The invention relates to a device for filling containers, comprising an arrangement for feeding filling material to at least one dosing system which forms a flow path in which there is a dosing valve which can be opened at least for the duration of the dosing processes in order to deliver the dosing amounts of the filling material to the pertinent containers by way of at least one filling line.
In the pertinent prior art, a system which economically enables automated molding (blow molding or vacuum molding), filling, and sealing of containers is known under the trademark bottelpackĀ®. When the indicated containers are to be filled with sensitive products, for example, pharmaceuticals, on the one hand the international standards for aseptic packaging must be satisfied, and on the other hand it must be ensured that during each filling process a specific dosing amount is filled in, and the quantity of the filling amount must be maintained with the greatest precision, especially when highly efficacious pharmaceuticals are involved.
To meet these requirements, in a device of the initially named type which is disclosed in document EP 0 418 080 B1, for each filling line which is assigned to a pertinent container to be filled, there is a dosing valve which opens and closes in a time-controlled manner by means of electromagnetic actuation, the opening time for each dosing process being chosen such that at a set buffer pressure of the filling material which is available in a dosing distributor, the desired dosing amount flows through the dosing valve during the opening time.
Based on this prior art, the object of the invention is to make available a device of the aforementioned type which is characterized by increased dosing accuracy compared to the prior art.
This object is achieved according to the invention by a device which has the features of claim 1 in its entirety.
Accordingly, one essential feature of the invention consists in that downstream of the dosing valve there is a controllable means by which a suction action can be produced on the flow path when the respective dosing processes are completed, specifically when the pertinent dosing valve closes. When the dosing process is ended, in the filling line this yields a suction action which causes return suction of the remaining liquid out of the filling line or at least prevents dripping of liquid afterwards. A maximum of dosing accuracy certainly can be achieved in this way.
In advantageous exemplary embodiments, between the dosing valve and the filling line there is a choke site, which constricts the flow path during the dosing processes, in the region of the choke site there being a movable control element which defines the width of the flow path depending on its position setting and which can be transferred into a position which widens the flow path at the choke site by forming a bypass when the means which produces the suction action is activated. The choke site, which in interaction with the time control of the opening time of the dosing valve determines the dosing amount, in interaction with the control element which defines the width of the flow path also forms a part of the means which produces the suction action and whose operating principle consists in that the movable control element forms a widening in the flow path as a bypass of the choke site, resulting in an enlargement of the inside volume of the flow path and thus an afterflow effect.
The arrangement in this connection can be advantageously made such that the means which produces the suction action is formed by a bypass valve designed as a diaphragm valve whose diaphragm which forms the movable control element with its one closing side delimits the flow path at the choke site and on whose other control side a negative pressure can be applied for producing a suction action in order to cause the diaphragm to execute a deflection motion which widens the flow path and whose lift produces the suction action on the filling line. In these exemplary embodiments the means which produces the suction action is characterized by an especially simple construction.
The dosing valve can also be formed by a diaphragm valve in a correspondingly advantageous manner.
An especially compact and simple structure of the dosing system can be achieved when the dosing valve and downstream bypass valve are diaphragm valves which are controlled by a joint diaphragm extending along the flow path.
In order to support the movement of the diaphragm both at the dosing valve and at the bypass valve into the rest position, i.e., into the respective closed position, and to elicit deflection movements out of the rest position, on the control side of the diaphragm opposite the closing side alternately an overpressure as the closing pressure and an underpressure as the opening pressure can be applied to the pertinent dosing valve and to the pertinent bypass valve by way of assigned control lines.
Advantageously, the arrangement can be made such that for a plurality of filling lines respectively assigned dosing units are combined in a dosing block, the input sides of the respective dosing valves being connected to a common distributor of the filling material which is under a set buffer pressure.
In such a design, in the dosing block there can be a diaphragm which is assigned to the dosing valves and bypass valves and which is common to the dosing system as a whole.
In operation with this dosing block, the diaphragm can be triggered jointly on the bypass valves from a common control line, while for the control sides of the diaphragm on the dosing valves, each filling line has its own control line for pressure and negative pressure.
The invention is detailed below using one exemplary embodiment shown in the drawings.
a to 4d show schematic sketches in illustration of the construction and manner of operation of the dosing valve means according to the exemplary embodiment of the invention.
The invention is explained below using one example in which the device contains a plurality of dosing systems, specifically according to
Of this device, only
a to 4d best illustrate how the dosing systems 5 work. As shown, on the dosing valve 29 and bypass valve 31 on the control side 37 of the diaphragm 33 there is a spherical cap-shaped space 43 into which a surface region of the diaphragm 33 can be deflected when negative pressure is applied to the control side 37 by way of the pneumatic connections 35 or 39, by which the opposite closing side 45 of the diaphragm 33 is raised out of the closed position and deflected into the respective space 43; this causes opening of the pertinent valve 29 or 31.
c and 4d illustrate the completion of the dosing process by closing of the dosing valve 29 (
As already mentioned, the dosing amount is determined by time control of the duration of opening of the respective dosing valve 29 via the individual pneumatic connection 35. The suction action on the filling lines 9 can be produced simultaneously for all dosing systems 5 by the pneumatic connection 39 which is common to them being triggered.
It should be noted that for conventional cleaning and sterilization measures as are carried out conventionally before the start of the production phases, the dosing valves 29 and the bypass valves 31 are controlled into the open position. Thus, the unchoked flow path 27 is available for throughflow of cleaning and sterilization media, that is to say, originating from the distributor of filling material 3 via the feed line 7, dosing system 5, and filling line 9 to the filling material channel 15 of the pertinent filling mandrel 11.
Number | Date | Country | Kind |
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10 2008 028 772.5 | Jun 2008 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2009/003706 | 5/26/2009 | WO | 00 | 10/21/2010 |