Atomic force microscopic analysis of hydrogen peroxide bleached kraft northern black spruce fibres

Hydrogen peroxide is a potent, relatively inexpensive oxidant that chemically degrades chromophoric components in pulps and textiles. Oxidation of cellulose is a byproduct of this process step that decreases the tensile strength of individual fibres. The residence time of pulp in the bleaching reactor must be optimized to achieve the desired brightness and minimizing fibre degradation. To evaluate the impact of peroxide bleaching at the microfibrillar level, a single black spruce tree was chosen and kraft pulped. Peroxide bleaching was conducted via benchtop polyethylene bag bleaching in a temperature-controlled waterbath. Atomic force microscopy (AFM) topographical images acquired before and after the bleaching step show dramatic changes in fibre structure consistent with delignification and defects in the surface topography. This was further verified by X-ray work at Brookhaven National Laboratory, NY, U.S.A.     

复配缓释凝胶吸附处理剂的制备及其除磷释氧性能

研制了海藻酸钠包埋壳聚糖凝胶小球和海藻酸钠/聚乙二醇4000复合包埋纳米过氧化钙缓释凝胶小球复配处理剂,考察其对水体中磷和有机物的去除效果及机理,采用X射线衍射、扫描电镜、元素能谱仪技术表征材料物化及形貌特征。该处理剂能够高效去除水中单一的磷和有机污染物,且对磷和甲基橙复合污染也具有较高的去除率;在实际河道水体中,该处理剂对高浓度的磷也具有较强的吸附能力,其缓慢释氧作用可保持水体溶解氧质量浓度在4.5 mg/L以上,为泥水界面处的好氧微生物提供了良好的好氧条件,可提高水体自净能力。     

Kinetic and spectral aspects in chemiluminescence system Eu(III)/HCO3/H2O2

Chemiluminescence (CL) of the systems containing Eu₂⁺ or HCO₃⁻ ions and hydrogen peroxide was studied. The kinetic curves and CL emission spectra of the systems were discussed. The emission spectrum of the system containing carbonates revealed two emission maxima: the first directly after initiation of the reaction by hydrogen peroxide and the second in several seconds after the first. On the basis of the characteristic bands in the CL spectrum the emitters in the system Eu₂⁺/HCO₃⁻/H₂O₂ were identified as: excited Eu³⁺ ions and excited products of carbonate decomposition. The emission bands for λ=600 and 420 nm appeared in a time distance of a few ten seconds.     

蒽醌法合成过氧化氢催化剂的研究进展

过氧化氢（H₂O₂, 俗称双氧水）, 由于其强氧化性常用作漂白剂、消毒剂, 同时也作化工原料。目前工业上生产过氧化氢的主要方法为蒽醌法, 全球近99%的产品均通过蒽醌法制得。研究具有高活性、高选择性及经济性的催化剂是合成过氧化氢所面对的最具挑战性的课题, 同时也是工业催化领域的研究热点之一。主要针对蒽醌法制过氧化氢催化剂, 综述了各种活性组分、载体及助剂在蒽醌加氢催化剂中的研究进展, 并简单探讨了各种活性组分的优缺点, 概括了各种载体、助剂的作用, 以期对过氧化氢催化剂的合成制备提供一些有益的启示。     

过氧化氢分光光度法测定湿法提钒工艺中钒

为了提高湿法提钒工艺过程控制效率,采用以过氧钒离子(VO(O₂)⁺)显色特性为基础的过氧化氢分光光度法测定钒含量,实现了样品中钒含量的现场快速测定。首先通过在试样溶液中加入适量氢氧化钠溶液,调整溶液pH值至9～10,然后加入过氧化氢将低价态钒全部氧化至钒(V),再加入硫酸调整溶液至酸性,钒(V)与过氧化氢在室温下形成稳定的红棕色过氧钒离子(VO(O₂)⁺),于450 nm处测定吸光度。钒质量浓度在2.0~400 mg/L内与吸光度值符合比尔定律。采用实验方法测定3种湿法冶金提钒液体试样(包括钒浸取溶液、钒盐沉淀后溶液以及废水等)中钒,结果的相对标准偏差(RSD,n=10)分别为0.38%、3.5%和7.6%;与高锰酸钾氧化-硫酸亚铁铵滴定法结果相一致。     

Preparation of alumina-doped yttria-stabilized zirconia nanopowders by microwave-assisted peroxyl-complex coprecipitation

Alumina-doped yttria-stabilized zirconia （ADYSZ） nanopowders were prepared by microwave-assisted peroxyl-complex coprecipitation （MAPCC） using ZrOCl2-8H2O, Y2O3 and AICly6H2O as starting materials, NH2-H2O as precipitant and H2O2 as complexant. The effects of adding H2O2 and microwave drying on the preparation and properties of ADYSZ were investigated. The precursors and nanopowders were studied by EDX, XRD, SEM and TEM techniques. The results show that the uniformity of component distribution within ADYSZ nanopowders is improved by adding appropriate dosage of H2O2. Complexing reaction between H2O2 and Zr^4＋ ion restrains the hydrolyzation and precipitation of Zr^4＋ ion. With the addition of H2O2, Al^3＋, y^3＋ and Zr^4＋ ions can be precipitated synchronously in a relatively narrow range of pH value. H2O2 also improves the filterability of the wet precipitate. The highly hydrophilic precipitates can be quickly and effectively separated from aqueous solution. During microwave drying process, the moisture of wet precursors is selectively heated. Quick expansion of steam vapor within the wet colloidal particles causes the aggregations burst into numerous tiny lumps. Compared with oven drying, microwave drying can not only shorten drying time but also reduce aggregation intensity of the resultant ADYSZ nanopowders.     

H_3PW_(12)O_(40)催化合成己二酸

以环己烯为原料,w(H2O2)=30%的过氧化氢为氧化剂,在草酸(H2C2O4)作为助剂的条件下,采用磷钨酸(H3PW12O40)作催化剂合成己二酸,结果表明,当n(环己烯)∶n(H3PW12O40)∶n(H2C2O4)∶n(H2O2)=100∶1∶1∶538,反应温度为92℃,反应时间为6h时,己二酸的收率可达70 1%。讨论了H3PW12O40加入量、环己烯加入量、过氧化氢加入量、反应时间、反应温度等因素对反应的影响。     

Evaluation of oxidative stability of canola oils by headspace analysis

Lipid oxidation is a major factor affecting flavor quality and shelf life of vegetable oils. Oxidative stability is therefore an important criterion by which oils are judged for usefulness in various food applications. In this study a method based on headspace analysis was developed to evaluate relative oxidative stability of canola oils. The method does not require the use of chemicals, involves minimal sample preparation, and can be performed on a relatively small sample size in comparison with traditional wet chemical methods. Canola oils freshly extracted in the laboratory from different seed samples were subjected to accelerated oxidation and analyzed for PV by standard methods and headspace volatiles by solid phase microextraction/GC-MS. Forward stepwise regression analysis of the data revealed a relationship between PV and headspace concentration of the volatile lipid oxidation products hexanal and trans,trans-2,4-heptadienal. The PV calculated using this formula correlated (R ²=0.73) with those measured by conventional methods. Presented in part at the 96th Annual Meeting of the AOCS, 1–4 May 2005, Salt Lake City, UT.     

催化氧化环己酮/环己醇清洁合成己二酸

以质量分数为 30 %的过氧化氢为氧化剂 ,Na2 WO4·2H2 O为催化剂 ,在酸性配体存在的条件下催化氧化环己酮 /环己醇清洁合成己二酸。反应在无溶剂、无相转移剂条件下进行 ,考察了各种不同配体及配体用量等对反应的影响。采用磺基水杨酸为配体 ,与Na2 WO4·2H2 O的摩尔比为 1∶2时 ,催化氧化环己酮和环己醇的己二酸的分离产率分别为 82 .1%和 6 8.6 %。并进一步考察了该催化体系对环己酮和环己醇混合物的催化性能。     

有机过氧化物对CPE硫化性能的影响

采用DCP或双2，5硫化CPE，通过改变硫化时间，研究CPE的硫化过程及性能。发现DCP对CPE的硫化速度快、硫化胶的物理机械性能好，但易使硫化胶产生异味；使用双2，5作硫化剂，则不产生异味，但其硫化速度较慢，双2，5的用量一般在4～4．5份之间为宜。