Elucidation of the Structure of Lignin-Carbohydrate Complexes in Ginkgo CW-DHP by 13C-2H Dual Isotope Tracer

To elucidate the chemical linkages between lignin and carbohydrates in ginkgo cell walls, 13C-2H-enriched cell wall-dehydrogenation polymers (CW-DHP) were selectively prepared with cambial tissue from Ginkgo biloba L. by feeding D-glucose-[6-2H2], coniferin-[α-13C], and phenylalanine ammonia-lyase (PAL) inhibitor. The abundant detection of 13C and 2H confirmed that D-glucose-[6-2H2] and coniferin-[α-13C] were involved in the normal metabolism of ginkgo cambial cells that had been effectively labelled with dual isotopes. In the ginkgo CW-DHP, ketal and ether linkages were formed between the C-α of lignin side chains and carbohydrates, as revealed by solid state CP/MAS 13C-NMR differential spectroscopy. Furthermore, the DMSO/TBAH ionic liquids system was used to fractionate the ball-milled CW-DHP into three lignin-carbohydrate complex (LCC) fractions: glucan–lignin complex (GL), glucomannan–lignin complex (GML), and xylan–lignin complex (XL). The XRD determination indicated that the cellulose type I of the GL was converted into cellulose type II during the separation process. The molecular weight was in the order of Ac-GL > Ac-GML > XL. The 13C-NMR and 1H-NMR differential spectroscopy of 13C-2H-enriched GL fraction indicated that lignin was linked with cellulose C-6 by benzyl ether linkages. It was also found that there were benzyl ether linkages between the lignin side chain C-α and glucomannan C-6 in the 13C-2H-enriched GML fraction. The formation of ketal linkages between the C-α of lignin and xylan was confirmed in the 13C-2H-enriched XL fraction.

Experimental Study on Ultra-Precision Polishing of Ti-6Al-4V by Ultraviolet-Induced Nanoparticle Colloid Jet Machining

Ti-6Al-4V is widely used in various fields of modern industry, but it is difficult to obtain an ultra-smooth surface of Ti-6Al-4V due to its poor machinability. In this article, ultraviolet-induced (UV-induced) nanoparticle colloid jet machining was utilized to carry out ultra-precision polishing of Ti-6Al-4V to improve the surface quality. The results of infrared differential spectroscopy before and after polishing show that new chemical bonds such as Ti-O-Ti (Al-O-Ti and V-O-Ti) appear on the Ti-6Al-4V workpiece surface, which indicates that the material of Ti-6Al-4V workpiece is removed through the chemical interaction between TiO2 nanoparticles and workpiece surface in the process of UV-induced nanoparticle colloid jet machining. The comparison of metallographic structure of Ti-6Al-4V before and after polishing shows that the chemical activity and material removal rate of the primary α phase in Ti-6Al-4V is higher than that of the remnant β phase in UV-induced nanoparticle colloid jet machining, which lead to the well-distributed nano-scale surface peaks and valleys at regular intervals on the polished Ti-6Al-4V workpiece surface. After polishing, the longitudinal residual stress on the surface of Ti-6Al-4V workpiece decreases from 75 MPa to 67 MPa and the transverse stress decreases from 13 MPa to 3 MPa. The surface roughness of Ti-6Al-4V workpiece is reduced from Sa 76.7 nm to Sa 2.87 nm by UV-induced nanoparticle colloid jet machining.

An improved TROPOMI tropospheric HCHO retrieval over China

We present an improved TROPOspheric Monitoring Instrument (TROPOMI) retrieval of formaldehyde (HCHO) over China. The new retrieval optimizes the slant column density (SCD) retrieval and air mass factor (AMF) calculation for TROPOMI observations of HCHO over China. Retrieval of HCHO differential SCDs (DSCDs) is improved using the basic optical differential spectroscopy (BOAS) technique resulting in lower noise and smaller random error, while AMFs are improved with a priori HCHO profiles from a higher resolution regional chemistry transport model. Compared to the operational product, the new TROPOMI HCHO retrieval shows better agreement with ground-based Multi-AXis Differential Optical Absorption Spectroscopy (MAX-DOAS) measurements in Beijing. The improvements are mainly related to the AMF calculation with more precise a priori profiles in winter. Using more precise a priori profiles in general reduces HCHO vertical column densities (VCDs) by 52.37 % (± 27.09 %) in winter. Considering the aerosol effect in AMF calculation reduces the operational product by 11.46 % (± 1.48 %) and our retrieval by 17.61 % (± 1.92 %) in winter. The improved and operational HCHO are also used to investigate the spatial–temporal characteristics of HCHO over China. The result shows that both improved and operational HCHO VCDs reach maximum in summer and minimum in winter. High HCHO VCDs mainly located over populated areas, i.e., Sichuan Basin and central and eastern China, indicate a significant contribution of anthropogenic emissions. The hotspots are more obvious on the map of the improved HCHO retrieval than the operational product. The result indicates that the improved TROPOMI HCHO retrieval is more suitable for the analysis of regional- and city-scale pollution in China.

An improved TROPOMI tropospheric HCHO retrieval over China

We present the improved retrieval of TROPOspheric Monitoring Instrument (TROPOMI) tropospheric formaldehyde (HCHO) over China. The new retrieval optimizes the slant column density (SCD) retrieval and air mass factor (AMF) calculation for TROPOMI observations of HCHO over China. HCHO SCDs are retrieved using the basic optical differential spectroscopy (BOAS) technique, while AMFs are calculated with a priori HCHO profile from a higher resolution regional chemistry transport model. Compared to the operational product, the new TROPOMI HCHO retrieval shows better agreement with the ground based Multi-AXis Differential Optical Absorption Spectroscopy (MAX-DOAS) measurements in China. The operational product in general overestimates HCHO VCDs by 14.01 %, while the improved HCHO only shows an underestimation of 3.67 %. The improvements are mainly related to the AMF calculation with higher resolution a priori profile (61.11 %), while the SCD retrieval only shows a minor effect of 0.15 %. The improved HCHO is also used to investigate the spatial-temporal characteristic of HCHO over China. The result shows that HCHO VCDs reach maximum in summer and minimum in winter. High HCHO VCDs mainly located over populated areas, i.e., Sichuan Basin, Central and Eastern China, indicating a significant contribution of anthropogenic emissions. The result indicates the improved TROPOMI HCHO is more suitable for the analysis of regional and city scale pollution in China.