Field of the invention The present invention relates to a method for producing cellulose carbamate (CCA) which can be further processed into regenerated cellulose products, such as fibers, films, or sponges, etc. More specifically, the present invention relates to an overall process for producing CCA from dissolving pulp (DP) and/or kraft pulp in a way that chemical pulp mill systems, steam, water, electricity, flue gas, wastewater treatment, and side streams of CCA production are utilized to improve the overall efficiency of whole process, and discharges of nitrogen compounds in the production of CCA are controlled.

Background of the invention

Cellulose carbamate (CCA) is an alkali-soluble cellulose derivative invented over 80 years ago. Due to alkali solubility properties, it is a good raw material for regenerated cellulose products.

CCA is manufactured by reacting cellulose with urea or urea radical at elevated temperatures. Typically, urea is used, and it reacts with cellulose according to reaction equations (1) and (2). In the carbamation reaction, urea starts to decompose when the temperature exceeds 133°C, and the intermediate products isocyanic acid and ammonia are formed, reaction equation (1). Isocyanic acid reacts further with OH-groups of cellulose by forming a carbamate group to the cellulose backbone (2). Ammonia gas, which is formed during cellulose carbamation, needs to be removed to prevent saturation of the product side of the reaction equation and to prevent the stopping of carbamation. Due to elevated temperature, the water is evaporated and the CCA thus formed is physically in solid form. It is a stable material which can be stored and transported. These properties make it an industrially viable product.

CCA can be manufactured from all types of chemical pulps, such as kraft pulp, pre-hydrolysis kraft pulp, soda-AQ pulp, sulfite pulp, neutral sulfite pulp, acid sulfite pulp or organosolv pulp. Common features in existing carbamate techniques are starting from dissolving pulp and pretreating of said pulp in order to activate it to reduce the DP ₀ (degree of polymerization). Usually the lowering of DP _o is done by mercerizing, by hydrolyzing with acidic or alkaline agent, by enzymes, by radiation, by catalysts and/or by mechanical means, such as milling.

US 2,134,825 discloses a process in which cellulose and urea are reacted at an elevated temperature to form an alkali-soluble product. US4404369 (FI 62318) discloses a method where an ammonia solution having urea dissolved therein is utilized and cellulose and urea are reacted at elevated temperatures to form an alkali-soluble product. WO03099872 discloses a process where cellulose is first activated with a mixture of urea and alkali, after which the liquid is pressed and the carbamation reaction is done at elevated temperatures by utilizing reactive extrusion equipment to form an alkali-soluble product. W02003064476 discloses a CCA production method where high process consistency and processing equipment are utilized, cellulose is pre-ground before mixing it with urea and a small amount of peroxide, and the mixture is reacted at elevated temperatures to form an alkali-soluble product. DE4443547 discloses a process for the preparation of cellulose carbamate by first hydrolyzing cellulose with hydrochloride acid in order to activate it before the carbamation reaction, after which it is reacted with urea at elevated temperatures to form an alkali-soluble product.

Dissolving pulp differs from the pulp intended for paper production. The production of dissolving pulp strives to create pulp with the highest possible cellulose concentration and the lowest possible concentration of hemicellulose, such as xylan, while striving to remove lignin from bleached paper pulp during the cooking and bleaching in such a way that as much cellulose and hemicellulose as possible remains in the paper pulp. In addition to the main component, cellulose - which is described as a-cellulose - paper pulp can contain up to 25% of hemicellulose, while dissolving pulp typically contains over 90% of ocellulose, and the amount of hemicellulose must be about under 5%.

The low hemicellulose concentration of dissolving pulp is typically sought by treat ing chips and/or pulp under strongly alkaline and acidic conditions. Dissolving pulp has conventionally been made either with a sulfite process or with a sulfate process equipped with acid prehydrolysis. If the sulfate process is used in the pro duction of dissolving pulp, before alkaline cooking, wood chips are typically subjected to prehydrolysis, where a significant amount of hemicellulose is removed under acidic conditions before the alkaline cooking. At the end of the fiberline, pulp is processed in bleaching stages similar to paper pulp, where the most important difference is the alkaline bleaching stages, which are carried out out at higher temperatures than in maximum yield-preserving bleaching. Furthermore, in order to produce viscose pulp, both sulfate cooking and sulfite cooking have typically cooked to a lower kappa than in paper pulp production. It is also known that in dissolving pulp production caustic extraction may be carried out after an acidic cooking process, or the chips are subjected an acid prehydrolysis stage at a high temperature and pressure before alkaline cooking. One preferred method for producing dissolving pulp is described in WO publication 2019170962. A chemical pulp mill is a closed process system where there exists a balance of certain elements, sodium and sulfur. Some inorganic elements, such as chlorine and potassium, enter process cycles with wood raw materials. They are removed when fly ash is taken away from the process balance. Due to the closed cycle, it is important to prevent or minimize the presence of non-process elements or totally new elements in pulp mill process cycles. Urea is needed when CCA is produced, and thus nitrogen is a new input to the process balance, and thus the amount of nitrogen needs to be minimized.

A major share of 99 million tons (62%) of the global fiber market is based on non renewable and non-biodegradable feedstock, known as synthetic textile fibers; 24.3% on cotton, which is non-ecological; and 6.6% on viscose, which is produced by using the hazardous chemical CS2 (carbon disulfide).

Viscose is the most commonly used method of producing cellulose-based regenerated fibers, and the viscose process that uses CS2 accounts for over 90% of the total volume of regenerated fibers. There are other methods that are used for products, such as Lyocell, produced with ionic liquids, which are more environmentally friendly but remain niche products due to their costs and chemical recovery challenges. CCA is an interesting alternative from current viscose fiber producers’ point of view due to minor changes in a viscose mill when moving to a carbamate process. The biggest advantage is that the CS2 chemical, which is harmful and toxic, is not used anymore, and thus the occupational health issues are much less crucial. The spinning system may be fully open, having no harmful and toxic CS2 gas emissions. Another big advantage is the higher spinning production capacity with current spinning equipment due to fast precipitation speed compared to viscose coagulation speed.

In view of the known processes, there is a need to develop an overall process concept, including a chemical pulp mill and a CCA manufacturing process for producing CCA to be used as a raw material for regenerated cellulose products. There is a particular need to provide an environmentally friendly arrangement for controlling harmful emissions and one new element in the process balance of a chemical pulp mill environment, nitrogen. Description of invention

It has surprisingly found that by integrating the cellulose carbamate production into a chemical pulp mill where dissolving pulp and/or Kraft pulp is produced, the benefits are greater from a technical and economical point of view when compared to any known solutions. The solution of the present invention is as defined in the appended claims.

In this application, the production of CCA is integrated into a chemical pulp mill where dissolving pulp and/or Kraft pulp is produced, in a such way that at least a portion of the chemicals used in the cellulose activation are produced by an integrated chemical recovery process of the pulp mill and discharges of nitrogen compounds in the production of CCA are controlled.

The CCA plant that produces CCA from dissolving pulp (DP) and/or kraft pulp with urea at an elevated temperature can be a process department at a chemical pulp mill. DP and/or kraft pulp is produced at the chemical pulp mill to be used in the CCA plant. Dissolving pulp and kraft pulp may be produced with the methods known in the art. The method typically comprises a pretreatment of cellulosic material, such as wood chips, cooking and bleaching.

The chemical pulp mill produces bleached fibrous cellulosic material. The fibrous cellulosic material may be derived from wood plant material, such as softwoods or hardwoods. It is also possible to use fibrous cellulosic material obtained from non wood lignocellulosic plant materials such as cotton, grass, bagasse, straws of grain crops, flax, hemp, sisal, abaca or bamboo.

The CCA plant, which produces CCA by reacting DP or kraft pulp with urea at an elevated temperature, can work with any known method which produces cellulose carbamate, but it is advantageous to use a method which does not use organic solvents or other chemicals foreign to the chemical pulp mill environment. CCA production methods that only use urea, or urea and sodium hydroxide and/or peroxide are the most suitable, because all the chemical residues or by-products can be utilized in the chemical pulp mill.

A required pre-treatment for the manufacturing of cellulose carbamate is the activation of the cellulose of dissolving pulp or kraft pulp. In the activation the degree of polymerization (DP ₀ ) is decreased. This can be carried out at a suitable stage of a chemical pulp mill fiberline, and/or at a separate stage between the chemical pulp mill fiberline and the CCA plant, and/or in the CCA plant. The activation, i.e. the decrease of the DP ₀ , can be performed according to different methods, which are suitable in the process environment of the chemical pulp mill. The activation may be carried out after the cooking or in connection with the bleaching at the chemical pulp mill. Advantageous activation methods are typically acid hydrolysis, alkali hydrolysis (merceration), ozone stage, peroxide treatment and peroxide addition in an oxygen stage.

A chemical pulp mill provides a CCA plant with process utilities, such as steam, electricity, and water, which are needed to manufacture cellulose carbamate.

The CCA plant can create waste streams from:

• CCA process carbamation reaction (ammonia)

• CCA process washing if washing of the product is needed (unreacted urea and by-products of carbamation) The present invention provides a method for the production of cellulose carbamate (CCA) from DP and/or kraft pulp and controlling discharges of nitrogen compounds in the production of cellulose carbamate, in which method dissolving pulp (DP) and/ or kraft pulp is produced at a chemical pulp mill, and the dissolving pulp and/or the kraft pulp are activated at the mill, at the CCA plant or between them. The activated DP or kraft pulp is reacted with urea to produce cellulose carbamate whereby ammonia is released. The cellulose carbamate production is integrated into the pulp mill having a flue gas system such that carbon dioxide from the flue gases is reacted with released ammonia to produce urea, which is used in the carbamate production.

The activation of dissolving pulp or kraft pulp, i.e. the decrease of DP ₀ , is done in the fiberline of the chemical pulp mill or at the CCA plant at the same time when CCA is manufactured. W02003064476 discloses a process for activating cellulose in the CCA manufacturing process. The activation of the dissolving pulp or the kraft pulp may be performed according to different methods, such as:

• acid hydrolysis, by using acid streams from the chemical pulp mill, such as sodium bisulfite, or fresh acid produced in a recovery cycle , e.g. H2S04 from sulfur-containing flue gases · alkali hydrolysis i.e. merceration, by using alkali streams from the chemical pulp mill

• ozone treatment and adjustment of the pulp pH, preferably with acid or alkali stream from the chemical pulp mill, or

• peroxide treatment in an 02-stage or at the CCA plant. Ammonia gas formed in the cellulose carbamation reaction is converted back to urea, to be used again in carbamation to minimize the CCA process chemical input, by using CO2, equations (3) and (4). A CO2 stream can be taken from the chemical pulp mill flue-gas system, especially from the lime kiln, and led to a CCA plant carbamation reactor, or to a separate process where urea is manufactured and reused in the CCA process. 2 l a;¾ ¾ l¾€C» f¾ (3)

Urea is produced by the reaction between ammonia and carbon dioxide (CO2). This is a two-step process, where the ammonia and carbon dioxide react to form ammonium carbamate, which is then dehydrated to urea. In the urea production process, ammonia and CO2 are introduced in gaseous form. Both components are liquefied in a high-pressure condenser and led to a high-pressure reactor, where ammonium carbamate is formed at an elevated temperature, e.g. 180— 190°C, reaction equation (5). This reaction is fast and exothermic.

An advantageous source of carbon dioxide is flue gases from a lime kiln, in which lime mud (CaCOs) is burnt to lime (CaO). The partial pressure of CO2 of lime kiln flue gases is higher than that of the flue gases of boilers, such as recovery boilers and power boilers, at the pulp mill, because the lime kiln flue gas includes CO2 from the combustion of fuel and also CO2 from the calcination reaction.

The nitrogen balance can be further controlled by using additional methods, if needed. Waste streams containing nitrogen compounds, such as unreacted urea, ammonia formed in carbamation reaction, thiourea or other by-products from the carbamation reaction, can be led fully or partly to a chemical pulp mill wastewater treatment plant, where they act as a nutrient source for micro-organisms, or to an anaerobic digestion system where biogas is produced. Another option is to lead nitrogen-containing waste streams fully or partly to an evaporation plant to produce dry fertilizers. With this process set-up, the amount of urea input to the CCA process can be minimized by utilizing unreacted residues.

Alkaline waste streams from the CCA plant, such as wastewater or ammonia gas, can be processed to the chemical pulp mill and used there to neutralize

• acidic hydrolysate from the dissolving pulp production (prehydrolysate),

• acidic washing filtrates from bleaching washers,

• acidic condensates from the evaporation plant, or

• other acidic process streams. These neutralized waste streams containing nitrogen can be further led to a chemical pulp mill wastewater treatment plant, where they act as a nutrient source for micro-organisms, or to anaerobic digestion to produce biogas.

Ammonia gas formed (reaction equation (1)) in a cellulose carbamation reaction can be utilized in the pulp mill flue-gas systems to minimize NOx emission, reaction equation (5) and (6). Ammonia can be in gaseous form or in dissolved solution form when utilized.

Carbon dioxide emissions are believed to be a major contributor to global warming. Consequently, it is advantageous to capture CO2 from flue gases of the pulp mill and utilize it as feedstock for urea.

Figure 1 is a schematic illustration of CCA production by integrating it into a chemical pulp mill where dissolving pulp or kraft pulp is produced.

The numbers and letters in FIG. 1 refer to the following streams and processing stages:

A. Chemical pulp mill

B. Cellulose carbamate (CCA) plant

1. Raw materials, chemical and process utilities needed to produce pulp

2. Cellulose carbamate

3. Urea

4. Dissolving pulp or kraft pulp

5. Slightly alkaline nitrogen-containing filtrate from CCA plant to neutralization, or to a wastewater treatment plant, or to an anaerobic digestion plant to biogas production at the pulp mill

6. Steam, water, electricity, and CO2 (urea recovery) from the pulp mill to the CCA production

7. Acidic or alkaline activation agent if the activation is done at the CCA plant

8. Ammonia to flue-gas systems to reduce NOx-emissions Raw material, such as wood chips, and chemicals, typically cooking chemicals, as well as process utilities are introduced (line 1) to a chemical pulp mill A, where dissolving pulp or kraft pulp is produced in a way known per se.

Dissolving pulp (DP) or kraft pulp is produced (line 4) at the chemical pulp mill in a way known per se. It is activated in the chemical pulp mill fiberline or at the CCA plant B.

A plant for a cellulose carbamate (CCA) production is integrated into the chemical pulp mill (line 6). CCA is produced by reacting a) activated DP or activated kraft pulp with urea at an elevated temperature. The dry matter content of DP or kraft pulp is about 40-90 %, and it is mixed efficiently with urea (from line 3), or b) DP or kraft pulp with urea (line 3) and with an activation agent (line 7) at an elevated temperature so that the activation of DP or kraft pulp is performed at the same time than CCA is produced. The dry matter content of DP or kraft pulp is about 40-90 %, and it is mixed efficiently with urea (from line 3) and with activation agent (line 7).

Then the final carbamation reaction is made in a steam-heated mixing reactor at a temperature of 130-160 °C. Ammonia is generated in the reaction. A small portion of the urea may not react, and it may be removed from the CCA product by washing. The CCA product is cooled, washed and dried, and then it is led to further processing (line 2).

Ammonia released from the carbamation process is scrubbed out of the reactor with steam and used to produce urea, which is recycled to the carbamation process. The amount of the urea supplied from an external source through line 3 can be decreased by producing urea internally. This is carried out by reacting ammonia with the carbon dioxide of flue gases from the pulp mill. An advantageous source for carbon dioxide is flue gases from a lime kiln, in which lime mud (CaCOs)is burnt to lime (CaO). The urea regeneration plant is preferably part of the CCA plant. Carbon dioxide is preferably captured from the flue gases. This can be performed by using conventional well-known methods, such as the monoethanolamine (MEA) absorption process and pressure swing adsorption (PSA) process. The urea production is a two-step process where the ammonia and carbon dioxide react to form ammonium carbamate, which is then dehydrated to urea. Ammonia and CO2 are introduced in gaseous form. Both components are liquefied in a high-pressure condenser and led to a high-pressure reactor where ammonium carbamate is formed at an elevated temperature, e.g. 180-190 °C, reaction equation (5). This reaction is fast and exothermic. The second reaction (6) is endothermic and does not go to completion. A solution comprising urea and ammonium carbamate is obtained. The ammonium carbamate present in the solution is decomposed to CO2 and NH ₃ in a recovery unit and recycled to the urea synthesis reactor. The urea process solution is led to the carbamation reactor.

A part of the released ammonia can be utilized also in pulp mill flue gas systems to minimize NOx emissions according to reaction equations (5) and (6). Ammonia can be in gaseous form or in dissolved form when it is led to the pulp mill (line 8). Slightly alkaline waste streams (line 5) comprising nitrogen compounds, such as unreacted urea, can be led fully or partly to a chemical pulp mill wastewater treatment plant. These waste streams can optionally or alternatively be led to an evaporation plant and produce dry fertilizers or to be led to biogas production or to be used as neutralizing agent to neutralize

• acidic hydrolysate from the dissolving pulp production (prehydrolysate),

• acidic washing filtrates from bleaching washers,

• acidic condensates from NCG gas condensation systems of the pulp mill evaporation plant, or

• other acidic process streams.

These neutralized waste streams containing nitrogen can be further led to a chemical pulp mill wastewater treatment plant, where they act as a nutrient source for micro-organisms, or to anaerobic digestion to produce biogas. The new method provides an efficient way to utilize available ammonia and carbon dioxide and thus control their emissions from the integrated CCA plant and pulp mill. The raw material, dissolving pulp or kraft pulp, is activated in the fiberline or at the CCA plant preferable by using chemicals produced by the pulp mill.