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Showing 1-7 of 7 results for "186783" within Papers
Chenfeng He et al.
Journal of colloid and interface science, 466, 168-177 (2016-01-02)
The effect of annealing on the surface hydrophilicity of various representative classes of hydrocarbon-based proton exchange membranes (PEMs) is investigated. In all cases, a more hydrophilic membrane surface develops after annealing at elevated temperatures. The annealing time also had some
C Eriksson et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 30(10), 871-877 (1992-10-01)
The herbicides dichlobenil (2,6-dichlorobenzonitrile), chlorthiamid (2,6-dichlorothiobenzamide) and their environmental degradation product 2,6-dichlorobenzamide are irreversibly bound and toxic to the olfactory mucosa following single injections in mice (Brandt et al., Toxicology and Applied Pharmacology 1990, 103, 491-501; Brittebo et al., Fundamental
Synthesis and properties of phenolphthalein-based polyarylene ether nitrile copolymers.
Li C, et al.
Materials Letters, 60(1), 137-141 (2006)
Chenchen Liu et al.
Polymers, 11(7) (2019-07-07)
Poly(arylene ether nitrile)s with sulfonic and carboxylic groups (SCPEN) were synthesized to investigate their electrical properties. This new series of copolymers were prepared by copolymerization of phenolphthalein, potassium hydroquinonesulfonate, and 2,6-difluorobenzonitrile, in different mole ratios. Their thermal, mechanical and dielectric
Xiaocan Liu et al.
Polymers, 11(9) (2019-08-31)
Porous materials with high specific surface area possess a broad application prospect in the treatment of wastewater. In this work, sulfonated poly(arylene ether nitrile) (SPEN) functionalized with a carboxylic acid group was successfully synthesized, which was subsequently transformed into SPEN
New polymer syntheses, 15 Syntheses of aromatic polyethers from difluorobenzonitriles and silylated diphenols.
Kricheldorf HR, et al.
Makromol. Chem., Rapid Commun., 8(11), 529-534 (1987)
Synthesis and laboratory evaluation of 1-(2,6-disubstituted benzoyl)-3-phenylureas, a new class of insecticides. II. Influence of the acyl moiety on insecticidal activity.
K Wellinga et al.
Journal of agricultural and food chemistry, 21(6), 993-998 (1973-11-01)
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