CS243904B1 - Polypropylene degradation activator - Google Patents
Polypropylene degradation activator Download PDFInfo
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- CS243904B1 CS243904B1 CS839862A CS986283A CS243904B1 CS 243904 B1 CS243904 B1 CS 243904B1 CS 839862 A CS839862 A CS 839862A CS 986283 A CS986283 A CS 986283A CS 243904 B1 CS243904 B1 CS 243904B1
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- disulfide
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- benzamidophenyl
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Abstract
Zmesi práškového alebo granulovaného izoitaktického polypropylénu s bis(o-benzamidofenylJdisulfidom sa degradovali za statických podmienok v komoře výtlačného plastoimera VP-05. Volbou teploty prispracovaní vzorky v intervale 255 až 300 °C, koncentrácie bis(o-benzamidofenyl) disulfidu od 0,02 do 1 % bjrnotnčetného a dížky termického namáhania od 1 do 30 minút možno dosiahnuť požadovaná hodnotu indexu toku taveniny. Bis(o-benzamidofenyljdisulfid možno použit ako aktivátor degradácie aj v přítomnosti stabilizačného systému.Mixtures of powdered or granular isotactic polypropylene with bis(o-benzamidophenyl)disulfide were degraded under static conditions in the chamber of a VP-05 extrusion plastometer. By selecting the sample processing temperature in the range of 255 to 300 °C, the concentration of bis(o-benzamidophenyl)disulfide from 0.02 to 1% by weight and the duration of thermal stress from 1 to 30 minutes, the desired melt flow index value can be achieved. Bis(o-benzamidophenyl)disulfide can be used as a degradation activator even in the presence of a stabilization system.
Description
Vynález sa týká použitia bis (o-benzamidofenyl) disulf idu alko aktivátora degradácie polypropylénu za účelom úpravy jeho molekulových charakteristik.The invention relates to the use of bis(o-benzamidophenyl) disulfide as an alcohol activator for the degradation of polypropylene for the purpose of modifying its molecular characteristics.
Komerčně typy polypropylénu určené pre výrobu vlákien a vstrekovaných výrobkov nevyhovuijú z hradiska molekulových charakteristik požiadavkám spracovatelov.Commercial types of polypropylene intended for the production of fibers and injection molded products do not meet the requirements of processors in terms of molecular characteristics.
Podlá typu výrobku požadujú sa polypropylény s hodnotami indexu toku taveniny do 50 g/10 minút, pričom u nás vyrábané typy polypropylénu majú hodnoty indexu toku taveniny do 11 g/10 minút.Depending on the type of product, polypropylenes with melt flow index values of up to 50 g/10 minutes are required, while the types of polypropylene produced in our company have melt flow index values of up to 11 g/10 minutes.
Sú možné dve cesty úpravy molekulových charakteristik; počas syntézy poilyméru vhodným nastavením polymerizačného systému, resp. dodatečnou úpravou hotového polymeru v procese spracovania pomocou aktivátorovi degradácie. Tento sposob súčasne umožňuje výrazné zúženie distrtbúcie molekulových hmotností.There are two possible ways of modifying the molecular characteristics; during the synthesis of the polymer by appropriate adjustment of the polymerization system, or by additional modification of the finished polymer during the processing process using a degradation activator. This method simultaneously allows a significant narrowing of the molecular weight distribution.
V súčasnosti sa na úpravu spracovatelsikých vlastností polypropylénu používá druhý sposob, pričom ako aktivátory degradácie sa používajú nízkomolekuloivé látky typu organických a anorganických peroxidov, dusíkaté zlúčeniny, sírne zlúčeniny a C-C iniciátory.Currently, the second method is used to modify the processing properties of polypropylene, using low-molecular substances such as organic and inorganic peroxides, nitrogen compounds, sulfur compounds and C-C initiators as degradation activators.
Potřeby polypropylénu s modifikovanými molekulovými charakteristikami sa doteraz riešili dovozom hotového modifikovaného' polyméru, resp. dovozom aktivátorov degradácie zo zahraničia.The need for polypropylene with modified molecular characteristics has so far been met by importing finished modified polymer or by importing degradation activators from abroad.
Uvedené nedostatky sú odstránené predmeitoim vynálezu, ktorého podstatou je použitie bis(o-benzaimldofenyl]disulfidu domácej výroby ,akoi aktivátora degradácie práškového polypropylénu, resp. práškového alebo granulovaného stabilizovaného polypropylénu, Degradácia zmesí polypropylénu s bis(o-benzamldofenyl)disulfidotm z východiskové]' hodnoty indexu toku taveniny použitého' typu polypropylénu do hodnot indexu toku taveniny 250 g/10 minút sa uskutečňuje v spracovatefskom zariadení v teplotnom Intervale 255 až 300 °C, pri koncentrácii bis (o-benzamidofenyl) disulf idu 0,02 až 1 % hmotnostně.The above-mentioned shortcomings are eliminated by the subject of the invention, the essence of which is the use of bis(o-benzamidophenyl) disulfide of domestic production as an activator of the degradation of powdered polypropylene, or powdered or granular stabilized polypropylene. The degradation of mixtures of polypropylene with bis(o-benzamidophenyl) disulfide from the initial melt flow index value of the type of polypropylene used to the melt flow index value of 250 g/10 minutes is carried out in a processing device in the temperature range of 255 to 300 °C, at a bis(o-benzamidophenyl) disulfide concentration of 0.02 to 1% by weight.
Doteraz sa bis(o-benzamidofenyl) disulfid používal aiko plastifikačné činidlo pri spracovaní kaučuku.Until now, bis(o-benzamidophenyl) disulfide has been used as a plasticizer in rubber processing.
Příklad 1Example 1
Zmesi práškového polypropylénu s bis(o-benzamidiofenyljdisulfidom sa spracovávali v komoře výtlačného· plastometra VP-05 za statických podmienok následovně: Vzorka sa pri zvolenej toplote nasypala, do tavnej komory plastifikačného valca a uzavřela sa piestom. Tryska sa upchala drotom. Po uplynutí zvolenej doby zádrže sa vzorka vytlačila vo formě struny, ktorá sa zgranulovala a z granúl sa zmeral index toku taveniny za štandardných podmienok (ČSN 64 0861).Mixtures of polypropylene powder with bis(o-benzamidiophenyl)disulfide were processed in the chamber of the VP-05 extrusion plastometer under static conditions as follows: The sample was poured into the melting chamber of the plasticizing cylinder at the selected temperature and closed with a piston. The nozzle was plugged with a wire. After the selected retention time, the sample was extruded in the form of a string, which was granulated and the melt flow index of the granules was measured under standard conditions (ČSN 64 0861).
Výsledky skúšky sú uvedené v tah. 1. Povodný nespracovaný práškový polypropylén mal hodnotu indexu toku taveniny 3,42 g/10 minút. Pre porovnáme sú uvedené aj výsledky pre vzorky neobsahujúce degradant.The test results are shown in Table 1. The raw polypropylene powder had a melt flow index of 3.42 g/10 minutes. The results for samples containing no degradant are also shown for comparison.
Tabulka 1Table 1
Teplota spracovania: 260 °C koncentrácia bis (o-benzamidofenyl ) disulf idu, % hmotnostně doba zádrže, minúty index toku taveniny, g/10 minútProcessing temperature: 260 °C concentration of bis (o-benzamidophenyl) disulfide, % by weight retention time, minutes melt flow index, g/10 minutes
2,612.61
12,7812.78
5 14,905 14.90
16,5016.50
3,513.51
7,467.46
0,07 5 11,520.07 5 11.52
20,2720.27
3,663.66
8,048.04
0,18 5 15,330.18 5 15.33
22,4522.45
3,763.76
8,718.71
0,35 5 17,220.35 5 17.22
25,4825.48
Příklad 2Example 2
Zmesi práškového polypropylénu s bis(o-benzamidofenyl) disulf idom otosahujúce konštanitné množstvo fennlickéhoi anfioxidantu 2,6-ditercbutyl-4-metylfenoilu 0,1 % hmotnostně sa spracovali rovnaiko ako bolo popísané v příklade 1.Mixtures of polypropylene powder with bis(o-benzamidophenyl) disulfide containing a constant amount of the phenolic antioxidant 2,6-di-tert-butyl-4-methylphenol of 0.1% by weight were processed in the same way as described in Example 1.
Výsledky pre teploty 260 a 270 °C a rožne koncentrácie degradantu a dížky termického namáhania sú uvedené v tabuíke 2.The results for temperatures of 260 and 270 °C and different degradant concentrations and thermal stress lengths are presented in Table 2.
Tabulka 2 teplota, °C doba zádrže, index toku taveniny, g/10 minut minuty pri koncentrácii bis (o-benzamidofenyl) disulf idu % hmotnostněTable 2 temperature, °C retention time, melt flow index, g/10 minutes minutes at the concentration of bis (o-benzamidophenyl) disulfide % by weight
Příklad 3 nyl ] disulf idoim o koncentrácii 0,56 % hmiotnostných sa degradovali v komoře výtlačZmesi komerčně stabilizovaného granulo- ného plastomera pri 260 a, 280 °C postupom váného polypropylénu s obchodným ozna- pcpísaným v příklade 1. cením Mosten 55 212 a indexem toku taive- Výsledné hodnoty indexov toku taveniny niny 0,6 g/10 minút s bis(o-benzamidofe- sú uvedené v tabuíke 3.Example 3 Mixtures of commercially stabilized granular plastomer with the trade name Mosten 55 212 and a melt flow index of 0.6 g/10 minutes were degraded in a compression chamber at 260 and 280 °C by the process described in Example 1. The resulting melt flow index values are given in Table 3.
Tabulka 3 index toku taveniny dlžka termického namáhania, g/10 minút minuty pre vzorky degradovanéTable 3 Melt flow index Thermal stress length, g/10 minutes minutes for degraded samples
kárskoím priemysle.the car industry.
Claims (3)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS839862A CS243904B1 (en) | 1983-12-23 | 1983-12-23 | Polypropylene degradation activator |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS839862A CS243904B1 (en) | 1983-12-23 | 1983-12-23 | Polypropylene degradation activator |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS986283A1 CS986283A1 (en) | 1985-09-17 |
| CS243904B1 true CS243904B1 (en) | 1986-07-17 |
Family
ID=5446891
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS839862A CS243904B1 (en) | 1983-12-23 | 1983-12-23 | Polypropylene degradation activator |
Country Status (1)
| Country | Link |
|---|---|
| CS (1) | CS243904B1 (en) |
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1983
- 1983-12-23 CS CS839862A patent/CS243904B1/en unknown
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| Publication number | Publication date |
|---|---|
| CS986283A1 (en) | 1985-09-17 |
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