- Home
- Search Results
- Page 1 of 1
Search for: All records
-
Total Resources3
- Resource Type
-
0000000003000000
- More
- Availability
-
30
- Author / Contributor
- Filter by Author / Creator
-
-
Zhu, Guanghui (3)
-
Chen, Huiyong (2)
-
Holdren, Scott (2)
-
Liu, Dongxia (2)
-
Wei, Lu (2)
-
Bai, Yuanyuan (1)
-
Berens, Samuel (1)
-
Chen, Yu-Sheng (1)
-
Liu, Yang (1)
-
Lively, Ryan P. (1)
-
Lyndon, Richelle (1)
-
Ma, Yao (1)
-
Pan, Yanbo (1)
-
Pang, Simon H. (1)
-
Shang, Wenjin (1)
-
Sholl, David S. (1)
-
Shulman, Emily (1)
-
Song, Kechen (1)
-
Sun, Runcang (1)
-
Tran, Dat T. (1)
-
- Filter by Editor
-
-
& Spizer, S. M. (0)
-
& . Spizer, S. (0)
-
& Ahn, J. (0)
-
& Bateiha, S. (0)
-
& Bosch, N. (0)
-
& Brennan K. (0)
-
& Brennan, K. (0)
-
& Chen, B. (0)
-
& Chen, Bodong (0)
-
& Drown, S. (0)
-
& Ferretti, F. (0)
-
& Higgins, A. (0)
-
& J. Peters (0)
-
& Kali, Y. (0)
-
& Ruiz-Arias, P.M. (0)
-
& S. Spitzer (0)
-
& Sahin. I. (0)
-
& Spitzer, S. (0)
-
& Spitzer, S.M. (0)
-
(submitted - in Review for IEEE ICASSP-2024) (0)
-
-
Have feedback or suggestions for a way to improve these results?
!
Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher.
Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?
Some links on this page may take you to non-federal websites. Their policies may differ from this site.
-
The separation of xylene isomers still remains an industrially challenging task. Here, porous purine-based metal–organic frameworks (MOFs) have been synthesized and studied for their potential in xylene separations. In particular, Zn(purine)I showed excellent para -xylene/ ortho -xylene separation capability with a diffusion selectivity of 6 and high equilibrium adsorption selectivity as indicated by coadsorption experiments. This high selectivity is attributed to the shape and size of the channel aperture within the rigid framework of Zn(purine)I.more » « less
-
Wei, Lu; Song, Kechen; Wu, Wei; Holdren, Scott; Zhu, Guanghui; Shulman, Emily; Shang, Wenjin; Chen, Huiyong; Zachariah, Michael R.; Liu, Dongxia (, Journal of the American Chemical Society)
-
Bai, Yuanyuan; Wei, Lu; Yang, Mengfei; Chen, Huiyong; Holdren, Scott; Zhu, Guanghui; Tran, Dat T.; Yao, Chunli; Sun, Runcang; Pan, Yanbo; et al (, Journal of Materials Chemistry A)The synthesis of hierarchical lamellar zeolites with a controlled meso-/microporous morphology and acidity is an expanding area of research interest for a wide range of applications. Here, we report a one-step synthesis of a hierarchical meso-/microporous lamellar MFI–Sn/Al zeolite ( i.e. , containing both Lewis acidic Sn- and Al-sites and a Brønsted acidic Al–O(H)–Si site) and its catalytic application for the conversion of glucose into 5-(ethoxymethyl)furfural (EMF). The MFI–Sn/Al zeolite was prepared with the assistance of a diquaternary ammonium ([C 22 H 45 –N + (CH 3 ) 2 –C 6 H 12 –N + (CH 3 ) 2 –C 6 H 13 ]Br 2− , C 22-6-6 ) template in a composition of 100SiO 2 /5C 22-6-6 /18.5Na 2 O/ x Al 2 O 3 / y SnO 2 /2957H 2 O ( x = 0.5, 1, and 2; y = 1 and 2, respectively). The MFI–Sn/Al zeolites innovatively feature dual meso-/microporosity and dual Lewis and Brønsted acidity, which enabled a three-step reaction cascade for EMF synthesis from glucose in ethanol solvent. The reaction proceeded via the isomerization of glucose to fructose over Lewis acidic Sn sites and the dehydration of fructose to 5-hydroxymethylfurfural (HMF) and then the etherification of HMF and ethanol to EMF over the Brønsted acidic Al–O(H)–Si sites. The co-existence of multiple acidities in a single zeolite catalyst enabled one-pot cascade reactions for carbohydrate upgrading. The dual meso-/microporosity in the MFI–Sn/Al zeolites facilitated mass transport in processing of bulky biomass molecules. The balance of both types of acidity and meso-/microporosity realized an EMF yield as high as 44% from the glucose reactant.more » « less
An official website of the United States government
