Homopolymers block copolymers and

Figure 1 Macromolecular architectures linear macromolecular chains (homopolymer, block-copolymer and statistical copolymer [14]), brushed-polymer (= linear chains attached to a polymer-chain brush-polymer, brush-copolymers [14]), star polymer [4], mikto-star-polymer [16], arborescent graft polymer (=repeated grafting of linear chains on a macromolecule [17,18]), dendrimer (= maximally branched, regular polymer [15])...

SHI Shibayama, M. and Osaka, N., Pressure- and temperatine-induced phase separation transition in homopolymer, block copolymer, and protein in water, Macromol. Symp., 291-292, 115, 2010. 

SpheruUte and Single Crystal Growth Rates.—Rate measurements have been made on homopolymers, block copolymers, and blends. - ... 

In a block copolymer, the different homopolymer subunits are connected together in one chain. In contrast, a graft copolymer contains sections of one homopolymer that have been grafted onto a chain of the other homopolymer. Block copolymers and graft copolymers are formed by controlling the conditions under which polymerization occurs. 

In general we have observed that homopolymer, block copolymers and polymer blends nanostructured by processing with CDs retain their unique solid-state organizations for considerable periods of time even at temperatures exceeding their Tg and I m values, where their chains are potentially mobile. For example, PET coalesced from its IC with y-CD continues to be rapidly crystallizable... 

Zhang J, Ren L, Hardy CG, Tang C (2012) Cobaltocenium-ctmtaining methacrylate homopolymers, block copolymers, and heterobimetallic polymers via RAFT polymeiizatioiL Macromolecules 45 6857-6863... 

Polymers are classified according to their chemical structures into homopolymers, copolymers, block copolymers, and graft copolymers. In a graft copolymer, sequences of one monomer are grafted onto a backbone of the other monomer and can be represented as follows ... 

In three dimensions, Ohta and Kurokawa [32] reported that a BCC arrangement was only slightly more favored than the FCC arrangement. In fact, many BCC structures have been reported for AB type block copolymers and the blends of homopolymer-block copolymer systems [27,33-35]. However, the lattice structure of the core-shell type polymer microspheres was FCC. This FCC formation resulted in the lower viscosity of... 

Two other forms of copolymers that can be prepared under certain conditions are called block copolymers and graft copolymers. Block copolymers are those in which different blocks of identical monomer units alternate with each other graft copolymers are those in which homopolymer branches of one monomer unit are "grafted" onto a homopolymer chain of another monomer unit. 

Copolymerization of two monomers gives a product with properties different from those of either homopolymer. Graft copolymers and block copolymers are two examples. 

The purpose of this review is to show how anionic polymerization techniques have successfully contributed to the synthesis of a great variety of tailor-made polymer species Homopolymers of controlled molecular weight, co-functional polymers including macromonomers, cyclic macromolecules, star-shaped polymers and model networks, block copolymers and graft copolymers. 

The transformation of the chain end active center from one type to another is usually achieved through the successful and efficient end-functionalization reaction of the polymer chain. This end-functionalized polymer can be considered as a macroinitiator capable of initiating the polymerization of another monomer by a different synthetic method. Using a semitelechelic macroinitiator an AB block copolymer is obtained, while with a telechelic macroinitiator an ABA triblock copolymer is provided. The key step of this methodology relies on the success of the transformation reaction. The functionalization process must be 100% efficient, since the presence of unfunctionalized chains leads to a mixture of the desired block copolymer and the unfunctionalized homopolymer. In such a case, control over the molecular characteristics cannot be obtained and an additional purification step is needed. 

Employing similar procedures, PPO-fc-POEGMA block copolymers and POEGMA-fc-PPO-fc-POEGMA triblock copolymers were prepared from the corresponding PPO macroinitiators [129]. The polymerizations were performed in a isopropanol/water (70/30) mixture at 20 °C using CuCl and bpy. The methacrylate monomer was almost quantitatively polymerized, and the polydispersities were lower than 1.25 in most cases. Less than 5% PPO homopolymer contamination was detected by SEC analysis. 

However, a PS-fo-PI/PI blend shows direct L G transitions without appearance of the PL phase. The L microdomain is more favourable than the PL phase since the volume fraction of the PI block component and the symmetry of microdomains is increased by the addition of PI homopolymer. Hence, the PL phase may not be formed as an intermediate structure if relatively high molecular weight PI homopolymer is added. The latter is not able to effectively fill the corners of the Wigner-Seitz cells in consequence packing frustration cannot be released and the PL phase is not favoured [152]. In contrast, the addition of low molecular weight PI homopolymer to the minor component of the PL phase reduces the packing frustration imposed on the block copolymers and stabilizes it [153]. Hence, transition from the PL to the G phase indicates an epitaxial relationship between the two structures, while the direct transition between L and G yields a polydomain structure indicative of epitaxial mismatches in domain orientations [152]. 

The structures of the dimethylsiloxane block copolymers and respective parent homopolymers prepared for use as positive, bilevel resist materials are shown in Figure 1. Most copolymers were synthesized with >10 wt % silicon. The selection of PDMSX block length and novolac chemical composition proved to be the two most critical variables in achieving adequate resolution. 

The range of properties of polymers can be greatly extended and varied by copolymerization of two or more monomers. The effects of radiation on copolymers would be expected to show similarities to the homopolymers, but major differences from linear relationships are often experienced. Aromatic groups in one monomer frequently show an intramolecular protective effect so that the influence of that monomer may be much greater than its mole fraction. The Tg of a copolymer is normally intermediate between the homopolymers, except for block copolymers, and this can cause a discontinuity in radiation degradation at a fixed temperature. 

The properties of polymer materials can e greatly extended by blending two or more homopolymers together. Blends may be classified as compatible or incompatible - although this does depend on the dimensions being considered. Compatibility is influenced by the molecular weight of the homopolymers and is enhanced in practice by incorporation of block copolymers and other compatibilizers. The effects of radiation on blends depend on the degree of compatibility and the extent of inter-molecular interaction (physically and chemically) between the different types of homopolymers. 

Draw representative structures for (a) homopolymers, (b) alternation copolymers, (c) random copolymers, (d) AB block copolymers, and (e) graft copolymers of styrene and acrylonitrile. 

The progressive decrease of the initial polymer molecular weight leads to segments of block copolymer, and to homopolymer of the monomer ... 

As is well known from free radical copolymerization theory, the composition of the copolymers will depend only on the propagation reaction. The relative ability of monomer to add to a growing chain is influenced by the nature of the last chain unit and by the relative concentration. Generally, chain transfer to monomer by polymer radicals will occur to an appreciable extent, and the final product will be made up of homopolymers, multisegment block copolymers, and branched and grafted structures. In the presence of two or more monomers,... 

---