Mothball

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Mothballs White coloured mothball (naphthalene ball) 20230315 180901.jpg
Mothballs
A packet of mothballs A packet of white coloured mothball (naphthalene ball) 20230315 180612.jpg
A packet of mothballs

Mothballs are small balls of chemical pesticide and deodorant, sometimes used when storing clothing and other materials susceptible to damage from silverfish, mold or moth larvae (especially clothes moths like Tineola bisselliella ).

Contents

Composition

Older mothballs consisted primarily of naphthalene, but due to naphthalene's flammability, many modern mothball formulations instead use 1,4-dichlorobenzene. The latter formulation may be somewhat less flammable, although both chemicals have the same NFPA 704 rating for flammability. The latter chemical is also variously labeled as para-dichlorobenzene, p-dichlorobenzene, pDCB, or PDB, making it harder to identify unless all these names and initialisms are known to a potential purchaser. Both of these formulations have the strong, pungent, sickly-sweet odor often associated with mothballs. Both naphthalene and 1,4-dichlorobenzene undergo sublimation, meaning that they transition from a solid state directly into a gas; this gas is toxic to moths and moth larvae. [1]

Due to the health risks of 1,4-dichlorobenzene, and flammability of naphthalene, other substances like camphor are sometimes used.

Uses

Mothballs are stored in air-tight bags made of a non-reactive plastic such as polyethylene or polypropylene (other plastics may be degraded or softened). The clothing to be protected should be sealed within airtight containers; otherwise the vapors will tend to escape into the surrounding environment. [1] Manufacturer's instructions regularly warn against using mothballs for any purpose other than those specified by the packaging, as such uses are not only harmful and noxious, they are also frequently considered illegal. [2] [1]

Although occasionally used as snake repellent, mothball use as a rodent, squirrel, or bat repellent is illegal in many areas, and tends to cause more annoyance and hazard to humans than to the target pest. [3] [1] However, mothballs continue to be advertised as squirrel repellent and are an ingredient in some commercial vermin and snake repellent products.

Health risks

The US Department of Health and Human Services (DHHS) has determined that 1,4-dichlorobenzene "may reasonably be anticipated to be a carcinogen". This has been indicated by animal studies, although a full-scale human study has not been done. [4] The National Toxicology Program (NTP), the International Agency for Research on Cancer (IARC) and the state of California consider 1,4-dichlorobenzene a carcinogen. [5]

Exposure to naphthalene mothballs can cause acute hemolysis (anemia) in people with glucose-6-phosphate dehydrogenase deficiency. [6] IARC classifies naphthalene as possibly carcinogenic to humans and other animals (see also Group 2B). [7] IARC points out that acute exposure causes cataracts in humans, rats, rabbits, and mice. Chronic exposure to naphthalene vapors is reported to also cause cataracts and retinal hemorrhage. [8] Under California's Proposition 65, naphthalene is listed as "known to the State to cause cancer". [9]

Research at the University of Colorado at Boulder revealed a probable mechanism for the carcinogenic effects of mothballs and some types of air fresheners. [10] [11]

In addition to their cancer risks, mothballs are known to cause liver and kidney damage. [1]

1,4-Dichlorobenzene is a neurotoxin. It has been abused as an inhalant, causing a variety of neurotoxic effects. [12] [13]

Mothballs containing naphthalene have been banned within the EU since 2008. [14] [15]

Alternatives

As discussed in more detail at Tineola bisselliella , alternatives to mothballs to control clothes moths include dry cleaning, freezing, thorough vacuuming, and washing in hot water. [16] Camphor is also used as a moth repellent, particularly in China. [17] Unlike naphthalene and dichlorobenzene, camphor has medicinal applications and is not regarded as a carcinogen, though it is toxic in large doses. Red cedar wood and oil is also used as an alternative moth repellent. [18]

Pheromone traps are also an effective diagnostic tool and can sometimes be an effective control tool to protect valuable clothing.

As a verb, "mothball" has a metaphorical usage, meaning "to stop work on an idea, plan, or job, but leaving it in such a way that work can continue in the future". [19] "Mothballed" is a common adjective to describe ships or aircraft which are stored for long periods, but not sent for scrapping.

The origins of this use of "mothballed" may have been reports that the ocean liner SS Normandie was "packed in mothballs" when in September 1939 it was 'interned' by the U.S. Government in New York. The papers reported a month later that "fourteen huge barrels of mothballs had been used to preserve carpets, draperies, and upoholstery". [20] The ship was at the time expected to remain in New York for the duration of the war, but after the attack on Pearl Harbor she was converted to a troop ship.

The US Navy planned to store fighting ships in 1945, but keep them ready for rapid return to service. By 1946 these ships were referred to as being "mothballed". The process however did not mention mothballs, but rust preventative coating, sealing compartments, removing equipment, and covering topside equipment, as well as protecting the hull. Mothballed ships were expected to be able to resume active service in just 10 days. [21] United States Navy reserve fleets are still informally referred to as the 'mothball fleet'.

See also

Related Research Articles

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<span class="mw-page-title-main">Roundup (herbicide)</span> Glyphosate-based herbicide made by Monsanto

Roundup is a brand name of herbicide originally produced by Monsanto, which Bayer acquired in 2018. Prior to the late-2010s formulations, it used broad-spectrum glyphosate-based herbicides. As of 2009, sales of Roundup herbicides still represented about 10 percent of Monsanto's revenue despite competition from Chinese producers of other glyphosate-based herbicides. The overall Roundup line of products represented about half of Monsanto's yearly revenue in 2009. The product is marketed to consumers by Scotts Miracle-Gro Company. In the late-2010s other non-glyphosate containing herbicides were also sold under the Roundup brand.

<span class="mw-page-title-main">Naphthalene</span> Chemical compound

Naphthalene is an organic compound with formula C
10
H
8
. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings. It is the main ingredient of traditional mothballs.

<span class="mw-page-title-main">1,4-Dichlorobenzene</span> Chemical compound

1,4-Dichlorobenzene (1,4-DCB, p-DCB, or para-dichlorobenzene, sometimes abbreviated as PDCB or para) is an aryl chloride and isomer of dichlorobenzene with the formula C6H4Cl2. This colorless solid has a strong odor. The molecule consists of a benzene ring with two chlorine atoms (replacing hydrogen atoms) on opposing sites of the ring.

<span class="mw-page-title-main">Camphor</span> Toxic, waxy, and transparent aromatic organic compound

Camphor is a waxy, colorless solid with a strong aroma. It is classified as a terpenoid and a cyclic ketone. It is found in the wood of the camphor laurel, a large evergreen tree found in East Asia; and in the kapur tree, a tall timber tree from South East Asia. It also occurs in some other related trees in the laurel family, notably Ocotea usambarensis. Rosemary leaves contain 0.05 to 0.5% camphor, while camphorweed (Heterotheca) contains some 5%. A major source of camphor in Asia is camphor basil. Camphor can also be synthetically produced from oil of turpentine.

<span class="mw-page-title-main">Glyphosate</span> Systemic herbicide and crop desiccant

Glyphosate is a broad-spectrum systemic herbicide and crop desiccant. It is an organophosphorus compound, specifically a phosphonate, which acts by inhibiting the plant enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSP). It is used to kill weeds, especially annual broadleaf weeds and grasses that compete with crops. Its herbicidal effectiveness was discovered by Monsanto chemist John E. Franz in 1970. Monsanto brought it to market for agricultural use in 1974 under the trade name Roundup. Monsanto's last commercially relevant United States patent expired in 2000.

<span class="mw-page-title-main">Lindane</span> Organochlorine chemical and an isomer of hexachlorocyclohexane

Lindane, also known as gamma-hexachlorocyclohexane (γ-HCH), gammaxene, Gammallin and benzene hexachloride (BHC), is an organochlorine chemical and an isomer of hexachlorocyclohexane that has been used both as an agricultural insecticide and as a pharmaceutical treatment for lice and scabies.

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<span class="mw-page-title-main">Pest control</span> Control of harmful species

Pest control is the regulation or management of a species defined as a pest; such as any animal, plant or fungus that impacts adversely on human activities or environment. The human response depends on the importance of the damage done and will range from tolerance, through deterrence and management, to attempts to completely eradicate the pest. Pest control measures may be performed as part of an integrated pest management strategy.

<span class="mw-page-title-main">Chemical hazard</span> Non-biological hazards of hazardous materials

Chemical hazards are hazards present in hazardous chemicals and hazardous materials. Exposure to certain chemicals can cause acute or long-term adverse health effects. Chemical hazards are usually classified separately from biological hazards (biohazards). Chemical hazards are classified into groups that include asphyxiants, corrosives, irritants, sensitizers, carcinogens, mutagens, teratogens, reactants, and flammables. In the workplace, exposure to chemical hazards is a type of occupational hazard. The use of personal protective equipment may substantially reduce the risk of adverse health effects from contact with hazardous materials.

<span class="mw-page-title-main">1,4-Dioxane</span> Chemical compound

1,4-Dioxane is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether. The compound is often called simply dioxane because the other dioxane isomers are rarely encountered.

<span class="mw-page-title-main">Ethylbenzene</span> Hydrocarbon compound; precursor to styrene and polystyrene

Ethylbenzene is an organic compound with the formula C6H5CH2CH3. It is a highly flammable, colorless liquid with an odor similar to that of gasoline. This monocyclic aromatic hydrocarbon is important in the petrochemical industry as a reaction intermediate in the production of styrene, the precursor to polystyrene, a common plastic material. In 2012, more than 99% of ethylbenzene produced was consumed in the production of styrene.

<span class="mw-page-title-main">Chloroprene</span> Chemical compound

Chloroprene (IUPAC name 2-chlorobuta-1,3-diene) is a chemical compound with the molecular formula CH2=CCl−CH=CH2. Chloroprene is a colorless volatile liquid, almost exclusively used as a monomer for the production of the polymer polychloroprene, better known as neoprene, a type of synthetic rubber.

IARC group 1 Carcinogens are substances, chemical mixtures, and exposure circumstances which have been classified as carcinogenic to humans by the International Agency for Research on Cancer (IARC). This category is used when there is sufficient evidence of carcinogenicity in humans. Exceptionally, an agent may be placed in this category when evidence of carcinogenicity in humans is less than sufficient, but when there is sufficient evidence of carcinogenicity in experimental animals and strong evidence in exposed humans that the agent (mixture) acts through a relevant mechanism of carcinogenicity.

IARC group 2B substances, mixtures and exposure circumstances are those that have been classified as "possibly carcinogenic to humans" by the International Agency for Research on Cancer (IARC) as This category is used when there is limited evidence of carcinogenicity in humans and less than sufficient evidence of carcinogenicity in experimental animals. It may also be used when there is insufficient evidence of carcinogenicity in humans but sufficient evidence in experimental animals. In some cases, an agent, mixture, or exposure circumstance with inadequate evidence of carcinogenicity in humans but limited evidence in experimental animals, combined with supporting evidence from other relevant data, may be included in this group.

IARC group 3 substances, chemical mixtures and exposure circumstances are those that can not be classified in regard to their carcinogenicity to humans by the International Agency for Research on Cancer (IARC). This category is used most commonly for agents, mixtures and exposure circumstances for which the level of evidence of carcinogenicity is inadequate in humans and inadequate or limited in experimental animals. Exceptionally, agents (mixtures) for which the evidence of carcinogenicity is inadequate in humans, but sufficient in experimental animals may be placed in this category when there is strong evidence that the mechanism of carcinogenicity in experimental animals does not operate in humans. Agents, mixtures and exposure circumstances that do not fall into any other group are also placed in this category.

<i>Tineola bisselliella</i> Species of moth

Tineola bisselliella, known as the common clothes moth, webbing clothes moth, or simply clothing moth, is a species of fungus moth. It is the type species of its genus Tineola and was first described by the Swedish entomologist Arvid David Hummel in 1823. It and a number of closely-related species are together known as the clothes moths due to their function as pests in human households. The specific name is commonly misspelled biselliella – for example by G. A. W. Herrich-Schäffer, when he established Tineola in 1853.

<span class="mw-page-title-main">Dichlorprop</span> Chemical compound

Dichlorprop is a chlorophenoxy herbicide similar in structure to 2,4-D that is used to kill annual and perennial broadleaf weeds. It is a component of many common weedkillers. About 4 million pounds of dichlorprop are used annually in the United States.

This is an index of articles relating to pesticides.

Naphthalene poisoning is a form of poisoning that occurs when naphthalene is ingested. Severe poisoning can result in haemolytic anaemia. Naphthalene was introduced in 1841 by Rossbach as an antiseptic to counteract typhoid fever. Although naphthalene was widely used industrially, only nine cases of poisoning have been reported since 1947 as of 1956, suggesting underdiagnosis of the condition. As a result, the condition has limited coverage within medical journals.

References

  1. 1 2 3 4 5 "What You Should Know About Mothballs: Protecting Your Children and Educating Childcare Providers" (PDF). ldh.la.gov. Louisiana Department of Health and Hospitals. Archived (PDF) from the original on June 11, 2021. Retrieved April 22, 2021.
  2. Uncommon Uses for Common Household Products. Frank W. Cawood and Associates. 2000. p. 126. ISBN   978-1-890957-39-1. Archived from the original on August 6, 2020. Retrieved November 3, 2016.
  3. "Problem Wildlife in the Garden and Yard". NPIC. National Pesticide Information Center. Archived from the original on October 23, 2020. Retrieved February 21, 2016.
  4. "ToxFAQs™ for Dichlorobenzenes". Toxic Substances Portal. Agency for Toxic Substances and Disease Registry. Archived from the original on November 26, 2020. Retrieved May 24, 2013.
  5. "p-dichlorobenzene (1,4-dichlorobenzene)" (PDF). Material Safety Data Sheet. Archived from the original (PDF) on May 22, 2013. Retrieved May 24, 2013.
  6. Santucci, K; Shah, B. (January 2000). "Association of naphthalene with acute hemolytic anemia". Academic Emergency Medicine. 7(1):42-7.
  7. "Some Traditional Herbal Medicines, Some Mycotoxins, Naphthalene and Styrene". IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. 82: 367. 2002. Archived from the original on March 25, 2016. Retrieved December 25, 2008.
  8. "Naphthalene". Air Toxics Web Site. US Environmental Protection Agency. Archived from the original on May 10, 2015. Retrieved May 24, 2013.
  9. Proposition 65 Archived July 29, 2019, at the Wayback Machine , Office of Environmental Health Hazard Assessment
  10. "Scientists May Have Solved Mystery Of Carcinogenic Mothballs" Archived October 10, 2008, at the Wayback Machine . Physorg.com. June 20, 2006.
  11. "Mothballs, air fresheners and cancer". Environmental Health Association of Nova Scotia. Archived from the original on February 22, 2020. Retrieved May 24, 2013.
  12. "Mothball sniffing warning issued" Archived November 27, 2020, at the Wayback Machine . BBC News. July 27, 2006.
  13. "Twin Girls with Neurocutaneous Symptoms Caused by Mothball Intoxication" Archived September 21, 2013, at the Wayback Machine . The New England Journal of Medicine. July 27, 2006.
  14. Gray, Kerrina (November 17, 2013). "Council warned against use of poisonous moth balls". Your Local Guardian. Newsquest (London) Ltd. Archived from the original on December 2, 2013. Retrieved November 23, 2012.
  15. Alderson, Andrew (November 15, 2008). "Holy straight bananas – now the Eurocrats are banning moth balls". The Telegraph. Archived from the original on January 3, 2014. Retrieved November 23, 2013.
  16. Eisenberg, Sheryl. "Mothballed". This Green Life. Natural Resources Defense Council. Archived from the original on May 22, 2013. Retrieved May 24, 2013.
  17. 国务院经贸办、卫生部关于停止生产和销售萘丸提倡使用樟脑制品的通知(国经贸调(1993)64号)
  18. Back, E.A.; Rabak, F. (1923). Red Cedar Chests as Protectors Against Moth Damage. Bulletin of the U.S. Department of Agriculture. U.S. Department of Agriculture. Archived from the original on March 11, 2022. Retrieved December 28, 2020.
  19. "Mothball". dictionary.cambridge.org. Cambridge Dictionary. Archived from the original on September 2, 2019. Retrieved September 2, 2019.
  20. "Normandie's Inactivity". Belfast Telegraph. October 9, 1939. p. 5.
  21. "A fleet in storage". Birmingham Daily Gazette. April 8, 1946. p. 5.