[Ferro List] More On tom's crud Testing (Keith)
Keith B
ferroist at comcast.net
Mon Jan 14 18:39:18 MST 2008
Hi Chris
There seem to be several potential or actual problems. The intent is to
end up with steel wire reinforcement which is durable in a sound and
durable OPC mortar matrix. It's probably desirable that the
reinforcement be strongly bonded to the matrix, but both because it's a
mesh and for reasons related to ligament behavior and as considered for
fiber reinforcement, that might be questioned.
Bearing the above in mind, the galvanizing is there to protect the steel
from rusting. It's assumed that it will passively isolate the steel
from the matrix environment and, if/when penetrated, protect it
sacrificially by galvanic action. It should not compromise the matrix
chemistry. Some loss of bond strength is expected and viewed as
unfortunate. It's known that bright zinc reacts rapidly with aqueous
calcium hydroxide, but assumed that action stops due to a self formed
barrier and/or change from slurry to a solid state environment.
In the real situation, the wire is vigorously flexed, probably impacted
and certainly exposed to abrasion as mortar is forced and vibrated both
past and against it. The mortar may not be a simple OPC mix, and that's
not well defined anyway regarding major let alone trace components.
Its cure is protracted to a notional solid state, but has known solid
state slow reactions in late cure which may or may not preserve a high
pH which is protective of steel - but a steel/zinc sandwich?...? Then,
of course, the OPC dries porous, very porous if workability has driven
the w/c ratio up, porous and structurally impaired if drying is too
fast. Late porosity allows water and atmospheric gases to act, plus
access by electrolytes, and any developed "crud zone" a damp water
channel adjacent the metal.
Considering all the above, one is inclined to question the wisdom of
galvanized versus plain steel, but if galvanized is to be used, it's
clear that the zinc must have protection at least through first cure. A
natural thin oxide/hydroxide coating may suffice, and one may maneuver
to limit the problems from its fragility. An all fines mix with rounded
particles would help, as might laying up the mesh and leaving it
unmolested for enough time for a displaced film to reform before
mudding, and certainly designing reinforcement to minimize need for
vigor to flood it with matrix. Martin Iorns technique is notably
gentle, for instance, and fewer layers and/or larger holes would help
for chicken wire or hardware cloth. Other than that, one's looking for
either a stronger and more tenacious thin barrier, or a thicker but
flexible one.
A hard barrier pretty much has to be thin to conform to flexure of the
wire and avoid the flaking likely with thicker coats. Ideally, it would
bond with the zinc and rapidly bond with curing OPC to both maximize
long term bond and rapidly recruit an incremental resistant coating to
further defend it. As it happens, a chromate coating does exactly that
and may be unique in doing so. Further, chromate ions adjacent zinc or
iron will preferentially plate out on their surfaces to molecular but
chemically protective thicknesses. There are other thin coatings, like
silica deposited from silicates, which offer chemical protection, but
they aren't easy to apply nor potentially self healing.
A "thick" coating could offer passive protection from gases,
electrolytes and other chemical action, and though soft enough to
conform to wire flexure, and actually offer mechanical protection during
emplacement. The downstream trade-off though, would likely be poor or
no bond to the matrix. That's what you get with vinyl or epoxy coated
steel. (How long does it take for a vinyl coated cyclone fence to
rust?) There is perhaps one interesting candidate though. That's
asphalt deposited from an emulsion. Further, it's probably possible to
spike such an emulsion with chromate; one could certainly asphalt coat a
chromated wire; and, one could probably dope asphalt with solids which
bond with OPC. As prepared in emulsions, the asphalt is a viscous
liquid becoming an amorphous solid. Leave it months to decades, and it
slowly crystallizes to a hard, bitumen solid - still clinging
tenaciously in air and watertight bond to its substrate. Deposited from
emulsion, it's a water displacer, and it bonds strongly to dry rust.
Doping with chromate or prior chromating should result in strong bonding
to zinc.
kb
Christopher Glasspool wrote:
> Keith or anyone having an idea on this:
> Seems to me that if galvanized material could be passivated by exposure to the elements then some other less innocuous material might be used to passivate the zinc other than adding chromium trioide to the mix design . Do you think wetting the galvy mesh with an acid or alkaloid might pre-passivate in a more efficent and speedy manner? Lime water maybe? Thanks, chris
>
>
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