Method for photodecomposing dye in contaminated aqueous solutions with sunlight

Patent metadata

Field	Value
Publication number	US-2024424485-A1
Application number	US-202418829388-A
Country	US
Kind code	A1
Filing date	Sep 10, 2024
Priority date	Jun 11, 2019
Publication date	Dec 26, 2024
Grant date	—

Abstract

An efficient photocatalyst nanocomposite comprising reduced graphene oxide, noble metal, and a metal oxide prepared by a one-step method that utilizes date seed extract as a reducing and nanoparticle determining size agent. The photocatalyst of the invention is a more effective sunlight photocatalyst than that prepared by traditional method in the photo decomposition of organic compounds in contaminated water.

First claim

1 . (canceled)

2 : The method of claim 12 , wherein the gold/zinc/graphene oxide photocatalyst nanocomposite comprises rGO in an amount in the range of 48 wt. % to 52 wt. % of the total weight of the nanocomposite.

3 - 8 . (canceled)

9 : The method of claim 12 , wherein the gold/zinc/graphene oxide photocatalyst nanocomposite comprises 5 mol. % of Au based on the molar amount of the ZnO.

10 - 11 . (canceled)

12 : A method for making a gold/zinc/graphene oxide photocatalyst nanocomposite and photodecomposing a dye in a contaminated aqueous composition comprising:
preparing a date seed extract suspension by grinding a date seed and heating the ground date seed in water at a temperature in the range of 60 to 100° C. for a time in the range of 1 to 5 hours to form an extract suspension mixture, separating solids from the extract suspension mixture to form an extract mixture, then evaporating water from the extract mixture to obtain crystals of the date seed extract, preparing an aqueous suspension of zinc acetate, chloroauric acid, and graphene oxide, wherein the zinc acetate and chloroauric acid are present in an equimolar ratio; mixing the aqueous suspension with the date seed extract to form a mixture, and heating the mixture at temperature in the range of 100-200° C. for a time in the range of 10 to 20 hours to form the gold/zinc/graphene oxide photocatalyst nanocomposite; wherein the gold/zinc/graphene oxide photocatalyst nanocomposite comprises Au nanoparticles, hexagonal wurtzite ZnO, and reduced graphene oxide (rGO); wherein the Au nanoparticles are present in an amount of 2 mol. % to 10 mol. % based on the molar amount of the ZnO nanoparticles and the rGO is present in an amount of 48 wt. % to 52 wt. % of the total weight of the gold/zinc/graphene oxide photocatalyst nanocomposite, wherein the Au nanoparticles have a diameter in the range of 15 to 20 nm and are homogeneously distributed on the ZnO nanoparticles and on the rGO: the ZnO nanoparticles have a diameter in the range of 30 to 40 nm and are present on the rGO; then mixing the gold/zinc/graphene oxide photocatalyst nanocomposite with the dye-contaminated aqueous composition to form a treatment mixture; and exposing the treatment mixture to sunlight for 0.5 to 5 hours to photodecompose the dye and form purified water.

13 - 19 . (canceled)

20 . The method of claim 12 , wherein the dye-contaminated aqueous composition comprises one or more dyes selected from the group consisting of methyl orange, methylene blue, indigo, and tyrian purple.

21 . The method of claim 12 , wherein the date seed extract comprises flavonoids and polyphenolic compounds.

22 . The method of claim 12 , wherein the aqueous suspension of zinc acetate, chloroauric acid and graphene oxide is obtained by mixing a 5 mol % solution of chloroauric acid with an aqueous zinc acetate solution.

23 . The method of claim 12 , wherein heating the mixture is carried out in an autoclave.

Assignees

• Univ Imam Abdulrahman Bin Faisal

Inventors

• Alomair Nuhad Abdullah
• Mohamed Hanan Hussein Amin

Classifications

• B01J2235/10

  Infrared [IR] · CPC title

• B01J35/45

  Nanoparticles · CPC title

• B01J2235/15

  X-ray diffraction · CPC title

• B01J2235/30

  Scanning electron microscopy; Transmission electron microscopy · CPC title

• B01J2235/00

  Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title