Method for producing bioresourced propionic acid from glycerol
US-9206110-B2 · Dec 8, 2015 · US
US2024228421A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024228421-A1 |
| Application number | US-202218148648-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 30, 2022 |
| Priority date | Dec 30, 2022 |
| Publication date | Jul 11, 2024 |
| Grant date | — |
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A composition and a method for preparing the same are provided. The method for preparing the composition includes providing a polyethylene terephthalate waste. The polyethylene terephthalate waste is subjected to a depolymerization in the presence of a catalyst and an alcoholysis agent to obtain a mixture, wherein an oxidizing atmosphere is continuously introduced into the depolymerization. The mixture is subjected to a solid-liquid separation to obtain a solid. The solid is subjected to a purification to obtain the composition.
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What is claimed is: 1 . A method for preparing a composition, comprising: providing a polyethylene terephthalate waste; subjecting the polyethylene terephthalate waste to a depolymerization in the presence of a catalyst and an alcoholysis agent to obtain a mixture, wherein an oxidizing atmosphere is continuously introduced into the depolymerization; subjecting the mixture to a solid-liquid separation, obtaining a solid; and subjecting the solid to a purification, obtaining the composition. 2 . The method as claimed in claim 1 , wherein the polyethylene terephthalate waste is polyethylene terephthalate bottle sheet, polyethylene terephthalate fabric, polyethylene terephthalate film, or a combination thereof. 3 . The method as claimed in claim 1 , wherein the catalyst comprises metal oxide, metal hydroxide, metal alkoxide, metal organic acid salt, metal carbonate, or a combination thereof. 4 . The method as claimed in claim 1 , wherein the catalyst comprises lithium oxide, lithium hydroxide, lithium acetate, lithium carbonate, sodium oxide, sodium hydroxide, sodium acetate, sodium carbonate, potassium oxide, potassium hydroxide, potassium acetate, magnesium oxide, magnesium hydroxide, magnesium acetate, carbonic acid Magnesium, calcium oxide, calcium hydroxide, calcium acetate, calcium carbonate, titanium oxide, titanium hydroxide, titanium acetate, titanium carbonate, zinc oxide, zinc hydroxide, zinc acetate, zinc carbonate, manganese oxide, manganese hydroxide, manganese acetate, manganese carbonate, tin acetate, antimony oxide, sodium methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, or a combination thereof. 5 . The method as claimed in claim 1 , wherein the alcoholysis agent is a dihydric alcohol. 6 . The method as claimed in claim 1 , wherein the alcoholysis agent is mono-ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, or a combination thereof. 7 . The method as claimed in claim 1 , wherein the oxidizing atmosphere comprises oxygen, ozone, or a combination thereof. 8 . The method as claimed in claim 1 , wherein the depolymerization has a temperature of 140° C. to 240° C., and the depolymerization has a process time of 0.5 hour to 8 hours. 9 . The method as claimed in claim 1 , wherein the purification comprises a recrystallization treatment. 10 . The method as claimed in claim 9 , wherein the purification further comprises an adsorption treatment. 11 . The method as claimed in claim 1 , wherein a ratio of a flow rate of the oxidizing atmosphere to a weight of the polyethylene terephthalate waste and the alcoholysis agent is 100 sccm/Kg to 3,000 sccm/Kg. 12 . A composition, comprising: 99.5 wt % to 99.997 wt % of a compound, wherein the compound is bis(2-hydroxyethyl) terephthalate, or a combination of bis(2-hydroxyethyl) terephthalate and bis(2-hydroxyethyl) terephthalate oligomer; 0.001 wt % to 0.25 wt % of mono(2-hydroxyethyl) terephthalate; and 0.001 wt % to 0.25 wt % of 2-hydroxyethyl[2-(2-hydroxyethoxy)ethyl]terephthalate, based on the weight of the composition. 13 . The composition as claimed in claim 12 , wherein the compound is a combination of bis(2-hydroxyethyl) terephthalate (BHET) and bis(2-hydroxyethyl) terephthalate oligomer, wherein an amount of bis(2-hydroxyethyl) terephthalate is 97 wt % to 99.897 wt %, and an amount of bis(2-hydroxyethyl) terephthalate oligomer is 0.1 wt % to 2.45 wt %, based on the weight of the composition. 14 . The composition as claimed in claim 12 , further comprising: 0.00001 wt % to 0.003 wt % of catalyst, based on the weight of the composition.
Titanium; Oxides or hydroxides thereof · CPC title
Terephthalic acid esters · CPC title
Preparation of carboxylic acid esters · CPC title
by reacting an ester group with a hydroxy group · CPC title
containing hydroxyl groups · CPC title
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