Unlock instant, AI-driven research and patent intelligence for your innovation.
Catalyst for ring-opening polymerization of cyclic ester and preparation method thereof
What is Al technical title?
Al technical title is built by PatSnap Al team. It summarizes the technical point description of the patent document.
A ring-opening polymerization, catalyst technology, applied in the field of cyclic ester ring-opening polymerization catalyst and its preparation
Active Publication Date: 2004-11-10
长春宸泰科技有限公司
View PDF0 Cites 34 Cited by
Summary
Abstract
Description
Claims
Application Information
AI Technical Summary
This helps you quickly interpret patents by identifying the three key elements:
Problems solved by technology
Method used
Benefits of technology
Problems solved by technology
These traditional catalysts are not selective for different configurations of lactide and when used to polymerize racemic lactide, only amorphous polymers are obtained
Method used
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more
Image
Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
Click on the blue label to locate the original text in one second.
Reading with bidirectional positioning of images and text.
Smart Image
Examples
Experimental program
Comparison scheme
Effect test
Embodiment 1
[0027] Embodiment 1: Catalyst Salmpen ( t Synthesis of Bu)AlEt,
[0028] Under the protection condition of stirring and inert gas, put 4ml of Schiff's base Salmpen ( t Bu)H 2 Toluene solution (1mol / L) and 4ml of AlEt 3 Toluene solution (1mol / L) is mixed, temperature control 80 ℃, stirs 48 hours, then cools down, vacuumizes and removes volatile matter, obtains product Salmpen ( t Bu)AlEt 2.24g, yield 95.1%. Elemental analysis results,
[0029] Calculated: C, 75.47; H, 9.76; N, 4.76; Found: C, 75.52; H, 9.59; N, 4.88.
Embodiment 2
[0030] Embodiment 2: Catalyst Salmpen ( t Bu)AlO i Synthesis of Pr
[0031] In addition to the AlEt in Example 1 3 Change aluminum isopropoxide into, and temperature of reaction changes outside 120 ℃, and other steps are identical with example 1, obtain product Salmpen ( t Bu)AlO i Pr 2.31g, yield 93.3%. Elemental analysis results, calculated value: C, 73.75; H, 9.61; N, 4.53; found value: C, 73.98; H, 9.87; N, 4.16.
Embodiment 3
[0032] Embodiment 3: Catalyst Salepen ( t Synthesis of Bu)AlEt
[0033] In addition to changing the Schiff base in Example 1 into Salepen ( t Bu)H 2 , the temperature of reaction is changed to 50 ℃, and other steps are identical with example 1, obtain product Salepen ( t Bu)AlEt 2.38g, yield 96.5%. Elemental analysis results, calculated value: C, 75.93; H, 9.97; N, 4.54; found value: C, 75.97; H, 10.21; N, 4.66.
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More
PUM
Property
Measurement
Unit
melting point
aaaaa
aaaaa
melting point
aaaaa
aaaaa
melting point
aaaaa
aaaaa
Login to View More
Abstract
The invention relates to a category of cyclic ester open loop polymerization catalyst and method for preparation, it also relates to the process for polymerizing racemic lactide by using these catalysts, wherein the catalysts are the product of the reaction between Schiff's base and aluminium triethide or aluminium isopropoxide, they exhibit stereoselectivity to the polymerization of racemic lactide, thus crystallinitypolylactic acid can be obtained through polymerizing racemic lactide.
Description
technical field [0001] The invention relates to a catalyst for ring-opening polymerization of cyclic esters, a preparation method thereof, and a method for stereoselectively polymerizing racemic lactide using the catalyst. technical background [0002] From an environmental protection point of view, polymers are required to be biodegradable in order to reduce waste disposal and pollution. Polylactic acid is a biocompatible and biodegradable polymer material. Compared with polyolefin, it has incomparably excellent characteristics in terms of environmental protection. At the same time, in the medical field, polylactic acid is more and more widely used, for example: it can be used as sutures, bone nails, bone rods, and drugcontrolled release carriers. [0003] Polylactic acid is generally obtained by ring-opening polymerization of lactide, and there have been a large number of patents and scientific documents disclosing the preparation of polylactic acid by ring-opening polym...
Claims
the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More
Application Information
Patent Timeline
Application Date:The date an application was filed.
Publication Date:The date a patent or application was officially published.
First Publication Date:The earliest publication date of a patent with the same application number.
Issue Date:Publication date of the patent grant document.
PCT Entry Date:The Entry date of PCT National Phase.
Estimated Expiry Date:The statutory expiry date of a patent right according to the Patent Law, and it is the longest term of protection that the patent right can achieve without the termination of the patent right due to other reasons(Term extension factor has been taken into account ).
Invalid Date:Actual expiry date is based on effective date or publication date of legal transaction data of invalid patent.