Aluminium amalgam (Al/Hg) Summary

G.Patton

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Introduction

Here you can find detailed information about aluminum amalgam, it's producing manuals from mercury nitrate or mercury chloride. There is a mercury nitrate synthesis manual with video instructions. Mercury chloride synthesis isn't described by reason that it's produce from mercury nitrate. Aluminum amalgam is one of a number of metal amalgams that is not described here for the reason that only aluminum amalgam is mainly used in synthetic routes of illicit drug production.

What is Amalgam

An amalgam is an alloy of mercury with another metal. It may be a liquid, a soft paste or a solid, depending upon the proportion of mercury. These alloys are formed through metallic bonding, with the electrostatic attractive force of the conduction electrons working to bind all the positively charged metal ions together into a crystal lattice structure. Almost all metals can form amalgams with mercury, the notable exceptions being iron, platinum, tungsten, and tantalum. Silver-mercury amalgams are important in dentistry, and gold-mercury amalgam is used in the extraction of gold from ore. Dentistry has used alloys of mercury with metals such as silver, copper, indium, tin and zinc.
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Aluminum can form an amalgam through a reaction with mercury. Aluminum amalgam may be prepared by either grinding aluminum pellets or wire in mercury, or by allowing aluminum wire or foil to react with a solution of mercuric chloride/mercuric sulfate. This amalgam is used as a reagent to reduce compounds, such as the reduction of nitro compounds to amines. The aluminum is the ultimate electron donor, and the mercury serves to mediate the electron transfer. The reaction itself and the waste from it contain mercury, so special safety precautions and disposal methods are needed. As an environmentally friendlier alternative, hydrides or other reducing agents can often be used to accomplish the same synthetic result. Another environmentally friendly alternative is an alloy of aluminum and gallium, which similarly renders the aluminum more reactive by preventing it from forming an oxide layer.

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Aluminum in air is ordinarily protected by a molecule-thin layer of its own oxide. This aluminum oxide layer serves as a protective barrier to the underlying aluminum itself and prevents chemical reactions with the metal. Mercury coming into contact with it does no harm. However, if any elemental aluminum is exposed (even by a recent scratch), the mercury may combine with it to form the amalgam. This process can continue well beyond the immediately exposed metal surface, potentially reacting with a large part of the bulk aluminum before it finally ends.

The presence of water in the solution is reportedly necessary; the electron rich amalgam will oxidize aluminum and reduce H+ from water, creating aluminum hydroxide (Al(OH)3) and hydrogen gas (H2). The electrons from the aluminum reduce mercuric Hg2+ ion to metallic mercury. The metallic mercury can then form an amalgam with the exposed aluminum metal. The amalgamated aluminum then is oxidized by water, converting the aluminum to aluminum hydroxide and releasing free metallic mercury. The generated mercury then cycles through these last two steps until the aluminum metal supply is exhausted.
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Preparation methods

Al/Hg amalgam from HgCl2 in MeOH solution
Set up a two-liter flat-bottom three-neck flask, and plugged one of the necks. Arrange a reflux condenser in the center hole. The apparatus was placed on stirrer/hotplate. Cut Reynolds Heavy Duty aluminum foil into about 1" squares, to make a total of 27.5g.
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5g of foil in 1" squares and 5g of foil and foil after 8-10 seconds of grinding in a Braun coffee grinder

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Closeup of foil balls and 27.5g foil in a 2000 mL flat-bottom flask

Put 5g batches into a small Braun coffee grinder and ground the foil for 8-10 seconds. The foil doesn't really get "ground", but it gets all balled up into little globs. This works amazingly well. It may sound weird to put your foil in a coffee grinder, but this is without question a breakthrough in the preparation of aluminum for the Al/Hg. Next, 400 mg of HgCl2 was dissolved in 750 mL of lab grade MeOH. When the MeOH was ready (all HgCl2 dissolved), it was also dumped in the flask and the condenser was put in place. It was stirred for 5-10 seconds every minute or so. In less than 10 minutes, faint bubbling was visible, the solution was gray, and the aluminum was distinctly less shiny. Some pieces had started to float. When the amalgam is ready, gas evolution stops.
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Amalgamation complete

Dry Al/Hg amalgam from Hg(NO3)2

We take 14 g of aluminum foil and tear it with our hands into pieces of 2x2, 3x3 cm in size. Be sure to tear, not cut, to increase the surface area. Place into a 3-necked round-bottomed flask and fill the foil completely with water.
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Now we are preparing the mercury salt. We take a mercury thermometer from the pharmacy, wrap it in paper, break it at the bottom tip. Pour all the mercury (~1-2 g) into a glass, where then add 4 mL of nitric acid (70%). Do not forget that mercury vapors are hazardous to health! To initiate the reaction, the glass had to be heated to about 50 degrees, stirring occasionally. All the mercury dissolved about for 30 minutes, and an orange gas, nitrogen oxide (IV), was released from the glass. The reaction equation is as follows:
Pipette 2 mL of the solution and place it in a round-bottom flask with foil. After about 5 minutes, the foil lost its shine, became dull, and a small layer of gray sludge (aluminum hydroxide) collected at the bottom of the flask. After 10-15 minutes, the reaction stops, this can be seen by the cessation of gas evolution.
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We drain the liquid and rinse the foil with water 3 times.
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Acetic essence is often used to produce hydrogen, but I "start" the reaction to produce hydrogen with water. Less acidic medium, which means less alkali must be added later. Many people ask the question: "How to remove this water?" There is no need to remove water anywhere, it reacts with aluminum and hydrogen is obtained: 2Al + 6H2O ---> 2Al (OH)3 + 3H2

How to use it

Al amalgam (Al/Hg) is widely used in reduction organic reactions of nitro-compounds to amines. Reduction reaction is a one-pot exothermic reaction with Al/Hg with organic unsaturated compound. Aluminium, water and mercury release hydrogen gas (H2) in reaction mixture and saturate organic compounds. You can meet Al/Hg reduction in most popular reactions such as Synthesis of amphetamine from P2NP via Al/Hg (video), Complete MDMA synthesis from sassafras oil, Synthesis and extraction of d-amphetamine (Nabenhower, 1942) and so on.
 
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Glede na wikipedijo je za proizvodnjo nitrata živega srebra(II) potrebna vroča in koncentrirana dušikova kislina, ali je to vseeno?
Reakcija z vročo dušikovo kislino je vsaj videti bolj burna, nastane veliko plina in to ni trajalo 10 minut.

Ali je pri živosrebrovem(II) nitratu in aluminiju treba upoštevati kakšno razmerje? Ali kako lahko določite pravilno količino, da dobite ustrezen amalgam.

Ali je napaka, če je v 0,1 ml raztopine dušikove kisline raztopljenih približno 50 mg nitrata živega srebra(II)? Ker sem prebral, da morate uporabiti kislo raztopino, da preprečite obarjanje produktov hidrolize.
Ali so še kakšne druge možnosti?
 

G.Patton

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Pozdravljeni
odgovor:

Približno razmerje je od 1:1300 do 1:650 (živosrebrov(II)nitrat proti Al v molih).
Ta kislina aktivira površino Al folije, da se začne reakcija s Hg. Veliko kisline bo pokvarilo izdelek za redukcijo. Ni je treba uporabljati.
Katere produkte hidrolize imate v mislih?
 

ACAB

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ok, torej ni nobene razlike, ali živemu srebru dodamo vročo dušikovo kislino ali hladno in jo nato segrejemo. Verjetno je druga metoda nežnejša.

To je razmeroma velik razpon, pri 50 g Al bi to pomenilo količino od 0,4 g do 0,9 g. Zdaj pa vem, zakaj povečanje krme ni dalo veliko večjega izkoristka, veliko premalo soli za tvorbo amalgama. Najlepša hvala!

Ali je bolje dati več živosrebrovega(II) nitrata ali le toliko, kolikor je potrebno? Vedno sem domneval, da je amalgamacija verižna reakcija, ki potrebuje le potisk, da popolnoma odreagira.
Kaj pomeni veliko kisline? Kisla raztopina pomeni, da imam v raztopini malo več kisline, kot je reagiralo.
Raztopil sem 21 g živega srebra v 70 ml 60 % HNO3, kar bi moralo dati koncentracijo 0,1 ml kisle raztopine na približno 50 mg nitrata živega srebra(II) in bi dal približno 50 ml HNO3 preveč.
To bi pomenilo približno 1 ml (0,5 g soli) kisle raztopine na 50 g Al. Ali je to že preveč kisline?
Mislim, da to pomeni monohidrat, oktahidrat in hemihidrat.
 

G.Patton

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Potrebna količina bi bila boljša, presežek Hg soli bo povzročil več odpadkov, ki vsebujejo Hg.
Mislil sem presežek kisline, vaša količina je v redu.
Mislim, da lahko presežek kisline upočasni reakcijo nastajanja Hg in Al(OH)3 v skladu z Le Chatelierjevim načelom.
 

ACAB

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Ok, razumem, tako da mi ni treba skrbeti zaradi produktov hidrolize, ampak da odvečna dušikova kislina zmoti mojo amalgamacijo.

Ravnal sem zelo teoretično po načelu želim 50 mg na 0,1 ml raztopine in vzel to formulo ter izračunal ostalo:
3HG + 8HNO3 --> 3HG(NO3)²+...+....
601,77g+504,08g -->1027,86g +...+...
2,93g+2,45g -->5g +...+...
5g nitrata živega srebra(II) + 10ml HNO3 = koncentracija 0,05g/0,1ml
70 ml HNO3 torej zahteva 21 g živega srebra.
Od 70 ml HNO3 bi moralo reagirati 17,15 g = 12,55 ml, preostanek (57 ml) pa bi bila kisla raztopina.

Kako bi bilo najbolje shraniti pripravljeno raztopino?
-Ali lahko dušikovo kislino destiliram? Kaj bi ostalo, čista živosrebrova sol? Vendar bi bilo to zaradi majhne količine zagotovo predrago.

-Ali naj raje dodam živo srebro in vse skupaj segrejem, da dobim večjo koncentracijo živosrebrove soli in manj kisline?
 

G.Patton

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Naredili ste napačno reakcijo in s tem tudi količine reagentov. Oglejte si mojo temo zgoraj, tam je pravilna reakcija.
Zatesnite jo nepredušno in jo postavite v hladilnik
Teh postopkov vam ni treba opraviti, človek. Če želite rešiti Hg v HNO3, ga morate segreti. Uporabite lahko povratni hladilnik, da se izognete izhlapevanju kisline.
 
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ACAB

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Toda gospod, reakcija
HG + 2HNO3 --> HG(NO3)² +NO2 + H2O
iz vašega prispevka ne more biti pravilna,
HG + 2HNO3 --> HG(NO3)²+ H2 bi bila pravilna, če bi bila, vendar bi verjetno morala biti ->
HG + 4HNO3 --> HG(NO3)² + 2NO2 + 2H2O, sicer število molekul na obeh straneh ni pravilno, manjkal bi en dušik in trije kisiki. Ali se strinjate z menoj glede tega? V vsakem primeru nastane dušikov dioksid (NO2), s čimer se 100 % strinjam, saj sem ga čutil.
Moja reakcija z dušikovim oksidom (NO)
3HG + 8HNO3 -->3HG(NO3)² + 2NO + 4H2O
bi bila prav tako pravilna, glede na število molekul, vendar je dušikov oksid brez vonja, zato to ne more biti prav, moja napaka.

Nimam pojma, zakaj lahko najdem toliko reakcij za HG + HNO3 in katera je prava.
Mislil sem, da moja raztopina ni prava, da je preveč kisla, vsaj tako sem vas razumel, in pomislil sem na dva načina "reševanja" moje raztopine, destilacijo ali koncentrat. Toda...
Kot ste pravkar zapisali, se zdi, da to navsezadnje ni potrebno.

Novo reakcijo bom potem, če se strinjate z mano, uporabil za izračun v prihodnosti, da določim pravilno količino živosrebrove soli.
 

G.Patton

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Da, imate prav! To je točno tako. Hvala za vaše obvestilo. NO2 je pravilen izdelek, rjav plin.
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Ohh, opravičujem se za nesporazum. Kislino lahko uparjate, vendar uporabite dobro prezračevani prostor in masko z rokavicami!
 
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diogenes

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Pozdravljeni Patton, poskusil sem dati folijo v mlinček za kavo (v skrajnem obupu), vendar nisem bil prepričan, ali bo delovalo, zato sem majhne kroglice pustil ob strani, potem pa sem prebral vaš zgornji prispevek in mi vlil novo upanje. Moje vprašanje je, ali se lahko uporablja tudi pri običajni metodi amalgamiranja ali samo z MeOH. To bi mi rešilo življenje, saj je raztrganje vse te folije zelo naporno. Hvala,
 

G.Patton

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Pozdravljen, Diogenes. Da, lahko.
 

diogenes

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Kako naj vem, kdaj so majhne kroglice (ki jih naredi mlinček za kavo) amalgamirane in pripravljene za uporabo. Na katere znake moram biti pozoren?

Ali prav tako dobro razumem, da reakcija pri uporabi metode z mlinčkom za kavo potrebuje več folije? Če da, kakšno je razmerje po vaših izkušnjah?
 

G.Patton

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Barve in mehurčki: V tem primeru je treba upoštevati tudi pravila, ki jih je treba upoštevati v kemijskih analizah. Ko je mehurčkanje končano, je pripravljeno za uporabo
ga morate prešteti po masi, rezanje in mešanje v mešalniku, ki se uporablja za povečanje kvadrature površine
 
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diogenes

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Hvala, Patton, poskusil bom in uporabil bom enako težo folije (čeprav je videti veliko manj kot to in eno uro krajši čas :) ).
 

MadHatter

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Zanima me, ali lahko namesto folije ali koščkov uporabimo aluminij v prahu? Nekaj takega, kot je nemški temni prah (200 očes - 2 mikrona). Če ga zmešate z živosrebrovim nitratom, kakšen bi bil rezultat?
 

ACAB

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Prebral sem, da ni tako dober, ker iz prahu ne moreš dobiti dobrega amalgama, ker prehitro reagira, sam ga še nikoli nisem poskusil, vedno pa se uporablja folija.
 

MadHatter

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Ok, zanimivo. Kje ste to prebrali, z veseljem bi to prebral tudi jaz! Pričakujem, da bo reakcija naravnost nasilna, kot so običajno reakcije z alu prahom, toda zakaj bi moral reakcijski čas vplivati na končni izdelek?
 

ACAB

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Žal ne morem zagotoviti povezave, mislim, da je bilo na starem forumu. Zagotovo nisva edina dva, ki meniva, da večja kot je površina, ki lahko reagira, potem je bolje, vendar v tem primeru verjetno ni tako, saj praktično vsi kuharji vedno delajo s folijo. Zakaj točno, ne morem povedati, žal mi je. Morda bi kakšen strokovnjak lahko odgovoril, zakaj se tu ne uporablja prah, ampak folija.

Reakcija lahko poteka tudi prehitro. Na primer, pri nadzorovani reakciji, ki enakomerno poteka dalj časa, je lahko pretvorba snovi veliko popolnejša kot pri kratki nasilni reakciji.
 

MadHatter

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Ah, okej, razumem. Ravno sem mislil na reakcijo za nastanek aluminijevega amalgama. Ampak potem je tu še redukcija P2NP ... Tu bi bil amalgam v prahu morda prehiter za delovanje.
 

ASheSChem

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za tehniko termometra potrebujemo le 70-odstotno dušikovo kislino ? (ni v redu za 60/65/69,5 %... ni enaka cena)
 
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