A novel proposal for all optical 3 to 8 decoder based on nonlinear ring resonators

In this paper, a 3 to 8 optical decoder was proposed using nonlinear photonic crystal ring resonators. For realizing the 3 to 8 decoder, we combined seven 1 to 2 optical decoders. In the proposed structure, X, Y and Z serve as input ports. By combination of these ports, one can control which output port to be ON. The maximum time delay of the proposed structure is about 6?ps.     

Influence of aliphatic polycarbonate middle block on mechanical and microstructural behaviour of triblock copolymers based on poly(l‐lactide) and polycarbonate

Three different ABA‐type triblock copolymers each containing biodegradable aliphatic polycarbonate as the middle block and poly(l ‐lactide) as the outer blocks were synthesized and the influence of the methylene chain length of the aliphatic polycarbonate middle block on various properties of the triblock copolymers was evaluated. Differential scanning calorimetry and wide‐angle X‐ray diffraction studies revealed that the incorporation of the outer blocks reduced the crystallinity of the middle aliphatic polycarbonate block. Variation of methylene chain length of the middle block led to a change in morphology from spherical to cylindrical as evidenced from atomic force microscopy studies. In addition, the mechanical properties of the block copolymers showed semi‐ductile to quasi‐brittle behaviour depending upon the composition of the middle block which was also confirmed using scanning electron microscopy. Dynamic mechanical analysis of the triblock copolymers indicated that storage modulus increased with a decrease in methylene chain length. © 2018 Society of Chemical Industry     

Advances in analysis of total uncertainties in a semi‐invasive residual stress measurement method

The ability to characterise residual stress distribution accurately and over different length scales, particularly deep into an engineering part, plays a significant role in assessing structural integrity. Two most commonly used techniques to measure residual stress fields deep into engineering components include neutron diffraction (ND) and deep‐hole drilling (DHD). As the measurements depend on several physical quantities, they are susceptible to error. The error or uncertainties may turn substantial and compromise the suitability of the results. Although noninvasive, the neutron diffraction technique is neither readily available nor portable and is limited to approximately 60‐mm‐thick specimen; errors associated with results become unacceptable at greater flight paths. Moreover, a mock‐up representing the engineering component is normally used in the ND technique. In contrast, the DHD technique is portable and measures residual stresses with high spatial resolution. An error propagation technique was applied to develop an error analysis procedure taking into consideration various stages of the DHD method and successfully applied to different DHD measurements. An essential feature comprising the effect of plasticity due to the creation of reference hole in the DHD procedure has not yet been taken into account in the error analysis procedure. This paper briefly describes how the uncertainties due to the creation of the initial reference hole can be determined. The effect of plasticity in the drilling procedure is quantified in this study. This error is combined with other sources of error and formulated to determine the total error. An incremental DHD technique was used to measure the complex triaxial residual stress field in an as‐welded circular disc, and the measured data were used to illustrate the total error using the error analysis method developed in the study.     

A theoretically-based novel protocol for the analytic treatment of the glass failure stresses associated with coaxial double ring test method

With the aim of validating a new standardized Coaxial Double Ring testing procedure, without overpressure and with fixed geometry, an ad hoc theoretical approach has been proposed here to rearrange the laboratory outcomes accounting for the effects of the geometric non-linearities associated with such a testing configuration. By borrowing this idea, once the experimental values of the failure load have been determined, it has been possible to obtain an expression in closed form (fully defined by only two coefficients) of the maximum tensile stress (σ_max) in the core of the specimen. Following this, in order to make the laboratory outcomes comparable and homogeneous, the σ_max-values have been then re-scaled to a common reference condition (equibiaxial stress on a reference area, σ_eqbx), by means of the use of a correction coefficient (K) able to determine, under a condition of equal probability of failure, the effective area (A_eff) of the tested specimens. After being corrected to account for the effects of the stress corrosion cracking (static fatigue effect), all re-scaled data have been finally interpreted using a Weibull-type statistical distribution to determine the main fractile values of the glass strength. Doing so, despite some unavoidable approximations, this procedure furnished a highly effective means of determining the bending strength of float glass. Unlike the pure numerical approach proposed in codes and literature, which requires to correct the experimental data via FEM simulation, the rationale behind the proposed approach is in fact to elaborate the experimental data through an analytic treatment of the problem, which would greatly facilitate the interpretation of the data as well as the standardization of the testing procedure.     

Electrocatalytic hydrogen evolution of highly dispersed Pt/NC nanoparticles derived from porphyrin MOFs under acidic and alkaline medium

Platinum (Pt)-based electrocatalysts often exhibit an excellent electrocatalytic activity for hydrogen evolution due to their best hydrogen bonding energy, but materials with high Pt content can easily cause aggregation and reduce their efficiency. In this article, Pt-based electrocatalysts with uniform dispersion and high efficiency were fabricated by a successive hydrothermal and calcination method, and the uniformly distributed Pt nanoparticle was mainly due to the anchoring effect of porphyrin ring in porphyrin MOFs, which made the minimized agglomerations as much as possible in the process of high temperature calcination. The results showed that the optimal Pt/NC-850 could reach current density of 10, 50 and 100 mA cm^?2 with only 17, 82 and 152 mV overpotentials, while the Pt/NC-850 also exhibited a superior stability and durability under acidic medium. Impressively, the Pt/NC-850 also had an excellent activity, good stability and durability under alkaline medium.     

Synthesis and characterization of copolymers with the same proportions of polystyrene and poly(ethylene oxide) compositions but different connection sequence by the efficient Williamson reaction

The AB type diblock PS‐b‐PEO and ABA type triblock PS‐b‐PEO‐b‐PS copolymers containing the same proportions of polystyrene (PS) and poly(ethylene oxide) (PEO) but different connection sequence were synthesized and investigated. Using the sequential living anionic polymerization and ring‐opening polymerization mechanisms, diblock PS‐b‐PEO copolymers with one hydroxyl group at the PEO end were obtained. Then, using the classic and efficient Williamson reaction (realized in a ‘click’ style), triblock PS‐b‐PEO‐b‐PS copolymers were achieved by a coupling reaction between hydroxyl groups at the PEO end of PS‐b‐PEO. The PS‐b‐PEO and PS‐b‐PEO‐b‐PS copolymers were well characterized by ¹H NMR spectra and SEC measurements. The critical micelle concentration (CMC) and thermal behaviors were also investigated by steady‐state fluorescence spectra and DSC, respectively. The results showed that, because the PEO segment in triblock PS‐b‐PEO‐b‐PS was more restricted than that in diblock PS‐b‐PEO copolymer, the former PS‐b‐PEO‐b‐PS copolymer always gave higher CMC values and lower crystallization temperature (T_c), melting temperature (T_m) and degree of crystallinity (X_c) parameters. © 2015 Society of Chemical Industry     

Controlled delivery of growth‐hormone‐releasing peptide 6 from the poly(lactic‐co‐glycolic acid)–poly(ethylene glycol)–poly(lactic‐co‐glycolic acid) copolymer and the effect of a growth‐hormone‐releasing peptide 6–copolymer hydrogel on the growth of rex rabbits

Growth‐hormone‐releasing peptide 6 (GHRP‐6) plays an important role in animal growth. However, there have been few studies focusing on the effect of GHRP‐6 on animal growth through controlled release systems. We synthesized the poly(lactic‐co‐glycolic acid) (PLGA)–poly(ethylene glycol) (PEG)–PLGA copolymer to investigate its controlled released effect on GHRP‐6 in vitro and to study the effect of a GHRP‐6–copolymer hydrogel on the growth of rex rabbits. The copolymer was synthesized with ring‐opening copolymerization and characterized by ¹H‐NMR. The interaction between GHRP‐6 and the copolymer was characterized by Fourier transform infrared spectroscopy and X‐ray diffraction. The body weight, serum level of insulin‐like growth factor 1 (IGF‐1), and hair coat quality were studied in rex rabbits. The results show that hydrogen bonds formed between the N? H group in GHRP‐6 and the C?O group in the copolymer. The release mechanism of GHRP‐6 was a combination of a diffusion‐controlled mechanism and an erosion‐controlled mechanism in the copolymer. The serum level of IGF‐1, hair coat quality, and body weight were all significantly higher in the GHRP‐6–copolymer hydrogel group than in the other groups. These results indicate that the copolymer effectively controlled the release of GHRP‐6. In addition, the GHRP‐6–copolymer hydrogel increased the synthesis of IGF‐1 for a prolonged period and, thereby, increased the rex rabbits' growth and hair coat quality. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40185.     

Preparation and properties of polyamide‐6‐based thermoplastic laminate composites by a novel in‐mold polymerization technique

In this work, a method for preparation of polyamide‐6 (PA6) based laminates reinforced by glass fiber‐ (GFL) or polyamide‐66 (PA66) textile structures (PL) via reactive injection molding is disclosed. It is based on in‐mold anionic polymerization of ε‐caprolactam carried out at 165°C in the presence of the respective reinforcements performed in newly developed prototype equipment whose design concept and operation are described. Both composite types were produced for reaction times of 20 min, with conversion degrees of 97–99%. Initial mechanical tests in tension of GFL samples displayed almost twofold increase of the Young's modulus and stress at break values when compared with the neat anionic PA6. The improvement was proportional to the volume fraction V_f of glass fiber fabric that was varied in the 0.16–0.25 range. A 300% growth of the impact strength was registered in PL composites with V_f of PA66 textile of 0.1. Removing the surface finish of the latter was found to be a factor for improving the adhesion at the matrix–fiber interface. The mechanical behavior of GFL and PL composites was discussed in conjunction with the morphology of the samples studied by optical and electron microscopy and the matrix crystalline structure as revealed by synchrotron X‐ray diffraction. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40083.     

Nonisothermal crystallization kinetics of poly(butylene terephthalate)/multiwalled carbon nanotubes nanocomposites prepared by in situ polymerization

Poly(butylene terephthalate)/multiwalled carbon nanotubes (PBT/MWNT) nanocomposites were prepared by in situ ring‐opening polymerization of cyclic butylene terephthalate oligomers (CBT). The nonisothermal crystallization behavior of the neat PBT and the PBT/MWNT nanocomposites was analyzed quantitatively. The results reveal that the combined Avrami/Ozawa equation exhibits great advantages in describing the nonisothermal crystallization of PBT and its nanocomposites. The presence of MWNTs has the nucleation effect promoting crystallization rate for the nanocomposites, and the maximum one is observed in the nanocomposite having 0.75 wt % MWNT content. On the other hand, the addition of MWNTs has the impeding effect reducing the chain mobility and retarding crystallization, which is confirmed by the crystallization activation energies. However, the nucleation effect of MWNTs plays the dominant role in the crystallization of PBT/MWNT nanocomposites, in other words, the incorporation of MWNTs is increasing the crystallization rate of the nanocomposites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40849.     

A new strategy for plasticizing and stabilization of PVC mixtures

This study was undertaken to examine possible use of classic tetravalent tin‐based heat stabilizers for the preparation of a polymer plasticizer: poly(ε‐caprolactone) (PCL) and simultaneous stabilization of PVC in PVC/PCL mixtures. PCL was prepared from ε‐caprolactone (CL) by polymerization initiated by tin‐containing organic compounds and successfully used to simultaneously plasticize and stabilize PVC. Moreover, conditions under which the polymerization of CL took place directly in situ during PVC/CL mixture processing were found. The procedure yielded homogeneous plasticized PVC/PCL mixtures, which were stable and contained >90% of the original monomer content. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41066.