Abstract:
The present invention relates to a process for treating polyolefin granules in a treatment vessel comprising the steps of: —Providing a bed of granules in liquid in said treatment vessel —Withdrawing a first stream of liquid from said treatment vessel, wherein said first stream of liquid contains hydrocarboneous compounds —introducing a first stream of vapour into said treatment vessel —Withdrawing a second stream of vapour from said treatment vessel wherein said second stream of vapour contains volatile hydrocarboneous compounds —Recovering the granules from said treatment vessel wherein said first stream of vapour has a temperature from Tb to Tb+10° C., wherein Tb is the boiling point of the liquid at the applied pressure, and said first stream of vapour produces an upwards rising vapour stream in said treatment vessel, the superficial vapour velocity of which is no more than 0.2 m/s, and a plant suitable for conducting said process.
Abstract:
A process for reducing the volatile organic compound content of granular plastomers having a density of equal to or lower than 883 kg/m3 and a MFR2 of 100.0 g/10 min or lower (ISO 1133 at 2.16 kg load and 190° C.), to below 65 ppm (VOC, VDA277), the process comprising the steps of providing a granular raw plastomer in a treatment vessel, the granular raw plastomer having a density of equal to or lower than 883 kg/m3, and a MFR2 of 100.0 g/10 min or lower (ISO 1133 at 2.16 kg load and 190° C.), and a volatile organic compound content (VOC, VDA277) of above 150 ppm, subjecting said granular raw plastomer to a gasflow within the range of 30 m3/(h t) to 150 m3/(h t) for an aeration time of less than 96 hours, whereby the gas has a minimum temperature of at least 26° C. measured at a gas inlet of the treatment vessel and a maximum temperature of 4° C. below the Vicat temperature (10 N, ISO 306) of the granular raw plastomer or 35° C. measured at the gas inlet of the treatment vessel, whatever value is lower; and recovering the granular plastomer.
Abstract:
Process for reducing the volatile organic compound content of plastomer having a density of equal to or lower than 883 kg/m3 and—a MFR2 of 100.0 g/l 0 min or lower (ISO 1133 at 2.16 kg load and 190° C.); to below 65 ppm(VOC, VDA277), the process comprising the steps of a) providing raw plastomer in granular form, the raw plastomer having a density of equal to or lower than 883 kg/m3; and a MFR2 of 100.0 g/10 min or lower (ISO 1133 at 2.16 kg load and 190° C.); and a volatile organic compound content (VOC, VDA277) of above 150 ppm, and the granules having an average D50 diameter of 2.5 to 4.5 mm b) subjecting said granular raw plastomer to at least one intensive hydrodynamic regime at a minimum temperature of at least 20° C. and a maximum temperature of 4° C. below the Vicat temperature (10 N, ISO 306) of the granular raw plastomer or 35° C., whatever value is lower, with the temperature measured at the gas inlet to the fast-fluidization regime, c) recovering the granular plastomer.
Abstract:
Process for reducing the volatile organic compound content of plastomer having a density of equal to or lower than 883 kg/m3 and—a MFR2 of 100.0 g/10 min or lower (ISO 1133 at 2.16 kg load and 190° C.); to below 65 ppm (VOC, VDA277), the process comprising the steps of a) providing raw plastomer in granular form, the raw plastomer having a density of equal to or lower than 883 kg/m3; and a MFR2 of 100.0 g/10 min or lower (ISO 1133 at 2.16 kg load and 190° C.); and a volatile organic compound content (VOC, VDA277) of above 150 ppm, and the granules having an average D50 diameter of 2.5 to 4.5 mm b) subjecting said granular raw plastomer to at least one intensive hydrodynamic regime at a minimum temperature of at least 20° C. and a maximum temperature of 4° C. below the Vicat temperature (10 N, ISO 306) of the granular raw plastomer or 35° C., whatever value is lower, with the temperature measured at the gas inlet to the fast-fluidization regime, c) recovering the granular plastomer.
Abstract:
An in-line blending process for polymers comprising: (a) providing two or more reactor-low pressure separator units (1,7) in parallel configuration, each reactor-low pressure separator unit comprising one reactor (2,8) fluidly connected to one low pressure separator (3,9) downstream and further a recycling line (5,11) connecting the low pressure separator (3,9) back to the corresponding reactor (2,8); (b) polymerizing olefin monomers having two or more carbon atoms in each of the reactors (2,8) in solution polymerisation; (c) forming an unreduced reactor effluents stream including a homogenous fluid phase polymer-monomer-solvent mixture in each of the reactors (2,8), (d) passing the unreduced reactor effluents streams from each of the reactors (2,8) through the corresponding low pressure separators (3,9), whereby the temperature and pressure of the low pressure separators (3,9) is adjusted such that a liquid phase and a vapour phase are obtained, whereby yielding a polymer-enriched liquid phase and a polymer-lean vapour phase, and (e) separating the polymer-lean vapour phase from the polymer-enriched liquid phase in each of the low-pressure separators (3,9) to form separated polymer-lean vapour streams and separated polymer-enriched liquid streams; (f) combining the polymer-enriched liquid streams from step (e) in a further low-pressure separator and/or a mixer (13) to produce a combined polymer-enriched liquid stream (16); (g) reintroducing the polymer-lean vapour streams from step (e) via recycling lines (5,11) into the corresponding reactors (2,8).
Abstract:
A process for providing an intermediate polyolefin polymer sample from a first polyolefin polymerization reactor coupled in series with a second polyolefin polymerization reactor and being connected by a connecting conduit.
Abstract:
The present invention relates to a polymerization process, comprising: a) supplying a feed containing ethylene and at least one alpha-olefin having 3 to 12 carbon atoms in a hydrocarbon solvent to a polymerization reactor, b) contacting the feed of step a) in the reactor with a catalyst to form a reaction mixture containing an ethylene-alpha-olefin co-polymer, c) withdrawing the reaction mixture from the polymerization reactor as a reactor outlet stream which comprises the ethylene-alpha-olefin co-polymer, unreacted monomer and comonomer, catalyst, and hydrocarbon solvent, d) heating the reactor outlet stream to a temperature which is at least 5° C. higher than the temperature of the reaction mixture at the outlet of the reactor for a time period of between 1 and 250 seconds in order to de-activate the polymerization catalyst, and e) separating hydrocarbon solvent, monomer and comonomer from the reactor outlet stream and recycling it back to the polymerization reactor without further purification steps.
Abstract:
A process for reducing the volatile organic compound content of granular plastomers having a density of equal to or lower than 883 kg/m3 and a MFR2 of 100.0 g/10 min or lower (ISO 1133 at 2.16 kg load and 190° C.), to below 65 ppm (VOC, VDA277), the process comprising the steps of providing a granular raw plastomer in a treatment vessel, the granular raw plastomer having a density of equal to or lower than 883 kg/m3, and a MFR2 of 100.0 g/10 min or lower (ISO 1133 at 2.16 kg load and 190° C.), and a volatile organic compound content (VOC, VDA277) of above 150 ppm, subjecting said granular raw plastomer to a gasflow within the range of 30 m3/(h t) to 150 m3/(h t) for an aeration time of less than 96 hours, whereby the gas has a minimum temperature of at least 26° C. measured at a gas inlet of the treatment vessel and a maximum temperature of 4° C. below the Vicat temperature (10 N, ISO 306) of the granular raw plastomer or 35° C. measured at the gas inlet of the treatment vessel, whatever value is lower; and recovering the granular plastomer.
Abstract:
Process for hydraulic conveying of polyolefin pellets comprising the steps of: (i) extruding molten polyolefin into strands and cutting the strands into pellets in an underwater pelletiser (A); (ii) withdrawing a first pellet suspension stream (1.1) from the pelletiser; (iii) concentrating the first pellet suspension stream in a first pellet separator (B); (iv) passing the concentrated pellet stream (1.4) to a hydraulic conveying line through a first vessel (D) and mixing it with water thereby producing a second pellet suspension stream (1.5); (v) withdrawing the second pellet suspension stream from the first vessel and passing it to a second pellet separator (E); (vi) separating the pellets from water in the second pellet separator thereby creating a second water stream (1.6) and a dry pellet stream (1.10) and passing the second water stream back to the first vessel; wherein any one of the first or second pellet suspension stream or the dry pellet stream comprises an antiblock.