Paper Pulp Bleaching Research Articles

On the electrosynthesis of sodium borohydride

Sodium borohydride (NaBH 4) is a versatile reducing agent used in many industrial processes. These include organic and pharmaceutical synthesis, wastewater treatment, and paper pulp bleaching. Additionally, it is a unique material in its ability to carry large amounts of hydrogen in a safe and innocuous form. In order for NaBH 4 to serve as a valuable support of the hydrogen economy, it is estimated that its cost must be reduced by at least one order of magnitude from its present price. Therefore, considerable research is required on the development of innovative NaBH 4 synthesis processes that have been reported in the open literature. It is anticipated that the most likely route to achieving the low-cost production of NaBH 4 lies in the electrochemical methods. A process for synthesising a NaBH 4 solution using a two-compartment electrolytic cell with conversion of metaborate to borohydride ions is described. Several cathode materials and electrolytic compositions are tested to select the most appropriate experimental conditions for the NaBH 4 electrosynthesis. To avoid erroneous results leading to false conclusions, the electrolysed solutions were in situ monitored by a newly developed potentiometric technique, whose resulting data are explained by thermodynamic and kinetic considerations.

Kinetic and biochemical properties of high and low redox potential laccases from fungal and plant origin

The electrochemical studies of laccase–mediator systems are aimed at understanding the mechanism of their redox transformation and their efficiency in both homogeneous and heterogeneous reactions; this topic has paramount application spanning from bleaching of paper pulp and the enzymatic degradation of lignin to the biosensors and biofuel cell development. In this paper four different laccases from Trametes hirsuta (ThL), Trametes versicolor (TvL), Melanocarpus albomyces (r-MaL) and Rhus vernicifera (RvL) were characterized from both biochemical and electrochemical points of view. Two of them (TvL and ThL) are high redox potential and two (RvL and r-MaL) are low redox potential laccases. The outline of this work is focused on the determination of catalytic and bioelectrochemical properties of these four enzymes in homogenous solution as well as immobilized onto electrode surface in the presence of a set of different redox mediators. The results measured in the homogenous reaction system correlated well with those measured with the immobilized enzymes. In addition, they are in good agreement with those reported with reference techniques, suggesting that the electrochemical methods employed in this work can be applied well in place of the traditional techniques commonly used for the kinetic characterization of laccases. These results are also discussed in terms of the known amino acid sequences and three-dimensional (3D) structures of the laccases.

Engineering and Applications of fungal laccases for organic synthesis

Laccases are multi-copper containing oxidases (EC 1.10.3.2), widely distributed in fungi, higher plants and bacteria. Laccase catalyses the oxidation of phenols, polyphenols and anilines by one-electron abstraction, with the concomitant reduction of oxygen to water in a four-electron transfer process. In the presence of small redox mediators, laccase offers a broader repertory of oxidations including non-phenolic substrates. Hence, fungal laccases are considered as ideal green catalysts of great biotechnological impact due to their few requirements (they only require air, and they produce water as the only by-product) and their broad substrate specificity, including direct bioelectrocatalysis.Thus, laccases and/or laccase-mediator systems find potential applications in bioremediation, paper pulp bleaching, finishing of textiles, bio-fuel cells and more. Significantly, laccases can be used in organic synthesis, as they can perform exquisite transformations ranging from the oxidation of functional groups to the heteromolecular coupling for production of new antibiotics derivatives, or the catalysis of key steps in the synthesis of complex natural products. In this review, the application of fungal laccases and their engineering by rational design and directed evolution for organic synthesis purposes are discussed.

Levels and congener distributions of PCDDs, PCDFs and dioxin-like PCBs in environmental and human samples: a review

The term “dioxins” is often used in a confusing way. In toxicological considerations—and also in the present report—the term is used to designate the PCDDs, the PCDFs and the coplanar (“dioxin-like”) PCBs, since these classes of compounds show the same type of toxicity. Because of the large number of congeners, relevant individual congeners are assigned with a toxic equivalency factor (TEF) that relate their toxicity to that of tetrachlorodibenzo-p-dioxin (TCDD) (2,3,7,8-TCDD) and are to be evaluated as dioxins. Each concentration of an individual congener in a mixture is multiplied with its TEF, and the resulting TCDD equivalents are added up and expressed as WHO-endorsed toxic equivalents (WHO-TEQ). Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) are mainly the by-products of industrial processes (such as metallurgical processing, bleaching of paper pulp, and the manufacturing of some herbicides and pesticides) but they can also result from natural processes like volcanic eruptions and forest fires. Waste incineration, particularly if combustion is incomplete, is among the largest contributors to the release of PCDDs and PCDFs into the environment. Due to their persistence, PCDDs, PCDFs and PCBs are part of the so-called persistent organic pollutants group of compounds that also include some chlorinated pesticides. Since they have a high lipophilicity and resist transformation, they bio-accumulate in animal and human adipose tissues. Consumption of food is considered as the major source of non-occupational human exposure to PCDD/Fs with foodstuffs from animal origin accounting for more than 90% of the human body burden. With meat, dairy, and fish products being the main contributors. The aim of the present review was to summarize experimental data regarding dioxin emissions from contaminated and uncontaminated biological and environmental samples, from the available literature. The information will be presented chronologically with respect to distribution in human milk, serum; food, water, air, soils and sediments.

Exploring the enzymatic parameters for optimal delignification of eucalypt pulp by laccase-mediator

Pycnoporus cinnabarinus laccase was compared with commercial laccases from Trametes villosa and Myceliophthora thermophila in terms of stability and mediator oxidation rates. Because of its high thermal stability and efficiency oxidizing 1-hydroxybenzotriazole (HBT), the P. cinnabarinus laccase was selected for totally chlorine free (TCF) bleaching of paper pulp, using HBT as mediator. Inactivation of laccase by HBT (50% in 4 h) decreased 20% in the presence of eucalypt kraft pulp. Laccase–HBT delignified (four points-decrease of kappa number with respect to the control) and bleached eucalypt pulp (6% ISO brightness increase) and subsequent alkaline treatment with hydrogen peroxide enhanced pulp brightness in 16% ISO. Short enzymatic treatment applied between oxygen delignification and peroxide bleaching stages enabled to obtain a final pulp with 90.3% ISO brightness and kappa number 5. The most significant improvement of pulp properties was produced during the first 2 h of laccase–HBT treatment, and no differences between enzyme performances at 65 and 50 °C were seen. Determination of hexenuronic acids, which contributed up to 50% to kappa number value after laccase-mediator treatment of eucalypt kraft pulp, provided a more realistic estimation of the final delignification rate that attained 81%. FTIR analysis of residual lignins from the treated pulps revealed strong modifications during laccase–HBT treatment.

Comparison of different fungal enzymes for bleaching high-quality paper pulps

Wild and recombinant hydrolases and oxidoreductases with a potential interest for environmentally sound bleaching of high-quality paper pulp (from flax) were incorporated into a totally chlorine free (TCF) sequence that also included a peroxide stage. The ability of feruloyl esterase (from Aspergillus niger) and Mn 2+-oxidizing peroxidases (from Phanerochaete chrysosporium and Pleurotus eryngii) to decrease the final lignin content of flax pulp was shown. Laccase from Pycnoporus cinnabarinus (without mediator) also caused a slight improvement of pulp brightness that was increased in the presence of aryl-alcohol oxidase. However, the best results were obtained when the laccase treatment was performed in the presence of a mediator, 1-hydroxybenzotriazol (HBT), enabling strong delignification of pulps. The enzymatic removal of lignin resulted in high-final brightness values that are difficult to attain by chemical bleaching of this type of pulp. A partial inactivation of laccase by HBT was observed but this negative effect was strongly reduced in the presence of pulp. The good results obtained with the same laccase expressed in A. niger at bioreactor scale, revealed the feasibility of using recombinant laccase for bleaching high-quality non-wood pulps in the presence of a mediator.

Efficient bleaching of non-wood high-quality paper pulp using laccase-mediator system

High-quality flax pulp was bleached in a totally-chlorine-free (TCF) sequence using a laccase-mediator system. Three fungal laccases (from Pycnoporus cinnabarinus, Trametes versicolor and Pleurotus eryngii) and two mediators, 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) and 1-hydroxybenzotriazole (HBT), were compared. P. cinnabarinus and T. versicolor laccases in the presence of HBT gave the best results in terms of high brightness and low lignin content (kappa number). The former laccase also resulted in the best preservation of cellulose and the largest removal of residual lignin as revealed by analytical pyrolysis, and was selected for subsequent TCF bleaching. Up to 90% delignification and strong brightness increase were attained after a laccase-mediator treatment followed by H 2O 2 bleaching. This TCF sequence was further improved by applying H 2O 2 under pressurized O 2. In this way, we obtained up to 82% ISO brightness (compared with 37% in the initial pulp, and 60% in the peroxide-bleached control) and very low kappa number (near 1). Good results were also found when the laccase-mediator treatment was performed in a bioreactor under pressurized oxygen. The pulp properties obtained, which could not be attained by conventional TCF bleaching of flax pulp, demonstrate the feasibility of enzymatic bleaching to substitute chlorine-containing reagents in manufacturing of these high-price paper pulps.

Electron transfer mediator systems for bleaching of paper pulp

The participation of biological agents in pulp bleaching systems has received a lot of attention from research teams around the world, driven by the environmental benefits that biobleaching could bring. Nature showed us the ability of some of its agents, such as wood-decaying fungi, to delignify and bleach wood and wood pulp. What we need to do is to enhance the efficiency of such agents to make them cope with the fast pace of our modern pulp mills. To do so, a profound understanding of the biobleaching system is required. Our efforts to discover new efficient mediators for the laccase-mediator system (LMS) brought us to use several techniques to analyse the reactions involved in mediated enzymatic delignification. Mostly based on electrochemistry, these techniques are reviewed in this paper, along with key results. Cyclic voltammetry was used to characterize electron transfer rates between each element of the LMS. We found, along with other authors, that the mediator redox potential has a great influence on its efficiency. We used bulk electrolysis to simulate the oxidative action of laccase on mediators and model compounds of lignin. Such electrolysis techniques allowed us to study mediated lignin oxidation outside of normal laccase working conditions. Finally, an electrolysis-based method for mediated pulp delignification that we developed, based upon our research on biobleaching, is presented.

Natural and recombinant fungal laccases for paper pulp bleaching.

Three laccases, a natural form and two recombinant forms obtained from two different expression hosts, were characterized and compared for paper pulp bleaching. Laccase from Pycnoporus cinnabarinus, a well known lignolytic fungus, was selected as a reference for this study. The corresponding recombinant laccases were produced in Aspergillus oryzae and A. niger hosts using the lacI gene from P. cinnabarinus to develop a production process without using the expensive laccase inducers required by the native source. In flasks, production of recombinant enzymes by Aspergilli strains gave yields close to 80 mg l(-1). Each protein was purified to homogeneity and characterized, demonstrating that the three hosts produced proteins with similar physico-chemical properties, including electron paramagnetic resonance spectra and N-terminal sequences. However, the recombinant laccases have higher Michaelian (Km) constants, suggesting a decrease in substrate/enzyme affinity in comparison with the natural enzyme. Moreover, the natural laccase exhibited a higher redox potential (around 810 mV), compared with A. niger (760 mV) and A. oryzae (735 mV). Treatment of wheat straw Kraft pulp using laccases expressed in P. cinnabarinus or A. niger with 1-hydroxybenzotriazole as redox mediator achieved a delignification close to 75%, whereas the recombinant laccase from A. oryzae was not able to delignify pulp. These results were confirmed by thioacidolysis. Kinetic and redox potential data and pulp bleaching results were consistent, suggesting that the three enzymes are different and each fungal strain introduces differences during protein processing (folding and/or glycosylation).

Practical applications of the Fenton reaction to the removal of chlorinated aromatic pollutants. Oxidative degradation of 2,4-dichlorophenol.

Chlorophenols (CPs) constitute a group of organic pollutants that are introduced into the environment as a result of several man-made activities, such as uncontrolled use of pesticides and herbicides, and as byproducts in the paper pulp bleaching. Promising removal technologies of chlorinated aromatics consist in the application of advanced oxidation processes (AOPs) that can provide an almost total degradation of a variety of contaminants. Among these, wide application find Fenton systems based on generation of reactive species having a high oxidizing power, such as hydroxyl radical HO*. Our objective was that of determining the overall degradation efficiency of the model compound 2,4-dichlorophenol (DCP) by thermal Fenton-type oxidation systems with a view toward defining in more details relevant process parameters, the effect of reaction temperature and of co-catalyst Cu2+. Reaction conditions were similar to those generally adopted as optimal in many practical applications, i.e. pollutant/Fe2+ (as FeSO4) ratio ca. 20, Fe2+/Cu2+ (co-catalyst) 2:1, pH adjusted and controlled at pH 3, and H2O2 in excess (up to four-fold over the stoichiometric amount required for complete mineralization). The results demonstrate that it is advantageous to carry out the reaction at a temperature markedly higher (70 degrees C) than ambient. The stepwise addition of H2O2 in aliquots yields an efficient transformation, while allowing a convenient control of the reaction exothermicity. Under these conditions, the essentially complete removal of the initial DCP is accomplished using just one equiv of H2O2 during 15 min; excess H2O2 (5 equivalents) yields extensive substrate mineralization. Also relevant, at 70 degrees C dechlorination of the initial DCP (and of derived reaction intermediates) is remarkably extensive (3-5% residual TOX), already with the addition of 1 equiv of H2O2. At the end of the reaction, IC and IC-MS analyses of the solution reveal that only low-molecular weight carboxylic acid (acetic, formic, oxalic, malonic, tartaric, etc.) contribute to the residual TOC. The whole of the results herein point to the advantage of performing the process at temperatures substantially higher than ambient (70 degrees C). Under the conditions adopted, almost complete degradation of the initial toxic compound can be achieved using hydrogen peroxide in fair excess (e.g., 3.5 equiv H2O2). In applying practical Fenton-type degradation systems to heavily polluted wastes, either for the pre-treatment of waters with a high COD value prior to biodegradation or for complete mineralization of pollutants, the set up of appropriate reaction conditions appears to be a key factor. Also, it is desirable to keep the concentration of iron salts within the lower limits in order to minimize the production and disposal of iron oxide sludges.

Retaining business customers through adaptation and bonding: a case study of HDoX

Business markets are complex. Sellers have to deal with customised demand, both passive and active markets, multi‐person interactions and interconnected relationships. Reports the case study of HDoX, a producer of hydrogen peroxide, an industrial chemical that has wide applications from the disinfecting of equipment in the foodstuffs industry to the bleaching of paper pulp. Focuses on HDoX’s practices for retention of its business customers, specifically, its industrial bulk users of hydrogen peroxide, through adaptation and bonding. HDoX’s customer retention practices are not part of an explicit retention plan but, instead, emerged as a result of HDoX’s continuous adaptation to customers and other members of its business network. The process of retaining industrial business customers is dynamic and contextualised and involves managing multi‐dimensional bonds between the seller, customers and other members of the business network.

Dioxin sources and industrial emissions control — a review

Dioxin, the collective term for polychlorinated dibenzo‐p‐dioxins and polychlorinated dibenzofurans, are generated during various chemical and high temperature processes. They have been shown to be toxic to humans and animals with 2,3,7,8‐tetrachloro‐dibenzo‐p‐dioxin (TCDD) exhibiting the greatest toxicity. Dioxin has been shown to exhibit immunotoxicity, reproductive and developmental toxicity in several animals. Epidemiological studies on groups of humans with prolonged or elevated exposure to dioxin have indicated increased cancer rates above threshold levels of exposure. Conversely, other studies have concluded that dioxin is a net anticarcinogen. There has been much study aimed at quantifying the relative contributions of the identified dioxin sources to the environmental load. Although some data suggests that burning of vegetation produces measurable amounts of dioxin it is rather industrial process waste streams which emit the greatest amounts. Processes implicated include organic chemical synthesis, metal processing, paper pulp bleaching and incineration of organic materials. Dioxin emission reduction strategies for high temperature processes have focussed upon the minimisation of the conditions at which dioxin forms in exhaust streams. Additionally, screening of process materials has been practised as have substitution of process chemicals in the pulp and paper bleaching industry.

Simultaneous purification and immobilization of Aspergillus niger xylanase on the reversibly soluble polymer Eudragit(TM) L-100.

The non-covalent immobilization of a commercial preparation of xylanase from A. niger was carried out on a reversibly soluble-insoluble enteric polymer Eudragit(TM) L-100. The immobilization of the xylanase activity by adsorption was simultaneously accompanied by removal of cellulase activity since the latter did not bind to the polymer. Thus, the soluble enzyme derivative may be useful for treatment of paper pulp bleaching in paper industry. The immobilized xylanase retained 60% of its activity toward xylan as the substrate. No change was observed in the pH optimum (5.5) of the enzyme upon immobilization. Only marginal increase in the K(m) of the free enzyme (3.6 mg ml(-1) to 5.0 mg ml(-1)) upon immobilization on the soluble polymer reflected that the enzyme-substrate binding continues to be efficient in spite of the macromolecular nature of the substrate. Fluorescence spectroscopy and UV difference spectroscopy were used to probe the change(s) in the enzyme structure upon immobilization. This change in structure was correlated with the "effectiveness factor" of the enzyme activity. CD spectra also showed that the enzyme undergoes drastic changes in the structure.

A comparison of enzyme-aided bleaching of softwood paper pulp using combinations of xylanase, mannanase and alpha-galactosidase.

Enzymatic pretreatment of softwood kraft pulp was investigated using xylanase A (XylA) from Neocallimastix patriciarum in combination with mannanase and alpha-galactosidase. Mannanase A (ManA) from Pseudomonas fluorescens subsp. cellulosa and ManA from Clostridium thermocellum, both family 26 glycosyl hydrolases, are structurally diverse and exhibit different pH and temperature optima. Although neither mannanase was effective in pretreating softwood pulp alone, both enzymes were able to enhance the production of reducing sugar and the reduction of single-stage bleached kappa number when used with the xylanase. Sequential incubations with XylA and P. fluorescens ManA produced the largest final kappa number reduction in comparison to control pretreated pulp. The release of galactose from softwood pulp by alpha-galactosidase A (AgaA) from P. fluorescens was enhanced by the presence of ManA from the same microorganism, and a single pretreatment with these enzymes, in combination with XylA. gave the most effective kappa number reduction using a single incubation. Results indicated that mixtures of hemicellulase activities can be chosen to enhance pulp bleachability.

Removal of organic contaminants in paper pulp treatment effluents by TiO 2 photocatalyzed oxidation

TiO 2 slurries under UV light irradiation were used for the oxidation and removal of the organic load of effluent from the bleaching of paper pulp. TOC was the main analytical parameter used to characterize the reaction progress, although COD, AOX and color also received periodic attention. Conditions such as the catalyst load, light intensity, pH, temperature, and concentration of O 2 and organic matter were changed through several series of experiments in order to determine their effect. A zero order kinetics accounts for the observed variation of TOC with time during most of the reaction, the rate constant being 0.25–0.40 ppm min −1 at 25 °C. This behavior is explained in terms of a Langmuir–Hinshelwood rate equation in a highly substrate concentrated system.

Family-10 and family-11 xylanases differ in their capacity to enhance the bleachability of hardwood and softwood paper pulps.

Enzyme-aided bleaching of softwood and hardwood kraft pulps by glycosyl hydrolase family-10 and -11 xylanases and a family-26 mannanase was investigated. The ability to release reducing sugar from pulp xylan and to enhance bleachability is not a characteristic shared by all xylanases. Of the six enzymes tested, two xylanases belonging to family 11 were most effective at increasing bleachability and improving final paper brightness. None of the enzymes had a deleterious effect on pulp fibre integrity. The efficiency of individual xylanases as bleach enhancers was not dependent on the source microorganism, and could not be predicted solely on the basis of the quantity or nature of products released from pulp xylan. Cooperative interactions between xylanase/xylanase and xylanase/mannanase combinations, during the pretreatment of softwood and hardwood pulps, were investigated. Synergistic effects on reducing-sugar release and kappa number reduction were elicited by a combination of two family-10 xylanases. Pretreatment of kraft pulp with mannanase A from Pseudomonas fluorescens subsp. cellulosa and any one of a number of xylanases resulted in increased release of reducing sugar and a larger reduction in kappa number than obtained with the xylanases alone, confirming the beneficial effects of family-26 mannanases on enzyme-aided bleaching of paper pulp.

5562803 Sequential bleaching of de-inked paper pulp with sodium bisulfite, dithionite and borohydride : Wang David L K; Meyers Patrick Hamburg, Germany assigned to Morton International Inc

5562803 Sequential bleaching of de-inked paper pulp with sodium bisulfite, dithionite and borohydride : Wang David L K; Meyers Patrick Hamburg, Germany assigned to Morton International Inc

Potent Bacterial Mutagens Produced by Chlorination of Simulated Poultry Chiller Water

Hypochlorite treatment of a simulated food-processing mixture produces 3,4-dichloromaleimide and 3,3-dichloro-4-(dichloromethylene)-2,5-pyrrolidinedione (C5HCl4NO2). The tetrachloro compound and two analogs, which can be synthesized from citraconic anhydride and itaconic anhydride, are direct-acting Ames mutagens in Salmonella typhimurium TA100 tester strain. These novel five-carbon cyclic imides are structurally similar to 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX), the principal mutagenic compound present in paper pulp bleaching liquors. Molecular structure analysis of the mutagens was based on X-ray crystallography, 13C NMR, and mass spectrometry of synthetic chlorinated imides with identical mass spectra and gas chromatographic retention indices. The tetrachloroimide accounts for much of the mutagenicity of the dichloromethane-extractable pH 2 fraction from chlorination of a simulated food-processing system consisting of chicken frankfurters. In the Ames TA100 tester strain it has a molecular mutagenicity of 1450 revertants/nmol without microsomal activation, making it the second most potent mutagen reported from a chlorination process. Keywords: Poultry chiller water; bacterial mutagens; chlorine disinfection byproducts; chlorinated imides

Glutathione and N-acetylcysteine inactivations of mutagenic 2(5H)-furanones from the chlorination of humics in water.

The mutagenic 2(5H)-furanones resulting from the chlorination of lignohumic substances in water disinfection and paper pulp bleaching are known to be inactivated by thiols. The objectives of the present study were to characterize the kinetics of an inactivating reaction, isolate and characterize products, and determine their mutagenicity in relation to the starting, mutagenic 2(5H)-furanones. The Salmonella typhimurium (TA100) mutagenicity of mucochloric acid (MCA) had a mean value of 2800 revertants/mumol from four assays and was twice as potent as the C-5 isopropyl ether of MCA (MCA-IPE), whose mutagenicity was determined in the same four assays. A second-order reaction of MCA with GSH at pH 7 was observed. The major product, making up 70% of the total product mixture, was identified as a 1.5:1 mixture of two diastereomers formed by sulfur displacement of the C-4 Cl atom from MCA. The major diastereomer was isolated from the 1.5:1 mixture. Connectivity of GSH to the MCA moiety in the product was established by 2D long-range coupling NMR and fully coupled 13C NMR. On the basis of circular dichroism, the major diastereomer had the S configuration at the hydroxyl-bearing, C-5 ring carbon. MCA-IPE reacted with GSH and N-acetylcysteine (NAC), giving 1:1 mixtures of two diastereomers, again by displacement of the C-4 Cl atom from MCA. A single diastereomer was isolated from the 1:1 MCA-IPE plus NAC reaction. Its structure, determined by X-ray crystallography, had the 5R,8R configuration and was in agreement with the ross structure deduced from the NMR analysis.(ABSTRACT TRUNCATED AT 250 WORDS)

Frontiers in Industrial Mycology

Production of speciality mushrooms in North America: shlitake and morels - T J Leonard and T J Volk Food fermentations: mucorales in ragi and related products - C W Hesseltine Genetic manipulation of beta/lactum antibiotic biosynthetic pathway - P L Skatrud, J Hoskins, J S Wood, M B Tobin, J R Miller, S Kovacevic, C A Cantwell and S W Queener New antibiotics - antifungals from Aspergillus - L D Boeck Heterologuous protein expression in filamentous fungi - S F Covert and D J Cullen Application of specific ectomycorrhizal fungi in world forestry - D H Marx, S B Maul and C E Cordell. Use of fungi in pulping wood: an overview of biopulping research - T K Kirk, R R Burgess and J W Koning, Jr Biological bleaching of kraft paper pulp - I D Reid and M G Paice White-rot fungi in the treatment of hazardous chemicals and wastes - R T Lamar, J A Glaser and T K Kirk Entomopathogenic fungi as bioinsecticides - D W Roberts and A E Hajek Role of production technology in mycoinsecticide development - C A Bradley, W E Black, R Kearnes and P Wood Principles in the development of biological control systems: employing Trichoderma species against soil-borne plant pathogenic fungi - X Jim, C K Hayes and G E Harman Bioherbicides - E E Trujillo.