Green and Effective Ammonium Carbonate-assisted Process for Drying Hemicellulose Obtained through Alkali Extraction of Bleached Bamboo Kraft Pulp

Hemicellulose has a wide range of applications,including that as an emulsifier for the food industry and raw material for the synthesis of bioethanol/biochemicals and biodegradable films.Hemicellulose is usually present as a spent liquor,such as the prehydrolysis liquor of the prehydrolysis kraft dissolving pulp production process and the alkali extraction liquor of the cold caustic extraction of pulp fibers.Due to its dilute nature,hemicellulose needs to be dried for practical utilization,and this is challenging.In this study,cellulose and hemicellulose in a bleached bamboo kraft pulp were separated using an alkali extraction process.Hemicellulose obtained from the extraction liquor was dried by an ammonium carbonate-assisted drying process.The effects of drying time and drying temperature were determined.Structure of the hemicellulose obtained by the ammonium carbonate-assisted drying process was similar to that of original hemicellulose,as revealed by detailed Fourier transform infrared and X-ray diffraction analyses.The novel drying method was more energy efficient and required a shorter drying time than the conventional freeze drying method,and the excellent solubility in alkaline solutions favored the chemical modification of hemicellulose.The dried hemicellulose can be used as a renewable raw material for the preparation of hydrogels and other substances such as bioethanol/biochemicals and biodegradable films.

Formation Process of Crystalline Ammonium Yttrium Carbonate Double Salt

The research was mainly based on the formation condition of crystalline ammoniu yttrium carbonate and the variation characteristics of PH value during the crystallization in which NH4HCO3 was used to precipitate yttrium ion. It is found that the crystallization process is always associated with the descent of pH. The pH of solution is controlled by the crystallization reaction of ammonium yttrium carbonate and the hydrolysis of NH4HCO3. Based on the pH variation, it can be judged whether the crystallization reaction occurs or not and the speed and the degree of crystallinity can be deterolfned. The precipitates were characterized by X- ray powder diffraction and differential thermal -thermogravimetric analysis. The results show that the crystallization is the process of NH4Y(CO3)2 formation and it is effected by feed ratio and feed method.

Effects of soil nitrate:ammonium ratio on plant carbon:nitrogen ratio and growth rate of Artemisia sphaerocephala seedlings

Can soil nitrate： ammonium ratios influence plant carbon： nitrogen ratios of the early succession plant？ Can plant carbon： nitrogen ratios limit the plant growth in early succession？ To address these two questions, we performed a two-factor （soil nitrate： ammonium ratio and plant density） randomized block design and a uniform-precision rotatable central composite design pot experiments to examine the relationships between soil nitrate： ammonium ratios, the carbon： nitrogen ratios and growth rate of Artemisia sphaerocephala seedlings. Under adequate nutrient status, both soil nitrate： ammonium ratios and plant density influenced the carbon： nitrogen ratios and growth rate of A. sphaerocephala seedlings. Under the lower soil nitrate： ammonium ratios, with the increase of soil nitrate： ammonium ratios, the growth rates of plant height and shoot biomass of A. sphaerocephala seedlings decreased significantly; with the increase of plant carbon： nitrogen ratios, the growth rates of shoot biomass of A. sphaerocephala seedlings decreased significantly. Soil nitrate： ammonium ratios affected the carbon： nitrogen ratios of A. sphaerocephala seedlings by plant nitrogen but not by plant carbon. Thus, soil nitrate： ammonium ratios influenced the carbon： nitrogen ratios of A. sphaerocephala seedlings, and hence influenced its growth rates. Our results suggest that under adequate nutrient environment, soil nitrate： ammonium ratios can be a limiting factor for the growth of the early succession plant.

Preparation of γ-Al2O3 via Hydrothermal Synthesis Using ρ-Al2O3 as Raw Material for Propane Dehydrogenation

γ-Al2O3 was prepared by hydrothermal synthesis usingρ-Al2O3 and urea as raw materials.In this work,the eff ects of the molar ratio of CO(NH2)2/Al and reaction temperature were investigated,and a Pt–Sn–K/γ-Al2O3 catalyst was prepared.The ammonium aluminum carbonate hydroxide(AACH),γ-Al2O3,and Pt–Sn–K/γ-Al2O3 were characterized by X-ray diff raction,scanning electron microscopy,transmission electron microscopy,N2 adsorption–desorption,thermogravimetry–differential thermal analysis,and NH3 temperature-programmed desorption techniques.The reactivity of Pt–Sn–K/γ-Al2O3 for propane dehydrogenation was tested in a micro-fixed-bed reactor.The results show thatγ-Al2O3 with a specific surface area of 358.1 m 2/g and pore volume of 0.96 cm 3/g was obtained when the molar ratio of CO(NH2)2/Al was 3:1 and the reaction temperature was 140℃.The alumina obtained by calcination of AACH has a higher specific surface area and larger pore volume than the industrial pseudo-boehmite does.The catalyst prepared from AACH as precursor showed high selectivity and conversion,which can reach 96.1%and 37.6%,respectively,for propane dehydrogenation.

Preparation of Nano-Alumina with Aluminum Scraps as Raw Materials

Ammonium aluminum carbonate hydroxide (AACH) was synthesized by the reaction of ammonium aluminum sulphate (AA) with ammonium hydrogen carbonate (AHC). AA was obtained by the reaction of NH4HSO4 with aluminum scraps as the raw materials. According to this method, AACH samples prepared were used to fabricate nano alumina powders by thermal decomposition. The microstructural properties of as-formed alumina were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), special surface analysis and inductively coupled plasma-atomic emission spectrometry (ICP-AES). Experimental observations revealed that highly pure (99.99%) α-alumina with mean diameter of 49 nm could be obtained.

Synthesis, Characterization and Flame-retardant Properties of Epoxy Resins and AACHH Composites

Flame retardant epoxy resins were prepared by a simple mixed method using ammonium aluminum carbonate hydroxy hydrate （AACHH） as a halogen-free flame retardant. The prepared samples were characterized by X-ray diffraction, thermogravimetric and differential scanning calorimetry, scanning electron microscope and limiting oxygen index（LOI） experiments. Effects of AACHH content on LOI of epoxy resins/AACHH composite and flame retardant mechanism were investigated and discussed. Results show that AACHH exhibites excellent flame-retardant properties in epoxy resin（EP）. When the content of AACHH was 47.4%, the LOI of EP reached 32.2%. Moreover, the initial and terminal decomposition temperature of EP increased by 48 ℃ and 40 ℃, respectively. The flame retarded mechanism of AACHH is due to the synergic flame retardant effects of diluting, cooling, decomposition resisting and obstructing.

Poriferan chitin as a template for hydrothermal zirconia deposition

Chitin is a thermostable biopolymer found in various inorganic-organic skeletal structures of numerous invertebrates including sponges （Porifera）. The occurrence of chitin within calcium- and silica-based biominerals in organisms living in extreme natural conditions has inspired development of new （extreme biomimetic） synthesis route of chitin-based hybrid materials in vitro. Here, we show for the first time that 3D-a-chitin scaffolds isolated from skeletons of the marine sponge Aplysina aerophoba can be effectively mineralized under hydrothermal conditions （150℃） using ammonium zirconium（IV） carbonate as a precursor of zirconia. Obtained chitin-ZrO2 hybrid materials were characterized by FT-IR, SEM, HRTEM, as well as light and confocal laser microscopy. We suggest that formation of chitin-ZrO2 hybrids occurs due to hydrogen bonds between chitin and ZrO2.