Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Znaleziono wyników: 2

Liczba wyników na stronie
first rewind previous Strona / 1 next fast forward last
Wyniki wyszukiwania
Wyszukiwano:
w słowach kluczowych:  proszki mineralne
help Sortuj według:

help Ogranicz wyniki do:
first rewind previous Strona / 1 next fast forward last
PL
W referacie przedstawiono wyniki eksperymentów pozwalających na ustalenie zależności pomiędzy powierzchnią właściwą proszku, a jego składem ziarnowym. Przedmiotem badań były piaski i marmury ze złóż "Biała Góra" i "Biała Marianna". Powierzchnię właściwą zmierzono metodą Blaine'a. Składy ziarnowe oznaczono precyzyjną metodą dyfraktometryczną. Przyjmując zasadę, że skład ziarnowy można opisać równaniem RRB, opracowano empiryczną zależność pomiędzy powierzchnią a składem ziarnowym proszku. Opracowana zależność może być stosowana do powierzchni poniżej 6100 cm /g. Przedstawiono dyskusję wyników.
EN
Results of experiment enabling establishment of relationship between specific surface and size distribution of powder were presented in this article. Sands and marbles from "Biała Góra" and "Biała Marianna" deposits were subject of tests. Specific surface was measured by Blaine method. Size distribution was indicated by precise diffractometric method. Considering that size distribution can be described by RRB equation, empirical relationship between surface and size distribution of powder was established. This relationship can be applied for surface below 6100 cm /g. Discussions on results were presented.
2
Content available remote Kompozyty polistyrenu z włóknami roślinnymi i proszkami mineralnymi
PL
Przedstawiono niektóre problemy związane z zastosowaniem włókien konopi, lnu i proszku tritlenku glinu jako napełniaczy do odpadowego ekspandowalnego polistyrenu. Stwierdzono, że włókna roślinne i napełniacz mineralny poprawiają wytrzymałość statyczną polimeru przy pewnym spadku wytrzymałości dynamicznej (udarności). Włókna, których efektywność jest bardzo zbliżona, dają bardziej wyraźną poprawę właściwości statycznych niż tritlenek glinu. Użycie wszystkich badanych napelniaczy zwiększa lepkość kompozytów, a w przypadku włókien intensyfikuje też zachowanie nienewtonowskie.
EN
Polystyrene and its copolymers are widely used in industry. Their contribution both to polymer production and polymer waste exceeds 10%. A relatively small part of this contribution (2%) falls to expandable polystyrene, but due to the very low density its waste becomes comparable with the total volume of other polymer waste. Additionally, the expandable polystyrene has a lower molecular weight, and hence the worse mechanical properties, in comparison with typical polystyrenes. It results in a number of serious problems connected with the management, e.g. recycling, of the waste. One of the possible ways of expandable polystyrene recycling is its modification. In this study the expanded polystyrene waste after densification with the two-roll-mill at ca. 120"C during 2 minutes and grinding was blended with hemp or flax fibers or with Al2O3 powder. The process was also carried out with the two-roll-mill at temperature 160°C during 10 min. The fiber in amount of 0:30% or the powder in amount of 0:20% was added to the molten polystyrene. The components were blended until the homogeneous blend was obtained. The samples for mechanical testing were prepared from grind by injection molding at 190°C. The Theological properties were measured using the grind. The relatively low temperatures and shear rates (shear stresses) on every processing stage were indispensable to prevent the polystyrene and plant fibers from strong thermomechanical degradation. The mechanical properties and melt flow index of waste polystyrene-plant fibers blends are presented in Table 1. The same properties of a standard polystyrene are given for comparison. It is evident from Table 1 that there are no significant differences in properties due to the kind of fibers. Both hemp and flax increase the static mechanical properties, especially the tensile and flexural strengths. The impact strength (dynamic property) shows a minimum at 10% fiber content. The impact strength is generally lower than that for pure polystyrene. The lack of dynamical toughening can be attributed to the loss of continuity of polystyrene phase and a weak adhesion between polymer and fiber. The rheological measurements have shown that the flow curves of polystyrene-fiber systems at 170,190 and 210°C can be adequately described by the power law. The constants K and n of the power law determined with a capillary rheometer are summarized in Table 2. Figures 1 and 2 present examples of the flow curves of polystyrene-hemp and polystyrene-flax compositions at 170°C. It can be seen that with increasing fiber content the constant K increases and the constant n decreases. It means that the fiber addition rises the viscosity of the system and simultaneously causes its rheological behavior more non-Newtonian. The qualitatively similar effect brings the temperature lowering. Table 3 presents the comparison of mechanical and rheological properties of waste and standard polystyrenes filled with Al2O3 powder. It can be seen that the powder addition increases the tensile strength (static property) and decreases the impact strength (dynamic property) and the flowability of the system in both cases. This behavior is similar to the systems with fibers discussed previously. However, for waste polystyrene blends a stronger tensile strength rise and a weaker impact strength fall than that for the standard polystyrene can be observed. It testifies probably to a better adhesion between polymer and powder in blends with waste polystyrene, which is due to its lower molecular weight. It follows from Tables 1 and 3 that the plant fibers are more efficient toughening agents for the waste polystyrene than the Al2O3j powder. A further improvement of their efficiency is possible by the simultaneous use of other modifications such as the addition of thermoplastic elastomers and preparation of the fiber surface with suitable adhesives.
first rewind previous Strona / 1 next fast forward last
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.