Method of treating waste plastic
A method of upgrading liquefied waste plastic (LWP) to a mixture of purified hydrocarbons is hereby provided. The method includes the steps of providing a feed including liquefied waste plastic (LWP) and a vacuum gas oil (VGO) stream and/or a heavy gas oil (HGO) stream to form a mixed stream, subjecting the mixed stream to hydrotreatment for removal of impurities and to produce a hydrotreated stream, subjecting the hydrotreated stream to hydrocracking to produce a hydrocracked stream including a mixture of purified hydrocarbons and fractionating the hydrocracked stream.
1 . A method of upgrading liquefied waste plastic (LWP) to a mixture of purified hydrocarbons, the method comprising:
providing a feed containing liquefied waste plastic (LWP), and containing a vacuum gas oil (VGO) stream and/or a heavy gas oil (HGO) stream to form a mixed stream;
subjecting said mixed stream to hydrotreatment for removal of impurities and to produce a hydrotreated stream;
subjecting the hydrotreated stream to hydrocracking to produce a hydrocracked stream containing a mixture of purified hydrocarbons; and
fractionating the hydrocracked stream containing a mixture of purified hydrocarbons.
2 . The method according to claim 1 , wherein the mixed stream comprises:
1 to 40 wt. % LWP, 5 to 30 wt. % LWP, or 5 to 25 wt. % LWP based on a total of the mixed stream, and a balance of the stream being VGO and/or HGO.
3 . The method according to claim 1 , wherein the LWP is produced as pyrolyzed waste plastic.
4 . The method according to claim 3 , wherein the pyrolyzed waste plastic is fractionated to one or more LWP fractions, and at least one of the LWP fractions is in the feed to be hydrotreated.
5 . The method according to claim 1 , wherein the LWP is subjected to pre-treatment before the hydrotreatment.
6 . The method according to claim 1 , wherein the hydrotreatment comprises:
use of at least one guard bed before hydrotreating the mixed stream.
7 . The method according to claim 1 , wherein the hydrotreatment and hydrocracking are performed in one unit, arranged in one vessel having a hydrotreatment section followed by a hydrocracking section.
8 . The method according to claim 1 , wherein the hydrotreatment is performed in a presence of a catalyst selected from sulfided NiMo, CoMo and a combination thereof, on alumina (Al 2 O 3 ) support.
9 . The method according to claim 1 , wherein the hydrotreatment is performed under conditions that include:
a temperature of 250-450° C., 330-420° C., or 390-410° C.;
a pressure of 30-250 bar, 130-180 bar, or 145-155 bar;
a hydrogen to oil volume ratio of 500-2000 L:L, about 900-1300 L:L, or about 1000-1200 L:L; and
a hydrocarbon liquid hourly space velocity (LHSV) of about 0.2 to 10.0 L/h, 1.5 to 2.7 L/h, and/or 1.8-2.5 L/h.
10 . The method according to claim 1 , wherein the hydrocracking is performed in a presence of a bifunctional catalyst comprising:
an acidic support and an active hydrogenation component, the acidic support being alumina, amorphous silica-alumina or a zeolite, and the active hydrogenation component being NiMo, NiW, Pd or Pt.
11 . The method according to claim 1 , wherein the hydrocracking is performed under conditions which include:
a temperature of 250-450° C., 370-420° C., or 390-410° C.;
a pressure of 50-250 bar, 140-160 bar, or 145-155 bar;
a hydrogen to oil volume ratio of 500-2000 L:L, about 900-1300 L:L, or 1000-1200 L:L; and
a hydrocarbon liquid hourly space velocity (LHSV) of about 0.5 to 5.0 L/h, 1.0 to 2.5 L/h, or 1.4 to 1.9 L/h.
12 . The method according to claim 1 , wherein the fractionating of the hydrocracked stream comprises:
performing a mixture of purified hydrocarbons such that at least two fractions are formed as a lighter and as a heavier fraction.
13 . The method according to claim 1 , comprising:
performing the fractionating such that at least three fractions are formed, of which a first heavier fraction is a fraction with components having a 5 wt. % distillation point of >380° C. and a second heavier fraction is a fraction with components having a 5 to 95 wt. % distillation range from 330 to 410° C., and a third fraction has a 95 wt. % distillation point of <370° C.
14 . The method according to claim 1 , comprising:
hydroisomerisation of the produced mixture of purified hydrocarbons either before the step of fractionating the produced mixture of purified hydrocarbons or after the step of fractionating the produced mixture of purified hydrocarbons.