FORM – 2
THE PATENTS ACT, 1970
(39 of l970)
&
THE PATENTS RULES, 2003
COMPLETE
Specification
(See Section 10; Rule 13)
IONIC LIQUID COMPOSITION
RELIANCE INDUSTRIES LIMITED
an Indian Company
of 3rd Floor, Maker Chamber - IV,
222, Nariman Point, Mumbai 400 021,
Maharashtra, India
Inventors:
1. JAIN SURESH SHANTILAL
2. ADURI PAVANKUMAR
3. RATNAPARKHI UDAY
4. UPPARA PARASU VEERA
THE FOLLOWING SPECIFICATION PARTICULARLY DESCRIBES THE INVENTION AND THE MANNER IN WHICH IT IS TO BE PERFORMED.

FIELD
The present disclosure relates to ionic liquids. Particularly, the present disclosure relates to ionic liquids containing composition for the manufacturing of aromatic carboxylic acids such as terephthalic acid.
Definition
In the context of the present disclosure, the term "ionic liquid" means a molecular composition comprising cationic and anionic counterparts interacting with each other by means including but not limited to electrostatic, covalent or semi-covalent bond. and said composition being in a phase including but not limited to liquid, semi-solid, viscous mass or a mixture thereof at a pre-determined temperature and pressure irrespective of the phase of occurrence of said composition at ambient temperature and pressure.
BACKGROUND:
Ionic liquids are liquids composed of ions that are fluid around or below 100°C. Ionic liquids, also referred to as room-temperature-molten salts, have attracted special attention for the past several years, owing to their potential uses as electrolytes for a variety of electrochemical devices such as lithium secondary batteries, solar cells, actuators, electric double-layer capacitors and the like, reaction media, and catalysts for organic syntheses.
Ionic liquids are used in a wide variety of applications. Recently, alkyl ionic liquids have been proposed as a promoter in the manufacturing of aromatic carboxylic acids such as terephthalic acid.
Terephthalic acid is an organic compound with formula C6H4(COOH)2. This colourless solid is a commodity chemical, used principally as a precursor to the polyester PET, used to make clothing and plastic bottles. World production in 1970 was around 1.75 million tonnes. By 2006, global purified terephthalic acid (PTA) demand had exceeded 30 million tonnes. There is a smaller, but nevertheless

significant, demand for terephthalic acid in the production of polybutylene terephthalate and several other engineering polymers.
US Patent No.7985875 discloses a process for preparing an aromatic carboxylic acid by liquid phase oxidation which comprises contacting a benzene or naphthalene compound having two or three C1-C4 alkyl, hydroxyalkyl or formyl groups with an oxygen-containing gas in the presence of a carboxylic acid solvent, a catalyst and a promoter in a reaction zone, the promoter is an ionic liquid comprising an organic cation selected from the group consisting of 1-alkylpyridinium and 1,3-dialkylimidazolium and an anion consisting essentially of bromide or iodide. However, the known alkyl ionic liquids though acts as a promoter in the manufacturing of terephthalic acid, they are not able to reduce the formation of impurities such as 4-carboxy-benzaldehyde (4-CBA).
Reducing the 4-CBA impurity in terephthalic acid is very important. If it exists in large quantities in terephthalic acid, acts a chain terminating agent during the PET polymerization process and hence desired PET molecular weight may not be achieved.
Accordingly, it is desired to develop ionic liquid/s containing composition which is capable of solubilizing not only the terephthalic acid and 4-CBA but also various other intermediates and side products, thereby reducing the formation of unwanted impurities and producing aromatic carboxylic acids such as terephthalic acid in highly pure form.
OBJECTS
Some of the objects of the present disclosure, which at least one embodiment herein satisfies, are as follows:
It is an object of the present disclosure to provide a composition containing ionic liquid/s which can act as a co-solvent as well as a promoter in the manufacturing of terephthalic acid.

It is another object of the present disclosure to provide a composition containing ionic liquids, which is capable of reducing the formation of undesired impurities such as 4-CBA when used in the manufacturing of aromatic carboxylic acids.
It is another object of the present disclosure to provide a process for the preparation of purified terephthalic acid in the presence of ionic liquid/s.
It is still another object of the present disclosure to provide a process for the preparation of purified terephthalic acid which can be carried out in a continuous manner.
It is yet another object of the present disclosure to provide a process for the preparation of purified terephthalic acid in which the thermo-oxidative loss of the ionic liquid is minimum.
It is a further object of the present disclosure to provide a process for the preparation of purified terephthalic acid in which the ionic liquid and the catalyst are recovered and recycled.
SUMMARY:
In accordance with the present disclosure there is provided a composition for preparing aryl carboxylic acid; said composition comprising:
wherein.
Ar is substituted or un-substituted aryl group.
- at least one ionic liquid of formula I. in an amount of 0.05 to 50 % of the total mass of the composition;


Z is (CH2)n, wherein n is an integer from 0 to 10.
Q+ is an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium, pyridinium, pyrrolidinium, morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium;
R is C1 to C20 linear or branched alkyl group or Ar-Z,
A"is an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonatses. phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides;
- at least one catalyst, in an amount of 0.01 to 5 % of the total mass of the composition,;
- at least one non-oxidizable polar solvent; and
at least one oxidizable multi-alkylated arylene compound with no two successive ring positions bearing alkyl group,
said composition adapted to reduce the formation of partially oxidized derivatives of said multi-alkylated arylene compound in a quantity less than 4000 ppm during the preparation of aryl carboxylic acid, said derivatives comprising at least one carboxylic acid moiety and at least one aldehyde moiety.
Typically, the proportion of the ionic liquid to the non-oxidizable polar solvent ranges
between 1:1 and 1:20.
Typically, the catalyst comprises at least one metal compound, the metal being
selected from the group consisting of cobalt, magnesium, chromium, copper, nickel,
vanadium, iron, molybdenum, tin, cerium, zirconium, cesium and titanium.
In one embodiment the catalyst is at least one selected from the group consisting of
cobalt acetate, manganese acetate, cerium acetate, potassium acetate, cesium acetate,

zirconium acetate, copper acetate, cobalt oxalate, manganese oxalate.cerium oxalate, potassium oxalate, cesium oxalate, zirconium oxalateand copper oxalate.
Typically, the non-oxidizable polar solvent is at least one solvent selected from the group consisting of acetic acid, methyl acetate ethyl acetate, propyl acetate, benzyl acetate, and water..
Typically, the ionic liquid of formula I is selected from the group consisting of 1-benzyl,3-methyl imidazolium chloride; 1-benzyl, 3-methyl imidazolium bromide; 1-benzyl, 3-methyl imidazolium acetate; 1-benzyl, 3-methyl imidazolium methane sulfonate; 1-benzyl, 3-methyl imidazolium phosphate; Benzyl tributyl phosphonium bromide; Benzyl tributyl ammonium bromide: 1-phenyl, 3-methyl imidazolium chloride; 1-phenyl, 3-methyl imidazolium bromide; 1-phenyl, 3-methyl imidazolium acetate; 1-phenyl, 3-methyl imidazolium methane sulfonate; 1-phenyl, 3-methyl imidazolium phosphate; Phenyl tributyl phosphonium bromide; Phenyl tributyl ammonium bromide; 1.3 di benzyl imidazolium chloride; 1,3 di benzyl imidazolium bromide; 1,3 di benzyl imidazolium acetate; 1,3 di benzyl imidazolium methane sulfonate; 1.3 di benzyl imidazolium phosphate; and combinations thereof.
In one embodiment, Ar is phenyl, Z is (CH2)n, wherein n is 1, Q+ is imidazolium group, R is methyl, and A" is bromide.
In another embodiment the composition further comprises at least one bromine source selected from the group consisting of HBr, NaBr, KBr, NH4Br, benzylbromide, monobromoacetic acid, di-bromo acetic acid, bromoacetyl bromide, tetrabromomethane and ethylene di-bromide.
In another embodiment the composition further comprises at least one mono alkyl ionic liquid comprising an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium, pyridinium, pyrrolidinium. morpholinium, quinolinium, isoquinolium. pyrazolium and piperidinium; and an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonates.

phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides.
Typically, the aryl carboxylic acid is at least one compound selected from the group consisting of terephthalic acid, isophthalic acid, p-toluic acid, m-toluic acid, 4-formyl benzoic acid, 3-formyl benzoic acid, .Naphthoic acid, Trimesic acid, benzoic acid, and substituted benzoic acid.
Typically, the oxidizable multi-alkylated arylene compound is at least one selected from the group consisting of para-xylene, meta-xylene, methylnaphthalene, mesitylene, toluene, substituted toluene and combinations thereof.
Typically, the partially oxidized derivative is at least one selected from the group consisting of 4-carboxy benzaldehyde, 3-carboxy benzaldehyde, p-tolualdehyde, m-tolualdehyde, naphthalenecarboxaldehyde, l,5-dicarboxilic,3-formyl-benzene, benzaldehyde, substituted benzaldehyde and combinations thereof.
In one embodiment the oxidizable multi-alkylated arylene compound is para-xylene. the non-oxidizable polar solvent is acetic acid, the partially oxidized derivative is 4-carboxy benzaldehyde and the aryl carboxylic acid is terephthalic acid.
In accordance with another aspect of the present disclosure there is provided a process for obtaining aryl carboxylic acid; said process comprising the following steps: a. preparing a composition comprising:
- at least one ionic liquid of formula I, in an amount of 0.05 to 50 % of the total mass of the composition;


wherein,
Ar is substituted or un-substituted aryl group,
Z is (CH2)n, wherein n is an integer from 0 to 10,
Q+ is an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium. pyridinium, pyrrolidinium, morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium;
R is C1 to C20 linear or branched alkyl group or Ar-Z.
A" is an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonatses, phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides;
- at least one catalyst, in an amount of 0.01 to 5 % of the total mass of the
composition;
- at least one non-oxidizable polar solvent; and
- at least one oxidizable multi-alkylated arylene compound with no two successive ring positions bearing alkyl group.
and
b. subjecting said composition to oxidation in the presence an oxidizing agent selected from the group consisting of air and oxygen at a temperature of 100 to 250 °C and at a pressure of 10 to 60 bar to obtain aryl carboxylic acid,
said process characterized by the formation of partially oxidized derivatives of said multi-alkylated arylene compound in a quantity less than 4000 ppm, said derivatives comprising at least one carboxylic acid moiety and at least one aldehyde moiety.

Typically, the proportion of the ionic liquid to the non-oxidizable polar solvent ranges between 1:1 and 1:20,
Typically, the the non-oxidizable polar solvent is at least one solvent selected from the group consisting of acetic acid, methyl acetate, ethyl acetate, propyl acetate, benzyl acetate, and water.
Typically, the ionic liquid of formula I is selected from the group consisting of 1-benzyl,3-methyl imidazolium chloride; 1-benzyl, 3-methyl imidazolium bromide; 1-benzyl. 3-methyl imidazolium acetate; 1-benzyl, 3-methyl imidazolium methane sulfonate: 1-benzyl, 3-methyl imidazolium phosphate; Benzyl tributyl phosphonium bromide; Benzyl tributyl ammonium bromide; 1-phenyl, 3-methyl imidazolium chloride; 1-phenyl, 3-methyl imidazolium bromide; 1-phenyl, 3-methyl imidazolium acetate; 1-phenyl, 3-methyl imidazolium methane sulfonate; 1-phenyl, 3-methyl imidazolium phosphate; Phenyl tributyl phosphonium bromide; Phenyl tributyl ammonium bromide; 1,3 di benzyl imidazolium chloride; 1,3 di benzyl imidazolium bromide; 1,3 di benzyl imidazolium acetate; 1,3 di benzyl imidazolium methane sulfonate; 1,3 di benzyl imidazolium phosphate; and combinations thereof.
In one embodiment, Ar is phenyl, Z is (CH2)n, wherein n is 1, Q+ is imidazolium group. R is methyl, and A' is bromide.
In one embodiment the process further comprises incorporation of at least one bromine source selected from the group consisting of HBr, NaBr, KBr, NH4Br, benzylbromide, monobromoacetic acid, di-bromo acetic acid, bromoacetyl bromide, tetrabromomethane and ethylene di-bromide in said composition. In another embodiment the process further comprises incorporation of at least one mono alkyl ionic liquid comprising an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium, pyridinium, pyrrolidinium, morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium; and an anion selected from the group

consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alky! sulfonates, phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides in said composition.
Typically, the aryl carboxylic acid is at least one compound selected from the group consisting of terephthalic acid, isophthalic acid, p-toluic acid, m-toluic acid, 4-formyl benzoic acid, 3-formyl benzoic acid, .Naphthoic acid, Trimesic acid, benzoic acid and substituted benzoic acid.
Typically, the oxidizable multi-alkylated arylene compound is at least one selected from the group consisting of para-xylene, meta-xylene, methylnaphthalene, mesitylene, toluene, substituted toluene and combinations thereof.
Typically, the partially oxidized derivative is at least one selected from the group consisting of 4-carboxy benzaldehyde, 3-carboxy benzaldehyde, p-toiualdehyde, m-tolualdehyde, naphthalenecarboxaldehyde, 1.5-dicarboxilic,3-formyl-benzene, benzaldehyde and substituted benzaldehyde.
In one embodiment the oxidizable multi-alkylated arylene compound is para-xylene, the non-oxidizable polar solvent is acetic acid, the partially oxidized derivative is 4-carboxy benzaldehyde and the aryl carboxylic acid is terephthalic acid.
Typically, the catalyst comprises at least one metal compound, the metal being selected from the group consisting of cobalt, magnesium, chromium, copper, nickel, vanadium, iron, molybdenum, tin, cerium, zirconium, cesium and titanium. In one embodiment the catalyst is at least one selected from the group consisting of cobalt acetate, manganese acetate, cerium acetate, potassium acetate, cesium acetate, zirconium acetate, copper acetate, cobalt oxalate, manganese oxalate,cerium oxalate, potassium oxalate, cesium oxalate, zirconium oxalate and copper oxalate.

Typically, the process is characterized by reduction in the thermo-oxidative loss of the ionic compound. Typically, the oxidation is carried out in a continuous manner for a time period of at least 6 hours without the need of replenishment of the ionic compound.
In another embodiment the process further comprises a step of separating and recycling the ionic compound, the carboxylic acid solvent and the catalyst.
DETAILED DESCRIPTION
The inventors of the present disclosure focused on developing a composition containing ionic liquid/s which can be used in the manufacturing of aryl carboxylic acids such as terephthalic acid. After conducting several experiments and trials, the inventors particularly found that aryl alkyl ionic liquids can be used as a promoter in the manufacturing of aryl carboxylic acids such as terephthalic acid. Further, it was found that when aryl alkyl ionic liquids are used not only as a promoter but also as a co-solvent, there is enhancement in the reaction rate. Still further, it was found that when aryl alkyl ionic liquid is used, as a promoter and co-solvent, during the manufacturing of aryl carboxylic acids such as terephthalic acid there is significant reduction in formation of undesired impurities such as 4-carboxy-benzaldehyde (4-CBA). The reason being the ionic liquid of the present disclosure is capable of solubilizing not only the terephthalic acid and 4-CBA but also various other intermediates and side products. It is advantageous to keep these intermediates in dissolved form in the ionic compounds, as they can be further oxidized into the desired product during the manufacturing of terephthalic acid. Thus the concentration of intermediates can be reduced during the oxidation stage itself, thereby eliminating hydrogenation stage as against the conventional manufacturing process. In accordance with the present disclosure there is provided a composition containing aryl alkyl ionic liquid for manufacturing of and carboxylic acid. The and carboxylic acid includes but is not limited to terephthalic acid, isophthalic acid, p-toluic acid, m-toluic acid, 4-formyl benzoic acid, 3-formyl benzoic acid, .Naphthoic acid, Trimesic acid, benzoic acid, substituted benzoic acid and combinations thereof.

The composition mainly consist of at least one ionic compound of Formula 1; at least one catalyst comprising at least one metal selected from the group consisting of cobalt, magnesium, chromium, copper, nickel, vanadium, iron, molybdenum, tin, cerium, zirconium, cesium and titanium; at least one non-oxidizable polar solvent; and at least one oxidizable multi-alkylated arylene compound with no two successive ring positions bearing alkyl group. Typically, the non-oxidizable polar solvent includes but is not limited to acetic acid, methyl acetate, ethyl acetate, propyl acetate, benzyl acetate, water, combinations thereof and the like. The oxidizable multi-alkylated arylene compound includes but is not limited to para-xylene. meta-xylene, methylnaphthalene, mesitylene, toluene, substituted toluene and combinations thereof.
The Ionic liquid employed in the composition of the present disclosure is represented by the following Formula:

wherein,
. Ar is substituted or un-substituted aryl group,
Z is (CH2)n, wherein n is an integer from 0 to 10,
Q+ is an organic cation selected from the group consisting of
quaternary ammonium, cholinium, sulfonium, phosphonium,
guanidinium, imidazolium, pyridinium, pyrrolidinium,
morpholinium, quinolinium, isoquinolium, pyrazolium and
piperidinium,
R is C1 to C20 linear or branched alkyl group or Ar-Z,
A" is an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl

sulfonates, phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides;
In accordance with the present disclosure the composition contains a specific proportion of the ionic compound, the catalyst and the non-oxidizable polar solvent. The amount of the ionic compound is maintained between 0.05 and 50 % of the total mass of the composition, whereas, the amount of the catalyst is maintained between 0.01 and 5 % of the total mass of the composition. In accordance with the present disclosure the proportion of the ionic liquid to the non-oxidizable polar solvent is maintained between 1:1 and 1:20.
In accordance with the present disclosure the compound of formula I is selected from the group consisting of l-benzyl,3-methyl imidazolium chloride; 1-benzyl, 3-methyl imidazolium bromide: 1-benzyl, 3-methyl imidazolium acetate; 1-benzyl, 3-methyl imidazolium methane sulfonate; 1-benzyl, 3-methyl imidazolium phosphate; Benzyl tributyl phosphonium bromide; Benzyl tributyl ammonium bromide; 1-phenyl, 3-methyl imidazolium chloride: 1-phenyl, 3-methyl imidazolium bromide: 1-phenyl, 3-methyl imidazolium acetate; 1-phenyl, 3-methyl imidazolium methane sulfonate; 1-phenyl, 3-methyl imidazolium phosphate: Phenyl tributyl phosphonium bromide; Phenyl tributyl ammonium bromide; 1,3 di benzyl imidazolium chloride; 1,3 di benzyl imidazolium bromide; 1,3 di benzyl imidazolium acetate; 1,3 di benzyl imidazolium methane sulfonate; 1,3 di benzyl imidazolium phosphate; and combinations thereof.
In one embodiment the catalyst includes but is not limited to cobalt acetate, manganese acetate, cerium acetate, potassium acetate, cesium acetate, zirconium acetate, copper acetate, cobalt oxalate, manganese oxa!ate,cerium oxalate, potassium oxalate, cesium oxalate, zirconium oxalateand copper oxalate.
In one embodiment, Ar is phenyl. Z is (CH2)n, wherein n is 1. Q is imidazolium group, R is methyl, A" is bromide and the compound of formula I is 1-benzyl, 3-methyl imidazolium bromide.

The composition of the present disclosure also includes at least one bromine source, as a promoter, which includes but is not limited to HBr, NaBr, KBr, NH4Br. benzylbromide, monobromoacetic acid, di-bromo acetic acid, bromoacetyl bromide, tetrabromomethane and ethylene di-bromide.
In another embodiment there is provided a composition which contains at least one mono alkyl ionic liquid along with at least one aryl alkyl ionic liquid. Typically, the mono
alkyl ionic liquid comprises an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium, pyridinium, pyrrolidinium, morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium; and an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonates, phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides.
It is also found that the composition containing a combination of aryl alkyl ionic liquid and alkyl ionic liquid can also provide pure aryl carboxylic acid such as terephthalic acid by reducing the formation of undesired impurities such as 4-carboxy-benzaldehyde(4-CBA).
The composition of the present disclosure reduces the formation of partially oxidized derivatives of said multi-alkylated arylene compound in a quantity less than 4000 ppm during the preparation of aryl carboxylic acid. The partially oxidized derivatives of said multi-alkylated arylene compound comprise at least one carboxylic acid moiety and at least one aldehyde moiety.
Typically, the partially oxidized derivative includes but is not limited to 4-carboxy benzaldehyde, 3-carboxy benzaldehyde, p-tolualdehyde. m-tolualdehyde, naphthalenecarboxaldehyde, l,5-dicarboxilic,3-formyl-benzene, benzaldehyde, substituted benzaldehyde and combination thereof.

In one embodiment the oxidizable multi-alkylated arylene compound is para-xylene, the non-oxidizable polar solvent is acetic acid, the partially oxidized derivative is 4-carboxy benzaldehyde and the aryl carboxylic acid is terephthalic acid.
The present disclosure also provides a process for obtaining aryl carboxylic acid. The aryl carboxylic acid includes but is not limited to terephthalic acid, isophthalic acid, p-toluic acid, m-toluic acid, 4-formyl benzoic acid, 3-formyl benzoic acid, .Naphthoic acid, Trimesic acid, benzoic acid, substituted benzoic acid and combinations thereof.
The process mainly involves two steps. In the first step a composition comprising at least one ionic liquid of formula I, in an amount of 0.05 to 50 % of the total mass of the composition;

wherein,
Ar is substituted or un-substituted aryl group,
Z is (CH2)n, wherein n is an integer from 0 to 10,
Q is an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium. guanidinium, imidazolium, pyridinium, pyrrolidinium, morpholinium, quinolinium. isoquinolium, pyrazolium and piperidinium;
R is C1 to C20 linear or branched alkyl group or Ar-Z,
A" is an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonatses. phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides;

at least one catalyst, in an amount of 0.01 to 5 % of the total mass of the composition; at least one non-oxidizable polar solvent; and at least one oxidizable multi-alkylated arylene compound with no two successive ring positions bearing alkyl group is prepared.
The non-oxidizable polar solvent employed in the process includes but is not limited to acetic acid, ethyl acetate, propyl acetate, benzyl acetate, benzyl acetate, water and the like. In the process of the present disclosure, the proportion of the ionic liquid to the non-oxidizable polar solvent is maintained between 1:1 and 1:20.
The oxidizable multi-alkylated arylene compound includes but is not limited to para-xylene, meta-xylene, methylnaphthalene, mesitylene, toluene, substituted toluene and combinations thereof.
In the second step, the obtained composition is subjected to oxidation in the presence an oxidizing agent selected from the group consisting of air and oxygen at a temperature of 100 to 250 °C and at a pressure of 10 to 60 bar to obtain aryl carboxylic acid. The process is characterized by the following features:
- the formation of partially oxidized derivatives of said multi-alkylated arylene compound during the preparation of aryl carboxylic acid is less than 4000 ppm.
- reduction in the thermo-oxidative loss of the ionic compound.
- the oxidation is carried out in a continuous manner for a time period of at least 6 hours without the need of replenishment of the ionic compound.
Jn accordance with the present disclosure the partially oxidized derivative includes but is not limited to 4-carboxy benzaldehyde, 3-carboxy benzaldehyde, p-tolualdehyde. m-tolualdehyde, naphthalenecarboxaldehyde, 1,5-dicarboxiIic,3-formyI-benzene, benzaldehyde, substituted benzaldehyde and combinations thereof.
In accordance with the present disclosure the ionic liquid of formula I includes but is not limited to 1-benzyl,3-methyl imidazolium chloride; 1-benzyl, 3-methyl imidazolium bromide; 1-benzyl, 3-methyl imidazolium acetate; 1-benzyl, 3-methyl imidazolium methane sulfonate; 1-benzyl, 3-methyl imidazolium phosphate; Benzyl

tributyl phosphonium bromide; Benzyl tributyl ammonium bromide; 1-phenyl, 3-methyl imidazolium chloride; 1-phenyl, 3-methyl imidazolium bromide; 1-phenyl, 3-methyl imidazolium acetate; 1-phenyl, 3-methyl imidazolium methane sulfonate; 1-phenyl, 3-methyl imidazolium phosphate; Phenyl tributyl phosphonium bromide: Phenyl tributyl ammonium bromide: 1.3 di benzyl imidazolium chloride: 1.3 di benzyl imidazolium bromide: 1.3 di benzyl imidazolium acetate; 1,3 di benzyl imidazolium methane sulfonate; 1,3 di benzyl imidazolium phosphate: and combinations thereof. In one embodiment, Ar is phenyl, Z is (CH2)n, wherein n is 1. Q+ is imidazolium group, R is methyl, and A" is bromide.
The process of the present disclosure also involves incorporation of at least one bromine source selected from the group consisting of HBr, NaBr, KBr, NH4Br, benzylbromide, monobromoacetic acid, di-bromo acetic acid, bromoacetyl bromide, tetrabromomethane and ethylene di-bromide in said composition.
In another embodiment the process further comprises incorporation of at least one mono alkyl ionic liquid comprising an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium, pyridinium, pyrrolidinium, morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium; and an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alky] sulfonates, phosphates, phosphonates, aky] phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides in said composition.
The process of the present disclosure also involves a step of separating and recycling the ionic compound, the carboxylic acid solvent and the catalyst. In one embodiment there is provided a process for the preparation of purified terephthalic acid. In the first step, a composition comprising at least one ionic liquid of Formula I; at least one catalyst: acetic acid: and para-xylene is prepared. In the second step, the obtained composition is subjected to oxidation in the presence of an oxidizing agent at a temperature of 100 to 250 °C and at a pressure of 10 to 60 bar to

obtain purified terephthalic acid. It is found that the formation of 4-carboxy benzaldehyde (4-CBA) during the preparation of aryl carboxylic acid is less than 4000 ppm.
The following examples illustrate the disclosure. The examples used herein are intended merely to facilitate an understanding of ways in which the embodiments herein may be practiced and to further enable those of skill in the art to practice the embodiments herein. Accordingly, the examples should not be construed as limiting the scope of the embodiments herein.
Examples:
Example 1: Thermal stability testing alky! ionic liquid
Thermal stability of 1-butyl, 3-methyl imidazolium chloride in the presence of air was studied at different temperatures at 20 bar pressure in a high pressure slurry reactor made of titanium. It was found that at 140 °C, there was a drastic uptake of oxygen. The sample was taken out and tested. It was found that found that it is decomposed.
Example 2: Thermal stability testing aryl alkyl ionic liquid
Example 1 was repeated using I-benzyl, 3-methyl imidazolium chloride in place of 1-butyl, 3-methyl imidazolium chloride. Decomposition onset temperature was found to be 180°C for this ionic salt.
Example 3: Preparation of terephthalic acid
Oxidation of p-xylene was carried out using acetic acid as a solvent by using cobalt acetate and manganese acetate as catalyst in the presence of 1-butyl, 3-methyl imidazolium bromide (550 ppm) as a promoter at 180 °C temperature and 20 bar pressure for 3 hours reaction time. The 4-CBA content in terephthalic acid was 15000 ppm.
Example 4: Preparation of terephthalic acid
Oxidation of p-xylene was carried out using acetic acid as a solvent by using cobalt acetate and manganese acetate as catalyst in the presence of 1-benzyl, 3-methyl

imidazolium bromide (4 %) as a promoter and as well as a co-solvent at 215°C temperature and 40 bar pressure for 3 hours reaction time. The 4-CBA content in terephthalic acid was 3100 ppm.
Example 5: Preparation of terephthalic acid
Oxidation of p-xylene was carried out using acetic acid as a solvent by using cobalt acetate and manganese acetate as catalyst in the presence of 1-benzyl, 3-methyl imidazolium bromide (4 %) as a promoter and as well as a co-solvent and 20% of 1-butyl, 3-methyl imidazolium acetate at 215 °C temperature and 40 bar pressure for 3 hours reaction time. The 4-CBA content in terephthalic acid was 4800 ppm.
Example 6: Preparation of benzoic acid from Toluene
Oxidation of Toluene was carried out using acetic acid as a solvent by using cobalt acetate and manganese acetate as catalyst in the presence of 1-benzyl, 3-methyl imidazolium bromide (4 %) as a promoter and as well as a co-solvent at 150 °C temperature and 40 bar pressure for 3 hours reaction time. Benzatdehyde was formed as a partially oxidized derivative.
Example 7: Preparation of Isophthalic acid from m-Xylene
Oxidation of m-xylene was carried out using acetic acid as a solvent by using cobalt acetate and manganese acetate as catalyst in the presence of 1-benzyl, 3-methyl imidazolium bromide (4 %) as a promoter and as well as a co-solvent at 215 °C temperature and 40 bar pressure for 3 hours reaction time. 3-Toluic acid and 3-carboxybenzaldehyde (3-CBA) were formed as partially oxidized derivatives.
Throughout this specification the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated element, integer or step, or group of elements, integers or steps, but not the exclusion of any other element, integer or step, or group of elements, integers or steps.

The use of the expression "a", "at least" or "at least one'' suggests the use of one or more elements or ingredients or quantities, as the use may be in the embodiment of the disclosure to achieve one or more of the desired objects or results.
The numerical values given for various physical parameters, dimensions and quantities are only approximate values and it is envisaged that the values higher or lower than the numerical value assigned to the physical parameters, dimensions and quantities fall within the scope of the disclosure and the claims unless there is a statement in the specification to the contrary.
While certain embodiments of the disclosure have been described, these embodiments have been presented by way of examples only, and are not intended to limit the scope of the disclosure. Variations or modifications in the composition of this disclosure, within the scope of the disclosure, may occur to those skilled in the art upon reviewing the disclosure herein. Such variations or modifications are well within the spirit of this disclosure.

We Claim:
]. A composition for preparing ary] carboxylic acid; said composition comprising:
i. at least one ionic liquid of formula I, in an amount of 0.05 to 50 % of the total mass of the composition;

wherein,
Ar is substituted or un-substituted aryl group,
Z is (CH2)n - wherein n is an integer from 0 to 10.
Q+ is an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium, pyridinium, pyrrolidinium, morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium;
R is C1 to C20 linear or branched alkyl group or Ar-Z,
A' is an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonates, phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides, and oxides:
ii. at least one catalyst, in an amount of 0.01 to 5 % of the total mass of the composition,;
iii. at least one non-oxidizable polar solvent; and
iv. at least one oxidizable multi-alkylated arylene compound with no two successive ring positions bearing alkyl group,

said composition adapted to reduce the formation of partially oxidized derivative of said multi-alkylated arylene compound in a quantity less than 4000 ppm during the preparation of aryl carboxylic acid, said derivatives comprising at least one carboxylic acid moiety and at least one aldehyde moiety.
2. The composition as claimed in claim 1, wherein the proportion of the ionic liquid to the non-oxidizable polar solvent ranges between 1:1 and 1:20.
3. The composition as claimed in claim 1, wherein the catalyst comprises at least one metal compound, the metal being selected from the group consisting of cobalt, magnesium, chromium, copper, nickel, vanadium, iron, molybdenum, tin, cerium, zirconium, cesium and titanium.
4. The composition as claimed in claim 1, wherein the catalyst is at least one selected from the group consisting of cobalt acetate, manganese acetate, cerium acetate, potassium acetate, cesium acetate, zirconium acetate, copper acetate, cobalt oxalate, manganese oxalate, cerium oxalate, potassium oxalate, cesium oxalate, zirconium oxalate and copper oxalate.
5. The composition as claimed in claim 1, wherein the non-oxidizable polar solvent is at least one solvent selected from the group consisting of acetic acid, methyl acetate, ethyl acetate, propyl acetate, benzyl acetate and water.
6. The composition as claimed in claim 1, wherein the ionic liquid of formula I is selected from the group consisting of 1-benzyl,3-methyl imidazolium chloride; 1-benzyl, 3-methy] imidazolium bromide: 1-benzyl, 3-methyl imidazolium acetate; 1-benzyl, 3-methyl imidazolium methane sulfonate; 1-benzyl, 3-methyl

imidazolium phosphate; Benzyl tributyl phosphonium bromide; Benzyl tributyl ammonium bromide; 1-phenyl, 3-methyl imidazolium chloride; 1-phenyl, 3-methyl imidazolium bromide; 1-phenyl, 3-methyl imidazolium acetate; 1-phenyl, 3-methyl imidazolium methane sulfonate; 1-phenyl, 3-methyl imidazolium phosphate; Phenyl tributyl phosphonium bromide: Pheny] tributyl ammonium bromide; 1,3 di benzyl imidazolium chloride; 1,3 di benzyl imidazolium bromide; 1,3 di benzyl imidazolium acetate; 1,3 di benzyl imidazolium methane sulfonate; 1,3 di benzyl imidazolium phosphate; and combinations thereof.
7. The composition as claimed in claim 1, wherein Ar is phenyl, Z is (CH2)n, wherein n is 1, Q+ is imidazolium group, R is methyl, and A" is bromide.
8. The composition as claimed in claim 1, further comprises at least one bromine source selected from the group consisting of HBr, NaBr, KBr, NH4Br, benzylbromide. monobromoacetic acid, di-bromo acetic acid, bromoacetyl bromide, tetrabromomethane and ethylene di-bromide.
9. The composition as claimed in claim 1, further comprises at least one mono alkyl ionic liquid comprising an organic cation selected from the group consisting of quaternary ammonium, cholinium, sulfonium, phosphonium, guanidinium, imidazolium, pyridinium, pyrrolidinium, morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium; and an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonates, phosphates, phosphonates, akyl phosphates, nitrates, nitrites-carbonates, acetates, bicarbonates, hydroxides and oxides.
10. The composition as claimed in claim 1, wherein the aryl carboxylic acid is at least one compound selected from the group consisting of terephthalic acid, isophthalic acid, p-toluic acid, m-toluic acid, 4-formyl benzoic acid, 3-formyl benzoic acid, ,Naphthoic acid. Trimesic acid, benzoic acid and substituted benzoic acid.

11. The composition as ciaimed in claim 1, wherein the oxidizable multi-alkylated
arylene compound is at least one selected from the group consisting of para-xylene, meta-xylene, methylnaphthalene, mesitylene, toluene and substituted toluene.
12. The composition as claimed in claim 1, wherein the partially oxidized derivative
is at least one selected from the group consisting of 4-carboxy benzaldehyde, 3-
carboxy benzaldehyde, p-tolualdehyde. m-tolualdehyde,
naphthalenecarboxaldehyde, 1.5-dicarboxilic,3-formyl-benzene, benzaldehyde and
substituted benzaldehyde.
13.The composition as claimed in claim 1, wherein the oxidizable multi-alkylated arylene compound is para-xylene, the non-oxidizable polar solvent is acetic acid, the partially oxidized derivative is 4-carboxy benzaldehyde and the aryl carboxylic acid is terephthalic acid.
14. A process for obtaining aryl carboxylic acid; said process comprising the following steps:
- preparing a composition comprising:

wherein,
Ar is substituted or un-substituted aryl group.
Z is (CH2)n, wherein n is an integer from 0 to 10,
i. at least one ionic liquid of formula I, in an amount of 0.05 to 50 % of the total mass of the composition;

Q+ is an organic cation selected from the group consisting of
quaternary ammonium, cholinium, sulfonium, phosphonium,
guanidinium, imidazolium, pyridinium, pyrrol rdini urn,
morpholinium, quinolinium, isoquinolium, pyrazolium and
piperidinium;
R is C1 to C20 linear or branched alkyl group or Ar-Z,
A* is an anion selected from the group consisting of chlorides,
bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl
sulfonatses, phosphates, phosphonates, akyl phosphates, nitrates,
nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides;
ii. at least one catalyst, in an amount of 0.01 to 5 % of the total mass of the composition;
iii. at least one non-oxidizable polar solvent; and
iv. at least one oxidizable multi-alkylated arylene compound with no two successive ring positions bearing alkyl group,
and
- subjecting said composition to oxidation in the presence an oxidizing agent selected from the group consisting of air and oxygen at a temperature of 100 to 250 °C and at a pressure of 10 to 60 bar to obtain aryl carboxylic acid.
said process characterized by the formation of partially oxidized derivatives of said multi-alkylated arylene compound in a quantity less than 4000 ppm, said derivatives comprising at least one carboxylic acid moiety and at least one aldehyde moiety.

15. The process as claimed in claim 14. wherein the proportion of the ionic liquid to the non-oxidizable polar solvent ranges between 1:1 and 1:20.
16. The process as claimed in claim 14, wherein the non-oxidizable polar solvent is at least one solvent selected from the group consisting of acetic acid, methyl acetate, ethyl acetate, propyl acetate, benzyl acetate and water.
17. The process as claimed in claim 14, wherein the ionic liquid of formula I is selected from the group consisting of 1 -benzyl,3-methyl imidazolium chloride; 1-benzyl, 3-methyl imidazolium bromide; 1-benzyl, 3-methyl imidazolium acetate; 1-benzyl, 3-methyl imidazolium methane sulfonate; 1-benzyl. 3-methyl imidazolium phosphate: Benzyl tributyl phosphonium bromide; Benzyl tributyl ammonium bromide; 1-phenyl, 3-methyl imidazolium chloride; 1-phenyl, 3-methyl imidazolium bromide; 1-phenyl, 3-methyl imidazolium acetate; 1-phenyl, 3-methyl imidazolium methane sulfonate; 1-phenyl, 3-methyl imidazolium phosphate; Phenyl tributyl phosphonium bromide; Phenyl tributyl ammonium bromide; 1,3 di benzyl imidazolium chloride; 1,3 di benzyl imidazolium bromide; 1,3 di benzyl imidazolium acetate; 1,3 di benzyl imidazolium methane sulfonate; 1,3 di benzyl imidazolium phosphate; and combinations thereof.
18. The process as claimed in claim 14, wherein Ar is phenyl, Z is (CH2)n, wherein n is 1, Q+ is imidazolium group, R is methyl, and A" is bromide.
19. The process as claimed in claim 14, further comprises incorporation of at least one bromine source selected from the group consisting of HBr, NaBr, KBr, NH4Br, benzyl bromide, monobromoacetic acid, di-bromo acetic acid, bromoacetyl bromide, tetrabromomethane and ethylene di-bromide in said composition.
20. The process as claimed in claim 14, further comprises incorporation of at least one mono alkyl ionic liquid comprising an organic cation selected from the group

consisting of quaternary ammonium, cholinium, sulfonium, phosphonium. guanidinium, imidazolium, pyridinium, pyrrolidinium. morpholinium, quinolinium, isoquinolium, pyrazolium and piperidinium; and an anion selected from the group consisting of chlorides, bromides, fluorides, iodides, mesylates, tosylates, sulfates, alkyl sulfonates, phosphates, phosphonates, akyl phosphates, nitrates, nitrites, carbonates, acetates, bicarbonates, hydroxides and oxides in said composition.
21. The process as claimed in claim 14, wherein the aryl carboxylic acid is at least one compound selected from the group consisting of terephthalic acid, isophfhalic acid, p-toluic acid, m-toluic acid, 4-formyl benzoic acid, 3-formyl benzoic acid, ^Naphthoic acid, Trimesic acid, benzoic acid and substituted benzoic acid.
22. The process as claimed in claim 14, wherein the oxidizable multi-alkylated arylene compound is at least one selected from the group consisting of para-xylene, meta-xylene, methylnaphthalene, mesitylene, toluene and substituted toluene.
23. The process as claimed in claim 14, wherein the partially oxidized derivative is at least one selected from the group consisting of 4-carboxy benzaldehyde, 3-carboxy benzaldehyde, p-tolualdehyde. m-tolualdehyde, naphthalenecarboxaldehyde, 1,5-dicarboxilic,3-formyl-benzene, benzaldehyde and substituted benzaldehyde .
24. The process as claimed in claim 14, wherein the oxidizable multi-alkylated arylene compound is para-xylene, the non-oxidizable polar solvent is acetic acid, the partially oxidized derivative is 4-carboxy benzaldehyde and the aryl carboxylic acid is terephthalic acid.
25.The process as claimed in claim 14, wherein the catalyst comprises at least one metal compound, the metal being selected from the group consisting of cobalt,

magnesium, chromium, copper, nickel, vanadium, iron, molybdenum, tin, cerium, zirconium, cesium and titanium.
26, The process as claimed in claim 14, wherein the catalyst is at least one selected
from the group consisting of cobalt acetate, manganese acetate, cerium acetate,
potassium acetate, cesium acetate, zirconium acetate, copper acetate, cobalt
oxalate, manganese oxalate,cerium oxalate, potassium oxalate, cesium oxalate,
zirconium oxalate and copper oxalate.
27. The process as claimed in claim 14, wherein said process characterized by
reduction in the thermo-oxidative loss of the ionic compound.
28, The process as claimed in claim 14, wherein said process characterized in that the
oxidation is carried out in a continuous manner for a time period of at least 6 hours
without the need of replenishment of the ionic compound.
29. The process as claimed in claim 14, further comprises a step of separating and
recycling the ionic compound, the carboxylic acid solvent and the catalyst.