CN109721904A - Polyvinyl alcohol film and combinations thereof and preparation method - Google Patents

Polyvinyl alcohol film and combinations thereof and preparation method Download PDF

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Publication number
CN109721904A
CN109721904A CN201711034910.1A CN201711034910A CN109721904A CN 109721904 A CN109721904 A CN 109721904A CN 201711034910 A CN201711034910 A CN 201711034910A CN 109721904 A CN109721904 A CN 109721904A
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China
Prior art keywords
polyvinyl alcohol
film
component
lubricant
slab
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Inventor
初立秋
徐萌
刘建叶
董穆
解娜
郭鹏
张琦
尹华
陈若石
白弈青
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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Sinopec Beijing Research Institute of Chemical Industry
China Petroleum and Chemical Corp
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Priority to CN201711034910.1A priority Critical patent/CN109721904A/en
Publication of CN109721904A publication Critical patent/CN109721904A/en
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Abstract

The present invention relates to polyvinyl alcohol film fields, and in particular, to polyvinyl alcohol film and combinations thereof and preparation method.The polyvinyl alcohol compositions contain polyvinyl alcohol, plasticizer, non-conductive functional filler, lubricant and optional auxiliary agent;The plasticizer contains component A, component B and component C;The component A is one of glycerine, ethylene glycol, polyethylene glycol and pentaerythrite or a variety of;The component B is one of magnesium chloride, magnesium nitrate, calcium chloride, copper sulphate and sodium acetate or a variety of;The component C is water.The present invention enables to the polyvinyl alcohol of wider alcoholysis degree range to be film-made through biaxial tension, and resulting polyvinyl alcohol film filler loading with higher and higher mechanical property.

Description

Polyvinyl alcohol film and combinations thereof and preparation method
Technical field
The present invention relates to polyvinyl alcohol film fields, and in particular, to polyvinyl alcohol film and combinations thereof and preparation side Method.
Background technique
Polyvinyl alcohol (PVA) is the non-petroleum base macromolecule that can be prepared from natural gas of industrialized production few in number Material, application range spread weaving, food, medicine, building, timber processing, papermaking, printing, agricultural, steel, producing high-molecular The fields such as work.The acid and alkali-resistance and organic solvent resistance of PVA is excellent, has splendid barrier property, and good biocompatibility can give birth to Object degradation.But because on its strand there are polyhydroxy structure, intramolecular and it is intermolecular produce very strong hydrogen bond, lead to its fusing point It is close with decomposition temperature, it is difficult thermoplastic processing, therefore its application is main at present or is based on solwution method technique, using solution curtain coating The disadvantages of method prepares PVA film there is complex steps, and film strength is poor.
Fast (the highest winding of the stretching ratio of biaxial tension method big (cross directional stretch multiplying power is up to 10 times or more), shaping speed Speed is up to hundreds of ms/min), high production efficiency, and the mechanical strength of obtained film, optical property and the thickness uniformity More preferably, but film forming is influenced significantly by process condition fluctuations, and film stretch process difficulty is big, has for film raw material Higher requirement.And due to the particularity of PVA processing, there are no the biaxial tension method process system researchs for PVA, so that Biaxial tension method prepares PVA film and is difficult to realize.
There are some researchs for PVA plasticising at present, it is desirable to which the plasticity that PVA is improved by the means such as being copolymerized, being blended makes it It is able to carry out thermoplasticity processing, to reduce its preparation cost, expands its use scope, but the research for thermoplasticity PVA film Also seldom.It is more at present be all design using melt-processed method prepare PVA film (such as CN106189010A, CN106189008A, CN101864132A and CN102391598A etc.), but it is all made of the tape casting or blowing prepares film, Both methods prepares film and comparatively requires raw material and technique all relatively low, and the performance of film is also compared with biaxial tension method Difference.
CN106189006A proposes to prepare PVA film using biaxial tension method, but its method need to use 95 (mol) % The PVA raw material of≤alcoholysis degree < 99.9 (mol) %, it is relatively narrow for the applicability of PVA;And the tensile strength of resulting PVA film It improves limited.
Summary of the invention
The purpose of the present invention is to provide a kind of novel polyvinyl alcohol film and combinations thereof and preparation method, the poly- second Enol film can have high filler content, and have both higher mechanical property.
To achieve the goals above, one aspect of the present invention provides a kind of polyvinyl alcohol compositions, and the composition contains poly- second Enol, plasticizer, non-conductive functional filler, lubricant and optional auxiliary agent;The plasticizer contains component A, component B and group Divide C;The component A is one of glycerine, ethylene glycol, polyethylene glycol and pentaerythrite or a variety of;The component B is chlorination One of magnesium, magnesium nitrate, calcium chloride, copper sulphate and sodium acetate are a variety of;The component C is water.
Second aspect of the present invention provides a kind of polyvinyl alcohol film containing above-mentioned composition.
Third aspect present invention provides a kind of preparation method of Biaxially-oriented polyethylene alcohol film, this method comprises:
(1) mixture of above-mentioned composition ingredient is provided;
(2) mixture is subjected to melting extrusion and is cast slab, obtain polyvinyl alcohol slab;
(3) polyvinyl alcohol slab is subjected to biaxial tension to form a film.
Fourth aspect present invention provides polyvinyl alcohol film prepared by the above method.
The present invention enables to the polyvinyl alcohol of wider alcoholysis degree range to be film-made through biaxial tension, and resulting polyvinyl alcohol Film filler loading with higher and higher mechanical property.
Specific embodiment
The endpoint of disclosed range and any value are not limited to the accurate range or value herein, these ranges or Value should be understood as comprising the value close to these ranges or value.For numberical range, between the endpoint value of each range, respectively It can be combined with each other between the endpoint value of a range and individual point value, and individually between point value and obtain one or more New numberical range, these numberical ranges should be considered as specific open herein.
One aspect of the present invention provides a kind of polyvinyl alcohol compositions, and the composition contains polyvinyl alcohol, plasticizer, non-conductive Functional filler, lubricant and optional auxiliary agent;The plasticizer contains component A, component B and component C;The component A is third One of triol, ethylene glycol, polyethylene glycol and pentaerythrite are a variety of;The component B be magnesium chloride, magnesium nitrate, calcium chloride, One of copper sulphate and sodium acetate are a variety of;The component C is water.
According to the present invention, the content of the component A, component B and component C can change in a wider range, in order to obtain It is more conducive to improve the filling effect and mechanical property of polyvinyl alcohol film, it is preferable that the component A, component B and component C's Weight ratio is 20-500:100:80-500, preferably 30-300:100:100-300, for example, 50-200:100:120-250, 80-150:100:150-200.
According to the present invention, the average molecular weight that the polyethylene glycol in the component A has is preferably 200-400.Described group Dividing A is preferably one of glycerine, the polyethylene glycol that average molecular weight is 200-400 and pentaerythrite or a variety of.
Preferably, the component B is one of magnesium chloride, magnesium nitrate and calcium chloride or a variety of.
In a preferred embodiment of the invention, the component A is glycerine and/or number-average molecular weight is 200- 400 polyethylene glycol, the component B are magnesium chloride and/or magnesium nitrate;Alternatively, the component A is pentaerythrite, the component B For calcium chloride.
According to the present invention, in order to obtain the polyvinyl alcohol film of more strong mechanical performance under high filling, it is preferable that described poly- The weight ratio of vinyl alcohol and plasticizer is 100:5-40, preferably 100:10-30, more preferably 100:15-25.Preferably, institute The weight ratio for stating polyvinyl alcohol and non-conductive functional filler is 100:30-200, preferably 100:50-100.Preferably, described The weight ratio of polyvinyl alcohol and lubricant is 100:0.5-5, preferably 100:1-3.
Wherein, composition of the invention is suitable for the polyvinyl alcohol of wider range alcoholysis degree, the degree of polymerization and partial size, preferably Ground, the alcoholysis degree of the polyvinyl alcohol are 80-99mol%, and the degree of polymerization is 1500 or more (preferably 1500-2500), and partial size is 90-500μm.The polyvinyl alcohol of low alcoholysis level is also suitable, such as the alcoholysis degree of the polyvinyl alcohol is 80-90mol%, is gathered Right is 1600-1800, and partial size is 100-300 μm.The polyvinyl alcohol of high alcoholysis degree is also suitable, such as the polyvinyl alcohol Alcoholysis degree be 95-99mol%, degree of polymerization 1700-2500, partial size be 320-400 μm.
According to the present invention, the non-conductive functional filler can be inorganic material, or organic material, or Person is their mixture.Preferably, the non-conductive functional filler be calcium carbonate, barium sulfate, talcum powder, zeolite, mica, Clay, silica, diatomite, kaolin, alumina, calcium sulfate, magnesium sulfate, calcium oxide, magnesia, entirely vulcanize Nano powder rubber, One of hud typed impact modifying agent, wood powder, bamboo powder and powdered rice hulls are a variety of.Wherein, the full vulcanization Nano powder rubber Specific example for example can for full vulcanization nanometer powder butadiene-styrene rubber, full vulcanization nanometer powder nitrile rubber, vulcanize nanometer entirely Powdery propylene acid esters rubber, full vulcanization nanometer powder carboxylic styrene-butadiene rubber, full vulcanization nanometer powder carboxy nitrile rubber, full vulcanization One of nanometer powder silicon rubber and full vulcanization nanometer powder butadiene-styrene-vinyl pyridine rubber are a variety of.
Non-conductive functional filler of the invention is preferably calcium carbonate, and especially average grain diameter is 0.05-10 μm, more preferably It is 0.1-5 μm, most preferably 0.5-2 μm of calcium carbonate particle.Using calcium carbonate particle as under non-conductive functional filler, Polyvinyl alcohol film of the invention will be assigned with lower cost and higher mechanical property.
According to the present invention, the lubricant can be selected from a variety of lubricants, it is preferable that the lubricant is poly- Glycols lubricant, fluoropolymer series lubricant agent, organic silicon lubricant, fatty alcohol type emollients, fatty acid lubrication Agent, fatty acid ester type emollients, stearic amide series lubricant agent, fatty acid metal soaps lubricant, alkane and oxidation of alkanes class One of lubricant and micro-and nano-particles series lubricant agent are a variety of.
Wherein, the polyethylene glycol series lubricant agent for example can be the PEG molecule that average molecular weight is 500-50000, It can also pass through other chemical modifications or physical modification by sealing end, grafting, crosslinking Treatment.
Wherein, the fluoropolymer series lubricant agent for example can be polytetrafluoroethylene (PTFE), Kynoar, polyhexafluoropropylene At least one of Deng, or other unimodal or multimodal fluoropolymers and crystallization or hemicrystalline fluoropolymer Object.
Wherein, the organo-silicic oil can be existing various using carbon, silicon atom as molecular backbone, with methyl, benzene The oligomer or oligomer of the organic groups such as base, alkoxy, vinyl are the compound of side chain.
Wherein, the fatty alcohol type emollients for example can in soft fat alcohol, tallow alcohol, tallow fatty alcohol etc. extremely Few one kind.
Wherein, the fatty acid lubricant for example can be with stearic acid and/or 12- hydroxy stearic acid.
Wherein, the fatty acid ester type emollients for example can be butyl stearate, stearic acid list glycerolipid, palmitinic acid ten At least one of six Arrcostabs, tearyl base ester etc..
Wherein, the stearic amide series lubricant agent for example can be stearic amide, oleamide, erucyl amide, n, At least one of n- ethylene bis stearic acid amide (EBS) etc..
Wherein, the fatty acid metal soaps lubricant for example can be lead stearate, calcium stearate, magnesium stearate, conjunction At at least one of calcium acetate etc..
Wherein, the alkane and oxidation of alkanes series lubricant agent for example can for atoleine, solid paraffin, polyethylene wax, At least one of polypropylene wax, ethylene oxide wax etc..
Wherein, the micro-and nano-particles series lubricant agent for example can be powdered rubber and/or aerosil particles.
According to the present invention, the composition can also contain auxiliary agent, and the auxiliary agent can be other to polyvinyl alcohol film Performance has a gain effect, and will not stretching film forming to polyvinyl alcohol film, mechanical property and high filling effect generate it is unfavorable Influence additive.The auxiliary agent for example can be one of antioxidant, acid absorbent and antistatic agent or a variety of.
Wherein, the antioxidant for example can be antioxidant 1010, antioxidant 1076, antioxidant 164, irgasfos 168, resist At least one of oxygen agent 264 etc..The content of the antioxidant can change in a wider range, the institute relative to 100 parts by weight Polyvinyl alcohol is stated, the content of the antioxidant is preferably 0.1-1 parts by weight.
Wherein, the acid absorbent can be for example at least one of hydrotalcite, calcium stearate, zinc stearate etc..The suction The content of sour agent can change in a wider range, relative to the polyvinyl alcohol of 100 parts by weight, the content of the acid absorbent Preferably 0.1-1 parts by weight.
Wherein, the antistatic agent for example can be sweet for ethoxylated alkylamine, ethoxylated alkyl acid amide, monostearate At least one of grease, sodium alkyl sulfonate etc..The content of the antistatic agent can change in a wider range, relative to 100 The polyvinyl alcohol of parts by weight, the content of the antistatic agent are preferably 0.1-1 parts by weight.
Second aspect of the present invention provides a kind of polyvinyl alcohol film containing above-mentioned composition.
As long as the polyvinyl alcohol film that the second aspect of the invention provides contains above-mentioned polyvinyl alcohol compositions, Content for example can be 80-100 weight %.
Third aspect present invention provides a kind of preparation method of Biaxially-oriented polyethylene alcohol film, this method comprises:
(1) mixture of above-mentioned composition ingredient is provided;
(2) mixture is subjected to melting extrusion and is cast slab, obtain polyvinyl alcohol slab;
(3) polyvinyl alcohol slab is subjected to biaxial tension to form a film.
According to the present invention, step (1) is mainly to provide the mixture of above-mentioned composition ingredient, in order to subsequent place Reason forms polyvinyl alcohol film.Preferably, step (1) includes: first to mix polyvinyl alcohol and plasticizer, is then re-introduced into non- Conducting functional filler, lubricant and optional auxiliary agent.It is highly preferred that the condition packet that polyvinyl alcohol and plasticizer are mixed Include: temperature is 50-90 DEG C (preferably 60-80 DEG C), and the time is 0.5-4h (preferably 1-2h).
The mixed process, which can be, is first heated to 50-90 DEG C for polyvinyl alcohol, then introduces plasticizer and is 50- in temperature 90 DEG C of mixing 0.5-4h.Introducing for the plasticizer can be by the way of disposably feeding intake, can also be using the side that feed intake step by step Formula, in order to improve the dispersion effect of plasticizer and polyvinyl alcohol, it is preferred to use the mode to feed intake step by step, it is preferable that the plasticising Agent is added in 5-60min and is finished.
According to the present invention, after polyvinyl alcohol and plasticizer being mixed, add non-conductive functional filler, lubricant and Before optional auxiliary agent, the mixture of polyvinyl alcohol and plasticizer first can be down to room temperature (such as 20-30 DEG C) and add non-lead again Electrically functional filler, lubricant and optional auxiliary agent, are then sufficiently mixed, and the mixing of above-mentioned composition ingredient is obtained Object.
According to the present invention, before carrying out step (2), the resulting mixture of step (1) can also be subjected to extruding pelletization and (squeezed The temperature being granulated out is 100-200 DEG C), resulting master batch is used for the operation of step (2);It is, of course, preferable to directly by step (1) Resulting mixture carries out the processing of step (2), to reduce loss of material, especially reduces the loss of plasticizer.
According to the present invention, by step (2) by the mixture carry out melting extrusion and be cast slab can be in casting machine It carries out, it is preferable that the temperature of the melting extrusion is 100-200 DEG C (preferably 110-160 DEG C);The curtain coating of the curtain coating slab Chilling roll temperature is 15-50 DEG C (preferably 20-40 DEG C).
According to the present invention, the structure for the film that the slab die head that the curtain coating slab uses can according to need acquisition is selected It selects, for example, single layer die can be used when needing to obtain the film with single layer structure;There is multilayer knot when needing to obtain When film (film with upper epidermis, sandwich layer and layer three-decker) of structure, the compound die head of multilayered structure can be used, and And at least one layer of (sandwich layer) connects with the extruder hopper equipped with above-mentioned polyvinyl alcohol compositions in the compound die head of multilayered structure Logical, at least one layer (sandwich layer) in the slab enabled in this way is the polyvinyl alcohol formed by above-mentioned polyvinyl alcohol compositions Layer, naturally it is also possible to be that the compound die head of the multilayered structure all connects with the extruder hopper equipped with above-mentioned polyvinyl alcohol compositions Logical, each layer in the slab enabled in this way is all the polyvinyl alcohol layer formed by above-mentioned polyvinyl alcohol compositions.
For this purpose, the polyvinyl alcohol slab is single layer structure or multilayered structure, preferably by upper epidermis, sandwich layer and layer The three-decker of composition, the upper epidermis, sandwich layer and layer are all the layer that polyvinyl alcohol compositions are formed.
According to the present invention, in step (3), the biaxial tension may include that Synchronos method stretching or the method for fractional steps stretch.Wherein, The Synchronos method stretching refers to carrying out film longitudinal (MD) simultaneously and laterally (TD) is stretched, and the method for fractional steps stretching refers to elder generation Film longitudinal stretching is carried out, then carries out film cross directional stretch.
Preferably, it includes first preheating polyvinyl alcohol slab that the Synchronos method, which stretches, then carries out MD and TD simultaneously It stretches.Preferably, the condition that the Synchronos method stretches includes: that draft temperature is 120-170 DEG C, and MD stretching ratio is 3 times or more (for example, 3-6 times), TD stretching ratio be 3 times or more (for example, 3-6 times), MD rate of extension for 300%/s or more (for example, 300%/s-500%/s), TD rate of extension is 300%/s or more (for example, 300%/s-500%/s)
Preferably, the method for fractional steps stretching includes: first to preheat polyvinyl alcohol slab, then first carries out MD stretching, Then progress TD stretching is preheated again.Preferably, the condition that the method for fractional steps stretches includes: that MD draft temperature is 80-100 DEG C, TD Draft temperature be 120-200 DEG C, MD stretching ratio be 3 times or more (for example, 3-6 times), TD stretching ratio for 3 times or more (such as Be 3-6 times), MD rate of extension be 100%/s or more (for example, 100%/s-200%/s), TD rate of extension be 100%/s with Upper (for example, 100%/s-200%/s).
According to the present invention, this method can carry out annealing setting processing to the film after stretching, can also be fixed without this Shape processing, in the case where carrying out setting processing namely this method further includes carrying out at annealing setting after step (3) to resulting film The temperature of reason, annealing setting processing is preferably 180-200 DEG C.The time of annealing setting processing is preferably 5-60s.To stretching Film afterwards, which carries out annealing setting processing, can play the role of improving film dimensions stability.
According to the present invention, this method can also include by resulting polyvinyl alcohol film carry out surface corona processing, cutting edge and Winding processing, surface corona processing, cutting edge and winding processing are the operation of this field routine, and the present invention has no this particularly It limits.
Fourth aspect present invention provides polyvinyl alcohol film prepared by the above method.
The resulting polyvinyl alcohol film mechanical property with higher of the present invention, the MD of the polyvinyl alcohol film stretch strong Degree for example can be 35MPa or more, especially 45MPa or more, preferably 70MPa or more, more preferably 75-150MPa;TD is drawn Stretching intensity for example can be 40MPa or more, especially 55MPa or more, preferably 80MPa or more, more preferably 85-160MPa; MD elongation at break for example can be 55% or more, preferably 60% or more, more preferably 70-100%;TD elongation at break example It such as can be 55% or more, preferably 60% or more, more preferably 60-70%;MD tensile modulus of elasticity for example can be 130MPa or more, preferably 200MPa or more, more preferably 300MPa or more, more preferably 340-700MPa;TD tensile elasticity Modulus for example can be 130MPa or more, preferably 200MPa or more, more preferably 300MPa or more, more preferably 350- 700MPa。
It is described for the resulting polyvinyl alcohol film of polyvinyl alcohol of higher alcoholysis degree (for example, 95-99mol%) The MD tensile strength of polyvinyl alcohol film for example can be 100MPa or more, preferably 110-150MPa;TD tensile strength is 110MPa or more, preferably 110-160MPa.MD elongation at break for example can be 60% or more, preferably 60-90%;TD is disconnected Splitting elongation for example can be 55% or more, more preferably 60-70%;MD tensile modulus of elasticity for example can for 200MPa with On, preferably 300-700MPa;TD tensile modulus of elasticity for example can be 200MPa or more, preferably 300-700MPa.
It is described for the resulting polyvinyl alcohol film of polyvinyl alcohol compared with low alcoholysis level (for example, 80-90mol%) The MD tensile strength of polyvinyl alcohol film for example can be 35MPa or more, especially 45MPa or more, preferably 70MPa or more, More preferably 75-90MPa;TD tensile strength for example can be 45MPa or more, especially 55MPa or more, preferably 80MPa with On, more preferably 85-110MPa.MD elongation at break for example can be 60% or more, preferably 70-100%;TD extension at break Rate for example can be 55% or more, preferably 60% or more, more preferably 60-70%;MD tensile modulus of elasticity for example can be 130MPa or more, preferably 200MPa or more, more preferably 300MPa or more, more preferably 340-600MPa;TD tensile elasticity Modulus for example can be 130MPa or more, preferably 200MPa or more, more preferably 300MPa or more, more preferably 350- 600MPa。
The present invention will be described in detail by way of examples below.
In following example: PEG200 be the average molecular weight for recovering fine chemistry industry research institute purchased from Tianjin be 200 it is poly- Ethylene glycol.PEG400 is to recover the polyethylene glycol that the average molecular weight of fine chemistry industry research institute is 400 purchased from Tianjin.Polyethylene Tensile strength, elongation at break and the tensile modulus of elasticity of alcohol film are that the method according to specified in GB/T 1040.3-2006 is surveyed ?.
Plasticizer preparation example
By according to the formula in table 1, component A, component B and component C are proportionally mixed, corresponding plasticizer is obtained.
Table 1
Note: the above component A and component B is measured with the pure material of substance listed in table.
Embodiment 1
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
(1) by 100 weight account polyethylene alcohol, (alcoholysis degree 88mol%, the degree of polymerization 1700, are purchased from Shanxi three by 180 μm of partial size Dimension group company) 60 DEG C are warming up to, the plasticizer E1 (finishing in 30min) of 15 parts by weight is gradually added dropwise;After finishing, temperature is protected It holds and is stirred 1h at 50 DEG C.After naturally cooling to 30 DEG C, the Kynoar lubricant that 1 parts by weight are added is (public purchased from 3M Take charge of the FX5911 trade mark), the calcium carbonate of 100 parts by weight (being purchased from Jiangxi Huaming nanometer calcium carbonate Co., Ltd, average grain diameter is 2 μm) With the antioxidant 1010 (being purchased from Switzerland's vapour bar chemistry (China) Co., Ltd, the same below) of 0.25 parts by weight, obtain after mixing To polyvinyl alcohol compositions;
(2) polyvinyl alcohol compositions made from step (1) are added to the model LCR400's of Labtech company, Sweden Melting extrusion is carried out in the sandwich layer extruder of multilayer extrusion casting machine and upper and lower surface layer extruder and is cast slab, and melting is squeezed Each section of temperature is 110-160 DEG C out, and curtain coating chilling roll temperature is 25 DEG C, is thus obtained by upper epidermis, sandwich layer and layer structure At polyvinyl alcohol slab;
(3) above-mentioned polyvinyl alcohol slab is put into the stretching clamp of film biaxial tension equipment, using two-way substep Stretch film comprising: first polyvinyl alcohol slab is preheated, then first carries out MD stretching, then preheats then progress TD drawing It stretches;Its condition includes: that the preceding preheating temperature of MD stretching is 90 DEG C, and MD draft temperature is 90 DEG C, and 3 times of MD stretching ratio, film MD is drawn Stretching rate is 100%/s;Preheating temperature is 140 DEG C before TD is stretched, and TD draft temperature is 140 DEG C, and TD stretching ratio is 4 times, thin Film TD rate of extension is 100%/s;Then the resulting film of biaxial tension is subjected to annealing setting processing 30s at 180 DEG C, obtained The film for being 25 μm to average thickness, is made of, each layer raw material is the poly- second of the present embodiment upper epidermis, sandwich layer and layer Enol composition.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 2
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
(1) by 100 weight account polyethylene alcohol, (alcoholysis degree 85mol%, the degree of polymerization 1500, are purchased from Shanxi three by 200 μm of partial size Dimension group company) 70 DEG C are warming up to, the plasticizer E2 (finishing in 25min) of 20 parts by weight is gradually added dropwise;After finishing, temperature is protected It holds and is stirred 1.5h at 60 DEG C.After naturally cooling to 30 DEG C, the polyethylene glycol lubricant that 2 parts by weight are added (is purchased from Switzerland Clariant Corporation, average molecular weight 10000), the calcium carbonate of 50 parts by weight (be purchased from Jiangxi Huaming nanometer calcium carbonate Co., Ltd, Average grain diameter is 2 μm), the irgasfos 168s of the antioxidant 1010 of 0.15 parts by weight and 0.25 parts by weight (be purchased from Switzerland's vapour bar chemistry (China) Co., Ltd), polyvinyl alcohol compositions are obtained after mixing;
(2) polyvinyl alcohol compositions made from step (1) are added to the model LCR400's of Labtech company, Sweden Melting extrusion is carried out in the sandwich layer extruder of multilayer extrusion casting machine and upper and lower surface layer extruder and is cast slab, and melting is squeezed Each section of temperature is 110-160 DEG C out, and curtain coating chilling roll temperature is 30 DEG C, is thus obtained by upper epidermis, sandwich layer and layer structure At polyvinyl alcohol slab;
(3) above-mentioned polyvinyl alcohol slab is put into the stretching clamp of film biaxial tension equipment, using two-way substep Stretch film comprising: first polyvinyl alcohol slab is preheated, then first carries out MD stretching, then preheats then progress TD drawing It stretches;Its condition include: MD stretch before preheating temperature be 100 DEG C, MD draft temperature be 100 DEG C, 4 times of MD stretching ratio, film MD Rate of extension is 100%/s;Preheating temperature is 135 DEG C before TD is stretched, and TD draft temperature is 135 DEG C, and TD stretching ratio is 5 times, Film TD rate of extension is 150%/s;The resulting film of biaxial tension is then subjected to annealing setting processing 10s at 200 DEG C, The film that average thickness is 25 μm is obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is the poly- of the present embodiment Vinyl alcohol compositions.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 3
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method described in embodiment 1, the difference is that:
Step (1): replacing E1 using the plasticizer E3 of 25 parts by weight, using the calcium carbonate of 200 parts by weight (purchased from Jiangxi China Bright nanometer calcium carbonate Co., Ltd, average grain diameter is by 1.5 μm) 2 μm of calcium carbonate is replaced, lubricant is using 1 parts by weight Glyceryl monostearate (is purchased from the standing grain major company Atmer163 trade mark);
Step (3): preheating temperature is 145 DEG C before TD is stretched, and TD draft temperature is 145 DEG C;
The film that average thickness is 25 μm is finally obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of the present embodiment.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 4-11
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method described in embodiment 1, unlike, the plasticizer E4-E11 for the parts by weight such as being respectively adopted replaces E1, The film that average thickness is 25 μm is finally respectively obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is this reality Apply the polyvinyl alcohol compositions of example.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 12
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method described in embodiment 1, the difference is that, the dosage of the plasticizer is 5 parts by weight;
The film that average thickness is 25 μm is finally obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of the present embodiment.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 13
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method described in embodiment 1, the difference is that, the dosage of the plasticizer is 35 parts by weight;
The film that average thickness is 25 μm is finally obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of the present embodiment.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 14
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method described in embodiment 1, the difference is that:
Step (3) replaces method of fractional steps biaxial tension namely the behaviour of the Synchronos method biaxial tension using Synchronos method biaxial tension Work includes: first to preheat polyvinyl alcohol slab, then carries out MD simultaneously and stretches and TD stretching;Its condition includes: preheating temperature Degree is 130 DEG C, and draft temperature is 130 DEG C, and 3.5 times of MD stretching ratio, MD rate of extension is 300%/s, and TD stretching ratio is 3.5 Times, TD rate of extension is 400%/s;
The film that average thickness is 25 μm is finally obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of the present embodiment.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 15
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method as described in example 4, unlike, using the alcoholysis degree 99mol%, poly- purchased from Ningxia Neng Hua company Right 2000 and 360 μm of partial size polyvinyl alcohol replace embodiment 4 in polyvinyl alcohol.
The film that average thickness is 25 μm is finally obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of the present embodiment.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 16
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method described in embodiment 15, the difference is that:
Step (3) replaces method of fractional steps biaxial tension namely the behaviour of the Synchronos method biaxial tension using Synchronos method biaxial tension Work includes: first to preheat polyvinyl alcohol slab, then carries out MD simultaneously and stretches and TD stretching;Its condition includes: preheating temperature Degree is 130 DEG C, and draft temperature is 130 DEG C, and 3.5 times of MD stretching ratio, MD rate of extension is 300%/s, and TD stretching ratio is 3.5 Times, TD rate of extension is 400%/s;
The film that average thickness is 25 μm is finally obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of the present embodiment.Gained biaxially oriented film performance is as shown in table 2.
Embodiment 17
The present embodiment is for illustrating polyvinyl alcohol film of the invention and combinations thereof and preparation method.
According to method described in embodiment 16, the difference is that, using the alcoholysis degree for being purchased from middle petrochemical industry Sichuan vinylon plant 97mol%, the degree of polymerization 1800 and 360 μm of partial size of polyvinyl alcohol replace the polyvinyl alcohol in embodiment 16.
The film that average thickness is 25 μm is finally obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of the present embodiment.Gained biaxially oriented film performance is as shown in table 2.
Comparative example 1-5
According to method described in embodiment 1, unlike, the plasticizer DE1-DE5 for the parts by weight such as being respectively adopted replaces E1, Rupture of membranes occurs in biaxial orientation process for comparative example 1-3, can not stretch, and is unable to get respective films, and comparative example 4-5 is finally respective The film that average thickness is 25 μm is obtained, is made of upper epidermis, sandwich layer and layer, each layer raw material is the poly- of this comparative example Vinyl alcohol compositions.Gained biaxially oriented film performance is as shown in table 2.
Comparative example 6-7
According to method described in embodiment 15, unlike, the plasticizer DE4-DE5 for the parts by weight such as being respectively adopted is replaced E4 finally respectively obtains the film that average thickness is 25 μm, is made of upper epidermis, sandwich layer and layer, each layer raw material is The polyvinyl alcohol compositions of this comparative example.Gained biaxially oriented film performance is as shown in table 2.
Comparative example 8
According to method described in embodiment 1, the difference is that, step (2) adds polyvinyl alcohol compositions made from step (1) The sandwich layer extruder and upper and lower surface layer for entering the multilayer extrusion casting machine of the model LCR400 to Labtech company, Sweden squeeze Melting extrusion and direct casting film-forming are carried out in machine out, the temperature that each section of melting extrusion is 110-160 DEG C, is cast chilling roll temperature It is 25 DEG C, thus directly obtains the cast film that average thickness is 25 μm, gained cast film performance is as shown in table 2.
Comparative example 9
According to method described in embodiment 1, the difference is that, this comparative example uses the upper blowing method of DR.COLLIN company, Germany Film blowing device extrusion and blow molding obtains polyvinyl alcohol film, and specific method is by polyvinyl alcohol compositions made from step (1) It is added in the hopper of upper blowing method film blowing device extruder, raw material is after the abundant fusion plastification of extruder, by the annular mouth of head Melt membrane tube is made in mould extrusion, after through compressed air inflation (blow-up ratio be 2.5 times), and it is poly- after vane is cooling blow molding to be made Alcohol film, film are the single layer structure that average thickness is 25 μm.Gained blown films porperties are as shown in table 2.
Table 2
It can be seen that by the data of table 2 using plasticizer provided in the present invention, enable to wider alcoholysis degree range Polyvinyl alcohol be film-made through biaxial tension, prepare resulting polyvinyl alcohol film intensity with higher.Wherein, especially excellent Under the proportion of choosing, MD and TD to tensile strength in 80MPa or more, MD elongation at break is in 75% or more, TD extension at break Rate is in 58% or more, MD tensile modulus of elasticity in 500MPa or more, and TD tensile modulus of elasticity is in 520MPa or more.
The preferred embodiment of the present invention has been described above in detail, and still, the present invention is not limited thereto.In skill of the invention In art conception range, can with various simple variants of the technical solution of the present invention are made, including each technical characteristic with it is any its Its suitable method is combined, and it should also be regarded as the disclosure of the present invention for these simple variants and combination, is belonged to Protection scope of the present invention.

Claims (16)

1. a kind of polyvinyl alcohol compositions, which is characterized in that the composition contains polyvinyl alcohol, plasticizer, non-conductive functionality Filler, lubricant and optional auxiliary agent;The plasticizer contains component A, component B and component C;The component A is glycerine, second One of glycol, polyethylene glycol and pentaerythrite are a variety of;The component B is magnesium chloride, magnesium nitrate, calcium chloride, copper sulphate With one of sodium acetate or a variety of;The component C is water.
2. composition according to claim 1, wherein the weight ratio of the component A, component B and component C are 20-500: 100:80-500, preferably 30-300:100:100-300.
3. composition according to claim 1 or 2, wherein the component A is glycerine, average molecular weight 200-400 Polyethylene glycol and one of pentaerythrite or a variety of;
The component B is one of magnesium chloride, magnesium nitrate and calcium chloride or a variety of.
4. composition described in any one of -3 according to claim 1, wherein the weight ratio of the polyvinyl alcohol and plasticizer For 100:5-40, preferably 100:10-30, more preferably 100:15-25;
Preferably, the weight ratio of the polyvinyl alcohol and non-conductive functional filler is 100:30-200, preferably 100:50- 100;
Preferably, the weight ratio of the polyvinyl alcohol and lubricant is 100:0.5-5, preferably 100:1-3.
5. composition described in any one of -4 according to claim 1, wherein the alcoholysis degree of the polyvinyl alcohol is 80- 99mol%, the degree of polymerization are 1500 or more, and partial size is 90-500 μm;
Preferably, the alcoholysis degree of the polyvinyl alcohol is 80-90mol%, and degree of polymerization 1600-1800, partial size is 100-300 μ m;
Preferably, the alcoholysis degree of the polyvinyl alcohol is 95-99mol%, and degree of polymerization 1700-2500, partial size is 320-400 μ m。
6. composition described in any one of -5 according to claim 1, wherein the non-conductive functional filler is carbonic acid Calcium, barium sulfate, talcum powder, zeolite, mica, clay, silica, diatomite, kaolin, alumina, calcium sulfate, magnesium sulfate, calcium oxide, Magnesia vulcanizes one of Nano powder rubber, hud typed impact modifying agent, wood powder, bamboo powder and powdered rice hulls or a variety of entirely, excellent It is selected as calcium carbonate;
Preferably, the lubricant is polyethylene glycol series lubricant agent, fluoropolymer series lubricant agent, organic silicon lubricant, rouge Fat alcohol type emollients, fatty acid lubricant, fatty acid ester type emollients, stearic amide series lubricant agent, fatty acid metal soap Series lubricant agent, alkane and one of oxidation of alkanes series lubricant agent and micro-and nano-particles series lubricant agent or a variety of.
7. composition described in any one of -6 according to claim 1, wherein the auxiliary agent is antioxidant, acid absorbent and resists One of electrostatic agent is a variety of.
8. a kind of polyvinyl alcohol film containing composition described in any one of claim 1-7.
9. a kind of preparation method of Biaxially-oriented polyethylene alcohol film, this method comprises:
(1) mixture of composition ingredient described in any one of claim 1-7 is provided;
(2) mixture is subjected to melting extrusion and is cast slab, obtain polyvinyl alcohol slab;
(3) polyvinyl alcohol slab is subjected to biaxial tension to form a film.
10. according to the method described in claim 9, wherein, step (1) includes: first to mix polyvinyl alcohol and plasticizer, Then it is re-introduced into non-conductive functional filler, lubricant and optional auxiliary agent;
Wherein, by the condition that polyvinyl alcohol and plasticizer mix include: temperature be 50-90 DEG C, time 0.5-4h.
11. method according to claim 9 or 10, wherein the temperature of the melting extrusion is 100-200 DEG C;The stream The curtain coating chilling roll temperature for prolonging slab is 15-50 DEG C.
12. the method according to any one of claim 9-11, wherein the polyvinyl alcohol slab be single layer structure or Multilayered structure, the three-decker being preferably made of upper epidermis, sandwich layer and layer.
13. the method according to any one of claim 9-12, wherein the biaxial tension include Synchronos method stretch or The method of fractional steps stretches;
It includes first preheating polyvinyl alcohol slab that the Synchronos method, which stretches, then carries out MD and TD simultaneously and stretches;It is described same Footwork stretch condition include: draft temperature be 120-170 DEG C, MD stretching ratio be 3 times or more, TD stretching ratio be 3 times with On, MD rate of extension is 300%/s or more, and TD rate of extension is 300%/s or more;
Method of fractional steps stretching includes: first to preheat polyvinyl alcohol slab, then first carries out MD stretching, then is preheated and laggard Row TD is stretched;The condition that the method for fractional steps stretches includes: that MD draft temperature is 80-100 DEG C, and TD draft temperature is 120-200 DEG C, MD stretching ratio is 3 times or more, and TD stretching ratio is 3 times or more, and MD rate of extension is 100%/s or more, and TD rate of extension is 100%/s or more.
14. the method according to claim 9 or 13, wherein this method further includes carrying out after step (3) to resulting film Setting of annealing is handled, and the temperature of annealing setting processing is 180-200 DEG C.
15. polyvinyl alcohol film made from the method as described in any one of claim 9-14.
16. polyvinyl alcohol film according to claim 15, wherein the MD tensile strength of the polyvinyl alcohol film is 35MPa or more, preferably 45MPa or more, more preferably 70MPa or more;TD tensile strength is 40MPa or more, preferably 55MPa More than, more preferably 80MPa or more;MD elongation at break is 55% or more, preferably 60% or more;TD elongation at break is 55% or more, preferably 60% or more;MD tensile modulus of elasticity be 130MPa or more, preferably 200MPa or more, more preferably 300MPa or more;TD tensile modulus of elasticity is 130MPa or more, preferably 200MPa or more, more preferably 300MPa or more.
CN201711034910.1A 2017-10-30 2017-10-30 Polyvinyl alcohol film and combinations thereof and preparation method Pending CN109721904A (en)

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