• Source: Tributyltin

Tributyltin (TBT) is an umbrella term for a class of organotin compounds which contain the (C4H9)3Sn group, with a prominent example being tributyltin oxide. For 40 years TBT was used as a biocide in anti-fouling paint, commonly known as bottom paint, applied to the hulls of oceangoing vessels. Bottom paint improves ship performance and durability as it reduces the rate of biofouling, the growth of organisms on the ship's hull. The TBT slowly leaches out into the marine environment where it is highly toxic toward nontarget organisms. TBT toxicity can lead to biomagnification or bioaccumulation within such nontarget organisms like invertebrates, vertebrates, and a variety of mammals. TBT is also an obesogen. After it led to collapse of local populations of organisms, TBT was banned.




Chemical properties


TBT, or tributyltin, tributylstannyl or tributyl stannic hydride compounds are organotin compounds. They have three butyl groups covalently bonded to a tin(IV) atom. A general formula for these compounds is (CH3CH2CH2CH2)3Sn−X. The −X is typically a chloride −Cl, hydroxide −OH, or a carboxylate RCO2−, where R is an organyl group. TBT is also known to be an endocrine disrupting compound, which influences biological activities such as growth, reproduction and other physiological processes.
TBT compounds have a low water solubility, a property that is ideal for antifouling agents. The toxicity of TBT prevents the growth of algae, barnacles, molluscs and other organisms on ships hulls. When introduced into a marine or aquatic environment, TBT adheres to bed sediments. TBT has a low Log Kow of 3.19 – 3.84 in distilled water and 3.54 for sea water, this makes TBT moderately hydrophobic. TBT compounds have a high fat solubility and tend to absorb more readily to organic matter in soils or sediment. The bioaccumulation of TBT in organisms such as molluscs, oysters and dolphins, have extreme effects on their reproductive systems, central nervous systems and endocrine systems. However, the adsorption of TBT to sediments is reversible and depends on pH level in the body of water.
TBT has a half-life of one or two weeks in marine water. When it accumulates in sediments its half life is about 2 years. TBT often bonds to suspended material and sediments, where it can remain and be released for up to 30 years. Studies have shown that 95% of TBT can be released from the sediments back into the aquatic environment. This absorption process can complicate quantification of TBT in an environment, since its concentration in the water is not representative of its availability.




Uses


Tributyltin (TBT) compounds are biocides. TBT's antifouling properties were discovered in the 1950s in the Netherlands by van der Kerk and coworkers. It prevents microorganisms from settling on the hull of a ship and poisons the organisms that end up settling. By the mid-1960s, it had become the most popular anti-fouling paint around the globe. TBT was mixed into paints to extend the life of antifouling coatings and ships were able to continue operations for a longer time frame. The paints ensured fuel efficiency and delayed costly ship repairs. It is also relatively inexpensive.
TBT is also an ingredient in some disinfectants, for example in combination with quaternary ammonium compounds. Additionally, TBT has been used in the fertilizer, textile, and wood industries. It has antifungal properties that make it useful for both the production of textiles and wood preservation, and in the creation of biocides for paired use with fertilizers. Another use of TBT is that they were used as stabilizers in compounds like polyvinyl chlorides. Due to this usage of TBT, there are a variety of consumer products where traces of TBT can be found, like in textile fabrics, plastic polymers, silicon, and many more.




Toxicity


The effects of antifouling paint go beyond the organisms that it is intended to kill. By poisoning barnacles, algae, and other organisms at the bottom of the food chain, the bioaccumulation of TBT increases over time affecting more and more of the bottom feeders of the aquatic food web environment, which are mainly invertebrates and are affected by TBT. There is a slight biomagnification of TBT that has been demonstrated in the lower part of the marine food chain (i.e., planktonic organisms, invertebrates, and fishes). However, the biomagnification of TBT into larger marine animals such as marine mammals is debatable. Toxic effects in some species occur at 1 nanogram per liter of water. Air pollution from TBT has not been noticed or considered significant enough to effect the environment. In the water, photodegradation and microorganisms can break down TBT and leach into the soil sediments.




= Bioaccumulation and biomagnification

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As TBT is most often used as a biofouling agent, it bioaccumulates in marine wildlife such as molluscs, with levels being higher in organisms and sediments in and around areas of high maritime activity, such as ports and harbours. The bioaccumulation increases over time, leading to a biomagnification in organisms higher up the food chain, although the biomagnification is not that considerable in size. As TBT can remain in the environment for up to 30 years due to often bonding to suspended material and sediments, it can remain in an ecosystem for a very long time. This means that bioaccumulation readily occurs in marine environments, which can lead to very high amounts of TBT being accumulated, especially in smaller organisms at the bottom of the food chain, which in turn has various health effects.




= Invertebrates

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Exposure to organotin compounds causes the development of male accessory sex organs in female prosobranch gastropods. This phenomenon has been termed imposex. TBT has been shown to affect invertebrate development. Marine snails, such as the dog whelk (Nucella lapillus), has often been used as an indicator species. In gastropods, the normal process of accessory sex organ development is retinoid dependent, as has been proven by the effect 9cisRA has on male penises. TBTs mimic the endogenous ligand of Retinoid X Receptor (9cisRA), and thus activates the signalling cascades that are retinoid acid dependent, promoting female penis growth.
There have been many theories as to why molluscs are affected by TBT. For example, previous literature has stated that TBT would cause the inhibition of aromatase which would lead to an increase in testosterone and therefore, causing imposex. It was theorized that TBT disrupts endocrine system by inhibiting cytochrome P450 molecule. Among its myriad functions, P450 converts androgen, which has male-hormone properties, into oestrogen, which has female hormone properties. It was theorized that the high concentration of androgen lead to the masculinization of females. Another indicator species is Chironomus riparius, a species of non-biting midge, which has been used to test the effects of TBT on development and reproduction at sublethal concentrations found in marine environments. Higher concentrations of TBT were found to increase the female population and the results are interesting because unlike the masculinization of the stengoglassan gastropods, feminization was present.




= Vertebrates

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Vertebrates become affected by the waters contaminated with TBT, as well as by consuming organisms that have already been poisoned. Oryzias latipes, commonly called Japanese rice fish, has been used as a model vertebrate organism to test for effects of TBT at developmental stages of the embryo. It was observed that developmental rate was slowed by TBT in a concentration-related manner and that tail abnormalities occurred. Illustrating the infiltration of TBT in the food chain, one study showed that most samples of skipjack tuna tested positive for presence of TBT. Tuna from waters around developing Asian nations had particularly high levels of TBT. Regulation of TBT is not enforced in Asia as rigorously as in Europe or US. Studies have shown that TBT is detrimental to the immune system. Research shows that TBT reduces resistance to infection in fish which live on the seabed and are exposed to high levels of TBT. These areas tend to have silty sediment like harbours and estuaries. TBT compounds have been described to interfere with glucocorticoid metabolism in the liver by inhibiting the activity of the enzyme 11beta-hydroxysteroiddehydrogenase type 2, which converts cortisol to cortisone.



Mammals

TBT can enter the diet of humans and other mammals such as whales, dolphins, dugongs, and sea otters. As of 2008 high levels of tributyltin have been detected in the livers of sea otters (Enhydra lutris) and stranded bottlenose dolphins. Otters dying of infectious causes tended to have higher levels of tissue butyltins than those dying of trauma or other causes. It was also reported by scientists that sea otters typically stay near boats and closed off marinas, which may have led to these organisms experiencing higher levels of butyltins. TBT has been shown to lead to immunosuppression in sea-otters and dolphins. TBT has also been linked to hearing loss in mammalian top predators such as toothed whales. In rats, the hypothalamus-pituitary-adrenal (HPA) axis can be affected by TBT. In the pituitary and adrenal glands, there have been findings of morphophysiological changes within rats affected by TBT. TBT can also affect humans as well. Humans can be exposed to these compounds and potentially experience headaches, fatigue, respiratory issues, and more. Long-term exposure can also lead to damage of some internal organs such as the kidneys and liver.




Regulation


Bans on TBT on boats less than 25 metres long first started in the 1980s. In 1990, the Marine Environment Protection Committee adopted Resolution MEPC 46(30), which recommended that the Government eliminate the use of TBT-containing antifouling paints on smaller vessels. This resolution was intended to be a temporary restriction until the International Maritime Organization could implement a ban of TBT anti-fouling agents for ships. Several countries followed and in 1997, Japan banned the production of TBT-based anti-fouling paints. The IMO began to use an Assembly resolution in 1999 that essentially wanted the MPEC to fix the severe environmental effects of the anti-fouling systems. This led to a worldwide ban on organotin compound applications on ships starting in 2003. In 2008, organotin compounds acting as biocide like TBT compounds were banned entirely in anti-fouling paint and included in the Rotterdam Convention and have been banned by the International Convention on the Control of Harmful Anti-fouling Systems on Ships of the International Maritime Organization. It states that ships cannot bear organotin compounds on their hulls or external parts or surfaces, unless there is a coating that forms a barrier so that organotin compounds cannot leach out to reduce exposure by allowing recovery to occur.




= Violations of the ban on TBT

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Although the ban on TBT use was proved to be effective on reducing the negative effects on the environment, some people that supplied them were still producing and selling them to other countries for a profit. Even though banned by some international agencies like the International Maritime Organization, TBT anti-fouling paints are still used in countries with poor regulation enforcement to this day, with the Caribbean being a prime example.




= U.S. Violations

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In November 2018, the US Department of Justice announced that three people they had charged and arrested in New Jersey for manufacturing and selling tributyltin based marine paint had pleaded guilty. The sentencing of these people was scheduled for February 2019.




See also


Triphenyltin
Organotin chemistry
Biomimetic antifouling coating




References






External links


Newcastle University Biofouling Group
"Ambient Aquatic Life Water Quality Criteria for Tributyltin (TBT)" United States Environmental Protection Agency, December 2003

Kata Kunci Pencarian:

• Obesogen
• Tributyltin
• Tributyltin chloride
• Tributyltin hydride
• Tin
• Tributyltin oxide
• Vinyl tributyltin
• Tributyltin azide
• Organotin chemistry
• Barton–McCombie deoxygenation
• Alcohol (chemistry)