Difference between revisions of "Cellulose nitrate"

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== Description ==
 
== Description ==
  
Some of the earliest synthetic resins were made from cellulose fibers. Cellulose nitrate was initially discovered by Henri Braconnot in 1833 (he named the compound xyloidine) and again in 1838 by Théophile-Jules Pelouze (he named the compound nitrimidine) when each man combined cellulose with nitric acid. The material was patented in 1846 by two other chemists and was initially used as an explosive (gun cotton). Nitrocellulose was developed for use as a plastic, when the chemistry was modified to control the degree of substitution (number of nitro groups on the chain). It was marketed in the U.S. as [[Celluloid]], a proprietary mixture of cellulose nitrate with [[camphor]] added as a plasticizer. Celluloid was molded into numerous shapes such as piano keys, billiard balls, ping pong balls, dolls, buttons and boxes. It was used to make inexpensive objects and decorations that imitated the appearance of [[ivory]], [[amber]], [[carnelian]], [[coral]], [[seashell]] and [[tortoiseshell]]. Cellulose nitrate was also used for photographic film (from the 1880s to 1920s) and animated drawing cels. Because of its instability, its use for cinematography was limited in 1912 and banned in 1951. In the early 20th century, cellulose nitrate was often used for clear lacquers, fabric dopes, adhesives, and high-gloss paints. During the 1940s and 50s, cellulose nitrate was commercially sold in mixed with natural resins ([[dammar]], [[shellac]], [[copal]], etc) as a waterproof varnish. Cellulose nitrate is inherently unstable and slowly decomposes at room temperature. Ultraviolet light, heat, and/or high humidities hasten its decomposition. Cellulose nitrate is still sold in adhesives, coatings, and explosives.
+
Some of the earliest synthetic resins were made from cellulose fibers. Cellulose nitrate was initially discovered by Henri Braconnot in 1833 (named xyloidine) and again in 1838 by Théophile-Jules Pelouze (named nitrimidine) when each man combined cellulose with nitric acid. The material was patented in 1846 by two other chemists and was initially used as an explosive (gun cotton). Nitrocellulose was developed for use as a plastic, when the chemistry was modified to control the degree of substitution (number of nitro groups on the chain). It was marketed in the U.S. as [[Celluloid]], a proprietary mixture of cellulose nitrate with [[camphor]] added as a plasticizer. Celluloid was molded into numerous shapes such as piano keys, billiard balls, ping pong balls, dolls, buttons and boxes. It was used to make inexpensive objects and decorations that imitated the appearance of [[ivory]], [[amber]], [[carnelian]], [[coral]], [[seashell]] and [[tortoiseshell]]. Cellulose nitrate was also used for photographic film (from the 1880s to 1920s) and animated drawing cels. Because of its instability, its use for cinematography was limited in 1912 and banned in 1951. In the early 20th century, cellulose nitrate was often used for clear lacquers, fabric dopes, adhesives, and high-gloss paints. During the 1940s and 50s, cellulose nitrate was commercially sold in mixed with natural resins ([[dammar]], [[shellac]], [[copal]], etc) as a waterproof varnish. Cellulose nitrate is inherently unstable and slowly decomposes at room temperature; its degradation is accelerated in the presence of ultraviolet light, heat, and/or high humidity. In spite of this, cellulose nitrate is still added to adhesives, coatings, and explosives; it is occasionally used in conservation as a coating for silver objects.
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
nitrocellulose; Zellulosenitrat (Deut.); nitrocellulose (Fr.); fulmicoton (Fr.); nitrocellulosa (It.); schietkatoen (Ned.); cellulosenitraat (Ned.); nitroceluloza (Pol.); nitrato de celulosa (Esp.); nitrocelulosa (Esp.); nitrato di cellulosa, celluloide (It.); nitrocelulose (Port.); trinitrocelulose (Port.); algodão-pólvora (Port.); bomullskrut (Sven.); nitrocellulosakrut (Sven.); nitrerad cellulosa (Sven.); nitro-cellulose; chardonnet; French ivory; pyroxylin; airplane wing dope, guncotton; gun-cotton; collodion; celloidin; celluidine; nitrocotton; photoxylin; xyloidine; nitrimidine
+
nitrocellulose; Zellulosenitrat (Deut.); nitrocellulose (Fr.); fulmicoton (Fr.); nitrocellulosa (It.); schietkatoen (Ned.); cellulosenitraat (Ned.); nitroceluloza (Pol.); nitrato de celulosa (Esp.); nitrocelulosa (Esp.); nitrato di cellulosa, celluloide (It.); nitrocelulose (Port.); trinitrocelulose (Port.); algodão-pólvora (Port.); bomullskrut (Sven.); nitrocellulosakrut (Sven.); nitrerad cellulosa (Sven.); nitro-cellulose; chardonnet; French ivory; pyroxylin; airplane wing dope, guncotton; gun-cotton; collodion; celloidin; celluidine; nitrocotton; photoxylin; nitrimidine
  
Examples: Celluloid; Xyloidine; Nitramidine; Parkesine; Zapon-lack [Dulux]; HMG [H.Marcel Guest]; Durofix [Rawplug]; Duco® cement [DuPont]; UHU Hart [Linger & Fischer, Germany];
+
Examples: Celluloid; Xyloidine; Xylonite; Nitramidine; Parkesine; Pyraline; Zapon-lack [Dulux]; HMG [H.Marcel Guest]; Durofix [Rawplug]; [[Duco]]® cement [DuPont]; UHU Hart [Linger & Fischer, Germany]; French Ivory; Ivoride
  
 
== Applications ==
 
== Applications ==
 
[[[SliderGallery rightalign|Cellulose nitrate FTIR.PNG~FTIR]]]
 
[[[SliderGallery rightalign|Cellulose nitrate FTIR.PNG~FTIR]]]
 +
* Hairbrushes, combs, fans, toys, jewelry, billiard balls
 +
* Substitutes for ivory, amber, carnelian, coral, seashell, tortoiseshell
 +
* Animation cels, Photographic film (banned in 1951)
 +
* Clear lacquers and adhesives; occasionally used to coat silver objects
  
== Risks ==
+
== Personal Risks ==
  
Highly flammable.  Explosion risk. Flash point = 13C (55F)  
+
Highly flammable.  It can easily be ignited and burns rapidly with intense heat. Emits toxic fumes when it’s burning
 +
<ref>https://www.govinfo.gov/content/pkg/GOVPUB-C13-3bd8f171acd7259f99f08f441194981b/pdf/GOVPUB-C13-3bd8f171acd7259f99f08f441194981b.pdf</ref>.
 +
There is also an explosion risk.   
  
Ultraviolet light, high temperatures and moisture accelerate degradation.  May adversely react with metals (lead, silver, tin, iron, copper and zinc).
+
With degradation, the pieces will exhibit cracking blistering, weeping, and fogging.
  
== Physical and Chemical Properties ==
+
ThermoFisher: [http://tools.thermofisher.com/content/sfs/msds/2015/RF1160_MTR-NARF_EN.pdf SDS]
  
BirefringentSoftening point 155-200C. No electical charge when rubbed with silk.
+
== Collection Risks ==
 +
Ultraviolet light, high temperatures and moisture accelerate degradation that emits gaseous nitric acidMay adversely react with metals (lead, silver, tin, iron, copper and zinc). Flammable and should be stored separate from other objects.
  
Soluble in ketones, esters, and ether alcohol mixtures.  Insoluble in water, ethanol, and hydrocarbons. Burns with a bright, violent flame; smells of nitrogen oxides. 
+
'''Links to Oddy Test results posted on AIC Wiki Materials Database Pages for individual materials below'''
  
One drop of diphenylamine solution (6% in conc. sulfuric acid) gives positive deep blue color for cellulose nitrate
+
[http://www.conservation-wiki.com/wiki/Oddy_Test_Results:_Exhibition_Adhesives_and_Tapes#Cellulose_nitrate0001 Cellulose Nitrate] tested in 2013.
  
{| class="wikitable"
+
==Environmental Risks ==
|-
 
! scope="row"| Density
 
| 1.34-1.40
 
|-
 
! scope="row"| Refractive Index
 
| 1.49-1.51
 
|}
 
  
== Additional Information ==
+
== Physical and Chemical Properties ==
  
° J.Reilly, "Celluloid Objects: Their Chemistry and Preservation" JAIC, 145-162, 1991. [http://aic.stanford.edu/jaic/articles/jaic30-02-003.html Link]
+
Soluble in ketones, esters, and ether alcohol mixtures.  Insoluble in water, ethanol, and hydrocarbons. Burns with a bright, violent flame; smells of nitrogen oxides. It does not produce an electical charge when rubbed with silk.  
  
° Museum Handbook, Part 1. Museums Collections. Web Edition. Appendix M. Management of Cellulose Nitrate and Cellulose Acetate Films, NPS, 2001. [http://www.cr.nps.gov/museum/publications/MHI/AppendM.pdf http://www.cr.nps.gov/museum/publications/MHI/AppendM.pdf]
+
One drop of diphenylamine solution (6% in conc. sulfuric acid) gives positive deep blue color for cellulose nitrate
  
 
+
* Density = 1.34-1.40
'''Links to Oddy Test results posted on AIC Wiki Materials Database Pages for individual materials below'''
+
* Refractive Index = 1.49-1.51
 
+
* Birefringent
[http://www.conservation-wiki.com/wiki/Oddy_Test_Results:_Exhibition_Adhesives_and_Tapes#Cellulose_nitrate0001 Cellulose Nitrate] tested in 2013
+
* Softening point 155-200C.
 +
* Flash point = 13C (55F)
  
 
== Comparisons ==
 
== Comparisons ==
Line 55: Line 56:
 
[[media:download_file_334.pdf|Physical Properties for Selected Thermoplastic Resins]]
 
[[media:download_file_334.pdf|Physical Properties for Selected Thermoplastic Resins]]
  
 +
== Resources and Citations ==
 +
<references/>
 +
* Contributions: Catherine Stephens, AIC Plastics Panel, 2020.
 +
 +
* Energetic Polymers: Binders and Plasticizers for Enhancing Performance by How Ghee Ang, Sreekumar Pisharath Weinheim : Wiley-VCH ; Chichester, 2012
  
 +
* J.Reilly, "Celluloid Objects: Their Chemistry and Preservation" JAIC, 145-162, 1991. [http://aic.stanford.edu/jaic/articles/jaic30-02-003.html Link]
  
== Sources Checked for Data in Record ==
+
* Museum Handbook, Part 1. Museums Collections. Web Edition. Appendix M. Management of Cellulose Nitrate and Cellulose Acetate Films, NPS, 2001. [http://www.cr.nps.gov/museum/publications/MHI/AppendM.pdf http://www.cr.nps.gov/museum/publications/MHI/AppendM.pdf]
  
 
* M.Kaufman, ''The First Century of Plastics'', The Plastics and Rubber Institute, London, 1963
 
* M.Kaufman, ''The First Century of Plastics'', The Plastics and Rubber Institute, London, 1963
Line 91: Line 98:
  
  
[[Category:Materials database]]
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[[Category:Materials database]][[Category:MWG]]

Latest revision as of 09:10, 24 May 2022

Cockade fan
MFA# 1976.388
Molded celluloid flowers
MFA # 2008.1361
Cellulose nitrate

Description

Some of the earliest synthetic resins were made from cellulose fibers. Cellulose nitrate was initially discovered by Henri Braconnot in 1833 (named xyloidine) and again in 1838 by Théophile-Jules Pelouze (named nitrimidine) when each man combined cellulose with nitric acid. The material was patented in 1846 by two other chemists and was initially used as an explosive (gun cotton). Nitrocellulose was developed for use as a plastic, when the chemistry was modified to control the degree of substitution (number of nitro groups on the chain). It was marketed in the U.S. as Celluloid, a proprietary mixture of cellulose nitrate with Camphor added as a plasticizer. Celluloid was molded into numerous shapes such as piano keys, billiard balls, ping pong balls, dolls, buttons and boxes. It was used to make inexpensive objects and decorations that imitated the appearance of Ivory, Amber, Carnelian, Coral, Seashell and Tortoiseshell. Cellulose nitrate was also used for photographic film (from the 1880s to 1920s) and animated drawing cels. Because of its instability, its use for cinematography was limited in 1912 and banned in 1951. In the early 20th century, cellulose nitrate was often used for clear lacquers, fabric dopes, adhesives, and high-gloss paints. During the 1940s and 50s, cellulose nitrate was commercially sold in mixed with natural resins (Dammar, Shellac, Copal, etc) as a waterproof varnish. Cellulose nitrate is inherently unstable and slowly decomposes at room temperature; its degradation is accelerated in the presence of ultraviolet light, heat, and/or high humidity. In spite of this, cellulose nitrate is still added to adhesives, coatings, and explosives; it is occasionally used in conservation as a coating for silver objects.

Synonyms and Related Terms

nitrocellulose; Zellulosenitrat (Deut.); nitrocellulose (Fr.); fulmicoton (Fr.); nitrocellulosa (It.); schietkatoen (Ned.); cellulosenitraat (Ned.); nitroceluloza (Pol.); nitrato de celulosa (Esp.); nitrocelulosa (Esp.); nitrato di cellulosa, celluloide (It.); nitrocelulose (Port.); trinitrocelulose (Port.); algodão-pólvora (Port.); bomullskrut (Sven.); nitrocellulosakrut (Sven.); nitrerad cellulosa (Sven.); nitro-cellulose; chardonnet; French ivory; pyroxylin; airplane wing dope, guncotton; gun-cotton; collodion; celloidin; celluidine; nitrocotton; photoxylin; nitrimidine

Examples: Celluloid; Xyloidine; Xylonite; Nitramidine; Parkesine; Pyraline; Zapon-lack [Dulux]; HMG [H.Marcel Guest]; Durofix [Rawplug]; Duco® cement [DuPont]; UHU Hart [Linger & Fischer, Germany]; French Ivory; Ivoride

Applications

FTIR

Cellulose nitrate FTIR.PNG

  • Hairbrushes, combs, fans, toys, jewelry, billiard balls
  • Substitutes for ivory, amber, carnelian, coral, seashell, tortoiseshell
  • Animation cels, Photographic film (banned in 1951)
  • Clear lacquers and adhesives; occasionally used to coat silver objects

Personal Risks

Highly flammable. It can easily be ignited and burns rapidly with intense heat. Emits toxic fumes when it’s burning [1]. There is also an explosion risk.

With degradation, the pieces will exhibit cracking blistering, weeping, and fogging.

ThermoFisher: SDS

Collection Risks

Ultraviolet light, high temperatures and moisture accelerate degradation that emits gaseous nitric acid. May adversely react with metals (lead, silver, tin, iron, copper and zinc). Flammable and should be stored separate from other objects.

Links to Oddy Test results posted on AIC Wiki Materials Database Pages for individual materials below

Cellulose Nitrate tested in 2013.

Environmental Risks

Physical and Chemical Properties

Soluble in ketones, esters, and ether alcohol mixtures. Insoluble in water, ethanol, and hydrocarbons. Burns with a bright, violent flame; smells of nitrogen oxides. It does not produce an electical charge when rubbed with silk.

One drop of diphenylamine solution (6% in conc. sulfuric acid) gives positive deep blue color for cellulose nitrate

  • Density = 1.34-1.40
  • Refractive Index = 1.49-1.51
  • Birefringent
  • Softening point 155-200C.
  • Flash point = 13C (55F)

Comparisons

General Characteristics of Polymers

Physical Properties for Selected Thermoplastic Resins

Resources and Citations

  • Contributions: Catherine Stephens, AIC Plastics Panel, 2020.
  • Energetic Polymers: Binders and Plasticizers for Enhancing Performance by How Ghee Ang, Sreekumar Pisharath Weinheim : Wiley-VCH ; Chichester, 2012
  • J.Reilly, "Celluloid Objects: Their Chemistry and Preservation" JAIC, 145-162, 1991. Link
  • M.Kaufman, The First Century of Plastics, The Plastics and Rubber Institute, London, 1963
  • History of Plastics: www.nswpmith.com.au/historyofplastics.html
  • B. Gascoigne, How to Identify Prints, Thames & Hudson, London, 2004
  • R. J. Gettens, G.L. Stout, Painting Materials, A Short Encyclopaedia, Dover Publications, New York, 1966
  • G.S.Brady, Materials Handbook, McGraw-Hill Book Co., New York, 1971 Comment: p. 171
  • Ralph Mayer, A Dictionary of Art Terms and Techniques, Harper and Row Publishers, New York, 1969 (also 1945 printing)
  • C.V.Horie, Materials for Conservation, Butterworth-Heineman, London, 1997
  • Matt Roberts, Don Etherington, Bookbinding and the Conservation of Books: a Dictionary of Descriptive Terminology, U.S. Government Printing Office, Washington DC, 1982
  • S.R.Trotman, E.R. Trotman, Textile Analysis, J.B. Lippincott Company, Philadelphia, 1932
  • Tom Rowland, Noel Riley, A-Z Guide to Cleaning, Conserving and Repairing Antiques, Constable and Co., Ltd., London, 1981
  • Pam Hatchfield, Pollutants in the Museum Environment, Archetype Press, London, 2002
  • Thomas B. Brill, Light Its Interaction with Art and Antiquities, Plenum Press, New York City, 1980
  • The Dictionary of Art, Grove's Dictionaries Inc., New York, 1996 Comment: "Plastic"; "Ivory"
  • Theodore J. Reinhart, 'Glossary of Terms', Engineered Plastics, ASM International, 1988