Analysis of CO 2 solubility and absorption heat into 1-dimethylamino-2-propanol solution

2017 ◽  
Vol 170 ◽  
pp. 3-15 ◽  
Author(s):  
Helei Liu ◽  
Hongxia Gao ◽  
Raphael Idem ◽  
Paitoon Tontiwachwuthikul ◽  
Zhiwu Liang
Keyword(s):  
2021 ◽  
Vol 765 (1) ◽  
pp. 012054
Author(s):  
V Rajiman ◽  
H N A Halim ◽  
A M Shariff ◽  
U F M Ali ◽  
M I H M Dzahir

Soft Matter ◽  
2015 ◽  
Vol 11 (19) ◽  
pp. 3936-3945 ◽  
Author(s):  
Sang Min Lee ◽  
Young Chan Bae

Schematic depiction of a core–shell structure composed of the PMMA core and the PHEMA shell, and the influence of three co-solvents on the volume transition temperature of the core–shell gels in 1-propanol solution.


2018 ◽  
Vol 63 (5) ◽  
pp. 1454-1459 ◽  
Author(s):  
Zulkifli Idris ◽  
Nithin B. Kummamuru ◽  
Dag A. Eimer

1990 ◽  
Vol 180 ◽  
Author(s):  
Mostafa M. Amini ◽  
Michael D. Sacks

ABSTRACTSingle-phase KNbO3 was prepared using bimetallic alkoxides. Potassium-niobium ethoxide, KNb(OC2H5)6, and potassium-niobium propoxide, KNb(OC3H7)6, were synthesized and subsequently hydrolyzed using several water concentrations. Potassium-deficient particles were rapidly precipitated when higher water concentrations were used and this resulted in the formation of a multiphase material after calcination. In contrast, single-phase KNbO3 powders could be prepared by two methods: (1) hydrolysis of KNb(OC3H7)6/propanol solutions using 1 mole water (per mole of propoxide) added as a water/propanol solution and (2) hydrolysis of KNb(OC2H5)6,/ethanol solutions using 1 mole of water (per mole of ethoxide) added as a water/methanol solution. The latter method was also used to form thin films of KNbO3.


2005 ◽  
Vol 09 (09) ◽  
pp. 646-650 ◽  
Author(s):  
Kuninobu Kasuga ◽  
Katsuyori Yashiki ◽  
Tamotsu Sugimori ◽  
Makoto Handa

1,4,8,11,15,18,22,25-octakis(p-t-butylbenzyloxy)phthalocyanine complexes of magnesium(II), nickel(II) and copper(II) were prepared by refluxing the propanol solution of 3,6-di(p-t-butylbenzyloxy)phthalonitrile in the presence of magnesium turnings. The complexes showed intense Q-bands between 740 and 750 nm in chloroform. The magnesium(II) complex showed an additional weak band at 807 nm in chloroform, while the nickel(II) and copper(II) did not. The Q-band of the magnesium(II) species was red-shifted with increase of acetic acid in the solvent mixture of chloroform and acetic acid; 745, (765, 807) and (810, 868 nm) in chloroform, 0.1% (v/v) acetic acid and 60% (v/v) acetic acid, respectively. The magnesium(II) complex has bands at 900 and 999 nm in trifluoroacetic acid. In the solvent mixture of 1% (v/v) acetic acid, the red-shift of the Q-band was larger for the magnesium(II) derivative, a little for the nickel(II) and scarcely for the copper(II), respectively. The shift was explained by protonation of the external nitrogen atoms of the phthalocyanine ring.


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