Frequency-angular resolving LiDAR using chip-scale acousto-optic beam steering.

Thanks to its superior imaging resolution and range, light detection and ranging (LiDAR) is fast becoming an indispensable optical perception technology for intelligent automation systems including autonomous vehicles and robotics1-3. The development of next-generation LiDAR systems critically needs a non-mechanical beam-steering system that scans the laser beam in space. Various beam-steering technologies4 have been developed, including optical phased array5-8, spatial light modulation9-11, focal plane switch array12,13, dispersive frequency comb14,15 and spectro-temporal modulation16. However, many of these systems continue to be bulky, fragile and expensive. Here we report an on-chip, acousto-optic beam-steering technique that uses only a single gigahertz acoustic transducer to steer light beams into free space. Exploiting the physics of Brillouin scattering17,18, in which beams steered at different angles are labelled with unique frequency shifts, this technique uses a single coherent receiver to resolve the angular position of an object in the frequency domain, and enables frequency-angular resolving LiDAR. We demonstrate a simple device construction, control system for beam steering and frequency domain detection scheme. The system achieves frequency-modulated continuous-wave ranging with an 18° field of view, 0.12° angular resolution and a ranging distance up to 115 m. The demonstration can be scaled up to an array realizing miniature, low-cost frequency-angular resolving LiDAR imaging systems with a wide two-dimensional field of view. This development represents a step towards the widespread use of LiDAR in automation, navigation and robotics.

Molecular scale behavior of xylan during solvent-controlled extraction and precipitation.

Solvent-controlled extraction and precipitation are the most fundamental methods for obtaining hemicellulose from lignocellulosic biomass and purification processes. However, the dissolution and precipitation mechanisms involved have scarcely been mentioned. In this study, the molecular scale behavior of xylan-type hemicellulose during solvent-controlled extraction and precipitation is investigated using molecular dynamics (MD) simulations and density functional theory (DFT) calculations. To bring the model closer to the real extracted xylan, a high degree of polymerization (DP100) of xylan is established, and hemicelluloses with low DP (DP15 and DP50) are also investigated. Four phenomena are explained at the molecular level, including the influence of the polymerization degree and side chain on the solubility of xylan in water, the improvement of the xylan's solubility in NaOH, the precipitation of xylan in ethanol, and the acetyl group preservation of xylan in DMSO. This study contributes to an increased understanding of the dissolution and precipitation mechanisms of hemicellulose and provides a resource for the simulation of high DP hemicellulose, which gives a theoretical basis for the efficient extraction of high-purity hemicellulose as well as economic biorefining.

Microwave-Assisted Oxalic Acid Pretreatment for the Enhancing of Enzyme Hydrolysis in the Production of Xylose and Arabinose from Bagasse.

In this study, highly-efficient hydrolysis of bagasse into xylose and arabinose sugars (C5 sugars) was developed by microwave-assisted oxalic acid pretreatment under mild reaction conditions. The effects of acid and hydrolysis conditions on the C5 sugar yields were discussed. The results showed that oxalic acid performed better than hydrochloric acid and maleic acid, and was a promising alternative to sulfuric acid for xylose production at the same acid concentration. The maximum yields of xylose (95.7%) and arabinose (91.5%) were achieved via the microwave-assisted oxalic acid pretreatment (120 °C, 10 min, 0.4 mol/L, solid-liquid ratio of 1:50 g/mL), indicating that almost all xylan-type hemicelluloses were released from the cell wall and hydrolyzed into C5 sugars. After pretreatment, more than 90% of the cellulose in the residual bagasse was converted to glucose (92.2%) by enzymatic hydrolysis. This approach could realize the highly-efficient hydrolysis of xylan from bagasse into C5 sugars, which would enhance the enzyme hydrolysis of treated bagasse into glucose.

A fractionation strategy of cellulose, hemicellulose, and lignin from wheat straw via the biphasic pretreatment for biomass valorization.

Developing an environmentally friendly and efficient pretreatment to utilize wheat straw is essential to a sustainable future. An acid biphasic system with 2-methyltetrahydrofuran (2-MeTHF) organic solvent and dilute p-toluenesulfonic acid (p-TsOH) were employed for the simultaneous fractionation of three components. Results showed that the biphasic system had excellent cellulose protection and high removal of hemicellulose and lignin. In detail, Under the optimal conditions (0.1 M p-TsOH, 2-MeTHF: H2O = 1:1 (v:v), 140 °C, 3 h), mostly cellulose retained in the residues (95.69%), 57.18% of lignin was removed and high yield of hemicellulose-based C5 sugars was achieved (77.49%). In the further process of dehydration of pre-hydrolysate dichloromethane (DCM) as an organic phase, the yield of furfural was 80.07% (170 °C-80 min). The saccharification of residue reached 95.82%. p-TsOH/2-MeTHF/H2O pretreatment was desirable for high selectivity fractionation. Important chemicals for bioenergy including furfural, monosaccharides and lignin are obtained.

CO2-Activation Nanofiber Carbon Paper as a High-Performance Interlayer for Trapping Polysulfides in Li-S Batteries.

Lithium-sulfur (Li-S) batteries have high theoretical energy density but low sulfur utilization due to the inherent insulating nature of sulfur and the shuttle effect of polysulfides. Herein, the CO2-activation carbon paper was prepared by poly(p-phenylenebenzobisoxazole) (PBO) nanofiber and was first applied as an interlayer for efficiently alleviating the shuttle effect of polysulfides in Li-S batteries. This interlayer exhibits good flexibility and strength with rich -C═O and -COOH functional groups on the three-dimensional porous structure, which improves chemical adsorption on Li2Sx species and ion rapid diffusion via interconnected diffusion channels and thus enhances the electrochemical kinetics. The initial specific capacity is 1367.4 mAh g-1 and remains 999.8 mAh g-1 after 200 cycles at 0.2C and 780.1 mAh g-1 at 5C, and the Coulombic efficiency is high, up to 99.8%, which is much better than that for the carbon paper without CO2 activation. The highly conductive flexible PBO carbon paper may bring breakthroughs in performance and thus lead to more practical applications of Li-S batteries.

Antimicrobial cellulose paper tuned with chitosan fibers for high-flux oil/water separation.

Separating films with both high efficiency and large flux are desperately needed to meet the rising demand for the treatment of oily wastewater, while traditional oil/water separation papers with high separation efficiency usually suffered from low flux due to the unsuitable size of filtration pores. Herein, we report a bio-based porous, superhydrophobic, and antimicrobial hybrid cellulose paper with tunable porous structures for high flux oil/water separation. The size of pores in the hybrid paper can be tuned by both physical supports provided by the chitosan fibers and the chemical shielding supplied by the hydrophobic modification. The hybrid paper with increased porosity (20.73 µm; 35.15 %) and excellent antibacterial properties can efficiently separate a wide range of oil/water mixtures, solely by gravity, with outstanding flux (maximum of 23,692.69 L m-2 h-1), tiny oil interception, and high efficiency of over 99 %. This work provides new sights in the development of durable and low-cost functional papers for rapid and efficient oil/water separation.

A highly stretchable, UV resistant and underwater adhesive hydrogel based on xylan derivative for sensing.

Hydrogels with fascinating adhesion have been demonstrated great potential in various applications. However, most hydrogels lose their adhesion in wet or underwater environments due to the influence of interfacial water. Inspired by mussel, an underwater adhesive hydrogel was facilely fabricated by introducing electrostatic interactions, which consisted of poly (acrylic acid) (PAA), quaternized xylan (QAX) and tannic acid (TA). In this hydrogel, -COO- from PAA, -N+(CH3)3 from QAX and catechol group from TA resembled amino acids with negative and positive charges and 3,4-dihydroxyphenylalanine units in mussel, which endowed the hydrogels with great underwater adhesion through multiple interactions. Notably, acrylic acid (AA) played a key role in the dispersion of the system. QAX, a biomass derived from plants with excellent properties, worked with PAA to construct hydrogel networks. The resultant hydrogels exhibited excellent mechanical properties including remarkable stretchability (>4000 %) and compressibility. Moreover, the hydrogels had superior UV-blocking (~99.96 %), and showed good adhesion both in air and underwater. The hydrogels can be exploited as a wearable sensor to monitor human motions and even subtle motions, which have the potential to be explored in human health monitoring.

A Review of Water-Resistant Cellulose-Based Materials in Pharmaceutical and Biomedical Application.

BACKGROUND: Cellulose, having huge reserves of natural polymers, has been widely applied in pharmaceutical and biomedicine fields due to its good biocompatibility, biodegradability, non-toxicity and excellent mechanical properties. At present, water- resistant metal-based and petroleum-based materials applied in the medical field have obvious problems of poor biocompatibility and high cost. Therefore, water-resistant cellulose- based materials with good biocompatibility and low price have become an attractive alternative. This review aims to summarize the preparation of water-resistant cellulose- based materials and their potential application in pharmaceutical and biomedical in recent years. METHODS: Common hydrophobic treatments of cellulose fibers or paper were overviewed. The preparation, properties and applications of water-resistant cellulose- based materials in the pharmaceutical and biomedical fields were summarized. RESULTS: Common hydrophobic treatments of cellulose fibers or paper were divided into chemical modification (graft polymerization, crosslinking, solution casting or dip-coating), physico-chemical surface modifications (plasma treatments, surface patterning, electrostatic spraying and electrowetting) and physical processing (electrostatic spinning, SAS process and 3D EHD printing). These hydrophobically processed cellulose fibers or paper could be prepared into various water-resistant cellulose-based materials and applied in pharmaceutical excipients, drug-loaded amphiphilic micelles, drug-loaded composite fibers, hydrophobic biocomposite film/coatings and paper-based detectors. They presented excellent water resistance and biocompatibility, low cytotoxicity and high drug loading ability, and stable drug release rate, etc., which could be used for water-insoluble drugs carriers, wound dressings, and medical testing equipment. CONCLUSION: Currently, water-resistant cellulose-based materials were mainly applied in water-insoluble drugs delivery carriers, wound dressing and medical diagnosis and presented great application prospects. However, the contradiction between hydrophobicity and mechanical properties of these reported water-resistant cellulose-based materials limited their wider application in biomedicine such as tissue engineering. In the future, attention will be focused on the higher hydrophobicity of water-resistant cellulose-based materials with excellent mechanical properties. In addition, clinical medical research of water-resistant cellulose-based materials should be strengthened.

Cellulose-based Biosensor for Bio-molecules Detection in Medical Diagnosis: A Mini-Review.

BACKGROUND: Biosensors are widely applied for the detection of bio-molecules in blood glucose , cholesterol, and gene. Cellulose as the most dominating natural polymer has attracted more and more interest, especially in the field of medicine such as advanced medical diagnosis. Cellulose could endow biosensors with improved biocompatibility, biodegradability and nontoxicity, which could help in medical diagnosis. This mini-review summarizes the current development of cellulose-based biosensors as well as their applications in medical diagnosis in recent years. METHODS: After reviewing recent years' publications we can say that, there are several kinds of cellulose used in biosensors including different cellulose derivatives, bacterial cellulose and nanocellulose. Different types of cellulose-based biosensors, such as membrane, nano-cellulose and others were briefly described in addition to the detection principle. Cellulose-based biosensors were summarized as in the previous papers. The description of various methods used for preparing cellulose-based biosensors was also provided. RESULTS: Cellulose and its derivatives with their unique chemical structure proved to be versatile materials providing a good platform for achieving immobilizing bioactive molecules in biosensors. These cellulose-based biosensors possess various desirable properties such as accuracy, sensitivity, convenience, low cost and fast response. Among them, cellulose paper-based biosensors have the advantages of low cost and easy operation. Nano-cellulose has unique properties such as a large aspect ratio, good dispersing ability and high absorption capacity. CONCLUSION: Cellulose displays a promising application in biosensors which could be used to detect different bio-molecules such as glucose, lactate, urea, gene, cell, amino acid, cholesterol, protein and hydroquinone. In future, the attention will be focused on designing miniaturized, multifunctional, intelligent and integrated biosensors. Creation of low cost and environmentally friendly biosensors is also very important.

Hemicellulose from Plant Biomass in Medical and Pharmaceutical Application: A Critical Review.

BACKGROUND: Due to the non-toxicity, abundance and biodegradability, recently more and more attention has been focused on the exploration of hemicellulose as the potential substrate for the production of liquid fuels and other value-added chemicals and materials in different fields. This review aims to summarize the current knowledge on the promising application of nature hemicellulose and its derivative products including its degradation products, its new derivatives and hemicellulosebased medical biodegradable materials in the medical and pharmaceutical field, especially for inmmune regulation, bacteria inhibition, drug release, anti-caries, scaffold materials and anti-tumor. METHODS: We searched the related papers about the medical and pharmaceutical application of hemicellulose and its derivative products, and summarized their preparation methods, properties and use effects. RESULTS: Two hundred and twenty-seven papers were included in this review. Forty-seven papers introduced the extraction and application in immune regulation of nature hemicellulose, such as xylan, mannan, xyloglucan (XG) and ß-glucan. Seventy-seven papers mentioned the preparation and application of degradation products of hemicellulose for adjusting intestinal function, maintaining blood glucose levels, enhancing the immunity and alleviating human fatigue fields such as xylooligosaccharides, xylitol, xylose, arabinose, etc. The preparation of hemicellulose derivatives were described in thirty-two papers such as hemicellulose esters, hemicellulose ethers and their effects on anticoagulants, adsorption of creatinine, the addition of immune cells and the inhibition of harmful bacteria. Finally, the preparations of hemicellulose-based materials such as hydrogels and membrane for the field of drug release, cell immobilization, cancer therapy and wound dressings were presented using fifty-five papers. CONCLUSION: The structure of hemicellulose-based products has the significant impact on properties and the use effect for the immunity, and treating various diseases of human. However, some efforts should be made to explore and improve the properties of hemicellulose-based products and design the new materials to broaden hemicellulose applications.

Preparation of Lignocellulose-Based Activated Carbon Paper as a Manganese Dioxide Carrier for Adsorption and in-situ Catalytic Degradation of Formaldehyde.

Formaldehyde is a colorless, highly toxic, and flammable gas that is harmful to human health. Recently, many efforts have been devoted to the application of activated carbon to absorb formaldehyde. In this work, lignocellulose-based activated carbon fiber paper (LACFP) loaded with manganese dioxide (MnO2) was fabricated for the adsorption and in-situ catalytic degradation of formaldehyde. LACFP was prepared by two-stage carbonization and activation of sisal hemp pulp-formed paper and was then impregnated with manganese sulfate (MnSO4) and potassium permanganate (KMnO4) solutions; MnO2 then formed by in situ growth on the LACFP base by calcination. The catalytic performance of MnO2-loaded LACFP for formaldehyde was then investigated. It was found that the suitable carbonization conditions were elevating the temperature first by raising it at 10°C/min from room temperature to 280°C, then at 2°C/min from 280 to 400°C, maintaining the temperature at 400°C for 1 h, and then increasing it quickly from 400 to 700°C at 15°C/min. The conditions used for activation were similar to those for carbonization, with the temperature additionally being held at 700°C for 2 h. The conditions mentioned above were optimized to maintain the fiber structure and shape integrity of the paper, being conducive to loading with catalytically active substances. Regarding the catalytic activity of MnO2-loaded LACFP, the concentration of formaldehyde decreased by 59 ± 6 ppm and the concentration of ΔCO2 increased by 75 ± 3 ppm when the reaction proceeded at room temperature for 10 h. The results indicated that MnO2-loaded LACFP could catalyze formaldehyde into non-toxic substances.

A new and highly efficient conservation treatment for deacidification and strengthening of aging paper by in-situ quaternization.

Ancient papers, facing the threat of acidification, aging and microbial corrosion, need to be repaired due to their significance of history, art and culture research. In this work, a new and highly efficient approach was proposed to deacidify and strengthen aging paper by in-situ quaternization for the conservation, in which MgO nanoparticles dispersed in hexamethyldisiloxane was coated on the paper surface and the aqueous alkaline solution and the 2, 3-epoxypropyl trimethyl ammonium chloride/isopropyl alcohol/water mixture were sprayed in a closed reactor. Results showed that properties of ageing papers were improved after MSCE-8/2 treatment. The pH value was in the range of 7.5-9.0 and the maximum amount of alkali storage was 220 mmol/Kg. The tensile strength and folding endurance were increased by 28.05% and 80%, respectively. The fluctuation range of brightness and chromatic aberration was 0.14 and 1.27. Moreover, treated paper also had the great anti-bacteria and anti-aging effects.

Efficient catalytic conversion of dilute-oxalic acid pretreated bagasse hydrolysate to furfural using recyclable ironic phosphates catalysts.

Efficient conversion of dilute-oxalic acid pretreated bagasse hydrolysate to furfural was developed using recyclable ironic phosphates (FePO4) catalysts in the modified heterogeneous system. The effects of reaction conditions on the furfural yields were investigated, and the stability and water solubility of catalysts were evaluated. Results showed that the maximum furfural yield of 88.7% was obtained in the modified biphasic system by FePO4 catalysts at 190 °C for 120 min. The catalyst could be recycled and reused in conversion of the xylose-rich hydrolysate into furfural due to the unique feature that the catalyst showed solid state at room temperature and could be gradually dissolved into the aqueous phase upon increasing the reaction temperature and time. The experiments of five-time recycles showed that the FePO4 catalyst exhibited excellent stability and catalytic performances.

A new approach to recycle oxalic acid during lignocellulose pretreatment for xylose production.

BACKGROUND: Dilute oxalic acid pretreatment has drawn much attention because it could selectively hydrolyse the hemicellulose fraction during lignocellulose pretreatment. However, there are few studies focusing on the recovery of oxalic acid. Here, we reported a new approach to recycle oxalic acid used in pretreatment via ethanol extraction. RESULTS: The highest xylose content in hydrolysate was 266.70 mg xylose per 1 g corncob (85.0% yield), which was achieved using 150 mmol/L oxalic acid under the optimized treatment condition (140 °C, 2.5 h). These pretreatment conditions were employed to the subsequent pretreatment using recycled oxalic acid. Oxalic acid in the hydrolysate could be recycled according to the following steps: (1) water was removed via evaporation and vacuum drying, (2) ethanol was used to extract oxalic acid in the remaining mixture, and (3) oxalic acid and ethanol were separated by reduced pressure evaporation. The total xylose yields could be stabilized by intermittent adding oxalic acid, and the yields were in range of 46.7-64.3% in this experiment. CONCLUSIONS: This sustainable approach of recycling and reuse of oxalic acid has a significant potential application for replacing traditional dilute mineral acid pretreatment of lignocellulose, which could contribute to reduce CO2 emissions and the cost of the pretreatment.

New Understandings of the Relationship and Initial Formation Mechanism for Pseudo-lignin, Humins, and Acid-Induced Hydrothermal Carbon.

The generation of pseudo-lignin as byproduct during the lignocellulose acidic pretreatment has been proposed for many years. However, the detailed formation mechanism is still unclear. Moreover, there is a lack of understanding in the initial reaction during the formation of humins (byproducts in furfural production) and acid-induced hydrothermal carbon (carbon material). In this work, the initial formation of these three substances were investigated. We first found the common feature of their formation process was that carbohydrate-hydrolyzed compounds could form black polymers by condensing in acidic media, but the difference was dependent on the reaction degree. Furthermore, the results revealed that oxidation was an accelerator for condensations during producing black polymers because oxidized compounds could enhance the acidity of the reaction system. However, condensations of oxidized compounds were more difficult to proceed. Meanwhile, during the initial stage, the dominating pathway was that furfural condensed with itself and isomerized xylose via aldol-condensation.

Production of xylooligosaccharides by microwave-induced, organic acid-catalyzed hydrolysis of different xylan-type hemicelluloses: Optimization by response surface methodology.

A feasible approach to produce xylooligosaccharides (XOS) using organic acids as catalysts by microwave-induced hydrolysis of different hemicelluloses was developed. The effects of different acids (oxalic acid, maleic acid, citric acid and sulfuric acid), acid concentration, reaction temperature and reaction time on the hemicelluloses hydrolysis were investigated. Results demonstrated that organic acid was more beneficial to the XOS production than the conventional sulfuric acid. Higher acid concentration, higher reaction temperature and longer reaction time accelerated the further depolymerization of XOS to form monosaccharide. Response surface methodology was employed to optimize the reaction conditions (temperature and time) for the production of XOS from beechwood xylan (BX), corncob hemicelluloses (CH) and recovered hemicelluloses from the industrial waste liquor of dissolving pulp (RH), respectively. The predicted highest XOS yields were achieved to 39.31% (126.54°C-7.95min), 27.29% (120.00°C-0min), 30.32% (122.63°C-15.85min), respectively, being close to the experimental value (39.42%, 27.46% and 30.89%) from BX, CH and RH, indicating the fitted models of XOS yield were in good agreement with the experimental results.

A feasible process for furfural production from the pre-hydrolysis liquor of corncob via biochar catalysts in a new biphasic system.

A feasible approach was developed to produce furfural from the pre-hydrolysis liquor of corncob via biochar catalysts as the solid acid catalyst in a new biphasic system with dichloromethane (DCM) as the organic phase and the concentrated pre-hydrolysis liquor (CPHL) containing NaCl as the aqueous phase. The biochar catalyst possessing many acidity groups (SO3H, COOH and phenolic OH groups) was prepared by the carbonization and sulfonation process of the corncob hydrolyzed residue. The influence of the catalytic condition on furfural yield and selectivity was comparatively studied. It was found that 81.14% furfural yield and 83.0% furfural selectivity were obtained from CPHL containing 5wt% xylose using this biochar catalyst in the CPHL-NaCl/DCM biphasic system at 170°C for 60min. In addition, with the regeneration process, this catalyst displayed the high performance and excellent recyclability.

Preparation of copper-chelate quaternized carboxymethyl chitosan/organic rectorite nanocomposites for algae inhibition.

Quaternized carboxymethyl chitosan/organic rectorite (QCMC/OREC) nanocomposites were rapidly prepared by intercalating QCMC into the layer of OREC under microwave irradiation. And then copper-chelate QCMC/OREC (QCMC/OREC-Cu) nanocomposites were obtained by mixing QCMC/OREC with CuSO4 solution. XRD and TEM results indicated that QCMC/OREC nanocomposites were obtained and QCMC was dispersed in the interlayer of OREC. Besides, FT-IR results revealed that the hydrogen bonds and electrostatic interaction in QCMC/OREC-Cu were both stronger than those in QCMC/OREC because of introducing the Cu(2+). The thermogravimetric analysis showed that the thermal stability of QCMC/OREC-Cu nanocomposites was higher than QCMC and QCMC/OREC. Algae inhibition assay revealed that QCMC/OREC-Cu nanocomposites had stronger antifouling activity than original QCMC and QCMC/OREC. This work provides important basis for developing novel antifouling materials.

Carboxymethyl chitosan/clay nanocomposites and their copper complexes: Fabrication and property.

To obtain environmentally friendly antifouling agent, an effort was made to intercalate carboxymethyl chitosan into the interlayer of organic montmorillonite to prepare carboxymethyl chitosan/organic montmorillonite nanocomposites and their copper complexes. In comparison, carboxymethyl chitosan-copper complexes were also obtained. Their structures were characterized by X-ray diffaraction, transmittance electron microscopy and Fourier transform infrared, and their thermal behavior and antimicrobial activity were discussed. The results revealed that the interlayer distance of carboxymethyl chitosan/organic montmorillonite nanocomposites enlarged with the increasing mass ratio of carboxymethyl chitosan to organic montmorillonite, when the mass ratio was at 20:1, the layer spacing of carboxymethyl chitosan/organic montmorillonite nanocomposites reached the maximum of 3.68 nm. As compared to other samples, carboxymethyl chitosan/organic montmorillonite-copper nanocomposites showed much higher thermal stability and inhibitory activity against Escherichia coli, the lowest minimum inhibition concentration was only 0.0003125% (w/v). The study provides a new method to find novel antifouling agent.