SEQUENTIAL SUBCRITICAL WATER EXTRACTION FOR RICE HUSK VALORIZATION, OBTAINING BIOACTIVE XYLANS AND CELLULOSE NANOCRYSTALS

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SEQUENTIAL SUBCRITICAL WATER EXTRACTION FOR RICE HUSK VALORIZATION, OBTAINING BIOACTIVE XYLANS AND CELLULOSE NANOCRYSTALS SHORT TERM SCIENTIFIC MISSION (STSM) Raquel Requena Peris Riga, 5 June Insitute of Food Engineering for Development Universitat Politècnica de València

THE INSTITUTIONS Duration: 01/09/2017 30/11/2017 Hosting Institution: Division of Glycoscience and Wallenberg Wood Science Center KTH Royal Institute of Technology Stockholm, Sweden. Home institution: Institute of Food Engineering for Development Universitat Politècnica de València Valencia, Spain

JUSTIFICATION Rice husks (RH) By-product from the food industry Hemicellulose fraction (20-30%) made up of substituted arabinoxylan (AX) with potential food, medical, and pharmaceutical applications. High cellulose content (30-40%) for producing cellulose nanocrystals (CNCs). Integral valorization 1) Sequential subcritical water extraction (SWE) 2) Alkali extraction AX: Bioactive compounds CNC: Reinforcement materials Food Packaging Materials Environmental friendly Preserve the molecular functionalities of the isolated hemicellulose fractions

EXPERIMENTAL DESIGN Alkali extracts (E-A) 1 st 2 nd 3 rd ALKALI PROCESS Lignin CNC-A Mill Alkali Treatments Alkali residue (R-A) Bleaching Treatments Bleached alkali residue (R-A-B) Acid Hydrolysis & Purification Raw Rice husk 20 mesh Rice husk HYDROTHERMAL PROCESS Subcritical water extraction (SWE) 5 15 30 60 SWE extracts (E-SWE) SWE residue (R-SWE) Bleaching Treatments Lignin Bleached SWE residue (R-SWE-B) Acid Hydrolysis & Purification CNC-SWE

WORKING PLAN Pretreatment: Wiley Mill ISOLATION OF THE HEMICELLULOSES Lower particle size improves the extraction Particle size: 20 mesh. A) Subcritical water extraction Sequential fractionation of hemicelluloses at different times: 5, 15, 30 and 60 min. 160 o C, deionised water Dionex ASE 350 B) Alkali extraction 4 wt% in NaOH (4.5 w/v) 80 ºC; 2h 3 different treatments Dialysis of the resulting extracts ISOLATION OF THE CNCS Bleaching 4 wt% in 1water:1buffer acetate: 1aqueous chlorite (1.7%) 5 different treatments at 80 ºC; 4h Acid Hydrolysis 4 wt% in 65 wt% sulphuric acid 45 ºc; 40 min. CNC purification 1. Successive centrifugations: until constant supernatant ph; 25000 g; 20 min 2. Dialysis: purified water 1 week 3. Sonication: 10 min; 7,125 W/ml 4. Centrifugation: remove higher particles Freeze-dry extracts and residues

WORKING PLAN CHARACTERIZATION OF THE RESIDUES Chemical composition analyses Soxhlet extraction NREL s LAP Klason lignin. Tappi method T222 om-06 Ash content TGA Monosaccharide composition Acid hydrolysis and HPAEC-PAD Scanning Electron Microscopy (SEM) Atomic Force Microscopy (AFM) Fourier Transform Infrared Spectrometry (FTIR) X-Ray Diffraction Analysis (XRD) Thermogravimetric Analysis (TGA)

WORKING PLAN CHARACTERIZATION OF THE EXTRACTS Monosaccharide composition Acid hydrolysis and HPAEC-PAD Molar mass distribution Size-Exclusion Chromatography Antioxidant activity. DPPH scavenging activity Antibacterial activity. MTT assay NAD H NAD + DPPH (ox) DPPH (red) MTT Formazan

RESULTS. Morphological changes of the residues Untreated rice husk Untreated rice husk Alkaline residue Bleached residue Alkaline residue Bleached residue SWE residue Bleached SWE residue Figure 1. Visual aspect of the samples after the different treatments SWE residue Bleached SWE residue Figure 2. SEM of the samples after the different treatments

RESULTS. Chemical composition of the residues Table 1. Yield and chemical composition (in %wt) after the different steps of the isolation of cellulose nanocrystals from rice husk Rice Husk Alkali process Hydrothermal process Alkaline Bleaching Hydrolysis SWE Bleaching Hydrolysis Yield a 100 54.4±0.1 65±2 69±1 58±1 Fuc <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 Ara 1.8±0.1 2.16±0.03 1.35±0.05 <0.1 0.4±0.1 0.4±0.1 <0.1 Rha <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 Gal 0.9±0.2 0.69±0.02 0.20±0.03 <0.1 <0.1 <0.1 <0.1 Glc 35.1±0.4 60±2 73.5±0.1 96±5 41±1 60±2 95±6 Xyl 17±1 12.2±0.2 17.0±0.4 1.0±0.1 11.1±0.2 15±3 <0.1 Man <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 GalA <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 GlcA <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 Total 55±1 75±2 92.0±0.2 96±5 53±1 60±2 95±6 carbohydrates Cellulose 35.1±0.4 60±2 73.5±0.1 96±5 41±1 60±2 95±6 Hemicellulose 19±2 15.0±0.2 18.4±0.3 1.0±0.1 11.6±0.2 15±3 <0.1 Klason lignin 33.8 20.5 9.0 N/A 39.5 25.0 N/A Ash 17.0±0.2 6±1 3.5±0.2 n.d 17±1 16.6±0.1 0.4±0.2 Extractives 5.46±0.01 - - - - - - a The gravimetric yields for each treatment were calculated based on the total dry weight (100%) of the previous treatment n.d: not detected; N/A: non applicable

RESULTS. Chemical structure of the residues (FTIR) Normalized absorbance Normalized absorbance Alkali process Hydrothermal process 3330 cm -1 1700 cm -1 1509 cm -1 1250 cm -1 3900 3500 3100 2700 2300 1900 1500 1100 700 3900 3500 3100 2700 2300 1900 1500 1100 700 λ (cm-1) λ (cm-1) RH R-A Alk Alk R-A-B bleached Alk CNC-A RH R-SWE SWE R-SWE-B bleached CNC-SWE Figure 3. FTIR spectra for the different materials obtained throughout both processes

RESULTS. Crystallinity of the residues (XRD) Table 2. Crystallinity index (CrI) after each step of both CNC isolation processes CrI (%) RH 40.1 ± 0.5 R-A 71.3 ± 0.8 R-A-B 72.3 ± 0.7 CNC-A 80.± 0.9 R-SWE 50.0 ± 2.1 R-SWE-B 58.4 ± 1.8 CNC-SWE 53.0 Figure 4. XRD patter of the residues along the conversion from macro to nano dimensions

Frequency (%) Frequency (%) RESULTS. Morphology of the CNCs (AFM) Aspect ratio (L/D) CNC-A = 30-70 CNC-SWE = 35-75 >10 L/D = 10-20 Good reinforcing Collazo-Bigliardi et al., 2018 material Johar et al., 2012 Particle Diameter (D) Particle Length (L) 25 20 CNC-A = 5.1±1.3 CNC-SWE = 5.2±1.2 25 20 CNC-A = 240±70 CNC-SWE = 270±70 15 15 10 10 5 5 0 3 3,5 4 4,5 5 5,5 6 6,5 7 7,5 Particle Diameter (nm) 0 130 160 190 220 250 280 310 340 370 400 430 460 Particle Length (nm) Figure 5. AFM analysis of the CNCs isolated from rice husk through the alkaline process and the hydrothermal process: particle diameter and length. Averaged diameter and length calculated from 100 individual CNC particles using AFM

RESULTS. Thermal behaviour of the residues (TGA) Table 3. Thermogravimetric parameters of the rice husk and their alkaline, bleached and hydrolyzed samples. Sample [25-150] o C [180-550] o C Mass loss (%) T max ( o C) T onset ( o C) Mass loss (%) T max ( o C) RH 2.77±0.04 70.3±0.9 252.3±1.3 55.0±0.4 345.4±0.8 R-A 3.01±0.05 67.2±2.1 274.6±0.5 63.6±1.3 330.8±0.1 R-A-B 2.86±0.09 60.5±4.2 303.0±0.3 74.7±0.2 346.8±0.1 CNC-A n.d n.d 223.1±3.2 14.2±2.8 271±6/315±6/416±5 R-SWE 2.13±0.10 59.3±0.4 318.3±0.3 59.9±0.3 363.8±0.5 R-SWE-B 2.63±0.01 55.03±0.6 301.8±1.3 63.5±0.4 344.4±0.1 CNC-SWE n.d n.d 173.9±2.4 8.3±0.4 216±1/354±2/421±1 Degradation patter of the CNCs 3 overlapping steps: 1 st at lower temperature: sulphate groups that catalyse the dehydration process of cellulose 2 nd breakdown of the more accessible region in the crystal interior 3rd at higher temperature: less accessible crystal interior of the CNCs

Monosacharyde composition (%) Monosacharyde composition (%) RESULTS. Monosaccharide composition of the extracts Hydrothermal process Alkali process 100 80 60 40 20 GlcA MeGlcA Xyl Gluc Gal Arab 100 80 60 40 20 GlcA GalA MeGlcA Xyl Gluc Gal Arab 0 5 min 15 min 30 min 60 min 0 1st 2nd 3rd Figure 6. Monosaccharide composition of the extracts after different times of SWE and after each consecutive alkaline extraction.

RESULTS. Monosaccharide composition of the extracts Table 4. Monosaccharide composition (in %wt) of the rice husk extracts resulting from the three consecutive alkaline extractions and the sequential fractionation by subcritical water extraction. Alkaline process 1 st 2 nd 3 rd Fuc <0.1 <0.1 <0.1 Ara 5.2±2.1 8.5±0.9 6.7±2.0 Rha <0.1 <0.1 <0.1 Gal 2.8±2.1 1.6±0.1 1.3±0.3 Glu 38.5±6.5 2.9±0.4 4.0±2.4 Xyl 33.6±5.5 60.4±2.6 47.0±9.6 Man <0.1 <0.1 <0.1 MeGlcA 0.6±0.2 2.9±0.4 2.7±1.0 GalA 0.3±0.1 0.6±0.1 0.3±0.1 GlcA 0.4±0.1 0.6±0.1 0.5±0.1 Xylan content (%) a 40±5 72±4 57±13 Total carbohydrates 81.3±10.2 77.5±3.9 62.4±10.6 Hydrothermal process 5 min 15 min 30 min 60 min <0.1 <0.1 <0.1 <0.1 1.7±0.1 12.8±0.9 12.1±1.0 7.6±0.5 <0.1 <0.1 <0.1 <0.1 <0.1 3.2±0.1 4.8±0.4 4.2±0.2 80.4±11.4 42.8±5.0 6.1±1.3 2.8±0.3 2.1±0.2 18.3±0.7 53.6±6.8 73.2±0.9 <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 2.3±0.4 2.2±0.3 <0.1 <0.1 <0.1 <0.1 <0.1 <0.1 0.8±0.1 0.7±0.1 3.8±0.3 31±2 69±7 83.7±1.4 85.5±11.6 77.0±6.3 79.7±8.9 90.7±1.7

w (log M) RESULTS. Molar mass distributions of the extracts w (log M) Alkali extraction 1,E+02 1,E+04 1,E+06 Molar mass (g mol -1 ) 1 st Alk1 2 nd Alk2 3 rd Alk3 SWE 1,E+02 1,E+04 1,E+06 Molar mass (g mol -1 ) Figure 7. Molar mass distributions of the rice husk extracts resulting from (A) the three consecutive alkaline extractions and (B) the sequential fractionation by subcritical water extraction 5 min SWE5 15 min SWE15 30 min SWE30 60 min SWE60 Table 5. Number-average molar mass (Mn) and weight-average molar mass (Mw) Mn Mw E-A-1 12150 271700 E-A-2 8784 35970 E-A-3 8128 35230 E-SWE-5min 36810 691700 E-SWE-15min 4291 250600 E-SWE-30min 3254 59990 E-SWE-60min 2705 6499 v v

RESULTS. Bioactivity of the hemicellulosic extracts % remaining DPPH % remaining DPPH Antioxidant activity 100 80 60 40 20 0 SWE-60 min extract 0 10 20 30 mg extract/mg DPPH EC50 = 9.6±0.6 mg/mg Actividad antimicrobiana 100 80 60 40 20 p-coumaric acid EC50 = 0.2 mg/mg ferulic acid EC50 = 20.8 mg/mg (Brand-Williams et al., 1995) 0 2 nd Alkali extract 0 200 400 600 mg extract/mg DPPH EC50 = 170±21 mg/mg 18-fold lower antioxidant activity SWE-60 min extract E. Coli MIC = 95 ± 2 mg/ml L. Innocua MIC = 55 ± 2 mg/ml 2 nd Alkali extract No antimicrobial activity

APPLICATIONS Arabinoxylans: Food packaging materials Food fomulations CNCs: Reinforcing materials Extend food shelflife Improving food quality Improving mechanical properties of packaging materials

Acknowledgement: ActInPak is supported by COST (European Cooperation in Science and Technology). COST is a funding agency for research and innovation networks. Our actions help connect research initiatives across Europe and enable scientists to grow their ideas by sharing them with their peers. This boosts their research, career and innovation. www.cost.eu ActInPak website: www.actinpak.eu