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Physics 115 General Physics II Session 9 Molecular motion and - PowerPoint PPT Presentation

Physics 115 General Physics II Session 9 Molecular motion and temperature Phase equilibrium, evaporation R. J. Wilkes Email: phy115a@u.washington.edu Home page: http://courses.washington.edu/phy115a/ 4/14/14 Physics 115 1 Lecture


  1. Physics 115 General Physics II Session 9 Molecular motion and temperature Phase equilibrium, evaporation • R. J. Wilkes • Email: phy115a@u.washington.edu • Home page: http://courses.washington.edu/phy115a/ 4/14/14 Physics 115 1

  2. Lecture Schedule (up to exam 1) Just joined the class? See course home page Today courses.washington.edu/phy115a/ for course info, and slides from previous sessions 4/14/14 Physics 115 2

  3. Announcements • Prof. Jim Reid is standing in for RJW this week • Exam 1 this Friday 4/18 , in class, formula sheet provided – YOU bring a bubble sheet , pencil, calculator (NO laptops or phones; NO personal notes allowed .) – We will post sample questions tomorrow, and go over them in class Thursday • Clicker responses from last week are posted, so you can check if your clicker is being detected. See link on class home page, http://courses.washington.edu/phy115a 4/14/14 3 Physics 115

  4. Gas Law: Avogadro’s number and R Last time Counting molecules to get N is difficult, so it is convenient to use Avagadro ’ s number N A , the number of carbon atoms in exactly 12 g (1 mole) of carbon. 1 mol = {molecular mass, A} grams of gas (For elements, what you see on the Periodic Table is A averaged over isotopes) N A = 6.022 x 10 23 molecules/mole and N = nN A , where n = number of moles of gas PV = nN A kT = nRT Notice: for real gases, Notice PV = energy: N-m PV / nT = 8.3J/(mol ⋅ K) only at low P R = N A k = 8.314 J/(mol ⋅ K) PV nRT = Ideal Gas Law, in moles Non-ideal gases R = “Universal gas constant” Good approx at low P for real gases 4/14/14 4 Physics 115

  5. Isotherm plots • PV=NkT results from many different observations: – Hold N, T constant and see how P, V vary: find PV = const → P = const V (with T and N fixed) Boyle ’ s Law For different T’s we get a set of (1/V)-shaped curves 4/11/14 5 Physics 115A

  6. Isobar plots – Hold N, P constant and see how V, T vary: find V = ( const ) T ( ) constant N , P Charles & Gay-Lussac Law For different P’s we get a set of linear plots 4/11/14 6 Physics 115A

  7. Example: Volume of an ideal gas • What volume is occupied by 1.00 mol of an ideal gas if it is at T = 0.00°C and P = 1.00 atm? PV nRT so = nRT V = P (1.00 mol) 0.08206 L atm/(mol K) (273.15 K ) [ ] ⋅ ⋅ = (1.00 atm) 22.41 L = – If we increase the V available, with same T: P must drop – If we increase the T, with V kept the same: P must rise • Standard Temperature and Pressure (STP) = 0°C, 1 atm – At STP, one mole of any ideal gas occupies 22.4 liters 4/14/14 7 Physics 115

  8. Example: heating and compressing a gas • An ideal gas initially has a volume = 2.00 L, temperature = 30.0°C, and pressure =1.00 atm. • The gas is heated to 60.0°C and compressed to a volume of 1.50 L – what is its new pressure? VT (2.0 L)(60.0 C 273.15 C ) ° + ° PV PV P P V T 1 2 (1.00 atm) (1.5 L)(30.0 = = 1 1 2 2 so = 2 1 C 273.15 C ) ° + ° T T 2 1 1 2 1.47 atm = – Notice: we must use Kelvin temperatures when applying ideal gas laws – what would result have been if we use the ratio (60/30)? 4/14/14 8 Physics 115

  9. Quiz 5 • Two containers with equal V and P each hold samples of the same ideal gas. Container A has twice as many molecules as container B. • Which is the correct statement about the absolute temperatures in containers A and B, respectively? A. T A = T B B. T A = 2 T B C. T A = (1/2)T B D. T A = (1/4) T B E. T A = (1/ √ 2)T B 4/14/14 9 Physics 115

  10. Quiz 5 • Two containers with equal V and P each hold samples of the same ideal gas. Container A has twice as many molecules as container B. • Which is the correct statement about the absolute temperatures in containers A and B, respectively? A. T A = T B B. T A = 2 T B ( ) ∝ 1/ n ( ) PV = nRT so T = PV / nR C. T A = (1/2)T B D. T A = (1/4) T B E. T A = (1/ √ 2)T B 4/14/14 10 Physics 115

  11. Relating gas laws to molecular motion • P, V, T are macroscopic quantities – Human-scale quantities, measurable on a table-top • Molecular motion ( x, v vs t ) = microscopic quantities • Kinetic theory of gases: connect micro to macro – Model for ideal gas • N is large, molecules are identical point-particles • Molecules move randomly • No inelastic interactions: collisions are always elastic – Recall: elastic means no loss of KE due to collision Elastic collision with wall means momentum (so, v ) component perpendicular to wall gets reversed Speed unchanged Vertical v unchanged Horizontal v reversed 4/14/14 11 Physics 115

  12. Calculate the pressure of a gas Change in horizontal momentum of molecule Δ p x = p x , f − p x , i = mv x − ( − mv x ) = 2 mv x Change is due to force exerted by wall: F Δ t = Δ p x , F ON WALL = − F BY WALL Average force exerted on wall by one molecule F AVG = Δ p x Δ t where Δ t = time between collisions = round-trip time 2 Δ t = 2 L / v x → F AVG = 2 mv x = mv x 2 L / v x L Assume symmetrical container (LxLxL): (doesn't matter in the end) $ 2 ' 2 AVG = F AVG mv x ) = mv x = 1 ( ) AVG 2 P → Adding up all molecules, PV = N m v x & ) & 2 A L V L % ( 4/14/14 12 Physics 115

  13. Defining temperature (again): molecular scale • Now we can connect macro to micro: ( 2 ) av → ( 2 ) av = 1 1 1 PV = NkT = 2 N 2 mv x 2 mv x 2 kT Nothing special about the x-direction: random motion means ( ) 2 ( ) 2 ( ) 2 ( ) 2 ( ) 2 ( ) 2 ( ) 2 ( ) 2 v v v and v v v v 3 v = = = + + = x y z x y z x av av av av av av av av (because random v components are independent of one another) The average translational kinetic energy of the molecules is: Deep and fundamental ! ( ) av = 3 1 2 mv 2 K translational av = 2 kT per molecule Avg KE of gas molecule is proportional to T, with Boltzmann constant as ( ) 1 2 3 3 K N mv NkT nRT = = = the factor trans 2 2 2 av Root-mean-square (RMS) - useful avg where quantity-squared is what matters: 3 N A kT 3 kT = 3 RT 3 RT ( ) av = v 2 ( ) av = v 2 and v RMS = = m molecule N A m molecule M MOLE M MOLE 4/14/14 13 Physics 115

  14. Example: RMS speed of gas molecules RMS means: take each molecule’s speed and square it, then find the average of those numbers, and THEN take the square root. In practice: we find the statistical speed distribution of the molecules, and use that to estimate RMS speed Oxygen gas (O 2 ) has a molar mass* M of about 32.0 g/mol, and hydrogen gas (H2) has a molar mass of about 2.00 g/mol. Assuming ideal-gas behavior, what is: Note: Walker says (a) the RMS speed of an oxygen molecule when “molecular mass” for molar the temperature is 300K (27°C), and mass – confusing. M X = grams in 1 mole of X, (b) RMS speed of a hydrogen molecule at the same m X = mass (in kg) of one X temperature molecule 3 RT 3(8.314 J/mol ⋅ K)(300 K) v O2 RMS = = 485 m/s = M O (0.0320 kg/mol) 3 RT 3(8.314 J/mol ⋅ K)(300 K) v H2 RMS = = 1,934 m/s = M H (0.0020 kg/mol) 4/14/14 14 Physics 115

  15. Probability Distributions Peak or mode = We give a 25 point quiz to N students, s with max and plot the results as a histogram , probability showing the number n i of students, or fraction f i = n i / N of students, for each possible score vs. score, from 0 to 25. Such plots represent distributions . For reasonably large N, we can use f i = n i / N to estimate the probability that a randomly selected student received a score s i . Notice, the fractions will add to 1 for all possible scores, so that Σ f i = 1 . In that case the histogram represents a normalized distribution function . We have the following relations: 1 n N f = 1 ∑ ∑ It’s not useful for = s n s f s ∑ ∑ = = i i av i i i i N class grades, but we i i i i could also calculate 1 the average squared = ∑ 2 2 s s f s = 2 2 2 s n s f s ∑ ∑ = = RMS av i i score: av i i i i N i i i 4/14/14 15 Physics 115

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