Homogeneous hydrolysis of 4,4’-Methylenediphenyl diisocyanate (MDI) in water

Author(s):  
Michael Neuland ◽  
Hans Allmendinger ◽  
Hans-Georg Pirkl ◽  
Robert J. West ◽  
Patrick M. Plehiers
ChemSusChem ◽  
2013 ◽  
Vol 6 (11) ◽  
pp. 2066-2068 ◽  
Author(s):  
Nima Nikbin ◽  
Stavros Caratzoulas ◽  
Dionisios G. Vlachos

1955 ◽  
Vol 58 (10) ◽  
pp. 790-795
Author(s):  
Taiseki Kunugi ◽  
Hiroshi Okada ◽  
Hideo Arai ◽  
Hisashi Machimoto

2011 ◽  
Vol 29 (4) ◽  
pp. 711-718 ◽  
Author(s):  
Qi Zhang ◽  
Yan Xiang ◽  
Ruxin Yang ◽  
Jiangju Si ◽  
Hong Guo

1957 ◽  
Vol 35 (9) ◽  
pp. 1010-1019 ◽  
Author(s):  
C. T. Bishop

A water soluble arabogalactan isolated from jack pine was shown to have a molar ratio of arabinose to galactose of 1:13, and a number average degree of polymerization of 53 ± 3. Fractionation data and electrophoresis indicated that the arabogalactan was homogeneous. Hydrolysis of the methyl ether of the polysaccharide yielded 2,3,5-tri-O-methyl-L-arabinose (4 moles); 2,3,4,6-tetra-O-methyl-D-galactose (12–13 moles); 2,3,4-tri-O-methyl-D-galactose (19 moles); 2,6-di-O-methyl-D-galactose (1 mole); and 2,4-di-O-methyl-D-galactose (14 moles). Some features of the structure of the arabogalactan are discussed on the basis of these results.


2012 ◽  
Vol 2012 ◽  
pp. 1-11 ◽  
Author(s):  
Václav Štengl ◽  
Tomáš Matys Grygar ◽  
Jana Velická ◽  
Jiří Henych ◽  
Snejana Bakardjieva

Nanometric particles of germanium-doped TiO2were prepared by homogeneous hydrolysis of TiOSO4and GeCl4in an aqueous solution using urea as the precipitation agent. Structural evolution during heating of these starting Ge-Ti oxide powders was studied by X-ray diffraction (XRD) and high-temperature X-ray powder diffraction (HTXRD). The morphology and microstructure changes were monitored by means of scanning electron microscopy (SEM), Raman and infrared spectroscopy (IR), specific surface area (BET), and porosity determination (BJH). The photocatalytic activity of all samples was determined by decomposition of Orange II dye under irradiation at 365 nm and 400 nm. Moderate doping with concentration upto value 2.05 wt.% positively influences azo dye degradation under UV and Vis light. Further improvement cannot be achieved by higher Ge doping. Effect of the annealing (200, 400, and 700°C) on photocatalysis and other properties has been assessed.


1951 ◽  
Vol 29 (9) ◽  
pp. 731-733 ◽  
Author(s):  
S. Epstein ◽  
C. A. Winkler

Measurements of the rates of alkaline hydrolysis of cyclotrimethylenetrinitramine (RDX) and cyclotetramethylenetetranitramine (HMX) in aqueous acetone show these two reactions to involve consecutive steps, the first of which is second order and rate controlling. Activation energies were estimated as 14 and 25 kcal. respectively. By establishing calibration curves, and controlling temperature, alkali concentration relative to concentration of explosive, and reaction time, the differential hydrolysis permits analysis of the HMX content of RDX(B) with an error of approximately ±0.2% HMX.


2014 ◽  
Vol 2014 ◽  
pp. 1-11
Author(s):  
Václav Štengl ◽  
Jiří Henych ◽  
Michaela Slušná ◽  
Tomáš Matys Grygar ◽  
Jana Velická ◽  
...  

Highly photoactive Ga3+-doped anatase modification of titania was prepared by homogeneous hydrolysis of aqueous solutions mixture of titanium oxo-sulphate TiOSO4and gallium(III) nitrate with urea. Incorporation of Ga3+into the anatase lattice has a clear positive effect on the photocatalytic activity under UV and Vis light irradiation up to a certain extent of Ga. Ga3+doping decreased the size of the crystallites, increased surface area, and affected texture of the samples. Higher amount of gallium leads to the formation of a nondiffractive phase, probably photocatalytically inactive. The titania sample with 2.18 wt.% Ge3+had the highest activity during the photocatalysed degradation in the UV and visible light regions; the total bleaching of dye Orange II was achieved within 29 minutes. Ga concentration larger than 5% (up to 15%) significantly inhibited the growth of the anatase crystal domains which formed the nondiffractive phase content and led to remarkable worsening of the photobleaching efficiency.


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