Bio-oil as Substitute of Phenol for Synthesis of Resol-type Phenolic Resin as Wood Adhesive

2017 ◽  
Vol 16 (3) ◽  
Author(s):  
Fangjia Dong ◽  
Mingcun Wang ◽  
Zhehui Wang
Keyword(s):  
Weight Ratio ◽  
Wood Adhesive ◽  
Exothermic Peak ◽  
Molar Ratio ◽  
Type I ◽  
Thermal Cure ◽  
Molar Ratios ◽  
Comprehensive Properties ◽  
Bio Oil ◽  
Resol Resin

AbstractThe bio-oil from fast pyrolysis of cornstalks was used as substitute of phenol to synthesize resol resin as an ideal wood adhesive. The effects of formaldehyde/phenol (F/P) molar ratios and oil/phenol (O/P) weight ratios on rehology, thermal cure, thermal resistance and adhension of plywoods were investigated. With the increase of bio-oil used in bio-resol, the gel time of the prepared bio-oil modified resol resin (bio-resol resin) increased gradually, and the exothermic peak temperature of thermal cure shifted slightly higher. It was found that the bio-resin with bio-oil/phenol = 0.5 (weight ratio) and F/P = 1.5 (molar ratio) had the best comprehensive properties. The plywoods made with the bio-resol resins fulfilled the standards of E0and type I plywood, implying the bio-resol resins was a new environment-friendly adhesive.

Characterization and Catalytic Performance of Modified SBA-16 in Liquid Phase Reaction

2018 ◽  
Vol 16 (8) ◽  
Author(s):  
Simsek Veli ◽  
Avci Pinar
Keyword(s):  
Acetic Acid ◽  
Liquid Phase ◽  
Batch Reactor ◽  
Weight Ratio ◽  
Catalytic Performance ◽  
Pluronic F127 ◽  
Molar Ratio ◽  
Phase Reaction ◽  
Molar Ratios ◽  
Liquid Phase Reaction

Abstract A new mesoporous silica SBA-16 (called SP-16) was prepared by the direct hydrothermal method using Pluronic F127 (triblock copolymer; EO106PO70EO106) as surfactant and TEOS (tetraethyl orthosilicate) as silica source. The catalyst property of the SBA-16 was attained by loading the STA (Silicotungstic acid) active compound. The loading contents of STA were determined between 5 % and 40 % based on weight ratio of W and Si (W/Si). Catalytic activities and sustainability of SP-16 (10–20 %, W/Si) catalysts were determined by esterification (liquid phase reaction methanol and acetic acid) reactions at 343-353K, under autogenic pressure, 1/1–1/2 feed molar ratios (methanol/acetic acid) and in the presence of 0.4 g catalyst in the semi-batch reactor for 6 - 24h. Acetic acid conversion values of 10 and 20 % catalysts with 1/1 molar ratio at the end of 24h were obtained as 32–52.9 % and 47–60 %, respectively. On the other hand, when 1/2 molar ratio at 353K was used, 20 % catalyst showed 82.2 % conversion. Moreover, a second reaction experiment of 10 % catalyst was also carried out in identical conditions in the presence of catalyst recovered after the first methyl acetate reaction. The first and second reaction results of 10 % catalyst indicated that catalytic activity and sustainability were preserved for both 6 and 24h analyses. The physical properties of the materials obtained were investigated by Nitrogen sorption at 77K (BET), X-ray diffraction (XRD), Fourier transform infrared spectroscopy(FT-IR), Multiple Internal Reflection (DRIFT), Thermo-gravimetry/Differential thermal analysis(TG/DTA), Scanning electron microscope (SEM) and MAPPING analysis methods.

scholarly journals Synthesis and characterization of ternary chitosan–TiO2–ZnO over graphene for photocatalytic degradation of tetracycline from pharmaceutical wastewater

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Hossein Asadzadeh Patehkhor ◽  
Moslem Fattahi ◽  
Mohammadreza Khosravi-Nikou
Keyword(s):  
Photocatalytic Degradation ◽  
Irradiation Time ◽  
Sol Gel ◽  
Weight Ratio ◽  
Molar Ratio ◽  
Operational Parameters ◽  
Pharmaceutical Wastewater ◽  
Operational Conditions ◽  
Molar Ratios

AbstractVarious nanocomposites of TiO2–ZnO, TiO2–ZnO/CS, and TiO2–ZnO/CS–Gr with different molar ratios were synthesized by sol–gel and ultrasound-assisted methods and utilized under UV irradiation to enhance the photocatalytic degradation of tetracycline. Characterization of prepared materials were carried out by XRD, FT-IR, FE-SEM, EDX and BET techniques. The TiO2–ZnO with the 1:1 molar ratio supported with 1:2 weight ratio CS–Gr (T1‒Z1/CS1‒Gr2 sample) appeared as the most effective material at the optimized operational conditions including the tetracycline concentration of 20 mg/L, pH = 4, catalyst dosage of 0.5 g/L, and 3 h of irradiation time. As expected, the graphene had a significant effect in improving degradation results. The detailed performances of the T1‒Z1/CS1‒Gr2 were compared with ternary nanocomposites from EDX and BET results as well as from the degradation viewpoint. This novel photocatalyst can be effective in actual pharmaceutical wastewater treatment considering the applied operational parameters.

scholarly journals Mechanism of Biomineralization Induced by Bacillus subtilis J2 and Characteristics of the Biominerals

Minerals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 218 ◽  
Author(s):  
Han ◽  
Wang ◽  
Zhao ◽  
Tucker ◽  
Zhao ◽  
...  
Keyword(s):  
Bacillus Subtilis ◽  
Hot Spot ◽  
Weight Ratio ◽  
Molar Ratio ◽  
Alkaline Condition ◽  
Carbonate Sedimentology ◽  
Molar Ratios ◽  
Nucleation Sites ◽  
Bacterium Bacillus Subtilis ◽  
Bacterium Bacillus

Abstract: Biomineralization induced by microorganisms has become a hot spot in the field of carbonate sedimentology; however, the mechanisms involved still need to be explored. In this study, the bacterium Bacillus subtilis J2 (GenBank MG575432) was used to induce the precipitation of calcium carbonate minerals at Mg/Ca molar ratios of 0, 3, 6, 9, and 12. Bacillus subtilis J2 bacteria released ammonia to increase pH, but the ammonia released only made the pH increase to 8.25. Carbonic anhydrase was also produced to catalyze the hydration of carbon dioxide, and this process released carbonate and bicarbonate ions that not only increased pH but also elevated carbonate supersaturation. The biominerals formed at a Mg/Ca molar ratio of 0 were spherulitic, elongated, dumbbell-shaped, and irregularly rhombohedral calcite; at a Mg/Ca molar ratio of 3, the biominerals were calcite and aragonite, the weight ratio of calcite decreased from 26.7% to 15.6%, and that of aragonite increased from 73.3% to 84.4% with increasing incubation time. At higher Mg/Ca molar ratios, the biominerals were aragonite, and the crystallinity and thermal stability of aragonite decreased with increasing Mg/Ca molar ratios. FTIR results showed that many organic functional groups were present on/within the biominerals, such as C–O–C, N–H, C=O, O–H, and C–H. HRTEM-SAED examination of the ultra-thin slices of B. subtilis J2 bacteria showed that nano-sized minerals with poor crystal structure had grown or been adsorbed on the EPS coating. The EPS of the B. subtilis J2 strain contained abundant glutamic acid and aspartic acid, which could be deprotonated in an alkaline condition to adsorb Ca2+ and Mg2+ ions; this made EPS act as the nucleation sites. This study may provide some references for further understanding of the mechanism of biomineralization induced by microorganisms.

scholarly journals Effect of Different Aluminum Substitution Rates on the Structure of Tobermorite

Materials ◽  
2019 ◽  
Vol 12 (22) ◽  
pp. 3765
Author(s):  
Liao ◽  
Li ◽  
Fang ◽  
Lu ◽  
Xu
Keyword(s):  
Exothermic Peak ◽  
Mas Nmr ◽  
Molar Ratio ◽  
Molar Ratios ◽  
Al Substitution ◽  
27Al Mas Nmr ◽  
Substitution Ratio ◽  
Ft Ir ◽  
Repulsive Forces ◽  
Aluminum Substitution

Tobermorite and Al-substituted tobermorite with varying Al/(Si + Al) molar ratios were synthesized via the static hydrothermal method. The effect of different Al substitution ratios on the structure of tobermorite was investigated by XRD, SEM–EDS, TG–DSC, FT–IR, 29Si, and 27Al MAS–NMR. The interplanar crystal spacing of (002) increased with the increment of the Al substitution ratio. The maximum ratio of the Al substitution for Si in the structure of tobermorite was about 15 at %, which was limited by the compositions of tobermorite and the electrostatic repulsive forces caused by Al substitution. The DSC curve of the tobermorite with an Al/(Al + Si) molar ratio of 0.15 showed a larger exothermic peak area at 850 °C, indicating that the Al-O-Si bond was formed in the structure of tobermorite and the Al participated in the recrystallization. The 29Si and 27Al MAS–NMR results confirmed that tetrahedral Al was introduced into the structure of the tobermorite. New silicon sites, Q2(1Al) and Q3(1Al), formed by the Al substitution for Si in bridging and non-bridging sites, were detected. Compared to the tobermorite without Al substitution, the adsorption capacity of Al-substituted tobermorite with Al/(Al + Si) = 0.15 to Na+ was improved by 44%.

scholarly journals Photocatalytic Reduction of CO2 to Methanol Using a Copper-Zirconia Imidazolate Framework

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 346
Author(s):  
Sonam Goyal ◽  
Maizatul Shima Shaharun ◽  
Ganaga Suriya Jayabal ◽  
Chong Fai Kait ◽  
Bawadi Abdullah ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalyst Support ◽  
Oxidation Potential ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molar Ratios ◽  
Optimum Parameters ◽  
Reduction Of Co2 ◽  
Enhanced Yield

A set of novel photocatalysts, i.e., copper-zirconia imidazolate (CuZrIm) frameworks, were synthesized using different zirconia molar ratios (i.e., 0.5, 1, and 1.5 mmol). The photoreduction process of CO2 to methanol in a continuous-flow stirred photoreactor at pressure and temperature of 1 atm and 25 °C, respectively, was studied. The physicochemical properties of the synthesized catalysts were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The highest methanol activity of 818.59 µmol/L.g was recorded when the CuZrIm1 catalyst with Cu/Zr/Im/NH4OH molar ratio of 2:1:4:2 (mmol/mmol/mmol/M) was employed. The enhanced yield is attributed to the presence of Cu2+ oxidation state and the uniformly dispersed active metals. The response surface methodology (RSM) was used to optimize the reaction parameters. The predicted results agreed well with the experimental ones with the correlation coefficient (R2) of 0.99. The optimization results showed that the highest methanol activity of 1054 µmol/L.g was recorded when the optimum parameters were employed, i.e., stirring rate (540 rpm), intensity of light (275 W/m2) and photocatalyst loading (1.3 g/L). The redox potential value for the CuZrIm1 shows that the reduction potential is −1.70 V and the oxidation potential is +1.28 V for the photoreduction of CO2 to methanol. The current work has established the potential utilization of the imidazolate framework as catalyst support for the photoreduction of CO2 to methanol.

scholarly journals Lipozyme 435-Mediated Synthesis of Xylose Oleate in Methyl Ethyl Ketone

Molecules ◽  
2021 ◽  
Vol 26 (11) ◽  
pp. 3317
Author(s):  
Maria Carolina Pereira Gonçalves ◽  
Jéssica Cristina Amaral ◽  
Roberto Fernandez-Lafuente ◽  
Ruy de Sousa Junior ◽  
Paulo Waldir Tardioli
Keyword(s):  
Oleic Acid ◽  
Methyl Ethyl Ketone ◽  
Molar Ratio ◽  
Methyl Ethyl ◽  
Sugar Ester ◽  
Molar Ratios ◽  
Emulsion Capacity ◽  
Ping Pong ◽  
Commercial Sugar ◽  
Repeated Use

In this paper, we have performed the Lipozyme 435-catalyzed synthesis of xylose oleate in methyl ethyl ketone (MEK) from xylose and oleic acid. The effects of substrates’ molar ratios, reaction temperature, reaction time on esterification rates, and Lipozyme 435 reuse were studied. Results showed that an excess of oleic acid (xylose: oleic acid molar ratio of 1:5) significantly favored the reaction, yielding 98% of xylose conversion and 31% oleic acid conversion after 24 h-reaction (mainly to xylose mono- and dioleate, as confirmed by mass spectrometry). The highest Lipozyme 435 activities occurred between 55 and 70 °C. The predicted Ping Pong Bi Bi kinetic model fitted very well to the experimental data and there was no evidence of inhibitions in the range assessed. The reaction product was purified and presented an emulsion capacity close to that of a commercial sugar ester detergent. Finally, the repeated use of Lipozyme 435 showed a reduction in the reaction yields (by 48 and 19% in the xylose and oleic acid conversions, respectively), after ten 12 h-cycles.

Appearance, corrosion properties, and leach resistance of spruce and pine wood treated with Mea modified micronized copper preservative (MCu)

Holzforschung ◽  
2014 ◽  
Vol 68 (4) ◽  
pp. 477-486 ◽  
Author(s):  
Myung Jae Lee ◽  
Sedric Pankras ◽  
Paul Cooper
Keyword(s):  
Wood Species ◽  
Wood Preservative ◽  
Molar Ratio ◽  
Corrosion Properties ◽  
Pine Wood ◽  
Molar Ratios ◽  
Copper Leaching ◽  
Mold Resistance ◽  
Refractory Wood

Abstract Canadian refractory wood species treated with micronized copper (MCu) wood preservative become mottled and streaky in appearance. To overcome this issue, the MCu system was modified by adding small amounts of monoethanolamine (Mea). The modified systems were evaluated to clarify the role of Mea in terms of leaching, corrosion, and mold resistance of MCu systems. The mottled and streaky surface on treated spruce was prevented at Mea/Cu molar ratios between 0.7 and 1.5. Copper leaching remained modest and was only slightly higher than that of MCu alone up to a Mea/Cu molar ratio of 1.2. However, adding even a small amount of Mea to the MCu formulation increased fastener corrosion compared with MCu. Protonated Mea increased as more Mea was added and was identified as the main corrosion-causing electrolyte in the system.

Hydrogen-bonded bent-core blue phase liquid crystal complexes containing various molar ratios of proton acceptors and donors

RSC Advances ◽  
2016 ◽  
Vol 6 (38) ◽  
pp. 32319-32327 ◽  
Author(s):  
Chun-Chieh Han ◽  
Yu-Chaing Chou ◽  
San-Yuan Chen ◽  
Hong-Cheu Lin
Keyword(s):  
Liquid Crystal ◽  
Chain Length ◽  
Alkyl Chain ◽  
Alkyl Chain Length ◽  
Chiral Center ◽  
Molar Ratio ◽  
Core Complex ◽  
Molar Ratios ◽  
Phase Liquid ◽  
Blue Phase

The molar ratio, alkyl chain length, lateral fluoro-substitution and the chiral center of H-bonded bent-core supramolecules would affect the BP ranges of BPLC complexes. H-bonded bent-core complex PIIIC9/AIIF* (3/7 mol mol−1) displayed the widest BPI range of ΔTBPI = 12 °C.

Reuse of Fried Oil to Obtain Biodiesel: Zeolites Y as a Catalyst

2007 ◽  
Vol 5 (1) ◽  
Author(s):  
A. Brito ◽  
M. E. Borges ◽  
R. Arvelo ◽  
F. Garcia ◽  
M. C. Diaz ◽  
...  
Keyword(s):  
Fixed Bed ◽  
Weight Ratio ◽  
Degree Of Conversion ◽  
Transesterification Reaction ◽  
Molar Ratio ◽  
Catalytic Reactor ◽  
Reaction Products ◽  
Waste Oil ◽  
Catalytic Effects ◽  
Fried Oil

The transesterification reaction is the most utilized process to obtain biodiesel. Fried oil transesterification reactions with methanol have been studied using several zeolites Y and interchanged with CsCl and KOH. The reaction has been carried out both in a slurry reactor and a fixed bed catalytic reactor. The catalytic effects of zeolites have been tested within a temperature range of 60-476°C, 2.5-5% catalyst/waste oil weight ratio, and 6:1 - 100:1 methanol/oil molar ratio. Cosolvents (THF, n-hexane) in the reaction feedstock effect have also been studied as well as catalyst regeneration effects. Viscosity of both the oil and the transesterification reaction products was determined as an initial guide to investigate the degree of conversion to biodiesel as well as FAME content by GC. When interchanged zeolites are used conversions are improved, getting the best yields (98% FAME) for the Y756 zeolite interchanged with KOH. Viscosities of the reaction product obtained reached values next to diesel standard ones.

scholarly journals BrO/SO<sub>2</sub> molar ratios from scanning DOAS measurements in the NOVAC network

2013 ◽  
Vol 5 (2) ◽  
pp. 1845-1870 ◽  
Author(s):  
P. Lübcke ◽  
N. Bobrowski ◽  
S. Arellano ◽  
B. Galle ◽  
G. Garzón ◽  
...  
Keyword(s):  
Molar Ratio ◽  
Optical Absorption Spectroscopy ◽  
Short Term ◽  
Dynamic Changes ◽  
Volcanic System ◽  
Molar Ratios ◽  
Remote Sensing Technique ◽  
Field Campaigns ◽  
Term Field

Abstract. The molar ratio of BrO to SO2 is, like other halogen/sulphur ratios, a~possible precursor for dynamic changes in the shallow part of a volcanic system. While the predictive significance of the BrO/SO2 ratio has not been well constrained yet, it has the major advantage that this ratio can be readily measured using the remote-sensing technique Differential Optical Absorption Spectroscopy (DOAS) in the UV. While BrO/SO2 ratios have been measured during several short-term field campaigns this article presents an algorithm that can be used to obtain long-term time series of BrO/SO2 ratios from the scanning DOAS instruments of the Network for Observation of Volcanic and Atmospheric Change (NOVAC) or comparable networks. Parameters of the DOAS retrieval of both trace gases are given and the influence of co-adding spectra on the retrieval error will be investigated. Difficulties in the evaluation of spectroscopic data from monitoring instruments in volcanic environments and possible solutions are discussed. The new algorithm is demonstrated by evaluating data from the NOVAC scanning DOAS systems at Nevado del Ruiz, Colombia encompassing almost four years of measurements between November 2009 and end of June 2013. This dataset shows variations of the BrO/SO2 ratio several weeks prior to the eruption on 30 June 2012.

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