DE10010826A1 - Verfahren zur Reduktion der Wasserdampfpermeabilität von Folien oder Beschichtungen - Google Patents
Verfahren zur Reduktion der Wasserdampfpermeabilität von Folien oder BeschichtungenInfo
- Publication number
- DE10010826A1 DE10010826A1 DE10010826A DE10010826A DE10010826A1 DE 10010826 A1 DE10010826 A1 DE 10010826A1 DE 10010826 A DE10010826 A DE 10010826A DE 10010826 A DE10010826 A DE 10010826A DE 10010826 A1 DE10010826 A1 DE 10010826A1
- Authority
- DE
- Germany
- Prior art keywords
- mixtures
- weight
- acid
- beeswax
- cellulose
- 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.)
- Withdrawn
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 117
- 229920000642 polymer Polymers 0.000 title claims abstract description 74
- 235000013871 bee wax Nutrition 0.000 title claims abstract description 34
- 239000012166 beeswax Substances 0.000 title claims abstract description 34
- 239000001993 wax Substances 0.000 title claims abstract description 32
- 229920002678 cellulose Polymers 0.000 title claims abstract description 29
- 229920002472 Starch Polymers 0.000 title claims abstract description 25
- 235000019698 starch Nutrition 0.000 title claims abstract description 25
- 239000001913 cellulose Substances 0.000 title claims abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 150000002148 esters Chemical class 0.000 title claims abstract description 22
- 239000008107 starch Substances 0.000 title claims abstract description 20
- 238000000576 coating method Methods 0.000 title claims abstract description 18
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 17
- 229920000728 polyester Polymers 0.000 claims abstract description 31
- 238000000034 method Methods 0.000 claims abstract description 26
- 239000000654 additive Substances 0.000 claims abstract description 24
- 125000003118 aryl group Chemical group 0.000 claims abstract description 18
- 230000035699 permeability Effects 0.000 claims abstract description 14
- 230000000996 additive effect Effects 0.000 claims abstract description 10
- 239000002253 acid Substances 0.000 claims description 28
- 150000001875 compounds Chemical class 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000011888 foil Substances 0.000 claims description 12
- 125000001931 aliphatic group Chemical group 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 11
- 150000002009 diols Chemical class 0.000 claims description 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 8
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 8
- 239000012948 isocyanate Substances 0.000 claims description 7
- 150000002513 isocyanates Chemical class 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 claims description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 229920000765 poly(2-oxazolines) Polymers 0.000 claims description 4
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 4
- 229960000834 vinyl ether Drugs 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 239000004952 Polyamide Substances 0.000 claims description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 150000001413 amino acids Chemical class 0.000 claims description 2
- 150000004985 diamines Chemical class 0.000 claims description 2
- 125000001033 ether group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 238000006068 polycondensation reaction Methods 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
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- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 235000010980 cellulose Nutrition 0.000 description 19
- -1 fats Chemical class 0.000 description 16
- 229920003232 aliphatic polyester Polymers 0.000 description 13
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 10
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 8
- 150000001991 dicarboxylic acids Chemical class 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
- 229920002988 biodegradable polymer Polymers 0.000 description 6
- 239000004621 biodegradable polymer Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000000945 filler Substances 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 239000002202 Polyethylene glycol Substances 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 239000001361 adipic acid Substances 0.000 description 5
- 235000011037 adipic acid Nutrition 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 229920001634 Copolyester Polymers 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 229920001400 block copolymer Polymers 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 239000004310 lactic acid Substances 0.000 description 4
- 235000014655 lactic acid Nutrition 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 3
- 150000002596 lactones Chemical class 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 3
- 229920000747 poly(lactic acid) Polymers 0.000 description 3
- 239000012744 reinforcing agent Substances 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 2
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- RKDVKSZUMVYZHH-UHFFFAOYSA-N 1,4-dioxane-2,5-dione Chemical compound O=C1COC(=O)CO1 RKDVKSZUMVYZHH-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- REKYPYSUBKSCAT-UHFFFAOYSA-N 3-hydroxypentanoic acid Chemical compound CCC(O)CC(O)=O REKYPYSUBKSCAT-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- JVTAAEKCZFNVCJ-REOHCLBHSA-N L-lactic acid Chemical compound C[C@H](O)C(O)=O JVTAAEKCZFNVCJ-REOHCLBHSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 229940081735 acetylcellulose Drugs 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 239000007850 fluorescent dye Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 229920005610 lignin Polymers 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 235000010603 pastilles Nutrition 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920001610 polycaprolactone Polymers 0.000 description 2
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- 229920001592 potato starch Polymers 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
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- 239000003381 stabilizer Substances 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
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- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- PVPBBTJXIKFICP-UHFFFAOYSA-N (7-aminophenothiazin-3-ylidene)azanium;chloride Chemical compound [Cl-].C1=CC(=[NH2+])C=C2SC3=CC(N)=CC=C3N=C21 PVPBBTJXIKFICP-UHFFFAOYSA-N 0.000 description 1
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- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- MWZJGRDWJVHRDV-UHFFFAOYSA-N 1,4-bis(ethenoxy)butane Chemical compound C=COCCCCOC=C MWZJGRDWJVHRDV-UHFFFAOYSA-N 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
- 229940043375 1,5-pentanediol Drugs 0.000 description 1
- PVBLJPCMWKGTOH-UHFFFAOYSA-N 1-aminocyclohexan-1-ol Chemical compound NC1(O)CCCCC1 PVBLJPCMWKGTOH-UHFFFAOYSA-N 0.000 description 1
- BVJYDVKFDDPCAW-UHFFFAOYSA-N 1-aminocyclopentan-1-ol Chemical compound NC1(O)CCCC1 BVJYDVKFDDPCAW-UHFFFAOYSA-N 0.000 description 1
- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- FQXGHZNSUOHCLO-UHFFFAOYSA-N 2,2,4,4-tetramethyl-1,3-cyclobutanediol Chemical compound CC1(C)C(O)C(C)(C)C1O FQXGHZNSUOHCLO-UHFFFAOYSA-N 0.000 description 1
- GZZLQUBMUXEOBE-UHFFFAOYSA-N 2,2,4-trimethylhexane-1,6-diol Chemical compound OCCC(C)CC(C)(C)CO GZZLQUBMUXEOBE-UHFFFAOYSA-N 0.000 description 1
- BTUDGPVTCYNYLK-UHFFFAOYSA-N 2,2-dimethylglutaric acid Chemical compound OC(=O)C(C)(C)CCC(O)=O BTUDGPVTCYNYLK-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- QEEZSWGDNCHFKC-UHFFFAOYSA-N 2-(4,5-dihydro-1,3-oxazol-2-ylmethyl)-4,5-dihydro-1,3-oxazole Chemical compound N=1CCOC=1CC1=NCCO1 QEEZSWGDNCHFKC-UHFFFAOYSA-N 0.000 description 1
- WVXLLHWEQSZBLW-UHFFFAOYSA-N 2-(4-acetyl-2-methoxyphenoxy)acetic acid Chemical compound COC1=CC(C(C)=O)=CC=C1OCC(O)=O WVXLLHWEQSZBLW-UHFFFAOYSA-N 0.000 description 1
- KFNAHVKJFHDCSK-UHFFFAOYSA-N 2-[2-(4,5-dihydro-1,3-oxazol-2-yl)ethyl]-4,5-dihydro-1,3-oxazole Chemical compound N=1CCOC=1CCC1=NCCO1 KFNAHVKJFHDCSK-UHFFFAOYSA-N 0.000 description 1
- VOGDKZZTBPDRBD-UHFFFAOYSA-N 2-[2-(4,5-dihydro-1,3-oxazol-2-yl)phenyl]-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC=C1C1=NCCO1 VOGDKZZTBPDRBD-UHFFFAOYSA-N 0.000 description 1
- HMOZDINWBHMBSQ-UHFFFAOYSA-N 2-[3-(4,5-dihydro-1,3-oxazol-2-yl)phenyl]-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC(C=2OCCN=2)=C1 HMOZDINWBHMBSQ-UHFFFAOYSA-N 0.000 description 1
- XRMPKRMBDKCXII-UHFFFAOYSA-N 2-[3-(4,5-dihydro-1,3-oxazol-2-yl)propyl]-4,5-dihydro-1,3-oxazole Chemical compound N=1CCOC=1CCCC1=NCCO1 XRMPKRMBDKCXII-UHFFFAOYSA-N 0.000 description 1
- GZQKJQLFIGBEIE-UHFFFAOYSA-N 2-[4-(4,5-dihydro-1,3-oxazol-2-yl)butyl]-4,5-dihydro-1,3-oxazole Chemical compound N=1CCOC=1CCCCC1=NCCO1 GZQKJQLFIGBEIE-UHFFFAOYSA-N 0.000 description 1
- ZDNUPMSZKVCETJ-UHFFFAOYSA-N 2-[4-(4,5-dihydro-1,3-oxazol-2-yl)phenyl]-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=C(C=2OCCN=2)C=C1 ZDNUPMSZKVCETJ-UHFFFAOYSA-N 0.000 description 1
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 description 1
- BUYHVRZQBLVJOO-UHFFFAOYSA-N 2-ethyl-2,4-dimethylhexane-1,3-diol Chemical compound CCC(C)C(O)C(C)(CC)CO BUYHVRZQBLVJOO-UHFFFAOYSA-N 0.000 description 1
- QNKRHLZUPSSIPN-UHFFFAOYSA-N 2-ethyl-2-(2-methylpropyl)propane-1,3-diol Chemical compound CCC(CO)(CO)CC(C)C QNKRHLZUPSSIPN-UHFFFAOYSA-N 0.000 description 1
- WVDGHGISNBRCAO-UHFFFAOYSA-N 2-hydroxyisophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1O WVDGHGISNBRCAO-UHFFFAOYSA-N 0.000 description 1
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 1
- ZAMLGGRVTAXBHI-UHFFFAOYSA-N 3-(4-bromophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)NC(CC(O)=O)C1=CC=C(Br)C=C1 ZAMLGGRVTAXBHI-UHFFFAOYSA-N 0.000 description 1
- CMELCQNRYRDZTG-UHFFFAOYSA-N 3-hydroxybutanoic acid Chemical class CC(O)CC(O)=O.CC(O)CC(O)=O CMELCQNRYRDZTG-UHFFFAOYSA-N 0.000 description 1
- IUPHTVOTTBREAV-UHFFFAOYSA-N 3-hydroxybutanoic acid;3-hydroxypentanoic acid Chemical compound CC(O)CC(O)=O.CCC(O)CC(O)=O IUPHTVOTTBREAV-UHFFFAOYSA-N 0.000 description 1
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 description 1
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 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
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/048—Forming gas barrier coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2467/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
- C08L91/06—Waxes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
- Paints Or Removers (AREA)
- External Artificial Organs (AREA)
- Biological Depolymerization Polymers (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Laminated Bodies (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Polyesters Or Polycarbonates (AREA)
Priority Applications (16)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10010826A DE10010826A1 (de) | 2000-03-08 | 2000-03-08 | Verfahren zur Reduktion der Wasserdampfpermeabilität von Folien oder Beschichtungen |
| PCT/EP2001/002491 WO2001066630A1 (de) | 2000-03-08 | 2001-03-06 | Verfahren zur reduktion der wasserdampfpermeabilität von folien oder beschichtungen |
| MXPA02007642A MXPA02007642A (es) | 2000-03-08 | 2001-03-06 | Procedimiento para la reduccion de la permeabilidad al vapor de agua de laminas o recubrimientos. |
| DE50100502T DE50100502D1 (de) | 2000-03-08 | 2001-03-06 | Verfahren zur reduktion der wasserdampfpermeabilität von folien oder beschichtungen |
| AT01909820T ATE247151T1 (de) | 2000-03-08 | 2001-03-06 | Verfahren zur reduktion der wasserdampfpermeabilität von folien oder beschichtungen |
| KR1020027011739A KR100697748B1 (ko) | 2000-03-08 | 2001-03-06 | 필름 또는 코팅의 수증기 투과성의 감소 방법 |
| AU2001237431A AU2001237431A1 (en) | 2000-03-08 | 2001-03-06 | Method for reducing the permeability of films or coatings to water vapour |
| JP2001565793A JP4880851B2 (ja) | 2000-03-08 | 2001-03-06 | フィルムまたはコーティングの水蒸気透過性を減少する方法 |
| CNB018060978A CN1283706C (zh) | 2000-03-08 | 2001-03-06 | 降低薄膜或涂层的水蒸气渗透率的方法 |
| EP01909820A EP1263859B1 (de) | 2000-03-08 | 2001-03-06 | Verfahren zur reduktion der wasserdampfpermeabilität von folien oder beschichtungen |
| BRPI0109072-0A BR0109072B1 (pt) | 2000-03-08 | 2001-03-06 | filme ou revestimento, processo para a redução da permeabilidade ao vapor d'água de filmes ou revestimentos, composição intermediária, uso da referida composição, e, uso de amido, celulose ou misturas destes. |
| ES01909820T ES2207604T3 (es) | 2000-03-08 | 2001-03-06 | Procedimiento para la reduccion de la permeabilidad al vapor de agua de laminas o de recubrimientos. |
| US10/204,969 US6727298B2 (en) | 2000-03-08 | 2001-03-06 | Method for reducing the permeability of films or coatings to water vapor |
| DK01909820T DK1263859T3 (da) | 2000-03-08 | 2001-03-06 | Fremgangsmåde til reduktion af foliers eller coatingers gennemtrængelighed for vanddamp |
| TW090105416A TWI224126B (en) | 2000-03-08 | 2001-03-08 | Process and composition for reducing the water-vapor permeability of films or coatings made from polymer compositions and film or coating obtainable from the polymer compositions |
| NO20024202A NO20024202D0 (no) | 2000-03-08 | 2002-09-03 | Fremgangsmåte for å redusere vanndamppermeabiliteten av filmer eller belegg |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10010826A DE10010826A1 (de) | 2000-03-08 | 2000-03-08 | Verfahren zur Reduktion der Wasserdampfpermeabilität von Folien oder Beschichtungen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10010826A1 true DE10010826A1 (de) | 2001-09-13 |
Family
ID=7633668
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10010826A Withdrawn DE10010826A1 (de) | 2000-03-08 | 2000-03-08 | Verfahren zur Reduktion der Wasserdampfpermeabilität von Folien oder Beschichtungen |
| DE50100502T Expired - Lifetime DE50100502D1 (de) | 2000-03-08 | 2001-03-06 | Verfahren zur reduktion der wasserdampfpermeabilität von folien oder beschichtungen |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE50100502T Expired - Lifetime DE50100502D1 (de) | 2000-03-08 | 2001-03-06 | Verfahren zur reduktion der wasserdampfpermeabilität von folien oder beschichtungen |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US6727298B2 (https=) |
| EP (1) | EP1263859B1 (https=) |
| JP (1) | JP4880851B2 (https=) |
| KR (1) | KR100697748B1 (https=) |
| CN (1) | CN1283706C (https=) |
| AT (1) | ATE247151T1 (https=) |
| AU (1) | AU2001237431A1 (https=) |
| BR (1) | BR0109072B1 (https=) |
| DE (2) | DE10010826A1 (https=) |
| DK (1) | DK1263859T3 (https=) |
| ES (1) | ES2207604T3 (https=) |
| MX (1) | MXPA02007642A (https=) |
| NO (1) | NO20024202D0 (https=) |
| TW (1) | TWI224126B (https=) |
| WO (1) | WO2001066630A1 (https=) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010075023A1 (en) * | 2008-12-15 | 2010-07-01 | E. I. Du Pont De Nemours And Company | Copolyesters with enhanced tear strength |
| WO2010077809A1 (en) * | 2008-12-15 | 2010-07-08 | E. I. Du Pont De Nemours And Company | Copolyesters with enhanced tear strength |
| WO2010077804A1 (en) * | 2008-12-15 | 2010-07-08 | E. I. Du Pont De Nemours And Company | Copolyesters with enhanced tear strength |
| EP2774951A1 (de) * | 2013-03-06 | 2014-09-10 | Basf Se | Polymermischungen enthaltend langkettige Polykondensate |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7030181B2 (en) * | 2001-04-11 | 2006-04-18 | Eastman Chemical Company | Films prepared from plasticized polyesters |
| US7285587B2 (en) * | 2002-12-20 | 2007-10-23 | Eastman Chemical Company | Flame retardant polyester compositions for calendering |
| US7235623B2 (en) * | 2003-11-26 | 2007-06-26 | Eastman Chemical Company | Polyester compositions for calendering |
| US7354653B2 (en) * | 2003-12-18 | 2008-04-08 | Eastman Chemical Company | High clarity films with improved thermal properties |
| JP4824579B2 (ja) * | 2003-12-18 | 2011-11-30 | イーストマン ケミカル カンパニー | 改善された熱的性質を有する高透明度フィルム |
| US20050137304A1 (en) * | 2003-12-18 | 2005-06-23 | Strand Marc A. | Process for calendering of polyesters |
| US8071695B2 (en) | 2004-11-12 | 2011-12-06 | Eastman Chemical Company | Polyeste blends with improved stress whitening for film and sheet applications |
| US8425591B1 (en) | 2007-06-11 | 2013-04-23 | Abbott Cardiovascular Systems Inc. | Methods of forming polymer-bioceramic composite medical devices with bioceramic particles |
| US8334342B2 (en) * | 2008-06-18 | 2012-12-18 | Basf Se | Glyoxal and methylglyoxal as additive for polymer blends |
| EP2498614B1 (en) * | 2009-09-14 | 2017-11-15 | Basf Se | Dispenser comprising a polyester membrane for control of mites in bee hives |
| CN103842452B (zh) | 2011-09-22 | 2017-05-31 | 凸版印刷株式会社 | 膜形成用组合物、层叠体、膜、片材基体、包装材料、膜形成用组合物的制造方法以及纤维素分散液的制造方法 |
| DE102013004554A1 (de) * | 2013-03-15 | 2014-09-18 | Clariant International Ltd. | Cellulose-haltige Lacksysteme |
| CN104130067B (zh) * | 2014-08-06 | 2016-08-24 | 昆明理工大学 | 一种缓控释肥包膜剂 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2292393A (en) * | 1939-08-01 | 1942-08-11 | Du Pont | Moistureproof sheet wrapping material |
| FR2659011B1 (fr) * | 1990-03-01 | 1994-09-30 | Oreal | Composition resistante a l'eau pour le revetement des cils, et son procede de preparation. |
| JPH04318074A (ja) * | 1991-04-17 | 1992-11-09 | Shinto Paint Co Ltd | 一時保護被膜組成物 |
| DE4127665A1 (de) | 1991-08-22 | 1993-02-25 | Beiersdorf Ag | Galenische matrix |
| IT1250901B (it) * | 1991-12-12 | 1995-04-21 | Novamont Spa | Articoli biodegradabili a base di amido. |
| US5213050A (en) | 1992-06-26 | 1993-05-25 | Damage Prevention Products, Inc. | Integrated paper cargo pallet |
| DE4237535C2 (de) * | 1992-11-06 | 2000-05-25 | Biotec Biolog Naturverpack | Biologisch abbaubare Polymermischung, ein Verfahren und eine Folie |
| US5844023A (en) | 1992-11-06 | 1998-12-01 | Bio-Tec Biologische Naturverpackungen Gmbh | Biologically degradable polymer mixture |
| ES2194863T3 (es) | 1992-11-30 | 2003-12-01 | Kv Pharm Co | Materiales farmaceuticos con enmascarado de sabor. |
| US5500465A (en) * | 1994-03-10 | 1996-03-19 | Board Of Trustees Operating Michigan State University | Biodegradable multi-component polymeric materials based on unmodified starch-like polysaccharides |
| DE4440850A1 (de) * | 1994-11-15 | 1996-05-23 | Basf Ag | Biologisch abbaubare Polymere, Verfahren zu deren Herstellung sowie deren Verwendung zur Herstellung bioabbaubarer Formkörper |
| DE4440858A1 (de) * | 1994-11-15 | 1996-05-23 | Basf Ag | Biologisch abbaubare Polymere, Verfahren zu deren Herstellung sowie deren Verwendung zur Herstellung bioabbaubarer Formkörper |
| US5861216A (en) | 1996-06-28 | 1999-01-19 | The United States Of America As Represented By The Secretary Of Agriculture | Biodegradable polyester and natural polymer laminates |
| DE19630232A1 (de) * | 1996-07-26 | 1998-01-29 | Wolff Walsrode Ag | Monoaxial gereckte, biologisch abbbaubare und kompostierbare Folie mit verbesserten Eigenschaften |
| DE19638488A1 (de) * | 1996-09-20 | 1998-03-26 | Basf Ag | Biologisch abbaubare Polyester |
| FI963935A7 (fi) | 1996-10-01 | 1998-04-02 | Upm Kymmene Oy | Polymeerikoostumus |
| CA2270362C (en) | 1996-11-05 | 2011-12-13 | Novamont S.P.A. | Biodegradable polymeric compositions comprising starch and a thermoplastic polymer |
| FR2756732B1 (fr) * | 1996-12-11 | 1999-01-08 | Oreal | Composition cosmetique comprenant l'association d'un polymere filmogene et d'une dispersion de cire fluoree, et utilisation de ladite association |
| TW397769B (en) * | 1997-04-30 | 2000-07-11 | Teijin Ltd | Lowly electrifiable composite polyester film |
| NL1006548C2 (nl) | 1997-07-10 | 1999-01-12 | Sara Lee De Nv | Biodegradeerbare folie. |
-
2000
- 2000-03-08 DE DE10010826A patent/DE10010826A1/de not_active Withdrawn
-
2001
- 2001-03-06 ES ES01909820T patent/ES2207604T3/es not_active Expired - Lifetime
- 2001-03-06 AU AU2001237431A patent/AU2001237431A1/en not_active Abandoned
- 2001-03-06 EP EP01909820A patent/EP1263859B1/de not_active Expired - Lifetime
- 2001-03-06 DE DE50100502T patent/DE50100502D1/de not_active Expired - Lifetime
- 2001-03-06 KR KR1020027011739A patent/KR100697748B1/ko not_active Expired - Fee Related
- 2001-03-06 US US10/204,969 patent/US6727298B2/en not_active Expired - Lifetime
- 2001-03-06 BR BRPI0109072-0A patent/BR0109072B1/pt not_active IP Right Cessation
- 2001-03-06 MX MXPA02007642A patent/MXPA02007642A/es active IP Right Grant
- 2001-03-06 WO PCT/EP2001/002491 patent/WO2001066630A1/de not_active Ceased
- 2001-03-06 AT AT01909820T patent/ATE247151T1/de not_active IP Right Cessation
- 2001-03-06 DK DK01909820T patent/DK1263859T3/da active
- 2001-03-06 JP JP2001565793A patent/JP4880851B2/ja not_active Expired - Fee Related
- 2001-03-06 CN CNB018060978A patent/CN1283706C/zh not_active Expired - Fee Related
- 2001-03-08 TW TW090105416A patent/TWI224126B/zh not_active IP Right Cessation
-
2002
- 2002-09-03 NO NO20024202A patent/NO20024202D0/no not_active Application Discontinuation
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010075023A1 (en) * | 2008-12-15 | 2010-07-01 | E. I. Du Pont De Nemours And Company | Copolyesters with enhanced tear strength |
| WO2010077809A1 (en) * | 2008-12-15 | 2010-07-08 | E. I. Du Pont De Nemours And Company | Copolyesters with enhanced tear strength |
| WO2010077804A1 (en) * | 2008-12-15 | 2010-07-08 | E. I. Du Pont De Nemours And Company | Copolyesters with enhanced tear strength |
| EP2774951A1 (de) * | 2013-03-06 | 2014-09-10 | Basf Se | Polymermischungen enthaltend langkettige Polykondensate |
Also Published As
| Publication number | Publication date |
|---|---|
| BR0109072A (pt) | 2003-06-03 |
| ATE247151T1 (de) | 2003-08-15 |
| CN1283706C (zh) | 2006-11-08 |
| JP4880851B2 (ja) | 2012-02-22 |
| JP2003525988A (ja) | 2003-09-02 |
| KR100697748B1 (ko) | 2007-03-22 |
| ES2207604T3 (es) | 2004-06-01 |
| EP1263859A1 (de) | 2002-12-11 |
| TWI224126B (en) | 2004-11-21 |
| CN1411489A (zh) | 2003-04-16 |
| EP1263859B1 (de) | 2003-08-13 |
| MXPA02007642A (es) | 2003-04-22 |
| US20030060542A1 (en) | 2003-03-27 |
| DE50100502D1 (de) | 2003-09-18 |
| NO20024202L (no) | 2002-09-03 |
| KR20020079948A (ko) | 2002-10-19 |
| US6727298B2 (en) | 2004-04-27 |
| WO2001066630A1 (de) | 2001-09-13 |
| AU2001237431A1 (en) | 2001-09-17 |
| BR0109072B1 (pt) | 2010-11-30 |
| NO20024202D0 (no) | 2002-09-03 |
| DK1263859T3 (da) | 2003-12-08 |
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Legal Events
| Date | Code | Title | Description |
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| 8130 | Withdrawal |