An Interpenetrating polymer network (IPN) is a polymer comprising two or more networks which are at least partially interlaced on a polymer scale but not covalently bonded to each other. The network cannot be separated unless chemical bonds are broken. [1] The two or more networks can be envisioned to be entangled in such a way that they are concatenated and cannot be pulled apart, but not bonded to each other by any chemical bond.
Interpenetrating polymer network (IPN): A polymer comprising two
or more networks which are at least partially interlaced on a molecular scale
but not covalently bonded to each other and cannot be separated unless chemical
bonds are broken.Note: A mixture of two or more pre-formed polymer networks is not an IPN. [2]
Semi-interpenetrating polymer network (SIPN): A polymer comprising one or
more networks and one or more linear or branched polymer(s) characterized by the
penetration on a molecular scale of at least one of the networks by at least some
of the linear or branched macromolecules.Note: Semi-interpenetrating polymer networks are distinguished from
interpenetrating polymer networks because the constituent linear or branched
polymers can, in principle, be separated from the constituent polymer network(s)
without breaking chemical bonds; they are polymer blends. [3]Sequential interpenetrating polymer network: Interpenetrating polymer network
prepared by a process in which the second component network is formed
following the formation of the first component network. [4]Sequential semi-interpenetrating polymer network: Semi-interpenetrating
polymer network prepared by a process in which the linear or branched
components are formed following the completion of the reactions that lead to
the formation of the network(s) or vice versa. [5]
Simply mixing two or more polymers does not create an interpenetrating polymer network (polymer blend), nor does creating a polymer network out of more than one kind of monomers which are bonded to each other to form one network (heteropolymer or copolymer).
There are semi-interpenetrating polymer networks (SIPN) [6] and pseudo-interpenetrating polymer networks. [7]
To prepare IPNs and SIPNs, the different components are formed simultaneously [8] [9] or sequentially. [10] [11]
The first known IPN was a combination of phenol-formaldehyde resin with vulcanized natural rubber made by Jonas Aylsworth in 1914. [12] However, this was before Staudinger's hypothesis on macromolecules and thus the terms "polymer" or "IPN" were not yet used. The first usage of the term "interpenetrating polymer networks" was first introduced by J.R. Millar in 1960 while discussing networks of sulfonated and unsulfonated styrene–divinylbenzene copolymers. [13]
Molecular intermixing tends to broaden the glass transition regions of some IPN materials compared to their component polymers. This unique characteristic provides excellent mechanical damping properties over a wide range of temperatures and frequencies due to a relatively constant and high phase angle. [14] In IPNs composed of both rubbery and glassy polymers, considerable toughening is observed compared to the constituent polymers. When the glassy component forms a discrete, discontinuous phase, the elastomeric nature of the continuous rubbery phase can be preserved while increasing the overall toughness of the material and its elongation at break. [15] On the other hand, when the glassy polymer forms a bicontinuous phase within the rubbery network, the IPN material can behave like an impact-resistant plastic. [15]
Most IPNs do not interpenetrate completely on a molecular scale, but rather form small dispersed or bicontinuous phase morphologies with characteristic length scales on the order of tens of nanometers. [12] However, since these length scales are relatively small, they are often considered homogeneous on a macroscopic scale. [12] The characteristic lengths associated with these domains often scale with the length of chains between crosslinks, and thus the morphology of the phases is often dictated by the crosslinking density of the constituent networks. [16] The kinetics of phase separation in IPNs can arise from both nucleation and growth and spinodal decomposition mechanisms, with the former producing discrete phases akin to dispersed spheres and the latter forming bicontinuous phases akin to interconnected cylinders. Contrary to many typical phase separation processes, coarsening, where the length scale of the phases tends to increase over time, can be impeded by the formation of crosslinks in either network. [12] Furthermore, IPNs are often able to maintain these complex morphologies over long periods of time compared to what could be achieved by simple polymer blends. [17]
IPNs have been used in automotive parts (including modern automotive paint), damping materials, medical devices, molding compounds, and in engineering plastics. [14] While many benefits come from the enhanced mechanical properties of the IPN materials, other characteristics such as resistance to solvent swelling can also make IPNs a material of commercial interest. [14] More recent applications and areas of research for IPNs include uses in drug delivery systems, energy storage materials, and tissue engineering. [18]
A polymer is a substance or material consisting of very large molecules called macromolecules, composed of many repeating subunits. Due to their broad spectrum of properties, both synthetic and natural polymers play essential and ubiquitous roles in everyday life. Polymers range from familiar synthetic plastics such as polystyrene to natural biopolymers such as DNA and proteins that are fundamental to biological structure and function. Polymers, both natural and synthetic, are created via polymerization of many small molecules, known as monomers. Their consequently large molecular mass, relative to small molecule compounds, produces unique physical properties including toughness, high elasticity, viscoelasticity, and a tendency to form amorphous and semicrystalline structures rather than crystals.
A gel is a semi-solid that can have properties ranging from soft and weak to hard and tough. Gels are defined as a substantially dilute cross-linked system, which exhibits no flow when in the steady-state, although the liquid phase may still diffuse through this system. A gel has been defined phenomenologically as a soft, solid or solid-like material consisting of two or more components, one of which is a liquid, present in substantial quantity.
In chemistry, a mixture is a material made up of two or more different chemical substances which are not chemically bonded. A mixture is the physical combination of two or more substances in which the identities are retained and are mixed in the form of solutions, suspensions and colloids.
In polymer chemistry, a copolymer is a polymer derived from more than one species of monomer. The polymerization of monomers into copolymers is called copolymerization. Copolymers obtained from the copolymerization of two monomer species are sometimes called bipolymers. Those obtained from three and four monomers are called terpolymers and quaterpolymers, respectively. Copolymers can be characterized by a variety of techniques such as NMR spectroscopy and size-exclusion chromatography to determine the molecular size, weight, properties, and composition of the material.
In chemistry and biochemistry, an oligomer is a molecule that consists of a few repeating units which could be derived, actually or conceptually, from smaller molecules, monomers. The name is composed of Greek elements oligo-, "a few" and -mer, "parts". An adjective form is oligomeric.
In organic chemistry and biochemistry, a side chain is a chemical group that is attached to a core part of the molecule called the "main chain" or backbone. The side chain is a hydrocarbon branching element of a molecule that is attached to a larger hydrocarbon backbone. It is one factor in determining a molecule's properties and reactivity. A side chain is also known as a pendant chain, but a pendant group has a different definition.
Amidines are organic compounds with the functional group RC(NR)NR2, where the R groups can be the same or different. They are the imine derivatives of amides (RC(O)NR2). The simplest amidine is formamidine, HC(=NH)NH2.
Gas phase ion chemistry is a field of science encompassed within both chemistry and physics. It is the science that studies ions and molecules in the gas phase, most often enabled by some form of mass spectrometry. By far the most important applications for this science is in studying the thermodynamics and kinetics of reactions. For example, one application is in studying the thermodynamics of the solvation of ions. Ions with small solvation spheres of 1, 2, 3... solvent molecules can be studied in the gas phase and then extrapolated to bulk solution.
A dispersion is a system in which distributed particles of one material are dispersed in a continuous phase of another material. The two phases may be in the same or different states of matter.
A telechelic polymer or oligomer is a prepolymer capable of entering into further polymerization or other reactions through its reactive end-groups. It can be used for example to synthesize block copolymers.
In IUPAC nomenclature of chemistry, a pendant group or side group is a group of atoms attached to a backbone chain of a long molecule, usually a polymer. Pendant groups are different from pendant chains, as they are neither oligomeric nor polymeric.
In materials science, a polymer blend, or polymer mixture, is a member of a class of materials analogous to metal alloys, in which at least two polymers are blended together to create a new material with different physical properties.
In chromatography, the retardation factor (R) is the fraction of an analyte in the mobile phase of a chromatographic system. In planar chromatography in particular, the retardation factor RF is defined as the ratio of the distance traveled by the center of a spot to the distance traveled by the solvent front. Ideally, the values for RF are equivalent to the R values used in column chromatography.
In chemistry, coalescence is a process in which two phase domains of the same composition come together and form a larger phase domain. In other words, the process by which two or more separate masses of miscible substances seem to "pull" each other together should they make the slightest contact.
In coordination chemistry, denticity refers to the number of donor groups in a given ligand that bind to the central metal atom in a coordination complex. In many cases, only one atom in the ligand binds to the metal, so the denticity equals one, and the ligand is said to be monodentate. Ligands with more than one bonded atom are called polydentate or multidentate. The denticity of a ligand is described with the Greek letter κ ('kappa'). For example, κ6-EDTA describes an EDTA ligand that coordinates through 6 non-contiguous atoms.
A chemical compound is a chemical substance composed of many identical molecules containing atoms from more than one chemical element held together by chemical bonds. A molecule consisting of atoms of only one element is therefore not a compound. A compound can be transformed into a different substance by a chemical reaction, which may involve interactions with other substances. In this process, bonds between atoms may be broken and/or new bonds formed.
In chemistry, a ring is an ambiguous term referring either to a simple cycle of atoms and bonds in a molecule or to a connected set of atoms and bonds in which every atom and bond is a member of a cycle. A ring system that is a simple cycle is called a monocycle or simple ring, and one that is not a simple cycle is called a polycycle or polycyclic ring system. A simple ring contains the same number of sigma bonds as atoms, and a polycyclic ring system contains more sigma bonds than atoms.
IUPAC Polymer Nomenclature are standardized naming conventions for polymers set by the International Union of Pure and Applied Chemistry (IUPAC) and described in their publication "Compendium of Polymer Terminology and Nomenclature", which is also known as the "Purple Book". Both the IUPAC and Chemical Abstracts Service (CAS) make similar naming recommendations for the naming of polymers.
Chain scission is a term used in polymer chemistry describing the degradation of a polymer main chain. It is often caused by thermal stress (heat) or ionizing radiation, often involving oxygen. During chain cleavage, the polymer chain is broken at a random point in the backbone to form two - mostly still highly molecular - fragments.
In chemical nomenclature, a descriptor is a notational prefix placed before the systematic substance name, which describes the configuration or the stereochemistry of the molecule. Some listed descriptors are only of historical interest and should not be used in publications anymore as they do not correspond with the modern recommendations of the IUPAC. Stereodescriptors are often used in combination with locants to clearly identify a chemical structure unambiguously.
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