Effect of the use of mineral filler on the properties of concrete

Engineers of the concrete technology are increasingly concerned with the material passing through a sieve of the size under 0.149 mm. Materials called very fine aggregate or mineral filler may affect the performance of concrete in an either positive or a negative way. Discussions on aggregate containing very fine material are vitally important. Washing the aggregate residue has been the sole way to solve this matter to date. This is mainly based on the debatable opinion that materials of this kind are regarded as clay material. The goal of the study was to determine how the content of mineral filler might affect properties of concrete. Two types of aggregates with different amounts of cement and mineral filler were used. Basically, mineral filler replaced sand. The effect of applying different amounts of mineral filler on concrete was then determined. The addition of 7-10% of mineral filler to fine aggregate (0-2 mm) was found to considerably improve the properties of concrete.     

Über das Spreiten von Lipiden auf der Haut

On the Spreading of Lipids on the Skin The spontaneous spreading of liquid lipids on human skin is an important property for the use value of such products in cosmetic and pharmaceutical preparations. A comparative evaluation procedure based on an impression method is described, by means of which it is possible to determine the spreading rates in a reproducible manner. The standardized spreading values of a number of lipids are discussed in comparison with their chemical structure and physico-chemical data such as viscosity and surface tension. None of these data series correlates entirely with the spreading rates of all the lipids tested. However, it is possible to assess relative spreading rates within similarly structured groups of compounds.     

Tissue variation in hydrocarbon composition in the rabbit

This study, which deals with the distribution of hydrocarbons in seven types of rabbit tissues, was done for the purpose of providing information that might help shed light on the biological relevance of the hydrocarbons in mammalian metabolism. Liver, kidneys, brain, spleen, skeletal muscle, perinephric adipose, and a sample of blood serum were collected from a single animal for analysis of their hydrocarbon composition. The analytical methodology consisted of solvent extraction, saponification (adipose), elution chromatography on hydrated alumina, and combined gas chromatography-mass spectrometry. Hydrocarbons were detected in all of the tissues examined at concentrations estimated to range from 0.1 to 0.01% of the total lipid extracted. Three quite distinct distribution modes were recognized. The bulk of the identified components consisted of normal, saturated, nonterpenoid hydrocarbons in the C₁₆ to C₃₃ range. Squalene, phytene, phytadiene, and pristane were the only terpenoids detected. Nonterepenoid branched (iso andanteiso) hydrocarbons were identified unequivocally and in significant amounts in the muscle only. The adipose was the only tissue which was relatively rich in monoalkenes, and its overall hydrocarbon composition closely resembled that of the feed. The results of the study are not consistent with metabolic inertness. The observed qualitative and quantitative differences might reflect function and metabolic activities of the individual organs in a way yet to be elucidated. Presented in part at the AOCS Spring Meeting, New Orleans, April, 1976.     

An anomaly in the necking behavior of polyethylene

Tensile creep measurements at constant load on nonoriented polyethylene have shown a marked transition at a certain stress level from a neck formation followed by instantaneous fracture to the formation of a neck which resists fracture for a considerable time. The transition, which shifts towards shorter time and higher nominal stress with increasing molecular weight, has been studied for 16 polyethylenes of different molecular weights, degrees of branching and crystalline structures. The marked. transition has only been observed for high density polyethylene of high molecular weight. Deformation measurements show a more distinct necking for the high density than for the medium density polyethylenes. This is consistent with current molecular deformation theories. A hypothesis for the transition is proposed based on the distinctness of the neck process in the high density polyethylene and the large difference in strength between the spherulitic structure and the fibrillar structure. The dependence of the transition on molecular weight is expected since the number of tic chains incrcrtses with increasing molecular weight.     

Kinetic investigations in heterogeneous reaction systems by wavefront analysis

In this paper the previously introduced wavefront analysis is extended to heterogeneous reaction systems, which consist of several reaction steps. It is shown how three mainly informations obtained at the wavefront, namely the damping of the wavefront, the time-gradients at the wavefront and the propagation velocity of the wavefront, can be used for kinetic investigations of a reaction step under consideration.     

Cold drawing of polyethylene terephthalate/polyethylene films

Films made from a 77/23 weight percent polyethylene terephthalate/polyethylene blend were stretched using an Instron apparatus. The structures of the samples were examined by methods which included ion beam etching and electron microscopy. The drawn samples exhibited a metallically lustrous and highly reflective surface up to a draw temperature, T_R, of 70°C and a draw ratio of about 5. Under certain conditions the change in structure caused by the stretching resulted in the formation of a highly uniform fibril-void structure. The voids are up to 3 μm in width and 160 μm in length and are formed primarily as a result of aggregation and then separation of the microfibrils of the individual polymer components.     

Polarographic behaviour of diisopropylaminoethane thiol hydrochloride

The polarographic behaviour of diisopropylaminoethanethiol HCl (RSH) has been studied in presence of 0·1 M LiCl at the dme. The effects of pH, supporting electrolyte, concentration, drop time and temperature on the characteristics of the wave have been investigated. The curves consist of two waves—a small pre-wave followed by a normal anodic wave over the entire pH range (2·60–12·60). The maximum number of moles absorbed on unit area is 3·98 × 10^?10 mole/cm², ie 2·4 × 10¹⁴ molecules/cm², which corresponds to an area 41·6 Ų per adsorbed molecule. The adsorption coefficient and molar adsorption energy are 6·34 × 10² and 26·34 kcal/mole respectively. The electrode reaction is reversible, diffusion-controlled and involves a one-electron tranfer process. The pK of the ?SH group is 10·6. Controlled-potential electrolysis, interaction with mercuric chloride and mathematical analysis reveal the depolarization of mercury with the formation of a Hg(I) complex, mercurous mercaptide RSHg, which rapidly changes to more stable mercuric complex (RS)₂Hg.     

Structure and properties of polyimide‐bonded magnets processed from prepolymers based on diacetyl derivatives of aromatic diamines and dianhydrides

We report a novel method of polyimide (PI) synthesis from prepolymers based on dianhydrides and diacetyl derivatives of aromatic diamines that facilitate the preparation of a melt processable mixture at 300 ± 10°C of the prepolymer and magnetic Nd‐Fe‐B alloy to provide PI‐bonded magnets with enhanced properties. It is shown that chemical structure of the prepolymers strongly influences viscosity behavior via crystallization of the oligoimide in the melt, leading to formation of PI with rigid‐rod like structure. This structural ordering of the prepolymers based on diacetyl derivative of diamine used in this study, if not controlled, leads to exponential increase of melt viscosity with time, making it practically impossible to prepare melt processable mixture of the magnetic particles and the PI prepolymers at elevated temperatures. The results obtained demonstrate that appropriate dianhydrides and diacetyl derivatives of diamines that do not lead to crystallization of oligoimides in prepolymer mixture can be used under controlled processing conditions to prepare melt‐processable PI‐bonded magnets containing rigid‐rod like PI structure that significantly increases thermal stability of the magnets. The temperature dependencies of the magnetic properties of the PI‐bonded magnets under conditions that they are likely to encounter during their service life were found to be remarkably similar to that of commercial thermoplastic magnets such as injection‐molded nylon magnets. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 478–485, 2006