Thermodynamics of Water and Water Solutions Questions ... · Thermodynamics of Water and Water...
Transcript of Thermodynamics of Water and Water Solutions Questions ... · Thermodynamics of Water and Water...
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Thermodynamics of Water and Water Solutions –Questions, Myths and some Answers
Georgios M. Kontogeorgis, Xiaodong Liang, Bjørn Maribo-Mogensen, Ioannis Tsivintzelis
Center for Energy Resources Engineering (CERE)Department of Chemical and Biochemical EngineeringTechnical University of Denmark
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Oil platforms in the North Sea(2007)982 oil and gas platforms in the North Sea. (drilling, service, etc) Great Britain and Norway own the majority of the oil and gas platforms, namely 590 and 193 respectively.
The Netherlands: 143 platforms Denmark: 53Germany: 3.
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Environmental challenges in oil & gas
• Decrease/optimize the amount of chemicals e.g. methanol and glycols (CPA, SAFT)
• Use more environmentally friendly chemicals e.g. antifreeze proteins
• CO2 – CCS
Photo: Petrobras
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SmartWater project
How injection of water of different salinity or other chemical modificationscan improve oil recovery
• Experimental: wettability alteration of the rock – effect of reservoir type
• Experimental: displacement experiments
• Experimental: oil-water interactions, emulsions
• Modeling: Flows in porous media with chemical transformations
Alexander ShapiroKaj ThomsenPhilip Fosbøl
MærskDONG
Collaboration with DTU-Byg and DTU-Kemi
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The book I read during Summer 2013vacations
”The most significant scientific discovery of this century””The most interesting science book I’ve ever read””As good as a Dan Brown novel”
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Outline
• Water (thermo) physical properties• Water structure and hydrophobic effect
• 1. Monomer fraction data (Experimental)
• 2. Association thermodynamic theories• Monomer fraction calculations from theories
• 3. A new theory and a new insight• Conclusions
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Lecture messages:The mystery of water’s structure and
water’s monomer fraction
• Water is one VERY strange molecule
• Water’s ”experimental” monomer fraction data
• Thermodynamic theories against ”experimental” monomer fraction data (XA)
• New theory links dielectric constant with XA resulting to alternative ”exper.” XA-data
• How do thermodynamic theories compare to new theory’s ”exp” XA-data ?
• Do all these give us insight into water’s structure ?
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What really matters is the hydrogen bonding!
8
potential energy r-6 (charge-dipole) r-2
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Hydrogen Bonds Dominate Properties
Molecule MW Dipole Moment (D)
Tb ( oC)
Ethane 30 0 -89
Formaldehyde 30 2.3 -21
Methanol 32 1.7 64
n-butane 58 0 -0.5
Acetone 58 3.0 56.5
Acetic Acid 60 1.5 118
n-Hexane 86 0 69
Ethyl propyl ether
88 1.2 64
1-pentanol 88 1.7 137
Israelachvili, 1985. Academic Press
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Water is a Liquid !!
http://chemed.chem.purdue.edu/genchem/topicreview/bp/ch14/liquids.php
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Water is a Liquid !!
http://chemed.chem.purdue.edu/genchem/topicreview/bp/ch14/liquids.php
H2O
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Water is a Liquid !!
http://chemed.chem.purdue.edu/genchem/topicreview/bp/ch14/liquids.php
HF19.5
-33.4 NH3
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Water is a Liquid !!
http://chemed.chem.purdue.edu/genchem/topicreview/bp/ch14/liquids.php
H2O
HF
100
19.5
-33.4 NH3
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Water is a VERY strange molecule!
http://chemed.chem.purdue.edu/genchem/topicreview/bp/ch14/liquids.php
H2O
HF
100
19.5
-33.4 NH3
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Water – 3D structure
The Physical Picture of Water HB Structure
H2O – liquid
H2S – gas
CH4 – gas
Why ?
0.1 nm
0.176 nm << 0.26 nm (vdW radii)
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Water has a high heat capacity
Cp=4.184 J/(g.K) [room T] – it takes a lot of time to warm up and cool down !
Why is EuropewarmerThanNorthernCanada ?
Gulf stream + Water salt content +Water heat capacity
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Water has a High Surface Tension value
liquids
n-Hexane
Toluene
Water
Mercury
)mJ(10 23
18
28
72
480
solids
Teflon
Polystyrene
NaCl
Tungsten
20
40
110
>1000
high
energy
interfaces
low energy
interfaces
not so well
defined
ambient
conditions
3/4 = hydrogenbonding, polar1/4 = dispersion
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Water ! High surface tension or what ?
”Jesus Christ” lizards in Costa Rica
Surface layers are less than 1 nm thick
Something more significant than a few extra bonds in thin film seems necessaryto account for water’s unusual surface properties ? (G.Pollack, Ch.16)
Photos from G. Pollack Book !
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Science News – On Line, March 1, 2003 Scientific American, Sept. 2003
Johannes M. Holmgren & Johan M. Persson M.Sc. Thesis (Lund, 2008)
Super hydrophobic surfaces – simply absence of hydrophilicity ? (Pollack)
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Water is not just the medium
Pure Water Water with Salts
0 50 100 150600
800
1000
1200
Density [
kg/m
3]
Model
Data
0 50 100 15040
60
80
100
Rel. S
tatic P
erm
ittivity
Temperature [oC]
Model
Data
0 1 2 3 4 5 620
40
60
80
NaC
l
r (Calc.)
r (Exp.)
0 1 2 3 4 5 620
40
60
80
MgC
l 2
Salt Concentration [mol/L]
Presence of ions decreases the static permittivity
Ion hydration shells are formed by e.g. water surrounding the molecules
Primitive models: solvent is a
dielectric continuum – not
explicitely treated, only
via its dielectric constant and
densityBjørn Maribo-Mogensen
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Anomalous dielectric constant of water
Israelachvili, 2011
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Water has very high solubility parameter
Solvent Sol.Parameter Polymer Sol.Parameter
MEK 18.5 Teflon 12.7
Hexane 14.9 PDMS 14.9
Styrene 19.0 PE 16.2
Cyclohexanone 19.0 PS 17.6
Acetone 19.9 PMMA 18.6
CCl4 17.6 PVC 19.4
Water 47.9 PET 21.9
Toluene 18.2 PAN 31.5
Solubility Parameter Values in (J/cm3)1/2
”Like” dissolves ”Like” V
RTHc
vap
2/1
321 8.1
cm
cal
But still universal solvent ! (salts,…)
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Water has a low free-volume – in the polymer range
Elbro’s free-volumeVf=V-Vw
Solvents
Polymers
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Water – an uncomparable molecule
water density versus temperature
0.95
0.96
0.97
0.98
0.99
1
1.01
-30 -10 10 30 50 70 90 110
temperature, C
wate
r d
en
sit
y,g
/ml
Full of hydrogen bondsand much more …
High Tb, Cp
HighPolarity (?)
Very highDielectricConstant
AndSurfacetension
4 C maximum
Tetrahedral structure (4 neighbors/molecule)Coulombic-type hydrogen bonds – not quasi-covalent
More openTetrahedra in ice
More dense (broken) tetrahedra inliquid
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Water density anomalies
F.Mallamace et al., 2007, Proc.Natl.Acad.Sci., 104(47), 18387 (MIT)
Maximum(277 K)
Minimum(203 K) – alsoFrom MD simulations
Use ofMonomerFractionDataAt all T(see later)
ScatteringRamanFTIRmeasurements
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Oil and Water don’t mix !
280 300 320 340 360 380 400 420 440 460 480
1E-7
1E-6
1E-5
1E-4
1E-3
0.01
0.1
Exp. data Tsonopoulos et al. (1983)
Exp. data Razzouk et al. (2010)
CPA, kij=0.0355
CPA, kij=0.0
Water in HC rich phase
m
ole
fra
ctio
n
Temperature / K
Hexane in water rich phase
Razzouk et al., 2010J.Chem.Eng.Data, 55: 1468
Water-hexane LLE
The minimum of the HC solubility in water
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Why don’t they mix ?
Prausnitz et al., 1999Gill and Wadso, 1976
An entropic effect
Almost equal to the water-HC interfacial energy
= -
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More structrured water in mixture!
Water alone5 nearest neighbors
3.0-3.5 H.Bonds/molecule
Water + alkanes
Water MORE structured !
4 H.Bonds/molecule3 H.Bonds/molecule in water-methanol
Water molecules stick together when the enemies appear !Water molecules simply love themselves too much !Water structure more important that the HBs !
Source: Israelachvili, Dixit et al., 2002 (Nature)
Alkane-alkane interactionAlso very strong >> vdW forces in free space(hydrophobic interaction, ”bond”!)
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Surfa
ce T
ensio
n
Concentration
non-ionic surfactant
Micelle Formation in Surfactant Solutions
airwater
CMC
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The micellization process – an entropic phenomenon (understood via the hydrophobic effect)
Surfactant Gibbs energy change
of micellization
(KJ/mol)
Enthalpy change of
micellization
(KJ/mol)
Entropy change of
micellization (J/K mol)
SDS -21.9 +2.51 +81.9
C12E6 -33.0 +16.3 +49.3
Dodecyl pyridinium
bromide
-21.0 -4.06 +56.9
N,N dimethyl
dodecyl amine oxide
-25.4 +7.11 +109.0
N-dodecyl-N,N-
dimethyl glycine
-25.6 -5.86 +64.9
Disorder Eventhough We Create Micelles ?
STHG
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Micellization is (almost always) an entropic effect, i.e. the driving force behind aggregation of surfactant molecules is a large
positive value of entropy of micellization! Why ?
Water alone
Water + surfactants
Water + micelles
The protagonist Is WATER !!
micelles
Did WaterRemember ?
DS
DS
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More maxima and minima in water properties
400
900
1400
1900
2400
280 330 380 430 480 530 580 630
Spe
ed
of
Sou
nd
(m
/s)
Temperature (K)
Exp
#1
#2
#3
#4
#540
60
80
280 330 380 430 480 530 580 630
Iso
ch
oric
He
at C
ap
acit
y (J
/m
ol-
K)
Temperature(K)
Exp
#1
#2
#3
#4
#5
Curves are PC-SAFT results with different parameter sets
http://www.lsbu.ac.uk/water/anmlies.htmlDiffusion vs. density
400350320300280260240220
Errington, 2001Nature, 409, 318
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Is all water the same ?
Natural water from Venezuela 40 000 more active than ordinary water –analyzed by Russians biophysicists
Water structure – water from country of origin – water not the same in all places in Earth
”Dead water” vs. Natural pure water from fountains (Dr. Korotkov)
Any good for ”Frappe” ?
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”Holly water”, ”Energized water” – do they really exist ?
http://www.johanngrander.com/
Johann Grander’s ”revitilized water”
Decorated in Austria
Bread rolls are fresherCoffee tastes betterUse in air conditioning unitsIn Austrian Casino….
Imported and used in Denmark in farms,By gardeners, and…
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Debated Grander water – Topsøe and Danisco also use it ?
• http://ing.dk/artikel/meta-science-vanvid-om-vand-120253
• http://ing.dk/blog/meta-science-uforklarlig-forklaring-126988
• http://ing.dk/artikel/dtu-professor-topsoe-og-danisco-til-grin-med-informationsvand-122709
• http://ing.dk/artikel/topsoe-og-danisco-jubler-over-rensende-mirakelvand-122331
• http://ing.dk/artikel/nysgerrige-danske-forskere-vil-teste-mystisk-vand-117658
• http://ing.dk/blog/vand-med-hukommelse-107016
• http://ing.dk/artikel/importor-af-mystisk-vandteknologi-kildevand-bliver-behandlet-med-naturmagneter-117616
• http://ing.dk/artikel/uforklarlig-vandteknologi-mystificerer-topsoe-og-danisco-117567
• http://ing.dk/artikel/ved-stuetemperatur-68350
Very Amazing Discussions
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Theories about water : ”The water memory debate”
French scientist Jacques Benveniste (80’s)Water seems to retain information from the molecules it interacted– ”water remembers”
Based on experiments with biologically active substances Water still has biological activity even after all biological molecules have vanished (full dilution + vigorous agitation!)
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”The water memory debate” – cont’d. Nature is upset
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”Gas hydrates” by water molecules around small dissolved nonpolar hydrophobic molecules
Israelachvili, 2011
Water can Participate in upTo 4 H-Bonds
More orderedWater than inBulk liquid
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Gas Hydrate Formation and the Memory of Water
” It is widely accepted [1-4] that it is easier (faster) to make hydrates from water that has previously been in hydrate form rather than directly from fresh water – i.e. if you place gas and water under pressure and cycle the temperature up and down to melt and reform hydrates, each subsequent temperature cycle downwards will form hydrates more quickly. In fact this is used as an experimental technique to run through experiments faster (this phenomenon is termed “memory water” by researchers in this field, although the term has none of the negative connotations of this idea in other branches of water science)”
Nicolas von Solms
Why on earth does this happen ?
Ack. Nicolas von Solms
Google: ”Water memory in gas hydrates”. 2 million hits – and heated debate !
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ProfessorMadeleine Ennis
Tried to disprove”water memory”Once and for allAnd her resultsShowed the exactOpposite !
”If the results areReal, she says,We may need toRewrite physicsAnd chemistry”
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Fights about water memory
Martin F. Chaplin (London South Bank U.)”The memory of water: an overviewHomeopathy, 2007, 96, 143
”Benveniste’s ideasadly makes no senseIt is a kind of desperation
If H.Bonds are lastingOnly a picosecondBefore they break andReform, how on earthIs the shape going toBe maintained”?
Philip Ball2011 Talk toRoyal Society of Chemistry
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Explanations for water memory?
Homopathy, 2007, 96, 143
Four very passionate articles on water memory
Yolene Thomas, 2007. The history of the memory of water. Homeopathy, 96, 151
Jose Teixeira, 2007. Can water possibly have a memory? A sceptical view. Homeopathy, 96, 158
V. Elia et al., 2007. The ”Memory of Water”: an almost deciphered enigma. Disspative structures inextremely dilute aqueous solutions. Homeopathy, 96, 163
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Four articles, Same year (2007) – Four opinions ?
Article Main Messages
Martin Chaplin, UK No such material as pure water existsLiquid water always contains other species such as H+ ionsIn the absence of other materials and surfaces, the HB pattern surrounding a solute does not persist when the solute is removedNumerous ”water memory” stories e.g. gas hydrates, etcMany explanations for the phenomenon, see previous slideGlass tubes and dissolved silica is one good explanationThe effect of shaking can be significant
Yolene Thomas, France Very emotional – in favor of J. BenvenisteRefers to Eni’s work, L. Rey and others who have ”proved” water memoryDigital Biology story – very exciting story ! But …
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Four articles, Same year (2007) – Four opinions ?
Article Main Messages
Jose Teixeira, France Quite criticalNo water clusters at all ! Except for micelles(surfactants)Any structure has a life of ps order (10-12 s)Presence of other molecules or dissolved gasescan explain some of the phenomenaWater is not pure water – full of impurities, whatelse is there in the so-called ”dilute” solutions ?
V. Elia, E.Napoli, R. Germano, Italy 10 years of experiments proving water memorydue to structuring and non-equilibrium status(Also many refs to others’ work, ”proofs”)Impurities have an effect but not the fullexplanation”within the solutions are molecular clusters of water molecules with HBs far from equilibriumconditions”
Water Memory = 463 mil. Hits in Google !
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Water structure – A big mystery
• Diverse models for water structure
• Complex – ”even water scientists occassionally have difficulties understanding one another’s theories”
• Most share a common feature: multiple states
• Martin Chaplin (London South Bank U., UK) web-site on water: http://www.lsbu.ac.uk/water/
• Rustum Roy et al. model
Ref. G.Pollack
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Water – an enduring mystery
• Article in Nature by Philip Ball (2008, 452, 291)
• Lars Pettersson, Anders Nilsson et al. theory in Science (2004, 304, 995) :
• ”Molecules in liquid water bind on average to just two others, forming chains and rings” (‘string theory’)
• ”The tetrahedral structure is not the only way to interpretprevious data on water structure from X-ray, neutron scattering and IR. The string model fits the results too, theysay”
• ”Two-state model with both classical tetrahedral structuresand chain/rings ones with denser & fewer hydrogen bonds”
• ”Cold water contains microscopic icebergs in a fluid sea” (Wilhelm Rontgen, 1982) and similar two-state models later(Henry Armstrong in 1920s, Oleg Samoilov in 1940s, WilseRobinson in 2000)
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How the Sweds see water
Y.Zubavicus and M.Grunze, May 2004. Science, 304, 974
Liquid water consists of Structures with two strongHydrogen bonds of each moleculeTo its neighbors, resulting in waterChains and rings
80% form 2-H bonds in Liquid waterRather than three or four as Assumed in most water-relatedStudies
Liquid water resembles top ice layers
More: Chemical Physics Letters(cover/frontiers article), 2008, 460: 387
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Fights in the pages of Science
• Smith et al. [group of Richard Saykally, U.California, Berkeley], October 2004, Science, 306, 851 ”Energetics of hydrogen bond network rearrangements in liquid water”: No way! We have tetrahedra, Only 10% HB broken – they have misintrepreted the data
• Nilsson et al., May 2005, Science, 308, 793a. Comment on ”Energetics….”
• Smith et al., May 2005, Science, 308, 793b. Response to Comment on ”Energetics…”
• My conclusion: Different interpretation of the same spectroscopic data ?
• More evidence for two-component water structure using femtosecond IR spectroscopy (Woutersen et al., 1997, Science, 278, 658)
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1. The experimental (?) monomer fraction data
• The data are shown in the next slides:
• Luck’s ”famous” data (1980)
• More data by other researchers – qualitativeagreement with Luck, showing somewhathigher monomer fractions
• ”New” data from Mallamace (MIT) showingvery high monomer fractions (do we interpretthe data correctly?)
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Free OH groups and percentage monomer fraction for pure water as a function of temperature [Luck, 1980]
% X1 = (XA)4
Von Solms et al., 2006, Ind.Eng.Chem.Res., 45, 5368
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Water monomer fraction data from varioussources Ioannis Tsivintzelis,
2013 (unpublished)
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
225 325 425 525 625 725 825Temperature / K
Mo
no
me
r F
rac
tio
n
Luck (1980) (Tranformed site fraction data, saturated water)
Luck (1980) (Monomer fraction data, saturated water)
Hoffman and Conradi (1997), 40 MPa
Hoffman and Conradi (1997), 30 MPa
Gorbaty and Kalinichev (1995), 50 MPa
IR and X-ray scattering
NMR
Other than Luck data: Both Liquid and supercritical water
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A more recent analysis from MIT
F.Mallamace et al., 2007, Proc.Natl.Acad.Sci., 104(47), 18387 (MIT)
Partially HB
Non HB
Random 3D(tetrahedral)Network
LDL
1,2 or 3BondsNot network
Monomer fractions
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Water monomer fraction data from various sources – cont’d (incl. Mallamace data)
Ioannis Tsivintzelis, 2013 (unpublished)
0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
25 125 225 325 425 525 625 725 825Temperature / K
Mo
no
me
r F
rac
tio
n
Luck (1980) (Tranformed site fraction data, saturated water)
Luck (1980) (Monomer fraction data, saturated water)
Mallamace et al. (2007)
Hoffman and Conradi (1997), 40 MPa
Hoffman and Conradi (1997), 30 MPa
Gorbaty and Kalinichev (1995), 50 MPa
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How many sites in water ?
M.Frosch, M. Bilde, O.F.Nielsen, 2010. J.Phys.Chem.A., 114: 11933
Many moreControversialStudies – see later
Two-stateLiquid WaterModels
”Room T: 43% of water molecules have4 hydrogen bonds,
the rest have fewer”
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Answers from molecular simulation ?
15%
5%
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More evidence for two-structure liquid water
F.Mallamace et al., 2007, Proc.Natl.Acad.Sci., 104(47), 18387 (MIT)
Partially HB
Non HB
Two different local HB structures: LDA (low density amorphous solid) and HDL (high density liquid)Two different local structures in liquid water: LDL (like LDA) open ”ice like” HB Network and HDL (not fully developed tetrahedral HB nextwork)HDL = NHB + PHBAbove 303 K (stable liquid) there is NO LDL (No ice-type 3D network!)
Tetrahedral
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Liquid water: 2, 3 or 4 hydrogen bonds – and how much of each one ?
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More controversies – effect of salts on water structure
Frosch, M., Bilde, M., Nielsen, O.F., 2010, J.Phys.Chem.A., 114, 11933& Dansk Kemi, 2011, 92,3, 26 ”Vand – en evig gåde”
% Hydrogen bonds (4 bonds) of waterIncreases with salt concentration
b = free water (NaCl-water)/free pure water < 1
Van’t Hoff factor for NaCl dissociation:i = id /b = (1+a) /b a = degree of dissociation
Clear change of water structure in presence of ions
Including change ofWater structureBrings van’t Hoff factorsClose to ”independent”Experimental data
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From water clustering to osmotic coefficients
Frosch, M., Bilde, M., Nielsen, O.F., 2010, J.Phys.Chem.A., 114, 11933
Osmotic coefficients from Raman spectroscopyAgree well with thermodynamic ones – when water structure change is accountedfor (together with electrolyte dissociation) Water structure effect crucial at higher concentrationsThe minimun explained by considering the dependence of the structure of water onelectrolyte - Similar results for other salts
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Another opinion…
Science, 2003, 301: 347
Y. Zhang and Paul Cremer, 2006, Current Opinion in Chemical Biology, 10: 658”Ions do not affect the bulk water properties” – numerous evidence for that !!
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What’s going on ?
• Are Luck’s ”famous” monomer fraction data for water wrong ?
• Is the tetrahedral structure of water wrong ? • Do we have many more ”free” (monomer) water
molecules than originally anticipated ? • Should we believe in a one or in a two- or in a
multi-state structure model for water ?• What type of structure is consistent with the
correct description of the thermodynamicproperties of water ?
• ...
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2. The theories (SAFT, CPA, NRHB) against monomer fraction data
Results summarized in the next slides:
• Theories in qualitative agreement with each other
• Theories not in very good agreement with Luck, etcdata
• All theories predict much ”more” hydrogen bonding or less monomer fraction than Luck’s data
• If we want to ”force” the theories to fit the monomer fraction data it can be done at the cost of getting i) strange parameters ii) poor phase behavior e.g. LLE for water-alkanes
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The SAFT model
Z = Zattr(disp) + Zrepuls(hs) + Zchain + Zassoc
),(,,, iiii BABA
iii m Chapman, Jackson, Radosz and Gubbins 1990
SAFT = Statistical Associating Fluid Theory
Wertheim’s articles in J. Stat. Physics (1986, 1987)(over 3000 citations)
”While brilliant areessentially incomprehensible”(J.M.Prausnitz)
Michael Wertheim
)1( ijjiij k
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Dec.10, 2010: 100 year anniversary from J. D. van der Waals Nobel Prize for Physics
Jose Valderrama, 2010. The legacy of van der Waals
2
RT aP
V b V
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SAFT – a theoretical concept
• Additive contributions from various effects (attraction, repulsion, chain, association)
• Wertheim theory for chain and association effects
• Segment concept
• Parameters with physical meaning
• Parameters following smooth trends / can be predicted from independent data
Z = Zattr(disp) + Zrepuls(hs) + Zchain + Zassoc
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SAFT – a family of models
SAFT Reference Citations (cit/year)
Original SAFT Chapman et al., 1990 943 (38)
Original SAFT (II) Huang and Radosz, 1990 899 (36)
Soft SAFT Vega and Blass, 1997 164 (7)
SAFT-VR Jackson et al., 1997 505 (28)
CPA Kontogeorgis et al., 1996 241 (13)
PC-SAFTsPC-SAFT
Gross and Sadowski, 2001Von Solms et al., 2003
755 (54)88 (7)
Source: Web of Science, July 1, 2014
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The concept of association – common in all
modelsProton donor site
Proton acceptor site
….. 2B
3B
…..
…..
….. 4C
Alkanols
R-OH
Primary amines
R-NH2
Water, glycols
….. 1A Aliphatic Acids
R-COOH
Glue-spot
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The concept and choice of association sites and schemes
Dimers
Oligomers
3D networks
+ amines
+ glycols
alkanolamines
Water: 3.5 sites ?
H1.5 O
Dixit et al.,2002 (Nature)
Chatzidimitriou-Dreismann, 2004
(Phys.Rev.Lett.)
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Acetic Acid (dimers)
Alcohols, phenols, amines (oligomers)
Water – 3D structureGlycols
Association models describe wellthe physics of association (in most cases)
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Extensive use of the association term – with success
• Water
• Alcohols, glycols
• Amines, organic acids
• Alkanolamines, glycolethers
• Diverse multifunctional (di-acids, polyphenolics)
• Exotic: ionic liquids, asphaltenes
70
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Three Recent Books with Association Models
2010 2010 201271
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Water-hydrocarbon LLE with CPA
72
280 300 320 340 360 380 400 420 440 460 480
1E-7
1E-6
1E-5
1E-4
1E-3
0.01
0.1
Exp. data Tsonopoulos et al. (1983)
Exp. data Razzouk et al. (2010)
CPA, kij=0.0355
CPA, kij=0.0
Water in HC rich phase
m
ole
fra
ctio
n
Temperature / K
Hexane in water rich phase
Razzouk et al., 2010J.Chem.Eng.Data, 55: 1468
Water-hexane LLE
The hydrophobic effect
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Water-hydrocarbon LLE with CPA
260 280 300 320 340 360 380 400 420 440 460 480 500 520 540
1E-6
1E-5
1E-4
1E-3
0.01
0.1
1
Water in Benzene rich phase
Benzene in water rich phase
Water in Hexane rich phase
mo
le fra
ctio
n
Temperature / K
Hexane in water rich phase
Kontogeorgis, Tsivintzelis et al., 2011, Fluid Phase Equilibria, 301: 244
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LLE with water and nC6 with PC-SAFT
1.0E-12
1.0E-10
1.0E-08
1.0E-06
1.0E-04
1.0E-02
1.0E+00
280 330 380 430 480
So
lub
ilit
y
Temperature (K)
Exp.
Exp. (W)
Gross (71.5% & 370%)
Grenner (32.1% & 15.4%)
Diamantonis (34.6% & 36.5%)
von Solms (99.9% & 8.50%)
Gross(0.039)Grenner (0.0571)*
Diamantonis (0.013)von Solms (0.05)+
* taken from Tsivintzelis, I. et. al, Ind. Eng. Chem. Res. 2008, 47, 5651
+ Arbitrarily set to 0.05
kij
Using optimum kij
Xiaodong Liang, 2012 (unpublished results)
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Good new LLE results for water-alkanes with the GC-PPC SAFT
De Hemptinne et al. [2011, IECR, 50: 7467]
Water (4C), used water/hexane LLE data for ”fine tuning” (CPA approach)
Good results due topolarity or ”CPA approach”?
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XA – calculations for water with 3 theories (4C)
250 300 350 400 450 500 550 600 650
0.0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
Exp. data
CPA
NRHB
sPC-SAFT
Fra
ctio
n o
f n
on
bo
nd
ed
site
s
Temperature / K
Kontogeorgis et al., 2010, FPE, 296: 219
% X1 = (XA)4
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XA – calculations for water with 3 theories (4C)
250 300 350 400 450 500 550 600 650
0.0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
Exp. data
CPA
NRHB
sPC-SAFT
Fra
ctio
n o
f n
on
bo
nd
ed
site
s
Temperature / K
Kontogeorgis et al., 2010, FPE, 296: 219
All theories predict more H-bonding than Luck’s data
% X1 = (XA)4
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XA – calculations for water with CPA and PC-SAFT (4C)
0
0.2
0.4
0.6
280 360 440 520 600
Free
sit
e fr
acti
on
Temperature (K)
Exp.
PCSAFT
CPA
PCSAFT (Trans. factor=1.4)
CPA (Trans. factor=1.3)
Liang et al., 2014 (accepted)
Recent study
Best PC-SAFTParameters(for water-alkane LLE)
Both models giveMuch lower XA thanLuck
The results can matchThe exp. Data bya multipl. Factor(artificial)
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Best parameters for water are NOT those thatreproduce the monomer fraction
0
10
20
30
40
50
60
70
80
-50 50 150 250 350 450
Temperature (oC)
% f
ree
-O
H g
rou
ps
(X
A)
LuckPC-SAFT (4C, m = 3.50)PC-SAFT (4C, m = 3.25)PC-SAFT (4C, m = 3.00)PC-SAFT (4C, m = 2.00)CPA (4C)PC-SAFT (4C, m = 1.50)
Grenner,06
Grenner, 07
Best XA sets:
Unusual
Parameters
+ Poor LLE
Grenner’s
parameters
give good
LLE results!
+ Poor XA
Grenner et al., 2007. Mol.Phys., 105, 1797
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Similar conclusion by recent study
Liang et al., 2014 (accepted)
0
0.2
0.4
0.6
280 360 440 520 600
Free
sit
e fr
acti
on
Temperture (K)
(b)
Exp.
W2B_1 W2B_2
W4C_1 W4C_2
W4C_3 W4C_4
1.E-7
1.E-6
1.E-5
1.E-4
1.E-3
1.E-2
1.E-1
1.E+0
270 340 410 480
So
lub
ilit
y
Temperature (K)
(b)
Exp. x W2B_1 (0.0349) W3B_1 (-0.0732)
W3B_C (0.0589) W4C_1 (0.0488) W4C_2 (0.0088)
Water-hexane LLE
HC in water Water in HC
4C-1 49.4 13.2
4C-2 46.4 34.6
4C-3 42.3 248
4C-4 58.8 505
Correlation results/1 kij
4C-3, 4C-4 Best for XA but worse for LLE4C-1, 4C-2 Best for LLE but worse for XA
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3. A new theory links dielectric constantwith monomer fraction
• Theory developed by Bjørn Maribo-Mogensen [J.Phys.Chem.B]
• Theory can be used to estimate dielectric constant usingmonomer fraction (XA ) from e.g. CPA or SAFT
• Alternatively if dielectric constant and density data areavailable, the new theory can be used to generate new ”exp” monomer fraction (exp if the theory is perfect!)
• Basic equations:
𝑔 =1
𝜇02
2𝜀𝑟 + 𝜀∞ 𝜀𝑟 − 𝜀∞𝜀𝑟 𝜀∞ + 2 2
9𝜀0𝑘𝐵𝑇𝑣
𝑁𝐴
1 − 𝑋𝐴 =𝑔 − 1
𝑧𝑐𝑜𝑠 𝛾 − 𝑔 − 1 𝑐𝑜𝑠 𝜃
𝜀∞ − 1
𝜀∞ + 2=
1
3𝜀0
𝑁𝐴𝑣𝛼0
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Bjørn Maribo-Mogensen, 2014 PhD Thesis
New theory predicts more H-bonding for water – in agreement to Association thermodynamic theoriesBut NOT in agreement to Luck data
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New theory vs. PC-SAFT vs. Luck
Xiaodong Liang, 2014, PhD thesis
0
0.2
0.4
0.6
280 360 440 520 600
Fre
e s
ite
fra
cti
on
Temperature (K)
Exp.
Calc.
PCSAFT
Using the new theory
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Some conclusions from monomer fraction study
• New theory for estimating dielectric constant can bealternatively used for estimating monomer or site fractions
• For methanol & water the theory yields lower XA values (more H-bonding than Luck); for ethanol it is the opposite
• XA for water from new theory are in better agreement with CPA + PC-SAFT values than with Luck data
• New theory can be used to obtain monomer fraction data for important compounds e.g. glycols for which no such data is available
• More input to water studies maybe can be obtained from measurements of the hydrophobic effect/free energy of hydration combined also with interfacial energies for water-alkanes
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Water – some personal final thoughts
• Monomer fraction data of water could give / could have given an idea about its structure
• I am not sure this is the case! (uncertainties in measurements and interpretation)
• Modern association theories can describe verywell many thermodynamic properties of waterincluding phase behavior (e.g. LLE water-alkanes)
• Association theories can predict the monomer fraction of water
• Poor agreement with ”published” monomer fraction data using the ”best” parameters for phase behavior
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Water – some personal final thoughts
• Recent theory relating dielectric constant and monomer fraction provides ”more” evidencethat association theories and the tetrahedralstructure are correct
• Other experimental studies disagree on whichwater structure is the correct
• Describing phase behavior or some of waterproperties does not necessarily mean weunderstand very much the water structure
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What have we learnt ?
• Water is a very/far too complex molecule – it should bevery hard to describe all properties with one theory
• Water – 4C is ”for us” still the best choice (CPA, SAFT association theories) – for phase equilibrium calculations
• (Maybe) No reason to re-think the water parameters ”from the practical point of view”
• (Maybe ) More advanced water theories can wait…
• (Maybe) Understanding of water structure is far more difficult than previously anticipated ?
• Maybe I have asked more questions than providedanswers (about water’s structure)
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David Chandler, UC Berkeley
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From C&EN, 14.12.2009 cont’d
Prof. Pavel Jungwirth (Academy of Sciences, Czech Republic):
”The primary problem with Pollack’s research is that it employsmacroscopic experiments to draw conclusions about waterstructure. Instead, microscopic tools such as spectroscopy and molecular simulations are the proper tools for investigating the molecular structure of water”
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From C&EN, 14.12.2009 cont’d
Prof. Pavel Jungwirth (Academy of Sciences, Czech Republic):
”The primary problem with Pollack’s research is that it employsmacroscopic experiments to draw conclusions about water structure. Instead, microscopic tools such as spectroscopy and molecularsimulations are the proper tools for investigating the molecularstructure of water”
Oh, Really !
Come On Now !!!
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We need more collaboration
“It is about time to get real practical answers. This center will provide answers to questions about water’s structure and its implications by (i) bringing together top scientists from Denmark and abroad in water research, working with “conventional” and with “provocative” theories, (ii) allowing ideas to be challenged and (iii) combining a multi-level approach which includes experimental, molecular simulation, theory (statistical mechanics) and modeling research.”
Application to DGF ”The proposed research ideas were not well developed”
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Socrates
Ἓν οἶδα ὅτι οὐδὲν οἶδα
"The one thing I know is that I know nothing"
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