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#Post#: 32--------------------------------------------------
Sofoline (So)
By: Chente Date: August 30, 2018, 2:59 am
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Sofoline is a chemical element with an atomic number of 14s,
symbol So. It is a toxic red translucent liquid and is
moderately reactive. Despite its toxicity, it has wide variety
of applications, being an important reactant in manufacturing
polymers, ceramics as well pesticides and raw material for
synthesizing medical drugs.
History
Sofoline was first identified by Maryl Marte in 2045 when she
noticed a clear red liquid is formed on the surface of heated
charcoal. It was not prepared in bulk amounts until in 2097
Bentyl Dcardes condensed sofoline dioxide and reduce it using
hydrogen.
Properties
[list]
[li]At standard room temperature and pressure, sofoline is a red
translucent liquid.[/li]
[li]It boils at 315.75 K (42.60 °C, 108.68 °F) to form a lime
green gas and freeze at 138.91 K (−134.24 °C,
−209.63 °F) to form a red translucent solid.[/li]
[li]The solid state is commonly known as red ice as it also have
the bizarre property of lower density than its liquid state in
addition to its transparency.[/li]
[li]Sofoline is quite similar to water in many physical aspects
except it has lower specific heat capacity, latent heat, less
volatile and is toxic, thus it’s commonly known as toxic water
or blood water.[/li]
[li]Sofoline can bond with each other to form long chains,
rings, branches etc. This allow sofoline to form diverse
compounds analogous to the organic compounds formed by carbon,
with all the carbon in the functional groups replaced by
sofoline. The ability for sofoline to expand valancy allows more
possible combinations than carbon.[/li]
[li]Sofoline has no biological role on carbon lifeforms such as
humans and carbon-synths and is toxic even in trace amounts. On
the other hand, sofoline is an essential macronutrient to
sofoline lifeforms, which is present as important biomolecules
in the place of carbon within their bodies as structural
components and food substances. Sofoline life ingests sofoganic
compounds to obtain energy for metabolism.[/li][/list]
Applications
Elemental sofoline
Owing to its oxidation state can be zero even in compounds; it
can be used in place of many metals as a bridging agent to
connect fragments of complex organic compounds together to
synthesize various important medical drugs, pesticides etc. The
So bridges can be removed easily leaving the finished product.
Sofoline can be attached to simple molecules to provide 'sticky
ends' which allow the molecules to polymerize easily. This
allows easy synthesis of important plastics. The disofoline bond
and the sofo group can be removed easily leaving the polymer
behind, or left within the polymer to produce self healing
plastics for specialized uses.
As a precursor to organosofoline and sofoganic compounds.
Due to the ease for sofoline to combine with other elements
esepcially hydrogen to form sofolane (SoH4), and the lower
activiation energy required to decompose sofolane into its
consituent elements than methane. It is commonly employed on gas
giants to harvest hydrogen from their atmospheres. In addition
it can also be used to concentrate deuterium and tritium for
fusion reactors used both in military and civillian
applications.
Sofoline compounds
Chlorosofolicacid (H4ClSo4) is sometimes used in place of
sulphuric acid to remove the oxide layer of metals. The various
sofochlorites are used in other applications ranging from
chemical additives to catalysts.
Sofoline nitride (SoN3) is used in various engine parts and
plating for automobiles, bearings, armour,nozzle for the plasma
thrusters and hull material for starships owing to its excellant
resistance to wear and high temperature.
Sofoline hydroxide (So(OH)5) is sometimes used in place of
sodium hydroxide for various applications (e.g. etching) except
food processing.
Sofoline chlorides (SoCln) and other sofoline halides are more
preferred to sulphur hexafluoride to be used to provide a
dielectric medium and inert medium as all sofoline halides are
inert towards most environment conditions owing to the bizarre
atomic properties of sofoline atoms and thus have low toxicity.
Nickel sofolide (NiSo) is an important catalyst used in the
refining of tsgnium.
The relatively weak So-H bond of sofolane allows it to become a
chemical feedstock for synthesis of various sofoganic compounds.
Safety and toxicity
Sofoline and its vapor are extremely toxic to non sofoline
lifeforms especially carbon lifeforms. Sofoline can easy
penetrate through the skin to enter the body and its high
affinity for hydrogen can allow it to bind strongly to tissues
and proteins. Sofoline is chemically similar to carbon thus
allow it to replace most carbon atoms within proteins and
important structures. This inhibits important enzymes and halts
physiological process such as respiration and result in death
within a few hours to minutes. A concentration at 0.1 ppm gives
headaches and vertigo which delays for an hour up to three
hours. Medical attention is required immediately after exposure.
Concentrations at 0.2-0.5 ppm deadens all symptoms and result in
death if untreated within 30 minutes Concentrations above 0.5
ppm causes permanent damage to major organs and can only be
treated using a time chamber together with the backup molecular
location blueprint of the individual to reverse the damage.
Sofoline hydroxide and chlorosofolic acid are corrosive and
oxidizing, which attacks tissues readily and standard
precautions of using corrosive chemicals apply.
Sofoline phosphide is extremely explosive and must be handled
with care.
Sofoline halides represent simple asphyxiation hazard with few
warning symptoms.
Other sofoline compounds are hazardarous and should be handled
carefully.
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