JP2021191697A - Aseptic filling machine and aseptic filling method - Google Patents

Abstract

To provide an aseptic filling machine and an aseptic filling method capable of reducing a size of the facilities to suppress initial investment, simplifying steps to reduce running costs and performing simultaneously molding and filling which are reliably aseptic.SOLUTION: The aseptic filling machine includes a heating part for heating a preform, a sterilizing part for sterilizing the heated a preform, a molding and filling part for filling a sterilized content into the sterilized preform at a high pressure to thereby mold the preform into a bottle and fill the content at the same time, and a sealing part for sealing the bottle filled with the content; before operating the aseptic filling machine, the molding and filling part and the sealing part are cleaned and sterilized in a state of non-inserting a stretching rod for stretching the preform in a longitudinal direction into a blow nozzle, and aseptic air is fed into the molding and filling part and the sealing part after sterilization to maintain the aseptic filling machine in an aseptic state.SELECTED DRAWING: Figure 1

Description

The present disclosure relates to an aseptic filling machine and an aseptic filling method for sterilizing a preform, molding the sterilized preform in a sterile atmosphere, and at the same time filling the contents.

Tea, sports drinks, milk drinks, drinks containing fruit juice, etc. are distributed in biaxially stretched polyethylene terephthalate (PET) bottles. Since these beverages may spoil if bacteria or the like are mixed during filling, the sterilized bottle is filled with the sterilized beverage in a sterile atmosphere and sealed with a sterilized cap. This process is continuously performed by one aseptic filling machine from molding the preform into a bottle to sealing.

As such a sterile filling machine, while transporting the preform, a disinfectant such as hydrogen peroxide is sprayed on the preform, and then the preform is heated to activate the disinfectant adhering to the surface and to activate the preform. An in-line system has been proposed in which the remodeling is raised to the molding temperature, and then the heated preform is molded into a bottle by a blow molding machine, the molded bottle is filled with beverages, etc., and capped to form a sterile package. (Patent Documents 1 and 2).

In addition, the preform is heated to the molding temperature, the heated preform is molded into a container, the molded container is sterilized, and the sterilized container is filled with the sterilized contents in an aseptic atmosphere. A sterile filling machine that seals a filled container with a sterilized lid material has also been proposed (Patent Documents 3 and 4).

The aseptic filling machine as described above is a long system because the preform is molded into a bottle and the molded bottle is filled with the contents. Therefore, it has been proposed to fill the preform with a beverage as a content at high pressure instead of the high-pressure gas used for blow molding the preform, and to perform molding and filling at the same time (Patent Documents 5 and 6). ).

In the method described in Patent Document 5, a stretch rod or an inner pipe is built in the core of a mold for injection molding a preform, and after injection molding, the preform outerly fitted to the core is introduced into the mold as it is and molded. It is a method in which sterility is maintained by filling, injection molding is continuously performed, and the core of injection molding is also used for blow molding, which is extremely complicated.

Further, Patent Document 6 is a method in which a preform is sterilized by steam or the like, and a liquid product is sent to a heated preform at a high pressure to form a bottle, and at the same time, the liquid product is filled in the bottle. In order to obtain sterile products by sending liquid products at room temperature, the process must be performed in a sterile atmosphere, which is costly, and there is a risk that bacterial contaminants will break through the protective measures during work and contaminate the product. It is said that it is always present, and the sterility at room temperature filling is not sufficient.

Japanese Patent Publication No. 2001-510104 Japanese Unexamined Patent Publication No. 2009-274740 Japanese Unexamined Patent Publication No. 2006-11195 Japanese Unexamined Patent Publication No. 2010-155631 Japanese Unexamined Patent Publication No. 2000-43129 Japanese Patent Publication No. 2011-506130

Conventionally, aseptic filling machines for bottles mold preforms into bottles and sterilize the bottles after molding. However, since a large amount of disinfectant is required and the equipment becomes excessive, the preform stage is used. Aseptic filling machines for sterilization are becoming widespread. However, after being sterilized at the preform stage, the preform is molded into a bottle and the molded bottle is filled with the contents, so the size of the entire aseptic filling machine is reduced compared to sterilizing the molded bottle. However, it is still long.

Therefore, it has been proposed that the preform is molded and filled into a bottle at the same time by filling the preform with the beverage as the content in the aseptic preform as in Patent Documents 5 and 6 at high pressure. .. However, it was insufficient to maintain sterility until the step of filling the sterilized preform at the same time as molding. Aseptic preforms may be contaminated by bacteria or the like before molding and filling, and Patent Document 6 recommends high-temperature filling. This is because even if the inner surface of the preform is contaminated by bacteria or the like by high-temperature filling, it can be sterilized by the heat of the contents to be filled. Products that are hot-filled and sealed must then be cooled, and there is also quality degradation of the contents, which does not take advantage of aseptic filling.

Patent Document 5 states that sterility is maintained because the core used in injection molding is molded and filled with the preform fitted, but the process is complicated and it is difficult to obtain high-speed productivity. Is.

There is a demand for a sterile filling machine that can simultaneously perform molding and filling with reliable sterility, by making the size of the equipment compact, reducing the initial investment, simplifying the process, and reducing the running cost. The present disclosure has been made to solve the above problems, and the preform bottle is filled with the sterilized contents at high pressure while maintaining the sterility of the sterilized preform. It is an object of the present invention to provide an aseptic filling machine and an aseptic filling method capable of simultaneously forming and filling.

The sterile filling machine according to the present disclosure is a heating unit that heats the preform, a sterilizing unit that sterilizes the preform, and the sterilized preform is filled with the sterilized contents at high pressure to fill the preform. It is a sterile filling machine provided with a molding filling part for molding into a bottle and a sealing part for sealing the bottle filled with the contents. The sterilizing part, the molding filling part and the sealing part are shielded by a chamber, and each part is sealed. Of the sterilizing part chamber, the molding filling part chamber and the sealing part chamber to be shielded, at least the molding filling part chamber and the cleaning device for cleaning the inside and the inner surface of the sealing part chamber, the sterilizing device for sterilizing, and at least the molding filling part chamber and the above-mentioned molding filling part chamber and A sterilizing air supply device for supplying sterilizing air is provided inside the sealing portion chamber, and the molding filling portion includes at least a mold, a blow nozzle, a stretching rod, a valve block, and a pressurizing device for pressurizing the contents. The drawing rod holding material for holding the stretching rod and the stretching rod holding material operating shaft are provided, and the stretching rod is configured to be non-inserted into the blow nozzle. The sterile filling machine according to another embodiment of the present disclosure includes a heating unit for heating the preform, a sterilizing unit for sterilizing the heated preform, and a sterilized content in the sterilized preform at high pressure. A sterile filling machine provided with a molding filling section for molding the preform into a bottle by filling, and a sealing section for sealing the bottle filled with the contents, wherein the sterilizing section, the molding filling section and the sealing section are provided. A sterilizer that sterilizes the inside and inside of the molded filling chamber and the sealed chamber, and at least the molding, at least among the sterilizing portion chamber, the molding filling portion chamber, and the sealing portion chamber in which the portions are shielded by a chamber and shielding each portion. A sterilizing air supply device for supplying sterilizing air is provided inside the filling portion chamber and the sealing portion chamber, and the molding filling portion pressurizes at least a mold, a blow nozzle, a drawing rod, a valve block, and the contents. A pressure device is provided, and a cup-shaped closing device that receives the discharge from the blow nozzle is provided, and a circulation path from the cup-shaped closing device to the pressurizing device, the valve block, and the blow nozzle is formed. It is configured as follows.

Further, in the aseptic filling machine according to the present disclosure, it is preferable that the aseptic air supply device is configured so that the pressure in the molding filling chamber is higher than the pressure in other chambers. Further, it is preferable that the aseptic filling machine according to another embodiment of the present disclosure is provided with a pre-sterilization section for sterilizing the preform in front of the heating section.

Further, it is preferable that the aseptic filling machine according to another embodiment of the present disclosure is provided with a cleaning device for cleaning the inside of the molded filling chamber and the sealed chamber.

Further, in the aseptic filling machine according to another embodiment of the present disclosure, it is preferable that the molding filling portion chamber includes a movable portion for holding the molding filling portion and a fixed portion for shielding the molding filling portion.

Further, in the aseptic filling machine according to another embodiment of the present disclosure, the sterilizing means of the preform in the sterilizing unit is a contact of the sterilizing agent gas or mist or a mixture thereof with the preform, and an electron beam. Irradiation, irradiation with light including ultraviolet rays, or contact with superheated steam is suitable for any one or two or more.

Further, in the aseptic filling machine according to another embodiment of the present disclosure, the sterilizing means of the preform in the pre-sterilizing unit is the contact of the sterilizing agent with the preform, the irradiation of an electron beam, and the light including ultraviolet rays. Irradiation, contact with hot water, or contact with superheated steam is preferable according to any one or two or more.

Further, in the aseptic filling machine according to another embodiment of the present disclosure, it is preferable that the pressurizing device is a high pressure plunger pump.

Further, it is preferable that the aseptic filling machine according to another embodiment of the present disclosure is provided with a stretching rod shielding chamber that shields the stretching rod.

Further, in the aseptic filling machine according to another embodiment of the present disclosure, it is preferable that a driving device for driving the stretching rod is provided at a position where the stretching rod is not inserted into the blow nozzle.

The aseptic filling method according to the present disclosure is a heating step for heating the preform, a sterilization step for sterilizing the preform, and a bottle of the preform by filling the sterilized contents with the sterilized contents at high pressure. It is an aseptic filling method having a molding and filling step of molding the contents into a bottle and at the same time filling the bottle with the contents, and a sealing step of sealing the bottle filled with the contents. The inside and inside of the chamber that is shielded from the outside are cleaned and sterilized, sterile air is supplied into the chamber, the sterility in the chamber is maintained, and the molding and filling step and the molding filling step and the inside of the chamber in which the sterility is maintained are maintained. When the sealing step is performed to clean and sterilize the inside and the inner surface of the chamber, the stretching rod for extending the preform in the longitudinal direction is not inserted into the blow nozzle to be joined to the mouth of the preform. .. The aseptic filling method according to another embodiment of the present disclosure includes a heating step of heating the preform, a sterilization step of sterilizing the heated preform, and a sterilized content of the sterilized preform at high pressure. It is an aseptic filling method having a molding filling step of molding the preform into a bottle by filling and at the same time filling the bottle with the contents, and a sealing step of sealing the bottle filled with the contents. In the chamber where the inside and the inner surface of the chamber that shields each part where the process and the sealing process are performed are sterilized, sterile air is supplied into the chamber, the sterility in the chamber is maintained, and the sterility is maintained. Before the molding and filling step and the sealing step are performed and the molding and filling step is performed, the discharge port of the blow nozzle that discharges the contents to the bottle is closed by a cup-shaped closing device, and the cup-shaped closing device is closed. By forming a pressurizing device for pressurizing the contents, a valve block for controlling the pressurized contents, and a circulation path leading to the blow nozzle, and circulating a cleaning agent or hot water in the circulation path. Clean or sterilize the inside of the contents of the pipe.

Further, in the aseptic filling method according to the present disclosure, it is preferable to spray sterile water into the chamber after cleaning and sterilizing the inside of the chamber. Further, it is preferable that the aseptic filling method according to another embodiment of the present disclosure includes a pre-sterilization step of sterilizing the preform before the heating step.

Further, in the aseptic filling method according to the present disclosure, when aseptic air is supplied into the chamber, it is preferable that the pressure in the chamber where the molding and filling step is performed is higher than the pressure in other chambers. Further, in the aseptic filling method according to another embodiment of the present disclosure, it is preferable to clean the inside and the inner surface of the chamber before sterilizing the inside and the inner surface of the chamber in which the molding filling step and the sealing step are performed. Is.

Further, in the aseptic filling method according to the present disclosure, it is preferable that the temperature of the cleaning liquid for cleaning the inside of the chamber is 50 ° C. or higher. Further, in the aseptic filling method according to another embodiment of the present disclosure, the sterilization step involves contact of the bactericidal gas or mist or a mixture thereof with the preform, irradiation with an electron beam, and light including ultraviolet rays. It is preferable to use either one or two or more of irradiation and contact with superheated steam.

Further, in the aseptic filling method according to another embodiment of the present disclosure, the pre-sterilization step involves contacting the preform with a bactericidal agent, irradiating an electron beam, irradiating light including ultraviolet rays, and contacting with warm water. It is suitable according to any one or more of the contacts of the superheated steam.

Further, in the sterile filling method according to another embodiment of the present disclosure, in the molding and filling step, the blow nozzle is joined to the top surface of the mouth of the preform, the mold is closed, and the preform is subjected to the longitudinal direction by a stretching rod. After stretching to, the pressurized content is controlled by a valve block to be introduced into the preform, the preform is stretched laterally, molded into a mold-shaped bottle, and at the same time, the content is molded into the preform. It is preferable to fill up to the vicinity of the lower end of the mouth of the reform.

Further, in the aseptic filling method according to another embodiment of the present disclosure, it is preferable to sterilize the inside of the chamber where the molding and filling step is performed with the stretch rod not inserted into the blow nozzle.

Further, in the aseptic filling method according to another embodiment of the present disclosure, it is preferable to wash the inside of the chamber where the molding and filling step is performed with the stretch rod not inserted into the blow nozzle.

Further, in the aseptic filling method according to another embodiment of the present disclosure, the flow path inside the blow nozzle is cleaned or sterilized so that the outer surface temperature of the blow nozzle is 60 ° C. or higher. It is preferable to sterilize the inside of the chamber where the molding and filling step is performed with hydrogen peroxide gas or mist or a mixture thereof.

Further, in the aseptic filling method according to another embodiment of the present disclosure, it is preferable to wash the inner surface of the mold while the mold is open while rotating the mold at a speed of 60 rpm or less. be.

According to the aseptic filling machine of the present disclosure, molding and filling can be performed at the same time by introducing the sterilized contents into the preform at a high pressure while maintaining the sterility of the sterilized preform. In addition, the aseptic filling machine of the present disclosure is much smaller than the conventional one by simplifying the process, and the initial investment cost can be suppressed. Further, according to the aseptic filling method of the present disclosure, as compared with the conventional method, molding and filling are performed at the same time, so that the process is simple and the running cost can be reduced. Moreover, it is possible to produce a product having high reliability for sterility.

It is a top view which shows the outline of an example of the aseptic filling machine which concerns on Embodiment 1 of this disclosure. The preform supply process which concerns on embodiment of this disclosure is shown. The preform heating step which concerns on embodiment of this disclosure is shown. The step of spraying a fungicide gas on a preform which concerns on embodiment of this disclosure is shown. The gas generator of the fungicide according to the embodiment of this disclosure is shown. The steps of irradiating the preform with an electron beam according to the embodiment of the present disclosure are shown. The light irradiation step including ultraviolet rays to the preform which concerns on embodiment of this disclosure is shown. The step of spraying superheated steam to the preform which concerns on embodiment of this disclosure is shown. It is sectional drawing which shows the molding filling part of the preform which concerns on embodiment of this disclosure. The apparatus which performs CIP and SIP in the molding filling part of the preform which concerns on embodiment of this disclosure is shown. The process of sealing the bottle according to the embodiment of the present disclosure is shown. It is a top view which shows the outline of the example of the aseptic filling machine which concerns on Embodiment 2 of this disclosure. The step of spraying a disinfectant on a preform which concerns on Embodiment 2 of this disclosure is shown.

Hereinafter, the first embodiment for carrying out the present disclosure will be described with reference to the drawings.

(Embodiment 1)
First, a heating unit that heats the preform supplied from the preform supply device to the temperature at which it is molded into a bottle, a sterilization unit that sterilizes the heated preform, and the contents sterilized into the sterilized preform at high pressure. An outline of the aseptic filling machine according to the first embodiment, which is provided with a molding filling part for forming a preform into a bottle by filling and simultaneously filling the contents, and a sealing part for sealing the bottle filled with the contents. It will be described with reference to FIG. 1, and the details of the aseptic filling machine and the aseptic filling method will be described with reference to the drawings. According to the first embodiment, the sterilized preform can be filled with the contents at the same time as molding, and a sterile product in which the contents are filled in the bottle can be obtained in a smaller number of steps as compared with the conventional case. ..

(Overview of the aseptic filling machine according to the first embodiment)
As shown in FIG. 1, the aseptic filling machine according to the present embodiment has a preform supply device 3 for supplying the preform 1, a heating unit 14 for heating the preform 1 to a temperature for forming the preform 1 into a bottle 2, and a heated pump. A sterilizing unit 6 that sterilizes the reform 1, a molding filling unit 21 that molds the preform 1 into a bottle 2 and at the same time fills the sterilized contents, and a seal that seals the bottle 2 filled with the contents with a sterilized cap 35. It has a part 26. Further, the sealed bottle 2 is placed on the discharge conveyor 31 and includes a discharge unit 30 to be discharged to the non-sterile zone.

The heating unit 14 is shielded by the heating unit chamber 18, the sterilizing unit 6 is shielded by the sterilizing unit chamber 5, the molding filling unit 21 is shielded by the molding filling unit chamber 22, and the sealing unit 26 and the discharging unit 30 are shielded by the sealing unit chamber 27. Since the heating unit 14 is located upstream of the sterilization unit 6 and is a non-sterile area, it does not have to be shielded by the chamber. The molding filling portion 21 and the sealing portion 26 may be shielded by a single chamber. Depending on the sterilizing means of the preform 1 in the sterilizing section 6, gas or mist of a sterilizing agent, a mixture thereof, or ozone is generated in the sterilizing section chamber 5. The sterilizing unit 6 is exhausted by the exhaust blower 33 through the exhaust gas treatment device 32 that detoxifies the gas or mist of the sterilizing agent, a mixture thereof, or ozone so that these do not flow into the heating unit 14.

A sterilizer is provided in at least the molding filling chamber 22 and the sealing chamber of the sterilizing chamber 5, the molding filling chamber 22 and the sealing chamber 27, and the inside of each chamber is sterilized before the start of operation of the aseptic filling machine. .. By sterilizing the preform 1, the inside of the sterilizing section chamber 5 may be sterilized, and it is not necessary to sterilize before operating the aseptic filling machine. The heating unit 14 is provided upstream of the sterilizing unit 6, and the inside of the heating unit chamber 18 does not have to be sterilized.

The disinfectant device includes a disinfectant spray nozzle and a disinfectant supply device that supplies the disinfectant to these nozzles. The disinfectant spray nozzle is, for example, a one-fluid spray or a two-fluid spray in which a disinfectant is mixed with compressed air and sprayed. The disinfectant spray nozzle is arranged so that the disinfectant adheres to the entire area in each chamber. The inside of each chamber is sterilized by the sprayed disinfectant. After the disinfectant is sprayed, sterile air at room temperature or heated is sprayed into each chamber to activate and further remove the disinfectant remaining in each chamber. The disinfectant may be washed away by spraying sterile water into each chamber before spraying sterile air. Further, since the contents may be scattered in the molding filling chamber 22 and the sealing chamber 27, it is preferable to wash them before sterilization.

At least, a sterile air supply device is provided in the molding filling chamber 22 and the sealing chamber 27, and after the inside of each chamber is sterilized, aseptic air sterilized by a sterilization filter is supplied into each chamber. The inside of the chamber is kept under positive pressure. A sterile air supply device may be provided in the heating section chamber 18 and the sterilization section chamber 5. Asepticity in the aseptic filling machine is maintained by keeping the inside of each chamber at a positive pressure by aseptic air. The pressure for holding the inside of each chamber at a positive pressure is set to be the highest in the molding filling chamber 22 and lower in the sealing chamber 27 than in the molding filling chamber 22. Since the sterilizer chamber 5 is exhausted, the pressure is maintained at substantially the same pressure as the atmospheric pressure. The sterilization chamber 5 is not provided with the aseptic air supply device, and the aseptic air in the molding filling chamber 22 may simply flow in. Further, an exhaust device may be provided in each chamber other than the sterilizer chamber 5 and used in combination with a sterile air supply device to maintain the inside of each chamber at an appropriate pressure. When the molding filling portion 21 and the sealing portion 26 are shielded by a single chamber, one aseptic air supply device and one exhaust device may be provided in a single chamber.

(Details of the aseptic filling machine and the aseptic filling method according to the first embodiment)
The preform 1 shown in FIG. 2 is continuously conveyed from the preform supply device 3 shown in FIG. 1 to the heating unit 14 by the preform transfer conveyor 4 at a desired speed.

The preform 1 in the embodiment of the present disclosure is a test tubular bottomed tubular body and is shown in FIG. The preform 1 is provided with the same mouth portion 1a as the bottle 2 shown in FIG. 11 at the beginning of its molding. A male screw is formed in the mouth portion 1a at the same time as the molding of the preform 1. Further, the preform 1 is formed with a support ring 1b for transportation in the lower part of the mouth portion 1a. The preform 1 or the bottle 2 is gripped by the gripper 34 via the support ring 1b and runs in the aseptic filling machine. Preform 1 is molded by injection molding, compression molding, or the like. The material of the preform 1 is made of a thermoplastic resin such as polyethylene terephthalate, polyethylene naphthalate, polypropylene, polyethylene, etc., and may be a single resin or a mixture thereof, or may contain a recycled thermoplastic resin. Further, in order to impart barrier properties, a thermoplastic resin such as an ethylene-vinyl alcohol copolymer or a polyamide having an aromatic amine as a monomer such as m-xylylenediamine may be contained as a layer or as a mixture.

As shown in FIG. 1, the preform 1 is supplied from the preform supply device 3 to the heating furnace transfer wheel 11 by the preform transfer conveyor 4. As shown in FIG. 2, the preform 1 supplied to the heating furnace transfer wheel 11 is gripped by the gripper 34 provided on the heating furnace transfer wheel 11 to grip the support ring 1b. After that, as shown in FIG. 3, the spindle 48 is released from the gripper 34, the spindle 48 is inserted into the mouth portion 1a of the preform 1, and the spindle 48 is conveyed to the heating furnace 19. As shown in FIG. 3, the preform 1 conveyed to the heating furnace 19 is heated to a temperature suitable for later blow molding by an infrared heater 15 or other heating means. A reflector 16 is provided on the opposite side of the infrared heater 15, and the heat radiated by the infrared heater 15 is reflected by the reflector 16, so that the preform 1 is efficiently heated. The temperature of the preform 1 to be heated is preferably 90 ° C to 130 ° C. The temperature of the mouth portion 1a of the preform 1 is suppressed to 70 ° C. or lower in order to prevent deformation and the like.

As shown in FIG. 3, the preform 1 has a spindle 48 inserted into the mouth portion 1a and is conveyed in the heating furnace 19 while rotating. Spindles 48 are provided on the endless chain 12 at regular intervals. The endless chain 12 is rotated by the pulleys 13a and 13b. By inserting the mandrel into the preform 1 instead of the spindle 48, it is possible to transport the preform 1 while rotating it in an inverted state.

The heated preform 1 is released from the spindle 48, gripped by the gripper 34, and conveyed to the sterilizing wheel 7 of the sterilizing unit 6 via the wheel 9.

The preform 1 conveyed to the sterilizing unit 6 is conveyed to a sterilizing wheel 7 provided with a large number of grippers 34 at a constant pitch, and is sterilized here. The sterilization step for sterilizing the preform 1 is performed by any one or more of contact with a gas or mist of a disinfectant or a mixture thereof, irradiation with an electron beam, irradiation with light including ultraviolet rays, and contact with superheated steam. The sterilization wheel 7 is provided with a sterilization means 8 for performing a sterilization step. The preform 1 is heated to the molding temperature in the heating unit 14, and the bactericidal effect is higher than that at room temperature.

Contact of the disinfectant gas or mist or a mixture thereof with the preform 1 means that the mist or a mixture thereof, in which the gas is liquefied by gasifying the disinfectant and cooling, is applied to the preform 1 as shown in FIG. It is to spray.

The disinfectant sprayed onto Preform 1 as a gas or mist or a mixture thereof preferably contains at least hydrogen peroxide. The content thereof is appropriately in the range of 0.5% by mass to 65% by mass. If it is less than 0.5% by mass, the bactericidal activity may be insufficient, and if it exceeds 65% by mass, it becomes difficult to handle for safety. More preferable is 0.5% by mass to 40% by mass, and when it is 40% by mass or less, it is easier to handle, and since the concentration of hydrogen peroxide is low, the residual amount of the disinfectant after sterilization can be reduced. The bactericidal agent contains water, but is one of alcohols such as methyl alcohol, ethyl alcohol, isopropyl alcohol, normal propyl alcohol and butyl alcohol, ketones such as acetone, methyl ethyl ketone and acetyl acetone, glycol ethers and the like. It may contain two or more kinds. Further, the bactericidal agent is an organic acid such as peracetic acid and acetic acid, an inorganic acid such as nitrate, a basic compound such as sodium hydroxide and potassium hydroxide, and a compound having a bactericidal effect such as sodium hypochlorite, chlorine dioxide and ozone. Additives such as a cationic surfactant, a nonionic surfactant, and a phosphoric acid compound may be contained.

The disinfectant gas or mist sprayed onto the preform 1 or a mixture thereof is obtained by the disinfectant gas generator 36 shown in FIG. The disinfectant gas generator 36 heats the disinfectant supply unit 37, which is a two-fluid spray nozzle that supplies the disinfectant in the form of drops, and the disinfectant supplied from the disinfectant supply unit 37 to a decomposition temperature or lower. It is provided with a vaporizing unit 38 for vaporizing. The disinfectant supply unit 37 introduces the disinfectant and the compressed air from the disinfectant supply path 37a and the compressed air supply path 37b, respectively, and sprays the disinfectant into the vaporization unit 38. The vaporization unit 38 is a pipe in which a heater 38a is sandwiched between the inner and outer walls, and the disinfectant blown into the pipe is heated and vaporized. The vaporized disinfectant gas is ejected from the disinfectant gas spray nozzle 39 to the outside of the vaporized portion 38. The vaporization unit 38 may be heated by dielectric heating or superheated steam instead of the heater 38a.

As the operating conditions of the disinfectant supply unit 37, for example, the pressure of the compressed air is adjusted in the range of 0.05 MPa to 0.6 MPa. At this time, the supply amount of compressed air is 50 L / min. ~ 300 L / min. Is appropriate. Further, the disinfectant may be dropped by gravity or pressure may be applied, and the supply amount of the disinfectant can be freely set. For example, the disinfectant is 1 g / min. ~ 100 g / min. It is supplied in the range of. Further, the inner surface of the vaporizing portion 38 is heated from 120 ° C. to 450 ° C. to gasify the sprayed fungicide.

The disinfectant gas is sprayed onto the preform 1 from the disinfectant gas spray nozzle 39 as shown in FIG. The disinfectant gas flows in two hands in the disinfectant gas spray nozzle 39, is sprayed from one nozzle 39a toward the inside of the preform 1, and from the other nozzle 39b toward the outer surface of the preform 1. Be sprayed. The disinfectant gas exits the disinfectant gas spray nozzle 39 and then flows into the preform 1 in the gas state, as a mist, or as a mixture thereof, or in the preform 1. Contact the outer surface.

The disinfectant gas or mist or mixture sprayed toward the inside of the preform 1 overflows from the mouth portion 1a of the preform 1 after flowing into the preform 1, but the overflowing disinfectant gas or the like The flow collides with the umbrella-shaped member 40, is guided to the inner surface of the umbrella-shaped member 40, changes the flow toward the outer surface of the preform 1, and comes into contact with the outer surface of the preform 1. When the annular groove 40a is provided in the umbrella-shaped member 40, the overflowing disinfectant gas or the like flows along the outer surface of the preform 1.

The amount of the disinfectant gas or mist or a mixture thereof to be sprayed is arbitrary, but the amount of the disinfectant is determined by the amount of the disinfectant supplied to the disinfectant gas generator 36 and the spraying time. A plurality of disinfectant gas generators 36 may be provided. The amount of spraying also varies depending on the size of preform 1. Disinfectant gas spraying The disinfectant gas or mist ejected from the nozzle 39 or a mixture thereof may be diluted with hot air and sprayed onto the preform 1.

When the disinfectant is hydrogen peroxide solution, the amount of hydrogen peroxide solution sprayed is as follows. The amount of hydrogen peroxide adhering to the preform 1 due to the hydrogen peroxide solution sprayed from the disinfectant gas spray nozzle 39 onto the preform 1 is converted into a hydrogen peroxide solution containing 35% by mass of hydrogen peroxide. Therefore, 0.0035 μL / cm ^{2 to} 0.35 μL / cm ² is preferable. The hydrogen peroxide concentration of the hydrogen peroxide solution sprayed on the preform 1 is preferably 2 mg / L to 20 mg / L, more preferably 5 mg / L to 10 mg / L.

The preform 1 sprayed with the disinfectant gas or mist or a mixture thereof is preferably aseptically air-rinsed with sterilized air. The nozzle for blowing sterile air to the preform 1 may be provided so as to face the mouth portion 1a of the preform 1, or a nozzle that follows the transport speed of the preform 1 may be inserted inside the preform 1. The sterile air rinse has the effects of activating the disinfectant sprayed on the preform 1 and removing the disinfectant sprayed on the inside of the preform 1 and foreign substances and dust existing inside. Aseptic air The rinsed air may be heated at room temperature. Heating is more effective in activating the disinfectant. Further, the sterile air rinse may be performed with the preform 1 upright or inverted. Inverting is more effective in eliminating foreign matter. Further, in order to eliminate foreign matter, it is preferable to suck the vicinity of the mouth portion 1a of the inverted preform 1. The amount of air blown is preferably 0.04 L / preform to 400 L / preform.

In the sterilization method of spraying the disinfectant gas or mist or a mixture thereof onto the preform 1, the disinfectant gas or mist or a mixture thereof is generated in the spraying step and the subsequent aseptic air rinsing step. Need to be exhausted. The exhausted air is detoxified by the exhaust gas treatment device 32 and discharged.

Irradiation of the electron beam to the preform 1 according to the embodiment of the present disclosure means that the electron beam is applied to the inner and outer surfaces of the preform 1 conveyed by the electron beam irradiation devices 42a, 42b and 42c as shown in FIG. It is to irradiate. The electron beam has a bactericidal action, and bacteria and the like adhering to the surface of the preform 1 are sterilized by irradiation with the electron beam. In FIG. 6, the electron beam is irradiated from three directions of the preform 1, but any method may be used as long as the inner and outer surfaces of the preform 1 are irradiated with the electron beam. For example, if the preform 1 is rotated, the electron beam irradiation device 42b becomes unnecessary. Further, even if a reflection mirror is provided above the mouth portion 1a of the preform 1 and the electron beam irradiated from the electron beam irradiation device 42a is introduced into the inside of the preform 1 from the upper part of the mouth portion 1a of the preform 1. I do not care. Further, a rod-shaped electron beam irradiating device may be inserted inside the preform 1 to irradiate the inner surface of the preform 1 with an electron beam.

The electron beam irradiation device 42a, 42b, 42c may have any structure. For example, there are a scanning type and a monofilament type, and a low output type having an output of 100 kV to 500 kV is preferable because it is easy to handle.

It is preferable to remove foreign substances adhering to the inner and outer surfaces of the preform 1 before irradiating the preform 1 with an electron beam. This is because if a foreign substance adheres to the surface of the preform 1, the electron beam is not irradiated to that portion, which may cause sterilization failure. In order to remove the foreign matter from the preform 1, the preform 1 is upright or inverted and blown with air or water before it is heated. When water is sprayed, it is necessary to further remove it, so spraying with air is preferable. Before blowing air, it is preferable to blow ionized air onto the preform 1 to eliminate static electricity. Further, it is preferable to provide a suction nozzle in the vicinity of the mouth portion 1a of the preform 1 to suck foreign matter and remove it to the outside of the aseptic filling machine. The step of removing the foreign matter of the preform 1 is preferably performed by the preform transfer conveyor 4 outside the heating unit 14, and after removing the foreign matter, the preform 1 is conveyed to the heating unit 14.

Since the electron beam changes oxygen into ozone, ozone is generated when oxygen is present in the atmosphere where the electron beam is irradiated. In order to remove the generated ozone, the inside of the sterilizer chamber 5 needs to be exhausted. The generation of ozone can be suppressed by replacing the atmosphere in which electron beam irradiation is performed with nitrogen or the like.

Irradiation of light containing ultraviolet rays to the preform 1 according to the embodiment of the present disclosure means that the inner and outer surfaces of the preform 1 are irradiated with light containing ultraviolet rays emitted from the light irradiation lamp 43 as shown in FIG. be. It is preferable to provide a light reflector 44 on the opposite side of the preform 1 with respect to the light irradiation lamp 43 to reflect the irradiated light and direct it toward the preform 1.

Ultraviolet rays contained in the irradiated light are a kind of electromagnetic waves having a wavelength of 100 nm to 380 nm. The irradiated light includes any of these wavelengths, and ultraviolet rays having a wavelength of 100 nm to 280 nm, which is called UV-C, are particularly effective for sterilization. Furthermore, it is the ultraviolet rays having a wavelength of 253.7 nm that has the most bactericidal effect, and it is optimal to include this.

The light irradiation lamp 43 that emits ultraviolet rays having a wavelength of 100 nm to 380 nm is a low-pressure mercury lamp, a high-pressure mercury lamp, a xenon flash lamp, or the like. In particular, the light irradiation lamp 43 is preferably a xenon flash lamp because the bactericidal effect of the light (wavelength: 100 to 950 nm) emitted from the xenon flash lamp in which xenon gas is sealed is high.

The bactericidal effect of irradiation with light including ultraviolet rays is proportional to the irradiation amount and irradiation time per unit area of light. However, since the light emitted by the xenon flash lamp has a higher sterilizing effect than the light emitted by the low-pressure mercury lamp or the high-pressure mercury lamp, it can be sufficiently sterilized by irradiation in a short time, and the preform 1 by irradiation with light can be sufficiently performed. It is possible to avoid an increase in the temperature of the mouth portion 1a.

The number of the light irradiation lamps 43 may be limited as long as the entire inner and outer surfaces of the preform 1 are irradiated with light containing ultraviolet rays. As shown in FIG. 7, a large number may be provided to irradiate the outer surface and the inner surface with light including ultraviolet rays. However, if the preform 1 is rotated, the light irradiation lamps 43 that irradiate the side surface of the preform 1 may be in one row. In order to irradiate the inner surface of the preform 1 with light containing ultraviolet rays, a light irradiation lamp 43 is provided facing the mouth portion 1a of the preform 1, and the light containing ultraviolet rays is emitted through the opening of the mouth portion 1a of the preform 1. It is preferable to irradiate the inner surface. Further, it is preferable to provide the light reflecting plate 44 in a dome shape toward the mouth portion 1a and efficiently irradiate the inner surface of the preform 1 with light including ultraviolet rays emitted from the light irradiation lamp 43. In order to irradiate the inner surface of the preform 1 with light containing ultraviolet rays, a rod-shaped light irradiation lamp may be inserted inside the preform 1 to irradiate the inner surface of the preform 1 with light containing ultraviolet rays. The shape of the light irradiation lamp 43 may be any shape such as a round shape, a rod shape, and a U shape.

The light reflector 44 shown in FIG. 7 has a purpose of efficiently irradiating the preform 1 with light including ultraviolet rays emitted from the light irradiation lamp 43. Therefore, it is provided on the opposite side of the preform 1 of the light irradiation lamp 43. The light reflector 44 may be a flat surface, a curved surface, a combination of a plurality of surfaces, or any shape. The configuration of the light reflector 44 may be any structure as long as it can reflect light including ultraviolet rays. For example, it is made of synthetic resin, metal, and glass, and its surface is smoothed. In order to make the surface smoother, coating, plating of metal, and vapor deposition of metal and metal oxide are performed. It may be a combination of.

Before irradiating the preform 1 with light containing ultraviolet rays, it is preferable to remove foreign substances adhering to the inner and outer surfaces of the preform 1. This is because if foreign matter adheres to the surface of the preform 1, the portion thereof is not irradiated with light including ultraviolet rays, which may cause sterilization failure. In order to remove the foreign matter from the preform 1, the preform 1 is upright or inverted and blown with air or water before it is heated. If water is sprayed, it is necessary to remove it, so spraying air is preferable. Before blowing air, it is preferable to blow ionized air onto the preform 1 to eliminate static electricity. Further, it is preferable to provide a suction nozzle in the vicinity of the mouth portion 1a of the preform 1 to suck foreign matter and remove it to the outside of the aseptic filling machine. The step of removing the foreign matter of the preform 1 is preferably performed by the preform transfer conveyor 4 outside the heating unit 14, and after removing the foreign matter, the preform 1 is conveyed into the heating unit 14.

Since light containing ultraviolet rays changes oxygen into ozone, ozone is generated when oxygen is present in the atmosphere in which light containing ultraviolet rays is irradiated. In order to remove the generated ozone, the inside of the sterilizer chamber 5 needs to be exhausted. The generation of ozone can be suppressed by replacing the atmosphere in which light including ultraviolet rays is irradiated with nitrogen or the like.

The contact of superheated steam with the preform 1 according to the embodiment of the present disclosure means that, as shown in FIG. 8, the superheated steam generated from the superheated steam generator 45 is blown from the superheated steam blowing nozzle 46 and the superheated steam blowing slit 47. It is to blow superheated steam on the inner and outer surfaces of Preform 1. Bacteria and the like adhering to the surface of preform 1 are sterilized by the heat of superheated steam.

The superheated steam is steam having a pressure of 0.1 MPa to 0.3 MPa, which is higher than the atmospheric pressure of 200 ° C. to 500 ° C. generated from water. The water passage pipe of the superheated steam generator 45 is heated by a heater or an induction coil to generate superheated steam. The generated superheated steam is ejected from the superheated steam blowing nozzle 46 and blown onto the inner surface of the preform 1. Further, the superheated steam generated by the superheated steam generator 45 is introduced into the superheated steam blowing slit 47, and the superheated steam is blown onto the outer surface of the preform 1.

The water supplied to the superheated steam generator 45 may be added with a bactericidal compound such as hydrogen peroxide. For example, the bactericidal effect is improved by adding 1% by mass to 5% by mass of hydrogen peroxide to water.

By rotating the preform 1, the superheated steam is efficiently sprayed on the outer surface. Further, the superheated steam blowing nozzle 46 may be inserted into the preform 1 to blow the superheated steam on the inner surface of the preform 1. Since it is sterilized by spraying for a short time, the mouth portion 1a is not deformed and the resin forming the preform 1 is not excessively heated. Further, the steam drain does not remain inside the preform 1, and the preform 1 can be conveyed to the molding filling portion 21 without removing the drain.

As described above, in the sterilizing unit 6, the preform 1 is subjected to contact with the sterilizing agent gas or mist or a mixture thereof, irradiation with an electron beam, and irradiation with light including ultraviolet rays by the sterilizing means 8 provided on the sterilizing wheel 7. , Is sterilized by any one or more methods of contact with superheated steam. Although the sterilizing means 8 is provided around the sterilizing wheel 7, one or two or more wheels may be provided in addition to the sterilizing wheel 7, and the sterilizing means may be provided on a plurality of wheels.

The inside of the sterilizing section chamber 5 may be sterilized by means such as spraying a sterilizing agent such as hydrogen peroxide solution into the sterilizing section chamber 5 before operating the aseptic filling machine. Therefore, a sterilizing agent spray nozzle is provided on the wall surface inside the sterilizing unit chamber 5. Further, a similar sterilizing agent spray nozzle may be provided to sterilize the surface of the sterilizing filter of the sterile air supply device in contact with the sterilizing section chamber 5 on the sterilizing section chamber 5 side.

The preform 1 sterilized by the sterilizing section 6 is gripped by the support ring 1b and conveyed to the molding filling wheel 20 of the molding filling section 21 via the wheel 10.

As shown in FIG. 9, the molding filling portion 21 includes a mold 23, a blow nozzle 49, a valve block 50, a stretching rod 51, and a pressurizing device 55. Further, a drive unit 62 for driving the molding filling unit 21 is provided. The molding filling section 21 must be washed and sterilized before operation and maintained aseptic during operation in order to ensure the sterility of the preform 1 and the bottle 2. Although the drive unit 62 is not shown, it includes a motor, a hydraulic device, an operation transmission means, an air cylinder, and the like. It is difficult to maintain sterility because the equipment of the drive unit 62 requires a lubricant and stains are accumulated.

As shown in FIG. 9, in order to ensure the sterility of the molding filling portion 21, the molding filling portion 21 is shielded by the molding filling portion chamber 22. The molding filling section 21 includes a cleaning device and a sterilizing device for cleaning and sterilizing the inside of the molding filling section chamber 22 before operation. Further, as shown in FIG. 9, the molding filling part chamber 22 holds the molding filling part 21 and isolates the molding filling part 21 from the driving part 62, and the movable part 63 and the fixing that shields the molding filling part 21 from the outside. It consists of a part 64. The movable portion 63 rotates about the double pipe 65 as a central axis. The molding filling portion 21 held by the movable portion 63 also rotates, and the preform 1 is molded into the bottle 2 and the contents are filled at the same time as the rotation.

When the mold 23 is closed from the wheel 10, the preform 1 is delivered to the molding filling wheel 20. After that, the blow nozzle 49 is joined to the mouth portion 1a of the preform 1, the drawing rod 51 is guided into the hole provided in the blow nozzle 49 and inserted into the preform 1, and the bottom surface of the preform 1 is formed into a mold 23. The stretching rod 51 stretches the preform 1 in the longitudinal direction until it comes into contact with the bottom surface of the. After that, the stretching rod 51 rises, and at the same time, the medium pressure content P1 and the high pressure content P2 are sequentially sent to the preform 1 by the operation of the solenoid valve of the valve block 50, the preform 1 is stretched laterally, and the mold is formed. It is molded into a shaped bottle 2 and at the same time filled with its contents.

The high pressure content P2 must be filled until the preform 1 is molded into a bottle in the shape of the mold 23. Therefore, the high-pressure content P2 is filled up to the lower end of the mouth portion 1a. If the bottle 2 is filled up to the vicinity of the upper end of the mouth portion 1a, the contents may overflow from the bottle 2 when the bottle 2 is molded and filled. The filling amount of the high-pressure content P2 must be controlled up to the vicinity of the lower end of the mouth portion 1a. The pressure of the medium pressure content P1 is 1 MPa to 2.5 MPa, and the pressure of the high pressure content P2 is 2.5 MPa to 4 MPa. As shown in FIG. 9, the medium pressure content P1 and the high pressure content P2 are obtained by pressurizing the content sterilized by a sterilizer (not shown) with the pressurizing device 55. The pressurizing device 55 is, for example, a multi-unit high-pressure plunger pump.

The molded bottle 2 is opened by the mold 23, gripped by the gripper 34 of the wheel 24, and conveyed from the molded filling chamber 22 to the wheel 25 in the sealed portion 28. The molding of the preform 1 into the bottle 2 and the filling performed at the same time are performed by opening and closing the mold 23 and opening and closing the mold 23 with the rotation of the movable portion 63 of the molding filling chamber 22 and the molding filling portion 21 held by the movable portion 63, and the stretching rod 51. It is carried out by repeating the descent and ascent of the medium pressure content P1 and the high pressure content P2 into the preform 1.

As shown in FIG. 9, the inside of the molding filling chamber 22 is maintained in an aseptic atmosphere when the aseptic filling machine is in operation. The drive unit 62 is provided in a non-sterile atmosphere. The aseptic atmosphere and the non-sterile atmosphere are separated by sealing the lower part of the movable part 63 by the liquid sealing device 66 provided in the lower part of the movable part 63. The liquid may be a liquid such as water, but peracetic acid (preferably 100 ppm or more and 3000 ppm or less as the concentration contained in the liquid) and hydrogen peroxide (1% by mass or more and 36% by mass or less are contained in the liquid). Is preferable.) A liquid containing a bactericidal agent such as) is preferable. The end face of the movable portion 63 immersed in the liquid of the liquid sealing device 66 is provided so as not to come into contact with the bottom of the liquid sealing device 66. The liquid is passed through both ends of the movable portion 63 immersed in the liquid sealing device 66. Therefore, when the inside of the molded filling portion chamber 22 is positively pressured by the supply of sterile air, the liquid level height of the liquid on the non-sterile atmosphere side of the liquid sealing device 66 is higher than the liquid level of the liquid on the sterile atmosphere side. It's getting higher.

As shown in FIG. 9, the medium pressure content P1 and the high pressure content P2 required for molding the preform 1 into the bottle 2 and filling them at the same time are provided in the double pipe 65 from the upper part of the molding filling portion 21. It is supplied by piping. The double pipe 65 and the fixing portion 64 are joined by a rotary joint 67. The medium pressure content P1 and the high pressure content P2 are introduced from the pipe in the double pipe 65 passing through the sterile atmosphere to the high pressure content supply manifold 68 in the non-sterile atmosphere. Since the medium pressure content P1 and the high pressure content P2 are supplied from the high pressure content supply manifold 68 to the valve block 50 held by the movable portion 63, the high pressure content supply manifold 68 is rotatable.

The inside of the molding filling chamber 22 is cleaned before the operation of the aseptic filling machine. Therefore, a cleaning device is provided in the molding filling chamber 22. As shown in FIG. 9, the cleaning device is a cleaning agent supply device that supplies a cleaning agent to the spray nozzle 56 and the spray nozzle 56 provided in the fixed portion 64 of the molding filling chamber 22. The spray nozzle 56 uses a two-fluid spray that mixes one fluid or a cleaning agent with compressed air and sprays the cleaning agent from the spray nozzle 56 before or at the same time as sterilizing the inside and the inner surface of the molding filling chamber 22. Spray into the filling chamber 22. Then, water or sterile water is sprayed from the nozzle 56 into the molding filling chamber 22 to wash away the cleaning agent.

Since the area where the inside of the mold 23 is opened is limited, in order to clean the inside of the mold 23, the spray nozzle 56 uses the area where the mold 23 is open (a short distance between the wheel 10 and the wheel 24). ), And the cleaning agent is sprayed while rotating the mold 23 at a speed of 60 rpm or less. This is because the cleaning effect of the inner surface of the mold 23 is improved by spraying the cleaning agent on the mold 23 that rotates at a relatively low speed. By cleaning, the outer surface of the mold 23, the blow nozzle 49, the stretching rod chamber 52, the valve block 50, etc. existing inside the molding filling chamber 22 and the inner surface of the molding filling chamber 22 are washed. The spraying pressure of the cleaning agent is at least 0.05 MPa or more, preferably 0.2 MPa or more.

As shown in FIG. 9, the stretching rod 51 is held by the stretching rod holding material 53. The operation of raising or lowering the stretching rod 51 is performed by operating the stretching rod holding material 53. The stretch rod holding material 53 moves up and down by the movement of the stretching rod holding material operating shaft 54. The drawing rod holding material 53 is operated by rotating the drawing rod holding material operating shaft 54 by a servomotor or by connecting the drawing rod holding material operating shaft 54 to a pneumatic cylinder. However, in the case of a pneumatic cylinder, it is necessary to sterilize the inside of the cylinder by introducing a sterilizing agent gas into the cylinder or to sterilize the air that generates pressure through a sterilizing filter. Further, the shaft that goes in and out of the pneumatic cylinder may be protected by a bellows. The stretching rod 51 may not be directly held by the stretching rod holding material 53, but may be raised and lowered using a magnetic material.

The stretching rod 51 is inserted into the blow nozzle 49, but since the content is filled in the preform 1 from the outer peripheral portion of the stretching rod 51, the stretching rod 51 comes into contact with the content. The stretching rod 51, the stretching rod holding material 53, and the stretching rod holding material operating shaft 54 are shielded by the stretching rod chamber 52 in order to prevent the contents adhering to the stretching rod 51 from scattering into the molding filling chamber 22. Will be done. Therefore, for cleaning the stretching rod 51, the stretching rod holding material 53, and the stretching rod holding material operating shaft 54, the cleaning agent is driven by the spray nozzle 56 provided in the stretching rod chamber 52 to drive the stretching rod 51 and the stretching rod holding. This is done by spraying on the material 53 and the drawing rod holding material operating shaft 54. The stretching rod chamber 52 is, for example, cylindrical, but may have any shape as long as it can shield the stretching rod 51, the stretching rod holding material 53, and the stretching rod holding material operating shaft 54.

When the stretching rod 51 is inserted into the blow nozzle 49, the inserted portion is not washed. Therefore, when cleaning the stretching rod 51, the stretching rod 51 is not inserted into the blow nozzle 49. Therefore, a driving device including a stretching rod holding material 53 and a stretching rod holding material operating shaft 54 is provided so that the stretching rod 51 rises from the blow nozzle 49 to a non-insertion position. Although FIG. 9 shows the mouth of the preform 1 facing up, the preform 1 may be inverted. In this case, the stretching rod 51 moves downward so that it is not inserted from the blow nozzle 49.

The cleaning agent is water containing an acidic compound or a basic compound. The water may be water sterilized by heating or filtration, pure water, ion-exchanged water, distilled water, or tap water. The acidic compound is an inorganic acid such as hydrochloric acid, nitrate or phosphoric acid, or an organic acid such as acetic acid, formic acid, octanoic acid, oxalic acid, citric acid, succinic acid or gluconic acid. The basic compound is an inorganic basic compound such as sodium hydroxide or potassium hydroxide, or an organic basic compound such as ethanolamine or diethylamine. In addition, non-alkali metal salts of organic acids, alkaline earth metal salts, ammonium salts, metal ion blocking agents such as ethylenediamine tetraacetic acid, anionic surfactants, cationic surfactants, polyoxyethylene alkylphenyl ethers and the like. Includes ionic surfactants, solubilizers such as sodium cumenesulfonate, acid-based polymers such as polyacrylic acid or metal salts thereof, corrosion inhibitors, preservatives, antioxidants, dispersants, defoaming agents, etc. But it doesn't matter. Further, since these cleaning liquids also have a bactericidal action when heated to 50 ° C. or higher, they may be used as a bactericidal agent for sterilizing the inside of the chamber.

After cleaning the inside and inner surface of the molding filling chamber 22, or at the same time, the inside and inner surface of the molding filling chamber 22 are sterilized. The disinfectant is sprayed into the molding filling chamber 22 from the spray nozzle 56. Therefore, a sterilizing device is provided in the molding filling chamber 22. As shown in FIG. 9, the sterilizer is a sterilizer supply device that supplies a sterilizer to the spray nozzle 56 and the spray nozzle 56 provided in the fixed portion 64 of the molding filling chamber 22. The spray nozzle 56 may be used in combination with the nozzle for spraying the cleaning agent, or may be provided separately. Further, the spray nozzle 56 is arranged so that the disinfectant adheres to the entire area in the molding filling chamber 22. The inside of the molded filling chamber 22 is sterilized by the sprayed disinfectant.

Since the area where the inside of the mold 23 is open is limited, in order to sterilize the inside of the mold 23, the spray nozzle 56 is an area where the mold is open (a short distance between the wheel 10 and the wheel 24). It is desirable to provide a large number of molds 23, and the disinfectant is sprayed while rotating the mold 23 at a speed of 60 rpm or less. By sterilization, the mold 23, the blow nozzle 49, the stretching rod chamber 52, the valve block 49, etc. existing inside the molding filling portion 22, and the inner surface of the molding filling portion chamber 22 are sterilized. The spray pressure of the fungicide is at least 0.05 MPa or more, preferably 0.2 MPa or more.

The inside of the stretching rod 51, the stretching rod holding material 53, the stretching rod holding material operating shaft 54, and the stretching rod chamber 52 is sterilized by a disinfectant sprayed from a spray nozzle 56 provided in the stretching rod chamber 52. Also in this case, the stretching rod 51 is not inserted into the blow nozzle 49.

As the disinfectant, the same as the gas or mist of the disinfectant used for disinfecting Preform 1 or a mixture thereof can be used. Further, a liquid disinfectant may be used. The liquid bactericidal agent preferably contains peracetic acid, and an equilibrium peroxide composition composed of peracetic acid, hydrogen peroxide, acetic acid and water is more preferable. The concentration of peracetic acid is preferably 500 mg / L to 4,000 mg / L. If it is less than 500 mg / L, the bactericidal activity is insufficient, and if it exceeds 4,000 mg / L, the concentration of peracetic acid is high, which may deteriorate the packing and other members used in the aseptic filling machine. In addition, a bactericidal agent containing bactericidal components such as hydrogen peroxide, sodium hypochlorite, chlorine dioxide, and ozone may be used as the liquid bactericidal agent. The liquid bactericide contains water, but alcohols such as methyl alcohol, ethyl alcohol, isopropyl alcohol, normal propyl alcohol and butyl alcohol, ketones such as acetone, methyl ethyl ketone and acetyl acetone, glycol ethers and the like 1 It may contain seeds or two or more species. Further, an inorganic acid such as nitric acid, a basic compound such as sodium hydroxide and potassium hydroxide, an additive such as a cationic surfactant, a nonionic surfactant, and a phosphoric acid compound may be contained. The disinfectant may be sprayed multiple times with different disinfectants. Further, the liquid bactericidal agent is heated to improve the bactericidal power.

After spraying the disinfectant from the spray nozzle 56, sterile water is sprayed over the entire area of the molded filling chamber 22 by using the spray nozzle 56 or by a separately provided nozzle. The sterile water is used to wash away the disinfectant remaining in the molding filling chamber 22. Aseptic water is heated at 121 ° C. or higher for 4 minutes or longer, or sterilized by passing through a sterilization filter. The sterile water sprayed into the molding filling chamber 22 is preferably heated to 60 ° C to 100 ° C.

After aseptic water is sprayed into the molding filling chamber 22, sterile air is sprayed into the molding filling chamber 22. The sterile air vaporizes and removes the sterile water remaining in the molding filling chamber 22. As shown in FIG. 9, an aseptic air supply device 57 is provided above the fixed portion 64 of the molding filling chamber 22 in order to blow sterile air into the molding filling chamber 22. The aseptic air supply device 57 includes a blower 58 and a sterilization filter 59. Further, aseptic air may be heated, and it is preferable to provide a sterile air heating device 60 between the blower 58 and the sterilization filter 59.

The air from the blower 58 is heated by the heating device 60, sterilized by the sterilization filter 59, and then becomes sterile hot air and is blown into the molding filling chamber 22. Aseptic air does not have to be heated, but by heating, sterile water is quickly removed. When the aseptic air is supplied to the molding filling chamber 22 in order to maintain the sterility in the molding filling chamber 22 during the operation of the aseptic filling machine, it is not always necessary to heat the sterile air.

Sterilization in the molding filling chamber 22 is performed, for example, by the following procedure. After spraying a cleaning agent containing sodium hydroxide, which is a basic compound, into the molding filling chamber 22, sterile water is sprayed to wash away the cleaning agent, and a disinfectant containing peracetic acid is sprayed into the molding filling chamber 22. Further, sterile water is sprayed to wash away the disinfectant, and then a gas or mist of peracetic acid solution similar to that used for disinfecting Preform 1 or a mixture thereof is sprayed into the molding filling chamber 22 to aseptically heat air. Is supplied and the inside of the molded filling part chamber 22 is dried to complete the sterilization.

When spraying a gas or mist of hydrogen peroxide solution or a mixture thereof, the blow nozzle 49 and the valve block 50 exposed in the molding filling chamber 22 by cleaning or sterilizing the flow path inside the blow nozzle 49. When the outer surface temperature of the above is 60 ° C. or higher and exposed to hydrogen peroxide gas or mist having a concentration of 5 mg / L or higher or a mixture thereof, the outer surface of these sites is preferably sterilized.

In the sterilization before the operation of the aseptic filling machine, the sterilizing agent is sprayed by the spray nozzle 56, so that the inner surface side of the sterilizing filter 59 is also sterilized.

The aseptic air that has passed through the sterilization filter 59 may be blown into the molding filling chamber 22 and exhausted by the exhaust device 61 provided in the molding filling chamber 22. Further, aseptic air may flow from the molding filling chamber 22 into the sterilizing chamber 5 and be exhausted from 33 to the exhaust blower provided in the sterilizing chamber 18.

By spraying the sterilizing agent into the molding filling chamber 22, the members exposed in the molding filling chamber 22 are sterilized. However, the inside of the pipes of the medium pressure content P1 and the high pressure content P2 of the blow nozzle 49 and the valve block 50, which are not exposed, is not cleaned and sterilized. Therefore, before operating the aseptic filling machine, the inside of the pipe is cleaned (CIP) and sterilized (SIP).

As shown in FIG. 10, CIP is performed by attaching a cup-shaped closing device 69 to the tip of the blow nozzle 49. A cleaning agent tank 70 is provided, the cleaning agent in the cleaning agent tank 70 is pumped by the cleaning agent supply pump 71, the cleaning agent is heated by the heating device 72 as necessary, and the cleaning agent is heated through the pressurizing device 55, and then the valve block. The cleaning agent is sent from 50 to the blow nozzle 49 and the stretching rod 51. The cleaning agent discharged from the blow nozzle 49 is received by the cup-shaped closing device 69 attached to the tip of the blow nozzle 49, and flows into the high-pressure content supply manifold 68 via the passage in the valve block 50. It returns to the cleaning agent tank 70 via the rotary joint 73 at the lower part of the drive unit 62 by the pipe inside the pipe body provided at the center of the drive unit 62. CIP is performed by circulating the cleaning agent in this circulation path. The order of the circulation routes may be changed as appropriate as long as all the parts in contact with the contents can be washed.

As the cleaning agent, the same cleaning agent as that used for cleaning the inside of the molded filling chamber 22 is used. Some detergents have a bactericidal action when heated to 50 ° C. or higher, and may be heated by the heating device 72.

As shown in FIG. 10, SIP is performed by supplying superheated steam to the pressurizing device 55 by the superheated steam supply device 74. The superheated steam supplied to the pressurizing device 55 is supplied to the blow nozzle 49 and the stretching rod 51 via the high-pressure content supply manifold 68 and the valve block 50. Further, the superheated steam discharged by the blow nozzle 49 is received by the cup-shaped closing device 69 mounted on the tip of the blow nozzle 49, and is discharged from the lower part of the drive unit 62. SIP is performed by the heat of superheated steam. Superheated steam is supplied at 121 ° C. or higher.

Further, SIP may be performed with warm water. SIP with hot water is performed by pumping sterile water heated by a sterile water supply pump 76 from a sterile water tank 75 as shown in FIG. The aseptic water to be pumped is heated to 70 ° C. to 100 ° C. by the heating device 72, and is fed from the valve block 50 to the blow nozzle 49 via the pressurizing device 55. Aseptic water discharged from the blow nozzle 49 is received by the cup-shaped closing device 69 attached to the tip of the blow nozzle 49, and flows into the high-pressure content supply manifold 68 via the passage in the valve block 50. It returns to the sterile water tank 75 via the rotary joint 73 at the lower part of the drive unit 62 by the pipe inside the pipe body provided at the center of the drive unit 62. SIP is performed by circulating hot water in this circulation path. The heating device 72 may be provided separately from the cleaning agent heating device. As long as all the parts in contact with the product liquid can be sterilized, the order of the circulation routes may be changed as appropriate.

The bottle 2 filled with the contents is conveyed to the sealing portion 26 via the wheel 24 shown in FIG. The bottle 2 is conveyed to the sealing wheel 25 provided in the sealing portion 26, and the cap 35 sterilized by the cap sterilizing device 28 is supplied to the sealing wheel 25 as shown in the figure, as in the sealing step shown in FIG. In addition, the cap 35 is wound around the mouth portion 1a of the bottle 2 by a capper (not shown), and the bottle 2 is sealed.

The sealed bottle 2 is delivered from the gripper 34 of the sealed wheel 25 to the gripper 34 of the discharge wheel 29 of the discharge unit 30. The bottle 2 delivered to the discharge wheel 29 is placed on the discharge conveyor 31. The bottle 2 placed on the discharge conveyor 31 is discharged from the inside of the sealed chamber 27 to the outside of the aseptic filling machine.

Before the operation of the aseptic filling machine, the inside of the sealed chamber 27 is cleaned by spraying a cleaning agent, washed away by spraying sterile water, sterilized by spraying a disinfectant, and sprayed with sterile water. Operations such as washing away the disinfectant and removing sterile water by blowing sterile air are performed. Further, while the aseptic filling machine is in operation, the aseptic air supplied by the aseptic air supply device provided in the aseptic chamber 27 keeps the pressure in the aseptic chamber 27 at a positive pressure, so that the inside of the aseptic chamber 27 is maintained. Asepticity is maintained. An exhaust device may be provided in the sealed chamber 27 in order to properly maintain the pressure in the sealed chamber 27.

In order to sterilize the inside of the sealed chamber 27 and maintain sterility, the inside of the sealed chamber 27 is supplied with a sterilizer that sterilizes the inside and the inner surface of the sealed chamber 27, and sterile air is supplied to the inside of the sealed chamber 27. A sterile air supply device is provided. A cleaning device for cleaning the inside of the sealed chamber 27 is also provided. The sterilizing device includes a spray nozzle for spraying the sterilizing agent into the sealing chamber 27 and a sterilizing agent supplying device for supplying the sterilizing agent to the spray nozzle. Further, the cleaning device includes a spray nozzle for spraying the cleaning agent into the sealing chamber 27 and a cleaning agent supply device for supplying the cleaning agent to the spray nozzle. As the disinfectant and the cleaning agent, the same disinfectant and the cleaning agent used for the disinfection and cleaning in the molding filling chamber 22 are used.

The second embodiment for carrying out the present disclosure will be described below with reference to the drawings.

(Embodiment 2)
First, the pre-sterilization section that sterilizes the preform supplied from the preform feeder, the heating section that heats the sterilized preform to the temperature at which it is molded into a bottle, the sterilization section that sterilizes the heated preform, and the sterilization section. By filling the preform with sterilized contents at high pressure, the preform is molded into a bottle, and at the same time, a molding filling part for filling the contents and a sealing part for sealing the bottle filled with the contents are provided. The outline of the sterile filling machine according to the second embodiment will be described with reference to FIG. 12, and the points different from the first embodiment will be further described. According to the second embodiment, since the preform is sterilized before the preform is heated, the sterilization after the heating can be simply performed, and the heat of the heated preform can be suppressed from being lowered. It is possible to fill the contents at the same time as molding the remodeling, and it is possible to obtain a sterile product in which the contents are filled in the bottle in a smaller number of steps than in the past.

(Overview of the aseptic filling machine according to the second embodiment)
As shown in FIG. 12, the aseptic filling machine according to the present embodiment has a preform supply device 3 for supplying the preform 1, a pre-sterilization unit 77 for sterilizing the preform 1, and a temperature for molding the preform 1 into a bottle 2. A heating unit 14 that heats up, a sterilizing unit 6 that sterilizes the heated preform 1, a molding filling unit 21 that molds the preform 1 into a bottle 2 and at the same time fills the sterilized contents, and a bottle filled with the contents. A sealing portion 26 for sealing 2 with a sterilized cap 35 is provided. Further, the sealed bottle 2 is placed on the discharge conveyor 31 and includes a discharge unit 30 to be discharged to the non-sterile zone.

The pre-sterilization section 77 is the pre-sterilization section chamber 78, the heating section 14 is the heating section chamber 18, the sterilization section 6 is the sterilization section chamber 5, the molding filling section 21 is the molding filling section chamber 22, and the sealing section 26 and the discharging section 30 are the sealing sections. Each is shielded by a chamber 27. Since the heating unit 14 is not a sterile area, it does not have to be shielded. Depending on the sterilizing means of the preform 1 in the pre-sterilizing unit 77, gas or mist of a disinfectant, a mixture thereof, or ozone is generated in the pre-sterilizing unit chamber 78. Similar to the sterilizing unit 6, the pre-sterilizing unit 77 is exhausted by the exhaust blower 82 through the exhaust gas treatment device 81 that detoxifies the gas or mist of the disinfectant, a mixture thereof, or ozone so that these do not flow into the heating unit 14. To. The other chambers are the same as in the first embodiment.

A sterilizer is provided in the pre-sterilizer chamber 78, and the inside of the pre-sterilizer chamber 78 may be sterilized before the start of operation of the aseptic filling machine. The inside of the pre-sterilization unit chamber 78 may be sterilized by sterilizing the preform 1, and it is not necessary to sterilize the inside of the pre-sterilization unit chamber 78 before operating the aseptic filling machine. The sterilizer is the same as the sterilizer provided in the sterilizer of the first embodiment.

(Details of the aseptic filling machine and the aseptic filling method according to the second embodiment)
The preform 1 shown in FIG. 2 is continuously conveyed from the preform supply device 3 shown in FIG. 12 to the pre-sterilization unit 77 at a desired speed by the preform transfer conveyor 4. Preform 1 is the same as that of the first embodiment.

The preform 1 conveyed to the pre-sterilization unit 77 is delivered to a pre-sterilization wheel 79 provided with a large number of grippers 34 at a constant pitch, and is sterilized here. The sterilization step for sterilizing the preform 1 is performed by any one or more of contact with a sterilizing agent, irradiation with an electron beam, irradiation with light including ultraviolet rays, contact with hot water, and contact with superheated steam. The sterilization wheel 79 is provided with a sterilization means 80 for performing a sterilization step. The preform 1 may be preheated with hot air before being sterilized. In order to preheat the preform 1, a wheel for preheating may be provided in front of the sterilization wheel 79. The bactericidal effect is improved by preheating the preform 1.

The contact of the fungicide with the preform 1 according to the second embodiment of the present disclosure means that the gas or mist of the fungicide or a mixture thereof is sprayed on the preform 1 as shown in FIG. 4, or as shown in FIG. This is done by spraying a liquid disinfectant onto the preform 1 that has been inverted. Spraying the disinfectant gas or mist or a mixture thereof onto the preform 1 is the same as in the first embodiment.

The liquid disinfectant is sprayed onto the inverted preform 1 as shown in FIG. The support ring 1b of the inverted preform 1 is gripped by the gripper 34, and the liquid disinfectant comes into contact with the entire inner surface of the preform 1 by the upward disinfectant spray nozzle 41a from the mouth portion 1a to the preform 1. Spray a liquid disinfectant on the inner surface. Further, the liquid disinfectant is sprayed onto the outer surface of the preform 1 by the downward disinfectant spray nozzle 41b so that the liquid disinfectant contacts the entire outer surface of the preform 1. The disinfectant spraying nozzle 41a may be provided so as to face the mouth portion 1a of the preform 1, or a nozzle 41a that follows the transport speed of the preform 1 may be provided so as to be inserted inside the preform 1. Further, the number of the disinfectant spraying nozzles 41b may be a plurality. Further, as long as the liquid disinfectant can come into contact with the inner and outer surfaces of the preform 1, the method may be to immerse the preform 1 in the liquid disinfectant instead of spraying the liquid disinfectant with a nozzle.

The liquid bactericidal agent preferably contains peracetic acid, and the liquid bactericidal agent is preferably an equilibrium peroxide composition composed of peracetic acid, hydrogen peroxide, acetic acid and water. The concentration of peracetic acid is preferably 500 mg / L to 4,000 mg / L. If it is less than 500 mg / L, the bactericidal activity is insufficient, and if it exceeds 4,000 mg / L, the concentration of peracetic acid is high, which may deteriorate the packing and other members used in the aseptic filling machine. In addition, a bactericidal agent containing bactericidal components such as hydrogen peroxide, sodium hypochlorite, chlorine dioxide, and ozone may be used as the liquid bactericidal agent. The liquid bactericide contains water, but alcohols such as methyl alcohol, ethyl alcohol, isopropyl alcohol, normal propyl alcohol and butyl alcohol, ketones such as acetone, methyl ethyl ketone and acetyl acetone, glycol ethers and the like 1 It may contain seeds or two or more species. Further, an inorganic acid such as nitric acid, a basic compound such as sodium hydroxide and potassium hydroxide, an additive such as a cationic surfactant, a nonionic surfactant, and a phosphoric acid compound may be contained.

The liquid disinfectant may be at room temperature, but is preferably heated to 40 ° C to 80 ° C. When heated, the bactericidal effect of the bactericidal agent is improved. The flow rate per one of the disinfectant spray nozzles 41a and 41b is 1 L / min. ~ 15 L / min. , Preferred 3 L / min. -10 L / min. Is appropriate. Further, the spraying time is appropriately 0.2 seconds to 5 seconds. The amount of the liquid disinfectant sprayed onto the preform 1 is determined by the flow rate and the spraying time of the disinfectant spray nozzles 41a and 41b, and is 0.05 ml / cm ^{2 to} 20 ml / cm with respect to the surface area of the preform 1. ² is preferable. If it is less than 0.05 ml / cm ² , sterilization will be insufficient, and if it ^{exceeds 20 ml / cm 2} , it will be excessive, resulting in waste of energy and disinfectant.

The preform 1 contacted with the liquid disinfectant is rinsed with sterile water to remove the adhered disinfectant. Aseptic water is produced by heating water at 121 ° C. or higher for 4 minutes or longer or by passing it through a sterilization filter. Further, the sterile water may be water treated under sterilizing conditions equal to or higher than the contents to be filled. For example, if the content to be filled is mineral water, the preform 1 may be rinsed with the mineral water to be filled. Rinsing of preform 1 with sterile water is performed by the same process and apparatus as the spraying of the disinfectant shown in FIG. The support ring 1b of the inverted preform 1 is gripped by the gripper 34, and sterile water is sprayed from the mouth portion 1a to the inner surface of the preform 1 by an upward nozzle so that the entire inner surface of the preform 1 is rinsed with sterile water. .. Further, sterile water is sprayed onto the outer surface of the preform 1 by a downward nozzle so that the entire area thereof is rinsed with sterile water. The upward nozzle may be provided so as to face the mouth portion 1a of the preform 1, or a nozzle that follows the transport speed of the preform 1 may be provided so as to be inserted inside the preform 1. Further, the number of downward nozzles may be multiple.

The temperature of sterile water is adjusted to 10 ° C to 80 ° C, preferably 30 ° C to 70 ° C. The flow rate per nozzle for spraying sterile water is 1 L / min. ~ 15 L / min. , Preferred 3 L / min. -10 L / min. Is appropriate. The spraying time is preferably 0.1 to 15 seconds. The amount of sterile water sprayed onto the preform 1 is determined by the flow rate of the nozzle and the spraying time, and is 0.05 ml / cm ^{2 to} 20 ml / with respect to the surface area of the preform 1.
It is preferably cm ^2. If it is less than 0.05 ml / cm ² , the rinse will be insufficient, and if it ^{exceeds 20 ml / cm 2} , it will be excessive and energy will be wasted.

It is preferable to remove the sterile water adhering to the preform 1 rinsed with sterile water by spraying sterile air on the inner and outer surfaces of the preform 1. The preform 1 is heated to the molding temperature by the heating unit 14, but heating unevenness occurs in the portion to which sterile water adheres, and there is a possibility that molding defects such as whitening and uneven thickness may occur in the bottle 2 to be molded. Is. Aseptic air is preferably compressed air rather than blower air, and the pressure of sterile air is 0.01 MPa or more, preferably 0.1 to 0.6 MPa. The inner diameter of the nozzle for blowing sterile air is φ1 mm to φ10 mm, preferably φ2 mm to φ8 mm.

When the disinfectant is hydrogen peroxide solution, the amount of hydrogen peroxide adhering to the preform 1 after sterile air rinsing is 0.0003 μL / cm ^{2 in terms of hydrogen peroxide solution containing 35% by mass of hydrogen peroxide.} A range of ~ 0.35 μL / cm ^{2 is suitable.} More preferably, it is 0.0004 μL / cm ^{2 to} 0.2 μL / cm ² . When the amount of hydrogen peroxide adhered is 0.0003 μL / cm ² or more, a sufficient bactericidal effect can be obtained. Further, when the amount of hydrogen peroxide adhered exceeds 0.35 μL / cm ² , the amount of the disinfectant remaining in the bottle 2 increases.

The irradiation of the electron beam, the irradiation of light including ultraviolet rays, and the contact of the superheated steam in the pre-sterilization unit 77 in the pre-sterilization step are the same as those in the first embodiment.

The contact of hot water with the preform 1 according to the second embodiment of the present disclosure is the same as the step of spraying the liquid disinfectant on the inverted preform 1 shown in FIG. It is done by spraying on the inner and outer surfaces. Bacteria and the like adhering to the surface of Preform 1 are sterilized by the heat of warm water. The support ring 1b of the inverted preform 1 is gripped by the gripper 34, and hot water is blown from the mouth portion 1a to the inner surface of the preform 1 by an upward nozzle so that the entire inner surface of the preform 1 is sterilized by the hot water. Further, on the outer surface of the preform 1, hot water is sprayed on the outer surface of the preform 1 by a downward nozzle so that the entire area is sterilized by the hot water. The upward nozzle may be provided so as to face the mouth portion 1a of the preform 1, or a nozzle that follows the transport speed of the preform 1 may be provided so as to be inserted inside the preform 1. Further, the number of downward nozzles may be multiple.

Hot water is water heated to 70 ° C to 100 ° C or sterile water. The flow rate per nozzle for spraying hot water is 1 L / min. ~ 15 L / min. , Preferred 3 L / min. -10 L / min. Is appropriate. The inner diameter of the nozzle is φ1 mm to φ10 mm, preferably φ2 mm to φ8 mm. The spraying time is preferably 0.1 to 15 seconds. Blowing amount of hot water into the preform 1 is determined by the flow rate and blowing time of the nozzle, it is preferred for the surface area of the preform 1 is ^{0.05ml / cm 2 ~20ml / cm 2} . If it is less than 0.05 ml / cm ² , sterilization is insufficient, and if it ^{exceeds 20 ml / cm 2} , it is excessive and wastes energy.

It is preferable that the hot water adhering to the preform 1 sterilized by the hot water is removed by blowing sterile air on the inner and outer surfaces of the preform 1. This is because the preform 1 is heated to the molding temperature by the heating unit 14, but heating unevenness may occur in the portion to which the hot water adheres, and molding defects such as whitening and uneven thickness may occur in the molded container. .. Since the preform 1 is further sterilized after heating, the air blown to the preform 1 does not have to be sterile air.

As described above, in the pre-sterilization unit 77, the pre-sterilization unit 77 uses the pre-sterilization means 80 provided on the pre-sterilization wheel 79 to contact the disinfectant, irradiate an electron beam, irradiate light including ultraviolet rays, and contact hot water. Sterilized by any one or more methods of contact with superheated steam. Although the pre-sterilization means 80 is provided around the pre-sterilization wheel 79, one or two or more wheels may be provided in addition to the pre-sterilization wheel 79, and the pre-sterilization means 80 may be provided on a plurality of wheels. In addition to the pre-sterilization wheel 79, sterilization may be performed by the preform supply device 3 or the preform transfer conveyor 4.

The inside of the pre-sterilization chamber 78 may be sterilized by means such as spraying a sterilizing agent such as hydrogen peroxide solution into the pre-sterilizing chamber 78 before the operation of the aseptic filling machine. Therefore, a sterilizing agent spray nozzle is provided on the wall surface inside the pre-sterilizing unit chamber 78. Further, in order to sterilize the surface of the sterilization filter of the sterile air supply device in contact with the pre-sterilization chamber 78 on the pre-sterilization chamber 78 side, a sterilizing agent spray nozzle may be provided.

The preform 1 sterilized by the pre-sterilization unit 77 is gripped by the gripper 34 with the support ring 1b and delivered to the heating furnace transfer wheel 11 via the wheel 81. The preform 1 transferred to the heating furnace transfer wheel 11 is heated by the heating unit 14 by the same process as in the first embodiment, and the heated preform 1 is sterilized by the sterilization unit 6 and sterilized. Is filled with the contents at the same time as the molding into the bottle by the molding filling part 21, the bottle 2 filled with the contents is sealed by the sealing part 26, and is discharged to the outside of the sterile filling machine through the discharging part 30.

Although the present disclosure is configured as described above, the present invention is not limited to the above-described embodiment. Various changes can be made within the gist of this disclosure, such as the machine.

1 ... Preform 2 ... Bottle 5 ... Sterilization part chamber 6 ... Sterilization part 14 ... Heating part 18 ... Heating part chamber 21 ... Molding filling part 22 ... Molding filling part chamber 23 ... Mold 26 ... Sealing part 27 ... Sealing part chamber 49 ... Blow nozzle 50 ... Valve block 51 ... Stretching rod 55 ... Pressurizing device 57 ... Sterile air supply device 62 ... Moving part 64 ... Fixed part 68 ... High pressure content supply chamber 69 ... Closing device 77 ... Pre-sterilization part

Claims (6)

A heating unit that heats the preform, a sterilizing unit that sterilizes the preform, a molding filling unit that molds the preform into a bottle by filling the sterilized preform with sterilized contents at high pressure, the above. A sterile filling machine equipped with a sealing part that seals a bottle filled with contents.
The sterilizing part, the molding filling part and the sealing part are shielded by a chamber, and at least of the sterilizing part chamber, the molding filling part chamber and the sealing part chamber that shield each part, the inside of the molding filling part chamber and the sealing part chamber. A cleaning device for cleaning the inner surface, a sterilizing device for sterilizing, and a sterile air supply device for supplying sterile air to at least the inside of the molding filling chamber and the sealing chamber are provided.
The molded filling section comprises at least a mold, a blow nozzle, a drawing rod, a valve block and a pressurizing device for pressurizing the contents.
An aseptic filling machine comprising a stretching rod holding material for holding the stretching rod and a stretching rod holding material operating shaft, and configured so that the stretching rod is not inserted into the blow nozzle. In the aseptic filling machine of claim 1,
The aseptic air supply device is a sterile filling machine configured to make the pressure in the molding filling chamber higher than the pressure in other chambers. A heating step for heating the preform, a sterilization step for sterilizing the preform, and a high-pressure filling of the sterilized contents into the preform to form the preform into a bottle and simultaneously forming the contents. It is a sterilizing filling method having a molding filling step of filling a bottle and a sealing step of sealing a bottle filled with contents.
The inside and inner surface of the chamber that shields each part where the molding filling step and the sealing step are performed from the outside are cleaned and sterilized, sterile air is supplied into the chamber, the sterility in the chamber is maintained, and the sterility is maintained. In the chamber where the above was maintained, the molding and filling step and the sealing step were performed.
An aseptic filling method in which the inside and the inner surface of the chamber are cleaned and sterilized without being inserted into a blow nozzle to which a stretch rod for extending the preform in the longitudinal direction is joined to the mouth of the preform. In the aseptic filling method according to claim 3,
An aseptic filling method in which aseptic water is sprayed into the chamber after cleaning and sterilizing the inside of the chamber. In the aseptic filling method according to claim 3 or 4.
A aseptic filling method in which when aseptic air is supplied into the chamber, the pressure in the chamber where the molding and filling step is performed is made higher than the pressure in other chambers. In the aseptic filling method according to any one of claims 3 to 5.
An aseptic filling method in which the temperature of the cleaning liquid for cleaning the inside of the chamber is 50 ° C. or higher.

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