United States Patent [191

[111

4,088,742

Homme, Jr.

[45]

May 9, 1978

[54]

CONTACT SULFURIC ACID PROCESS

956,049

EMPLOYING DOUBLE
CONVERSION/DOUBLE ABSORPTION
[75] Inventor: Arthur C. Homme, Jr., Basking
Ridge, NJ.

Tucker et al., 80; Emission Control from Acid Plants,

Chemical Engineering Progress, vol. 67, #5, May 1971,

Morristown, NJ.

[21] Appl. No.: 772,191

[22] Filed:
Feb. 25, 1977
[51] Int. Cl.
001B 17/72;C01B 17/68
US. Cl. ............................... .. 423/522; 423/533.
Field of Search ....................... .. 423/522, 533-535

[56]

United Kingdom ............... .. 423/535

OTHER PUBLICATIONS

[73] Assignee: Allied Chemical Corporation,

[52]
[58]

4/ 1964

References Cited

U.S. PATENT DOCUMENTS

3,350,169

10/1967

Rinckhoff .......................... .. 423/522

3,653,828
3,525,586
3,443,896

4/
5/1969
8/1970
1972

Dreclsel
Conner
Furkert et
eteta1.
a1. ..................... .. 423/522

FOREIGN PATENT DOCUMENTS

1,467,010

12/1968

1,567,403

5/1972

Germany ........................... .. 423/522

Germany

1,177,117

9/1964

Germany ........................... .. 423/522

pp. 57-63.
Primary Examiner--O. R. Vertiz
Assistant Examiner-Gary P. Straub
Attorney, Agent, or Firm-Gerhard H. Fuchs; Ernest A.
Polin

[57]

ABSTRACT

Improvement in the contact sulfuric acid process em

ploying double conversion, double absorption using a

cold, sulfur dioxide-containing feed gas stream obtained
from a wet gas puri?cation plant, which involves by
passing a portion of the cold feed gas stream around the
primary conversion and intermediate absorption sec
tions, and introducing it directly into the secondary
conversion section, results in energy savings by reduc
ing amount of power required to transport the gas
through the plant, and by increasing the amount of
recoverable heat of reaction from the secondary con
version section.

423/522

8 Claims, 3 Drawing Figures

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4,088,742

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4,088,742

4,08 8,742

CONTACI SULFURIC ACID PROCESS

EMPLOYING DOUBLE CONVERSION/DOUBLE
ABSORPTION
BACKGROUND OF THE INVENTION
The present invention relates to an improvement in
the contact sulfuric acid process. More particularly, the

the process self-sustaining. For that reason, Furkert et

al. suggested addition of pure, dry sulfur in the form of
solid granules or in liquid form to the gas stream prior to
its introduction into the secondary conversion stage, so
that the sulfur melts and is ignited immediately and very

quickly delivers the required heat in order to maintain

the oxidation in the second conversion stage. Furkert et

al.s suggestion, while operable, presents certain equip

present invention relates to an improvement in the

ment problems in that it requires special means for intro
contact sulfuric acid process employing the double 10 ducing the elemental sulfur. Furthermore, elemental
conversion-double absorption steps operating on cold
sulfur may not be available at the plant, for example,
sulfur dioxide-containing feed gas obtained from a wet
when the plant is operating on sulfur dioxide-containing

gas puri?cation plant.

In the contact sulfuric acid process, a gas stream

containing both sulfur dioxide and free oxygen is passed

through a catalyst, after having been preheated to the
kindling temperature of the catalyst, if necessary, to
effect oxidation of the sulfur dioxide to form sulfur

trioxide, followed by cooling the gas stream to tempera

gas obtained by roasting of sulfur ores.

Disadvantages of use of shell-and-tube type heat ex
changers for'preheating the feed gas stream to the sec
ondary conversion stage are overcome by employing
heat sink type heat exchangers, as described by Mareski '

et al. Canadian Pat. No. 975,927. The higher heat recov

ery possible with less expensive and less corrosion sus

ture within the range of about 400 to about 550 F and 20

ceptible pebble bed type heat exchangers as described
contacting it with strong sulfuric acid to effect selective
by
Mareski et al. may indeed avoid need for burning
absorption of the sulfur trioxide. The oxidation of sulfur
sulfur in the gas stream, as required by Furkert et al., in
dioxide to sulfur trioxide is an equilibrium reaction;
the event the gas stream being fed to the secondary
complete oxidation of the sulfur dioxide cannot be
achieved in the presence of the'sulfur trioxide which is 25 conversion stage contains at least about one percent of
sulfur dioxide. Nevertheless, the pebble bed heat ex
being formed. However, the equilibrium can be shifted
changers required by Mareski et al. are bulky, and at
toward the sulfur trioxide by removing the sulfur triox
least two of these are required. These are alternately
ide from the reaction mixture. Therefore, it is common
heated and cooled by alternating the direction of the
practice to subject the gas stream from which sulfur

trioxide has been selectively removed by scrubbing

with strong sulfuric acid to a second conversion by
passing it through a catalyst mass, after preheating it to

the kindling temperature of the catalyst. Thereafter it is

again cooled and passed through a second absorber
wherein it is contacted with strong sulfuric acid to
scrub sulfur trioxide therefrom. The exit gas from the
second absorber, which now contains only trace
amounts of unconverted sulfur dioxide, is vented to the

atmosphere.

gases ?owing through them, so that they require rela

tively close operator attention.

It has also been proposed to employ shell-and-tube

type heat exchangers for preheating the feed gas stream
to the secondary conversion stage to effect indirect heat
exchange contact with exit gases from that stage, as
described by Furkert et al., and to supply the additional
amount of heat which may be required to bring the feed

gas stream to the kindling temperature of the catalyst by

indirectly contacting it with products of combustion of
fossil fuel, as, for example, described by W. G. Toka and

As previously noted, the feed gas stream containing

both sulfur dioxide and free oxygen must, before intro
duction into the catalyst mass, be heated to at least the
kindling temperature of the catalyst which, in the case

J. R. Burley in Chemical Engineering Practice, Vol. 67,

No. 5, p. 57 et seq. (May 1971).

of the commonly employed vanadium catalyst, is in the

on a hot sulfur dioxide-containing feed gas stream ob

Of course, in a contact sulfuric acid plant operating

order of about 780 to about 800 F. In a sulfuric acid 45 tained by combustion of brimstone, suf?cient heat is

plant wherein the sulfur dioxide-containing feed gas

stream is obtained by combustion of brimstone, this

available to preheat the gases prior to introduction into

the secondary conversion stage by indirect heat ex
presents no problem since the gases obtained by com
change with the hot gas from the brimstone combus
bustion of brimstone are at a temperature above that
tion, or by indirect heat exchange contact with con
kindling temperature, and excess heat can be recovered 50 verter gases from the ?rst conversion stage, or alterna
from the gas stream, as by passing it through a waste
tively, by introducing hot sulfur dioxide-containing
heat boiler prior to introducing it into the converter
gases from the brimstone burner directly into the sec
containing the catalyst. Also, the oxidation of sulfur
ondary conversion stage, as described by P. Rinckhoff,
dioxide to sulfur trioxide is an exothermic reaction, so
in U.S. Pat. No. 3,350,169. The Rinckhoff procedure of
that heat is generated in the conversion, which can be 55 introducing hot products of combustion of brimstone
recovered, if desired.
directly into the secondary conversion stage seems to be
In a sulfuric acid plant employing the double conver
equivalent to Furkert et al.s procedure of introducing
sion-double absorption process steps, as above de
sulfur into that gas stream. In each case, the desired
scribed, the gases obtained from the intermediate ab
effect is provision of heat by combustion of sulfur.
sorber must be preheated prior to introducing them into 60 However, the expedient of Rinckhoff et al. is not avail
the second conversion stage. This can be effected under
utilization of the heat generated in the second conver
sion stage, as shown by Furkert et al. in U.S. Pat. No.

able in a contact sulfuric acid plant employing a cold

sulfur dioxide-containing feed gas stream obtained from

a wet gas purification plant.
3,443,896. However, since the temperature differentials
It is an object of the present invention to provide a
involved here are relatively small, impracticably large 65 double conversion-double absorption contact sulfuric
heat exchangers of the shell-and-tube type would be
acid process, using cold sulfur dioxide-containing feed
required, and even then the heat available from reaction
gas obtained from a wet gas purification plant, having
in the secondary stage is generally insuf?cient to make
reduced energy requirements.

4,088,742

It is a further object to provide such process wherein

size of equipment required for the primary conversion

and intermediate absorption steps is reduced, wherein
power requirements to transport the gas stream through
the primary conversion and intermediate absorption
steps are reduced, and wherein external heat require
ments for preheating the feed gas stream to the second
ary conversion step are minimized.

SUMMARY OF THE INVENTION

The present invention provides a process for making
sulfuric acid by catalytic oxidation of sulfur dioxide
from a cold sulfur dioxide-containing feed gas stream
from a wet gas puri?cation plant, involving the steps of:
(a) dividing said cold feed gas stream into a ?rst and
a second stream, said second stream comprising
from about 1 to about 30 percent by volume of the
total gas stream;

sulfur trioxide; cooling the gas stream and contacting it

with sulfuric acid to effect absorption of sulfur trioxide

therefrom, wherein the improvement comprises: divid

ing the cold sulfur dioxide-containing feed gas stream
5 into a ?rst and a second stream, said second stream

comprising from about 1 to about 30 percent by volume

of the total gas stream, and by-passing said second gas
stream around the primary contact and intermediate
absorption sections, and combining it with the gas
10 stream from the intermediate absorption section prior to
its introduction into the secondary contact section.
The procedure of the present invention has at least

three advantages. First, it affords substantial savings in

energy required for operation of the process by reduc
ing the amount of energy necessary to transport the gas
stream through the apparatus, in that that amount of
energy which would otherwise be required for trans

porting the by-passed portion of the sulfur dioxide-con

(b) preheating the ?rst gas stream to the kindling

taining gas stream through the primary contact and
temperature of the catalyst;
20 intermediate absorption stages is dispensed with. Sec
(c) passing the preheated ?rst gas stream through a
ond, since less gas is passed through the primary con
primary contact section containing catalyst to ef
version and intermediate absorption sections, smaller
fect oxidation of part of the sulfur dioxide to sulfur
sized equipment will suf?ce for these sections, resulting
trioxide;
in important savings in cost of equipment and required
(d) cooling the gas stream from the primary contact 25 amount of catalyst. Third, by virtue of introduction of
section to temperature between about 400 and
sulfur dioxide-containing gas of higher sulfur dioxide
about 500 F;
content directly into the secondary contact section, the
(e) contacting the gas stream so cooled with sulfuric
total amount of heat generated in that section by the
acid in an intermediate absorption section to effect

absorption of sulfur trioxide therefrom;

oxidation of sulfur dioxide to sulfur trioxide is in

30 creased, and the additional heat becomes available for

(f) combining the gas stream from the intermediate

absorption section with said second gas stream
obtained in step a), above, and preheating the com
bined gas stream to the kindling temperature of the

preheating the gas stream from the intermediate absorp

tion section, thereby reducing the amount of heat which

from step g), below, augmented by indirect heat

vented to the atmosphere following the ?nal absorption

step is slightly increased. This increase, however, is

must be supplied by an external heat source, such as by

a combustion of fossil fuel. There is a slight penalty in
catalyst by indirect heat exchange with hot gases 35 that the amount of sulfur dioxide in the gas stream

exchange with an external heat source, if neces

sary;

(g) passing the preheated combined gas stream

through a secondary contact section containing
catalyst to effect oxidation of sulfur dioxide con
tained therein to sulfur trioxide;
(h) cooling the gas stream from the secondary contact
section to temperature between about 300 and

minor and can be controlled within desired limits by

controlling the amount of sulfur dioxide-containing gas

40 stream which is by-passed around the primary conver

sion and intermediate absorption sections.

In addition, the improved process of the present in
vention permits facile and precise control of the amount
of free sulfur dioxide contained in the exit gas stream at

about 420 F by indirect heat exchange with the 45 or below a desired ?xed level. This may be readily
gas stream to be introduced into the secondary
accomplished by continually or intermittently monitor
contact section; followed by
ing the sulfur dioxide content of the exit gas, as by
(i) contacting the cooled gas stream with sulfuric acid
means of a sensor, and then automatically controlling
to effect absorption of sulfur trioxide therefrom.
the amount of sulfur dioxide-containing feed gas which
In another aspect, the present invention provides an 50 is by-passed around the primary contact and intermedi
improvement in the contact sulfuric acid process em

ate absorption sections by means of a control valve,

ploying the double conversion-double absorption pro

cedure using a cold sulfur dioxide-containing feed gas

which may be automatically controlled responsive to

sensor reading. Since variations in degree of by-pass
stream from a wet gas puri?cation plant, involving
will result in variations in the amount of heat generated
preheating the gas stream to the kindling temperature of 55 within the secondary contact section, the amount of
the catalyst and passing it through a primary contact
heat applied from an external heat source is then prefer
section containing catalyst to effect oxidation of sulfur
ably controlled by sensing the temperature of the gas
dioxide to sulfur trioxide; cooling the gas stream and
stream entering the secondary contact section and vary
contacting it with sulfuric acid in an intermediate ab
ing the amount of fuel supplied for preheating respon
sorption section to effect absorption of sulfur trioxide 60 sive to sensed temperature changes, as by an automatic
therefrom; preheating the gas stream from the interme
control valve.

diate absorption section by indirect heat exchange

contact with the exit gas stream from the secondary

absorption section, if desired, and augmented by indi

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is further illustrated by the

rect heat exchange with an external heat source, if nec 65 annexed drawings, wherein

essary; followed by passing the preheated gas stream

through a secondary contact section containing catalyst

FIG. 1 is a schematic flow diagram illustrating the

essential process steps and apparatus employed there

to effect oxidation of sulfur dioxide contained therein to

for;

4,088,742

FIG. 2 is a schematic ?ow diagram of a contact sulfu

?ltration, such as in coke boxes or by electrostatic pre

cipitation.

ric acid plant employing a cold sulfur dioxide-contain

ing feed gas stream obtained from a wet gas puri?cation

As the ?nal step in the wet puri?cation operation, the

plant, employing cold gas by-pass around the primary

moisture laden gases are dried to reduce the water con

conversion and intermediate absorption sections in ac

tent to between about 0.005 and 0.02 grams of water per

cordance with the present invention; and

standard cubic foot, desirably not higher than about

0.015 grams of water per standard cubic foot, preferably

FIG. 3 is a schematic ?ow diagram of the essential

processing steps and equipment employed therefor as in
FIG. 1, but further illustrating means for sensing sulfur

less than about 0.01 grams of water per standard cubic

foot. Excessive amounts of water in the cold feed gas
dioxide content in the exit gas stream and for control 10 stream will cause corrosion of equipment and formation
of sulfuric acid mist that will result in a visible absorber
ling the degree of cold gas by-pass responsive thereto,

exit. Drying is usually accomplished by passing the gas

stream through packed towers irrigated by drying acid
containing from about 80 to about 99 percent by weight

as well as further optional means which may be em-_

ployed in conjunction therewith for controlling the

amount of heat applied by an external heat source to the

of sulfuric acid. The water content of the gases will be

gas stream entering the secondary conversion section.

DETAILED DESCRIPTION OF THE
INVENTION OF THE PREFERRED
EMBODIMENTS AND OF THE BEST MODE
PRESENTLY CONTEMPLATED FOR ITS
PRACTICE

related to the strength of the sulfuric acid employed for

drying, stronger acids resulting in lower water content.
The temperature of the gas stream from the wet gas

puri?cation plant usually is at about ambient tempera

20 ture, say in the order of about 60 to about 100 F.

The puri?ed cold sulfur dioxide-containing feed gas

stream will generally contain of from about 8 to about

The cold sulfur dioxide-containing feed gas stream

employed for making sulfuric acid in accordance with

12 percent by volume of sulfur dioxide, and generally of

from about 7 to about 11 percent by volume oxygen, the

the method of the present invention is a gas stream
which has been cooled and/or scrubbed for removal of 25 balance comprising inert gases, such as nitrogen and
carbon dioxide.
impurities therefrom by contacting it with water or

The principle of operation of the process of the pres

ent
invention is explained in further detail with refer
about 50 percent by weight of H2804, followed by
ence
to FIG. 1. Cold sulfur dioxide-containing feed gas,
drying it, as by contacting it with sulfuric acid of higher 30
that
is
to say, sulfur dioxide-containing feed gas which
concentration, say in about the order of 60 Be. or
is
below
kindling temperature of the catalyst mass is
above. Usually, it is obtained by roasting of sul?de ores,
supplied by means of a blower (not shown) through
such as pyrites, copper sul?de, zinc sul?de and others,
cold gas feedline 11. That feed gas stream is divided into
or by thermal decomposition impurities-containing sul

weak sulfuric acid, say sulfuric acid containing less than

a ?rst stream and' a second stream. The ?rst stream is

furic acid, such as spent sulfuric acid from a pickling 35

passed through heat exchange means 1, wherein it is

operation, sludge acid from oil re?ning operation, or

heated to kindling temperature of the catalyst mass (in

the order of about 780 to about 800 F) by indirect heat
exchange with exit gas from primary contact means 2.
Preheated feed gas from heat exchange means 1 is intro
duced into primary contact means via line 13. Primary

spent acid from sulfonation or nitration operations.

Sulfur dioxide-containing gases obtained from these

sources, that is to say, from metal sul?de roasting and

sludge acid decomposition operations, are too highly

contaminated with impurities to permit their direct

contact means 2 comprises one or more beds of catalyst,

introduction into a contact plant. For that reason, such

gases are usually subjected to a series of puri?cation

which may any of the known sulfur dioxide oxidation

catalyst such as platinum, vanadium oxides, such as
steps, which may comprise dust removal, cooling and
vanadium pentoxide, iron oxide or other oxidation cata
scrubbing and mist removal, in each instance followed 45 lysts suitable for the oxidation reaction. Such oxidation

by drying.

catalyst is generally deposited in form of cylindrical

Dust removal is required since dust contained in the

feed gas would rapidly plug packed towers and car
talyst beds. Dust removal may be effected by passing

rods, worms or irregularly shaped granules, or in any

other suitable form within a converter vessel having
suf?cient volume to achieve at least partial conversion
of the sulfur dioxide to sulfur trioxide. Catalytic oxida
tion of sulfur dioxide to sulfur trioxide is exothermic. To

the feed gas stream through large baffled chambers,

electrostatic precipitators, tangential dust collectors
and the like. Usually, in the dust removal section the
temperature of the gas stream is maintained in the range
of about 650 to 1000 F to minimize condensation and
sulfation of equipment. Dust removal may be omitted in

prevent the heat of reaction from deteriorating the cata

lyst mass from excessive temperature rise, it is usual
practice to employ a plurality of converters, say, at least
two, perhaps three converters, through which the gas is
passed serially, for partial conversion of its sulfur diox
ide content to sulfur trioxide. Gas exiting from each
converter may be passed through a suitable cooling

gas puri?cation operations involving sulfur dioxide

containing gas streams obtained by thermal decomposi
tion of sludge acid.
Following removal of gross dust contamination, as
above-described, it is usual practice to contact the gas

means, such as a heat exchanger, or cooling may be

effected by introduction of ambient air after each con

version step. In any event, heat of reaction generated in
the oxidation reaction of the sulfur dioxide is utilized in
heat exchange means 1 to preheat the cold sulfur diox

stream with water or weak sulfuric acid to cool it and to

remove the remaining dust. This is usually achieved

through use of sprays or in packed towers. The weak

acid is circulated through and cooled by use of shell-and

tube-type heat exchangers of acid resisting material,

such as carbon. The gases from the scrubbing step con
tain considerable amounts of water vapor and sulfuric

acid mist. The sulfuric acid mist is usually removed by

ide containing feed gas to the kindling temperature of

65

the catalyst.
In heat exchange means 1 the partially converted gas
is cooled to temperature in the order of about 400 to
about 550 F, preferably from about 400 to about 440

4,088,742
F, and is then introduced through line 14 into intermedi

catalyst, which is in the neighborhood of about 780 to

about 800 F, it is next passed through line 16 into heat

ate absorption means 3 wherein it is contacted with

concentrated sulfuric acid to selectively absorb sulfur

trioxide therefrom. Intermediate absorption means 3 is
provided with suitable internal means for effecting effi
cient gas liquid contact, such as Raschig rings or other
suitable packing, bubble cap trays or sieve trays. Usu
ally, the gas stream rises within the absorber counter

exchange means 5 wherein heat is applied from a source

external of the sulfuric acid process. That heat may, for

example, be supplied by combustion of fuel, such as oil

or gas. From heat exchange 5, the mixed gas stream is

passed through line 17 into the secondary contact

means 6, which may comprise one or more converters

current to the downward flow of the concentrated

packed with catalyst, as described above in connection
sulfuric acid. The concentrated sulfuric acid stream 10 with discussion of primary contact means 2. In second

preferably enters the absorber with a concentration of

ary contact means 6 remaining sulfur dioxide is oxidized

to sulfur trioxide in conventional manner, and the exit
gas is cooled to temperature within the range of from

about 99 percent by weight sulfuric acid, although other

sulfuric acid concentrations can be used consistent with

conventional practice. Sulfur trioxide is absorbed from

the gas phase into the sulfuric acid stream to form sulfu

about 300 to about 440 F by passing it via line 18

5

through heat exchange means 4, wherein it gives off

ric acid having concentration of, say, about 99.5 percent

by weight. As is conventional, the resultant sulfuric acid
phase may be withdrawn from the absorber and divided

part of its heat to the cold mixed gas stream, as above

described. From heat exchange means 4 the mixed gas
stream is passed via line 19 into ?nal absorption means

into a recycle stream and a product stream. Water or

7, wherein sulfur trioxide is scrubbed therefrom by

weak sulfuric acid is added to the recycle stream in 20 contacting it with strong sulfuric acid in the manner
order to maintain its concentration at desired level, as is
above described in connection with discussion of inter
conventional. Temperature of the absorber acid is usu
mediate absorption means 3, and the exit gas stream
ally maintained within the range of about 220 to about
from ?nal absorption means 7 is vented to the atmo
235 F.
sphere via exit stack 20, after ?rst passing it through a
The gas stream from the intermediate absorption 25 mist ?lter (not shown), if desired.
means may comprise in the order of about 0.5 to about
Movement of the gas stream through the apparatus is
2 percent by volume of sulfur dioxide, 10 to about 11
effected by suitable blower means (not shown) associ

percent by volume of oxygen, the balance principally

comprising nitrogen. It is desirable to maintain the sul

ated with cold gas feed line 11, as well as line 15. The
blower means in line 15 is located downstream from the

fur dioxide content of that gas stream below about 2

point where cold gas by-pass line enters line 13.

It is, of course, possible to introduce the cold by-pass

percent by volume, preferably below about 1 percent by

volume, in order to minimize sulfur dioxide contamina

sulfur dioxide stream into the secondary contact means
tion of the sulfuric acid product from the intermediate
at a point other than ahead of heat exchange means 4, as
absorption means. If desired, the exit gas from the inter
by introducing it into the gas stream entering heat ex
mediate absorption means may be passed through a mist 35 change means 5 or entering secondary contact means 6.
?lter (not shown) and it is then mixed with the second
Thus, it may be introduced as by means of line 120
stream, which is the cold by-pass stream, which has
and/or 1212, both shown in broken lines, between heat
been by-passed around heat exchange means 1, primary
exchange means 4 and heat exchange means 5, and/or
contact means 2, and intermediate absorption means 3
between heat exchange means 5 and secondary means 6,
by means of cold gas by-pass line 12. The by-passed 40 as may be desired. That would, however, require that
cold gas stream comprises from about 1 to about 30
the gases in heat exchange 4 and/or 5 are brought to
percent by volume of the total feed gas steam, prefera
temperature suf?ciently high so that the temperature of
bly from about 10 to about 15 percent by volume. Desir
the mixed gas stream downstream from the point where
ably, the volume of the cold sulfur dioxide by-pass
the cold-by-pass stream is introduced would be suf?
stream is regulated such that the sulfur dioxide content 45 cient to reach a kindling temperature of the catalyst
of the gas stream being introduced into secondary
mass.
contact means 6 comprises from about 2 to about 4
The method of the present invention as explained
percent by volume of sulfur dioxide, preferably from
above in connection with discussion of FIG. 1 provides
about 2 to about 3 percent by volume of sulfur dioxide,
signi?cant energy savings, on two accounts. First, en
depending on the maximum amount of sulfur dioxide
ergy requirements to move the gas stream through heat
permitted in the exit gas stream to be vented into the
exchange means 1, primary contact means 2, and inter
atmosphere. Lower sulfur dioxide levels in the exit gas
mediate absorption means 3 are reduced by by-passing
stream will, of course, result from lower sulfur dioxide
the cold by-passing stream around these pieces of equip
content in the feed gas stream to the secondary contact
ment. The energy saved corresponds to the difference
means.

The mixed gas stream in line 15, which is at a temper

ature within the range of from about 180 to about 200

F, must next be preheated to the kindling temperature

55 between the energy required to pass a total feed gas

stream at the rate at which is supplied through heat

exchange means 1, primary contact means 2 and inter
mediate absorption means 3, with associated lines, as

of the catalyst mass in the secondary contact means.

against passing only part of the total feed gas stream
This is effected in a series of two heat exchange means. 60 through these pieces of equipment and by-passing the
The mixed cold gas stream is ?rst passed into and
remaining part around it. Secondly, by providing a

through heat exchange means 4-, wherein is it indirectly

higher gas strength in the mixed gas stream downstream
contacted with the exit gas stream from secondary
from the intermediate absorption means 3, more sulfur
contact means 6, thereby heating it to a temperature
dioxide is available in secondary contact means 6 for
within the range from about 550 to about 580 F, 65 oxidation into sulfur trioxide, which results in genera
which is still below the kindling temperature of the
tion of additional heat from the oxidation, which addi
catalyst in the secondary contact means. To bring the
tional heat can be imparted to the cold mixed gas stream
mixed gas stream to the kindling temperature of the
in heat exchange means 4, thereby reducing the amount

4,08 8,742

of externally supplied heat which must be supplied in

10

It should be recognized that detail design of the indi

The ?rst gas stream leaves absorber 51 at a tempera

ture of about 225 to about 230 F and contains about
1.1 percent by volume of sulfur dioxide. That ?rst gas
stream is next mixed with the second (by-pass) gas
stream, to obtain a mixed gas stream containing about

vidual pieces of equipment employed in the method of

2.7 percent by volume of sulfur dioxide. The mixed gas

heat exchange means 5 in order to bring the gas stream

to the kindling temperature of the catalyst in the sec
ondary contact means.

the invention process, and their operation, are within

the capabilities of one of ordinary skill in the art.
With reference to FIG. 2, a cold sulfur dioxide-con
taining feed gas stream obtained from a wet gas puri?
cation plant is introduced to the conversion system via
feed line 61 at a rate of 60,000 SCFM. The feed gas
stream contains about 11 percent by volume of sulfur

from about 190 to about 590 F and from about 590 to

about 790 F. Both heat exchangers 34 and 35, are of

dioxide, 12 percent by volume of oxygen, the balance

being inert gases such as nitrogen and carbon dioxide.
The feed gas stream is moved through the system by

the mixed gas stream is brought into indirect heat ex

change contact with the exit gas from secondary cata

stream has a temperature of about 180 to about 190 F.

The mixed gas stream is passed through heat exchang

ers 34 and 35 by means of blower 22 via lines 73 and 74.

In heat exchangers 34 and 35 the mixed gas stream is

respectively heated to temperature within the range of

shell-and-tube type construction. In heat exchanger 34

lyst bed 44, in heat exchanger 35 it is brought into indi

means of blower 21. Downstream from blower 21 the
feed gas stream is split into two streams, a ?rst gas 20 rect heat exchange contact with products of combus
tion of fossil fuel, say natural gas or oil.
stream in line 62, and a second gas stream in line 63. The
second gas stream passed through line 63 comprises

After passage through heat exchangers 34 and 35, the

about 10 to about 25 percent by volume of the total feed

gas stream. Assuming the second gas stream to be about
12 percent by volume of the total feed gas stream, it

mixed gas stream, now preheated to the kindling tem

amounts to about 7,800 SCFM.

oxidized to sulfur trioxide, under heating of the gas

stream to temperature within the range of from about
825 to about 860 F. That gas stream next is passed via

The ?rst gas stream is serially passsed through heat

exchangers 31, 32 and 33, which are of shell-and-tube
type construction. The temperature of the ?rst gas
stream at the exits of these heat exchangers is as follows:

out heat exchanger 31 about 680 F; out heat exchanger

32 about 740 F, and; out heat exchanger 33 about 800
F. From heat exchanger 33, the ?rst gas stream, which
is now preheated to the kindling temperature of the

catalyst, is passed to and through ?rst catalyst bed 41 by

means of line 64. In catalyst bed 41, part of the sulfur
dioxide contained in the feed gas stream is oxidized to

sulfur trioxide with resultant temperature rise of the gas

stream to about 1140 F. The gas stream is next passed

via line 65 through heat exchanger 33 therein it is

cooled to temperature in the order of about 820 to

about 840 F by indirect heat exchange with incoming

feed gas, as above described, and is next passed via line
66 to a second catalyst bed 42, wherein again part of the
remaining sulfur dioxide is oxidized to sulfur trioxide
under heating of the gas stream to temperature in the
order of about 940 F. The exit gas from second catalyst

bed 42 is passed via line 67 through heat exchanger 32

wherein it is cooled to temperature in the order of about
820 F, to be routed via line 68 through third catalyst

bed 43, wherein again- part of the remaining sulfur diox

perature of the catalyst, is passed through secondary

catalyst bed 44 wherein reamining sulfur dioxide is

line 76 through heat exchanger 34 wherein its tempera

ture is reduced to within about 440 to about 450 F, and
is then introduced into ?nal absorber 52 via line 77. In
?nal absorber 52, the gas stream is contacted with sulfu

ric acid containing about 99 percent H2SO4 by weight,

in the manner above described in connection with ab

sorption in intermediate absorber 51, to scrub remaining

sulfur trioxide from the gas stream. The exit gas stream
from absorber 52 is vented to the atmosphere via line 78

after passage through an optional mist ?lter (not

shown). The exit gas stream vented to the atmosphere
contains about 830 ppm of sulfur dioxide.

Reverting momentarily to the step of heating the

mixed gas stream in heat exchanger 35 by indirect heat
exchange with products of combustion, a fuel, such as
gas or oil, is supplied through line 80, and is burned in
preheated air supplied via line 81. The resultant prod
ucts of combustion are passed through heat exchanger
35, wherein they preheat the mixed gas stream to the
kindling temperature of the catalyst. Combustion air is
introduced by means of blower 23 via line 82, and is

passed for preheating through heat exchanger 35,

wherein it is brought into indirect heat exchange

contact with gas from heat exchanger 35, which repre

ide is oxidized to sulfur trioxide under heat rise to about 55 sents the partially cooled products of combustion of the

940 F. Catalyst beds 41, 42 and 43 together comprise

the primary contact means. In the gas stream exiting

from third catalyst bed 43, about 91.5 percent of the

sulfur dioxide originally contained therein have been

converted to sulfur trioxide. The exit gas stream is then

passed via line 69 through heat exchanger 31, wherein it

fuel. Products of combustion so cooled in heat ex

changer 36 are exhausted to the atmosphere via line 84.

The Table below summarizes bene?cial results ob

tained by the improvement of the present invention

when applied to a contact sulfuric acid plant employing

double conversion-double absorption, as above

is cooled to temperature in the order of about 435 to
described, operating on a cold sulfur dioxide-containing
about 440 F, to be introduced via line 70 into interme
feed gas stream obtained from a wet gas puri?cation
diate absorber 51 wherein it is contacted with sulfuric 65 plant, containing about 11 percent by volume of sulfur
acid of about 99 percent by weight of HZSQ, having
dioxide, 12 percent by volume of oxygen, the balance
temperature of about 230 F, to selectively absorb sulfur
being inert gases, supplied at a rate of about 65,000
trioxide therefrom.
SCFM.

4,088,742

11

12

TABLE
Without Split

First Catalyst Bed,

Liters Catalyst
Second Catalyst Bed,
Liters Catalyst
Third Catalyst Bed,
Liters Catalyst
Pressure Drop, Primary

Feed, Conven-

Invention

tional Process

Process

47,000

39,100

52,500

40,300

71,300

52,300

87

50

55

44

Saved
Units

Conversion and Inter

mediate Absorption
Sections, Inches H2O

Pressue Drop, Secondary

Conversion and Final

Absorption Sections,
Inches H2O
Oil Consumption,

32,800

4,800

14.6

12,500,000 4,870,000

28,00

28.0

Barrels/Year

Electricity Consumed,
KWH/Year

17,370,000

The improvement of the present invention, as de- 20 sulfur dioxide content in the exit gases to the predeter
scribed above in connection with FIG. 1, permits sub
mined level.
stantial reduction in the size of equipment for the pri
It should be recognized that any change in the
mary contact and intermediate absorption sections, and
amount of cold feed gas that it by-passed around the
it results in substantial reduction in fuel consumption
primary contact and intermediate absorption sections
and electric power consumption. correspondingly 25 will alter the amount of heat generated within the sec
smaller or larger reductions may be obtained by de
ondary contact means, for reasons above explained.
creasing or increasing the proportion of the sulfur diox
Therefore it would be desirable to employ means for

ide-containing feed gas stream which is by-passed

around the primary contact and intermediate absorption

sections. This, however is accompanied by the penalty

automatically controlling the temperature entering the

30

of somewhat higher sulfur dioxide content of the exit

gas stream, and the degree of by-pass, upon which the
sulfur dioxide content of the exit gas stream to a sub

secondary contact means by varying the amount of

externally applied heat to heat exchange means 5. This
may be accomplished by provision of temperature sen
sor 103 in line 17, which is operatively connected to a
fuel control valve 104 which increases or decreases the
fuel ?ow responsive to decrease or increase in tempera

stantial degree depends, will have to be consistent with

such regulations as may govern permissible S02 content 35 ture of the gases passing through line 17 as sensed by
of the exit gas stream.
sensor 103. Conjoint employment of the sulfur dioxide
The improvement of the present invention also pro
control means in the exit gas by the joint operation of
vides a facile method for controlling the sulfur dioxide
sensor 101 and control valve 102, in conjunction with
content of the exit gas stream. In this connection, refer
heat control by means of heat sensor 103 and fuel con
ence is made to FIG. 3. The equipment and gas flow 40 trol valve 104, will serve to maximize the bene?ts to be
shown in FIG. 3 are identical to that shown in FIG. 1,
gained by the improvement of the present invention.
vexcept that certain control means, to be discussed in
Since various changes may be made in carrying out

detail below, are shown superimposed in heavy lines.

Thus, there is provided in exit stack 20, a sensor 101
which continually monitors the 50; content of the exit
gases. Such sensors are known and available. Sensor 101 4

is operatively connected to control valve 102. Control

valve 102 regulates the amount of sulfur dioxide-con

taining feed gas which is passed through cold gas by

the improved process of my invention without depart

ing from its scope and essential characteristics, all mat
ter contained in the above descriptions shall be inter
preted as illustrative only, the scope of my invention

being de?ned by the appended claims.

I claim:

1. The process for making sulfuric acid by catalytic

pass line 12 responsive to signals received from sensor 50 oxidation of sulfur dioxide from a cold sulfur dioxide
101. Sensor 101 and control valve 102 are programed
containing gas stream from a wet gas puri?cation plant

employing conventional process control equipment to

maintain sulfur dioxide content of the gases in exit stack

20 at a predetermined level. Should the sulfur dioxide
content in the exit gases rise above that level, sensor 101 55
will send a signal to control valve 102 responsive to
which control valve 102 will function to reduce the
amount of cold sulfur dioxide feed gas which is passed

involving the steps of:

(a) dividing said cold gas stream into a ?rst and a
second stream, said second stream comprising from
about 1 to about 30 percent by volume of the total

gas stream;
(b) preheating the ?rst gas stream to the kindling

around the primary contact and intermediate absorption

sections via line 12, thereby reducing the sulfur dioxide

temperature of the catalyst;

(c) passing the preheated ?rst gas stream through a
primary contact section containing catalyst to ef

content which enters the secondary contact means and,

fect oxidation of part of the sulfur dioxide to sulfur

consequently, reducing the sulfur dioxide content in the

exit gases. Conversely, should sensor 101 detect a re
duction in the sulfur dioxide content of the exit gases, a

signal will be given to control valve 102 to increase the 65

amount of cold gas that is by-passed, thereby increasing
the sulfur dioxide content of the gases entering the
secondary contact means and consequently bringing the

trioxide;
(d) cooling the gas stream from the primary contact
section to temperature between about 400 and

about 550 F;
(e) contacting the gas stream so cooled with sulfuric
acid in an intermediate absorpti: 2'.- section to effect

absorption of sulfur trioxidc therefrom;

13

4,088,742

(f) combining the gas stream from the intermediate

absorption section with said second gas stream
obtained in step a), above, and preheating the com

14

4. The process of claim 2 wherein further the com

bined gas stream obtained in step f) contains from about

2 to about 4 percent by volume of sulfur dioxide.
5. The process of claim 3 wherein further the com
bined gas stream obtained in step f) contains from about
2 to about 4 percent by volume of sulfur dioxide.
6. The process of claim 1 wherein said second gas
stream comprises from about 10 to about 15 percent by

bined gas stream to the kindling temperature of the

catalyst by indirect heat exchange with hot gases

from step g), below, augmented by indirect heat
exchange with an external heat source, if neces
sary;

volume of the total gas stream, wherein the gas stream

obtained from the intermediate absorption section in

step e) contains from about 0.5 to about 2 percent by

(g) passing the preheated combined gas stream

through a secondary contact section containing

volume of sulfur dioxide, and wherein further the com

catalyst to effect oxidation of sulfur dioxide con

tained therein to sulfur trioxide;
(h) cooling the gas stream from the secondary contact
section to temperature between about 300 and
about 450 F by indirect heat exchange with the
gas stream to be introduced into the secondary

bined gas stream obtained in step f) contains from about

2 to about 4 percent by volume of sulfur dioxide.
' 7. The process of claim 1 wherein said second gas

stream comprises from about 10 to about 15 percent by

volume of the total gas stream, wherein the gas stream

obtained from the intermediate absorption section in

step e) contains less than about 1 percent by volume of
contact section; followed by
20 sulfur dioxide, and wherein the combined gas stream
(i) contacting the cooled gas stream with sulfuric acid
obtained in step t) contains from about 2 to about 4
to effect absorption of sulfur trioxide therefrom.
percent by volume of sulfur dioxide.
2. The process of claim 1 wherein the gas stream
8. The process of claim 1 with the further steps of
obtained from the intermediate absorption section in
sensing the sulfur dioxide content in the gas stream
obtained in step i) from contacting the cooled gas
step e) contains from about 0.5 to about 2 percent by
stream with sulfuric acid to effect absorption of sulfur
volume of sulfur dioxide.
trioxide therefrom, and regulating the volume of said
3. The process of claim 1 wherein the gas stream
second stream obtained in step a) to maintain the sulfur
obtained from the intermediate absorption section in
dioxide content in the gas stream obtained in step i) at
step e) contains less than about 1 percent by volume of
predetermined level.
sulfur dioxide.
i
*
t
i
t

35

50

55

65