JP2006298949A - Resin composition for lactic acid-based resin and its utilization - Google Patents
Resin composition for lactic acid-based resin and its utilization Download PDFInfo
- Publication number
- JP2006298949A JP2006298949A JP2005117791A JP2005117791A JP2006298949A JP 2006298949 A JP2006298949 A JP 2006298949A JP 2005117791 A JP2005117791 A JP 2005117791A JP 2005117791 A JP2005117791 A JP 2005117791A JP 2006298949 A JP2006298949 A JP 2006298949A
- Authority
- JP
- Japan
- Prior art keywords
- lactic acid
- resin
- resin composition
- general formula
- acid resin
- 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
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- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 title claims abstract description 171
- 229920005989 resin Polymers 0.000 title claims abstract description 105
- 239000011347 resin Substances 0.000 title claims abstract description 105
- 239000004310 lactic acid Substances 0.000 title claims abstract description 84
- 235000014655 lactic acid Nutrition 0.000 title claims abstract description 84
- 239000011342 resin composition Substances 0.000 title claims abstract description 44
- 150000001875 compounds Chemical class 0.000 claims abstract description 31
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000004056 anthraquinones Chemical class 0.000 claims abstract description 7
- 125000004450 alkenylene group Chemical group 0.000 claims abstract description 5
- 125000000732 arylene group Chemical group 0.000 claims abstract description 5
- 150000001768 cations Chemical class 0.000 claims abstract description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 5
- 238000002425 crystallisation Methods 0.000 claims description 37
- 230000008025 crystallization Effects 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 11
- 239000008107 starch Substances 0.000 claims description 11
- 235000019698 starch Nutrition 0.000 claims description 11
- 229920000881 Modified starch Polymers 0.000 claims description 9
- 239000004368 Modified starch Substances 0.000 claims description 9
- 235000019426 modified starch Nutrition 0.000 claims description 9
- 229920006230 thermoplastic polyester resin Polymers 0.000 claims description 9
- 229920008262 Thermoplastic starch Polymers 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 230000001737 promoting effect Effects 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 abstract description 6
- 229960000448 lactic acid Drugs 0.000 description 74
- 239000000126 substance Substances 0.000 description 17
- -1 limethylolpropane Chemical compound 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 11
- 238000002156 mixing Methods 0.000 description 11
- 238000000465 moulding Methods 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 9
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 7
- 238000001746 injection moulding Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229920000747 poly(lactic acid) Polymers 0.000 description 7
- 239000004626 polylactic acid Substances 0.000 description 7
- 239000004594 Masterbatch (MB) Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 6
- JVTAAEKCZFNVCJ-REOHCLBHSA-N L-lactic acid Chemical group C[C@H](O)C(O)=O JVTAAEKCZFNVCJ-REOHCLBHSA-N 0.000 description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- JVTAAEKCZFNVCJ-UWTATZPHSA-N D-lactic acid Chemical group C[C@@H](O)C(O)=O JVTAAEKCZFNVCJ-UWTATZPHSA-N 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000000813 microbial effect Effects 0.000 description 4
- 244000005700 microbiome Species 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 229930182843 D-Lactic acid Chemical group 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000000137 annealing Methods 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 229940022769 d- lactic acid Drugs 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 3
- 150000003839 salts Chemical group 0.000 description 3
- 150000005846 sugar alcohols Polymers 0.000 description 3
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical compound O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- MKJXYGKVIBWPFZ-UHFFFAOYSA-L calcium lactate Chemical compound [Ca+2].CC(O)C([O-])=O.CC(O)C([O-])=O MKJXYGKVIBWPFZ-UHFFFAOYSA-L 0.000 description 2
- 239000001527 calcium lactate Substances 0.000 description 2
- 229960002401 calcium lactate Drugs 0.000 description 2
- 235000011086 calcium lactate Nutrition 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 150000002596 lactones Chemical class 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 150000003606 tin compounds Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- YXTDAZMTQFUZHK-ZVGUSBNCSA-L (2r,3r)-2,3-dihydroxybutanedioate;tin(2+) Chemical compound [Sn+2].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O YXTDAZMTQFUZHK-ZVGUSBNCSA-L 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- JJTUDXZGHPGLLC-ZXZARUISSA-N (3r,6s)-3,6-dimethyl-1,4-dioxane-2,5-dione Chemical compound C[C@H]1OC(=O)[C@H](C)OC1=O JJTUDXZGHPGLLC-ZXZARUISSA-N 0.000 description 1
- RKDVKSZUMVYZHH-UHFFFAOYSA-N 1,4-dioxane-2,5-dione Chemical compound O=C1COC(=O)CO1 RKDVKSZUMVYZHH-UHFFFAOYSA-N 0.000 description 1
- SCRCZNMJAVGGEI-UHFFFAOYSA-N 1,4-dioxane-2,5-dione;oxepan-2-one Chemical compound O=C1COC(=O)CO1.O=C1CCCCCO1 SCRCZNMJAVGGEI-UHFFFAOYSA-N 0.000 description 1
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- MLFIYYDKLNZLAO-UHFFFAOYSA-N 2-aminoethane-1,1-diol Chemical compound NCC(O)O MLFIYYDKLNZLAO-UHFFFAOYSA-N 0.000 description 1
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 1
- SKEZDZQGPKHHSH-UHFFFAOYSA-J 2-hydroxypropanoate;tin(4+) Chemical compound [Sn+4].CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O.CC(O)C([O-])=O SKEZDZQGPKHHSH-UHFFFAOYSA-J 0.000 description 1
- KDSNLYIMUZNERS-UHFFFAOYSA-O 2-methylpropanaminium Chemical compound CC(C)C[NH3+] KDSNLYIMUZNERS-UHFFFAOYSA-O 0.000 description 1
- UOBYKYZJUGYBDK-UHFFFAOYSA-N 2-naphthoic acid Chemical compound C1=CC=CC2=CC(C(=O)O)=CC=C21 UOBYKYZJUGYBDK-UHFFFAOYSA-N 0.000 description 1
- ULKFLOVGORAZDI-UHFFFAOYSA-N 3,3-dimethyloxetan-2-one Chemical compound CC1(C)COC1=O ULKFLOVGORAZDI-UHFFFAOYSA-N 0.000 description 1
- LPUBRQWGZPPVBS-UHFFFAOYSA-N 3-butoxypropan-1-amine Chemical compound CCCCOCCCN LPUBRQWGZPPVBS-UHFFFAOYSA-N 0.000 description 1
- JOZZAIIGWFLONA-UHFFFAOYSA-N 3-methylbutan-2-amine Chemical compound CC(C)C(C)N JOZZAIIGWFLONA-UHFFFAOYSA-N 0.000 description 1
- 229940006015 4-hydroxybutyric acid Drugs 0.000 description 1
- JJTUDXZGHPGLLC-IMJSIDKUSA-N 4511-42-6 Chemical compound C[C@@H]1OC(=O)[C@H](C)OC1=O JJTUDXZGHPGLLC-IMJSIDKUSA-N 0.000 description 1
- PHOJOSOUIAQEDH-UHFFFAOYSA-N 5-hydroxypentanoic acid Chemical compound OCCCCC(O)=O PHOJOSOUIAQEDH-UHFFFAOYSA-N 0.000 description 1
- HUKPVYBUJRAUAG-UHFFFAOYSA-N 7-benzo[a]phenalenone Chemical compound C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=CC=CC2=C1 HUKPVYBUJRAUAG-UHFFFAOYSA-N 0.000 description 1
- GDALETGZDYOOGB-UHFFFAOYSA-N Acridone Natural products C1=C(O)C=C2N(C)C3=CC=CC=C3C(=O)C2=C1O GDALETGZDYOOGB-UHFFFAOYSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920000954 Polyglycolide Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- MBIDWOISWGGCJD-UHFFFAOYSA-N [O].[Bi].[Bi] Chemical class [O].[Bi].[Bi] MBIDWOISWGGCJD-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- FZEYVTFCMJSGMP-UHFFFAOYSA-N acridone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3NC2=C1 FZEYVTFCMJSGMP-UHFFFAOYSA-N 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229920003232 aliphatic polyester Polymers 0.000 description 1
- SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 description 1
- OYFUVZBROQZLCL-UHFFFAOYSA-K aluminum;4-tert-butylbenzoate;hydroxide Chemical compound [OH-].[Al+3].CC(C)(C)C1=CC=C(C([O-])=O)C=C1.CC(C)(C)C1=CC=C(C([O-])=O)C=C1 OYFUVZBROQZLCL-UHFFFAOYSA-K 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- GSCLMSFRWBPUSK-UHFFFAOYSA-N beta-Butyrolactone Chemical compound CC1CC(=O)O1 GSCLMSFRWBPUSK-UHFFFAOYSA-N 0.000 description 1
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- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
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Landscapes
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Abstract
Description
本発明は、乳酸系樹脂用樹脂組成物及び前記樹脂組成物を用いて得られる乳酸系樹脂成形品に関する。また、本発明は、乳酸系樹脂の結晶化を促進させる方法に関する。 The present invention relates to a resin composition for a lactic acid resin and a lactic acid resin molded product obtained using the resin composition. The present invention also relates to a method for promoting crystallization of a lactic acid resin.
熱可塑性樹脂は比較的安価で軽量、耐蝕性や加工性に優れていることから、今日では機械部品、精密部品、電気・電子機器部品、日用雑貨類、工業部品、繊維などその用途展開は多岐にわたっている。
近年、従来の熱可塑性樹脂の特徴に加え、微生物によって最終的に水と二酸化炭素に分解される微生物崩壊性の樹脂が広く市場に展開されてきている。微生物崩壊性樹脂は自然界に廃棄前は耐蝕性を有するが、廃棄後は自然界の微生物により最終的に水と二酸化炭素にまで分解される。よって微生物崩壊性樹脂は、従来の難分解性の高分子樹脂と比較して自然循環型の素材であり、環境負荷軽減の観点から今後益々の需要増加が見込まれている。
Thermoplastic resins are relatively inexpensive, lightweight, and have excellent corrosion resistance and processability. Today, their applications such as mechanical parts, precision parts, electrical / electronic equipment parts, daily goods, industrial parts, and textiles are being developed. There are a wide variety.
In recent years, in addition to the characteristics of conventional thermoplastic resins, microbial disintegrating resins that are finally decomposed into water and carbon dioxide by microorganisms have been widely deployed in the market. The microorganism-disintegrating resin has corrosion resistance before being discarded in nature, but after being discarded, it is finally decomposed into water and carbon dioxide by the microorganisms in nature. Therefore, the microbial degradable resin is a natural circulation type material as compared with the conventional hard-to-decompose polymer resin, and an increase in demand is expected in the future from the viewpoint of reducing the environmental load.
非石化資源を原料とした代表的な微生物崩壊性樹脂であるポリ乳酸は、優れた透明性や加工性でフィルムや繊維等でその用途を拡大している。また、ポリ乳酸は結晶性樹脂なので、結晶化度を上げることで耐熱性の向上を図ることができるが、結晶化速度が遅いため、例えば射出成形において成形金型を結晶化可能な温度に設定し、一定時間アニーリングすることによって結晶化させているが、このアニーリング時間が長いという問題があった。このためひとつの成形品において結晶化状態がばらついたり、結晶化可能な温度でアニーリングしても成形品が変形しやすかったり、生産コストの上昇等、乳酸系樹脂の普及を妨げる大きな要因となっている。 Polylactic acid, which is a typical microbial-disintegrating resin made from non-fossil resources, is expanding its application with films, fibers, etc. due to its excellent transparency and processability. In addition, since polylactic acid is a crystalline resin, heat resistance can be improved by increasing the degree of crystallization, but because the crystallization speed is slow, for example, in injection molding, the mold is set to a temperature at which it can be crystallized. However, although it is crystallized by annealing for a certain time, there is a problem that this annealing time is long. For this reason, the crystallized state varies in one molded product, and the molded product is easily deformed even when annealed at a temperature at which crystallization is possible. Yes.
特許文献１では結晶化剤として乳酸カルシウム等の乳酸塩や安息香酸塩が開示されているが、それだけでは結晶化が不十分のため、更にアニーリング工程が必要であった。 Patent Document 1 discloses lactate and benzoate such as calcium lactate as a crystallization agent, but the crystallization is insufficient by itself, so that an annealing step is further required.
特許文献２では、結晶化剤としてタルク、シリカ、乳酸カルシウム等を使用して射出成形を試みたが、結晶化速度が遅い上、成形品が脆いため、耐熱性や耐衝撃性が低かった。
特許文献３で結晶化剤としてポリグリコール酸及びその誘導体を使用しているが、特許文献２の記載と矛盾があり技術的内容を正確に判断できない。
In Patent Document 2, although talc, silica, calcium lactate and the like are used as a crystallization agent, injection molding is attempted. However, since the crystallization speed is slow and the molded product is brittle, heat resistance and impact resistance are low.
In Patent Document 3, polyglycolic acid and its derivatives are used as crystallization agents, but there is a contradiction with the description in Patent Document 2 and the technical contents cannot be judged accurately.
特許文献４には、植物系ワックスを混合溶融し、結晶化させながら成形する技術が開示されているが、結晶化しても成形品の脱型が容易ではなく生産効率が悪い上、成形品の剛性が低かった。 Patent Document 4 discloses a technique of mixing and melting a plant-based wax and crystallizing it. However, even if it is crystallized, it is not easy to remove the molded product and the production efficiency is low. The rigidity was low.
本発明の目的は、優れた成形性及び耐熱性を有する乳酸系樹脂成形品を提供することである。 An object of the present invention is to provide a lactic acid resin molded product having excellent moldability and heat resistance.
本発明者らは前記した課題を解決すべく鋭意研究を重ねた結果、本発明に到ったものである。
即ち、（１）乳酸系樹脂（Ａ）と、一般式（１）で示される化合物とを含む乳酸系樹脂用樹脂組成物である。
一般式（１）
That is, it is a resin composition for a lactic acid resin containing (1) a lactic acid resin (A) and a compound represented by the general formula (1).
General formula (1)
（２）熱可塑性ポリエステル樹脂、澱粉、変性澱粉からなる群から１種以上選択される樹脂（Ｂ）と、一般式（１）で示される化合物とを含む乳酸系樹脂用樹脂組成物である。 (2) A resin composition for a lactic acid resin comprising a resin (B) selected from the group consisting of a thermoplastic polyester resin, starch, and modified starch, and a compound represented by the general formula (1).
（３）乳酸系樹脂（Ａ）と、熱可塑性ポリエステル樹脂、澱粉、変性澱粉からなる群から１種以上選択される樹脂（Ｂ）と、一般式（１）で示される化合物とを含む乳酸系樹脂用樹脂組成物である。 (3) A lactic acid series comprising a lactic acid series resin (A), a resin (B) selected from the group consisting of a thermoplastic polyester resin, starch, and modified starch, and a compound represented by the general formula (1) It is a resin composition for resin.
（４）請求項１〜３いずれか記載の乳酸系樹脂組成物を用いて得られる成形品であって、一般式（１）で示される化合物が０．０１〜５０重量％である乳酸系樹脂成形品である。 (4) A molded product obtained by using the lactic acid resin composition according to any one of claims 1 to 3, wherein the compound represented by the general formula (1) is 0.01 to 50% by weight. It is a molded product.
（５）一般式（１）で示される化合物を用いる乳酸系樹脂の結晶化促進方法である。 (5) A method for promoting crystallization of a lactic acid resin using a compound represented by the general formula (1).
本発明の乳酸系樹脂用樹脂組成物は、乳酸系樹脂（Ａ）と、一般式（１）で示される化合物とを含むので、成形品製造の際に乳酸系樹脂の結晶化が促進できる。 Since the resin composition for lactic acid-based resins of the present invention contains the lactic acid-based resin (A) and the compound represented by the general formula (1), crystallization of the lactic acid-based resin can be promoted during the production of a molded product.
本発明の乳酸系樹脂用樹脂組成物は、熱可塑性ポリエステル樹脂、澱粉、変性澱粉からなる群から１種以上選択される樹脂（Ｂ）と、一般式（１）で示される化合物とを含むので、成形品製造の際に乳酸系樹脂の結晶化が促進できる。 Since the resin composition for lactic acid-based resins of the present invention contains a resin (B) selected from the group consisting of thermoplastic polyester resin, starch and modified starch, and a compound represented by the general formula (1). The crystallization of the lactic acid resin can be promoted during the production of the molded product.
本発明の乳酸系樹脂用樹脂組成物は、乳酸系樹脂（Ａ）と、熱可塑性ポリエステル樹脂、澱粉、変性澱粉からなる群から１種以上選択される樹脂（Ｂ）と、一般式（１）で示される化合物とを含むので、成形品製造の際に乳酸系樹脂の結晶化が促進できる。 The resin composition for a lactic acid resin of the present invention includes a lactic acid resin (A), a resin (B) selected from the group consisting of a thermoplastic polyester resin, starch, and modified starch, and a general formula (1). Therefore, the crystallization of the lactic acid resin can be promoted during the production of a molded product.
上記乳酸系樹脂用樹脂組成物を用いて得られる本発明の成形品は、一般式（１）で示される化合物が０．０１〜５０重量％なので、成形性及び耐熱性が良好である。 The molded product of the present invention obtained using the above resin composition for lactic acid resin has good moldability and heat resistance because the compound represented by the general formula (1) is 0.01 to 50% by weight.
本発明の乳酸系樹脂の結晶化促進方法は、一般式（１）で示される化合物を用いるので、乳酸系樹脂の成形加工工程が短縮でき生産性が優れると共に成形品の成形性及び耐熱性が良好である。 Since the method for promoting crystallization of a lactic acid resin of the present invention uses the compound represented by the general formula (1), the molding process of the lactic acid resin can be shortened, the productivity is excellent, and the moldability and heat resistance of the molded product are improved. It is good.
＜乳酸系樹脂（Ａ）＞
本発明で用いられる乳酸系樹脂（Ａ）は、ポリ乳酸ホモポリマーの他、ポリ乳酸コポリマーを含む。また、ポリ乳酸ホモポリマー及び／又はポリ乳酸コポリマーを主体とするブレンドポリマーであっても良い。
<Lactic acid resin (A)>
The lactic acid resin (A) used in the present invention includes a polylactic acid copolymer in addition to a polylactic acid homopolymer. Further, it may be a blend polymer mainly composed of a polylactic acid homopolymer and / or a polylactic acid copolymer.
乳酸系樹脂（Ａ）の重量平均分子量（Ｍｗ）は、ＧＰＣ分析によるポリスチレン換算で５万〜５０万が好ましく、１０万〜２５万が更に好ましい。重量平均分子量が５万未満では実用上必要な物性が得られない場合があり、一方、重量平均分子量が５０万を超えると、成形性不良になり易い場合がある。 The weight average molecular weight (Mw) of the lactic acid-based resin (A) is preferably 50,000 to 500,000, more preferably 100,000 to 250,000 in terms of polystyrene by GPC analysis. When the weight average molecular weight is less than 50,000, physical properties necessary for practical use may not be obtained. On the other hand, when the weight average molecular weight exceeds 500,000, moldability may be easily deteriorated.
また、乳酸系樹脂（Ａ）におけるＬ−乳酸単位及びＤ−乳酸単位の構成モル比Ｌ／Ｄは、１００／０〜０／１００のいずれであっても良いが、高い融点を得るにはＬ−乳酸またはＤ−乳酸のいずれかの単位を７５モル％以上、更に高い融点を得るにはＬ−乳酸またははＤ−乳酸のいずれかの単位を９０モル％以上含むことが好ましい。 In addition, the constituent molar ratio L / D of the L-lactic acid unit and the D-lactic acid unit in the lactic acid-based resin (A) may be 100/0 to 0/100, but in order to obtain a high melting point, L -It is preferable to contain at least 75 mol% of units of lactic acid or D-lactic acid, and 90 mol% or more of either unit of L-lactic acid or D-lactic acid in order to obtain a higher melting point.
ポリ乳酸コポリマーは、乳酸モノマー又はラクチドと共重合可能な他の成分とが共重合されたものである。他の成分としては、２個以上のエステル結合形成性の官能基を持つジカルボン酸、多価アルコール、ヒドロキシカルボン酸、ラクトン等及びこれらの構成成分より成る各種ポリエステル、各種ポリエーテル、各種ポリカーボネート等が挙げられる。 The polylactic acid copolymer is obtained by copolymerizing a lactic acid monomer or other component copolymerizable with lactide. Other components include dicarboxylic acids having two or more ester bond-forming functional groups, polyhydric alcohols, hydroxycarboxylic acids, lactones, etc., and various polyesters, polyethers, polycarbonates, and the like comprising these components. Can be mentioned.
ジカルボン酸の例としてコハク酸、アジピン酸、アゼライン酸、セバシン酸、テレフタル酸、イソフタル酸等が挙げられる。 Examples of dicarboxylic acids include succinic acid, adipic acid, azelaic acid, sebacic acid, terephthalic acid, isophthalic acid and the like.
多価アルコールの例としてビスフェノールにエチレンオキサイドを付加反応させたものなどの芳香族多価アルコール、エチレングリコール、プロピレングリコール、ブタンジオール、ヘキサンジオール、オクタンジオール、グリセリン、ソルビタン、リメチロールプロパン、ネオペンチルグリコール等の脂肪族多価アルコール、ジエチレングリコール、トリエチレングリコール、ポリエチレングリコール、ポリプロピレングリコール等のエーテルグリコール等が挙げられる。 Examples of polyhydric alcohols include aromatic polyhydric alcohols such as those obtained by addition reaction of bisphenol with ethylene oxide, ethylene glycol, propylene glycol, butanediol, hexanediol, octanediol, glycerin, sorbitan, limethylolpropane, neopentyl glycol And aliphatic glycols such as diethylene glycol, triethylene glycol, polyethylene glycol, and polypropylene glycol.
ヒドロキシカルボン酸の例としてグリコール酸、ヒドロキシブチルカルボン酸、その他特開平６−１８４４１７号公報に記載されているもの等が挙げられる。 Examples of the hydroxycarboxylic acid include glycolic acid, hydroxybutylcarboxylic acid, and others described in JP-A-6-184417.
ラクトンとしてグリコリド、ε−カプロラクトングリコリド、ε−カプロラクトン、β−プロピオラクトン、δ−ブチロラクトン、β−又はγ−ブチロラクトン、ピバロラクトン、δ−バレロラクトン等が挙げられる。 Examples of the lactone include glycolide, ε-caprolactone glycolide, ε-caprolactone, β-propiolactone, δ-butyrolactone, β- or γ-butyrolactone, pivalolactone, and δ-valerolactone.
本発明で用いられる乳酸系樹脂（Ａ）は、従来公知の方法で合成されるものである。すなわち特開平７−３３８６１号公報、特開昭５９−９６１２３号公報、高分子討論会予稿集第４４巻、３１９８−３１９９頁に記載のような乳酸モノマーからの直接脱水縮合、又は乳酸環状二量体ラクチドの開環重合によって合成することができる。 The lactic acid resin (A) used in the present invention is synthesized by a conventionally known method. That is, direct dehydration condensation from a lactic acid monomer as described in JP-A-7-33861, JP-A-59-96123, Polymer Proceedings Proceedings Vol. 44, pages 3198-3199, or lactic acid cyclic dimer Can be synthesized by ring-opening polymerization of lactide.
直接脱水縮合を行う場合、Ｌ−乳酸、Ｄ−乳酸、ＤＬ−乳酸、又はこれらの混合物のいずれの乳酸を用いても良い。また、開環重合を行う場合においてもＬ−ラクチド、Ｄ−ラクチド、ＤＬ−ラクチド、ｍｅｓｏ−ラクチド、又はこれらの混合物いずれのラクチドを用いても良い。 When performing direct dehydration condensation, any lactic acid of L-lactic acid, D-lactic acid, DL-lactic acid, or a mixture thereof may be used. Moreover, when performing ring-opening polymerization, you may use the lactide of any of L-lactide, D-lactide, DL-lactide, meso-lactide, or these mixtures.
ラクチドの合成、精製及び重合操作は、例えば米国特許４０５７５３７号明細書、公開欧州特許出願第２６１５７２号明細書、Ｐｏｌｙｍｅｒ Ｂｕｌｌｅｔｉｎ,１４,４９１−４９５（１９８５）及びＭａｋｒｏｍｏｌ Ｃｈｅｍ, １８７, １６１１−１６２８ （１９８６）等の文献に様々に記載されている。 Lactide synthesis, purification and polymerization procedures are described, for example, in U.S. Pat. ) And the like.
この重合反応に用いる触媒は特に限定されるものではなく、公知の乳酸重合用触媒を用いることができる。例えば乳酸スズ、酒石酸スズ、ジカプリル酸スズ、ジラウリル酸スズ、ジパルミチン酸スズ、ジステアリン酸スズ、ジオレイン酸スズ、α−ナフトエ酸スズ、β−ナフトエ酸スズ、オクチル酸スズ等のスズ系化合物、粉末スズ、酸化スズ； 亜鉛末、ハロゲン化亜鉛、酸化亜鉛、有機亜鉛系化合物； テトラプロピルチタネート等のチタン系化合物； ジルコニウムイソプロポキシド等のジルコニウム系化合物； 三酸化アンチモン等のアンチモン系化合物； 酸化ビスマス(III) 等のビスマス系化合物； 酸化アルミニウム、アルミニウムイソプロポキシド等のアルミニウム系化合物等を挙げることができる。 The catalyst used for this polymerization reaction is not particularly limited, and a known catalyst for lactic acid polymerization can be used. For example, tin compounds such as tin lactate, tin tartrate, dicaprylate, dilaurate, dipalmitate, tin distearate, dioleate, tin α-naphthoate, tin β-naphthoate, tin octylate, powder Tin powder, zinc oxide, zinc oxide, organic zinc compounds; titanium compounds such as tetrapropyl titanate; zirconium compounds such as zirconium isopropoxide; antimony compounds such as antimony trioxide; bismuth oxide Bismuth compounds such as (III); Aluminum compounds such as aluminum oxide and aluminum isopropoxide.
これらの中でも、スズ又はスズ化合物からなる触媒が活性の点から特に好ましい。これらの触媒の使用量は、例えば開環重合を行う場合、ラクチドに対して０．００１〜５重量％程度が好ましい。 Among these, a catalyst made of tin or a tin compound is particularly preferable from the viewpoint of activity. For example, when ring-opening polymerization is performed, the amount of these catalysts used is preferably about 0.001 to 5% by weight with respect to lactide.
重合反応は上記触媒の存在下、触媒種によって異なるが、通常１００〜２２０℃の温度で行うことができる。また、特開平７−２４７３４５号公報に記載のような２段階重合を行うことも好ましい。 Although the polymerization reaction varies depending on the type of catalyst in the presence of the catalyst, it can usually be carried out at a temperature of 100 to 220 ° C. It is also preferable to carry out two-stage polymerization as described in JP-A-7-247345.
本発明において、乳酸系樹脂（Ａ）は、乳酸系樹脂用樹脂組成物においては基材樹脂として、乳酸系樹脂成形品においては希釈樹脂として用いられる。 In the present invention, the lactic acid resin (A) is used as a base resin in a resin composition for a lactic acid resin, and as a diluted resin in a lactic acid resin molded article.
＜樹脂（Ｂ）＞
本発明における樹脂（Ｂ）は、熱可塑性ポリエステル樹脂、澱粉、変性澱粉からなる群から１種以上選択されたものである。
熱可塑性ポリエステル樹脂としては、脂肪族ポリエステル系樹脂の他、芳香族ポリエステル、微生物または植物より合成されたポリエステル樹脂等が挙げられる。
<Resin (B)>
The resin (B) in the present invention is one or more selected from the group consisting of thermoplastic polyester resin, starch, and modified starch.
Examples of the thermoplastic polyester resin include aliphatic polyester resins, aromatic polyesters, polyester resins synthesized from microorganisms or plants, and the like.
澱粉または変性澱粉としては、とうもろこし、米、芋、馬鈴薯、麦等から得られる澱粉、またはその澱粉に天然油脂等を共重合させたもの、あるいは澱粉を主成分としてラクトース、グルコース等の糖類、糖蜜、カゼイン等の微生物の摂取し好適な有機物質で修飾されたものが挙げられる。 As starch or modified starch, starch obtained from corn, rice, rice bran, potato, wheat, or the like, or a product obtained by copolymerizing starch with natural fats and oils, or sugars such as lactose or glucose, molasses mainly composed of starch And those modified with organic substances suitable for ingestion of microorganisms such as casein.
樹脂（Ｂ）の例として、具体的には市販された微生物崩壊性樹脂等が挙げられる。例えば昭和高分子社製や日本触媒社製のポリブチレンサクシネート、ポリエチレンサクシネート、ポリブチレンサクシネートアジペート、ダイセル化学社製のポリカプロラクトン、モンサント社製のポリ（３−ヒドロキシ酪酸−ＣＯ−３−ヒドロキシ吉草酸）（Ｐ（３ＨＢ−３ＨＶ））やポリ（３−ヒドロキシ酪酸−ＣＯ−４−ヒドロキシ酪酸）（Ｐ（３ＨＢ−４ＨＢ））やポリ（３−ヒドロキシ酪酸−ＣＯ−３−ヒドロキシプロピオネート）（Ｐ（３ＨＢ−３ＨＰ））、三菱ガス化学社製のユーペック（ポリエステルポリカーボネート）、日本コーンポール社製変性澱粉樹脂等が挙げられる。 Specific examples of the resin (B) include commercially available microbial disintegrating resins. For example, polybutylene succinate, polyethylene succinate, polybutylene succinate adipate manufactured by Showa Polymer Co., Ltd. or Nippon Shokubai Co., Ltd., polycaprolactone manufactured by Daicel Chemical Industries, poly (3-hydroxybutyric acid-CO-3- Hydroxyvaleric acid (P (3HB-3HV)) and poly (3-hydroxybutyric acid-CO-4-hydroxybutyric acid) (P (3HB-4HB)) and poly (3-hydroxybutyric acid-CO-3-hydroxypropio) Nate) (P (3HB-3HP)), Upec (polyester polycarbonate) manufactured by Mitsubishi Gas Chemical Company, modified starch resin manufactured by Nippon Corn Pole, and the like.
＜一般式（１）で示される化合物＞
本発明においては、一般式（１）で示される化合物を乳酸系樹脂の結晶化剤として用いる。
一般式（１）
In the present invention, the compound represented by the general formula (1) is used as a crystallization agent for a lactic acid resin.
General formula (1)
Ｑとして表される化合物としては置換基を有していてもよい複素環、または置換基を有していてもよい芳香族多環、または置換基を有していてもよいアントラキノンを表す。
例えばナフタレン、アントラセン、フェナンスレン、ピレン、クリセン、インドール、チアゾール、ベンズイミダゾール、キノリン、アクリドン、アントラキノン、フェノチアジン、キナゾリン、カルバゾール、ベンザンスロン、ペリレン等が挙げられる。
The compound represented by Q represents a heterocyclic ring which may have a substituent, an aromatic polycycle which may have a substituent, or an anthraquinone which may have a substituent.
Examples include naphthalene, anthracene, phenanthrene, pyrene, chrysene, indole, thiazole, benzimidazole, quinoline, acridone, anthraquinone, phenothiazine, quinazoline, carbazole, benzanthrone, and perylene.
Ａは直接結合、または−Ｏ−、−ＳＯ２−、−ＣＯ−、−Ｓ−、−ＣＯＮＨ−、−ＳＯ２ＮＨ−で置換されても良い炭素数１〜２０で構成された、アルキレン基、アルケニレン基、あるいはアリーレン基を表す。 A is a direct bond or an alkylene group composed of 1 to 20 carbon atoms which may be substituted with —O—, —SO 2 —, —CO—, —S—, —CONH— or —SO 2 NH—. Represents an alkenylene group or an arylene group.
Ｚは−ＳＯ３Ｍ、−ＣＯＯＭを表し、Ｍは１〜３価のカチオンの一当量を表し、例えば水素原子、ナトリウム、カリウム、カルシウム、バリウム、マンガン、ニッケル、ストロンチウム等の金属あるいはジメチルアンモニウム、トリメチルアンモニウム、ジエチルアンモニウム、トリエチルアンモニウム、ヒドロキシエチルアンモニウム、ジヒドロキシエチルアンモニウム、２−エチルヘキシルアンモニウム、ピリジニウムピペリジニウム、ジメチルアミノプロピルアンモニウム、モルフォリニウム、ラウリルアンモニウム、ステアリルアンモニウム、オレイルアンモニウム、ヘキシルアンモニウム、１，２−ジメチルプロピルアンモニウム、ブチルアンモニウム、イソブチルアンモニウム、ブトキシプロピルアンモニウム、デシルオキシプロピルアンモニウム等が挙げられる。 Z represents —SO 3 M, —COOM, and M represents one equivalent of a monovalent to trivalent cation, such as a metal such as a hydrogen atom, sodium, potassium, calcium, barium, manganese, nickel, strontium, or dimethylammonium, Trimethylammonium, diethylammonium, triethylammonium, hydroxyethylammonium, dihydroxyethylammonium, 2-ethylhexylammonium, pyridiniumpiperidinium, dimethylaminopropylammonium, morpholinium, laurylammonium, stearylammonium, oleylammonium, hexylammonium, 1, 2-dimethylpropylammonium, butylammonium, isobutylammonium, butoxypropylammonium, decyloxy B pills and ammonium.
一般式（１）の具体的な化合物を表１に挙げた。これらの造塩物も用いることができる。結晶化促進剤は成形品における着色の自由が広がるので、無色または着色程度が低い方がより好ましい。例えば、表１に記載の化合物記号（ａ）のアルミニウム塩は薄いレモン色であり好ましく用いられる。 Specific compounds of the general formula (1) are listed in Table 1. These salt forms can also be used. The crystallization accelerator is more colorless or has a lower degree of coloring because the freedom of coloring in the molded product is widened. For example, the aluminum salt of the compound symbol (a) shown in Table 1 has a light lemon color and is preferably used.
＜その他の成分＞
本発明の乳酸系樹脂用樹脂組成物または乳酸系樹脂成形品には、必要に応じて着色剤、酸化防止剤、紫外線吸収剤、光安定剤、熱安定剤、難燃剤、架橋剤等の通常プラスチック加工の際に常用されている添加剤を加える事が出来る。また、使用し得る着色剤に特に制限はなく、例えばカーボンブラックアゾ、ジスアゾ、キナクリドン、アントラキノン、フラバントロン、ペリレン、ジオキサジン、縮合アゾ、アゾメチン、又はメチン系等の各種有機顔料等が挙げられる。
<Other ingredients>
The resin composition for a lactic acid resin or a lactic acid resin molded product of the present invention usually contains a colorant, an antioxidant, an ultraviolet absorber, a light stabilizer, a heat stabilizer, a flame retardant, a crosslinking agent, etc. as necessary. Additives commonly used in plastic processing can be added. The colorant that can be used is not particularly limited, and examples thereof include carbon black azo, disazo, quinacridone, anthraquinone, flavantron, perylene, dioxazine, condensed azo, azomethine, and methine-based various organic pigments.
さらに本発明における乳酸系樹脂組成物には、必要に応じて、従来公知の可塑剤、酸化防止剤、熱安定剤、光安定剤、紫外線吸収剤、顔料、着色剤、各種フィラー、帯電防止剤、離型剤、香料、滑剤、難燃剤、発泡剤、充填剤、抗菌・抗カビ剤、他の核形成剤等の各種添加剤が配合されていても良い。 Further, in the lactic acid resin composition in the present invention, conventionally known plasticizers, antioxidants, heat stabilizers, light stabilizers, ultraviolet absorbers, pigments, colorants, various fillers, antistatic agents are optionally added. Various additives such as mold release agents, fragrances, lubricants, flame retardants, foaming agents, fillers, antibacterial / antifungal agents, and other nucleating agents may be blended.
＜乳酸系樹脂用樹脂組成物＞
本発明の乳酸系樹脂用樹脂組成物における基材樹脂としては、前記した乳酸系樹脂（Ａ）、樹脂（Ｂ）、または乳酸系樹脂（Ａ）と樹脂（Ｂ）の組み合わせの３種類がある。更にこれらの樹脂以外の樹脂も必要に応じて添加することができる。
本発明の乳酸系樹脂用樹脂組成物は、上記の基材樹脂と、一般式（１）で示される化合物とを配合し、エクストルーダー、ニーダー、ロールミル、バンバリミキサー等の混練機を用いて得られる。
本発明の乳酸系樹脂用樹脂組成物は、成形品製造の際に希釈樹脂（乳酸系樹脂（Ａ））と混合して成形されるいわゆるマスターバッチであってもよいし、また、そのままの組成で成形されるコンパウンドであってもよい。
乳酸系樹脂用樹脂組成物の形状は特に規定しないが、マスターバッチとして使用される場合は共に混合される希釈樹脂の形状と同一であれば加工時の分離発生防止などの点から好ましい。
<Resin composition for lactic acid resin>
The base resin in the resin composition for a lactic acid resin of the present invention includes the above-described three types of lactic acid resin (A), resin (B), or a combination of the lactic acid resin (A) and the resin (B). . Furthermore, resins other than these resins can be added as necessary.
The resin composition for a lactic acid-based resin of the present invention is obtained by blending the above base resin and the compound represented by the general formula (1) and using a kneader such as an extruder, kneader, roll mill, or Banbury mixer. It is done.
The resin composition for a lactic acid resin of the present invention may be a so-called masterbatch that is molded by mixing with a diluted resin (lactic acid resin (A)) during the production of a molded product, or may be a composition as it is. It may be a compound molded in
The shape of the resin composition for lactic acid-based resins is not particularly specified, but when used as a masterbatch, it is preferable from the standpoint of preventing separation during processing if it is the same as the shape of the diluted resin mixed together.
本発明の乳酸系樹脂用樹脂組成物における一般式（１）で示される化合物の含有量は、樹脂組成物や成形品の製造が容易である観点から５０重量％以下が好ましい。より好ましくは３０重量％以下であり、０．０１〜１０重量％の範囲が特に好ましい。 The content of the compound represented by the general formula (1) in the resin composition for a lactic acid resin of the present invention is preferably 50% by weight or less from the viewpoint of easy production of the resin composition and molded product. More preferably, it is 30 weight% or less, and the range of 0.01-10 weight% is especially preferable.
＜乳酸系樹脂成形品＞
本発明の乳酸系樹脂成形品は、乳酸系樹脂用樹脂組成物がマスターバッチの場合は、成形品製造の際に希釈樹脂として乳酸系樹脂（Ａ）と混合して成形される。また、コンパウンドの場合はそのままの組成で成形される。
<Lactic acid resin molded products>
When the resin composition for lactic acid resin is a master batch, the lactic acid resin molded product of the present invention is molded by mixing with the lactic acid resin (A) as a dilution resin when the molded product is produced. In the case of a compound, it is molded with the composition as it is.
本発明の乳酸系樹脂成形品における一般式（１）で示される化合物の含有量は０．０１〜５０重量％である。この範囲であれば、乳酸系樹脂の結晶化を促進させることができる。０．０１重量％未満では、結晶化ピーク温度や結晶化熱量は確認できるものの再現性があまりない上冷却時間も長くなり成形性が良好でない。より好ましくは０．０１〜３０重量％であり、０．０１〜１０重量％の範囲が特に好ましい。 The content of the compound represented by the general formula (1) in the lactic acid resin molded product of the present invention is 0.01 to 50% by weight. Within this range, crystallization of the lactic acid resin can be promoted. If it is less than 0.01% by weight, the crystallization peak temperature and the amount of crystallization heat can be confirmed, but the reproducibility is not so much and the cooling time becomes long, and the moldability is not good. More preferably, it is 0.01-30 weight%, and the range of 0.01-10 weight% is especially preferable.
一般に射出成形による乳酸系樹脂成形品は、成形品を成形するときに成形金型を結晶化可能な温度に設定し、一定時間アニーリングすることによって結晶化させている。樹脂が結晶化したか否かは、走査型示差熱量計（ＤＳＣ）における発熱ピーク（結晶化ピーク）の有無により分かる。結晶化ピークや結晶化熱量が認められない場合は、結晶化が起こっていないと考えられる。
本発明においては、成形品の組成におけるＤＳＣの結晶化ピーク温度が９０〜１３０℃、更に１００〜１１５℃が好ましい。
In general, a lactic acid-based resin molded product by injection molding is crystallized by setting a molding die to a temperature at which crystallization can be performed and molding it for a certain period of time. Whether or not the resin has crystallized can be determined by the presence or absence of an exothermic peak (crystallization peak) in a scanning differential calorimeter (DSC). When no crystallization peak or heat of crystallization is observed, it is considered that crystallization has not occurred.
In the present invention, the DSC crystallization peak temperature in the composition of the molded product is preferably 90 to 130 ° C, more preferably 100 to 115 ° C.
本発明における結晶化ピーク温度及び結晶化熱量は、走査型示差熱量計（Ｓｅｉｋｏ Ｉｎｓｔｒｕｍｅｎｔｓ Ｉｎｃ社製、ＤＳＣ−６２００）で測定した値である。更に詳しくは、３ｍｇのペレットサンプルを３０℃／分で２０〜２２０℃まで昇温し、さらに１分間保持してサンプルを均質化した後、１０℃／分の速度で５０℃まで降温させ、その過程において結晶化ピーク温度及び結晶化熱量を測定した値である。 The crystallization peak temperature and crystallization heat amount in the present invention are values measured with a scanning differential calorimeter (DSC-6200, manufactured by Seiko Instruments Inc.). More specifically, a 3 mg pellet sample was heated to 20-220 ° C. at 30 ° C./min, held for 1 minute to homogenize the sample, and then cooled to 50 ° C. at a rate of 10 ° C./min. It is the value which measured the crystallization peak temperature and the crystallization heat quantity in the process.
成形品の成形方法は、一般のプラスチックと同様の射出成形、押し出し成形、中空成形、回転成形、粉末成形、真空成形、圧縮成形等、公知の方法が挙げられる。 Examples of the molding method of the molded product include known methods such as injection molding, extrusion molding, hollow molding, rotational molding, powder molding, vacuum molding, and compression molding similar to those for general plastics.
成形品の具体例としては機械部品、精密部品、電気・電子機器部品、日用雑貨類、工業部品、繊維、容器、キャップ、フィルム、テープ等が挙げられる。これらは積層構造を有していても良い。更に詳しくは自動車のダッシュボード、コンソール、ドア内張り、ピラー、開閉ハンドルノブ、フロアカーペット、シートカバー等の内装材、バンパー、ドア開閉ハンドルノブ、給油口フタ、フェンダー、ドアミラー、マッドガード等の外装品、弁当箱等が挙げられる。 Specific examples of the molded product include mechanical parts, precision parts, electrical / electronic equipment parts, daily goods, industrial parts, fibers, containers, caps, films, tapes, and the like. These may have a laminated structure. In more detail, interior materials such as automobile dashboards, consoles, door linings, pillars, opening / closing handle knobs, floor carpets, seat covers, bumpers, door opening / closing handle knobs, filler caps, fenders, door mirrors, mudguards, Examples include lunch boxes.
以下に実施例を挙げて本発明をさらに具体的に説明する一般式（２）で示される化合物が、本発明はこれらの実施例に限定されるものではない。実施例中「部」は「重量部」、「％」は「重量％」をいう。
実施例及び比較例における成形品の組成とＤＳＣの値は表２及び表３、成形品の評価結果は表４に示した。
The compound represented by the general formula (2), which further specifically explains the present invention with reference to the following examples, is not intended to limit the present invention. In the examples, “parts” means “parts by weight” and “%” means “% by weight”.
The compositions and DSC values of the molded products in Examples and Comparative Examples are shown in Tables 2 and 3, and the evaluation results of the molded products are shown in Table 4.
[実施例１]
（乳酸系樹脂用樹脂組成物の製造）
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％と、表１に記載の化合物記号（ａ）のアルミニウム塩１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の乳酸系樹脂組成物を得た。
(Production of resin composition for lactic acid resin)
After pre-blending 99% of lactic acid resin (Laysia H-100, manufactured by Mitsui Chemicals) and 1% of the aluminum salt of the compound symbol (a) described in Table 1, the mixture was kneaded and granulated with an extruder, and pelletized. A lactic acid resin composition was obtained.
（成形品の製造）
上記樹脂組成物を６０℃の熱風乾燥機で１２時間乾燥し、射出成形機（東芝機械社製 ＩＳ７５Ｅ 成形温度＝２００℃、金型設定温度１０５℃、射出一次設定圧力＝６０％、冷却固化時間１分間）を用いて成形板（２×３ｍｍ角、厚さ２ｍｍ）を成形した。
(Manufacture of molded products)
The resin composition was dried for 12 hours with a hot air dryer at 60 ° C., and injection molding machine (IS75E manufactured by Toshiba Machine Co., Ltd., molding temperature = 200 ° C., mold set temperature 105 ° C., injection primary set pressure = 60%, cooling solidification time. A molded plate (2 × 3 mm square, 2 mm thickness) was molded using 1 minute).
（評価）
（１）成形品製造前の樹脂組成物（成形品と同じ組成のもの）における結晶化ピーク温度及び結晶化熱量の測定
成形品製造前の、６０℃の熱風乾燥機で１２時間乾燥した後の樹脂組成物について、結晶化ピーク温度及び結晶化熱量を、走査型示差熱量計（Ｓｅｉｋｏ Ｉｎｓｔｒｕｍｅｎｔｓ Ｉｎｃ社製、ＤＳＣ−６２００）で測定した。樹脂組成物３ｍｇのサンプルを３０℃／分で２０〜２２０℃まで昇温し、さらに１分間保持してサンプルを均質化した後、１０℃／分の速度で５０℃まで降温させ、その過程において結晶化ピーク温度、結晶化熱量を測定した。
(Evaluation)
(1) Measurement of crystallization peak temperature and crystallization calorie in resin composition (same composition as molded product) before production of molded product After drying with a hot air dryer at 60 ° C. for 12 hours before production of molded product About the resin composition, the crystallization peak temperature and the crystallization calorie | heat amount were measured with the scanning differential calorimeter (The Seiko Instruments Inc company make, DSC-6200). A sample of 3 mg of the resin composition was heated to 20 to 220 ° C. at 30 ° C./min, held for 1 minute to homogenize the sample, and then cooled to 50 ° C. at a rate of 10 ° C./min. The crystallization peak temperature and crystallization heat quantity were measured.
（２）成形品における成形性
射出成形用金型からの成形品の脱型状態を目視評価した。
良好：脱型が容易。
不良：脱型しない、または脱型するが成形不良。
(2) Moldability in molded product The mold release state of the molded product from the injection mold was visually evaluated.
Good: Demolding is easy.
Defect: Does not demold, or demold, but molding failure.
（３）成形品の耐熱性
簡易的に以下の方法で行った。槽内温度８５℃の熱風オーブン中に、２枚の成形板の２×３ｍｍ角の平滑面同士を重ねて１時間静置した後、２枚の成形板の接触面の付着状態を観察し評価した。
良好：２枚の成形板は付着していない（成形の際に充分結晶化された成形板は耐熱性が向上しているため接触面の溶着が少ない。）。
不良：２枚の成形板は付着している（成形の際に結晶化されていない、または充分でなかった成形板は耐熱性が向上せず接触面の溶着が著しい。）。
(3) Heat resistance of molded product This was simply carried out by the following method. In a hot air oven at 85 ° C. in the tank, the 2 × 3 mm square smooth surfaces of the two molded plates were placed on each other and allowed to stand for 1 hour, and then the adhesion state of the contact surfaces of the two molded plates was observed and evaluated. did.
Good: The two molded plates are not attached (the molded plate sufficiently crystallized at the time of molding has improved heat resistance, so that the contact surface is less welded).
Defective: Two molded plates are adhered (a molded plate that is not crystallized or insufficient during molding does not have improved heat resistance and has a significant contact surface weld).
[実施例２]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９０％と、表１に記載の化合物記号（ａ）のアルミニウム塩１０％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Example 2]
90% of lactic acid resin (Laysia H-100 manufactured by Mitsui Chemicals) and 10% of the aluminum salt of the compound symbol (a) shown in Table 1 were previously blended, and then kneaded and granulated with an extruder, and pelletized. A resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[実施例３]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９．９９％と、表１に記載の化合物記号（ａ）のアルミニウム塩０．０１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Example 3]
A lactic acid resin (Laissia H-100, Mitsui Chemicals, Inc.) 99.99% and an aluminum salt 0.01% of the compound symbol (a) shown in Table 1 were previously blended and then kneaded and granulated with an extruder. A pellet-shaped resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[実施例４]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）５０％と、表１に記載の化合物記号（ａ）のアルミニウム塩５０％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Example 4]
50% lactic acid resin (Laysia H-100 manufactured by Mitsui Chemicals) and 50% aluminum salt of the compound symbol (a) shown in Table 1 were previously blended and then kneaded and granulated with an extruder, and pelletized. A resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[実施例５]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％と、実施例４の樹脂組成物（マスターバッチとして用いた。）１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Example 5]
99% lactic acid resin (Laysia H-100 manufactured by Mitsui Chemicals) and 1% of the resin composition of Example 4 (used as a masterbatch) were blended in advance and then kneaded and granulated with an extruder, and then pelleted. A resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[実施例６]
熱可塑性ポリエステル樹脂（昭和高分子社製 ビオノーレ３００１）５０％と、表１に記載の化合物記号（ａ）のアルミニウム塩５０％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物（マスターバッチ）を得た。
その後、このマスターバッチ１％と、乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Example 6]
After blending in advance 50% of a thermoplastic polyester resin (Bionore 3001 manufactured by Showa Polymer Co., Ltd.) and 50% of the aluminum salt of the compound symbol (a) shown in Table 1, the mixture is kneaded and granulated with an extruder, and pelletized A resin composition (master batch) was obtained.
Thereafter, 1% of the master batch and 99% of lactic acid resin (Lacia H-100 manufactured by Mitsui Chemicals) were blended in advance, and then kneaded and granulated with an extruder to obtain a pellet-shaped resin composition. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[比較例１]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）を６０℃の熱風乾燥機で１２時間乾燥した後、実施例１と同様に行い成形品を得、評価を行った。
[Comparative Example 1]
A lactic acid resin (Laissia H-100 manufactured by Mitsui Chemicals, Inc.) was dried with a hot air dryer at 60 ° C. for 12 hours, and then a molded product was obtained and evaluated in the same manner as in Example 1.
[比較例２]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％と、脂肪酸金属塩系造核材（シェルジャパン社製ＡＬ−ＰＴＢＢＡ）１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Comparative Example 2]
After pre-blending 99% of lactic acid resin (Laisia H-100 made by Mitsui Chemicals) and 1% fatty acid metal salt nucleating material (AL-PTBBA made by Shell Japan), knead and granulate with an extruder, A pellet-shaped resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[比較例３]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％と、モンタン酸ナトリウム塩造核材（クラリアントジャパン社製Ｌｉｃｏｍｏｎｔ ＮａＶ １０１）１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Comparative Example 3]
After pre-blending 99% of lactic acid resin (Laysia H-100 made by Mitsui Chemicals) and 1% sodium montanate nucleating material (Licomont NaV 101 made by Clariant Japan), knead and granulate with an extruder, A pellet-shaped resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[比較例４]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％と、モンタン酸カルシウム塩造核材（クラリアントジャパン社製Ｌｉｃｏｍｏｎ ＣａＶ １０２）１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Comparative Example 4]
After pre-blending 99% of lactic acid resin (Laisia H-100 made by Mitsui Chemicals) and 1% calcium montanate salt nucleating material (Licomon CaV 102 made by Clariant Japan), knead and granulate with an extruder, A pellet-shaped resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[比較例５]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％と、リン酸エステル金属塩系造核材（旭電化工業社製アデカスタブＮＡ１１）１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Comparative Example 5]
After pre-blending 99% of lactic acid resin (Laysia H-100 made by Mitsui Chemicals) and 1% phosphate metal salt nucleating material (Adeka Stub NA11 made by Asahi Denka Kogyo Co., Ltd.), kneading and granulation with an extruder As a result, a pellet-shaped resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[比較例６]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）９９％と、ソルビトール系造核材（新日本理化社製ゲルオールＭＤ）１％を予めブレンドした後、押出機にて混練造粒し、ペレット状の樹脂組成物を得た。その後は実施例１と同様に行い成形品を得、評価を行った。
[Comparative Example 6]
After pre-blending 99% of lactic acid resin (Laysia H-100 made by Mitsui Chemicals) and 1% sorbitol nucleating material (Gerall MD made by Shin Nippon Chemical Co., Ltd.), kneaded and granulated with an extruder, and pelletized A resin composition was obtained. Thereafter, the molded product was obtained in the same manner as in Example 1 and evaluated.
[比較例７]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）を６０℃の熱風乾燥機で１２時間乾燥した後、金型設定温度を１０５℃から３０℃に変更した以外は実施例１と同様に行い成形品を得、評価を行った。
[Comparative Example 7]
Lactic acid-based resin (Laysia H-100, manufactured by Mitsui Chemicals, Inc.) was dried in a hot air dryer at 60 ° C. for 12 hours, and then molded in the same manner as in Example 1 except that the mold setting temperature was changed from 105 ° C. to 30 ° C. The product was obtained and evaluated.
[比較例８]
乳酸系樹脂（三井化学社製 レイシアＨ−１００）を６０℃の熱風乾燥機で１２時間乾燥した後、射出成形の際の冷却固化時間を５分間、１０分間、３０分間に変更した以外は実施例１と同様に行った。しかし、射出成形機シリンダ中に滞留している溶融樹脂が熱劣化していずれも成形できなくなった為、試験を中止した。特に冷却固化時間が長時間のものほど熱劣化度が激しかった。
[Comparative Example 8]
This was carried out except that lactic acid-based resin (Laysia H-100 manufactured by Mitsui Chemicals, Inc.) was dried with a hot air dryer at 60 ° C. for 12 hours, and then the cooling and solidifying time during injection molding was changed to 5 minutes, 10 minutes, and 30 minutes. Performed as in Example 1. However, the test was stopped because the molten resin staying in the cylinder of the injection molding machine could not be molded due to thermal deterioration. In particular, the longer the cooling and solidification time, the more severe the heat degradation.
本発明の乳酸系樹脂成形品は透明性、加工性、微生物崩壊性の他、耐熱性が必要とされる用途にも展開できる。
また、本発明の乳酸系樹脂の結晶化促進方法により、乳酸系樹脂成形品の生産工程が短縮できると共に良好な成形品が得られる。
The lactic acid-based resin molded product of the present invention can be used for applications that require heat resistance in addition to transparency, processability, and microbial disintegration.
In addition, the lactic acid resin crystallization promoting method of the present invention can shorten the production process of the lactic acid resin molded product and obtain a good molded product.
Claims (5)
一般式（１）
General formula (1)
A method for promoting crystallization of a lactic acid resin using a compound represented by the general formula (1).
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| JP2016529375A (en) * | 2013-08-29 | 2016-09-23 | アーケマ・インコーポレイテッド | Biodegradable polymer composition with improved impact resistance |
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| JP2000198908A (en) * | 1999-01-06 | 2000-07-18 | Mitsui Chemicals Inc | Method for molding resin |
| JP2000239498A (en) * | 1999-02-17 | 2000-09-05 | Nippon Shokubai Co Ltd | Polyester resin composition |
| JP2005008712A (en) * | 2003-06-17 | 2005-01-13 | Toray Ind Inc | Automobile part |
| JP2005023260A (en) * | 2003-07-04 | 2005-01-27 | Toray Ind Inc | Electrical/electronic component |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016529375A (en) * | 2013-08-29 | 2016-09-23 | アーケマ・インコーポレイテッド | Biodegradable polymer composition with improved impact resistance |
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