U.S. patent application number 13/662250 was filed with the patent office on 2013-08-15 for apparatus for preparing an ionic liquid catalyst for disposal.
This patent application is currently assigned to Chevron U.S.A. Inc.. The applicant listed for this patent is Shawn Stephen Healy, Hye Kyung Cho Timken, Shawn Shlomo Winter. Invention is credited to Shawn Stephen Healy, Hye Kyung Cho Timken, Shawn Shlomo Winter.
Application Number | 20130209324 13/662250 |
Document ID | / |
Family ID | 48945706 |
Filed Date | 2013-08-15 |
United States Patent
Application |
20130209324 |
Kind Code |
A1 |
Timken; Hye Kyung Cho ; et
al. |
August 15, 2013 |
APPARATUS FOR PREPARING AN IONIC LIQUID CATALYST FOR DISPOSAL
Abstract
We provide an apparatus for preparing a used catalyst for
disposal, comprising: a. a vessel used to hydrolyze a used ionic
liquid catalyst comprising an anhydrous metal halide, to produce a
hydrolyzed product; and b. a separator used to separate a liquid
phase and a solid phase from the hydrolyzed product; wherein the
liquid phase comprises a non-water-reactive aqueous phase and a
hydrocarbon phase; and wherein the solid phase comprises a solid
portion of the hydrolyzed product, that is not water reactive.
Inventors: |
Timken; Hye Kyung Cho;
(Albany, CA) ; Healy; Shawn Stephen; (Eagle
Mountain, UT) ; Winter; Shawn Shlomo; (Salt Lake
City, UT) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Timken; Hye Kyung Cho
Healy; Shawn Stephen
Winter; Shawn Shlomo |
Albany
Eagle Mountain
Salt Lake City |
CA
UT
UT |
US
US
US |
|
|
Assignee: |
Chevron U.S.A. Inc.
San Ramon
CA
|
Family ID: |
48945706 |
Appl. No.: |
13/662250 |
Filed: |
October 26, 2012 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
13396121 |
Feb 14, 2012 |
|
|
|
13662250 |
|
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Current U.S.
Class: |
422/187 |
Current CPC
Class: |
A62D 2203/10 20130101;
B01J 19/00 20130101; B01J 31/0284 20130101; A62D 3/35 20130101;
B01J 31/26 20130101; B01J 2231/323 20130101; B01J 8/006 20130101;
B01J 31/0298 20130101; B01J 8/005 20130101 |
Class at
Publication: |
422/187 |
International
Class: |
B01J 19/00 20060101
B01J019/00 |
Claims
1. An apparatus for preparing a used catalyst for disposal,
comprising: a. a vessel, holding a basic solution, used to
hydrolyze a used ionic liquid catalyst comprising an anhydrous
metal halide, to produce a hydrolyzed product, wherein a hydrogen
halide gas is evolved and dissolved into the basic solution in the
vessel; and b. a separator used to separate a liquid phase and a
solid phase from the hydrolyzed product; wherein the liquid phase
comprises a non-water-reactive aqueous phase having a pH of 4 to 10
and a hydrocarbon phase; and wherein the solid phase is not water
reactive.
2. The apparatus of claim 1, wherein the used ionic liquid catalyst
is selected from the group consisting of a
hydrocarbyl-substituted-pyridinium chloroaluminate, a
hydrocarbyl-substituted-imidazolium chloroaluminate, a quaternary
amine chloroaluminate, a trialkyl amine hydrogen chloride
chloroaluminate, an alkyl pyridine hydrogen chloride
chloroaluminate, and mixtures thereof.
3. The apparatus of claim 1, wherein the anhydrous metal halide is
selected from the group consisting of AlCl.sub.3, AlBr.sub.3,
GaCl.sub.3, GaBr.sub.3, InCl.sub.3, InBr.sub.3, and mixtures
thereof.
4. The apparatus of claim 1, wherein the basic solution comprises a
base selected from the group consisting of LiOH, NaOH, KOH, CsOH,
RbOH, Mg(OH).sub.2, Ca(OH).sub.2, Sr(OH).sub.2, NH.sub.4OH,
Ba(OH).sub.2, and mixtures thereof.
5. The apparatus of claim 1, wherein less than a full charge of the
used ionic liquid catalyst is removed from a hydrocarbon conversion
process unit such that the hydrocarbon conversion process unit
operates continuously.
6. The apparatus of claim 1, wherein the used ionic liquid catalyst
comprises conjunct polymer.
7. The apparatus of claim 1, additionally comprising a
liquid/liquid separator used to separate the liquid phase into the
non-water-reactive aqueous phase from the hydrocarbon phase.
8. The apparatus of claim 1, wherein the hydrogen halide gas is
neutralized.
9. The apparatus of claim 1, wherein the used ionic liquid catalyst
comprises one or more corrosion metals other than aluminum and the
one or more corrosion metals, or products thereof, are collected in
the solid phase.
10. The apparatus of claim 1, wherein a hydrolysis is performed
continuously by adding the used ionic liquid catalyst to the vessel
while the hydrolyzed product is taken out of the vessel.
11. The apparatus of claim 1, wherein greater than 80 wt % of the
anhydrous metal halide is hydrolyzed and collected in the solid
phase.
12. The apparatus of claim 1, wherein the vessel is fabricated of a
metal, a plastic, a resin, or a glass.
13. The apparatus of claim 1, wherein the vessel is designed to
give turbulent flow so that thorough mixing of the used ionic
liquid catalyst and a basic solution will result.
14. The apparatus of claim 1, wherein the separator is a gravity
filter or a pressure rapid filter.
Description
[0001] This application is a divisional of U.S. patent application
Ser. No. 13/396,121, filed Feb. 14, 2012, in Group Art Unit 1736;
and herein incorporated in its entirety.
TECHNICAL FIELD
[0002] This application is directed to an apparatus for preparing a
used ionic liquid catalyst for disposal.
BACKGROUND
[0003] Ionic liquid catalysts need to be safely disposed of after
use. Without treatment, they can be highly water reactive and
unsafe to handle or dispose of.
SUMMARY
[0004] This application provides an apparatus for preparing a used
catalyst for disposal, comprising:
[0005] a. a vessel used to hydrolyze a used ionic liquid catalyst
comprising an anhydrous metal halide, to produce a hydrolyzed
product; and [0006] b. a separator used to separate a liquid phase
and a solid phase from the hydrolyzed product; wherein the liquid
phase comprises a non-water-reactive aqueous phase and a
hydrocarbon phase; and wherein the solid phase comprises a solid
portion of the hydrolyzed product, that is not water reactive.
BRIEF DESCRIPTION OF THE DRAWINGS
[0007] FIG. 1 is a diagram of a flow chart with one embodiment for
hydrolysis of ionic liquid catalyst.
DETAILED DESCRIPTION
[0008] Anhydrous metal-halide-containing used ionic liquid catalyst
is treated for safe and economic disposal by hydrolyzing the used
ionic liquid catalyst followed by separation which produces a
non-water-reactive aqueous phase, a hydrocarbon phase and a solid
phase.
[0009] Prior to the treatment by the process the used catalyst is
water reactive and unsuitable for disposal by usual methods. "Water
reactive" means that the composition will violently react with
moisture, sometimes leading to release of toxic gases, explosions,
or fire. Water reactive substances are dangerous when wet because
they undergo a chemical reaction with water. This reaction can
release a gas that presents a toxic health hazard. In addition, the
heat generated when water contacts such materials is often enough
for the mixture to spontaneously combust or explode.
Ionic Liquid Catalyst
[0010] Ionic liquid catalysts comprising an anhydrous metal halide
are very effective for catalyzing a hydrocarbon conversion process.
Examples of hydrocarbon conversion processes are paraffin
alkylation, olefin dimerization, olefin oligomerization, concurrent
alkylation and oligomerization, isomerization, and aromatic
alkylation. The hydrocarbon conversion process can be one used to
make gasoline, middle distillate, base oil, or petrochemical
components.
[0011] The ionic liquid catalyst comprising an anhydrous metal
halide is composed of at least two components which form a complex.
The first component of the ionic liquid catalyst comprises an
anhydrous metal halide which provides Lewis Acid functionality to
the catalyst. The metal halide is selected from compounds of Group
13 metals, including anhydrous aluminum halides, alkyl aluminum
halide, gallium halide, and alkyl gallium halide. Specific metal
halides, such as AlCl.sub.3, AlBr.sub.3, GaCl.sub.3, GaBr.sub.3,
InCl.sub.3, InBr.sub.3, and mixtures thereof could be in the used
ionic liquid catalyst. The periodic table by the International
Union of Pure and Applied Chemistry (IUPAC), version date 22 Jun.
2007, is used for defining the Group 13 metals.
[0012] In order to maintain the catalytic activity of the anhydrous
metal halide containing ionic liquid catalyst, the metal halide is
kept in an anhydrous condition. Anhydrous metal halides are water
reactive which means the anhydrous metal halides react with
moisture in the atmosphere, in hydrocarbon feeds, or in water. The
reaction with moisture tends to be very vigorous and generates
toxic hydrogen halide gas and the reaction converts a portion or
all of the metal halides into metal hydroxide and hydrated metal
halides.
[0013] The second component making up the ionic liquid catalyst is
an organic salt or mixture of salts. These salts can be
characterized by the general formula Q+A-, wherein Q+ is an
ammonium, phosphonium, boronium, iodonium, or sulfonium cation and
A- is a negatively charged ion such as Cl.sup.-, Br.sup.-,
ClO.sub.4.sup.-, NO.sub.3.sup.-, BF.sub.4.sup.-, BCl.sub.4.sup.-,
PF.sub.6.sup.-, SbF.sub.6.sup.-, AlCl.sub.4.sup.-, TaF.sub.6.sup.-,
CuCl.sub.2.sup.-, FeCl.sub.3.sup.-, HSO.sub.3.sup.-,
RSO.sub.3.sup.-, SO.sub.3CF.sub.3.sup.---, alkyl-aryl sulfonate,
and benzene sulfonate (e.g., 3-sulfurtrioxyphenyl). In one
embodiment the second component is selected from those having
quaternary ammonium halides containing one or more alkyl moieties
having from about 1 to about 12 carbon atoms, such as, for example,
trimethylamine hydrochloride, methyltributylammonium halide, or
substituted heterocyclic ammonium halide compounds, such as
hydrocarbyl-substituted-pyridinium halide compounds for example
1-butylpyridinium halide, benzylpyridinium halide, or
hydrocarbyl-substituted-imidazolium halides, such as for example,
1-ethyl-3-methyl-imidazolium chloride.
[0014] In one embodiment, the second component making up the ionic
liquid catalyst is an organic salt that is hygroscopic in nature
and has a tendency to attract and hold water molecules from the
surrounding environment. With these ionic liquid catalysts, in
order to maintain the integrity of the ionic liquid catalyst and
its catalytic performance, both the anhydrous metal halides and the
organic salts are thoroughly dried before the catalyst synthesis,
and moisture-free conditions are maintained during the catalytic
reaction.
[0015] In one embodiment the ionic liquid catalyst is selected from
the group consisting of hydrocarbyl-substituted-pyridinium
chloroaluminate, hydrocarbyl-substituted-imidazolium
chloroaluminate, quaternary amine chloroaluminate, trialkyl amine
hydrogen chloride chloroaluminate, alkyl pyridine hydrogen chloride
chloroaluminate, and mixtures thereof. For example, the used ionic
liquid catalyst can be an acidic haloaluminate ionic liquid, such
as an alkyl substituted pyridinium chloroaluminate or an alkyl
substituted imidazolium chloroaluminate of the general formulas A
and B, respectively.
##STR00001##
[0016] In the formulas A and B; R, R.sub.1, R.sub.2, and R.sub.3
are H, methyl, ethyl, propyl, butyl, pentyl or hexyl group, X is a
chloroaluminate. In one embodiment the X is AlCl.sub.4.sup.-,
Al.sub.2Cl.sub.7.sup.-, or Al.sub.3Cl.sub.10.sup.-. In the formulas
A and B, R, R.sub.1, R.sub.2, and R.sub.3 may or may not be the
same. In one embodiment the ionic liquid catalyst is
N-butylpyridinium
heptachlorodialuminate[NBuPy.sup.+][Al.sub.2Cl.sub.7.sup.-]. In one
embodiment the used ionic liquid catalyst is
1-Ethyl-3-methylimidazolium heptachlorodialuminate
[emim.sup.+][Al.sub.2Cl.sub.7.sup.-].
Used Ionic Liquid Catalyst
[0017] After the ionic liquid catalyst has been used to catalyze a
hydrocarbon conversion process it can become deactivated, or no
longer needed, for further hydrocarbon conversions. We refer to
this catalyst as used ionic liquid catalyst.
[0018] In one embodiment the used ionic liquid catalyst comprises a
cation selected from the group of an alkyl-pyridinium, an
alkyl-imidazolium, or a mixture thereof. In another embodiment the
used ionic liquid catalyst can have the general formula RR'R''
NH.sup.+Al.sub.2Cl.sub.7.sup.-, wherein N is a nitrogen containing
group, and wherein RR' and R'' are alkyl groups containing 1 to 12
carbons, and where RR' and R'' may or may not be the same.
[0019] In one embodiment, the used ionic liquid catalyst is the
full charge from a hydrocarbon conversion process. In another
embodiment, the used ionic liquid catalyst is a portion of the full
charge of catalyst from a hydrocarbon conversion process. In one
embodiment, less than a full charge of used ionic liquid catalyst
is removed from a hydrocarbon conversion reactor or process unit
such that the hydrocarbon conversion reactor or process unit
operates continuously. The used ionic liquid catalyst can be
drained from the process unit, and may also be referred to as spent
ionic liquid catalyst. For example, the used ionic liquid catalyst
can be less than 20 wt %, less than 15 wt %, less than 10 wt %,
less than 5 wt %, or less than 1 wt % of the full charge of
catalyst in the hydrocarbon conversion process unit. By removing
less than the full charge of catalyst, the hydrocarbon conversion
process can operate continuously, with gradual removal and addition
of fresh or reactivated ionic liquid catalyst without stopping or
disrupting the process.
Residual Hydrocarbon or Conjunct Polymer
[0020] In one embodiment the used ionic liquid catalyst
additionally comprises residual hydrocarbon or conjunct polymer.
Residual hydrocarbon or conjunct polymer can be formed and built up
in the used ionic liquid catalyst during hydrocarbon conversion
processes. The term conjunct polymer was first used by Pines and
Ipatieff to distinguish these polymeric molecules from other
polymers. Unlike some other polymers which are compounds formed
from repeating units of smaller molecules by controlled or
semi-controlled polymerizations, "conjunct polymers" are
"pseudo-polymeric" compounds formed asymmetrically from two or more
reacting units by concurrent acid-catalyzed transformations
including polymerization, alkylation, cyclization, additions,
eliminations and hydride transfer reactions. Consequently, the
produced "pseudo-polymeric" may include a large number of compounds
with varying structures and substitution patterns. The skeletal
structures of "conjunct polymers", therefore, range from the very
simple linear molecules to very complex multi-ring featured
molecules. Some examples of the likely polymeric species in
conjunct polymers were reported by Miron et. al. (Journal of
Chemical and Engineering Data, 1963), and Pines (Chem. Tech.,
1982). Conjunct polymers are also commonly known to those in the
refining industry as "red oils" due to their reddish-amber color or
"acid-soluble oils" due to their high uptake in the catalyst phase
where paraffinic products and hydrocarbons with low olefinicity and
low functional groups are usually immiscible in the catalyst phase.
In this application, the term "conjunct polymers" also includes
ASOs (acid-soluble-oils), red oils, and C12+ alkylates. Residual
hydrocarbon can be unreacted starting materials from the
hydrocarbon conversion process, or products from the hydrocarbon
conversion process that are not separately collected.
[0021] One way to dispose of used ionic liquid catalyst is
incineration. Incineration is not only an expensive disposal option
but also the water-reactive nature of the used ionic liquid
catalyst makes incineration difficult. As the used ionic liquid
catalyst is exposed to the moisture during the incineration step,
it can generate toxic and corrosive gas and corrosive materials
that can damage the incineration equipment. Thus, there is a need
for a safer and more cost efficient disposal process for used ionic
liquid catalysts. We have found that spent ionic liquid catalyst
can be converted to environmentally friendly materials by
controlled hydrolysis and can be disposed of in a cost efficient
manner.
Hydrolysis
[0022] The used ionic liquid is hydrolyzed with water or with a
basic solution. The hydrolysis conditions can be chosen carefully
so that the reaction heat is controlled and the hazardous gas
formed during the hydrolysis is captured by the hydrolysis solution
medium. In one embodiment, the hydrolysis uses a basic solution
comprising water and a base that is strong enough to neutralize an
acid formed by the used ionic liquid catalyst and water. In one
embodiment the base that can be used for the hydrolysis is a base
that hydrolyzes completely, and forms a basic solution with a pH of
10 or higher. Examples of bases include LiOH, NaOH, KOH, CsOH,
RbOH, Mg(OH).sub.2, Ca(OH).sub.2, Sr(OH).sub.2, NH.sub.4OH,
Ba(OH).sub.2, and mixtures thereof. In one embodiment, the cation
of the base is an alkali metal, an alkaline earth metal, or
ammonium hydroxide. In another embodiment, the hydrolysis vessel
holds a basic solution comprising a base selected from the group
consisting of LiOH, NaOH, KOH, CsOH, RbOH, Mg(OH)2, Ca(OH)2,
Sr(OH)2, NH4OH, Ba(OH)2, and mixtures thereof.
[0023] The basic solution can contain from 1 wt % to 60 wt % of the
base, 5 wt % to 30 wt % of the base, 8 wt % to 25 wt % of the base,
or 10 wt % to 20 wt % of the base, depending on the solubility and
strength of the base used.
[0024] In one embodiment, the used ionic liquid catalyst and basic
solution are mixed together at a molar ratio of used ionic liquid
catalyst to base of 0.5:1 to 1:20, 1:1 to 1:15, or 1:1 to 1:10. The
temperature under which the hydrolysis is performed is from
-20.degree. C. to 90.degree. C. The pressure under which the
hydrolysis is performed is from 80 to 2500 kPa. In one embodiment,
the hydrolyzing is done at ambient temperature and pressure. In one
embodiment, the hydrolyzing occurs in less than a week, less than
50 hours, and in some embodiments can occur in less than 10 hours,
or less than 1 hour. In one embodiment the hydrolyzing occurs
between 1 minutes and 60 minutes, between 10 minutes and 45
minutes, or between 15 minutes and 40 minutes. In one embodiment
the hydrolysis proceeds continuously by adding used ionic liquid
catalyst into the hydrolysis vessel while the hydrolyzed product is
taken out. Residence time of the mixture of used ionic liquid
catalyst and aqueous solution in the hydrolysis vessel of the
continuous unit can range from 10 minutes to 10 hours.
[0025] In one embodiment the hydrolysis reaction can be controlled
carefully in order to control the reaction temperature and
pressure. To control the exotherm associated with the hydrolysis,
one could adjust the feed rate of ionic liquid to the hydrolysis
solution medium. A cooling coil can be added to control the
hydrolysis temperature and to minimize the vaporization of
hydrolysis medium, which is typically water. In some embodiments it
is desirable to control the hydrolysis temperature to less than
90.degree. C., less than 70.degree. C., or less than 50.degree.
C.
[0026] The hydrolysis can be performed with or without stirring or
with recirculation through a pump. In one embodiment the used ionic
liquid catalyst is added slowly to the basic solution. Adding the
used ionic liquid catalyst slowly can help control the hydrolysis
temperature. The hydrolysis can be performed continuously,
semi-continuously, or in batches.
[0027] In one embodiment, the vessel used for the hydrolyzing is
fabricated of a metal, a plastic, a resin, or a glass. The vessel
can be agitated or mixed by any suitable method such as stirring or
recirculation around the vessel via a pump. In one embodiment the
vessel is designed to give turbulent flow so that thorough mixing
will result. Since the hydrolysis can be quite exothermic, in some
embodiments, cooling coil(s) or fan(s) can be used to maintain the
proper temperature.
[0028] After the hydrolysis, the final pH of the mixture of the
used ionic liquid catalyst and the basic solution can be adjusted.
Alternatively, the pH of the basic solution can be adjusted to
reach a target pH for disposal. In one embodiment, the hydrolysis
conditions are controlled to reach an acceptable, near neutral pH
for the non-water-reactive aqueous phase. At a near neutral pH, the
aqueous phase can be treated as a non-hazardous waste stream and
can be sent to non-hazardous effluent waste handling facilities. In
one embodiment, the pH of the non-water-reactive aqueous phase is 4
to 10, 5 to 9, or 6 to 8.
[0029] In one embodiment, a hydrogen halide gas is evolved during
the hydrolysis and the hydrogen halide gas dissolves into the basic
solution and is neutralized (i.e., reacted with the base). For
example, when hydrolyzing a used ionic liquid catalyst comprising a
chloroaluminate, hydrogen chloride can be evolved and dissolved
into the basic solution. Capturing the hydrogen chloride into the
basic solution and neutralizing it prevents the release of a toxic
and corrosive gas into the atmosphere.
[0030] The hydrolysis step produces solid particles that form a
slurry in the liquid phase. For example, when hydrolyzing a used
ionic liquid catalyst comprising a chloroaluminate, a slurry
containing solid precipitates comprising aluminum hydroxide,
aluminum oxide and hydrated aluminum chloride forms.
Separation of Liquid and Solid Phases
[0031] The hydrolyzed product containing solid and liquid phases is
separated by a separator, employing, for example, filtration or
centrifugation to separate the liquid phase from the solid phase.
In one embodiment, the liquid phase contains mostly residual
hydrocarbon and the aqueous phase of the hydrolyzed product, which
is non-water-reactive. In one embodiment, the separated liquid
phase contains less than 5 wt %, less than 2 wt %, or less than 1
wt % of the solid material in the hydrolyzed product.
[0032] Either prior to or during the liquid-solid separation, an
organic polymer or inorganic coagulant can be added to the
hydrolyzed product to make the separation of the liquid phase from
the solid phase more efficient and/or to reduce any chemically
bound water in the solid phase.
[0033] Filtration can be a method used for separation of the
hydrolyzed product into the liquid phase and the solid phase. Any
filter and filter media that effects good separation of the liquid
phase from the solid phase can be used. The filter is a
semi-permeable barrier placed perpendicular to or across a liquid
flow. The filter media and depth is sized according to the size and
amount of particles in the solid phase. In one embodiment, the
filter is either a gravity or pressure rapid filter.
[0034] The filter can operate either up-flow, down-flow, or at
angles in-between. Examples of filter media that can be used in the
filter include a deep bed (e.g., greater than 3'' up to 50'') of
sand or anthracite on a large particle bed support. Mixed media
filter beds can also be used.
[0035] In one embodiment, the solid phase is rinsed with a
hydrocarbon, water, or both to remove hydrocarbon products and/or
water soluble products held in the solid phase. The rinsate can be
added to the liquid phase or separately handled.
Solid Phase
[0036] The solid phase separated from the hydrolyzed product
comprises a solid phase of the hydrolyzed product that is not water
reactive. It can be safely handled or disposed of as waste or could
be sent to a coker unit. In some embodiments, the solid phase
requires no further processing to be disposed of in a landfill. In
some embodiments the solid waste comprises residual materials that
require it be disposed of as hazardous waste.
[0037] In one embodiment, the solid phase comprises reaction
products formed by the hydrolysis of the anhydrous metal halide in
the used ionic liquid. For example, when hydrolyzing a used ionic
liquid catalyst comprising a chloroaluminate, a slurry containing
solid precipitates comprising aluminum hydroxide, aluminum oxide
and hydrated aluminum chloride forms. In one embodiment, greater
than 75 wt %, greater than 80 wt %, or greater than 90 wt % of the
anhydrous metal halide is hydrolyzed and collected in the solid
phase. In one embodiment, the solid phase comprises less than 40 wt
%, less than 30 wt %, or less than 20 wt % of water and residual
hydrocarbon.
[0038] In one embodiment, the solid phase comprises metal that can
come from one or more corrosion metals, or products thereof.
Examples of corrosion metals are those included in steel alloys,
such as Al, Co, Cr, Cu, Fe, Mn, Mo, Nb, Ni, Ti, V, W, and mixtures
thereof. Examples of products of corrosion metals are metal
hydroxides, oxides, or chlorides. Removal of the corrosion metals
can make the liquid phase more suitable for waste effluent
treatment or other uses.
Separating Hydrocarbon Phase from the Liquid Phase
[0039] In one embodiment, the liquid phase is further separated
into an aqueous phase and a hydrocarbon phase in a liquid/liquid
separator. The separating is done using any liquid/liquid separator
that separates the components of the liquid phase between two
immiscible solvent phases of different densities. The separating
can be done using gravity, such as in a separatory funnel or
dropping funnel. The separating can also be done using a
centrifuge, especially where the volume to be separated is very
large or the separation is desired to be done quickly, such as in
less than an hour, less than 30 minutes, or less than 10
minutes.
[0040] The aqueous phase can be easily handled by several means,
including by disposal as aqueous waste, sent to an effluent
treatment facility, or sent to a facility to recover NaOH. The
hydrocarbon phase can be used in subsequent refining operations as
fuel or recycled in a refinery hydrocarbon pool. For example, the
hydrocarbon phase can be separated and used as a solvent or feed to
a refining process. In one embodiment, the hydrocarbon phase can be
used as a feed for a coker unit, a feed to a base oil or distillate
plant; or used as a fuel oil.
EXAMPLES
Example 1
Used Ionic Liquid Catalyst Comprising Anhydrous Metal Halide
[0041] In this example we used N-butylpyridinium
heptachlorodialuminate
(C.sub.5H.sub.5C.sub.4H.sub.9Al.sub.2Cl.sub.7) ionic liquid
catalyst. This catalyst had the following composition:
TABLE-US-00001 Element Wt % Al 12.4 Cl 56.5 C 24.6 H 3.2 N 3.3
[0042] The above catalyst was used for C3/C4 olefins alkylation
with isobutane to make alkylate gasoline. During the alkylation the
used catalyst accumulated 5 wt % of conjunct polymer. The used
catalyst also accumulated trace amounts of Fe, Ni, Cu and Cr from
corrosion byproducts in the alkylation process.
Example 2
Hydrolysis of Used Ionic Liquid Catalyst
[0043] 173.3 g of 15 wt % NaOH solution was prepared in a 1 L
beaker equipped with an overhead stirrer. While stirring, 58.66 g
of the used ionic liquid catalyst from Example 1 was added slowly
to the NaOH solution over a 36 minute period at a rate to control
the exotherm from the hydrolysis to less than 50 deg C. A brown
slurry was formed and the final pH of the solution with the brown
slurry was about 5. The brown slurry was filtered to capture an
aluminum hydroxide/oxide solid as a wet filter cake.
[0044] The filter cake was rinsed with heptane and de-ionized water
to remove any strippable hydrocarbon from the filter cake and to
add the strippable hydrocarbon to the liquid filtrate. 78.8 g of
rinsed wet filter cake was recovered. The liquid filtrate was
separated further to a hydrocarbon phase and an aqueous phase using
a separatory funnel. The hydrocarbon phase was dried to remove the
heptane solvent, and 0.34 g of heavy hydrocarbon having a brownish
yellow color was recovered.
[0045] The boiling point distribution of the recovered hydrocarbon
phase was measured by gas chromatography for high temperature
distillation using ASTM D 6352-04 (Reapproved 2009), "Standard Test
Method for Boiling Range Distribution of Petroleum Distillates in
Boiling Range from 174 to 700.degree. C. by Gas Chromatography",
and the results are shown below.
TABLE-US-00002 % Temperature, C. (F.) IBP 204 (399) 10 303 (578) 30
354 (670) 50 394 (742) 70 443 (830) 90 539 (1003) FBP 720
(1328)
[0046] The boiling point distribution data showed that the
recovered hydrocarbon phase had a final boiling point greater than
700 deg. C. This heavy hydrocarbon would be a useful product for
many purposes, including a feed for a coker unit or a fuel oil.
Example 3
Material Balance of Hydrolyzed Product Streams
[0047] Elemental analyses of the aqueous phase and solid phase from
Example 2 were performed. The elemental analysis showed that the
aqueous phase contained mainly Na, Al, N, C, and very low corrosion
metal ion concentrations (below instrument detection limits). The
elemental analysis of the solid phase (rinsed wet filter cake) from
Example 2 indicated that the bulk (i.e., greater than 70 wt %) of
the corrosion metals were captured in the solid phase.
[0048] Elemental material balances around Example 2 were calculated
to understand how the key elements of the feed composition of the
used ionic liquid catalyst and basic solution were redistributed in
the hydrolyzed product phases. The tables below show the
distribution of key elements in the feeds (ionic liquid
catalyst+NaOH solution) and in the resulting different hydrolyzed
product phases (hydrocarbon phase, non-water-reactive aqueous
phase, and the solid phase).
[0049] Feed Composition:
TABLE-US-00003 Used Ionic Conjunct NaOH Element Liquid Cat., Wt %
Polymer, Wt % Solution, Wt % C 86 14 0 N 100 0 0 Cl 99 1 0 Al 100 0
0 Na 0 0 100 Fe 100 0 0
[0050] Product Composition:
TABLE-US-00004 Aqueous Hydrocarbon Solid Phase (Wet Element Phase,
Wt % Phase, Wt % Filter Cake), Wt % C 68 2.1 30 N 52 <1 48 Cl 82
<1 18 Al 0.3 <1 99.7 Na 84 <1 16 Fe 3 0 97
[0051] The compositional analysis indicated that greater than 99.5
wt % of the anhydrous aluminum chloride in the used ionic liquid
catalyst was converted to solids (e.g., aluminum hydroxide and
aluminum oxide) and collected in the wet filter cake. It is
believed that most of the N-butylpyridinium chloride stayed intact
during the hydrolysis process. The compositional analysis suggested
that over 50 wt % of the N-butylpyridinium chloride was dissolved
in the aqueous phase and the rest was deposited on the wet filter
cake. Most of the NaOH solution was converted to NaCl and was
dissolved in the aqueous phase. Most of the corrosion metal
products, as noted by Fe, were deposited in the solid phase that
was collected in the wet filter cake.
[0052] The transitional term "comprising", which is synonymous with
"including," "containing," or "characterized by," is inclusive or
open-ended and does not exclude additional, unrecited elements or
method steps. The transitional phrase "consisting of" excludes any
element, step, or ingredient not specified in the claim. The
transitional phrase "consisting essentially of" limits the scope of
a claim to the specified materials or steps "and those that do not
materially affect the basic and novel characteristic(s)" of the
claimed invention.
[0053] For the purposes of this specification and appended claims,
unless otherwise indicated, all numbers expressing quantities,
percentages or proportions, and other numerical values used in the
specification and claims, are to be understood as being modified in
all instances by the term "about." Furthermore, all ranges
disclosed herein are inclusive of the endpoints and are
independently combinable. Whenever a numerical range with a lower
limit and an upper limit are disclosed, any number falling within
the range is also specifically disclosed.
[0054] Any term, abbreviation or shorthand not defined is
understood to have the ordinary meaning used by a person skilled in
the art at the time the application is filed. The singular forms
"a," "an," and "the," include plural references unless expressly
and unequivocally limited to one instance.
[0055] All of the publications, patents and patent applications
cited in this application are herein incorporated by reference in
their entirety to the same extent as if the disclosure of each
individual publication, patent application or patent was
specifically and individually indicated to be incorporated by
reference in its entirety.
[0056] This written description uses examples to disclose the
invention, including the best mode, and also to enable any person
skilled in the art to make and use the invention. Many
modifications of the exemplary embodiments of the invention
disclosed above will readily occur to those skilled in the art.
Accordingly, the invention is to be construed as including all
structure and methods that fall within the scope of the appended
claims. Unless otherwise specified, the recitation of a genus of
elements, materials or other components, from which an individual
component or mixture of components can be selected, is intended to
include all possible sub-generic combinations of the listed
components and mixtures thereof.
* * * * *