Polyurea Elastomer Systems with Improved Adhesion to Substrates

Total Page:16

File Type:pdf, Size:1020Kb

Polyurea Elastomer Systems with Improved Adhesion to Substrates Europäisches Patentamt *EP000986593B1* (19) European Patent Office Office européen des brevets (11) EP 0 986 593 B1 (12) EUROPEAN PATENT SPECIFICATION (45) Date of publication and mention (51) Int Cl.7: C08G 18/10, C08G 18/66, of the grant of the patent: C08G 18/50, C09D 175/02, 02.01.2002 Bulletin 2002/01 B05D 7/00 (21) Application number: 98918777.8 (86) International application number: PCT/US98/08443 (22) Date of filing: 27.04.1998 (87) International publication number: WO 98/55525 (10.12.1998 Gazette 1998/49) (54) POLYUREA ELASTOMER SYSTEMS WITH IMPROVED ADHESION TO SUBSTRATES POLYHARNSTOFF-ELASTOMERSYSTEME MIT VERBESSERTER HAFTUNG AUF SUBSTRATEN SYSTEMES ELASTOMERES DE POLYUREE A ADHERENCE AMELIOREE SUR DES SUBSTRATS (84) Designated Contracting States: (72) Inventor: PRIMEAUX, Dudley, Joseph, II BE CH DE ES FR GB LI NL SE Elgin, TX 78621 (US) (30) Priority: 05.06.1997 US 869385 (74) Representative: Winkler, Andreas, Dr. 03.04.1998 US 54979 FORRESTER & BOEHMERT Pettenkoferstrasse 20-22 (43) Date of publication of application: 80336 München (DE) 22.03.2000 Bulletin 2000/12 (56) References cited: (73) Proprietor: HUNTSMAN PETROCHEMICAL EP-A- 0 344 512 US-A- 5 415 499 CORPORATION US-A- 5 442 034 US-A- 5 626 917 Austin, Texas 78752 (US) US-A- 5 631 341 Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention). EP 0 986 593 B1 Printed by Jouve, 75001 PARIS (FR) EP 0 986 593 B1 Description Field of the Invention 5 [0001] The invention relates to aliphatic and aromatic polyurea elastomers and processes for making the same, and, in one aspect, more particularly relates to methods and compositions for making aliphatic and aromatic polyurea elas- tomers having improved adhesion to wet substrates via use of a special polyurethane primer which can penetrate the substrate. The polyurea systems may be applied via spray, 2-part caulk, pour, brush-on or other method, 10 Background of the Invention [0002] Spray elastomer systems are commonly recognized as coating materials, with aliphatic and aromatic isocy- anate spray polyurea elastomer systems being particularly useful when employed in this capacity. This two-component technology is based on an isocyanate quasi-prepolymer and an amine coreactant, often an amine resin blend. 15 [0003] It is further known to use spray polyurea elastomer coatings as liners on the inside of rail cars, and on surfaces such concrete, wood, etc. Such coatings should be highly conformal to the surface sprayed and should have excellent adhesion to the surface for the lifetime of the coating. Increasingly strict environmental regulations continue to reduce the volatile organic compound (VOC) emissions permitted during the application of such coatings. These requirements have forced the coatings to have higher solids and lower solvent contents and/or be entirely water-based systems. 20 [0004] The following excerpt from G. H. Brevoort, "Current Trends and Issues in Railcar Painting and Lining," Journal of Protective Coatings and Linings, December, 1991, is instructive. [0005] "Without a doubt, the driving force in the past decade to develop high solids, improved protective coatings and linings with reduced VOCs has come from The Clean Air Act and its amendments. [0006] "Some residual benefits accrue from the use of high solids, VOC-conformant coatings and linings. For exam- 25 ple, the number of gallons required is fewer, which results in fewer containers to ship, handle, open, apply and dispose of. While the price per gallon is higher, the contents per container are greater and go further so that fewer gallons are required. Much less solvent is being packaged, shipped and emitted. Often, the actual material cost for a job is reduced with more concentrated, high-solids products. Most important, many in the industry, including individual users, are being environmentally responsible. 30 [0007] "It is not easy to formulate high solids, VOC-conformant coatings and linings. Solvents are not just removed and replaced with more solids. Among the problems encountered are maintaining suspension of the mixed products (non-settling), maintaining their application and handling characteristics, producing coatings with the ability to build adequate drying and recoating times for practical use. Leveling of the applied coating film to create a smooth appear- ance has been particularly difficult to achieve." 35 [0008] One advantage of spray polyurea technology is that no foaming is noted even if the elastomer system is applied to a wet substrate. However, in some cases the moisture acts as a barrier to mechanical/chemical adhesion. There are commercially available water emulsifiable isocyanates used as substrate primers for spray elastomer sys- tems. For wet substrates, these primers have poor penetration properties, giving poor elastomer coating system ad- hesion and possible foaming. 40 [0009] There is thus a continuing need to develop new systems to address the varied requirements of spray polyurea coatings. Various known polyurea systems have been employed which address some of these parameters. [0010] For example, U.S. Pat. No. 5,266,671 to Dudley J. Primeaux, II of Huntsman Petrochemical Corporation describes a spray polyurea elastomer which exhibits improved resistance to abrasion. The elastomer includes an isocyanate, an amine terminated polyoxyalkylene polyol, a chain extender and a chemically sized filler material. The 45 isocyanate is preferably a quasi-prepolymer of an isocyanate and a material selected from at least one polyol, a high molecular weight polyoxyalkyleneamine or a combination thereof. A method for making a spray polyurea elastomer which is substantially resistant to abrasion is also disclosed. [0011] Spray polyurea elastomers made from an (A) component and a (B) component, where the (A) component has a quasi-prepolymer made from an isocyanate and an active hydrogen-containing material, such as a polyoxy- 50 alkylenepolyamine, is described in U.S. Pat. No. 5,442,034 to Dudley J. Primeaux, II of Huntsman Petrochemical Corporation. The (B) component includes an amine resin, such as an amine-terminated polyoxyalkylene polyol which may be the same or different from the polyoxyalkylene polyamine of the quasi-prepolymer. The viscosity of the (A) component is reduced by the inclusion of an organic, alkylene carbonate, such as ethylene carbonate, propylene carbonate, butylene carbonate, dimethyl carbonate and the like. The alkylene carbonate also serves as a compatibilizer 55 between the two components, thus giving an improved mix of the system. [0012] U.S. Patent 5,415,499 discloses a method of repairing manholes by spraying polyurea on the surface. An aqueous silane solution is used as a primer. [0013] EP 0 344 512-A2 discloses polyurethane formulations where castor oil is employed as an ingredient. 2 EP 0 986 593 B1 Summary of the Invention [0014] Accordingly, it is an object of the present invention to provide a polyurea elastomer system, which can be applied via spraying or otherwise, which can be directly applied to a wet substrate with little or no foaming. 5 [0015] It is another object of the present invention to provide a polyurea elastomer system which has excellent ad- hesion to a substrate over which it is applied, even if the substrate is wet. [0016] Another object of the invention is to provide a polyurea elastomer system where the polyurea elastomer may be applied over a primer even when the primer is not completely cured. [0017] In carrying out these and other objects of the invention, there is provided, in one form, a polyurea elastomer 10 system having a primer, where the primer contains a water emulsifiable isocyanate, and a hydrophobic, primary hy- droxyl-containing compound. The system also employs a polyurea elastomer which contains a quasi-prepolymer of an isocyanate, and an active hydrogen-containing material; at least one amine resin; and at least one amine-terminated chain extender. 15 Detailed Description of the Invention [0018] It has been discovered that by utilizing a water emulsifiable isocyanate, and by using castor oil instead of water, a primer system with good penetration to the wet substrate can be realized. Even prior to cure of the primer, a fast cure spray polyurea elastomer system can be applied, thus giving a complete elastomer system with excellent 20 adhesion to wet substrates. Indeed, the primer may be immediately coated with the spray polyurea elastomer. Any residual moisture would not cause any foaming problems with the spray polyurea elastomer. [0019] In one embodiment, the primer is prepared such that an excess of isocyanate groups would be present. This would permit an actual chemical bond between the primer and the spray polyurea elastomer. Without being bound by any particular theory, the castor oil appears to allow the isocyanate to penetrate through the moisture into the substrate 25 before curing. [0020] The polyurea spray elastomer part of the system, in one embodiment of the invention, may be prepared by mixing an isocyanate component with a resin blend component, a blend of polyoxyalkylene diamines and/or triamines and amine-terminated chain extenders, in high pressure impingement mix spray equipment and can be directly applied to a primed substrate. The inventive polyurea elastomer system is expected to have excellent flexibility and elongation. 30 Superior abrasion and impact resistance are also anticipated advantages of the system. [0021] The polyurea spray elastomer systems of this invention contain no solvents and thus have little or no VOCs. They are thus considered 100% solids systems to comply with VOC requirements. [0022] Polyurea spray systems cure rapidly even under low ambient temperature conditions.
Recommended publications
  • Polyurea-Containing Reaction Injection Molded Elastomers
    Europaisches Patentamt (19) European Patent Office © Publication number: 0 092 672 Office europeen des brevets A2 © EUROPEAN PATENT APPLICATION © Application number: 83102703.2 © Int. CI.3: C 08 G 18/50 C 08 G 18/32, C 08 G 18/65 @ Date of filing: 18.03.83 B 29 D 27/00 © Priority: 23.04.82 US 371377 © Applicant: TEXACO DEVELOPMENT CORPORATION 2000 Westchester Avenue White Plains New York 1 0650(US) © Date of publication of application: 02.11.83 Bulletin 83/44 @ Inventor: Dominguez, RichardJoseph Gilbert 3107 Canter Lane © Designated Contracting States: Austin Texas 78759(US) DE FR GB IT SE © Representative: Burnside, Michael et al, c/o Michael Burnside & Partners 2 Serjeants' Inn Fleet Street London EC4Y1HLIGB) © Polyurea-containing reaction injection molded elastomers. The invention relates to reaction injection molded elastomers containing a minor amount of polyurea linkages derived from high molecular weight amine terminated polyethers, a hydroxyl terminated chain extender and a polyisocyanate. The reaction injection molded (RIM) elas- tomers of this invention are useful, for example, as auto- mobile body parts. This invention concerns the field of reaction in- jection molded elastomers. United States Patents 4,254,069 and 4,272,618 concern the curing of RIM polyurethane elastomers. In the Glossary of these patents, a "polyol" is defined as a di- or greater functionality high molecular weight alcohol or an amine terminated molecule composed of ether groups. In the discussion of chain extenders in these patents, low molecular weight hydroxyl terminated molecules; e.g., ethylene glycol, are disclosed. However, the actual examples are of polyether polyurethanes using polyols (hy- droxyl terminated) of high molecular weight.
    [Show full text]
  • Influence of Hard Segment Content and Diisocyanate Structure on the Transparency and Mechanical Properties of Poly(Dimethylsilox
    polymers Article Influence of Hard Segment Content and Diisocyanate Structure on the Transparency and Mechanical Properties of Poly(dimethylsiloxane)-Based Urea Elastomers for Biomedical Applications Natascha Riehle 1,2, Kiriaki Athanasopulu 1,2, Larysa Kutuzova 1,2, Tobias Götz 3, Andreas Kandelbauer 2 , Günter E. M. Tovar 3,4 and Günter Lorenz 2,* 1 Reutlingen Research Institute, Reutlingen University, Alteburgstr. 150, 72762 Reutlingen, Germany; [email protected] (N.R.); [email protected] (K.A.); [email protected] (L.K.) 2 Center for Process Analysis & Technology (PA&T), School of Applied Chemistry, Reutlingen University, Alteburgstrasse 150, 72762 Reutlingen, Germany; [email protected] 3 Institute of Interfacial Process Engineering and Plasma Technology IGVP, University of Stuttgart, Nobelstr. 12, 70569 Stuttgart, Germany; [email protected] (T.G.); [email protected] (G.E.M.T.) 4 Fraunhofer-Institute for Interfacial Engineering and Biotechnology IGB, Nobelstr. 12, 70569 Stuttgart, Germany * Correspondence: [email protected]; Tel.: +49-7121-271-2027 Abstract: The effect of hard segment content and diisocyanate structure on the transparency and mechanical properties of soft poly(dimethylsiloxane) (PDMS)-based urea elastomers (PSUs) was in- Citation: Riehle, N.; Athanasopulu, vestigated. A series of PSU elastomers were synthesized from an aminopropyl-terminated PDMS (Mn: − K.; Kutuzova, L.; Götz,
    [Show full text]
  • Polyurea Elastomers
    WHAT IS A POLYUREA ELASTOMER? A polyurea is a polymer based on the reaction of an isocyanate with a polyamine. It is mixed at high temperature (around 80°C) to initiate rapid polymerization. The resulting polymer is highly elastomeric – that is, it has a high capacity to deform (stretch) and recover. Coatings based on polyurea elastomer also exhibit extraordinary toughness and resistance to impact, tear and abrasion. Furthermore, polyurea polymers cure at lower temperatures, and operate at much greater extremes of temperature than other polymers. Polyurea elastomer coatings are 100% solids, and contain no volatile organic components (zero VOC) and are therefore virtually odourless. They cure within minutes, so flooring and equipment can undergo maintenance with minimal disruption. This combination of properties offers unique opportunities for true Application OF Dulux Flexituff® Polyurea is by plural polyurea elastomer coatings in the protective coatings industry. spray and takes only a few seconds to cure WHAT IS A POLYUREA HYBRID? A true polyurea elastomer is the product of the reaction of a poly- isocyanate component and an amine-terminated resin (polyamine). A polyurethane is the product of the reaction of a poly-isocyanate component and a polyol. Polyurea forms a tough, rubber-like layer that is seamless and extremely resilient to impact Polyurethanes have significantly different properties from polyurea elastomers. A polyurethane is generally hard and of low flexibility and therefore an ideal finish coat as part of a protective coating system over steelwork, car bodies and other rigid, dimensionally stable substrates not normally exposed to high mechanical impact. A polyurea hybrid is the product of the reaction between an isocyanate and a mixture of polyol and polyamine reactants.
    [Show full text]
  • The True Polyurea Spray Elastomer Story: Chemistry, Advances and Applications
    The True Polyurea Spray Elastomer Story: Chemistry, Advances and Applications Dudley J. Primeaux II, PCS * Owner / Consultant Primeaux Associates LLC 161 Forest Drive Elgin, Texas 78621-5552 USA 1-512-285-4870 [email protected] Lee Hanson and Ray V. Scott The Hanson Group LLC 340 Hurstbourne Lane, Suite 210 Duluth, Georgia 30097 USA 1-770-495-9554 www.hansonco.net Monday, September 11, 2006 4:15 – 4:45 pm "Presented at a meeting of the Thermoset Resin Formulators Association at the Hyatt Regency Montreal in Montreal, Quebec, Canada, September 11 through 12, 2006. This paper is presented by invitation of TRFA. It is publicly distributed upon request by the TRFA to assist in the communication of information and viewpoints relevant to the thermoset industry. The paper and its contents have not been reviewed or evaluated by the TRFA and should not be construed as having been adopted or endorsed by the TRFA.” * Presenter ABSTRACT: The polyurea elastomer coating / lining technology has shown some very significant inroads since the introduction of the technology back in the late 1980’s and has grown in use by significant volumes since the initial start in the early 1990’s. As “polyurea” is a description of a complete technology area, there are a variety of systems / formulations / chemistry available and this has become very confusing. Recent technical developments have pushed the technology into new use areas including concrete coatings / linings, steel coatings, traffic deck systems and specialty coating uses. This paper will take a look at the polyurea technology, formulation basics and chemical advancements as well as application and performance.
    [Show full text]
  • 100% Solids Polyurethane and Polyurea Coatings Technology
    049CWM0303.pdf !"#$%#&'!!()$*!+,!!+-./!0% 100% Solids Polyurethane and Polyurea Coatings Technology he need for corrosion pro- tection has provided a When it comes to corrosion protection, great challenge for today’s how do these technologies stack up? coatings industry to for- mulate and to provide By Shiwei William Guan coatings products that can Madison Chemical Industries meet various combined requirements. These standing about the differences among tems’ structure, properties and appli- include environmental the three systems as well as the cation characteristics and provides Tand safety compliance such as volatile advantages and disadvantages of each guidelines on the selection of the three organic compound (VOC) content, system’s application and performance. coating systems by highlighting the cost-effectiveness, appearance and A lot of hype also exists, especially development of several new systems of high performance. with respect to 100% solids elastomer- 100% solids polyurethane and The ideal corrosion protection coat- ic polyurea coatings, which needs to be polyurea coatings technology and their ing system must be environmentally put in perspective by providing an application in high-performance corro- friendly, worker-safe, durable and able accurate gauge to decide whether a sion protection. These new systems to expose little or no metal/substrate polyurea or polyurethane is the best include modifications by ceramic surface to the environment while choice for an application. and/or anti-microbial additives and the being resistant to environmental, This paper reviews the basic chem- world’s first 100% solids, rigid and mechanical and chemical damage istry and development of three coat- aliphatic polyurethane coatings. from the initial stage of handling and ings systems currently available: installation through its entire service 100% solids elastomeric polyurethane, Chemistry and Development life.
    [Show full text]
  • Polyurea Basic Concepts Rev 0918 1
    Polyurea Basic Concepts Rev 0918_1 Primeaux Associates LLC Informal Casual Atmosphere • Welcome to the Polyurea Basic Concepts Course • Follow a PowerPoint Presentation – Course Manual • Ask questions when you have them • Get to know the people in the room – Material suppliers – Equipment suppliers – Contractors – Inspectors – Consultants – Newcomers to the business Introductions • Instructor – Dudley Primeaux II, PCS, CCI – > 50 Technical Publications – Named inventor on > 30 Patents • Class Self Introductions Polyurea Basics, Rev 0918.1 1 Primeaux Associates LLC Polyurea Disclaimer • Not all polyurea’s are created equal • Material covered & physical properties do not apply to all polyurea’s • Many different aspects determine a successful application of polyurea – Material selection for project – Surface preparation – Equipment setup & use – Application techniques What is Polyurea? Polyurea Basics, Rev 0918.1 2 Primeaux Associates LLC What is a “Polyurea”? “Polyurea” is a description of a technology and it in itself is not a coating / lining material. Polyurea Technology • Polyurea is a thermoset material, not a thermoplastic • As with all thermoset materials, there is some “shrinkage” associated with cure • Can be between 0.5 – 5.0% linear! Polyurea Basics, Rev 0918.1 3 Primeaux Associates LLC Polyurea Technology Polyurea Technology Typical Shrinkage, general values Hardness, Shore D Elongation, % Shrinkage, % 60 – 70 < 100 3 – 5 % 50 – 60 ~200 – 250 2 – 4 % 40 – 50 ~250 – 500 1.5 – 2.5 % < 35 ~250 – 800 0.5 – 1.0 % Polyurea Basics, Rev 0918.1 4 Primeaux Associates LLC Polyurea Definition •A pure polyurea coating / elastomer is derived from the reaction product of a polyisocyanate component and an amine-terminated resin blend. For reference purposes, a polyurethane / polyurea hybrid coating / elastomer is the reaction product of a polyisocyanate component and a resin blend component.
    [Show full text]
  • Elastocoat®: Polyurea • Strong • Seamless • Crack-Bridging • Durable
    150 years Elastocoat®: Polyurea • strong • seamless • crack-bridging • durable 1 150 years Content Chemistry of polyurea Properties of polyurea Polyurea benefits Applications Spray product portfolio Product testing 2 150 years Chemistry of Polyurea Spray Elastomers Polyurea is an elastomer made from two reactive components with a volume mixing ratio of 1:1. O O OCN NCO R H2N R' NH2 R R' * + * N N N N isocyanate- H H H H n prepolymer amine resin polyurea Isocyanate components: Resin components: MDI-based prepolymers Polyetheramines for aromatic systems Amine chain extenders HDI- or IPDI-based Other diamines (e.g. DMDC) for aliphatic systems Pigments Additives 3 150 years Polyurea Spray Elastomers Benefits Fast reactivity, set and cure - rapid return to service Relative processing insensitivity Temperature tolerant: cures even below 0 °C Moisture tolerant: no foaming even at 99 % rH Broader processing window 4 150 years Polyurea Spray Elastomers Benefits Wider application window 5 150 years Polyurea Spray Elastomers Benefits Flexible, seamless and resilient, in comparison to other systems 6 150 years Polyurea Spray Elastomers Benefits Rapid application even on vertical areas Relatively unlimited application thickness Good adhesion to many substrates with correct surface preparation (metal, concrete and wood) 7 150 years Polyurea – Unique Properties, High Performance Polyurea Polyurethane Epoxy Gel time + 0 - Moisture insensitivity ++ 0 + Elongation + 0 -- Hardness 0 0 + Tensile strength ++ 0 - Abrasion resistance ++ 0 +
    [Show full text]
  • Technology and Future Prospects for Lightweight Plastic Vehicle Structures
    ANLIESDITM-138 Technology and Future Prospects for Lightweight Plastic Vehicle Structures by F. Stodolsky, R.M. Cuenca, and P.V. Bonsignore Center for Transportation Research, Energy Systems Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, Illinois 60439 August 1997 Work sponsored by United States Department of Energy, Assistant Secretary for Energy Efficiency and Renewable Energy, Office of Transportation Materials TRISWION OF MIS DOCUMENT is UNlJMm @ This report is printed on recycled paper. .. II DISCLAIMER This report was prepared as an account of work sponsored by an agenq of the United States Government Neither the United States Government nor any agency thereof, nor any of their empioyees, make any warranty, express or impiied, or aoumes any legal liabili- ty or respolsibiiity for the accuracy, cornpletewss, or usefdness of any infomaation, appa- ratus, produd, or process disdosed, or represents that its use wouid not infringe privately owned rights Refmnce herein to any specific annmerdal product, pmcess, or service by trade name, trademark, manufacturer, or othemise does not mlymnstitute or imply its endorsement, namnmbbbn, or favoring by the United States Government or any agency tbereof. The views and opinions of authors expressed herein do not neeessar- ily state or reflect those of the United States Government or any agency thereof. DISCLAIMER Portions of this document may be illegible electronic image products. Images are produced from the best available original document. Preface Most information for this report was obtained in 1994, and early drafts of this report were completed in 1995. While significant advances have been reported in the field of automotive plastics over the past three years, the authors feel their conclusions are still valid.
    [Show full text]
  • Finding a Green Alternative to Vinyl Resin Coatings – Final Report
    Finding a Green Alternative to Vinyl Resin Coatings – Final Report Research and Development Office Science and Technology Program (Final Report) ST-2017-8835-1, 8540-2017-49 U.S. Department of the Interior Bureau of Reclamation Research and Development Office November 2017 Mission Statements The U.S. Department of the Interior protects America’s natural resources and heritage, honors our cultures and tribal communities, and supplies the energy to power our future. The mission of the Bureau of Reclamation is to manage, develop, and protect water and related resources in an environmentally and economically sound manner in the interest of the American public. The following form is a Standard form 298, Report Documentation Page. This report was sponsored by the Bureau of Reclamations Research and Development office. For more detailed information about this Report documentation page please contact David Tordonato at 303-445-2394. THIS TEXT WILL BE INVISIBLE. IT IS FOR 508 COMPLIANCE OF THE NEXT PAGE. Disclaimer: This document has been reviewed under the Research and Development Office Discretionary peer review process https://www.usbr.gov/research/peer_review.pdf consistent with Reclamation's Peer Review Policy CMP P14. It does not represent and should not be construed to represent Reclamation's determination, concurrence, or policy. REPORT DOCUMENTATION PAGE Form Approved OMB No. 0704-0188 T1. REPORT DATE T2. REPORT TYPE T3. DATES COVERED November 2017 Research T4. TITLE AND SUBTITLE Finding a Green Alternative to Vinyl Resin Coatings 5a. CONTRACT NUMBER XXXR4524KS-RR4888FARD160100011 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 1541 (S&T) 6. AUTHOR(S) 5d. PROJECT NUMBER 8835 David Tordonato (303) 445-2394 [email protected] 5e.
    [Show full text]
  • Chemistry, Comparisons & Facts
    CHEMISTRY,CHEMISTRY, COMPARISONSCOMPARISONS andand FACTSFACTS regardingregarding POLYURETHANESPOLYURETHANES andand POLYUREASPOLYUREAS CHEMISTRYCHEMISTRY Part A Part B ++ == POLYURETHANEPOLYURETHANE Isocyanate Part A ++ Part B == POLYUREAPOLYUREA Isocyanate PolyurethanePolyurethane ReactionReaction HH OO RR--NCONCO ++ RR1--OHOH RR--NN--CC--OO--RR1 (Isocyanate) (Polyol) (POLYURETHANE) PolyureaPolyurea ReactionReaction OO RR--NCONCO ++ RR1--NHNH2 RR--NHNH--CC--NHNH--RR1 (Isocyanate) (Amine) (POLYUREA) Isocyanate Types DEFINITIONDEFINITION POLYURETHANEPOLYURETHANE // POLYUREAPOLYUREA FuturaFutura && HuntsmanHuntsman define:define: PolyureaPolyurea asas havinghaving >80%>80% amineamine contentcontent inin thethe “B”“B” component.component. PolyurethanePolyurethane asas havinghaving >80%>80% polyolpolyol contentcontent inin thethe “B”“B” component.component. PolyurethanePolyurethane // PolyureaPolyurea HybridHybrid asas aa materialmaterial betweenbetween thethe aboveabove criteria.criteria. POLYURETHANEPOLYURETHANE DevelopedDeveloped duringduring WWWW II.II. SolventSolvent basedbased becamebecame popularpopular inin thethe 1970’s.1970’s. SolventSolvent freefree developeddeveloped inin thethe 1980’s.1980’s. EarlyEarly usesuses werewere asas coatingscoatings forfor PolyurethanePolyurethane foamfoam roofing.roofing. POLYUREAPOLYUREA DevelopedDeveloped inin thethe earlyearly 1980’s.1980’s. TexacoTexaco (Huntsman)(Huntsman) hashas patentpatent onon rawraw materials.materials. WorkedWorked closelyclosely withwith FuturaFutura toto developdevelop
    [Show full text]
  • Meso-Scale Computational Investigation of Polyurea Microstructure and Its Role in Shockwave Attenuation/Dispersion
    Volume 2, Issue 3, 163-188. DOI: 10.3934/matersci.2015.3.163 Received date 12 March 2015, Accepted date 18 June 2015, Published date 01 July 2015 http://www.aimspress.com/ Research article Meso-scale computational investigation of polyurea microstructure and its role in shockwave attenuation/dispersion Mica Grujicic *, Jennifer Snipes , and S. Ramaswami Department of Mechanical Engineering, Clemson University, Clemson SC 29634, USA * Correspondence: E-mail: [email protected]; Tel: +864-656-5639; Fax: +864-656-4435. Abstract: In a number of recently published studies, it was demonstrated that polyurea possesses a high shockwave-mitigation capacity, i.e. an ability to attenuate and disperse shocks. Polyurea is a segmented thermoplastic elastomer which possesses a meso-scale segregated microstructure consisting of (high glass-transition temperature, Tg) hydrogen-bonded discrete hard domains and a (low Tg) contiguous soft matrix. Details of the polyurea microstructure (such as the extent of meso-segregation, morphology and the degree of short-range order and crystallinity within the hard domains) are all sensitive functions of the polyurea chemistry and its synthesis route. It has been widely accepted that the shockwave-mitigation capacity of polyurea is closely related to its meso-phase microstructure. However, it is not presently clear what microstructure-dependent phenomena and processes are responsible for the superior shockwave-mitigation capacity of this material. To help identify these phenomena and processes, meso-scale coarse-grained simulations of the formation of meso-segregated microstructure and its interaction with the shockwave is analyzed in the present work. It is found that shockwave-induced hard-domain densification makes an important contribution to the superior shockwave-mitigation capacity of polyurea, and that the extent of densification is a sensitive function of the polyurea soft-segment molecular weight.
    [Show full text]
  • Preparation of Polyurea Microcapsules by Interfacial Polymerization of Isocyanate and Chitosan Oligosaccharide
    materials Article Preparation of Polyurea Microcapsules by Interfacial Polymerization of Isocyanate and Chitosan Oligosaccharide Fuqiang Yu 1,2, Ying Wang 2, Yan Zhao 3,*, Jingyu Chou 2 and Xiaowu Li 1,* 1 Department of Materials Physics and Chemistry, School of Materials Science and Engineering, and Key Laboratory for Anisotropy and Texture of Materials, Ministry of Education, Northeastern University, Shenyang 110819, China; [email protected] 2 State Key Laboratory for the Discovery and Development of Novel Pesticides, Shenyang Sinochem Agrochemicals R&D Co., Ltd., Shenyang 110021, China; [email protected] (Y.W.); [email protected] (J.C.) 3 Jihua Laboratory, Nanhai, Foshan 528200, China * Correspondence: [email protected] (Y.Z.); [email protected] (X.L.) Abstract: (2-((1-(4-chlorophenyl)-1H-pyrazol-3-yl)oxy)-N-(3,4-dichlorophenyl)-propanamide) is a new oil-soluble compound with good fungicidal activity against Rhizoctonia solani. Chitosan oligosac- charide (COS) is the depolymerization product of chitosan and can be developed into biological pesticides, growth regulators, and fertilizers due to its various bioactivities. COS is an oligomer of β- (1 ! 4)-linked d –glucosamine and can be taken as a polyamine. In this study, microcapsules were prepared by interfacial polymerization of oil-soluble methylene diphenyl diisocyanate and water-soluble COS. The effects of several key preparation parameters, e.g., emulsifier dosage, agita- tion rate during emulsification, and core/shell ratio, on properties of the microcapsules such as the encapsulation efficiency, particle size, and size distribution were investigated. The microcapsules Citation: Yu, F.; Wang, Y.; Zhao, Y.; were characterized by infrared spectroscopy, thermogravimetric analysis, and scanning electron Chou, J.; Li, X.
    [Show full text]