7 Solutions/Solubility, Diffusion, Tension, & Fluid Physics Flashcards
Solute
Solid, liquid, or gas dissolved in solvent
Solute particles must be surrounded by solvent particles
Solvent
Substance into which a solute is dissolved
Dissolving agent
Body fluid solvent = water
Solution
Homogenous mixture of two or more components
Particles include atoms, ions, or molecules
Solute dissolved in solvent
Ex: Sugar and water (both polar)
Suspension
Solution where the solute CANNOT be dissolved in the solvent
Ex: Oil (non-polar) and water
Colloid Solution
Particles exist in solution somewhere between a TRUE solution and a TRUE suspension
Size of particles - between those found in solutions and suspensions
Mixed in way that remain evenly distributed w/out settling out
Solubility
Polar dissolves in polar
↑ temperature ↑ solubility
Heat (↑ temp) & energy (stirring) breaks intermolecular forces
H2O dissolves polar substances better than ethanol d/t H2O more polar (dipole-dipole & hydrogen bonding)
Solids - dissolution in solvent directly proportional to temp (100g dextrose in 100ml H2O will slightly displace volume d/t dextrose particles take up space b/w H2O molecules)
↑ temp ↑ solubility (solid in liquid)
Gases - solubility dependent on solvent nature and temp
↑ temp ↓ solubility (gas in liquid)
Endothermic & exothermic reactions
Solution Strength CALCULATION
Solute grams per 100mL solvent = % solution
Percent = per 100
0.9% NaCl = 0.9g NaCl / 100mL
Molar solution - solute moles per 1L solvent
NaCl = 23 + 35AMU = 58g/mol
0.9g NaCl / 100mL = 9g / 1L
(9g/L) / (58g/mol) = 0.155 moles
Henry’s Law
Amount gas dissolved in liquid directly proportional to the pressure applied to the gas as it overlies the liquid
Temperature also affects gas solubility (inversely proportional)
40mmHg pressure applied therefore 40mmHg pressure from gas molecules w/in the solution
Diffusion
Process by which substance spreads through the space available to it by random molecular motion
Molecules more from area of high to low concentration
Pressure gradient ∆P
P1 - P2 > 0
Graham’s Law
Describes gas movement from one compartment to another through a porous membrane (diffusion) or small opening such as an orifice (effusion)
Diffusion α 1/√Molecular Weight
Directly proportional to solubility
Larger, more cumbersome molecules = less diffusion
Graham’s Law CALCULATION
Diffusion coefficient = Gas solubility / √Molecular weight
= Gas 1 Diffusion Rate / Gas 2 Diffusion Rate
= (Gas 1 Solubility / Gas 2 Solubility) x (√Gas 2 MW /√Gas 1 MW)
Given solubility - Gas A 20x more soluble than Gas B
Relative rate of diffusion
Fick’s Law
Describes gas volume that diffuses across membrane per minute
Diffusion rate = (Area x Diffusion coefficient x ∆P) / Membrane thickness
r/t alveolar capillary membrane
↑ surface area ↑ diffusion
↑ thickness ↓ diffusion
Turbulent Flow
Density more important
Influences probability that interactions b/w fluid molecules will occur
↑ density = ↑ molecules per unit area therefore ↑ change molecular collisions ↑ drag (resistance) ↓ flow
Gas Diffusion/Effusion
Diffusion - porous membrane; gradual gas mixing d/t motion of component particles
Effusion - escape of gaseous molecules via small opening (orifice) into evacuated space
α 1/√MW
α 1/√Density
Less dense gas ↑ diffusion/effusion
Bunsen Solubility Coefficient α
Gas volume in liquid unit at 0°C and 760mmHg
Expressed as numerical value for particular gas in given liquid
= mL gas per 1 mL H2O