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Decomposition of hydrogen peroxide by the lignin-combined manganese in pulp bleaching

机译:木质素组合锰在纸浆漂白中的过氧化氢分解

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For hydrogen peroxide bleaching, its efficiency and selectivity are apparently affected by the accumulation of transition metal ions in the bleaching system. Lignin contains a rich number of functional groups, such as phenolic hydroxyl and carboxyl, therefore it is a very good combiner for the accumulation of transition metal ions, especially in the case of hydrogen peroxide bleaching of high yield pulp, where high amount of lignin is dissolved or dispersed in the bleaching stream. The mechanism of lignin-combined metal ion in decomposing hydrogen peroxide may be very different compared to that of the free metal ions dissolved in solution. Understanding the difference shall be important in finding good methods in improving the hydrogen peroxide bleaching efficiency. In this study, the effect of manganese ion in aqueous solution and lignin-combined manganese on decomposing hydrogen peroxide under typical pulp bleaching conditions was investigated. A variety of bleaching stabilizers, ethylenediaminetetraacetic acid (EDTA), sodium silicate (Na_2SiO_3) and magnesium sulfate (MgSO_4), were added individually or in combination, to investigate their effects in controlling the free manganese induced or lignin-combined manganese induced hydrogen peroxide decomposition. Fourier Transform Infrared Spectroscopy (FT-IR), Elemental Analyses, Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES), were used to study the chemical features of the lignin-manganese composites, as well as the amount of metal ions present in the solution or adsorbed on lignin. The results showed that the hydrogen peroxide decomposition in the presence of manganese and lignin can be represented by a pseudo-first-order kinetics. The decomposition of hydrogen peroxide by free manganese ion under alkaline condition was different to that by lignin-combined manganese. EDTA added individually showed the most positive effect on reducing the decomposition of peroxide by free manganese in solution, with a pseudo-first-order rate constant (k_(obs)) of 2.57*10~(-4) min~(-1). Synergistic effect of manganese and lignin on peroxide decomposition was found to be exist, with a pseudo-first-order rate constant (k_(obs)) of 6.53* 10~(-4) min~(-1), without any common additions added. Hydrogen peroxide is the most important bleaching chemical in the production of elemental chlorine free (ECF) and totally chlorine free (TCF) pulp bleaching. Unfortunately, transition metals, especially manganese, is sensitive to catalyze decomposition of hydrogen peroxide, under certain condition of bleaching. A lot of studies involving manganese-induced peroxide decomposition have been done to control the invalid decomposition for peroxide bleaching, especially for manganese ions . As a result, pulp slurry is dealt with either acid washes or chelating washing prior to the peroxide stage, which has shown to greatly improve the removal of metal ions. Unfortunately, there is still residual metals to introduce peroxide decomposition, after washing processes. Therefore several technologies for peroxide stabilization have been developed, such as magnesium sulfate, sodium silicate and diethylenetriaminepentaacetic acid. In fact, manganese is present in many different states during the bleaching process, such as "nonequilibrium" suspended particles, oligomer dynamic equilibrium with carboxylic groups of fiber, and oligomer chelated with residual lignin by forming coordinate bonds with phenolic groups . In the case of high yield pulping, peroxide bleaching is produced together with pulping process, with certain content of dissolved lignin in flows or residual lignin from pulp fiber. Lignin is an amorphous, polyphenolic, highly cross-linked polymer consisting of certain numbers of active carboxyl and hydroxyl (phenolic or not) sites that would be readily available for complexation with metal ions. In fact, lignin have already proved to be suitable for heavy metals removal from waste water. As a result
机译:对于过氧化氢漂白,其效率和选择性显然受到漂白系统中过渡金属离子的积累的影响。木质素含有丰富的官能团,例如酚羟基和羧基,因此它是一种非常好的组合器,用于过渡金属离子的积累,特别是在高产浆的过氧化氢漂白的情况下,其中大量木质素是溶解或分散在漂白流中。与溶解在溶液中的游离金属离子的相比,木质素组合的金属离子在分解过氧化氢中的机制可能非常不同。了解差异对于在改善过氧化氢漂白效率方面的良好方法方面是重要的。在本研究中,研究了在典型的纸浆漂白条件下在水溶液中锰离子和木质素组合锰的影响。单独或组合加入各种漂白稳定剂,乙二胺四乙酸(EDTA),硅酸钠(Na_2SiO_3)和硫酸镁(MgSO_4),以研究它们在控制自由锰诱导或木质素组合锰诱导的过氧化氢分解中的作用。傅里叶变换红外光谱(FT-IR),元素分析,电感耦合等离子体原子发射光谱法(ICP-AES)用于研究木质素 - 锰复合材料的化学特征,以及存在的金属离子量溶液或吸附在木质素上。结果表明,锰和木质素存在下的过氧化氢分解可以由伪一阶动力学表示。通过自由锰离子在碱性条件下分解过氧化氢的分解与木质素组合锰不同。 EDTA在溶液中单独添加了对通过游离锰进行过氧化锰的分解的最积极效果,具有2.57×10〜(-4)分钟的伪一阶速率常数(K_(OB))〜(-1) 。发现锰和木质素对过氧化物分解的协同作用被存在,具有6.53×10〜(-4)分钟〜(-1)的伪一阶速率常数(K_(OB)),没有任何常见的添加添加。过氧化氢是基元氯(ECF)和完全氯(TCF)纸浆漂白的生产中最重要的漂白化学品。不幸的是,在某些漂白条件下,过渡金属,尤其是锰,尤其是致催化过氧化氢的分解。已经进行了许多涉及锰诱导的过氧化物分解的研究以控制过氧化物漂白的无效分解,特别是对于锰离子。结果,在过氧化物阶段之前,用酸性洗涤或螯合洗涤纸浆浆料,其显示大大改善了金属离子的去除。不幸的是,洗涤过程后,仍有残留的金属在过氧化物分解中引入过氧化物分解。因此,已经开发了几种过氧化物稳定化的技术,例如硫酸镁,硅酸钠和二亚乙基三胺丙酸。事实上,在漂白过程中,锰存在于许多不同的状态下,例如“非QuigibiRim”悬浮颗粒,寡聚物动力平衡,通过形成与酚醛基团的坐标键与残留的木质素螯合的低聚物。在高屈服制浆的情况下,过氧化物漂白与制浆过程一起产生,具有一定含量的流量或来自纸浆纤维的残留木质素中的溶解木质素。木质素是由一定数量的活性羧基和羟基(酚类或不)位点组成的无定形,多酚,高度交联聚合物,其将易于与金属离子络合。事实上,木质素已经证明是适合从废水中去除的重金属。其结果

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