Yes, the solution will be salts of metals and the acids at pH7.
Our drinking water still contains metals at PH 7 , so saying the solution has No metals, absolutely none, is just not true, luckily most of our drinking water is treated by the earth for our wells, and by water technicians for city waters, and the toxic heavy metals have been removed for the most part making water safer to drink.
What is flushed into a sewer by the people living upriver is treated for drinking water by the people living downriver.( living in the city downriver you can just hope that man is doing his job properly), and they are not contaminating your drinking water and their sewer facilities are working upriver, and also they are doing their job properly.
If you drink from a well or a spring just hope your neighbor is not dumping salts from his attempts to learn to dissolve metals in acids, thinking his solutions are safe to dump on the ground that makes his roses grow big and pretty from the all of the metal nitrate salts involved...
metal + acid = salts
salt of the metals and acids
What you dispose of is not gone.
If I have an acidic solution with heavy metals the solution will contain metal cations and the acids anions along with the acidic hydronium ions in solution H
3O, basically, ions of any metal or metal ions of that alloy previously involved some of these metals we may need to stay healthy (in small quantities) can be toxic to our environment or our health in larger quantities, several of the metals we are involved within our scrap metal alloys or electronic or other scrap are heavy metal poisons.
Once we put metals and acid together in solution, all kinds of reactions can be taking place with byproducts forming in solution.
Evaporating an acidic solution can besides evaporate water, drive reactions forward, drive the more volatile components out of solution and begin to push out the metal and acid ions as the lesser soluble salts crystalize out of solution, one acid and metal can push another acid out of solution and even change the metal salt involved in solution...
Many of these ionic salts of metals and acids can be insoluble salts,( see solubility rules) others are fairly soluble but can be pushed out of solution by an overload of how many ions the concentrated solution can hold, just as adding table salt to hot water there comes a point where the ionic solution will hold not more ions and adding more salt it leaves NaCl in the bottom of the glass, the temperature also plays a role on the solubility of metal salts
If I use copper to cement and recover the values from solution, I still have an acidic copper solution with the other toxic heavy metals left in this acidic solution (any metal that was involved in the alloy of the scrap being dissolved).
Adding iron metal will displace most of the copper ions from solution converting them to copper metal, as the iron and its metals alloys dissolve into solution as ions, as iron gives up electrons to the copper ions...
Besides copper the iron will displace other metals from solution (basically contaminating the copper powder with toxic heavy metals) metals Like Cadmium, cobalt, nickel, lead, antimony, arsenic, bismuth can contaminate the copper metal and salts of metal dragged down with everything else...
Now adding sodium hydroxide will help to convert the acids to salts, depleting the hydronium ions involved in the solution, raise the pH, and begin to form metal hydroxides. as you raise the pH towards being more basic many metal ions will become more insoluble to the point we can begin to remove them as salts of the metals and or hydroxides of the metals. as we raise the pH to PH7 (neutral many of the metal salts become more insoluble metals like iron form hydroxides and precipitate out of solution given time along with more of the copper ions metals that give strong color to the solution...
Even though the solution may become more clear with most of the copper and iron which give color removed at this pH of 7 (neutral) we are not done removing the toxic heavy metals,.
Many metals that may precipitate in a basic solution (when we add hydroxide or an alkaline solution) and then they can dissolve again as we add more caustic soda or alkali's redissolving the precipitate to form soluble metal hydroxide or metal complexes, they may precipitate being slightly basic and then dissolve again as the solution becomes more basic the amphoteric metals.
we need to raise the pH even further to remove more toxic metals, viewing the chart
We see:
Ferric ions (iron) are least soluble somewhere around pH 4.
Copper and chromium least soluble around pH 7 to 8, with chromium being amphoteric begins to redissolve back into solution as we raise the pH to make the solution more basic.
Zinc, nickel, cadmium, and lead are at their minimum solubility at around pH of 10 to 11, with lead and cadmium being amphoteric...
Silver complexes may stay in a solution that is extremely basic, but then we are not discussing silver complexes here.
So raising our waste solution to pH 10 or 11 we can precipitate out most (but not all) of the heavy toxic metals like zinc, nickel, and lead.
Then lowering the pH to 7-8 to precipitate metals most of (but not all of ) the remaining copper and chromium
we do not remove all of the metals in the process, we do not eliminate all of the heavy toxic metals, but we make the solution safe to dispose of (properly) making the solution a much less toxic salt solution.
I go a step further and evaporate my salt solutions to dry salts (some then reused, and other are disposed of properly).
The cemented metals like your copper are not pure and contain other metals and salts of metals that may be more toxic than the metal you cemented from solution, to begin with...
The hydroxides and salts can be dried and disposed of properly, normally, and legally that is all that is normally required before properly disposing of the hydroxides.
Even though they are fairly insoluble now does not mean they are not still water-soluble, so here I also go a step further than necessary dealing with my waste, I roast the hydroxide red hot in an oxidizing environment in order to convert these metal hydroxide salts to the more stable oxides.
Note we did not remove all of the toxic metals from the solution this salt of the acid still holds very reactive metals and traces of toxic metals...
Further discussion not related to our waste treatment:
we do not need to, for our waste, but we could remove more of the traces of the toxic metals using sulfide precipitation and then chelating agents and fine filtering to remove more of the ions from our salts solution.
The remaining salt solution after we are done beside very reactive metals, sodium, potassium, or other reactive metal ions (cations), we also have the ions of the acids left in solution, nitrates, chlorides, sulfates, fluorides or whatever the solution involved with previously in the pot we made this mess in...
To further treat the solution to make it purer the use of Ion exchange is often used which can displace one metal for another metal ion, which may become more insoluble at a different temperature or pressure or will react chemically different.