IP Library Granted Patent US 12,440,810
Granted Patent B1
US 12,440,810 · App. 19/243,763 · Granted Oct 14, 2025

Method for photocatalytic degradation of organic pollutants

Inventors: Umair Baig (Dhahran, SA); Abdul Waheed (Dhahran, SA)
Assignee: KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS
B01D71/68B01D71/0211B01D71/481B82Y30/00
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Quick Facts
Patent No.
US 12,440,810
App. No.
19/243,763
Granted
Oct 14, 2025
Kind
B1
Abstract

A membrane including a polysulfone/polyethylene terephthalate (PSf/PET) support and an active layer on an outer surface of the PSf/PET support. The active layer comprises reacted units of a diacyl chloride compound, a tetra-amine compound, and a nanocomposite including graphitic carbon nitride and polypyrrole. The membrane of the present disclosure is self-cleaning following exposure to radiation and finds application in water decontamination and de-salination.

Claims (29)

1. A method for photocatalytically degrading an organic pollutant in an aqueous solution, comprising:

exposing a photocatalytic membrane to the aqueous solution containing the organic pollutant to adsorb at least a portion of the organic pollutant onto the photocatalytic membrane; then

irradiating the photocatalytic membrane with solar light to degrade the organic pollutant;

wherein the photocatalytic membrane comprises:

a polysulfone/polyethylene terephthalate (PSf/PET) support; and

an active layer on an outer surface of the PSf/PET support,

wherein the active layer comprises reacted units of:

a diacyl chloride compound;

a tetra-amine compound; and

a nanocomposite comprising graphitic carbon nitride and polypyrrole.

2. The method of claim 1 , wherein the graphitic carbon nitride is bonded to at least one terminal end of the polypyrrole in the nanocomposite.

3. The method of claim 1 , wherein the graphitic carbon nitride has triazine and heptazine rings.

4. The method of claim 1 , wherein the graphitic carbon nitride is in the form of nanosheets.

5. The method of claim 4 , wherein the nanosheets have a thickness of 10-100 nm.

6. The method of claim 1 , wherein the diacyl chloride compound is an aromatic ring substituted with two acyl chloride groups.

7. The method of claim 1 , wherein the tetra-amine compound is a linear or branched aliphatic amine with of 2-50 carbons and four amine groups.

8. The method of claim 1 , wherein the photocatalytic membrane has 0.01 to 5 wt % of the nanocomposite based on the total weight of the active layer.

9. The method of claim 1 , wherein particles of the active layer have a globular shape.

10. The method membrane of claim 1 , wherein particles of the active layer are not agglomerated.

11. The method of claim 1 , wherein particles of the active layer have an average size of 50-200 nm.

12. The method of claim 1 , wherein the photocatalytic membrane comprises 50-70 at. % carbon, 25-35 at. % sulfur, 5-15 at. % oxygen, and 1-10 at. % nitrogen, based on a total number of atoms in the photocatalytic membrane.

13. The method of claim 1 , wherein the photocatalytic membrane has a surface roughness of less than 24 nm.

14. The method of claim 1 , wherein the photocatalytic membrane has a water contact angle of less than 90°.

15. The method an of claim 1 , wherein the active layer of the photocatalytic membrane covers at least 95% of the outer surface of the polysulfone/polyethylene terephthalate (PSf/PET) support.

16. The method of claim 1 , wherein the photocatalytic membrane is porous, having pores with an average diameter of less than 1 nm.

17. The method of claim 1 , wherein the photocatalytic membrane has a permeate flux of 40 to 100 L m −2 h −1 at 10-30 bar.

18. The method of claim 1 , wherein the photocatalytic membrane rejects at least 60% of inorganic salts.

19. The method of claim 1 , wherein the photocatalytic membrane is self-cleaning following exposure to the solar light.

20. The membrane of claim 19 , wherein the solar light includes radiation having a wavelength of from 400-700 nm.

Continuity (1)
Continuation 18084085 · Dec 19, 2022
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