IP Library Granted Patent US 9,950,315
Granted Patent B2
US 9,950,315 · App. 14/842,301 · Granted Apr 24, 2018

Ni—MgO—ZnO solid catalysts for syngas preparation and process for the preparation thereof

Inventors: Rajaram Bal (Dehradun, IN); Rajib Kumar Singha (Dehradun, IN); Chandrashekar Pendem (Dehradun, IN); Laxmi Narayan Siva Kumar Konathala (Dehradun, IN); Ankur Bordoloi (Dehradun, IN); Sandeep Saran (Dehradun, IN)
Assignee: Council of Scientific & Industrial Research
B01J23/80B01J37/009B01J37/031B01J37/04B01J37/08C01B3/40C01B2203/0238C01B2203/1058C01B2203/1076C01B2203/1241Y02P20/142Y02P20/52
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Quick Facts
Patent No.
US 9,950,315
App. No.
14/842,301
Granted
Apr 24, 2018
Kind
B2
Abstract

The present invention provides a process and catalyst for the production of synthesis gas (a mixture of CO and H 2 ) by reforming of methane with carbon dioxide. The process provides a direct single step selective vapor phase dry reforming of methane with carbon dioxide to produce synthesis gas over Ni—MgO—ZnO catalyst between temperature range of 600° C. to 800° C. at 1 atmospheric pressure. The process provides a methane conversion of 5-95% with H 2 to CO mole ratio of 0.83-1.2.

Claims (11)

1. A process for the preparation of a Ni—MgO—ZnO solid catalyst, the catalyst comprising:

a) Ni in the range of 2-10%,

b) MgO in the range of 2-10% and

c) ZnO in the range of 90-95%,

wherein the said process comprises the steps of:

i. dissolving Zinc nitrate hexahydrate and Magnesium nitrate hexahydrate in water,

ii. adding Nickel nitrate hexahydrate in water to the mixture as obtained in step (i) followed by stirring to obtain a homogenous mixture;

iii. adding a solution of CTAB (cetyltrimethylammonium bromide) in ethanol to the mixture as obtained in step (ii) with stirring for period in the range of 1 to 2 hours followed by adding hydrazine hydrate with adjusting the pH of the solution in the range of 8-12 to obtain a solution,

iv. stirring the solution as obtained in step (iii) for a period in the range of 1-3 hours followed by autoclaving for period in the range of 12 to 48 hours at a temperature in the range of 160 to 180° C. to obtain a precipitate;

v. filtering the precipitate as obtained in step (iv) with water and drying at a temperature ranging between 60 to 110° C. for a time period ranging between 12-20 hours followed by calcining at a temperature in the range of 400-750° C. for a time period of 4-8 hours to obtain the Ni—MgO—ZnO catalyst.

2. The process as claimed in claim 1 , wherein the Ni to Ni—MgO—ZnO of the catalyst varied in the range of 2 to 10%.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY NAME PREVIOUSLY RECORDED ON REEL 036831 FRAME 0046. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Apr 5, 2016
From: RAJARAM, BAL; KUMAR, SINGHA RAJIB; CHANDRASHEKAR, PENDEM; SIVAKUMAR, KONATHALA LAXMI NARAYAN; ANKUR, BORDOLOI; SANDEEP, SARAN
To: COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH
Reel/Frame 038360/0974 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2015
From: BAL, RAJARAM; SINGHA, RAJIB KUMAR; PENDEM, CHANDRASHEKAR; KONATHALA, LAXMI NARAYAN SIVA KUMAR; BORDOLOI, ANKUR; SARAN, SANDEEP
To: COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH
Reel/Frame 036831/0046 →
Priority Claims (1)
IN 2508/DEL/2014 · Sep 2, 2014 · national
Continuity (1)
Related Publication 20160059217A1 · Mar 3, 2016