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Title:
METHOD OF REMOVAL OF CARBONYL COMPOUNDS ALONG WITH ACID GASES FROM CRACKED GAS IN ETHYLENE PROCESS
Document Type and Number:
WIPO Patent Application WO/2004/003110
Kind Code:
A1
Abstract:
A method for inhibiting and dissolving polymeric deposits on the internal surfaces of a caustic wash unit system in a hydrocarbon cracking process wherein said deposits result from polymerization of at least one component contained within a feed stream of said caustic wash unit system. The method comprises the step of introducing into said stream an effective amount of a compound selected from a group consisting of alkali metal salts of oxo acids of sulfur, alkali metal salts of acids of lactam, alkali metal salts of acids of sultam, alkali metal salts of amino acids, alkaline earth metal salts of acids of sultam, alkaline earth metal salts of amino acids, lactam, sultam, amino acids, and combinations thereof, wherein said effective amount inhibits polymerization and dissolves said deposits.

Inventors:
SUBRAMANIYAM MAHESH (IN)
Application Number:
PCT/IN2002/000195
Publication Date:
January 08, 2004
Filing Date:
September 30, 2002
Export Citation:
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Assignee:
DORF KETAL CHEMICALS INDIA PVT (IN)
SUBRAMANIYAM MAHESH (IN)
International Classes:
C07C7/00; C07C11/04; C07C11/167; C10G19/02; C10G55/04; C10G70/06; C10G75/04; (IPC1-7): C10G19/02; C07C7/11; C07C7/20; C10G70/04; C10G70/06; C10G75/04
Domestic Patent References:
WO2002036715A12002-05-10
Foreign References:
EP0824142A21998-02-18
EP0264280A21988-04-20
EP1116778A12001-07-18
DE2333588A11975-02-06
US5264114A1993-11-23
Attorney, Agent or Firm:
Joshi, Hiral Chandrakant (501 Vishwananak, Andheri - Chakala Road, Opp. Hindustan Lever, Andheri, Mumbai 9 Maharashtra, IN)
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Claims:
CLAIMS What is claimed is:
1. A method for inhibiting and dissolving polymeric deposits on the internal surfaces of a caustic wash unit system in a hydrocarbon cracking process wherein said deposits result from polymerization of at least one component contained within a feed stream of said caustic wash unit system, comprising the step of : introducing into said stream an effective amount of a compound selected from a group consisting of alkali metal salts of oxo acids of sulfur, alkali metal salts of acids of lactam, alkali metal salts of acids of sultam, alkali metal salts of amino acids, alkaline earth metal salts of acids of sultam, alkaline earth metal salts of amino acids, lactam, sultam, amino acids, and combinations thereof, wherein said effective amount inhibits polymerization and dissolves said deposits.
2. A method according to claim 1, wherein said hydrocarbon cracking process produces hydrocarbons selected from a group consisting of ethylene and butadiene.
3. The method according to claim 1, wherein said alkali metal salts of oxo acids of sulfur are a compound selected from a group consisting of sodium salt of oxo acid of sulfur compounds, sodium dithionite, sodium metabisulfite, sodium sulfite and sodium bisulfite.
4. The method according to claim 1, wherein the amino acid is selected from a group consisting of 6aminohexanoic acid, glycine, taurine, sulfanilic acid, beta alanine, NH2 (CHX) YOZOH and isomers of the foregoing (Where X=112, Y = S or C and Z=12).
5. The method according to claim 1, wherein the lactam is selected from the group consisting of epsilon caprolactum, isomers of epsilon caprolactum and substituted derivatives of epsilon caprolactum.
6. The method of claim I, wherein the amino acid comprises amino caproic acid derived from epsilon caprolactum.
7. The method of claim l, wherein the amino acid is the acid salt of amino caproic acid with an acid selected from a group consisting of hydrochloric acid, sulfuric acid, perchloric acid and organic acid.
8. The method of claim 7, wherein the organic acid is an organic acid capable of hydrolyzing epsilon caprolactum.
9. The method of claim 7, wherein the organic acid is an organic acid capable of forming a salt with 6aminohexanoic acid.
10. The method of claim 1, wherein the component contained within the feed stream is derived from carbonyl compounds.
11. The method of claim 1, wherein the amino acid is amino caproic acid made from alkaline hydrolysis of epsilon caprolactum using an agent selected from the group consisting of potassium hydroxide, sodium hydroxide, lithium hydroxide, calcium hydroxide, magnesium hydroxide, organic or inorganic bases capable of reacting with epsilon caprolactum such that an amino and an carboxyl group are created, and combinations thereof.
12. The method of claim 10, wherein the amino acid is amino caproic acid and the component in the feed stream is carbonyl and the molar ratio of said carbonyl to mixture of amino acid and alkali or alkaline earth metal salts of oxo acids of sulfur is between 1 : 10 and 1: 0. 01.
13. The method of claim 10, wherein the amino acid is an amino caproic acid sodium salt and the component in the feed stream is carbonyl and the molar ratio of carbonyl compound to amino acid is between 1: 10 to 1: 0.01.
14. The method of claim 1, wherein the caustic wash unit system further comprises an alkaline scrubber of pH greater than 7.
15. The method of claim 1, wherein the caustic wash unit system further comprises a caustic scrubber.
16. The method of claim 1, wherein the caustic wash unit system further comprises an amine scrubber.
17. The method of claim 1, wherein the amino acid consists of a compound selected from a group of aliphatic amino acids, aromatic amino acids, straight chain aliphatic amino acids, branched chain aliphatic amino acids, cyclic amino acids, isomers of the foregoing.
18. The method of claim 1, wherein the amino acid has at least one carboxyl group.
19. The method of claim l, wherein the amino acid has at least one sulfoxyl group.
20. The method of claim 1, wherein the amino acid has more than one amino group.
21. The method of claim 1, wherein the hydrocarbon cracking process includes the cracking process of liquid as well as gaseous hydrocarbons for producing olefins ; and wherein superior solubilization occurs over inhibiting and dispersion of deposits formed during said process.
22. The method of claim 1, wherein the amino acid is used neat or in a mixture.
23. The method of claim 1, wherein the lactam is selected from a group consisting of isomers of lactams and substituted derivatives of lactams.
24. The method of claim 1, wherein the sultam is selected from a group consisting of isomers of sultams and substituted derivatives of sultams.
25. The method of claim 1, wherein the sultam can be hydrolyzed with acids or bases selected from a group consisting of potassium hydroxide, sodium hydroxide, lithium hydroxide, calcium hydroxide, magnesium hydroxide, and organic and inorganic bases.
26. The method of claim 1, wherein the amino acid is a derivative of the structure (HOOZ) WPH(CH2) XNH2 (where X=1 to 6, Z=C or heteroatom S, W= I to 4 and PH is phenyl ring).
27. The method of claim 1, wherein the amino acid is a derivative of the structure ((HOOZ)(CH2) x) wPH(CH2) yNH2 (where X>0, Y>0, Z =C or heteroatom S, W=1 to 4 and PH is phenyl ring).
28. The method according to claim 1, wherein there are present molecules that dissolve the polymer formed in the caustic wash unit system and any downstream units associated therewith.
29. The method of claim 1, wherein sultam and the component in the feed stream is carbonyl and the molar ratio of carbonyl to amino acid is between 1 : 10 and 1: 0. 01 30. The method of claim 1, wherein lactam is epsilon caprolactam and the component in the feed stream is carbonyl and the molar ratio of carbonyl to lactam or sultam is between 1 : 10 and 1 : 0. 01 31. The method of claim 1, wherein the amino acid and the lactam or sultam can be used neat or in a mixture.
30. 32 The method of claim 1, wherein the components are in solid or liquid state.
31. 33 The method of claim 1, wherein the lactam or sultam is used neat or in a mixture.
32. 34 The method of claim 1, wherein the effective amount introduced into said stream is added in a single dosage or periodic dosages wherein the effective amount may be neat or a mixture.
33. 35 The method of claim 1, wherein the effective amount may be used in combination with an inhibiting agent.
34. 36 The method of claim 1, wherein the stream comprises at least one carbonyl compound and the effective amount is introduced either before, at the same time, or after said stream enters said caustic wash unit system.
Description:
METHOD OF REMOVAL OF CARBONYL COMPOUNDS ALONG WITH ACID GASES FROM CRACKED GASES IN ETHYLENE PROCESS TECHNICAL FIELD OF THE INVENTION: The present invention generally relates to a method of removing undesired by- products from pyrolytic cracking of hydrocarbons. The invention specifically relates to a method for removal of acetaldehyde and other carbonyl compounds along with other acidic gases like H2S and C02 that are formed when cracked gasses enter a caustic tower or an amine unit within an ethylene plant, where the cracked gases are produced in a pyrolysis heater during the pyrolytic cracking of hydrocarbons.

BACKGROUND OF THE INVENTION: In pyrolytic cracking operations, feedstock such as ethane, propane, naphtha, kerosene, gas oil, fuel oil and the like undergo"cracking, "i. e. the removal of hydrogen, to form unsaturated hydrocarbons. Pyrolytic cracking also tends to produce oxygenated hydrocarbons, including carbonyl compounds such as acetaldehyde. In a typical operation, the cracked effluent stream is quenched, fractionated and compressed. Acidic contaminants such as hydrogen sulfide, carbon dioxide and mercaptans are then typically removed from the effluent.

During the operation of scrubbing these gases with caustics or amines, some oxygenated compounds are removed. At the same time, however, the basic conditions in the scrubber tend to cause base-induced condensation reactions of the carbonyl compounds, including aldehydes (e. g., acetaldehyde) and/or ketones, which in turn result in the formation of polymers. These polymers are deposited on the internal surfaces of the scrubber. As the mass of polymer grows, it leads to fouling and can eventually obstruct the flow of liquids through the system. This is undesirable, as the operating system must be shutdown for a significant amount of time in order to remove the deposited polymer and clean the equipment.

In the past, polymerization of oxygenated compounds, such as carbonyl-containing organics in basic solutions, has been prevented by adding amine compounds such as hydroxylamine hydrochloride, hydroxylamine sulfate, hydrazine, carbohydrazides and the like. Several patents relate to methods of inhibiting carbonyl fouling.

U. S. Pat. No. 4,673, 489, granted to Roling, discloses using hydroxylamine and its salts of hydrochloric acid and sulfuric acid to inhibit polymer formation caused by condensation reactions of aldehydes contained in caustic scrubber units. One disadvantage of the method is that the additive has to be used in almost molar proportion.

U. S. Pat. No. 4,952, 301, granted to Awbrey, discloses using ethylenediamines with the molecular formula NH2 (CH2CH2NH) xH where x is an integer ranging from 1 to about 10 to inhibit carbonyl based fouling, particularly aldehyde fouling, that often occurs during caustic scrubbing of liquid or gas phase hydrocarbon streams in the base wash unit.

U. S. Pat. No. 5,264, 114, granted to Dunbar, discloses the use of amine compounds to inhibit the deposition of foulants during caustic washing of the hydrocarbon gases contaminated with the carbonyl compounds which comprises of treating the said hydrocarbon gases with an aqueous amine solution wherein the said aqueous amine solution comprises water and an amine compound having a concentration range of 2 ppm to about 5000 ppm and wherein the said amine compound is selected from a group of organic compounds of the formula RNH2 and R2NH wherein the R is selected from the group of alkyl or aryl groups.

U. S. Pat. No. 5,160, 425, granted to Lewis, discloses Carbohydrazide as useful for inhibiting polymeric fouling deposits during the caustic scrubbing of pyrolytically-produced hydrocarbons contaminated with oxygen-containing compounds.

U. S. Pat. No. 5,288, 394, granted to Lewis et al., describes and claims a method of inhibiting formation of polymeric fouling deposits during the caustic scrubbing of a hydrocarbon stream contaminated with oxygenated compounds with a basic washing solution

having pH greater than 7 comprising: adding to said hydrocarbon stream a sufficient amount of a compound containing at least one hydrazide compound for inhibiting formation and deposition of fouling materials.

U. S. Pat. No. 5, 194, 143, granted to Roling, describes and claims a method for inhibiting the formation of polymeric based fouling deposits during the basic washing of olefins containing hydrocarbon contaminated with oxygenated compounds comprising about 1 to 10,000 parts per million acetoacetate ester compound having the formula CH3COCH2CxHy where x is an integer from about 1 to about 8 and y is an integer from about 3 to about 17.

U. S. Pat. No. 5,220, 104, granted to McDaniel et al. , discloses the use of percarbonate salts for the same purpose.

U. S. Pat. No. 5,770, 041, granted to Lewis et al. , describes the use of certain aldehydic compounds without alpha hydrogen atoms or non-enolizable aldehydes like formaldehyde, glyoxal, etc. as aldol inhibitor, but again in this case the said inhibitor has to be used in at least thrice the molar ratio per mole of carbonyl species.

U. S. Pat. No. 5,714, 055, granted to Lewis et al. , discloses the use of certain organic amine inhibitors like sulfanilic acid for inhibiting the aldol condensation in extremely severe fouling conditions, but this patent does not disclose the use of said inhibitor for dissolving the polymer once made.

The prior art systems treat caustic towers with an injection of a compound to inhibit the aldol condensation mechanism. In order to inhibit aldol condensation, the prior art systems mostly use additives that are organic in nature and contribute to chemical oxygen demand for caustic used in the scrubbing process. In addition, the prior art additives typically require that additive to reactant molar ratios be of at least 1: 1 for effective performance.

Further, the adducts of high molecular weight polymers with these compounds tend to be

insoluble in the basic system. Thus, the prior art additives are ineffective for the purposes of maintaining unobstructed flow through the system and reducing significant maintenance time for removing polymer deposits and cleaning the equipment.

A current practice in the industry is to treat the weak caustic with gasoline or another aromatic fraction in order to remove the polymers before sending it to the spent caustic oxidation unit, in order to prevent fouling there. The resulting gasoline-containing stream causes disposal and operational problems, however. Likewise, routing the gasoline- containing stream to other operating units can cause problems due to the presence of the caustic, as it may effect pH, catalyst and reaction parameters.

Another current practice in the industry is to treat the caustic tower with organic additives, and despite the various advances in the art it remains desirable to provide an alternative method to improve the performance of this particular unit in the industry. There have also been shortcomings when any of these additives have been used concurrently to provide a synergistic effect in such systems.

Hence, it is desirable to provide a method for preventing fouling that does not create problems in equipment downstream of the scrubber and that does not pose significant environmental problems.

SUMMARY OF THE INVENTION : One embodiment of the present invention discusses a method of using the caustic/amine scrubber to scavenge acidic gases like HzS and C02, and additionally scavenge carbonyl compounds without posing any polymerization problems. Another embodiment of the present invention includes a method for scavenging oxygenated hydrocarbons without posing polymerization problems and without interfering with plant operations or with the operation of the individual process units.

One embodiment of the present invention includes a method that provides additional advantages of reducing the concentration of oxygenated hydrocarbons, particularly carbonyl compounds, in equipment and in product streams. Yet another embodiment of the present invention includes a method for inhibiting oxygenated hydrocarbon fouling that does not interfere with overall plant operations or operations of the individual processes. The method in this embodiment provides the additional advantage of reducing the concentration of oxygenated hydrocarbons, particularly carbonyl compounds, in equipment and streams. An alternative embodiment of the present invention includes use of certain inorganic salts, (e. g. alkali metal salts of oxo acids of sulfur, alkali metal salts of acids of lactam, alkali metal salts of acids of sultam, alkali metal salts of amino acids, alkaline earth metal salts of acids of sultam, alkaline earth metal salts of acids of amino acids, lactam, sultam, amino acids, and combinations thereof) that prevent the polymer formed by aldol condensation and further dissolve said polymer. The dissolution is observed in synergistic compositions.

Also, the present invention can be used along with caustic in the caustic tower, in that the invention can be premixed with the caustic used for making the scrubbing solution.

BRIEF DESCRIPTION OF THE DRAWINGS: Figs. 1A and 1B depict chemical compounds useful in the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS: The present invention includes a method for inhibiting and dissolving the polymeric deposits formed in caustic or alkaline scrubbers which are used for scrubbing acidic gases such as carbon dioxide and hydrogen sulfide from the effluent streams formed during the pyrolytic cracking of hydrocarbons such as naphtha, ethane, and propane. The cracking operations also produce oxygenated compounds such as vinyl acetate or acetaldehyde, which undergo polymerization under the alkaline conditions in the scrubber. Upon hydrolysis under

alkaline conditions, vinyl acetate releases acetaldehyde which contributes further to the buildup of polymeric deposits One embodiment of the present invention includes a method wherein certain inorganic salts like sodium dithionite, sodium metabisulphite, and sodium bisulphate are used to mitigate fouling. Said inorganic salts are blended with aliphatic amino acids (including but not limited to 6-amino caproic acid) to mitigate the effects of polymerization in the system in synergistic combination. The blends of inorganic salts and aliphatic amino acids, particularly 6-amino caproic acid, not only prevent but also dissolve the polymers formed by the aldol condensation described above.

Another embodiment of the present invention includes a method wherein a combination of inorganic salts and certain lactams (including but not limited to epsilon caprolactam (molecular weight 113) ) is used to mitigate the effects of polymerization in the system. The blend of the inorganic salt and caprolactam not only prevents but also dissolves the polymers formed by the aldol condensation described above.

In one embodiment of the present invention, when amino acids or lactams are used along with the inorganic salts, particularly sodium dithionite, they react with both the low and high molecular weight polymers such that the reacted adduct is soluble in the caustic solution. Thus, the amino acid and the inorganic salts in synergistic ratio solublize the polymers formed and prevent precipitation and fouling of the equipment. The present additives have the dual advantage of working as polymerization inhibitors by reacting with acetaldehydes as well as solublizing any existing polymers by reacting with them.

In one embodiment of the present invention, amino acids that are particularly useful include but are not limited to 6-amino acids such as the amino hexanoic acid made from epsilon caprolactum, glycine, or taurine, or any compound having one of the structures as shown in Figs. lA and IB. Also suitable are the derivatives, isomers, and inorganic or

organic salts of these compounds. These structures are representatives of only some embodiments of the present invention, however one skilled in the art will recognize that modifications to the embodiments may be made without departing from the scope of the claimed invention.

These said compounds, described in the preceding paragraph, are effective polymerization inhibitors for aldol condensation reactions. For the purposes of this invention, an acetaldehyde polymer may be defined as having 2 or more repeating units of acetaldehyde. These said compounds are effective scavengers for carbonyl compounds found in any hydrocarbon stream. Said compounds are also effective polymerization inhibitors for aldol condensation reactions, as well as agents for solubilizing any polymers that may already have been formed by that mechanism.

In one embodiment of the present invention, the inorganic salts may be added to the alkaline scrubber in an amount representing a molar ratio of carbonyl to inorganic salt is from about 1: 0. 01 to about 1 : 25 mole. Preferably the inorganic salt is added to the alkaline scrubber in an amount representing a molar ratio of carbonyl to inorganic salt from about 1 : 0.05 to 1: 0.005.

In another embodiment of the present invention, the amino acid and the previously mentioned inorganic salts may be added to the alkaline scrubber in an amount representing a molar ratio of carbonyl to the mixture of amine and the inorganic salts is from about 1 : 0.01 to about 1: 25 mole. Preferably the mixture of amino acid and the inorganic salt is added to the alkaline scrubber in an amount representing a molar ratio of carbonyl to mixture from about 1: 0.05 to 1: 0.005 In yet another embodiment of the present invention, the lactam and the previously mentioned inorganic salts may be added to the alkaline scrubber in an amount representing a molar ratio of carbonyl to the mixture of lactam and the inorganic salts from about 1 : 0.01 to

about 1 : 25 mole. Preferably the lactam and the inorganic salts are added to the alkaline scrubber in amount representing a molar ratio of carbonyl to lactam and the inorganic salts from about 1 : 0.5 to 1: 0.25 In one embodiment of the present invention, salt of an amino acid or pure amino acid or combinations thereof are added either as neat product or as an aqueous solution containing 0.05 to greater than 60 weight percent of the amino acid. In one embodiment, 18 weight percent of amino acid is used.

In one embodiment of the present invention, the lactam can be added either as neat product or as an aqueous solution containing 0.05 to greater than 60 weight percent of the amino acid, with 18 or 38 weight percent preferred.

In yet another embodiment, the preferred amount of additive ranged from 0.5 to 1,000, 000 parts of inhibitor per one million parts of the aqueous scrubbing medium used in the caustic wash system. Preferably, 25 to 200 ppm of additive was used.

The following Examples are merely illustrative of some embodiments of the present invention and the manners in which it can be performed, and are not intended to limit the scope of the claimed invention in any way.

Example 1 To a clean four necked round bottom flask, equipped with a thermometer, stirrer and condenser, caprolactum (18 g, 0.1593 mole), sodium hydroxide (7 g, 0.175 g) and 75.0 g water were added. The mixture was well agitated and heated to 105°C to 120°C for a period of six hours. Small samples were periodically withdrawn and checked for conversion using HPLC. The conversion of epsilon caprolactum to six amino hexanoic acid was greater than 75%.

Example 2 20 ml of 10% NaOH solution was added to a 50 ml stoppered conical flask. A desired inhibitor in solution or in solid form was then added, followed by the addition of 1 ml vinyl acetate. The mixture is shaken well and kept in an oven for 24 hrs at 55°C. One blank run was prepared wherein all reagents except the inhibitor were added. At the end of 24 hours the contents of the flask were visually checked for clarity or any deposits, and UV readings were measured. The following results were obtained as shown in Table 1.

Table 1 The following results were average readings from two to three identical runs with the same composition and reaction parameters. Expt. Compounds gms Mole % Absorbance Observation No. Ratio Transmittance at 720 nm at 800 nm 1 Blank nil nil 0.5 2.5 Red hazy liquid with precipitate 1 Sodium 0.2075 0.125 68.5 0.2575 Red slightly dithionite hazy liquid 2 Sodium 0.4715 0.250 89.55 0. 0475 Red clear liquid dithionite 3 Sodium 0.943 0.5 90 0.042 Faint red clear dithionite liquid 4 Sodium 1. 886 1. 0 80. 35 0. 09 Colorless liquid dithionite 5 Sodium 0.1281 0.0625 0.466 2.54 Red hazy liquid metabisulphite 6 Sodium 0.2562 0.125 80.7 0.179 Red clear liquid metabisulfite 7 Sodium 0.549 0.25 86.4 0.113 Red clear liquid metabisulfite 8 Sodium 2. 089 1. 0 87. 3 0. 066 Red clear liquid metabisulfite 1 I Sodium 0.140 0.125 2.8 1.80 Hazy red liquid bisulfite 12 Sodium 0.338 0.30 86.1 0.133 Red clear liquid bisulfite 13 Sodium 0.563 0.50 86 0.1035 Red clear liquid bisulfite 14 Sodium 1. 127 1. 0 89.1 0.092 Red clear liquid bisulfite

17 Sodium sulfite 0.170 0.125 0. 35 2. 653 Red hazy liquid 18 Sodium sulfite 0.682 0.5 83.6 0.130 Red clear liquid 19 Sodium sulfite 1. 365 1.0 89. 2 0. 08 Red clear liquid 20 Sodium sulfate 1. 539 1.0 5.9 1.904 Hazy liquid with gummy polymer 21 Sodium 1.496 1.0 4.4 1.332 Same as above hydrogen sulfate Example 3 20 mi of 10 % NaOH solution was pipetted into a 50 ml stoppered conical flask. To this was added 1 ml of vinyl acetate solution. The mixture was shaken well and kept in an oven for 15 minutes. During this period, the vinyl acetate was hydrolyzed and polymerized to form insoluble products. After 15 minutes the desired amount of inhibitor was added. One control sample was prepared without inhibitor. The flask was shaken well and kept in an oven for 24 hours. After 24 hours the flask was checked visually for clarity and any deposits.

In some cases UV transmittance was measured for comparison. The results are shown in Table 2.

Table 2 : After Polymerization Expt Compounds gms Mole Moles Total % Absorbance Observation . s of Moles Transmittan at 720 nm No. ce at 800nm 1 blank nil nil nil nil 0.5 2.5 Red turbid liquid with polymer particles 2 Sodium 0.943 0. 5------0. 5 62.5 0.202 Yellow clear Dithionite liquid with few particles 3 Amino 0.125 0.087 0.087 0.5 2.709 Same as caproic acid above 4 Sodium 0. 943 0.5 0.0879 0.5879 77.05 0.1125 Red clear Dithionite + transparent Amino liquid caproic acid 0. 125 5 Sodium 0.943 0.5 0.5879 85.7 0.07 Red clear dithionite + transparent Example 1 liquid 0. 3ml 0.087 6 caprolactum 0.367 0.3 0.3 11. 4 1. 095 Hazy red 3 liquid with particles 7 Sodium 0.943 0.5 0.3 0.8 69.7 0.171 Clear red dithionite + liquid with caprolactam few particles 0.367 3 Table 3: Before Polymerization Expt Compounds gms Motes Moles Total % Absorbance Observation . no of of moles transmittance at 720 nm at 800nm I Sodium 0. 1------0. 1 18. 5 0.842 Red hazy Dithionite liquid 2 Amino 0. 0372-----0. 026 0.026 0.3 2.571 Closer to caproic acid blank 3 Sodium 0.1886 0.1 0.026 0. 126 82 0.183 Red clear Dithionite + 0.0372 transparent Amino liquid caproic acid 4 Sodium 0. 1886 0. 1 0. 026 0. 126 81. 0 0. 210 Red clear dithionite + transparent Example I liquid 0. 09ml 5 Sodium 0.1886 0.1 0.160 0.260 86. 7 0.1195 Red clear dithionite + transparent sulfanilic liquid acid 0. 3 6 Sulfanilic 0.30 0.160 0.160 0.2 2.872 Red brown acid hazy with particles 7 caprolactum 0.3673 0.3 0.3 0. 4 2.783 Dark red slight hazy liquid with some dispersed particles 8 Caprolactum 0.1836 0.1 0.15 0.250 82.9 0.176 Red clear + sodium transparent dithionite liquid 0. 1886

9 Sodium 0.1853 0.1 0.09 0.190 93. 3 0.067 Faint Red metabisulfit clear e + sodium transparent dithionite 0. 1866 liquid 10 Sodium 0.1132 0.06 0.0625 0.123 81 0.285 Red clear dithionite + transparent Amino liquid caproic acid 0.0888 11 Amino 0.0888 0.0625 0.0625 0.3 2.872 Same as caproic acidblank The basic wash systems in which the present treatments were useful for inhibiting fouling include amine acid gas scrubber and caustic wash systems.

Example 4: Caustic Solution Stability 0.3 mole strength of sodium dithionite was prepared in 10 % NaOH solution. The performance of this sodium dithionite solution was tested periodically. To 20 mi of the solution, I ml vinyl acetate was added and shaken well. The flask was kept in the oven at 55°C for 24 hrs. The details of the result are listed in Table 4.

Table 4: Caustic Solution Stability Sr. Hours % Absorbance @ 720 Observation No. Transmittance nm at 800 nm 1 24 hrs 90. 3 0. 122 Red clear transparent liquid 2 192 85. 3 0. 145 Red clear transparent liquid 3 240 87. 9 0. 140 Red clear transparent liquid 4 360 90. 9 0. 129 Red clear transparent liquid 5 480 87. 3 0. 142 Red clear transparent liquid Example 5: Sodium Metabisulfite 0.2 mole strength of sodium dithionite was prepared in 10 % NaOH solution. The performance of this sodium dithionite solution was tested periodically. To 20 ml of the solution, 1 ml vinyl acetate was added and shaken well. The flask was kept in the oven at 55°C for 24 hrs. The details of the result are listed in Table 5.

Table 5: Sodium Metabisulfite Sr. Hours % Absorbance @ 720 Observation No. Transmittance nm at 800 nm 1 24 hrs 90. 7 0. 095 Red clear transparent liquid 2 72 90. 8 0. 109 Red clear transparent liquid 3 168 90. 3 0. 105 Red clear transparent liquid 4 216 88. 7 0. 118 Red clear transparent liquid 5 336 90. 4 0. 116 Red clear transparent liquid While the present invention has been described herein in terms of various embodiments, one of ordinary skill in the art will recognize that modifications to the embodiments can be made without departing from the scope of the claimed invention.