EP2019730A1

EP2019730A1 - Oxidation catalyst for the purification of nitrogen gas containing organic impurities

Info

Publication number: EP2019730A1
Application number: EP06842729A
Authority: EP
Inventors: Sreenivasa Rao Gajula; Rajeshwar Dongara; Raghvendra Char Pavagada; Ramaswamy Krishnamurthy Konda; Bhimarao Anand Halgeri; Mohan Singaram; Sudhir Singh
Original assignee: Indian Petrochemicals Corp Ltd
Current assignee: Reliance Industries Ltd
Priority date: 2006-05-02
Filing date: 2006-08-29
Publication date: 2009-02-04
Also published as: EP2019730A4; WO2007125539A1

Abstract

An oxidation catalyst for the purification of nitrogen gas containing organic impurities. The catalyst comprises sulphated alumina with a sulphate loading of 1-20 percent weight alumina. The sulphated alumina is impregnated with an aqueous solution of a noble metal complex formed with a complexing agent. The noble metal content of the catalyst is 0.1 to 1 percent weight alumina and the surface penetration of the noble metal on the alumina is 100-150 microns. Also a method of preparing the oxidation catalyst by sulphating alumina with a sulphating agent to a sulphate loading of 1- 20 percent weight alumina; drying the alumina at 110-160ºC; calcining the alumina at 520-560ºC; complexing a noble metal in 0.1 to 1 percent weight alumina with a complexing agent; impregnating the sulphated alumina with an aqueous solution of the noble metal complex; drying the catalyst material at 110-160ºC; calcining the catalyst material at 520-560°C; reducing the catalyst material with hydrogen at 470-500ºC; and passivating the catalyst material by cooling it down to 25-50ºC in an inert atmosphere.

Description

TITLE OF THE INVENTION Oxidation catalyst for the purification of nitrogen gas containing organic impurities

FIELD OF THE INVENTION

This invention relates to an oxidation catalyst for the purification of nitrogen gas containing organic impurities, particularly nitrogen gas containing impurities formed of organic compounds from a polymerization reactor like solid-state polycondensation reactor used for the production of aromatic polyester resins.

This invention also relates to a method for the preparation of an oxidation catalyst for the purification of nitrogen gas containing organic impurities, particularly nitrogen gas containing impurities formed of organic compounds from a polymerization reactor like solid-state polycondensation reactor used for the production of aromatic polyester resins.

BACK GROUND OF THE INVENTION

During polymerization of polymers like aromatic polyester resins such as polyethylene terephthalate (PET) resin in polymerization reactors like solid state polycondensation (SSP) reactor, an inert gas such as nitrogen is run through the reactor to strip the developing polymer of the organic impurities which are generally formed of aldehydes and glycols (acetaldehyde and ethylene glycol in the case of polyethylene terephthalate) and glycol oligomers. The impurities being stripped from the polymers accumulate in the nitrogen gas stream. Generally the impurities are present in the nitrogen gas from a SSP reactor, in quantities, defined as methane equivalent of, up to about 2000-3000 ppm (parts per million) by weight or more. The inert gas from a SSP reactor is purified by oxidation of the organic impurities to CO₂ in an oxidation reactor using oxygen or gas containing oxygen (generally air) in excess of the stoichiometric quantity with regard to the organic impurities. The oxidation reaction is carried out at a temperature between 500 and 600⁰C by circulating the inert gas stream over a catalyst bed formed of a support coated with platinum or platinum and palladium. The oxidation is controlled so that the gaseous stream at the outlet of the oxidation reactor contains oxygen not in excess of 50-500 ppm. Due to the veiy high requirement of nitrogen in the polymerization and crystallization units of the SSP reactor, the gas hourly space velocity (GHSV₅ h^'') ^'όf nitrogen in the oxidation reactor is very high. Therefore, the catalyst should oxidize'ithe hydrocarbon impurities at very short contact times. The high oxygen content in the gaseous stream coming out of the oxidation reactor is reduced by subjecting the gaseous stream to a deoxidation treatment with hydrogen. The gaseous stream is then dried by circulating it on. a silica gel molecular sieve or other beds of drying materials so as to eliminate the water stripped from the polymer chips and generated in the oxidation and deoxidation stages before being recycled to the SSP reactor. 5

_; Guido et al in US 5547652 teaches a process for the purification of recycle inert gas stream containing organic impurities and leaving a SSP reactor. Oxygen or oxygen containing gas is added to the gas stream in a stoichiometric quantity with respect to the organic impurities or in such an excess amount that the gas at the outlet of the oxidation reactor contains upto 10 ppm

10 of oxygen. Oxidation is carried out at 250 to 600⁰C, preferably 250 to 350⁰C using a catalyst comprising Pt or mixtures of Pt and Pd supported on an inert porous support. The catalyst is preferably Pt and Pd supported on gamma alumina having a porosity of 0.4-0.6 cm³/g. The stoichiometry of the oxidation reaction is monitored by an oxygen analyzer like zirconia sensor connected to the outlet of the oxidation reactor. The gaseous stream leaving the oxidation

15 reactor is recycled to the SSP reactor after drying to remove water present.

Guido et al in US 5612011 further teaches a process for the purification of recycle inert ga's stream containing organic impurities and leaving a SSP reactor. Oxygen or oxygen containing gas is added to the gas stream containing impurities and the impurities are oxidized in an 0 oxidation reactor using a catalyst comprising Pt or mixtures of Pt and Pd supported on an inert porous support at 250 to 600⁰C, preferably 250 to' 35O⁰C. The quantity of oxygen used is in such an excess that the gas at the outlet of the oxidation reactor contains greater than 10 ppm but less than or equal to 250 ppm of oxygen. Preferably the catalyst comprises Pt and' Pd supported on gamma alumina having a porosity of 0.5 - 0.6cm³/g, preferably 0.4 - 0.6cm³/g^'.^λ ■ _; 5 "^' •

James et al in US 6749821 teaches a process for the purification of a recycle inert gas stream leaving a polymerization reactor from organic impurities. Oxygen or a gas containing oxygen is added to the gas stream and the organic impurities in the gas stream are oxidized in εln oxidization reactor using a catalyst impregnated with a metal including platinum. All of the ^0 metal impregnated on the catalyst is in a substantially reduced state, the reduction having carried out in a gas containing hydrogen. The oxidation is carried out at a temperature less than 300⁰C preferably 250⁰C using oxygen or gas containing oxygen substantially stoichiometric quantity with respect to the organic impurities such that the gas leaving the oxidation reactor contains no greater than 250 ppm oxygen. The gas leaving the oxidation reactor is dried and recycled to the polymerization reactor. The support for the catalyst comprises activated alumina; platinum is dispersed on the surface of the catalyst; and the catalyst includes 0.1 to 2.0 wt% platinum.

5 OBJECTS OF INVENTION

■^■ An object of the invention is to provide an oxidation catalyst which has improved activity, for the purification of nitrogen gas either generated or recycled containing organic impurities, particularly impurities formed of organic compounds from a polymerization reactor like solid state polycondensation (SSP) reactor used for the production of aromatic polyester resins.

ΪO v- Another object of the invention is to provide an oxidation catalyst which reduces the , heat requirement of the process for the purification of nitrogen gas either generated or^' recycled containing organic impurities, particularly impurities formed of organic compounds from a polymerization reactor like solid state polycondensation (SSP) reactor used for the 15 production of aromatic polyester resins.

Another object of the invention is to provide a method for the preparation of an oxidation catalyst for the purification of nitrogen gas either generated or recycled containing organic impurities, particularly impurities formed of organic compounds from a polymerization j 20 reactor like solid state polycondensation (SSP) reactor used for the production of aromatic p polyester resins, which catalyst has improved activity.

Another object of the invention is to provide a method for the preparation of an oxidation catalyst for the purification of nitrogen gas either generated or recycled containing organic 25 impurities, particularly impurities formed of organic compounds from a polymerization reactor like solid state polycondensation reactor used for the production of aromatic polyester resins, which catalyst reduces the heat requirement of the process for -the purification of nitrogen gas containing organic impurities.

30 DETAILED DESCRIPTION OF INVENTION

According to the invention there is provided an oxidation catalyst for the purification of nitrogen gas containing organic impurities, the catalyst comprising sulphated alumina with -a sulphate loading of 1 - 20 percent weight alumina, the sulphated alumina being

^'■* impregnated with an aqueous solution of a noble metal complex formed with a complexiηg 6 000324

^'ft * agent, the noble metal content of the catalyst being 0.1 to 1 percent weight alumina and ^"the surface penetration of the noble metal on the alumina being 100 - 150 microns.

According to the invention there is also provided a method of preparing an oxidation catalyst for the purification of nitrogen gas containing organic impurities, the method comprising the steps of :

i) sulphating alumina with a sulphating agent to a sulphate loading of 1 - 20 percent weight alumina;

ii) drying the alumina of step (i) at 110-160⁰C;

iii) calcining the alumina of step(ii) at 520-560⁰C;

iv) complexing a noble metal in 0.1 to 1 percent weight alumina with a complexing*- agent;

v) impregnating the sulphated alumina of step (iii) with an aqueous solution of thέ' noble metal complex obtained by step (iv);

vi) drying the catalyst material of step (v) at 110 - 160⁰C;

vii) calcining the catalyst material of step (vi) at 520 - 560⁰C;

viii) reducing the catalyst material of step (vii) with hydrogen at 470 - 500⁰C; and

ix) passivating the catalyst material of step (viii) by cooling it down to 25 - 50⁰C in. an inert atmosphere.

The sulphate loading of the alumina is preferably 1 to 10 percent weight alumina and still preferably 2.4 percent weight alumina. Preferably the alumina comprises gamma alumina spheres having average diameter of 3 - 4 mm, apparent bulk density of 0.3 to 1.0 g/cc, surface area of 100 to 500 m²/g, pore volume of 0.1 to 1 cc/g, pore diameter of 20 to 300A and crush strength of 6 to 8 kg. Preferably, the noble metal content of the catalyst is 0.5 006/000324

percent weight alumina. Preferably the surface penetration of the noble metal on the alumina is 100 microns. The noble metal is selected from platinum or platinum group and is preferably platinum. The platinum is obtained from platinum source selected from chloroplatinic acid, ammonium chloroplatinate, bromoplatinic acid, platinum chloridS, platinum tetrachloride hydrate, platinum dichlorocarboxyl dichloride or dinitrodiamirip. platinum and is preferably chloroplatinic acid. The complexing agent is selected from thiomalic acid or thio glycolic acid and is preferably thiomalic acid. The sulphating agent is selected from sulphuric acid or ammonium sulphate and is preferably sulphuric acid. Preferably the noble metal catalyst is complexed with the complexing agent in 0.3 percent weight alumina.

The catalyst of the invention can be advantageously used for purification of nitrogen gas either generated or recycled containing organic impurities particularly impurities formed of organic compounds from a polymerization reactor like solid state polycondensation (SSP) reactor used for the production of aromatic polyester resins. The sulphate species on the alumina provide pathway for the total oxidation of the hydrocarbon which involves the breaking of a C-C bond instead of H-abstraction. The surface sulfate promotes the dissociative adsorption of hydrocarbon on noble metal such as Pt, which results in higher activity^"11 fpr hydrocarbon oxidation. Hydrocarbon chemisorption on PtZAl₂Os is increased by surface sulfates on gamma-alumina. The highly oxidized Pt species are generated during oxidatϊoη reaction. The electronegative sulfate (SO₄ ^2") deposit which lies in close proximity to the edge of Pt atoms would withdraw electron density from the Pt atom, conferring on Pt species a higher positive charge. A new catalytic site consisting of adjacent cationic (oxidized Pt species) and anionic (SO₄ ^2') moieties would then develop and facilitate the initial C-H bond activation. An interfacial sulphate species plays a key role in the increased activity of the catalyst and activation of hydrocarbon molecule. Pt sites are required for the activation of oxygen and subsequent oxidation of alkyl species. The complexing agent helps to restrict the penetration of the active metal to the surface of alumina. The catalyst exhibits increased activity correspondingly increasing the polymerization. The catalyst decreases the hydrocarbon light off temperature thereby reducing the heat requirement of the oxidation", reaction. The invention is also economical for the above reasons.

The catalyst of the invention may be regenerated in situ by carbon removal using known methods (Indian Patent No 179243). The following experimental examples are presented as illustration of the invention and are not intended as undue limitations on the generally broad scope of the invention as set out in the claims.

EXAMPLE I

A 0.057 molar concentration solution of 45 ml of chloroplatinic acid and 0.3 wt % thiomaϊϊc acid in deionized water were mixed and stirred for 1 hour in a flask. The solution was aged^'ϊpr

48 hours and adjusted to a volume of 100 ml with deionized water. 100 gms of gamma; alumina spheres having average diameter of 3.5 mm, apparent bulk density of 0.42 g/cc, crush strength of 8.0 kg, surface area of 165 m2 Ig, pore volume of 0.1 cc/g and pore diameter of

100 A was added into the flask containing the aged chloroplatinic acid complex and mixed

^■ v^; thoroughly. The catalyst material was dried at 15O⁰C for 12 hours in an air flowing oven and taken in a quartz glass tube and calcined in a tubular electrical furnace in flowing air at 54O⁰C for 4 hour. The calcined material was reduced in a reduction reactor in hydrogen gas flow at 485⁰C for 4 hours. The reactor was cooled down to 5O⁰C and the flow Was switched from hydrogen to nitrogen for the passivation of the active material. The catalyst had a platinum content of 0.5 wt-%. The distribution of platinum on the alumina surface was about 100 microns deep as found out by EDXA (Energy Dispersive X-ray Analysis)

EXAMPLE 2

The procedure of Example 1 was followed using lOOg sulphated gamma alumina. The sulphation was carried out by soaking the alumina in 200 ml, IN sulphuric acid solution: After 4 hrs of soaking, the excess liquid was decanted and the solid was dried at 12O⁰C for 12 Hrs and calcined at 54O⁰C for 4 hrs to get sulphated alumina which was mixed with chloroplatinic acid complex and processed further as described in Example 1. The distribution of platinum on the alumina surface was about 100 microns deep as found out by EDXA.

EXAMPLE 3

Evaluation of the catalysts of Examples 1 and 2 vis-a-vis the catalyst prepared by the procedure of Example 1 of US 6749821 for hydrocarbon oxidation was carried out in a continuous flow fixed bed reactor for generating methane and propane oxidation temperature curves as shown in Figs 1 and 2 of the accompanying drawings. Gas hourly space velocity was kept constant at 9000 Hr^"1 for the reactions. A gas mixture stream of oxygen and methane^ or propane and nitrogen (as carrier gas) was used. The flow rates of hydrocarbon and oxygen were adjusted as per stoichiometry. Hydrocarbon analyzer analyzed feed mixture inlet composition. Conversions were calculated based on the unconverted hydrocarbon across the catalyst bed at various reactor temperatures. Fig 1 clearly shows that propane oxidation light off temperature of the catalyst of Example 1 and catalyst of US 6749821 is 190⁰C, whereas that of the catalyst of Example 2 is 170⁰C which is 20⁰C less. Light off temperature of catalyst (T₅o- Value) is defined as the temperature at which 50% conversion of hydrocarbon takes place. The catalyst of the invention improves the lightoff temperature by 20⁰C and enchances the catalytic activity throughout. Fig 2 clearly show that the methane light off temperature of catalysts of Examples 1 and 2 is 477⁰C wherfi'as that of US 6749821 is 495°C. Catalyst of Example 2 of the invention shows increased activity throughout from 400⁰C onwards as compared to the catalysts of Example 1 and US 6749821.

EXAMPLE 4

Catalysts of Examples 1 and 2 were tested in a pilot reactor with plant process conditions and nitrogen stream from the gas recycle loop of a polymerization reactor. The pilot reactor was a twin parallel reactor, one comprising the catalyst and the other without any catalyst (blank). The catalysts of Examples 1 and 2 were alternated in the said one reactor. The gas stream from the polymerization reactor was passed through both the reactors. Down stream of these reactors had scrubbers to collect the reactor effluent in deionized water for COE) (Chemical Oxygen Demand) and TOC (Total Organic Carbon) analysis. The reactor when used with the catalyst of Example 2 showed a conversion of 99% and when used with the catalyst of Example 1 showed conversion of 92%. The evaluation tests were run fof^?a duration of 10 days.

Claims

CLAIMS :

1.An oxidation catalyst for the purification of nitrogen gas containing organic impurities, ϊhe catalyst comprising sulphated alumina with a sulphate loading of 1 - 20 percent weight alumina, the sulphated alumina being impregnated with an aqueous solution of a noble metal complex formed with a complexing agent, the noble metal content of the catalyst being 0.1 to 1 percent weight alumina and the surface penetration of the noble metal on the alumina being 100 - 150 microns.

2.An oxidation catalyst as claimed in claim 1, wherein the sulphated alumina is with*a sulphate loading of 1 - 10 percent weight alumina.

3.An oxidation catalyst as claimed in claim 1, wherein the sulphated alumina is with a sulphate loading of 2.4 percent weight alumina.

4.An oxidation catalyst as claimed in any one of claims 1 to 3, wherein the alumina comprises gamma alumina spheres having average diameter of 3 - 4 mm, apparent bulk density of 0.3 to 1.0 g/cc, surface area of 100 to 500 m²/g, pore volume of 0.1 to 1 cc/g, pore diameter' of 20 to 300A and crush strength of 6 to 8 kg.

5. An oxidation catalyst as claimed in any one of claims 1 to 4, wherein the noble metal content of the catalyst is 0.5 percent weight alumina.

6. An oxidation catalyst as claimed in any one of claims 1 to 5, wherein the surface penetration of the noble metal on the alumina is 100 microns.

7. An oxidation catalyst as claimed in any one of claims 1 to 6, wherein the noble metal iβ platinum.

8. An oxidation catalyst as claimed in claim 7, wherein the platinum is obtained from chloroplatinic acid.

9. An oxidation catalyst as claimed in any one of claims 1 to 7, wherein the complexing agent is thiomalic acid.

10. A method of preparing an oxidation catalyst for the purification of nitrogen gas containing organic impurities, the method comprising the steps of :

i) sulphating alumina with a sulphating agent to a sulphate loading of 1 - 20 percent, weight alumina;

ii) drying the alumina of step (i) at 110-160⁰C;

iii) calcining the alumina of step(ii) at 520-560⁰C;

iv) complexing a noble metal in 0.1 to 1 percent weight alumina with a complexing,\ agent;

v) impregnating the sulphated alumina of step (iii) with an aqueous solution of the noble metal complex obtained by step (iv);

vi) drying the catalyst material of step (v)'at 110 - 160°C;

vii) calcining the catalyst material of step (vi) at 520 - 560⁰C;

ix) passivating the catalyst material of step (viii) by cooling it down to 25 - 50⁰C in an inert atmosphere.

11. A method as claimed in claim 10, wherein the sulphation of the alumina is carried out to a sulphate loading of 1 to 10 percent weight alumina or 2.4 percent weight alumina.

12. A method as claimed in claim 10 or 11, wherein the sulphating agent is sulphuric acid.

13. A method as claimed in any one of claims 10 to' 12, wherein the noble metal catalyst is complexed with the complexing agent in 0.3 percent weight alumina.

14. A method as claimed in any one of claims 10 to 13, wherein the surface penetration of the noble metal on the alumina is 100 microns.

15. A method as claimed in any one of claims 10 to 14, wherein the noble metal is platinum..

16. A method as claimed in claim 15, wherein the platinum is obtained from chloroplatinic , acid.

17. A method as claimed in any one of claims 10 to 16, wherein the complexing agent is thiomalic acid.