CN1970621A - Highly ductile, abrasive-wearable self-lubricant polyformaldehyde material and its preparation method - Google Patents
Highly ductile, abrasive-wearable self-lubricant polyformaldehyde material and its preparation method Download PDFInfo
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- CN1970621A CN1970621A CN 200610022223 CN200610022223A CN1970621A CN 1970621 A CN1970621 A CN 1970621A CN 200610022223 CN200610022223 CN 200610022223 CN 200610022223 A CN200610022223 A CN 200610022223A CN 1970621 A CN1970621 A CN 1970621A
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- polyoxymethylene
- polyoxyethylene
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Abstract
The invention discloses a high-density, abrasion-proof self-lubricating polyformaldehyde material and making method, which comprises the following steps: drying 50-99% polyformaldehyde at 60-90 deg.c for 4-6h; adding 1-50% polyethylene oxide, 0.01-1% polyformaldehyde stabilizer, 0.01-1% formaldehyde and 0.01-1% formaldehyde adsorbent into high-speed stirrer to blend evenly; fusing at 170-200 deg.c to squeeze; cooling the squeezed material below crystallizing temperature of polyethylene oxide with cooling speed at 50-80deg.c/min; obtaining the product with high flexibility between the interior of polyformaldehyde spherulite and spherulite.
Description
Technical field
The present invention relates to a kind of high tenacity, high wear-resistence self-lubricating polyformaldehyde material and preparation method thereof, belong to polymer processing field.
Background technology
Polyoxymethylene (polyoxymethylene) is a kind of important engineering plastics, has excellent physical and mechanical properties, as high strength, high rigidity, outstanding fatigue performance, creep resistant, self lubricity and wear resistant, be that specific tenacity often is used to non-ferrous metal and alloy replacing thing comparatively near one of resin kind of metal in all plastics.Polyoxymethylene is divided into homopolymerization type and copoly type two classes, and homopolymerization type polyoxymethylene is developed in nineteen fifty-nine by U.S. Dupond company, the copoly type polyoxymethylene by U.S. Cekanese company in exploitation in 1961.POM is very easily crystallization in the process of forming process, generates larger-size spherocrystal, and notch sensitivity is big, and notched Izod impact strength is low.POM and other properties-correcting agent consistency are poor, are difficult to toughness reinforcing.Simultaneously, POM is used for making driving member more, needs the excellent friction polishing machine.Toughness reinforcing and antifriction is the important research content (Wang Duoren, synthetic resins and engineering plastics production technology, Beijing, China Light Industry Press, 2001,8) of POM modification.
The polyoxymethylene toughening modifying mainly contains blending and modifying and modification by copolymerization, the properties-correcting agent of blending and modifying is elastomerics or rubber, as paracril (NBR), terpolymer EP rubber, polystyrene elastomerics (as the segmented copolymer of vinylbenzene and divinyl), polyester elastomer (as terephthaldehyde's acid butyl ester and poly-tetramethyl-di-alcohol segmented copolymer), polyamide-based elastomerics (as nylon-6 and poly-tetramethylethylene glycol segmented copolymer, polyurethane elastomer (TPU) etc.But polyoxymethylene and most elastomer compatibility are poor, only have TPU and polyoxymethylene that certain consistency is arranged, and toughening modifying is effective, and has realized commercialization.Modification by copolymerization is made main chain with polyoxymethylene, by graft copolymerization or block copolymerization, with polyolefin copolymer, butadiene type multipolymer, polyvinyl acetate, polymethylmethacrylate etc. are made side chain, or in the polyoxymethylene polymerization process, introduce and properties-correcting agent consistency side chain preferably, with the properties-correcting agent blend, can solve polyoxymethylene does not have side group, the problem of toughness reinforcing difficulty again, but complex process, production cost height (Flexman E A, Hdeng D D, Snyder H L, PolymPrep, [J], 1988,29:189～192; Masamoto J., Polym., [J], 2000,41:7283～7287).The method of improving the polyoxymethylene friction and wear behavior mainly contains following several: add the lower macromolecular materials of frictional coefficient such as tetrafluoroethylene, ultrahigh molecular weight polyethylene(UHMWPE); Add lubricating oil and lubricated lipids such as silicone oil, mineral oil, grease; Add fibrous materials such as glass, carbon fibre, aramid fiber; Add inorganic powder class lubricant etc.Though the friction and wear behavior of blend is improved, other mechanical properties decrease amplitudes of blend are bigger, and over-all properties is relatively poor.Yet when performance was improved on the one hand to polyoxymethylene, the performance of others can descend to some extent generally,, be difficult to realize simultaneously toughness reinforcing and lubricating modification (Chen J Y, Cao Y et al., Wear to polyoxymethylene, [J], 2006,260:1342～1348; WangH T, Liu W M et al., Polym.Mater.Sci.Eng., [J], 1997,13 (2): 126～128).
Polyoxyethylene is a kind of macromolecular material of high-crystallinity, has high tenacity at normal temperatures, because the low polymeric solid lubricant that is often used as of fusing point.Document does not also have the report of polyoxyethylene modified polyacetal now.
Summary of the invention
The objective of the invention is at polyoxymethylene performance shortcomings and the deficiencies in the prior art and a kind of high tenacity is provided, wear-resistant self-lubricating polyformaldehyde material and preparation method thereof, be characterized in utilizing better consistency between polyoxyethylene and the polyoxymethylene, pass through melt blending, extrudate sharply is cooled to below the Tc of polyoxyethylene, speed of cooling is 50～80 ℃/min, between polyoxymethylene spherocrystal inside and spherocrystal, form the polyoxyethylene crystallizing layer, this structure not only can increase reactive force between the polyoxymethylene spherocrystal, improve the impact resistance of polyoxymethylene, can also effectively stop polyoxymethylene to contact with slipping plane, increase the oilness of polyoxymethylene, realize that synchronously polyoxymethylene is toughness reinforcing and lubricated, preparation has the polyoxymethylene blends of high tenacity and high-antiwear self-lubricating, widens the use range of polyoxymethylene.
Purpose of the present invention is realized that by following technical measures wherein said raw material umber is parts by weight except that specified otherwise.
The starting raw material recipe ingredient of high tenacity, wear-resistant self-lubricating polyformaldehyde material is:
Polyformaldehyde resin: 50～99 parts
Peo resin: 50～1 parts
Polyoxymethylene thermo-stabilizer: 0.01～1 part
Formaldehyde absorption agent: 0.01～1 part
Formic acid absorption agent: 0.01～1 part
Wherein the melting index of polyoxymethylene is homopolymer or the multipolymer of 1～25g/10min; The molecular weight of polyoxyethylene is 20,000 to 6,800,000.
The polyoxymethylene thermo-stabilizer is any one in antioxidant 264, antioxidant 1010 or the nylon-6.
The formaldehyde absorption agent is Dyhard RU 100 or trimeric cyanamide.
The formic acid absorption agent is magnesium hydroxide or aluminium hydroxide.
The preparation method of high tenacity, the poly-property formaldehyde materials of wear-resistant self-lubricating
With 99～50 parts of polyoxymethylene in 60～90 ℃ of dryings of temperature 4～6 hours, then with 1～50 part of polyoxyethylene, mix in each 0.01～1 part of adding homogenizer of 0.01～1 part of polyoxymethylene stablizer and formaldehyde and formic acid absorption agent, extrude in 170～200 ℃ of melt blendings of temperature, extrudate sharply is cooled to below the Tc of polyoxyethylene, speed of cooling is greater than 50 ℃/min, obtains having the polyoxyethylene crystallizing layer and is mixed in polyoxymethylene spherocrystal inside or ball intergranular high tenacity, wear-resistant self-lubricating polyformaldehyde material.
Because higher, the spherulite size of polyoxymethylene degree of crystallinity is big, the interface interaction power between the spherocrystal is relatively poor, so its notch sensitivity is bigger, notched Izod impact strength is low.On the microcosmic, polyoxyethylene passes through melt blending, between polyoxymethylene spherocrystal inside and spherocrystal, form the polyoxyethylene crystallizing layer, see for details shown in attached Fig. 1 and 2, this structure not only can increase reactive force between the polyoxymethylene spherocrystal, improve the impact resistance of polyoxymethylene, can also effectively stop polyoxymethylene to contact, increase the oilness of polyoxymethylene with slipping plane; On the macroscopic view, high tenacity polyoxyethylene disperse phase evenly sees for details shown in the accompanying drawing 3, causes crazing or shear zone easily, absorbs more impact energy, improves the blend notched Izod impact strength.In addition, because the fusing point of polyoxyethylene is lower, be about 68 ℃, the heat that produces in the friction process makes the polyoxyethylene fusion, and separates out in the middle of matrix at leisure, forms one deck lubricant film at frictional interface, thereby improve the friction and wear behavior of polyoxymethylene, see for details shown in the accompanying drawing 4.Simultaneously, the tiny abrasive dust that is present in frictional interface has been isolated steel loop surface and body material effectively, has reduced contact area greatly, and plays the effect of solid antifriction anti-wear agent, thereby has effectively improved the friction and wear behavior of polyoxymethylene/polyoxyethylene blend.Therefore polyoxyethylene can effectively improve the notched Izod impact strength of polyoxymethylene simultaneously and reduce frictional coefficient and wear loss.The blend performance data is detailed to be shown in Table 1.
Table 1 is the mechanical property and the friction and wear behavior of pure polyoxymethylene and modified polyacetal of the present invention.
The present invention has the following advantages:
1, polyoxyethylene melt blending, work in-process is controlled its morphological structure, improves the toughness and the friction and wear behavior of polyoxymethylene simultaneously;
2, the peo resin consumption is few, and the production cost of polyformaldehyde composite material is lower;
3, this method technology is simple, easy to implement.
Description of drawings
Fig. 1 is the polarized light microscopy photo that polyoxyethylene forms polyoxyethylene sheet crystal layer in polyoxymethylene/polyoxyethylene blend in polyoxymethylene spherocrystal inside
Fig. 2 is the polarized light microscopy photo that polyoxyethylene forms polyoxyethylene sheet crystal layer in polyoxymethylene/polyoxyethylene blend between the polyoxymethylene spherocrystal
Fig. 3 is the dispersive SEM photo of polyoxyethylene in the polyoxymethylene matrix in polyoxymethylene/polyoxyethylene blend
Fig. 4 is the SEM photo that polyoxyethylene is separated out from matrix in polyoxymethylene/polyoxyethylene blend friction process
Embodiment
Below by embodiment the present invention is carried out concrete description; be necessary to be pointed out that once more that present embodiment only is used for the present invention is further specified; can not be interpreted as limiting the scope of the invention, the person skilled in the art in this field can make some nonessential improvement and adjustment according to the content of foregoing invention:
Embodiment 1
With 396g copoly type polyoxymethylene in 90 ℃ of baking ovens of temperature after dry 4 hours, with molecular weight be 20,000 polyoxyethylene 4g, each 1.2g of antioxidant 264, aluminium hydroxide and trimeric cyanamide, add in the homogenizer and mix, extrude in 170 ℃ of following melt blendings of temperature again, extrudate sharply is cooled to below the Tc of polyoxyethylene, speed of cooling is 60 ℃/min, obtains having the polyformaldehyde material that the polyoxyethylene crystallizing layer is mixed in the structure of polyoxymethylene spherocrystal inside.Its notched Izod impact strength is 7.5kJ/m
2, tensile strength is 54MPa, and elongation at break is 50%, and frictional coefficient is 0.21, and the polishing scratch width is 4.5mm.
Embodiment 2
With 360g copoly type polyoxymethylene in 90 ℃ of baking ovens of temperature dry 6 hours, with the 40g molecular weight 500,000 peo resin, 2g antioxidant 1010,2g Dyhard RU 100,1.5g after mixing in the magnesium hydroxide adding homogenizer, under 210 ℃ of temperature, extrude by melt blending, extrudate sharply is cooled to below the Tc of polyoxyethylene, speed of cooling is 50 ℃/min, obtains having the polyformaldehyde material that the polyoxyethylene crystallizing layer is mixed in structure between the polyoxymethylene spherocrystal.Its notched Izod impact strength is 16kJ/m
2, tensile strength is 43MPa, and elongation at break is 82%, and frictional coefficient is 0.17, and the polishing scratch width is 3mm.
Embodiment 3
It with the 80g molecular weight 6,800,000 peo resin, with the copoly type polyoxymethylene of 320g after 90 ℃ of temperature are descended dry 4～6 hours, each 1.8g of nylon-6, magnesium hydroxide and trimeric cyanamide, join mix in the homogenizer after, insert in the twin screw extruder and extrude in 210 ℃ of melt blendings of temperature, extrudate sharply is cooled to below the Tc of polyoxyethylene, speed of cooling is 80 ℃/min, obtains having the polyformaldehyde material that the polyoxyethylene crystallizing layer is mixed in the structure of polyoxymethylene spherocrystal inside.Its notched Izod impact strength is 14kJ/m
2, tensile strength is 45MPa, and elongation at break is 75%, and frictional coefficient is 0.18, and the polishing scratch width is 4.03mm.
Table 1 is the mechanical property and the friction and wear behavior of pure polyoxymethylene and modified polyacetal of the present invention
Claims (5)
1, a kind of high tenacity, wear-resistant self-lubricating polyformaldehyde material is characterized in that the recipe ingredient of this polyformaldehyde material is by weight:
50～99 parts of polyoxymethylene
50～1 parts of polyoxyethylenes
0.01～1 part of polyoxymethylene thermo-stabilizer
0.01～1 part in formaldehyde absorption agent
0.01～1 part in formic acid absorption agent
Wherein the melting index of polyoxymethylene is homopolymer or the multipolymer of 1～25g/10min; The molecular weight of polyoxyethylene is 20,000 to 6,800,000.
2, high tenacity, wear-resistant self-lubricating polyformaldehyde material according to claim 1 is characterized in that the polyoxymethylene thermo-stabilizer is any one in antioxidant 264, antioxidant 1010 or the nylon-6.
3, high tenacity, wear-resistant self-lubricating polyformaldehyde material according to claim 1 is characterized in that the formaldehyde absorption agent is Dyhard RU 100 or trimeric cyanamide.
4, high tenacity, wear-resistant self-lubricating polyformaldehyde material according to claim 1 is characterized in that the formic acid absorption agent is magnesium hydroxide or aluminium hydroxide.
5, as the preparation method of high tenacity, wear-resistant self-lubricating polyformaldehyde material as described in one of claim 1～4, it is characterized in that this method may further comprise the steps:
With polyoxymethylene 99～50 weight parts, in 60～90 ℃ of dryings of temperature 4～6 hours, then with polyoxyethylene 1～50 weight part, mix in each 0.01～1 weight part adding homogenizer of polyoxymethylene stablizer 0.01～1 weight part and formaldehyde and formic acid absorption agent, extrude in 170～200 ℃ of melt blendings of temperature, extrudate sharply is cooled to below the Tc of polyoxyethylene, 50～80 ℃/min of speed of cooling obtains having the polyoxyethylene crystallizing layer and is mixed in polyoxymethylene spherocrystal inside or ball intergranular high tenacity, wear-resistant self-lubricating polyformaldehyde material.
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102382417A (en) * | 2011-09-30 | 2012-03-21 | 深圳市科聚新材料有限公司 | Polyoxymethylene stabilizing agent and preparation method thereof |
| CN102108182B (en) * | 2009-12-28 | 2012-12-26 | 上海日之升新技术发展有限公司 | Polyformaldehyde material for transmission and conduction parts and preparation method thereof |
| CN103172969A (en) * | 2013-02-07 | 2013-06-26 | 钭礼俊 | Polyformaldehyde modified material and preparation method thereof |
| CN105504662A (en) * | 2015-12-30 | 2016-04-20 | 成都新柯力化工科技有限公司 | Polyformaldehyde wire material for 3D printing and preparation method thereof |
| CN105597515A (en) * | 2016-01-01 | 2016-05-25 | 东莞市正林化工科技有限公司 | Formaldehyde absorbent and preparing method thereof |
| CN106243611A (en) * | 2016-08-31 | 2016-12-21 | 江苏互胜新材料科技有限公司 | Polyformaldehyde high stable basis master batch and preparation method thereof |
| CN106633609A (en) * | 2016-12-13 | 2017-05-10 | 无锡市四方达高分子材料有限公司 | Abrasion-resistant plastic gear |
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| CN101885896B (en) * | 2010-07-23 | 2012-08-29 | 北京化工大学 | High-toughness wear-resistant polyformaldehyde composition and preparation method thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPH04168144A (en) * | 1990-10-31 | 1992-06-16 | Toray Ind Inc | Polyacetal resin composition |
| CN1176154C (en) * | 2002-12-17 | 2004-11-17 | 四川大学 | Nano composite polyformaldehyde material and its prepn |
| CN1233731C (en) * | 2003-12-16 | 2005-12-28 | 云南云天化股份有限公司 | Modified polyformaldehyde/ thermoplastic polyaminoester elastomer blend and its preparation method and use |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102108182B (en) * | 2009-12-28 | 2012-12-26 | 上海日之升新技术发展有限公司 | Polyformaldehyde material for transmission and conduction parts and preparation method thereof |
| CN102382417A (en) * | 2011-09-30 | 2012-03-21 | 深圳市科聚新材料有限公司 | Polyoxymethylene stabilizing agent and preparation method thereof |
| CN103172969A (en) * | 2013-02-07 | 2013-06-26 | 钭礼俊 | Polyformaldehyde modified material and preparation method thereof |
| CN105504662A (en) * | 2015-12-30 | 2016-04-20 | 成都新柯力化工科技有限公司 | Polyformaldehyde wire material for 3D printing and preparation method thereof |
| CN105597515A (en) * | 2016-01-01 | 2016-05-25 | 东莞市正林化工科技有限公司 | Formaldehyde absorbent and preparing method thereof |
| CN106243611A (en) * | 2016-08-31 | 2016-12-21 | 江苏互胜新材料科技有限公司 | Polyformaldehyde high stable basis master batch and preparation method thereof |
| CN106633609A (en) * | 2016-12-13 | 2017-05-10 | 无锡市四方达高分子材料有限公司 | Abrasion-resistant plastic gear |
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Assignee: Sichuan Senpu Pipe Co., Ltd. Assignor: Sichuan University Contract record no.: 2011510000295 Denomination of invention: Highly ductile, abrasive-wearable self-lubricant polyformaldehyde material and its preparation method Granted publication date: 20080702 License type: Exclusive License Open date: 20070530 Record date: 20110922 |