Semi- and fully interpenetrating polymer networks based on polyurethane–polyacrylate systems. VI. Polyurethane–poly(methyl acrylate-co-ethyl acrylate) semi-1-interpenetrating polymer networks

Dynamic mechanical and longitudinal sonic velocity measurements have been made on a series of semi-1-IPNs in which the network component is a polyurethane and the linear constituent a copolymer of methyl acrylate and ethyl acrylate. Dynamic mechanical analysis reveals phase separation. The shifting of the polyurethane glass transition in both the tan δ? and the E″–temperature plots indicates that some mixing occurs. The longitudinal sonic velocity results indicate that the polyurethane is present as a continuous phase in all the materials investigated.     

An analysis of transport phenomena for multi-solid particle systems at higher reynolds numbers by a standard karman—pohlhausen method—I Momentum transfer

Using the concentric spheres free surface model and a standard 4th polynomial Karman—Pohlansen method, the dimensionless tangential stress distribution, and the dimensionless pressure distribution around a solid sphere in a swarm, and the viscous, form and total drag coefficient for multi-solid particle systems were computed numerically at higher Reynolds numbers. The void function obtained from the drag coefficient for multiparticle system was comparative to the experimental data. The friction factor for multi-particle systems so computed agreed with the experimental data of packed and distended beds.     

Extraction of lipids from cottonseed tissue: VI. Ultrastructural morphology of isolated pigment glands

Cottonseed pigment glands, isolated from the underflow fraction of the liquid cyclone process, were examined with an electron microscope. The glands were circumscribed by a layer of tangentially flattened cells. Subjacent to the flattened cells were partially lysed cells containing recognizable remnants of cell walls. Within the lumens or matrices of the glands were myriads of pigment spherules measuring 0.1–1.5 µ in diameter. These spherules remained within the glands, even though gland walls were ruptured mechanically. Since aggregates of pigment spherules devoid of gland walls were observed in the gland-rich fraction, it was concluded that maintenance of intact pigment glands was not a requisite for successful separation of gossypol from other cottonseed components with the liquid cyclone process. Avoiding dispersion of aggregated spherules from the glandular matrix was probably just as important as maintaining intact gland walls during mechanical separation of gossypol from other cottonseed components.     

Telerobot-enabled HUB-CI model for collaborative lifecycle management of design and prototyping

The HUB-CI model is investigated in a telerobotic system in a client/server network to manage the lifecycle of engineering design and prototyping. The purpose of this platform is to support collaborative engineering design and proof of concept to enhance distributed team collaboration and resource utilization. The suggested platform is exemplified in two collaboration support tools and a physical prototyping platform. Structured Co-Insight Management is developed to support innovative idea exchanges and the consensus decision-making during the design process. Conflict/error detection management helps preventing conflicts and errors during the lifecycle of design and development. Physical collaboration over the network occurs when a team controls the telerobot operation during prototyping and testing in design cycles. A pilot system is implemented with a group project for the design of an electronic circuit (including both hardware and software designs). The functional assessment method is used to compare this platform to other collaborative design tools. The system presented offers unique qualitative advantages as an integrated collaboration support system.     

Role of adhesive–substrate compatibility in adhesion

For substrates such as polyesters having limited capacity for hydrogen bonding or other specific interactions, thermodynamic compatibility of the substrate and adhesive is shown to be a key factor in promoting bondability to the substrate. Such compatibility occurs, as shown by Abere, when the cohesive energy densities (CED) or solubility parameters (δ = √CED) of substrate and adhesive are matched. Investigations with polyester film-adhesive-film model systems with the use of a variety of nonpolar (hydrocarbon) and polar (chlorinated compounds, ethers, esters) adhesives illustrate how compatibility promotes bondability to poly(ethylene terephthalate). The poor adhesion of polyester fibers to resorcinol–formaldehyde–latex (RFL) adhesives is attributed to the incompatibility of resorcinol (δ = 16.0) with the polyester (δ = 10.3). Adhesion to RFL was improved by substituting the more compatible n-hexyl resorcinol (δ = 12.5) for resorcinol in RFL adhesives. Currently, the best adhesive systems for polyester tire yarns are those (e.g., isocyanate–epoxy) involving formation of urethane polymers having matching δ values with poly(ethylene terephthalate).     

Crystalline complex between poly(γ-methyl l-glutamate) and dimethyl phthalate

The crystalline complex between poly(γ-methyl l-glutamate) (PMLG) and dimethyl phthalate (DMP) has been formed in films cast from a solution in dichloroethane. It has the stoichiometry of 1 mol of DMP to three or four residues of PMLG and shows two definite characteristics in X-ray diffraction patterns; one is the large hexagonal unit cell with the edge of around 28 Å and another the ‘extra’ 5.07 Å meridional reflection which can not be interpreted by a PMLG α-helical conformation. The structural examination for the films with various DMP contents is carried out by X-ray, viscoelastic, and d.s.c. measurements and the following structure is proposed for the crystalline complex. Four PMLG are associated to form a group which is hexagonally packed and DMP molecules, located in the gaps between groups, form a specific favourable helical structure along PMLG chains in which the van der Waals stacking of benzene rings of DMP is significant.     

Surfactants as replacements for natural lipids in bread baked from defatted wheat flour

Petroleum ether (PE) extracted 1.00% total free lipids (0.70% nonpolar and 0.30% polar) and 2-propanol (PrOH) extracted 1.36% total free and bound lipids (0.73% nonpolar and 0.63% polar) from wheat flour; the lipid fractions were characterized by thin layer chromatography. PE- or PrOH-defatted flours were baked after reconstitution with total, nonpolar, or polar wheat flour lipids; or with equivalent amounts of nonionic sucrose monopalmitate (SMP), ethoxylated monoglycerides (EMG) — each with a hydrophile-lipophile balance (HLB) of 14.0 or anionic sodium stearoyl-2-lactylate (SSL) — with an HLB value of 9.0. Defatted flours supplemented with surfactants alone or in combination with wheat flour lipids were used in bread with no-shortening and with 3%-shortening. The importance of the polar flour lipids in breadmaking was verified. The lipids in wheat flour were essential for maximizing the beneficial effects of shortening on breadmaking quality. Nonionic SMP or EMG completely replaced both PE-extractable wheat flour free total lipids ( or their non-polar or polar fractions) and 3% shortening; nonionic surfactants with high HLB were better than the anionic SSL for replacing free flour lipids. No surfactant completely replaced unfractionated PrOH-extracted lipids (free + bound) and shortening or total polar flour lipids (free + bound). All surfactants, especially anionic SSL, added with PrOH-extracted polar lipids improved the overall bread-making properties of the PrOH-defatted flour both in the absence and in the presence of shortening. Presented at the AOCS Meeting, New York, May 1977     

A generalized method for correcting instrument spreading in gel permeation chromatography

A general method of chromatogram correction for skewed instrument spreading in gel permeation chromatography is presented. The correction method is so general that there is no restriction on the shape of the spreading function. It admits nonsymmetric, non-Gaussian as well as nonconvolution type. Aspects of solution techniques are discussed and an illustrative example is given to elucidate the method.     

Synergistic Influence of Poly(4-Vinylpyridine) and Potassium Iodide on Inhibition of Corrosion of Mild Steel in 1M HCl

The corrosion and inhibition behavior of mild steel in 1 M HCl in the presence of poly(4-vinylpyridine)(P4VP) and potassium iodide (KI) was investigated using weight loss measurements, potentiodynamic polarization studies and impedance measurements. The inhibition efficiency increased with increasing P4VP concentration. The inhibiting action of P4VP is considerably enhanced by the addition of potassium iodide. The adsorption of this compound either alone or in combination with iodide ions on the metal surface is found to obey Lamgmir's adsorption isotherm. The experimental results suggest that the presence of iodide ions in the solution increases the surface coverage and, therefore, indicate the joint adsorption of P4VP and iodide ions. On the other hand, it was found that the inhibiting effect of P4VP and (P4VP + KI) increased with increasing temperature of the corrosion medium. The presence of these species in the solution decreases the double layer capacitance and increases the charge transfer resistance, both derived from Nyquist plots obtained from a.c. impedance studies. The variation of charge transfer resistance with time suggests that the inhibitive action of (P4VP + KI) depends mainly on the protective inhibitor film formed on the steel surface.     

Synthesis and characterization of poly(1,8-diethynylnaphthalene)

Summary The cyclopolymerization of 1,8-diethynylnaphthalene(DEN) and its copolymerization with diethyl dipropargylmalonate(DEDPM) were carried out by various transition metal catalysts. MoCl₅-based catalyst was found to be very effective and gave almost a quantitative polymer yield. The resulting dark-brown homopolymer(PDEN) was partially soluble in chloroform, tetrahydrofuran, and dimethyl sulfoxide, whereas copolymer (1:1) with number avaerage molecular weight of 2.1x10⁴ by GPC showed good solubility in those solvents. The structure of the polymers was analysed by IR, NMR, and UV-VIS spectroscopies. From the spectral and solubility data, it is proposed that cyclized products with the conjugated system are formed. Room temperature conductivities of the I₂-doped homo and copolymer were found to be about 7.5x10^-3 and 5.1x10^-3 S/cm, respectively.