Celluloid

9.5 mm motion picture film

Celluloids are a class of compounds created from nitrocellulose and camphor, with added dyes and other agents. Generally considered the first thermoplastic, it was first created as Parkesine in 1856^[1] and as Xylonite in 1869, before being registered as Celluloid in 1870. Celluloid is easily molded and shaped, and it was first widely used as an ivory replacement.

The main use was in movie and photography film industries, which used only celluloid films prior to acetate films that were introduced in the 1950s. Celluloid is highly flammable, difficult and expensive to produce and no longer widely used, although its most common uses today are in table tennis balls, musical instruments and guitar picks.^[2]

History

Nitrocellulose

Nitrocellulose-based plastics slightly predate celluloid. Collodion, invented in 1848 and used as a wound dressing and an emulsion for photographic plates, is dried to a celluloid-like film.

Alexander Parkes

The first celluloid as a bulk material for forming objects was made in 1855 in Birmingham, England, by Alexander Parkes, who was never able to see his invention reach full fruition, after his firm went bankrupt due to scale-up costs.^[3] Parkes patented his discovery after realising a solid residue remained after evaporation of the solvent from photographic collodion.

Parkes patented it as a clothing waterproofer for woven fabrics in the same year. Later in 1862, Parkes showcased Parkesine at the Great Exhibition in London, where he was awarded a bronze medal for his efforts. The introduction of Parkesine is generally regarded as the birth of the plastics industry.^[3]

John Wesley Hyatt

In the 1860s, an American, John Wesley Hyatt, acquired Parkes's patent and began experimenting with cellulose nitrate with the intention of manufacturing billiard balls, which until that time were made from ivory. He used cloth, ivory dust, and shellac, and on April 6, 1869, patented a method of covering billiard balls with the addition of collodion. With assistance from Peter Kinnear and other investors,^[4] Hyatt formed the Albany Billiard Ball Company (1868–1986) in Albany, New York, to manufacture the product. In 1870, John and his brother Isaiah patented a process of making a "horn-like material" with the inclusion of cellulose nitrate and camphor.^[5] Alexander Parkes and Daniel Spill (see below) listed camphor during their earlier experiments, calling the resultant mix "xylonite", but it was the Hyatt brothers who recognized the value of camphor and its use as a plasticizer for cellulose nitrate. Isaiah Hyatt dubbed his material "celluloid" in 1872.

Daniel Spill and legal disputes

Newark, New Jersey, industrial production complex of the Celluloid Company (c. 1890)

English inventor Daniel Spill had worked with Parkes and formed the Xylonite Co. to take over Parkes' patents, describing the new plastic products as Xylonite. He took exception to the Hyatts' claims and pursued the brothers in a number of court cases between 1877 and 1884. Initially the judge found in Spill's favour, but ultimately it was judged that neither party held an exclusive claim and the true inventor of celluloid/xylonite was Alexander Parkes, due to his mention of camphor in his earlier experiments and patents.^[6] The judge ruled all manufacturing of celluloid could continue both in Spill's British Xylonite Company and Hyatts' Celluloid Manufacturing Company.

Celluloid and sterling silver pen.

The name Celluloid actually began as a trademark of the Celluloid Manufacturing Company, first of Albany, NY, and later of Newark, New Jersey, which manufactured the celluloids patented by John Wesley Hyatt. Hyatt used heat and pressure to simplify the manufacture of these compounds. Over the years, celluloid has become the normal term used for this type of plastic. In 1878 Hyatt was able to patent a process for injection moulding thermoplastics, although it took another 50 years before it could be realised commercially, and in later years celluloid was used as the base for photographic film.^[7]

Photography

English photographer John Carbutt founded the Keystone Dry Plate Works in 1879 with the intention of producing gelatin dry plates.^[8] The Celluloid Manufacturing Company was contracted for this work by means of thinly slicing layers out of celluloid blocks and then removing the slice marks with heated pressure plates. After this, the celluloid strips were coated with a photosensitive gelatin emulsion. It is not certain exactly how long it took for Carbutt to standardize his process, but it occurred no later than 1888. A 15-inch-wide (380 mm) sheet of Carbutt's film was used by William Dickson for the early Edison motion picture experiments on a cylinder drum Kinetograph. However, the celluloid film base produced by this means was still considered too stiff for the needs of motion picture photography.

By 1889, more flexible celluloids for photographic film were developed, and both Hannibal Goodwin and the Eastman Kodak Company obtained patents for a film product (Ansco, which purchased Goodwin's patent when he died, was eventually successful in an infringement suit against Kodak). This ability to produce photographic images on a flexible material (as opposed to a glass or metal plate) was a crucial step toward the advent of motion pictures.

Uses

Celluloid doll

Table tennis balls

A Seth Thomas black mantel clock, a typical late 19th century American style. The "serpentine" and "stone" of the pillars are made of celluloid glued to wood.

All movie and photography films prior to acetate films in the fifties were made of celluloid. Its high flammability was legendary since it self explodes when exposed to temperatures over 150 °C in front of a hot movie projector beam.

Celluloid was useful for creating cheaper jewellery, jewellery boxes, hair accessories and many items that would earlier have been manufactured from ivory, horn or other expensive animal products. It was often referred to as "Ivorine" or "French Ivory". It was also used for dressing table sets, dolls, picture frames, charms, hat pins, buttons, buckles, stringed instrument parts, accordions, fountain pens, cutlery handles and kitchen items. The main disadvantage the material had was that it was flammable. Items made in celluloid are collectible today and increasingly rare in good condition. It was soon overtaken by Bakelite and Catalin. Table tennis balls are also made from celluloid.

Shelf clocks and other furniture items were often covered with celluloid in a manner similar to veneer. This celluloid was printed to look like expensive woods, or materials like marble or granite. The Seth Thomas clock company called its celluloid clock material "adamantine". Celluloid enabled clockmakers to make the typical late Victorian style of black mantel clock in such a way that the wooden case appeared to be black marble, and the various pillars and other decorative elements of the case looked like semi-precious stone.^[9]

Flaming celluloid pattern on an accordion.

Celluloid remains in use for musical instruments, especially accordions and guitars. Celluloid is very robust and easy to mold in difficult forms, and has great acoustic performance as cover for wooden frames since it does not block wood's natural pores. Instruments covered with celluloid can easily be recognized by the material's typical nacre-like flaming pattern. Thick celluloid panels are cooked in a bain-marie which turns them into a leather-like substance. Panels are then turned on a mold and allowed to harden for as long as three months.

Formulation

A typical formulation of celluloid might contain 70 to 80 parts nitrocellulose, nitrated to 11% nitrogen, 30 parts camphor, 0 to 14 parts dye, 1 to 5 parts ethyl alcohol, plus stabilizers and other agents to increase stability and reduce flammability.

Production

Celluloid is made from a mixture of chemical such as nitrocellulose, camphor, alcohol, as well as colorants and fillers depending on the desired product. The first step is transforming raw cellulose into nitrocellulose by conducting a nitration reaction. This is achieved by exposing the cellulose fibers to an aqueous solution of nitric acid; the hydroxyl groups (-OH) will then be replaced with nitrate groups (-NO2) on the cellulose chain. The reaction can produce mixed products, depending on the degree of substitution of nitrogen, or the percent nitrogen content on each cellulose molecule; cellulose nitrate has 2.8 molecule of nitrogen per molecule of cellulose. It was determined that sulfuric acid was to be used as well in the reaction in order to first, catalyze the nitric acid groups so it can allow for the substitution onto the cellulose, and second, allow for the groups to easily and uniformly attach to the fibers, creating a better quality nitrocellulose. The product then must be rinsed to wash away any free acids that did not react with the fibers, dried, and kneaded. During this time, a solution of 50% camphor in alcohol is added, which then changes the macromolecule structure of nitrocellulose into a homogeneous gel of nitrocellulose and camphor. The chemical structure is not well understood, but it is determined that it is one molecule of camphor for each unit of glucose. After the mixing, the mass is pressed into blocks at a high pressure and then is fabricated for its specific use.^[10]

Nitrating cellulose is extremely flammable process in which even factory explosions are not uncommon. Many western celluloid factories closed after hazardous explosions, and only two factories in China remain in business.

Environmental hazards

Deterioration

Many sources of deterioration in celluloid exist, such as thermal, chemical, photochemical, and physical. The most inherent flaw is as celluloid ages, the camphor molecules are ‘squeezed’ out of the mass due to the unsustainable pressure used in the production. That pressure causes the nitrocellulose molecules to bind back to each other or crystallize, and this results in the camphor molecules being shoved out of the material. Once exposed to the environment, camphor can undergo sublimation at room temperature, leaving the plastic as brittle nitrocellulose. Also, with exposure to excess heat, the nitrate groups can break off and expose nitrogen gases, such as nitrous oxide and nitric oxide,^[11] to the air.

Another factor that can cause this is excess moisture, which can accelerate deterioration of nitrocellulose with the presence of nitrate groups, either newly fragmented from heat or still trapped as a free acid from production. Both of these sources allow the accumulation of nitric acid, a main component of acid rain that leads to corrosion of the environment. Another form of deterioration, Photochemical, is severe in celluloid because it absorbs ultraviolet light well. The absorbed light leads to chain-breakage and stiffening.^[12]

Accordions even over 100 years old covered with thick celluloid might be in pristine condition, while on the other hand thin celluloid film reels are often melted in an unrecognisable solid block after tens of decades in storage.

See also

• Green eyeshade

References

External links

Wikimedia Commons has media related to Celluloids.

Look up celluloid in Wiktionary, the free dictionary.

• "Celluloid" Plastics Historical Society
• "History of Plastics" Society of the Plastics Industry