Reducing waste contamination from animal-processing plants by anaerobic thermophilic fermentation and by flesh fly digestion

There is currently no market in Israel for the large amounts of waste from fish- and poultry-processing plants. Therefore, this waste is incinerated, as part of the measures to prevent the spread of pathogens. Anaerobic methanogenic thermophilic fermentation (AMTF) of wastes from the cattle-slaughtering industry was examined previously, as an effective system to treat pathogenic bacteria, and in this article, we discuss a combined method of digestion by thermophilic anaerobic bacteria and by flesh flies, as a means of waste treatment. The AMTF process was applied to the wastes on a laboratory scale, and digestion by rearing of flesh fly (Phaenicia sericata) and housefly (Musca domestica) larvae on the untreated raw material was done on a small scale and showed remarkable weight conversion to larvae. The yield from degradation of poultry waste by flesh fly was 22.47% (SD = 3.89) and that from fish waste degradation was 35.34% (SD = 12.42), which is significantly higher than that from rearing houseflies on a regular rearing medium. Bacterial contents before and after thermophilic anaerobic digestion, as well as the changes in the chemical composition of the components during the rearing of larvae, were also examined.     

Synthesis of Cyclopropyl Ethers and Cyclopropanols by Carbene Transfer – Acetolysis of Cyclopropyl p-Toluenesulfonates

The reaction of chloromethyl phenyl ether with butyllithium in olefins yields phenoxy-cyclopropanes. 1-Chloro-1-phenoxycyclopropanes can be prepared in a similar manner, though the yields are poor. Alkoxycyclopropanes are formed when dichloromethyl alkyl ethers are treated with methyllithium/lithium iodide in the presence of olefins. Cyclopropanols can be obtained in good yields by reaction of (β-chloroethoxy)cyclopropanes either with butyl- or ethyllithium or with bases. – As was shown by acetolysis experiments with cyclopropyl p-toluenesulfonates having a known steric configuration, the rearrangement of a cyclopropyl derivative into an allyl cation proceeds in accordance with the Woodward-Hoffmann-DePuy rule. The solvolysis of exo-bicyclo[n.1.0]alkyl p-toluene-sulfonates is assumed to proceed via “semi-open” intermediates, which are somewhere between an allyl cation and a cyclopropyl cation.     

Verwendung von Carboxylpapier in der Papierchromatographie

Zusammenfassung Bei der Chromatographie auf Carboxylpapier herrschen definierte Ionenaustauschvorgänge vor, die sich theoretisch näherungsweise ableiten lassen. Durch Variation von Carboxylgehalt und austauschfähigem Kation im Papier, sowie vonph-Wert, Pufferkapazität und Kationenstärke in der entwickelnden Lösung ist es möglich, die für die chromatographische Trennung der drei basischen Aminosäuren günstigsten Bedingungen festzustellen. Es ist zu erwarten, daß sich auf Carboxylpapier weitere, kationenbildende Stoffe trennen lassen, die sich entweder in ihrer Affinität zur Oxycellulose oder in ihrer Basizität oder in beidem voneinander unterscheiden.Die Arbeit wurde durch wertvolle Kritik von Herrn Professor Dr. Th. Wieland gefördert. Wesentliche Anregungen stammen auch von Herrn Dr. W. Vollmer. Im Labor wurden die Chromatogramme sämtlich von Frau E. v. Dungen ausgeführt.     

A 13C endor study on Copper(II)/Zinc(II) bis-(diethyl-dithiocarbamate) Cu/Zn(et2dtc)2

¹³C ENDOR spectra of Cu(et₂dtc)₂ substituted into a single crystals of Zn(et₂dtc)₂ are reported. The symmetry of the incorporated guest molecule appears to be considerably influenced by the Zn(et₂dtc)₂ host lattice. The unexpectedly large isotropic ¹³C hfs coupling can be understood assuming a “transannular overlap” mechanism.     

Use of S-matrix approach to develop a theory of perturbations in 1/Z

On the basis of the S-matrix approach, a theory of perturbations in 1/Z is developed; the energy of a multielectron system is written in the form of a double series in powers of andZ and a method of determining the coefficients of this series in a j-j coupling scheme is given. The method is applied to configurations of the type , and numerical results are given for the wavelength of transitions between several states of the isoelectronic as sequence of carbon, illustrating the good agreement between experiment and theory.Translated from Izvestiya Vysshikh Uchebnikh Zavedenii, Fizika, No. 8, pp. 59–63, August, 1978.     

Structure, activity and selectivity of V2O5-TiO2 catalysts for o-xylene conversion

The formation of needle shaped crystallites of V₆O₁₃ at low V concentrations on V₂O₅-anatase coated catalysts explains the low selectivity for phthalic anhydride during o-xylene oxidation. The (010) plane of V-oxide, most active for selective oxidation of o-xylene, is not accessible and the contact of this plane with the anatase faces promotes the anatase-rutile transformation and the incorporation and blocking of V⁴⁺ ions.

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V₆O₁₃ V , V₂O₅-, -. (010) , -, , - V⁺⁴.

     

Unconventional nucleotide analogues. 3. 4-(N1-pyrimidyl)-2-aminobutyric acids

Alkylation of 4-ethoxy-2-hydroxypyrimidines (10a, b), via their anions, provides a convenient procedure for preparing N₁-substituted derivatives. Reaction of 10a, b with t-butyl 4-bromo-2-benzyloxycarbamidobutyrate (17) gives good yields of the N₁-alkylated products 18a, b. The latter have been converted to uracil- (20a), thymine- (20b) and cytosine- (21) substituted -aminobutyric acids.