Hydrolytic degradation of poly(oxyethylene)–poly-(ε-caprolactone) multiblock copolymers

The degradation of poly(oxyethylene)–poly(ε-caprolactone) (POE–PCL) multiblock copolymers was investigated at 37°C in a 0.13M, pH 7.4 phosphate buffer selected to mimic in vivo conditions. The copolymers were obtained by coupling polycaprolactone diols and poly(ethylene glycol) diacids using dicyclohexylcarbodiimide as coupling agent. Various techniques, such as weighing, size exclusion chromatography, infrared, ¹H nuclear magnetic resonance, differential scanning calorimetry, and X-ray diffractometry, were used to monitor changes in total mass, water absorption, molar mass, thermal properties, degree of crystallinity, and composition. The results showed that introduction of POE sequences considerably increased the hydrophilicity of the copolymers as compared with PCL homopolymers. Nevertheless, the degradability of PCL sequences was not enhanced due to the phase separation between the two components. Significant morphological changes were also observed during the degradation. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68: 989–998, 1998     

Rapid Bonding of Ti3SiC2 and Ti3AlC2 by Pulsed Electrical Current Heating

Inspired by pressure resistance welding of metallic materials, herein we describe how two MAX phases—Ti₃SiC₂ and Ti₃AlC₂—were successfully joined by a rapid electric current heating method in a pulsed electric current sintering furnace. No welding agent was employed and the total processing time was less than 6 min. When the bulk temperature of the joint couple exceeded 1070°C, good joints, with shear strength above 50 MPa, were achieved in both homo‐ and heterojunction joints.     

Influence of a metallic filler on polyurethane formation

The addition of metallic fillers is recognized to impart improvement of acoustic properties to polyurethane-based materials used for marine applications. The system under consideration was obtained by the reaction of a triisocyanateterminated prepolymer with 1,4-butanediol, in the presence of various concentrations of lead powder. With increasing lead content, gelation time is reduced and an Einstein-type law does not apply. The kinetics of the reaction were determined by Fourier transform infrared spectroscopy. Deviation from the classic second order is observed for the filled systems, and the higher the lead content, the more important the deviation is, showing undoubtedly the catalytic effect of the metallic powder.     

Mineral Fillers in Intumescent Fire Retardant Formulations — Criteria for the Choice of a Natural Clay Filler for the Ammonium Polyphosphate/Pentaerythritol/Polypropylene System

Addition of natural clay materials in intumescent polypropylene-based formulations (additive: ammonium polyphosphate and pentaerythritol) leads either to a decrease or to an increase of their fire retardant performances versus the chemical or the physical characteristics of the clay materials. A study of the factors affecting these performances has been carried out using linear and principal components analysis. This analysis shows that the results of the evaluation tests (LOI and UL 94) are affected in different ways by the adduct of the different clay material and that an increase in the LOI is not necessarily related to an increase in the UL 94 classification. LOI values are improved by the presence of the montmorillonite and of illite clay minerals which may react with acidic phosphate to form active carbonization catelysts, in addition, the results of the LOI test are improved by the presence of quartz and other foreign minerals in the clay materials. This study discusses the part played by the different constitutive minerals in the formation of defects in the polymer chain during the mixing process. It is proposed that the presence of these defects leads to a change in fire retardant performance.     

Experimental Study of the Radiodepolymerization of Starch

The radiodepolymerization of starch is studied by means of investigating the variations of intrinsic viscosity and of the rate of water-soluble products. The experimental results corroborate the theoretical laws proposed in an earlier paper. Special study of watersoluble products shows how the theoretical laws can be used to investigate the chemical functions radioinduced on the chains of dextrins.     

Identification of ritual blood in African artifacts using TOF-SIMS and synchrotron radiation microspectroscopies

A new protocol is implemented to demonstrate the presence of blood in the patina of African art objects from Mali. Divided into three steps, the protocol first consists in demonstrating the presence of proteins and localizing them in the sample's cross sections using time-of-flight secondary ion mass spectrometry (TOF-SIMS) and synchrotron-based infrared microspectrometry (microFT-IR). In a second time, TOF-SIMS is used to investigate heme, which is a blood marker. If heme is missing, which could mean that it is too degraded to be detected, X-ray microfluorescence (microXRF) and X-ray absorption near-edge microspectroscopy (microXANES) are used to prove the presence of iron in the protein area and to get a fingerprint of its chemical environment. This permits us thus to demonstrate that iron is indeed linked with proteins and not with mineral phases of the sample. Coupled with the ritual context of the objects, this constitutes a proof of the use of blood. Thanks to this protocol, which has the major advantage of avoiding false positive results, the presence of blood has been demonstrated in seven out of the eight studied samples.     

Tracer Studies in Laboratory Beach Simulating Tidal Influences

Bioremediation of oil spills on tidally influenced beaches commonly involves the addition of a nutrient solution to the contaminated region of the beach at low tide to stimulate the growth of indigenous oil-degrading bacteria. Maximizing the residence time of nutrients in the beach and subsequently their contact time with microorganisms is a main goal for successful bioremediation. Therefore, understanding the effects of the tide on water flow and solute transport in a beach is an essential task for designing a nutrient application strategy. We investigated these effects by conducting a tracer study in a laboratory beach simulating nutrient application on natural beaches. The study consisted of applying, at low tide, a conservative tracer solution onto the beach surface near the high-tide line and monitoring its movement in the beach subsurface. The tidal motion caused the applied plume to move downward and seaward. The downward movement occurred during rising tides, while the seaward movement occurred mainly during falling tides. The results indicate that nutrients should be applied at the high-tide line during low tides. Guidelines for scaling up the results to natural beaches are provided along with an example.