Sannino Filomena, Pansini Michele, Marocco Antonello, Bonelli Barbara, Garrone Edoardo, Esposito Serena
Department of Agriculture Sciences, Università di Napoli "Federico II", Via Università 100, 80055 Portici (NA), Italy.
Department of Civil and Mechanical Engineering, Università degli Studi di Cassino e del Lazio Meridionale, Via G. Di Biasio 43, 03043 Cassino (FR), Italy.
Phys Chem Chem Phys. 2015 Nov 21;17(43):28950-7. doi: 10.1039/c5cp05085e.
The simple means adopted for investigating H-Y zeolite acidity in water is the pH-dependence of the amount of a basic molecule adsorbed under isochoric conditions, a technique capable of yielding, under equilibrium conditions, an estimate of the pKa value of the involved acidic centres: the behaviour with temperature of adsorbed amounts yields instead some information on thermodynamics. Simazine (Sim, 2-chloro-4,6-bis(ethylamino)-s-triazine) was chosen as an adsorbate because its transverse dimension (7.5 Å) is close to the opening of the supercage in the faujasite structure of H-Y (7.4 Å). In short term measurements, Sim adsorption at 25 °C occurs only at the outer surface of H-Y particles. Two types of mildly acidic centres are present (with pKaca. 7 and ca. 8, respectively) and no strong one is observed. Previous adsorption of ammonia from the gas phase discriminates between the two. The former survives, and shows features common with the silanols of amorphous silica. The latter is suppressed: because of this and other features distinguishing this site from silanol species (e.g. the formation of dimeric Sim2H(+) species, favoured by coverage and unfavoured by temperatures of adsorption higher than ambient temperature) a candidate is an Al based site. We propose a Lewis centre coordinating a water molecule, exhibiting acidic properties. This acidic water molecule can be replaced by the stronger base ammonia, also depleting inner strong Brønsted sites. A mechanism for the generation of the two sites from surface Brønsted species is proposed. Long term adsorption measurements at 25 °C already show the onset of the interaction with inner strongly acidic Brønsted sites: because of its size, activation is required for Sim to pass the supercage openings and reach inner acidic sites. When adsorption is run at 40-50 °C, uptake is much larger and increases with temperature. Isochoric measurements suggest a pKa value of ca. 3 compatible with its marked acidic nature, although attainment of equilibrium conditions is questionable. Measurements at 60 °C (both isochors and DRIFT) show the onset of changes at the outer surface brought about by the presence of hot water. Control experiments run with USY (Ultra Stabilized zeolite Y), featuring wormholes and cavities rendering accessible internal sites, show the extensive involvement of internal Brønsted sites already at 25 °C.
在水中研究H-Y沸石酸度所采用的简单方法是,在等容条件下,碱性分子吸附量对pH的依赖性,该技术能够在平衡条件下估算所涉及酸性中心的pKa值:吸附量随温度的变化则能提供一些关于热力学的信息。选择西玛津(Sim,2-氯-4,6-双(乙氨基)-s-三嗪)作为吸附质,是因为其横向尺寸(7.5 Å)接近H-Y八面沸石结构中超笼的开口(7.4 Å)。在短期测量中,25℃下西玛津的吸附仅发生在H-Y颗粒的外表面。存在两种类型的弱酸性中心(pKa分别约为7和8),未观察到强酸性中心。先前从气相中吸附氨可区分这两种酸性中心。前者保留下来,表现出与无定形二氧化硅的硅醇相同的特征。后者受到抑制:基于此以及该位点与硅醇物种的其他区别特征(例如二聚体Sim2H(+)物种的形成,受覆盖度影响且在高于环境温度的吸附温度下不利于形成),推测该位点是基于铝的位点。我们提出一个路易斯中心与一个水分子配位,表现出酸性性质。这个酸性水分子可被更强的碱氨取代,同时也会消耗内部的强布朗斯特位点。提出了一种由表面布朗斯特物种产生这两种位点的机制。25℃下的长期吸附测量已经显示出与内部强酸性布朗斯特位点相互作用的开始:由于西玛津的尺寸,它需要活化才能通过超笼开口并到达内部酸性位点。当在40 - 50℃下进行吸附时,吸附量要大得多且随温度升高而增加。等容测量表明其pKa值约为3,与其显著的酸性性质相符,尽管达到平衡条件存在疑问。60℃下的测量(等容线和漫反射红外傅里叶变换光谱)显示热水的存在导致外表面开始发生变化。用具有蠕虫孔和空洞从而使内部位点可及的超稳Y型沸石(USY)进行的对照实验表明,在25℃时内部布朗斯特位点就已广泛参与吸附过程。