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C orrosion Solution pH 2 4 6 8 10 C orrosion R ate (g/cm 2 *m in) 0 1e-7 2e-7 3e-7 4e-7 M AP BAP KBAP KM AP LG-770 LHG -8 C orrosion Solution pH 2 4 6 8 10 C orrosion R ate (g/cm 2 *m in) 0 5e-7 1e-6 2e-6 2e-6 KAP Aqueous Corrosion Data Corrosion performed with ~1cm 3 samples in 100mL of DI water, 1mM NH 4 OH, or 1mM HCl The lowest dissolution rates occur at neutral pH with basic conditions accelerating corrosion to a greater extend than acidic conditions

Aqueous Corrosion Data

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Aqueous Corrosion Data. Corrosion performed with ~1cm 3 samples in 100mL of DI water, 1mM NH 4 OH, or 1mM HCl The lowest dissolution rates occur at neutral pH with basic conditions accelerating corrosion to a greater extend than acidic conditions. pH Changes of Corrosion Solutions. - PowerPoint PPT Presentation

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Page 1: Aqueous Corrosion Data

Corrosion Solution pH

2 4 6 8 10

Co

rro

sio

n R

ate

(g

/cm

2 *min

)

0

1e-7

2e-7

3e-7

4e-7

MAP BAP KBAP KMAP LG-770 LHG-8

Corrosion Solution pH

2 4 6 8 10

Co

rro

sio

n R

ate

(g

/cm

2 *min

)

0

5e-7

1e-6

2e-6

2e-6

KAP

Aqueous Corrosion Data

• Corrosion performed with ~1cm3 samples in 100mL of DI water, 1mM NH4OH, or 1mM HCl

• The lowest dissolution rates occur at neutral pH with basic conditions accelerating corrosion to a greater extend than acidic conditions

Page 2: Aqueous Corrosion Data

pH Changes of Corrosion Solutions

• Except for KAP see very little change for the acid and DI water solutions.

• The basic solution, however, shows a larger pH shift to go along with the increased dissolution rates on the previous slide.

Dissolution time (days)

0 5 10 15 20 25 30

pH

Ch

ang

e

-2.2

-2.0

-1.8

-1.6

-1.4

-1.2

-1.0

-0.8

-0.6

-0.4

-0.2

KAP MAP BAP KBAP KMAP

Dissolution time (days)

0 5 10 15 20 25 30

pH

Ch

an

ge

-0.2

-0.1

0.0

0.1

0.2

0.3

0.4 KAP MAP BAP KBAP KMAP

Dissolution time (days)

0 5 10 15 20 25 30p

H C

ha

ng

e

-2.5

-2.0

-1.5

-1.0

-0.5

0.0

0.5

KAP MAP BAP KBAP KMAP

1mM HCl pH 2.5 initially

DI water pH 6.0 initially

1mM NH4OH pH 10.5 initially

Page 3: Aqueous Corrosion Data

1/T (*1000 ºK)

0.0027 0.0028 0.0029 0.0030 0.0031 0.0032 0.0033 0.0034

ln D

iss

olu

tio

n R

ate

(g

/cm

3 *min

)-20

-18

-16

-14

-12KAP KMAP KBAP MAP BAP

Arrhenius Fit of Dissolution Data

23.0 (+/- 2.8)KAP

19.2 (+/- 2.9)MAP

18..4 (+/- 1.3)BAP

11.2 (+/- 0.73)KBAP

9.9 (+/- 2.3)KMAP

Ea (kcal/mole)Glass

23.0 (+/- 2.8)KAP

19.2 (+/- 2.9)MAP

18..4 (+/- 1.3)BAP

11.2 (+/- 0.73)KBAP

9.9 (+/- 2.3)KMAP

Ea (kcal/mole)Glass

• Samples were corroded at temperatures from 25 to 90ºC

• The data was fit to an arrhenius equation to calculate dissolution activation energies

• The table shows the calculated energies for several of the studied glass samples

Page 4: Aqueous Corrosion Data

Time (min)

0 1 2 3 4 5 6 7 8 9 10

Vo

lum

e o

f 0.

001M

NH

4OH

Ad

ded

(m

L)

0

2

4

6

8

10

12

14

16KAP KBAP KMAP MAP BAP

pH stat Titration of Glass Samples

8.61.8KAP

6.40.48KMAP

5.50.36KBAP

2.30.32BAP

4.20.22MAP

G (kcal/mol)SlopeGlass

8.61.8KAP

6.40.48KMAP

5.50.36KBAP

2.30.32BAP

4.20.22MAP

G (kcal/mol)SlopeGlass•The slope of the curves at longer times is compared to the free energy of hydration of the oxides in the table.

•The graph to right shows the pH stat curves for the glasses at a pH of 9.2.•KAP reacts at a much faster rate than the other glasses.

Page 5: Aqueous Corrosion Data

Initial Reaction of Glass Species

• The short term pH shift of the glass samples can give a description of the number of reactive groups on the surface of each glass sample.

• The samples shown here are for glasses with an initial pH 9.2

• KAP shows the most shift, with KMAP close.

Time (sec)

0 100 200 300 400 500 600

pH

( -

log

[H+]

)

8.4

8.5

8.6

8.7

8.8

8.9

9.0

9.1

9.2

KAPMAPKMAPBAP KBAP

Delta Ghydration (kcal/mole)

1 2 3 4 5 6 7 8 9

pH

Sh

ift

-0.2

-0.1

0.0

0.1

0.2

0.3

0.4

0.5

0.6BAP MAP KBAP KMAP KAP

Page 6: Aqueous Corrosion Data

Starting pH of System ( -log[H+] )

7 8 9 10

OH

Ad

sorb

ed b

y G

lass

(m

ole

s)d

uri

ng

fir

st 6

0s

1e-8

1e-7

1e-6

1e-5KAPKMAPKBAPBAPMAP

4 5 6 7 8 9

1e-11

1e-10

1e-9

1e-8

1e-7

1e-6

1e-5

pH shift measurements of Glasses

• Glass is added to a solution of desired pH and the shift in pH for the first 60s is measured. This is used to calculated the moles of OH adsorbed by the glass surface.

• While there is some scatter as of yet, it can be seen that KAP and KMAP appear to follow the same trend.

• The other glass are somewhat lower than this trend initially and all of the glasses begin to come together near a pH of 7.

Page 7: Aqueous Corrosion Data

Predominance Diagrams for KAP and KBAP

2 4 6 8 10 12

-6

-4

-2

0

2

Lo

g [

PO

43 ]

TO

T

pH

K +

K H P O 4

[ e ]T O T

= 1 0 0 .0 0 m M

[ K + ]T O T

= 1 0 .0 0 m M

[ A l 3 + ]T O T

= 1 0 .0 0 m M

2 4 6 8 10 12

-7

-5

-3

-1

1

Lo

g [

K+

] TO

T

pH

H 2 P O 4H 3 P O 4

K H P O 4

B a 3 (P O 4 )2 (s )

[ e ]T O T

= 1 0 0 .0 0 m M

[ B a 2 + ]T O T

= 1 5 .0 0 m M

[ A l 3 + ]T O T

= 1 0 .0 0 m M

[ P O 43 ]

T O T= 6 0 .0 0 m M

•For KBAP appear to see multiple stable phases present at lower pH, but only one system shown at basic pH•KAP on the other hand shows little other than the K+ ion for most of the plot.

•Further study of the diagrams may provide clues into the reactions affecting glass dissolution in each species.

Page 8: Aqueous Corrosion Data

Weathering of Glass Samples

Temperature (ºC)

50 100 150 200 250 300 350 400 450

Wei

gh

t L

oss

(%

)

86

88

90

92

94

96

98

100

5 Days10 Days14 Days

0 Days

7 hours3 Hours

1 Day

AdsorbedWater

ReactedWater

• KAP powder was weathered for different times at 80% RH and 50ºC

• Samples were removed and TGA experiments performed to determine weight loss

• Samples show two weight loss regions, possibly one due to surface adsorbed water and the other due to reacted species.

Page 9: Aqueous Corrosion Data

ERD for H depth profilesKAP Glass

(mole%: 30K20.10Al2O3

.60P2O5)

0.0E+00

5.0E+21

1.0E+22

1.5E+22

2.0E+22

2.5E+22

-0.2 0 0.2 0.4 0.6 0.8 1

Depth (microns)

Co

nce

ntr

atio

n (

H/c

m3 )

Unreacted

1 day, 50 deg, 80% RH

22 MeV Si+5 Elastic Recoil Detection

• ERD was performed on a series of glass samples to measure the hydrogen depth profiles as a function of corrosion time at 50ºC and 80%RH.

• After only one day of corrosion KAP has corroded beyond the depth limit of the ERD measurement.

Page 10: Aqueous Corrosion Data

ERD of KMAP and KBAPKMAP Glass

(mole%: 15K20.15MgO.10Al2O3

.60P2O5)

0.0E+00

5.0E+21

1.0E+22

1.5E+22

2.0E+22

2.5E+22

-0.2 0 0.2 0.4 0.6 0.8 1

Depth (microns)

Co

nce

ntr

atio

n (

H/c

m3 )

Unreacted

1 day, 50 deg, 80% RH

1 week, 50 deg, 80% RH

22 MeV Si+5 Elastic Recoil Detection

KBAP Glass(mole%: 15K20

.15BaO.10Al2O3.60P2O5)

0.0E+00

5.0E+21

1.0E+22

1.5E+22

2.0E+22

2.5E+22

-0.2 0 0.2 0.4 0.6 0.8 1

Depth (microns)

Co

nce

ntr

atio

n (

H/c

m3 )

Unreacted

1 day, 50 deg, 80% RH

1 week, 50 deg, 80% RH

22 MeV Si+5 Elastic Recoil Detection

• KMAP shows less water to begin with, but by 1 week of corrosion KMAP and KBAP have roughly the same depth profiles.

Page 11: Aqueous Corrosion Data

•Liquid Chromatography provides information about chain distributions..•The top figure shows the distribution for a series of weathered KMAP glasses.•Orthophosphate units replace longer chains with weathering.•The bottom figure compares the changes in average chain length for the KMAP and KAP glasses.

Corrosion Time (days)

0 2 4 6 8 10 12 14

Ave

rag

e C

hai

n L

eng

th (

# P

O4

an

ion

s)

2

4

6

8

10KAP KMAP

Chain Length (# PO4 anions, m indicates ring)

1 2 3M 3 4M 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29

Per

cen

t o

f to

tal P

ho

sph

oru

s

0

5

10

15

20

25

30

35 0 Days2 Days5 Days10 Days14 Days

Chain Distribution of Weathered Layer

Page 12: Aqueous Corrosion Data

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

x16

MAS-NMR of KBAP Weathering• The spectra on the left are 31P MAS spectra of the KBAP

glasses after 0, 1, and 7 days of corrosion at 50ºC and 80%RH.

• The spectra on the right are the 1H-31P Cp-MAS spectra showing the phosphorus resonances that interact with water in the samples.

• The water has very little effect on the overall spectra of the glasses and is mostly interacting with Q1 and Q0 units in the glass structure.

Page 13: Aqueous Corrosion Data

• The spectra on the left are 31P MAS spectra of the KAP glasses after 0, 1, and 7 days of corrosion at 50ºC and 80%RH.

• The spectra on the right are the 1H-31P Cp-MAS spectra showing the phosphorus resonances that interact with water in the samples.

• In this case the water has a large effect on the overall spectra showing a number of new resonances due to the presence of a variety of PO4-OHx units.

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

-100-5050 0 ppm

x8

MAS-NMR of KAP Weathering

Page 14: Aqueous Corrosion Data

2d spectra of the KAP 7 Day sample

• The 31P profile is on the x-axis and the 1H on the y-axis in the plot.• The 2D spectra shows the presence of two different species of water.

The 1H species at 5ppm is due to adsorbed water and can be seen interacting with a number of different phosphorus environments.

• The 15ppm 1H is due to more strongly interacting water, most likely in the form of P-OH only seen attached to most likely Q1 units.

Page 15: Aqueous Corrosion Data

-80-70-60-50-40-30-20-1070 60 50 40 30 20 10 0 ppm

KAP 7days

1H-27Al CPMAS

27Al Direct MAS

32,000 scans

-80-70-60-50-40-30-20-1070 60 50 40 30 20 10 0 ppm

KBAP 7days1H-27Al CPMAS

27Al Direct MAS

232,000 scans

27Al Spectra of Corroded Glasses

• 27Al spectra of KAP and KBAP show that much less of the Al is correlated to 1H in the corroded samples than in the bulk glass.

• Partially this is due to the limited reaction depth of the water, but may also be due to an inhibiting effect of aluminum keeping OH groups away from the phosphate species.

Page 16: Aqueous Corrosion Data

Thin Film XRD of Weathered Surfaces

2Theta (º)

10 20 30 40 50 60 70

Dif

fra

cte

d In

ten

sit

y (c

ps

)

KAP

BAP

KBAP

•KH2PO4 crystals on appear KAP surface and AlPO4 crystals on the surface of BAP and KBAP in addition to the KH2PO4 .

Page 17: Aqueous Corrosion Data

Additional Crystal Species

• What can be seen for the KBAP spectra is that additional species such as K2HPO4 and Al(OH)3 can be used to describe some of the peaks.

Angle 2 Theta (º)

10 20 30 40 50 60 70

Inte

ns

ity

(cp

s)

0

20

40

60

80

100

120K2HPO4 crystal

AL(OH)3 crystal

• Additional species such as Ba3(PO4)2, AlOOH, and Ba(OH)2 may also be present.

• At this moment, however, the low angle peak can only be due to AlPO4

Page 18: Aqueous Corrosion Data

Optical Microscopy Images of Fibers

• LG-770 fibers before and after dipping in LN2

• There appears to be no noticeable difference between the two fibers

• LHG-8 from the same pull showing a wide range of surface features.

• LHG-8 also showed no change in surface characteristics before and after LN2 dipping

• All fibers were corroded for ~3 weeks at 100% RH at room temperature

Before

After

Page 19: Aqueous Corrosion Data

Fresh Pulled Fiber 14 Days Drierite 14 days 100% RH

LG-770

LHG-8

AFM images of Glass Fibers

Page 20: Aqueous Corrosion Data

Failure Strain Data for 1 week• In the prior slide see that

LG-770 fibers show a small number of large corrosion points ~ 50nm in height and 1mm in diameter with little to no roughness of the surface other than that.

• LHG-8 exhibits more surface roughness, ~5nm, but lacks the large peaks seen in LG-770.

Relative Humitidy (RH%)

20 40 60 80 100

Fai

lure

Str

ain

(%

)

2.0

2.5

3.0

3.5

4.0

4.5

5.0

5.5

LHG-8LG-770

•Strength data for 1 week of corrosion at a variety of RH’s.

•Both glasses appear to follow the same trend.

Page 21: Aqueous Corrosion Data

Upcoming Work• Work planned for this spring and summer includes:

– Corrosion and Weathering of KCAP and CAP samples for comparison to the rest of the data. It may be that KMAP acts more like KAP due to some ionic radii comparisons which KCAP may give more insight to.

– Further NMR correlation measurements to determine which species are being preferentially attacked during the weathering process.

– pH stat and drift measurements in the acidic region to determine if the same trends continue.– Liquid NMR measurements of short term corrosion surfaces to determine the weathering

and hydrolysis rates of each glass surface.– Calculation of more predominance diagrams to look for the effect of stable solution species

on corrosion rates.– Further weathering tests in more humidity/temperature environments for trending of

corrosion.– Study of Iron phosphates looking specifically on the affect of modifier composition on the

corrosion stability of glasses.

• I am also looking at using this data to compare to some of the strength and fatigue measurements on glass fibers that Nate and Adam have performed to see if it can help explain some of their results.