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Using Archimedes Principle
Using Archimedes Principle
To cite this article: R. P. Taylor, S. T. McClain & J. T. Berry (1999) Uncertainty analysis of metal-
casting porosity measurements using Archimedes' principle, International Journal of Cast Metals
Research, 11:4, 247-257, DOI: 10.1080/13640461.1999.11819281
Article views: 24
Download by: [The UC San Diego Library] Date: 30 May 2017, At: 00:18
Uncertainty analysis of metal-casting porosity
measurements using Archimedes' principle
l
i=l
(2) - X 8R
Bx-.....!._ (5)
' - R ax.l
Comparing Equations (1) and (2) shows the addition
of a correction factor in terms of the cup diameter, De, The bias in the result is computed in a similar manner
the basket wire diameter, Db, and the number of wires, except correlations between biases must be accounted
N, suspending the basket. for:
To show the importance of the correction factor,
consider the example based on typical data from
our laboratory. A porosity-free cast-aluminum alloy
sample with a theoretical density, Pth = 2.685 gjml,
yields Ws = 15.8078 g, and Wsb- Wb = 9.9228 g using
water with PL = 0.9985 gjml. Substituting into where bx,xk is the covariance and 8ik is the Kronecker
Equation (1) delta:
8· - { 1 i= k (7)
P = 100 [1.o _ (o.oo75) zk- 0 i =/= k
app 2.685
The 95% level of confidence uncertainty is then given
X ( 15.8078 )] _ O 1l as:
15.8078- 9.9228 - .
Neglecting the added buoyancy results in an apparent
porosity of 0.11% for this porosity-free example.
Substituting into Equation (2) with, N = 2, De =
6.426cm, and Db= 0.1524cm gives Papp = -0.004%, where t95 is the appropriate multiplier based on the
which is much closer to the actual value of 0%. student-t distribution. As pointed out by Coleman and
Therefore, for porosities of the order of 1%, a signifi- Steele, Equation (8) can be approximated in most
cant error will result if the added buoyancy is engineering applications by taking t 95 = 2, which
neglected. For all cases in this paper, Equation (2) gives:
will be used.
Uncertainty analysis
The detailed uncertainty-analysis model is based on where PR and BR are the 95% level of confidence
that of Coleman and Steele. 7 The experimental result estimates of precision and bias limit.
+ 2BwsbBwb ( ~:) c:::) tivity coefficient mean that uncertainties in the weight
measurements are magnified, perhaps by several
orders of magnitude, when porosity is computed.
+2BwsBwb(~J (~:) When porosity of the order of 1% needs to be deter-
mined, great care must be taken in the weight measure-
ments. These sensitivities are greatly reduced at higher
+ 20neeDb ( i:e) (£:) (11) values of porosity.
Increasing the relative density of the liquid strongly
Here the only correlated bias uncertainties are those decreases the sensitivity coefficients. Using a liquid that
between the three weights and the one between the cup has a specific gravity of 1.5 (ethyl phthalate as reported
and basket wire diameters. Correlation of the uncer- by Villar) increases PL! Pth to 0.55. 3 This results in
tainties occur when the uncertainties in two measure- ~ensitivity coefficients of iiw, ~ 150, iiw,b ~ 200, and
ments arise in whole or in part from the same elemental Bwb ~ 40, which is a reduction by a factor of 2. _
sources. Here the same mass balance was used for the Fig. 6 shows a plot of the absolute value of ePth
weights, hence, the bias uncertainty in each weight is versus P. For porosity less than 1%, the sensitivity
the bias uncertainty in the mass balance, and all increases rapidly. For a porosity of 0.1 %, the magni-
uncertainties in the weights are perfectly correlated. tude is 1000. The sensitivity coefficient for PL has
The same is true for the diameters, since they were identical magnitude. Therefore, for porosities of the
measured with the same set of calipers. A more order 1% or less, the values for PL and Pth must be
detailed discussion of correlated biases can be found known with very good accuracy. Fig. 7 shows the
in Brown et al. 8 absolute value of iin, versus P. The curve has a similar
Inspecting Equations (10) and (11) shows that not shape to the one in Fig. 6, but the magnitude is much
only do the levels of the uncertainties in each measure- less. The sensitivity coefficient for Db has an identical
ment matter, but the amount that this is magnified by magnitude. For P greater than 0.2%, the sensitivity is
the sensitivity coefficients is also very important. If the less than 1. Uncertainties in the diameters are expected
300
flws
200
100
0
0.2 0.4 0.6 0.8 1.0
PJPth
Fig. 3 Sensitivity coefficients with respect to W8
to have negligible influence on the uncertainty in water. The weight of the sample and basket in water
porosity when compared with the influence of the was recorded. The sample was removed from the
other measurements. basket, and the basket was replaced in the balance
and weighed in water. The temperature of the water
was then recorded. The density of the water was
Numerical example determined from the table in ASTM B311-93. Equa-
A numerical example of porosity measurement uncer- tion (2) was then used to calculate the percentage
tainty is presented for four samples of cast-aluminum porosity of the sample. The procedure was repeated
alloy 356 ranging in size from 3 to 15 g. The equipment for all of the samples.
used for the measurements was a Mettler H748AR The bias and random uncertainty of each measure-
mechanical balance, digital calipers, a 200ml beaker, a ment was determined in a variety of ways. A common
basket made from insulated copper wire, and a small way of determining the random uncertainty of a
Archimedean bench made of balsa wood. Water was measurement is to determine the standard deviation
used as the reference fluid. of a number of measurements. The precision limit, the
The particular procedure used was very similar to 95% level of confidence estimate of precision, is then
the procedure presented in ASTM B311-93. Distilled the product ofthe student-t value based on the sample
water was obtained and about 0.5 g of detergent was size and the standard deviation of the measurement. If
added per gallon of water. Both the water and samples a large sample size is assumed, the precision limit is
were allowed to reach the ambient temperature in the simply twice the standard deviation limit of the mea-
laboratory. The sample was then weighed in air. The surements. The bias limit, the 95% level of confidence
Archimedean bench and the beaker were placed in the estimate of bias, is an estimate of the fixed or systematic
balance, and the sample and basket were hung from error of the measuring device. In some cases, the bias
the balance so that the sample was submerged in the limit is estimated based on the available information
400
300
~sb i
. I
200 ·'-; r-- -- --- --- ---
~--
·l.
100
80
..... 60
~
20
PJPth
Fig. 5 Sensitivity coefficients with respect to Wb
1000
I
I
800 -1-·---··--·-
I
600
o;th
400
0 2 3 4 5
p
I
I
2.0 ---t
I
I
_ _l __ _
I I
I I
I I
1.0 --1 --- -- r- --
1 I
I I
0.5 ---+ -- - - + -- f-- ---
1 I I
I I I
0.0 L--~_:===+=====+=======i==~
0 2 3 4 5
p
and best engineering judgement. Guidance on estimat- times each. The standard deviations of both the mea-
ing bias limits can be found in Coleman and Steele. 9 surements were 0.0001 g. Since the standard deviations
The precision limit of the measurement of the of the measurements were the same, the standard
sample weights in air was determined by measuring deviations of the all of the dry weight measurements
the weights of a 5 g sample and a 15 g sample fifteen were taken to be 0.0001 g. By measuring calibrated
Table 1 Summary of the component diameter and precision limits were determined to be
uncertainties 0.150 cm and 0.004 cm for the wire basket and
6.433cm and 0.106cm for the beaker. The biases of
Measurement Bias Limit. B Precision Limit. P
the diameter measurements were estimated to be the
resolution of the calipers, 0.001 cm.
Ws 0.0002 g 0.0001 g The final component uncertainties to be estimated
Wsb 0.0002 g 0.0070 g are the uncertainties of the theoretical density of the
wb 0.0002 g 0.0048 g alloy. Unfortunately, this is the most difficult uncer-
Pw 0.0001 g/cm 3 0.0001 g/cm 3 tainty to estimate. Slight differences in alloy composi-
De 0.001 cm 0.106cm
0.001 cm 0.004cm
tion can change the theoretical density. Sigworth et al.
Dw
Pth 0.0006 g/cm 3 0.0015 g/cm 3 noted that Sr-modification of aluminum A356
increased the theoretical density from 2.6672 gfcm 3 to
2.6775 g/cm 3 . 10 The localised effects of macrosegrega-
tion of elements, especially those of atomic weights
standards and using best engineering judgement, the which are greater than those of the principle alloying
bias limit of all measurements made with the mechan- element (for example, copper or iron in aluminum
ical balance was estimated to be 0.0002 g. Because all alloys) have previously been cited 11 and are difficult
weight measurements were made with the same balance, to overcome unless knowledge of the element's con-
all weight measurement biases are correlated. centration profile is known. Higher iron contents in
There are many sources of random uncertainty in the similar alloys, such as aluminum alloy 356, can
wet measurements Wsb and Wb. During the measure- increase the theoretical density to over 2. 7 g/cm3 . 12
ments in water, bubbles can attach to the sample or the The theoretical density and the bias and precision
basket, water can seep into any surface pits on the uncertainty limits of the samples used here, Sr-modified
sample, small variations in water level can be caused and grain refined aluminum alloy 356, were determined
by losing water that adheres to the sample or basket, for the sample created from the same melt with the
or convective currents may cause variations in the highest measured density. The porosity was measured
measured weight of the sample. The standard devia- using metallography and image analysis, and the the-
tion of the weights of the sample and basket in water oretical density of the sample was determined from:
and the standard deviation of the weight of the basket
in water were determined by repeating the measure- lOOps
Pth =lOO_ p (12)
ments thirty-one times for an 18 g bar of wrought
3
aluminum alloy 6061-T6. The standard deviation of The value for the density was 2.7251 g/cm , with
3 3
Wsb was 0.0035 g. The standard deviation of Wb was Bprh = 0.0006gfcm and Pprh = 0.0015gfcm . Table I
0.0024 g. Thus, the precision limits of Wsb and Wb were presents a summary of the component uncertainties.
0.0070 g and 0.0048 g, respectively. The densities of four samples of cast-aluminum alloy
The density of the water was determined by measur- 356 were determined. The dry weights of the samples 1,
ing the temperature of the water and reading the 2, 3, and 4 were 3.0779 g, 7.2684 g, 11.6569 g, and
density of the water based on the table presented in 15.3101 g, respectively. Table 2 summarises the infor-
ASTM B311-93. The uncertainties associated with mation gathered for each of the samples. These values
density of the water are caused by the uncertainties along with the uncertainty estimates in Table 1 were
in the water temperature measurement. The thermo- substituted into Equations (10) and (11) to compute
meter used had a bias limit of 0.5 oc and a precision the precision and bias uncertainties. The overall uncer-
limit of 0.5 ac. From the table in ASTM B311-93, an tainty, Up, was determined using Equation (9). Table 3
error of0.5 ac correlates to an error of0.0001 g/cm 3 in presents the porosity of each sample and the uncer-
the water density. Hence, the bias limit and the preci- tainty of each of the measurements.
sion limit of the density of the water are 0.0001 g/cm 3 . Table 3 shows that the uncertainty in the porosity
The diameters of the wire basket and the diameter of measurement was unacceptable for the smaller samples.
the 200 ml beaker were determined with digital cali- The porosity of sample 1 was found to be 1.8143 ±
pers. Each diameter was measured fifteen times. The 0.7264 or 40% of the porosity measurement. The
Table 3 The sample porosities and uncertainties for a precision component uncertainty, and
c2 = R2e .e Bx;BxJ (16)
Sample Porosity% Bp Pp Up Xz X} XX
I J
Sample 1 1.82 0.026 0.73 0.73 for a correlated bias term between the component
Sample 2 1.64 0.024 0.31 0.31 biases of X; and J0. By the definition of the NPC,
Sample 3 1.58 0.024 0.19 0.19 the sum of the NPCs for all component uncertainties
Sample 4 1.43 0.024 0.15 0.15 must equal unity. Table 4 presents the NPCs for all
component uncertainties of the four porosity measure-
ments. The NPCs are listed in decreasing order of
uncertainty of the porosity measurement of sample 2 contribution.
was better, but it was still unacceptable at 0.3114. The Table 4 reveals that the precision errors in the
porosity measurements of samples 3 and 4 were accept- measurements of Wsb and Wb dominate the total
able in that their uncertainties are about 10% of the uncertainty of a porosity measurement. Pwsb and
porosity measurements. Table 3 also shows the domi- Pwb contribute more than 99% of the total uncertainty
nance of precision errors in the uncertainty of the in porosity of sample 1 to 91 % of the total uncertainty
porosity measurements. The precision components in the porosity of sample 4. The only other measure-
were all at least seven times the bias uncertainties. ments which contribute more than 0.1% to the total
While Table 3 shows that the total uncertainty of uncertainty in any one porosity measurement are the
each porosity measurement is dominated by precision bias and precision of the theoretical density of the
errors, a normalized criterion will reveal which com- alloy, the bias and precision of the density ofthe water,
ponent uncertainty causes the most uncertainty in the and the precision of the diameter of the basket wire.
resulting porosity measurement. A common normal- The maximum contributions of Pp 1h, Bp 1h, PPL' BpL,
ized criterion is the normalized percentage contribu- and PDb are 5.5%, 2.0%, 0.41 %, 0.41 %, and 0.14%,
tion (NPC), presented in Equation (13) in terms of respectively, in the porosity measurement of sample 4.
Equations (4) and (6). Table 4 also demonstrates that when one weight
2
NPC = £_ (13) measurement is subtracted from another, such as
u~ ( Wb- Wsb) in Equation (2), the correlated bias term
where: Bwsb, Wb cancels the contributions of both of the bias
1.0 .------,-1---~~--~~---
1 I I
0.8 1-----+----+------+----
~
0 I I I
c:
1-----L ___ j__________L___ _
~<D 0.6
0
c:
0
I I I
:::J o I I I
0.4 1------0-9---T---~----
~
t
o 0
Fig. 8 Effect of using the mean of J measurements of Wb and Wsb on the total uncertainty in porosity
correlated, neither of the biases contributes any uncer- water (u = 0.073 N/m). 14 The lower surface tension
tainty to the reduced data. should reduce the random uncertainty of Wsb and
The domination of precision in the uncertainty of a W6 due to bubble formation. Bubble formation is a
porosity measurement leads to an effective method of source of random uncertainty in any weight measure-
reducing the total uncertainty of a porosity measure- ments in water. By using a denser fluid with a lower
ment. If the average of several measurements is found surface tension, bubble formation should be greatly
and used to compute the porosity, the uncertainty is reduced.
reduced from the uncertainty with one measurement.
If Wsb and W 6 are each measured J times and the mean
of each value is used in Equation (2), the appropriate
precision limits areY Conclusions
The example demonstrated that the main source of
and P-wb
Pw uncertainty in the porosity measurement is the preci-
=--b
/] (17)
sion of Wsb and Wb. The precision in Wsb and W 6
Fig. 8 shows the effect of the number of measurements contributed over 90% of the uncertainty in the poros-
of Wsb and W 6 on the total uncertainty of sample 1. ity measurements of samples of 15 g or less. In samples
Averaging four readings of Wsb and W 6 decreases the less than 10 g, the precision in W.,6 and W6 caused
uncertainty by about one half. Using more than 10 the uncertainty in the porosity measurement to be
readings adds little to the fidelity of the porosity unacceptable. By making repeated measurements of
determination. Table 5 shows the recomputed uncer- Wsb and Wb, the precision limits were reduced, and the
tainties when three measurements of Wsb and W 6 are uncertainty of a porosity measurement was signifi-
used. The reduction in uncertainty of samples 1 and 2 cantly lowered.
is seen to be significant. The uncertainty analysis model revealed that the
Fluids denser than water that are used to lower the fluid used in the porosity determination greatly affects
normalized sensitivity coefficients may produce an extra the normalized sensitivity coefficients of W., W56 , and
benefit. Tetrachloroethylene (s.g. = 1.6, u = 0.032 Njm) Wb. While water is normally used for porosity deter-
may also lower the uncertainty of a porosity measure- mination, choosing a fluid such as ethyl phthalate
ment because its surface tension is about half that of (s.g. = 1.5) or tetrachloroethylene (s.g. = 1.6) can
reduce the sensitivity coefficients of w., w.b, and wb
by a factor of 2 for aluminum alloys. A reduction in the
Table 5 The sample porosities and uncertainties normalized sensitivity coefficients will reduce the
with the average of three weighings in uncertainty in the porosity measurement.
water Thin section castings and adequately degassed and
fed castings can contain low levels of porosity. To
measure the porosity with fidelity, the simple applica-
Sample Porosity% Bp Pp Up
tion of Archimedes' principle using water and single
Sample 1 1.82 0.026 0.42 0.42
measurements may need to be altered. By choosing a
Sample 2 1.64 0.024 0.18 0.18 suitable liquid and by making repeated measurements,
Sample 3 1.58 0.024 0.11 0.12 Archimedes' principle is useful in determining the
Sample 4 1.43 0.024 0.093 0.096 porosity of small cast specimens with low levels of
porosity.
Nomenclature
B - buoyant force
BR - biaslimitoftheresult Fig. 9 Archimedes' principle
DZ~D~D~)
D, - P 8Dc - (D~ - ND~) 2
PLws(1 +
PL ws
Ps = Ws- (Wsh- Wb) (l- 9 )
X Pth = -iJD (11-8)
(Ws-(Wsb-Wb)-AWs) '
Using Equation (1-5) the corrected porosity formula is:
The one parameter that can be controlled to try
_
100 1
PL) W
_ ( Pth s
(l
+ ND1 ))
D~ - ND~
(1-10)
to minimise the sensitivity coefficients is the relative density
of the liquid PLI Pth· To study this, it is convenient to convert
p - ws - ( wsb - wh) the coefficients into functions of porosity and relative density
( using the relationships:
Pth ) =Ws ( 1- 100
fV,h-Wb=Ws ( 1-p;A _pA ) (11-9)
100
Appendix 11
Derivation of the pyknometry sensitivity
wb = wdb(1- ;~) (11-10)
B - ws 8P (11-12)
w,- p aws
Wdb 100- P (l _ Pth PL)
(j _ Ws100 Ph Pth
(Ws- (Wsb- Wb))(Ws- (Wsb- Wb)- AWs) (11-13)
w,- ( 100 )
A 100-P- 1
(11-2)
O--D; 1 (11-16)
2 2 2
PL- Dc - ND b ( 1 N Db ) ( 100
- - - - 1)
+ D~ - ND~ 100- P
(11-14) (11-17)
(11-15)
The first three coefficients are strong functions of both P and
(j _ _ 2ND;D~ pL!Pth. The last four are not dependent on PLI Pth but are
D• - (D~ - ND~)2 strong functions of P.