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Copyright of Acta Stomatologica Croatica is the property of Acta Stomatologica Croatica and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

The underutilized cement-rich fine fraction of concrete-based demolition waste is a potential sorbent for aqueous metal ion contaminants. In this study, crushed concrete fines (CCF) were found to exclude 33.9 mg g−1 of Cr3+, 35.8 mg g−1 of Ni2+, and 7.16 mg g−1 of Sr2+ from ~1000 ppm single metal nitrate solutions (CCF:solution 25 mg cm−3) under static batch conditions at 20 °C after 3 weeks. The removal of Sr2+ followed a pseudo-second-order reaction (k2 = 3.1 × 10−4 g mg−1 min−1, R2 = 0.999), whereas a pseudo-first-order model described the removal of Cr3+ (k1 = 2.3 × 10−4 min−1, R2 = 0.998) and Ni2+ (k1 = 5.7 × 10−4 min−1, R2 = 0.991). In all cases, the principal mechanism of interaction was the alkali-mediated precipitation of solubility-limiting phases on the surface of the CCF. Four consecutive deionized water leaching procedures (CCF:water 0.1 g cm−3) liberated 0.53%, 0.88%, and 8.39% of the bound Cr3+, Ni2+, and Sr2+ species, respectively. These findings indicate that CCF are an effective sorbent for the immobilization and retention of aqueous Cr3+ and Ni2+ ions, although they are comparatively ineffectual in the removal and sustained exclusion of Sr2+ ions. As is commonly noted with Portland cement-based sorbents, slow removal kinetics, long equilibrium times, the associated release of Ca2+ ions, high pH, and the formation of loose floc may preclude these materials from conventional wastewater treatments. This notwithstanding, they are potentially suitable for incorporation into permeable reactive barriers for the containment of metal species in contaminated groundwaters, sediments, and soils. [ABSTRACT FROM AUTHOR]

Construction and demolition activities generate approximately two thirds of the world’s waste, with concrete-based demolition material accounting for the largest proportion. Primary aggregates are recovered and reused, although the cement-rich fine fraction is underutilised. In this study, single metal batch sorption experiments confirmed that crushed concrete fines (CCF) are an effective sorbent for the maximum exclusion of 45.2 mg g−1 Cd2+, 38.4 mg g−1 Co2+ and 56.0 mg g−1 MoO4 2− ions from aqueous media. The principal mechanisms of sorption were determined, by scanning electron microscopy of the metal-laden CCF, to be co-precipitation with Ca2+ ions released from the cement to form solubility limiting phases. The removal of Co2+ and MoO4 2− ions followed a zero-order reaction and that of Cd2+ was best described by a pseudo-second-order model. The Langmuir model provided the most appropriate description of the steady state immobilisation of Cd2+ and Co2+, whereas the removal of MoO4 2− conformed to the Freundlich isotherm. Long equilibration times (>120 h), loose floc formation and high pH are likely to limit the use of CCF in many conventional wastewater treatment applications; although, these properties could be usefully exploited in reactive barriers for the management of contaminated soils, sediments and groundwater. [ABSTRACT FROM AUTHOR]

Landfilling and stockpiling unrecycled colored container glass represents a considerable failure in sustainability with respect to the conservation of energy and mineral resources. In this study, the single-step hydrothermal synthesis of low-silica zeolites from a mixture of waste green container glass and aluminum foil (Al:Si = 1) in 4 M NaOH(aq) at 125 °C was followed at 1, 3, 7 and 14 days. The principal phases, sodalite and cancrinite, appeared within 1 day accompanied by minor quantities of hydrogarnet and tobermorite arising from a stoichiometric excess of calcium ions in the parent glass. Products of 63, 67, 71 and 72% crystallinity were obtained at 1, 3, 7 and 14 days, respectively, with partial successive conversion of sodalite to cancrinite over time. Ion-exchange and catalytic applications of sodalite and cancrinite arise from the high anionic charge of the 1:1 ratio of alternating SiO44- and AlO45- units within their aluminosilicate frameworks. In this respect, the uptake capacity of the 14-day zeolitic product for Cu2+ and Cd2+ ions (1.58 meq g-1 and 1.66 meq g-1, respectively) was within the expected range for zeolites and compared favorably with those reported for other inorganic sorbents derived from industrial and municipal wastes. The 14-day product was also found to be an effective basic heterogeneous catalyst for the Knoevenagel condensation reaction. [ABSTRACT FROM AUTHOR]

Copyright of Acta Odontologica Latinoamericana: AOL is the property of Acta Odontologica Latinoamericana and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

ObjectiveTo determine whether the antimicrobial nature of a fatty acid chelate temporary dental cement can be enhanced by the addition of 5% cetyl pyridinium chloride (CPC). Materials and methodsThe temporary cement, Cavex Temporary was employed, and additions of CPC were made to either the base or the catalyst paste prior to mixing the cement. Release of CPC from set cement specimens was followed using reverse-phase HPLC for a period of up to 2 weeks following specimen preparation. Potential interactions between Cavex and CPC were examined by Fourier transform infrared spectroscopy (FTIR) and antimicrobial effects were determined using zone of inhibition measurements after 24 h with disc-shaped specimens in culturedStreptococcus mutans. ResultsFTIR showed no interaction between CPC and the components of the cement. CPC release was found to follow a diffusion mechanism for the first 6 h or so, and to equilibrate after approximately 2 weeks, with no significant differences between release profiles when the additive was incorporated into the base or the catalyst paste. Diffusion was rapid, and had a diffusion coefficient of approximately 1 × 10−9 m2 s−1in both cases. Total release was in the range 10–12% of the CPC loading. Zones of inhibition around discs containing CPC were significantly larger than those around the control discs of CPC-free cement. ConclusionsThe antimicrobial character of this temporary cement can be enhanced by the addition of CPC. Such enhancement is of potential clinical value, though furtherin vivowork is needed to confirm this. [ABSTRACT FROM AUTHOR]