JPH0152175B2 - - Google Patents
Info
- Publication number
- JPH0152175B2 JPH0152175B2 JP58053178A JP5317883A JPH0152175B2 JP H0152175 B2 JPH0152175 B2 JP H0152175B2 JP 58053178 A JP58053178 A JP 58053178A JP 5317883 A JP5317883 A JP 5317883A JP H0152175 B2 JPH0152175 B2 JP H0152175B2
- Authority
- JP
- Japan
- Prior art keywords
- density polyethylene
- heat
- bag
- low density
- linear low
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- 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
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/40—General aspects of joining substantially flat articles, e.g. plates, sheets or web-like materials; Making flat seams in tubular or hollow articles; Joining single elements to substantially flat surfaces
- B29C66/41—Joining substantially flat articles ; Making flat seams in tubular or hollow articles
- B29C66/43—Joining a relatively small portion of the surface of said articles
- B29C66/431—Joining the articles to themselves
- B29C66/4312—Joining the articles to themselves for making flat seams in tubular or hollow articles, e.g. transversal seams
-
- 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
- B29C2793/00—Shaping techniques involving a cutting or machining operation
- B29C2793/0063—Cutting longitudinally
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0018—Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0019—Combinations of extrusion moulding with other shaping operations combined with shaping by flattening, folding or bending
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/001—Combinations of extrusion moulding with other shaping operations
- B29C48/0022—Combinations of extrusion moulding with other shaping operations combined with cutting
-
- 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
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/09—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels
- B29C48/10—Articles with cross-sections having partially or fully enclosed cavities, e.g. pipes or channels flexible, e.g. blown foils
-
- 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
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/71—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
-
- 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
- B29K2023/04—Polymers of ethylene
- B29K2023/06—PE, i.e. polyethylene
-
- 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
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0037—Other properties
- B29K2995/0049—Heat shrinkable
-
- 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
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0037—Other properties
- B29K2995/0063—Density
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は包装袋の製造方法に関するものであ
る。詳しくは線状低密度ポリエチレンを用いたヒ
ートシール強度の大きい包装袋を製造する方法に
関するものである。
通常、線状低密度ポリエチレンを用いてインフ
レーシヨン成形し、ヒートシールにより包装用の
袋を製造した場合、袋の胴部強度は強いが、ヒー
トシール部の強度が極めて低くなり実用上問題が
あつた。
これは後述する線状低密度ポリエチレンの分子
構造上、線状低密度ポリエチレンは溶融延伸等に
より分子配向を付与して熱収縮性を持たせようと
しても強い収縮性を持たせることができないた
め、ヒートシールを行なつた際ヒートシール部が
熱収縮を起さず、フイルム肉厚が減少してしま
い、ヒートシール強度が出ないものである。
本発明者等は、線状低密度ポリエチレンを用い
て良好なヒートシール強度を有する包装袋を得る
べく種々検討の結果、特定の線状低密度ポリエチ
レンに特定の樹脂を特定量配合し、特定の条件下
にインフレーシヨン成形を行なうことにより目的
を達成し本発明を完成した。
すなわち、本発明の要旨はメルトインデツクス
0.2〜2g/10分、流動比18〜35の線状低密度ポ
リエチレンにメルトインデツクス0.1〜2g/10
分、流動比30〜70の低密度ポリエチレンを5〜70
重量%配合した混合物をブローアツプ比0.9〜
1.5、ドラフト率10〜40の条件下にインフレーシ
ヨン成形し、得られた筒状フイルムを引取方向に
対して交差する方向を長手方向としてヒートシー
ル及び切断することを特徴とする包装袋の製造方
法に存する。
以下に本発明を更に詳細に説明する。
本発明に用いられる線状低密度ポリエチレンと
は、エチレンと他のα−オレフインとの共重合物
であり、従来の高圧法により製造された低密度ポ
リエチレン樹脂とは異なる。線状低密度ポリエチ
レンは、例えばエチレンと、他のα−オレフイン
としてブテン、ヘキチン、オクテン、デセン、4
メチルペンテン−1等を4〜17重量%程度、好ま
しくは5〜15重量%程度共重合したものであり中
低圧法高密度ポリエチレン製造に用いられるチー
グラー型触媒又フイリツプス型触媒を用いて製造
されたものであり、従来の高密度ポリエチレンを
共重合成分により短い枝分かれ構造とし、密度も
この短鎖枝分かれを利用して適当に低下させ0.91
〜0.95g/cm3程度としたものであり、従来の低密
度ポリエチレンより直鎖性があり、高密度ポリエ
チレンより枝分かれが多い構造のポリエチレンで
ある。
このような線状低密度ポリエチレンをヒートシ
ールした際ヒートシール部の収縮が少ないのは線
状密度ポリエチレンの分子構造は上述のように短
鎖枝分かれであるため、ヒートシールの際に分子
間に熱弛緩が起こるためと考えられる。
メルトインデツクス0.2〜2g/10分、流動比
18〜35のものが用いられる。メルトインデツク
ス、及び流動比がこの範囲を外れると包装袋とし
た際の胴部の強度が低下し好ましくない。
線状低密度ポリエチレンに配合される低密度エ
チレンホモポリマー及びエチレンと他の共重合成
分との共重合体を含むものである。
共重合成分としては、酢酸ビニル、エチルアク
リレート、メチルアクリレート等のビニル化合
物、ヘキセン、プロピレン、オクテン、4−メチ
ルペンテン−1等の炭素数3以上のオレフイン類
等が挙げられる。共重合成分の共重合量としては
0.5〜18重量%、好ましくは2〜10重量%程度で
ある。これらの低密度ポリエチレンは通常の高圧
法(1000〜3000Kg/cm2)により、酸素、有機過酸
化物等のラジカル発生剤を用いラジカル重合によ
り得たものであるのが望ましいが、流動比が35〜
70(35を含まず)の線状低密度ポリエチレンで代
用することも可能である。これらの低密度ポリエ
チレンの中でも酢酸ビニル含有量0.5〜18重量%
ましくは2〜10重量%のエチレン−酢酸ビニル共
重合体が特に好ましい。
本発明方法においてメルトインデツクスとは
JIS K6760に準拠し190℃で測定した値であり、
流動比とは、上記メルトインデツクス測定器を用
い、せん断力106ダイン/cm2(荷重11131g)と
105ダイン/cm2(1113g)との押出量(g/10分)
との比であり、
流動比=荷重11131gでの押出量(10分間)/荷重1113
gでの押出量(10分間)
で算出される。
流動比は用いられる樹脂の分子量分布の目安で
あり、流動比の値が小さければ分子量分布は狭
く、流動比の値が大きければ分子量分布は広いこ
とを表わしている。
本発明においては、すなわち、分子量分布の狭
い線状低密度ポリエチレンに分子量分布の広い低
密度ポリエチレンを配合する点に大きな特徴を有
するものである。
前述したように胴部に充分な強度を有する袋を
製造しようとした場合、流動比18〜35の線状低密
度ポリエチレンを用いるのが必要であるが、線状
低密度ポリエチレン単独では、ヒートシール部の
強度が著しく低下してしまうことは前記した通り
である。本発明においてはこの線状低密度ポリエ
チレンのヒートシール強度を向上させる目的で分
子量分布の広い低密度ポリエチレンを配合するも
のである。
分子量分布の広い低密度ポリエチレンは長鎖分
岐を有し、かつ溶融弾性が高いためインフレーシ
ヨン成形時に分子配向が起りやすくこのような樹
脂によつて得たフイルムはヒートシール時に分子
配向を受けた方向に収縮し、フイルムの元の厚さ
より厚くなりヒートシール部の強度が向上するの
である。
前記した線状低密度ポリエチレンに低密度ポリ
エチレンを配合することにより前記した低密度ポ
リエチレンの収縮効果を線状低密度ポリエレンに
付与することができるか、もしくは低密度ポリエ
チレンの収縮効果を線状低密度ポリエチレンが打
消してしまうかは成形を行ない種々検討すること
となるが、本発明の混合物を特定の条件下にイン
フレーシヨン成形することにより良好なヒートシ
ール性を有する、すなわちヒートシール部が収縮
により厚さの増加する現象を生起することが見出
された。
その成形条件とは、ブローアツプ比を0.9〜1.5
とし、ドラフト率を10〜40としてインフレーシヨ
ン成形することである。
ここでドラフト率とは下記式によつて得られ
る。
ドラフト率=∫m/∫f・G/t・1/BUR
式中、記号は下記の通り。
G:ダイスリツトの幅
t:得られたフイルムの厚み
∫m:ダイスリツトから押出される樹脂の密度
∫f:フイルムの密度
BUR:ブローアツプ比
ブローアツプ比を1.5以上とするとヒートシー
ル時にヒートシールの長手方向の収縮が生起し袋
胴部の配向と逆方向の歪が発生するため得られた
袋のヒートシール端部の強度が低下し、破袋の原
因となる。
ドラフト率は10以下ではヒートシール時良好な
収縮が生起せず40以上とすれば袋の胴部自体の分
子配向が一方向に大きくなりすぎ胴部自体の引裂
けの生起する原因となる。
以下に実施例を示し本発明を更に詳細に説明す
るが、本発明はその要旨を越えない限り以下の実
施例に限定されるものではない。
実施例 1
線状低密度ポリエチレン{メルトインデツクス
(Ml):1g/10分、流動比:20、密度:0.920
g/cm3、共重合成分:ブテン−1、共重合量:10
重量%}に高圧法低密度ポリエチレン{Ml:0.4
g/10分、流動比:45:、密度:0.924g/cm3、
三菱化成工業(株)製、ノバテツク−L F100}(ノ
バテツクは三菱化成工業(株)の登録商標)を30重量
%を配合し、モダンマシナリー社製、デルサ65φ
押出機に環状スリツト径200φ、リツプクリアラ
ンス3mmのインフレーシヨンダイ及び冷却用エア
ーリングを取付けたインフレーシヨン成形機を用
い、押出量50Kg/hr、ブローアツプ比(BUR)
1.4、ドラフト率24の条件下にフイルム厚150μの
インフレーシヨンフイルムを得た。
得られたインフレーシヨンフイルムを長さ670
cm、幅440cmの筒状フイルムに切断し、ニユーロ
ング社製HS22B−2型ヒートシーラー(加熱部
長さ150mm、加熱部クリアランス0.3mm、冷却部長
さ:150mm、冷却部クリアランス1mm)を用いて
ヒートシール温度(加熱部表面温度)250℃、冷
却部温度30℃、フイルム送り速度15m/秒の条件
下に筒状フイルムの開口部の一方を端部から1.5
cmの位置でヒートシールした、ヒートシール部は
フイルムの引取方向(縦方向)に収縮を起して、
元のフイルム厚さより厚くなつていた。
得られた袋に20Kgの肥料を充填し、開口部を前
記と同様の条件でヒートシールし落袋試験用の包
装袋を得た。
落袋試験は、上記20Kgの肥料を充填した袋をヒ
ートシール後18〜24時間推積して放置した後、包
装袋の胴部が床面と平行でヒートシール部が床面
と略垂直となるようにして20袋を落下させる(横
落下)ことにより試験を行ない破袋率を求めた。
落下条件は室温を−5℃とし落下高さ1.5m、
1袋当り落下回数5回とした。破袋率は試験に用
いた包装袋の破袋した袋の百分率で求めた。
また、ヒートシール部の状態を把握するためイ
ンフレーシヨンフイルムの熱収縮率を測定した。
熱収縮率の測定はフイルムの任意の位置から直
径6mmの円形試験片を切り出し、これを表面温度
200℃のホツトプレート上に5秒間置き、縦方向
(フイルム引取方向)、及び横方向(フイルム幅方
向)の長さの変化を元の長さに対する百分率で表
わした。なお、縦方向の収縮率が大きければ、ヒ
ートシール時のフイルム引取方向の収縮率が大と
なり、ヒートシール部強度が向上することが認め
られている。
結果第1表に示した。
比較例 1
線状低密度ポリエチレン(Ml:2g/10分、
流動比20、密度:0.918g/cm3、共重合成分:ブ
テンー1、共重合量:10重量%)のみを用い、す
なわち、低密度ポリエチレンを混合せずに、他は
実施例1と同様にインフレーシヨン成形、ヒート
シールを行ない包装袋を得た。
得られた包装袋につき落袋試験、熱収縮率の測
定を行なつた。
結果を第1表に示した。
The present invention relates to a method of manufacturing a packaging bag. Specifically, the present invention relates to a method of manufacturing a packaging bag with high heat-sealing strength using linear low-density polyethylene. Normally, when packaging bags are manufactured using linear low-density polyethylene by inflation molding and heat sealing, the body of the bag is strong, but the strength of the heat sealing part is extremely low, which poses a practical problem. It was hot. This is because, due to the molecular structure of linear low-density polyethylene, which will be described later, linear low-density polyethylene cannot be made to have strong shrinkability even if you try to give it heat-shrinkability by imparting molecular orientation by melt-stretching or the like. When heat-sealing is performed, the heat-sealed portion does not undergo thermal contraction, the film thickness decreases, and heat-sealing strength is not achieved. As a result of various studies in order to obtain a packaging bag with good heat-sealing strength using linear low-density polyethylene, the present inventors blended a specific amount of a specific resin into a specific linear low-density polyethylene, By performing inflation molding under these conditions, the objective was achieved and the present invention was completed. In other words, the gist of the present invention is the melt index
Melt index 0.1 to 2 g/10 to linear low density polyethylene with flow ratio 18 to 35, 0.2 to 2 g/10 min.
minutes, low density polyethylene with a flow ratio of 30 to 70.
The blow-up ratio of the mixture containing % by weight is 0.9~
1.5. Manufacture of a packaging bag characterized by inflation molding under the condition of a draft rate of 10 to 40, heat sealing and cutting the obtained cylindrical film with the longitudinal direction in the direction intersecting the taking direction. It lies in the method. The present invention will be explained in more detail below. The linear low-density polyethylene used in the present invention is a copolymer of ethylene and other α-olefins, and is different from low-density polyethylene resins produced by conventional high-pressure methods. Linear low-density polyethylene contains, for example, ethylene and other α-olefins such as butene, hextine, octene, decene,
It is a copolymer of about 4 to 17% by weight, preferably about 5 to 15% by weight of methylpentene-1, etc., and is produced using a Ziegler type catalyst or Phillips type catalyst used in the production of high density polyethylene by medium and low pressure process. The conventional high-density polyethylene is made into a short branched structure using a copolymer component, and the density is appropriately lowered to 0.91 using this short chain branching.
~0.95 g/cm 3 , and is a polyethylene with a structure that is more linear than conventional low-density polyethylene and more branched than high-density polyethylene. When such linear low-density polyethylene is heat-sealed, the shrinkage of the heat-sealed portion is small because the molecular structure of linear low-density polyethylene is short-chain branched as mentioned above, so heat is generated between the molecules during heat-sealing. This is thought to be due to relaxation. Melt index 0.2-2g/10min, flow ratio
18 to 35 are used. If the melt index and flow ratio are out of this range, the strength of the body when used as a packaging bag decreases, which is not preferable. It includes a low-density ethylene homopolymer blended with linear low-density polyethylene and a copolymer of ethylene and other copolymer components. Examples of copolymerization components include vinyl compounds such as vinyl acetate, ethyl acrylate, and methyl acrylate, and olefins having 3 or more carbon atoms such as hexene, propylene, octene, and 4-methylpentene-1. As for the copolymerization amount of copolymerization components,
The amount is about 0.5 to 18% by weight, preferably about 2 to 10% by weight. These low-density polyethylenes are preferably obtained by radical polymerization using a radical generator such as oxygen or an organic peroxide using a normal high-pressure method (1000 to 3000 Kg/cm 2 ), but if the fluidity ratio is 35 ~
70 (excluding 35) linear low-density polyethylene may be substituted. Among these low-density polyethylenes, vinyl acetate content is 0.5 to 18% by weight.
Particularly preferred is 2 to 10% by weight of ethylene-vinyl acetate copolymer. What is melt index in the method of the present invention?
Values measured at 190℃ in accordance with JIS K6760,
The fluidity ratio is calculated using the above melt index measuring device with a shear force of 10 6 dynes/cm 2 (load 11131 g).
Extrusion rate (g/10 min) with 10 5 dynes/cm 2 (1113g)
Flow ratio = Extrusion amount at load 11131g (10 minutes) / Load 1113
Calculated by the extrusion amount in g (10 minutes). The fluidity ratio is a measure of the molecular weight distribution of the resin used; a small fluidity ratio value indicates a narrow molecular weight distribution, and a large fluidity ratio value indicates a wide molecular weight distribution. A major feature of the present invention is that low-density polyethylene with a wide molecular weight distribution is blended with linear low-density polyethylene with a narrow molecular weight distribution. As mentioned above, when trying to manufacture a bag with sufficient strength for the body, it is necessary to use linear low-density polyethylene with a flow ratio of 18 to 35. As mentioned above, the strength of the parts is significantly reduced. In the present invention, low density polyethylene having a wide molecular weight distribution is blended in order to improve the heat sealing strength of the linear low density polyethylene. Low-density polyethylene, which has a wide molecular weight distribution, has long chain branches and high melt elasticity, so molecular orientation tends to occur during inflation molding.Films made from such resins undergo molecular orientation during heat sealing. This causes the film to shrink in the direction of the film, making it thicker than its original thickness and improving the strength of the heat-sealed portion. By blending low-density polyethylene with the above-mentioned linear low-density polyethylene, the shrinkage effect of the above-mentioned low-density polyethylene can be imparted to the linear low-density polyethylene, or the shrinkage effect of low-density polyethylene can be imparted to the linear low-density polyethylene. Whether or not the polyethylene is canceled out will need to be investigated after molding, but by inflation molding the mixture of the present invention under specific conditions, it has good heat-sealability, that is, the heat-sealed part shrinks. It was found that the phenomenon of increasing thickness occurs due to the increase in thickness. The molding conditions include a blow-up ratio of 0.9 to 1.5.
Inflation molding is performed with a draft rate of 10 to 40. Here, the draft rate is obtained by the following formula. Draft rate = ∫m/∫f・G/t・1/BUR In the formula, the symbols are as follows. G: Width of the die slit t: Thickness of the obtained film ∫m: Density of the resin extruded from the die slit ∫f: Density of the film BUR: Blow-up ratio When the blow-up ratio is set to 1.5 or more, the longitudinal Shrinkage occurs and distortion occurs in the direction opposite to the orientation of the bag body, which reduces the strength of the heat-sealed end of the resulting bag, causing the bag to break. If the draft rate is less than 10, good shrinkage will not occur during heat sealing, and if it is more than 40, the molecular orientation of the body of the bag will become too large in one direction, causing tearing of the body. EXAMPLES The present invention will be explained in more detail by way of examples below, but the present invention is not limited to the following examples unless it exceeds the gist thereof. Example 1 Linear low density polyethylene {melt index (Ml): 1 g/10 min, flow ratio: 20, density: 0.920
g/cm 3 , copolymerization component: butene-1, copolymerization amount: 10
Weight%} to high pressure low density polyethylene {Ml: 0.4
g/10 minutes, flow ratio: 45:, density: 0.924 g/cm 3 ,
Contains 30% by weight of Novatek-L F100 (manufactured by Mitsubishi Chemical Industries, Ltd.) (Novatek is a registered trademark of Mitsubishi Chemical Industries, Ltd.), and manufactured by Modern Machinery Co., Ltd., Delsa 65φ
The extruder was equipped with an inflation molding machine with an annular slit diameter of 200φ, an inflation die with a lip clearance of 3 mm, and a cooling air ring, with an extrusion rate of 50 kg/hr and a blow-up ratio (BUR).
An blown film with a film thickness of 150μ was obtained under the conditions of 1.4 and draft ratio of 24. The length of the resulting blown film is 670 mm.
cm, width 440 cm, and heat-sealed using a Newlong HS22B-2 type heat sealer (heating section length: 150 mm, heating section clearance: 0.3 mm, cooling section length: 150 mm, cooling section clearance: 1 mm). (Surface temperature of heating part) 250℃, temperature of cooling part 30℃, film feed speed 15m/sec.
The heat-sealed part that was heat-sealed at the cm position shrinks in the film take-up direction (vertical direction),
It was thicker than the original film thickness. The obtained bag was filled with 20 kg of fertilizer, and the opening was heat-sealed under the same conditions as described above to obtain a packaging bag for the drop bag test. In the drop bag test, a bag filled with 20 kg of fertilizer was left for 18 to 24 hours after being heat-sealed, and then the body of the packaging bag was parallel to the floor and the heat-sealed part was approximately perpendicular to the floor. A test was conducted by dropping 20 bags in such a manner (sideways drop), and the bag breakage rate was determined. Drop conditions were room temperature -5℃, fall height 1.5m,
Each bag was dropped 5 times. The bag breakage rate was calculated as the percentage of bags that were broken among the packaging bags used in the test. In addition, the thermal shrinkage rate of the inflation film was measured in order to understand the condition of the heat-sealed portion. To measure the heat shrinkage rate, cut out a circular test piece with a diameter of 6 mm from any position on the film, and then
The film was placed on a hot plate at 200° C. for 5 seconds, and changes in length in the longitudinal direction (direction in which the film was taken) and in the transverse direction (direction of film width) were expressed as a percentage of the original length. It is recognized that if the shrinkage rate in the longitudinal direction is large, the shrinkage rate in the film take-off direction during heat sealing will be large, and the strength of the heat-sealed portion will be improved. The results are shown in Table 1. Comparative example 1 Linear low density polyethylene (Ml: 2g/10min,
Fluidity ratio: 20, density: 0.918 g/cm 3 , copolymerization component: butene-1, copolymerization amount: 10% by weight), that is, without mixing low-density polyethylene, but otherwise in the same manner as in Example 1. A packaging bag was obtained by inflation molding and heat sealing. The obtained packaging bags were subjected to a drop bag test and the heat shrinkage rate was measured. The results are shown in Table 1.
【表】
*:−の付号は収縮せずに元の長さより延
びたことを示す。
実施例 2
実施例1で用いた高圧法低密度ポリエチレンに
替え、高圧法低密度ポリエチレン{三菱化成工業
(株)製、ノバテツクーLT0110、Ml:0.74g/10
分、流動比:55、密度0.929}を10重量%配合し
たほかは実施例1と同様にして包装袋を得た。
得られた包装袋につき実施例1で示したと同様
の方法により落袋試験、熱収縮率測定を行なつ
た。
結果を第2表に示す。
実施例 3、4
実施例1で用いた高圧法低密度ポリエチレンに
替えエチレン−酢酸ビニル共重合体{三菱油化(株)
製、商品名:ユカロンHE60、酢酸ビニル含有量
6重量%、Ml:0.4g/10分、流動比40、密度:
0.927g/cm3}を40重量%配合したもの(実施列
3)、エチレン−酢酸ビニル共重合体{三菱油化
(株)製、商品名:ユカロンX−341、酢酸ビニル含
有量7重量%、Ml:0.2/10分、流動比50、、密
度:0.935g/cm3}を25重量%配合したもの(実
施例4)を用いたほかは、実施例1と同様にして
包装袋を得た。
得られた包装袋につき実施例1で示したと同様
の方法により落袋試験、熱収縮率測定を行なつ
た。
結果を第2表に示す。[Table] *: The minus sign indicates that the material has expanded beyond its original length without shrinking.
Example 2 High-pressure low-density polyethylene used in Example 1 was replaced with high-pressure low-density polyethylene {Mitsubishi Chemical Industries, Ltd.
Manufactured by Novatec Co., Ltd. LT0110, Ml: 0.74g/10
A packaging bag was obtained in the same manner as in Example 1, except that 10% by weight of 10% by weight of 10% by weight of 10% by weight, flow ratio: 55, density 0.929} was added. The obtained packaging bag was subjected to a drop bag test and a heat shrinkage rate measurement in the same manner as shown in Example 1. The results are shown in Table 2. Examples 3 and 4 Ethylene-vinyl acetate copolymer was used in place of the high-pressure low-density polyethylene used in Example 1 {Mitsubishi Yuka Co., Ltd.
Manufactured by Yucalon HE60, vinyl acetate content 6% by weight, Ml: 0.4g/10min, fluidity ratio 40, density:
0.927g/cm 3 } (Example row 3), ethylene-vinyl acetate copolymer {Mitsubishi Yuka Co., Ltd.
Co., Ltd., product name : Yucalon A packaging bag was obtained in the same manner as in Example 1 except that Example 4) was used. The obtained packaging bag was subjected to a drop bag test and a heat shrinkage rate measurement in the same manner as shown in Example 1. The results are shown in Table 2.
【表】
実施例 5、6
実施例1で用いた高圧法低密度ポリエチレンに
替えエチレンー酢酸ビニル共重合体{三井ポリケ
ミカル(株)製、商品名:ミラソンAce30N、酢酸ビ
ニル含有量6重量%、Ml=0.5g/10分、流動比
40、密度:0.928g/cm3}を40重量%配合したも
の(実施例5)、エチレン−酢酸ビニル共重合体
{三井ポリケミカル(株)製、商品名:ミラソンH625
−4、酢酸ビニル含有量5.9重量%、Ml=0.24
g/10分、流動比45、密度:0.933g/cm3}を60
重量%配合したもの(実施例6)を用い、押出量
を35Kg/hrとしたほかは実施例1と同様にして包
装袋を得た。
得られた包装袋につき落下条件の室温を−10℃
としたほかは実施例1で示したと同様の方法によ
り落袋試験、熱収縮率測定を行なつた。
結果を表3に示す。[Table] Examples 5 and 6 Ethylene-vinyl acetate copolymer used in place of high-pressure low-density polyethylene used in Example 1 {manufactured by Mitsui Polychemical Co., Ltd., trade name: Mirason Ace30N, vinyl acetate content 6% by weight, Ml=0.5g/10min, fluidity ratio
40, density: 0.928 g/cm 3 } (Example 5), ethylene-vinyl acetate copolymer {manufactured by Mitsui Polychemical Co., Ltd., product name: Mirason H625
-4, vinyl acetate content 5.9% by weight, Ml=0.24
g/10 min, flow ratio 45, density: 0.933 g/cm 3 } to 60
A packaging bag was obtained in the same manner as in Example 1, except that the weight percent blend (Example 6) was used and the extrusion rate was 35 Kg/hr. The room temperature of the drop condition for the obtained packaging bag is -10℃.
A drop bag test and a heat shrinkage rate measurement were carried out in the same manner as in Example 1, except that The results are shown in Table 3.
Claims (1)
比18〜35の線状低密度ポリエチレンにメルトイン
デツクス0.1〜2g/10分、流動比30〜70の低密
度ポリエチレンを5〜70重量%配合した混合物を
ブローアツプ比0.9〜1.5、ドラフト率10〜40の条
件下にインフレーシヨン成形し、得られた筒状フ
イルムを引取方向に対して交差する方向を長手方
向としてヒートシール及び切断することを特徴と
する包装袋の製造方法。 2 線状低密度ポリエチレンは密度0.915〜0.935
g/cm3のものであることを特徴とする特許請求の
範囲第1項に記載の方法。 3 低密度ポリエチレンは密度0.915〜0.940g/
cm3のものであることを特徴とする特許請求の範囲
第1項又は第2項に記載の方法。 4 低密度ポリエチレンは酢酸ビニル含有量0.5
〜18重量%のエチレン−酢酸ビニル共重合体であ
ることを特徴とする特許請求の範囲第1項乃至第
3項のいずれかに記載の方法。 5 ヒートシールはヒートシール部を230〜280℃
の温度でフイルム同志が融着するまで加熱し、そ
の後ヒートシール部を自由状態とすることにより
ヒートシール部に収縮を生起させることを特徴と
する特許請求の範囲第1項乃至第4項のいずれか
に記載の方法。[Scope of Claims] 1. Linear low density polyethylene with a melt index of 0.2 to 2 g/10 minutes and a flow ratio of 18 to 35 and 5 pieces of low density polyethylene with a melt index of 0.1 to 2 g/10 minutes and a flow ratio of 30 to 70. A mixture containing ~70% by weight was inflation-molded under conditions of a blow-up ratio of 0.9-1.5 and a draft rate of 10-40, and the resulting cylindrical film was heat-sealed with the longitudinal direction intersecting the drawing direction. and a method for producing a packaging bag, which comprises cutting the bag. 2 Linear low density polyethylene has a density of 0.915 to 0.935
2. A method according to claim 1, characterized in that it is of g/cm 3 . 3 Low density polyethylene has a density of 0.915 to 0.940g/
3. The method according to claim 1 or 2, characterized in that it is of cm 3 . 4 Low density polyethylene has a vinyl acetate content of 0.5
4. A method according to any one of claims 1 to 3, characterized in that the amount of ethylene-vinyl acetate copolymer is ~18% by weight. 5 Heat-seal the heat-sealed part at 230-280℃
Any one of claims 1 to 4, characterized in that the heat-sealed portion is heated until the films are fused to each other at a temperature of Method described in Crab.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58053178A JPS59178221A (en) | 1983-03-29 | 1983-03-29 | Preparation of packaging bag |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58053178A JPS59178221A (en) | 1983-03-29 | 1983-03-29 | Preparation of packaging bag |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59178221A JPS59178221A (en) | 1984-10-09 |
| JPH0152175B2 true JPH0152175B2 (en) | 1989-11-08 |
Family
ID=12935608
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58053178A Granted JPS59178221A (en) | 1983-03-29 | 1983-03-29 | Preparation of packaging bag |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59178221A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60108446A (en) * | 1983-11-18 | 1985-06-13 | Mitsubishi Petrochem Co Ltd | Method for filling and packaging |
| JPS61213236A (en) * | 1985-03-20 | 1986-09-22 | Mitsui Petrochem Ind Ltd | Olefin resin composition having excellent sealability in presence of foreign material and film composed of said composition |
| JPH0649808B2 (en) * | 1985-07-26 | 1994-06-29 | 三井石油化学工業株式会社 | Olefin resin composition excellent in foreign matter sealability |
| DE3851667T2 (en) * | 1987-07-13 | 1995-02-16 | Mitsubishi Chem Ind | Linear polyethylene film and process for its manufacture. |
-
1983
- 1983-03-29 JP JP58053178A patent/JPS59178221A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59178221A (en) | 1984-10-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4499241A (en) | Composition for cold drawn film | |
| EP0270932B1 (en) | Monolayer polyethylene shrink film | |
| JPH0428745B2 (en) | ||
| JPH0354048B2 (en) | ||
| EP0409615B1 (en) | Tough monolayer shrink film for products containing moisture | |
| EP0404368A2 (en) | Blends of linear low density polyethylene and low density polyethylene and films for shrink-wrapping therefrom | |
| JP2785403B2 (en) | Film production method | |
| JPH0450887B2 (en) | ||
| JPH0826193B2 (en) | Butene-1 Propylene Copolymer Composition Rich in Butene | |
| JPH0724926A (en) | Packaging bag manufacturing method | |
| JP2836156B2 (en) | Method for producing stretched polyethylene film | |
| JP2625813B2 (en) | Manufacturing method of packaging bag | |
| JPH0549459B2 (en) | ||
| JP2615931B2 (en) | Film production method | |
| JPH0517021B2 (en) | ||
| JPH0564173B2 (en) | ||
| JPH07100348B2 (en) | Film production method | |
| JPS59178221A (en) | Preparation of packaging bag | |
| JP3015114B2 (en) | Manufacturing method of packaging bag | |
| JPH0353930A (en) | Manufacture of packing bag | |
| US4481334A (en) | Composition for drawn film, cold drawn film made of said composition and process for manufacture of said film | |
| JPH0624789B2 (en) | Double packaging bag manufacturing method | |
| JPS60245541A (en) | Manufacture of packaging bag | |
| JPH0419931B2 (en) | ||
| JP2557472B2 (en) | Film production method |