Photostabilization of cationic UV-cured coatings in the presence of nanoTiO2

The effect of TiO₂ nanoparticles for sun-weathering protection of UV-cured coatings is investigated. TiO₂ is either introduced in the form of nanoparticles in the photocurable formulations or generated in situ via sol–gel process. Cured films containing comparable amounts of TiO₂ were weathered for 800 h under UV irradiation and compared with free-TiO₂ coating. The TiO₂ presence induces a clear lower mass loss decrease during weathering as well as a lower gel content decrease. The TiO₂ screen effect is also confirmed by a lower alkyl-band reduction monitored by FT-IR during weathering. The TiO₂ generated in situ via sol–gel gives rise to transparent coatings without interfering with photopolymerization process and therefore without compromising UV-cured film properties.     

Photocrosslinking of stilbene-modified polymers

The reactions of trans-2,5-dimethoxy-4′-aminostilbene with poly(maleic anhydride-co-methylvinyl ether) and trans-2,5-dimethoxy-4′-isocyanatostilbene with poly(oxy-1,4-phenyleneisopropylidene:1,4-phenyleneoxy-2-hydroxytrimethylene) yield polymeric systems which undergo rapid crosslinking upon short exposure to ultraviolet light. The extent of photocrosslinking as a function of exposure time was determined by the decrease of the trans-stilbene ultraviolet absorption at 350 nm.     

The stress cracking of polyamides by metal salts. Part III. Metal thiocyanates

The stress cracking of polyamide (nylon 6) by a number of metal thiocyanates in aqueous and nonaqueous solutions has been investigated. Lithium, zinc and cobalt_II thiocyanates were the most active and their activity was compared with that of the corresponding metal halides. Stress cracking parameters were determined and the mechanism of cracking studied by infrared techniques. The action of metal thiocyanates on nylon 6 is similar to that of the corresponding metal halides. Some metal cobaltothiocyanates were also found to be active stress cracking agents.     

Compatibilization of inorganic particles for polymeric nanocomposites. Optimization of the size and the compatibility of ZnO particles

Summary The synthesis of in-situ hydrophobic functionalized ZnO nanoparticles via an emulsion process is systematically investigated. Different parameters are varied, such as precursor salt concentration and ultrasonification, to optimize the size and the size distribution of the ZnO particles. Particles with a size below 25 nm and surrounded by a hydrophobic polymer shell can be easily obtained. The influence of the polymeric shell on the compatibility with different polymeric matrices is described. Due to the small size of the inorganic particles and the excellent hydrophobization, highly transparent inorganic/organic nanocomposites can be obtained by spin-coating and extrusion.     

A new method for measuring the transfer of oxygen in liquids. MeasurementS of oxygen transfer from bubbles in water and in water + 1-butanol

At the base of a column of liquid 20 cm in diameter and well over 1 m in height, oxygen bubbles of constant volume were formed and released with a frequency of approximately one bubble per second. Measurements were carried out on bubbles with volumes ranging from 0·2 to 2 cm³. The mass transfer per bubble was determined by measuring the increase in oxygen concentration of the liquid phase with an oxygen electrode and counting the number of bubbles. The results were reproducible within 3 per cent, and it is probable that still better results are attainable with this method.The measurements were initially performed in distilled water to test the apparatus. Later, water—butanol mixtures were employed in order to determine the influence of butanol on the mass transfer. The results of the latter experiments have been checked with a theory published previously [23, 24]. Theory and results appear to be in satisfactory agreement.     

Converter refractories from Satkinsk dolomitic magnesite

Conclusions Satkinsk dolomitic magnesite fired in a rotary kiln using a cycle employed for Styl'sk dolomite can be used to obtain sintered powder with an apparent density 3.15 g/cm³.Compared with the currently produced tarred dolomite-magnesite refractories, the tar-bonded converter refractories made on the basis of powder produced from dolomitic magnesite are characterized by higher densities, strength, and resistance to hydration.Thus, Satkinsk dolomitic magnesite which is hardly used at the present time is a promising raw material for producing converter refractories.Translated from Ogneupory, No. 8, pp. 15–20, August, 1971.     

The relation of synergist to antioxidant in fats

Summary Citric and ascorbic acids delayed substantially the rate of peroxide accumulation, during the induction period, of lard which contained pro-oxidant levels ofα-tocopherol or NDGA. While low levels (.025%) of both acids showed effective synergistic action withα-tocopherol, higher levels were proportionately less effective. Tocopherol had a marked protective effect on ascorbic and phosphoric acids in autoxidizing lard. Evidence indicates that ascorbic and citric acid function as synergists in natural fats and oils by inhibiting the antioxidant catalysis of peroxide decomposition. This concept is discussed in relation to current theories of the mechanism of synergist action. Journal Paper No. 742 of the Purdue University Agricultural Experiment Station, Lafayette, Ind.     

Lipolysis of trivernolin by pancreatic lipase

Vernolic acid (cis-12,13-epoxy-cis-9-oetadece-noic acid) occurs as the triglyceride in the seed ofVernonia anthelmintica. Incubation of the seed produces a 1,3-divernolin. To determine whether the structure of trivernolin is responsible for the apparent secondary ester position specificity of the natural enzyme, trivernolin and tri-olein, were incubated with pancreatic lipase and the free fatty acids and monoglycerides were determined after 5 and 15 min digestion periods. The preponderance of 2-monoglyceride produced by the action of pancreatic lipase was interpreted to indicate that the structure of trivernolin was not solely responsible for the secondary position specificity of theV. anthelmintica lipase toward trivernolin.     

The difficultly extractable lipides of cottonseed meats,their composition and effect on the refining characteristics of the crude oils

Summary and Conclusions Crude lipides fractions were produced from raw, tempered, and cooked meats from two lots of cottonseed by a series of successive stepwise extractions, designed to obtain fractional portions of the total lipides in the order of the difficulty of their extraction. The proximate composition of the crude lipides fractions was determined. It was found that the composition of successive lipides fractions varied with the degree of exhaustiveness of extraction. The fractions obtained by more exhaustive extraction contained greater amounts of undesirable non-neutral oil material and lesser amounts of desirable neutral oil. It was also established that the method used in preparing meats for extraction was of paramount importance in its effect on the composition of the crude lipides obtained. The crude lipides fractions from raw and tempered meats contained large amounts of impurities while the crude lipides fractions similarly obtained from cooked meats were relatively low in impurities. Crude oils equivalent to varying degrees of total lipides extraction were reconstituted from the crude lipides fractions and evaluated for refining characteristics. The impurities content of the reconstituted oils varied as the degree of total lipides extraction and increases in the impurities content of the oils were generally reflected in disproportionate increases in refining losses and/or refined oil color. The oils obtained from the cooked meats at all degrees of extraction were outstandingly low in refining losses as compared to the oils from the raw and the tempered meats. Presented in two parts at the spring meeting, American Oil Chemists’ Society, New Orleans. La., Apr. 18–20, 1955, and at the fall meeting, Philadelphia, Pa., Oct. 10–12, 1995. One of the laboratories of the Southern Utilization Research Branch, Agricultural Research Service, U. S. Department of Agriculture.