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Page 1: 1 Hydrogen Storage Useful refs: See

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Hydrogen Storage Useful refs:See http://people.bath.ac.uk/cestjm/Shared/DTC/ch50182-Mays-Day2/

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Energy White Paper

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Why Hydrogen for Energy?2H2 + O2 = 2H2O + Energy

Three Major Attractions(1) Clean combustion of a non-toxic fuel

(2) Delivered energy / mass is very high

(energy gain / electron best of all the chemical elements)

(3) Offers greatest potential for “Sustainable Energy Future”

FUEL CONTENTS OF POLLUTING MATTER IN FUMES (Kg/Kg of fuel)

Formula

CO2

SO2

NOx

Dust and Unburned

Matter

H2O

Pb(C2H5)4

C 1.893 0.012 0.008 0.1 0.633 0 CH4 2.75 0.03 0.0075 0 2.154 0

C8H17 3.09 0.010 0.0115 0.85 1.254 0.001 H2 0 0 0.016 0 7 0

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• Economic recyclable/rechargeable vessels

• Near ambient temperature pressure operation

• High hydrogen storage capacity/small volume

• Fast recharge and discharge kinetics

• Impact Safety

• Tolerant to trace poisoning

Hydrogen Storage Systems for Mobile Applications

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• On a weight basis H2 has nearly three times the

energy content of gasoline. – 120 MJ/kg vs. 44 MJ/kg (LHV)

• On a volume basis the situation is reversed. – 3 MJ/L (5000 psi), 8 MJ/L (LH2) vs. 32 MJ/L

• Physical storage of hydrogen is bulky.• Capacity of reversible chemical storage at useful T, P is low.• Other challenging issues include energy efficiency, cost, and safety.

Storing enough hydrogen on vehicles to achieve greater than 300 miles driving range is difficult.

On-Board Hydrogen Storage Challenge

JoAnn Milliken, US DOE Status Report, 22 Oct 2002

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0 10 20 30 40 50 60 70 80 90 1000

10

20

30

40

50

60

70

80

90

100

20.4 K

87 kg m-3 [Silvera, Rev Mod Phys 52 (1980) 393]

critical point

solid

normal boiling point

real gasideal gas

real gas

de

nsi

ty / k

g m

-3

pressure / MPa

triple point

77 K

298 K

ideal gas

liqu

id d

ensi

ties

0 10 20 30 40 50 60 70 80 90 1000

10

20

30

40

50

60

70

80

90

100

20.4 K

87 kg m-3 [Silvera, Rev Mod Phys 52 (1980) 393]

critical point

solid

normal boiling point

real gasideal gas

real gas

de

nsi

ty / k

g m

-3

pressure / MPa

triple point

77 K

298 K

ideal gas

liqu

id d

ensi

ties

0 10 20 30 40 50 60 70 80 90 1000

10

20

30

40

50

60

70

80

90

100

20.4 K

87 kg m-3 [Silvera, Rev Mod Phys 52 (1980) 393]

critical point

solid

normal boiling point

real gasideal gas

real gas

de

nsi

ty / k

g m

-3

pressure / MPa

triple point

77 K

298 K

ideal gas

liqu

id d

ensi

ties

Leachman’s EOS for Normal HydrogenLeachman, et al. J Phys Chem Ref Data 38 (2009) 721

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Cryogenic Storage of Hydrogen

Spherical designs best S/V

3% / day boil off (@ 20 K)

Insulation bulky

40% liquefaction penalty

High pressure options

Liq H2

Liq N2

Steel/Aluminium

Low emmittance multilayers

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Compression Storage of Hydrogen

Composite H2 Cylinder – 12 wt%

Conformable geometricsHigher wt% via increased pressureHeating on filling

H2 : 350 bar

Glass/Carbon fibreAluminium/Thermoplastic

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Advanced Materials for Hydrogen-Storage: 3 Strategic Challenges

I. Storage Capacity ≥ 6.5 wt%II. Reversibility of thermal absorption / desorption

cycles (at an accessible temperature)III. Low cost, low toxicity, low risk of explosion, etc.

(Source: www.doe.gov)

There is, as yet, no material known to meet simultaneously all of these requirements

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Volume of 4 kg of hydrogen compacted in different ways, with size relative to the size of a car.

Mg2NiH4 LaNi5H6 H2 (liquid) H2 (200 bar)

Schlapbach and Züttel, Nature, 15 Nov 2001

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Carbon

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15Reversibly stored amount of hydrogen on various carbon materials versus the specific surface area of the samples.

Louis Schlapbach & Andreas Züttel, Nature 414, 15 Nov 2001

= nanotube samples (best-fit line indicated)

= other nanostructured carbon samples

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Magnesium-based Storage Materials

Problems associated with magnesium:

• Stability of the MgH2.

• Surface oxidation of magnesium based powders.

• Slow diffusion of hydrogen through MgH2.

Possible Solutions:

• Milling to develop a nanocrystalline material.

• Introduction of catalysts to dissociate hydrogen by co-milling or by developing multilayers.

• Alloying with other metals such as Ni, Al etc….

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Conclusions

Mobile

• Carbon Nanotubes - Less than 0.5 wt% uptake at RT. Adsorption related to surface area.- There may be a means of creating high hydrogen storage capacity CNT, but despite a large global effort, it remains elusive and lacking independent verification.

• Milled Magnesium + Alloys - Continuing to optimise milling conditions / PGM additions, in an effort to produce a practical on-board auto hydrogen store.- Operating Temperature still a problem

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• Low-cost storage material

• Able to scale up storage solution to large-scale?

• Relatively high hydrogen storage capacity

• Reasonably fast recharge and discharge kinetics

• Tolerant to trace poisoning

• Long-term cycling

Hydrogen Storage Systems for Stationary Applications

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zeolite A zeolites X and Y zeolite RHO.

The corners on each framework represent Si or Al and these are linked by oxygen bridges represented by the lines on the frameworks

Zeolite Framework Structures

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Zeolite A – Si-Al network.

Zeolite Preparation

• Hydrothermal Procedure

• Ion exchange using metal nitrate

• Characterisation•XRD

•SEM with EDX

•BET surface area (N2 at 77K)

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H2 uptake (wt.%)Material -196ºC RT 270ºCNaA 1.54 0.28 0.30CdA 1.14 0.25 0.30MgA 1.19 - -NaCsRHO 0.00 0.18 0.20CdRHO 0.08 0.19 0.25LiX 2.15 - -NaX 1.79 - 0.25CdX 1.42 - -MgX 1.61 - 0.28CuX - - 0.25NaY 1.81 - -CdY 1.47 - -MgY 1.74 - -

Hydrogen uptake in Zeolites

-196°C

-196°C

15bar H2

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Wt% Hydrogen plotted against BET surface area for activated carbon and zeolites samples.

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Conclusions

Stationary

Activated CarbonSignificant amounts of hydrogen can be stored reversibly (up to 4wt%) at 77 K and 15 bar.

Zeolites- Up to 2wt% at 77 K and 15 bar.- Hydrogen storage capacity of certain zeolites can be increased by manipulation of the zeolite exchangeable cations, e.g. Zeolite RHO

Unfortunately, at room temperature storage properties are below 1wt%, for both activated carbon and zeolites.

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THE STORAGE OF HYDROGEN IN SOLIDS

• Carbon: A deeper understanding of the unique interaction between H2 (H) and carbon;

– nature of physi-, vs chemi-sorption, in nanostructured carbon– the role of dangling bonds.

• Light Hydrides: A deeper understanding of the thermodynamics and kinetics of decomposition / absorption reactions and (intermediate) processes;

– metallicity, chemical reactivity and electronic states,– innovation in the synthesis and stabilisation (handling) of hydrides.

• Nanostructured Porous Solids: The tailoring of pore geometry, and (interior) chemical reactivity for hydrogen activation, storage and release;

– the interaction between H2 (H) and porous solids.