Case studies on sugar production from underutilized woody biomass using sulfite chemistry

IF 0.6 4区 农林科学 Q4 MATERIALS SCIENCE, PAPER & WOOD Tappi Journal Pub Date : 2015-10-01 DOI:10.32964/TJ14.9.577
J. Zhu, M. S. Chandra, R. Gleisner, William Gilles, Johnway Gao, G. Marrs, Dwight Anderson, J. Sessions
{"title":"Case studies on sugar production from underutilized woody biomass using sulfite chemistry","authors":"J. Zhu, M. S. Chandra, R. Gleisner, William Gilles, Johnway Gao, G. Marrs, Dwight Anderson, J. Sessions","doi":"10.32964/TJ14.9.577","DOIUrl":null,"url":null,"abstract":"We examined two case studies to demonstrate the advantages of sulfite chemistry for pretreating underutilized woody biomass to produce sugars through enzymatic saccharification. In the first case study, we evaluated knot rejects from a magnesium-basedsulfite mill for direct enzymatic sugar production.We found that the sulfite mill rejects are an excellent feedstock for sugar production. In the second study, we presented SPORL (sulfite pretreatment to overcome the recalcitrance of lignocelluloses),a sulfite pretreatment process based on modified sulfite pulping for robust bioconversion of softwood forest residues. Sulfite pulping technology is well developed, with proven commercial scalability, and sulfite pretreatment is a strong contender for commercial adoption. woody biomass through enzymatic saccharification. Application: Mills can consider sulfite chemistry, which has the advantage of high-yield sugar production from roducing sugars from underutilized woody biomass for pretreating woody biomass for sugar production using Pcan be a potential revenue stream for pulp mills enzymes. Unlike pulping, where the goal is to achieve without competing with feedstock for pulp production. as much as delignification as possible while preserving To efficiently release sugar from woody biomass through hemicelluloses, pretreating biomass for sugar production enzymatic saccharification, a pretreatment step is does not need to achieve complete delignification required to remove the strong recalcitrance of wood but requires significant dissolution of hemicelluloses polymer matrix to biological deconstruction [1]. Several [8] to produce a porous substrate to improve cellulose chemical-including pulping processes have been studied accessibility to cellulase. The dissolution of hemicelluloses for pretreating woody biomass [2-6]. However, limited can also fractionate hemicelluloses into the form of successes were achieved in terms of good sugar yield. monomeric sugars, which is very desirable for biomass Sulfite chemistry has several unique characteristics that biorefining. The ability of delignification by sulfite under are considered disadvantages for pulping; for example, acidic conditions can facilitate hemicellulose dissolution at deploymerization of hemicelluloses often results in pulps high temperatures to reduce reaction time while partially with low strength and yield [7]. Furthermore, acidic or solubilizing and sulfonating lignin. Table I lists the utility bisulfite pulping requires low temperature and prolonged of the characteristics of sulfite chemistry for enzymatic time for delignification to avoid lignin condensation at saccharification of woody biomass by comparing with low pH. However, these disadvantages can be beneficial their effects on wood pulping [9-13]. SEPTEMBER 2015 I VOL. 14 NO. 9 I TAPPI JOURNAL 577 9 We have demonstrated the robust performance of sulfite pretreatment to overcome the recalcitrance of lignocelluloses (SPORL), based on modified sulfite pulping for ethanol production from a variety of woods including hybrid poplar and softwoods [9,14-17]. All these studies used pulp mill wood chips (i.e., competing feedstock with lumber and fiber productions). In this study we will demonstrate sulfite chemistry for high yield sugar production from two underutilized feedstocks, sulfite mill rejects and Douglas-fir harvest forest residue. Case study 1 was a study of glucose production from magnesium sulfite pulp mill rejects, and case study 2 was a study of high titer sugar production from Douglas-fir harvest forest residue by SPORL. A few studies have demonstrated that sulfite mill rejects are highly digestible for sugar production [18-20]. The main char­ acteristic of the present sulfite mill rejects was from magne­ sium sulfite pulping of softwood, different from ammonia sul­ fite pulping in previous studies. The metal base may affect enzyme activities for sugar production, which warrants the present study. Softwood forest residues are available in large quantities in the United States, but are highly recalcitrant to enzymatic saccharification due to high lignin content. Few studies reported sugar production from softwood forest resi­ due. Our previous study was conducted at a laboratory scale of 150 g ovendry (o.d.) forest residue [21]. We will demonstrate sulfite pretreatment at a pilot scale and using a sulfite solution prepared according to pulp mill practice; that is, bubbling sul­ fur dioxide (SO2) into a hydroxide solution instead of using commercial sodium bisulfite with sulfuric acids to adjust pH reported in all our previous studies [9,14-17,21]. In view of the mature technology for sulfite pulping, this study has practical importance, especially considering colo­ cating sugar production on kraft pulp mills for recovery chem­ icals as well as making use of underutilized woody biomass at pulp mills. MATERIALS AND METHODS Case study 1: Sulfite mill rejects Sulfite mill rejects were obtained from Cosmo Specialty Fibers Inc. (Cosmopolis, WA, USA). The mill produces high-grade dissolving pulp from softwood using magnesium sulfite with magnesium recovery. The rejects were unbleached reject knots with a typical particle size of 2 in. The collected rejects had a moisture content of approximately 70% and were shipped to the USDA Forest Service, Forest Products Labora­ tory (FPL), in Madison, WI, USA. Burning these rejects at the mill did not produce much heat due to the high moisture con­ tent (private communication with two sulfite mills). The asreceived rejects were then directly disk milled in a 12-in. laboratory disk refiner (Andritz Sprout-Bauer Atmospheric Refiner; Springfield, OH, USA) using two disks with plate pat­ tern DB2-505 at a disk plate gap of 1 mm, approximately 10 times larger than that used for typical mechanical pulping. The energy consumption for refining was minimal at approx­ imately 100 W-h/kg because of the large plate gap used. Case study 2: Douglas-fir harvest forest residue The Douglas-fir forest residue was from a regeneration harvest Douglas-fir stand in Lane County, OR, USA, and owned by Weyerhaeuser Co. Forest residue was chosen because of its lower cost than wood, and competing for feedstock with pulp and lumber production can be avoided. A horizontal drum fixed-hammer grinder (Model 4710B, Peterson Pacific Corp.; Eugene, OR, USA) equipped with a combination of 76and 102-mm grates was used to grind road piles of the residue (Fig. 1). The ground residue was shipped to Weyerhaeuser Co. at Federal Way, WA, USA, by truck. The moisture content of the residue measured at arrival was 43.9%. A gyratory screen (Black-Clawson; Middleton, OH, USA) equipped with a 44.5-mm (1.75-in.) diameter round-hole punched-plate top deck was used to remove oversized particles and a 3.2-mm (1/8-in.) clear-opening woven wire bottom screen (6 wires/ in. mesh) to remove fines. The oversize fraction was further hammer milled, which resulted in near zero oversized parti­ cles and 14.9% fines from the 9.8% original screen oversize fractions. The total rejection of fines was 9.0%. Fractionation through screening was found to selectively remove bark and ash [22,23]. The accept forest residue labeled as FS-10 was then air-dried to a moisture content of 15% before being shipped to the FPL. A sulfite pretreatment (SPORL) was applied to 61.75 kg FS-10 of 81.4% moisture using a pilot-scale rotating digester of 390 L [24]. A dilute sulfite solution was prepared by bubbling 3.3 kg SO2 at a gauge pressure of 34.5 kPa into a 139-L solution containing 1.25 kg (95% purity) calcium hydroxide. The resultant total SO, and calcium bisulfite charge on o.d. weight FS-10 was 6.6 wt% and 6.46 wt%, respectively. The FS-10 was steamed after loading into the digester to result in a final pretreatment liquor-to-o.d. wood ratio of 3.55:1 (L/kg). This gave an equivalent true combined SO, concentration in the cooking liquor of 1.15 wt% and true free SO, concentration of 0.68 wt%. These SO, loadings are significantly lower than the approximately 8 wt% total SO, (at liquor-to-wood ratio of 4:1) typically used in sulfite pulp mills, or a reduction of 80%. To accommodate facility limitations at sulfite mills, the pretreatment temperature was conducted to 145°C, slightly higher than typical sulfite pulping temperature. It took ap­ proximately 37 min for the 390-L digester to be heated to T = 145°C using a steam jacket. The temperature was main­ tained for another 240 min to result in an effective pretreat­ ment duration, tT145, approximately within the calculated time of 225-270 min based on optimal pretreatment condition of T = 180°C for tT180 = 25-30 min [9], as in Eq. (1):","PeriodicalId":22255,"journal":{"name":"Tappi Journal","volume":null,"pages":null},"PeriodicalIF":0.6000,"publicationDate":"2015-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tappi Journal","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.32964/TJ14.9.577","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MATERIALS SCIENCE, PAPER & WOOD","Score":null,"Total":0}
引用次数: 7

Abstract

We examined two case studies to demonstrate the advantages of sulfite chemistry for pretreating underutilized woody biomass to produce sugars through enzymatic saccharification. In the first case study, we evaluated knot rejects from a magnesium-basedsulfite mill for direct enzymatic sugar production.We found that the sulfite mill rejects are an excellent feedstock for sugar production. In the second study, we presented SPORL (sulfite pretreatment to overcome the recalcitrance of lignocelluloses),a sulfite pretreatment process based on modified sulfite pulping for robust bioconversion of softwood forest residues. Sulfite pulping technology is well developed, with proven commercial scalability, and sulfite pretreatment is a strong contender for commercial adoption. woody biomass through enzymatic saccharification. Application: Mills can consider sulfite chemistry, which has the advantage of high-yield sugar production from roducing sugars from underutilized woody biomass for pretreating woody biomass for sugar production using Pcan be a potential revenue stream for pulp mills enzymes. Unlike pulping, where the goal is to achieve without competing with feedstock for pulp production. as much as delignification as possible while preserving To efficiently release sugar from woody biomass through hemicelluloses, pretreating biomass for sugar production enzymatic saccharification, a pretreatment step is does not need to achieve complete delignification required to remove the strong recalcitrance of wood but requires significant dissolution of hemicelluloses polymer matrix to biological deconstruction [1]. Several [8] to produce a porous substrate to improve cellulose chemical-including pulping processes have been studied accessibility to cellulase. The dissolution of hemicelluloses for pretreating woody biomass [2-6]. However, limited can also fractionate hemicelluloses into the form of successes were achieved in terms of good sugar yield. monomeric sugars, which is very desirable for biomass Sulfite chemistry has several unique characteristics that biorefining. The ability of delignification by sulfite under are considered disadvantages for pulping; for example, acidic conditions can facilitate hemicellulose dissolution at deploymerization of hemicelluloses often results in pulps high temperatures to reduce reaction time while partially with low strength and yield [7]. Furthermore, acidic or solubilizing and sulfonating lignin. Table I lists the utility bisulfite pulping requires low temperature and prolonged of the characteristics of sulfite chemistry for enzymatic time for delignification to avoid lignin condensation at saccharification of woody biomass by comparing with low pH. However, these disadvantages can be beneficial their effects on wood pulping [9-13]. SEPTEMBER 2015 I VOL. 14 NO. 9 I TAPPI JOURNAL 577 9 We have demonstrated the robust performance of sulfite pretreatment to overcome the recalcitrance of lignocelluloses (SPORL), based on modified sulfite pulping for ethanol production from a variety of woods including hybrid poplar and softwoods [9,14-17]. All these studies used pulp mill wood chips (i.e., competing feedstock with lumber and fiber productions). In this study we will demonstrate sulfite chemistry for high yield sugar production from two underutilized feedstocks, sulfite mill rejects and Douglas-fir harvest forest residue. Case study 1 was a study of glucose production from magnesium sulfite pulp mill rejects, and case study 2 was a study of high titer sugar production from Douglas-fir harvest forest residue by SPORL. A few studies have demonstrated that sulfite mill rejects are highly digestible for sugar production [18-20]. The main char­ acteristic of the present sulfite mill rejects was from magne­ sium sulfite pulping of softwood, different from ammonia sul­ fite pulping in previous studies. The metal base may affect enzyme activities for sugar production, which warrants the present study. Softwood forest residues are available in large quantities in the United States, but are highly recalcitrant to enzymatic saccharification due to high lignin content. Few studies reported sugar production from softwood forest resi­ due. Our previous study was conducted at a laboratory scale of 150 g ovendry (o.d.) forest residue [21]. We will demonstrate sulfite pretreatment at a pilot scale and using a sulfite solution prepared according to pulp mill practice; that is, bubbling sul­ fur dioxide (SO2) into a hydroxide solution instead of using commercial sodium bisulfite with sulfuric acids to adjust pH reported in all our previous studies [9,14-17,21]. In view of the mature technology for sulfite pulping, this study has practical importance, especially considering colo­ cating sugar production on kraft pulp mills for recovery chem­ icals as well as making use of underutilized woody biomass at pulp mills. MATERIALS AND METHODS Case study 1: Sulfite mill rejects Sulfite mill rejects were obtained from Cosmo Specialty Fibers Inc. (Cosmopolis, WA, USA). The mill produces high-grade dissolving pulp from softwood using magnesium sulfite with magnesium recovery. The rejects were unbleached reject knots with a typical particle size of 2 in. The collected rejects had a moisture content of approximately 70% and were shipped to the USDA Forest Service, Forest Products Labora­ tory (FPL), in Madison, WI, USA. Burning these rejects at the mill did not produce much heat due to the high moisture con­ tent (private communication with two sulfite mills). The asreceived rejects were then directly disk milled in a 12-in. laboratory disk refiner (Andritz Sprout-Bauer Atmospheric Refiner; Springfield, OH, USA) using two disks with plate pat­ tern DB2-505 at a disk plate gap of 1 mm, approximately 10 times larger than that used for typical mechanical pulping. The energy consumption for refining was minimal at approx­ imately 100 W-h/kg because of the large plate gap used. Case study 2: Douglas-fir harvest forest residue The Douglas-fir forest residue was from a regeneration harvest Douglas-fir stand in Lane County, OR, USA, and owned by Weyerhaeuser Co. Forest residue was chosen because of its lower cost than wood, and competing for feedstock with pulp and lumber production can be avoided. A horizontal drum fixed-hammer grinder (Model 4710B, Peterson Pacific Corp.; Eugene, OR, USA) equipped with a combination of 76and 102-mm grates was used to grind road piles of the residue (Fig. 1). The ground residue was shipped to Weyerhaeuser Co. at Federal Way, WA, USA, by truck. The moisture content of the residue measured at arrival was 43.9%. A gyratory screen (Black-Clawson; Middleton, OH, USA) equipped with a 44.5-mm (1.75-in.) diameter round-hole punched-plate top deck was used to remove oversized particles and a 3.2-mm (1/8-in.) clear-opening woven wire bottom screen (6 wires/ in. mesh) to remove fines. The oversize fraction was further hammer milled, which resulted in near zero oversized parti­ cles and 14.9% fines from the 9.8% original screen oversize fractions. The total rejection of fines was 9.0%. Fractionation through screening was found to selectively remove bark and ash [22,23]. The accept forest residue labeled as FS-10 was then air-dried to a moisture content of 15% before being shipped to the FPL. A sulfite pretreatment (SPORL) was applied to 61.75 kg FS-10 of 81.4% moisture using a pilot-scale rotating digester of 390 L [24]. A dilute sulfite solution was prepared by bubbling 3.3 kg SO2 at a gauge pressure of 34.5 kPa into a 139-L solution containing 1.25 kg (95% purity) calcium hydroxide. The resultant total SO, and calcium bisulfite charge on o.d. weight FS-10 was 6.6 wt% and 6.46 wt%, respectively. The FS-10 was steamed after loading into the digester to result in a final pretreatment liquor-to-o.d. wood ratio of 3.55:1 (L/kg). This gave an equivalent true combined SO, concentration in the cooking liquor of 1.15 wt% and true free SO, concentration of 0.68 wt%. These SO, loadings are significantly lower than the approximately 8 wt% total SO, (at liquor-to-wood ratio of 4:1) typically used in sulfite pulp mills, or a reduction of 80%. To accommodate facility limitations at sulfite mills, the pretreatment temperature was conducted to 145°C, slightly higher than typical sulfite pulping temperature. It took ap­ proximately 37 min for the 390-L digester to be heated to T = 145°C using a steam jacket. The temperature was main­ tained for another 240 min to result in an effective pretreat­ ment duration, tT145, approximately within the calculated time of 225-270 min based on optimal pretreatment condition of T = 180°C for tT180 = 25-30 min [9], as in Eq. (1):
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用亚硫酸盐化学从未充分利用的木质生物质中制糖的案例研究
我们研究了两个案例研究,以证明亚硫酸盐化学在预处理未充分利用的木质生物质通过酶糖化生产糖方面的优势。在第一个案例研究中,我们评估了镁基亚硫酸盐厂用于直接酶促糖生产的结渣。我们发现亚硫酸盐废渣是一种优良的制糖原料。在第二项研究中,我们提出了SPORL(亚硫酸盐预处理以克服木质纤维素的顽固性),这是一种基于改性亚硫酸盐纸浆的亚硫酸盐预处理工艺,用于软木林残留物的强大生物转化。亚硫酸盐制浆技术发展良好,具有成熟的商业可扩展性,亚硫酸盐预处理是商业应用的有力竞争者。通过酶糖化的木质生物质。应用:工厂可以考虑亚硫酸盐化学,它的优点是通过从未充分利用的木质生物质中生产糖来高产糖,因为使用Pcan预处理木质生物质用于制糖是纸浆工厂酶的潜在收入来源。与纸浆不同,纸浆的目标是在不与原料竞争的情况下实现纸浆生产。为了通过半纤维素有效地从木质生物质中释放糖,预处理生物质用于制糖的酶解糖化,预处理步骤不需要达到去除木材强顽固性所需的完全脱木质素,而是需要大量溶解半纤维素聚合物基质进行生物解构。研究了几种制备多孔底物以改善纤维素化学制浆过程的方法,包括纤维素酶的可及性。半纤维素的溶解预处理木质生物质[2-6]。然而,有限的半纤维素也可以分馏成成功的形式,在良好的糖产量方面取得了成功。亚硫酸盐化学中非常理想的单体糖具有几个独特的特点,可以进行生物精制。亚硫酸盐脱木质素的能力被认为是制浆的缺点;例如,酸性条件可以促进半纤维素的溶解,在半纤维素的展开过程中,通常会导致纸浆温度升高,以减少反应时间,而部分纸浆强度低,收率低。此外,酸性或增溶磺化木质素。表1列出了亚硫酸盐制浆的效用,与低ph相比,亚硫酸盐制浆需要较低的温度和较长的亚硫酸盐化学特性来进行脱木质素的酶促时间,以避免木质生物质糖化时木质素的缩聚。然而,这些缺点对木材制浆的影响是有益的[9-13]。2015年9月I卷14期我们已经证明了亚硫酸盐预处理在克服木质纤维素(SPORL)的顽固性方面的强大性能,基于改性亚硫酸盐制浆,从各种木材(包括杂交杨树和软木)中生产乙醇[9,14-17]。所有这些研究都使用纸浆厂的木屑(即与木材和纤维产品竞争的原料)。在这项研究中,我们将展示亚硫酸盐化学对两种未充分利用的原料的高产糖生产,亚硫酸盐厂废渣和道格拉斯冷杉采伐森林残留物。案例研究1是利用亚硫酸镁纸浆厂废渣生产葡萄糖的研究,案例研究2是利用SPORL利用道格拉斯冷杉采伐林渣生产高滴度糖的研究。一些研究表明,亚硫酸盐磨渣对制糖具有高度可消化性[18-20]。与以往研究的硫酸铵制浆不同,亚硫酸镁制浆废渣的主要特征是针叶木材的亚硫酸盐废渣。金属碱可能会影响糖生产酶的活性,这是值得研究的。在美国,针叶林残留物大量可用,但由于木质素含量高,对酶糖化具有很强的抗性。很少有研究报道软木林残渣制糖。我们以前的研究是在实验室规模150 g (od)森林残留物[21]进行的。我们将在中试规模上演示亚硫酸盐预处理,并使用根据纸浆厂实践制备的亚硫酸盐溶液;即将二氧化硫(SO2)冒泡到氢氧化物溶液中,而不是使用商业亚硫酸钠和硫酸来调节pH值,我们之前的研究都有报道[9,14-17,21]。鉴于亚硫酸盐制浆技术的成熟,本研究具有重要的现实意义,特别是考虑到硫酸盐纸浆厂的染色制糖以回收化学物质以及利用纸浆厂未充分利用的木质生物质。 我们研究了两个案例研究,以证明亚硫酸盐化学在预处理未充分利用的木质生物质通过酶糖化生产糖方面的优势。在第一个案例研究中,我们评估了镁基亚硫酸盐厂用于直接酶促糖生产的结渣。我们发现亚硫酸盐废渣是一种优良的制糖原料。在第二项研究中,我们提出了SPORL(亚硫酸盐预处理以克服木质纤维素的顽固性),这是一种基于改性亚硫酸盐纸浆的亚硫酸盐预处理工艺,用于软木林残留物的强大生物转化。亚硫酸盐制浆技术发展良好,具有成熟的商业可扩展性,亚硫酸盐预处理是商业应用的有力竞争者。通过酶糖化的木质生物质。应用:工厂可以考虑亚硫酸盐化学,它的优点是通过从未充分利用的木质生物质中生产糖来高产糖,因为使用Pcan预处理木质生物质用于制糖是纸浆工厂酶的潜在收入来源。与纸浆不同,纸浆的目标是在不与原料竞争的情况下实现纸浆生产。为了通过半纤维素有效地从木质生物质中释放糖,预处理生物质用于制糖的酶解糖化,预处理步骤不需要达到去除木材强顽固性所需的完全脱木质素,而是需要大量溶解半纤维素聚合物基质进行生物解构。研究了几种制备多孔底物以改善纤维素化学制浆过程的方法,包括纤维素酶的可及性。半纤维素的溶解预处理木质生物质[2-6]。然而,有限的半纤维素也可以分馏成成功的形式,在良好的糖产量方面取得了成功。亚硫酸盐化学中非常理想的单体糖具有几个独特的特点,可以进行生物精制。亚硫酸盐脱木质素的能力被认为是制浆的缺点;例如,酸性条件可以促进半纤维素的溶解,在半纤维素的展开过程中,通常会导致纸浆温度升高,以减少反应时间,而部分纸浆强度低,收率低。此外,酸性或增溶磺化木质素。表1列出了亚硫酸盐制浆的效用,与低ph相比,亚硫酸盐制浆需要较低的温度和较长的亚硫酸盐化学特性来进行脱木质素的酶促时间,以避免木质生物质糖化时木质素的缩聚。然而,这些缺点对木材制浆的影响是有益的[9-13]。2015年9月I卷14期我们已经证明了亚硫酸盐预处理在克服木质纤维素(SPORL)的顽固性方面的强大性能,基于改性亚硫酸盐制浆,从各种木材(包括杂交杨树和软木)中生产乙醇[9,14-17]。所有这些研究都使用纸浆厂的木屑(即与木材和纤维产品竞争的原料)。在这项研究中,我们将展示亚硫酸盐化学对两种未充分利用的原料的高产糖生产,亚硫酸盐厂废渣和道格拉斯冷杉采伐森林残留物。案例研究1是利用亚硫酸镁纸浆厂废渣生产葡萄糖的研究,案例研究2是利用SPORL利用道格拉斯冷杉采伐林渣生产高滴度糖的研究。一些研究表明,亚硫酸盐磨渣对制糖具有高度可消化性[18-20]。与以往研究的硫酸铵制浆不同,亚硫酸镁制浆废渣的主要特征是针叶木材的亚硫酸盐废渣。金属碱可能会影响糖生产酶的活性,这是值得研究的。在美国,针叶林残留物大量可用,但由于木质素含量高,对酶糖化具有很强的抗性。很少有研究报道软木林残渣制糖。我们以前的研究是在实验室规模150 g (od)森林残留物[21]进行的。我们将在中试规模上演示亚硫酸盐预处理,并使用根据纸浆厂实践制备的亚硫酸盐溶液;即将二氧化硫(SO2)冒泡到氢氧化物溶液中,而不是使用商业亚硫酸钠和硫酸来调节pH值,我们之前的研究都有报道[9,14-17,21]。鉴于亚硫酸盐制浆技术的成熟,本研究具有重要的现实意义,特别是考虑到硫酸盐纸浆厂的染色制糖以回收化学物质以及利用纸浆厂未充分利用的木质生物质。 材料和方法案例研究1:亚硫酸盐磨废渣亚硫酸盐磨废渣来自Cosmo特种纤维公司(cosmopolitan, WA, USA)。该工厂采用亚硫酸镁和镁回收技术,以软木为原料生产高档溶解纸浆。废品为未漂白的废品结,典型粒径为2英寸。收集的次品含水量约为70%,并被运往美国威斯康星州麦迪逊市的美国农业部林业局林产品实验室(FPL)。由于高含水率(与两个亚硫酸盐工厂的私人通信),在工厂燃烧这些废渣不会产生太多热量。然后,将收到的次品直接在12英寸的钻头中进行圆盘铣削。实验室盘式精炼机(Andritz sproutt - bauer大气精炼机;Springfield, OH, USA)使用两个圆盘,其板型为DB2-505,盘板间隙为1mm,约为典型机械制浆的10倍。由于使用了大的板间隙,精炼的能耗最小,约为100 W-h/kg。道格拉斯杉木林渣来自美国俄勒冈州莱恩县道格拉斯杉木林分的再生收获,为惠好公司所有。选择道格拉斯杉木林渣是因为它比木材成本低,可以避免与纸浆和木材生产竞争原料。卧式滚筒定锤磨床(4710B型,Peterson Pacific Corp.;Eugene, OR, USA)配备了76和102毫米的组合格栅,用于研磨残渣的道路桩(图1)。地面残渣用卡车运往位于美国华盛顿州联邦大道的Weyerhaeuser Co.。到达时测得的残渣水分含量为43.9%。旋转屏幕(布莱克-克劳森;Middleton, OH, USA)配备了直径44.5 mm (1.75 in)的圆孔冲孔板顶部甲板,用于去除超大颗粒,以及3.2 mm (1/8 in)的透明编织丝底部筛网(6丝/ in)。网)去除细粒。对超细颗粒进行进一步的锤磨,使原始筛分超细颗粒的9.8%变为近零的超细颗粒和14.9%的细颗粒。罚款总拒收率为9.0%。通过筛选进行分馏可以选择性地去除树皮和灰分[22,23]。然后将标记为FS-10的接受森林残留物风干至水分含量为15%,然后运往FPL。在390l[24]的中试旋转消化器上,对61.75 kg FS-10进行了亚硫酸盐预处理(SPORL),含水率为81.4%。在表压34.5 kPa下,将3.3 kg SO2泡入含有1.25 kg(95%纯度)氢氧化钙的139 l溶液中,制得稀亚硫酸盐溶液。得到的总so6和亚硫酸钙电荷在od重量FS-10上分别为6.6%和6.46%。FS-10在装载到消化器后进行蒸煮,以进行最后的预处理。木材比为3.55:1 (L/kg)。由此得出,蒸煮液中真正的组合SO浓度为1.15 wt%,真正的游离SO浓度为0.68 wt%。这些SO的负荷量明显低于通常用于亚硫酸盐纸浆厂的总SO的约8 wt%(在酒木比为4:1时),或减少80%。为了适应亚硫酸盐厂的设备限制,预处理温度为145℃,略高于典型的亚硫酸盐制浆温度。使用蒸汽夹套将390-L蒸煮器加热到T = 145°C大约需要37分钟。再保持温度240 min,使有效预处理时间tT145大致在根据tT180 = 25-30 min[9]的最佳预处理条件T = 180℃计算的225-270 min时间内,如式(1)所示: 材料和方法案例研究1:亚硫酸盐磨废渣亚硫酸盐磨废渣来自Cosmo特种纤维公司(cosmopolitan, WA, USA)。该工厂采用亚硫酸镁和镁回收技术,以软木为原料生产高档溶解纸浆。废品为未漂白的废品结,典型粒径为2英寸。收集的次品含水量约为70%,并被运往美国威斯康星州麦迪逊市的美国农业部林业局林产品实验室(FPL)。由于高含水率(与两个亚硫酸盐工厂的私人通信),在工厂燃烧这些废渣不会产生太多热量。然后,将收到的次品直接在12英寸的钻头中进行圆盘铣削。实验室盘式精炼机(Andritz sproutt - bauer大气精炼机;Springfield, OH, USA)使用两个圆盘,其板型为DB2-505,盘板间隙为1mm,约为典型机械制浆的10倍。由于使用了大的板间隙,精炼的能耗最小,约为100 W-h/kg。道格拉斯杉木林渣来自美国俄勒冈州莱恩县道格拉斯杉木林分的再生收获,为惠好公司所有。选择道格拉斯杉木林渣是因为它比木材成本低,可以避免与纸浆和木材生产竞争原料。卧式滚筒定锤磨床(4710B型,Peterson Pacific Corp.;Eugene, OR, USA)配备了76和102毫米的组合格栅,用于研磨残渣的道路桩(图1)。地面残渣用卡车运往位于美国华盛顿州联邦大道的Weyerhaeuser Co.。到达时测得的残渣水分含量为43.9%。旋转屏幕(布莱克-克劳森;Middleton, OH, USA)配备了直径44.5 mm (1.75 in)的圆孔冲孔板顶部甲板,用于去除超大颗粒,以及3.2 mm (1/8 in)的透明编织丝底部筛网(6丝/ in)。网)去除细粒。对超细颗粒进行进一步的锤磨,使原始筛分超细颗粒的9.8%变为近零的超细颗粒和14.9%的细颗粒。罚款总拒收率为9.0%。通过筛选进行分馏可以选择性地去除树皮和灰分[22,23]。然后将标记为FS-10的接受森林残留物风干至水分含量为15%,然后运往FPL。在390l[24]的中试旋转消化器上,对61.75 kg FS-10进行了亚硫酸盐预处理(SPORL),含水率为81.4%。在表压34.5 kPa下,将3.3 kg SO2泡入含有1.25 kg(95%纯度)氢氧化钙的139 l溶液中,制得稀亚硫酸盐溶液。得到的总so6和亚硫酸钙电荷在od重量FS-10上分别为6.6%和6.46%。FS-10在装载到消化器后进行蒸煮,以进行最后的预处理。木材比为3.55:1 (L/kg)。由此得出,蒸煮液中真正的组合SO浓度为1.15 wt%,真正的游离SO浓度为0.68 wt%。这些SO的负荷量明显低于通常用于亚硫酸盐纸浆厂的总SO的约8 wt%(在酒木比为4:1时),或减少80%。为了适应亚硫酸盐厂的设备限制,预处理温度为145℃,略高于典型的亚硫酸盐制浆温度。使用蒸汽夹套将390-L蒸煮器加热到T = 145°C大约需要37分钟。再保持温度240 min,使有效预处理时间tT145大致在根据tT180 = 25-30 min[9]的最佳预处理条件T = 180℃计算的225-270 min时间内,如式(1)所示:
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Tappi Journal
Tappi Journal 工程技术-材料科学:纸与木材
CiteScore
1.30
自引率
16.70%
发文量
59
审稿时长
6-12 weeks
期刊介绍: An internationally recognized technical publication for over 60 years, TAPPI Journal (TJ) publishes the latest and most relevant research on the forest products and related industries. A stringent peer-review process and distinguished editorial board of academic and industry experts set TAPPI Journal apart as a reliable source for impactful basic and applied research and technical reviews. Available at no charge to TAPPI members, each issue of TAPPI Journal features research in pulp, paper, packaging, tissue, nonwovens, converting, bioenergy, nanotechnology or other innovative cellulosic-based products and technologies. Publishing in TAPPI Journal delivers your research to a global audience of colleagues, peers and employers.
期刊最新文献
Rice straw-based sustainable food packaging material with improved strength and barrier properties: Development and characterization Kraft pulp viscosity as a predictor of paper strength: Its uses and abuses Using bleaching stage models for benchmarking hardwood ECF bleach plants Pulp and paper mills: The original biorefineries — past performance and limitations to future opportunities Cross-flow separation characteristics and piloting of graphene oxide nanofiltration membrane sheets and tubes for kraft black liquor concentration
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1