Low chlorine dioxide bleaching of kraft pulp using nitrous acid treatment

被引:0
作者
Kishino, M [1 ]
Ohi, H
机构
[1] Hokkaido Forest Prod Res Inst, Asahikawa, Hokkaido 0710198, Japan
[2] Univ Tsukuba, Inst Agr & Forest Engn, Tsukuba, Ibaraki 3058572, Japan
来源
MOKUZAI GAKKAISHI | 2001年 / 47卷 / 04期
关键词
kraft pulp; bleaching; nitrous acid; chlorine dioxide; dioxins;
D O I
暂无
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
Non-chlorine bleaching of hardwood kraft pulp (LUKP) with a small addition of chlorine dioxide was investigated. Nitrous acid (Ak) treatment conducted at pH 1.3 and 70-90 degreesC for 30-180 min was proposed as the pre-treatment of oxygen (O) beaching. The A(k) treatment distinctly degraded the syringyl lignin model compounds veratrylglycerol-beta -syringyl ether (VS) by the C alpha -C beta cleavage yielding veratraldehyde, and kraft lignin was also degraded. The kappa number (Kn) of pulp decreased during the A(k) treatment. O bleaching was improved by the A(k) pre-treatment. A(k)-O bleaching gave a higher viscosity level than Ak-peroxide bleaching. Dioxins and coplanar polychlorinated biphenyls (PCBs) formed by chlorine dioxide (D) bleaching with a very large excess of chlorine dioxide following A(k)-O were determined. Formation of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) was a little above the minimum level of detection, but 2,3,7,8-tetrachlorodibenzofran (TCDF) was clearly determined. It was shown that an excess of chlorine dioxide may possibly cause formation of TCDFs. Therefore the sequence using the A(k)-O bleaching and a small addition of chlorine dioxide, A(k)-O-D, was proposed for LUKP.
引用
收藏
页码:344 / 349
页数:6
相关论文
共 10 条
[1]  
Adler E., 1952, SVENSK PAPPERSTIDN, V55, P245
[2]  
CRAWFORD RJ, 1991, TAPPI J, V74, P159
[3]  
Dence C. W., 1996, PULP BLEACHING PRINC, P812
[4]   Sulfuric acid bleaching of kraft pulp III: reactivity of kraft pulping-resistant structures under acidic conditions [J].
Ikeda, T ;
Tomimura, Y ;
Magara, K ;
Ishihara, M ;
Hosoya, S .
JOURNAL OF WOOD SCIENCE, 1999, 45 (05) :417-424
[5]  
Kishino M, 1996, MOKUZAI GAKKAISHI, V42, P95
[6]   STEREOCHEMICAL ASSIGNMENT OF THE THREO AND ERYTHRO FORMS OF 2-(2,6-DIMETHOXYPHENOXY)-1-(3,4-DIMETHOXYPHENYL)-1,3-PROPANEDIOL FROM X-RAY ANALYSES OF THE SYNTHETIC INTERMEDIATES (Z)-2-(2,6-DIMETHOXYPHENOXY)-3-(3,4-DIMETHOXYPHENYL)-2-PROPENOIC ACID AND THREO-2-(2,6-DIMETHOXYPHENOXY)-3-(3,4-DIMETHOXYPHENYL)-3-HYDROXYPROPANOIC ACID [J].
LUNDQUIST, K ;
STOMBERG, R ;
VONUNGE, S .
ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1987, 41 (07) :499-510
[7]   Cleavage of C alpha-C beta bonds of lignin model compounds by nitrite and nitric acid [J].
Ohi, H ;
Kishino, M .
HOLZFORSCHUNG, 1997, 51 (04) :343-348
[8]   SYNTHESIS AND C-13 NMR SPECTROSCOPIC CHARACTERIZATION OF 6 DIMERIC ARYLGLYCEROL-BETA-ARYL ETHER MODEL COMPOUNDS REPRESENTATIVE OF SYRINGYL AND P-HYDROXYPHENYL STRUCTURES IN LIGNINS - ON THE ALDOL REACTION IN BETA-ETHER PREPARATION [J].
SIPILA, J ;
SYRJANEN, K .
HOLZFORSCHUNG, 1995, 49 (04) :325-331
[9]  
Vuorinen T, 1999, J PULP PAP SCI, V25, P155
[10]  
Wiegand P, 1999, TAPPI J, V82, P135