Composition and a process for reducing aromatics from a hydrocarbon feedstock

Abstract

The present disclosure relates to a composition for reducing aromatics from a hydrocarbon feedstock. The composition comprises a solvent mixture. The solvent mixture includes a primary solvent, a first co-solvent, a second co-solvent, and a secondary solvent. The present disclosure also relates to a process for reducing aromatics from a hydrocarbon feedstock.

Claims

1. A composition for reducing polycyclic aromatics (PCA) to less than 3 wt % from a hydrocarbon feedstock, said composition comprising a solvent mixture, wherein said solvent mixture comprises: a) N-Methyl-2-Pyrrolidone (NMP) as a primary solvent in an amount ranging from 70 vol % to 95 vol % of the total solvent mixture; b) monoethylene glycol as a first co-solvent in an amount ranging from 2 vol % to 20 vol % of the total solvent mixture; c) propylene glycol as a second co-solvent in an amount ranging from 1 vol % to 20 vol % of the total solvent mixture; and water as a secondary solvent in an amount ranging from 2 vol % to 4 vol % of the total solvent mixture.

2. The composition as claimed in claim 1, wherein said hydrocarbon feedstock is at least one selected from the group consisting of lube oil distillate, naphtha, and deasphalted oil.

3. A process for reducing polycyclic aromatics (PCA) to less than 3 wt % from said hydrocarbon feedstock using the composition as claimed in claim 1, said process comprising the following steps: X. contacting said solvent mixture with said hydrocarbon feedstock in a pre-determined ratio ranging from 1:1 to 2.5:1, and at a pre-determined temperature ranging from 50 C. to 150 C., while stirring at a pre-determined rate ranging from 300 rpm to 650 rpm for a pre-determined time period ranging from 2 hours to 4 hours, to obtain a biphasic mixture comprising an extract phase containing aromatics and a raffinate phase; and Y. separating said extract phase from said biphasic mixture to obtain said raffinate phase with reduced polycyclic aromatics (PCA) content.

4. The process as claimed in claim 3, wherein said extract phase is separated from said biphasic mixture, in the process step Y, to obtain said raffinate phase with aromatics content less than 3 wt %.

5. The process as claimed in claim 3, being a liquid-liquid extraction process.

6. The process as claimed in claim 3, wherein in the process step X, the flow of said hydrocarbon feedstock is counter-current to the flow of said solvent mixture.

Description

DETAILED DESCRIPTION

(1) As described herein above, the content of polycyclic aromatics in a hydrocarbon feedstock should be less than 3 wt % as per the industry standards. This is because, aromatics are carcinogenic, and several legal norms stipulate that the hydrocarbon feedstock having the content of polycyclic aromatics greater than 3 wt % shall be indicated as toxic.

(2) However, conventionally, an extract phase and a raffinate phase obtained by a liquid-liquid extraction method contain polycyclic aromatics above the permissible limit, specifically in an amount in the range of 15 wt % to 25 wt % and 6 wt % to 10 wt % respectively.

(3) The present disclosure, therefore, envisages a composition and a process for reducing aromatics from a hydrocarbon feedstock.

(4) The hydrocarbon feedstock can be at least one selected from the group consisting of lube oil distillate, naphtha, and deasphalted oil (DAO).

(5) The composition comprises a solvent mixture. The solvent mixture includes a primary solvent, a first co-solvent, a second co-solvent, and a secondary solvent.

(6) The primary solvent can be N-Methyl-2-Pyrrolidone (NMP).

(7) The amount of the primary solvent can be in the range of 70 vol % to 95 vol % of the total solvent mixture.

(8) The first co-solvent and the second co-solvent facilitate in increasing the selectivity for aromatics in the hydrocarbon feedstock, i.e. the co-solvents facilitate in increasing the solubility of aromatics in N-Methyl-2-Pyrrolidone (NMP).

(9) The first co-solvent and the second solvent are selected from the group consisting of an amide, a glycol, and a paraffinic hydrocarbon.

(10) The amide can be at least one selected from the group consisting of N, N-Di methylformamide and N,N-dimethylpropionamide.

(11) The glycol can be least one selected from the group consisting of monoethylene glycol, propyleneglycol, and diethylene glycol.

(12) The paraffinic hydrocarbon can be least one selected from the group consisting of N-Hexane and N-decane.

(13) The first co-solvent can be in the range of 2 vol % to 20 vol % of the total solvent mixture.

(14) The second co-solvent can be in the range of 1 vol % to 20 vol % of the total solvent mixture.

(15) The secondary solvent acts as an anti-solvent.

(16) Particularly, the secondary solvent controls the solubilizing power of N-Methyl-2-Pyrrolidone (NMP) for solubilizing aromatics in N-Methyl-2-Pyrrolidone (NMP).

(17) The secondary solvent can be water.

(18) The secondary solvent can be in the range of 2 vol % to 4 vol % of the total solvent mixture.

(19) The process for reducing aromatics from the hydrocarbon feedstock using the composition is carried out in the steps described herein below.

(20) In the first step, the hydrocarbon feedstock is contacted with the solvent mixture in a pre-determined ratio ranging from 1:1 to 2.5:1, and at a pre-determined temperature ranging from 50 C. to 150 C., while stirring at a pre-determined rate ranging from 300 rpm to 650 rpm for a pre-determined time period ranging from 2 hours to 4 hours, to obtain a biphasic mixture comprising an extract phase containing aromatics and a raffinate phase.

(21) In the second step, the extract phase is separated from the biphasic mixture to obtain the raffinate phase with reduced aromatics content.

(22) In accordance with the present disclosure, the extract phase is separated from the biphasic mixture, in the second process step, to obtain the raffinate phase with polycyclic aromatics content less than 3 wt %.

(23) The process of the present disclosure being a liquid-liquid extraction process.

(24) In the first process step, the flow of the hydrocarbon feedstock can be counter-current to the flow of the solvent mixture.

(25) The present disclosure is further described in light of the following experiment which is set forth for illustration purpose only and not to be construed for limiting the scope of the disclosure.

EXPERIMENTAL DETAILS

Experiment 1

(26) The following laboratory scale experiment can be scaled up to industrial/commercial scale.

(27) 280 ml of NMP, 25 ml of monoethylene glycol (first co-solvent), 5 ml of propyleneglycol (second co-solvent) and 10 ml of water were added and mixed in a first reaction vessel to form a composition comprising a solvent mixture.

(28) In a second reaction vessel, 200 ml of a hydrocarbon feedstock (lube oil distillate) was contacted with 320 ml of the composition at 90 C. while stirring at 500 rpm for 2 hours to obtain a biphasic mixture comprising an extract phase containing aromatics and a raffinate phase.

(29) After settling of the phases, the extract phase was separated from the biphasic mixture to obtain the raffinate phase containing lower amount of aromatics and higher amount hydrocarbons, particularly PCA.

(30) The refractive index of the raffinate phase was determined, to determine the quality of the raffinate phase using a refractometer, and the PCA content of the raffinate phase was determined using IP-346 method. The results obtained are tabulated in Table-1.

(31) TABLE-US-00001 TABLE 1 Amount of Amount of hydrocarbons Refractive PCA (wt %) in the index of the in the Sr. raffinate raffinate raffinate No Composition phase phase phase 1 97 vol % NMP and 57.1% 1.4720 6 3 vol % water 2 92 vol % NMP, 58.5% 1.4715 4 3 vol % water, and 5 vol % co-solvents 3 87 vol % NMP, 60.1% 1.4718 2.5 3 vol % water, and 10 vol % co-solvents 4 82 vol % NMP, 60.6% 1.4725 2 3 vol % water, and 15 vol % co-solvents 5 77 vol % NMP, 61%. 1.4730 2 3 vol % water, and 20 vol % co-solvents

Inference

(32) From Table-1, it can be inferred that, with increase in the amount of co-solvents in the composition, the refractive index of the raffinate phase and the amount of PCA in the raffinate phase are reduced.

Experiment 2

(33) The following experiment was performed on a commercial scale.

(34) Based on the promising results obtained on laboratory scale (experiment-1), the developed process was tried on commercial scale in one of the solvent extraction units of the applicant. The commercial trials were conducted with a feed (the lube oil distillate). The lube oil distillate was fed at a rate of 42 m.sup.3/hr into the unit. A composition comprising a solvent mixture was added in the lube oil distillate such that the ratio of the composition and the lube oil distillate was 1.6. A base case data (as shown in Table-2) was obtained for 3 days prior to the start of plant trials. A mixture of co-solvents was injected into the unit at certain percentages (ranging from 2.0 to 10.0%) in two stages and the performance was observed. No operational issues were observed during the trial, and all the parameters such as extractor tower temperature, the composition to feed ratio, and all other operating parameters were kept the same as the base case. The raffinate yield and product properties were continuously monitored. The results of the plant trials indicated that the raffinate yield improved by 1.5 wt % for the operation.

(35) The refractive index of the raffinate phase was determined, to determine the quality of the raffinate phase using a refractometer, and the PCA content of the raffinate phase was determined using IP-346 method. The results obtained are tabulated in Table-2.

(36) TABLE-US-00002 TABLE 2 Amount of Amount of hydrocarbons Refractive PCA (wt %) in the index of the in the Sr. raffinate raffinate raffinate No Composition phase (%) phase phase 1 97 vol % NMP and 60.01 1.4728 6.2 3 vol % water (base case) 2 92 vol % NMP, 61.2 1.4725 3.8 3 vol % water, and 5 vol % co-solvents 3 87 vol % NMP, 61.62 1.4724 2.9 3 vol % water, and 10 vol % co-solvents

Inference

(37) From Table-2, it can be inferred that, with increase in the amount of co-solvents in the composition, the refractive index of the raffinate phase and the amount of PCA in the raffinate phase are reduced.

Technical Advances and Economical Significance

(38) The present disclosure described herein above has several technical advantages including, but not limited to, the realization of a composition and a process that: reduces the amount of aromatics, particularly PCA, from the hydrocarbon feedstock.

(39) The disclosure has been described with reference to the accompanying embodiments which do not limit the scope and ambit of the disclosure. The description provided is purely by way of example and illustration.

(40) The embodiments herein and the various features and advantageous details thereof are explained with reference to the non-limiting embodiments in the following description.

(41) Descriptions of well-known components and processing techniques are omitted so as to not unnecessarily obscure the embodiments herein.

(42) The foregoing description of the specific embodiments so fully revealed the general nature of the embodiments herein that others can, by applying current knowledge, readily modify and/or adapt for various applications such specific embodiments without departing from the generic concept, and, therefore, such adaptations and modifications should and are intended to be comprehended within the meaning and range of equivalents of the disclosed embodiments. It is to be understood that the phraseology or terminology employed herein is for the purpose of description and not of limitation. Therefore, while the embodiments herein have been described in terms of preferred embodiments, those skilled in the art will recognize that the embodiments herein can be practiced with modification within the spirit and scope of the embodiments as described herein.