Benzene Nitration Arabic
Benzene Nitration Arabic
Benzene Nitration Arabic
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OXIDATION (reading.php?idm=38330)
ETHYNYLATION (reading.php?idm=37820)
NITRATION
Nitration is the insertion of a nitro group (-NO2) into an organic compound, usually through the agency of the reaction of a hydrocarbon with
nitric acid. Concentrated sulfuric acid may be used as a catalyst.
Both straight chain and ring-type carbon compounds can be nitrated; alkanes yield nitroparaffins. The process for the production of
nitrobenzene from benzene involves the use of mixed acid (Fig. 1), but there are other useful nitrating agents, e.g., inorganic nitrates, oxides
of nitrogen, nitric acid plus acetic anhydride, and nitric acid plus phosphoric acid. In fact, the presence of sulfuric acid in quantity is vital to the
success of the nitration because it increases the solubility of the hydrocarbon in the reaction mix, thus speeding up the reaction, and promotes
the ionization of the nitric acid to give the nitronium ion (NO2+), which is the nitrating species. Absorption of water by sulfuric acid favors the
nitration reaction and shifts ther eaction equilibrium to the product.
Nitration offers a method of making unreactive paraffins into reactive substances without cracking. Because nitric acid and nitrogen oxides
are strong oxidizing agents, oxidation always accompanies nitration. Aromatic nitration reactions have been important particularly for the
manufacture of explosives. Nitrobenzene is probably the most important nitration product.
Certain esters of nitric acid (cellulose nitrate, glyceryl trinitrate) are often referred to as nitro compounds (nitrocellulose, nitroglycerin), but this
terminology should be avoided. Vapor-phase nitration of paraffin hydrocarbons, particularly propane, can be brought about by uncatalyzed
contact between a large excess of hydrocarbon and nitric acid vapor at around 400oC, followed by quenching. A multiplicity of nitrated and
oxidized products results from nitrating propane; nitromethane, nitroethane, nitropropanes, and carbon dioxide all appear, but yields of useful
products are fair. Materials of construction must be very oxidation-resistant and are usually of ceramic-lined steel. The nitroparaffins have
found limited use as fuels for race cars, submarines, and model airplanes. Their reduction products, the amines, and other hydroxyl
compounds resulting from aldol condensations have made a great many new aliphatic yntheses possible because of their ready reactivity.
Nitration reactions are carried out in closed vessels that are provided with an agitating mechanism and means for controlling the reaction
temperature. The nitration vessels are usually constructed of cast iron and steel, but often acid-resistant alloys, particularly chrome-nickel
steel alloys, are used. Plants may have large (several hundred gallon capacity) nitration vessels operating in a batch mode or small
continuous units. The temperature is held at about 50oC, governed by the rate of feed of benzene. Reaction is rapid in well-stirred and
continuous nitration vessels. The reaction products are decanted from the spent acid and are washed with dilute alkali. The spent acid is sent
to some type of recovery system and yields of 98 percent can be anticipated.
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Considerable heat evolution accompanies the nitration reaction, oxidation increases it, and the heat of dilution of the sulfuric acid increases
it still further. Increased temperature favors dinitration arid oxidation, so the reaction must be cooled to keep it under control. Good heat
transfer can be assured by the use of jackets, coils, and good agitation in the nitration vessel. Nitration vessels are usually made of stainless
steel, although cast iron stands up well against mixed acid.
When temperature regulation is dependent solely on external jackets, a disproportional increase in nitration vessel capacity as compared
with jacket surface occurs when the size of the machine is enlarged. Thus, if the volume is increased from 400 to 800 gallons, the heat-
exchange area increases as the square and the volume as the cube of the expanded unit. To overcome this fault, internal cooling coils or
tubes are introduced, which have proved satisfactory when installed on the basis of sound calculations that include the several thermal factors
entering into this unit
process.
A way of providing an efficient agitation inside the nitration vessel is essential if local overheating is to be mitigated. Furthermore, the
smoothness of the reaction depends on the dispersion of the reacting material as it comes in contact with the change in the nitration vessel so
that a fairly uniform temperature is maintained throughout the vessel. Nitration vessels are usually equipped with one of three general types
of agitating mechanism: (1) single or double impeller, (2) propeller or turbine, with cooling sleeve, and (3) outside tunnel circulation. The
single-impeller agitator consists of one vertical shaft containing horizontal arms. The shaft may be placed off center in order to create rapid
circulation past, or local turbulence at, the point of contact between the nitrating acid and the organic compound.
The double-impeller agitator consists of two vertical shafts rotating in opposite directions, and each shaft has a series of horizontal arms
attached.
The lower blades have an upward thrust, whereas the upper ones repel the liquid downward. This conformation provides a reaction mix that
is essentially homogeneous. The term sleeve-and-propeller agitation is usually applied when the nitration vessel is equipped with a vertical
sleeve through which the charge is circulated by the action of a marine propeller or turbine. The sleeve is usually made of a solid bank of acid-
resisting cooling coils through which cold water or brine is circulated at a calculated rate. In order to obtain the maximum efficiency with this
type of nitration vessel, it is essential to maintain a rapid circulation of liquid upward or downward in the sleeves and past the coils.
الكيمياء العضوية
أي المواد التي تحتوي على عناصر الكربون والهيدروجين واالوكسجين، ويدرس بنية وخواص وتفاعالت المركبات والمواد العضوية.هي أحد فروع علم الكيمياء
وكذلك دراسة البنية تتضمن استخدام المطيافية (مثل رنين.)والنتروجين واحيانا الكبريت (كل ما يحتويه تركيب جسم الكائن الحي مثال البروتين يحوي تلك العناصر
إلى عناصر أخرى و.مغناطيسي نووي) ومطيافية الكتلة والطرق الفيزيائية والكيميائية األخرى لتحديد التركيب الكيميائي والصيغة الكيميائية للمركبات العضوية
. كيمياء عضوية فلزية و كيمياء عضوية ال فلزية-:تشمل
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