Hydrogen Bonding in Polymeric Materials

Author(s):  
Liangliang Xia ◽  
Ming Zhou ◽  
Hongjun Tu ◽  
wen Zeng ◽  
xiaoling Yang ◽  
...  

The preparation of room-temperature self-healing polymeric materials with good healing efficiency and high mechanical strength is challenging. Two processes are essential to realise the room-temperature self-healing of materials: (a) a...


Segmented thermoset polymeric materials properties mainly classified through its carbonyl hydrogen bonding. The addition of graphite particle loading in polymeric materials tailored the functional characteristic of the composites. Therefore, the carbonyl hydrogen bonding in the hard segments of the synthesized segmented ultraviolet (UV) curable thermoset polyurethanes-graphite (TPU-G) composites was identified. This composites based green polymer incorporated with varying graphite particles loading were prepared through slip casting method which cure upon UV light. These result in an enhancement of the carbonyl hydrogen bonding which tribute to degree of phase separation (DPS %) in the TPU-G composites ranged from 10-20%, as compared to that in the pure TPU. In addition, the spectroscopy detects the formation of carbonyl hydrogen groups within the TPU-G composites although they are prone to chain scission and undergo photo oxidation subjected to ultraviolet (UV) curing. Upon UV curing, higher graphite weight loading (TPU-G20, TPU-G25 and TPU-G30 composites), shows higher and stable DPS% value, attribute to soft segment- soft segment and hard segment- hard segment establishment. Therefore, the graphite particles dominantly absorb the incident radiation instead of thermoset polyurethane without changing its based.


2018 ◽  
Vol 5 (6) ◽  
pp. 180564 ◽  
Author(s):  
Kristin M. Hutchins

The design, synthesis and property characterization of new functional materials has garnered interest in a variety of fields. Materials that are capable of recognizing and binding with small molecules have applications in sensing, sequestration, delivery and property modification. Specifically, recognition of pharmaceutical compounds is of interest in each of the aforementioned application areas. Numerous pharmaceutical compounds comprise functional groups that are capable of engaging in hydrogen-bonding interactions; thus, materials that are able to act as hydrogen-bond receptors are of significant interest for these applications. In this review, we highlight some crystalline and polymeric materials that recognize and engage in hydrogen-bonding interactions with pharmaceuticals or small biomolecules. Moreover, as pharmaceuticals often exhibit multiple hydrogen-bonding sites, many donor/acceptor molecules have been specifically designed to interact with the drug via such multiple-point hydrogen bonds. The formation of multiple hydrogen bonds not only increases the strength of the interaction but also affords unique hydrogen-bonded architectures.


1995 ◽  
Vol 49 (9) ◽  
pp. 1311-1316 ◽  
Author(s):  
Dimitris Tsiourvas ◽  
Constantinos M. Paleos ◽  
Jane Anastassopoulou ◽  
Theophile Theophanides

The FT-IR/ATR technique has been employed in the investigation of the forces leading to the organization of a number of polymeric materials exhibiting thermotropic liquid crystalline character. Two types of compounds have been studied, i.e., one bearing the carboxylic polar group near the main chain and the other at the end of the side chain. Intermolecular and intramolecular hydrogen bonding between the carboxylic groups was found to lead to the formation of “facing” and “sideways” structures. Enhanced stability of these supramolecular structures was obtained by the presence of intramolecular hydrogen bonds between the amide groups, resulting in the formation of smectic phases. Furthermore, it has been found that the strengthening of hydrogen bonding between carboxylic groups is associated with a weakening of hydrogen bonds between the amide groups.


2008 ◽  
Vol 47-50 ◽  
pp. 258-261 ◽  
Author(s):  
Hai Bao Lv ◽  
Yan Ju Liu ◽  
Dong Xing Zhang ◽  
Jin Song Leng ◽  
Shan Yi Du

Recently, there is interest in triggering shape recovery of shape-memory polymers(SMPs) by novel non-external heating. In this paper, many hard works have been carried out to make SMP induced by solution. The main challenge in the development of such polymer systems is the conversion of solution-induced effects at the molecular level to macroscopic movement of working pieces. This paper presents a systematic study on the effects of solution on the glass transition temperature (Tg). The results reveal that the hydrogen bonding of shape memory polymer (SMP) was aroused by the absorbed solution that significantly reduces Tg of polymer. The mechanism behind it is solution firstly intenerates polymeric materials till the Tg of polymer lowered down to the temperature of ambient, then hydrogen bonding interaction improves the flexibility of polymeric macro-molecular chains. Thus, the shape memory effect (SME) can undergo solution-driven shape recovery. In addition, it provides a new approach that the SMP can be induced by applying non-energy stimulus. The Dynamic Mechanical Analyzer (DMA) results reveal that the modulus of polymer was softened gradually with immersion time increasing. The experimental result is approximate to the theory.


2019 ◽  
Vol 10 (33) ◽  
pp. 4519-4523 ◽  
Author(s):  
Yuichiro Kobayashi ◽  
Tomohiro Hirase ◽  
Yoshinori Takashima ◽  
Akira Harada ◽  
Hiroyasu Yamaguchi

Polymeric materials were prepared by cross-linking them with two independent non-covalent interactions, namely hydrogen bonding and metal–ligand interactions.


1977 ◽  
Vol 50 (5) ◽  
pp. 934-944 ◽  
Author(s):  
S. Dzierża ◽  
J. Janáček

Abstract Polyurethane elastomers are a numerous group of polymeric materials of wide practical application. They are usually formed by polyaddition of diisocyanates with hydroxyl-terminated polyesters or polyethers in the presence of low molecular weight diols or diamines as chain extenders. One may consider urethane elastomers to be block copolymers, consisting of moderately flexible long linear polyester or polyether segments and relatively stiff segments of aromatic and urethane groups. The length and structure of each block can be easily controlled. Crosslinking by an excess of diisocyanate can occur only at the stiff segments, and the number of branch points can also be controlled. The properties of these elastomers can be widely changed using components of different structures and varying their quantitative ratios. They are the results of a combination of segment flexibility, crosslinking, chain entanglement, orientation of segments, hydrogen bonding and other van der Waals forces, as well as rigidity of aromatic units. In the urethane systems, hydrogen bonding and other van der Waals forces, play a much more pronounced role than in familiar olefin-derived elastomers. Although polyurethane elastomers have very good mechanical properties at room temperature, their application is strongly limited by rapid deterioration of properties which takes place at elevated temperatures. The decay of mechanical properties of polyurethane is caused by the breaking of hydrogen and other secondary bonds, as well as by the presence of relatively weak crosslinks that make up their network. The properties of polyurethanes at elevated temperatures may, perhaps, be improved by forming additional crosslinks, besides the typical ones. Some efforts concerning this problem have been published. The aim of our study was to obtain and check the properties of polyurethane elastomers having unsaturated bonds, on which some additional crosslinks were expected to be formed in the presence of a suitable crosslinking agent.


Author(s):  
D. L. Misell

In the electron microscopy of biological sections the adverse effect of chromatic aberration on image resolution is well known. In this paper calculations are presented for the inelastic and elastic image intensities using a wave-optical formulation. Quantitative estimates of the deterioration in image resolution as a result of chromatic aberration are presented as an alternative to geometric calculations. The predominance of inelastic scattering in the unstained biological and polymeric materials is shown by the inelastic to elastic ratio, I/E, within an objective aperture of 0.005 rad for amorphous carbon of a thickness, t=50nm, typical of biological sections; E=200keV, I/E=16.


Author(s):  
Martin J. Mahon ◽  
Patrick W. Keating ◽  
John T. McLaughlin

Coatings are applied to appliances, instruments and automobiles for a variety of reasons including corrosion protection and enhancement of market value. Automobile finishes are a highly complex blend of polymeric materials which have a definite impact on the eventual ability of a car to sell. Consumers report that the gloss of the finish is one of the major items they look for in an automobile.With the finish being such an important part of the automobile, there is a zero tolerance for paint defects by auto assembly plant management. Owing to the increased complexity of the paint matrix and its inability to be “forgiving” when foreign materials are introduced into a newly applied finish, the analysis of paint defects has taken on unparalleled importance. Scanning electron microscopy with its attendant x-ray analysis capability is the premier method of examining defects and attempting to identify their root cause.Defects are normally examined by cutting out a coupon sized portion of the autobody and viewing in an SEM at various angles.


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