Rapid in situ synthesis of MgAl-LDH on η-Al2O3 for efficient hydrolysis of urea in wastewater

Author(s):  
Chenyuan Guo ◽  
Shuguang Shen ◽  
Meina Li ◽  
Ying Wang ◽  
Jing Li ◽  
...  
2018 ◽  
Vol 18 (7) ◽  
pp. 4714-4719 ◽  
Author(s):  
Abdullah M Al-Enizi ◽  
Robert M Brooks ◽  
M. M Ahmad ◽  
M. M El-Halwany ◽  
Mohamed H El-Newehy ◽  
...  

2016 ◽  
Vol 5 (1) ◽  
pp. 708-713 ◽  
Author(s):  
Heri Satria ◽  
Kosuke Kuroda ◽  
Takatsugu Endo ◽  
Kenji Takada ◽  
Kazuaki Ninomiya ◽  
...  

2004 ◽  
Vol 550 (1-3) ◽  
pp. 26-34 ◽  
Author(s):  
Jianxin Tang ◽  
Nongyue He ◽  
Libo Nie ◽  
Pengfeng Xiao ◽  
Hong Chen

2004 ◽  
Vol 19 (11) ◽  
pp. 3290-3297 ◽  
Author(s):  
Toshinobu Yogo ◽  
Tomoe Yamamoto ◽  
Wataru Sakamoto ◽  
Shin-ichi Hirano

Nanocrystalline BaTiO3 particle–polymer hybrid was synthesized by polymerization and hydrolysis of [2-(methacryloxy)ethoxy]triisopropoxytitanium (MEPT) and barium alkoxide. The precursor for hybrid was synthesized from prepolymerized MEPT and barium alkokide, which was then hydrolyzed to form BaTiO3 particle–polymer hybrids below 100 °C. BaTiO3 particles increased in crystallinity when the amount of water for hydrolysis increased. The nanocrystalline particles were identified to be BaTiO3 by electron diffraction. Nanometer-sized BaTiO3 particle–polymer hybrid was shaped to a film with a dielectric constant of 8.2 at 10 kHz. A suspension consisting of the hybrid and silicone oil responded to a direct-current field, exhibiting a typical electrorheological behavior.


ChemPlusChem ◽  
2019 ◽  
Vol 84 (4) ◽  
pp. 382-386 ◽  
Author(s):  
Chenlu Yang ◽  
Yana Men ◽  
Yuezhi Xu ◽  
Lijing Liang ◽  
Ping Cai ◽  
...  

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.


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