 -0.29 0.00 0.00 0.00
100 ◦F
R-600a 10.03 10.03 10.03 10.03 4.68 4.68 0.42 0.00 0.00
R-134a -3.55 -3.55 0.00 0.00 0.00 0.00
R-410a 0.12 0.00 0.00 0.00
R-600a -3.15 -3.15 -3.15 -3.15 -2.89 -2.89 0.41 0.00 0.00
R-134a -0.05 -0.05 0.00 0.00 0.00 0.00
R-410a 0.01 0.00 0.00 0.00
R-600a 4.19 4.19 4.19 4.19 4.14 4.14 1.89 0.00 0.00
R-134a -1.23 -1.23 0.00 0.00 0.00 0.00
R-410a 1.83 0.00 0.00 0.00
105
Liquid HT Coefficient Percent Change With Respect to Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 1.18 0.00 3.62 0.00 -2.87 0.00 0.00 0.00
R-152a 0.00 0.00 7.21 -2.37 -3.70 -1.05 0.00 0.00
40 ◦F
R-600a 0.99 0.99 0.99 0.99 0.04 0.04 -0.04 0.00 0.00
R-134a 1.20 1.20 0.00 0.00 0.00 0.00
R-410a -0.50 0.00 0.00 0.00
R-22 5.35 5.35 5.35 -0.47 -0.47 0.00 0.00 0.00 0.00
R-152a 2.03 2.03 2.03 0.47 0.47 0.18 0.00 0.00 0.00
100 ◦F
R-600a 1.81 1.81 1.81 1.81 -0.06 -0.06 -0.19 0.00 0.00
R-134a 1.71 1.71 0.00 0.00 0.00 0.00
R-410a -0.07 0.00 0.00 0.00
106
Vapor Friction Factor Percent Change With Respect to 2013
Refrigerant 1981 1985 1989 1993 1997 2001 2005 2009 2013
R-22 0.83 0.83 0.83 0.49 0.49 0.00 0.00 0.00 0.00
R-152a 0.44 0.00 0.00 0.00
40 ◦F
R-600a 0.70 0.70 0.70 0.70 0.35 0.35 0.00 0.00 0.00
R-134a 0.45 0.45 0.00 0.00 0.00 0.00
R-410a 0.20 0.00 0.00 0.00
R-600a 0.83 0.83 0.83 0.83 0.83 0.83 0.00 0.00 0.00
R-134a 0.78 0.78 0.00 0.00 0.00 0.00
R-410a 0.74 0.00 0.00 0.00
R-600a 0.959 0.981 0.981 0.981 0.044 0.044 -0.016 0.000 0.000
R-134a 1.260 1.260 0.000 0.000 0.000 0.000
R-410a -0.597 0.000 0.000 0.000
R-22 5.090 5.348 5.348 -0.453 -0.453 0.000 0.000 0.000 0.000
R-152a 2.071 2.075 2.075 0.485 0.485 0.176 0.000 0.000 0.000
100 ◦F
R-600a 1.717 1.818 1.818 1.818 -0.063 -0.063 0.022 0.000 0.000
R-134a 1.724 1.724 0.000 0.000 0.000 0.000
R-410a -0.402 0.000 0.000 0.000
R-600a 1.056 0.790 0.790 0.790 0.627 0.636 0.126 0.000 0.000
R-134a 0.514 0.514 0.000 0.000 0.000 0.000
R-410a 0.343 0.000 0.000 0.000
R-600a 1.324 0.747 0.747 0.747 1.039 1.023 0.000 0.000 0.000
R-134a 0.903 0.903 0.000 0.000 0.000 0.000
R-410a 1.088 0.000 0.000 0.000
108
Vapor ΔP Percent Change With Respect to Previous Edition
Refrigerant 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
R-22 -0.28 0.00 -0.28 0.00 -0.32 0.00 0.00 0.00
R-152a -0.44 0.00 0.00
40 ◦F
109
APPENDIX C
0.0
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.0
Percent Change %
-10.0
-15.0
-20.0
-25.0
-30.0
Years
110
Percent Change Previous Edition, Vapor Viscocity, 40
Degrees F
1.00
0.50
0.00
Percent Change %
-1.00
-1.50
-2.00
-2.50
-3.00
Years
2.00
1.00
Percent Change %
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1.00
-2.00
-3.00
-4.00
-5.00
Years
111
Percent Change Previous Edition, Liquid Thermal
Conductivity, 40 Degrees F
4.00
2.00
0.00
Percent Change %
-4.00
-6.00
-8.00
-10.00
Years
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2.00
Percent Change %
-4.00
-6.00
-8.00
-10.00
-12.00
-14.00
Years
112
Percent Change Previous Edition, Vapor Thermal
Conductivity, 40 Degrees F
5.00
4.00
3.00
Percent Change %
2.00
1.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1.00
-2.00
-3.00
Years
8.00
6.00
Percent Change %
4.00
2.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2.00
-4.00
-6.00
Years
113
Percent Change From 2013, Surface Tension, 40 Degrees F
2
0
1981 1985 1989 1993 1997 2001 2005 2009 2013
Percent Change %
-1
-2
-3
-4
-5
-6
Year
0
Percent Change %
-4
-6
-8
-10
Year
114
Percent Change Previous Edition, Surface Tension, 40
Degrees F
6
4
Percent Change %
0
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1
-2
Years
6
Percent Change %
0
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2
-4
Years
115
Percent Change From 2013, Liquid Specific Heat, 40
Degrees F
10.00
5.00
Percent Change %
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
-10.00
-15.00
Year
4.00
3.00
Percent Change %
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
-2.00
-3.00
-4.00
Year
116
Percent Change Previous Edition, Liquid Specific Heat, 40
Degrees F
30.00
25.00
20.00
Percent Change %
15.00
10.00
5.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.00
-10.00
Years
3.00
2.00
Percent Change %
1.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1.00
-2.00
-3.00
-4.00
Years
117
Percent Change From 2013, Vapor Specific Heat, 40
Degrees F
10.00
5.00
Percent Change %
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
-10.00
-15.00
Year
10.00
Percent Change %
5.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
-10.00
-15.00
Year
118
Percent Change Previous Edition, Vapor Specific Heat, 40
Degrees F
20.00
15.00
Percent Change %
10.00
5.00
0.00
85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.00
-10.00
Years
20.00
15.00
Percent Change %
10.00
5.00
0.00
85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.00
-10.00
-15.00
Years
119
Percent Change From 2013, Liquid Enthalpy, 100 Degrees F
2.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-2.00
-4.00
Percent Change %
-6.00
-8.00
-10.00
-12.00
-14.00
-16.00
-18.00
Year
30.00
25.00
Percent Change %
20.00
15.00
10.00
5.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.00
Years
120
Percent Change Previous Edition, Liquid Enthalpy, 100
Degrees F
25.00
20.00
Percent Change %
15.00
10.00
5.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.00
Years
-1.00
-1.50
-2.00
-2.50
-3.00
-3.50
-4.00
-4.50
Year
121
Percent Change Previous Edition, Vapor Enthalpy, 100
Degrees F
4.50
4.00
3.50
Percent Change %
3.00
2.50
2.00
1.50
1.00
0.50
0.00
-0.50 81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
Years
4.00
Percent Change %
3.00
2.00
1.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1.00
Years
122
Percent Change From 2013, Liquid Density, 40 Degrees F
0.30
0.25
0.20
Percent Change %
0.15
0.10
0.05
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.05
-0.10
Year
0.30
0.20
Percent Change %
0.10
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.10
-0.20
-0.30
Year
123
Percent Change Previous Edition, Liquid Density, 40
Degrees F
0.10
0.05
0.00
Percent Change %
-0.10
-0.15
-0.20
-0.25
-0.30
Years
0.20
0.10
Percent Change %
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.10
-0.20
-0.30
-0.40
Years
124
Percent Change From 2013, Vapor Specific Volume, 40
Degrees F
0.80
0.60
0.40
Percent Change %
0.20
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.20
-0.40
-0.60
-0.80
Year
1.50
Percent Change %
1.00
0.50
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.50
-1.00
Year
125
Percent Change Previous Edition, Vapor Specific Volume,
40 Degrees F
0.80
0.60
0.40
Percent Change %
0.20
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.20
-0.40
-0.60
-0.80
-1.00
Years
0.50
Percent Change %
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.50
-1.00
-1.50
-2.00
Years
126
Liquid Reynolds Number Percent Change From 2013, 100
Fahrenheit
5.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-5.00
Percent Change %
-10.00
-15.00
-20.00
-25.00
Year
25.00
20.00
Percent Change %
15.00
10.00
5.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-5.00
Years
127
Vapor Reynolds Number Percent Change From 2013, 100F
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
Percent Change %
-1.00
-2.00
-3.00
-4.00
-5.00
-6.00
Year
5.00
4.00
Percent Chage %
3.00
2.00
1.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1.00
-2.00
-3.00
Years
128
Vapor Prandtl Number Precent Change From 2013, 40F
8.00
7.00
6.00
5.00
Percent Change %
4.00
3.00
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
-2.00
-3.00
Year
2.00
1.00
0.00
Percent Change %
-3.00
-4.00
-5.00
-6.00
-7.00
Years
129
NuD,L Percent Change with Respect to 2013, 40F
2.00
1.00
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-1.00
Percent Change %
-2.00
-3.00
-4.00
-5.00
-6.00
-7.00
-8.00
Year
0.50
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
Percent Change %
-0.50
-1.00
-1.50
-2.00
-2.50
-3.00
-3.50
Year
130
NuD,L Percent Change with Respect to Previous Edition, 40F
10.00
8.00
6.00
Percent Change %
4.00
2.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-2.00
-4.00
Years
2.00
1.50
Percent Change %
1.00
0.50
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.50
-1.00
Years
131
Vapor HT Coefficient Percent Change With Respect to
2013, 40F
1.00
0.50
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
Percent Change %
-0.50
-1.00
-1.50
-2.00
-2.50
-3.00
-3.50
Year
3.00
Percent Change %
2.00
1.00
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1.00
-2.00
Years
132
Vapor HT Coefficient Percent Change With Respect to
Previous Edition, 100F
1.50
1.00
0.50
Percent Change %
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.50
-1.00
-1.50
-2.00
-2.50
Years
2.00
1.50
Percent Change %
1.00
0.50
0.00
1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.50
-1.00
Year
133
Liquid Friction Factor Percent Change With Respect to
Previous Edition, 40F
1.00
0.50
0.00
Percent Change %
-1.00
-1.50
-2.00
-2.50
-3.00
Years
1.10
0.90
Percent Change %
0.70
0.50
0.30
0.10
-0.10 1981 1985 1989 1993 1997 2001 2005 2009 2013
-0.30
-0.50
Year
134
Vapor Friction Factor Percent Change With Respect to
Previous Edition, 100F
0.60
0.40
0.20
0.00
Percent Change %
0.50
0.00
Percent Change %
-1.00
-1.50
-2.00
-2.50
-3.00
Years
135
Vapor Friction Factor Percent Change With Respect to
Previous Edition, 40F
0.10
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.10
Percent Change %
-0.20
-0.30
-0.40
-0.50
-0.60
Years
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-1.00
Percent Change %
-2.00
-3.00
-4.00
-5.00
-6.00
-7.00
Years
136
Vapor Friction Factor Percent Change With Respect to
Previous Edition, 100F
1.00
0.50
Percent Change %
0.00
81-'85 85-'89 89-'93 93-'97 97-'01 01-'05 05-'09 09-'13
-0.50
-1.00
-1.50
Years
137