CN1111556C - 一种多元胺与胍盐聚合物及其制备方法 - Google Patents
一种多元胺与胍盐聚合物及其制备方法 Download PDFInfo
- Publication number
- CN1111556C CN1111556C CN 00125721 CN00125721A CN1111556C CN 1111556 C CN1111556 C CN 1111556C CN 00125721 CN00125721 CN 00125721 CN 00125721 A CN00125721 A CN 00125721A CN 1111556 C CN1111556 C CN 1111556C
- Authority
- CN
- China
- Prior art keywords
- polyamine
- polymer
- guanidinesalt
- guanidine salt
- salt polymer
- 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.)
- Expired - Lifetime
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- 229920000642 polymer Polymers 0.000 title claims abstract description 27
- 150000002357 guanidines Chemical class 0.000 claims abstract description 19
- 238000002360 preparation method Methods 0.000 claims abstract description 9
- 150000001412 amines Chemical class 0.000 claims abstract description 5
- 229920000768 polyamine Polymers 0.000 claims description 21
- 239000000126 substance Substances 0.000 claims description 14
- -1 acryl Chemical group 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 238000010792 warming Methods 0.000 claims description 8
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 6
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 6
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 125000002252 acyl group Chemical group 0.000 claims description 4
- LPKCJFLRJWWIDI-UHFFFAOYSA-N (diaminomethylideneamino)phosphonic acid Chemical compound NC(N)=NP(O)(O)=O LPKCJFLRJWWIDI-UHFFFAOYSA-N 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical group CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 claims description 3
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 claims description 3
- MJFQUUWPZOGYQT-UHFFFAOYSA-O diaminomethylideneazanium;nitrate Chemical compound NC(N)=[NH2+].[O-][N+]([O-])=O MJFQUUWPZOGYQT-UHFFFAOYSA-O 0.000 claims description 3
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims description 3
- 239000004312 hexamethylene tetramine Substances 0.000 claims description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 125000004031 fumaroyl group Chemical group C(\C=C\C(=O)*)(=O)* 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 125000003099 maleoyl group Chemical group C(\C=C/C(=O)*)(=O)* 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 claims description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- 229960001124 trientine Drugs 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 8
- 238000000354 decomposition reaction Methods 0.000 abstract description 5
- 229920005989 resin Polymers 0.000 abstract description 3
- 239000011347 resin Substances 0.000 abstract description 3
- 230000000844 anti-bacterial effect Effects 0.000 abstract description 2
- 239000007790 solid phase Substances 0.000 abstract description 2
- 229920000891 common polymer Polymers 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 238000010094 polymer processing Methods 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- 230000009257 reactivity Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 10
- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine group Chemical group NC(=N)N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 7
- 125000003368 amide group Chemical group 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 4
- 150000001408 amides Chemical class 0.000 description 4
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000007306 functionalization reaction Methods 0.000 description 2
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000002516 radical scavenger Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000002411 thermogravimetry Methods 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- 229940123208 Biguanide Drugs 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
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 230000009435 amidation Effects 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 230000002000 scavenging effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940083542 sodium Drugs 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 description 1
- 229960004306 sulfadiazine Drugs 0.000 description 1
- 229960002135 sulfadimidine Drugs 0.000 description 1
- QPPBRPIAZZHUNT-UHFFFAOYSA-N sulfamerazine Chemical compound CC1=CC=NC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 QPPBRPIAZZHUNT-UHFFFAOYSA-N 0.000 description 1
- 229960002597 sulfamerazine Drugs 0.000 description 1
- ASWVTGNCAZCNNR-UHFFFAOYSA-N sulfamethazine Chemical compound CC1=CC(C)=NC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 ASWVTGNCAZCNNR-UHFFFAOYSA-N 0.000 description 1
- 238000000214 vapour pressure osmometry Methods 0.000 description 1
Landscapes
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Abstract
Description
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN 00125721 CN1111556C (zh) | 2000-10-19 | 2000-10-19 | 一种多元胺与胍盐聚合物及其制备方法 |
Applications Claiming Priority (1)
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---|---|---|---|
CN 00125721 CN1111556C (zh) | 2000-10-19 | 2000-10-19 | 一种多元胺与胍盐聚合物及其制备方法 |
Publications (2)
Publication Number | Publication Date |
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CN1350022A CN1350022A (zh) | 2002-05-22 |
CN1111556C true CN1111556C (zh) | 2003-06-18 |
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CN 00125721 Expired - Lifetime CN1111556C (zh) | 2000-10-19 | 2000-10-19 | 一种多元胺与胍盐聚合物及其制备方法 |
Country Status (1)
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100406496C (zh) * | 2003-07-23 | 2008-07-30 | 上海塑杰科技有限公司 | 一种多元胺与胍盐聚合物及其在抗菌聚酯和聚酰胺材料中的应用 |
WO2020073784A1 (zh) | 2018-10-10 | 2020-04-16 | 桂林新先立抗菌材料有限公司 | 一种抗菌聚合物及其制备方法 |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101210062B (zh) * | 2006-12-27 | 2010-05-19 | 华东理工大学 | 一种抗菌聚合物材料 |
CN101812160B (zh) * | 2009-02-23 | 2012-05-30 | 上海富元塑胶科技有限公司 | 一种聚烯烃功能化母粒及其制备方法和应用 |
CN102517668B (zh) * | 2011-11-15 | 2014-04-09 | 青岛大学 | 一种功能性丝瓜络再生纤维及其制备方法 |
US9670149B2 (en) | 2013-06-17 | 2017-06-06 | 3M Innovative Properties Company | Process for preparing guanidino-functional monomers |
CN104855416B (zh) * | 2015-05-27 | 2018-02-16 | 武汉桀升生物科技有限公司 | 一种耐高温复合抗菌剂及其制备方法 |
CN106009856A (zh) * | 2016-07-27 | 2016-10-12 | 上海巨峰化工有限公司 | 一种胍盐抗菌涂料 |
CN107254045B (zh) * | 2017-05-26 | 2021-05-18 | 天津大学 | 一种胍类聚合物杀菌剂的制备方法 |
CN108587273A (zh) * | 2018-05-24 | 2018-09-28 | 南京中森挤出机械有限公司 | 船舶用外层防污涂料及其制备方法 |
CN109535418B (zh) * | 2018-10-10 | 2019-08-30 | 桂林新先立抗菌材料有限公司 | 一种抗菌织物材料及其制备方法 |
CN109535571B (zh) * | 2018-10-10 | 2021-02-19 | 桂林新先立抗菌材料有限公司 | 一种注塑材料及其制备方法 |
CN109208174B (zh) * | 2018-10-10 | 2019-09-27 | 桂林新先立抗菌材料有限公司 | 一种熔喷无纺布及其制备方法 |
CN109503832A (zh) * | 2018-10-18 | 2019-03-22 | 上海高聚生物科技有限公司 | 一种聚环氧丙基己基胍盐酸盐及其制备方法 |
CN109232325B (zh) * | 2018-10-24 | 2021-04-06 | 中国石油化工股份有限公司 | 一种用于油田污水处理的杀菌剂及制备方法 |
CN109371500A (zh) * | 2018-10-30 | 2019-02-22 | 中国工程物理研究院核物理与化学研究所 | 一种抗菌提铀纤维及其制备方法 |
CN110577639A (zh) * | 2019-08-09 | 2019-12-17 | 上海高聚生物科技有限公司 | 一种聚五亚甲基胍盐及其制备方法和应用 |
CN110777442A (zh) * | 2019-11-06 | 2020-02-11 | 吉林师范大学 | 衣康酸胍基苯乙烯共聚消毒纤维制备方法 |
CN111484698B (zh) * | 2020-04-27 | 2022-08-16 | 上海应用技术大学 | 一种胍盐酸盐抗菌剂改性马来酸酐接枝共聚聚丙烯复合材料的制备方法 |
CN112521600A (zh) * | 2020-11-13 | 2021-03-19 | 上海明涌新材料有限公司 | 一种胍盐聚合物及其制备方法与用途 |
CN113508820A (zh) * | 2021-06-29 | 2021-10-19 | 中海油天津化工研究设计院有限公司 | 一种油溶性高效杀菌剂及其制备方法 |
CN114369188A (zh) * | 2021-11-18 | 2022-04-19 | 山东志存科技有限公司 | 一种大分子杀菌剂-聚烯烃卡巴嘧啶的合成工艺 |
CN114317131A (zh) * | 2021-12-06 | 2022-04-12 | 山东志存科技有限公司 | 一种强力杀菌去污洗衣片及制作工艺 |
-
2000
- 2000-10-19 CN CN 00125721 patent/CN1111556C/zh not_active Expired - Lifetime
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100406496C (zh) * | 2003-07-23 | 2008-07-30 | 上海塑杰科技有限公司 | 一种多元胺与胍盐聚合物及其在抗菌聚酯和聚酰胺材料中的应用 |
WO2020073784A1 (zh) | 2018-10-10 | 2020-04-16 | 桂林新先立抗菌材料有限公司 | 一种抗菌聚合物及其制备方法 |
JP2022504411A (ja) * | 2018-10-10 | 2022-01-13 | 桂林新先立抗菌材料有限公司 | 抗菌性ポリマーおよびその調製方法 |
JP7107534B2 (ja) | 2018-10-10 | 2022-07-27 | 桂林新先立抗菌材料有限公司 | 抗菌性ポリマーおよびその調製方法 |
US11773220B2 (en) | 2018-10-10 | 2023-10-03 | Guilin Zheqi Technology Co., Ltd | Antibacterial polymer and preparation method thereof |
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Publication number | Publication date |
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CN1350022A (zh) | 2002-05-22 |
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Address after: 541003 No. 3 Pingshan North Road, Guilin, the Guangxi Zhuang Autonomous Region Patentee after: Guilin Xinxianli Antibacterial Material Co.,Ltd. Address before: 541003 No. 3 Pingshan North Road, Guilin, the Guangxi Zhuang Autonomous Region Patentee before: Guilin Chi Chi Feng Feng antibacterial material Co., Ltd. |
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