2020 - MD&A MENTIONS -
Typically, at brine well locations, a shallow, fresher groundwater zone is first encountered, which is underlain by a transitional interface with increasing salt concentrations leading to consistent brine concentrations at depth.
WHAT, IF ?
PE ( Schlumberger ) kept the cores for soil analysis...
check the Li content in the soils, from / surface to initial shallow aquifer.
What if there was a span of, 50m to the first, aquifer and soils contained Li ?
Could my idea of pumping brines from lower strata - check for other Li bomds, then,
extracting ( lithium ) using plant tech - treating the spent brine to a state of deionized water with a fortification of ozone, for higher odds of...creating new ( multi - bonds ) then, impregnating the 0 - 50m upper strata, allowing the treated water to seep down to the shallow - aquifers - enriching these, aquifers with the intent to, pump and exploit more lithium.
Another idea...
is simply pumpimg up the shallow ( brines ) stripping the brines of, mimeral - bonds
converting to deionized water, with addition of ozone injection - and redistributing the
hybridized water back into the shallow aquifers...allow, to sit and allow the hydrogen molecule
+ oxygen + ozone...to do its job of rebonding with - sediment comtact zones...to ultimately
rebomd with more minerals...the key here is...the above formula oc pure water with ozone,
has several - free - vacant seats - which allow new mimerals to bond.
For example - if one were to send downhole mimeral water, expecting thecmimeral water, to
Bond with more lithium...it would not be feasable due to the mimeral water has already occupied bomds with the waters molecules...hence, strippimg the water, to a free unbomded deionized state...allows for new bomds, to occur.
Has PE ever...
checked the brines for, sodium lithiim bonds...?
Lithium could have formed a, tetrabond...whereas the lab may, miss the triad - bomd
and pass it off as, sodium chloride brine.
Also...if tenova is on thier game...
if there's sufficient sodium chloride in the brines...
One could postulate the sodium might have stooen the chloride bond quicker than the, lithium.
Think of it as...some salts bond, quicker, easier, than, another...maybe sodium is, quicker,
than lithium...
If so...then, another idea would be...to target the sodiim chloride, in a deparate extraction phase
and separate the chloride bond from the sodium....since each are, indigenous from the basin,
one could have a chloride value in,which to use back down, hole...to admimister to key areas
to bond more lithium... making use of what is already there, to assist with extraction.
Also....( gotta laugh ) i had forgot PE had acquired nevada lithium's + advantage lithium claims
that are, adjacent, to albermarle...interesting.
Which brings up the subject of...
I hope, Schlumberger considers revising the PEA and tacks on these exrra brine, holes, from nevada, energy and advantage....and also, factors in, retesting all former holes, testing the brine with an acid at least 10% dilute, to see if anyblithium was hiding with another bond...then, take a poke at, acreassesment of 2017 resource estimate, to see if they can reinstate the amount of, lithiim brime without a restriction on, amount of brines - due to the use of a - plant extraction - which llows for brines to be resent back down hole.
Lastly, in the 2018 PEA ...
Mentions, the basin is a closed basin - and pitch of aquifers slopes to albermarle.
if this is at, all accurate - it would mean the brine comes from PE's claims and streams towards
albermarles....so how is it the southern brine ( holes ) revealed weaker brines, while albermarles
are, 300 ppm ?
If the aquifers run from PE's side...then, pe should also have 300 ppm.
hence = retest the, older plugged brine holes with a 10% - dilute acid added to the, brines.
see if the lithium, was hiding with in a bond to another element
Wango~
Excuse the typos...cracked screen on tab...
But also, the ecitor box has a hyper text going, on.
Seems to change my words even when typing....grrr...