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By Rudolf Keller

In the electrolysis of neodymium oxide from a molten fluoride electrolyte, anode effects may occur at the carbon anodes, interfering with smooth cell operation. In laboratory experiments, we attempted to circumvent this problem by selecting electrolytes with a high oxide concentration, possibly at relatively low rare earth content, but cathodic deposition was not satisfactory. A regime at higher cell voltage was discovered to yield good cell performance, but evolution of considerable amounts of fluorocarbon compounds suggested that a reactive treatment of the off-gases would be necessary for environmental acceptability. Subsequent experimentation at low cell voltage revealed conditions for satisfactory operation without occurrence of anode effects and without formation of any CF4 or C2F8.

Jan 1, 1997

By Y. W. Miao

Along the south-west coast of Taiwan is about 550,000 metric tons of heavy sand deposit containing about 10 % black monazite. The Institute has developed a separation process to recover the individual rare earths and the developed process has been commercialized by a local private company. The decomposition of the local black monazite by sodium hydroxide through hydrothermal and fusion methods has been investigated. In the hydrothermal process 4.5 wt. % of aqueous alkali solution was used in an autoclave. In the fusion process, caustic soda (9.8% NaOH) was employed in am open cylindrical reactor. The same product of hydrous rare earth oxides were obtained and then dissolved by hydrochloric acid and the p-H adjusted in order to separate the thorium from the rare earths. After filtration, the filtrate contained rare earth chloride and the cake contained mainly the silica and thorium hydroxide. Both methods give a yield of 90 % with respect to the rare earths recovery. A detailed description of operation and comparison of the two methods are given.

Jan 1, 1989

By Ejike Emmanuel, Nwoye Chukwuka, Ogwuegbu Martin, Asuwaji Ayuk, Onyedika Gerald

"Microwave pre-treatment of cassiterite ore prior to leaching was carried out in an attempt to obtain high grade of Sn02 and to conserve the total energy expended during processing. Microwave treatment was selected due to the presence of associated minerals which behaves differently to microwave energy. Studies in this work showed that microwave pretreatment of cassiterite ore can be applied to increase the recovery of tin oxide within 5 minutes of leaching. Microwave treatment of the ore resulted in mineral liberation at all particle sizes. Tin oxide was separated from the major impurities via leaching in potassium hydroxide solution and precipitation, resulting in 98% Sn02 at pH 7.IntroductionIn the nineties, the available techniques used for ore processing and analysis in Nigeria was the solution methods of either alkaline fusion or acid digestion [1,2]. A process in which cassiterite is made acid soluble by reduction to SnO2 , which stabilizes by glass formation and the tin was extracted by leaching the glass with sulphuric acid, followed by electrowinning was reported [3,4]. In another study, Baba et al [5] studied the dissolution kinetics of a Nigerian casiterite ore in hydrochloric acid solution. The effects of acid concentration,temperature, particle size and stirring speed were examined. It was found that the dissolution rates of cassiterite depends on hydrogen ion concentration, H+, stirring speed and ore particle dimensions. These were believed to report low data due to incomplete solubilization of the ore minerals in aqeous medium [6]. Analytical chemists have used microwave heating devices routinely for the dissolution of metals, minerals and various chemical products in chemical analysis [7,8]. It offers faster heating rate and consequently faster dissolution rate than conventional heating. The principle of the dissolution of analytical samples has been applied to the leaching of various minerals contained in an ore or concentrate sample. Some researchers [9, 10] conducted microwave assisted leaching of laterite ores containing oxides of nickel, cobalt, and iron. The metals of these mineral components were converted into their chlorides by microwave heating (1200 W, 2450 MHz, Nz atmosphere) a mixture of the ore and ammonium chloride between l 77°C and 312° C for 4-5 min, followed by water leaching at 80° C for 30 min. Nickel and cobalt extractions were 70% and 85%, and respectively, and are comparable with roasting at 300°C in a conventional rotary kiln for 2 hours."

Jan 1, 2013

By Lidong Teng, Seshadri Seetharaman, Aida Abbasalizadeh

0In the present paper, the feasibility of the recovery of dysprosium from spent Nd-Fe- B magnets containing approximately 9 wt% Dy was investigated by using molten salt process. The salt bath consisted of a mixture of NaCl-KCl-LiCl corresponding to the ternary eutectic composition. AlCl3 was used as a chlorinating agent in order to enable an efficient dissolution of metal in the molten salt phase in the salt bath. The metal chloride which is formed as the result of chemical reaction between the metal in magnet and AlCl3, is subsequently subjected to electrolysis in order to be deposited on the cathode. Graphite rods were dipped in the salt bath as electrodes and alumina crucibles were used as the containers for the electrolytic cells.

Jan 1, 2014

By Tobias Pröll, Bernhard Kronberger, Joachim Rohovec, Werner Hölt, Hermann Hofbauer

"As this is only a first draft, more precise explanations as well as detailed schemes, figures and plots will be included in the final draft. The description og the 100 kW test rig will also be mor detailed as construction is ongoing and will be finished during the summer. Furthermore simulations are to be finished shortly; so details on combustibles and gas concentrations will also be included in the final draft.AbstractOxyFuel combustion is a key technology for the efficient separation of CO2 from fuel combus¬tion (especially coal). Since coal plays a minor role in the Austrian energy mix the application of OxyFuel towards other fuels (biomass, waste fuels) is interesting to reduce greenhouse gas emissions from Austrian energy sector. The investigation of OxyFuel technology for alter¬native fuels is also interesting from a strategic point of view in order to generate knowledge for operation of capture ready cofiring and waste/sludge-incineration plants. OxyFuel uses a synthetic mixture of 02 and recycled exhaust gas where the 02 content may vary. This supplementary degree of freedom allows improved operation especially for low calorific fuels. Heavy fuel oil addition for low calorific combustibles can be omitted when using OxyFuel combustion. Application of alternative fuels (wood, waste wood, municipal waste, sewage sludge) in a 100-kW CFB plant is investigated in combination with process simulation.IntroductionOxyFuel combustion is discussed as one of the key technologies for the efficient separation of CO2 from combustion of fossil fuels (especially coal). Since coal plays only a minor role as primary energy source in Austria, the broadening of the scope towards OxyFuel of other fuels like biomass or waste fuels is necessary to reduce greenhouse gas emissions from Austrian energy sector. The investigation of OxyFuel technology for alternative fuels besides the large coal-oriented projects is interesting also from the strategic point of view. The presented project aims at the generation of knowledge in order to design and operate capture ready cofiring and waste/sludge incineration plants."

Jan 1, 2008

By Haldun Kurama, Cenk Karakurt, Ilker Bekir Topçu

"The usage of binders or pozzolanic materials in the production of concrete is not new. However, in recent years, the use of the pozzolanic siliceous material such as natural zeolite and coal combustion ash (CBA) has received re-attention due to the generated considerable interest in the economical use of both naturally occurring raw materials, recycling of the waste material and saved energy. In this study, the potential and utilization opportunities of natural zeolites and bottom ash (BA) in concrete applications were reviewed. Case studies, conducted to determine the possible usage of the natural zeolite and BA in concrete production, i.e. light weight concrete (LWC) were also presented. The physical and mechanical properties of cured concretes were examined to find out the competitive material usage on the final product properties. Autoclaved aerated concrete (AAC) with 1.1 nm tobermorite (5CaO 6SiO2 5H2O) as binder is a lightweight construction material that mainly uses in place of concrete to manufacture various building materials, including blocks, panels, slabs and the like. The material is a mixture of sand, lime, cement, gypsum, water and an expanding agent, which causes the raw material to rise like bread dough, with countless small air pores. AAC can be molded and cut into precisely dimensioned units and cured in an autoclave, which steam cures the concrete under pressure. During this process, the ingredients combine to form the calcium silicate hydrate gels that establish the special properties of the finished product. The process produces a material that is only one-fourth to one-third the weight of a conventional concrete block (bulk density of 400-800 kg /m3) of the same size. Regular AAC offers considerable advantages over other construction materials such as high thermal and sound insulation, excellent fire resistance, high resource and energy efficiency, low environmental impact, and finally outstanding structural performance (especially for earthquake zones) [1]. Its lightweight also makes it easy to use during construction, and its aerated structure gives it better thermal insulation and sound absorption properties than conventional concrete."

Jan 1, 2008

By Xiping Chen, Wangxing Li, Jiemi Zhou

"Desulfurization methods suitable for anode-grade petroleum coke (coke for short) used in primary aluminum industry are coke desulfurization during calcination, desulfurization in soakage and desulfurization in mediums. Coke desulfurization during calcination is discussed in this paper. Influences of calcination temperature, holding time and coke granularity on coke desulfurization were discussed. Experimental results show that calcination temperature has a remarkable influence on coke desulfurization. When the temperature is high enough desulfurization ratio of coke can reach 85% only by calcination. Holding time has a definite influence on coke desulfurization, but desulfurization ratio is low at the temperature of 900~1300°C. The influence of holding time is obvious when calcination temperature surpasses 1400°C. The influence of coke granularity is smaller compared with calcination temperature and holding time.IntroductionPetroleum coke is main raw material for carbon anode in primary aluminum industry, and its weight percentage in carbon anode is about seven percent. Green coke can not be directly used for anode production because of its immanent moisture and volatiles. Green coke must be calcined in order to meet the request of anode production. Calcination is a heat-treatment process during which green coke is heated to a given temperature to remove volatiles, moisture and some sulfur. Real density, strength, electrical conductivity and anti-oxidation ability of petroleum coke can be improved by calcination and calcined coke can be received [1, 3, 4]. Sulfur in calcined coke finally goes into carbon anode. During baking or aluminum smelting, the sulfur in anode ultimately changes into SO2 and emits from anode into the atmosphere. Excess SO2 easily leads to acid rain which brings heavy pollution to the environment [1, 2]. With the development of Chinese aluminum industry, consumption of anode-grade petroleum coke increases year by year, the total consumption in 2007 surpassed 4.5 million tones and the yearly emission of SO2 from aluminum smelters has exceeded 270 kilotones. From 2005 Chinese government began to limit the emission of SO2 from primary aluminum industry, so desulfurization of anode-grade petroleum coke becomes more and more urgent. Some relationship need to be found and used to guide desulfurization of petroleum coke."

Jan 1, 2008

By V. V. Kutumbarao, M. T. Nimje, G. Balasubramanian

Wastes from the aluminium industry such as red mud from the alumina refinery, fly ash from the captive power plant and spent pot lining from the smelter, have been successfully converted into glass-ceramic products. The process involves addition of a small quantity of glass former along with traces of nucleating agents to aid crystallization, to a specific mixture ofred mud, fly ash and spent pot lining, followed by melting at around 1300°C and vitrification by cooling. The resultant glass is then converted into a glass- ceramic by a suitable heat treatment at around 700 - 750°C. The glass-ceramic products show excellent wear resistance, besides possessing an aesthetic appearance. The major application foreseen for such products is as decorative tiles in the building industry.

Jan 1, 2000

By Jr. Pomykala, B. J. Jody, E. J. Daniels

Each year, about five (5) million ton of shredder residues are landfilled in the United States. ·Similar quantities are landfilled in Europe and the Pacific Rim. Landfilling of these residues results in a cost to the existing recycling industry and also represents a loss of material resources that are otherwise recyclable. In this paper, we outline the resources recoverable from typical shredder residues and describe technology that we have developed to recover these resources.

Jan 1, 2000

By Daniel Helm

The first industrial application of direct solvent extraction of nickel from hypersaline sulfate feed solutions has highlighted the need to investigate the influence of chloride on the extraction behaviour nickel in the presence of calcium using Versatic 10 and the solubility characteristics of gypsum. Temperature-solubility curves for gypsum in various aqueous electrolytes were prepared. The solubility of gypsum is increased significantly by the presence of sulfate ions, while chloride ions decrease it for a given temperature. The anion effects of chloride and sulfate on the extraction of calcium and nickel by Versatic 10 corresponded well with the complexing ability of the anions. It was shown that the presence of chloride shifts the extraction isotherms for both metals significantly to the left, while decreasing the selectivity of Versatic 10 for nickel over calcium. The loading of nickel onto Versatic 10 in this system was shown to be at a maximum within 3 seconds, while calcium extraction took between 4 ? 5 seconds to load to a maximum. Chloride ions had no influence on loading kinetics of nickel, but depressed the rate of calcium loading. It was shown that in the presence of an excess of nickel, calcium loading is effectively eliminated, and that calcium is scrubbed from Versatic 10 within 2.5 seconds of contact with nickel electrolyte.

Jan 1, 2003

By M. Cassir

"The unique properties of molten carbonates offer a large scope of applications in the field of energy. In effect, these molten salts are in the center of chemical and electrochemical reactions involving carbon and carbonaceous species, carbon dioxide and carbon monoxide, significant for energy generation or even for the production of fuels. Moreover, such media have also an oxidative character; they dissolve molecular oxygen and oxygen reduced species, O 2-, O22- and hypothetically o-, which may have an important role in waste treatments, homogeneous catalysis and synthesis of oxides. In this presentation, an overview will be given on the principal physicochemical properties of molten carbonates, before focusing on their main known application, the molten carbonate fuel cell (MCFC). Progress in other new fuel cells applications will also be analyzed, such as direct carbon fuel cell (DCFC), hybrid carbon fuel cell (HDCFC) and composite high-temperature fuel cells combining the features of MCFC and solid oxide fuel cell (SOFC). Afterwards, membranes for the separation and capture of C02 will be reviewed. Finally, other topics, as the oxidative coupling of methane in molten carbonates, will be briefly mentioned.IntroductionIn the thirty past years, the molten carbonate science and advances have been mainly dedicated to the understanding and optimization of the molten carbonate fuel cell (MCFC), which is still a major issue in the heart of a new vision of energy development. More recently, new topics related to other kinds of fuel cells (DCFC, composite SOFC/MCFC systems) and C02 capture have emerged and are concentrating important research and technological efforts. Moreover, new fields of implementation, related to molten carbonates, are also present: geology, glasses, production of nanocarbon particles etc. Considering other areas where this molten phase plays a major role, such as catalysis, waste destruction, surface treatment, it can be confirmed that the field of molten carbonates is very rich and offers many opportunities for fundamental science and competitive applications. Whatever their specific application, molten carbonates activity is associated to more efficient energy systems with low production of C02 and, in a prospective sense, to non-polluting energy using the value of C02. A recent event, the International Workshop on Molten Carbonates & Related Topics, IWMC201 I, held in Paris in 2011 , have put in evidence the importance to improve and exploit this investigation and technological domain."

Jan 1, 2012

By Sunil Jayasekera

This paper describes the results of a study carried out to examine the feasibility of electrolytic recovery of silver from cyanide leach liquor generated from a Western Australian silver mine tailings using a novel high mass transfer electrowinning cell. The proposed circuit involves heap leaching and electrowinning in a closed loop. The filter-press-like closed electrode arrangement of the cell allowed much improved mass transfer of metal ions to the cathode surface, making direct electrowinning of metals from dilute solutions feasible. The tests were conducted both in the laboratory and at large scale using a prototype with ~1.0 m2 cathode area. The results showed that the recovery of silver from as low as 250 mg L-1tenor was feasible. The silver deposit produced with the prototype cell was non-adherent and powdery and could be readily removed from the closed cell. A system was developed so that silver powder was discharged continuously during the run.

Jan 1, 2003

By Uday Pal

In direct reduction processes for iron and steel making, significant amounts of Fe-C alloy droplets are generated and these remain suspended in relatively low FeO (around 5%) containing slags. Earlier workers have found that when the FeO content in the slag is <5%, the decarburization reaction becomes extremely slow (virtually ceases to occur) even though the alloy droplet contains a significant amount of carbons (2-3%). Understanding this rate controlling kinetic phenomena is crucial to designing an&apos; optimum direct steel making process. We studied decarburization of Fe-C particles by low FeO (<5%) containing CaO-SiO2A12O3 slags and found that by putting both the droplet and the slag in direct contact with an inert electronically conductive member that extends deep inside the slag bulk were able to quickly and completely decarburize the droplets. A detailed description and an explanation of the process will be presented.

Jan 1, 1995

By V. G. Papangelakis

The implementation of a flow-through yttria-stabilized zirconia (YSZ) sensor for pH measurements in high temperature and concentrated electrolyte systems relevant to hydrometallurgical processing of nickeliferous laterites is discussed. Instrumentation involved the use of a custom made flow-through titanium electrochemical cell. Accuracy and validity of the pH measurements at temperatures up to 250C were assessed using concentrated sulphate process solutions ranging from synthetic binary sulphuric acid ? water solutions to progressively multicomponent metal ? sulphate solutions simulating laterite Pressure Acid Leach conditions. The measurements were also compared with theoretical models using recently obtained thermodynamic data. A difference of ±0.25 pH units was observed between measured and calculated pH values at temperatures. This is an acceptable difference given that these are the first direct high temperature pH measurements ever on the concentrated acidic sulphate solutions. This result is encouraging more research for the development of industrial electrochemical systems for direct pH measurements in autoclaves.

Jan 1, 2003

By Tong Deng

Clean processing of copper converter slags for reclaiming cobalt and copper could be a challenge. An innovative and environmentally benign approach for recovering metal values from such a slag was developed in the present work. Curing the slag with sulfuric acid, without re-smelting or roasting as currently practiced in the industry, made it amenable to leaching, and more than 95% of the cobalt and up to 90% of the copper was extracted, together with iron, by water leaching, leaving silica behind in a residue. Copper in the leach liquor was recovered by cementation with iron, and the dissolved iron crystallized as ferrous sulfate monohydrate. Cobalt in the pregnant solution rich in iron was recovered by either cementation or sulfide precipitation. Chemical and mineralogical characterization of the slag and its products were examined and compared to determine the nature of the changes occurring during curing and leaching. Operating variables were also investigated and optimized.

Jan 1, 2003

By M. H. Ghandehari

Sintered (Pr,Sm)Co5 displays a multi-phase microstructure in which closely related intermetallic compounds are formed during the process of fabricating useful magnets from over-stoichiornetric compositions. These compounds have much lower magnetic crystalline anisotropies compared to those of SmCo5 and PrCo5. Despite a careful control of the microstructure in producing "single phase" PrCo5 base magnets, sufficient concentrations of the lower anisotropy phases are formed which act as nucleation centers for domain reversal, resulting in a drop in coercivity. This article describes the use of sintering additives, primarily oxides, to prevent the formation of the magnetically soft phases in the final microstructure.

Jan 1, 1989

By Alice Barreto Bevitori, Frederico Muylaert Margem, Renan Sopeletto Carreiro, Sergio Neves Monteiro, Isabela Leão Amaral da Silva

"The ramie fiber is one of the strongest lignocellulosic fibers with applications ranging from simple items such as fabrics and ropes to engineering composites for automobile parts and building panels. Characterization of the ramie fiber has recently been conducted for physical and mechanical properties. In principle, thinner ramie fiber could be comparatively stronger and consequently more effective as a composite reinforcement. In this work an attempt to correlate the ramie fiber elastic modulus obtained in tensile test with its corresponding diameter, precisely measured by means of a profile projector, was carried out. Tensile results analyzed by the Weibul1 statistic showed a significant increase in elastic modulus with decreasing the diameter of ramie fiber. Scanning electron microscopy observation of the fracture of selected ruptured fiber revealed possible mechanisms that could justify the elastic modulus/diameter inverse dependence.IntroductionEngineering applications of natural fibers obtained from cellulose-rich plants, also known as lignocellulosic fibers, are currently being the focus of attention. In fact, they are considered an enviromnental1y correct alternative to substitute synthetic fibers such as the glass fiber, associated with an intensive intake of energy during production, as reinforcement of polymer composites [1-4]. In recent years there has been a growing tendency towards the use of lignocellulosic fiber composites in several industrial sectors from civil constructions to car making. In particular, the automotive industry is expanding the number of both interior and exterior components made of natural fiber composites [5]."

Jan 1, 2012

By M. Sripathy, K. V. Sharmal

"The conventional fiber reinforced plastic does not participate in the plastic deformation or enter the large plastic deformation state during collision. On the other hand, sandwich structure allows more plastic deformation, which improves the energy absorption efficiency. The objective of this study is focused on the investigation of the crushing of sandwich structure made from sisal / coir / bamboo/ glass fabrics as reinforcement and with polyester resin to form the composites skin and with polyurethane foam as the core. Experiments were conducted, showing that the underlying crushing mechanism of sandwich structures is very different from that of solid-section thin-walled structures. When a sandwich is subjected to crushing, the core deforms in the shear mode and the face bends independently. The damage is through the width zone of crushed foam core accompanied by a residual crushing in the foam. It is shown that such damage causes a significant reduction of compressive strength. Results show that glass/polyester and bamboo/polyester skin based sandwich structures have superior compressive strength. Coir /polyester based sandwich structure come next to glass/polyester sandwich structures in this aspect which is then followed by Sisal /polyester based sandwich structures.IntroductionCellular polymeric foam sandwich structures are often employed in shock mitigating applications. The cellular polymeric foam has several favorable properties, such as, low density, relatively high strength-to weight ratio and a significant degree of crushability. This high crushability is the result of the large void ratio in such materials, which also facilitates the collapse of cell walls via bending and buckling [1]. A few feasibility studies on FRP sandwich panels show that the panels efficiently provided high mechanical performance for minimum weight [2]."

Jan 1, 2012

By D. F. Liub, Z. Y. Liu, W. Y. Xue, Y. F. Shenb, Y. D. Wang

"The microstructure characteristics and deformation behavior of ultrafme grained (UFO) 304SS fabricated by accumulative rolling and armealing have been investigated by means of tensile tests, electron-backscatter-diffraction (EBSD) and transmission electron microscopy (TEM) techniques. The volume fraction of martensite phase decreases with increasing armealing temperature. In the grain sizes ranging from 300 nm to 10 µm, the strength held Hall-Petch relationship. The sample with an average grain size of 300 nm exhibited extra high yield strength of 1700 MPa and a tensile strength of 1780 MPa, while the elongation retains 12%. The limited uniform elongation in the UFO materials could be explained in terms of plastic instability. Very interestingly, for the bulk material with an average grain size of 1.200 µm, the high yield strength and uniform elongation were simultaneously achieved to be as 1000 MPa and 18%, respectively.IntroductionUltra-high strengths have been achieved in elemental metals by employing heavy plastic deformation, or by creating ultra-fine-grained (UFO) structure. Here UFO materials are defined as polycrystalline solids with property-controlling microstructural features below the 1 µm level. Typical processing routes include severe plastic deformation (SPD) [1, 2], which decomposes the grains through dislocation accumulation and reorganization (polygonization). Several different kinds of SPD process for bulk materials are typically as equal-charmel angular pressing (ECAP) [3], high-pressure torsion (HPT) [4] and accumulative roll-bonding (ARB) [5]. One of the main motivations for such a push for the very small grain sizes stems from the expectation of unprecedented mechanical strength, as predicted by the well-known Hall-Petch relationship that projects a continuous rise of strength with decreasing grain size [6]. However, these ultra-high strength metals no longer have the high ductility typical of their conventional coarse-grained counterparts, because the undesirable inhomogeneous deformation on the microstructure level can lead to the early onset of failure, severely limiting the useful ductility [2]. Recently, the interesting strategies have been performed to increasing simultaneously the ductility and strength ofUFG pure copper and nanostructured alloys by Zhao et al [7, 8]. In a pure copper, a high ductility has been achieved without sacrificing strength by introducing a high density of pre-existing twins and a large fraction of high-angle grain boundaries. Their encouraging results trigger our motivation to obtain high strength and ductility from the commercially bulk material."

Jan 1, 2013

By Wellington Pereira Inácio, Frederico Muylaert Margem, Artur Camposo Pereira, Sergio Neves

"Natural fibers are currently gaining attention as reinforcement of polymer composites for uses in engineering parts for automobile and building construction. In spite of environmental, economical and societal advantages, the natural lignocellulosic fibers are not as uniform in their dimension and properties as compared to synthetic. In recent works it was found that the variation in strength could be correlate to the equivalent diameters for several lignocellulosic fibers including the sisal fibers. In the present work an investigation on a possible correlation of the equivalent diameter with changes in density and elastic modulus was carried out. Precise measurements of the equivalent diameter, conducted in a profile projector, were correlated with the density and the elastic modulus by means of the Weibull statistic analysis. The results showed that an inverse correlation with the diameter also applies for both the density and the elastic modulus with a high degree of precision. SEM observation of the sisal fiber in structure and fracture aspects strongly indicate that defects and microfibril participation could be responsible for the inverse correlation.IntroductionAccording to Kalia [1], cellulose-based fibers are currently being pushed owing to their ""green"" image. Contrary to synthetic glass fiber, extensively used in our modem technology, these lignocellulosic fibers are renewable and can be incinerated at the end of the material's lifetime without adding pollution in the atmosphere moreover, the amount of CO2 released during incineration process is negligible as compared to the corresponding amount taken up by the plant throughout its lifetime. Even if an industrial processing equivalent of C02 release is added, the lignocellulosic fiber is considered neutral with respect to the emission of gases responsible for the global warming [2]."

Jan 1, 2012