Patent Application
20200407207
The present invention relates to a plant for treating receptacles, for example bottles made of plastic or the like, adapted to be filled with a pourable product, preferably a pourable food product, even more preferably sterilised.
In particular, the present invention relates to a plant for producing the above-mentioned receptacles from known preforms, for filling the receptacles with the pourable product and for applying caps to the receptacles (i.e., capping them).
Plants for treating receptacles are known, which are adapted to contain, in particular to be filled with, a pourable product, preferably a pourable food product, even more preferably sterilised.
Generally, receptacles treated in the above-mentioned plants are defined by bottles, containers or the like.
In the present description, by the term “treated”, “treatment” or the like, it is to be understood, either alone or in combination, the forming, filling and capping processes of the above-mentioned receptacles.
Typically, a treatment plant of the above-mentioned type essentially comprises:
The need for ensuring a suitable aseptic condition of the receptacles during the treatment process is known in the art, in order to guarantee quality and safety standards envisaged for the consumers.
Consequently, plants of the above-mentioned type further comprise an isolation chamber, housing at least partially, at least the filling unit and the capping unit and configured to internally delimit a controlled atmosphere, so that the filling and capping units can operate in sterile and/or aseptic conditions.
The isolation chamber therefore defines a sterile and/or aseptic environment of the treatment plant, required to guarantee the above-mentioned operating conditions.
In order to create said sterile and/or aseptic conditions, a typical treatment plant further comprises a plurality of filtering units, each of which is configured to filter the air to be introduced into the isolation chamber, usually sucked-up from the external environment by suction means, such as for example fans, creating, in this manner, the controlled atmosphere inside the isolation chamber.
As is known, the filtering units are operatively interposed between the external environment and the isolation chamber, in particular arranged at a boundary wall of the isolation chamber that separates the external environment from the controlled environment.
In particular, each filtering unit may comprise one or more filters of a known type (for example, HEPA or ULPA filters) and one or more fans operatively coupled to the corresponding filters. The fans convey, in use, the air from the external environment towards the relative filters; said air is then filtered (sterilised and/or made aseptic) and introduced inside the isolation chamber.
The isolation chamber is configured, therefore, to operate in overpressure conditions with respect to the external environment.
In some cases, also the above-mentioned forming unit is housed in the same isolation chamber or in a respective further isolation chamber of the above-mentioned type, the latter typically being fed with filtered air but not containing a sterile and/or aseptic controlled atmosphere.
The need to periodically control the above-mentioned filtering unit is known in the art, in order to guarantee the aforesaid quality and safety standards (aseptic standards usually required by the competent authorities of the sector).
It is therefore necessary to perform periodic controls, typically performed manually by an operator, which entails stoppage of the treatment plant, emptying the isolation chamber from the relative production batch, opening the isolation chamber, with corresponding interruption of the aseptic/sterile conditions, and the required transient period after controls for recalibrating the optimal operating conditions in order to resume the treatment process.
Albeit the plants of the above-mentioned type represent a valid solution for treating—forming, filling and capping—receptacles adapted to contain a pourable product, the Applicant has observed that these are still susceptible to further improvements. In particular, the need is felt to reduce the stoppages of the plant, avoid recalibration times and improve the aseptic quality inside the isolation chamber.
The object of the present invention is to achieve a plant for treating receptacles, which is more reliable and less costly, and enables to meet at least some of the needs specified above and connected to the treatment plants of the known type.
According to the invention, this object is achieved by a treatment plant as claimed in the attached claims.
For a better understanding of the present invention, a preferred non-limiting embodiment thereof will be described in the following, purely by way of example and with the aid of the attached drawings, wherein;
With reference to the attached figures, number 1 indicates as a whole a plant for treating receptacles 2 which are adapted to contain a pourable product, preferably a pourable food product, even more preferably sterilised, such as carbonated beverages (for example, sparkling water, soft drinks and beer) or still beverages (for example water, fruit juices, tea, sport drinks, wine, emulsions, yoghurt, etc.)
In particular, the plant 1 is adapted to produce receptacles 2, in the example described bottles made of plastic, from preforms 3, to fill receptacles 2 with the pourable product and to subsequently cap the filled receptacles with the respective caps 4 (
In this regard, the plant 1 comprises, at least:
In an alternative embodiment not illustrated, the plant 1 comprises only one or any combination of the forming unit 5, filling unit 6 and capping unit 7.
Therefore, in the following description, by the term “treatment” it is intended the forming and/or filling and/or capping process of the receptacles 2.
As is known, the forming unit 5 comprises a kiln 10 for preheating the preforms 3 and a forming device 11, arranged operatively downstream of the kiln 10 and configured to shape the previously heated preforms 3, so as to obtain the receptacles 2 of the desired shape.
Preferably, forming takes place by means of blowing inside the preheated preforms 3, which expand until assuming the pre-established shape imparted thereto by the forming device 11.
The filling unit 6 is arranged operatively downstream of the forming unit 5 and comprises a conveyor, in the example described a carousel 12, configured to receive the formed receptacles 2, to feed them along a transfer path, shaped as an arc of a circle and to fill them with the pourable product, in a manner known and not described in detail.
The capping unit 7 is arranged operatively downstream of the filling unit 6 and comprises a conveyor, in the example described a carousel 13 configured to receive the caps 4 from an inlet conveyor not described in detail, to receive the receptacles 2 filled by the carousel 12, to feed them along a corresponding transfer path shaped as an arc of a circle, to support them in a rotatable manner and cap them with the corresponding caps 4, in a manner known and not described in detail.
After being capped, the receptacles 2 are then fed to the outlet conveyor 8 for possible subsequent labelling, packaging and storage operations.
In order to guarantee that the treatment process is carried out according to the pre-established foodstuff quality and safety standards, the plant 1 further comprises an isolation chamber 14 (
In use, the isolation chamber 14 is configured to delimit, i.e. to contain therein, a controlled atmosphere controlled in sterile and/or aseptic conditions. Therefore, the isolation chamber 14 defines a sterile and/or aseptic environment of the plant 1. In this manner, the filling unit 6 and the capping unit 7 can operate in sterile and/or aseptic conditions, to guarantee the aforementioned standards.
Conveniently, the isolation chamber 14 is delimited by a boundary wall 15 that separates and seals in a fluid tight manner the environment inside the isolation chamber 14 from the external environment.
In order to create the above-mentioned sterile and/or aseptic conditions inside the isolation chamber 14 and, thus, constitute the controlled atmosphere, the treatment plant 1 comprises at least a filtering unit 16 adapted to filter a gas, in this specific example air, to be introduced inside the isolation chamber 14.
In detail, as can be seen in
In use, the air, after having been conveyed by the fan 17 towards the filtering member 18, is filtered/sterilised and subsequently introduced inside the isolation chamber 14.
As the isolation chamber 14 is sealed, it is configured to operate in overpressure conditions with respect to the external environment.
Conveniently, the filtering unit 16 is arranged at the wall 15, in particular is fixed to the wall 15, with the fan 17 facing the external environment and the filtering member 18 facing the environment inside the isolation chamber 14.
In greater detail, the treatment plant 1 comprises a duct 19 that fluidically connects the filtering unit 16 with the isolation chamber 14.
More precisely, the duct 19 is adapted to contain, in use, the controlled atmosphere and, therefore, can be considered an extension (and therefore an integral part) of the isolation chamber 14. Consequently, the wall 15 externally delimits the duct 19.
In an alternative embodiment not illustrated, the treatment plant 1 is not provided with any duct 19 and the filtering unit 16 is arranged directly on the wall 15 delimiting the isolation chamber 14.
According to the invention, the treatment plant 1 further comprises a test device 20 housed inside the isolation chamber 14, immersed, in use, in the controlled atmosphere and configured to perform one or more test operations on the filtering unit 16, in particular on the filtering member 18.
In detail, the test (or check and/or control) operations comprise:
Preferably, the test device 20 comprises a particle counter.
It is specified that by the expression “culture medium” it is intended, in the present description, any element adapted to support and/or host one or more known microbiological cultures.
In an embodiment, said culture medium could be defined by one or more strips of support material that can be contaminated with a known microbiological culture.
In an embodiment, the test device 20 comprises means for depositing the above-mentioned culture medium, defined for example by one (or more) of the above-mentioned, preferably adhesive, strips, and means for analysing the culture medium.
In practice, the initially sterile strip, is adapted to be arranged inside the duct 19, and therefore in the isolation chamber 14, at the filtering unit 16. Preferably, the test device 20 is configured to deposit the strip downstream of a sterilising unit of the filtering unit 16, arranged upstream of the filtering member 18 and configured to sterilise the filtering member 18.
After a certain period of time, the test device 20 is configured to analyse the strip and to detect (check) the presence or absence of possible microbiological cultures formed, during the treatment process, on the strip itself.
In this manner, the efficiency of the sterilising unit, and therefore of the filtering unit 16, can be easily checked during the treatment process and without interrupting the treatment process itself.
In light of what has been described above, the test device 20 is configured to carry out:
According to another aspect of the present invention, the test device 20 is movable inside the isolation chamber 14 and, therefore, inside the controlled atmosphere contained, in use, therein.
In detail, the test device 20 is carried by a robotic arm 21, conveniently arranged inside the isolation chamber 14 and thus apt to be immersed inside the controlled atmosphere.
Preferably, the robotic arm 21 is arranged in the duct 19 and is appropriately positioned so as to control the movement of the test device 20 at the filtering member 18 of the filtering unit 16.
In use, the robotic arm 21 is controllable, for example by means of a control unit, known and not illustrated, to move the test device 20 at, i.e. in the proximity of, the filtering member 18 to detect and measure a quantity of the particles of contaminating agents possibly present downstream of the filtering element 18 and that, therefore, are introduced in the duct 19 and in the isolation chamber 14.
The above-mentioned detection can be carried out during the treatment process (filling and/or capping) of receptacles 2, without the need to stop the treatment plant 1.
Therefore, the above-mentioned test operations are carried out automatically by means of the robotic arm 21 and without the manual intervention of any operator, during the filling and capping processes.
According to this preferred and non-limiting embodiment, the robotic arm 21 is fixed to an internal wall 22 of the duct 19 in particular is flanged to the internal wall 22, and is coupled in a mobile manner to a fixed support base 23 arranged outside of the duct 19 and therefore outside of the isolation chamber 14.
Expediently, the robotic arm 21 is coupled to the support base 23 by means of a coupling flange 24, schematically illustrated in
Conveniently, the test device 20 is mounted on a free end portion of the robotic arm 21 so as to be able to easily reach the pre-set operating area.
Expediently, the robotic arm 21 is provided with six degrees of freedom.
From an examination of the features of the treatment plant 1 according to the present invention the advantages that it allows to obtain are evident.
In particular, thanks to the presence of the test device 20 arranged in a mobile manner inside the isolation chamber 14 and carried by the robotic arm 21, which is also arranged inside the isolation chamber 14, it is possible to carry out the test operations during, and without interrupting, the treatment process of the receptacles 2 (and therefore on the fly), in an automatic manner. In this manner, the stoppages of the treatment plant 1 are drastically reduced, and the transitory times required for recalibration of the optimal sterile and/or aseptic operating conditions of the controlled atmosphere, are avoided.
Furthermore, this results in an improved aseptic and/or sterile condition of the controlled atmosphere, since there is no interruption of the aseptic and/or sterile conditions each time it is necessary to carry out the test operations.
In addition, thanks to the configuration described above, tests can be carried out on the efficiency of the filtering unit 16 during, and without interrupting, the treatment process, which otherwise, in the absence of the configuration according to the present invention, would require the presence of an appropriate separation structure. The architecture of the treatment plant 1 is, therefore, extremely simplified.
It is clear that modifications and variations can be made to the treatment plant 1 described and illustrated here without thereby departing from the scope defined by the claims.
In particular, the treatment plant 1 could comprise, furthermore, a further isolation chamber that houses the forming unit 5 and is configured to contain a respective controlled atmosphere.
In this case, the controlled atmosphere of said isolation chamber is preferably formed by filtered air but not sterilised and/or aseptic air.
In order to create said controlled atmosphere, the treatment plant 1 could comprise a further filtering unit for filtering the air to be introduced inside the isolation chamber.
Conveniently, the treatment 1 could comprise a further robotic arm, substantially identical to the robotic arm 21 and carrying a test device 20, to carry out test operations on the further filtering unit.
In addition, the treatment plant 1 could comprise a single isolation chamber housing the forming 5, filling 6 and capping 7 units and supplied by a single filtering unit.
Furthermore, the treatment plant 1 could comprise two or more robotic arms 21 carrying as many test devices 20 and arranged inside the isolation chamber 14.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102019000010134 | Jun 2019 | IT | national |
