Polymer Networks IPNs

This novel class of polymers, together with simultaneous interpenetrating networks (SIN s) and interpenetrating elastomeric networks (lEN s) 

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Hyperbranched polyurethanes are constmcted using phenol-blocked trifunctional monomers in combination with 4-methylbenzyl alcohol for end capping (11). Polyurethane interpenetrating polymer networks (IPNs) are mixtures of two cross-linked polymer networks, prepared by latex blending, sequential polymerization, or simultaneous polymerization. IPNs have improved mechanical properties, as weU as thermal stabiHties, compared to the single cross-linked polymers. In pseudo-IPNs, only one of the involved polymers is cross-linked. Numerous polymers are involved in the formation of polyurethane-derived IPNs (12). 

Interpenetrating Polymer Network (IPN) A subclass of PBs reserved for the mixture of two polymers where both components form a continuous phase and at least one is synthesized or crosslinked in the presence of the other [8]. 

To prepare an interpenetrating polymer network (IPN) structure, PU networks having ACPA units were immersed with MMA and polymerized. PU-PMMA semi-lPN thus formed was given improved interfacial strength between PU and PMMA phases and showed flexibility with enforced tear strength [65,66]. 

The advances in polymer blending and alloying technology have occurred through three routes (1) similar-rheology polymer pairs, (2) miscible polymers such as polyphenylene oxide and polystyrene, or (3) interpenetrating polymer networks (IPNs). All these systems were limited to specific polymer combinations that have an inherent physical affinity for each other. However with... 

An interpenetrating polymer network (IPN) is defined as a material comprising two or more networks which are at least partly interlaced on a molecular scale, hut not covalently bonded to each other. These networks caimot he separated unless chemical bonds are broken. Two possible methods exist for preparing them, as follows ... 

The ultimate goal of bulk modification endows with the polymer-specific surface composition or a specific property for a given application. The bulk modification can be classified into blending, copolymerization, interpenetrating polymer networks (IPNs), etc. 

Radio-chemical graft copolymerization with good efficiency on halogenated polyolefins has been carried out by contacting the substrate with monomer (styrene) vapor [158,159]. Interpenetrating polymer network (IPN) could be made by grafting the monomers on preirradiated substrates... 

Polymers with Spatially Graded Morphologies Designed from Photo-Induced Interpenetrating Polymer Networks (IPNs)... 

Interpellet porosity, 25 294 Interpenetrated wall matrix, in hollow-fiber membranes, 76 15 Interpenetrating polymer networks (IPNs), 79 834... 

Frisch, H. L. Du, Y. Schultz, M. Interpenetrating Polymer Network (IPN) Materials. In Polymer Networks. Principles of Their Formation Structure and Properties-, Stepto, R. F. T., Ed. Blackie Academic London, 1998 pp 186-214. 

So, interpenetrating polymer networks (IPNs) with a weight ratio of vinyl alcohol residue in PVA to acrylic acid monomer 4 6 exhibit positive swelling changes with temperature but IPNs 6 4 evidence negative swelling ones [48],... 

Materials known as interpenetrating polymer networks, IPN s, contain two or more polymers, each in network form (6 9), A practical restriction requires that at least one of the polymer networks has been formed (i.e. polymerized or crosslinked) in the immediate presence of the other. Two major types of synthesis have been explored, both yielding distinguishable materials with different morphologies and physical properties. 

Simultaneous Interpenetrating Networks. An interpenetrating polymer network, IPN, can be defined as a combination of two polymers in network form, at least one of which was polymerized or synthesized in the presence of the other (23). These networks are synthesized sequentially in time. A simultaneous interpenetrating network, SIN, is an IPN in which both networks are synthesized simultaneously in time, or both monomers or prepolymers mixed prior to gelation. The two polymerizations are independent and non-interfering in an SIN, so that grafting or internetwork crosslinking is minimized (23-26). 

This is a theoretical study on the entanglement architecture and mechanical properties of an ideal two-component interpenetrating polymer network (IPN) composed of flexible chains (Fig. la). In this system molecular interaction between different polymer species is accomplished by the simultaneous or sequential polymerization of the polymeric precursors [1 ]. Chains which are thermodynamically incompatible are permanently interlocked in a composite network due to the presence of chemical crosslinks. The network structure is thus reinforced by chain entanglements trapped between permanent junctions [2,3]. It is evident that, entanglements between identical chains lie further apart in an IPN than in a one-component network (Fig. lb) and entanglements associating heterogeneous polymers are formed in between homopolymer junctions. In the present study the density of the various interchain associations in the composite network is evaluated as a function of the properties of the pure network components. This information is used to estimate the equilibrium rubber elasticity modulus of the IPN. 

Interpenetrating polymer networks (IPNs) continue to excite both fundamental and technological interest. 

Since the start of modern interpenetrating polymer network (IPN) research in the late sixties, the features of their two-phased morphologies, such as the size, shape, and dual phase continuity have been a central subject. Research in the 1970 s focused on the effect of chemical and physical properties on the morphology, as well as the development of new synthetic techniques. More recently, studies on the detailed processes of domain formation with the aid of new neutron scattering techniques and phase diagram concepts has attracted much attention. The best evidence points to the development first of domains via a nucleation and growth mechanism, followed by a modified spinodal decomposition mechanism. This paper will review recent morphological studies on IPN s and related materials. 

Polyurethane-acrylic coatings with interpenetrating polymer networks (IPNs) were synthesized from a two-component polyurethane (PU) and an unsaturated urethane-modified acrylic copolymer. The two-component PU was prepared from hydroxyethylacrylate-butylmethacrylate copolymer with or without reacting with c-caprolactonc and cured with an aliphatic polyisocyanate. The unsaturated acrylic copolymer was made from the same hydroxy-functional acrylic copolymer modified with isocyanatoethyl methacrylate. IPNs were prepared simultaneously from the two-polymer systems at various ratios. The IPNs were characterized by their mechanical properties and glass transition temperatures. 

A substantial number of definitions in the terminology section are either of physical quantities or are expressed mathematically. In such cases, there are recommended symbols for the quantities and, when appropriate, corresponding SI units. Other terms have eommon abbreviations. The following format is used to indicate these essential eharaeteristics name of term (abbreviation), symbol, SI unit unit. Typical examples are tensile stress, interpenetrating polymer network (IPN). If there are any, alternative names or synonyms follow on the next line, and the definition on the sueeeeding lines. 

Macromers can also be used as cross-linkers between already formed polymers when both ends are active. These functional groups could be either two vinyl ends or two Lewis acids or bases such as two hydroxyl or amine groups. Interpenetrating polymer networks (IPNs) and related structures such as dendrites and stars can also be formed using macromers. 

Polymer blends and interpenetrating polymer networks (IPNs) are different from copolymers but like copolymers are used to bring together the properties of different polymers [Paul et al., 1988]. The total of all polymer blends (produced by both step and chain reactions) is estimated at about 3% of the total polymer production—about 3 billion pounds per year in the United States. There is considerable activity in this area since new products can be obtained and markets expanded by the physical mixing together of existing products. No new polymer need be synthesized. 

An interpenetrating polymer network (IPN) (Sec. 2-13c-3) is obtained by carrying out a polymerization with crosslinking in the presence of another already crosslinked polymer [Klempner... 

In this chapter, temperature responsive swelling-shrinking changes in hydrogels were reviewed from the view point of polymer-water interaction and polymer-polymer interaction. In particular, characteristics of interpenetrating polymer networks (IPN) constructed of two distinct polymers which lead to novel temperature-responsive swelling changes were discussed... 

A number of liquid crystalline polyphosphazenes with mesogenic side groups have been prepared (48—50). Polymers with nonlinear optical activity have also been reported (51). Polyphosphazene membranes have been examined for gas, liquid, and metal ion separation, and for filtration (52—54). There is interest in phosphazene—organic copolymers, blends, and interpenetrating polymer networks (IPNs) (55—61) to take advantage of some of the special characteristics of phosphazenes such as flame retardance and low temperature flexibility. A large number of organic polymers with cydophosphazene substituents have been made (62). 

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