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Introduction

Increasing global consumption and the threat of anthropogenic climate change put

pressure on the global society to increase resource efficiency and reduce CO

2

emissions.

Current production of primary silicon and ferrosilicon alloys are characterized by high

energy requirements and significant emission of climate gases. Elkem consumes

roughly 12 TWh of energy (electricity and carbon based reductants combined) and

emits an estimated 1.3 MT of CO

2

annually. In an effort to dramatically improve on

these numbers, Elkem has proclaimed its ambitions to develop a novel silicon and

ferrosilicon production process with the prospect of major reductions in overall energy

consumption and close to zero CO

2

emissions from fossil carbon sources.

The novelty of the process lies in the direct integration between the silicon production

process and a charcoal production facility, thereby enabling an additional reduction in

energy consumption and CO

2

emissions. In combination with an energy recovery

facility, the energy recovery factor of the total system will far outweigh that of

conventional silicon-furnace heat recovery systems. The integrated charcoal, metal and

energy recovery process has been termed

Carbon Neutral Metal Production

(CNMP

for short). The integration with charcoal production introduces by-products that are

novel to the conventional silicon production process; gases and condensate from

pyrolysis, bark, and fines from biomass and charcoal handling. Consequently, this

requires a new heat recovery system, boilers, handling, and more. There are also

uncertainties coupled to the charcoal production, such as identifying process conditions

for charcoal production in order to fulfil satisfactory specifications, as well as

understanding how process conditions affect mass and energy distribution between the

two by-products (gas and condensate).

Charcoal production is a subject that has been studied for centuries or millennia and

several reviews are available on the topic [1-6]. The distinction between fast and slow

pyrolysis refers to the heating rate of the fuel. Slow pyrolysis, is typically conducted at

heating rates ranging from 1-5 °C/min, whilst during fast pyrolysis the heating rates are

in the 100-1000 °C/s range. The heating rate is the most important factor influencing

the yield of liquids; increased heating rate results in increased yield of liquids. The

upper liquid yield limit is around 75 % on mass basis [7]. In order to obtain such high

yields, a short vapour residence time (in the literature a vapour residence time of less

than 2 s seems to be the generally agreed upon number) is necessary since the pyrolysis

vapours react through secondary reactions and form gases and additional char through

polymerization. If charcoal is of interest, prolonging the vapour residence time has

showed to be positive in regards of charcoal yield since this promotes secondary, char

forming reactions. This can be accomplished by limiting the amount of purge gas or by

using large particles or thick beds thus introducing a mass transfer limitation from the

biomass to the gas phase. The coupling to soak time (hold time) at maximum process

temperature here becomes analogous; i.e. if the pyrolysis vapours are allowed to react

with the charcoal for longer period of time more will be converted through secondary

reaction to gas and additional charcoal [8, 9]. Fixed carbon content increases rapidly

and roughly linearly with pyrolysis temperature from 300 to 400 °C (fixed carbon

content 20-70 %) and then slows down reaching a maximum value at around 90 % at

800 °C [10] provided that sufficient residence time is given for the fuel particles.

In preceding work, it was identified early on that the carbonization technology needs to

be integrated with existing infrastructure used in the silicon production process in order

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