U.S. patent application number 12/168510 was filed with the patent office on 2009-02-05 for water-soluble phenylenediamine compositions and methods for stabilizing ethylenically unsaturated compounds and monomers.
This patent application is currently assigned to GENERAL ELECTRIC COMPANY. Invention is credited to Sherif Eldin, John Link.
Application Number | 20090032768 12/168510 |
Document ID | / |
Family ID | 33298911 |
Filed Date | 2009-02-05 |
United States Patent
Application |
20090032768 |
Kind Code |
A1 |
Link; John ; et al. |
February 5, 2009 |
WATER-SOLUBLE PHENYLENEDIAMINE COMPOSITIONS AND METHODS FOR
STABILIZING ETHYLENICALLY UNSATURATED COMPOUNDS AND MONOMERS
Abstract
Compositions and methods for inhibiting polymerization of
ethylenically unsaturated monomers are provided. The compositions
include a water-soluble phenylenediamine composition.
Inventors: |
Link; John; (Humble, TX)
; Eldin; Sherif; (Bellaire, TX) |
Correspondence
Address: |
HOFFMANN & BARON, LLP
6900 JERICHO TURNPIKE
SYOSSET
NY
11791
US
|
Assignee: |
GENERAL ELECTRIC COMPANY
Fairfield
CT
|
Family ID: |
33298911 |
Appl. No.: |
12/168510 |
Filed: |
July 7, 2008 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
11786826 |
Apr 13, 2007 |
7414162 |
|
|
12168510 |
|
|
|
|
10422521 |
Apr 24, 2003 |
|
|
|
11786826 |
|
|
|
|
Current U.S.
Class: |
252/182.12 |
Current CPC
Class: |
C09K 15/20 20130101;
C07C 215/16 20130101; C09K 15/22 20130101; C09K 15/28 20130101 |
Class at
Publication: |
252/182.12 |
International
Class: |
C09K 3/00 20060101
C09K003/00 |
Claims
1.-10. (canceled)
11. A composition resistant to polymerization comprising: (a) an
ethylenically unsaturated monomer, and (b) one or more
water-soluble compounds of the following formula: ##STR00021##
wherein at least one of R.sup.1, R.sup.2, and R.sup.3 is
##STR00022## R.sup.1, R.sup.2 and R.sup.3 are independently
selected from H, C.sub.1-C.sub.18 alkyl, hydroxyalkyl,
--O--R.sup.6, --S--R.sup.6, --N--(R.sup.7)(R.sup.8), aryl, and
##STR00023## R.sup.5 is selected from the group consisting of H,
alkyl, hydroxyalkyl, --O--R.sup.6, --S--R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl; Z comprises one or more
substituents selected from the group consisting of hydrogen, alkyl,
alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heterocyclo,
--CN, --NO.sub.2, --O--R.sup.6, --S--R.sup.6, and
--N(R.sup.7)(R.sup.8), R.sup.6, R.sup.7 and R.sup.8 are
independently selected form the group consisting of hydrogen,
alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl and
heterocyclo; and wherein said composition is water-soluble.
12. The composition of claim further comprising a solvent.
13.-21. (canceled)
Description
FIELD OF THE INVENTION
[0001] The present invention relates to water-soluble
phenylenediamine compositions and methods for inhibiting
polymerization of ethylenically unsaturated hydrocarbons.
BACKGROUND OF THE RELATED TECHNOLOGY
[0002] During the refining process, hydrocarbon streams are
frequently exposed to elevated temperatures, which can lead to
premature polymerization of the desired monomer. The premature
polymerization results in reduction of the amount of the desired
monomer end-products as well as a loss in efficiency caused by
fouling and deposit formation within the processing equipment.
[0003] In order to reduce or prevent polymer formation, stabilizing
or inhibitor compositions have been introduced into the hydrocarbon
stream at or upstream of a location where polymerization is likely
to occur, such as where distillation is performed.
[0004] Phenylenediamines (PDA's) are widely used as antioxidants
and polymerization inhibitors. However, their use is limited to
hydrocarbon streams where the PDA is soluble. A number of patents
relate to the use of various PDA's, combinations of different PDA's
and combinations of PDA's with other inhibitors to stabilize
hydrocarbon fluids.
[0005] Among these patents is U.S. Pat. No. 6,200,461 to Eldin
which describes methods and compositions for inhibiting the
polymerization of ethylenically unsaturated hydrocarbons under both
processing and storage conditions by the addition of combinations
of aminophenol compounds and either PDA or hydroxylamine. Other
combinations have also been used. These include inhibitor
combinations containing a PDA with an oxime compound and a
hydroxylamine as shown in U.S. Pat. No. 5,489,718 to Arhancet.
Other examples include the combination of a PDA and a hydroxylamine
as shown in U.S. Pat. No. 5,396,004 to Arhancet and a PDA with a
hydroxytoluene compound as shown In U.S. Pat. No. 5,416,258 to
Arhancet et al.
[0006] Examples of specific PDA compounds may be found in U.S. Pat.
No. 4,929,778 to Roling which describes compositions including a
PDA compound which has at least one N--H bond and a hindered phenol
useful for inhibiting the polymerization of styrene during elevated
temperature processing, storage and shipment. U.S. Pat. No.
4,774,374 to Abruscato et al. discloses an oxygenated species
formed by the reaction of oxygen and an
N-aryl-N'-alkyl-p-phenylenediaminie.
[0007] While each of these references provides compositions and
methods that reduce premature polymerization of ethylenically
unsaturated monomers, they are generally limited to hydrocarbon
processing and storage where they are soluble, which does not
include where water is present. Therefore, the currently available
PDA inhibitors do not adequately address the concerns of the
prevention of premature polymerization of a monomers with
water-solubility, where a water phase is present.
[0008] Therefore, it would be desirable to provide a water-soluble
composition for the reducing and or preventing the polymerization
of ethylenically unsaturated monomers. Desirably, the composition
will include a water-soluble phenylenediaminie composition which
acts as an antioxidant/free-radical polymerization inhibitor.
SUMMARY OF THE INVENTION
[0009] The present invention provides a water-soluble
phenylenediamine composition which also functions as an
antioxidant/free-radical polymerization inhibitor. The compounds
are of the following formula:
##STR00001##
[0010] wherein at least one of R.sup.1, R.sup.2, and R.sup.3 is
##STR00002##
[0011] R.sup.1, R.sup.2 and R.sup.3 are independently selected from
H, alkyl, hydroxyalkyl, --O--R.sup.6, --S--R.sup.6, --C(O)R.sup.6,
--C(S)R.sup.6, --N--(R.sup.7)(R.sup.8), aryl, and
##STR00003##
[0012] R.sup.5 is selected from the group consisting of H, alkyl,
hydroxyalkyl, O, S, --O--R.sup.6, --S--R.sup.6,
--N--(R.sup.7)(R.sup.6), and aryl;
[0013] Z comprises one or more substituents selected from the group
consisting of hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl,
cycloalkenyl, aryl, heterocyclo, --CN, --NO.sub.2, --O--R.sup.6,
--S--R.sup.6, and --N--(R.sup.7)(R.sup.8); and
[0014] R.sup.6, R.sup.7 and R.sup.8 are independently selected from
the group consisting of hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, cycloalkenyl, aryl and heterocyclo. Desirably, the
compound corresponds the following formula:
##STR00004##
[0015] The compounds of formula (I), above, may be added to a
composition including an ethylenically unsaturated monomer to
produce a composition resistant to polymerization. The addition of
the water-soluble phenylenediamine composition of the present
invention to the monomer composition may occur during synthesis or
processing or storage of the composition.
[0016] The compounds of the present invention include a reaction
product of a phenylenediamine compound of the following
formula:
##STR00005##
[0017] wherein at least one of R.sup.1, R.sup.2 and R.sup.3 is
H.
[0018] R.sup.1, R.sup.2 and R.sup.3 are independently selected from
the group consisting of, alkyl, hydroxyalkyl, --O--R.sup.6,
--S--R.sup.6, --C(O)R.sup.6, --C(S)R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl;
[0019] Z comprises one or more substituents selected from the group
consisting of hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl,
cycloalkenyl, aryl, heterocyclo, --CN.sub.1--NO.sub.2,
--O--R.sup.6, --S--R.sup.6, and --N(R.sup.7)(R.sup.8); and
[0020] R.sup.6, R.sup.7 and R.sup.8 are independently selected from
the group consisting of hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, cycloalkenyl, aryl and heterocyclo,
[0021] with a heterocylic compound of the following formula:
##STR00006##
[0022] wherein R.sup.5 is selected from the group consisting of H,
alkyl, hydroxyalkyl, --O--R.sup.6, --S--R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl.
[0023] Another aspect of the present invention provides a method of
preparing a water-soluble phenylenediamine composition including
the step of reacting a phenylenediamine compound of the following
formula:
##STR00007##
wherein at least one of R.sup.1, R.sup.2 and R.sup.3 is H and
[0024] R.sup.1, R.sup.2 and R.sup.3 are independently selected from
the group consisting of, alkyl, hydroxyalkyl, --O--R.sup.6,
--S--R.sup.6, --C(O)R.sup.6, --C(S)R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl;
[0025] Z comprises one or more substituents selected from the group
consisting of hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl,
cycloalkenyl, aryl, heterocyclo, --CN, --NO.sub.2, --O--R.sup.6,
--S--R.sup.6, and --N(R.sup.7)(R.sup.8); and
[0026] R.sup.6, R.sup.7 and R.sup.8 are independently selected from
the group consisting of hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, cycloalkenyl, aryl and heterocyclo,
[0027] with a heterocylic compound of the following formula:
##STR00008##
[0028] wherein R.sup.5 is selected from the group consisting of H,
alkyl, hydroxyalkyl, --O--R.sup.6, --S--R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl. Desirably, the phenylenediamine
compound is 1,4-phenylenediamine.
[0029] A further aspect of the present invention provides a method
of reducing or inhibiting fouling and deposit formation during
hydrocarbon processing including the step of administering an
effective amount of one or more water-soluble compounds of the
following formula to a hydrocarbon stream at or upstream of a
location where said fouling and/or said deposit formation may
occur:
##STR00009##
[0030] wherein at least one of R.sup.1, R.sup.2, and R.sup.3 is
##STR00010##
[0031] R.sup.1, R.sup.2 and R.sup.3 are independently selected from
H, C.sub.1-C.sub.18 alkyl, hydroxyalkyl, --O--R.sup.6,
--S--R.sup.6, --N--(R.sup.7)(R.sup.8), aryl, and
##STR00011##
[0032] R.sup.5 is selected from the group consisting of H, alkyl,
hydroxyalkyl, --O--R.sup.6, --S--R.sup.6, --N--(R.sup.7)(R.sup.8),
and aryl;
[0033] Z comprises one or more substituents selected from the group
consisting of hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl,
cycloalkenyl, aryl, heterocyclo, --CN, --NO.sub.2, --O--R.sup.6,
--S--R.sup.6, and --N(R.sup.7)(R.sup.8);
[0034] R.sup.6, R.sup.7 and R.sup.8 are independently selected form
the group consisting of hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, cycloalkenyl, aryl and heterocyclo; and wherein
[0035] said composition is water-soluble
DETAILED DESCRIPTION OF THE INVENTION
[0036] The present invention includes compounds of the formula:
##STR00012##
[0037] wherein the NHR.sup.3 group may be present in any of the
ortho, para, and meta positions,
[0038] at least one of R.sup.1, R.sup.2, and R.sup.3 is
##STR00013##
[0039] R.sup.1, R.sup.2 and R.sup.3 are independently selected from
H, alkyl, hydroxyalkyl, --O--R.sup.6, --S--R.sup.6, --C(O)R.sup.6,
--C(S)R.sup.6, --N--(R.sup.7)(R.sup.8), aryl, and
##STR00014##
[0040] R.sup.5 is selected from the group consisting of H, alkyl,
hydroxyalkyl, O, S, --O--R.sup.6, --S--R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl;
[0041] Z comprises one or more substituents selected from the group
consisting of hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl,
cycloalkenyl, aryl, heterocyclo, --CN, --NO.sub.2, --O--R.sup.6,
--S--R.sup.6, and --N(R.sup.7)(R.sup.6); and
[0042] R.sup.6, R.sup.7 and R.sup.8 are independently selected from
the group consisting of hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, cycloalkenyl, aryl and heterocyclo. Desirably, the
second amine group is in the para position, corresponding to the
following formula:
##STR00015##
[0043] The term "alkyl" is meant to include substituted or
unsubstituted, straight or branched chain saturated hydrocarbon
groups, desirably having 1 to 20 carbons in the main chain.
Examples of unsubstituted groups include methyl, ethyl, propyl,
isopropyl, n-butyl, t butyl, isobutyl, pentyl, hexyl, isohexyl,
heptyl, 4,4-dimethyl pentyl, octyl, 2,2,4-trimethylpentyl, nonyl,
decyl, undecyl, dodecyl, and the like. Substituents may include
halogen, hydroxy, or aryl groups.
[0044] The term "hydroxyalkyl" is meant to include an alkyl group
as described above with at least one hydroxy group substituent.
[0045] The term "alkenyl" is meant to include substituted or
unsubstituted, straight or branched chain hydrocarbon groups
including at least one carbon to carbon double bond in the chain,
and desirably including 2 to 10 carbons in the normal chain.
Examples of such unsubstituted alkenyl groups include ethenyl,
propenyl, isobutenyl, butenyl, pentenyl, hexenyl, heptenyl,
octenyl, nonenyl, decenyl, and the like. Substituents may include
those as described above.
[0046] The term "alkynyl", is meant to include substituted or
unsubstituted, straight and branched chain hydrocarbon groups
including at least one carbon to carbon triple bond in the chain,
and preferably having 2 to 10 carbons in the normal chain. Examples
of such unsubstituted groups include ethynyl, propynyl, butynyl,
pentynyl, hexynyl, heptynyl, octynyl, nonynyl, decynyl, and the
like. Substituents may include those as described above.
[0047] The term "cycloalkyl" is meant to include substituted or
unsubstituted, saturated cyclic hydrocarbon ring systems,
preferably containing 1 to 3 rings and 3 to 7 carbons per ring.
Exemplary unsubstituted such groups include cyclopropyl,
cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl,
cyclodecyl, cyclododecyl, and adamantyl. Exemplary substituents
include one or more alkyl groups as described above, or one or more
groups described above as alkyl substituents.
[0048] The term "cycloalkenyl" is meant to include hydrocarbon ring
systems which may be substituted or unsubstituted as described
above for cycloalkyl, further containing at least one carbon to
carbon double bond forming a partially unsaturated ring. These may
also include substituents as described above.
[0049] The terms "heterocyclo" or "heterocyclic" are meant to
include substituted or unsubstituted, fully saturated or
unsaturated, aromatic or non-aromatic cyclic groups having at least
one heteroatom (such as N, O, and S) in at least one ring,
desirably monocyclic or bicyclic groups having 3-6 atoms in each
ring. The heterocyclo group may be bonded through any carbon or
heteroatom of the ring system. Examples of heterocyclic groups
include, without limitation, thienyl, furyl, pyrrolyl, pyridyl,
imidazolyl, pyrrolidinyl, piperidinyl, azepinyl, indolyl,
isoindolyl, quinolinyl, isoquinolinyl, benzothiazolyl,
benzoxazolyl, benzimidazolyl, benzoxadiazolyl, and benzofurazanyl.
These may also include substituents as described above.
[0050] The term "aryl" is meant to include substituted or
unsubstituted monocyclic, bicyclic or tricyclic aromatic groups,
desirably including one or two rings which contain only carbon ring
atoms and 6 to 12 ring carbons. The term "aryl" can also refer to
an aryl group fused to a monocyclic cycloalkyl or monocyclic
heterocycle in which the point(s) of attachment is/are on the
aromatic portion. Examples of aryl groups include phenyl, biphenyl,
and naphthyl. Aryl rings fused to cycloalkyls are include indanyl,
indenyl, and tetrahydronaphthyl. Examples of aryl groups fused to
heterocyclic groups include 2,3-dihydrobenzofuranyl, benzopyranyl,
1,4-benzodioxanyl, and the like. Substituents may include those as
described above as well as nitro groups.
[0051] The water-soluble phenylenediamine compounds of the present
invention may be formed by the reaction of a phenylenediamine
compound of the following formula:
##STR00016##
[0052] wherein at least one of R.sup.1, R.sup.2 and R.sup.3 is
H;
[0053] R.sup.1, R.sup.2 and R.sup.3 are independently selected from
the group consisting of, alkyl, hydroxyalkyl, --O--R.sup.6,
--S--R.sup.6, --C(O)R.sup.6, --C(S)R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl;
[0054] Z comprises one or more substituents selected from the group
consisting of hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl,
cycloalkenyl, aryl, heterocyclo, --CN, --NO.sub.2, --O--R.sup.6,
--S--R.sup.6, and --N(R.sup.7)(R.sup.8); and
[0055] R.sup.6, R.sup.7 and R.sup.8 are independently selected from
the group consisting of hydrogen, alkyl, alkenyl, alkynyl,
cycloalkyl, cycloalkenyl, aryl and heterocyclo,
[0056] with a heterocylic compound of the following formula:
##STR00017##
[0057] wherein R.sup.5 is selected from the group consisting of H,
alkyl, hydroxyalkyl, --O--R.sup.6, --S--R.sup.6,
--N--(R.sup.7)(R.sup.8), and aryl. Desirably, the heterocyclic
compound is propylene oxide or butylene oxide
[0058] This reaction produces a mixture of reaction products that
may be separated by any of a variety of means known in the art,
including chromatography. For example, the reaction of
1,4-phenylenediamine with the substituted heterocyclic compound may
produce a mixture of five different products as shown in the
following reaction scheme:
##STR00018##
[0059] Similarly, where the phenylenediamine staring material
includes a non-hydrogen substitution, the products of the reaction
with the substituted heterocyclic compound are shown by the
reaction scheme as shown below.
##STR00019##
[0060] The reaction of 1,4-phenylenediamine with propylene oxide
will also produce a mixture of products which include
N,N'-dihydroxypropylphenylenediamine,
N,N-dihydroxypropylphenylenediamine,
N-hydroxypropylphenylenediamine,
N,N,N'-trihydroxypropylphlenylenediamine, and
N,N,N',N'-tetrahydryoxypropylphenylenediamine.
[0061] The phenylenediamine compounds of the present invention are
useful as antioxidant/free-radical polymerization inhibitors. In
other words, they are useful to stabilize hydrocarbon compositions
including ethylenically unsaturated monomers by inhibiting
polymerization. They are useful as inhibitors under both process
and storage conditions including where the monomers are subjected
to elevated temperatures, for example up to about 125.degree.
C.
[0062] The water-soluble phenylenediamine compositions are useful
with a variety of ethylenically unsaturated monomers. These
include, but are not limited to vinyl aromatic compounds such as
styrene, substituted styrene, divinylbenzene, vinyl toluene, and
vinyl naphthalene, and other ethylenically unsaturated monomers
such as acrylic acid, alkyl acrylates, acrylonitrile, butadiene,
dicyclopentadiene, cyanoacrylates, isoprene, and propylene.
[0063] For the methods of the present invention, the useful
water-soluble phenylenediamine compositions will retain at least
one "--NH" group for effective polymerization inhibition. The
effective amount of the water-soluble phenylenediamine composition
having at least one "--NH" group used in the methods of the present
invention as a polymerization inhibitor is that amount which is
sufficient to affect inhibition of polymerization and will vary
according to the conditions under which the monomer is synthesized,
processed, and/or stored. There are several factors that will
affect the amount of inhibitor that is required. Factors that will
require an increase in the amount of inhibitor are increased
monomer concentration and increased temperature.
[0064] Generally, an effective concentration of the water-soluble
phenylenediamine compositions of the present invention will range
from about 0.5 ppm to about 2000 ppm, more desirably from about 1
ppm to about 50 ppm. The compositions may be used in many
hydrocarbon processing steps where premature polymerization is
likely to occur including hydrocarbon cracking processes,
preheating, distillation, hydrogenation, extraction, etc, The
water-soluble phenylenediamine composition may be added at a
location upstream of these process locations.
[0065] The water-soluble phenylenediamine compositions may be added
to a water stream, hydrocarbon stream or to a monomer composition
alone, or after first being premixed with a solvent. Where a premix
of the water-soluble phenylenediamine composition is desired, it
may be first combined with a solvent such as water or an organic
solvent including, but not limited to methanol, ethanol, acetone,
pyridine, nitrobenzene, n-hexadecane, n-hexane, methylene chloride,
dimethyl sulphoxide, chloroform, carbon tetrachloride, benzene,
glycols, esters and ethers.
[0066] Other inhibitors or antifoulants known in the art may be
combined with the waters soluble phenylenediamine compounds of the
present invention. These may include other phenylenediamines,
hydroxylamines, nitroxides, and hindered phenols. When a
compositions containing an additional phenylenediamine composition
is desired, the additional phenylenediamine may correspond to the
following formula:
##STR00020##
wherein R.sup.a, R.sup.b and R.sup.c are independently selected
from the group consisting of H, C.sub.1-C.sub.18 alkyl,
hydroxyalkyl, --O--R.sup.6, --S--R.sup.6, --N--(R.sup.7)(R.sup.6),
and aryl.
[0067] The water-soluble phenylenediamine compositions of the
present invention have a wider variety of uses as compared to
conventional phenylenediamine inhibitors. For example, during
processing of acrylonitrile, there is contact with water and
consequent fouling and deposit formation in the water sections. A
phenylenediamine composition that is not water-soluble will not be
effective as an inhibitor in this situation.
[0068] PDA's such as
N-(1,4-dimethylpentyl)-N'-phenyl-p-phenylenediamine and
N-(1,3-dimethylbutyl)-N-phenyl-p-phenylenediamine are not miscible
with water. Instead, when they are added to water, they separate,
forming two distinct layers, a PDA layer and a water layer.
However, the PDA's of the present invention are completely miscible
with water, When they are added to water, the PDA's of the present
invention do not form a separate layer, i.e., a partition between
the aqueous and hydrocarbon phases where it provides vinyl monomer
free radical polymerization inhibition.
[0069] The features and advantages of the present invention are
more fully shown by the following examples which are provided for
purposes of illustration and are not to be construed as limiting
the invention in any way.
EXAMPLES
[0070] Acrylonitrile was chosen to represent reactive vinyl
monomers. The water-soluble phenylenediamines (PDA's) of the
present invention were tested in acrylonitrile. Comparative testing
was also performed using conventional polymerization inhibitors.
The comparative inhibitor compositions are shown in TABLE 1, while
the inventive inhibitor compositions which were tested are shown in
TABLE 2. The parenthesis after the inhibitor names indicates the
weight ratio of two or more inhibitors in the composition.
TABLE-US-00001 TABLE 1 Comparative Inhibitor Compositions
Composition Inhibitor(s) A Blank B Hydroquinone C
N-(1,3-dimethylbutyl)-N-phenyl-p-phenylenediamine D
Benzoquinonediimide E Benzoquinonediimide/Hydroquinone (1:1) F
Hydroquinone/N-(1,3-dimethylbutyl)-N-phenyl-p- phenylenediamine
(1:1) G Hydroquinone/N-(1,4-dimethylpentyl)-N'-phenyl-p-
phenylenediamine (1:1) H N-(1,4-dimethylpentyl)-N'-phenyl-p-
phenylenediamine
TABLE-US-00002 TABLE 2 Inventive Inhibitor Compositions Composition
Inhibitor(s) I N,N,N',N'-Tetrahydroxypropylphenylenediamine J
N-hydroxypropylphenylenediamine and N,N'-
dihydroxypropylphenylenediamine (reaction mixture) K
N-hydroxypropylphenylenediamine and N,N'-
dihydroxypropylphenylenediamine (reaction mixture)/ Hydroquinone
(1:1) L N-hydroxypropylphenylenediamine and N,N'-
dihydroxypropylphenylenediamine (reaction mixture)/
Benzoquinonediimide (1:1)
[0071] For each of the experiments, acrylonitrile was heated under
an inert atmosphere in glass tubes. A single inhibitor composition
(A-L) was added to each tube. In the first experiment, tubes
containing acrylonitrile were dosed with 2 ppm of various
inhibitors and were heated at 110.degree. C.
[0072] For the second experiment, 35 ppm azobisobutyronitrile
(AIBN), a free radical polymerization initiator, was also added to
each tube to simulate conditions where fee radical concentrations
are relatively high. The second experiment was conducted at
66.degree. C.
[0073] For each experiment, the performance of the inhibitor
performance was judged by the length of the induction time for
polymerization, i.e., the formation of visible polymer, as the
reaction mixture turned turbid and white polyacrylonitrile started
to deposit. The results of both experiments are shown in TABLE 3,
below.
TABLE-US-00003 TABLE 3 Results of Acrylonitrile Study Induction
Time to Polymerization Experiment 2 (with polymerization initiator)
Composition Experiment 1 (hours) (minutes) A 1 15 B 2.2 132 C 106
n/a D 508 n/a E 528 160 F n/a 183 G n/a 195 H n/a 230 I 4 49 J 106
290 K 168 n/a L 278 n/a
[0074] As can be seen from TABLE 3, the inventive compositions J, K
and L performed better than the comparative compositions that
included the known polymerization inhibitors hydroquinone,
N-(1,4-dimethylpentyl)-N'-phenyl-p-phenylenediamine, and
N-(1,3-dimethylbutyl)-N-phenyl-p-phenylenediamine. In addition,
inventive composition J has the advantage of being water-soluble
which increases the variety of potential uses.
[0075] While there have been described what are presently believed
to be the preferred embodiments of the invention, those skilled in
the art will realize that changes and modifications may be made
thereto without departing from the spirit of the invention, and it
is intended to include all such changes and modifications as fall
within the true scope of the invention.
* * * * *