scholarly journals Application of Vinyl ether Copolymers for Surface Modification of Carbon Black

Author(s):  
A. V. Perchenok ◽  
E. V. Suvorova ◽  
A. A. Farmakovskaya ◽  
V. Kohlert

In this work, the possibility of stabilizing aqueous dispersed systems of carbon with vinyl ether copolymers of various composition and structure was investigated. It was shown that the presence of hydrophobic fragments in the macromolecule chain plays a significant role and positively affects the results of stabilization of aqueous dispersions of carbon particles. It was shown that the composition and molecular architecture of the stabilizing copolymer strongly affects the stabilizing ability in studied systems. Studies have shown that the use of a polymeric stabilizer in combination with ultrasonic treatment of dispersed systems makes it possible to obtain stable, homogeneous, highly dispersed suspensions. At the same time, it was demonstrated that a strong increase in the time and intensity of ultrasonic treatment of the system does not lead to a significant improvement in the results

2016 ◽  
Vol 16 (11) ◽  
pp. 6823-6840 ◽  
Author(s):  
Pauli Paasonen ◽  
Kaarle Kupiainen ◽  
Zbigniew Klimont ◽  
Antoon Visschedijk ◽  
Hugo A. C. Denier van der Gon ◽  
...  

Abstract. Atmospheric aerosol particle number concentrations impact our climate and health in ways different from those of aerosol mass concentrations. However, the global, current and future anthropogenic particle number emissions and their size distributions are so far poorly known. In this article, we present the implementation of particle number emission factors and the related size distributions in the GAINS (Greenhouse Gas–Air Pollution Interactions and Synergies) model. This implementation allows for global estimates of particle number emissions under different future scenarios, consistent with emissions of other pollutants and greenhouse gases. In addition to determining the general particulate number emissions, we also describe a method to estimate the number size distributions of the emitted black carbon particles. The first results show that the sources dominating the particle number emissions are different to those dominating the mass emissions. The major global number source is road traffic, followed by residential combustion of biofuels and coal (especially in China, India and Africa), coke production (Russia and China), and industrial combustion and processes. The size distributions of emitted particles differ across the world, depending on the main sources: in regions dominated by traffic and industry, the number size distribution of emissions peaks in diameters range from 20 to 50 nm, whereas in regions with intensive biofuel combustion and/or agricultural waste burning, the emissions of particles with diameters around 100 nm are dominant. In the baseline (current legislation) scenario, the particle number emissions in Europe, Northern and Southern Americas, Australia, and China decrease until 2030, whereas especially for India, a strong increase is estimated. The results of this study provide input for modelling of the future changes in aerosol–cloud interactions as well as particle number related adverse health effects, e.g. in response to tightening emission regulations. However, there are significant uncertainties in these current emission estimates and the key actions for decreasing the uncertainties are pointed out.


2011 ◽  
Vol 5 (1) ◽  
pp. 59-65 ◽  
Author(s):  
Nikolay Bulychev ◽  
◽  
Edward Kisterev ◽  
Yulia Ioni ◽  
Ondine Confortini ◽  
...  

2016 ◽  
Vol 11 (2) ◽  
pp. 121
Author(s):  
N. Bulychev ◽  
E. Kisterev ◽  
H. Reimann ◽  
C. Schaller ◽  
C.D. Eisenbach

The surface modification of titanium dioxide in aqueous dispersions of specially tailor-made periodic acrylic acid/isobutylene copolymers, poly(acrylic acid)/polystyrene graft copolymers, and hydrophobically modified polyethyleneoxide urethane (HEUR) by ultrasonic treatment was studied. The pigment surface modification by the above copolymers was comparatively investigated regarding conventional adsorption as contrasted to an ultrasonic treatment assisted procedure. The course and efficiency of the polymer adsorpption onto the pigment surface was quantified by electrokinetic sonic amplitude measurements. The higher efficiency of the pigment surface coating by the copolymers as achieved by ultrasonic treatment varies with the copolymer architecture and is a consequence of ultrasonically induced pigment surface activation.


2021 ◽  
Vol 16 ◽  
pp. 127-133 ◽  
Author(s):  
A. V. Perchenok ◽  
E. V. Suvorova ◽  
A. A. Farmakovskaya ◽  
V. Kohlert

The stability of aqueous dispersed systems of TiO2 and Fe2O3 microparticles in the presence of a water-soluble polymer - ethylhydroxyethylcellulose (EHEC) - has been studied under the condition of using two methods of mechanoactivation of the pigment surface - processing them in a disintegrator and in an ultrasonic field. It is shown that in the absence of a polymer stabilizer, an intense effect on aqueous dispersed systems of pigments leads to rapid coagulation of particles. In the presence of EHEC, a small stabilizing effect is observed, which is significantly enhanced when processing dispersed systems in a disintegrator and in an ultrasonic field. In this case, the stability of dispersed systems depends little on the method of mechanoactivation of their surface, but significantly depends on the duration of the intense exposure.


2019 ◽  
Vol 8 (4) ◽  
pp. 4137-4140

The surface modification of titanium dioxide in aqueous dispersions of specially tailor-made periodic acrylic acid/isobutylene copolymers by ultrasonic treatment was studied. The pigment surface modification by the above copolymers was comparatively investigated regarding conventional adsorption as contrasted to an ultrasonic treatment assisted procedure. The course and efficiency of the polymer adsorption onto the pigment surface was quantified by electrokinetic sonic amplitude measurements. The higher efficiency of the pigment surface coating by the copolymers as achieved by ultrasonic treatment and is a consequence of ultrasonically induced pigment surface activation.


This paper describes a spectroscopic investigation into the light emission o f flames burning at pressures up to 40 atm. Both premixed and diffusion flames are investigated. It shows that the equipartitioning of energy released by chemical reaction is faster at high pressure. This leads to the suppression of unstable radicals which are observed in low-pressure flames. The total light intensity of flames burning with air is little pressure-dependent; however, continuous gas radiation and emission from carbon particles become predominant at higher pressures. The radiation of oxygen flames is mainly determined by the increase in temperature of flames burning at high pressure. This leads to a strong increase in the emission from those products which are present in equilibrium such as OH and O 2 . Continuous gas radiation increases very strongly with pressure and two types of continua can readily be distinguished. the carbon monoxide flame continuum and the hydrogen flame continuum. The first continuum has been attributed by Gaydon to the process CO + O —> CO 2 + hv and this is supported by the present investigation. It is proposed that the second continuum is due to the association OH + OH -> H 2 O 2 + hv , and experimental evidence presented in this paper is in agreement with this. Continua occurring in hydrocarbon flames are a superposition of the two described above. This continuous gas radiation is responsible for m ost of the light em itted from highpressure flames.


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