Shear-induced pre-crystallization structures of long chain branched polypropylene under steady shear flow near the melting temperature

Shear-induced crystallization of a long chain hyper-branched polypropylene (LCB-PP, denoted PP-3) was carried out at a relatively high temperature of 170 °C, close to its melting temperature of 158 °C. Small-angle X-ray scattering (SAXS) showed that the intensity ratio of the normal to the perpendicular to the shear (V/H) was always larger than 1 for PP-3, indicating that shish-like structures were predominately formed and further growth to kebab was suppressed in PP-3. The crystallization behavior of PP-3 can be explained by the nature of PP-3 that there were a large amount of crystallization nuclei due to their branching points, and the point-like precursors formed from these nuclei were arrayed linearly along the shear direction and transformed into thread-like precursors or premature shishs; however, owing to the large amount of branching, further progress in crystallization was suppressed.     

Effects of Various Preparation and Polymerization Procedures on the Isospecific Nature of TiCl3-Based Polypropylene Catalysts

Summary As one of a series approaches in using two-component and three-component donor-free Ziegler–Natta catalysts, in this preliminary work, the effects of various preparation and polymerization conditions including catalyst preparation by wet- or dry- grinding, the type of cocatalyst, with or without pretreatment of catalyst by cocatalyst before polymerization, Al/Ti molar ratio and polymerization temperature, etc., on the isospecific nature of active sites of the TiCl₃ catalyst were studied through a systematic characterization of the PPs by a combination of GPC, ¹³C-NMR with TREF method. It was demonstrated that the types of Al-alkyl cocatalysts play the most dominant role in determination of isospecificity of activate sites and its distribution. A plausible mechanism (Scheme 1) regarding the formation of isospecific active sites with different stability in terms of Ti–Al bimetallic complexing depending on the type of cocatalyst had been proposed. Except the catalyst grinding method, other factors eg., pretreatment, temperature, and Al/Ti molar ratio, etc. did not show obvious effects on the isospecific nature of active sites.     

Smart sunglasses based on electrochromic polymers

Smart sunglasses based on electrochromic polymers are proposed and developed in this study. This article discusses the design, processing, and the optical and electrical performance of a prototype smart sunglasses based on cathodic electrochromic (EC) polymers, which show several merits compared with traditional materials for sunglasses lens as well as other smart window materials. It is a multilayer design of device. The conjugated polymer, poly[3,3‐dimethyl‐3,4‐dihydro‐2H‐thieno [3,4‐b] [1,4]dioxepine] (PProDOT‐Me₂), is utilized as the electrochromic working layer. The counter layer of the device is vanadium oxide (V₂O₅) film, which serves as an ion storage layer. There is also a polymer gel electrolyte acting as the ionic transport layer, sandwiched between the working and counter layers. The characteristics of the prototype device are reported, including transmittance (%T), driving power, response time, open circuit memory, and lifetime. POLYM. ENG. SCI., 2008. © 2008 Society of Plastics Engineers     

Kinetic parameters for anodic oxidation of hypochlorite ion on Pt and Pt oxide electrodes in alkaline solution

Kinetic parameters for the anodic oxidation of hypochlorite ion have been determined by means of normal pulse voltammetry by using a platinum disk as the working electrode. By using the working electrode that formed an oxide film by electrochemical pretreatment, the effect of the lattice oxygen of the surface oxide on the reaction was also examined. The measurement results were analyzed by the classical method, and then the analytical results were evaluated by digital simulation. The normal pulse voltammogram of the hypochlorite ion showed quasi-reversible oxidation waves. The apparent rate constant was calculated to be 5.0-8.1 × 10⁻⁴ cm s⁻¹, depending on the electrode surface state. At the low-concentration range of <4.0 mg Cl dm⁻³, the oxidation current was concentration dependent at the cathodically polarized electrode, while it became independent after the anodic polarization.     

Preparation and properties of biodegradable network poly(ester-carbonate) elastomers

Biodegradable elastomeric network poly(ester-carbonate)s were prepared from multifunctional aliphatic carboxylic acids such as tricarballylic acid (Y_t) or trimesic acid (Y) and polycarbonate diols (PCD) with molecular weights of 1000 and 2000 g/mol. Prepolymers prepared by a melt polycondensation were cast from dimethylformamide solution and postpolymerized at 270 °C for 40-80 min to form a network. The resultant films were transparent, flexible and insoluble in organic solvents. WAXS exhibited the crystalline peaks due to polycarbonate segments for the network films from PCD₂₀₀₀, while those from PCD₁₀₀₀ were amorphous. The tensile properties were determined for these network films at the temperatures 22, 30, 40 and 50 °C. These films showed elastomeric properties at all temperatures measured. The elongation at break was much higher for the films from PCD₂₀₀₀ (208-434%) than those from PCD₁₀₀₀ (40-120%), and decreased with increasing temperatures. The weight losses of the network films degraded in the buffer solution of Rhizopus delemar lipase at 37 °C increased with time, suggesting that these network films are biodegradable. The degradation rate of the network films from Y_t is faster than that from Y. The GPC curves showed that the lipase hydrolyzed both the ester linkages between Y or Y_t and PCD as well as polycarbonate moiety in the network polymer.     

Radiation‐initiated graft polymerization of methylmethacrylate onto poly(tetrafluoroethylene): Characterization by 1H‐NMR

A broad‐line ¹H‐NMR study was carried out to examine the local structure of poly(methylmethacrylate) (PMMA) grafted onto Poly(tetrafluoroethylene) (PTFE). The NMR spectra were observed for three different samples with 1.0, 5.4, and 7.0 wt % PMMA over the temperature range from 150 to 380 K. With the help of selectively deuterated PMMA (PMMA‐d₅ and PMMA‐d₈)‐grafted samples, the NMR spectra were analyzed in terms of two components—a Gaussian (G) component, and a Lorentzian (L) component. Based on the second moments (〈ΔH²〉) analysis, the L and G components were attributed to the ¹H–¹H dipolar interactions within one CH₃ group and the interactions of CH₃ groups that are closely located in aggregated PMMA chains. Combining the results with the temperature dependence of 〈ΔH²〉 and the angular resolved XPS, the location and rotational motion of PMMA grafted onto PTFE are discussed. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1386–1394, 1999     

Determination of residual avoparcin in chicken muscle by HPLC with ultraviolet and amperometric detection

An analytical method was developed for determination of residual avoparcin in chicken muscle by measuring alpha- and beta-avoparcin, major components of the pharmaceutical preparation avoparcin, using HPLC with UV and amperometric detectors. The analytical HPLC was run on a Cosmosil 5C18-AR column (4.6 mm x 25 cm) with a gradient formed from A: 2.5% acetic acid, 0.01 mol/L sodium heptane sulfonic acid-acetonitrile (88.5:11.5) (pH 4.0) and B: 2.5% acetic acid-acetonitrile (10:90), using UV and amperometric detection (AMD) with glassy-carbon electrode (+900 mV). Avoparcin was extracted from chicken muscle by homogenization with methanol-0.2 mol/L sulfuric acid (6:4) followed by centrifugation after pH adjustment to 4 with 1 mol/L sodium hydroxide. The supernatant was evaporated to dryness, and the residue was dissolved in water. The aqueous layer was adjusted to pH 4 by adding 1 mol/L sodium hydroxide. Then it was purified on a Sep-Pak tC18 plus ENV cartridge. The cartridge was washed with water, and retained substances were eluted with 50% methanol. The eluate was evaporated to dryness under reduced pressure. The residue was dissolved in water and determined by HPLC. Recoveries of avoparcin spiked in chicken muscle were 73.1-88.1% at levels of 2-10 micrograms/g. The detection limits were 0.5 microgram/g (UV) and 0.2 microgram/g (AMD).     

$V_rm DD$-Hopping Accelerators for On-Chip Power Supply Circuit to Achieve Nanosecond-Order Transient Time

A V_DD-hopping accelerator for on-chip power supply circuits is proposed and the effectiveness of the accelerator circuit is experimentally verified. The quick dropper with the linear regulator enables nanosecond-order transient time in on-chip distributed power supply systems. The measured transition time is less than 5 ns with a load circuit equivalent to 25-k logic gates in 0.18-mum CMOS. This is to be compared with the case without the accelerator of the order of mus and thus the acceleration by two orders of magnitude is achieved. Extensions of the basic approach are also discussed including implementation of the quick dropper for a switching DC-DC converter, the control stability improvement, automatic timing generation, and the parasitic element effects of the power lines     

Scattering of a Gaussian Beam by Stepped Index Luneberg Lens

The scattering and focusing characteristics of a Gaussian beam with phase distribution is studied by a stepped index Luneberg lens. A model experiment was performed using a six-layer spherical lens. Two kinds of beams, that is, broad and narrow beam are examined for the incident Gaussian beam. We find that focusing effect of a narrow beam is wholly lower than that of a broad beam. The focal point is also shifted toward outer of sphere because of phase lag for the beam source. The spot size equals almost the wavelength for the various beam parameters.     

Design impact of positive temperature dependence on drain currentin sub-1-V CMOS VLSIs

In sub-1-V CMOS designs, especially around 0.5-V CMOS designs, on-state drain current of MOSFETs shows positive temperature dependence, being different from the negative temperature dependence in the conventional voltage designs. Combined with low threshold voltage less than 0.2 V, the possibility of temperature instability increases. This paper describes possible temperature instabilities in the low-voltage regime by using circuit simulation environments incorporating temperature change in time and experiments using MOSFETs and the 32-bit adder circuit in quarter-micrometer CMOS technology with a low threshold voltage of 0.25 V