Polymer Gels History of the Term Paper

Excerpt from Term Paper :

Advancement of nanotechnology has gained significant attention in the self -- assembling characteristic of a variety of molecules, which is a vital requirement for the growing bottom -- up design of nanoscale structures. When these molecules go through molecular self -- congregation, the consequential structural elements, for instance nanotubes or vesicles, can be further transformed to give specific charactistics to the components. Like nanotubes can be covered with metals or partially -- conducting substances to fabricate nanowires.

Smart polymeric gels are classified on various structural properties. Superporous hydrogels (SPHs) are utilized to augment the responsiveness of hydrogels. In this case, the augmented responsiveness to stimuli is accomplished by manufacturing interconnected absorbent networks. Superporous hydrogels (SPHs) correspond to a rapid -- swelling group of hydrogels with pore dimensions much bigger than the usual network of a normal hydrogel. These were firstly created as modern gastric retention devices to augment the duration of drugs stay in the stomach. Normally network size of a usual hydrogel is less than 100 nm whereas the pore size of Superporous hydrogel varies from below 1 ?m to greater than 1,000 ?m. The distension kinetics of Superporous hydrogels is much quicker than that of usual hydrogels. This dissimilarity can be understood by explaining the dissimilarity in morphology of both the types of hydrogels. As the network size of usual hydrogels is diminutive, the puffiness in such fairly closed systems is restricted by dispersion of water across the glassy polymer matrix. Conversely, SPHs contain huge interconnected pores that cause the capillary ingestion of water.

Super porous Hydrogels

Shape -- memory polymers represent one more group of smart biomaterials and carry out its job by an omnipresent method present in our day -- to -- day lives. Take an example of the built-in memorizing capacity of an expandable rubber band that is stretched and then left to relax; if the entropic energy linked to the enlarged rubber band can be stored to be utilize later on, then it will be considered as shape -- memory based application. Reactions triggered by shape -- memory and stimuli -- responsiveness are interconnected. Actually, stimuli -- receptiveness can be thought as a conventional instance of the shape -- memory property in substances. Substances are said to display a shape -- memory effect if they can change their shape and get fixed into a short-term shape, and contain the capability to get the original, enduring shape only on coming in contact to an external stimulus. The shape -- memory alloys were the foremost shape -- memory objects to be discovered. This discovery was then utilized in various applications, like toys, "shrink -- to -- fit" pipe couplers for airplanes, solid state heat engines and therapeutic usage in orthopedics, orthodontics, and heart surgical procedures.

Lastly, protein hydrogels develop a complete new group of biomaterials by copying and incorporating the self -- assembling codes from surrounding in smart hybrids. Drawbacks of hydrogels manufactured by conventional methods, for instance crosslinking copolymerizaton, exhibit deficiency of accurate control of structural organization and the hysteresis connected to "on" and "off" alterations. Protein engineering put forwards potent solutions to reduce these limitations by developing distinct supramolecular structures.

protein engineering

4. Relative advantages and disadvantages of the polymer in the application

Within the field of biomaterials examination, stimuli -- sensitive hydrogels or smart 4 hydrogels are getting more stability and hence becoming more popular in its application. Reaction to a stimulus is a fundamental part of living systems. Imitating this characteristic of living systems may give a reasonable solution to a lot of the present day biomedical problems. Smart hydrogels act in response to various stimuli, that is in the form of temperature, pH, radiance, stress, electric field, chemicals, or ionic potency, or a mixture of these all. Such hydrogels possess the capability of giving response to small alterations in ambient stimuli and display remarkable property modifications. In order to react really smart, a biomaterial modification in hydrogel microstructures needs to be rapid and reversible. Nevertheless, the foremost challenge with usual stimuli -- responsive hydrogels is the slow reaction time to stimulus and the hysteres is connected to the now and then states. One technique to get rid of this disadvantage is to have slim and undersized hydrogels without considerably altering their mechanical properties. Another challenge is to create hydrogels that deteriorate as a result of proper ambient stimulus in the body. This is in comparison to the modern technology where hydrogels mortify at a fixed pace when getting implant in the body. For instance, proteolytic stimulus, that is, biochemical indicators from cells in the surrounding of an implanted biomaterial scaffold may vigorously transduce signaling cues if the scaffold can mortify and amend its infrastructure in a stimuli reactive approach. In this case, the motivation is the cascade of biochemical indicators from the cells in the surrounding area of the biomaterial.

Hydrogel -- based microvalves possess several advantages over traditional microvalves, that include comparatively uncomplicated fabrication, no exterior control obligation, no integrated electronics, and creation of greater amount of displacement force. Nevertheless, electronically controllable hydrogel microvalves, relying on heat sensitive hydrogels, propose greater accuracy in flow intonation and signal actuation.

One more difficullty in the manufacture of smart hydrogels is to compose hydrogels bio-compatible such that the immune system does not start out immunogenic response inside body. In reality, extracellular matrix mimetic biomaterial hydrogels that avoid reactions from the immune system can also be characterized as smart hydrogels, that react vigorously to stimuli from the host tissue. The composition of such ECM -- mimetics intends to copy the ECM, although in a much simpler way, taking the fundamental nature of the structural and practical parameters of the extracellular matrix mimetic biomaterial.

5. Recommendation about how to design and process polymers to improve their performance in the application

Properties of Polymer gels can be managed by slightly altering the microstructure of the polymer main structure and the flanking liquid, if exist. The potency of the gel, which is distinguished by the equilibrium modulus, is normally comparative to the compactness of crosslinks with harder gels having an elevated compactness of crosslinks a gel can be made more flexible by enhancing the gap between crosslinks either by augmenting molecular weight of the polymer chain linking the crosslinks or thinning the gel with a fluid. Fluid in the gel which is not component of the crosslinked complex is recognized as the sol and possibly will made up of a solvent for instance water, small chain polymers or lengthy entangled polymers. The network of crosslinked polymer is normally recognized as the gel. Alternately, faults can be included to the network. For a specified crosslink compactness, the best end-linked polymer gel where each and every polymer chain is attached at both ends to crosslinks and each and every crosslink is attached completely to the polymer network will possess the maximum modulus. In case of a disproportion among the quantity of polymer chains and crosslinker, faults occur into the system like loops and floppy ends, that ends up in a softer gel. Gels that are produced by random course of action for instance irradiation will result in formation of networks containing a number of defects. Hence, for a specific application, there are several techniques to regulate the properties of a polymer gel to increase performance by controlling microstructure of gels and processing conditions.

Works Cited

Annaka, Masahiko and Tanaka, Toyoichi, Multiple phases of polymer gels, Nature, ISSN 0028-0836, 2005, pp. 430-432

Darmawan, Adi; Smart, Simon; Julbe, Anne; Diniz da Costa, Joao Carlos, Iron Oxide Silica Derived from Sol-Gel Synthesis, Materials, ISSN, Volume 4, Issue 2, 2011, pp. 448-456

Heitfeld, Kevin a, Smart membranes: Hydroxypropyl cellulose for flavor delivery, ISBN 9780549027560, 2007, 15.

Hu, Jinlian, Adaptive and Functional Polymers, Textiles and Their Applications, ISBN 1848164750, 2011, p. 416

Lei, Yu, Supramolecular Polymeric Networks via Hydrogen Bonding in Ionic Liquids, 2012, ISBN 1267855339.

Maeda, Shingo; Hara, Yusuke; Yoshida, Ryo; Hashimoto, Shuji, Active polymer gel actuators, International journal of molecular sciences, ISSN 1422-0067, Volume 11, Issue 1, 2010, pp. 52-66

Osada, Yoshihito; Okuzaki, Hidenori; Hori, Hirofumi, a Polymer Gel with Electrically Driven Motility, Nature, ISSN 0028-0836, 2002, pp. 242-244

Osada, Yoshihito; Ping Gong, Jian; Tanaka, Yutaka, Polymer Gels, Journal of Macromolecular Science, Part C: Polymer Reviews, ISSN 1532-1797, Volume 44, Issue 1, 2004, pp. 87-112

Schreiner, LJ; Olding, T; McAuley, KB, Polymer gel dosimetry, Journal of Physics: Conference…

Cite This Term Paper:

"Polymer Gels History Of The" (2013, February 18) Retrieved August 16, 2017, from

"Polymer Gels History Of The" 18 February 2013. Web.16 August. 2017. <

"Polymer Gels History Of The", 18 February 2013, Accessed.16 August. 2017,