IP Library Granted Patent US 12,465,895
Granted Patent B2
US 12,465,895 · App. 19/243,771 · Granted Nov 11, 2025

Porous water decontamination membrane

Inventors: Umair Baig (Dhahran, SA); Abdul Waheed (Dhahran, SA)
Assignee: KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS
B01D71/68B01D71/0211B01D71/481B82Y30/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,465,895
App. No.
19/243,771
Granted
Nov 11, 2025
Kind
B2
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 (25)

1 . A porous water decontamination membrane, comprising:

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

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

wherein the crosslinked polyamide active layer comprises reacted units of:

a diacyl chloride compound;

a tetra-amine compound; and

a homogeneous nanocomposite comprising graphitic carbon nitride nanosheets and polypyrrole;

wherein the graphitic carbon nitride nanosheets are bonded to at least one terminal end of the polypyrrole in the nanocomposite.

2 . The membrane of claim 1 , wherein the graphitic carbon nitride nanosheets has triazine and hepta zine rings.

3 . The membrane of claim 1 , wherein the graphitic carbon nitride nanosheets have a thickness of 10-100 nm.

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

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

6 . The membrane of claim 1 , wherein the membrane has 0.01 to 5 wt % of the nanocomposite based on the total weight of the crosslinked polyamide active layer.

7 . The membrane of claim 1 , wherein particles of the crosslinked polyamide active layer have a globular shape.

8 . The membrane of claim 1 , wherein particles of the crosslinked polyamide active layer are not agglomerated.

9 . The membrane of claim 1 , wherein particles of the crosslinked polyamide active layer have an average size of 50-200 nm.

10 . The membrane of claim 1 , having 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 membrane.

11 . The membrane of claim 1 , having a surface roughness of less than 24 nm.

12 . The membrane of claim 1 , having a water contact angle of less than 90°.

13 . The membrane of claim 1 , wherein the crosslinked polyamide active layer covers at least 95% of the outer surface of the polysulfone/polyethylene terephthalate (PSf/PET) support.

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

15 . The membrane of claim 1 , having a permeate flux of 40 to 100 L m −2 h −1 at 10-30 bar.

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

17 . The membrane of claim 1 , wherein the membrane is self-cleaning following exposure to radiation.

18 . The membrane of claim 17 , wherein the radiation is from 400-700 nm.

Continuity (2)
Continuation 18084085 · Dec 19, 2022
Related Publication 20250312754A1 · Oct 9, 2025
References Cited (10)
US 11426343B2 · Chiatello et al. · 2022 [cited by applicant]
US 20140319044A1 · Giannelis et al. · 2014 [cited by applicant]
US 20230330644A1 · Faisal · 2023 [cited by examiner]
CN 103680996B · 2017 [cited by applicant]
CN 111018041A · 2020 [cited by examiner]
CN 112156662A · 2021 [cited by examiner]
CN 112495436A · 2021 [cited by applicant]
CN 112156662B · 2021 [cited by applicant]
Balakumar, et al. ; Synergistic temary porous CN-PPy-MMt nanocomposite for efficient photocatalytic metronidazole mineralization performance, mechanism, and pasthways ; Environmental Science: Nano, Issue 8 ; 2021 ; Abst… [cited by applicant]
Zhou, et al. ; Uniformly assembled polypyrrole-covered bacterial cellulose/g-C3N4 flexible nanofiber membrane for catalytic degradation of tetracycline hydrochloride ; Journal of Water Process Engineering, vol. 47 ; Jun… [cited by applicant]