Density Absolute Error
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just how much the measured value is likely to deviate from the unknown, true, value of the quantity. The art of estimating these deviations should probably be called uncertainty analysis, but for historical reasons is referred to as
Absolute Error Example
error analysis. This document contains brief discussions about how errors are reported, the kinds of errors absolute error definition that can occur, how to estimate random errors, and how to carry error estimates into calculated results. We are not, and will not be,
Relative Error Definition
concerned with the “percent error” exercises common in high school, where the student is content with calculating the deviation from some allegedly authoritative number. Significant figures Whenever you make a measurement, the number of meaningful digits that you write down absolute error physics implies the error in the measurement. For example if you say that the length of an object is 0.428 m, you imply an uncertainty of about 0.001 m. To record this measurement as either 0.4 or 0.42819667 would imply that you only know it to 0.1 m in the first case or to 0.00000001 m in the second. You should only report as many significant figures as are consistent with the estimated error. The quantity 0.428 m is said to have absolute error and relative error in numerical analysis three significant figures, that is, three digits that make sense in terms of the measurement. Notice that this has nothing to do with the "number of decimal places". The same measurement in centimeters would be 42.8 cm and still be a three significant figure number. The accepted convention is that only one uncertain digit is to be reported for a measurement. In the example if the estimated error is 0.02 m you would report a result of 0.43 ± 0.02 m, not 0.428 ± 0.02 m. Students frequently are confused about when to count a zero as a significant figure. The rule is: If the zero has a non-zero digit anywhere to its left, then the zero is significant, otherwise it is not. For example 5.00 has 3 significant figures; the number 0.0005 has only one significant figure, and 1.0005 has 5 significant figures. A number like 300 is not well defined. Rather one should write 3 x 102, one significant figure, or 3.00 x 102, 3 significant figures. Absolute and relative errors The absolute error in a measured quantity is the uncertainty in the quantity and has the same units as the quantity itself. For example if you know a length is 0.428 m ± 0.002 m, the 0.002 m is an absolute error. The relative error (also called the fractional error) is obtained by dividing the absolute error in the quantity by the quantity itself. The rel
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Absolute Error Formula
help here? Sign up for a free 30min tutor trial difference between absolute error and relative error with Chegg Tutors Dismiss Notice Dismiss Notice Join Physics Forums Today! The friendliest, high quality science
Fractional Error Formula
and math community on the planet! Everyone who loves science is here! Finding the maximum/absolute error in calculating the density of a metal sample. Sep 27, 2012 http://www.owlnet.rice.edu/~labgroup/pdf/Error_analysis.htm #1 nerdy_hottie 1. The problem statement, all variables and given/known data "You are measuring the density of a metal sample. You have determined that the mass of the sample is 63.8 grams, and your error in this result is plus or minus 0.1 g. The volume of the sample is 8.8 +/- 0.1 https://www.physicsforums.com/threads/finding-the-maximum-absolute-error-in-calculating-the-density-of-a-metal-sample.639389/ cm^3. What is the maximum error (in g/cm^3) in your measurement of the sample density? " 2. Relevant equations density=mass/volume For z = x/y: δz/z = δx/x + δy/y 3. The attempt at a solution Well, filling into the equation for δz/z and substituting this for δρ/ρ and solving for δρ: δρ=ρ(δm/m + δv/v) =(63.8g/8.8cm^3)(0.1g/63.8g + 0.1cm^3/8.8cm^3) =(7.25g/cm^3)(0.01293) =0.0937g/cm^3 However, it says this answer is incorrect. Any hints on where I am going wrong? nerdy_hottie, Sep 27, 2012 Phys.org - latest science and technology news stories on Phys.org •Game over? Computer beats human champ in ancient Chinese game •Simplifying solar cells with a new mix of materials •Imaged 'jets' reveal cerium's post-shock inner strength Sep 27, 2012 #2 szynkasz Maybe it should be done in this way: [tex]\rho_{max}=\frac{m+\Delta m}{V-\Delta V}\\ \rho_{min}=\frac{m-\Delta m}{V+\Delta V}\\ \Delta\rho=max\left(\rho-\rho_{min},\rho_{max}-\rho\right) [/tex] Last edited: Sep 27, 2012 szynkasz, Sep 27, 2012 Sep 27, 2012 #3 nerdy_hottie I'm not quite sure I u
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a quick overview of the site Help Center Detailed answers to any questions you might have Meta Discuss the workings and policies of this site About Us Learn more about Stack Overflow the company Business Learn more about hiring developers or posting ads with us Physics Questions Tags Users Badges Unanswered Ask Question _ Physics Stack Exchange is a question and answer site for active researchers, academics and students of physics. Join them; it only takes a minute: Sign up Here's how it works: Anybody can ask a question Anybody can answer The best answers are voted up and rise to the top How to correctly solve density tolerance up vote 0 down vote favorite I want to know if my solution to a textbook problem has any major problems with it. Here is the problem: Ethanol has a given density of 0.789 g/mL at 20 degrees Celsius and isopropanol has a given density of 0.785 g/mL at 20 degrees Celsius. A chemist analyzes a substance using a pipet that is accurate to $\pm 0.02$ mL and a balance accurate to $\pm 0.003$ g. Is this equipment precise enough to distinguish between ethanol and isopropanol? And here is my solution: We can calculate with tolerances in the same way we calculate measurements. The mass tolerance of $\pm 0.003$ g has three significant figures. The volume tolerance of $\pm 0.02$ mL has two significant figures. The density tolerance will therefore have two significant figures. $\pm 0.003 \text{ g} / \pm 0.02 \text{ mL} = \pm 0.15 \text{ g/mL}$.In order to distinguish between ethanol and isopropanol, whose densities differ by 0.789 - 0.785 g/ mL, or 0.004 g/ mL, we need a precision smaller than half the difference, or 0.002 g/mL. But we can only measure density to within 0.15 g/mL of the actual value. Therefore, this equipment is not precise enough to distinguish between ethanol and isopropanol. But what I don't like or feel is right about dividing the tolerances like that is that having a smaller tolerance (more precise) for volume in the denominator blows up (bad) your density tolerance. Shouldn't higher precision (smaller tolerance) of either pipet OR balance result in higher precision (smaller