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Selective conversion of cellobiose and cellulose into gluconic acid in water in the presence of oxygen, catalyzed by polyoxometalate-supported gold nanoparticles

机译:多金属氧酸盐负载的金纳米粒子催化下,在氧气存在下,纤维二糖和纤维素在水中的选择性转化为葡萄糖酸

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摘要

Gold nanoparticles loaded onto Keggin-type insoluble polyoxometalates (Cs _xH _(3-x)PW _(12)O _(40)) showed superior catalytic performances for the direct conversion of cellobiose into gluconic acid in water in the presence of O _2. The selectivity of Au/Cs _xH _(3-x)PW _(12)O _(40) for gluconic acid was significantly higher than those of Au catalysts loaded onto typical metal oxides (e.g., SiO _2, Al _2O _3, and TiO _2), carbon nanotubes, and zeolites (H-ZSM-5 and HY). The acidity of polyoxometalates and the mean-size of the Au nanoparticles were the key factors in the catalytic conversion of cellobiose into gluconic acid. The stronger acidity of polyoxometalates not only favored the conversion of cellobiose but also resulted in higher selectivity of gluconic acid by facilitating desorption and inhibiting its further degradation. On the other hand, the smaller Au nanoparticles accelerated the oxidation of glucose (an intermediate) into gluconic acid, thereby leading to increases both in the conversion of cellobiose and in the selectivity of gluconic acid. The Au/Cs _xH _(3-x)PW _(12)O _(40) system also catalyzed the conversion of cellulose into gluconic acid with good efficiency, but it could not be used repeatedly owing to the leaching of a H ~+-rich hydrophilic moiety over long-term hydrothermal reactions. We have demonstrated that the combination of H _3PW _(12)O _(40) and Au/Cs _(3.0)PW _(12)O _(40) afforded excellent yields of gluconic acid (about 85 %, 418 K, 11 h), and the deactivation of the recovered H _3PW _(12)O _(40)-Au/Cs _(3.0)PW _(12)O _(40) catalyst was not serious during repeated use. Crazy glu: Cellulose was oxidized into gluconic acid by combining polyoxometalate (POM)-supported Au nanoparticles (NPs) and acidic POMs. Au-NP size and POM acidity are the determining factors in the selective oxidation of glucose and cellobiose.
机译:负载在Keggin型不溶性多金属氧酸盐(Cs _xH _(3-x)PW _(12)O _(40)上的金纳米颗粒显示出优异的催化性能,可在O _2存在下将纤维二糖直接转化为葡萄糖酸。 Au / Cs _xH _(3-x)PW _(12)O _(40)对葡萄糖酸的选择性显着高于负载在典型金属氧化物(例如SiO _2,Al _2O _3和TiO _2),碳纳米管和沸石(H-ZSM-5和HY)。多金属氧酸盐的酸度和金纳米粒子的平均大小是纤维二糖催化转化为葡萄糖酸的关键因素。多金属氧酸盐的强酸度不仅有利于纤维二糖的转化,而且通过促进解吸并抑制其进一步降解而导致葡萄糖酸具有更高的选择性。另一方面,较小的Au纳米颗粒加速了葡萄糖(中间体)氧化为葡萄糖酸,从而导致纤维二糖的转化率和葡萄糖酸的选择性均增加。 Au / Cs _xH _(3-x)PW _(12)O _(40)体系还催化了纤维素向葡萄糖酸的高效转化,但由于H〜的浸出而不能重复使用。长期水热反应中富含+的亲水部分。我们已经证明,H _3PW _(12)O _(40)和Au / Cs _(3.0)PW _(12)O _(40)的组合提供了极好的葡糖酸收率(约85​​%,418 K, 11 h),并且在重复使用期间,回收的H _3PW _(12)O _(40)-Au / Cs _(3.0)PW _(12)O _(40)催化剂的失活并不严重。疯狂的谷氨酸:通过将多金属氧酸盐(POM)负载的金纳米颗粒(NPs)和酸性POM结合起来,纤维素被氧化为葡萄糖酸。 Au-NP大小和POM酸度是葡萄糖和纤维二糖选择性氧化的决定因素。

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