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- Balducci, Francesco, et al.
(author)
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A formaldehyde-free adhesive for particleboards based on soy flour, magnesium oxide, and a plant-derived enzymatic hydrolysate
- 2020
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In: BioResources. - : North Carolina State University. - 1930-2126. ; 15:2, s. 3087-3102
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Journal article (peer-reviewed)abstract
- An adhesive for particleboards based on natural materials was prepared. Soy flour (38.9 wt%), magnesium oxide (MgO) (2.8 wt%), and a hydrolysate from an agricultural crop (13.9 wt%) were mixed with water and ground in a ball mill at 44% solids. The solubility and interaction of the soy flour proteins and the proteins contained in the plant hydrolysate were triggered by the strong basic environment created by MgO in the presence of water. The natural adhesive appeared to be thermally stable at temperatures from 130 °C to 240 °C, with unchanged mass and no major signals in the thermal analysis curves. These results, together with a viscosity of 510 Pa·s at 25 °C, suggested a good operability of the adhesive. Three-layered particleboards were manufactured with weight combinations of natural adhesive and polyamidoamine-epichlorohydrin (PAE) of 0%:100%, 33%:67%, 50%:50%, 67%:33%, and 100%:0%. The natural adhesive showed inferior internal bond strength and poor water resistance compared with urea-formaldehyde-bonded boards. Addition of the PAE significantly improved the internal bond and swelling, and for all the combinations these properties were comparable or, in most cases, better than in the urea-formaldehyde controls. All boards were formaldehyde-free, while the natural adhesive itself released no dangerous volatile substances
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| 2. |
- Marchetti, Fabio, et al.
(author)
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Zinc(II) Complex with Pyrazolone-Based Hydrazones is Strongly Effective against Trypanosoma brucei Which Causes African Sleeping Sickness
- 2022
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In: Inorganic Chemistry. - : American Chemical Society (ACS). - 0020-1669 .- 1520-510X. ; 61:34, s. 13561-13575
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Journal article (peer-reviewed)abstract
- Two pyrazolone-based hydrazones H2L′ [in general, H2L′ in detail, H2L1 = 5-methyl-2-phenyl-4-(2-phenyl-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)ethyl)-2,4-dihydro-3H-pyrazol-3-one, H2L2 = (Z)-5-methyl-2-phenyl-4-(2-phenyl-1-(2-(pyridin-2-yl)hydrazineyl)ethylidene)-2,4-dihydro-3H-pyrazol-3-one] were reacted with Zn(II) and Cu(II) acceptors affording the complexes [Zn(HL1)2(MeOH)2], [Cu(HL1)2], and [M(HL2)2] (M = Cu or Zn). X-ray and DFT studies showed the free proligands to exist in the N-H,N-H tautomeric form and that in [Zn(HL1)2(MeOH)2], zinc is six-coordinated by the N,O-chelated (HL1) ligand and other two oxygen atoms of coordinated methanol molecules, while [Cu(HL1)2] adopts a square planar geometry with the two (HL1) ligands in anti-conformation. Finally, the [M(HL2)2] complexes are octahedral with the two (HL2) ligands acting as κ-O,N,N-donors in planar conformation. Both the proligands and metal complexes were tested against the parasite Trypanosoma brucei and Balb3T3 cells. The Zn(II) complexes were found to be very powerful, more than the starting proligands, while maintaining a good safety level. In detail, H2L1 and its Zn(II) complex have high selective index (55 and >100, respectively) against T. brucei compared to the mammalian Balb/3T3 reference cells. These results encouraged the researchers to investigate the mechanism of action of these compounds that have no structural relations with the already known drugs used against T. brucei. Interestingly, the analysis of NTP and dNTP pools in T. brucei treated by H2L1 and its Zn(II) complex showed that the drugs had a strong impact on the CTP pools, making it likely that CTP synthetase is the targeted enzyme.
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