MATSE 403 Paper

5
MATSE 403Final Paper Part III: Stateof theart Advances/ Production/ Synthesis Daniel Cook Introduction  As mentioned in previous portions of  this paper, Magnesium is an ideal candidate as a biodegradable material. It is highly biocompatible (approximately threehundred milligrams per day is the recommended daily intake), has a high primary stability, and has a superior strength to weight ratio. Even with such promising characteristics Magnesium has yet to make a significant contribution in the field biomaterials. A major factor preventing its application is its high rate of  corrosion invivo. High rates of  corrosion are the source of  two problems. First, magnesium corrodes invivo through the following equation:  2  As can be seen from this one mole of  magnesium produces one mole of  hydrogen gas, causing a large accumulation of  subcutaneous gas bubbles. The second issue with high corrosion rates is the tissue the implant is supporting will not have sufficient time to heal before the implant completely corrodes. This is most evident in bone fracture and stent use. Both bone and arteries require approximately six weeks to fully heal, meaning the implant must last this amount of  time. This section of  the paper will look at what methods are being investigated to control the problem of  rapid corrosion.  Alloying  Alloying magnesium with more corrosion resistant materials is the first method being investigated. Two of  the main alloys currently being researched are WE43 and AZ91D. The composition of  these alloys are as follows: WE43 Element Weight Percent Yttrium 4.11 Neodymium 2.28 Rhenium 0.98 Zirconium 0.45 Dysprosium 0.27 Magnesium 91.91  AZ91D Element Weight Percent Aluminum 8.1 Zinc 1 Silicon 0.3 

Transcript of MATSE 403 Paper

Page 1: MATSE 403 Paper

8/8/2019 MATSE 403 Paper

http://slidepdf.com/reader/full/matse-403-paper 1/5

MATSE 403 ‐ Final Paper

Part III: State ‐of ‐the ‐art Advances/ Production/ Synthesis

Daniel Cook

Introduction

As mentioned in previous portions of this paper, Magnesium is an ideal candidate as a biodegradable

material. It is highly biocompatible (approximately three ‐hundred milligrams per day is the

recommended daily intake), has a high primary stability, and has a superior strength to weight ratio.

Even with such promising characteristics Magnesium has yet to make a significant contribution in the field biomaterials. A major factor preventing its application is its high rate of corrosion in‐vivo. High rates

of corrosion are the source of two problems. First, magnesium corrodes in‐vivo through the following

equation:

2 ↔

As can be seen from this one mole of magnesium produces one mole of hydrogen gas, causing a large accumulation of subcutaneous gas bubbles. The second issue with high corrosion rates is the tissue the

implant is supporting will not have sufficient time to heal before the implant completely corrodes. This

is most evident in bone fracture and stent use. Both bone and arteries require approximately six weeks to fully heal, meaning the implant must last this amount of time. This section of the paper will look at what methods are being investigated to control the problem of rapid corrosion.

Alloying

Alloying magnesium with more corrosion resistant materials is the first method being investigated. Two of the main alloys currently being researched are WE43 and AZ91D. The composition of these alloys are as follows:

WE43Element Weight Percent Yttrium 4.11 Neodymium 2.28 Rhenium 0.98 Zirconium 0.45

Dysprosium 0.27 Magnesium 91.91

AZ91DElement Weight Percent Aluminum 8.1 Zinc 1 Silicon 0.3

Page 2: MATSE 403 Paper

8/8/2019 MATSE 403 Paper

http://slidepdf.com/reader/full/matse-403-paper 2/5

Manganese 0.13 Magnesium 90.47

There are two methods used to produce these alloys, depending on the intended application. The first method is die casting. This method is used when the implant needs to be a bulk metal, such as when

the implant is used for bone repair. Die casting involves heating the metals until they reach a molten state. Pressure is then used to force this liquid into a mold where it cools and hardens, forming the

alloy.

The second method for production is electron beam physical vapor deposition. This method is preferred when the alloy must be very thin (micrometers range), or when the implant must have a very specific surface morphology. These requirements are common to stent use. In this method electrons ejected

from a charged tungsten filament bombard the metals, causing them to vaporize. The vapor containing

the metals then precipitates, forming a thin solid alloy.

The purpose of adding these metals to pure magnesium is that they provide electrochemical protection, as well as acting as hardeners. From an electrochemical perspective, all of the listed alloying metals are

more noble than magnesium thus providing cathodic protection. From a physical point ‐of ‐view many of the metals, specifically aluminum, zinc, and the rare earth metals cause solid solution strengthening.

Solid solution strengthening helps prevent dislocations from easily sliding, thus increasing the yield strength of the material.

The benefit of alloying can be seen by looking at table x which displays the experimental corrosion rate

of both WE43 and AZ91D tested in simulated body fluid at thirty seven degrees Celsius.

Alloy Corrosion Rate (mm/year) AZ91D 2.8 WE43 6.9 Pure Magnesium 105

Coatings It is immediately apparent that the addition of alloying elements significantly decreases the rate of corrosion. However even with such drastic drops in corrosion rate, some issues still remain. While bulk

metal applications can typically be made thicker to increase the amount of time before total

degradation, applications of thin films typically have very tight space requirements meaning increasing the thickness of the implant is not viable. This is where another, more recent, research topic in magnesium biomaterials has taken hold. This new topic involves the formation of a very thin coating on top of the magnesium implant.

Page 3: MATSE 403 Paper

8/8/2019 MATSE 403 Paper

http://slidepdf.com/reader/full/matse-403-paper 3/5

The idea make the

corrode fi The first

magnesiusolution f

Experime

showed atable y.

Material Pure MaAZ91D Magnesiu

Another

increases

The hydr

to keep t

ehind provi

coating mat

rst, saving th

oating being

m thin films. or twenty ‐fo

ntal corrosio significant d

nesium

m with Hydr

enefit to the

cell prolifera

xide coating e pH in a via

ing a thin su

rial more co

e magnesiu

investigated

It is formed r hours. Th

rate measu

ecrease in co

oxide Coatin

hydroxide ction on its su

accomplishe

ble range, as

rface coating

rrosion resist implant fro

is magnesiu

by soaking a coating is f

2

rements for rrosion, even

ating is not

rface. This ca

s this cell pro

well as provi

on top of thant than sta

immediate

hydroxide.

magnesium rmed throu

hin film mag when comp

Corrosi105 2.8 0.252

nly the bioc

n be seen in

liferation by ding a better

e magnesium

dard magne corrosion.

This coating

hin film in oh the followi

nesium treat

ared to untr

on rate (mm

ompatibility

figure z:

decreasing h surface for

or magnesi

sium. This co

is very easy

e molar soding reaction:

ed with the ated alloys,

/year)

of the coatin

ydrogen gas ell adhesion.

m alloys is tating will the

to synthesize

ium hydroxid

ydroxide co

ummarized i

, but it actu

evolution, h While the

n

on

e

ting n

lly

lping

Page 4: MATSE 403 Paper

8/8/2019 MATSE 403 Paper

http://slidepdf.com/reader/full/matse-403-paper 4/5

coating st

over untr

The seco

first appl

then immthis coati

This coati

little sup

following magnesiu

This figur

magnesiu

applied.

In additio

advantag

expandin

environm

coating hcan be ill

ill lacks the ceated magne

d coating ga

ing a hydrox

ersed in a fog is:

ng is still in itorting corro

figure comp

m:

shows that m. The coat

oth these fa

n to the theo

. In applica and contra

ent to by ‐pa

wever, thes

strated as:

ell density of

sium.

rnering atten

ide coating aty percent h

s infancy sta

ion rate evid

res the brea

the breakdo

d sample al

ctor generall

retical reduc

ions such as ting of blood

s the coatin

e cracks natu

the simulate

tion is a mag described adrofluoric a

es in terms ence. Howe

kdown volta

n voltage is o has a lowe

y correspond

tion in corro

stents, the c vessels caus and directly

rally passiva

d body fluid,

nesium fluor

bove. Once

id solution f

2 →

f being used

er some ele

es of pure m

much higher

r current den to a lower c

ion rate, the nstant mech

e cracks to f attack the pe and form t

it still provid

ide coating. his coating i

or ninety ‐six

as a corrosi

ctrochemical agnesium to

for the fluor

sity through

orrosion rate

fluoride coa

anical strain rm in the co

ure magnesi

he hydroxide

es a significa

This coating i applied to t

hours. The r

n inhibitor, analysis has the fluoride

ide coating tout the rang in practice.

ting also pro

put on the iating. These

m implant. coating expl

nt improvem

s produced bhe implant, ieaction form

o there is ve

been done. coated

an the unco of voltages

ides a mech

plant from tcracks allow

ith the fluo

ained above.

ent

y is

ing

ry he

ated

nical he the

ride This

Page 5: MATSE 403 Paper

8/8/2019 MATSE 403 Paper

http://slidepdf.com/reader/full/matse-403-paper 5/5

Conclusi

As can be

rate of co

as a biod

stage. Ad

coatings i

on

seen, alloyin

rrosion to an

gradable ma

ditional corr

n‐vivo to pro

g and the ap acceptable lterial. Howe

sion data fove biocompa

plications of evel. These ver more res

r the coating

tibility.

oatings to pdvances giv

earch must b must be ob

ure magnesi great promi

e done befo

tained, as we

m can signifi

se to the fut

re it reaches

ll as testing

icantly alter tre of magne

a commercia

f the alloys

he sium l

nd