US20050249905A1 - Polyolefin container having certain shrink characteristics and method of making such containers - Google Patents
Polyolefin container having certain shrink characteristics and method of making such containers Download PDFInfo
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- US20050249905A1 US20050249905A1 US11/137,046 US13704605A US2005249905A1 US 20050249905 A1 US20050249905 A1 US 20050249905A1 US 13704605 A US13704605 A US 13704605A US 2005249905 A1 US2005249905 A1 US 2005249905A1
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- container
- polypropylene
- preform
- bottle
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/0005—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor characterised by the material
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D1/00—Containers having bodies formed in one piece, e.g. by casting metallic material, by moulding plastics, by blowing vitreous material, by throwing ceramic material, by moulding pulped fibrous material, by deep-drawing operations performed on sheet material
- B65D1/02—Bottles or similar containers with necks or like restricted apertures, designed for pouring contents
- B65D1/0207—Bottles or similar containers with necks or like restricted apertures, designed for pouring contents characterised by material, e.g. composition, physical features
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C35/00—Heating, cooling or curing, e.g. crosslinking or vulcanising; Apparatus therefor
- B29C35/02—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould
- B29C35/08—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation
- B29C35/0805—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation
- B29C2035/0822—Heating or curing, e.g. crosslinking or vulcanizing during moulding, e.g. in a mould by wave energy or particle radiation using electromagnetic radiation using IR radiation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/78—Measuring, controlling or regulating
- B29C49/783—Measuring, controlling or regulating blowing pressure
- B29C2049/7831—Measuring, controlling or regulating blowing pressure characterised by pressure values or ranges
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/78—Measuring, controlling or regulating
- B29C49/783—Measuring, controlling or regulating blowing pressure
- B29C2049/7832—Blowing with two or more pressure levels
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/78—Measuring, controlling or regulating
- B29C49/786—Temperature
- B29C2049/7861—Temperature of the preform
- B29C2049/7862—Temperature of the preform characterised by temperature values or ranges
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/78—Measuring, controlling or regulating
- B29C2049/7879—Stretching, e.g. stretch rod
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/07—Preforms or parisons characterised by their configuration
- B29C2949/0715—Preforms or parisons characterised by their configuration the preform having one end closed
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/07—Preforms or parisons characterised by their configuration
- B29C2949/072—Preforms or parisons characterised by their configuration having variable wall thickness
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/07—Preforms or parisons characterised by their configuration
- B29C2949/081—Specified dimensions, e.g. values or ranges
- B29C2949/0811—Wall thickness
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/07—Preforms or parisons characterised by their configuration
- B29C2949/081—Specified dimensions, e.g. values or ranges
- B29C2949/082—Diameter
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/07—Preforms or parisons characterised by their configuration
- B29C2949/0861—Other specified values, e.g. values or ranges
- B29C2949/0862—Crystallinity
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/22—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at neck portion
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/24—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at flange portion
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/26—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at body portion
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/20—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer
- B29C2949/28—Preforms or parisons whereby a specific part is made of only one component, e.g. only one layer at bottom portion
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/3024—Preforms or parisons made of several components characterised by the number of components or by the manufacturing technique
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2949/00—Indexing scheme relating to blow-moulding
- B29C2949/30—Preforms or parisons made of several components
- B29C2949/3032—Preforms or parisons made of several components having components being injected
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/02—Combined blow-moulding and manufacture of the preform or the parison
- B29C49/06—Injection blow-moulding
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/08—Biaxial stretching during blow-moulding
- B29C49/087—Means for providing controlled or limited stretch ratio
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/08—Biaxial stretching during blow-moulding
- B29C49/10—Biaxial stretching during blow-moulding using mechanical means for prestretching
- B29C49/12—Stretching rods
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/42—Component parts, details or accessories; Auxiliary operations
- B29C49/4205—Handling means, e.g. transfer, loading or discharging means
- B29C49/42093—Transporting apparatus, e.g. slides, wheels or conveyors
- B29C49/42095—Rotating wheels or stars
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/10—Polymers of propylene
- B29K2023/12—PP, i.e. polypropylene
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2067/00—Use of polyesters or derivatives thereof, as moulding material
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2623/00—Use of polyalkenes or derivatives thereof for preformed parts, e.g. for inserts
- B29K2623/10—Polymers of propylene
- B29K2623/12—PP, i.e. polypropylene
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/712—Containers; Packaging elements or accessories, Packages
- B29L2031/7158—Bottles
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
Definitions
- Injection stretch blow molding is a process of producing thermoplastic articles, such as liquid containers. This process involves the initial production of a preform articles by injection molding. Then, the preform article that after reheating is subjected to stretching and gas pressure to expand (blow) the preform article against a mold surface to form a container.
- a first type is a single stage process in which a preform is made on a machine and allowed to cool somewhat to a predetermined blow molding temperature. While still at this elevated temperature, the preform is stretch blow molded into a container on the same machine, as part of a single manufacturing procedure. This is a one step or so-called “single stage” manufacturing procedure.
- the temperature of the preform is cooled (reduced) following preform formation from about 230° C. to about 120-140° C. The preform is not returned to ambient temperature, but instead is blown to a container while at about 120 to 140° C.
- Another type of process is a two stage process.
- preforms first are formed in an injection machine. Then, preforms are cooled to ambient temperature. In some cases, preforms are shipped from one location to another (or from one company to another) prior to stretch blowing the preforms into containers.
- preforms are heated from an initial ambient temperature to an elevated temperature for stretch blowing on a molding machine to form a container.
- the injection machine and the molding machine typically are located apart from one another in such a two stage procedure.
- Two stage manufacturing processes are sometimes referred to as “reheat stretch blow molding” (RSBM) processes, because preform articles formed in the first stage are subsequently reheated during the second stage of manufacture to form finished containers.
- RSBM reheat stretch blow molding
- FIG. 1 shows a typical polypropylene container that may be manufactured according to the process of the invention
- FIG. 2A is a schematic flow diagram showing the processing steps employed in the first stage of the two stage process, which relates to injection manufacture of preform articles;
- FIG. 2B illustrates processing steps in the second stage of manufacturing in accord with the invention, wherein a preform article is stretch blow molded to form a container;
- FIG. 3 is a side view of a conventional thick-walled preform article
- FIG. 3A shows a side cross-sectional view of the conventional preform article of FIG. 3 ;
- FIGS. 3B and 3C show a first embodiment of a relatively thin walled preform with an external profile that may be employed in the invention
- FIG. 4 shows a side view of a second preform that may be used in the invention, i.e. a relatively thin-walled preform article according to the practice of the invention, in which the preform article optionally may have a profile on the inside rather than the outside of the preform article structure;
- FIG. 4A shows a cross-sectional view of the thin-walled preform article of FIG. 4 ;
- FIG. 5 is a longitudinal sectional view of an injection molding assembly for the production of a preform article
- FIG. 6 is an illustration of stage two of the manufacturing process, showing a vertical cross-sectional view of stretch blow mold apparatus that is used to produce the containers from a perform, in this view showing a start up position with the preform article in place;
- FIG. 7 is a view of the apparatus of FIG. 6 showing the mold closed on the preform article.
- FIG. 8 shows a fully blown container with a stretch rod and swage in a down position with the container decompressing in the mold.
- a two-stage process of injection stretch blow molding polypropylene to form a container is disclosed in the practice of the invention.
- a first stage of this process comprises forming a preform article.
- a second subsequent stage comprises reheating and blow molding the preform article to form a container.
- the invention is directed to both preform articles and containers, in addition to the specific method or process for forming these products. Surprisingly beneficial results have been achieved in the practice of the invention.
- a polypropylene container is made by an injection stretch blow molding two stage process.
- the container has:
- a process having at least the following steps. First, a chemical composition comprising at least in part polypropylene is provided. This chemical composition provides a melt flow index in the range of between about 6 and about 50 grams/10 minutes, according to ASTM D 1238 at 230 degrees C./2.16 kg.
- the chemical composition is injected into a mold at a fill rate of greater than about 5 grams of chemical composition per second. This injection may be made through an orifice or gate, as further described herein.
- a preform article is formed in a mold. The preform article is removed from the mold. The preform article includes a closed end adapted for subsequent second stage reheating and stretch blow molding. The closed end may be integral with a side wall. The side wall of the preform provides a thickness of less than about 3.5 mm, in one aspect of the invention.
- melt flow index MFI
- resins polypropylene chemical compositions
- the invention has overcome limitations in the art, in part by the unexpected discovery that processing parameters may be established to impart necessary conditions and benefits to form superior polypropylene-based preforms.
- This invention facilitates efficient and cost-effective production of clear, low haze polypropylene articles from preforms using injection to make a preform, followed in some instances by stretch blow molding to form a container.
- the advantages of the process disclosed herein comprise, among other things, appropriate selection of melt flow polypropylene resins, appropriate selection of nucleating and clarifying agents, appropriate thickness of performs, appropriate rate or speed of injecting the resin for preform production, and also perhaps the appropriate gate width during preform production. Surprisingly, it has been found that there are ranges for each of these criteria which cause stretch blow molded articles to be produced at high rates with superior clarity.
- Polypropylene has long been known to exist in several forms, and essentially any known form could be used in the practice of the invention. Thus, the invention is not limited to any particular type of polypropylene.
- Isotactic propylene iPP
- sPP syndiotactic polypropylene
- container articles produced in accordance with the criteria noted above exhibit specific haze to thickness ratios, and such is within the scope of the present invention.
- the invention provides a vast improvement in polypropylene injection stretch blow-molded article technology whereby efficient methods of producing very clear articles is accorded as proper replacements for previous PET types.
- the practice of the invention makes it possible to provide injection stretch blow-molded polypropylene articles that may be produced at very high rates and exhibit substantially uniform clarity levels.
- the invention may provide polypropylene preforms that facilitate production of very low haze container articles with injection stretch blow molding in a very efficient manner.
- One application of the invention provides improved containers, wherein such containers (or bottles) exhibit low haze levels.
- DMDBS 1,3-O-2,4-bis(3,4-dimethylbenzylidene) sorbitol
- Millad® 3988 1,3-O-2,4-bis(3,4-dimethylbenzylidene) sorbitol
- Such a compound provides highly effective haze reductions within polypropylenes with concomitant low taste and odor problems.
- Disubstituted DBS compounds are broadly described in U.S. Pat. Nos. 5,049,605 and 5,135,975 to Rekers. As it is, in terms of providing excellent clarity, particularly within the neck and bottom regions of target injection stretch blow-molded polypropylene bottle articles within this invention, DMDBS is a useful compound for such a result.
- thermoplastic nucleator in terms of high crystallization temperatures is available from Milliken & Company using the tradename HPN-68TM.
- HPN-68TM thermoplastic nucleating compounds that may be employed in the practice of the invention are disclosed in U.S. Pat. Nos. 6,465,551 and 6,534,574.
- the HPN-68TM compound is disodium bicyclo[2.2.1]heptanedicarboxylate.
- the ability to provide highly effective crystallization, or, in this specific situation, control targeted levels of crystallization within polypropylene preforms prior to injection stretch blow molding sometimes is facilitated by utilization of such a nucleating agent. Low amounts of this additive can be provided to produce the desired and intended amorphous-crystalline combination within the target performs.
- Other nucleating agents can be employed in the practice of the invention.
- the polypropylene polymers employed in the practice of the invention may include homopolymers (known as HPs), impact or block copolymers (known as ICPs)(combinations of propylene with certain elastomeric additives, such as rubber, and the like), and random copolymers (known as RCPS) made from at least one propylene and one or more ethylenically unsaturated comonomers.
- HPs homopolymers
- ICPs impact or block copolymers
- RCPS random copolymers
- co-monomers if present, constitute a relatively minor amount, i.e., about 10 percent or less, or about 5 percent or less, of the entire polypropylene, based upon the total weight of the polymer.
- co-monomers may serve to assist in clarity improvement of the polypropylene, or they may function to improve other properties of the polymer.
- Co-monomer examples include acrylic acid and vinyl acetate, polyethylene, polybutylene, and other
- Polypropylene provides an average molecular weight of from about 10,000 to about 2,000,000, preferably from about 30,000 to about 300,000, and it may be mixed with additives such as polyethylene, linear low density polyethylene, crystalline ethylenepropylene copolymer, poly(1-butene), 1-hexene, 1-octene, vinyl cyclohexane, and polymethylpentene, as examples.
- additives such as polyethylene, linear low density polyethylene, crystalline ethylenepropylene copolymer, poly(1-butene), 1-hexene, 1-octene, vinyl cyclohexane, and polymethylpentene, as examples.
- Other polymers that may be added to the base polypropylene for physical, aesthetic, or other reasons, include polyethylene terephthalate, polybutylene terephthalate, and polyamides, among others.
- Resin compositions utilized to produce the preform articles and injection stretch blow-molded containers of the invention can be obtained by adding a specific amount of a nucleating agent/clarifying agent directly to the polypropylene, either in dry form or in molten form, and mixing them by any suitable means while in molten form to provide a substantially homogenous formulation.
- a concentrate containing as much as about 20 percent by weight of a nucleator/clarifier in a polypropylene masterbatch may be prepared and be subsequently mixed with the resin.
- the desired nucleator/clarifier may be present in any type of standard polypropylene additive form, including, without limitation, powder, prill, agglomerate, liquid suspension, and the like, particularly comprising dispersion aids such as polyolefin (e.g., polyethylene) waxes, stearate esters of glycerin, waxes, mineral oil, and the like.
- dispersion aids such as polyolefin (e.g., polyethylene) waxes, stearate esters of glycerin, waxes, mineral oil, and the like.
- any form may be exhibited by such a combination or composition including such combination made from blending, agglomeration, compaction, and/or extrusion.
- the produced resins are then utilized to form preforms, as noted herein, which are then subsequently utilized to form the desired container articles in an injection stretch blow molding procedure.
- organoleptic improvement additives be added for the purpose of reducing the migration of degraded benzaldehydes from reaching the surface of the desired article.
- organoleptic improvement additive is intended to encompass such compounds and formulations as antioxidants (to prevent degradation of both the polyolefin and possibly the target alditol derivatives present within such polyolefin), acid neutralizers (to prevent the ability of appreciable amounts of residual acids from attacking the alditol derivatives), and benzaldehyde scavengers (such as hydrazides, hydrazines, and the like, to prevent the migration of foul tasting and smelling benzaldehydes to the target polyolefin surface).
- Polypropylene compositions having an melt flow index (MFI) of between about 6 and about 60 are useful in the practice of the invention. Furthermore, MFI values of between about 13 and about 35 are particularly useful in the practice of the invention, as further described below.
- MFI melt flow index
- the thickness and design of the target preform is important for a number of reasons.
- the thickness of such an article should be thin, as compared with the thickness of previously produced polypropylene preforms. This facilitates low haze results as noted above, and also facilitates utilization within prior PET injection stretch blow molding machinery.
- the side wall thickness of preforms desirably may be less than about 3.5 mm for effective results. In some applications, side wall thickness of between about 1.5 mm and 3.5 is very useful. Some applications may use a thickness of as much as 4.0 mm, as set forth in Table A.
- a gate as further described herein, comprises the opening through which liquid chemical composition (polypropylene and additive mixture) is admitted into the preform mold cavity.
- the gate diameter employed during preform production is particularly important, and may be related to other processing variables.
- a gate diameter of 1.5 mm may be used.
- a gate diameter of 3.8 mm has been used.
- Other gate sizes could be used as well, but each factor or factor must be adjusted to account for gate diameter. Gate diameters between about 1.5 mm and 3.8 mm can be advantageously employed in the practice of the invention.
- FIG. 1 shows a stretch blow molded polypropylene container that may be manufactured in accordance with the practice of the invention.
- Container 10 (sometimes referred to herein as a “bottle”) is shown.
- the container 10 of FIG. 1 has a relatively concave bottom 11 , a cylindrical main sidewall 12 , a conical upper portion 13 , and a thickened externally threaded neck 14 on the convergent end of the upper portion 13 .
- a neck ring 15 provides a physical point of reference, and may be used to carry the container 10 along processing machinery during manufacture and subsequent filling of the container 10 .
- the container 10 may be of any desired size or shape with sizes of from 0.5 to 4 liters being very useful, for example.
- the neck 14 usually is rigid to support a pressure retaining screw type cap (not shown). Thus, the neck 14 may be many times the thickness of the sidewall 12 . Furthermore, the conical upper portion 13 may be gradually thickened as it approaches neck 14 .
- FIG. 2A a flow schematic is provided showing the steps in the first stage of a two-stage stretch blow molding process.
- a two stage (two step) procedure is provided for production of containers 10 .
- FIG. 2A shows the first stage of the manufacturing procedure, that is, the injection molding process of preforms production.
- a chemical composition containing polypropylene is acquired from a source, such as a polypropylene manufacturer.
- the polypropylene-containing chemical composition may comprise a homopolymer, copolymer or other polymeric composition.
- the chemical composition may contain various additives, including (for example) nucleating agents, antioxidants, lubricants, s-scavengers, UV absorbers and the like, as further described herein.
- the polypropylene chemical composition is provided into an injection machine and heated. The heated chemical composition then is injected at a relatively high rate of speed through a valve or “gate”, and into the mold of the injection machine. A preform article is formed in a mold. The preform article is cooled and removed from the mold.
- FIG. 2B shows a second stage of a two-stage stretch blow molding process.
- a preform article (which may or may not have been manufactured at a location distant from the stretch blow molding apparatus) is converted to a container 10 .
- a preform article (usually at ambient temperature) is provided in a stretch blow molding machine. Then, the preform article is heated from ambient temperature to an elevated temperature.
- the elevated temperature employed is also known as the “orientation” temperature, and it is typically in the range of about 120-130° C. for random copolymers.
- the inner surface temperature of the preform needs to be sufficiently high to ensure that containers have the best optical properties. This has been found to be one important variable in the stretch blow molding process which sometimes determines whether the container will be transparent or hazy.
- the preform article is sufficiently softened, the preform is stretch blow molded into a container 10 .
- the formed container 10 is cooled and removed from the stretch mold apparatus.
- FIGS. 3-3A show a thick-walled polypropylene preform having a relatively thick side wall 80 (in this example, the side wall thickness is about 5 mm).
- the preform article 60 shown in FIG. 3 includes a closed end 62 and an open end 72 . Furthermore, a neck 66 is shown, with threads 68 at the base of the neck 66 . A main body portion 64 with side wall 80 is shown. It is common for polypropylene-based preforms 60 such as that shown in FIG. 3 to have a side wall 80 having a thickness of about 5 mm, or more.
- This preform article 60 happens to also be “stepped out” or tapered at each end, on its exterior profile.
- a “profile” is found on the exterior of many preform articles.
- the size of the threads at the open end 72 are fixed, and cannot be subject to variation.
- FIG. 3B and corresponding FIG. 3C show a first embodiment of a thin walled preform article that may be employed in the practice of the invention. It should be noted that the invention may include the use of “stepped out” preforms with an exterior profile, such as shown in FIGS. 3 B/ 3 C so long as the preforms are less than about 3.5 mm in side wall width.
- one discovery of the invention is that thin-walled preforms, in conjunction with processing conditions presented herein, provide surprisingly unexpected results as compared to conventional thick walled preforms.
- FIGS. 3 B/ 3 C a preform 90 having thin side wall 91 is shown.
- a preform article 115 having a relatively thin side wall may be employed, as further described herein and as shown in FIGS. 4-4A .
- the geometry of the preform article 115 of FIG. 3 shows a tapered neck 114 , and a main body portion 102 with side walls 101 and 104 that are approximately parallel to each other along their length. Furthermore, a closed end portion 116 tapers from the main body portion 102 . Threads 110 are provided adjacent the open end 103 of preform article 115 .
- a transition area 105 represents the tapering region of the side wall 101 into the neck 114 .
- a preform article 115 of the invention is shown in which the outer wall surfaces 109 a - b of the preform article are generally parallel and straight, forming a substantially symmtrical tube on its outer dimension from a point near the closed end 116 to a point near the open end 103 .
- the inner wall 108 of the preform 115 is profiled due to a transition zone 105 .
- the preform article 115 engages a mold so as to make a container 10 of the appropriate geometry.
- profiled it is meant that a given wall has a changing angle or slope which deviates from 180 degrees.
- the invention may in some embodiments take advantage of a profiled inner wall 108 , as opposed to a profiled exterior wall, as is common in the conventional devices (see FIGS. 3-3A ).
- the use of a profiled inner wall 108 has been found to be a useful feature in application of the preform 115 to container 10 manufacture.
- One reason for this fact is that it facilitates the use of relatively uniform outer wall dimensions.
- preforms 115 can be used that have differing inner wall 108 profile for various container sizes, while still exhibiting a common outer dimension or shape. This is useful in manufacturing, to avoid or minimize tooling and/or machinery changes for each size preform 115 that may be used to make containers 10 of various sizes.
- a relatively uniform outer dimension to the preform articles 115 may provide an advantage that may be realized in the practice of the invention. It should be recognized that the use of a profiled inner wall 108 is not required in the practice of the invention, but is one useful manner of practicing the invention. Thus, preforms having either an exterior profile or an exterior profile may be used in the practice of the invention.
- FIG. 5 shows a schematic vertical cross-sectional view of an injection molding machine for making preform articles in a first stage.
- a preform article 115 may be 10 formed in an injection molding unit 120 having a barrel 121 fed by an hopper 122 and ejecting the melt through a round nose nozzle 123 .
- a chemical composition i.e. polypropylene-containing pellets or portions, with optional additives or optional nucleating agents, etc) is provided into inlet hopper 122 .
- Barrel 121 rotatably mounts a melting and mixing screw 124 with a non-return valve nose 125 .
- Heater bands 126 may be provided in the barrel 121 .
- Crystalline polypropylene stretch blow mold formulations are fed through the hopper 122 into the barrel 121 where they are advanced by the melting and mixing screw 124 to a molten condition at the valve end 125 whereupon the screw is advanced to the dotted line position where the valve nose 125 will force the molten material through the nozzle orifice 127 .
- Gate 137 a received a determined the amount of liquid flow that proceeds into the molding cavity 135 .
- Other similar apparatus could be used to form a preform, which achieves the same or similar result as that shown in FIG. 5 .
- the apparatus includes a two-part mold 130 with a first core part 131 and a second molding cavity defining part 132 .
- the part 131 has a cylindrical core 133 with a hemispherical end 134 .
- the part 132 has a molding cavity 135 with a hemispherical bottom end 136 fed by a conduit 137 .
- the end wall of the part 132 has a recess 138 receiving the rounded nose of the nozzle 123 .
- the molten plastics material ahead of the valve 125 may be ejected through the orifice 127 by moving the screw rod to the dotted line position as shown in FIG. 5 .
- the molten material will flow through the conduit 137 into the mold cavity 135 .
- the surface of core 133 and the molding cavity surfaces 135 and 136 typically are polished, but may be treated as well to facilitate the ejection of preforms 115 .
- Steel is a desired metal for manufacture of such mold surfaces 135 .
- Chilled mold temperatures from about 11-20 degrees C. may be employed.
- the gate 137 a refers is the opening between the point at which the liquid polypropylene is injected and the actual core 134 of the mold cavity 135 .
- Gate size is a parameter that may vary for different applications.
- the size of the gate 137 a can be important in the manufacture of preformed articles 115 . This is because the size of the gate 137 a determines the shear forces applied to the molten polypropylene as it is injected into the mold cavity.
- the size of gate 137 a will affect the filing rate.
- the size of the gate 137 a will in some cases determine the rate by at which the chemical composition may be injected, which affects the ultimate clarity of the containers 10 produced by the preformed article 115 in the second stage of the container 10 manufacture (see FIG. 2B ).
- Gate diameter may vary, depending upon the application. The invention is not limited to any particular gate diameter, but it has been found that diameters between about 1.5 mm and about 3.8 mm are useful, and may be found in equipment in the industry. It may be an advantage in the practice of the invention to be capable of employing gate diameter settings that already are in existence and used on existing commercial PET processing equipment.
- the injection rate usually is relatively slow. Cavity filling time is typically about 1 to about 4.5 total seconds to fill mold cavity 135 . This corresponds generally to an injection rate greater than about 5 grams/second. In other cases, the rate may be between about 5 and about 22 grams per second. Table A shows various parameters that may be advantageously employed in the practice of the invention.
- the mold 130 Upon solidification of the preform article 115 in the mold 130 , the mold 130 is opened by withdrawing part 131 (and core 133 ) from part 132 . The preform 115 is stripped from the mold.
- melt flow index also known as the melt flow rate
- melt flow index is an important factor in the manufacturing of preform articles 115 .
- melt flow index is measured according to American Society of Testing Materials ASTM D-1238. This testing method is a nationally (or internationally) known standard. It is a standard test method for measuring the melt flow rates of thermoplastics. Unless otherwise indicated herein, all references to melt flow index, melt flow rate, MFI, or MFR, refer to measurements according to this industry standard. For polypropylene, measurements are at 230 degrees C., and using 2.16 kg, as per this standard.
- the more viscous is a material at a given temperature the lower will be the MFI value of that material.
- a given polymer or copolymer composition will have an MFI that is specified by a manufacturer.
- each particular type of polypropylene-containing composition to be employed in the practice of the invention will have a given or predetermined MFI.
- the MFI is also determined and affected by the length of the polymer chains in a given polypropylene composition. The longer the polymeric chains, the more viscous the material. The more viscous the material, the lower the MFI value will be for a given composition.
- MFI values are important in determining the speed at which a chemical composition may be fed into an injection mold cavity to form a preform article. This is true because the MFI also will affect the clarity of the final container which is produced from the preform. By clarity, it is meant the degree of haze that will be present in a given container 10 made according to the invention. In general, the higher percentage of haze in the container 10 , the less transparent is the container 10 produced in the invention. Higher levels of haze are undesirable.
- One unexpected result of the invention is that it has been found that using a given polymeric composition having a predetermined melt flow index, and injecting that composition at a fill rate of greater than about 5 grams per second, a highly desired preform article may be formed. Furthermore, it has been found that the sidewall thickness of the preform is very important in container manufacture. In the practice of the invention, a preform article 115 with a side wall thickness of less than about 3.5 millimeters has proved to be very desirable. This achieves a high productivity of container manufacture while still maintaining a low degree of haze, i.e. a clear container. Cycle time necessary to make a preform article 115 is significantly reduced by using a preform design with a minimum side wall thickness.
- Hot plastic polypropylene is capable of cooling in the preform mold more quickly using a reduced wall thickness for the preform stage. This facilitates faster preform cycle times, thereby increasing the number of preform articles 115 that can be made in a given period of time, increasing manufacturing capacity and efficiency.
- Stage two (step 2 ) of manufacture is shown generally in FIG. 2B , and FIGS. 6-8 .
- a preform article 115 is taken at ambient temperature, and then uniformly heated.
- the preform article 115 is placed in a stretch blow mold apparatus 140 in a position with its open end 103 resting on a platform 141 on a base 142 surrounding a reciprocal swage 143 .
- the closed end 116 of the preform 115 is shown near the center of FIG. 6 .
- the apparatus freely receives the retracted end of the stretch rod 144 of the apparatus 140 .
- the molding dies 145 of the apparatus 140 are in an opened condition. Threaded neck forming wall portions 146 are shown, as well as tapered cone forming portions 147 , cylindrical main body forming portions 148 , and concave bottom forming portions 149 .
- a rotary system is employed to transfer preforms using transfer wheels equipped with grippers into a blow mold cavity.
- rotary stretch blow molding equipment is known in the art, and may be applied in the practice of the invention. From the open position of FIG. 6 the apparatus 140 is closed to the position of FIG. 7 with the mold halves 145 coming together and with the swage 143 extended into the open end of the preform 115 so that the neck and thread forming portions 146 of the die can mold the thick neck 114 of the bottle on the preform 115 . The projection of the swage 143 into the position of FIG. 7 also moves the stretch rod 144 against the closed end 116 of the preform 115 .
- the apparatus 140 is further activated to eject the stretch rod 144 beyond the swage 143 into closely spaced relation from the bottom forming portion 149 of the dies 145 thereby effecting a stretching of the preform 115 to the full height of the dies.
- the stretch rod 144 and the swage 143 are retracted from the container 10 .
- the gas pressure in the bottle is released, and the dies 45 are separated.
- a blowing agent is introduced into the preform article 115 forming an axially elongated and hoop stretched balloon in the closed die.
- the balloon (not shown) is blown into a finished container 10 , as shown in FIG. 8 , with the polypropylene material biaxially stretched to produce a strong container 10 .
- Roughness on the inner container 10 surface has a negative influence on the container clarity. If, during reheating of the preform 115 (within the window of process stability), the temperature in the skin-layer (at the side of the core) is insufficiently high, the material undesirably may be ruptured apart during the stretch blow molding (stage two) process, resulting in a rough inner container 10 surface and containers 10 having low clarity. Additionally, it has been observed that a low amount of “pre-blowing” (intermediate shape of the stretched and pre-blown preform part, i.e. before the final pressure is applied) may contribute to a relatively rough inner container 10 surface (i.e. undesirable high haze) for the same reason. More specifically the primary pressure, flow of air and pre-blow time usually need to be sufficiently high to prevent that the material gets ruptured apart what gives the part an undesirable high haze.
- variables that are important in the practice of the invention include, for example, injection speed, MFI of the polypropylene-containing resin, the preform article thickness. In some instances, the gate diameter used during injection of the preform article is a factor. These factors may be optimized and correlated to each other for a given container application, as in the Critical Filling Rate Model set forth below. It is possible using the practice of the invention to maximize productivity of the preform and to maximize productivity polypropylene containers in a two-stage stretch blow molding process.
- a preform thickness may be of a value less than about 3.5 mm. Thickness is measured along side walls 101 , 104 as shown in FIG. 4A , measured as the maximum or thickest portion of the side wall. In yet another embodiment of the invention, the preform thickness may be in the range of about 2-3.5 mm. Furthermore, in the practice of the invention it has been found that an injection fill rate into the cavity mold of greater than about 5 grams of chemical composition (resin) per second is quite useful. Furthermore, in other aspects of the invention it is advantageous to use a cavity mold fill rate of between 5 and 22 grams per second.
- Table A shows a correlation between processing variables in the practice of the invention.
- the MFI values and preform wall thickness values are correlated to the optimized injection mold filling rate in the practice of the invention. It is important to note in Table A that for a given preform wall thickness an increase in the MFI value allows an operator to use a higher injection mold filling rate while still obtaining containers 10 of sufficient clarity.
- a greater preform wall thickness at a given level of MFI value enables an operator employing the invention to use an injection mold filling rate which is greater, resulting in faster production, reduced cycle times, and good container clarity.
- Table A reports values for a (valve) gate thickness of 1.5 mm.
- the use of a wider gate such as about 3.8 mm can result in a filling rate of about 13 g/sec at a MFI value of 13. This compares to the data in Table A in which a MFI of 13 at a (valve) gate diameter of 1.5 mm was successfully employed using an injection speed of about 5-6 g/sec.
- a (valve) gate diameter of 3.8 mm at MFI value 20 may result in an injection speed of about 22 g/sec. This value of 22 g/sec may be compared to the injection speed shown in Table A (valve diameter 1.5 mm) of 5-7 g/s.
- the invention makes it possible to achieve a rate of container production of at least about 1500 containers per hour per mold.
- Example 1 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/sec) I-1 RB307MO 1.5 0.5 50.6 I-2 RB307MO 1.5 1.0 25.3 I-3 RB307MO 1.5 1.5 16.9 I-4 RB307MO 1.5 2.0 12.7 I-5 RB307MO 1.5 2.5 10.1 I-6 RB307MO 1.5 3.0 8.4 I-7 RB307MO 1.5 3.5 7.2 I-8 RB307MO 1.5 4.0 6.3 I-9 RE420MO 13 0.5 50.6 I-10 RE420MO 13 1.0 25.3 I-11 RE420MO 13 1.5 16.9 I-12 RE420MO 13 2.0 12.7 I-13 RE420MO 13 2.5 10.1 I-14 RE420MO 13 3.0 8.4 I-15 RE420MO 13 3.5 7.2 I-16 RE420MO 13 4.0 6.3 I-17 RF365MO 20 0.5 50.6 I-18 RF365MO 20 1.0 25.3 I-19 RF365MO 20 1.5 16.9 I-20 RF365MO 20 2.0 12.7 I-21 RF365MO 20 2.5 10.1 I
- Example 2 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/cc) II-1 RB307MO 1.5 0.5 40.6 II-2 RB307MO 1.5 1.0 20.3 II-3 RB307MO 1.5 1.5 13.5 II-4 RB307MO 1.5 2.0 10.2 II-5 RB307MO 1.5 2.5 8.1 II-6 RB307MO 1.5 3.0 6.8 II-7 RB307MO 1.5 3.5 5.8 II-8 RB307MO 1.5 4.0 5.1 II-9 RE420MO 13 0.5 40.6 II-10 RE420MO 13 1.0 20.3 II-11 RE420MO 13 1.5 13.5 II-12 RE420MO 13 2.0 10.2 II-13 RE420MO 13 2.5 8.1 II-14 RE420MO 13 3.0 6.8 II-15 RE420MO 13 3.5 5.8 II-16 RE420MO 13 4.0 5.1 II-17 RF365MO 20 0.5 40.6 II-18 RF365MO 20 1.0 20.3 II-19 RF365MO 20 1.5 13.5 II-20 RF365MO 20 2.0 10.2 II-21 RF365MO 20 2.5 8.1
- Example 3 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/cc) III-1 RB307MO 1.5 0.5 34.6 III-2 RB307MO 1.5 1.0 17.3 III-3 RB307MO 1.5 1.5 11.5 III-4 RB307MO 1.5 2.0 10.2 III-5 RB307MO 1.5 2.5 6.9 III-6 RB307MO 1.5 3.0 5.8 III-7 RB307MO 1.5 3.5 4.9 III-8 RB307MO 1.5 4.0 4.3 III-9 RE420MO 13 0.5 34.6 III-10 RE420MO 13 1.0 17.3 III-11 RE420MO 13 1.5 11.5 III-12 RE420MO 13 2.0 10.2 III-13 RE420MO 13 2.5 6.9 III-14 RE420MO 13 3.0 5.8 III-15 RE420MO 13 3.5 4.9 III-16 RE420MO 13 4.0 4.3 III-17 RF365MO 20 0.5 34.6 III-18 RF365MO 20 1.0 17.3 III-19 RF365MO 20 1.5 11.5 III-20 RF365MO 20 2.0 10.2 III-21 RF365MO 20 2.5 6.9
- Polypropylene bottles (330 ml) were on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 1.
- This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps.
- Pre-blow pressure was 6 bar & final pressure was 8 bar. After optimization, the bottle productivity for the preforms with 4 mm thickness was 820 bph/cav.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- Polypropylene bottles (330 ml) were blown at high speed on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 2.
- This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps.
- Pre-blow pressure was 6 bar & final pressure was 8 bar.
- the bottle productivity for the preforms with 3 mm thickness was 1,030 bph/cav.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- Polypropylene bottles (330 ml) were blown at high speed on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 3.
- This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps.
- Pre-blow pressure was 6 bar & final pressure was 8 bar. After optimization, the bottle productivity for the preforms with 2 mm thickness was 1,200 bph/cav.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- Polypropylene bottles (500 ml) were blown at high speed (1500 bottles/cavity/hour) on a Sidel SBO-8 Series II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 1.
- Axial stretch ratio is 2.5/1
- Machine settings were adjusted to accommodate high clarity, high speed bottle production.
- Preforms were subjected to a pre-blow pressure of 3 Bar for 0.9 seconds with the preform inner temperature set to about 125°-130° C. and the outer temperature set to about 120°-125° C. Heating power distribution was managed in the range of 90%.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or excellent (a fully blown bottle with outstanding optical clarity).
- Polypropylene bottles (500 ml) were blown at high speed (1,500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 2.
- Axial stretch ratio is 2.5/1
- Machine settings were adjusted to accommodate high clarity, high speed bottle production.
- Preforms were subjected to a pre-blow pressure of 4.5 Bar for 0.4 seconds & nozzle for 3 rotations open activated at ‘point zero’.
- Blowing time is 0.8 sec & Exhaust time is 0.4 sec.
- Stretch speed is 1,384 m/sec & a standard stretch rod with 14 mm diameter was used.
- Preform temperature is about 120-130° C.
- % GP 65%.
- This example used 100% was ventilation to cool the preform surface.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- Polypropylene bottles (500 ml) were blown at high speed (1,500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 3.
- Axial stretch ratio is 2.5/1
- Machine settings were adjusted to accommodate high clarity, high speed bottle production.
- Preforms were subjected to a pre-blow pressure of 4 Bar for 0.4 seconds & nozzle for 3 rotations open activated at ‘point zero’.
- Blowing time is 0.8 sec & Exhaust time is 0.4 sec.
- Stretch speed is 1,384 m/sec & a standard stretch rod with 14 mm diameter was used.
- Preform temperature is about 115-127° C.
- % GP 45%. Used 100% ventilation to cool the preform surface.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown put), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- the preforms (ref. Table X) were produced on a two-cavity mold (only one cavity installed) 100 ton Netstal injection molding machine with a variable injection time (0.5-4.0 sec) and a constant cooling time of 10 sec. Melt temperature was 230° C. Temperature of the cooling water was 13° C. The holding pressure time was 4.5 sec. Total cycle time was around 20 sec (not optimized). A valve gate with a diameter of 1.5 mm was used.
- the preforms have a wall thickness of 3 mm and a bottle weight of about 20.3 g.
- Polypropylene bottles (330 ml, ref. Table XI) were produced blown at high speed on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 10.
- This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps.
- Pre-blow pressure was 6 bar & final pressure was 8 bar.
- the bottle productivity for the preforms with 3 mm thickness was 1,030 bph/cav.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- Polypropylene bottles (500 ml, table XII) were produced at high speed (1,500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 10.
- Axial stretch ratio is 2.5/1
- Machine settings were adjusted to accommodate high clarity, high speed bottle production.
- Preforms were subjected to a pre-blow pressure of 4.5 Bar for 0.4 seconds & nozzle for 3 rotations open activated at ‘point zero’.
- Blowing time is 0.8 sec & Exhaust time is 0.4 sec.
- Stretch speed is 1,384 m/sec & a standard stretch rod with 14 mm diameter was used.
- Preform temperature is about 120-130° C.
- % GP 65%.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- the preforms were produced on a two-cavity mold (only one cavity installed) 100 ton Netstal injection molding machine with a variable injection time (0.5-4.0 sec) and a constant cooling time of 10 sec. Melt temperature was 240° C. Temperature of the cooling water was 13° C. The holding pressure time was 8.4 sec. Total cycle time was around 25 sec (not optimized).
- a valve gate with a diameter of 1.5 mm was used.
- the preforms have a wall thickness of 3 mm and a bottle weight of about 20.3 g. These preforms were later blown into bottles as explained in subsequent examples.
- TABLE XIII Example 13 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/cc) XIII-1 HPMT230 30 0.5 50.6 XIII-2 HPMT230 30 1.0 25.3 XIII-3 HPMT230 30 1.5 16.9 XIII-4 HPMT230 30 2.0 12.7 XIII-5 HPMT230 30 2.5 10.1 XIII-6 HPMT230 30 3.0 8.4 XIII-7 HPMT230 30 3.5 7.2 XIII-8 HPMT230 30 4.0 6.3 XIII-9 RF365MO 20 2.5 50.6 XIII-10 RF365MO 20 3.0 25.3 XIII-11 RF365MO 20 3.5 16.9 XIII-12 RF365MO 20 4.0 12.7 XIII-13 RF365MO 20 0.5 10.1 XIII-14 RF365MO 20 1.0 8.4 XIII-15 RF
- Polypropylene bottles (500 ml) having a narrow neck were produced at high speed (1500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 13.
- the following stretch ratios were used: axial stretch ratio of 2.63/1, radial stretch ratio of 3.08 and a total stretch ratio of 8.10/1.
- Machine settings were adjusted to accommodate high clarity, high speed bottle production.
- the temperature measured at the outer side of the preform was 143.5° C. and 152.5° C. at the inner side of the preform.
- Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
- the thickness of preforms is measured along the side walls 101 , 104 as shown in FIG. 4A , measured at the widest portion of the side walls 101 , 104 .
- Thickness of containers such as for purposes of percent haze/thickness ratios is measured at the point at which the haze has been measured (see below), using a Magna-Mike 8500 Hall effect thickness gauge.
- haze has been measured on a BYK-Gardner hazemeter by ASTM Standard Test Method D1003-61 modified by use of an 0.2′′ aperture.
- the area in which haze could be measured reliably was in relatively small areas less than about 0.5′′ in area.
- Samples were obtained from sample containers (bottles) at a relatively flat point approximately mid-way to the bottom of the bottle after the transition point.
- a thickness modified haze was calculated for each sample where (H/t) is defined as the haze divided by the thickness at the point where the haze was measured.
- Roughness on the inner container 10 surface has a negative influence on the container clarity. If, during reheating of the preform 115 (within the window of process stability), the temperature in the skin-layer is insufficiently high, the material undesirably may be ruptured apart during the stretch blow molding (stage two) process, resulting in a rough inner container 10 surface and containers 10 having low clarity.
- Preforms were made with fill rates ranging from 5.5 to 40.2 grams per second utilizing two different resins—Borealis RF365 MO (20 MI RCP) and Atofina 7525 (12 MI RCP). Three different injection valve gates were utilized in the preform production—1.5, 3.0, and 3.8 mm.
- Haze was measured in the middle of the bottle on the third rib of the bottle from the top using a BYK Gardner hazemeter. In general, it has been found that haze is dependent upon fill rate. There is a strong increase in haze in both of the resins with increasing fill rate. The Borealis resin reaches a minimum % haze at a faster fill rate than does the Atofina resin, indicating an interaction and influence of the Ml of the resin with fill rate.
- valve gate diameter There is an effect of the valve gate diameter as it can be seen that the change in haze of both of the resins (see attached Table XV).
- a 3.8 mm valve gate shows a different dependency of % haze on fill time than do the 1.5 and 3.0 mm gates.
- the resin MI there is an effect of the resin MI on the haze.
- the 10 MI Atofina resin has a different haze response to the fill rate and gate diameter, than does the 20 MI Borealis resin.
- FIG. 12 is also illustrative of the effect of pre-blow time and pressure on container percent (%) haze.
- Pre-blow pressure 1 bar (very hazy in panel) 2 bar (slightly hazy in panel) 4 bar (clear) 5 bar (clear) 7 bar (clear) 10 bar (clear).
- Pre-blow time 0 sec (very hazy in panel) 0.05 sec (slightly hazy in panel) 0.1 sec (slightly hazy) 0.2 sec (clear) 0.4 sec (OK) 0.8 sec (OK)
- a polypropylene container is made by an injection stretch blow molding two stage process.
- the container has:
- a clear bottle may be produced by two stages, injection molding into a preform and then stretch blow the preform into the final clear bottle. Such bottles exhibit a certain percentage of free shrinkage in the axial direction. This is known as a “free shrinkage test” or “shrinkage test”, for purposes of this specification and claims.
- Sample D (the comparative example) bottle apparently exhibits the highest shrinkage ratio among all tested. It also has the highest wall thickness among all bottles tested.
- wall thickness of the preform is one of the critical factors to make good quality and clear ISBM polypropylene bottles with good productivity.
- the current invention designs the preform with the wall thickness of 3.5 mm or less, while the prior art is above that.
- the comparative bottle has the wall thickness of 4.9 mm, while the first three bottles out of this invention have the wall thickness of 2.8 mm and 3.5 mm.
- the shrinkage behavior is similar provided all bottles are made of polypropylene random copolymer.
- the wall thickness of the shrunk bottle relates closely to the preform wall thickness.
- the comparable example bottle has the highest shrunk bottle wall thickness, largely due to the fact that the preform is high in wall thickness. This would be one way of differentiating the bottles based on the current inventive preform design or a prior art preform design.
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Abstract
The two stage production of clear, low-haze, injection stretch blow molded polypropylene container articles with advantageous free shrink characteristics is disclosed. In the first processing stage, a preform article is manufactured on an injection molding machine. In a second and subsequent step, which may occur remotely from apparatus used in the first step, the preform article is heated and stretch blown into a container. The process may employ the selection of processing parameters to produce preform articles that facilitate stretch blow molding at relatively high rates of speed, while still maintaining an appropriate polypropylene polymer morphology that results in clear, low haze containers. Free shrink may be improved and measured. Furthermore, a haze, MFI, and wall thickness of containers subjected to a free shrinkage test following manufacture may be used to estimate or predict the processing parameters used to manufacture the container.
Description
- This application is a continuation in part of U.S. Ser. No.10/764,234 entitled “PROCESS FOR MAKING INJECTION STRETCH BLOW MOLDED POLYPROPYLENE ARTICLES” (Milliken File No. 5729), filed Jan. 23, 2004; and also claims priority to previously filed United States provisional patent application Ser. No. 60/575,447 entitled “MOLDED CONTAINERS HAVING ADVANTAGEOUS FREE SHRINK CHARACTERISTICS” (Milliken File 5729B), filed on May 28, 2004.
- Injection stretch blow molding is a process of producing thermoplastic articles, such as liquid containers. This process involves the initial production of a preform articles by injection molding. Then, the preform article that after reheating is subjected to stretching and gas pressure to expand (blow) the preform article against a mold surface to form a container.
- There are several different processes that employ stretch blow molding. A first type is a single stage process in which a preform is made on a machine and allowed to cool somewhat to a predetermined blow molding temperature. While still at this elevated temperature, the preform is stretch blow molded into a container on the same machine, as part of a single manufacturing procedure. This is a one step or so-called “single stage” manufacturing procedure. In a typical single stage blow molding process for polypropylene, the temperature of the preform is cooled (reduced) following preform formation from about 230° C. to about 120-140° C. The preform is not returned to ambient temperature, but instead is blown to a container while at about 120 to 140° C.
- Another type of process is a two stage process. In a two stage process, preforms first are formed in an injection machine. Then, preforms are cooled to ambient temperature. In some cases, preforms are shipped from one location to another (or from one company to another) prior to stretch blowing the preforms into containers. In the second stage of the two-stage process, preforms are heated from an initial ambient temperature to an elevated temperature for stretch blowing on a molding machine to form a container. The injection machine and the molding machine typically are located apart from one another in such a two stage procedure. Two stage manufacturing processes are sometimes referred to as “reheat stretch blow molding” (RSBM) processes, because preform articles formed in the first stage are subsequently reheated during the second stage of manufacture to form finished containers.
- There has been a long felt need in the industry of container manufacturing to provide polypropylene materials, preforms, and container articles in a process that will afford a cost-effective manufacture of low-haze, high clarity products. A process of employing polypropylene in a manner that will result in highly efficient preform and container production at a minumum cost with a fast cycle time is very desirable. Furthermore, a process of treating a finished container to estimate or identify the processes used to manufacture the container also would be quite useful.
- The invention will now be described by way of example with reference to the drawings:
-
FIG. 1 shows a typical polypropylene container that may be manufactured according to the process of the invention; -
FIG. 2A is a schematic flow diagram showing the processing steps employed in the first stage of the two stage process, which relates to injection manufacture of preform articles; -
FIG. 2B illustrates processing steps in the second stage of manufacturing in accord with the invention, wherein a preform article is stretch blow molded to form a container; -
FIG. 3 is a side view of a conventional thick-walled preform article; -
FIG. 3A shows a side cross-sectional view of the conventional preform article ofFIG. 3 ; -
FIGS. 3B and 3C show a first embodiment of a relatively thin walled preform with an external profile that may be employed in the invention; -
FIG. 4 shows a side view of a second preform that may be used in the invention, i.e. a relatively thin-walled preform article according to the practice of the invention, in which the preform article optionally may have a profile on the inside rather than the outside of the preform article structure; -
FIG. 4A shows a cross-sectional view of the thin-walled preform article ofFIG. 4 ; -
FIG. 5 is a longitudinal sectional view of an injection molding assembly for the production of a preform article; -
FIG. 6 is an illustration of stage two of the manufacturing process, showing a vertical cross-sectional view of stretch blow mold apparatus that is used to produce the containers from a perform, in this view showing a start up position with the preform article in place; -
FIG. 7 is a view of the apparatus ofFIG. 6 showing the mold closed on the preform article; and -
FIG. 8 shows a fully blown container with a stretch rod and swage in a down position with the container decompressing in the mold. - Reference now will be made to the embodiments of the invention, one or more examples of which are set forth below. Each example is provided by way of explanation of the invention, not as a limitation of the invention. In fact, it will be apparent to those skilled in the art that various modifications and variations can be made in this invention without departing from the scope or spirit of the invention.
- A two-stage process of injection stretch blow molding polypropylene to form a container is disclosed in the practice of the invention. A first stage of this process comprises forming a preform article. A second subsequent stage comprises reheating and blow molding the preform article to form a container. The invention is directed to both preform articles and containers, in addition to the specific method or process for forming these products. Surprisingly beneficial results have been achieved in the practice of the invention.
- In the invention, it is possible to identify the manner of making a container that has been made by a two step process (and other process variables) by employing a free shrink process as set forth below in Example 17. In the invention, a polypropylene container is made by an injection stretch blow molding two stage process. The container has:
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- a) a side wall providing a haze value of less than 3 according to ASTM D 1003,
- b) an MFI (melt flow index) between about 6 g/10 min and about 50 g/10 min according to ASTM D 1238;
- c) wherein the average wall thickness of the container after subjecting the container to the free shrinkage test (see Example 17 below) is less than about 1.8 mm.
- In the first stage of forming a preform article, a process is provided having at least the following steps. First, a chemical composition comprising at least in part polypropylene is provided. This chemical composition provides a melt flow index in the range of between about 6 and about 50 grams/10 minutes, according to ASTM D 1238 at 230 degrees C./2.16 kg.
- Further, the chemical composition is injected into a mold at a fill rate of greater than about 5 grams of chemical composition per second. This injection may be made through an orifice or gate, as further described herein. A preform article is formed in a mold. The preform article is removed from the mold. The preform article includes a closed end adapted for subsequent second stage reheating and stretch blow molding. The closed end may be integral with a side wall. The side wall of the preform provides a thickness of less than about 3.5 mm, in one aspect of the invention.
- Processing parameters are employed in the practice of the invention to produce preform articles that facilitate fast and efficient stretch blow molding to produce containers having a desirably low haze. The melt flow index (MFI) of the polypropylene chemical compositions (i.e. resins) will be tuned to the injection speed of resin in molding the preform article, the thickness and structure of the preform article, and the proper selection of injection gate diameter during such the preform production stage. Each of these factors are important to the successful production of desirable low-haze container articles. Improved containers, preforms, and processing conditions are within the scope of this invention.
- The invention has overcome limitations in the art, in part by the unexpected discovery that processing parameters may be established to impart necessary conditions and benefits to form superior polypropylene-based preforms. This invention facilitates efficient and cost-effective production of clear, low haze polypropylene articles from preforms using injection to make a preform, followed in some instances by stretch blow molding to form a container.
- The advantages of the process disclosed herein comprise, among other things, appropriate selection of melt flow polypropylene resins, appropriate selection of nucleating and clarifying agents, appropriate thickness of performs, appropriate rate or speed of injecting the resin for preform production, and also perhaps the appropriate gate width during preform production. Surprisingly, it has been found that there are ranges for each of these criteria which cause stretch blow molded articles to be produced at high rates with superior clarity.
- Polypropylene has long been known to exist in several forms, and essentially any known form could be used in the practice of the invention. Thus, the invention is not limited to any particular type of polypropylene. Isotactic propylene (iPP) may be described as having the methyl groups attached to the tertiary carbon atoms of successive monomeric units on the same side of a hypothetical plane through the polymer chain, whereas syndiotactic polypropylene (sPP) generally may be described as having the methyl groups attached on alternating sides of the polymer chain.
- Additionally, container articles produced in accordance with the criteria noted above exhibit specific haze to thickness ratios, and such is within the scope of the present invention. The invention provides a vast improvement in polypropylene injection stretch blow-molded article technology whereby efficient methods of producing very clear articles is accorded as proper replacements for previous PET types.
- The practice of the invention makes it possible to provide injection stretch blow-molded polypropylene articles that may be produced at very high rates and exhibit substantially uniform clarity levels. The invention may provide polypropylene preforms that facilitate production of very low haze container articles with injection stretch blow molding in a very efficient manner. One application of the invention provides improved containers, wherein such containers (or bottles) exhibit low haze levels.
- An effective clarifying agent, that also functions as a nucleator, for polypropylene is 1,3-O-2,4-bis(3,4-dimethylbenzylidene) sorbitol (hereinafter DMDBS), available from Milliken & Company under the trade name Millad® 3988. Such a compound provides highly effective haze reductions within polypropylenes with concomitant low taste and odor problems. Disubstituted DBS compounds are broadly described in U.S. Pat. Nos. 5,049,605 and 5,135,975 to Rekers. As it is, in terms of providing excellent clarity, particularly within the neck and bottom regions of target injection stretch blow-molded polypropylene bottle articles within this invention, DMDBS is a useful compound for such a result.
- An effective thermoplastic nucleator in terms of high crystallization temperatures is available from Milliken & Company using the tradename HPN-68™. Other like thermoplastic nucleating compounds that may be employed in the practice of the invention are disclosed in U.S. Pat. Nos. 6,465,551 and 6,534,574. The HPN-68™ compound is disodium bicyclo[2.2.1]heptanedicarboxylate. The ability to provide highly effective crystallization, or, in this specific situation, control targeted levels of crystallization within polypropylene preforms prior to injection stretch blow molding sometimes is facilitated by utilization of such a nucleating agent. Low amounts of this additive can be provided to produce the desired and intended amorphous-crystalline combination within the target performs. Other nucleating agents can be employed in the practice of the invention.
- The polypropylene polymers employed in the practice of the invention may include homopolymers (known as HPs), impact or block copolymers (known as ICPs)(combinations of propylene with certain elastomeric additives, such as rubber, and the like), and random copolymers (known as RCPS) made from at least one propylene and one or more ethylenically unsaturated comonomers. Generally, co-monomers, if present, constitute a relatively minor amount, i.e., about 10 percent or less, or about 5 percent or less, of the entire polypropylene, based upon the total weight of the polymer. Such co-monomers may serve to assist in clarity improvement of the polypropylene, or they may function to improve other properties of the polymer. Co-monomer examples include acrylic acid and vinyl acetate, polyethylene, polybutylene, and other like compounds.
- Polypropylene provides an average molecular weight of from about 10,000 to about 2,000,000, preferably from about 30,000 to about 300,000, and it may be mixed with additives such as polyethylene, linear low density polyethylene, crystalline ethylenepropylene copolymer, poly(1-butene), 1-hexene, 1-octene, vinyl cyclohexane, and polymethylpentene, as examples. Other polymers that may be added to the base polypropylene for physical, aesthetic, or other reasons, include polyethylene terephthalate, polybutylene terephthalate, and polyamides, among others.
- Resin compositions utilized to produce the preform articles and injection stretch blow-molded containers of the invention can be obtained by adding a specific amount of a nucleating agent/clarifying agent directly to the polypropylene, either in dry form or in molten form, and mixing them by any suitable means while in molten form to provide a substantially homogenous formulation. Alternatively, a concentrate containing as much as about 20 percent by weight of a nucleator/clarifier in a polypropylene masterbatch may be prepared and be subsequently mixed with the resin. Furthermore, the desired nucleator/clarifier (and other additives, if desired) may be present in any type of standard polypropylene additive form, including, without limitation, powder, prill, agglomerate, liquid suspension, and the like, particularly comprising dispersion aids such as polyolefin (e.g., polyethylene) waxes, stearate esters of glycerin, waxes, mineral oil, and the like. Essentially any form may be exhibited by such a combination or composition including such combination made from blending, agglomeration, compaction, and/or extrusion. The produced resins are then utilized to form preforms, as noted herein, which are then subsequently utilized to form the desired container articles in an injection stretch blow molding procedure.
- In particular, it is contemplated that certain organoleptic improvement additives be added for the purpose of reducing the migration of degraded benzaldehydes from reaching the surface of the desired article. The term “organoleptic improvement additive” is intended to encompass such compounds and formulations as antioxidants (to prevent degradation of both the polyolefin and possibly the target alditol derivatives present within such polyolefin), acid neutralizers (to prevent the ability of appreciable amounts of residual acids from attacking the alditol derivatives), and benzaldehyde scavengers (such as hydrazides, hydrazines, and the like, to prevent the migration of foul tasting and smelling benzaldehydes to the target polyolefin surface).
- Polypropylene compositions having an melt flow index (MFI) of between about 6 and about 60 are useful in the practice of the invention. Furthermore, MFI values of between about 13 and about 35 are particularly useful in the practice of the invention, as further described below.
- An injection speed of the chemical composition (i.e. polypropylene and various additives) into a preform cavity mold at a fill rate of greater than about 5 grams of chemical composition per second has been found to be particularly valuable in the practice of the invention. Table A shows values for various parameters that may be employed in the practice of the invention, as further discussed herein.
- In addition to the injection speed of the specific MFI resin, the thickness and design of the target preform is important for a number of reasons. The thickness of such an article should be thin, as compared with the thickness of previously produced polypropylene preforms. This facilitates low haze results as noted above, and also facilitates utilization within prior PET injection stretch blow molding machinery. The side wall thickness of preforms desirably may be less than about 3.5 mm for effective results. In some applications, side wall thickness of between about 1.5 mm and 3.5 is very useful. Some applications may use a thickness of as much as 4.0 mm, as set forth in Table A.
- A gate, as further described herein, comprises the opening through which liquid chemical composition (polypropylene and additive mixture) is admitted into the preform mold cavity. The gate diameter employed during preform production is particularly important, and may be related to other processing variables. A wider gate during injection into the mold cavity, coupled with the particular speed or speed range at which the resin is injected, facilitates greater control and influence upon the degree of polymer crystal orientation resulting therefrom. In the practice of the invention, a gate diameter of 1.5 mm may be used. In other applications, a gate diameter of 3.8 mm has been used. Other gate sizes could be used as well, but each factor or factor must be adjusted to account for gate diameter. Gate diameters between about 1.5 mm and 3.8 mm can be advantageously employed in the practice of the invention.
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FIG. 1 shows a stretch blow molded polypropylene container that may be manufactured in accordance with the practice of the invention. Container 10 (sometimes referred to herein as a “bottle”) is shown. Thecontainer 10 ofFIG. 1 has a relatively concave bottom 11, a cylindricalmain sidewall 12, a conicalupper portion 13, and a thickened externally threadedneck 14 on the convergent end of theupper portion 13. Aneck ring 15 provides a physical point of reference, and may be used to carry thecontainer 10 along processing machinery during manufacture and subsequent filling of thecontainer 10. - The
container 10 may be of any desired size or shape with sizes of from 0.5 to 4 liters being very useful, for example. Theneck 14 usually is rigid to support a pressure retaining screw type cap (not shown). Thus, theneck 14 may be many times the thickness of thesidewall 12. Furthermore, the conicalupper portion 13 may be gradually thickened as it approachesneck 14. - Turning now to
FIG. 2A , a flow schematic is provided showing the steps in the first stage of a two-stage stretch blow molding process. In the invention, a two stage (two step) procedure is provided for production ofcontainers 10.FIG. 2A shows the first stage of the manufacturing procedure, that is, the injection molding process of preforms production. A chemical composition containing polypropylene is acquired from a source, such as a polypropylene manufacturer. The polypropylene-containing chemical composition may comprise a homopolymer, copolymer or other polymeric composition. Furthermore, the chemical composition (also known as a “resin”) may contain various additives, including (for example) nucleating agents, antioxidants, lubricants, s-scavengers, UV absorbers and the like, as further described herein. The polypropylene chemical composition is provided into an injection machine and heated. The heated chemical composition then is injected at a relatively high rate of speed through a valve or “gate”, and into the mold of the injection machine. A preform article is formed in a mold. The preform article is cooled and removed from the mold. -
FIG. 2B shows a second stage of a two-stage stretch blow molding process. In the second stage, a preform article (which may or may not have been manufactured at a location distant from the stretch blow molding apparatus) is converted to acontainer 10. A preform article (usually at ambient temperature) is provided in a stretch blow molding machine. Then, the preform article is heated from ambient temperature to an elevated temperature. The elevated temperature employed is also known as the “orientation” temperature, and it is typically in the range of about 120-130° C. for random copolymers. - The inner surface temperature of the preform needs to be sufficiently high to ensure that containers have the best optical properties. This has been found to be one important variable in the stretch blow molding process which sometimes determines whether the container will be transparent or hazy. When the preform article is sufficiently softened, the preform is stretch blow molded into a
container 10. The formedcontainer 10 is cooled and removed from the stretch mold apparatus. -
FIGS. 3-3A show a thick-walled polypropylene preform having a relatively thick side wall 80 (in this example, the side wall thickness is about 5 mm). Thepreform article 60 shown inFIG. 3 includes aclosed end 62 and anopen end 72. Furthermore, aneck 66 is shown, withthreads 68 at the base of theneck 66. Amain body portion 64 withside wall 80 is shown. It is common for polypropylene-basedpreforms 60 such as that shown inFIG. 3 to have aside wall 80 having a thickness of about 5 mm, or more. - This
preform article 60 happens to also be “stepped out” or tapered at each end, on its exterior profile. Thus, a “profile” is found on the exterior of many preform articles. In many cases, the size of the threads at theopen end 72 are fixed, and cannot be subject to variation. -
FIG. 3B and correspondingFIG. 3C show a first embodiment of a thin walled preform article that may be employed in the practice of the invention. It should be noted that the invention may include the use of “stepped out” preforms with an exterior profile, such as shown in FIGS. 3B/3C so long as the preforms are less than about 3.5 mm in side wall width. - Thus, one discovery of the invention is that thin-walled preforms, in conjunction with processing conditions presented herein, provide surprisingly unexpected results as compared to conventional thick walled preforms. In the FIGS. 3B/3C a
preform 90 havingthin side wall 91 is shown. - The geometry of a preform article is important in the manufacturing of
containers 10. In the practice of the invention, apreform article 115 having a relatively thin side wall may be employed, as further described herein and as shown inFIGS. 4-4A . The geometry of thepreform article 115 ofFIG. 3 shows atapered neck 114, and amain body portion 102 withside walls closed end portion 116 tapers from themain body portion 102.Threads 110 are provided adjacent theopen end 103 ofpreform article 115. Atransition area 105 represents the tapering region of theside wall 101 into theneck 114. - In
FIG. 4 , apreform article 115 of the invention is shown in which the outer wall surfaces 109 a-b of the preform article are generally parallel and straight, forming a substantially symmtrical tube on its outer dimension from a point near theclosed end 116 to a point near theopen end 103. Theinner wall 108 of thepreform 115 is profiled due to atransition zone 105. When blown in stage two of manufacture, thepreform article 115 engages a mold so as to make acontainer 10 of the appropriate geometry. - By “profiled”, it is meant that a given wall has a changing angle or slope which deviates from 180 degrees. Thus, the invention may in some embodiments take advantage of a profiled
inner wall 108, as opposed to a profiled exterior wall, as is common in the conventional devices (seeFIGS. 3-3A ). The use of a profiledinner wall 108 has been found to be a useful feature in application of thepreform 115 tocontainer 10 manufacture. One reason for this fact is that it facilitates the use of relatively uniform outer wall dimensions. Thus, preforms 115 can be used that have differinginner wall 108 profile for various container sizes, while still exhibiting a common outer dimension or shape. This is useful in manufacturing, to avoid or minimize tooling and/or machinery changes for eachsize preform 115 that may be used to makecontainers 10 of various sizes. - Thus, a relatively uniform outer dimension to the
preform articles 115 may provide an advantage that may be realized in the practice of the invention. It should be recognized that the use of a profiledinner wall 108 is not required in the practice of the invention, but is one useful manner of practicing the invention. Thus, preforms having either an exterior profile or an exterior profile may be used in the practice of the invention. -
FIG. 5 shows a schematic vertical cross-sectional view of an injection molding machine for making preform articles in a first stage. Apreform article 115 may be 10 formed in aninjection molding unit 120 having abarrel 121 fed by anhopper 122 and ejecting the melt through around nose nozzle 123. A chemical composition (i.e. polypropylene-containing pellets or portions, with optional additives or optional nucleating agents, etc) is provided intoinlet hopper 122.Barrel 121 rotatably mounts a melting and mixingscrew 124 with anon-return valve nose 125.Heater bands 126 may be provided in thebarrel 121. Crystalline polypropylene stretch blow mold formulations are fed through thehopper 122 into thebarrel 121 where they are advanced by the melting and mixingscrew 124 to a molten condition at thevalve end 125 whereupon the screw is advanced to the dotted line position where thevalve nose 125 will force the molten material through thenozzle orifice 127.Gate 137 a received a determined the amount of liquid flow that proceeds into themolding cavity 135. Other similar apparatus could be used to form a preform, which achieves the same or similar result as that shown inFIG. 5 . - The apparatus includes a two-
part mold 130 with afirst core part 131 and a second moldingcavity defining part 132. Thepart 131 has acylindrical core 133 with ahemispherical end 134. Thepart 132 has amolding cavity 135 with a hemisphericalbottom end 136 fed by aconduit 137. The end wall of thepart 132 has arecess 138 receiving the rounded nose of thenozzle 123. - With the apparatus in the position of
FIG. 4 the molten plastics material ahead of thevalve 125 may be ejected through theorifice 127 by moving the screw rod to the dotted line position as shown inFIG. 5 . The molten material will flow through theconduit 137 into themold cavity 135. - The surface of
core 133 and the molding cavity surfaces 135 and 136 typically are polished, but may be treated as well to facilitate the ejection ofpreforms 115. Steel is a desired metal for manufacture of such mold surfaces 135. Chilled mold temperatures from about 11-20 degrees C. may be employed. - One feature employed when injection
molding preform articles 115, as shown inFIG. 5 , is theGate 137 a. Thegate 137 a refers is the opening between the point at which the liquid polypropylene is injected and theactual core 134 of themold cavity 135. Gate size is a parameter that may vary for different applications. The size of thegate 137 a can be important in the manufacture of preformedarticles 115. This is because the size of thegate 137 a determines the shear forces applied to the molten polypropylene as it is injected into the mold cavity. The size ofgate 137 a will affect the filing rate. The size of thegate 137 a will in some cases determine the rate by at which the chemical composition may be injected, which affects the ultimate clarity of thecontainers 10 produced by the preformedarticle 115 in the second stage of thecontainer 10 manufacture (seeFIG. 2B ). - To improve the economics of making polypropylene preforms, it may be important to inject chemical compositions quickly (shorter preform cycle time) into the
mold cavity 135. However, when injecting quickly, the clarity of thecontainer 10 produced may be compromised because of the characteristics imparted to thepreform article 115 during such mold fill step. Thus, using a relatively wide or large gate 37 a allows one to inject at a faster rate while still achieving the same or sufficient clarity in the final container. In some applications, this is desirable. Gate diameter may vary, depending upon the application. The invention is not limited to any particular gate diameter, but it has been found that diameters between about 1.5 mm and about 3.8 mm are useful, and may be found in equipment in the industry. It may be an advantage in the practice of the invention to be capable of employing gate diameter settings that already are in existence and used on existing commercial PET processing equipment. - The injection rate usually is relatively slow. Cavity filling time is typically about 1 to about 4.5 total seconds to fill
mold cavity 135. This corresponds generally to an injection rate greater than about 5 grams/second. In other cases, the rate may be between about 5 and about 22 grams per second. Table A shows various parameters that may be advantageously employed in the practice of the invention. - Upon solidification of the
preform article 115 in themold 130, themold 130 is opened by withdrawing part 131 (and core 133) frompart 132. Thepreform 115 is stripped from the mold. - The melt flow index (MFI), also known as the melt flow rate, is an important factor in the manufacturing of
preform articles 115. In general, melt flow index is measured according to American Society of Testing Materials ASTM D-1238. This testing method is a nationally (or internationally) known standard. It is a standard test method for measuring the melt flow rates of thermoplastics. Unless otherwise indicated herein, all references to melt flow index, melt flow rate, MFI, or MFR, refer to measurements according to this industry standard. For polypropylene, measurements are at 230 degrees C., and using 2.16 kg, as per this standard. - In general, the more viscous is a material at a given temperature, the lower will be the MFI value of that material. For example, a given polymer or copolymer composition will have an MFI that is specified by a manufacturer. Thus, each particular type of polypropylene-containing composition to be employed in the practice of the invention will have a given or predetermined MFI. The MFI is also determined and affected by the length of the polymer chains in a given polypropylene composition. The longer the polymeric chains, the more viscous the material. The more viscous the material, the lower the MFI value will be for a given composition.
- MFI values are important in determining the speed at which a chemical composition may be fed into an injection mold cavity to form a preform article. This is true because the MFI also will affect the clarity of the final container which is produced from the preform. By clarity, it is meant the degree of haze that will be present in a given
container 10 made according to the invention. In general, the higher percentage of haze in thecontainer 10, the less transparent is thecontainer 10 produced in the invention. Higher levels of haze are undesirable. - One unexpected result of the invention is that it has been found that using a given polymeric composition having a predetermined melt flow index, and injecting that composition at a fill rate of greater than about 5 grams per second, a highly desired preform article may be formed. Furthermore, it has been found that the sidewall thickness of the preform is very important in container manufacture. In the practice of the invention, a
preform article 115 with a side wall thickness of less than about 3.5 millimeters has proved to be very desirable. This achieves a high productivity of container manufacture while still maintaining a low degree of haze, i.e. a clear container. Cycle time necessary to make apreform article 115 is significantly reduced by using a preform design with a minimum side wall thickness. Hot plastic (polypropylene) is capable of cooling in the preform mold more quickly using a reduced wall thickness for the preform stage. This facilitates faster preform cycle times, thereby increasing the number ofpreform articles 115 that can be made in a given period of time, increasing manufacturing capacity and efficiency. - Stage two (step 2) of manufacture is shown generally in
FIG. 2B , andFIGS. 6-8 . Apreform article 115 is taken at ambient temperature, and then uniformly heated. Thepreform article 115 is placed in a stretchblow mold apparatus 140 in a position with itsopen end 103 resting on a platform 141 on abase 142 surrounding areciprocal swage 143. Theclosed end 116 of thepreform 115 is shown near the center ofFIG. 6 . The apparatus freely receives the retracted end of thestretch rod 144 of theapparatus 140. The molding dies 145 of theapparatus 140 are in an opened condition. Threaded neck formingwall portions 146 are shown, as well as taperedcone forming portions 147, cylindrical mainbody forming portions 148, and concavebottom forming portions 149. - Alternatively, and in some embodiments, it may be that a rotary system is employed to transfer preforms using transfer wheels equipped with grippers into a blow mold cavity. Thus, rotary stretch blow molding equipment is known in the art, and may be applied in the practice of the invention. From the open position of
FIG. 6 theapparatus 140 is closed to the position ofFIG. 7 with the mold halves 145 coming together and with theswage 143 extended into the open end of thepreform 115 so that the neck andthread forming portions 146 of the die can mold thethick neck 114 of the bottle on thepreform 115. The projection of theswage 143 into the position ofFIG. 7 also moves thestretch rod 144 against theclosed end 116 of thepreform 115. - From the position of
FIG. 7 theapparatus 140 is further activated to eject thestretch rod 144 beyond theswage 143 into closely spaced relation from thebottom forming portion 149 of the dies 145 thereby effecting a stretching of thepreform 115 to the full height of the dies. As shown inFIG. 8 , thestretch rod 144 and theswage 143 are retracted from thecontainer 10. The gas pressure in the bottle is released, and the dies 45 are separated. A blowing agent is introduced into thepreform article 115 forming an axially elongated and hoop stretched balloon in the closed die. The balloon (not shown) is blown into afinished container 10, as shown inFIG. 8 , with the polypropylene material biaxially stretched to produce astrong container 10. - Roughness on the
inner container 10 surface has a negative influence on the container clarity. If, during reheating of the preform 115 (within the window of process stability), the temperature in the skin-layer (at the side of the core) is insufficiently high, the material undesirably may be ruptured apart during the stretch blow molding (stage two) process, resulting in a roughinner container 10 surface andcontainers 10 having low clarity. Additionally, it has been observed that a low amount of “pre-blowing” (intermediate shape of the stretched and pre-blown preform part, i.e. before the final pressure is applied) may contribute to a relatively roughinner container 10 surface (i.e. undesirable high haze) for the same reason. More specifically the primary pressure, flow of air and pre-blow time usually need to be sufficiently high to prevent that the material gets ruptured apart what gives the part an undesirable high haze. - In the practice of the invention, it is important that several variables and factors be correlated to each other. Variables that are important in the practice of the invention include, for example, injection speed, MFI of the polypropylene-containing resin, the preform article thickness. In some instances, the gate diameter used during injection of the preform article is a factor. These factors may be optimized and correlated to each other for a given container application, as in the Critical Filling Rate Model set forth below. It is possible using the practice of the invention to maximize productivity of the preform and to maximize productivity polypropylene containers in a two-stage stretch blow molding process.
- In one particularly useful aspect of the invention, a preform thickness may be of a value less than about 3.5 mm. Thickness is measured along
side walls FIG. 4A , measured as the maximum or thickest portion of the side wall. In yet another embodiment of the invention, the preform thickness may be in the range of about 2-3.5 mm. Furthermore, in the practice of the invention it has been found that an injection fill rate into the cavity mold of greater than about 5 grams of chemical composition (resin) per second is quite useful. Furthermore, in other aspects of the invention it is advantageous to use a cavity mold fill rate of between 5 and 22 grams per second. - Table A shows a correlation between processing variables in the practice of the invention. In Table A, the MFI values and preform wall thickness values are correlated to the optimized injection mold filling rate in the practice of the invention. It is important to note in Table A that for a given preform wall thickness an increase in the MFI value allows an operator to use a higher injection mold filling rate while still obtaining
containers 10 of sufficient clarity. Thus, as a result of the practice of the invention it is possible to reduce the cycle time as compared to prior art processes, and yet still obtain containers of relatively low haze and high quality. - Looking from left to right in Table A, a greater preform wall thickness at a given level of MFI value enables an operator employing the invention to use an injection mold filling rate which is greater, resulting in faster production, reduced cycle times, and good container clarity.
- Table A reports values for a (valve) gate thickness of 1.5 mm. In the practice of the invention, the use of a wider gate such as about 3.8 mm can result in a filling rate of about 13 g/sec at a MFI value of 13. This compares to the data in Table A in which a MFI of 13 at a (valve) gate diameter of 1.5 mm was successfully employed using an injection speed of about 5-6 g/sec. Furthermore, it has been found in the practice of the invention that using a (valve) gate diameter of 3.8 mm at MFI value 20 may result in an injection speed of about 22 g/sec. This value of 22 g/sec may be compared to the injection speed shown in Table A (valve diameter 1.5 mm) of 5-7 g/s.
TABLE A Processing Variables Correlated to Injection Mold Filling Rate for Invention* Preform Wall Thickness MFI 2 mm 3 mm 4 mm 1.5 Poor Poor Poor Clarity Clarity Clarity 13 4-5 g/s 4-5 g/s 5-6 g/s 20 5 g/s 5-7 g/s 7-10 g/s 30 6-7 g/s 10-13 g/s 13-17 g/s 45 11 g/s 20 g/s N/A
*Values in Table A are provided for a (valve) gate diameter of 1.5 mm.
- Measurements of percent haze/thickness ratios have been obtained on
various containers 10 in the practice of the invention. It has been found that a percent haze/thickness reported as percent haze/mils with a value of less than about 0.05 is particularly highly desirable. - In the practice of the invention, it is possible in a manufacturing operation to achieve a rate of container production of greater than about 900 containers per hour per mold. In other applications, it is possible to provide a stretch blow molding step in a manufacturing operation at a rate of container production of at least about 1200 containers per hour per mold. In an even more desirable aspect, the invention makes it possible to achieve a rate of container production of at least about 1500 containers per hour per mold.
- Commercial random copolymer resins containing Millad 3988 (Borealis) were used to produce preforms as indicated in Table I. The preforms were produced on a two-cavity mold (only one cavity installed) 100 ton Netstal injection molding machine with a variable injection time (0.5-4.0 sec) and a constant cooling time of 22 sec. Melt temperature was 230° C. Temperature of the cooling water was 13° C. The holding pressure time was 9.2 sec. Total cycle time was around 37 sec (not optimized). A valve gate with a diameter of 1.5 mm was used. The preforms have a wall thickness of 4 mm and a bottle weight of about 25.3 g. These preforms were later blown into bottles as explained in subsequent examples.
TABLE I Example 1 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/sec) I-1 RB307MO 1.5 0.5 50.6 I-2 RB307MO 1.5 1.0 25.3 I-3 RB307MO 1.5 1.5 16.9 I-4 RB307MO 1.5 2.0 12.7 I-5 RB307MO 1.5 2.5 10.1 I-6 RB307MO 1.5 3.0 8.4 I-7 RB307MO 1.5 3.5 7.2 I-8 RB307MO 1.5 4.0 6.3 I-9 RE420MO 13 0.5 50.6 I-10 RE420MO 13 1.0 25.3 I-11 RE420MO 13 1.5 16.9 I-12 RE420MO 13 2.0 12.7 I-13 RE420MO 13 2.5 10.1 I-14 RE420MO 13 3.0 8.4 I-15 RE420MO 13 3.5 7.2 I-16 RE420MO 13 4.0 6.3 I-17 RF365MO 20 0.5 50.6 I-18 RF365MO 20 1.0 25.3 I-19 RF365MO 20 1.5 16.9 I-20 RF365MO 20 2.0 12.7 I-21 RF365MO 20 2.5 10.1 I-22 RF365MO 20 3.0 8.4 I-23 RF365MO 20 3.5 7.2 I-24 RF365MO 20 4.0 6.3 I-25 RG460MO 30 0.5 50.6 I-26 RG460MO 30 1.0 25.3 I-27 RG460MO 30 1.5 16.9 I-28 RG460MO 30 2.0 12.7 I-29 RG460MO 30 2.5 10.1 I-30 RG460MO 30 3.0 8.4 I-31 RG460MO 30 3.5 7.2 I-32 RG460MO 30 4.0 6.3 I-33 RJ370MO 45 0.5 50.6 I-34 RJ370MO 45 1.0 25.3 I-35 RJ370MO 45 1.5 16.9 I-36 RJ370MO 45 2.0 12.7 I-37 RJ370MO 45 2.5 10.1 I-38 RJ370MO 45 3.0 8.4 I-39 RJ370MO 45 3.5 7.2 I-40 RJ370MO 45 4.0 6.3 - Commercial random copolymer resins containing Millad 3988 (Borealis) were used to produce preforms as indicated in Table II. The preforms were produced on a two-cavity mold (only one cavity installed) 100 ton Netstal injection molding machine with a variable injection time (0.5-4.0 sec) and a constant cooling time of 10 sec. Melt temperature was 230° C. Temperature of the cooling water was 13° C. The holding pressure time was 4.5 sec. Total cycle time was around 20 sec (not optimized). A valve gate with a diameter of 1.5 mm was used. The preforms have a wall thickness of 3 mm and a bottle weight of about 20.3 g. These preforms were later blown into bottles as explained in subsequent examples.
TABLE II Example 2 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/cc) II-1 RB307MO 1.5 0.5 40.6 II-2 RB307MO 1.5 1.0 20.3 II-3 RB307MO 1.5 1.5 13.5 II-4 RB307MO 1.5 2.0 10.2 II-5 RB307MO 1.5 2.5 8.1 II-6 RB307MO 1.5 3.0 6.8 II-7 RB307MO 1.5 3.5 5.8 II-8 RB307MO 1.5 4.0 5.1 II-9 RE420MO 13 0.5 40.6 II-10 RE420MO 13 1.0 20.3 II-11 RE420MO 13 1.5 13.5 II-12 RE420MO 13 2.0 10.2 II-13 RE420MO 13 2.5 8.1 II-14 RE420MO 13 3.0 6.8 II-15 RE420MO 13 3.5 5.8 II-16 RE420MO 13 4.0 5.1 II-17 RF365MO 20 0.5 40.6 II-18 RF365MO 20 1.0 20.3 II-19 RF365MO 20 1.5 13.5 II-20 RF365MO 20 2.0 10.2 II-21 RF365MO 20 2.5 8.1 II-22 RF365MO 20 3.0 6.8 II-23 RF365MO 20 3.5 5.8 II-24 RF365MO 20 4.0 5.1 II-25 RG460MO 30 0.5 40.6 II-26 RG460MO 30 1.0 20.3 II-27 RG460MO 30 1.5 13.5 II-28 RG460MO 30 2.0 10.2 II-29 RG460MO 30 2.5 8.1 II-30 RG460MO 30 3.0 6.8 II-31 RG460MO 30 3.5 5.8 II-32 RG460MO 30 4.0 5.1 II-33 RJ370MO 45 0.5 40.6 II-34 RJ370MO 45 1.0 20.3 II-35 RJ370MO 45 1.5 13.5 II-36 RJ370MO 45 2.0 10.2 II-37 RJ370MO 45 2.5 8.1 II-38 RJ370MO 45 3.0 6.8 II-39 RJ370MO 45 3.5 5.8 II-40 RJ370MO 45 4.0 5.1 - Commercial random copolymer resins containing Millad 3988 (Borealis) were used to produce preforms as indicated in Table III. The preforms were produced on a two-cavity mold (only one cavity installed) 100 ton Netstal injection molding machine with a variable injection time (0.5-4.0 sec) and a constant cooling time of 10 sec. Melt temperature was 230° C. Temperature of the cooling water was 13° C. The holding pressure time was 2 sec. Total cycle time was around 20 sec (not optimized). A valve gate with a diameter of 1.5 mm was used. The preforms have a wall thickness of 2 mm and a bottle weight of about 17.3 g. These preforms were later blown into bottles as explained in subsequent examples.
TABLE III Example 3 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/cc) III-1 RB307MO 1.5 0.5 34.6 III-2 RB307MO 1.5 1.0 17.3 III-3 RB307MO 1.5 1.5 11.5 III-4 RB307MO 1.5 2.0 10.2 III-5 RB307MO 1.5 2.5 6.9 III-6 RB307MO 1.5 3.0 5.8 III-7 RB307MO 1.5 3.5 4.9 III-8 RB307MO 1.5 4.0 4.3 III-9 RE420MO 13 0.5 34.6 III-10 RE420MO 13 1.0 17.3 III-11 RE420MO 13 1.5 11.5 III-12 RE420MO 13 2.0 10.2 III-13 RE420MO 13 2.5 6.9 III-14 RE420MO 13 3.0 5.8 III-15 RE420MO 13 3.5 4.9 III-16 RE420MO 13 4.0 4.3 III-17 RF365MO 20 0.5 34.6 III-18 RF365MO 20 1.0 17.3 III-19 RF365MO 20 1.5 11.5 III-20 RF365MO 20 2.0 10.2 III-21 RF365MO 20 2.5 6.9 III-22 RF365MO 20 3.0 5.8 III-23 RF365MO 20 3.5 4.9 III-24 RF365MO 20 4.0 4.3 III-25 RG460MO 30 0.5 34.6 III-26 RG460MO 30 1.0 17.3 III-27 RG460MO 30 1.5 11.5 III-28 RG460MO 30 2.0 10.2 III-29 RG460MO 30 2.5 6.9 III-30 RG460MO 30 3.0 5.8 III-31 RG460MO 30 3.5 4.9 III-32 RG460MO 30 4.0 4.3 III-33 RJ370MO 45 0.5 34.6 III-34 RJ370MO 45 1.0 17.3 III-35 RJ370MO 45 1.5 11.5 III-36 RJ370MO 45 2.0 10.2 III-37 RJ370MO 45 2.5 6.9 III-38 RJ370MO 45 3.0 5.8 III-39 RJ370MO 45 3.5 4.9 III-40 RJ370MO 45 4.0 4.3 - Polypropylene bottles (330 ml) were on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 1. Axial stretch ratio is 1.9/1, Hoop Stretch ratio=2.5/1 & Total Stretch Ratio=4.8/1. This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps. Pre-blow pressure was 6 bar & final pressure was 8 bar. After optimization, the bottle productivity for the preforms with 4 mm thickness was 820 bph/cav. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE IV Example 4 Bottles MFI Injection (g/10 Speed % Haze/ Bottle Example sec) (g/cc) thickness Quality IV-1 1.5 50.6 1.252 Acceptable IV-2 1.5 25.3 Acceptable IV-3 1.5 16.9 Acceptable IV-4 1.5 12.7 1.530 Acceptable IV-5 1.5 10.1 Acceptable IV-6 1.5 8.4 Acceptable IV-7 1.5 7.2 Acceptable IV-8 1.5 6.3 Acceptable IV-9 13 50.6 Acceptable IV-10 13 25.3 Acceptable IV-11 13 16.9 Acceptable IV-12 13 12.7 Acceptable IV-13 13 10.1 Acceptable IV-14 13 8.4 Average IV-15 13 7.2 0.067 Excellent IV-16 13 6.3 0.043 Excellent IV-17 20 50.6 Acceptable IV-18 20 25.3 Acceptable IV-19 20 16.9 Acceptable IV-20 20 12.7 Average IV-21 20 10.1 0.782 Average IV-22 20 8.4 Excellent IV-23 20 7.2 Excellent IV-24 20 6.3 0.036 Excellent IV-25 30 50.6 1.191 Acceptable IV-26 30 25.3 0.150 Acceptable IV-27 30 16.9 0.062 Excellent IV-28 30 12.7 Excellent IV-29 30 10.1 Excellent IV-30 30 8.4 Excellent IV-31 30 7.2 0.075 Excellent IV-32 30 6.3 Excellent IV-33 45 50.6 NA IV-34 45 25.3 NA IV-35 45 16.9 NA IV-36 45 12.7 NA IV-37 45 10.1 NA IV-38 45 8.4 NA IV-39 45 7.2 NA IV-40 45 6.3 0.072 NA - Polypropylene bottles (330 ml) were blown at high speed on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 2. Axial stretch ratio is 1.9/1, Hoop Stretch ratio=2.4 & Total Stretch Ratio=4.6/1. This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps. Pre-blow pressure was 6 bar & final pressure was 8 bar. After optimization, the bottle productivity for the preforms with 3 mm thickness was 1,030 bph/cav. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE V Example 5 Bottles MFI Injection (g/10 Speed % Haze/ Bottle Example sec) (g/cc) thickness Quality V-1 1.5 40.6 Acceptable V-2 1.5 20.3 Acceptable V-3 1.5 13.5 Acceptable V-4 1.5 10.2 Acceptable V-5 1.5 8.1 Acceptable V-6 1.5 6.8 Acceptable V-7 1.5 5.8 Acceptable V-8 1.5 5.1 2.143 Acceptable V-9 13 40.6 Acceptable V-10 13 20.3 Acceptable V-11 13 13.5 Acceptable V-12 13 10.2 Acceptable V-13 13 8.1 Acceptable V-14 13 6.8 Acceptable V-15 13 5.8 Average V-16 13 5.1 Excellent V-17 20 40.6 Acceptable V-18 20 20.3 Acceptable V-19 20 13.5 Acceptable V-20 20 10.2 Average V-21 20 8.1 Average V-22 20 6.8 0.132 Average V-23 20 5.8 Excellent V-24 20 5.1 0.056 Excellent V-25 30 40.6 0.125 Acceptable V-26 30 20.3 Acceptable V-27 30 13.5 Acceptable V-28 30 10.2 Excellent V-29 30 8.1 Excellent V-30 30 6.8 Excellent V-31 30 5.8 0.075 Excellent V-32 30 5.1 Excellent V-33 45 40.6 Acceptable V-34 45 20.3 Average V-35 45 13.5 Excellent V-36 45 10.2 Excellent V-37 45 8.1 Excellent V-38 45 6.8 Excellent V-39 45 5.8 Excellent V-40 45 5.1 Excellent - Polypropylene bottles (330 ml) were blown at high speed on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 3. Axial stretch ratio is 1.9/1, Hoop Stretch ratio=2.4 & Total Stretch Ratio=4.4/1. This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps. Pre-blow pressure was 6 bar & final pressure was 8 bar. After optimization, the bottle productivity for the preforms with 2 mm thickness was 1,200 bph/cav. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE VI Example 6 Bottles MFI Injection (g/10 Speed % Haze/ Bottle Example sec) (g/cc) thickness Quality VI-1 1.5 34.6 Acceptable VI-2 1.5 17.3 Acceptable VI-3 1.5 11.5 Acceptable VI-4 1.5 10.2 Acceptable VI-5 1.5 6.9 Acceptable VI-6 1.5 5.8 Acceptable VI-7 1.5 4.9 Acceptable VI-8 1.5 4.3 Acceptable VI-9 13 34.6 Acceptable VI-10 13 17.3 Acceptable VI-11 13 11.5 Acceptable VI-12 13 10.2 Acceptable VI-13 13 6.9 Acceptable VI-14 13 5.8 Acceptable VI-15 13 4.9 Acceptable VI-16 13 4.3 Average VI-17 20 34.6 Acceptable VI-18 20 17.3 Acceptable VI-19 20 11.5 Acceptable VI-20 20 10.2 Acceptable VI-21 20 6.9 Acceptable VI-22 20 5.8 Average VI-23 20 4.9 Excellent VI-24 20 4.3 Excellent VI-25 30 34.6 Acceptable VI-26 30 17.3 Acceptable VI-27 30 11.5 Acceptable VI-28 30 10.2 Acceptable VI-29 30 6.9 Excellent VI-30 30 5.8 Excellent VI-31 30 4.9 Excellent VI-32 30 4.3 Excellent VI-33 45 34.6 Acceptable VI-34 45 17.3 Average VI-35 45 11.5 Excellent VI-36 45 10.2 Excellent VI-37 45 6.9 Excellent VI-38 45 5.8 Excellent VI-39 45 4.9 Excellent VI-40 45 4.3 0.087 Excellent - Polypropylene bottles (500 ml) were blown at high speed (1500 bottles/cavity/hour) on a Sidel SBO-8 Series II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 1. Axial stretch ratio is 2.5/1, Hoop Stretch ratio=2.63 & Total Stretch Ratio=6.57/1. Machine settings were adjusted to accommodate high clarity, high speed bottle production. Preforms were subjected to a pre-blow pressure of 3 Bar for 0.9 seconds with the preform inner temperature set to about 125°-130° C. and the outer temperature set to about 120°-125° C. Heating power distribution was managed in the range of 90%. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or excellent (a fully blown bottle with outstanding optical clarity).
TABLE VII Example 7 Bottles MFI Injection (g/10 Speed % Haze/ Bottle Example sec) (g/cc) thickness Quality VII-1 1.5 50.6 Acceptable VII-2 1.5 25.3 Acceptable VII-3 1.5 16.9 Acceptable VII-4 1.5 12.7 Acceptable VII-5 1.5 10.1 Acceptable VII-6 1.5 8.4 Acceptable VII-7 1.5 7.2 Acceptable VII-8 1.5 6.3 1.500 Acceptable VII-9 13 50.6 Acceptable VII-10 13 25.3 Acceptable VII-11 13 16.9 1.474 Acceptable VII-12 13 12.7 0.494 Acceptable VII-13 13 10.1 0.283 Average VII-14 13 8.4 0.205 Average VII-15 13 7.2 0.075 Excellent VII-16 13 6.3 0.089 Excellent VII-17 20 50.6 Acceptable VII-18 20 25.3 0.895 Acceptable VII-19 20 16.9 0.250 Acceptable VII-20 20 12.7 0.111 Acceptable VII-21 20 10.1 0.467 Acceptable VII-22 20 8.4 0.211 Average VII-23 20 7.2 0.086 Excellent VII-24 20 6.3 0.068 Excellent VII-25 30 50.6 Acceptable VII-26 30 25.3 Acceptable VII-27 30 16.9 Average VII-28 30 12.7 0.079 Excellent VII-29 30 10.1 Excellent VII-30 30 8.4 Excellent VII-31 30 7.2 Excellent VII-32 30 6.3 0.068 Excellent VII-33 45 50.6 Excellent VII-34 45 25.3 Excellent VII-35 45 16.9 Excellent VII-36 45 12.7 Excellent VII-37 45 10.1 Excellent VII-38 45 8.4 Excellent VII-39 45 7.2 Excellent VII-40 45 6.3 Excellent - Polypropylene bottles (500 ml) were blown at high speed (1,500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 2. Axial stretch ratio is 2.5/1, Hoop Stretch ratio=2.54 & Total Stretch Ratio=6.36/1. Machine settings were adjusted to accommodate high clarity, high speed bottle production. Preforms were subjected to a pre-blow pressure of 4.5 Bar for 0.4 seconds & nozzle for 3 rotations open activated at ‘point zero’. Blowing time is 0.8 sec & Exhaust time is 0.4 sec. Stretch speed is 1,384 m/sec & a standard stretch rod with 14 mm diameter was used. Preform temperature is about 120-130° C. Heating profile: Z1=75%, Z2=90%, Z3=70%, Z4=70%, Z5=65% & Z6=70% with Z1, Z5 & Z6 in an advanced position. % GP=65%. This example used 100% was ventilation to cool the preform surface. Total heating time, 14.65 sec, stabilization time=6.0 sec & final stabilization time=4.5 sec. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE VIII Example 8 Bottles MFI Injection (g/10 Speed % Haze/ Bottle Example sec) (g/cc) thickness Quality VIII-1 1.5 40.6 Acceptable VIII-2 1.5 20.3 Acceptable VIII-3 1.5 13.5 Acceptable VIII-4 1.5 10.2 Acceptable VIII-5 1.5 8.1 Acceptable VIII-6 1.5 6.8 Acceptable VIII-7 1.5 5.8 Acceptable VIII-8 1.5 5.1 1.316 Acceptable VIII-9 13 40.6 Acceptable VIII-10 13 20.3 Acceptable VIII-11 13 13.5 Acceptable VIII-12 13 10.2 Acceptable VIII-13 13 8.1 Acceptable VIII-14 13 6.8 Acceptable VIII-15 13 5.8 0.087 Average VIII-16 13 5.1 0.074 Excellent VIII-17 20 40.6 Acceptable VIII-18 20 20.3 Acceptable VIII-19 20 13.5 Acceptable VIII-20 20 10.2 0.153 Average VIII-21 20 8.1 Average VIII-22 20 6.8 Excellent VIII-23 20 5.8 Excellent VIII-24 20 5.1 0.084 Excellent VIII-25 30 40.6 Acceptable VIII-26 30 20.3 Acceptable VIII-27 30 13.5 0.094 Average VIII-28 30 10.2 Excellent VIII-29 30 8.1 Excellent VIII-30 30 6.8 Excellent VIII-31 30 5.8 Excellent VIII-32 30 5.1 0.082 Excellent VIII-33 45 40.6 Acceptable VIII-34 45 20.3 0.192 Average VIII-35 45 13.5 Excellent VIII-36 45 10.2 Excellent VIII-37 45 8.1 Excellent VIII-38 45 6.8 Excellent VIII-39 45 5.8 Excellent VIII-40 45 5.1 0.072 Excellent - Polypropylene bottles (500 ml) were blown at high speed (1,500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 3. Axial stretch ratio is 2.5/1, Hoop Stretch ratio=2.54 & Total Stretch Ratio=6.36/1. Machine settings were adjusted to accommodate high clarity, high speed bottle production. Preforms were subjected to a pre-blow pressure of 4 Bar for 0.4 seconds & nozzle for 3 rotations open activated at ‘point zero’. Blowing time is 0.8 sec & Exhaust time is 0.4 sec. Stretch speed is 1,384 m/sec & a standard stretch rod with 14 mm diameter was used. Preform temperature is about 115-127° C. Heating profile: Z1=72.5%, Z2=26%, Z3=26%, Z4=32.8%, Z5=26% & Z6=55.5% with Z1, Z5 & Z6 in an advanced position. % GP=45%. Used 100% ventilation to cool the preform surface. Total heating time is 14.65 sec, stabilization time=6.0 sec & final stabilization time=4.5 sec. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown put), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE IX Example 9 Bottles MFI Injection (g/10 Speed % Haze/ Bottle Example sec) (g/cc) thickness Quality IX-1 1.5 34.6 3.462 Acceptable IX-2 1.5 17.3 2.722 Acceptable IX-3 1.5 11.5 2.300 Acceptable IX-4 1.5 10.2 2.053 Acceptable IX-5 1.5 6.9 2.250 Acceptable IX-6 1.5 5.8 2.000 Acceptable IX-7 1.5 4.9 2.000 Acceptable IX-8 1.5 4.3 1.824 Acceptable IX-9 13 34.6 2.537 Acceptable IX-10 13 17.3 1.739 Acceptable IX-11 13 11.5 1.833 Acceptable IX-12 13 10.2 0.545 Acceptable IX-13 13 6.9 0.154 Acceptable IX-14 13 5.8 0.146 Acceptable IX-15 13 4.9 0.160 Acceptable IX-16 13 4.3 0.115 Average IX-17 20 34.6 2.591 Acceptable IX-18 20 17.3 1.250 Acceptable IX-19 20 11.5 2.000 Acceptable IX-20 20 10.2 1.077 Acceptable IX-21 20 6.9 0.200 Acceptable IX-22 20 5.8 0.107 Average IX-23 20 4.9 0.186 Average IX-24 20 4.3 Excellent IX-25 30 34.6 Acceptable IX-26 30 17.3 Acceptable IX-27 30 11.5 Acceptable IX-28 30 10.2 Average IX-29 30 6.9 0.143 Average IX-30 30 5.8 Excellent IX-31 30 4.9 Excellent IX-32 30 4.3 0.100 Excellent IX-33 45 34.6 1.000 Acceptable IX-34 45 17.3 0.387 Acceptable IX-35 45 11.5 0.143 Average IX-36 45 10.2 Excellent IX-37 45 6.9 Excellent IX-38 45 5.8 Excellent IX-39 45 4.9 Excellent IX-40 45 4.3 0.092 Excellent - Several compounds were produced on a Killion single screw extruder at a temperature 230° C. using 25 g/10 min random copolymer polypropylene fluff. The preforms (ref. Table X) were produced on a two-cavity mold (only one cavity installed) 100 ton Netstal injection molding machine with a variable injection time (0.5-4.0 sec) and a constant cooling time of 10 sec. Melt temperature was 230° C. Temperature of the cooling water was 13° C. The holding pressure time was 4.5 sec. Total cycle time was around 20 sec (not optimized). A valve gate with a diameter of 1.5 mm was used. The preforms have a wall thickness of 3 mm and a bottle weight of about 20.3 g. These preforms were later blown into bottles as explained in subsequent examples.
TABLE X Example 10 Preforms Injection Injection Loading Time Speed Example Nucleator (ppm) (sec) (g/cc) X-1 NA-21 2000 0.5 50.6 X-2 NA-21 2000 1.0 25.3 X-3 NA-21 2000 1.5 16.9 X-4 NA-21 2000 2.0 12.7 X-5 NA-21 2000 2.5 10.1 X-6 NA-21 2000 3.0 8.4 X-7 NA-21 2000 3.5 7.2 X-8 NA-21 2000 4.0 6.3 X-9 NA-11 1000 0.5 50.6 X-10 NA-11 1000 1.0 25.3 X-11 NA-11 1000 1.5 16.9 X-12 NA-11 1000 2.0 12.7 X-13 NA-11 1000 2.5 10.1 X-14 NA-11 1000 3.0 8.4 X-15 NA-11 1000 3.5 7.2 X-16 NA-11 1000 4.0 6.3 X-17 HPN-68 1000 0.5 50.6 X-18 HPN-68 1000 1.0 25.3 X-19 HPN-68 1000 1.5 16.9 X-20 HPN-68 1000 2.0 12.7 X-21 HPN-68 1000 2.5 10.1 X-22 HPN-68 1000 3.0 8.4 X-23 HPN-68 1000 3.5 7.2 X-24 HPN-68 1000 4.0 6.3 X-25 AlptBBA 1000 0.5 50.6 X-26 AlptBBA 1000 1.0 25.3 X-27 AlptBBA 1000 1.5 16.9 X-28 AlptBBA 1000 2.0 12.7 X-29 AlptBBA 1000 2.5 10.1 X-30 AlptBBA 1000 3.0 8.4 X-31 AlptBBA 1000 3.5 7.2 X-32 AlptBBA 1000 4.0 6.3 X-33 CaHHPA 1500 0.5 50.6 X-34 CaHHPA 1500 1.0 25.3 X-35 CaHHPA 1500 1.5 16.9 X-36 CaHHPA 1500 2.0 12.7 X-37 CaHHPA 1500 2.5 10.1 X-38 CaHHPA 1500 3.0 8.4 X-39 CaHHPA 1500 3.5 7.2 X-40 CaHHPA 1500 4.0 6.3 X-41 M3905 2000 0.5 50.6 X-42 M3905 2000 1.0 25.3 X-43 M3905 2000 1.5 16.9 X-44 M3905 2000 2.0 12.7 X-45 M3905 2000 2.5 10.1 X-46 M3905 2000 3.0 8.4 X-47 M3905 2000 3.5 7.2 X-48 M3905 2000 4.0 6.3 X-49 M3988 2000 0.5 50.6 X-50 M3988 2000 1.0 25.3 X-51 M3988 2000 1.5 16.9 X-52 M3988 2000 2.0 12.7 X-53 M3988 2000 2.5 10.1 X-54 M3988 2000 3.0 8.4 X-55 M3988 2000 3.5 7.2 X-56 M3988 2000 4.0 6.3 X-57 — — 0.5 50.6 X-58 — — 1.0 25.3 X-59 — — 1.5 16.9 X-60 — — 2.0 12.7 X-61 — — 2.5 10.1 X-62 — — 3.0 8.4 X-63 — — 3.5 7.2 X-64 — — 4.0 6.3 - Polypropylene bottles (330 ml, ref. Table XI) were produced blown at high speed on a two-cavity Chia-Ming stretch blow molding machine designed to blow polypropylene bottles from preforms described in Example 10. Axial stretch ratio is 1.9/1, Hoop Stretch ratio=2.4 & Total Stretch Ratio=4.6/1. This machine is equipped with 3 heater boxes per cavity & uses 1000 Watt IR lamps. Pre-blow pressure was 6 bar & final pressure was 8 bar. After optimization, the bottle productivity for the preforms with 3 mm thickness was 1,030 bph/cav. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE XI Example 11 Bottles Injection Loading Speed % Haze/ Bottle Example Nucleator (ppm) (g/cc) thickness Quality XI-1 NA-21 2000 50.6 2.048 Acceptable XI-2 NA-21 2000 25.3 1.500 Average XI-3 NA-21 2000 16.9 0.130 Excellent XI-4 NA-21 2000 12.7 0.079 Excellent XI-5 NA-21 2000 10.1 0.074 Excellent XI-6 NA-21 2000 8.4 0.076 Excellent XI-7 NA-21 2000 7.2 0.100 Excellent XI-8 NA-21 2000 6.3 0.052 Excellent XI-9 NA-11 1000 50.6 2.000 Acceptable XI-10 NA-11 1000 25.3 0.739 Average XI-11 NA-11 1000 16.9 0.132 Excellent XI-12 NA-11 1000 12.7 0.100 Excellent XI-13 NA-11 1000 10.1 0.111 Excellent XI-14 NA-11 1000 8.4 0.087 Excellent XI-15 NA-11 1000 7.2 0.096 Excellent XI-16 NA-11 1000 6.3 0.086 Excellent XI-17 HPN-68 1000 50.6 Acceptable XI-18 HPN-68 1000 25.3 1.565 Average XI-19 HPN-68 1000 16.9 Excellent XI-20 HPN-68 1000 12.7 Excellent XI-21 HPN-68 1000 10.1 Excellent XI-22 HPN-68 1000 8.4 Excellent XI-23 HPN-68 1000 7.2 Excellent XI-24 HPN-68 1000 6.3 0.121 Excellent XI-25 AlptBBA 1000 50.6 Acceptable XI-26 AlptBBA 1000 25.3 0.304 Average XI-27 AlptBBA 1000 16.9 Excellent XI-28 AlptBBA 1000 12.7 Excellent XI-29 AlptBBA 1000 10.1 Excellent XI-30 AlptBBA 1000 8.4 Excellent XI-31 AlptBBA 1000 7.2 Excellent XI-32 AlptBBA 1000 6.3 0.186 Excellent XI-33 CaHHPA 1500 50.6 Acceptable XI-34 CaHHPA 1500 25.3 0.880 Average XI-35 CaHHPA 1500 16.9 Excellent XI-36 CaHHPA 1500 12.7 Excellent XI-37 CaHHPA 1500 10.1 Excellent XI-38 CaHHPA 1500 8.4 Excellent XI-39 CaHHPA 1500 7.2 Excellent XI-40 CaHHPA 1500 6.3 0.100 Excellent XI-41 M3905 2000 50.6 Acceptable XI-42 M3905 2000 25.3 0.240 Average XI-43 M3905 2000 16.9 Average XI-44 M3905 2000 12.7 Excellent XI-45 M3905 2000 10.1 Excellent XI-46 M3905 2000 8.4 Excellent XI-47 M3905 2000 7.2 Excellent XI-48 M3905 2000 6.3 0.067 Excellent XI-49 M3988 2000 50.6 Acceptable XI-50 M3988 2000 25.3 1.826 Average XI-51 M3988 2000 16.9 Average XI-52 M3988 2000 12.7 Excellent XI-53 M3988 2000 10.1 Excellent XI-54 M3988 2000 8.4 Excellent XI-55 M3988 2000 7.2 Excellent XI-56 M3988 2000 6.3 0.058 Excellent XI-57 — — 50.6 Acceptable XI-58 — — 25.3 1.917 Average XI-59 — — 16.9 Excellent XI-60 — — 12.7 Excellent XI-61 — — 10.1 Excellent XI-62 — — 8.4 Excellent XI-63 — — 7.2 Excellent XI-64 — — 6.3 0.083 Excellent - Polypropylene bottles (500 ml, table XII) were produced at high speed (1,500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 10. Axial stretch ratio is 2.5/1, Hoop Stretch ratio=2.54 & Total Stretch Ratio=6.36/1. Machine settings were adjusted to accommodate high clarity, high speed bottle production. Preforms were subjected to a pre-blow pressure of 4.5 Bar for 0.4 seconds & nozzle for 3 rotations open activated at ‘point zero’. Blowing time is 0.8 sec & Exhaust time is 0.4 sec. Stretch speed is 1,384 m/sec & a standard stretch rod with 14 mm diameter was used. Preform temperature is about 120-130° C. Heating profile: Z1=75%, Z2=90%, Z3=70%, Z4=70%, Z5=65% & Z6=70% with Z1, Z5 & Z6 in an advanced position. % GP=65%. The invention employed 100% ventilation to cool the preform surface. Total heating time is 14.65 sec, stabilization time=6.0 sec & final stabilization time=4.5 sec. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE XII Example 12 Bottles Injection Loading Speed % Haze/ Bottle Example Nucleator (ppm) (g/cc) thickness Quality XII-1 NA-21 2000 50.6 Acceptable XII-2 NA-21 2000 25.3 Average XII-3 NA-21 2000 16.9 Excellent XII-4 NA-21 2000 12.7 Excellent XII-5 NA-21 2000 10.1 Excellent XII-6 NA-21 2000 8.4 Excellent XII-7 NA-21 2000 7.2 Excellent XII-8 NA-21 2000 6.3 0.088 Excellent XII-9 NA-11 1000 50.6 Acceptable XII-10 NA-11 1000 25.3 Average XII-11 NA-11 1000 16.9 Excellent XII-12 NA-11 1000 12.7 Excellent XII-13 NA-11 1000 10.1 Excellent XII-14 NA-11 1000 8.4 Excellent XII-15 NA-11 1000 7.2 Excellent XII-16 NA-11 1000 6.3 0.115 Excellent XII-17 HPN-68 1000 50.6 Acceptable XII-18 HPN-68 1000 25.3 Average XII-19 HPN-68 1000 16.9 Excellent XII-20 HPN-68 1000 12.7 Excellent XII-21 HPN-68 1000 10.1 Excellent XII-22 HPN-68 1000 8.4 Excellent XII-23 HPN-68 1000 7.2 Excellent XII-24 HPN-68 1000 6.3 0.116 Excellent XII-25 AlptBBA 1000 50.6 Acceptable XII-26 AlptBBA 1000 25.3 Average XII-27 AlptBBA 1000 16.9 Excellent XII-28 AlptBBA 1000 12.7 Excellent XII-29 AlptBBA 1000 10.1 Excellent XII-30 AlptBBA 1000 8.4 Excellent XII-31 AlptBBA 1000 7.2 Excellent XII-32 AlptBBA 1000 6.3 0.164 Excellent XII-33 CaHHPA 1500 50.6 Acceptable XII-34 CaHHPA 1500 25.3 Average XII-35 CaHHPA 1500 16.9 Excellent XII-36 CaHHPA 1500 12.7 Excellent XII-37 CaHHPA 1500 10.1 Excellent XII-38 CaHHPA 1500 8.4 Excellent XII-39 CaHHPA 1500 7.2 Excellent XII-40 CaHHPA 1500 6.3 0.100 Excellent XII-41 M3905 2000 50.6 Acceptable XII-42 M3905 2000 25.3 Excellent XII-43 M3905 2000 16.9 Excellent XII-44 M3905 2000 12.7 Excellent XII-45 M3905 2000 10.1 Excellent XII-46 M3905 2000 8.4 Excellent XII-47 M3905 2000 7.2 Excellent XII-48 M3905 2000 6.3 0.048 Excellent XII-49 M3988 2000 50.6 Acceptable XII-50 M3988 2000 25.3 Average XII-51 M3988 2000 16.9 Excellent XII-52 M3988 2000 12.7 Excellent XII-53 M3988 2000 10.1 Excellent XII-54 M3988 2000 8.4 Excellent XII-55 M3988 2000 7.2 Excellent XII-56 M3988 2000 6.3 0.076 Excellent XII-57 — — 50.6 Acceptable XII-58 — — 25.3 Average XII-59 — — 16.9 Excellent XII-60 — — 12.7 Excellent XII-61 — — 10.1 Excellent XII-62 — — 8.4 Excellent XII-63 — — 7.2 Excellent XII-64 — — 6.3 0.062 Excellent - A commercial homopolymer resin containing Millad 3988 (Mosten MT 230 from Chemopetrol, MFI=30) & random copolymer (Borealis RF365 MO, MFI=20) was used to produce preforms as indicated in Table XIII. The preforms were produced on a two-cavity mold (only one cavity installed) 100 ton Netstal injection molding machine with a variable injection time (0.5-4.0 sec) and a constant cooling time of 10 sec. Melt temperature was 240° C. Temperature of the cooling water was 13° C. The holding pressure time was 8.4 sec. Total cycle time was around 25 sec (not optimized). A valve gate with a diameter of 1.5 mm was used. The preforms have a wall thickness of 3 mm and a bottle weight of about 20.3 g. These preforms were later blown into bottles as explained in subsequent examples.
TABLE XIII Example 13 Preforms MFI Injection Injection (g/10 Time Speed Example Resin sec) (sec) (g/cc) XIII-1 HPMT230 30 0.5 50.6 XIII-2 HPMT230 30 1.0 25.3 XIII-3 HPMT230 30 1.5 16.9 XIII-4 HPMT230 30 2.0 12.7 XIII-5 HPMT230 30 2.5 10.1 XIII-6 HPMT230 30 3.0 8.4 XIII-7 HPMT230 30 3.5 7.2 XIII-8 HPMT230 30 4.0 6.3 XIII-9 RF365MO 20 2.5 50.6 XIII-10 RF365MO 20 3.0 25.3 XIII-11 RF365MO 20 3.5 16.9 XIII-12 RF365MO 20 4.0 12.7 XIII-13 RF365MO 20 0.5 10.1 XIII-14 RF365MO 20 1.0 8.4 XIII-15 RF365MO 20 1.5 7.2 XIII-16 RF365MO 20 2.0 6.3 - Polypropylene bottles (500 ml) having a narrow neck were produced at high speed (1500 bottles/cavity/hour) on a Sidel SBO-8 Series-II stretch blow molding machine designed to blow PET preforms using the polypropylene preforms described in Example 13. The following stretch ratios were used: axial stretch ratio of 2.63/1, radial stretch ratio of 3.08 and a total stretch ratio of 8.10/1. Machine settings were adjusted to accommodate high clarity, high speed bottle production. In case of the Chemopetrol MT230 resin (homopolymer with a MFI of about 30 g/10 min) the temperature measured at the outer side of the preform was 143.5° C. and 152.5° C. at the inner side of the preform. In case of the Borealis RF 365 MO (random copolymer with a MFI of 20 g/10 min) the temperature measured at the outer side of the preform was 127.5° C. and 134.8° C. at the inner side of the preform. Bottle quality was judged at the time of production to be Unacceptable (poorly blown bottle or blown out), Acceptable (a fully blown bottle with moderate optical properties), Average (a fully blown bottle with improved optical properties), or Excellent (a fully blown bottle with outstanding optical clarity).
TABLE XIV Example 14 Bottles MFI Injection (g/10 Speed % Haze/ Bottle Example sec) Resin (g/cc) thickness Quality XIV-1 30 MT230 50.6 2.427 Acceptable (HP) XIV-2 30 MT230 25.3 Acceptable (HP) XIV-3 30 MT230 16.9 0.583 Acceptable (HP) XIV-4 30 MT230 12.7 0.373 Average (HP) XIV-5 30 MT230 10.1 0.256 Excellent (HP) XIV-6 30 MT230 8.4 0.274 Excellent (HP) XIV-7 30 MT230 7.2 0.265 Excellent (HP) XIV-8 30 MT230 6.3 0.163 Excellent (HP) XIV-9 20 RF 50.6 50.6 Acceptable 365MO XIV-10 20 RF 25.3 25.3 Acceptable 365MO XIV-11 20 RF 16.9 16.9 Acceptable 365MO XIV-12 20 RF 12.7 12.7 Acceptable 365MO XIV-13 20 RF 10.1 10.1 Acceptable 365MO XIV-14 20 RF 8.4 8.4 Acceptable 365MO XIV-15 20 RF 7.2 7.2 Average 365MO XIV-16 20 RF 6.3 6.3 Excellent 365MO - For purposes of this specification, the thickness of preforms is measured along the
side walls FIG. 4A , measured at the widest portion of theside walls - Thickness of containers (bottles), such as for purposes of percent haze/thickness ratios is measured at the point at which the haze has been measured (see below), using a Magna-Mike 8500 Hall effect thickness gauge.
- For purposes of this specification, haze has been measured on a BYK-Gardner hazemeter by ASTM Standard Test Method D1003-61 modified by use of an 0.2″ aperture. The area in which haze could be measured reliably was in relatively small areas less than about 0.5″ in area. Samples were obtained from sample containers (bottles) at a relatively flat point approximately mid-way to the bottom of the bottle after the transition point. A thickness modified haze was calculated for each sample where (H/t) is defined as the haze divided by the thickness at the point where the haze was measured.
- Roughness on the
inner container 10 surface has a negative influence on the container clarity. If, during reheating of the preform 115 (within the window of process stability), the temperature in the skin-layer is insufficiently high, the material undesirably may be ruptured apart during the stretch blow molding (stage two) process, resulting in a roughinner container 10 surface andcontainers 10 having low clarity. - Preforms were made with fill rates ranging from 5.5 to 40.2 grams per second utilizing two different resins—Borealis RF365 MO (20 MI RCP) and Atofina 7525 (12 MI RCP). Three different injection valve gates were utilized in the preform production—1.5, 3.0, and 3.8 mm. Four different conditions were used to produce the SBM bottles—Condition 1 is with % Production Power=80% (Oven Temperature=74° C.) and Preblow=0.7 seconds, Condition 2% Production Power=83% (Oven Temperature=79° C.) and Preblow=0.7 seconds, Condition 3% Production Power=80% (Oven Temperature=74° C.), Preblow=0.2 seconds, and Condition 4% Production Power=77% (Oven Temperature=74° C.) and Preblow=0.7 seconds. Percent Production Power controls the temperature of the preform. Preblow is the time at which preblow begins with respect to the beginning of engagement of the stretch rod to the bottom of the preform.
- Haze was measured in the middle of the bottle on the third rib of the bottle from the top using a BYK Gardner hazemeter. In general, it has been found that haze is dependent upon fill rate. There is a strong increase in haze in both of the resins with increasing fill rate. The Borealis resin reaches a minimum % haze at a faster fill rate than does the Atofina resin, indicating an interaction and influence of the Ml of the resin with fill rate.
- There is an effect of the valve gate diameter as it can be seen that the change in haze of both of the resins (see attached Table XV). A 3.8 mm valve gate shows a different dependency of % haze on fill time than do the 1.5 and 3.0 mm gates. Additionally, there is an effect of the resin MI on the haze. The 10 MI Atofina resin has a different haze response to the fill rate and gate diameter, than does the 20 MI Borealis resin.
TABLE XV Fill Rate Conditions and Results Gate Resin Diameter Thickness MFI (mm) Fill Rate (g/sec) Haze (mil) Haze/Thickness 20 1.5 40.2 42.1 17.6 2.39 27.7 20.6 15.5 1.33 20.3 21.8 14.2 1.54 17.3 7.49 13.9 0.54 13.9 3.71 14.6 0.25 12.0 2.57 14.6 0.18 10.5 2.45 14.7 0.17 9.2 1.48 14.8 0.10 8.5 1.98 15.4 0.13 5.7 1.85 14.9 0.12 20 3.0 38.0 46 14 3.29 27.7 46.3 15.8 2.93 20.1 14.1 15.1 0.93 16.9 5.49 16.7 0.33 14.2 3.56 13.5 0.26 12.2 1.71 13.5 0.13 10.8 1.7 14.6 0.12 9.5 0.99 14.8 0.07 8.7 1.3 14 0.09 5.5 2.04 13.6 0.15 20 3.8 38.0 35.9 15.7 2.29 27.0 7.04 16.5 0.43 20.1 5.98 14.3 0.42 16.9 3.15 15.1 0.21 14.2 2.09 15.1 0.14 12.1 2.27 13.5 0.17 10.8 1.58 13.2 0.12 9.5 1.36 14.5 0.09 8.3 1.53 13.4 0.11 5.5 1.7 13.8 0.12 10 1.5 38.7 41 17.6 2.33 30.4 44 15.9 2.77 20.3 39 15.5 2.52 16.9 31.1 15.2 2.05 13.9 18.3 14 1.31 11.9 18.6 13.4 1.39 10.6 14.4 13.9 1.04 9.2 4.53 16.6 0.27 8.6 3.76 13.6 0.28 5.7 2.5 14.2 0.18 10 3.8 37.4 51 16.3 3.13 28.0 39.2 16.9 2.32 20.1 20.8 15.6 1.33 16.9 29.4 13.2 2.23 14.2 22 14.7 1.50 12.2 6.22 15.3 0.41 10.8 4.5 14.4 0.31 9.5 3.85 12.5 0.31 8.3 2.3 15.7 0.15 5.5 1.99 12.9 0.15 - The effect of pre-blow pressure and pre-blow time on bottle transparency was demonstrated.
FIG. 12 is also illustrative of the effect of pre-blow time and pressure on container percent (%) haze.Pre-blow pressure: 1 bar (very hazy in panel) 2 bar (slightly hazy in panel) 4 bar (clear) 5 bar (clear) 7 bar (clear) 10 bar (clear). Pre-blow time: 0 sec (very hazy in panel) 0.05 sec (slightly hazy in panel) 0.1 sec (slightly hazy) 0.2 sec (clear) 0.4 sec (OK) 0.8 sec (OK) - In the invention, it is possible to identify the manner of making a container that has been made by a two step process (and other process variables) by employing a free shrink process as set forth in this example. In the invention, a polypropylene container is made by an injection stretch blow molding two stage process. The container has:
-
- a) a side wall providing a haze value of less than 3 according to ASTM D 1003,
- b) an MFI (melt flow index) between about 6 g/10 min and about 50 g/10 min according to ASTM D 1238;
- c) wherein the average wall thickness of the container after subjecting the container to the free shrinkage test is less than about 1.8 mm.
- A clear bottle may be produced by two stages, injection molding into a preform and then stretch blow the preform into the final clear bottle. Such bottles exhibit a certain percentage of free shrinkage in the axial direction. This is known as a “free shrinkage test” or “shrinkage test”, for purposes of this specification and claims.
- If the initial bottle length is Lo, and the length of the bottle after the shrinkage is L, then the axial free shrinkage ratio is
% FSA=100*(Lo−L)/Lo - Testing was carried out according to the following procedures:
-
- 1) Prepare a hot oil bath equilibrated at 155-157 degree C.
- 2) Pick the bottle to be tested, make two small holes (about 3 mm) at the bottom of the bottle
- 3) Measure the initial bottle length, which is Lo in the above equation. Also measure the wall thickness of the bottle, measure it at the middle point between the top and the bottom of the bottle, pick 8 locations along the perimeter to do the measurements, and calculate the average of these eight measurements to be the wall thickness of this bottle
- 4) Sink the bottle upside down into the oil bath, the holes on the bottom allow the air to get out, make sure that the bottle does not touch the wall of the hot oil bath
- 5) Start counting time when the bottom of the bottle touches the oil
- 6) Let the bottle stay in the oil bath for 3-5 minutes, then take the shrunk bottle out of the oil bath slowly (the mouth pointing down so that hot oil can get out easily)
- 7) Put the bottle into a room temperature oil bath to cool for 1 minute
- 8) Take the shrunk bottle out and let it sit for 10 minutes
- 9) Measure, the length of the shrunk bottle, which is L in the above equation
- 10) Measure the wall thickness of the shrunk bottle—measure it at the middle point between the top and the bottom of the shrunk bottle, pick 8 locations along the perimeter to do the measurements, and calculate the average of these eight measurements to be the wall thickness of this shrunk bottle
- 11) For one kind of bottle, do five repeats at least. The average length and wall thickness of the shrunk bottle can be used for calculations for shrinkage ratio or drawing conclusions.
- Four types of the ISBM polypropylene bottles were used for this study, the first three examples (A, B, C) were made from the preforms based on the current inventive design, while the last one (D) is a comparative example based on prior art. Results of the shrinkage test are reported in Table XVI. Please note that preform dimensions are out of the preform design, length of the ISBM bottle is also out of design. While the thickness of the ISBM bottle, the length and thickness of the shrunk bottle were measured according to the above procedures. Numbers in the Table XVI below include measurements which are average numbers based on several measurements.
TABLE XVI Results of the Free Shrinkage Study of ISBM Bottles preform dimension ISBM bottle shrunk bottle (mm) dimension (mm) dimension (mm) Sample length thickness length thickness length thickness % FSA A 102.6 2.8 195.8 0.41 106 0.977 46.1 B 107.0 3.5 208.7 0.65 111 1.732 46.9 C 102.6 2.8 155.8 0.74 104 1.426 33.1 D 94.46 4.9 219.4 0.72 108 1.921 50.6 (comparative example) - Sample D (the comparative example) bottle apparently exhibits the highest shrinkage ratio among all tested. It also has the highest wall thickness among all bottles tested. Previous discussions have demonstrated that wall thickness of the preform is one of the critical factors to make good quality and clear ISBM polypropylene bottles with good productivity. The current invention designs the preform with the wall thickness of 3.5 mm or less, while the prior art is above that. In this example, the comparative bottle has the wall thickness of 4.9 mm, while the first three bottles out of this invention have the wall thickness of 2.8 mm and 3.5 mm.
- Though it is difficult to shrink the ISBM bottle completely back to the preform size, the shrinkage behavior is similar provided all bottles are made of polypropylene random copolymer. As a result, the wall thickness of the shrunk bottle relates closely to the preform wall thickness. Based on the data in the table, the comparable example bottle has the highest shrunk bottle wall thickness, largely due to the fact that the preform is high in wall thickness. This would be one way of differentiating the bottles based on the current inventive preform design or a prior art preform design.
Claims (23)
1. A polypropylene container made by an injection stretch blow molding two stage process, said container having a side wall, wherein:
a) said side wall provides a haze value of less than about 3 according to ASTM D 1003,
b) said polypropylene provides an MFI between about 6 g/10 min and about 50 g/10 min according to ASTM D 1238;
c) wherein the average wall thickness of said container after subjecting said container to the free shrinkage test is less than about 1.8 mm.
2. The polypropylene container according to claim 1 wherein said haze of said side wall of the polypropylene container is less than about 2, measured according to ASTM D 1003.
3. A polypropylene container according to claim 1 wherein the haze of the side wall of the polypropylene container is less than about 1, measured according to ASTM D 1003.
4. A polypropylene container according to claim 1 wherein the wall thickness of the container after subjecting the container to the free shrinkage test is less than about 1.6 mm.
5. A polypropylene container according to claim 1 wherein the wall thickness of the container after subjecting the container to the free shrinkage test is less than about 1.5 mm.
6. A polypropylene container according to claim 1 wherein the wall thickness of the bottle after subject to the free shrinkage test is less than 1.4 mm.
7. A polypropylene container according to claim 1 wherein the wall thickness of the bottle after subject to the free shrinkage test is less than about 1.2 mm.
8. A polypropylene container according to claim 1 wherein the wall thickness of the bottle after subject to the free shrinkage test is less than about 1.0 mm.
9. A polypropylene container according to claim 2 wherein the wall thickness of the bottle after subject to the free shrinkage test is less than about 1.6 mm.
10. A polypropylene container according to claim 2 wherein the wall thickness of the bottle after subject to the free shrinkage test is less than about 1.4 mm.
11. A polypropylene container according to claim 2 wherein the wall thickness of the bottle after subject to the free shrinkage test is less than about 1.2 mm.
12. A polypropylene resin container made by injection stretch blow molding two stage process with the following characteristics:
a) haze of the side wall of the polypropylene resin container of less than about 3 according to ASTM D 1003,
b) MFI of the polypropylene resin is between 6 g/10 min and 50 g/10 min according to ASTM D 1238,
c) the average wall thickness of the container is less than 0.8 mm,
d) the axial free shrinkage ratio (% FSA) is no more than about 50%.
13. A polypropylene container according to claim 12 wherein the haze of the side wall of the polypropylene container is less than about 2 according to ASTM D 1003.
14. A polypropylene container according to claim 12 wherein the haze of the side wall of the polypropylene container is less than about 1 according to ASTM D 1003.
15. A polypropylene container according to claim 12 wherein the wall thickness of the container is less than about 0.7 mm.
16. A polypropylene container according to claim 12 wherein the wall thickness of the container is less than about 0.6 mm.
17. A polypropylene container according to claim 12 wherein the wall thickness of the container is less than 0.5 mm.
18. A polypropylene container according to claim 12 wherein the shrinkage ratio is no more than 45%.
19. A polypropylene container according to claim 12 wherein the shrinkage ratio is no more than 40%.
20. A polypropylene container according to claim 13 wherein the wall thickness of the container is less than 0.7 mm.
21. A polypropylene container according to claim 13 wherein the wall thickness of the container is less than 0.6 mm.
22. A polypropylene container according to claim 13 wherein the shrinkage ratio is no more than 45%.
23. A polypropylene container according to claim 13 wherein the shrinkage ratio is no more than 40%.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/137,046 US20050249905A1 (en) | 2004-01-23 | 2005-05-25 | Polyolefin container having certain shrink characteristics and method of making such containers |
EP05754304A EP1748931A4 (en) | 2004-05-28 | 2005-05-26 | Polyolefin container having certain shrink characteristics and method of making such containers |
BRPI0511638-4A BRPI0511638A (en) | 2004-05-28 | 2005-05-26 | polyolefin container having certain shrinkage characteristics, and the process of producing such containers |
PCT/US2005/018522 WO2005118407A2 (en) | 2004-05-28 | 2005-05-26 | Polyolefin container having certain shrink characteristics and method of making such containers |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/764,234 US20050161866A1 (en) | 2004-01-23 | 2004-01-23 | Process of making two-stage injection stretch blow molded polypropylene articles |
US57544704P | 2004-05-28 | 2004-05-28 | |
US11/137,046 US20050249905A1 (en) | 2004-01-23 | 2005-05-25 | Polyolefin container having certain shrink characteristics and method of making such containers |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US10/764,234 Continuation-In-Part US20050161866A1 (en) | 2004-01-23 | 2004-01-23 | Process of making two-stage injection stretch blow molded polypropylene articles |
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US20050249905A1 true US20050249905A1 (en) | 2005-11-10 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US11/137,046 Abandoned US20050249905A1 (en) | 2004-01-23 | 2005-05-25 | Polyolefin container having certain shrink characteristics and method of making such containers |
Country Status (4)
Country | Link |
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US (1) | US20050249905A1 (en) |
EP (1) | EP1748931A4 (en) |
BR (1) | BRPI0511638A (en) |
WO (1) | WO2005118407A2 (en) |
Families Citing this family (2)
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EP1870225A1 (en) * | 2006-06-21 | 2007-12-26 | Total Petrochemicals Research Feluy | Stretching/blowing conditions in one-stage injection-stretch-blow-moulding |
US11873133B2 (en) * | 2021-04-20 | 2024-01-16 | Drug Plastics & Glass Company, Inc. | Bottle, injection blow molding core rod for the bottle and related method |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4177239A (en) * | 1977-04-20 | 1979-12-04 | Bekum Maschinenfabriken Gmbh | Blow molding method |
US4357288A (en) * | 1980-02-25 | 1982-11-02 | Deacon Machinery, Inc. | Method of making clear transparent polypropylene containers |
US5066222A (en) * | 1989-03-14 | 1991-11-19 | Bekum Maschinenfabriken Gmbh | Method and apparatus for heating and conveying plastic preforms prior to mold blowing operations |
US5135975A (en) * | 1989-09-20 | 1992-08-04 | Milliken Research Corporation | Bis(3,4-dialkylbenzylidene) sorbitol acetals and compositions containing same |
US5326258A (en) * | 1992-04-11 | 1994-07-05 | Bekum Maschinenfabriken Gmbh | Method and apparatus for heating preform blanks composed of partly crystalline synthetic resins produced by injection molding |
US5783232A (en) * | 1996-12-03 | 1998-07-21 | Bekum Maschinenfabriken Gmbh | Blow molding machine using reheat method for producing hollow plastic articles |
US6129961A (en) * | 1998-08-27 | 2000-10-10 | Toyo Boseki Kabushiki Kaisha | Polyester resin and production method thereof |
US6627278B1 (en) * | 1998-11-30 | 2003-09-30 | Fort James Corporation | Injection blow-molded disposable tumbler and method of making same |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0151741A3 (en) * | 1983-12-13 | 1985-09-25 | MITSUI TOATSU CHEMICALS, Inc. | Injection stretch-blow molded container and resin composition therefor |
-
2005
- 2005-05-25 US US11/137,046 patent/US20050249905A1/en not_active Abandoned
- 2005-05-26 BR BRPI0511638-4A patent/BRPI0511638A/en not_active IP Right Cessation
- 2005-05-26 EP EP05754304A patent/EP1748931A4/en not_active Withdrawn
- 2005-05-26 WO PCT/US2005/018522 patent/WO2005118407A2/en not_active Application Discontinuation
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4177239A (en) * | 1977-04-20 | 1979-12-04 | Bekum Maschinenfabriken Gmbh | Blow molding method |
US4357288A (en) * | 1980-02-25 | 1982-11-02 | Deacon Machinery, Inc. | Method of making clear transparent polypropylene containers |
US5066222A (en) * | 1989-03-14 | 1991-11-19 | Bekum Maschinenfabriken Gmbh | Method and apparatus for heating and conveying plastic preforms prior to mold blowing operations |
US5135975A (en) * | 1989-09-20 | 1992-08-04 | Milliken Research Corporation | Bis(3,4-dialkylbenzylidene) sorbitol acetals and compositions containing same |
US5326258A (en) * | 1992-04-11 | 1994-07-05 | Bekum Maschinenfabriken Gmbh | Method and apparatus for heating preform blanks composed of partly crystalline synthetic resins produced by injection molding |
US5783232A (en) * | 1996-12-03 | 1998-07-21 | Bekum Maschinenfabriken Gmbh | Blow molding machine using reheat method for producing hollow plastic articles |
US6129961A (en) * | 1998-08-27 | 2000-10-10 | Toyo Boseki Kabushiki Kaisha | Polyester resin and production method thereof |
US6627278B1 (en) * | 1998-11-30 | 2003-09-30 | Fort James Corporation | Injection blow-molded disposable tumbler and method of making same |
Also Published As
Publication number | Publication date |
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WO2005118407A3 (en) | 2007-03-01 |
EP1748931A2 (en) | 2007-02-07 |
BRPI0511638A (en) | 2008-01-02 |
WO2005118407A2 (en) | 2005-12-15 |
EP1748931A4 (en) | 2007-06-27 |
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