JP2023520281A - クロロスルホン化ポリ(プロピレンカーボネート)及びその製造方法、ならびに使用 - Google Patents
クロロスルホン化ポリ(プロピレンカーボネート)及びその製造方法、ならびに使用 Download PDFInfo
- Publication number
- JP2023520281A JP2023520281A JP2022544661A JP2022544661A JP2023520281A JP 2023520281 A JP2023520281 A JP 2023520281A JP 2022544661 A JP2022544661 A JP 2022544661A JP 2022544661 A JP2022544661 A JP 2022544661A JP 2023520281 A JP2023520281 A JP 2023520281A
- Authority
- JP
- Japan
- Prior art keywords
- propylene carbonate
- poly
- chlorosulfonated
- present disclosure
- chlorosulfonated poly
- 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.)
- Granted
Links
- -1 poly(propylene carbonate) Polymers 0.000 title claims abstract description 367
- 229920000379 polypropylene carbonate Polymers 0.000 title claims abstract description 194
- 238000004519 manufacturing process Methods 0.000 title claims description 17
- 239000000463 material Substances 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 17
- 239000000853 adhesive Substances 0.000 claims abstract description 15
- 230000001070 adhesive effect Effects 0.000 claims abstract description 15
- 239000003973 paint Substances 0.000 claims abstract description 7
- 238000006243 chemical reaction Methods 0.000 claims description 31
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 claims description 18
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 15
- 238000005580 one pot reaction Methods 0.000 claims description 12
- 239000012752 auxiliary agent Substances 0.000 claims description 11
- 239000003153 chemical reaction reagent Substances 0.000 claims description 11
- 239000002270 dispersing agent Substances 0.000 claims description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 8
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 7
- 230000035484 reaction time Effects 0.000 claims description 7
- 238000006116 polymerization reaction Methods 0.000 claims description 6
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 claims description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 4
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 239000000454 talc Substances 0.000 claims description 4
- 229910052623 talc Inorganic materials 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims 1
- 239000000047 product Substances 0.000 abstract description 24
- 239000000460 chlorine Substances 0.000 abstract description 12
- 229910052801 chlorine Inorganic materials 0.000 abstract description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract description 7
- 230000003993 interaction Effects 0.000 abstract description 5
- 239000012467 final product Substances 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 abstract description 4
- 238000013461 design Methods 0.000 abstract description 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract description 3
- 230000002195 synergetic effect Effects 0.000 abstract description 3
- 230000003213 activating effect Effects 0.000 abstract description 2
- 239000013585 weight reducing agent Substances 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- 238000000921 elemental analysis Methods 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- 238000005259 measurement Methods 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 230000008901 benefit Effects 0.000 description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000001257 hydrogen Chemical group 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 241000698776 Duma Species 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
- 125000001309 chloro group Chemical group Cl* 0.000 description 4
- 238000009841 combustion method Methods 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 238000005227 gel permeation chromatography Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 238000011160 research Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 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 3
- 239000012530 fluid Substances 0.000 description 3
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229920002681 hypalon Polymers 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 238000002715 modification method Methods 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000004611 spectroscopical analysis Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 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
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- 206010057040 Temperature intolerance Diseases 0.000 description 1
- 229920006125 amorphous polymer Polymers 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 150000005676 cyclic carbonates Chemical class 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 230000008543 heat sensitivity Effects 0.000 description 1
- 238000007602 hot air drying Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/02—Aliphatic polycarbonates
- C08G64/0208—Aliphatic polycarbonates saturated
- C08G64/0225—Aliphatic polycarbonates saturated containing atoms other than carbon, hydrogen or oxygen
- C08G64/0233—Aliphatic polycarbonates saturated containing atoms other than carbon, hydrogen or oxygen containing halogens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/42—Chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/02—Aliphatic polycarbonates
- C08G64/0208—Aliphatic polycarbonates saturated
- C08G64/0225—Aliphatic polycarbonates saturated containing atoms other than carbon, hydrogen or oxygen
- C08G64/025—Aliphatic polycarbonates saturated containing atoms other than carbon, hydrogen or oxygen containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D169/00—Coating compositions based on polycarbonates; Coating compositions based on derivatives of polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J169/00—Adhesives based on polycarbonates; Adhesives based on derivatives of polycarbonates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W90/00—Enabling technologies or technologies with a potential or indirect contribution to greenhouse gas [GHG] emissions mitigation
- Y02W90/10—Bio-packaging, e.g. packing containers made from renewable resources or bio-plastics
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyesters Or Polycarbonates (AREA)
- Adhesive Tapes (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
[式中、xは、0又は1である。yは、0~3の整数である。mは、重合度である。]
20gのポリ(プロピレンカーボネート)(PPC)と、分散剤として3gのシリカ(SiO2)とを、3つ口フラスコに投入し、機械攪拌した。常温状態で5.4gの塩化スルホニル(SO2Cl2)を投入し、その後、油浴槽中で110℃に昇温し、水酸化ナトリウム溶液でオフガスを処理しながら、60minクロロスルホン化反応し、その後、直ちにシャーレに入れて、室温で冷却し、半透明ゲル状態のクロロスルホン化ポリ(プロピレンカーボネート)を得た。
20gのポリ(プロピレンカーボネート)(PPC)と、分散剤として3gのシリカ(SiO2)とを3つ口フラスコに投入し、機械攪拌を行った。常温状態で、5.4gの塩化スルホニル(SO2Cl2)を添加し、その後、油浴槽中で110℃に昇温し、水酸化ナトリウム溶液でオフガスを処理しながら、70minクロロスルホン化反応し、その後、直ちにシャーレに入れて、室温で冷却し、透明で半流動状態のクロロスルホン化ポリ(プロピレンカーボネート)を得た。
20gの塩化ポリ(プロピレンカーボネート)(CPPC)を3つ口フラスコに投入し、機械攪拌を行い、常温状態で5.4gの塩化スルホニル(SO2Cl2)を添加し、その後、油浴槽中で110℃に昇温し、水酸化ナトリウム溶液でオフガスを処理しながら、70minクロロスルホン化反応し、その後、直ちにシャーレに入れて、室温で冷却し、乳黄色で流動状態のクロロスルホン化ポリ(プロピレンカーボネート)を得た。
20gの塩化ポリ(プロピレンカーボネート)(CPPC)と、分散剤として3gのシリカ(SiO2)とを、3つ口フラスコに投入し、機械攪拌を行い、同時に、10.8gの塩化スルホニル(SO2Cl2)と4.7gのジオクチルフタレート(DOP)とを混合し、ジオクチルフタレートは、有機溶媒固定剤として塩化スルホニルの分解温度を向上させるために用いられる。常温状態で、3つ口フラスコに混合液を添加し、水酸化ナトリウム溶液でオフガスを処理しながら、その後、油浴槽中で80℃に昇温し、60minクロロスルホン化反応し、室温で冷却し、淡黄色の粉末及び塊体とが混合したクロロスルホン化ポリ(プロピレンカーボネート)を得た。
Claims (11)
- 前記mは、10~500であることを特徴とする請求項1に記載のクロロスルホン化ポリ(プロピレンカーボネート)。
- 前記クロロスルホン化ポリ(プロピレンカーボネート)の数平均分子量が2000~110000ダルトンであることを特徴とする請求項1に記載のクロロスルホン化ポリ(プロピレンカーボネート)。
- 前記クロロスルホン化ポリ(プロピレンカーボネート)は、生分解性材料であることを特徴とする請求項1に記載のクロロスルホン化ポリ(プロピレンカーボネート)。
- ポリ(プロピレンカーボネート)及び/又は塩化ポリ(プロピレンカーボネート)とクロロスルホン化試薬とをクロロスルホン化反応させた後、クロロスルホン化ポリ(プロピレンカーボネート)を得る工程を含むことを特徴とするクロロスルホン化ポリ(プロピレンカーボネート)の製造方法。
- 前記クロロスルホン化試薬は、塩化スルホニル、クロロスルホン酸及び二酸化硫黄ガスのうちの1種又は2種以上を含み、
前記ポリ(プロピレンカーボネート)及び/又は塩化ポリ(プロピレンカーボネート)とクロロスルホン化試薬との質量比が1.5:1~7.4:1であることを特徴とする請求項5に記載の製造方法。 - 前記クロロスルホン化反応の温度が60~120℃であり、
前記クロロスルホン化反応の時間が20~120minであることを特徴とする請求項5に記載の製造方法。 - 前記クロロスルホン化反応の原料は、助剤をさらに含み、
前記ポリ(プロピレンカーボネート)及び/又は塩化ポリ(プロピレンカーボネート)と助剤との質量比が20:1~20:4であることを特徴とする請求項5に記載の製造方法。 - 前記助剤は、分散剤を含み、
前記分散剤は、シリカ、ホワイトカーボン、炭酸カルシウム及びタルクのうちの1種又は2種以上を含むことを特徴とする請求項8に記載の製造方法。 - 前記クロロスルホン化ポリ(プロピレンカーボネート)の製造は、ワンポット反応により行われることを特徴とする請求項5に記載の製造方法。
- 請求項1~4のいずれか1項に記載のクロロスルホン化ポリ(プロピレンカーボネート)又は請求項5~10のいずれか1項に記載の製造方法により製造されたクロロスルホン化ポリ(プロピレンカーボネート)の、粘着剤、粘着ステッカー又は塗料分野への使用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110233721.7 | 2021-03-03 | ||
CN202110233721.7A CN113004509B (zh) | 2021-03-03 | 2021-03-03 | 一种氯磺化聚丙撑碳酸酯及其制备方法 |
PCT/CN2021/101997 WO2022183637A1 (zh) | 2021-03-03 | 2021-06-24 | 氯磺化聚丙撑碳酸酯及其制备方法和用途 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2023520281A true JP2023520281A (ja) | 2023-05-17 |
JP7381144B2 JP7381144B2 (ja) | 2023-11-15 |
Family
ID=76403352
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2022544661A Active JP7381144B2 (ja) | 2021-03-03 | 2021-06-24 | クロロスルホン化ポリ(プロピレンカーボネート)及びその製造方法、ならびに使用 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20240209147A1 (ja) |
EP (1) | EP4303249A1 (ja) |
JP (1) | JP7381144B2 (ja) |
CN (1) | CN113004509B (ja) |
WO (1) | WO2022183637A1 (ja) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113004509B (zh) * | 2021-03-03 | 2022-09-06 | 中国科学院长春应用化学研究所 | 一种氯磺化聚丙撑碳酸酯及其制备方法 |
CN115232590B (zh) * | 2022-07-29 | 2024-06-25 | 中国科学院长春应用化学研究所 | 一种压敏胶组合物及其制备方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4104264A (en) * | 1977-05-05 | 1978-08-01 | Air Products & Chemicals, Inc. | End capped polyalkylene carbonates having improved thermal stablity |
CN103881078A (zh) * | 2014-04-17 | 2014-06-25 | 中国科学院长春应用化学研究所 | 氯化聚丙撑碳酸酯及其制备方法 |
CN105218820A (zh) * | 2015-10-19 | 2016-01-06 | 昆明理工大学 | 一种二氧化硫、二氧化碳与环氧化合物共聚物的制备方法 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2272901B (en) * | 1992-11-25 | 1997-01-15 | Tosoh Corp | Process for the preparation of chlorinated polyolefin and chlorosulfonated polyolefin |
US7687595B2 (en) * | 2007-08-06 | 2010-03-30 | Sabic Innovative Plastics Ip B.V. | Sulfonated telechelic polycarbonates |
CN102153683B (zh) | 2011-01-13 | 2012-10-17 | 杭州新元化工技术开发有限公司 | 一种气固液三相反应制备氯磺化聚乙烯的方法 |
ITMI20131513A1 (it) * | 2012-09-13 | 2014-03-14 | Ptt Global Chemical Public Co Ltd | Composizione di carbonato di polialchilene a stabilita' termica migliorata, e metodo di preparazione della stessa |
CN103012630A (zh) * | 2012-12-26 | 2013-04-03 | 长春工业大学 | 用磺酰氯作氯磺化剂制备氯磺化聚乙烯的方法 |
CN104449521B (zh) * | 2014-12-23 | 2017-08-25 | 中国科学院长春应用化学研究所 | 一种热熔胶组合物及其制备方法 |
CN107793732B (zh) | 2017-11-24 | 2020-01-31 | 中国科学院长春应用化学研究所 | 一种改性聚丙撑碳酸酯的制备方法 |
CN109666138B (zh) * | 2018-12-28 | 2021-01-08 | 中国科学院长春应用化学研究所 | 一种脂肪族聚碳酸酯的制备方法 |
CN113004509B (zh) * | 2021-03-03 | 2022-09-06 | 中国科学院长春应用化学研究所 | 一种氯磺化聚丙撑碳酸酯及其制备方法 |
-
2021
- 2021-03-03 CN CN202110233721.7A patent/CN113004509B/zh active Active
- 2021-06-24 US US17/799,162 patent/US20240209147A1/en active Pending
- 2021-06-24 JP JP2022544661A patent/JP7381144B2/ja active Active
- 2021-06-24 WO PCT/CN2021/101997 patent/WO2022183637A1/zh active Application Filing
- 2021-06-24 EP EP21923604.9A patent/EP4303249A1/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4104264A (en) * | 1977-05-05 | 1978-08-01 | Air Products & Chemicals, Inc. | End capped polyalkylene carbonates having improved thermal stablity |
CN103881078A (zh) * | 2014-04-17 | 2014-06-25 | 中国科学院长春应用化学研究所 | 氯化聚丙撑碳酸酯及其制备方法 |
CN105218820A (zh) * | 2015-10-19 | 2016-01-06 | 昆明理工大学 | 一种二氧化硫、二氧化碳与环氧化合物共聚物的制备方法 |
Also Published As
Publication number | Publication date |
---|---|
US20240209147A1 (en) | 2024-06-27 |
WO2022183637A1 (zh) | 2022-09-09 |
EP4303249A1 (en) | 2024-01-10 |
CN113004509A (zh) | 2021-06-22 |
JP7381144B2 (ja) | 2023-11-15 |
CN113004509B (zh) | 2022-09-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2023520281A (ja) | クロロスルホン化ポリ(プロピレンカーボネート)及びその製造方法、ならびに使用 | |
CN106751613B (zh) | 一种高韧性聚乳酸及其制备方法 | |
CN109206625A (zh) | 一种物理分相超分子动态聚合物及其应用 | |
CN110408012A (zh) | 1,2-聚丁二烯橡胶增韧改性聚乳酸的制备方法 | |
CN111978531B (zh) | 纤维素接枝型全生物降解高分子材料及其制备方法 | |
CN102532465A (zh) | 超支化聚氨酯的制备方法与改性聚乳酸树脂及其制备方法 | |
CN102977319A (zh) | 可降解聚乳酸两嵌段共聚物、制备方法及其在改性聚乳酸中的应用 | |
CN107955321A (zh) | 汽车内饰件用抗紫外塑料 | |
CN116970242B (zh) | 一种硫酸钙晶须增强聚丙烯及其制备方法 | |
CN108341937A (zh) | 一种生物基含碳酸酯结构的聚酯及其制备方法和应用 | |
CN114891183A (zh) | 一种水性聚氨酯改性淀粉分散液及其制备方法 | |
CN109206826A (zh) | 一种物理分相动态聚合物及其应用 | |
CN104292391A (zh) | 一种不饱和酸酐接枝氯化聚乙烯熔融生产法 | |
CN113402702A (zh) | 阻燃可降解pbs及其制备方法 | |
CN102093717A (zh) | 磺化聚醚砜/TiO2纳米复合材料及其制备方法 | |
CN110903606B (zh) | 一种植物油基复合材料及其制备方法 | |
CN109206824A (zh) | 一种物理分相超分子动态聚合物及其应用 | |
CN109180961B (zh) | 一种激光响应的P(AM-co-St)@Bi2O3复合水凝胶的制备方法和应用 | |
CN113527978A (zh) | 一种生物基热熔型标线涂料及其制备方法 | |
CN112694587A (zh) | 一种基于双向修复结构的自修复聚氨酯及其制备方法和应用 | |
CN111763354B (zh) | 一种耐热改性热塑性淀粉包装材料及其制备方法 | |
Parreño Jr et al. | Sulfur copolymers (SDIB) from inverse vulcanization of elemental sulfur (S8) for polymer blend | |
CN118087307A (zh) | 一种基于纤维素肉桂酸酯的纸制品防油防水涂料、纸制品及其制备方法 | |
CN108727917A (zh) | 一种抗日晒车用粉末涂料及其制备方法 | |
CN108948629B (zh) | 一种高耐候性环保高分子材料及其制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20220720 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20230620 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20230913 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20231024 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20231026 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 7381144 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |