Effect of Solvent Type on High-Temperature Thermal Gradient Interaction Chromatography of Polyethylene and Ethylene-1-Octene Copolymers

2014 ◽  
Vol 216 (1) ◽  
pp. 38-48 ◽  
Author(s):  
Abdulaziz Alghyamah ◽  
João B. P. Soares
Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 204
Author(s):  
Yu Li ◽  
Chumin Liang ◽  
Xunzhong Zou ◽  
Jinzhong Gu ◽  
Marina V. Kirillova ◽  
...  

Three 2D coordination polymers, [Cu2(µ4-dpa)(bipy)2(H2O)]n∙6nH2O (1), [Mn2(µ6-dpa)(bipy)2]n (2), and [Zn2(µ4-dpa)(bipy)2(H2O)2]n·2nH2O (3), were prepared by a hydrothermal method using metal(II) chloride salts, 3-(2′,4′-dicarboxylphenoxy)phthalic acid (H4dpa) as a linker, as well as 2,2′-bipyridine (bipy) as a crystallization mediator. Compounds 1–3 were obtained as crystalline solids and fully characterized. The structures of 1–3 were established by single-crystal X-ray diffraction, revealing 2D metal-organic networks of sql, 3,6L66, and hcb topological types. Thermal stability and catalytic behavior of 1–3 were also studied. In particular, zinc(II) coordination polymer 3 functions as a highly active and recoverable heterogeneous catalyst in the mild cyanosilylation of benzaldehydes with trimethylsilyl cyanide to give cyanohydrin derivatives. The influence of various parameters was investigated, including a time of reaction, a loading of catalyst and its recycling, an effect of solvent type, and a substrate scope. As a result, up to 93% product yields were attained in a catalyst recoverable and reusable system when exploring 4-nitrobenzaldehyde as a model substrate. This study contributes to widening the types of multifunctional polycarboxylic acid linkers for the design of novel coordination polymers with notable applications in heterogeneous catalysis.


1969 ◽  
Vol 30 (1-2) ◽  
pp. 50-56 ◽  
Author(s):  
B.E. Fryxell ◽  
E.A. Aitken

2012 ◽  
Vol 312 (1) ◽  
pp. 88-96 ◽  
Author(s):  
Zhe Zhou ◽  
Rongjuan Cong ◽  
Yiyong He ◽  
Manjiri Paradkar ◽  
Mehmet Demirors ◽  
...  

2005 ◽  
Vol 61 (11-12) ◽  
pp. 587-593 ◽  
Author(s):  
W. Kiridena ◽  
C. DeKay ◽  
N. D. Villiere ◽  
W. W. Koziol ◽  
C. F. Poole

1998 ◽  
Vol 35 (8) ◽  
pp. 905-922 ◽  
Author(s):  
Haiming Yang ◽  
Kurt Kyser ◽  
Kevin Ansdell

Metamorphic assemblages differ between the metasedimentary MacLean Lake belt and the adjacent Central Metavolcanic belt in the La Ronge domain, Trans-Hudson Orogen. The former consists of meta-arkoses, psammitic gneisses, metaconglomerates, and calc-silicate gneisses of upper amphibolite facies (600-740°C, 440-660 MPa) with local migmatization, whereas the latter is comprised mainly of metavolcanic and plutonic rocks, with minor metasedimentary schists of greenschist to lower amphibolite facies (480-630°C, 520-560 MPa). Petrographic evidence indicates that peak metamorphic conditions were reached towards the end of D1 deformation during which the Central Metavolcanic belt was thrust onto the MacLean Lake belt along the McLennan Lake tectonic zone, which separates the two belts. Peak metamorphic assemblages did not undergo retrograde alteration during D2 deformation, indicating that high temperature was maintained during D2 deformation. Differences in pressure (P) and temperature (T) between the northeastern and southwestern parts of the Central Metavolcanic belt may have resulted from tilting along strike after peak metamorphism. Peak temperatures increase gradually from the Central Metavolcanic belt to MacLean Lake belt across the McLennan Lake tectonic zone. Peak pressures in the two belts are similar, implying that the Central Metavolcanic belt thrust sheet was probably thin. The P-T data for the MacLean Lake belt indicate a relatively high thermal gradient (40-50°C/km), similar to that in the metasedimentary Kisseynew domain in the orogen.


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