CN1190373C - 处理木质纤维素材料的方法 - Google Patents
处理木质纤维素材料的方法 Download PDFInfo
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- CN1190373C CN1190373C CNB018081150A CN01808115A CN1190373C CN 1190373 C CN1190373 C CN 1190373C CN B018081150 A CNB018081150 A CN B018081150A CN 01808115 A CN01808115 A CN 01808115A CN 1190373 C CN1190373 C CN 1190373C
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- reactor
- methane
- fermentation
- acid
- liquid
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- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 description 1
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- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 241001148470 aerobic bacillus Species 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
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- 229910052782 aluminium Inorganic materials 0.000 description 1
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- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
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- JYYOBHFYCIDXHH-UHFFFAOYSA-N carbonic acid;hydrate Chemical compound O.OC(O)=O JYYOBHFYCIDXHH-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
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- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 1
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- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical class [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 description 1
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- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
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- 150000002085 enols Chemical class 0.000 description 1
- 238000006911 enzymatic reaction Methods 0.000 description 1
- WIZOZORCIQKFQD-UHFFFAOYSA-N ethane methane Chemical compound C.C.C.C.C.C.CC WIZOZORCIQKFQD-UHFFFAOYSA-N 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
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- 150000002191 fatty alcohols Chemical class 0.000 description 1
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- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
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- 238000005194 fractionation Methods 0.000 description 1
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- 239000011121 hardwood Substances 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- SURQXAFEQWPFPV-UHFFFAOYSA-L iron(2+) sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Fe+2].[O-]S([O-])(=O)=O SURQXAFEQWPFPV-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 238000012417 linear regression Methods 0.000 description 1
- AGBQKNBQESQNJD-UHFFFAOYSA-N lipoic acid Chemical compound OC(=O)CCCCC1CCSS1 AGBQKNBQESQNJD-UHFFFAOYSA-N 0.000 description 1
- 239000006194 liquid suspension Substances 0.000 description 1
- 229940050906 magnesium chloride hexahydrate Drugs 0.000 description 1
- DHRRIBDTHFBPNG-UHFFFAOYSA-L magnesium dichloride hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-] DHRRIBDTHFBPNG-UHFFFAOYSA-L 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- CNFDGXZLMLFIJV-UHFFFAOYSA-L manganese(II) chloride tetrahydrate Chemical compound O.O.O.O.[Cl-].[Cl-].[Mn+2] CNFDGXZLMLFIJV-UHFFFAOYSA-L 0.000 description 1
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- 230000002906 microbiologic effect Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
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- 230000007935 neutral effect Effects 0.000 description 1
- QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- GTTYPHLDORACJW-UHFFFAOYSA-N nitric acid;sodium Chemical compound [Na].O[N+]([O-])=O GTTYPHLDORACJW-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen(.) Chemical compound [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
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- 230000000050 nutritive effect Effects 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- JJVNINGBHGBWJH-UHFFFAOYSA-N ortho-vanillin Chemical compound COC1=CC=CC(C=O)=C1O JJVNINGBHGBWJH-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 238000006213 oxygenation reaction Methods 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 150000007965 phenolic acids Chemical class 0.000 description 1
- 238000011020 pilot scale process Methods 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 235000007715 potassium iodide Nutrition 0.000 description 1
- 229960004839 potassium iodide Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
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- 229960002477 riboflavin Drugs 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 239000012898 sample dilution Substances 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000002444 silanisation Methods 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 229940001516 sodium nitrate Drugs 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- COBXDAOIDYGHGK-UHFFFAOYSA-N syringaldehyde Natural products COC1=CC=C(C=O)C(OC)=C1O COBXDAOIDYGHGK-UHFFFAOYSA-N 0.000 description 1
- 229960002663 thioctic acid Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
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- 150000004788 tropolones Chemical class 0.000 description 1
- 235000011912 vitamin B7 Nutrition 0.000 description 1
- 239000011735 vitamin B7 Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000009156 water cure Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
- 239000007218 ym medium Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P5/00—Preparation of hydrocarbons or halogenated hydrocarbons
- C12P5/02—Preparation of hydrocarbons or halogenated hydrocarbons acyclic
- C12P5/023—Methane
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F9/00—Multistage treatment of water, waste water or sewage
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/06—Ethanol, i.e. non-beverage
- C12P7/08—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate
- C12P7/10—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate substrate containing cellulosic material
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F11/00—Treatment of sludge; Devices therefor
- C02F11/06—Treatment of sludge; Devices therefor by oxidation
- C02F11/08—Wet air oxidation
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/28—Anaerobic digestion processes
- C02F3/286—Anaerobic digestion processes including two or more steps
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F3/00—Biological treatment of water, waste water, or sewage
- C02F3/34—Biological treatment of water, waste water, or sewage characterised by the microorganisms used
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P2201/00—Pretreatment of cellulosic or lignocellulosic material for subsequent enzymatic treatment or hydrolysis
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/10—Biological treatment of water, waste water, or sewage
Abstract
Description
整个糖类* | 31.8±0.5克/升 |
干燥物质 | 55.4±0.9克/升 |
有机质 | 44.5±0.9克/升 |
PH值 | 7.3±0.2 |
化学需氧量** | 61.4±1.6克/升 |
凯氏氮** | 0.12±0.01克/升 |
醋酸 | 2.0±0.1克/升 |
啤酒糖酵母的发酵 | 迈氏热厌氧杆菌A3M4的发酵 | 总量 | |||
克/升 | 总量百分比 | 克/升 | 总量百分比 | 克/升 | |
平均值 | 5.3±1.0 | 94% | 0.3±0.2 | 6% | 5.6±1.0 |
样本 | 取样时间 | 滞留时间 | 流量 | 入口COD含量 | 出口COD含量 | COD减少量 |
(天)* | (天) | (毫升/天) | (克/升) | (克/升) | (百分比w/w) | |
R1 | 76 | 2.0 | 100 | 27.2 | 4.5 | 84 |
R2 | 102 | 1.3 | 159 | 25.7 | 4.9 | 81 |
R3 | 107 | 1.0 | 200 | 26.7 | 5.7 | 79 |
R4 | 110 | 1.0 | 200 | 28.9 | 5.4 | 81 |
抑制物 | 入口(ppm) | 出口(ppm) | 减少量(%) |
2-呋喃甲酸 | 5.61 | 0.00 | 100 |
4-水杨醛 | 3.46 | 0.35 | 90 |
4-水杨酸 | 15.72 | 0.4 | 97 |
香草酸 | 60.74 | 0.62 | 99 |
高香草酸 | 25.08 | 0.69 | 97 |
丁香酸 | 45.53 | 0.00 | 100 |
丁香醇 | 7.43 | 0.96 | 87 |
乙酰香兰酮 | 5.40 | 1.13 | 79 |
乙酰丁兰酮 | 28.11 | 0.97 | 97 |
进料 | WSSE | WSWO | 单位 |
水解产物 | |||
水解产物中麦草的浓度 | 60 | 60 | 克/升 |
COD/TS-关系 | 1.1 | 1.1 | 克/升 |
预处理后TS的损失量 | 2% | 8% | 克/升 |
COD的转化程度 | 82% | 85% | 克/升 |
比甲烷产量 | 0.35 | 0.35 | 升-CH4/-COD |
麦草中半纤维素的含量 | 28% | 28% | 克/升 |
麦草中纤维素的含量 | 37% | 37% | 克/升 |
半纤维素的回收率 | 60% | 70% | 克/升 |
半纤维素的回收率 | 90% | 80% | 克/升 |
葡萄糖与纤维素的关系 | 1.11 | 1.11 | 克/升 |
木糖与半纤维素的关系 | 1.14 | 1.14 | 克/升 |
计算 | |||
葡萄糖产量 | 22.2 | 19.7 | 克/升 |
木糖产量 | 11.5 | 13.4 | 克/升 |
COD损失(转化为乙醇的糖类) | 36 | 35 | 克-COD/升 |
水解产物中的初始COD | 65 | 61 | 克-COD/升 |
用于生产甲烷的剩余COD | 29 | 25 | 克-COD/升 |
甲烷产量 | 8.28 | 7.58 | 升-CH4/升-水解产物 |
比甲烷产量 | 138 | 126 | 米3-CH4/吨-麦草 |
因子 | 参数 | 低水平 | 高水平 | 单位 |
A | 温度 | 185 | 195 | 摄氏度 |
B | 碳酸钠 | 6.5 | 2 | 克/升 |
C | 氧气 | 6 | 12 | ×105帕斯卡 |
D | 反应时间 | 10 | 15 | 分钟 |
起始物或反应物 | 温度:时间:氧气压力:碳酸钠: | 185摄氏度10分钟6×105帕斯卡6.5克/升 | 185摄氏度10分钟12×105帕斯卡2克/升 | 185摄氏度15分钟6×105帕斯卡2克/升 | 185摄氏度15分钟12×105帕斯卡6.5克/升 | 195摄氏度10分钟6×105帕斯卡2克/升 | 195摄氏度10分钟12×105帕斯卡6.5克/升 | 195摄氏度15分钟6×105帕斯卡6.5克/升 | 195摄氏度15分钟12×105帕斯卡2克/升 | 麦草 |
固体部分NCWM半纤维素木质素纤维素转化能力液体部分葡萄糖木糖阿拉伯糖总糖PH回收率半纤维素纤维素总量 | (克)(%w/w)(%w/w)(%w/w)(%w/w)(%w/w)(克/100克)(克/100克)(克/100克)(克/100克)-(%)(%)(%) | 31.713.913.88.461.853.73.68.72.014.37.759.294.379.2 | 38.217.120.08.053.538.14.36.31.311.94.769.6102.488.3 | 36.316.114.79.058.638.14.08.71.614.24.864.1105.787.8 | 30.514.710.44.867.562.12.99.62.314.86.056.599.781.2 | 36.218.612.39.758.039.33.810.21.515.54.763.6103.986.5 | 29.315.77.65.667.867.72.69.92.314.85.952.099.876.9 | 28.413.78.07.767.463.22.810.12.515.46.153.293.376.1 | 28.621.83.27.165.166.33.210.51.014.73.841.691.770.1 | 6025.127.98.737.014.1-----100100100 |
种类 | 化合物 | 温度:时间:氧气压力:碳酸钠: | 185摄氏度10分钟6×105帕斯卡6.5克/升 | 185摄氏度10分钟12×105帕斯卡2克/升 | 185摄氏度15分钟6×105帕斯卡2克/升 | 185摄氏度15分钟12×105帕斯卡6.5克/升 | 195摄氏度10分钟6×105帕斯卡2克/升 | 195摄氏度10分钟12×105帕斯卡6.5克/升 | 195摄氏度15分钟6×105帕斯卡6.5克/升 | 195摄氏度15分钟12×105帕斯卡2克/升 |
糖类酸类呋喃类酚类 | 葡萄糖木糖阿拉伯糖甲酸乙酸乙醇酸乳酸苹果酸柠檬酸草酸琥珀酸5-羟甲基糖醛2-糖醛2-呋喃甲酸酚愈创木酚丁香酚4-羟基苯甲醛香草醛丁香醛4-羟基苯乙酮加拿大麻素乙酸丁香酮4-羟基苯甲酸香草酸丁香酸p-香豆酸阿魏酸 | (克/100克)(克/100克)(克/100克)(克/100克)(克/100克)(克/100克)(克/100克)(克/100克)(克/100克)(克/100克)(克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克)(毫克/100克) | 3.568.712.042.191.920.490.430.100.070.030.830002171512712645135128 | 4.266.311.333.611.680.58n.d.a0.210.000.010.260331313559233740103912185 | 4.018.661.560.721.520.590.170.1900.010.240051623666354846637232412 | 2.879.582.327.122.571.51n.d.0.310.090.010.400053502215158311846865 | 3.7510.191.513.041.610.730.220.17000.25032619639745051056428282416 | 2.579.942.335.772.121.45n.d.0.270.030.010.38001151963554417156516112371817 | 2.8410.062.526.222.602.023.290.240.070.010.470075321325283614706404866 | 3.2310.510.986.452.271.16n.d.0.230.070.010.411513516285558969814661178461214 |
总量 | (克/100克) | 20.49 | 18.52 | 17.97 | 26.95 | 21.86 | 25.31 | 30.63 | 25.97 |
酚类mg/l | 啤酒糖酵母,起始时 | 啤酒糖酵母,结束时迈氏热厌氧杆菌,起始时 | 迈氏热厌氧杆菌,结束时,Ww-处理,起始时 | Ww-处理,结束时 |
酚 | 4.5 | 3.9 | 3.8 | 0.9 |
愈创木酚 | 8.5 | 8.0 | 8.2 | 0.0 |
丁香酚 | 2.3 | 2.8 | 3.6 | 0.0 |
4-羟基苯甲醛 | 13.7 | 0.9 | 0.6 | 0.0 |
香草醛 | 10.6 | 1.9 | 1.1 | 0.1 |
丁香醛 | 3.6 | 3.2 | 2.6 | 0.3 |
4-羟基苯乙酮 | 2.8 | 2.5 | 2.7 | 0.2 |
加拿大麻素 | 5.0 | 5.0 | 4.9 | 0.2 |
乙酸丁香酮 | 17.4 | 19.0 | 20.0 | 1.9 |
2-呋喃甲酸 | 7.2 | 6.2 | 6.5 | 0.0 |
4-羟基苯甲酸 | 23.7 | 22.8 | 26.0 | 0.0 |
香草酸 | 32.3 | 31.2 | 30.6 | 0.1 |
丁香酸 | 20.2 | 16.1 | 19.0 | 0.1 |
p-香豆酸 | 5.0 | 5.1 | 4.7 | 0.0 |
阿魏酸 | 2.1 | 3.4 | 3.0 | 0.2 |
总酚 | 158.8 | 131.9 | 137.4 | 4.0 |
乙酸 | 23.5 | 23.0 | 33.2 | 1.8 |
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ATE411971T1 (de) | 2008-11-15 |
US20020192774A1 (en) | 2002-12-19 |
CN1443141A (zh) | 2003-09-17 |
ES2315272T3 (es) | 2009-04-01 |
DE60136267D1 (de) | 2008-12-04 |
WO2001060752A1 (en) | 2001-08-23 |
EP1259466B1 (en) | 2008-10-22 |
EP1259466A1 (en) | 2002-11-27 |
DK1259466T3 (da) | 2009-01-05 |
CA2400336A1 (en) | 2001-08-23 |
US6555350B2 (en) | 2003-04-29 |
AU2001233621A1 (en) | 2001-08-27 |
CA2400336C (en) | 2010-04-27 |
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