Preparation of polymer modified bitumen (PMB) from polyethylene terephthalate (PET) derived polyamido amine

Patent metadata

Field	Value
Publication number	US-9528001-B2
Application number	US-201514659089-A
Country	US
Kind code	B2
Filing date	Mar 16, 2015
Priority date	Mar 26, 2014
Publication date	Dec 27, 2016
Grant date	Dec 27, 2016

Abstract

The present invention relates a novel approach to prepare Polymer Modified Bitumen by using terephthalamide additives, derived from PET, for improving bitumen quality. Particularly, the present invention provides a process to utilize waste PET, which is a threat to environment and is available commercially in different physical forms, for conversion into industrially useful additive for bituminous product.

First claim

We claim:

1. A process for preparing modified bitumen, the process comprising of:
(i) reacting polyethylene terephthalate (PET) with amines or polyamines to obtain amido amines or polyamido amines;
(ii) reacting the amido amines or polyamido amines as obtained in step (i) with isocyanate or polyisocyanate and bitumen in a solvent to obtain modified bitumen.

2. The process as claimed in claim 1 , wherein amido amines or polyamido amines are reacted with isocyanate or polyisocyanate, prior to reacting with bitumen.

3. The process as claimed in claim 1 , wherein amido amines or polyamido amines; isocyanate or polyisocyanate; and bitumen are reacted simultaneously.

4. The process as claimed in claim 1 , wherein amido amines, or polyamido amines are present in 0.05-30% wt/wt of bitumen.

5. The process as claimed in claim 1 , wherein the isocyanates or polyisocyanates are present in 0.05-30% wt/wt of bitumen.

6. The process as claimed in claim 1 , wherein the reaction is conducted at a temperature of 50° C. to 190° C.

7. The process as claimed in claim 1 , wherein the reaction is conducted for a period of 10 minutes to 8 hours.

8. The process as claimed in claim 1 , wherein amines or polyamines are selected from the group comprising ethylene diamine, triethylene tetramine, propylene diamine, trimethylene diamine, hexamethylene diamine, decamethylene diamine, octamethylene diamine, di(heptamethylene)triamine, tripropylene tetramine, tetraethylene pentamine, trimethylene diamine, pentaethylene hexamine, di(trimethylene)triamine, N-(2-aminoethyl)piperazine, 1,4-bis(2-aminoethyl)piperazine, an aromatic polyamine selected from phenylene and napthylene diamines or hydrazines such as hydrazine, organo-hydrazines having hydrocarbon-based substituents of up to about 30 carbon atoms.

9. The process as claimed in claim 1 , wherein isocyantes or polyisocyanates are selected from the group comprising hexamethylene diisocyanate (HDI), trimethyl hexamethylene diisocyanate (HMDI), ethylene diisocyanate, ethylidene diisocyanate, propylene, butylene diisocyanate, diisocyanate dichlorohexaméthylène, furfurylidene diisocyanate, cycloaliphatic polyisocyanates, like isophorone diisocyanate (IPDI), cyclopentylene-1,3-diisocyanate, cyclohexylenedimethylene-1-diisocyanate, cyclohexylene-1,2-diisocyanate, and mixtures thereof, aromatic polyisocyanates like the 4,4′-diphenyl diisocyanate (MDI) and its isomers, such as 2,4′- and 2,2′-diphenylmethane diisocyanate, toluene diisocyanate (TDI) and isomers thereof, particularly the 2,4- and 2,6-toluene diisocyanate, 2,2-diphenylpropane-4′-diisocyanate, p-phenylene diisocyanate, m-phenylene diisocyanate, xylene diisocyanate, 1,4-naphthalene diisocyanate, 1,5-naphthalene diisocyanate, azobenzene-4,4′-diisocyanate, diphenyl sulfone-4,4′-diisocyanate, 1-chlorobenzene-2,4-diisocyanate, 4,4′,4″-triisocyanatotripheriyl methane, 1,3,5-triisocyanato-tetraisocyanate, and mixtures thereof.

10. The process as claimed in claim 1 , wherein the solvent is selected from dimethyl formamide (DMF), dimethyl sulphoxide (DMSO), acetone, methylethyl ketone, tetrahydrofuran (THF), ethyl acetate, benzene, toluene, chlorobenzene, hexane, cylohexane, xylene and dichloro methane (DCM).

11. The process as claimed in claim 1 , wherein the polyisocyante is diisocyanates, selected from MDI and its isomers, TDI and its isomers, HDI, IPDI and derivatives thereof.

12. The process as claimed in claim 1 , wherein amido amines or polyamido amines and isocyanate or polyisocyanate are reacted to obtain a polyurea.

13. A bituminous cement mixture comprising polyurethane or polyurea polymers as claimed in claim 12 , in body of bitumen.

14. A bituminous concrete comprising bituminous cement mixture of claim 1 and an aggregate.

Assignees

• Indian Oil Corp Ltd

Inventors

• Bhatnagar Akhilesh Kumar
• Padhan Rabindra Kumar
• Gupta Anurag Ateet
• Raman Naduhatty Selai

Classifications

• C08L75/02

  Polyureas · CPC title

• C08L75/12

  from compounds containing nitrogen and active hydrogen, the nitrogen atom not being part of an isocyanate group · CPC title

• C08G18/603

  Polyamides · CPC title

• C08G73/028

  Polyamidoamines · CPC title

• C08L75/00

  Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers · CPC title