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Characterization and enhancement of carboxyl groups in softwood kraft pulps during oxygen delignification.

机译:氧脱木素过程中针叶牛皮纸浆中羧基的表征和增强。

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This study first examined the kinetic changes of fiber carboxyl group content in bulk fiber, polysaccharide, and residual lignin of oxygen delignified pulps during onestage oxygen delignification of a low kappa (32.5) kraft pulp. The carboxyl group contents determined in different chemical components of oxygen delignified pulps were used to establish the distribution of carboxyl groups in lignin and pulp polysaccharide and decouple the responses from residual lignin and polysaccharide. Following this study, two high kappa (∼ 49.0) SW kraft pulps prepared were delignified through twostage oxygen delignification. Fiber carboxyl group profiles of these pulps were elucidated to investigate the effect of lignin content of incoming unbleached kraft pulps on fiber carboxyl group formation. Due to a limitation to enhance fiber carboxyl groups only by parameter optimization during one- and two- stage oxygen delignification, a catalytic oxidation program was developed to enhance fiber carboxyl group content by 52.2-116.0% employing 0.10-0.18% of a bismuth ruthenium pyrochlore oxide catalyst during oxygen delignification. The mechanism of fiber carboxyl group formation through the catalytic oxidation was proposed. The main factor on carboxyl group formation in pulp carbohydrate was identified to follow the order: NaOH > oxygen pressure> reaction temperature through a 3-factor at 3-level (L933) orthogonal experimental design and the optimal conditions were found at 2.5% NaOH, 85-100°C, and 800-960 kPa O2 during the catalytic oxidation.; ECF bleaching study was also conducted on these pulps with higher amount of fiber carboxyl group enhanced at early pulping and oxygen delignification processes. The bleaching results demonstrated that the early-stage enhanced fiber carboxyl groups were partially retained through ECF bleaching. Additionally, fiber carboxyl groups of fully bleached kraft pulps were ∼20% different from typical bleaching protocols, depending on bleaching chemicals used and the bleaching sequences such as DEDED, (D+C)EDED, ODEDD, and OQPZP.; This study finally demonstrated that an increase of fiber carboxyl groups by 17.4-62.1% through chemical oxidation resulted in reduced fiber curl, increased fiber WRVs, 4.3-25.5% increase in paper tensile index at comparable pulp viscosity; and 4.4-30.1% increase in paper dry tensile stiffness.
机译:这项研究首先研究了低卡伯(32.5)牛皮纸浆的一级氧脱木质素过程中,氧脱木质素纸浆中散装纤维,多糖和残留木质素中纤维羧基含量的动力学变化。用氧脱木素纸浆的不同化学成分确定的羧基含量可用于建立木质素和纸浆多糖中羧基的分布,并分离残留木质素和多糖的响应。这项研究之后,通过两阶段的氧气脱木质素处理,将制备的两种高卡伯(〜49.0)SW牛皮纸浆脱木质素。阐明了这些纸浆的纤维羧基轮廓,以研究未漂白的牛皮纸浆中木质素含量对纤维羧基形成的影响。由于仅在一阶段和两阶段氧脱木质素过程中通过参数优化来增强纤维羧基的局限性,因此开发了一种催化氧化程序,以使用0.10-0.18%的铋钌烧绿石将纤维羧基含量提高52.2-116.0%。氧脱木素过程中的氧化物催化剂。提出了通过催化氧化形成纤维羧基的机理。确定了纸浆碳水化合物中羧基形成的主要因素,其顺序为:NaOH>氧气压力>通过三水平三因子正交试验设计的反应温度(L933),发现最佳条件为2.5%NaOH, 85-100°C和800-960 kPa O2的催化氧化过程。还对这些纸浆进行了ECF漂白研究,这些纸浆在早期制浆和氧脱木质素过程中具有较高的纤维羧基基团含量。漂白结果表明,早期增强的纤维羧基通过ECF漂白被部分保留。另外,完全漂白的牛皮纸浆的纤维羧基与典型的漂白方案相差约20%,这取决于所用的漂白剂和漂白顺序,例如DEDED,(D + C)EDED,ODEDD和OQPZP。这项研究最终证明,在相当的纸浆粘度下,通过化学氧化使纤维羧基增加17.4-62.1%,可减少纤维卷曲,增加纤维WRV,使纸张拉伸指数增加4.3-25.5%。和纸干拉伸刚度增加4.4-30.1%。

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