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Svetsaren_nr2 definitief (Page 1) - Esab

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The susceptibility to localised corrosion also increases<br />

with rising temperatures and with increasing oxidising<br />

capacity of the environment. Strong oxidisers such as<br />

chlorine dioxide (ClO 2 ) and ozone (O 3 ) used in pulp<br />

bleaching, therefore play an important role from the<br />

point of view of localised and general corrosion<br />

susceptibility.<br />

The weld metal microstructure plays a major role<br />

with respect to local corrosion resistance. The<br />

corrosion behaviour of weld metal differs from that of<br />

the more homogeneous base metal that has been<br />

manufactured by rolling and subsequent heat treatment.<br />

A solidified weld metal, instead, remains in the<br />

”as-cast” condition, showing far more pronounced inhomogeneity<br />

than the base metal. The main reasons for<br />

this inhomogeneity are the microsegregation which<br />

takes place during weld solidification and the uneven<br />

partitioning of alloying elements between different<br />

phases during phase transformations. In high-alloyed<br />

austenitic stainless steel welds, the microsegregation of<br />

Mo and Cr in particular leads to a remarkably inhomogeneous<br />

weld composition. After weld solidification,<br />

the dendrite cores are, therefore, depleted in<br />

Cr and Mo, whereas the interdendritic regions are<br />

enriched in these elements. Consequently, the dendrite<br />

cores are more easily attacked in a chloride-containing<br />

environment, which results in inadequate corrosion<br />

resistance unless the weld composition is overalloyed.<br />

The corrosion resistance of a weld may also be created<br />

by the precipitation of Cr- carbides and intermetallic<br />

phases such as sigma-phase in the weld metal<br />

microstructure [1-7].<br />

To avoid the above mentioned problems, the weld<br />

composition is normally overalloyed to eliminate local<br />

underalloyed regions from the weld microstructure. To<br />

achieve this, it has been generally recommended to use<br />

Ni-based consumables when welding high-alloyed<br />

stainless steels. For example, the welding of 254 SMO -<br />

steel (6 %Mo) is usually carried out with a high Mocontaining<br />

(9 %Mo), Ni-base consumable. For 654<br />

SMO (7.5 %Mo), the Mo- content of the consumable is<br />

increased to 15 %.<br />

The use of overalloyed Ni-base consumables has<br />

some limitations, however. The weldability of these<br />

consumables is technically quite demanding, as a result<br />

of the more viscous weld pool behaviour, and a skilful<br />

welder is therefore needed to avoid weld imperfections.<br />

The weld fusion line may also show inadequate<br />

corrosion resistance due to the formation of an<br />

unmixed zone in the dissimilar joint, see Fig. 2. This is<br />

due to the fact that the unmixed zone solidifies in a<br />

similar manner as the base metal, leaving a pronounced<br />

microsegregation in this narrow weld region.<br />

General corrosion in highly oxidising<br />

conditions<br />

In highly oxidising conditions, such as in ClO 2 - bleaching,<br />

the dominant corrosion mechanism may change<br />

from localised corrosion to the so called transpassive<br />

Fig. 2. Schematic presentation of different weld zones [8].<br />

dissolution which causes general corrosion in the base<br />

and weld metals. The resistance to general corrosion in<br />

highly oxidising conditions depends not only on<br />

composition but also on pH, temperature, and on the<br />

oxidising potential (ClO 2 - content) of the environment.<br />

Research studies as well as practical experience<br />

have shown that Ni-base alloys and stainless steels<br />

display a different behaviour in ClO 2 -bleaching<br />

environments. With stainless steels, the transpassive<br />

corrosion rate increases with the oxidising potential of<br />

the environment as well as with increasing Cr-, Ni- and<br />

Mo- contents of the steel. At low pH- values (< 2),<br />

there is no striking difference between stainless steels<br />

and Ni-based alloys. As soon as the pH- value exceeds<br />

3, the transpassive corrosion rate of stainless steels<br />

decreases, while that of the Ni-based alloys increases.<br />

Consequently, the dissolution rate of Ni-based alloys is<br />

more pronounced in neutral solutions than in acid<br />

environments [9-12].<br />

Both Ni-based alloys and stainless steels display an<br />

increased transpassive corrosion in oxidising conditions<br />

when the Cr-, Ni- and Mo- contents of the alloys are<br />

increased. This is due to the fact that all these elements<br />

display more pronounced dissolution rates in oxidising<br />

conditions.<br />

General corrosion of welds in highly oxidising<br />

conditions<br />

To take account of the possibility of general corrosion,<br />

the composition of a weld metal must be optimised to<br />

minimise transpassive dissolution. This is important,<br />

especially when the localised corrosion resistance of a<br />

weld has been maximised with Ni-based consumables,<br />

without noticing any enhanced risk of general<br />

dissolution. There is clear evidence that, in oxidising<br />

and acidic conditions (pH = 3-6), Ni-based weld metals<br />

can display a relatively rapid general dissolution via<br />

transpassive mechanisms. Important alloying elements<br />

(Cr and Mo), which are added to increase localised<br />

corrosion resistance, as well as Ni added to maintain an<br />

austenitic microstructure, have shown to be harmful<br />

with respect to general corrosion resistance. This has<br />

led to development work on new welding consumables<br />

and welding techniques that take both corrosion<br />

mechanisms into account.<br />

It has been demonstrated experimentally that the<br />

40 • <strong>Svetsaren</strong> no. 2 • 2002

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