CN1458187A - Polyester resin composition, polyester resin modifier and resin formed article - Google Patents

Polyester resin composition, polyester resin modifier and resin formed article Download PDF

Info

Publication number
CN1458187A
CN1458187A CN 02119941 CN02119941A CN1458187A CN 1458187 A CN1458187 A CN 1458187A CN 02119941 CN02119941 CN 02119941 CN 02119941 A CN02119941 A CN 02119941A CN 1458187 A CN1458187 A CN 1458187A
Authority
CN
China
Prior art keywords
polyester
tackifier
resin
high molecular
vibrin
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.)
Pending
Application number
CN 02119941
Other languages
Chinese (zh)
Inventor
堀井万平
菅原秀纪
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ANLONG CHEMICALS Co Ltd
Original Assignee
ANLONG CHEMICALS Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by ANLONG CHEMICALS Co Ltd filed Critical ANLONG CHEMICALS Co Ltd
Priority to CN 02119941 priority Critical patent/CN1458187A/en
Priority to CN 200610006240 priority patent/CN1955220A/en
Publication of CN1458187A publication Critical patent/CN1458187A/en
Pending legal-status Critical Current

Links

Images

Abstract

The present invention aims to produce various products with different shapes with polyester resin as main material. Into polyester resin, tackifier with melt flow rate below 20 g/10 min listed in item 4 of JISK7210 table 1 is added to increase the viscosity of the melt. Especially, to regenerated polyester resin, polymerizing agent with functional group capable of reacting with polyester resin is also added together with the tackifier.

Description

Polyester and resin composition, polyester resin modifier and resin forming article
Invention field
The present invention relates to the modified polyester and resin composition of melt viscosity, change the polyester resin modifier of vibrin melt viscosity, and by the formed resin forming article of polyester and resin composition.
Prior art
Because the melt viscosity of vibrin is very low; so in extrusion molding that does not comprise drawing process or injection molded technology; melts hangs because of deadweight from the mouth mould of extrusion shaper or the nozzle of injection molding machine, and the phenomenon that occurs hanging, for the very difficulty that is shaped.Can only be with the extrusion molding that comprises drawing process or injection molded technology or blow molding technology at this for the shaping of vibrin, can only be to be limited to film like, fibrous, container-like but the problem that occurs is the shape of these process formings.As long as comprise in other words: drawing process, according to the molecular orientation of drawing force change vibrin, melt viscosity just uprises, and the phenomenon that hangs of last note just is not easy to take place.
Nearest regeneration for the vibrin molding waste materials such as PET bottle that use, become the problem of concern, because of the thermally treating polyester resin in when regeneration lower molecular weightization that becomes, make melt viscosity become more and more lower, the problems referred to above have become more deep volt attitude.Even for example become the shaping thing, that is the vibrin shaping thing of lower molecular weightization just also, and its physical strength very deterioration that becomes also has a lot of problems in the use.
Always, in order to improve vibrin, particularly the melt viscosity of recycled polyester resin adds vibrin such as containing epoxy group(ing) and makes polymer quantize with the resin that contains the functional group that can react.This method is used always.
But above-mentioned polymer quantification method quantizes that for polymer certain limit is arranged, and the problem that can not obtain sufficient melt viscosity for the extrusion molding of recycled polyester resin is particularly arranged.
Summary of the invention
The objective of the invention is to provide a kind of polyester and resin composition, this polyester and resin composition is formed by vibrin with according to the tackifier of JISK7210 table 1 condition 4 melt flow rate (MFR)s (MFR) below 20g/10 divides, the vibrin of 100 Quality Mgmt Dept is added as far as possible the tackifier of 2~100 Quality Mgmt Dept, under the situation for recycled polyester tree tree, preferably add vibrin and the high molecular agent that contains the functional group that can react again especially.These tackifier and this high molecular agent preferably recently mix with 1: 1~10: 1 quality.Also have, the functional group of this high molecular agent generally is an epoxy group(ing).
And the present invention also provides a kind of polyester resin modifier, this polyester resin modifier contain melt flow rate (MFR) (MFR) below 20g/10 divides tackifier and vibrin and the high molecular agent that contains the functional group that can react.These tackifier are that polypropylene and synthetic rubber mix the polymkeric substance that forms, and these tackifier and high molecular agent recently mix with 6: 4~9: 1 quality as far as possible.
The present invention also provides a kind of resin forming article, and this resin forming article is formed by above-mentioned polyester and resin composition.This resin forming article is manufactured according to extrusion molding or injection molded, and this polyester and resin composition need not to carry out predrying before shaping again, and the moisture that also need not to outgas in shaping is removed and dewatered processing, just may be extruded to be shaped or injection molded.
Below describe the present invention in detail.
Brief description of drawings
Fig. 1 has been to use the chart that concerns between the shearing rate of various tackifier and high molecular agent sample and the melt viscosity.
Fig. 2 has added the chart that concerns between the shearing rate of sample of various amount modifier As and the melt viscosity.
Fig. 3 is the chart that concerns that has added between the shearing rate of sample of various amount properties-correcting agent B and the melt viscosity.
Fig. 4 is the chart that concerns that has added between the forming temperature of sample of various amount modifier As and the helical length.
Fig. 5 is the chart that concerns that has added between the forming temperature of sample of various amount properties-correcting agent B and the helical length.
The embodiment of invention
Vibrin
Vibrin of the present invention is the resulting resin of esterification of the above carboxylic acid of above polyvalent alcohol of binary and binary, such as, ethylene glycol terephthalate (PET) (hereinafter to be referred as PET), butylene terephthalate etc.
The present invention is useful for the recycled polyester resin especially.
Tackifier
Tackifier of the present invention are in order to increase the melt viscosity of vibrin.As such tackifier, will select the resin or the elastomerics of high melt viscosity for use.Following illustration is these tackifier once, as, the elastomerics of polyolefin resins such as polyethylene, polypropylene, ethylene-ethyl acrylate copolymer or elastomerics, styrene-butadiene-styrene block copolymer (SBS), vinylbenzene-polyethylene-butadiene-styrene block copolymer styrenics such as (SEBS), or above-mentioned polyolefin resin and above-mentioned styrenic elastomerics and and elastomeric polymkeric substance.As above-mentioned synthetic rubber, such as being acrylic rubber, isobutylene-isoprene copolymer, polyethylene-polypropylene rubber (EPR, EPDM), silica gel, urethanes, fluoridize class rubber, polysulfide rubber, grafting (modification) rubber, divinyl rubber, synthetic polyisoprene, neoprene, polyisoprene rubber, polyisobutylene rubber, butyl rubber, acrylonitrile-butadiene rubber, styrene butadiene rubbers (SBR), acrylonitrile-butadiene rubber (NSR), pyridine-divinyl rubber, styrene isoprene rubber, vinyl cyanide-neoprene, vinylbenzene-neoprene etc.
As the tackifier that high tackify effect is arranged is polypropylene and above-mentioned elastomeric polymer alloy.And EPR or EPDM or SBR that good intermiscibility is preferably arranged with polypropylene as above-mentioned synthetic rubber.Also have as the polymkeric substance of above-mentioned tackifier as use the recycled polyester resin, under pre-dried situation after the extrusion molding water-cooled, resin is not easy flavescence or caking.
The melt flow rate (MFR) of above-mentioned tackifier (MFR) be according to JISK7210 table 1 condition 4 (190 ℃ of test temperatures, test weight 21.18 (N)) for the measuring method of standard, be 0.5~20g/10 branch, preferred 0.5~10g/10 branch is more preferably 0.5~5g/10 branch.Above-mentioned tackifier normally add 2~100 Quality Mgmt Dept for 100 Quality Mgmt Dept's vibrin, and preferably 3~50 Quality Mgmt Dept are more preferably and add 10~20 Quality Mgmt Dept.Under the situation of addition less than 2 Quality Mgmt Dept of above-mentioned tackifier, the tackify effect is not remarkable, and the phenomenon that the rigidity of goods also has a reduction when surpassing 100 Quality Mgmt Dept occurs.
With regard to the present invention, above-mentioned tackifier not merely are the melt viscosities that increases vibrin, also can be in order to improve its thermotolerance, and shock-resistance, dimensional stability, rigidity etc. and add.
The high molecular agent
As for the present invention, particularly resemble recycled polyester resin this lower molecular weightization, become under the low-down situation for melt viscosity, use the high molecular agent.Mainly use the functional group's of energy and vibrin reaction resin or elastomerics as above-mentioned high molecular agent.
As the functional group of energy and the reaction of polyester material fat, such as, epoxy group(ing), carboxyl, isocyanate group etc. are wherein preferably used and vibrin has the very epoxy group(ing) of hyperergy.As resin that this functional group is arranged or elastomerics ethylene-methyl methacrylate glycidyl ester (GMA) multipolymer, ethylene-acrylic acid copolymer, ethene-ethene copolymers such as different acrylonitrile copolymer are arranged mainly, polypropylene grafted ethene copolymer with the graft copolymerization of above-mentioned ethene copolymer ethene, contain epoxy group(ing) SBS, contain the SEBS of epoxy group(ing), the EEA that contains epoxy group(ing), the SBS that contains carboxyl, the SEBS that contains carboxyl, contain the EEA of carboxyl etc., and the difference of the solubility parameter of above-mentioned high molecular agent and tackifier is preferably in 1.
The tackifier that are used for above-mentioned high molecular agent preferably select to use the tackifier of main chain of the same race.Such as being to resemble under the situation of olefines of polyethylene, EEA, EPR or EPDM-sample for tackifier, ethylene-methyl methacrylate glycidyl ester (GMA) multipolymer, ethylene-acrylic acid copolymer as the high molecular agent, ethene-olefines high molecular agent such as isocyanic acid vinyl ester copolymers are selected, for tackifier is under the situation of SBS or SEBS, the SBS that contains epoxy group(ing), the SEBS that contains epoxy group(ing), the high molecular agent that contains the SBS of carboxyl, the SBS such as SEBS that contains carboxyl or SEBS class is selected.For the addition of the above-mentioned high molecular agent of vibrin 100 Quality Mgmt Dept 0.1~100 Quality Mgmt Dept normally, but 0.3~50 quality height preferably is more preferably 1.0~20 Quality Mgmt Dept.
When the addition of above-mentioned high molecular agent during in discontented 0.1 Quality Mgmt Dept, the high molecular effect can not be given full play to the effect of dissolving mutually for tackifier, but when surpassing 100 Quality Mgmt Dept, and this effect is not significant to be changed and become saturated.
The mixture ratio of mixed above-mentioned tackifier and above-mentioned high molecular agent 1: 1~10: 1 mass ratio preferably usually in above-mentioned vibrin.The addition that is to say the high molecular agent also lacks than tackifier, if addition is more than 1/10 of tackifier, the high molecular effect just can be brought into play fully, if but addition is the equivalent that surpasses tackifier, it is saturated that the polymer effect will become, and extrusion molding is also just hindered.
Polyester resin modifier
Can be modulated into polyester resin modifier to above-mentioned tackifier and above-mentioned high molecular agent mixing.This situation is that the mixture ratio of these tackifier and this polymeric agent is as aforementioned, 1: 1~10: 1, but preferably mix with 6: 4~9: 1 mass ratio.With regard to the best tackifier of above-mentioned properties-correcting agent is above-mentioned polypropylene and elastomeric polymkeric substance, preferably also uses EPR, EPDM, SBR as synthetic rubber.
Other compositions
As for the present invention, in order further to improve the thermotolerance of polyester and resin composition, shock-resistance, dimensional stability, rigidity etc., can add following composition, such as, styrene isoprene rubber (SIR), styrene-ethylene copolymers, poly-(alpha-methyl styrene)-polyhutadiene-(alpha-methyl styrene) multipolymer (α-MeS-B-α-MeS), poly-(alpha-methyl styrene)-polyisoprene-poly-(alpha-methyl styrene), butadiene-styrene copolymer (BS), ethylene-propylene-ethylidene multipolymer, vinyl-vinyl acetate copolymer, ethene-1-butadienecopolymer, ethylene-propylene-ethidine-norbornene copolymer, ethylene-propylene-dicyclopentadiene copolymer, ethylene-propylene-1,4 hexadiene multipolymers, ethene-1-divinyl-ethidine-norbornene copolymer, ethene-1-divinyl-1,4 hexadiene multipolymer, vinyl cyanide-neoprene (NCR), vinylbenzene-neoprene resin or elastomericss such as (SCR), lime carbonate, magnesiumcarbonate, barium sulfate, calcium sulfate, calcium sulfite, calcium phosphate, calcium hydroxide, magnesium hydroxide, aluminium hydroxide, magnesium oxide, titanium dioxide, ferric oxide, zinc oxide, aluminum oxide, silicon-dioxide, diatomite, rhombspar, gypsum, talcum, clay, asbestos, mica, glass fibre, Calucium Silicate powder, wilkinite, white carbon black, black wood charcoal is black, iron powder, aluminium powder, feldspar, blast furnace slag, flying dust (volcanic ash), cement, the weighting agent of zirconia powder etc., fire retardant, antioxidant, antiaging agent, UV light absorber, charged preventor, crystallization promotor, whipping agent, dyestuff, the tinting material of pigment etc.Mentioned component also can be added in the modifier.
(prescription)
The blending means of mentioned component preferably dry type is mixed, and particularly the compound particles granulation of tackifier and high molecular agent, the crushed material of hybrid polyester resin in particle preferably mixes laminar crushed material, then injection molded again.
Described as preceding note for vibrin of the present invention 100 Quality Mgmt Dept, tackifier add more than 3 Quality Mgmt Dept, the high molecular agent is added under the above polyester and resin composition situation of 1 Quality Mgmt Dept, even in the regeneration of the vibrin that contains moisture in the said composition or in forming technology, add water decomposition, and by degraded, this by degraded vibrin also because above-mentioned high molecular agent and by high molecular, and also because its melt viscosity of above-mentioned tackifier also by tackify, so the predrying or degassing in shaping before shaping, moisture remove etc. processing become unnecessary.
Embodiment 1 (new vibrin)
Dicarboxylic acid units is, 100 moles of % of terephthalic acid, diol units is, 98 moles of % of ethylene glycol, glycol ether 2 rubs and shows % and get, the ethylene glycol terephthalate unit is to use (PET) that accounts for 98% mole of the full component unit of repetition, in the prescription of table 1, tackifier A (new LDPE (film grade) (LDPE): MFR 4.0g/10 branch), tackifier B (reactivity-TPO: polypropylene-EPR polymkeric substance, MFR 0.69/10 minute) each self-drying type of above-mentioned tackifier mixes, use the キ ャ ピ ロ ゲ ラ Off of Japan smart machine society system, mouth die orifice footpath 1mm, measure 270 ℃ of temperature, measure melt viscosity under the condition of 300 seconds warm up time, and barrel temperature is 260~270 ℃, mold (mould) temperature: 25~85 ℃ of molding surface, the about 1000kgf/cm of injection pressure 2Condition under injection molded, make the plate of 175mm * 12.7mm, thickness 4mm, and reprocess this plate and make 64mm * 12.7mm, the test film of notch depth 2.54mm (JISK7110) has been measured its shock-resistance.It the results are shown in Table 1.
Table 1
Sample No. (embodiment 1) 1 ?2 ?3 ?4 ?5
PET (Quality Mgmt Dept) 100 ?100 ?100 ?100 ?100
Tackifier (Quality Mgmt Dept) ?A(LDPE) ?10 ?20
B (reactive TPO) ?10 ?20
Melt viscosity ?1.22×10 2sec -1*1 4500 ?5800 ?6200 ?6500 ?7100
?2.43×10 3sec -1*1 3100 ?2400 ?2800 ?2000 ?1900
The IZOD impact value *2(kj/m 2) 2.6 ?5.4 ?6.8 ?5.2 ?6.4
*1: shearing rate *2: according to JISK7110
As shown in table 1, according to the addition of tackifier, the melt viscosity of PET (shearing rate 1.22 * 10 2Sec -1) phenomenon that hangs does not appear when extrusion molding, and increase to that 5000 pools are above, shock-resistance also is enhanced.
Embodiment 2 (recycled polyester resin)
Use is predrying 4 hours PET bottle waste product crushed material under 150 ℃ of conditions, in the prescription of table 2, dry type mixes tackifier A, tackifier B, tackifier C (EEA, the MFR0.6g/10 branch), tackifier D (SEBS, MFR 2.3g/10 branch) injection molded and under the same condition of high molecular agent A (SBS that contains epoxy group(ing)) tackifier, high molecular agent B (styrene-grafted ethene-GMA multipolymer), high molecular agent C (ethene-GMA multipolymer) and embodiment 1, make same test film, and similarly measured rerum natura with embodiment 1.It the results are shown in Table 2.
Table 2
Sample No. (embodiment 2) ????1 ??2 ????3 ????4 ????5 ????6 ????7 ????8 ????9 ????10
Regenerative PET (Quality Mgmt Dept) ????100 ??100 ????100 ????100 ????100 ????100 ????100 ????100 ????100 ????100
Tackifier (Quality Mgmt Dept) ????A(LDPE) ??14 ????13 ????7
B (reactive TPO) ????14 ????14 ????1 ????7
????C(EEA) ????14 ????13 ????7
????D(SEBS) ????14 ????1 ????7
High molecular agent (Quality Mgmt Dept) A (SBS that contains epoxy group(ing)) ??4 ????4 ????4 ????4
????B(PS-g-EGMA) ????4 ????4 ????4
????C(EGMA) ????4 ????4
Tackifier: high molecular agent (recipe ratio) ???7∶2 ??7∶2 ????7∶2 ????7∶2 ????7∶2 ????7∶2 ????7∶2 ????7∶2 ????7∶2 ????7∶2
Melt viscosity (pool) ????1.22×10 2sec -1*3 ???1380 ??3240 ????4440 ????5200 ????4380 ????3460 ????4810 ????3960 ????4210 ????4100
????2.43×10 3sec -1*3 ???930 ??830 ????1490 ????1500 ????1400 ????870 ????1120 ????1210 ????920 ????1080
The IZOD impact value *4(kj/m 2) ???1.4 ??7.8 ????5.1 ????5.2 ????7.0 ????5.9 ????7.6 ????5.8 ????5.6 ????6.4
The xanthochromia of (140 ℃) when dry Have Do not have Do not have Have Have Do not have Have Do not have Do not have
Caking when dry Have Do not have Do not have Have Have Have Have Have Do not have
*3: shearing rate *4: according to JISK7110
Even as shown in table 2, according to the addition of tackifier and high molecular agent by the lower molecular weight change the recycled polyester resin, its melt viscosity (shearing rate 1.22 * 10 2Sec -1) also be increased, and shock-resistance is also increased substantially.Be used as the sample No.3 of the reactivity-TPO of tackifier use in addition, 4 and 10 when drying, does not have xanthochromia, caking phenomenon also do not occur.
With regard to above sample NO.1,2,3,4,6,8 and 10 change its shearing rate (Sec separately -1), measure its melt viscosity separately then.It the results are shown in Table 3 and Fig. 1.
Table 3
Melt viscosity (pool)
Sample No. (embodiment 2)
?1 ?2 ?3 ?4 ?6 ?8 ?10
?1.22×10 1sec -1 ?2060 ?15500 ?8490 ?7380 ?9250 ?12200 ?13520
?2.43×10 1sec -1 ?1110 ?9150 ?4560 ?7350 ?4890 ?7830 ?6040
?6.08×10 1sec -1 ?1160 ?4840 ?5160 ?6140 ?2320 ?5030 ?4860
?1.22×10 2sec -1 ?1380 ?3240 ?4440 ?5200 ?3460 ?4810 ?4210
?2.43×10 2sec -1 ?1310 ?2460 ?3540 ?4120 ?2520 ?3280 ?3680
?6.08×10 2sec -1 ?1210 ?1760 ?2700 ?2830 ?1640 ?1950 ?2210
?1.22×10 3sec -1 ?1100 ?1270 ?2100 ?2130 ?1230 ?1600 ?1930
?2.43×10 3sec -1 ?930 ?830 ?1490 ?1500 ?870 ?1120 ?920
The phenomenon that hangs (during injection molded) Have Do not have Do not have Do not have Do not have Do not have Do not have
As table 3 and shown in Figure 1, sample No.2 of the present invention, 3,4,6,8 and 10 shearing rate near 0 state under, compared with the sample No.1 that do not have to add regenerative PET, appoint and all to have shown higher melt viscosity by a kind of sample, and the phenomenon that hangs of the front end place vibrin of the nozzle when injection molded also is prevented from.Shearing rate when also having relative extrusion molding is near 10 2Sec -1The situation of shearing rate under, sample No.2,3,4,6,8 and 10, compared with sample No.1, any sample is all higher, and when injection molded, the phenomenon that hangs of shaping thing also is prevented from, the possibility that abnormity is shaped also can be predicted.
This that is to say sample No.2,3,4, under 6,8 and 10 the situation, when extruding according to extrusion shaper, thickness is very average, the wire molding is just obtained smoothly, under the situation of sample No.1, the thickness inequality of wire molding, thin part has just become fragment.
On the other hand, relatively the shearing rate during injection molded 10 3Sec -1During above shearing rate, sample No.2, all near the melt viscosity of sample No.1, the formedness of injection molded also can be predicted for 3,4,6,8 and 10 melt viscosity, any sample wherein.
Embodiment 3
Mix above-mentioned tackifier A (LDPE) 72.2 quality %, tackifier D (SEBS) 5.6 quality %), high molecular agent A (SBS that contains epoxy group(ing)) 22.2 quality % modulation polyester modification agent A, remix tackifier B (the 75 quality % of reactivity-TPO), high molecular agent B (styrene-grafted ethene-GMA multipolymer) 25 modulation polyester modification agent B.
Respectively with regard to above-mentioned modifier A and properties-correcting agent B, add 5 quality %, 10 quality %, 15 quality % in the regenerative PET that in embodiment 2, uses, find out the relation of shearing rate and melt viscosity.It the results are shown in Figure 2 and Fig. 3.
As shown in Figures 2 and 3, add modifier A and properties-correcting agent B5 quality %, the phenomenon that hangs just is prevented from, and abnormity is shaped and also becomes possibility, and the formedness of injection molded also can be predicted.
Also have, aspect the regenerative PET that has added modifier A and properties-correcting agent B, under the condition of 260~280 ℃ of scopes of forming temperature, carry out injection molded in the mould that has the spirrillum chamber, determine the helical length in the die cavity, it the results are shown in Figure 4 and Fig. 5.
According to Fig. 4 and Fig. 5, add modifier A and properties-correcting agent B5 weight %, the situation that helical length and nothing are added is more than on an equal basis, also according to modifier A and properties-correcting agent B, show the good flowability of each sample melts in mould, injection molded is not only hindered, and is modified on the contrary.
Embodiment 4
Mainly use following tackifier as tackifier; tackifier A (new LDPE (film grade) (LDPE): MFR 4.0g/10 branch); tackifier B (reactivity-TPO, MFR 0.6g/10 branch); mainly use following high molecular agent as the high molecular agent; high molecular agent A (SBS that contains epoxy group(ing)); high molecular agent B (styrene-grafted ethene-GMA multipolymer EGMA-g-PS) SBS; above-mentioned tackifier and above-mentioned high molecular agent prescription, after the mixing back of combination roller, pulverizing, granulating, modulate polyester resin modifier according to table 4 and table 5.
The waste product crushed material (regenerative PET) of above-mentioned each properties-correcting agent and PET bottle according to the prescription shown in table 4 and the table 5, is carried out that dry type is mixed, fusion is mixed in extrusion shaper then, extrudes ribbon from nozzle at last, in water, cut off again, make apparent granulation with cutting knife.Just not dry each particulate material of filling a prescription, also to measure machine (trade(brand)name Capillo graph) with regard to the melt viscosity that each particle sample uses Japan smart machine company to make, at mouth die orifice footpath 1mm, measure 270 ℃ of temperature, measure melt viscosity under the condition of 300 seconds warm up time.It the results are shown in Table 4 and table 5
210~256 ℃ of barrel temperatures, screw rod; φ 30,2 of reverse directions, full helical (fullflight), L/D=2.5, venting hole (open vent), 100rpm, mouthful mould; 3.5 * 15mm, tape formula mouth mould (ribbon dye), extrusion molding under the condition of buffer layer (breaker strip) is arranged, observe the phenomenon of confirming to hang (the shape volt retentivity of the resin that comes out from the mouth mould according to naked eyes, the situation that hangs that occurs because of deadweight), it the results are shown in Table 4 and table table 5.
Table 4
Sample No. (embodiment 4) ?1 ??2 ?3 ?4 ?5 ??6 ?7 ?8
Regenerative PET (Quality Mgmt Dept) ?100 ??100 ?100 ?100 ?100 ??100 ?100 ?100
Tackifier (Quality Mgmt Dept) ????A(LDPE) ?3 ??10 ?3 ?15 ?20 ??100 ?100
B (reactive TPO) ?3
A (SBS that contains epoxy group(ing)) ?1 ??1 ?3 ?5 ?20 ??10 ?20
????B(PS-g-EGMA) ?1
Tackifier: high molecule ratio agent (recipe ratio) ?3∶1 ?10∶1 ?1∶1 ?3∶1 ?1∶1 ??10∶1 ?5∶1 ?3∶1
Melt viscosity (pool) ????6.08×10 1sec -1*5 ?640 ?960 ?700 ?2170 ?3410 ??3010 ?4120 ?660
????1.22×10 2sec -1*5 ?720 ?850 ?710 ?1370 ?2280 ??2280 ?2830 ?720
????2.43×10 2sec -1*5 ?620 ?720 ?580 ?840 ?1670 ??1560 ?2020 ?540
Extrude situation *5 ?○ ?○ ?○ ?○ ?○ ??○ ?○ ?○
*5: shearing rate
*6: *: the phenomenon that hangs significantly, zero is arranged: the phenomenon that hangs is improved
Table 5
Sample No. (embodiment 4) ??9 ??10 ??11 ??12 ??13 ??14 ??15 ??16
Regenerative PET (Quality Mgmt Dept) ??100 ??100 ??100 ??100 ??100 ??100 ??100 ??100
Tackifier (Quality Mgmt Dept) ?A(LDPE) ??15 ??13
B (reactive TP0) ??15 ??100 ??15 ??7
?D(SEBS) ??15 ??15 ??1 ??7
High molecular agent (Quality Mgmt Dept) A (SBS that contains epoxy group(ing)) ??5 ??5 ??4
?B(PS-g-EGMA) ??5 ??20 ??5 ??5 ??4
Tackifier: high molecule ratio agent (recipe ratio) ??3∶1 ??5∶1 ??3∶1 ??3∶1 ??3∶1 ??3∶1 ??7∶2 ??7∶2
Melt viscosity (pool) ?6.08×10 1sec -1*7 ??3110 ??8800 ??3880 ??4710 ??1730 ??3470 ??2250 ??3920
?1.22×10 2sec -1*7 ??2470 ??6100 ??3140 ??3740 ??1460 ??2650 ??1830 ??3220
?2.43×10 2sec -1*7 ??1210 ??4100 ??2530 ??2840 ??1250 ??1920 ??1410 ??2690
Extrude situation *8 ??○ ??○ ??○ ??○ ??○ ??○ ??○ ??○
*7: shearing rate
*8: *: the phenomenon that hangs significantly, zero is arranged: the phenomenon that hangs is improved
[comparative example)
As the comparative example of the foregoing description, according to the prescription shown in the table 6, and the method mensuration melt viscosity same with the foregoing description, confirm the phenomenon that hangs in extrusion molding, whether to occur.It the results are shown in Table 6.
Table 6
Sample No. (comparative example) ?1 ??2 ???3 ????4 ???5 ????6
Regenerative PET (Quality Mgmt Dept) ?100 ??100 ???100 ????100 ???100 ????100
Tackifier (Quality Mgmt Dept) ??A(LDPE) ???1 ????0.5 ???120 ????300
High molecular agent (Quality Mgmt Dept) A (SBS that contains epoxy group(ing)) ???1 ????1 ???20 ????20
Tackifier: high molecular agent (recipe ratio) ???1∶1 ????1∶2 ???6∶1 ????15∶1
Melt viscosity (pool) ??6.08×10 1sec -1*9 ?1160 ??490 ???420 ????530 ???4980 ????4050
??1.22×10 2sec -1*9 ?1380 ??200 ???540 ????460 ???3270 ????3080
??2.43×10 2sec -1*9 ?1310 ??60 ???500 ????340 ???2360 ????2350
Extrude situation *10 ?○ ??× ???× ????× ???○ ????○
Predrying (150 ℃, 4 hours) Have Do not have Do not have Do not have Do not have Do not have
*9: shearing rate
*10: *: the phenomenon that hangs significantly, zero is arranged: the phenomenon that hangs is improved
The sample No.1 of the comparative example shown in the table 6 has been to use in the thermostat container of 150 ℃ of temperature by predrying 4 hours regenerative PET.
With reference to the result shown in table 4 and the table 5, by pre-dried embodiment (sample No.1~sample No.16), wherein the resin combination of any prescription, the phenomenon that hangs all are not prevented from.
As for the sample NO.2 of the comparative example that does not add tackifier shown in the table 6 and high molecular agent, the sample No.3 that tackifier are discontented with the comparative example of 3 Quality Mgmt Dept, and discontented 3 Quality Mgmt Dept of tackifier, the high molecular agent is at the sample No.4 of the comparative example of the following addition of equivalent, because of all not obtaining necessary melt viscosity through predrying for extrusion molding etc., and the serious phenomenon that hangs appears.
Under the situation of regenerative PET 100 Quality Mgmt Dept being added the above tackifier of 100 Quality Mgmt Dept, (in comparative example sample No.5, be 120 Quality Mgmt Dept, in comparative example sample No.6, be 300 Quality Mgmt Dept), for extrusion molding etc. sufficient melt viscosity has been arranged, as long as resin combination of the present invention has had necessary melt viscosity at extrusion molding etc., necessity that regenerative PET (vibrin) 100 Quality Mgmt Dept are not added most tackifier, the tackifier that added volume on the contrary can make the intermiscibility of tackifier and vibrin worsen on the contrary, the infringement molding (such as, with the molding of comparative example sample No.6 formed thereby) problem of cosmetic look will take place, so do not wish too much to add tackifier.
From the shaping thing of the resin combination formed thereby shown in the foregoing description, the aesthetic property of its outward appearance is good, and should sufficient shock-resistance have been arranged the shaping thing.Even should the shaping thing be that the foaming and molding thing is also passable.
The melt viscosity of vibrin is according to the interpolation of above-mentioned tackifier and modified, particularly to do the lower molecular weight change the recycled polyester resin add the high molecular agent again, its melt viscosity is just increased significantly, the phenomenon that hangs of shaping thing that hangs when phenomenon and extrusion molding of the vibrin that comes out from nozzle when injection molded is just sent out and is prevented from, not only injection molded is kept well, and shock-resistance is also modified.
When the also useful polyester and resin composition that contains tackifier and high molecular agent carries out injection molded or extrusion molding.With regard to unnecessary vibrin is carried out predrying or attract dewatering, that is to say that pre-dried cost of equipment of the expense of needn't deflorating and design have the cost of equipment of the special extrusion shaper of venting hole, and saved dewatered time and trouble.
Thereby only limit in the past laminar, fibrous, the container-like vibrin shaping thing different shape that can be shaped now, the vibrin that particularly is used in the polyester and resin composition of the present invention is regenerating resins such as exhausted PET bottle, so the regeneration rate just improves relatively.

Claims (12)

1, a kind of polyester and resin composition is characterized in that, this polyester and resin composition is by vibrin and formed according to the tackifier of JISK7210 table 1 condition 4 melt flow rate (MFR)s (MFR) below 20g/10 divides.
2, polyester and resin composition as claimed in claim 1, the vibrin of 100 Quality Mgmt Dept added the tackifier of 2~100 Quality Mgmt Dept.
3, polyester and resin composition as claimed in claim 1 or 2, it is characterized in that, in polyester and resin composition, add vibrin again and have the functional group's that can react high molecular agent.
4, polyester and resin composition as claimed in claim 3 is characterized in that, these tackifier and this high molecular agent recently mix with 1: 1~10: 1 quality.
5, as claim 3 or 4 described polyester and resin compositions, this vibrin is the recycled polyester resin.
6, as claim 3 or 4 or 5 described polyester and resin compositions, the functional group of this high molecular agent is an epoxy group(ing).
7, a kind of polyester resin modifier, this polyester resin modifier contain melt flow rate (MFR) (MFR) below 20g/10 divides tackifier and vibrin and the high molecular agent that has the functional group that can react.
8, polyester resin modifier as claimed in claim 7 is characterized in that, these tackifier are that polypropylene and synthetic rubber mix the polymkeric substance that forms.
As claim 7 or 8 described polyester resin modifiers, it is characterized in that 9, these tackifier and high molecular agent recently mix with 6: 4~9: 1 quality.
10, a kind of resin forming article is characterized in that, this resin forming article is to be formed by the described polyester and resin composition of the arbitrary claim of claim 1~6.
11, resin forming article as claimed in claim 10 is characterized in that, this resin forming article is manufactured according to extrusion molding or injection molded.
12, resin forming article as claimed in claim 10, this resin forming article is formed by claim 3 or 4 or 5 described polyester and resin compositions, and that this polyester and resin composition need not to carry out before shaping again is predrying, the moisture that also need not to outgas in shaping is removed the processing of removing with moisture, just can be extruded and be shaped or injection molded.
CN 02119941 2002-05-13 2002-05-13 Polyester resin composition, polyester resin modifier and resin formed article Pending CN1458187A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN 02119941 CN1458187A (en) 2002-05-13 2002-05-13 Polyester resin composition, polyester resin modifier and resin formed article
CN 200610006240 CN1955220A (en) 2002-05-13 2002-05-13 Polyester resin composite and polyester resin medifier and resin molding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 02119941 CN1458187A (en) 2002-05-13 2002-05-13 Polyester resin composition, polyester resin modifier and resin formed article

Related Child Applications (1)

Application Number Title Priority Date Filing Date
CN 200610006240 Division CN1955220A (en) 2002-05-13 2002-05-13 Polyester resin composite and polyester resin medifier and resin molding

Publications (1)

Publication Number Publication Date
CN1458187A true CN1458187A (en) 2003-11-26

Family

ID=29426911

Family Applications (2)

Application Number Title Priority Date Filing Date
CN 02119941 Pending CN1458187A (en) 2002-05-13 2002-05-13 Polyester resin composition, polyester resin modifier and resin formed article
CN 200610006240 Pending CN1955220A (en) 2002-05-13 2002-05-13 Polyester resin composite and polyester resin medifier and resin molding

Family Applications After (1)

Application Number Title Priority Date Filing Date
CN 200610006240 Pending CN1955220A (en) 2002-05-13 2002-05-13 Polyester resin composite and polyester resin medifier and resin molding

Country Status (1)

Country Link
CN (2) CN1458187A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102120868A (en) * 2011-04-08 2011-07-13 扬州三星塑胶有限公司 Toughening process for high-tensile-strength recycled polyester sheet
CN103741326A (en) * 2013-12-17 2014-04-23 江苏金太阳纺织科技有限公司 Method for preparing wear-proof cotton and linen fabric
CN109943903A (en) * 2019-03-14 2019-06-28 宁波三邦超细纤维有限公司 Regenerative environment-friendly superfine fibre and preparation method thereof
CN110004516A (en) * 2019-03-14 2019-07-12 宁波三邦超细纤维有限公司 Regenerative environment-friendly antibacterial functions fiber and preparation method thereof
CN110004517A (en) * 2019-03-14 2019-07-12 宁波三邦超细纤维有限公司 Original liquid coloring regenerative environment-friendly functional fibre and preparation method thereof
CN110042516A (en) * 2019-03-14 2019-07-23 宁波三邦超细纤维有限公司 Coloured Chinese fiber crops composite antibacterial superfine fibre and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101023650B1 (en) * 2008-12-11 2011-03-22 제일모직주식회사 Environmentally Friendly Thermoplastic Resin Composition Using Recycled Polyester Resin

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102120868A (en) * 2011-04-08 2011-07-13 扬州三星塑胶有限公司 Toughening process for high-tensile-strength recycled polyester sheet
CN103741326A (en) * 2013-12-17 2014-04-23 江苏金太阳纺织科技有限公司 Method for preparing wear-proof cotton and linen fabric
CN103741326B (en) * 2013-12-17 2015-03-25 葛小飞 Method for preparing wear-proof cotton and linen fabric
CN109943903A (en) * 2019-03-14 2019-06-28 宁波三邦超细纤维有限公司 Regenerative environment-friendly superfine fibre and preparation method thereof
CN110004516A (en) * 2019-03-14 2019-07-12 宁波三邦超细纤维有限公司 Regenerative environment-friendly antibacterial functions fiber and preparation method thereof
CN110004517A (en) * 2019-03-14 2019-07-12 宁波三邦超细纤维有限公司 Original liquid coloring regenerative environment-friendly functional fibre and preparation method thereof
CN110042516A (en) * 2019-03-14 2019-07-23 宁波三邦超细纤维有限公司 Coloured Chinese fiber crops composite antibacterial superfine fibre and preparation method thereof

Also Published As

Publication number Publication date
CN1955220A (en) 2007-05-02

Similar Documents

Publication Publication Date Title
CN1036142C (en) Cleaning resin composition
CN1482165A (en) Wood plastic foamed material and machine-shaping process thereof
CN1575226A (en) Moulding comprising plastic and reinforced by natural fibre
CN1502652A (en) Reinforcing toughening material of polyolefine/inorganic powder compound material and use thereof
CN114479289B (en) Scratch-resistant polypropylene composite material with high impact resistance and high stripping performance, and preparation method and application thereof
CN1458187A (en) Polyester resin composition, polyester resin modifier and resin formed article
CN106641953A (en) Preparation process of automobile lamp outer cover
JP3042008B2 (en) Blow blow molding
CN1295276C (en) Light diffusion resin composition
JPH0698673B2 (en) Blow hollow molded products
CN105237996B (en) Recycled polycarbonate reinforced and toughened through isomeric crosslinking method and preparation method of recycled polycarbonate
JP2020158699A (en) Method for producing regenerated resin composition
JPH09263667A (en) Vinyl chloride resin composition
JP3961270B2 (en) Method for producing foamed polyester resin molded product
JP3728693B2 (en) Polyester resin composition and hollow profile extrusion molded product
EP3315547A1 (en) Cleaning agent for cleaning polymer processing equipment, method for producing it and its use
JPS6356894B2 (en)
CN1110519C (en) Compositions based on ABS polymerizates or on their blends, and flexible products obtained from these compositions
CA2459283A1 (en) Method and apparatus for stabilizing material physical properties of recyclable bumpers
JP2020158698A (en) Regenerated resin composition
CN1137937C (en) Process for preparing styrene-acrylonitrile-butadiene resin dedicated for dashboard of car
JP3371565B2 (en) Cleaning additives
JP4536269B2 (en) Pencil or pencil-type cosmetics using polyethylene terephthalate resin
CN1099442C (en) Modified polyester
US20040209985A1 (en) Resin composition for injection molding

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
REG Reference to a national code

Ref country code: HK

Ref legal event code: DE

Ref document number: 1060585

Country of ref document: HK

C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C12 Rejection of a patent application after its publication
RJ01 Rejection of invention patent application after publication
REG Reference to a national code

Ref country code: HK

Ref legal event code: WD

Ref document number: 1060585

Country of ref document: HK