Field of the Invention

The present invention relates to delignification and bleaching of cellulosic wood pulp fibers for use in papeπαa ing and to the production of a pulp having reduced halogen concentrations, and good brightness and viscosity. Background of the Invention.

Chlorine-based chemicals, such as chlorine, chlo¬ rine dioxide, and hypochlorite, have been used in pulp bleaching for several decades, and continue to be used for removing lignin and bleaching the pulp to high brightness. In general terms, the extent of bleaching, hence the degree of brightness obtained, is determined by the type of pulp being bleached and the proposed end use of the paper product. For example, groundwood pulp may be intended for use in making linerboard which does not need to exhibit a high brightness. In this situation less bleaching may be employed. In other examples, kraft pulps intended for use in making fine writing papers require different bleaching circumstances which will produce the desired brightness in the final paper product. In all instances, however, where chlorine-based bleaching agents have been employed in the prior art, there are produced chlorinated organics. These compounds are generally insoluble and substantial quantities are swept from the pulp with the effluent from one or more of the stages of the bleaching sequence. A relatively smaller percentage of such chlorinated organics remain in the pulp and eventually appear in the paper product.

In chlorine-based bleaching processes, the "C" factor of the pulp is employed as a measure of the chlorina¬ tion charge required for a specific pulp. By definition, the "C ¹¹ factor refers to the effective chlorination charge and is equal to the chlorine dioxide plus the chlorine in the charge (expressed in terms of effective chlorine) , divided by the Kappa number of the pulp. Generally, it is

stated in the prior art that higher "C" factors produce brighter pulps, but that a "C" factor of about 0.22 provides maximum brightness in a pulp without unacceptable degrada¬ tion of the cellulosic fibers (e.g. reduced strength) . Thus, it has been common heretofore when seeking maximum brightness of the pulp, (in the range of 70-85% GE) to use large "C" fac-tors, i.e. larger quantities of chlorine- containing bleaching agent.

In the past decade, there has been a growing concern about the environmental impact of chlorinated organ¬ ic compounds in bleach plant effluent. Also, public concern for the disposal of paper containing organically bound chloride has been increasing. Undesirable chlorinated organics such as dioxin have been detected in the exhaust gases of incinerators burning municipal wastes containing chloride, including, for example, paper products made from chlorine bleached pulps. West German environmental regula¬ tions, for example, propose restricting the total chloride residue for packaging material including wood pulp to less than 200 ppm. The allowable adsorbed organic halogens (AOX) discharged in the effluent per ton of wood pulp has been restricted to 2.0 kg or less. More stringent regulations are expected in the near future.

Several options have been proposed or practiced to reduce or eliminate chlorinated organics in the bleaching process. The most straightforward method is to substitute non-chlorine bleaching chemicals, such as oxygen, peroxides, ozone, peracetic acid, etc. for chlorine-based bleaching chemicals. Unfortunately, no chlorine-free bleaching proc¬ ess has been developed with the ability to produce accept¬ able pulp properties (such as brightness or viscosity) at an acceptable bleaching cost.

Another option to reduce the discharge of chlori¬ nated organic compounds is to reduce the chlorine usage in the first stage of the bleaching process. Two alternatives that produce no significant degradation of pulp properties have been commercialized for this purpose. These are (a)

extended delignification in the cooking stage and (b) oxygen delignification. These alternatives, with proper extrac¬ tion, reduce the lignin content of brown stock going into the bleach plant. They do not, however, reduce the chlori¬ nated organic compounds in the bleached pulp and effluent to sufficiently low levels.

A third option to reduce the generation of chlori¬ nated organics in a bleaching process is to substitute chlorine dioxide for chlorine. Chlorine dioxide is a rela¬ tively strong oxidant compared to chlorine; to achieve the same degree of delignification, it requires only about thirty-eight weight percent chlorine dioxide on the pulp compared with one hundred weight percent of chlorine. However, these prior art processes are of the DEDED type wherein the chlorination stage (D) is followed by the con¬ ventional extraction (E) and additional chlorination (D) stages. The pulp and the discharge effluents resulting from this prior art option contain higher concentrations of chlorinated organics than are acceptable and/or desirable. Processes using both oxygen delignification and chlorine dioxide substitution have been suggested but do not achieve the regulated concentrations of chlorine-containing residues in either the pulp or the effluent. Summary of the Invention

In accordance with the method of the present invention, a cellulosic wood pulp is initially contacted with a chlorine-based bleaching agent as the first-stage of a bleaching sequence. This chlorination agent preferably is primarily chlorine dioxide, but may contain free chlorine. Contrary to the prior art, after this initial D stage and prior to any extraction (E) stage, the pulp is processed through an ozonation stage. After the ozonation stage, the pulp is processed through the customary extraction, further bleaching, etc. stages. Importantly, and as noted to be contrary to the prior art, the ozonation takes place immedi¬ ately following chlorination and prior to extraction. It has been recognized heretofore that ozone as a strong oxi-

dant tends to degrade the pulp and that any use of ozone on pulp should be preceded with an acid wash, for example to remove heavy metals known to be harmful to the stability of ozone and/or decomposition products that may cause low pulp properties (e.g. strength) . Contrary to such prior art, the present inventor has found that without an acid wash stage the ozonation can take place immediately following an ini¬ tial chlorine dioxide (D) or chlorine dioxide/free chlorine mixture (D _c ) bleaching stage. In this regard, it is to be understood that preferably there is a conventional water washing of the pulp between the stages of the bleaching sequence. This washing is not deemed to be a "stage", but rather is in the nature of a dilution of the aqueous phase of the pulp. For example, the quantity of water commonly used provides a dilution factor of between about 1 and about 3. It has been found that the wash water need not be "clean" or "fresh" water. For example, recirculated water which contains considerable residues from previous usage has been used successfully.

Among the several unexpected advantages provided by the present method, it has been found that the ozone treatment not only provides delignification and bleaching but also oxidizes substantial quantities of the chlorinated lignin residues left over from the chlorination stage. This oxidative activity converts substantial quantities of the insoluble chlorinated organics to inorganic chlorine- containing compounds and/or to chlorinated organics that are soluble in the liquor present in the ozonation stage. The oxidation of these chlorinated residues by the ozone thus not only reduces the chlorinated organic content in the wood pulp, but also reduces the adsorbed chlorinated organics discharged in the effluent. These converted inorganic chlorides, generally, are not environmentally hazardous. The result is a pulp having good brightness, acceptable viscosity, and reduced chlorinated organic content. Nota¬ bly, such desirable results are obtained by employing as few as four stages in the bleaching sequence, and employing

lower total effective chlorine charges in the chlorination stage than heretofore known to be possible.

Specifically, the present inventors, using their improved method, have produced wood pulp which has less than 200 ppm total organic chloride (TOC1) residue. TOC1 as used herein refers to the total organically bound chlorine content of the pulp resulting from the bleaching sequence unless indicated otherwise. TOC1 is essentially insoluble. The effluent discharge from the bleaching process of the disclosed method has less than 2.0 kg adsorbed organic halides (AOX) per ton of wood pulp. AOX, as the term is used herein refers to the sum of the AOX, i.e. adsorbed organic halides, of the several stages of bleaching, i.e. AOX of the D_ stage plus AOX of the Z stage plus AOX of the E stage and plus AOX of the D ₂ stage, unless indicated otherwise. As noted, the pulp produced by the present invention has a brightness and viscosity that meet or exceed the requirements of industrial papermaking.

Therefore, it is an object of the present inven¬ tion to provide a method for the preparation of cellulosic wood pulp fibers for use in papermaking that can provide wood pulps with lowered residual chlorine content and efflu¬ ents with lowered levels of adsorbed organic halides (AOX) while retaining or enhancing the characteristics of bright¬ ness and pulp viscosity within acceptable ranges.

It is another object of the present invention to provide such an improved method for bleaching cellulosic pulp that is both economical and readily adaptable to the current papermaking industry. These and other objects will be recognized from the present description including the Figures. Brief Description of the Figures

FIGURES 1-5 are graphic representations, computer- generated from mathematical models depicting the relation¬ ship of ozone charge and chlorination factor in obtaining various values of the brightness, viscosity and total chlo¬ ride on pulp.

In accordance with the present invention, an aqueous slurry of cellulosic wood fibers as is commonly produced by conventional digestion means in the papermaking industry is processed through sequential stages of a bleach¬ ing operation. Softwoods, hardwoods or mixtures thereof may be processed employing the present invention. Following digestion, the slurry preferably is processed directly to the bleaching sequence disclosed herein. If desired, it may be subjected to such treatment as oxygenation, ozonation or other oxidation prior to entering the present sequence, but with attendant increased expense.

In the first stage of the present sequence, the pulp slurry is treated with a chlorine-based agent, i.e. chlorine dioxide or a mixture of chlorine dioxide and free chlorine. Preferably in this stage the oxidant is princi¬ pally chlorine dioxide. Consistent with the industry prac¬ tices, the term, D, is employed to represent a bleaching stage employing chlorine dioxide, with Dη_, representing the first D stage of a sequence. The term D _c , represents a stage employing chlorine dioxide plus free chlorine. In a D _c stage, the chlorine dioxide and free chlorine are inter¬ mixed prior to introduction to the bleaching apparatus, and therefore are introduced to the pulp simultaneously as a single process stream, as opposed to first adding the chlorine dioxide and free chlorine as separate process streams.

Following the D-^ stage, and with or without an intervening washing, the pulp is processed through an ozona¬ tion stage, Z. Heretofore, it has been taught in the indus¬ try that ozone tends to be decomposed by certain of the non-cellulosic components of the pulp. Contrary to the prior art, in the present invention the pulp moves from the D-_ stage directly to the Z stage without an intervening extraction, E, stage. In the Z stage, the pulp is contacted with ozone in a reaction tower, for example, for a period of time and employing sufficient ozone to effect oxidation of substantial quantities of the chlorinated lignins and/or

other chlorinated components of the pulp, in addition to the contribution of the ozone toward further delignification. Many of the oxidized chlorine-based lignins, residues, etc. commonly are soluble in the environment of the Z stage. Other of the oxidized compounds are soluble in an alkaline solution such as is present in an E stage. Thus, these oxidized chlorine-based compounds are solubilized into the liquor and extracted from the pulp during washing and/or extraction following the Z stage. This liquor effluent may then be processed as necessary to recover desirable chlo¬ rine-containing compounds or to destroy or render harmless other of the compounds. The pulp may be further processed through any of several selected stages, and preferably a complete sequence will include an extraction stage following the ozonation stage. Such extraction stage may be enhanced with oxygen, E ₀ , or peroxide, E _p , a combination of oxygen and peroxide, E _0+p , or other enhancer. The extraction stage is followed by a further bleaching stage, preferably using chlorine dioxide. As desired, washes may be employed be¬ tween selected stages, e.g. between the E and D ₂ stages.

To facilitate a further understanding of the invention, the following examples are given primarily for purposes of illustrating certain more specific details thereof.

Southern softwood kraft pulp with Kappa number of 32.3 and an initial viscosity of 30.3 cP was used as the wood pulp slurry for all of the following Examples except as otherwise noted. The series of Examples used various combi¬ nations of the following bleaching stages:

0 stage: Prechlorination oxygen delignification was conducted in a reactor for 1 hr. at 85°C, with 3% sodium hydroxide, 40-80 psig oxygen pressure and 0.5% magnesium sulfate on the pulp at a consistency of 10%.

D→C stage: In the sequential chlorine dioxide substitution stage, chlorine dioxide was added to the pulp and mixed; after 20 seconds, chlorine was added and the pulp was well mixed; this stage was conducted in a reactor for 40

min. at 50°C with a consistency of 3-10%.

C stage: Chlorination was conducted in a reactor for 30 to 40 min. at 45°C with a consistency of 3%, with chlorine of the desired charge.

D stage: Chlorine dioxide addition was conducted at 50 to 70°C with a consistency of 10%;

D _c stage: Where the chlorine was present in the chlorine dioxide as free chlorine, the chlorine was intro¬ duced simultaneously with the chlorine dioxide.

Z stage: The ozone stage was conducted under a pH of about 2-5 at room temperature for 40 to 90 min. with a consistency of 1%;

E stage: Extraction was conducted for 60 min. at 70°C with a consistency of 10% and with desired sodium hydroxide charge;

E ₀ stage: Extraction enhanced with oxygen was conducted under conditions similar to the E stage with an initial oxygen pressure of 40-50 psig that was gradually reduced to 0 psig;

E _p stage: Extraction enhanced with peroxide was conducted under conditions similar to the E stage with a 0.4-0.6% hydrogen peroxide charge;

^E o + _p ^sta 9 ^e: Extraction enhanced with oxygen and peroxide was conducted under conditions similar to the E ₀ stage with a 0.4% to 0.6% hydrogen peroxide charge;

Washings: The slurry was washed with distilled water in a screen box or funnel between each stage; the stage labeled (DZ) is a D stage followed immediately by a Z stage without intermediate washing.

EXAMPLE 1-5 Several prior art bleaching sequences employing procedures well known in the art were run on Southern pine softwood kraft pulp having a Kappa number of 32.3. These sequences employed the usual chlorine stages with and with¬ out chlorine dioxide substitution. The results are shown in Table I. As expected, good brightness and viscosity values were noted, except when an oxygenation stage was employed prior to chlorination (Example 3) . This latter Example showed the deterioration of the pulp (low viscosity) that has been noted in the prior art. Of these Examples, only the D→C E _0+p DED produced significant reduction in the total chloride on the pulp, but such reduction was obtained only at the expense of two additional stages.

Table 1.

Total Organic Chloride Chloride Pulp Pulp

Bleaching Chemical Charge on Pulp on Pulp Brightness Viscosity Example Sequence (% on Oven Dried (OP) Pulp) ⁽ M ⁾ * (ppm) (GE %) (cP) C Facto

D-C ^J o+p D

D→CE _0+p D 220 190 86.1 (83.3)** 22.5 0.22 1.66 — 2.9 3 0.8

D-C ''O+p

D-CE _0+p DED 195 150 88.5 (86.5) 20.8 0.22

1.66—2.9 0.8 0.4 0.3

0D-CE _0+p D 215 170 86.8 (34.8) 14.3 0.22

1.15—2 3 0.7

C E _Q D

CE _C D 314 300 84.7 (80.3) 23.8 0.22

7.25 4.35 0.7

C E D E D

CEDED 345* 320 86.7 (83.0). 27.0 0.22 7.25 4 0.7 0.5 0.5

Remarks :

* Estimated by the sum of inorganic and organic chlorides ** Reverted brightness (at 105"C for 1 hr) . *** Oxygen pulp with kappa number = 22.3, viscosity = 21.8 cP

EXAMPLES 6-13 In Examples 6-13 the pulp employed was the same as in Examples 1-5. Examples 6-13 involved bleaching sequences using an ozone bleaching stage. Table 2 shows the proper¬ ties of the pulps of these Examples. Employing ozonation prior to chlorination, Examples 6, 7, 10 and 12, produced pulps of low brightness, except in Examples 7 and 12 where additional and costly extraction and chlorination stages were added. Quite unexpectedly, Examples 8 and 9 (DZED) where ozonation was employed after chlorination, produced pulps of good brightness and viscosity plus low total chlo¬ ride on the pulp. Notably, Examples 8 and 9 (DZED) employed 20% and 7% less chlorine dioxide than Example 11 (DZEDED) plus the fact that the DZED sequence with its fewer stages yielded better viscosity values and almost equal brightness values. Further, the brightness obtained by the DZED se¬ quence is almost equal to the brightness obtained in the more costly prior art CEDED sequence (cf. Ex. 10 and Ex. 5) .

Table 2.

Total Organic

Chloride Chloride Pulp Pulp

Bleaching Chemical Charge on Pulp on Pulp Brightness Viscosity Example Seσuence (% on Oven Dried (OP) Pulp) (pom) (ppm) (GE %) (cP) C Factor

Z E D

ZED DCD ND 78.9 (N.D.)** 16.5

2 2.5 1.5

Z E D E D

ZEDED 75* 57 87.9 (85.2) 14.4

2 2.5 1.5 0.5 0.5 D Z E D

DZED ND ND 84.7 (N.D.) 19.0 0.11 1.37 1.0 2.5 0.7

D Z E D

DZED 101* 80 86.5 (82.7) 16.8 0.11 1.4 1.0 2.5 1.0

Z D E D

10 ZDED ND ND 79.0 (N.D.) 23.5 0.11 1.0 1.37 2.5 0.7

D Z E D E D

11 DZEDED 77* 65 89.0 (85.3) 15.8 0.11 1.37 1.0 2.5 0.7 0.5 0.5

Table 2 . continued

Total Organic Chloride Chloride Pulp Pulp

Bleaching Chemical Charge on Pulp on Pulp Brightness scosity

Example Sequence (% on Oven Dried (OD) Pulo) (ppm) (pom) (GE %) (cP) C Factor Z D E D E D

12 ZDEDED 150* 140 87.2 (84. •2) 21.8 0.11 1.0 1.37 2.5 0.7 0.5 0.5

D Z E D

13 ODZED 99 70 86.6 (84 .0) 14.4 0.14 1.2 0.5 2.0 0.7

( 1) N. D. : not determined.

(2) Kappa NO. of 32.3

* Estimated by the sum of inorganic and organic chlorides .

** Reverted brightness.

EXAMPLES 14-19

Examples 14-16 employed Southern softwood kraft pulp having a Kappa number of 27.3. Table 3 shows certain properties of the resultant bleached pulps. From Table 3 it is noted that enhancement of the extraction stage (e.g. E _Q , _p , or E ₀₊ p in the preferred DZED bleaching sequence permits the use of less chlorine dioxide in the D stage and produces a pulp of substantially equivalent brightness and viscosity to the pulp produced using a DZED sequence without such enhancement.

Examples 17-19 employed Southern hardwood kraft pulp having a Kappa of 14.9. Table 3 also shows the proper¬ ties of the resultant bleached pulps of these examples. These pulps showed high viscosity and good brightness values as well as relatively low T0C1 values employing total chlo¬ rine dioxide amounts less than the total chlorine dioxide amounts employed in obtaining substantially equivalent brightness and viscosity values for softwood pulp. For either softwood or hardwood pulps, the total chlorine diox¬ ide employed in these Examples 14-19 is substantially less than the total chlorine dioxide employed to obtain equiva¬ lent brightness and viscosity values without employing ozone after chlorination.

TABLE 3

Organic

Pulp Chloride Bleaching Kappa C On Pulp Brightness Viscosity Example Sequence No. Factor % Chemical on Pulp (ppm) (% .G.E.) (cP)

D Z E _p D

14 PZEpD 27.3 0.12 1.24 0.6 3% N _a OH 0.5 110 86.3 (ND) IS.2

0.5% H ₂ 0 ₂

D Z E_ D

15 DZE ₀ D 27.3 0.12 1.24 0.6 3 0.5 140 86.0 (ND) 16.2

D Z

16 DZE _0+p D 27.3 0.12 1.24 0.6 3%N-,OH 0.5 110 87.0 (ND) 14.7 0.5% H ₂ 0 ₂ D Z E _n D

17 DZE ₀ D 14.9 0.12 0.7 0.4 1.5 0.6 120 85.9 (82.1) 18.6

18 DZEpD 14.9 0.12 0.7 0.4 1.5 0.6 130 85.8 (81.7) 18.8

19 DZE _0+p D( ² ^ 14.9 0.12 0.7 0.4 1.5 0.6 120 86.5 (82.1) 18.6

EXAMPLES 20-54 A laboratory D _C ZED bleaching sequence was studied using a central composite statistically designed experiment which varied the D _c stage chlorination factor and fraction of chlorine dioxide charge, and ozone charge in the Z stage. The pulp had a Kappa number of 32.3. The results are shown in Table 4. In Table 4, Examples 24, 29-32, 34, 38-41, 45, 47-49 and 54 represent actual run data which served as the basis for the statistically designed experimental data of the remaining examples. From this data it may be concluded that to obtain a pulp brightness of about 85% GE or higher and a viscosity of at least about 18 cP, the preferred chlorination factor is about 0.12 and the ozone charge is about 1.1%. This holds true for chlorine dioxide which includes up to about 50% free chlorine. All of the pulps of Examples 20-38 showed low TOCl and AOX values, each being within present regulatory limits. Most surprisingly, howev¬ er, it was found that by using a lower chlorination factor (e.g. 0.12) which results in substantial savings in the cost of chlorine-based bleaching agent, one can use ozone per¬ centages of about 1% and obtain a three-fold reduction in AOX values.

TABLE 4

% Charge Total

(as ιeffective chlorine) Organic Cl AOX Pulp

Bleaching C CIO, (% on 'oven dried (OD) pulp) on pulp Total Brightness Viscosity

Example Sequence Factor ( % ) D C Z D ³ (ppm) (kσ/BDT) (% GE) (cP)

20 DZED 0.037 100 1.20 0.00 0.9 1.0 60 0.1 55.0 23.5

21 D _C ZED 95 1.14 0.06 1.0 1.0 40 0.1 58.0 22.2

22 D _C ZED 90 1.08 0.12 1.0 1.0 65 0.1 59.0 22.0

23 D _C ZED 80 0.96 0.24 1.1 1.0 50 0.2 62.0 21.0

24 D _C ZED 50 0.60 0.60 0.8 1.0 360 0.49 47.0 21.8

25 DZED 0.07 100 2.26 0.00 1.2 1.0 20 0.2 76.0- 20.2

26 D _C ZED 95 2.14 0.12 1.3 1.0 20 0.2 80.0 20.0

27 D _C ZED 90 2.03 0.23 1.3 1.0 50 0.3 79.0 19.5

28 D _C ZED 80 1.81 0.45 1.3 1.0 100 0.35 78.0 19.0

29 D _C ZED 80 1.81 0.45 1.0 1.0 240 0.61 65.1 20.14

30 D _C ZED 80 1.81 0.45 0.5 1.0 440 0.40 46.5 25.72

31 D _C ZED 20 0.45 1.81 0.5 1.0 725 1.75 43.8 23.78

32 D _C ZED 20 0.45 1.81 1.1 1.0 220 1.51 63.0 18.82

33 DZED 0.12 100 3.88 0.00 1.1 1.0 100 0.4 85.0 18.6

34 DZED 100 3.88 0.00 0.8 1.0 170 0.7 79.6 21.9

TABLE , continued

% Charge Total

(as effective chlorine) Organic Cl AOX Pulp

Bleaching C CIO _? (% on oven dried (OD) pulp) on pulp Total Brightness Viscosity

Example Sequel Factor (%> D C Z D ³ (ppm) (kq/BDT ^" ι (% GE) (CP)

35 D _C ZED 95 3.67 0.19 1.1 1.0 125 0.5 85.0 18.5

36 D _C ZED 90 3.49 0.39 1.1 1.0 150 0.6 84.0 18.0

37 D _C ZED 80 3.10 0.78 1.1 1.0 200 0.8 83.0 17.8

38 D-ZED 50 1.94 1.94 0.3 1.0 370 2.98 72.7 18.62

39 D _C ZED 50 1.94 1.94 0.8 1.0 380 2.70 72.3 18.90

40 D _C ZED 50 1.94 1.94 1.3 1.0 255 2.34 84.7 15.86

41 D _C ZED 0 0.00 3.83 0.8 1.0 440 4.41 67.4 17.43

42 DZED 0.17 100 5.50 0.00 0.7 1.0 100 0.9 87.5 20.2

43 D _C ZED 95 5.22 0.28 0.7 1.0 125 1.0 87.5 20.0

44 D _C ZED 90 4.95 0.55 0.7 1.0 150 1.2 87.0 19.5

45 D _C ZED 80 4.40 1.10 1.1 1.0 170 2.52 88.1 15.76

46 D _C ZED 80 4.40 1.10 0.7 1.0 200 1.4 86.0 19.1

47 D _C ZED 80 4.40 1.10 0.5 1.0 280 3.21 84.2 21.37

48 D _C ZED 20 1.10 4.40 1.1 1.0 250 6.94 86.3 14.87

TABLE 4, Continued

% Charge Total

(as effective chlorine) Organic Cl AOX Pulp

Bleaching C C10 ₂ (% on oven dried (OD) PUlP) on pulp Total Brightness Viscosity

Example Sequence Factor (%) D C Z D ³ (ppm) fkq/BDT) (% GE) (cP)

49 D _C ZED 20 1.10 4.40 0.5 1.0 380 5.91 76.9 19.82

50 DZED 0.20 100 6.46 0.00 0.3 1.0 95 1.3 88.0 25.2

51 D _C ZED 95 6.14 0.32 0.3 1.0 125 1.5 83.0 24.8

52 D _C ZED 90 5.81 0.65 0.3 1.0 150 1.8 87.5 24.6

53 D _C ZED 80 5.17 1.29 0.3 1.0 200 2.0 87.0 24.2

54 D _C ZED 50 3.23 3.23 0.8 1.0 215 5.63 88.8 15.49

/ 1 \ ."___._.» -JO ^■ _

(2) Preceded by an alkaline extraction with 3% sodium hydroxide charge.

(3) Based on predicted data, except examples 24, 29-32, 34 , 38-41, 45 , 47-49 and 54.

Table 5 shows the adsorbed organic halogens (AOX) generated in the bleaching stages of the sequences of Exam¬ ples 1-3, 9, 11 and 14. Examples 1 and 2 showed AOX levels in excess of the desired 2.0 kg per ton of wood pulp. A pre-delignification stage, as in Example 3, produced efflu¬ ent within the 2.0 kg level, but Example 3, had high levels of chloride in the wood pulp (see Table 2) . Examples 9, 11 and 14 involved stages of chlorine dioxide bleaching fol¬ lowed by ozonation. Example 9 represented a preferred sequence, DZED, and produced effluent well below the target¬ ed AOX level. Example 14 showed that pre-delignification with oxygen can improve the AOX level, but at the expense of the cost associated with the additional stage (0) . Notably, the 4-stage DZED (Example 9) sequence produced a lower AOX value than the more costly 6-stage DZEDED (Example 11) sequence.

Table 5

AOX (kg/BDT) in Effluent

Example Sequence Stages Total

D--C E _0+p D

D→CE _0+p P 2.20

0.86 1.3 0.04

D—C ^o+ D E D

D- ^* -CE _0+p DED 2.23 0.86 1.3 0.04 0.02 0.01

D—C E _0+p D

0D-CE _o+p D 1.27

0.71 0.5 0.06

D Z E D

DZED 0.43

0.13 0.2 0.06 0.04

D Z E D E P

11 DZEDED 0.63

1.37 1.0 2.5 0.7 0.5 0.5

D Z E P

14 ODZED 0.32

0.17 0.09 0.04 0.02

Experimental data were subjected to regression analysis of pulp brightness, viscosity and TOCl on chlorina¬ tion factor, fraction of chlorine dioxide charge in the D _c stage and ozone charge in the second stage (D _C ZED sequence) . The results are depicted graphically in Figures 1-5. From these Figures, at 100% chlorine dioxide in the D _c stage, it may be seen that as one accepts a lower viscosity, equal amounts of ozone can be employed with lower quantities of chlorine dioxide ("C" factor) while still maintaining high brightness and low TOCl values. This relationship holds true when the chlorine dioxide charge includes up to 80% chlorine dioxide (see Figs. 4 and 5) , the actual ranges being somewhat condensed when employing greater than about 50% free chlorine in the mixture.

It may be seen from the foregoing that the present invention provides for a method of preparation of cellulosic wood pulp fibers for use in papermaking that reduces the total chloride residue in the wood pulp to less than 200 ppm and the AOX discharge per ton of wood pulp to less than 2.0 kg. In addition, the wood pulp has a brightness greater than 85% GE and a viscosity above about 14 centipoises. Also, the method is economical and readily adaptable to the current papermaking industry.

From the Examples, it will be noted that the percentage of ozone, based on oven dry weight of pulp, employed varies as a function of the "C" factor, the effec¬ tive ratio of "C" factor to % ozone being between about 0.11 and 0.6, and preferably between about 0.2 and 0.6 for mini¬ mizing the TOCl and AOX values while maximizing the bright¬ ness and viscosity values of the pulp.

Various features of the invention which are believed to be novel are set forth in the appended claims.

EXAMPLES 55-56

In Table 6, there are shown the results of two runs in which the dioxin content of the pulp and effluent was determined. Southern pine kraft pulp, with 1% reject from cooking, having a Kappa No. of 30.3 and a viscosity of 35 cP was employed in both examples. In Example 55, a control run indicative of prior art bleaching sequences that do not employ ozone, but which do include oxygen and perox¬ ide enhanced extraction, there was no detectable tetrachlor- odibenzodioxin (TCDD) . In this example, there was detected 2.5 ppt of tetrachlorodibenzofuran (TCDF) . In the effluent from this run there was detected 2.5 ppt and 30.3 ppt of TCDD and TCDF, respectively,

In Example 56, a DZE ₀ D sequence in accordance with the present invention, there were no dioxins (TCDD or TCDF) detected in either the pulp or the effluent.

TABLE 6

DETERMINATION OF DIOXINS

Dioxins (unit = ppt)

Bleaching Brightness AOX OCl

Example Seσuences Conditions (% GE) (kq/TP) (ppm) TCDD TCDF

55 D->CE _0+p D 86.5 (81.0) 2.78 210 Pulp ND 2.5 Effluent 2.5 30.3

1.53%-*2.67% 3% NaOH

0.4% H ₂ 0 ₂ 0.8%

56 DZE ₀ D D Z E ₀ D 85.3 (80.0) 0.49 100 Pulp ND ND Effluent ND ND

1.27% 1.0% 2% 0.8%

Remarks:

1. First chlorination stage was conducted at 45"C for 30 minutes. 2. Eo, E _0+p was conducted in Quantum Reactor at 10% CSC, 75"C for 1 hour at 45 psig 0 ₂ pressure, gradually reduced to 0 psig.

3. Final D stage was conducted at 10% CSC, 70'C for 2.5 hours.

4. Not detectable.

EXAMPLE 57 Table 7 presents the results of a bleaching se¬ quence in accordance with the present invention in which the ozonated pulp at a pH of 12.7 was processed directly to an alkaline extraction stage (enhanced with oxygen) without an intervening water washing (ZE ₀ ) . In this Example 57, the GE brightness of the pulp and its viscosity were lower than when the pulp was washed with water between the Z and E stages, but these parameter values were still in a range that is acceptable for certain pulps. The TOCl of the on pulp was 128 ppm, well below present regulated standards.

TABLE 7 DZED SEQUENCE UNDER ALKALINE OZONATION CONDITIONS

Brightness Viscosity TOCl

Example Sequence Conditions % GE CP ppm

57 D(ZE _Q )D D Z D 81.3 (77.5) 11 128

1.15% 3% NaOH 3% 0.8% 34% consistency