Lead(II) nitrate: Difference between revisions
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| ExternalSDS = [http://www.inchem.org/documents/icsc/icsc/eics1000.htm ICSC 1000], [http://www.mallbaker.com/americas/msds/english/L3130_msds_us_Default.pdf MallBaker MSDS] |
| ExternalSDS = [http://www.inchem.org/documents/icsc/icsc/eics1000.htm ICSC 1000], [http://www.mallbaker.com/americas/msds/english/L3130_msds_us_Default.pdf MallBaker MSDS]{{dead link|date=September 2017 |bot=InternetArchiveBot |fix-attempted=yes }} |
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| EUClass = Repr. Cat. 1/3<br />Toxic ('''T''')<br />Harmful ('''Xn''')<br />Dangerous for the environment ('''N''') |
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In 1597, the German [[alchemy|alchemist]] [[Andreas Libavius]] first described the compound, coining the medieval names of ''plumb dulcis'' and ''calx plumb dulcis'', meaning "sweet lead", because of its taste.<ref name="libavius">{{cite book|first = Andreas|last = Libavius|authorlink = Andreas Libavius|title = Alchemia Andreæ Libavii|location = Francofurti|publisher = Iohannes Saurius|year = 1595}}</ref> Although originally not understood during the following centuries, the [[decrepitation]] property of lead(II) nitrate led to its use in matches and special [[explosive material|explosives]] such as [[lead(II) azide|lead azide]].<ref name="pyrotechnica">{{cite journal|title = Lead nitrate as an oxidizer in blackpowder|journal = Pyrotechnica |volume = 4 |date = October 1978|pages=16–18|first = J. B.|last = Barkley|publisher = Pyrotechnica Publications|location = [[Post Falls, Idaho]]}}</ref> |
In 1597, the German [[alchemy|alchemist]] [[Andreas Libavius]] first described the compound, coining the medieval names of ''plumb dulcis'' and ''calx plumb dulcis'', meaning "sweet lead", because of its taste.<ref name="libavius">{{cite book|first = Andreas|last = Libavius|authorlink = Andreas Libavius|title = Alchemia Andreæ Libavii|location = Francofurti|publisher = Iohannes Saurius|year = 1595}}</ref> Although originally not understood during the following centuries, the [[decrepitation]] property of lead(II) nitrate led to its use in matches and special [[explosive material|explosives]] such as [[lead(II) azide|lead azide]].<ref name="pyrotechnica">{{cite journal|title = Lead nitrate as an oxidizer in blackpowder|journal = Pyrotechnica |volume = 4 |date = October 1978|pages=16–18|first = J. B.|last = Barkley|publisher = Pyrotechnica Publications|location = [[Post Falls, Idaho]]}}</ref> |
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The production process was and still is chemically straightforward, effectively dissolving [[lead]] in aqua fortis ([[nitric acid]]), and subsequently harvesting the [[Precipitation (chemistry)|precipitate]]. However, the production remained small-scale for many centuries, and the commercial production of lead(II) nitrate as raw material for the manufacture of other lead compounds was not reported until 1835.<ref name=britannica1911>{{cite web|url = http://www.1911encyclopedia.org/Lead|title = Lead|publisher = [[Encyclopædia Britannica Eleventh Edition]]|accessdate = 2006-10-11}}</ref><ref name=macgregor>{{cite book|first = John|last = Macgregor|title = Progress of America to year 1846|publisher = Whittaker & Co|location = London|year = 1847|isbn = 0-665-51791-2}}</ref> In 1974, the [[United States|U.S.]] consumption of lead compounds, excluding pigments and [[gasoline]] additives, was 642 tons.<ref name="greenwood">{{cite book| first = Norman N.|last = Greenwood|author2=Earnshaw, A. |year = 1997|title = Chemistry of the Elements|edition = 2nd|pages= 388, 456|location = Oxford|publisher = Butterworth-Heinemann|isbn = 0-7506-3365-4}}</ref> |
The production process was and still is chemically straightforward, effectively dissolving [[lead]] in aqua fortis ([[nitric acid]]), and subsequently harvesting the [[Precipitation (chemistry)|precipitate]]. However, the production remained small-scale for many centuries, and the commercial production of lead(II) nitrate as raw material for the manufacture of other lead compounds was not reported until 1835.<ref name=britannica1911>{{cite web|url = http://www.1911encyclopedia.org/Lead|title = Lead|publisher = [[Encyclopædia Britannica Eleventh Edition]]|accessdate = 2006-10-11|deadurl = yes|archiveurl = https://web.archive.org/web/20061005054333/http://www.1911encyclopedia.org/Lead|archivedate = 2006-10-05|df = }}</ref><ref name=macgregor>{{cite book|first = John|last = Macgregor|title = Progress of America to year 1846|publisher = Whittaker & Co|location = London|year = 1847|isbn = 0-665-51791-2}}</ref> In 1974, the [[United States|U.S.]] consumption of lead compounds, excluding pigments and [[gasoline]] additives, was 642 tons.<ref name="greenwood">{{cite book| first = Norman N.|last = Greenwood|author2=Earnshaw, A. |year = 1997|title = Chemistry of the Elements|edition = 2nd|pages= 388, 456|location = Oxford|publisher = Butterworth-Heinemann|isbn = 0-7506-3365-4}}</ref> |
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== Structure == |
== Structure == |
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Most commercially available lead(II) nitrate, as well as [[laboratory]]-scale material, is produced accordingly.<ref name="adlam">{{cite book|last = Adlam|first = George Henry Joseph|author2=Price, Leslie Slater |title = A [[Higher School Certificate (UK)|Higher School Certificate]] Inorganic Chemistry|location = London|publisher = John Murray|year = 1938}}</ref> Supply is in 25 kilogram bags up to 1000 kilogram [[Flexible intermediate bulk container|big bags]], and in laboratory containers, both by general producers of laboratory chemicals and by producers of lead and [[Inorganic compounds by element#Lead (Plumbum)|lead compounds]]. No large-scale production has been reported. |
Most commercially available lead(II) nitrate, as well as [[laboratory]]-scale material, is produced accordingly.<ref name="adlam">{{cite book|last = Adlam|first = George Henry Joseph|author2=Price, Leslie Slater |title = A [[Higher School Certificate (UK)|Higher School Certificate]] Inorganic Chemistry|location = London|publisher = John Murray|year = 1938}}</ref> Supply is in 25 kilogram bags up to 1000 kilogram [[Flexible intermediate bulk container|big bags]], and in laboratory containers, both by general producers of laboratory chemicals and by producers of lead and [[Inorganic compounds by element#Lead (Plumbum)|lead compounds]]. No large-scale production has been reported. |
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In nitric acid treatment of lead-containing wastes, e.g., in the processing of lead–[[bismuth]] wastes from lead refineries, impure solutions of lead(II) nitrate are formed as [[by-product]]. These solutions are reported to be used in the [[gold cyanidation]] process.<ref name="sidech">{{cite web|title = Product catalog; other products|url = http://www.sidech.be/products.html|publisher = Sidech|location = Tilly, Belgium|accessdate = 2008-01-05}}</ref> |
In nitric acid treatment of lead-containing wastes, e.g., in the processing of lead–[[bismuth]] wastes from lead refineries, impure solutions of lead(II) nitrate are formed as [[by-product]]. These solutions are reported to be used in the [[gold cyanidation]] process.<ref name="sidech">{{cite web|title = Product catalog; other products|url = http://www.sidech.be/products.html|publisher = Sidech|location = Tilly, Belgium|accessdate = 2008-01-05}}{{dead link|date=September 2017 |bot=InternetArchiveBot |fix-attempted=yes }}</ref> |
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== Reactions == |
== Reactions == |
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== Safety == |
== Safety == |
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{{main article|Lead poisoning}} |
{{main article|Lead poisoning}} |
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Lead(II) nitrate is toxic, and ingestion may lead to acute lead poisoning, as is applicable for all soluble lead compounds.<ref name="icsc">{{cite web|title = Lead nitrate, Chemical Safety Card 1000|url = http://www.inchem.org/documents/icsc/icsc/eics1000.htm |publisher = [[International Labour Organization]], International Occupational Safety and Health Information Centre|date=March 1999|accessdate = 2008-01-19}}</ref> All [[Inorganic compounds by element#Lead (Plumbum)|inorganic lead compounds]] are classified by the [[International Agency for Research on Cancer]] (IARC) as [[List of IARC Group 2A carcinogens|probably carcinogenic to humans]] (Category 2A).<ref name="IARC1">{{cite journal|publisher=[[International Agency for Research on Cancer]] |year=1987 |url=http://monographs.iarc.fr/ENG/Monographs/suppl7/suppl7.pdf |format=PDF |title=Inorganic and Organic Lead Compounds |journal=IARC Monographs on the Evaluation of Carcinogenic Risks to Humans |volume=Suppl. 7 |accessdate=2008-01-19 |pages= 239 |deadurl=yes |archiveurl=https://web.archive.org/web/20080306134819/http://monographs.iarc.fr/ENG/Monographs/suppl7/suppl7.pdf |archivedate=2008-03-06 |df= }}</ref> They have been linked to [[renal cell carcinoma|renal cancer]] and [[glioma]] in experimental animals and to renal cancer, [[brain tumor|brain cancer]] and [[lung cancer]] in humans, although studies of workers exposed to lead are often complicated by concurrent exposure to [[arsenic]].<ref name="IARC2">{{cite journal|publisher = [[International Agency for Research on Cancer]]|year = 2006|url = http://monographs.iarc.fr/ENG/Monographs/vol87/volume87.pdf|format = PDF|title = Inorganic and Organic Lead Compounds|journal = IARC Monographs on the Evaluation of Carcinogenic Risks to Humans|volume = 87|isbn=92-832-1287-8|accessdate = 2008-01-01|author = World Health Organization, International Agency for Research on Cancer}}</ref> Lead is known to substitute for [[zinc]] in a number of [[enzyme]]s, including [[porphobilinogen synthase|δ-aminolevulinic acid dehydratase]] (porphobilinogen synthase) in the [[heme|haem]] biosynthetic pathway and [[Nucleotidase|pyrimidine-5′-nucleotidase]], important for the correct metabolism of [[DNA]] and can therefore cause fetal damage.<ref name=mohammed>{{cite journal|last = Mohammed-Brahim|first = B.|author2 = Buchet, J.P. |author3=Lauwerys, R. |title = Erythrocyte pyrimidine 5'-nucleotidase activity in workers exposed to lead, mercury or cadmium|journal = Int Arch Occup Environ Health|year = 1985|volume = 55|issue = 3|pages = 247–52|pmid = 2987134|doi = 10.1007/BF00383757}}</ref> |
Lead(II) nitrate is toxic, and ingestion may lead to acute lead poisoning, as is applicable for all soluble lead compounds.<ref name="icsc">{{cite web|title = Lead nitrate, Chemical Safety Card 1000|url = http://www.inchem.org/documents/icsc/icsc/eics1000.htm |publisher = [[International Labour Organization]], International Occupational Safety and Health Information Centre|date=March 1999|accessdate = 2008-01-19}}</ref> All [[Inorganic compounds by element#Lead (Plumbum)|inorganic lead compounds]] are classified by the [[International Agency for Research on Cancer]] (IARC) as [[List of IARC Group 2A carcinogens|probably carcinogenic to humans]] (Category 2A).<ref name="IARC1">{{cite journal|publisher=[[International Agency for Research on Cancer]] |year=1987 |url=http://monographs.iarc.fr/ENG/Monographs/suppl7/suppl7.pdf |format=PDF |title=Inorganic and Organic Lead Compounds |journal=IARC Monographs on the Evaluation of Carcinogenic Risks to Humans |volume=Suppl. 7 |accessdate=2008-01-19 |pages= 239 |deadurl=yes |archiveurl=https://web.archive.org/web/20080306134819/http://monographs.iarc.fr/ENG/Monographs/suppl7/suppl7.pdf |archivedate=2008-03-06 |df= }}</ref> They have been linked to [[renal cell carcinoma|renal cancer]] and [[glioma]] in experimental animals and to renal cancer, [[brain tumor|brain cancer]] and [[lung cancer]] in humans, although studies of workers exposed to lead are often complicated by concurrent exposure to [[arsenic]].<ref name="IARC2">{{cite journal|publisher = [[International Agency for Research on Cancer]]|year = 2006|url = http://monographs.iarc.fr/ENG/Monographs/vol87/volume87.pdf|format = PDF|title = Inorganic and Organic Lead Compounds|journal = IARC Monographs on the Evaluation of Carcinogenic Risks to Humans|volume = 87|isbn = 92-832-1287-8|accessdate = 2008-01-01|author = World Health Organization, International Agency for Research on Cancer|deadurl = yes|archiveurl = https://web.archive.org/web/20071021091930/http://monographs.iarc.fr/ENG/Monographs/vol87/volume87.pdf|archivedate = 2007-10-21|df = }}</ref> Lead is known to substitute for [[zinc]] in a number of [[enzyme]]s, including [[porphobilinogen synthase|δ-aminolevulinic acid dehydratase]] (porphobilinogen synthase) in the [[heme|haem]] biosynthetic pathway and [[Nucleotidase|pyrimidine-5′-nucleotidase]], important for the correct metabolism of [[DNA]] and can therefore cause fetal damage.<ref name=mohammed>{{cite journal|last = Mohammed-Brahim|first = B.|author2 = Buchet, J.P. |author3=Lauwerys, R. |title = Erythrocyte pyrimidine 5'-nucleotidase activity in workers exposed to lead, mercury or cadmium|journal = Int Arch Occup Environ Health|year = 1985|volume = 55|issue = 3|pages = 247–52|pmid = 2987134|doi = 10.1007/BF00383757}}</ref> |
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== See also == |
== See also == |
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* {{cite journal|title = Lead|url = https://www.cdc.gov/niosh/npg/npgd0368.html|publisher = National Institute for Occupational Safety and Health|journal = NIOSH Pocket Guide to Chemical Hazards|date=September 2005|id = NIOSH 2005-149| accessdate = 2008-01-19}} |
* {{cite journal|title = Lead|url = https://www.cdc.gov/niosh/npg/npgd0368.html|publisher = National Institute for Occupational Safety and Health|journal = NIOSH Pocket Guide to Chemical Hazards|date=September 2005|id = NIOSH 2005-149| accessdate = 2008-01-19}} |
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* {{cite journal|title = Lead and Lead Compounds Fact Sheet|url = http://www.npi.gov.au/database/substance-info/profiles/50.html|journal = National Pollutant Inventory|publisher = Australian Government, Department of the Environment and Water Resources|date=July 2007| accessdate = 2008-01-19| archiveurl = https://web.archive.org/web/20080111154608/http://www.npi.gov.au/database/substance-info/profiles/50.html| archivedate = January 11, 2008}} |
* {{cite journal|title = Lead and Lead Compounds Fact Sheet|url = http://www.npi.gov.au/database/substance-info/profiles/50.html|journal = National Pollutant Inventory|publisher = Australian Government, Department of the Environment and Water Resources|date=July 2007| accessdate = 2008-01-19| archiveurl = https://web.archive.org/web/20080111154608/http://www.npi.gov.au/database/substance-info/profiles/50.html| archivedate = January 11, 2008}} |
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* {{cite journal|title = Lead|url = http://www.afhh.org/hhe/hhe_lead.htm|journal = A Healthy home environment, Health hazards|publisher = US Alliance for healthy homes |
* {{cite journal|title = Lead|url = http://www.afhh.org/hhe/hhe_lead.htm|journal = A Healthy home environment, Health hazards|publisher = US Alliance for healthy homes|accessdate = 2008-01-19|deadurl = yes|archiveurl = https://web.archive.org/web/20080220005525/http://www.afhh.org/hhe/hhe_lead.htm|archivedate = 2008-02-20|df = }} |
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* {{cite web|title = Demonstration movie: Bright Orange Yellow How can you get it|url = http://www.metacafe.co.il/watch/330392/bright_orange_yellow_how_can_you_get_it|accessdate = 2008-01-19}} |
* {{cite web|title = Demonstration movie: Bright Orange Yellow How can you get it|url = http://www.metacafe.co.il/watch/330392/bright_orange_yellow_how_can_you_get_it|accessdate = 2008-01-19}} |
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;Material Safety Data Sheets |
;Material Safety Data Sheets |
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* [http://physchem.ox.ac.uk/MSDS/LE/lead_nitrate.html MSDS for lead nitrate, PTCL, Oxford University] |
* [http://physchem.ox.ac.uk/MSDS/LE/lead_nitrate.html MSDS for lead nitrate, PTCL, Oxford University] |
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* {{cite web|url= http://www.proscitech.com.au/cataloguex/msds/c151.pdf |title=MSDS for lead nitrate, ProSciTech }} {{small|(126 [[Kibibyte|KiB]])}} |
* {{cite web |url= http://www.proscitech.com.au/cataloguex/msds/c151.pdf |title= MSDS for lead nitrate, ProSciTech }}{{dead link|date=September 2017 |bot=InternetArchiveBot |fix-attempted=yes }} {{small|(126 [[Kibibyte|KiB]])}} |
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* [https://web.archive.org/web/20060328120306/http://www.sciencestuff.com/msds/C1980.html MSDS for lead nitrate, Science Stuff Inc] |
* [https://web.archive.org/web/20060328120306/http://www.sciencestuff.com/msds/C1980.html MSDS for lead nitrate, Science Stuff Inc] |
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* [http://avogadro.chem.iastate.edu/MSDS/Pb(NO3)2.htm MSDS for lead nitrate, Iowa State University] |
* [http://avogadro.chem.iastate.edu/MSDS/Pb(NO3)2.htm MSDS for lead nitrate, Iowa State University] |
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* [https://srmors.nist.gov/msds/view_msds2pdf.cfm?msds=991 MSDS for lead nitrate, NIST] |
* [https://srmors.nist.gov/msds/view_msds2pdf.cfm?msds=991 MSDS for lead nitrate, NIST]{{dead link|date=September 2017 |bot=InternetArchiveBot |fix-attempted=yes }} |
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{{featured article}} |
{{featured article}} |
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Revision as of 11:18, 24 September 2017
_nitrate_1.jpg)
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| Names | |||
|---|---|---|---|
| IUPAC name
Lead(II) nitrate
| |||
| Other names
Lead nitrate
Plumbous nitrate Lead dinitrate Plumb dulcis | |||
| Identifiers | |||
3D model (JSmol)
|
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| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.030.210 | ||
PubChem CID
|
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| RTECS number |
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| UNII | |||
| UN number | 1469 | ||
CompTox Dashboard (EPA)
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| |||
| |||
| Properties | |||
| Pb(NO3)2 | |||
| Molar mass | 331.2 g/mol[1] | ||
| Appearance | White colourless crystals | ||
| Density | 4.53 g/cm3 (20 °C)[1] | ||
| Melting point | 470 °C (878 °F; 743 K)[1] decomposes | ||
| 376.5 g/L (0 °C) 597 g/L (25 °C)[1] 1270 g/L (100 °C) | |||
| Solubility in nitric acid in ethanol in methanol |
insoluble 0.4 g/L 13 g/L | ||
| −74.0·10−6 cm3/mol[2] | |||
Refractive index (nD)
|
1.782[3] | ||
| Structure | |||
| Face-centred cubic, cP36 | |||
| Pa3, No. 205[4] | |||
a = 0.78586 nm[4]
| |||
Lattice volume (V)
|
0.4853 nm3 | ||
Formula units (Z)
|
4 | ||
| Hazards | |||
| NFPA 704 (fire diamond) | |||
| Flash point | Non-flammable | ||
| Lethal dose or concentration (LD, LC): | |||
LDLo (lowest published)
|
500 mg/kg (guinea pig, oral)[5] | ||
| Safety data sheet (SDS) | ICSC 1000, MallBaker MSDS[permanent dead link] | ||
| Related compounds | |||
Other anions
|
Lead(II) sulfate Lead(II) chloride Lead(II) bromide | ||
Other cations
|
Tin(II) nitrate | ||
Related compounds
|
Thallium(III) nitrate Bismuth(III) nitrate | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |||
-nitrate-unit-cell-3D-balls.png)
-nitrate-xtal-3D-SF.png)
Lead(II) nitrate is an inorganic compound with the chemical formula Pb(NO3)2. It commonly occurs as a colourless crystal or white powder and, unlike most other lead(II) salts, is soluble in water.
Known since the Middle Ages by the name plumb dulcis, the production of lead(II) nitrate from either metallic lead or lead oxide in nitric acid was small-scale, for direct use in making other lead compounds. In the 19th century lead(II) nitrate began to be produced commercially in Europe and the United States. Historically, the main use was as a raw material in the production of pigments for lead paints, but such paints have been superseded by less toxic paints based on titanium dioxide. Other industrial uses included heat stabilization in nylon and polyesters, and in coatings of photothermographic paper. Since around the year 2000, lead(II) nitrate has begun to be used in gold cyanidation.
Lead(II) nitrate is toxic, an oxidizing agent, and is categorised as probably carcinogenic to humans by the International Agency for Research on Cancer. Consequently, it must be handled and stored with the appropriate safety precautions to prevent inhalation, ingestion and skin contact. Due to its hazardous nature, the limited applications of lead(II) nitrate are under constant scrutiny.
History
Since the Middle Ages, lead(II) nitrate has been produced as a raw material for the production of coloured pigments in lead paints, such as chrome yellow (lead(II) chromate), chrome orange (lead(II) hydroxide chromate) and similar lead compounds. These pigments were used for dyeing and printing calico and other textiles.[6]
In 1597, the German alchemist Andreas Libavius first described the compound, coining the medieval names of plumb dulcis and calx plumb dulcis, meaning "sweet lead", because of its taste.[7] Although originally not understood during the following centuries, the decrepitation property of lead(II) nitrate led to its use in matches and special explosives such as lead azide.[8]
The production process was and still is chemically straightforward, effectively dissolving lead in aqua fortis (nitric acid), and subsequently harvesting the precipitate. However, the production remained small-scale for many centuries, and the commercial production of lead(II) nitrate as raw material for the manufacture of other lead compounds was not reported until 1835.[9][10] In 1974, the U.S. consumption of lead compounds, excluding pigments and gasoline additives, was 642 tons.[11]
Structure
The crystal structure of solid lead(II) nitrate has been determined by neutron diffraction.[12][13] The compound crystallizes in the cubic system with the lead atoms in a face-centred cubic system. Its space group is Pa3Z=4 (Bravais lattice notation), with each side of the cube with length 784 picometres.
The black dots represent the lead atoms, the white dots the nitrate groups 27 picometres above the plane of the lead atoms, and the blue dots the nitrate groups the same distance below this plane. In this configuration, every lead atom is bonded to twelve oxygen atoms (bond length: 281 pm). All N–O bond lengths are identical, at 127 picometres.
Research interest in the crystal structure of lead(II) nitrate was partly based on the possibility of free internal rotation of the nitrate groups within the crystal lattice at elevated temperatures, but this did not materialise.[13]
Preparation and production
Lead(II) nitrate can be obtained by dissolving metallic lead in aqueous nitric acid:[11][14]
- Pb + 4 HNO3 → Pb(NO3)2 + 2 NO2 + 2 H2O
More commonly, it is obtained by dissolving lead(II) oxide in nitric acid:[11]
- PbO + 2 HNO3 → Pb(NO3)2 + H2O
In either case, since the solvent is concentrated nitric acid (in which lead(II) nitrate has very low solubility) and the resulting solution contains nitrate ions, anhydrous crystals of lead(II) nitrate spontaneously form as a result of the common ion effect:[14]
Most commercially available lead(II) nitrate, as well as laboratory-scale material, is produced accordingly.[15] Supply is in 25 kilogram bags up to 1000 kilogram big bags, and in laboratory containers, both by general producers of laboratory chemicals and by producers of lead and lead compounds. No large-scale production has been reported.
In nitric acid treatment of lead-containing wastes, e.g., in the processing of lead–bismuth wastes from lead refineries, impure solutions of lead(II) nitrate are formed as by-product. These solutions are reported to be used in the gold cyanidation process.[16]
Reactions
Apart from lead(II) acetate, lead(II) nitrate is the only common soluble lead compound. Lead(II) nitrate readily dissolves in water to give a clear, colourless solution.[17] As an ionic substance, the dissolution of lead(II) nitrate involves dissociation into its constituent ions.
- Pb(NO3)2 (s) → Pb2+ (aq) + 2 NO−
3 (aq)
When concentrated sodium hydroxide solution is added to lead(II) nitrate solution, basic nitrates are formed, even well past the equivalence point. Up through the half equivalence point, Pb(NO3)2·Pb(OH)2 predominates, then after this point Pb(NO3)2·5Pb(OH)2 is formed. No simple Pb(OH)2 is formed up to at least pH 12.[14][18]
Complexation
Lead(II) nitrate is associated with interesting supramolecular chemistry because of its coordination to nitrogen and oxygen electron-donating compounds. The interest is largely academic, but with several potential applications. For example, combining lead nitrate and pentaethylene glycol (EO5) in a solution of acetonitrile and methanol followed by slow evaporation produces a new crystalline material [Pb(NO3)2(EO5)].[19] In the crystal structure for this compound, the EO5 chain is wrapped around the lead ion in an equatorial plane similar to that of a crown ether. The two bidentate nitrate ligands are in trans configuration. The total coordination number is 10, with the lead ion in a bicapped square antiprism molecular geometry.
The complex formed by lead(II) nitrate, lead(II) perchlorate and a bithiazole bidentate N-donor ligand is binuclear, with a nitrate group bridging the lead atoms with coordination number of 5 and 6.[20] One interesting aspect of this type of complexes is the presence of a physical gap in the coordination sphere; i.e., the ligands are not placed symmetrically around the metal ion. This is potentially due to a lead lone pair of electrons, also found in lead complexes with an imidazole ligand.[21]
This type of chemistry is not unique to the nitrate salt; other lead(II) compounds such as lead(II) bromide also form complexes, but the nitrate is frequently used because of its solubility properties and its bidentate nature.
Oxidation and decomposition
Lead(II) nitrate is an oxidizing agent. Depending on the reaction, this may be due to the Pb2+(aq) ion, which has a standard reduction potential (E0) of −0.125 V, or the nitrate ion, which under acidic conditions has an E0 of +0.956 V.[22] The nitrate would function at high temperatures or in an acidic condition, while the lead(II) works best in a neutral aqueous solution.
When heated, lead(II) nitrate crystals decompose to lead(II) oxide, oxygen and nitrogen dioxide.
- 2 Pb(NO3)2 (s) → 2 PbO (s) + 4 NO2 (g) + O2 (g)
Because of this property, lead nitrate is sometimes used in pyrotechnics such as fireworks.[8]
Solubility
Lead(II) nitrate is soluble in water but is almost insoluble in nitric acid.
| The System of Pb(NO3)2-HNO3-H2O At 26°, 40°, 59.5°, and 80 °C.[23] | |||
| Temperature | Composition of saturated solution, Wt.% | Density | |
|---|---|---|---|
| °C | Pb(NO3)2 | HNO3 | g/L |
| 26 | 37.41 | 0 | 1434 |
| 24.75 | 4.93 | 1253 | |
| 12.22 | 12.96 | 1162 | |
| 4.26 | 25.99 | 1183 | |
| 0.53 | 50.26 | 1266 | |
| 0.06 | 63.84 | 1333 | |
| 0.008 | 71.35 | 1387 | |
| 40 | 42.16 | 0 | 1516 |
| 29.24 | 4.78 | 1350 | |
| 16.46 | 12.23 | 1224 | |
| 5.86 | 26.37 | 1201 | |
| 0.78 | 48.94 | 1278 | |
| 0.1 | 61.98 | 1345 | |
| 59.5 | 33.77 | 4.04 | 1443 |
| 20.82 | 11.39 | 1284 | |
| 1.01 | 49.08 | 1268 | |
| 0.15 | 62.4 | 1323 | |
| 0.03 | 70.54 | 1360 | |
| 80 | 52.45 | 0 | 1692 |
| 43.41 | 3.92 | 1528 | |
| 24.52 | 10.72 | 1352 | |
| 11.17 | 25.54 | 1209 | |
| 1.7 | 48.55 | 1233 | |
| 0.25 | 62.65 | 1290 | |
| 0.05 | 70.71 | 1321 | |
Applications
Because of the hazardous nature of lead(II) nitrate, there is a preference for using alternatives in industrial applications. In the formerly major application of lead paints, it has largely been replaced by titanium dioxide.[24] Other historical applications of lead(II) nitrate, such as in matches and fireworks, have declined or ceased as well. Current applications of lead(II) nitrate include use as a heat stabiliser in nylon and polyesters, as a coating for photothermographic paper, and in rodenticides.[11]
On a laboratory scale, lead(II) nitrate provides one of two convenient and reliable sources of dinitrogen tetroxide. By carefully drying lead(II) nitrate and then heating it in a steel vessel, nitrogen dioxide is produced, which dimerizes into the desired compound.
- 2 NO2 ⇌ N2O4
To improve the leaching process in the gold cyanidation, lead(II) nitrate solution is added. Although a bulk process, only limited amounts (10 to 100 milligrams lead(II) nitrate per kilogram gold) are required.[25][26] Both the cyanidation itself, as well as the use of lead compounds in the process, are deemed controversial due to the compounds' toxic nature.
In organic chemistry, lead(II) nitrate has been used as an oxidant, for example as an alternative to the Sommelet reaction for oxidation of benzylic halides to aldehydes.[27] It has also found use in the preparation of isothiocyanates from dithiocarbamates.[28] Because of its toxicity it has largely fallen out of favour, but it still finds occasional use, for example as a bromide scavenger during SN1 substitution.[29]
Safety
Lead(II) nitrate is toxic, and ingestion may lead to acute lead poisoning, as is applicable for all soluble lead compounds.[30] All inorganic lead compounds are classified by the International Agency for Research on Cancer (IARC) as probably carcinogenic to humans (Category 2A).[31] They have been linked to renal cancer and glioma in experimental animals and to renal cancer, brain cancer and lung cancer in humans, although studies of workers exposed to lead are often complicated by concurrent exposure to arsenic.[32] Lead is known to substitute for zinc in a number of enzymes, including δ-aminolevulinic acid dehydratase (porphobilinogen synthase) in the haem biosynthetic pathway and pyrimidine-5′-nucleotidase, important for the correct metabolism of DNA and can therefore cause fetal damage.[33]
See also
- Pigments containing lead, such as White lead, Naples Yellow, and Red lead
- Historical compounds, such as Muriatic acid, Vitriol, sugar of lead, and Sal mirabilis
References
- ^ a b c d Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.70. ISBN 1-4398-5511-0.
- ^ Haynes, William M., ed. (2011). CRC Handbook of Chemistry and Physics (92nd ed.). Boca Raton, FL: CRC Press. p. 4.133. ISBN 1-4398-5511-0.
- ^ Patnaik, Pradyot (2003). Handbook of Inorganic Chemical Compounds. McGraw-Hill. p. 475. ISBN 0-07-049439-8.
- ^ a b Nowotny, H.; Heger, G. (1986). "Structure refinement of lead nitrate". Acta Crystallographica Section C Crystal Structure Communications. 42 (2): 133. doi:10.1107/S0108270186097032.
- ^ "Lead compounds (as Pb)". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
- ^ Partington, James Riddick (1950). A Text-book of Inorganic Chemistry. MacMillan. p. 838.
- ^ Libavius, Andreas (1595). Alchemia Andreæ Libavii. Francofurti: Iohannes Saurius.
- ^ a b Barkley, J. B. (October 1978). "Lead nitrate as an oxidizer in blackpowder". Pyrotechnica. 4. Post Falls, Idaho: Pyrotechnica Publications: 16–18.
- ^ "Lead". Encyclopædia Britannica Eleventh Edition. Archived from the original on 2006-10-05. Retrieved 2006-10-11.
{{cite web}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Macgregor, John (1847). Progress of America to year 1846. London: Whittaker & Co. ISBN 0-665-51791-2.
- ^ a b c d Greenwood, Norman N.; Earnshaw, A. (1997). Chemistry of the Elements (2nd ed.). Oxford: Butterworth-Heinemann. pp. 388, 456. ISBN 0-7506-3365-4.
- ^ Hamilton, W. C. (1957). "A neutron crystallographic study of lead nitrate". Acta Crystallogr. 10 (2): 103–107. doi:10.1107/S0365110X57000304.
- ^ a b Nowotny, H.; G. Heger (1986). "Structure refinement of lead nitrate". Acta Crystallogr. C. 42 (2): 133–35. doi:10.1107/S0108270186097032.
- ^ a b c Othmer, D. F. (1967). Kirk-Othmer Encyclopedia of Chemical Technology. Vol. 12 (Iron to Manganese) (second completely revised ed.). New York: John Wiley & Sons. p. 272. ISBN 0-471-02040-0.
- ^ Adlam, George Henry Joseph; Price, Leslie Slater (1938). A Higher School Certificate Inorganic Chemistry. London: John Murray.
- ^ "Product catalog; other products". Tilly, Belgium: Sidech. Retrieved 2008-01-05.[permanent dead link]
- ^ Ferris, L. M. (1959). "Lead nitrate—Nitric acid—Water system". Journal of Chemicals and Engineering Date. 5 (3): 242–242. doi:10.1021/je60007a002.
- ^ Pauley, J. L.; M. K. Testerman (1954). "Basic Salts of Lead Nitrate Formed in Aqueous Media". Journal of the American Chemical Society. 76 (16): 4220–4222. doi:10.1021/ja01645a062.
- ^ Rogers, Robin D.; Andrew H. Bond; Debra M. Roden (1996). "Structural Chemistry of Poly (ethylene glycol). Complexes of Lead(II) Nitrate and Lead(II) Bromide". Inorg. Chem. 35 (24): 6964–6973. doi:10.1021/ic960587b. PMID 11666874.
- ^ Mahjoub, Ali Reza; Ali Morsali (2001). "A Dimeric Mixed-Anions Lead(II) Complex: Synthesis and Structural Characterization of [Pb2(BTZ)4(NO3)(H2O)](ClO4)3 {BTZ = 4,4'-Bithiazole}". Chemistry Letters. 30 (12): 1234. doi:10.1246/cl.2001.1234.
- ^ Shuang-Yi Wan; Jian Fan; Taka-aki Okamura; Hui-Fang Zhu; Xing-Mei Ouyang; Wei-Yin Sun; Norikazu Ueyama (2002). "2D 4.82 Network with threefold parallel interpenetration from nanometre-sized tripodal ligand and lead(II) nitrate". Chem. Commun. (21): 2520–2521. doi:10.1039/b207568g.
{{cite journal}}: Unknown parameter|last-author-amp=ignored (|name-list-style=suggested) (help) - ^ Hill, John W.; Petrucci, Ralph H. (1999). General Chemistry (2nd ed.). Upper Saddle River, New Jersey: Prentice Hall. p. 781. ISBN 0-13-010318-7.
- ^ Ferris, L. M. (1960). "Lead Nitrate-Nitric Acid-Water System". Journal of Chemical & Engineering Data. 5 (3): 242. doi:10.1021/je60007a002.
- ^ "Historical development of titanium dioxide". Millennium Inorganic Chemicals. Archived from the original on October 21, 2007. Retrieved 2008-01-04.
{{cite web}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Habashi, Fathi (1998). Recent advances in gold metallurgy. Vol. 13. pp. 43–54.
{{cite book}}:|journal=ignored (help) - ^ "Auxiliary agents in gold cyanidation". Gold Prospecting and Gold Mining. Retrieved 2008-01-05.
- ^ Schulze, K. E. (1884). "Über α- und β-Methylnaphtalin". Chemische Berichte. 17: 1530. doi:10.1002/cber.188401701384.
- ^ Dains, F. B.; Brewster, R. Q.; Olander, C. P. "Phenyl isothiocyanate". Organic Syntheses; Collected Volumes, vol. 1, p. 447.
- ^ Rapoport, H.; Jamison, T. (1998). "(S)-N-(9-Phenylfluoren-9-yl)alanine and (S)-Dimethyl-N-(9-phenylfluoren-9-yl)aspartate". Organic Syntheses; Collected Volumes, vol. 9, p. 344.
- ^ "Lead nitrate, Chemical Safety Card 1000". International Labour Organization, International Occupational Safety and Health Information Centre. March 1999. Retrieved 2008-01-19.
- ^ "Inorganic and Organic Lead Compounds" (PDF). IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Suppl. 7. International Agency for Research on Cancer: 239. 1987. Archived from the original (PDF) on 2008-03-06. Retrieved 2008-01-19.
{{cite journal}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ World Health Organization, International Agency for Research on Cancer (2006). "Inorganic and Organic Lead Compounds" (PDF). IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. 87. International Agency for Research on Cancer. ISBN 92-832-1287-8. Archived from the original (PDF) on 2007-10-21. Retrieved 2008-01-01.
{{cite journal}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - ^ Mohammed-Brahim, B.; Buchet, J.P.; Lauwerys, R. (1985). "Erythrocyte pyrimidine 5'-nucleotidase activity in workers exposed to lead, mercury or cadmium". Int Arch Occup Environ Health. 55 (3): 247–52. doi:10.1007/BF00383757. PMID 2987134.
External links
- Woodbury, William D. (1982). "Lead". Mineral yearbook metals and minerals. Bureau of Mines: 515–42. Retrieved 2008-01-18.
- "Lead". NIOSH Pocket Guide to Chemical Hazards. National Institute for Occupational Safety and Health. September 2005. NIOSH 2005-149. Retrieved 2008-01-19.
- "Lead and Lead Compounds Fact Sheet". National Pollutant Inventory. Australian Government, Department of the Environment and Water Resources. July 2007. Archived from the original on January 11, 2008. Retrieved 2008-01-19.
- "Lead". A Healthy home environment, Health hazards. US Alliance for healthy homes. Archived from the original on 2008-02-20. Retrieved 2008-01-19.
{{cite journal}}: Unknown parameter|deadurl=ignored (|url-status=suggested) (help) - "Demonstration movie: Bright Orange Yellow How can you get it". Retrieved 2008-01-19.
- Material Safety Data Sheets
- MSDS for lead nitrate, PTCL, Oxford University
- "MSDS for lead nitrate, ProSciTech" (PDF).[permanent dead link] (126 KiB)
- MSDS for lead nitrate, Science Stuff Inc
- MSDS for lead nitrate, Iowa State University
- MSDS for lead nitrate, NIST[permanent dead link]