7782-49-2 Usage
Introduction
Selenium was discovered by Berzelius and Gahn in1817 while investigating the lead chamber process for making sulfuric acid. They initially believed that the bottom of the lead chamber generating an offensive odor was due to presence of tellurium, a sulfur group element that was discovered thirty-five years earlier. Further studies indicated a new element, the chemical properties of which were very similar to tellurium. This new element was named selenium, derived from the Greek word selene, meaning moon. The name followed tellus, the Latin word for earth given to tellurium which chemically resembled the new element. Willoughby Smith in 1873 discovered photoresistivity in this metal; i.e., as the intensity of light exposure on the metal increased, its current resistance decreased.
Selenium is a very rare element. The metal does not occur in nature in free elemental form. Its abundance in the earth’s crust is about 0.05 mg/kg. It occurs in certain copper ores and sometimes with native sulfur. Some selenium containing minerals are eucairite, CuAgSe; clausthalite, PbSe; naumannite, Ag2Se; crookesite, (CuTlAg)2Se; and zorgite, PbCuSe.
Chemical Properties
Different sources of media describe the Chemical Properties of 7782-49-2 differently. You can refer to the following data:
1. Selenium is a nonmetal (or semimetallic) element (also referred to as a metalloid). It belongs to Group 16 (Group VIA) of the periodic table, located between sulfur and tellurium.
The chemical properties of selenium are similar to sulfur. Selenium combines with metals and many nonmetals directly or in aqueous solution. It does not react directly with hydrogen fluoride or hydrogen chloride but decomposes hydrogen iodide to liberate iodine and yield hydrogen selenide. The selenides resemble sulfides in appearance, composition, and properties. It may form halides by reacting vigorously with fluorine and chlorine, but the reactions with bromine and iodide are not as rapid. It reacts with oxygen to form a number of oxides, the most stable of which is selenium dioxide.
2. Jewelers most frequently encounter selenium in the form of brass-black and gun-bluing
compounds. Selenium print toner used by photographers is sometimes used by jewelers
as a metal-coloring solution. These coloring mixtures usually contain selenic acid. Selenic
acid can release hydrogen selenide gas that can cause illness, and used daily, it might
enlarge the liver and spleen. Tellurium is sometimes used in association with selenium.
3. Selenium exists in three forms: a red amor-
phous powder, a gray form, and red crystals. Occurs as an
impurity in most sulfide ores. Selenium, along with tellu-
rium, is found in the sludges and sediments from electro-
lytic copper refining. It may also be recovered in flue dust
from burning pyrites in sulfuric acid manufacture.
Physical Properties
Selenium exists in several allotropic forms. Three distinct forms are (1)amorphous (2)crystalline and (3)metallic:
Amorphous forms exhibit two colors, occurring as a red powder of density 4.26g/cm3 that has a hexagonal crystal structure and a black vitreous solid of density 4.28g/cm3. The red amorphous selenium converts to the black form on standing. Amorphous selenium melts at 60 to 80°C; insoluble in water; reacts with water at 50°C when freshly precipitated; soluble in sulfuric acid, benzene and carbon disulfide.
Crystalline selenium exhibits two monoclinic forms: an alpha form constituting dark red transparent crystals, density 4.50 g/cm3. The alpha form converts to a metastable beta form of hexagonal crystal structure when heated to about 170°C. Both the crystalline forms are insoluble in water; soluble in sulfuric and nitric acids; very slightly soluble in carbon disulfide. Also, both the crystalline forms convert into gray metallic modification on heating.
The gray metallic form of selenium is its most stable modification. It constitutes lustrous gray to black hexagonal crystals; density 4.18 g/cm3 at 20°; melts at 217°C; soluble in sulfuric acid and chloroform; very slightly soluble in carbon disulfide; insoluble in alcohol.
All forms of selenium vaporize at 684.8°C.
Application
Selenium has many industrial uses, particularly electronic and solid-state applications, which have increased phenomenally in recent years. This is attributed to its unique properties: (1) it converts light directly to electricity (photovoltaic action); (2) its electrical resistance decreases with increased illumination (photoconductivity); and (3) it is able to convert alternating current to direct current.
Selenium is used in photoelectric cells, solar cells, and as a rectifier in radio and television sets. It also was used historically in exposure meters in photography and as an ingredient of toning baths. It is used in photocopying documents. In the glass industry it is incorporated to pigments to color pink, orange, and ruby-red glass. Other applications are as a metallic base in preparing electrodes for arc light; as an additive to stainless steel; in chrome plating bath for inducing microcracks for corrosion control; in vulcanization of rubber; as a catalyst; and as a flame-proofing agent for electric switchboard cables.
Although a toxic metal, selenium in trace amounts is a nutritional element. Trace amounts added to cattle food are effective against muscular dystrophy in sheep and cattle.
Production
Selenium is recovered from anode muds or slimes in electrolytic refining of copper. Anode mud is treated with sulfuric acid and roasted. Selenium is converted to its dioxide, which vaporizes and is collected in a wet scrubber system.
Alternatively, raw anode slimes are aerated with hot dilute sulfuric acid to remove copper. Slimes are then mixed thoroughly with sodium carbonate and roasted in the presence of sufficient air. Sodium selenate formed is leached with water. Hydrochloric acid is added to this selenate solution. Treatment with sulfur dioxide precipitates elemental selenium. Alternatively, the selenate solution is evaporated to dryness. Sodium selenate is reduced to sodium selenide by heating with carbon at high temperatures. Sodium selenide is leached with water. Air is blown over the solution. Selenide is oxidized to elemental selenium which precipitates.
In another process known as soda-niter smelting, a slight variation of the above method, after removal of copper anode slimes are mixed with sodium carbonate and silica and charged to the furnace. First, slags are removed. To the molten mass, caustic soda and potassium nitrate are added. Selenium and tellurium separate into the slags. The slags are cooled, crushed, and leached with water. Sulfuric acid is added. This precipitates tellurium as dioxide. Sulfur dioxide is then passed through the solution precipitating elemental selenium.
Selenium obtained by the above methods is about 99% pure. High purity metal may be obtained by refining this commercial grade material. Commercial grade selenium is distilled to form highly purified metal. Another refining method involves melting the crude metal and bubbling hydrogen through it. Hydrogen selenide so formed is decomposed at 1,000°C. A third method involves oxidizing selenium to its dioxide and reducing the latter with ammonia at 600 to 800°C.
Selenium was recovered earlier from flue dusts from lead and copper sulfide ores. This process is now obsolete and no longer used.
Reactions
The chemical properties of selenium fall between sulfur and tellurium. Thus, selenium reacts with oxygen similarly to sulfur, forming two oxides, selenium dioxide, SeO2 and trioxide, SeO3. The metal combines with halogens forming their halides. With nonmetals, selenium forms binary compounds exhibiting oxidation states +4 and +6.
Selenium reacts with electropositive metals and hydrogen forming selenides, where its oxidation state is –2. Thus, it combines with sodium to form sodium selenide, Na2Se. When the metal is heated with hydrogen below 250°C, the product is hydrogen selenide, H2Se.
The metal is not attacked by hydrochloric acid, nor does it react with dilute nitric and sulfuric acids. High purity selenium reacts slowly with concentrated nitric acid. The crude metal, however, dissolves in cold concentrated nitric acid.
When fused with caustic soda or caustic potash, sodium selenate, or potassium selenate, Na2SeO4, or K2SeO4 is obtained.
Molten selenium combines with most metals forming selenides. Such metal selenides include Ag2Se, Cu2Se, HgSe, ZnSe, CdSe, PbSe, FeSe, FeSe2, and Sb2Se3.
Selenium dissolves in sulfur and tellurium in all proportions.
Toxicity
Although an essential nutrient metal at trace concentrations, selenium is highly toxic at moderate concentrations. Some of its compounds, such as hydrogen selenide, are very toxic. Exposure to Se metal fumes can cause severe irritation of eyes, nose and throat. The metal is listed by the US EPA as one of the priority pollutant metals in the environment.
Description
Selenium was discovered in 1817 by J?ns Jacob Berzelius.
Especially noted was the similarity of the new element to the
previously known tellurium. Selenium is an essential trace
element atw0.1 ppm in diets. Selenium is a biologically active
part of a number of important proteins, particularly enzymes
involved in antioxidant defense mechanisms, thyroid hormone
metabolism, and redox control of intracellular reactions. In
humans and animals, selenium plays a role in protecting
tissues from oxidative damage as a component of glutathione
peroxidase.
Physical properties
Selenium is a soft metalloid or semimetal that is similar to tellurium, located just belowit in the oxygen group, and sulfur, which is just above it in the same group. Selenium hasseveral allotropic forms that range from a gray metallic appearance to a red glassy appearance.These allotropic forms also have different properties of heat, conductivity, and density. In itsamorphous state, it is a red powder that turns black and becomes crystalline when heated.Crystalline selenium has a melting point of 220°C, a boiling point of 685°C, and a densityof 4.809 g/cm3.
Isotopes
There are a total of 35 isotopes of selenium. Five of these are stable, anda sixth isotope has such a long half-life that it is also considered stable: Se-82 =0.83×10+20 years. This sixth isotope constitutes 8.73% of selenium’s abundance in theEarth’s crust, and the other five stable isotopes make up the rest of selenium’s abundanceon Earth.
Origin of Name
Named for the Greek word selene, meaning “moon.” Jons Jacob Berzelius
(1779–1848) discovered selenium and named it after the mineral called “eucairite,”
which in Greek means “just in time.”
Occurrence
Selenium is the 67th most abundant element in Earth’s crust. It is widely spread over theEarth, but does not exist in large quantities. As a free element it is often found with the elementsulfur.There is only one mineral ore that contains selenium: eucairite (CuAgSe). Although rich inselenium, it is too scarce to be of commercial use. Almost all selenium is recovered from theprocessing of copper and the manufacturing of sulfuric acid as a leftover sludge by-product.This makes selenium’s recovery profitable. Recovering it from eucairite is not profitable.Selenium is found in Mexico, Bosnia, Japan, and Canada. It can be found in recoverablequantities in some soils in many countries.
Characteristics
Crystalline selenium is a p-type semiconductor. It acts as a rectifier that can change electriccurrent from alternating current (AC) to direct current (to DC). It has photovoltaic proper ties, meaning it is able to convert light (radiant) energy that strikes it into electrical energy.Selenium’s resistance to the flow of electricity is influenced by the amount of light shining onit. The brighter the light, the better the electrical conductivity.Selenium burns with a blue flame that produces selenium dioxide (SeO2). Selenium willreact with most metals as well as with nonmetals, including the elements in the halogen group17.
History
Discovered by Berzelius in 1817,
who found it associated with tellurium, named for the Earth.
Selenium is found in a few rare minerals, such as crooksite and
clausthalite. In years past it has been obtained from flue dusts
remaining from processing copper sulfide ores, but the anode
muds from electrolytic copper refineries now provide the
source of most of the world’s selenium. Selenium is recovered
by roasting the muds with soda or sulfuric acid, or by smelting
them with soda and niter. Selenium exists in several allotropic
forms. Three are generally recognized, but as many as six
have been claimed. Selenium can be prepared with either an
amorphous or crystalline structure. The color of amorphous
selenium is either red, in powder form, or black, in vitreous
form. Crystalline monoclinic selenium is a deep red; crystalline
hexagonal selenium, the most stable variety, is a metallic
gray. Natural selenium contains six stable isotopes. Twentynine
other isotopes and isomers have been characterized. The
element is a member of the sulfur family and resembles sulfur
both in its various forms and in its compounds. Selenium exhibits
both photovoltaic action, where light is converted directly
into electricity, and photoconductive action, where the
electrical resistance decreases with increased illumination.
These properties make selenium useful in the production of
photocells and exposure meters for photographic use, as well
as solar cells. Selenium is also able to convert a.c. electricity
to d.c., and is extensively used in rectifiers. Below its melting
point, selenium is a p-type semiconductor and is finding
many uses in electronic and solid-state applications. It is
used in xerography for reproducing and copying documents,
letters, etc., but recently its use in this application has been
decreasing in favor of certain organic compounds. It is used
by the glass industry to decolorize glass and to make rubycolored
glasses and enamels. It is also used as a photographic
toner, and as an additive to stainless steel. Elemental selenium
has been said to be practically nontoxic and is considered to
be an essential trace element; however, hydrogen selenide and
other selenium compounds are extremely toxic, and resemble
arsenic in their physiological reactions. Hydrogen selenide in
a concentration of 1.5 ppm is intolerable to man. Selenium
occurs in some soils in amounts sufficient to produce serious
effects on animals feeding on plants, such as locoweed, grown in such soils. Selenium (99.5%) is priced at about $250/kg. It
is also available in high-purity form at a cost of about $350/kg
(99.999%).
Uses
Different sources of media describe the Uses of 7782-49-2 differently. You can refer to the following data:
1. selenium is a trace mineral used for years in topical preparations for its anti-fungal properties. Selenium has been shown to have other protective effects such as repairing DnA, reducing the DnA-binding of carcinogens, and suppressing gene mutations. In laboratory studies, skin lotions containing selenium compounds have been shown to decrease uV-induced skin damage such as inflammation, blistering, and pigmentation.
2. Selenium is used in the manufacture of colored glass, in photocells, in semiconductors,as a rectifier in radio and television sets, andas a vulcanizing agent in the manufacture ofrubber.Klaus Schwartz in 1957 discovered thattrace amounts of selenium in the feed protectedvitamin E-deficient rats from dietaryliver necrosis. Soon, thereafter, several animaland epidemiology studies showed thatits presence in the diet could provide protectiveaction in humans against several degenerativediseases including cirrhosis, cancer,diabetes and Keshan disease, a juvenile cardiomyopathy.The range between its beneficialand toxic character, however, is veryclose and, therefore, the daily dietary intakeshould be appropriately monitored (Naverro-Alarcon and Lopez-Martinez 2000). Thereis no accurate estimate of human requirementsof dietary selenium. Extrapolation ofanimal data to humans suggest an averagedaily requirement in the range 50 to 200 μg.Longnecker et al. (1991) observed no evidenceof adverse effects from selenium inhuman health at a daily intake level as highas 724 μg..
3. The photosensitive nature of selenium makes it useful in devices that respond to theintensity of light, such as photocells, light meters for cameras, xerography, and electric “eyes.”Selenium also has the ability to produce electricity directly from sunlight, making it ideal foruse in solar cells. Selenium possesses semiconductor properties that make it useful in the electronicsindustry, where it is a component in some types of solid-state electronics and rectifiers.It is also used in the production of ruby-red glass and enamels and as an additive to improvethe quality of steel and copper. Additionally, it is a catalyst (to speed up chemical reactions)in the manufacture of rubber.Selenium is an essential trace element for both plants and animals, and it is a diet supplementin animal feed as well as for humans.
Production Methods
Selenium (Se), a nonmetallic element of the sulfur group, is
widely distributed in nature. It is obtained along with tellurium
as a by-product of metal ore refining, chiefly from
copper deposits. About 16 ton is mined a year globally.
The global refinery production of selenium, excluding the
U.S. production, increased from about 1,400 metric ton in
2000 to about 1510 metric ton in 2008 and 1500
in 2009.
Because selenium is present in fossil fuels, up to 90% of
the selenium content in ambient air is emitted during their
combustion. Air pollution concentrations averaged from
0.38 ng/m3 in remote areas to 13 ng/m3 in urban areas.
The mass medium particle diameter was 0.92 mm. The
worldwide emissions of 10,000 tons/year from natural
sources exceed the atmospheric emissions from anthropogenic
sources (5100 ton). However, 41,000 tons is emitted
into the aquatic ecosystems. The largest contributors are
electric power generating plants that produce 18,000 ton;
manufacturing processes account for 12,000 ton.
Most of the world’s selenium today is provided by
recovery from anode muds of electrolytic copper
refineries. Selenium is recovered by roasting these muds
with soda or sulfuric acid or by melting them with a soda
and niter.
Definition
Different sources of media describe the Definition of 7782-49-2 differently. You can refer to the following data:
1. A metalloid element
existing in several allotropic forms
and belonging to group 16 of the periodic
table. It occurs in minute quantities in sulfide
ores and industrial sludges. The common
gray metallic allotrope is very
light-sensitive and is used in photocells,
solar cells, some glasses, and in xerography.
The red allotrope is unstable and reverts
to the gray form under normal
conditions.
Symbol: Se; m.p. 217°C (gray); b.p.
684.9°C (gray); r.d. 4.79 (gray); p.n. 34;
r.a.m. 78.96.
2. selenium: Symbol Se. A metalloidelement belonging to group 16 (formerlyVIB) of the periodic table; a.n.34; r.a.m. 78.96; r.d. 4.81 (grey); m.p.217°C (grey); b.p. 684.9°C. There are anumber of allotropic forms, includinggrey, red, and black selenium. Itoccurs in sulphide ores of other metalsand is obtained as a by-product(e.g. from the anode sludge in electrolyticrefining). The element is asemiconductor; the grey allotrope islight-sensitive and is used in photocells,xerography, and similar applications.Chemically, it resemblessulphur, and forms compounds withselenium in the +2, +4, and +6 oxidation states. Selenium was discoveredin 1817 by J?ns Berzelius.
General Description
Selenium is a reddish colored powder that may become black upon exposure to air. Selenium is toxic by ingestion. Selenium is used to manufacture electronic components and rubber.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
SELENIUM, silicon, or sulfur ignites in fluorine gas at ordinary temperatures [Mellor 2:11-13 1946-47]. A mixture of barium carbide and selenium heated to 150° C becomes incandescence [Mellor 5:862 1946-47]. Calcium carbide and selenium vapor react with incandescence [Mellor 5:862 1946-47]. A moist mixture of selenium and chlorates, except the alkali chlorates, becomes incandescent. Selenium reacts violently with chromium trioxide [Mellor 11:233 1946-47]. Reaction of selenium and silver bromate (also potassium bromate) is violently explosive [Mellor 2, Supp1:763 1956]. Freshly reduced selenium reacts vigorously with nitric acid. Trace amounts of organic matter probably influenced the reaction [J. Chem. Soc. 1938 p.391]. The reaction between zinc and selenium or tellurium is accompanied by incandescence [Mellor 4:476-480 1946-47].
Hazard
The fumes and gases of most selenium compounds are very toxic when inhaled. SeO2 andSeS2 are toxic if ingested and very irritating to the skin. They are also carcinogenic.Although some compounds of selenium are poisonous, as an element it is essential in traceamounts for humans. It is recommended that 1.1 to 5 milligrams of selenium be included inthe daily diet. This amount can be maintained by eating seafood, egg yokes, chicken, milk,and whole grain cereals. Selenium assists vitamin E in preventing the breakdown of cells andsome chemicals in the human body.
Health Hazard
The toxicity of selenium and its compoundsvaries substantially. Sodium seleniteis highly toxic; many sulfur compoundsof selenium are much less toxic. The targetorgans are the respiratory tract, liver,kidneys, blood, skin, and eyes. The sign ofacute poisoning is a garlic-like odor in thebreath and sweat. The other symptoms areheadache, fever, chill, sore throat, and bronchitis.Chronic intoxication can cause loss ofhair, teeth, and nails, depression, nervousness,giddiness, GI disturbances dermititis,blurred vision, and a metallic taste. Althoughinhalation toxicity is severe in test animals,oral toxicity is of low order. Chronic exposurecould cause a disease known as selenosis,characterized by a variety of neurologicalabnormalities. The LD50 values for seleniumcompounds vary with the compounds.
Matoba et al. (1986) reported a case offatal suicidal ingestion of “Super Blue”containing 4% selenious acid. Autopsy examinationshowed highest levels of Se in thelung, kidney and stomach of the patient.Death resulted from pulmonary edema, necrosisof proximal tubules and congestion of thekidney.
Paul and coworkers (1989) have investigatedthe antidotal actions of several compoundson the acute toxicity of seleniumin rats. Male Wistar rats were injectedsodium [75Se]selenite subcutaneously inthis study. Intraperitoneal administration ofdiethyldithiocarbamate or treatment withcitrate salt of bismuth, antimony, orgermanium, administered subcutaneously,reduced selenium-induced loss of bodyweight in the animals. Germanium citrateand bis(carboxyethyl)germanium sesquioxidepromoted increases in the 24-hour urinaryexcretion of selenium when administered 15minutes after sodium selenite.
The chemical species of selenium causingits toxic actions and the molecular target,however, are not well established. Guptaand Porter (2002) attributed selenite as thepotent inhibitor of the enzyme squalenemonooxygenase in cholesterol biosynthesis.Such inhibition by selenite, as well as,methylselenol was slow and irreversibleon purified recombinant human squalenemonooxygenase thus indicating a covalentbinding to the enzyme. Their study alsoshowed that presence of dithiol enhancedthe inhibition by selenite, suggesting theformation of a more toxic species, possiblyselenide. High doses of selenite werefound to cause cytotoxicity inducing 8-hydroxydeoxy-guanosine in DNA of primaryhuman keratinocytes (Li Shen et al. 2001).These authors investigated the interaction ofselenite and selenomethionine, the commondietary selenium antioxidants (to reduceoxidative stress) with other antioxidantsin DNA damage. Synergistic effects wereobserved between selenite and trolox (awater-soluble Vitamin E). On the other handCuSo4 played a protective role in seleniteinducedcytotoxicity, DNA oxidative damage and apoptosis. Haratake et al. (2005) studiedthe reaction of glutathione selenotrisulfide,an important intermediate in the metabolismof selenite with human hemoglobin. Thestudy showed that selenotrisulfide reactedrapidly with hemoglobin under physiologicalconditions.
Fire Hazard
Combustible material: may burn but does not ignite readily. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
Flammability and Explosibility
Nonflammable
Agricultural Uses
Selenium (Se) is a metalloid element belonging to Group
16 (formerly VIB) of the Periodic Table. It is an
essential ingredient in the forage for animals to prevent
muscular dystrophy or white muscle disease which
weakens the heart of cattle and sheep.
However, selenium is not essential for plants, and its
uptake by plants varies. Certain species of Astrugals
absorb more selenium than others because of a special
amino acid in them. Plants like mustard, cabbage and
onions absorb moderate amounts of selenium. This
absorbed selenium accumulates in the tissues of these
plants, and no treatment can remove it. The excess soil
selenium content can be corrected by the addition of
barium chloride or calcium sulphate, which may form
insoluble selenate.
Chemically, selenium resembles sulphur. Its total
concentration in most soils is between 0.1 and 0.3 ppm as
selenides, elemental selenium, selenites, selenates and
organic selenium compounds. The selenium uptake is the
highest in basic soil and the lowest in neutral soil.
There has been some concern about the increased
selenium deficiencies in cattle due to a negative effect of
sulphate on the selenate ion uptake by crops. Such
livestock disorders are severe after a wet summer. This is
due to a lowered soil redox potential, converting selinium
into forms unavailable for plant uptake. This is also
pronounced in soils with increased nitrate deposition
which converts the selenate and selenite into elemental
selenium or its gaseous form. On the other hand, winter
forage is seen to contain higher amounts of selenium.
Phosphate rocks and superphosphates containing 20
ppm or more of selenium may be sufficient for plants to
protect the livestock from being deficient in selenium.
Fertilization programs to produce selenium-adequate
forage, specifically suited to grazing animals, are a
subject of continuing interest. Fertilization with selenites
is preferred to other easily available selenates in view of
the former's slow-acting nature. Fertilization with
selenites is preferred also because they produce a lesser
level of selenium in plants than selenates do. Selenium of
roughly 75 g/ha for forages and 15 g/ha for foliar
application is satisfactory.
Biotechnological Applications
Selenium is a component of a number of proteins. Selenium can exist as an anion at biological pH, which makes it able to both give and accept electrons. The best understood physiological functions of selenium are two enzyme functions. One of these functions is done as part of a family of proteins named glutathione peroxidase (one is found inside of cells, another is outside cells in places like the plasma).
Glutathione peroxidase is part of the body's antioxidant defense network by eliminating peroxides, including hydrogen peroxide, which can be both precursors and products of free radicals. Selenium also functions in an enzyme that is part thyroid hormone synthesis. A more recently discovered selenium enzyme is known as thioredoxin reductase, which seems to have a number of regulatory roles within cells, and seems to affect antioxidant defense by in?uencing electron ?ow in some reactions. One interesting point about this enzyme is that in rats, the enzyme activities can be increased by elevating selenium intake above those normally considered adequate.
Safety Profile
Poison by intravenous route. When heated to decomposition it emits toxic fumes of Se. See also SELENIUM and SELENIUM COMPOUNDS
Potential Exposure
Most of the selenium produced is used
in the manufacture of selenium rectifiers. It is also utilized
as a pigment for ruby glass, paints, and dyes; as a vulcaniz-
ing agent for rubber; a decolorizing agent for green glass; a
chemical catalyst in the Kjeldahl test; as an insecticide; in
the manufacture of electrodes, selenium photocells, sele-
nium cells, and semiconductor fusion mixtures; in photo-
graphic toning bathes; and for dehydrogenation of organic
compounds. It is also used in veterinary medicine and in
antidandruff shampoos. Se is used in radioactive scanning
for the pancreas and for photostatic and X-ray xerography.
It may be alloyed with stainless steel; copper, and cast
steel. Selenium is a contaminant in most sulfide ores of
copper, gold, nickel, and silver; and exposure may occur
while removing selenium from these ores.
Veterinary Drugs and Treatments
Depending on the actual product and species, vitamin E/selenium
is indicated for the treatment or prophylaxis of selenium-tocopherol
deficiency (STD) syndromes in ewes and lambs (white muscle
disease), sows, weanling and baby pigs (hepatic necrosis, mulberry
heart disease, white muscle disease), calves and breeding cows
(white muscle disease), and horses (myositis associated with STD).
Vitamin E may be useful as adjunctive treatment of discoid lupus
erythematosus, canine demodicosis, and acanthosis nigricans in dogs. It may also be of benefit in the adjunctive treatment of hepatic
fibrosis or adjunctive therapy of copper-associated hepatopathy
in dogs.
Environmental Fate
Although selenium occurs naturally in the environment found
in rocks and soil, it can also be released by both natural and
manufacturing processes. However, forms of selenium can be
transformed (changed) in the environment. Weathering of
rocks to soil may cause low levels of selenium in water or it may
cause it to be taken up by plants and naturally released into the
air. Volcanic eruptions are suspected of contributing to selenium
in air, and soils in the areas around volcanoes tend to
have enriched amounts of selenium.
Selenium has multiple oxidation states (valence states)
including -2, 0, +4, and +6. The type of selenium found is
a result of its oxidation state, which may vary according to
ambient conditions, such as pH and microbial activity. Selenium
enters the air from burning coal or oil. Most of the selenium in
air is bound to fly ash and to suspended particles. The elemental
selenium that may be present in fossil fuels forms selenium
dioxide during combustion (burning). Selenium dioxide can
then form selenious acid with water or sweat. Selenium anhydride is released during the heating of copper, lead, and zinc
ores when there is selenium in them. Hydrogen selenide
decomposes rapidly in air to form elemental selenium and
water, thus eliminating the danger from this compound formost
people, except those who are exposed to it in their workplace.
Airborne particles of selenium, such as in coal ash, can settle
on soil or surface water. Disposal of selenium in commercial
products and waste could also contribute to selenium levels in
soil. But the amount of selenium released to soil from fly ash
and hazardous waste sites has not been measured. The forms
and fate of selenium in soil depend largely on the acidity of the
surroundings and its interaction with oxygen. In theory,
at equilibrium with no oxygen present, deep-soil selenium may
be present as elemental selenium. In the absence of oxygen
when the soil is acidic, the amount of biologically available
selenium should be low. Elemental selenium that cannot
dissolve in water and other insoluble forms of selenium (such
as selenium sulfide and heavy metal selenides) are less mobile
and will usually remain in the soil, posing less of a risk for
exposure. Active agricultural or industrial processes may
increase the amount of biologically available selenium by
decreasing the acidity of the soil and increasing the oxygen and
the soluble selenium compounds. Selenium compounds that
can dissolve in water are very mobile. For example, selenates
and selenites are water-soluble, and thus mobile, so there is an
increased chance of exposure to them. Irrigation drainage
waters may result in increased selenium entering the surface
water. Other factors that may affect the rates at which selenium
moves through the soil are temperature, moisture, time, season
of year, concentration of water-soluble selenium, organic
matter content, and microbiological activity.
Shipping
UN3283 Selenium compound, solid, n.o.s.,
Hazard Class: 6.1; Labels: 6.1-Poisonous material,
Technical Name Required.
Purification Methods
Dissolve selenium in small portions in hot conc HNO3 (2mL/g), filter and evaporate to dryness to give selenious acid which is then dissolved in conc HCl. Pass SO2 gas through the solution whereby selenium (but not tellurium) precipitates. It is filtered off and washed with conc HCl. This purification process is repeated. The selenium is then converted twice to the selenocyanate by treating with a 10% excess of 3M aqueous KCN (CARE), heated for half an hour on a sand-bath and filtered. Add an equal weight of crushed ice to the cold solution, followed by an excess of cold, conc HCl, with stirring (in an efficient fume cupboard as HCN is evolved) which precipitates selenium powder. This is washed with water until colourless, and then with MeOH and is heated in an oven at 105o. Finally it is fused for 2hours in vacuo. It is cooled, crushed and stored in a desiccator [Tideswell & McCullough J Am Chem Soc 78 3036 1956].
Toxicity evaluation
Selenium in the body can be grouped in three main categories:
selenium in proteins, nonprotein selenium species, and selenoamino
acids. The most prevalent selenium species include
selenocysteine, selenomethionine, and inorganic forms of selenium
(selenite and selenate). Little is known about the specific
biochemical mechanisms by which selenium and selenium
compounds exert their acute toxic effects but may involve redox
cycling. Generally, water-soluble forms are more easily absorbed
and are generally of greater acute toxicity. Sulfhydryl enzymes are
attacked by soluble selenium compounds.
Excess selenium results in liver atrophy, necrosis, and
hemorrhage.
Incompatibilities
Reacts violently with strong acids and
strong oxidizers, chromium trioxide; potassium bromate;cadmium. Reacts with incandescence on gentle heating
with phosphorous and metals, such as nickel, zinc, sodium,
potassium, platinum. Reacts with water @ 50 ? C forming
flammable hydrogen and selenious acids.
Waste Disposal
Powdered selenium: dispose
in a chemical waste landfill. When possible, recover
selenium and return to suppliers
Precautions
During use and handling of selenium, occupational workers should be careful to avoid
contact with the skin. Selenium compounds are considered very damaging to the liver,
and hazardous.
Check Digit Verification of cas no
The CAS Registry Mumber 7782-49-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7782-49:
(6*7)+(5*7)+(4*8)+(3*2)+(2*4)+(1*9)=132
132 % 10 = 2
So 7782-49-2 is a valid CAS Registry Number.
InChI:InChI=1/Se
7782-49-2Relevant articles and documents
Hydrothermal synthesis, characterization, and magnetic properties of cubic MnSe2/Se nanocomposites material
Sobhani, Azam,Salavati-Niasari, Masoud
, p. 93 - 101 (2014)
The cubic MnSe2/Se nanocomposites were produced under hydrothermal condition, by reduction of SeCl4to Se and Se2-, and reaction of the reduced selenium with Mn2+ion during the next step, in the presence of different surfactants using hydrazine as reductant. The main factors affecting the morphology, the particle size and the phase of the products, such as surfactant, reductant and its amount, reaction temperature and time were studied. The pure Se or a mixture of Se and MnSe2nanorods were obtained in the presence of different surfactants and small amounts of hydrazine. The cubic MnSe2/Se nanocomposites were formed at 120 °C for 12 h or longer periods of time, in the presence of polyethylene glycol (PEG) and large amounts of hydrazine. The size of the as-prepared cubes decreases with increasing the reaction time. With increasing temperature of reaction from 120°C to 180°C, the morphology of the products changes from cubes to the mixture of nanorods and nanoparticles.
Small molecule-controlled spontaneous growth of rose-like Se crystals at room temperature
Deng, Da-Wei,Yu, Jun-Sheng,Pan, Yi
, p. 1129 - 1134 (2008)
The spontaneous growth of rose-like Se crystals in aqueous solutions at room temperature is reported. The formation of rose-like Se crystals is based on the oxidation of Na2Se in the presence of thioglycerol solution at pH = 11 in a dark ambient atmosphere. In alkaline solutions, the growth evolution of rose-like Se crystals with aging time was followed by scanning electron microscopy (SEM), and an interesting formation process from initial Se monomers to amorphous Se (a-Se) spheres, and to the final rose-like complex structures of Se crystals was observed. Seven kinds of small molecules with different structures, including 1-thioglycerol (TG), mercaptamine (MA), L-cysteine (L-cys), 3-mercaptopropionic acid (MPA), thioglycolic acid (TGA), glycerol (GLY), and Lserine (L-ser), were used to manipulate the growth of Se crystals. The experimental results show that the structures of the small molecules play a key role in the growth of the Se crystals. The presence of thiols in the structure of the small molecules is favorable for the formation of the aggregates of Se crystals, and other termini, such as -NH2, -OH, or -COO-, will determine whether the aggregates of Se crystals are made up of Se slices or Se prisms. These observations suggest that the ligand molecules have a crucial effect on the nucleation, monomers, and growth of nanocrystals. The selection of ligands can be extended to other important materials for further preparation of nanocrystals with desired shapes. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
Preparation, Structure, and Properties of the Mo/Se Ions 2-Se)2(H2O)6>(2+) and 3-Se)4(H2O)12>(5+)
Henkel, G.,Kampmann, G.,Krebs, B.,Lamprecht, G. J.,Nasreldin, M.,Sykes, A. G.
, p. 1014 - 1016 (1990)
Preparation of the MoV2 di-μ-selenido aqua ion, 2-Se)2(H2O)6>(2+), has enabled the cuboidal mixed-valence (3.25) ion 3-Se)4(H2O)12>(5+) to be obtained; characterisation of both complexes including crystal str
Selenium adsorption on Cs-covered Si(100) 2 × 1 surfaces
Sotiropoulos,Kamaratos
, p. 637 - 641 (2004)
This report involves the study of Se adsorption on caesiated Si(100) 2 × 1 surfaces in ultra high vacuum (UHV) using low energy electron diffraction, Auger electron spectroscopy, thermal desorption spectroscopy and work function measurements. Selenium atoms on Cs/Si(100) 2 × 1 surface adsorb initially on uncaesiated portions of Si and subsequently on the Cs overlayer. The presence of Se increases the binding energy of Cs on Si(100). For Cs and Se coverages above 0.5 ml CsSe and CsxSe ySiz, compound formation was observed. The coadsorption of Se and Cs induces a high degree of surface disorder, while desorption most probably causes surface etching. The presence of Cs on Si(100) 2 × 1 surfaces prevents the diffusion of Se into the Si substrate and greatly suppresses the formation of SiSe2 and SiSe3, detected when Se is adsorbed on clean Si(100) 2 × 1 surfaces.
Studies of stoichiometry of electrochemically grown CdSe deposits
Bieńkowski, Krzysztof,Strawski, Marcin,Maranowski, Bartosz,Szklarczyk, Marek
, p. 8908 - 8915 (2010)
The proper deposition bath composition for electrochemical synthesis of the CdSe deposit in the hexagonal structure of the right elemental stoichiometry, and photoreacting as an n-type semiconductor which can be used as a stable photoanode is investigated. The deposits were prepared by a cyclic potentiodynamic technique and the concentration of Cd2+ and SeO 32- in the deposition baths varied from 10-4 M to 0.1 M, and from 10-5 M to 10-3 M, respectively. The electrochemical, the X-ray diffraction (EDS and XRD), and the photoactivity studies of a number of deposits have shown that application of the solution composition following Cd:Se = 5:1 results in deposition of the stoichiometric CdSe. The detected ratio of reagents is explained on the base of reaction mechanism and necessary excess of cadmium ions preventing CdSe deposit dissolution. The procedure of CdSe electrosynthesis was developed to yield of a direct semiconductor in the hexagonal structure. The necessity for cadmium cations excess is explained on the basis of the mixed electrochemical/chemical deposition mechanism.
Keller, E.
, p. 771 - 778 (1897)
Structural-morphological and biological properties of selenium nanoparticles stabilized by bovine serum albumin
Valueva,Borovikova,Koreneva,Nazarkina,Kipper,Kopeikin
, p. 1170 - 1173 (2007)
Nanostructures formed during the reduction of ionic selenium in the selenite-ascorbate redox system in an aqueous solution of bovine serum albumin (BSA) were studied using static and dynamic light scattering and flow birefringence. It was established that this process results in the formation of stable aggregates of selenium nanoparticles that adsorb BSA molecules. It was found that highly-ordered superhigh-molecular-weight spherical nanostructures with high density and unique morphology are formed. Experiments with a cell culture of promyelocytic leukemia HL-60 showed that BSA adsorbed on selenium nanoparticles can inhibit the growth of tumor cells and deactivate free radicals with an efficiency comparable with that of sodium selenite.
Synthesis and Application of Monomeric Chalcogenolates of 13 Group Elements
?i?ica, Tomá?,Milasheuskaya, Yaraslava,R??i?ková, Zdeňka,Němec, Petr,?vanda, Pavel,Zmrhalová, Zuzana Olmrová,Jambor, Roman,Bou?ka, Marek
, p. 4229 - 4235 (2019)
Utilization of the N,C,N-chelating ligand L (L={2,6-(Me2NCH2)2C6H3}?) in the chemistry of 13 group elements provided either N→In coordinated monomeric chalcogenides LIn(μ-E4) (E=
Synthesis of Se nanoparticles by using TSA ion and its photocatalytic application for decolorization of cango red under UV irradiation
Yang,Shen,Xie,Liang,Zhang
, p. 572 - 582 (2008)
In this study, we describe a size-controlled synthesis of selenium nanoparticles based on the reduction of selenious acid (H2SeO3) by UV-irradiated tungstosilicate acid (H4SiW12O40, TSA) solution which serves both as reducing reagent and stabilizer. The nanoparticles are characterized by ultraviolet-visible spectroscopy (UV-vis), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), X-ray photoelectron spectroscopy (XPS), the Raman spectra, transmission electron microscopy (TEM) and Zetasizer, respectively. The characteristic catalytic behavior of the Se nanoparticles is established by studying the decolorization of cango red in the presence of UV light. It is obvious that selenium catalyzes the reaction efficiently. The results show that the rate of dye decolorization varies linearly with the nanoparticle concentration and the rate of dye decolorization decreases with the size of the Se nanoparticles increasing.
Selenium-modified titanium dioxide photochemical diode/electrolyte junctions: Photocatalytic and electrochemical preparation, characterization, and model simulations
De Tacconi, Norma R.,Chenthamarakshan,Rajeshwar, Krishnan,Tacconi, Eugenio J.
, p. 11953 - 11960 (2005)
The photoelectrochemical behavior of TiO2 thin film electrodes, photocatalytically modified with Se islands, is described. The TiO2 thin films were electrodeposited on transparent conducting oxide glass substrates. The resultant electrode forms a n-TiO2p-Se photochemical diode which, in turn, contacts an electrolyte phase. Both transient photocurrent profiles (in response to excitation light that is switched on or off) and steady-state current-potential curves in response to chopped irradiation are considered. We show that the relative dominance of the contributions from the TiO2 and Se components to the overall response of the photochemical diode/electrolyte junction crucially depends on the wavelength distribution of the excitation light source. A simple equivalent circuit representation of this junction is presented, comprised of a photodiode in parallel with two photodiodes connected in series back-to-back. Simulations of the transient and steady-state photoelectrochemical response of this system are presented, and are shown to be in good agreement with the corresponding experimental profiles. ? 2005 American Chemical Society.
Thermodynamics of glass/crystal transformation in Se58Ge 42-xPbx (9 ≤ x ≤ 20) glasses
Deepika,Saxena, Narendra S.
, p. 28 - 35 (2010)
This article reports the thermodynamics of Se58Ge 42-xPbx (9 ≤ x ≤ 20) glassy alloys determined from the heat of fusion and specific heat capacity measurements. A differential scanning calorimetry method has been employed for the determination of thermodynamic quantities such as entropy, enthalpy, and Gibbs free energy differences between the glassy and crystalline phase of these alloys as a function of temperature. An effort has also been made to determine the stability of these glasses using the data obtained from different thermodynamic quantities. This study reveals that stability of the samples increases with the increase of lead (Pb) content in the glassy alloys.
Synthesis of anatase Se/Te-TiO2 nanorods with dominant {100} facets: Photocatalytic and antibacterial activity induced by visible light
Lin, Zong-Hong,Roy, Prathik,Shih, Zih-Yu,Ou, Chung-Mao,Chang, Huan-Tsung
, p. 302 - 309 (2013)
A facile method for the preparation of Te- and Se/Te-doped anatase TiO 2 nanorods (NRs) with exposed {100} facets, which provides high photocatalytic and antibacterial activity under irradiation with visible light, is developed. Sodium titanate nanotubes are formed from commercial TiO 2 nanoparticles (P25) in NaOH through a hydrothermal reaction. The as-prepared Na-titanate nanotubes are then used to form Te-TiO2 nanotubes in the presence of tellurite (TeO32-) ions and NaBH4. Upon further hydrothermal reaction, the Te-TiO2 nanotubes are transformed to form Te-TiO2 NRs that further form Sen/Te-TiO2 NRs through a reduction of selenite (SeO 32-) ions with NaBH4. The Te-TiO2 NRs and Sen/Te-TiO2 NRs have highly active {100} facets and thus provide the photocatalytic activities for the generation of ×OH at 2.5 and 4.5 times higher than that of commercial P25, respectively. The Te-TiO2 and Sen/Te-TiO2 NRs exhibit higher antibacterial activities against E. coli and S. aureus than P25 when activated by visible light. These stable and biocompatible Te-TiO2 and Se n/Te-TiO2 NRs hold great potential as potent antibacterial agents.
Schott, H. F.,Swift, E. H.,Yost, D. M.
, p. 721 - 721 (1928)
Electrochemical approach for selenization of stacked Cu-In layers for formation of crystalline CuInSe2
Gujar,Shinde,Park, Jong-Won,Lee, Hyun Kyung,Jung, Kwang-Deog,Joo, Oh-Shim
, p. E131-E135 (2008)
We report an electrochemical approach to form crystalline CuIn Se2 (CIS) films onto indium-tin-oxide substrates via thermal treatment to Se-coated Cu-In alloy. The simultaneous deposition of Cu-In alloy with optimum thickness was obtained by an electrochemical method from a mixture of aqueous solutions of CuS O4 and In2 (S O4)3 at constant potential. Further, the electrochemical method was used for deposition of elemental Se onto the priorly deposited Cu-In alloy film. To produce CIS films, Se-coated Cu-In alloy films were annealed in argon atmosphere at different temperatures ca. 350-450°C for 30 min. The Cu-In alloy, Se-coated Cu-In alloy, and thermally treated films were characterized using X-ray diffraction to identify the phases and scanning electron microscopy to observe the surface morphology.
Structural and optical properties of amorphous selenium prepared by plasma-enhanced CVD
Nagels,Sleeckx,Callaerts,Tichy
, p. 49 - 52 (1995)
The preparation of layers of amorphous Se by plasma-enhanced CVD using the hydride H2Se as precursor gas is described. Information concerning the structure of the films was obtained from Raman spectroscopy. The spectra of amorphous Se indicated that the dominant molecular structure is the eight-membered ring and/or a chain with Se8 molecular fragments. This material exhibited reversible photodarkening when illuminated at 77 K. In order to explain this phenomenon, we propose a mechanism which takes into account the role of the lone-pair electron orbitals of Se in their contribution to structural ordering. Illumination can cause a distortion in the normal bonding direction between nearest-neighbour Se atoms and induce in this way intrinsic defect states located at the band edges. In the photo-darkened state, optical transition will occur between these defect states.
Chemically deposited se thin films and their use as a planar source of selenium for the formation of metal selenide layers
Bindu,Nair,Nair
, p. C526-C534 (2006)
Selenium thin films of thickness ～300 nm were deposited from a solution of sodium selenosulfate of pH 4.5. These films are amorphous, but they are crystalline and photoconductive through annealing for 15 min at 150- 200 C. In this paper we present the properties of these films and their use as a planar source of selenium vapor (1.7× 10-6 mol cm2 of the film) to react with metal films to form metal selenide layers. For this, metal films of Ag, Sn, In, Cu, Sb, etc., deposited by thermal evaporation, are kept in contact with the Se-thin film and are heated at temperatures typically a chemically deposited thin film of Sb2 S3, AgSbSe2 is produced through heating at 200- 300 C. Photovoltaic structures SnO2: F-CdS- Sb2 S3 - AgSbSe2 fabricated this way show open-circuit voltage >500 mV and short-circuit current density of 2-5 mA cm2.
Deposition of selenium thin layers on gold surfaces from sulphuric acid media: Studies using electrochemical quartz crystal microbalance, cyclic voltammetry and AFM
Cabral, Murilo Feitosa,Pedrosa, Valber A.,Machado, Sergio Antonio Spinola
, p. 1184 - 1192 (2010)
In this paper we report here new considerations about the relationship between the mass and charge variations (m/z relationship) in underpotential deposition (UPD), bulk deposition and also in the H2Se formation reaction. Nanogravimetric experiments were able to show the adsorption of H2SeO3 on the AuO surface prior to the voltammetric sweep and that, after the AuO reduction, 0.40 monolayer of H2SeO3 remains adsorbed on the newly reduced Au surface, which was enough to gives rise to the UPD layer. The UPD results indicate that the maximum coverage with Seads on polycrystalline gold surface corresponds to approximately 0.40 monolayer, in good agreement with charge density results. The cyclic voltammetry experiments demonstrated that the amount of bulk Se obtained during the potential scan to approximately 2 Se monolayers, which was further confirmed by electrochemical quartz crystal microbalance (EQCM) measurements that pointed out a mass variation corresponding of 3 monolayers of Se. In addition, the Se thin films were obtained by chronoamperometric experiments, where the Au electrode was polarized at +0.10 V during different times in 1.0 M H2SO4 + 1.0 mM SeO2. The topologic aspects of the electrodeposits were observed in Atomic Force Microscope (AFM) measurements. Finally, in highly negative potential polarizations, the H2Se formation was analyzed by voltammetric and nanogravimetric measurements. These finding brings a new light on the selenium electrodeposition and point up to a proposed electrochemical model for molecule controlled surface engineering.
Development of a hydrothermal method to synthesize spherical znse nanoparticles: Appropriate templates for hollow nanostructures
Gharibe, Soodabe,Afshar, Shahrara,Vafayi, Leila
, p. 37 - 44 (2014)
Hydrothermal method was used to synthesize pure ZnSe nanosphere materials. The effects of the reducing agent amount, the reaction time and temperature were investigated on the purity of ZnSe. Also, the effects of surfactants such as sodium dodecyl sulfate (SDS) (anionic) and cetyl trimethylammonium bromide (CTAB) (cationic) were studied on the morphology of ZnSe. The prepared nanospheres were characterized using XRD, SEM, TEM and UV-Vis spectroscopy. Through these techniques, it was found that the pure ZnSe nanoparticles have a zinc blend structure and in a spherical form with average diameter of 30 nm.
Preparation of single-crystalline selenium nanowires in the presence of ethylenediaminetetramethylenephosphonic acid
Lei, Yun,Yao, Lide,He, Yuping,Wang, Shiquan,Yu, Richeng,Zou, Bingsuo
, p. 330 - 331 (2006)
Selenium nanowires have been synthesized by using 2-mercaptoethylamine- depleted CdSe nanoparticles as selenium source and ethylenediaminetetramethylenephosphonic acid as chelating agent. The products were characterized by X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, and UV-vis spectrophotometry. The result shows that the selenium nanowires are single crystals grown along the [001] direction of hexagonal lattice. The optical measurement shows a blue shift relative to the bulk hexagonal selenium, and the optical bandedge might be attributed to the interchain interactions within a hexagonal selenium crystal. Copyright
Sorum, C. H.,Edwards, J. O.
, p. 2318 - 2322 (1952)
Electrochemical synthesis of selenium nanotubes by using CTAB soft-template
Zhang, Sheng-Yi,Zhang, Juan,Liu, Yi,Ma, Xiang,Chen, Hong-Yuan
, p. 4365 - 4370 (2005)
The single-crystalline Se nanotubes were synthesized on the surface of Au sheet electrode by cyclic voltammetry. In synthesis process, cetyltrimethyl ammonium bromide (CTAB) was used as soft-template. The formation mechanism of Se nanotubes was discussed.
Riley oxidation: A forgotten name reaction for synthesis of selenium nanoparticles
Shah, Chetan P.,Dwivedi, Charu,Singh, Krishan K.,Kumar, Manmohan,Bajaj, Parma N.
, p. 1213 - 1217 (2010)
A simple wet chemical method, involving reaction of acetone with selenium dioxide, has been developed, to synthesize polyvinyl alcohol-stabilized selenium nanoparticles. The method is capable of producing nanoparticles in the size range of about 100-300 nm, under ambient conditions. The synthesized nanoparticles can be separated easily from the aqueous sols by a high-speed centrifuge, and can be re-dispersed in aqueous medium by a sonicator. The effect of concentrations of selenium dioxide, acetone and PVA on the size of the selenium nanoparticles has been studied. The size of the selenium nanoparticles has been found to increase with increase in the reaction time as well as the concentration of selenium dioxide, while it decreases with increase in the concentration of the stabilizer, PVA. The synthesized selenium nanoparticles have been characterized by UV-visible optical absorption spectroscopy, X-ray diffraction, energy dispersive X-ray analysis, differential scanning calorimetry, atomic force microscopy, scanning electron microscopy and transmission electron microscopy techniques.
XRD, SEM and photoelectrochemical characterization of ZnSe electrodeposited on Cu and Cu-Sn substrates
Ju?knas, Remigijus,Avi?inis, Darius,Kalinauskas, Putinas,Selskis, Algirdas,Giraitis, Raimondas,Pak?tas, Vidas,Karpavi?ien, Violeta,Kanapeckait, Stase,Mockus, Zenius,Kondrotas, Rokas
, p. 118 - 123 (2012)
XRD, SEM and photoelectrochemical examinations of deposits formed on the Cu substrate by electrochemical deposition in a water solution containing 0.2 mol dm-3 of ZnSO4 and 0.002 mol dm-3 of H 2SeO3 were performed. Formation of Cu2Se x at potentials positive to that of electrochemical deposition of ZnSe was proved by the XRD technique. The formation of Cu2Se x continued even after deposition due to further diffusion of the deposited Se into Cu. A nano-crystalline ZnSe of cubic structure was electrodeposited at a potential of -0.62 V vs. Ag/AgCl electrode and XRD examination of deposits formed using cyclic potential scanning and pulse plating revealed the presence of hexagonal ZnSe along with the cubic one. A photoelectrochemical characterization proved that the electrodeposited ZnSe was a p-type semiconductor. A significant amount of Cu2Sex was formed during annealing of ZnSe electrodeposited on the Cu substrate although only traces of copper selenide were detected before the annealing. ZnSe, SnSe and a small quantity of Cu2Sex were detected by XRD after annealing of ZnSe electrodeposited on the Cu-Sn/Mo/glass substrate.
Gutbier, A.,Engeroff, F.
, p. 193 - 193 (1914)
Reactivity of Ionic Liquids: Reductive Effect of [C4C1im]BF4 to Form Particles of Red Amorphous Selenium and Bi2Se3 from Oxide Precursors
Knorr, Monika,Schmidt, Peer
, p. 125 - 140 (2020/12/17)
Temperature-induced change in reactivity of the frequently used ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate ([C4C1im]BF4) is presented as a prerequisite for the rational screening of reaction courses in material synthesis. [C4C1im]BF4 becomes active with oxidic precursor compounds in reduction reaction at ?≥200 °C, even without the addition of an external reducing agent. The reaction mechanism of forming red amorphous selenium from SeO2 is investigated as a model system and can be described similarly to the Riley oxidation. The reactive species but-1-ene, which is formed during the decomposition of [C4C1im]BF4, reacts with SeO2 and form but-3-en-2-one, water, and selenium. Elucidation of the mechanism was achieved by thermoanalytical investigations. The monotropic phase transition of selenium was analyzed by the differential scanning calorimetry. Beyond, the suitability of the single source oxide precursor Bi2Se3O9 for the synthesis of Bi2Se3 particles was confirmed. Identification, characterization of formed solids succeeded by using light microscopy, XRD, SEM, and EDX.
