JPH08510213A - 改良塩基性カルシウムカルボキシレート - Google Patents
改良塩基性カルシウムカルボキシレートInfo
- Publication number
- JPH08510213A JPH08510213A JP6524676A JP52467694A JPH08510213A JP H08510213 A JPH08510213 A JP H08510213A JP 6524676 A JP6524676 A JP 6524676A JP 52467694 A JP52467694 A JP 52467694A JP H08510213 A JPH08510213 A JP H08510213A
- Authority
- JP
- Japan
- Prior art keywords
- calcium
- acid
- weight
- carbon
- content
- 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
Links
- 239000011575 calcium Substances 0.000 title claims abstract description 37
- 229910052791 calcium Inorganic materials 0.000 title claims abstract description 35
- -1 calcium carboxylate Chemical class 0.000 title claims abstract description 24
- 239000002253 acid Substances 0.000 claims abstract description 24
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 16
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 239000000344 soap Substances 0.000 claims abstract description 11
- 239000004032 superbase Substances 0.000 claims abstract description 11
- 150000002148 esters Chemical class 0.000 claims abstract description 9
- 239000004014 plasticizer Substances 0.000 claims abstract description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 6
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 3
- 150000007513 acids Chemical class 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000012429 reaction media Substances 0.000 claims description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims 2
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims 1
- 239000000920 calcium hydroxide Substances 0.000 claims 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims 1
- 239000000292 calcium oxide Substances 0.000 claims 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims 1
- 239000001569 carbon dioxide Substances 0.000 claims 1
- 229910002092 carbon dioxide Inorganic materials 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 238000003756 stirring Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 229920000915 polyvinyl chloride Polymers 0.000 abstract description 7
- 239000004800 polyvinyl chloride Substances 0.000 abstract description 7
- 239000003381 stabilizer Substances 0.000 abstract description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 13
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 3
- 159000000007 calcium salts Chemical class 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 150000004715 keto acids Chemical class 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- NZQMQVJXSRMTCJ-UHFFFAOYSA-N 3-Methyl-hexanoic acid Chemical compound CCCC(C)CC(O)=O NZQMQVJXSRMTCJ-UHFFFAOYSA-N 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 2
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- QJRRBVNPIKYRQJ-UHFFFAOYSA-N 10-methylundecanoic acid Chemical compound CC(C)CCCCCCCCC(O)=O QJRRBVNPIKYRQJ-UHFFFAOYSA-N 0.000 description 1
- OILUAKBAMVLXGF-UHFFFAOYSA-N 3,5,5-trimethyl-hexanoic acid Chemical compound OC(=O)CC(C)CC(C)(C)C OILUAKBAMVLXGF-UHFFFAOYSA-N 0.000 description 1
- DGZZHLSSAUIDSX-UHFFFAOYSA-N 3-ethyloctanoic acid Chemical compound CCCCCC(CC)CC(O)=O DGZZHLSSAUIDSX-UHFFFAOYSA-N 0.000 description 1
- HHGZJCMMPUJXIF-UHFFFAOYSA-N 4,5-dimethylhexanoic acid Chemical compound CC(C)C(C)CCC(O)=O HHGZJCMMPUJXIF-UHFFFAOYSA-N 0.000 description 1
- CNQGBTJIGDAYTK-UHFFFAOYSA-N 4-ethylnonanoic acid Chemical compound CCCCCC(CC)CCC(O)=O CNQGBTJIGDAYTK-UHFFFAOYSA-N 0.000 description 1
- AWQSAIIDOMEEOD-UHFFFAOYSA-N 5,5-Dimethyl-4-(3-oxobutyl)dihydro-2(3H)-furanone Chemical compound CC(=O)CCC1CC(=O)OC1(C)C AWQSAIIDOMEEOD-UHFFFAOYSA-N 0.000 description 1
- OEOIWYCWCDBOPA-UHFFFAOYSA-N 6-methyl-heptanoic acid Chemical compound CC(C)CCCCC(O)=O OEOIWYCWCDBOPA-UHFFFAOYSA-N 0.000 description 1
- XZOYHFBNQHPJRQ-UHFFFAOYSA-N 7-methyloctanoic acid Chemical compound CC(C)CCCCCC(O)=O XZOYHFBNQHPJRQ-UHFFFAOYSA-N 0.000 description 1
- OAOABCKPVCUNKO-UHFFFAOYSA-N 8-methyl Nonanoic acid Chemical compound CC(C)CCCCCCC(O)=O OAOABCKPVCUNKO-UHFFFAOYSA-N 0.000 description 1
- VSAJTRPXXNCHGB-UHFFFAOYSA-N 9-methyl-decanoic acid Chemical compound CC(C)CCCCCCCC(O)=O VSAJTRPXXNCHGB-UHFFFAOYSA-N 0.000 description 1
- 102100035474 DNA polymerase kappa Human genes 0.000 description 1
- 101710108091 DNA polymerase kappa Proteins 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- ZCZLQYAECBEUBH-UHFFFAOYSA-L calcium;octadec-9-enoate Chemical compound [Ca+2].CCCCCCCCC=CCCCCCCCC([O-])=O.CCCCCCCCC=CCCCCCCCC([O-])=O ZCZLQYAECBEUBH-UHFFFAOYSA-L 0.000 description 1
- 238000010960 commercial process Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007037 hydroformylation reaction Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/126—Acids containing more than four carbon atoms
- C07C53/128—Acids containing more than four carbon atoms the carboxylic group being bound to a carbon atom bound to at least two other carbon atoms, e.g. neo-acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/414—Preparation of superbasic salts
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/126—Acids containing more than four carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0091—Complexes with metal-heteroatom-bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB939309946A GB9309946D0 (en) | 1993-05-14 | 1993-05-14 | Improved basic calcium carboxylates |
| GB9309946.3 | 1993-05-14 | ||
| PCT/EP1994/001566 WO1994026686A1 (en) | 1993-05-14 | 1994-05-13 | Improved basic calcium carboxylates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH08510213A true JPH08510213A (ja) | 1996-10-29 |
Family
ID=10735473
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6524676A Pending JPH08510213A (ja) | 1993-05-14 | 1994-05-13 | 改良塩基性カルシウムカルボキシレート |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0698007A1 (enExample) |
| JP (1) | JPH08510213A (enExample) |
| GB (1) | GB9309946D0 (enExample) |
| TW (1) | TW251306B (enExample) |
| WO (1) | WO1994026686A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5519076A (en) * | 1994-02-24 | 1996-05-21 | Nissan Ferro Organic Chemical Co, Ltd. | Halogen-containing resin composition |
| JPH07286080A (ja) * | 1994-02-24 | 1995-10-31 | Nissan Fuero Yuki Kagaku Kk | ハロゲン含有樹脂組成物 |
| US5919741A (en) * | 1998-01-20 | 1999-07-06 | The Lubrizol Corporation | Overbased carboxylate gels |
| US6835328B2 (en) | 2002-07-08 | 2004-12-28 | Crompton Corporation | Overbased metal carbonate/carboxylate microemulsions and halogen-containing polymers containing same |
| US20040006165A1 (en) * | 2002-07-08 | 2004-01-08 | Julius Fakinlede | Overbased metal carbonate/carboxylate microemulsions and halogen-containing polymers containing same |
| ITVA20110032A1 (it) * | 2011-11-29 | 2013-05-30 | Lamberti Spa | Composizioni di sali surbasici di calcio carbossilato/carbonato |
| CN111718655A (zh) * | 2020-07-01 | 2020-09-29 | 中山华明泰科技股份有限公司 | 一种复合异辛酸钙制备方法及应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1528804A (fr) * | 1967-04-27 | 1968-06-14 | Prod Chim Et De Synthese Soc D | Stabilisants liquides au plomb pour les polymères et copolymères du chlorure de vinyle |
| FR2592391B1 (fr) * | 1985-12-30 | 1988-02-05 | Charbonnages Ste Chimique | Savons de calcium possedant une reserve de basicite elevee. |
| GB9121736D0 (en) * | 1991-10-14 | 1991-11-27 | Exxon Chemical Patents Inc | Improved overbased carboxylates |
-
1993
- 1993-05-14 GB GB939309946A patent/GB9309946D0/en active Pending
-
1994
- 1994-05-13 EP EP94918321A patent/EP0698007A1/en not_active Withdrawn
- 1994-05-13 JP JP6524676A patent/JPH08510213A/ja active Pending
- 1994-05-13 WO PCT/EP1994/001566 patent/WO1994026686A1/en not_active Ceased
- 1994-06-09 TW TW83105255A patent/TW251306B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| TW251306B (enExample) | 1995-07-11 |
| WO1994026686A1 (en) | 1994-11-24 |
| GB9309946D0 (en) | 1993-06-30 |
| EP0698007A1 (en) | 1996-02-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN106631779B (zh) | 多元醇酯及其在卤代乙烯基聚合物加工中的应用 | |
| EP2118047B1 (en) | Glycerol esters | |
| US3723489A (en) | Metal derivatives of 3,5-di-t-butyl-4-hydroxyphenyl propionic acid | |
| CN87101635A (zh) | 用钯催化剂将不饱合烯烃化合物羰基化的方法 | |
| JPH08510213A (ja) | 改良塩基性カルシウムカルボキシレート | |
| US3939201A (en) | Esters | |
| JP2004527634A5 (enExample) | ||
| US4220570A (en) | Stabilizer combination for vinyl chloride polymers containing partial esters of pentaerythritol with fatty acids | |
| CN1863759A (zh) | 粉状高碱性无定形碱土金属盐及其制备方法 | |
| US6649585B1 (en) | Processes for preparing superbasic zinc soaps and methods of using said soaps | |
| DE60312685T2 (de) | Komplexe von metallsalzen mit organischen säuren und beta-diketonen und methoden zu deren darstellung | |
| EP0804404A1 (en) | Basic zinc carboxylates | |
| US2528803A (en) | Preparation of metallic soaps | |
| US5302644A (en) | Stabilizers containing ketofatty acid glycerides for Ca/Zn-stabilized PVC molding compounds | |
| EP0304149A2 (en) | High-solids coating compositions | |
| US4014910A (en) | Process for the preparation of an (ar)alkane carboxylic acid | |
| US5021598A (en) | Process for making bismuth carboxylates | |
| EP0837094A2 (en) | Basic calcium carboxylates | |
| WO1992006945A1 (en) | Metal carboxylates | |
| US3365403A (en) | Process of producing solutions of metal soaps of epoxidized fatty acids in an alkyl phenol | |
| CA1168262A (en) | Treatment of dibasic esters with alkali metal borohydrides, permanganates or methylates | |
| US4656210A (en) | Stabilized polyvinyl chloride molding compositions | |
| JP2613214B2 (ja) | 新規なハロゲン含有樹脂組成物 | |
| US3970631A (en) | Triesters of triethanolmethane and monocarboxylic acids as plasticizers for polyvinyl chloride | |
| US6448314B1 (en) | Use of monohydrate zinc acetylacetonate as halogenated polymer stabilizer and preparation method |