速生桉木低污染制浆漂白及纸浆纤维性质的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
桉树生长快,制浆造纸性能优良,是我国“林纸一体化”工程中重点推广的速生树种之一,发展桉树制浆对促进我国造纸工业的可持续发展具有重要意义。本论文以我国南方的速生桉木为原料,进行了硫酸盐法蒸煮、氧脱木素和无元素氯(ElementalChlorine Free,简称ECF)漂白的研究,并分析了纤维性质对纸浆打浆性质和纸页性质的影响,为速生桉木的清洁制浆提供理论依据和技术支持。
     采用实验设计与分析软件MODDE对速生桉木硫酸盐法蒸煮进行了实验设计和结果分析,由MODDE数学模型的分析结果可知,有效碱用量、硫化度、蒸煮温度和保温时间对速生桉木硫酸盐浆的蒸煮结果均有明显的影响,且影响的程度各自不一。在某一卡伯值条件下,纸浆的细浆得率、黏度和白度不能同时达到最优化水平。MODDE可以根据蒸煮工艺条件预测蒸煮结果,当蒸煮条件为:有效碱用量17%,硫化度29.5%,蒸煮温度150℃,保温时间135 min时,MODDE预测的蒸煮结果为:卡伯值18.1(上下限分别为21.5和15.3),细浆得率50.3%(上下限分别为51.2%和49.5%),白度34.1%ISO(上下限分别为36.1%ISO和32.2%ISO),黏度1429 mL/g(上下限分别为1627 mL/g和1232 mL/g)。MODDE也具有优化蒸煮工艺的功能,在要求达到的蒸煮指标时,分别设定细浆得率、黏度和白度的最大化权重,在给定的卡伯值范围内,可以制定出合适的蒸煮工艺条件(有效碱用量、硫化度、蒸煮温度、保温时间);同样,细浆得率、白度或黏度也可作为目标进行蒸煮工艺的优化。
     在硫酸盐法蒸煮过程中,蒸煮温度、有效碱用量和保温时间对纸浆己烯糖醛酸的含量均有明显的影响,而硫化度则对纸浆中己烯糖醛酸的含量影响不大。较低的蒸煮温度、较低的有效碱用量和较短的保温时间有利于降低纸浆中己烯糖醛酸的含量,且纸浆的细浆得率也较高。
     研究了用碱量、温度、氧压和时间对桉木硫酸盐浆(卡伯值为17.1)氧脱木素的影响。较为优化的氧脱木素工艺条件为:用碱量2%,温度100℃,氧压0.5 MPa,时间60min,此时氧脱木素浆的卡伯值为9.5,白度为58.4%ISO,黏度为795 mL/g。添加表面活性剂能进一步提高氧脱木素的脱木素率,提高纸浆白度,而纸浆的黏度只略有下降。三种表面活性剂(S1,S2和S3)较适宜的用量均为0.2%左右,其中表面活性剂S3的效果最好。当S3的用量从0增加至0.2%时,氧脱木素浆的白度从58.4%ISO升高至62.3%ISO,卡伯值从9.5降低至8.1,黏度从795 mL/g降低至744 mL/g。
     木素红外光谱和~(31)P-NMR谱的分析结果表明,桉木原料木素中的酯键在硫酸盐法蒸煮过程中易被氧化而断裂,木素被降解:原料木素中的紫丁香型木素单元在蒸煮和氧脱木素过程中溶出较多:在蒸煮和氧脱木素过程中,苯环的侧链断裂溶出,苯环上的甲氧基被脱除。桉木经硫酸盐法蒸煮后,木素结构中侧链上的连接键也发生了断裂,使脂肪羟基的含量增大;蒸煮过程中,木素之间的连接结构发生断裂,使得木素中酚羟基的含量增大;此外,蒸煮也使得木素原料中稳定的内酯或酯发生水解,使木素的羧基数量增加。氧脱木素过程中,木素结构单元发生了开环反应,使羧基含量增加,酚羟基含量减少。此外,木素侧链的氧化也使脂肪族羟基的含量减少,羧基的含量增加。
     对卡伯值为24.1(CK1)和17.1(CK2)的桉木硫酸盐浆分别进行了ODQP和DQP漂白。CK1浆经氧脱木素后卡伯值降至16.9,在有效氯用量为2.5%,H_2O_2用量为2.5%时,ODQP漂白浆的白度达到86.1%ISO,黏度为783 mL/g;CK2浆在有效氯用量为4.0%,H_2O_2用量为2.5%时,DQP漂白浆的白度为85.4%ISO,黏度为706 mL/g。相同打浆度下,DQP浆的抗张指数和耐破指数比ODQP浆高,而撕裂指数则是后者高;抗张指数相同时,ODQP浆的撕裂指数高于DQP浆;ODQP浆比DQP浆容易打浆。氧脱木素作为硫酸盐法蒸煮的继续可以降低后续漂白药品的用量,改善漂白选择性。
     CK2浆在有效氯用量为4.0%,H_2O_2用量为2.5%时,DQP和(DQ)P漂白浆均能达到85%ISO以上的白度,且具有较好的白度稳定性。(DQ)段适宜的终点pH值为3.5~4。相同打浆度下,DQP浆的抗张指数和耐破指数都比(DQ)P浆好,(DQ)P浆的撕裂指数高于DQP浆;抗张指数相同时,(DQ)P浆的撕裂指数较高。(DQ)P浆较容易打浆。(DQ)P两段短流程漂白可得到与DQP三段漂非常接近的结果,将D段和Q段合并为一段(DQ)在技术上是可行的。两段漂所需要的设备投资、能耗和运行成本比三段漂少,具有明显的优势和潜在的应用前景。当漂白浆的白度均为84%ISO左右时,与CK2 O(DQ)P漂白浆相比,CK2 O~*(DQ)P(O~*为表面活性剂S3强化的氧脱木素)漂白浆所消耗的漂白化学品的量更少,即氧脱木素段添加合适的表面活性剂能有效降低漂白化学品用量。达到相同打浆度时,O~*(DQ)P浆需要消耗较多的打浆能耗,但其抗张指数、撕裂指数和耐破指数均高于O(DQ)P浆;抗张指数相同时,O~*(DQ)P浆的撕裂指数较高。对白度为85%左右的CK2漂白浆来说,DQP和(DQ)P的强度性能最高,O~*(DQ)P次之,O(DQ)P最低。
     与桉木漂白浆相比,麦草漂白浆很容易打浆,其主要原因是由于麦草漂白浆中较高的细小组分含量和半纤维素含量。打浆后,桉木纤维润胀并分丝帚化,纸浆的各项强度指标快速增大。麦草漂白浆经打浆后其纸页强度性能的上升幅度较小,其主要原因是麦草浆打浆过程产生大量的细小组分,而主要不是纤维的分丝帚化;打浆度相同时,桉木漂白浆的各项纸页强度性能要比麦草漂白浆的好得多。
     桉木漂白浆的纤维素含量高,半纤维素含量适中,因而打浆后纸页的强度性质得到较大改善;麦草漂白浆的半纤维素(尤其是木聚糖)含量高,而纤维素的含量相对较低,因而易打浆而强度的上升幅度较小。桉木漂白浆纤维的总电荷比麦草漂白浆高,打浆过程中纤维的总电荷基本保持不变但表面电荷明显增加;麦草漂白浆纤维的表面电荷比桉木浆低,且打浆过程中纤维的表面电荷变化非常少,说明其纤维表面的细纤维化程度没有桉木浆好,故其强度的改善没有桉木浆好。采用位错(dislocation)值可以表征制浆漂白过程中纤维的损伤程度。桉木漂白浆经打浆后,桉木浆纤维的位错值变化不大,而麦草浆纤维的位错值随打浆度的上升而明显增大,这也是导致打浆度相同时桉木漂白浆纸页强度比麦草漂白浆更好的原因之一。纸浆细小组分的性质影响着纸页的各项性质。麦草浆含有大量的细小组分,约为35%~47%,大部分为杂细胞,;筛分除去细小组分后,麦草浆的滤水性能明显改善,强度性质和光学性质也都有所提高。而桉木浆中的细小组分主要是纤维碎片和细小纤维,筛分除去细小组分后,纸页的抗张指数和耐破指数明显降低,而撕裂指数提高。
Eucalyptus grows fast and behaves well in pulp and paper making,it is one of the fast-growing trees which are developed emphasisly in the "Forestry-pulp-paper integration" project,and the utilization of fast-growing eucalyptus is important for the sustainable development of China's paper industry.Researches on kraft cooking,oxygen delignification and elemental chlorine free(ECF) bleaching of fast-growing eucalyptus were carried out in this thesis;the effects of fiber properties on pulp beating and sheet properties were also studied;which will provide the fundamental base and technique support for the clean pulping and bleaching of fast-growing eucalyptus.
     The modelling and design software(MODDE) was used for the design and evaluation of the kraft cooking experiments of fast-growing eucalyptus.Based on the MODDE mathematic model of kraft cooking,it can be learned that the variations of effective alkali charge,sulfidity, temperature and time affected the pulp properties significantly,for the pulp with a given Kappa number,pulp screened yield,viscosity and brightness could not be maximized simultaneously.Mathematic model is based on the cooking experiments,it could predict pulp properties at a given cooking conditions,at the cooking conditions of effective alkali charge 17%,sulfidity 29.5%,temperature 150℃,time 135 min,the pulp properties predicted by model were:Kappa number 18.1(upper 21.5,lower 15.3),screened yield 50.3%(upper 51.2%,lower 49.5%),brightness 34.1%ISO(upper 36.1%ISO,lower 32.2%ISO) and viscosity 1429 mL/g(upper 1627 mL/g,lower 1232 mL/g).The kraft cooking can also be optimized by model:as the target Kappa number was set up and the weight of screened yield, viscosity and brightness were mamximized with different values(from 0 to 1),the optimal cooking conditions,including effective alkali charge,sulfidity,temperature and time,could be established.Similarly,screened yield,brightness or viscosity can also be as a target for the technological optimization.
     During the kraft cooking process,the temperature,effective alkali charge and time affected the pulp HexA content significantly,and the variation of sulfidity did not influence the pulp HexA content.Lower temperature,lower effecitve alkali charge and shorter time resulted in a pulp with lower HexA content and higher screened yield.
     The effects of alkali charge,temperature,pressure and time on oxygen delignification were studied.For eucalyptus kraft pulp with Kappa number 17.1,the optimized oxygen delignification conditions were:alkali charge 2%,temperature 100℃,O_2 pressure 0.5 MPa, time 60 min;and the oxygen delignifed pulp with Kappa number 9.5,brightness 58.4%ISO, viscosity 795 mL/g was obtained.The utilization of surfactant during oxygen delignification process could improve the delignification efficiency and pulp brightness,and pulp viscosity decreased slightly.The oxygen delignification reinforced with three different surfactants(S1, S2 and S3) were also carried out,the optimized charges of the three surfactants were all 0.2%, and surfactant S3 led to better results than the others.With the charge of S3 increasing from 0 to 0.2%,pulp Kappa number decreased from 9.5 to 8.1,brightness increased from 58.4%ISO to 62.3%ISO and viscosity decreased from 795 mL/g to 744 mL/g.
     Changes of lignin structure during kraft cooking and oxygen delignification were analysis by means of FTIR and ~(31)P-NMR.The results showed that during kraft cooking process the ester links between lignin units were cleaved,more syringyl lignin units were dissolved,the contents of aliphatic OH,phenolic OH and COOH groups in residual lignin increased apparently.The oxygen delignification process resulted in the increase on the content of COOH groups and decrease on the content of phenolic OH groups which indicated that the phenolic rings were partially opened during oxygen delignification process,COOH groups were formed at the same time.The oxidization of lignin side chains led to increase of COOH groups and decrease of aliphatic OH.
     Two different eucalyptus pulps with Kappa numbers of 24.1(CK1) and 17.1(CK2) were prepared by kraft cooking process,the ODQP and DQP bleaching sequences were applied to these two kraft pulps respectively.After oxygen delignification,the Kappa number of CK1 decreased from 24.1 to 16.9,which was close to that of CK2,meaning that the kraft pulping was extended by the oxygen delignification.The bleaching results showed that ODQP pulp with the 86.1%ISO brightness and 783mL/g viscosity was obtained from CK1 pulp when the active chlorine charge was 2.5%,H_2O_2 charge was 2.5%;the DQP pulp with 85.4%ISO brightness and 706 mL/g viscosity was also obtained from CK2 pulp at the active chlorine charge of 4.0%,H_2O_2 charge of 2.5%.The property testing of the sheets made from the 86.1%ISO ODQP pulp and 85.4%ISO DQP pulp indicated that the ODQP pulp had better tear index and less beating energy consumption at a given beating degree but lower tensile index and burst index compared with those of the DQP pulp.Kraft cooking extended by oxygen delignification can improve pulp bleachability.
     The DQP and(DQ)P bleaching sequences were applied to CK2 pulp.The bleaching results showed that the DQP pulp with brightness 85.4%ISO and(DQ)P pulp with brightness 85.3%ISO were obtained when the active chlorine charge was 4.0%,H_2O_2 charge was 2.5%. The brightness of the(DQ)P pulp was not sensitive to the variation of the pH value in(DQ) stage in the pH range of 2 to 4,the pulp brightness didn't change significantly.The property testing of the sheets made from the DQP and(DQ)P bleached pulps indicated that both pulps had very good strength properties,the(DQ)P pulp had better tear index and less beating energy consumption at a given beating degree but lower tensile index and burst index compared with those of the DQP pulp.The experiment results indicate that it is feasible to combine D stage and Q stage into a(DQ) stage.
     O(DQ)P and O~*(DQ)P(O~*:Oxygen delignification reinforced with surfactant S3) bleachings were carried out with CK2 pulp.With the same final brightness about 84%ISO, O~*(DQ)P pulp consumed less active chlorine and peroxide compared with the O(DQ)P pulp; although O~*(DQ)P pulp needed a higher beating energy,the tensile index,tear index and burst index of the pulp were better than those of O(DQ)P pulp at the same ~oSR value.Generally, the strength properties of DQP and(DQ)P pulps were superior to those of O(DQ)P and O~*(DQ)P pulps.
     Wheat straw bleached pulps responded to refining more easily than eucalyptus bleached pulps and that the differences were due mainly to the higher contents of fines and xylan in the wheat straw pulps.During the beating process,the strength property of the eucalyptus pulps developed fastly because of the fiber swelling and fiber laminating;in the case of wheat straw bleached pulps,large amount of fines were formed instead of fiber swelling and fiber laminating during beating,which resulted in a very limited increase in pulp strength property. At a given beating degree,the strength properties of eucalyptus bleached pulps were much better than those of wheat straw bleached pulps.
     The eucalyptus bleached pulps had higher cellulose contents and moderate hemi-cellulose contents,which led to significant progress on the pulp strength properties; although wheat straw bleached pulps were easily beaten,the lower contents of cellulose and higher contents of hemi-cellulose(especially xylan) resulted in limited improvement on pulp strength properties.At a given beating degree,the eucalyptus bleached pulps had higher total fiber charges than those of wheat straw bleached pulps,and the total fiber charges were not affected by the beating;the surface fiber charges of eucalyptus bleached pulps were higher than that of wheat straw bleached pulps at a given beating degree,and were developed by beating.
     The initial number of dislocation was higher and that the number increased more rapidly during beating for wheat straw fibers than for eucalyptus fibers.These results may explain the lower and slower development of the strength properties of paper sheets prepared from wheat straw pulps than in that from eucalyptus pulps.The fines had a significant effect on sheet properties.Wheat straw pulps had a very high content of fines(35%~47%).Removal of fines from the wheat straw pulps improved not only the drainability of the pulps suspension but also the mechanical and optical sheet properties,this indicated that the fines in the wheat straw pulps acted mainly as filler with low bonding properties.Removing the fines from eucalyptus pulps led to a decrease on sheet tensile index and burst index,an increase on sheet tear index,and it could be learned that the fines in the eucalyptus pulps was beneficial to the pulp strength properties.
引文
[1]陆晓鸣.中国造纸工业发展趋势研究[J].中华纸业,2005,26(9):6-14
    [2]余贻骥.值得关注的中国造纸工业[J].江苏造纸.2005(3):2-8
    [3]中国造纸协会.中国造纸工业2004年度报告[J].造纸信息,2005(5):1-6
    [4]中国造纸协会.中国造纸工业2005年度报告[J].江苏造纸,2006(2):2-6
    [5]中国造纸协会.中国造纸工业2006年度报告[J].造纸信息,2007(6):4-14
    [6]曹朴芳,曹振雷,邝仕均.我国造纸工业原料结构调整战略研究(上)[J].中国造纸,2003,22(5):55-63
    [7]白嘉雨,徐大平,徐建民.大力种植桉树人工林实现造纸工业可持续发展[J].中华纸业,2006,27(4):13-15
    [8]中国造纸协会.造纸工业“十五”发展的导向指针[J].纸和造纸,2001(4):5-10
    [9]王祝雄.我国森林资源概况和对林纸结合的意见[J].中华纸业,2001,22(10):6-8
    [10]张锡瀛.关于加强规划措施促进林纸结合的意见[J].中华纸业,2000,21(10):9-12
    [11]黄文荣,陈中豪.无污染漂白技术是造纸工业可持续发展的方向[J].西南造纸,2003(1):7-10
    [12]李忠正.中国造纸工业发展的大趋势[J].江苏造纸,2006(1):2-8
    [13]谢直兴,严代碧.桉树人工林现状及其可持续发展[J].四川林业科技,2006,27(1):76-81
    [14]余贻骥.浅谈发展桉木浆生产和人工桉树林种植[J].纸和造纸,2005(5):22-23
    [15]杨懋暹.开发桉树是有效缓解中国制浆用材短缺的有效途径[J].中华纸业,2005,26(12):29-30
    [16]徐大平.桉树速生丰产林-我国林浆纸一体化的必然选择[J].中华纸业,2006,27(4):14-25
    [17]中国造纸学会.中国桉树种植与制浆造纸研讨会纪要[J].中华纸业,2005,26(11):22-23
    [18]甘家齐.开发利用桉树制浆造纸加快林纸一体化进展的探讨[J].中华纸业,2005,26(11):10-15
    [19]殷亚方,姜笑梅,吕建雄,等.国外桉树人工林资源和木材加工利用现状[J].世界林业研究,2001,14(2):35-41
    [20]温远光,刘世荣,陈放,等.桉树工业人工林的生态问题与可持续经营[J].广西科 学院学报,2005,21(1):13-18
    [21]殷亚方,姜笑梅,吕建雄,等.我国桉树人工林资源和木材利用现状[J].木材工业,2001,15(5):12-25
    [22]McDonough T.,Thomas J..Oxygen Delignification.Pulp Bleaching-Principles and Practice[M].Eds.Carlton,W.Dence and Douglas W.Reeve.Atlanta:Tappi Press,1996:213-239
    [23]陈嘉翔.高效清洁制浆漂白新技术[M].北京:中国轻工业出版社.1992
    [24]安国兴.纸浆氧脱木素技术的现状和发展趋势[J].中国造纸,1998,17(4):58-59
    [25]Kamishima H.,Fujii T.and Akamatsu I..Protective agents for carbohydrates in ozone bleaching of unbleached Kraft pulps:Ⅱ.Screening of protective agent for carbohydrates in ozone bleaching[J].Shikoku Kogyo Gijutsu Shikensho Kenkyu Hokoku 1985(9):15-30
    [26]Olm,L.and Teder,A..The kenetics of oxygen bleaching[J].Tappi Journal,1979,62(12):43-46
    [27]Ericsson B.,Lindgren B.and Theander O..Factor influencing the carbohydrate degradation under oxygen-alkali bleaching[J].Svensk Papperstidning.1971(22):757-765
    [28]Kishimoto T.and Nakatsubo F..Non-chlorine bleaching of Kraft pulp.Ⅳ:Oxidation of methyl-4-O-ethyl-β-D-glucopyranoside with Fenton's reagent:Effects of pH and oxygen[J].Holzforschung.1998,52(2):180-184
    [29]Iribarne J.and Schroeder L..High-pressure oxygen delignification of Kraft pulp part Ⅰ:kinetics[J].Tappi Journal,1997,80(10):241-250
    [30]Lindgren B.O.and Walding J..Reactions of nitrated Kraft lignin in an alkaline oxygen bleaching stage[J].Tappi Journal,1997(10):119-123
    [31]Yasumoto M.,Matsumoto Y.and Ishizu A..A model study on the degradation mechanism of carbohydrate during oxygen delignification[C].7~(th) International Symposium on Wood and Pulping Chemistry,Beijing,China,1993:192-196
    [32]Yokoyama T..The role of peroxide species in carbohydrate degradation during oxygen bleaching.Part Ⅱ:Effect of oxygen pressure on the degradation of lignin and carbohydrate model compounds and on reaction selectivity[J].Journal of Pulp and Paper Science.1996,22(5):1151-1154
    [33]Samuelson O.and Otjeg U..Oxygen bleaching of kraft pulps pretreated with nitrogen oxides[J].Cellulose Chemistry and Technology,1996(30):95-104
    [34]Collins.Terrence..New efficient selective TCF wood pulping bleaching[C].Tappi Pulping Conference Proceedings,1998:1291-1300
    [35]Poukka,O.,Isotalo,I.and Gullichsen,J..Optimal delignification degrees of cooking and oxygen/alkali stage in production of ECF bleached softwood kraft pulp[J].Paperi ja Puu-Paper and Timber,1999,81(4):316-324
    [36]Agarwal S.B.,Genco J.M.,Cole B.,et al.Kinetics of oxygen delignification[J].Journal of Pulp and Paper Science,1999,25(10):361-366
    [37]Gratzl J.S..The Chemical basis of pulp bleaching with oxygen,hydrogen peroxide and ozone-a short review[J].Papier ja Puu,1992,10A(10):v1-v8
    [38]Guay D.,Cole B.W.,Fort Jr.R.C.,et al.Mechanisms of oxidative degradation of carbohydrates during oxygen delignification[C].I.S.W.P.C.,Yokohoma,Japan,1999
    [39]Gierer J.,Jansbo K.and Reitberger T..A study on the selectivity of bleaching with oxygen-containing species[J].Holzforschung,1989,43(6):391-396
    [40]Argyropoulos D.,Liu Y.and Ahazi B..Salient reactions in lignin during pulping and bleaching[C].88~(th) Annual PAPTAC Meeting,Montreal,Canada,2002,p.A165-A170
    [41]Hausman M.C..A mechanistic study of the degradation of lignin model compounds with oxygen species[D].Ph.D.Thesis,University of Maine,1999
    [42]McGrouther Kim G..Cellulose degradation during oxygen delignification[C].10~(th)International Symposium on Wood and Pulping Chemistry,1999:239-245
    [43]Lindeberg O.and Sundin,S..On the degradation of cellulose during oxygen delignification[J].Svensk Papperstidning,1978(15):485-488
    [44]Yasumoto M.,Matsumoto Y.and Ishizu A..A model study on the degradation mechanism of carbohydrate during oxygen delignification[C].7~(th) International Symposium on Wood and Pullping Chemistry,Beijing,China,1993:192-196
    [45]Landucci L.and Sanyer N..Influence of transition metals in oxygen pulping[J].Tappi Journal,1975,58(2):60-63
    [46]Kang G.J.,Ni Y.and van Heiningen..Effect of selected chemical in recycled filtrate in the selectivity during O_2 delignification[C].Tappi Conference Proceedings.1998:243-249
    [47]Swan,Brita and Akerblom,Inga-Stina.The solubility of magnesium ions in alkaline solution in the presence of some complex-forming agents[J].Svensk Papperstidning,1977,80(11):346-349
    [48]Yasumoto M.,Matsumoto Y.and Meshisuta G..The role of peroxide species in carbohydrate degradation during oxygen bleaching.Part Ⅲ:Effect of metal ions on the reaction selectivity between lignin and carbohydrate model compounds[J].Journal of Pulp and Paper Science,1999,25(2):42-46
    [49]Yokoyama T.,Matsumoto Y.and Meshitsuka G..A model study on the degradation mechanisms of carbohydrate during oxygen bleaching-effect of oxygen perssure on the reaction selectivity[C].8~(th) International Symposium on Wood and Pulping Chemistry,Helsinki,Finland,1995:315-322
    [50]Monica E.K.,and Gierer Josef..Hydorxyl radicals in oxygen bleaching[C].3~(rd)International Symposium on Wood and Pulping Chemistry,1985:209-210
    [51]Sjostrom E.,and Valttila O..Inhibition of carbohydrate degradtion during oxygen bleaching[J].Paperi ja Puu.1972(11):695-705
    [52]Samuelson O.and Ojteg U..Behavior of calcium,magnesium and manganese compounds during oxygen bleaching of Kraft pulps[J].Journal of Wood Chemistry and Technology,1995,15(3):303-328
    [53]Samuelson O.and Otjeg U..Manganese and magnesium during oxygen bleaching of wood pulp[J].Nordic Pulp and Paper Research Journal,1994(4):259-266
    [54]Samuelson O.and Otjeg U..Optimization of the pretreatment of Kraft pulp with nitrogen dioxide[J].Tappi Journal,1991(6):155-161
    [55]Samuelson O.and Otjeg U..NO_2 treatment of Kraft pulp followed by oxygen bleaching:Influence of black liquor[J].Tappi Journal,1990(2):141-146
    [56]Samuelson O.and Otjeg U..Influence of sodium carboxylates and spent liquor on NO_2treatment of Kraft pulp[J].Nordic Pulp and Paper Research Journal,1988(4):203-209
    [57]Samuelson O.and Sjoberg L..Oxygen bleaching of Kraft and polysulfide pulps[J].Tappi Journal,1979(12):47-50
    [58]Samuelson O.and Sjoberg L..Degradation of carbohydrates during oxygen bleaching[J].Svensk Papperstidnig,1969(72):662-666
    [59]Samuelson O.,Sjoberg L.and Marklund A..The Prenox Process-Experiences from a pilot plant installation[C].Tappi Pulping Conference Proceedings,1986:49-54
    [60]Johansson E.and Ljunggren S..The reactivity of lignin model compounds and the influence of metal ions during bleaching with oxygen and hydrogen peroxide[C].7~(th)International Symposium on Wood and Pulping Chemistry,Beijing,China,1993:180-187
    [61]Allison and Robert W..Efficient ozone and peroxide bleaching of alkaline pulps from Pinus radiata[J].Appital Journal,1982,36(1):42-46
    [62]邱玉桂.郑志彤.林中选,等.Soda-AQ麦草浆氧气漂白的强化[J].广东造纸,1996(2):14-17
    [63]Jakara J.,Paren A.and Nyman J..Production and use of different peracids in chemical pulp bleaching[J].Paperi ja Puu,1998,80(4):281-287
    [64]Gierer Josef.Chemistry of delignfication,Part 2:Reactions of lignins during bleaching[J].Journal of Wood Science and Technology,1986(20):1-33
    [65]陈晋阳,柳士忠,董俊萍等.Keggin结构钨钼磷混配杂多酸盐的合成和性质研究[J].湖北大学学报(自然科学版),1998,20(1):73-76
    [66]王雅珍,马立群,杨玉林.杂多酸的催化、阻聚作用[J].精细化工,2000,17(4):228-231
    [67]Evtuguin D.V.and Neto C.P..Bleaching of kraft pulp by oxygen in the presence of polyoxometalates[J].Pulp and Paper Science,1998,24(4):133
    [68]Evtuguin D.V.,Neto C.P..Lignin degradation in oxygen delignification catalysed by [PMo_7V_5O_(40)]~(8-) polyanion.Part Ⅰ Study on wood lignin[J].Holzforschung,2000,54(4):381
    [69]Weinstock I.A..Selective transition-metal catalysis of oxygen delignification using water-soluble salts of polyoxometalate(POM) anions[J].Holzforschung,1998,52(3):311-318
    [70]Kroschwitz Jaqueline and Howe-Grant Mary.Antioxidants[J].Kirk-Othmer Encyclopedia of Chemical Technology.1997(3):424-445
    [71]Cole B..The Effect of substrate,solvent,and structure on reactions of thiols with quinones[C].9~(th) International Symposium on Wood and Pulping Chemistry,Montreal,Canada,1997:KI-1 to K1-6
    [72]Johansson E.E.,Lind J.and Ljunggren S..Aspects of the chemistry of cellulose degradation and the effect of ethylene glycol during ozone delignification of kraft pulps[J].Journal of Pulp and Paper Science,2000,26(7):239-244
    [73]Sawyer D.T..Metal-gluconate complexes[J].Journal of Chemical Abstracts,1964:633-645
    [74]Bennacer E.M.,Kiruyshina M.F.and Zarubin M.Y..Effect of organic solvents on cleavage of beta-alkyl-O-arylic and glucosidic bonds kinetics[C].5~(th) International Symposium on Wood and Pulping Chemistry,Raleigh,U.S.A.,1989:139-146
    [75]Lai Y.and Mun S.P..The chemical aspects of acid delignification processes:I Role of aryl-ether hydrolysis in aspen[J].Holzforschung,1994,48(3):203-206
    [76]Evtuguin D.,Neto C.P.and Pedrosa De Jesus.Delignification by oxygen in the presence of polyoxometalates:Mechanism proposal and possible applications[C].9~(th) International Symposium of Wood and Pulping Chemistry, Montreal, Canada, 1997(25): 1-4
    [77] Colodette J. L. and Santos de Campos A. S.. Improvements in a process for delignifying lignocellulosic pulp by means of oxygen[P]. European Patent 0524127A2, 1993
    [78] Duggirala and Prasad Y.. Evaluation of surfactants as digester additives for kraft softwood pulping[J]. Tappi Journal, 1999, 82(11):121-127
    [79] Naddeo and Ronald C.. Cheaning and bleaching of secondary fiber[P]. US Patent 5, 234.544,1993
    
    [80] 黄干强.ECF还是TCF—湛江木浆厂漂白工艺方案的思考.广东造纸,1998,(1):18-20
    
    
    [81] Retthauer E.W., Kraus H.W. and Dodmenico A. Dioxin Perspectives[M]. Plenum Press. New York and London, 1991
    [82] Kishino M., Ohi, H. Low chlorine dioxide bleaching of kraft pulp using nitrous acid treatment[J]. Mokuzai Gakkaishi/Journal of the Japan Wood Research Society, 2001, 47(4): 344-349
    [83] Mcdonough T.J, Berry R.M., Berts J.L. et al. Chlorine dioxide in the chlorination stage-A summary of existing pubulished information[C]. International Pulp Bleaching Conference Proceeding, Quebec City, Canada, June 18-21,1985, Vol.1: 143-153
    [84] Reeve D.W. Chlorine Dioxide in Delignification in: Pulp Bleaching Principles and Pracice[M]. Eds. C.W.Dence and D.W.Reeve Atlanta, TAPPI Press, 1996:261-290
    [85] Axegard P. Effect of ClO_2 substitution on bleaching efficiency and the formation of organically bound chlorine-Part 2[J]. Journal of Pulp Paper Science, 1986, 12(3): 67
    [86] Munro F.C., Chandrasekaran S., Cook C.R.et al. Impact of high chlorine dioxide substitution for chlorine on the oxygen delignified pulp at Espanola, Proc[C]. TAPPI Pulping Conf., Seattle, Washington(Oct.1989)
    [87] Ni Y., Kubes G.T. and Van Heiningen A.R.P. Reduction of the formation of organically bound chlorine during ClO_2 bleaching[J]. Journal of Pulp and Paper Science, 1994, 20(4): 103
    [88] Reeve D.W., Weishar K.M. and Li L. Process Modifications to dcrease orgnochlorine formation during chlorine dioxide delignification[J]. Journal of Pulp and Paper Science, 1995,21(6): 197
    [89] Lachenal D., Joncourt M.J., Froment P. et al. Reduction of The formation of AOX during chlorine dioxide bleaching[J]. Journal of Pulp and Paper Scince, 1998,24(1): 14-17
    [90] Brage C., Eriksson T., Gierer G.. Reaction of chlorine dioxide with lignins in unbleached pulps.Part Ⅰ[J].Holzforschung,1991,45(1):23-30
    [91]Dence C.W.Chemistry of Chemical Pulp Bleaching In:Pulp Bleaching Principles and Practice[M].Eds.C.W.Dence and D.W.Reeve Atlanta,TAPPI Press,1996:125-159
    [92]Mckague A.B.,Kang G.J.,Reeve D.W.Reaction of a lignin model dimer with chlorine and chlorine dioxide[J].Holzforschung,1993(47):497-500
    [93]Brage C.,Eriksson T.,Gierer G.Reaction of chlorine dioxide with lignins in unbleached pulps.Part Ⅱ[J].Holzforschung,1991,45(2):147-152
    [94]Ni Y.,Shen X.,Van Heiningen A.R.P.Studies on the reactions of phenolic and non-Phenolic lignin model compounds with chlorine dioxide[J].Journal Wood Chemistry and Technology,1994,14(2):243-262
    [95]黄干强.螯合作用与过氧化氢漂白[J].广东造纸,1996(4):12-15
    [96]秦梦华,石淑兰.过氧化氢漂白的几个机理[J].纸和造纸,1994(3):6-7
    [97]Paavilainen L..Importance of cross-dimensional fiber properties and coarsess for the characterization of softwood sulphate pulp[J].Paperi ja Puu,1993(79):343-351
    [98]Page D.H.,A theory for the tensile strength of paper[J].Tappi Journal,1969(52):674-681
    [99]Seth R.S.,Page D.H..Fiber properties and tearing resistance[J].Tappi Journal,1988(71):103-107
    [100]Laine J.,Hynynen R.,Stenius P..The effect of surface chemical composition and charge on the fiber and paper properties of unbleached and bleached kraft pulps.The fundamentals of papermaking materials[C].Transactions of the 11~(th) Fundamental Research Symposium,Cambridge,UK,September 1997:859-891
    [101]Paavilainen L.,Effects of sulphate cooking parameters on the papermaking[J].Paperi ja Puu,1989.71(4):356-363
    [102]Gumagul N.,Page D.H..The difference between dry and rewetted zero-span tensile strength of paper[J].Tappi Journal,1989(72):164-167
    [103]Lindstrom T.,Wagberg,L.,Larsson T..On the nature of joint strength in paper-A review of dry and wet strength resins used in paper manufacture.13~(th) Fundamental Research Symposium,2005,Cambridge UK
    [104]Retulainen E.,Ebeling K..Fiber-to-fiber bonding and ways of characterizing bond strength[J].Appita Journal,1992,46(4):282-288
    [105]Campbell W.B..The mechanism of bonding[J].Tappi Journal,1959,42(12):999-1001
    [106]Scallan A.M.,Grignon J..The effect of cations on pulp and paper properties[J].Svensk Papperstidn,1979,82(4):40-47
    [107] Spiegelberg H.L.. The effect of hemicelluloses on the mechanical properties of individual pulp fibers[J]. Tappi Journal, 1966(49):388-396
    [108] Paavilainen L.. Conformability, flexibility and collapsibility of sulphate fibers[J]. Paperi ja Puu, 1993(75):689-702
    [109] Fors C.. The effect of fiber charge on web consolidation in papermaking, in Pulp and Paper Chemistry and Technology[D]. Ph.D Thesis, 2000, Royal Institute of Technology, Stockholm, p.78
    [110] Sjostrom E., Wood Chemistry. Fundamentals and Applications[M]. Second edition ed. 1993, San Diego: Academic press. 292
    [111] Buchert J., Teleman A., Carlsson G., et al. Effects of pulping and bleaching on the surface composition of kraft pulps[C]. The 8~(th) International Symposium on Wood and Pulping Chemistry, Helsinki, Finland, 1995,2: p. 567-573.
    [112] Sjostrom E.. The origin of charge on cellulosic fibers[J]. Nordic Pulp and Paper Research Journal, 1989,4(2): 90-93
    [113] Chai X.-S., Hou Q. X., Zhu, J.Y.. Carboxyl groups in wood fibers: Part II. The fate of carboxyl groups during alkaline delignification and its application for fiber yield prediction in alkaline pulping[J]. Industrial engineering chemistry research, 2003(42): 5440-5444
    [114] Croon I., Enstrom B. F.. The 4-O-methyl-D-glucuronic acid groups of birch xylan during sulfate pulping[J]. Tappi Journal, 1961,44(12): 870-874
    [115] Axelsson S., Croon I., Enstrom, B.. Dissolution of hemicelluloses during sulfate pulping. Part I. Isolation of hemicelluloses from the cooking liquor at different stages of a birch soda cooking[J]. Svensk Papperstidn, 1962,65(18):693-697
    [116] Hamilton J.K., Buchert J., Teleman A., et al. The behavior of hemicelluloses during pulping. I. Examination of the xylose-containing hemicelluloses associated with hardwood and softwood[J]. Tappi Journal, 1958,41(12):803-811
    [117] Buchert J., Teleman A., Harjunpaa V., et al. Effect of cooking and bleaching on the structure of xylan in conventional pine kraft pulp[J]. Tappi Journal, 1995, 78(11):125-130
    [118] Chakar F.S., Lenong A., Ragauskas A.J., et al. Influence of hexenuronic acids on US bleaching operations[J]. Tappi Journal, 2000, 83(11): 62
    [119] Johansson M.H., Samuelson O.. The formation of end groups in cellulose during alkali cooking[J]. Carbohydrate Research, 1974(34):33-43
    [120] Laine J.. Effect of ECF and TCF bleaching on the charge properties of kraft pulp[J]. Paperi ja Puu,1997a,79(8):551-559
    [121]Zhang Y.,Sjogren B.,Engstrand P.,et al.Determination of charged groups in mechanical pulp fibers and their influence on pulp properties[J].J.Wood Chem.Technol.,1994,14(1):83-102
    [122]Heijnesson A.,Simonson R.,Westermark U..Metal ion content of material removed from the surface of unbleached kraft fibers[J].Holzforschung,1995,49(1):75-80
    [123]Gellerstedt G.,Lindfors E.-L..Hydrophilic groups in lignin after oxygen bleaching[J].Tappi J.,1987.70(6):119-122
    [124]Gierer J.,Chemistry of delignification.Part 2:Reaction of residual lignins during bleaching[J].Wood Sci.Technol.,1986.20(1):1-33
    [125]Gellerstedt G.,Lindfors E.L..On the structure and reactivity of residual lignin in kraft pulp fibers[C].International Pulp Bleaching Conference.1991:73-75
    [126]Scallan A.M.,Grignon J..Effect of cations on pulp and paper properties[J].Svensk Papperstidn.,1979.82(4):40-47
    [127]Sheng-Li Chen,Shuangfei Wang,and Lucian A.Lucia.New insights into the fundamental nature of lignocellulosic fiber surface charge[J].Journal of Colloid and Interface Science,2004(275):392-397
    [128]Scallan A.M..The effect of acidic groups on the swelling of pulps:a review[J].Tappi J.,1983.66(11):73-75
    [129]Scallan A.M.,Tigerstrom A.C..Swelling and elasticity of the cell walls of pulp fibers[J].J.Pulp Pap.Sci.,1992,18(7):273-277
    [130]Engstrand P.,Sjogren B.,Olander K.,et al.The significance of carboxylic groups for the physical properties of mechanical pulp fiber[C].6~(th) International Symposium Wood Pulping Chemistry,Melboune,Australia,1991:75-79
    [131]Barzyk D.L.,Ragauskas A.J.,Ellis R.L..The effect of acid group content on the properties of cotton fibers[C].AIChE Symposium Series.Fundamentals and Applications in Pulping,Papermaking,and Chemical Preparation,1997:146-151
    [132]Seth R S.The measurement and significance of fines[J].Pulp and Paper Canada,2003,104(2):41
    [133]管永刚.细小纤维功能的多重性与弊病[J].黑龙江造纸,2003(1):24-27
    [134]Patel M.,Trivedi R..Variations in strength and bonding properties of fines from filler,fiber and their aggregates[J].Tappi journal,1994,77(3):185
    [135]劳嘉葆.阔叶木的原细小纤维和表面电荷对AKD施胶的影响[J].国际造纸,2004, 23(3):41-42
    [136]窦正远.蔗渣化机浆中细小纤维组分对漂白性能的影响[J].纸和造纸,1996(3):40-41
    [137]Sirvio J,Nurminen I..Systematic changes in paper properties caused by fines[J].Pulp and Paper Canada,2004,105(8):39
    [138]许桂红.造纸过程中单程留着作用的重要意义[J].造纸科学与技术,2004,23(1):57-59
    [139]陈嘉翔.新闻纸用脱墨浆分级后漂白的研究[J].纸和造纸,2003(5):30-32
    [140]石淑兰,何福望.制浆造纸分析与检测[M].北京:中国轻工业出版社,2003
    [141]MODDE 7 User Guide and Tutorial[M].IID2014,by Umetrics AB,2003.
    [142]Eriksson L.,Johansson E.,Kettaneh-Wold N.and Wold,S.(2001):Multi and Megavariate Data Analysis,Principles and Application[M],Umetrics Academy,ISBN 91-973730-1-X,Umetrics AB,Umea.
    [143]Shimizu K.Wood and Cellulosic Chemistry[M].New York:Marcel Dekker,1991:177-214
    [144]邬义明.植物纤维化学(第二版)[M].北京:轻工业出版社,1991:242-245
    [145]Clayton W D.The alkaline degradation of some hardwood 4-O -methyl-D-glucuronoxylans [J].Svensk Papperstidning,1963,66(4):115-124
    [146]Johansson M and Samuelson O.Epimerization and degradation of 2-O -(4 -O -methyl-D -glucopyranosyluronic acid) -D -xylitol in alkaline medium[J].Carbohydrate Research,1977,54(2):295-299
    [147]Shimizu K.β-elimination of 2 -O -(4 -O -methyl -α-D -glucopyranosyluronic acid) -D -xylose with methylsulphinyl carbanion and hydrolysis of the hex -4-enopyranosiduronic linkage[J].Carbohydrate Research,1981,92(2):219-224
    [148]Teleman A,Harjunpaa V,Tenkanen M.,et al.Characterisation of 4 -deoxy -β-L -threo -hex -4 -enopyranosyluronic acid attached to xylan in pine kraft pulp and pulping liquor by ~1H and ~(13)C-NMR spectroscopy[J].Carbohydrate Research,1995,272(1):55-71
    [149]Siltala M,Winberg K,Henricson K et al.Mill scale application for selective hydrolysis of hexenuronic acids groups in TCF bleaching of kraft pulp[C].In:Proceedings of International Pulp Bleaching Conference,Book 1,Helsinki,Finland,1998:279-287
    [150]Vuorinen T,Buchert J,Telemen A.,et al.Selective hydrolysis of hexenuronic acid groups and its application in ECF and TCF bleaching of kraft pulps[C].In:Proceedings of International Pulp Bleaching Conference,Book 1,Washington D.C.1996:43-51
    [151] Vuorinen T, Fagerstrom P, Rasanen E., et al. Selective hydrolysis of hexenuronic acid groups opens new possibilities for development of bleaching processes[C]. In: Proceedings of 9~(th) International Symposium of Wood and Pulping Chemistry, Montreal, Canada, 1997:M4-1-4
    [152] Chai X. S., Zhu J. Y., Li J.. A simple and rapid method to determine hexeneuronic acid groups in chemical pulps[J]. Journal of Pulp and Paper Science, 2001,27(5): 165-170
    [153] Chai X.S., Yoon S.H., Zhu J.Y., Li J.. The fate of hexenuronic acid groups during alkaline pulping of loblolly pine[J]. Journal of Pulp and Paper Science, 2001, 27(12):407-411
    [154] Chai X.S., Luo Q., Yoon S.H., Zhu J.Y.. The fate of hexenuronic acid groups during kraft pulping of hardwoods[J]. Journal of Pulp and Paper Science, 2001, 27(12):403-406
    [155] Gierer J.. Mechanisms of bleaching with oxygen-containing species[C]. Proceedings of the International Symposium on Wood and Pulping Chemistry. Paris, 1987(1):279
    [156] Gierer Josef, Reitberger Torbjorn and Yang Erquan, et al. Formation and involvement of radicals in oxygen delignification studied by the autoxidation of lignin and carbohydrate model compounds[J]. Journal of Wood Chemistry and Technology. 2001, 21(4):313-341
    [157] Reitberger T., Gierer J., Yang E., et al. Involvement of oxygen-derived free radicals in chemical and biological degradation of lignin. in oxidative delignification chemistry-fundamentals and catalysis[M]. ACS Symposium Series 785, Argyropoulos, D. S., American Chemical Society, Washington, D C, 2001, Chapter 15:255
    [158] Gierer J.. Mechanisms of bleaching with oxygen-containing species[C]. Proceedings of the International Symposium on Wood and Pulping Chemistry. CTAPI, Beijing, China, 1993(1):301
    [159] Gierer J.. The role of superoxide anion radicals in delignification[C]. Proceedings of the International Symposium on Wood and Pulping Chemistry. CTAPI, Beijing, China, 1993(1):240
    [160] Gierer Josef, Yang Erquan and Reitberger Torbjorn.. On the significance of the superoxide radical (O_2·~- /HO·) in oxidative delignification, studied with 4-t-butylsyringol and 4-t-butylguaiacol. Part I. The mechanism of aromatic ring opening[J]. Holzforschung. 1994,48(5):405-414
    [161] Gierer J.. Formation and involvement of superoxide (O_2·~-/HO·) and hydroxyl (HO) radicals in TCF bleaching processes:A review[J].Holzforschung.1997(51):34-46
    [162]Swan B.and Gustavsson R..Bleaching cellulose pulp in the presence of formaldehyde[P].US Patent 4-004-967,1997
    [163]Schuchmann M.N.,Bothe E.,von Sonntag J.,et al.Reaction of HO· radicals with benzoquinone in aqueous solutions,a pulse radiolysis study[J].J.Chem.Soc..1998(2):791
    [164]Guay D.F..Mechanisms of oxidative degradation of carbohydrates during oxygen delignification[D].Ph.D.Thesis,University of Maine,1999
    [165]赵建,李雪芝,石淑兰等.桉木常规KP浆和RDH浆的氧脱木素研究(Ⅰ)[J].中国造纸学报,2003,18(1):31-35
    [166]Rodriguze A.,Jimznez L.,Ferrer J.L.Use of oxygen in the delignification and bleaching of pulps[J].Appita Journal.2007,60(1):17-22
    [167]Allen L.,Schofield M.,Faubert M.,et al.Improved deresination during oxygen delignification.Part Ⅱ:Effects of blended surfactant addition[J].Pulp and Paper Canada.2005,106(2):41-43
    [168]Eriksson O.and Lindgren B.O..About the linkage between lignin and hemicelluloses in wood[J].Svensk Paperstiding.1997(80):59-63
    [169]Minor J.L..Chemical linkage of pine polysaccarides to lignin[J].Journal of Wood Chemistry and Technology.1982,2(1):1-16
    [170]Iverson T..Lignin-carbohydrate bonds in a lignin-carbohydrate complex isolated from spruce[J].Journal of Wood Chemistry and Technology.1985(19):243-251
    [171]Tamminen T.L.and Hortling B.R..Isolation and characterization of residual lignin[M].Tappi Press.Atlanta,1999:1-42
    [172]Gellerstedt G.,Pranda J.and Lindfors E.-L..Structural and molecular properties of residual birch kraft lignins[J].Journal of Wood Chemistry and Technology.1994,14(4):467-482
    [173]Lachenal D.,Fernandes J.C.and Froent P..Behaviour of residual lignin in kraft pulp during bleaching[C].Proceedings of the 1994 International Pulp Bleaching Conference.1994:41-45
    [174]Argyropoulos D.S.,Sun Y.and Palus E..Isolation of residual kraft lignin in high yield and purity[J].Journal of Pulp and Paper Science,2002,28(2):50-54
    [175]Jiang,Z.H.and Argyropoulous,D.S..The stereoselective degradation of arylglycerol-beta-aryl ethers during kraft pulping[J].Journal of Pulp and Paper Science. 1994,20(7):183-188
    [176]Granata A.and Argyropoulous D.S..2-chloro-4,4,5,5-tetramethyl-1,2,3-dioxaphosholane.A reagent for the accurate determination of the uncondensed and condensed phenolic moieties in lignins[J].Journal of Agriculture and Food Chemistry.1995(43):1538-1544
    [177]Sun Y.and Argyropoulous D.S..A comparison of the reactivity and efficiency of ozone,chlorine dioxide,dimehtyldioxirane and hydrogen peroxide with residual kraft lignin[J].Holzforschung.1996,50(2):175-182
    [178]Argyropoulous D.S.,Bolker H.I.,Heitner.C.,et al.~(31)P-NMR spectroscopy in wood chemistry.Part Ⅴ.Qualitative analysis of lignin functional groups[J].Journal of Wood Chemistry and Technology.1993,13(2):187-212
    [179]Argyropoulous D.S..~(31)P-NMR spectroscopy in wood chemistry.A review of recent progress[C].International Symposium on Wood and Pulping Chemistry Proceedings,Beijing,China,May 25-28,1993(2):776-786
    [180]Lundquist K..NMR studies of lignins.2.Interpretation of the ~1H-NMR spectrum of acetylated birch lignin[J].Acta Chemica Scandinavica.1979,B33(1):27-30
    [181]陈方,陈嘉翔.桉木木素的付立叶变换红外光谱研究[J].纤维素科学与技术,1994,2(2):14-20
    [182]陈昌华,李静,苏茂尧,陈中豪.影响尾叶桉酶解木素制备的因素研究[J].纤维素科学与技术,1998,6(2):61-67
    [183]Argyropoulos D.S.,Sun Y.and Palus E..Isolation of residual kraft lignin in high yield and purity[J].Journal of Pulp and Paper Science,2002,28(2):50-54
    [184]Granata A.and Argyropoulous D.S..2-chloro-4,4,5,5-tetramethyl-1,2,3-dioxaphosholane.A reagent for the accurate determination of the uncondensed and condensed phenolic moieties in lignins[J].Journal of Agriculture and Food Chemistry.1995(43):1538-1544
    [185]Argyropoulous D.S.,Bolker H.I.,Heitner.C.,et al.~(31)p-NMR spectroscopy in wood chemistry.Part Ⅴ.Qualitative analysis of lignin functional groups[J].Journal of Wood Chemistry and Technology.1993,13(2):187-212
    [186]刘玉.三倍体毛白杨EMCC蒸煮和TCF漂白及其木素结构变化的研究[D].华南理工大学博士学位论文,2005(6):52-63
    [187]付时雨.尾叶桉硫酸盐浆漆酶介体体系生物漂白及脱木素机理研究[D].华南理工大学博士学位论文.2000(6):77
    [188]Chang H.M..Isolation of lignin from pulp[A].In:Yin S.Y.,Demc,C.W.(Eds),Methods in Lignin Chemistry,Springer series in wood sciences.1992:72-76
    [189]陈嘉翔,余家鸾.植物纤维化学结构的研究方法[M].华南理工大学出版社,1989:146-147
    [190]Parsad B.,Gratzl J.S.,Kirkman A.,Jameel H.,Rost T..High-kappa pulping and extended oxygen delignification decreases recovery cycle load[J].Tappi J.,1994.77(11):135-147
    [191]Dyer T.J.,Johnston D.C.,Ragauskas A.J.Improved bleaching performance with reduced cost:Optimizing ECF bleaching technologies with a poor man's O[C].in 2001TAPPI Pulping Conference.2001.Seattle,WA,United States.
    [192]Jiang J.E.,Greenwood B.F.,Phillips J.R.,et al..Combining modified continuous cooking with two-stage oxygen bleaching for optimal extended delignification[R].In Eur.Pulp Pap.Week 4th Int.Conf.New Avail.Tech.Current Trends.1992.Bologna,England.
    [193]Santos C.A.,Shackford L.D.,Miller W.J.,et al..Extended oxygen delignification for increased yield using pulps produced with conventional and modified cooking[C].In International Pulp Bleaching Conference.2000.Halifax,NS,Canada.
    [194]Steffes F.,Bokstrom M.,Norden S..Pulp yield improvements using two-stage extended oxygen delignification[C],in 1998 TAPPI Breaking the Pulp Yield Barrier Symposium.1998.Atlanta,GA:TAPPI Press.
    [195]Yang R.,Lucia L.,Ragauskas A.J.,et al.Oxygen delignification chemistry and its impact on pulp fibers[J].J.Wood Chem.Technol.,2003.23(1):13-29
    [196]曹邦威.纸浆漂白的最新进展-两段短流程漂白[J].中华纸业,2006,27(5):43-46
    [197]谢来苏,詹怀宇.制浆原理与工程[M].北京:中国轻工业出版社,2001
    [198]杨桂花,陈嘉川.二氧化氯的制备及其应用[J].山东轻工业学院学报,2004:18(4):1-4
    [199]Dahlman O;Jacobs A;Liljenberg A and Olsson A.I.Analysis of carbohydrates in wood and pulps employing enzymatic hydrolysis and subsequent capillary zone elecrophoresis[J].J.Chromatography,2000,891(1):157-174
    [200]Nishi K.Bhardwaj,Viet Hoang,Kien L.N..A comparative study of the effect of refining on physical and electrokinetic properties of various cellulosic fibres[J].Bioresource Technology,2007(98):1647-1654
    [201]Subrahmanyam S.V.,Godiyal R.D.,Sharma A.K.,et al..Effect of refining energy on the pulp properties of nonwoods[J].IPPTA,2000,12(2):1-18
    [202]Wai N.N and Murakami K.Characteristics of kraft pulp from Burmese bamboo[C].International Symposium on Wood Pulping Chemistry.Tsukuba science city,Japan 23-27 May 1983:188-193
    [203]Rao A.R.K;Srinivasan G and Maheshwari H.K.Effect of beating on bamboo fibres[J].Indian Pulp and Paper,February-March 1978:35-46
    [204]Mista D.K.Industrial experiences & problems involved in stock preparation & paper making utilizing non-wood fibrous materials[M].Non-wood Plant Fibre Pulping,Progress Rep.No6.TAPPI CAR no 58,1975:7-22
    [205]隆言泉.造纸原理与工程[M].北京,中国轻工业出版社,1994
    [206]Nishi K.Bhardwaj,Tuan D.Duong,Viet Hoang,et al.Determination of fiber charge components of Lo-Solids unbleached kraft pulps[J].Journal of Colloid and Interface Science,274(2004):543-549
    [207]Lindstrom T..Chemical factors affecting the behaviour of fibres during papermaking[J].Nordic Pulp Pap.Res.J.,1992,7(4):181-192
    [208]Laine J.,Stenius P..Effect of charge on the fibre and paper properties of bleached industrial kraft pulps[J].Pap.Puu-Pap.Timber,1997,79(4):257-266
    [209]Zhang Y.,Sjogren B.,Engstrand P.,et al.Determination of charged groups in mechanical pulp fibers and their influence on pulp properties[J].J.Wood Chem.Technol.,1994,14(1):83-102
    [210]Fardim P.,Duran N..Modification of fibre surfaces during pulping and refining as analysed by SEM,XPS and ToF-SIMS[J].Colloid.Surf.,2003,223(1-3):263-276
    [211]Nyholm K.,Ander P.,Bardage S.and Daniel G..Dislocations in pulp fibres-their origin,characteristics and importance-a review[J].Nordic Pulp Paper Res.J.,2001(4):376-384
    [212]Mohlin U-B and Homatowska J.Fibre and sheet properties of Acacia and Eucalyptus[J].Appita Journal,2006,59(3):225-230
    [213]Nikhil,C.B and Sarajit B.Studies on the improvement of pulp strength by fractionation and blending technique[J].Appita Journal,1981,34(6):485-491
    [214]Ljusgren I;Wiberg B;Tubek Lindblom A and Persson T.Papermaking potential of Scandinavian softwood pulp together with non-wood pulp[C].New Technologies in Non-wood Fiber Pulping and Papermaking,5~(th) INWFPPC,Guangzhou,China,2006:281-286

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700