CN1314426A - Modified polyurethane elastomer material and its preparing method and use - Google Patents

Modified polyurethane elastomer material and its preparing method and use Download PDF

Info

Publication number
CN1314426A
CN1314426A CN 00114428 CN00114428A CN1314426A CN 1314426 A CN1314426 A CN 1314426A CN 00114428 CN00114428 CN 00114428 CN 00114428 A CN00114428 A CN 00114428A CN 1314426 A CN1314426 A CN 1314426A
Authority
CN
China
Prior art keywords
lignin
nitration
elastomer material
polyurethane elastomer
castor oil
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
Application number
CN 00114428
Other languages
Chinese (zh)
Other versions
CN1116330C (en
Inventor
张俐娜
黄进
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wuhan University WHU
Original Assignee
Wuhan University WHU
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Wuhan University WHU filed Critical Wuhan University WHU
Priority to CN 00114428 priority Critical patent/CN1116330C/en
Publication of CN1314426A publication Critical patent/CN1314426A/en
Application granted granted Critical
Publication of CN1116330C publication Critical patent/CN1116330C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Polyurethanes Or Polyureas (AREA)
  • Biological Depolymerization Polymers (AREA)

Abstract

The modified polyurethane elastomer material is prepared by mixing nitrolignin, castor oil type polyurethane, chain expander, 1,4-bytanediol and solvlent tetrahydrofuran and curing at proper condition. Compared with existing polyurethane, the modified polyurethane has obviously raised tensile strength and extension at break, and it has elasticity of restoring deformation completely similar to that of rubber and may be biologically degraded. It may be used as biologically degraded paint and film material in medicine, daily use, chemical industry, environment protection and other fields.

Description

Modified polyurethane elastomer material and its production and use
The present invention relates to a kind of modified polyurethane elastomer material and its production and use, specifically a kind of castor oil type polyurethane elastomer material that contains a small amount of nitration of lignin and its production and use, belong to filed of functional, also belong to the natural polymer field.
Xylogen is used as fuel mostly as the byproduct of paper industry, but it is considered to have the potentiality that become chemical industry basic raw material and preparation Biodegradable material with nontoxic, low-cost and biodegradable characteristics.Up to now, utilize xylogen to prepare plastics (United States Patent (USP), 4131573,1978), resin (Canadian Patent, 654728,1962) and tackiness agent (United States Patent (USP), 3931072,1976; Material and as research (United States Patent (USP), 2610954,1962 of rubber accelerator such as 3886101,1974); German Patent, 1165844,1964) remarkable progress (Progress in Polymer Science, 17,611,1992 have been obtained; The polymer circular, 4,240,1992).But these researchs are mostly at sulfonated lignin and kraft paper xylogen, and the applied research of byproduct-alkali lignin that the southern alkaline process of China is obtained does not appear in the newspapers as yet.Interpenetrating polymer networks is a powerful measure of improving material property in the polymeric material field.Resins, epoxy-castor oil type polyurethane grafting interpenetrating polymer networks material is with the increase of epoxy resin content, and the tensile strength of its material increases but elongation at break reduces (Journal of Applied Polymer Science, 70,1649,1998); Polystyrene-Viscotrol C urethane interpenetrating polymer networks material shows the plasticity (Polymer Engineering and Science, 18,200,1978) of polystyrene gradually with the increase of polystyrene content.
The purpose of this invention is to provide a kind of polyurethane elastomer material of modification-contain castor oil type polyurethane elastomer material of nitration of lignin and its production and use, mechanical properties such as the tensile strength of this modified polyurethane elastomer material, elongation at break should be than being significantly improved before the modification, and can be used as biodegradable preventing water coating and mould material.
For achieving the above object, the technical solution adopted in the present invention is as follows:
A kind of modified polyurethane elastomer material, it be with isocyanato (NCO) and hydroxyl (molar ratio OH) is 2.0 castor oil type polyurethane prepolymer, 1,4-butyleneglycol and nitrogen content 6.32%, weight-average molecular weight 0.5~2.0 * 10 4Nitration of lignin be dissolved in respectively in the tetrahydrofuran solvent, mix then, solidified 6~8 hours down and obtain at 15-40 ℃ respectively, the massfraction of the nitration of lignin wherein ratio of material total mass (nitration of lignin with) is 1~6%.
A kind of method for preparing the polyurethane elastomer material of above-mentioned modification: with tetrahydrofuran (THF) do solvent be made into respectively massfraction be 28.6% isocyanato (NCO) and hydroxyl (molar ratio OH) be 2.0 castor oil type polyurethane prepolymer, 18.4% 1, the solution of 4-butyleneglycol and 1.0~5.9% nitration of lignin, mix by 1: 1: 1 volume ratio then, curing made the polyurethane film that contains nitration of lignin (massfraction is 1~6%) in 6~8 hours under 15-40 ℃ respectively, promptly contained the castor oil type polyurethane elastomer material of nitration of lignin.
According to technical scheme of the present invention, the preparation method of described nitration of lignin is: after 20 gram bamboo wood alkali lignins (byproduct of paper industry) and the mixing of 35mL nitrosonitric acid, drip the 22mL diacetyl oxide, in cryosel stirred in water bath 12~18 hours, the solid sediment that reaction is obtained was repeatedly with the frozen water washing and surpass centrifugal settling and obtain neutral, nitrogen content 6.32%, weight-average molecular weight 0.5~2.0 * 10 then 4Nitration of lignin; It has good solubility in ethyl acetate and tetrahydrofuran (THF).
According to technical scheme of the present invention, the preparation of castor oil type polyurethane prepolymer is with reference to the method (Macromolecules, 12,360,1979) of L.H.Sperling.Viscotrol C dehydration one hour under 100 ℃, the pressure of 20mmHg is heavily steamed before tolylene diisocyanate uses.Viscotrol C is added dropwise to tolylene diisocyanate lentamente 40 ℃ of following stirring reactions 2 hours.The mass ratio of Viscotrol C and tolylene diisocyanate is 57: 29, the conversion obtain isocyanato (NCO) and hydroxyl (molar ratio OH) is 2.0.
Modified polyurethane elastomer material of the present invention has excellent mechanical property, and biodegradable.Therefore, this material can be used as super quality and competitive price, biodegradable, pollution-free green coating and mould material, also can be used as new resilient material and is used for fields such as medicine, daily, chemical industry and environmental protection.
Modified polyurethane elastomer material of the present invention is to have introduced a small amount of nitration of lignin when synthetic preparation, make the material after the modification all increase nearly one times by graft crosslinking reaction, show that nitration of lignin is very effective to the enhancing and the toughening effect of polyurethane material than mechanical properties such as the tensile strength of original castor oil type polyurethane and elongation at breaks; Graft reaction has taken place between nitration of lignin and castor oil type polyurethane in the testimonial material in infrared spectra, transmission electron microscope etc. as a result, simultaneously the stronger hydrogen bond of intermolecular existence and thermostability is improved.Material presents good consistency and two kinds of intermolecular networks obviously increase, and causes intensity and elastic raising thus.The material that obtains has the elasticity of rubber like, and its tensile deformation can recover fully.This material also has biodegradable in addition, can be used as water-repellancy green coating component or biodegradable functional film material and is used for the green chemical industry field.The byproduct that the present invention utilizes this inexpensive, abundant, biodegradable paper industry of alkali lignin is as one of raw material of preparation modified polyurethane elastomer material, both reach the purpose that increases mechanical properties such as tensile strength of material and elongation at break simultaneously, improved the economic value added that alkali lignin uses again.That therefore should invent is high in technological content, has the characteristics of easy exploiting utilization and changing waste into valuables.
The present invention is a nitrating agent with nitrosonitric acid and diacetyl oxide, makes nitration of lignin with the reaction of bamboo wood alkali lignin, and makes castor oil type polyurethane coating or the mould material that contains nitration of lignin first.A small amount of nitration of lignin has very strong reactive behavior, and it and castor oil type polyurethane reaction form the intermolecular cross-linking network, thereby its intensity and elasticity are improved greatly.What should particularly point out is that tensile strength of material and the elongation at break that obtains increased nearly one times simultaneously, and presents the stress-strain feature of rubber.Therefore this invention has significant technical progress.
Below in conjunction with specific embodiment technical scheme of the present invention is further described:
Embodiment 1
20 gram bamboo wood alkali lignins and 35mL nitrosonitric acid are mixed back dropping 22.5mL diacetyl oxide, constantly stirred 18 hours in the cryosel water-bath, the solid sediment that reaction is obtained washs and surpasses centrifugal settling with frozen water repeatedly and obtains neutral, nitrogen content 6.32%, weight-average molecular weight 1.1 * 10 then 4Nitration of lignin; It has good solubility in ethyl acetate and tetrahydrofuran (THF).
Viscotrol C dehydration one hour under 100 ℃, the pressure of 20mmHg is heavily steamed before tolylene diisocyanate uses.Viscotrol C is added dropwise to tolylene diisocyanate lentamente 40 ℃ of following stirring reactions 2 hours.The mass ratio of Viscotrol C and tolylene diisocyanate is 57: 29, the conversion obtain isocyanato (NCO) and hydroxyl (molar ratio OH) is 2.0.
With tetrahydrofuran (THF) do solvent be made into respectively massfraction be 28.6% castor oil type polyurethane prepolymer, 18.4% 1, the solution of 4-butyleneglycol and 1.4% nitration of lignin, mix by 1: 1: 1 volume ratio then, on the tetrafluoroethylene plate, make the polyurethane film that contains nitration of lignin (massfraction is 1.4%) by the hydrostomia method, solidification value is 20 ± 2 ℃, 8 hours set times.The film that the mechanical property of this film obtains than comparative example 1 has increased nearly one times.
Embodiment 2
The preparation method of polyurethane film who contains nitration of lignin (massfraction is 2.9%) is with embodiment 1, and the massfraction that only adds nitration of lignin-tetrahydrofuran solution is 2.8%.The tensile strength of this film and elongation at break all increase than the material that embodiment 1 obtains.
Embodiment 3
Reduce at the suitable but elongation at break of 35 ± 2 ℃ of tensile strengths of solidifying the polyurethane film that obtained in 6 hours down and film that embodiment 1 obtains according to embodiment 1 proportioning raw materials and method, compare mechanical property with comparative example 2 and be significantly improved.
Embodiment 4
Solidify the polyurethane film that obtained in 6 hours according to embodiment 2 proportioning raw materials and method down at 35 ± 2 ℃.Compare with the film that embodiment 2 obtains, the tensile strength of this film quite and elongation at break increase; Compare with the film that embodiment 3 obtains, the tensile strength and the elongation at break of this film all are significantly improved.Particularly the film that obtains than comparative example 1 and 2 of its elongation at break has increased more than one times.
Embodiment 5
The preparation method of polyurethane film who contains nitration of lignin (massfraction is 5.5%) is with embodiment 1, the massfraction that only adds nitration of lignin-tetrahydrofuran solution be 5.4% and solidification value be 35 ± 2 ℃, 6 hours set times.The film that this tensile strength of material and embodiment 3 obtain is suitable, but elongation at break increases.Comparative example 1
Method by embodiment 1 makes the castor oil type polyurethane prepolymer.Making solvent with tetrahydrofuran (THF), to be made into massfraction respectively be 1 of 28.6% castor oil type polyurethane prepolymer and 18.4%, the 4-butyleneglycol, mix by 1: 1 volume ratio then, on the tetrafluoroethylene plate, make the castor oil type polyurethane film by the hydrostomia method, solidification value is 20 ± 2 ℃, 8 hours set times.Comparative example 2
Method with comparative example 1 makes the castor oil type polyurethane film, but solidification value is 35 ± 2 ℃, 6 hours set times.
The mechanical property of subordinate list 1 nitration of lignin-castor oil type polyurethane film
The feature mechanical property
Nitration of lignin content temperature of reaction σ b/ MPa ε b/ %
10 20 ± 2 ℃ 11.73 126 of comparative example
1 1.4% 20 ± 2 ℃ 20.80 211 of embodiment
2 2.9% 20 ± 2 ℃ 22.85 239 of embodiment
20 35 ± 2 ℃ 14.15 106 of comparative example
3 1.4% 35 ± 2 ℃ 20.07 164 of embodiment
4 2.9% 35 ± 2 ℃ 22.90 258 of embodiment
Embodiment annotates for 5 5.5% 35 ± 2 ℃ 19.88 215: Mechanics Performance Testing records on the CMT6503 instrument of Shenzhen SANS testing tool company with reference to State Standard of the People's Republic of China GB4456-84, and draw speed is 100mm/min.

Claims (5)

1. modified polyurethane elastomer material, it is characterized in that: it is that molar ratio by isocyanato and hydroxyl is 2.0 castor oil type polyurethane prepolymer, 1,4-butyleneglycol and nitration of lignin are dissolved in the tetrahydrofuran solvent respectively, mix then, solidify 6~8 hours gained down at 15-40 ℃, wherein the massfraction of nitration of lignin is 1~6%.
2. method for preparing the described modified polyurethane elastomer material of claim 1, it is characterized in that: with tetrahydrofuran (THF) do solvent be made into respectively massfraction be the molar ratio of 28.6% isocyanato and hydroxyl be 2.0 castor oil type polyurethane prepolymer, 18.4% 1, the solution of 4-butyleneglycol and 1.0~5.9% nitration of lignin, mix by 1: 1: 1 volume ratio then, solidify the product that obtained in 6~8 hours down at 15-40 ℃ respectively and be the castor oil type polyurethane elastomer material that contains nitration of lignin.
3. method according to claim 2 is characterized in that: the nitrogen content of described nitration of lignin is 6.32%, weight-average molecular weight is 0.5~2.0 * 10 4
4. nitration of lignin according to claim 3 is to prepare gained by following method, it is characterized in that: after 20 gram bamboo wood alkali lignins and the mixing of 35mL nitrosonitric acid, drip the 22mL diacetyl oxide, in cryosel stirred in water bath 12~18 hours, the solid sediment that reaction is obtained was repeatedly with the frozen water washing and surpass centrifugal settling and obtain nitration of lignin then.
5. the described modified polyurethane elastomer material of claim 1 is as biodegradable coating or mould material.
CN 00114428 2000-03-16 2000-03-16 Modified polyurethane elastomer material and its preparing method and use Expired - Fee Related CN1116330C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 00114428 CN1116330C (en) 2000-03-16 2000-03-16 Modified polyurethane elastomer material and its preparing method and use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 00114428 CN1116330C (en) 2000-03-16 2000-03-16 Modified polyurethane elastomer material and its preparing method and use

Publications (2)

Publication Number Publication Date
CN1314426A true CN1314426A (en) 2001-09-26
CN1116330C CN1116330C (en) 2003-07-30

Family

ID=4584112

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 00114428 Expired - Fee Related CN1116330C (en) 2000-03-16 2000-03-16 Modified polyurethane elastomer material and its preparing method and use

Country Status (1)

Country Link
CN (1) CN1116330C (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1302072C (en) * 2005-10-12 2007-02-28 太原理工大学 Modified polyurethane composition and preparation thereof
CN100469810C (en) * 2001-06-15 2009-03-18 独立行政法人产业技术综合研究所 Lignin-containing polyurethane and process for producing the same
CN102260366A (en) * 2010-05-29 2011-11-30 比亚迪股份有限公司 Water-soluble polyurethane and preparation method thereof, and water-soluble ink composition containing water-soluble polyurethane and preparation method thereof
CN109485824A (en) * 2018-10-12 2019-03-19 华南理工大学 A kind of thermosetting property lignin-base polyurethane elastomer of recyclable processing and preparation method thereof
CN110318699A (en) * 2014-03-07 2019-10-11 株式会社吴羽 The manufacturing method of drilling tool decomposability rubber component
CN113103560A (en) * 2021-04-14 2021-07-13 中国科学技术大学 High-strength polyurethane material and preparation method thereof

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100469810C (en) * 2001-06-15 2009-03-18 独立行政法人产业技术综合研究所 Lignin-containing polyurethane and process for producing the same
CN1302072C (en) * 2005-10-12 2007-02-28 太原理工大学 Modified polyurethane composition and preparation thereof
CN102260366A (en) * 2010-05-29 2011-11-30 比亚迪股份有限公司 Water-soluble polyurethane and preparation method thereof, and water-soluble ink composition containing water-soluble polyurethane and preparation method thereof
CN102260366B (en) * 2010-05-29 2014-04-02 比亚迪股份有限公司 Water-soluble polyurethane and preparation method thereof, and water-soluble ink composition containing water-soluble polyurethane and preparation method thereof
CN110318699A (en) * 2014-03-07 2019-10-11 株式会社吴羽 The manufacturing method of drilling tool decomposability rubber component
CN110318699B (en) * 2014-03-07 2021-12-07 株式会社吴羽 Method for manufacturing decomposable rubber member for drilling tool
CN109485824A (en) * 2018-10-12 2019-03-19 华南理工大学 A kind of thermosetting property lignin-base polyurethane elastomer of recyclable processing and preparation method thereof
CN113103560A (en) * 2021-04-14 2021-07-13 中国科学技术大学 High-strength polyurethane material and preparation method thereof
CN113103560B (en) * 2021-04-14 2022-05-13 中国科学技术大学 High-strength polyurethane material and preparation method thereof

Also Published As

Publication number Publication date
CN1116330C (en) 2003-07-30

Similar Documents

Publication Publication Date Title
Ciobanu et al. Properties of lignin–polyurethane films prepared by casting method
CN104628982B (en) A kind of preparation method of alkali lignin base water polyurethane
CN101429417A (en) High-adhesive property watersoluble polyurethane adhesion agent and method of producing the same
CZ304264B6 (en) Process for preparing polyurethane materials containing lignin and polyurethane material prepared in such a manner
US20240262953A1 (en) Thermoplastic elastomer with excellent resilience and high strength and preparation method thereof
Li et al. Synthesis of cationic waterborne polyurethane via thiol-ene click reaction and catechol chemistry to improve the performance of soybean meal adhesives
CN1116330C (en) Modified polyurethane elastomer material and its preparing method and use
CN110003638B (en) Calcium carbonate high-filling biodegradable film and preparation method thereof
CN108707322B (en) Method for preparing high-impact-toughness polylactic acid compound by reactive blending of vegetable oil derivatives
CN114891183A (en) Waterborne polyurethane modified starch dispersion liquid and preparation method thereof
CN111607062B (en) Biomass polyurethane foam material and preparation method thereof
CN112980376A (en) Waterborne polyurethane adhesive and preparation method thereof
CN115417998B (en) Biodegradable self-repairing rubber elastomer and preparation method and application thereof
CN1104456C (en) Semi interpenetration polymer network material and its preparing method and use
CN111205426B (en) Preparation method of low-temperature-resistant polyurethane elastomer
CN113307941B (en) Acrylate oligomer and preparation method and application method thereof
CN111826117B (en) Two-component polyurethane sealing heat-insulating glue
CN115433442A (en) Biodegradable tough composite material and preparation method thereof
CN115028986A (en) Cable sheath material and preparation method thereof
CN1583853A (en) Elastic material containing nitrated casing glycan, its preparing method and use thereof
CN1273528C (en) Half interpenetration polymer network materal and preparation process and application thereof
CN112961475A (en) Biodegradable plastic and preparation method thereof
CN118374258B (en) Adhesive and preparation method thereof
CN114524958B (en) Preparation method of degradable barrier film
CN111019331B (en) Polyester elastomer film and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee