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The use of tricyclic copolymer latex (AMPS) can effectively improve the carbonation resistance of sulphoaluminate cement. This paper investigated polymer AMPS and polycarboxylic acid to modify sulphoaluminate cement materials by exploring the carbonation level of sulphoaluminate cement paste and mortar and the strength before and after carbonation. Then, the optimal dosage of polymer and polycarboxylic acid was obtained so that the carbonation resistance of sulphoaluminate cement reached the best state. The compressive strength was significantly improved by adding AMPS for sulphoaluminate cement paste and mortar. After carbonation, the strength decreased and combined with the carbonation level; it was concluded that the carbonation resistance of sulphoaluminate cement materials was the best when the optimal dosage of AMPS and polycarboxylic acid was 5% and 1.8%, respectively. Due to the addition of AMPS, the hydrated calcium aluminosilicate (C-A-S-H) and hydrated calcium silicate (C-S-H) gels, generated by the hydration of sulphoaluminate cement and the surface of unreacted cement particles, are wrapped by AMPS particles. The water is discharged through cement hydration. The polymer particles on the surface of the hydration product merge into a continuous film, which binds the cement hydration product together to form an overall network structure, penetrating the entire cement hydration phase and forming a polymer cement mortar with excellent structural sealing performance. To prevent the entry of CO2 and achieve the effect of anti-carbonation, adding polycarboxylic acid mainly improves the sample's internal density to achieve the anti-carbonation purpose.

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In view of the disadvantages of polycarboxylic acid grinding aids, such as poor reinforcement effect and cumbersome synthesis process, a new type of polycarboxylic acid grinding aid was prepared to meet the requirements of multifunctional admixture for cement concrete. The polycarboxylate grinding aid (PC) was prepared using acrylic acid, sodium allyl sulfonate, and isoprenol polyoxyethylene ether (TPEG) as raw materials, and ammonium persulfate as initiator in the nitrogen atmosphere. The effect of PC and its compound with triethanolamine (TEA) and triisopropanolamine (TIPA) on cement particle size and strength, and hydration process and structures of hydrated products were investigated. Moreover, the grinding mechanism of grinding aids was also proposed. The results indicate that the PC has good performance in both grinding and high-efficiency water-reducing. The average particle diameter of cement was reduced by 3.65 µm when 0.03 wt% of PC was added as grinding aid. Moreover, a high initial fluidity of the cement paste, 290 mm, could be reached when 0.08 wt% of PC was added. The fluidity loss of cement paste after 30 min and 60 min was 265 mm and 260 mm, respectively. After PC compounding with TEA and TIPA, 4.07 µm and 4.7 µm of the average particle size of the cement can be reduced, respectively. Based on the investigations on the hydration rate of cement hydration, the phases, and the microstructures of the hardened slurry, it could be concluded that grinding aids can change the hydration process of cement and improve the morphologies and structures of hydration products without influence on the type of hydrated products. Note that the compounded grinding aids, such as PC with TEA or PC with TIPA, can more effectively enhance the early and late strength of cement. This shows excellent comprehensive performance. In this study, a new type of polycarboxylic acid grinding aid was prepared to meet the requirements of the versatility of cement concrete additives, and to simplify the synthesis process, reduce production costs, improve the grinding effect, and improve the performance of cement concrete.

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Since there are not many studies on the application of polymeric surfactants in viscosity reduction emulsification of heavy oil, a series of polyether carboxylic acid-sulfonate polymeric surfactants were synthesized. The viscosity reduction performance and the effect of different chain lengths on the viscosity reduction effect were also investigated. The viscosity reduction, emulsification, wetting, and foaming performance tests showed that the viscosity reduction performance of this series of polymeric surfactants was excellent, with the viscosity reduction rate exceeding 95%, and the viscosity was reduced to 97 mPa·s by the polymeric surfactant with a molecular weight of 600 polyethers. It was also concluded that among the three surfactants with different side chains, the polymeric surfactant with a polyether molecular weight of 600, which is the medium side-chain length, had the best viscosity reduction performance. The study showed that the polyether carboxylic acid-sulfonate polymer surfactant had a promising application in the viscosity reduction of heavy oil.

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Dissolved black carbon (DBC), the water-soluble component of black carbon, which is formed by incomplete combustion of fossil fuels or biochar, takes up about 10% of dissolved organic matter (DOM) in river water. However, the distribution of DBC in water environment especially in source water is not clear and as an important component of DOM, whether DBC can produce disinfection byproducts (DBPs) like other DOM during disinfection remains unknown. In this study, the DBC concentrations in seventeen source water samples from East China were measured. The concentrations of DBC in the source water samples ranged from 60 to 270 µg/L, which were positively correlated with UV254 absorbance and chemical oxygen demand. The levels of DBC in wet season were higher than that in dry season. The average concentrations of DBC in different types of source water samples followed the order of reservoir > canal > lake > river. DBC could only be removed by 20% during the simulated coagulation, and further generate different categories of DBPs during chlorination, among which the concentrations of haloacetic acids (HAA) were the highest. The results indicated that DBC widely distributes in source water and is an important precursor of HAAs and THMs during chlorination.

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RESUMEN

The composition and radiative forcing of light-absorbing brown carbon (BrC) aerosol remain poorly understood. Polycyclic aromatics (PAs) are BrC chromophores with fused benzene rings. Understanding the occurrence and significance of PAs in BrC is challenging due to a lack of standards for many PAs. In this study, we quantified polycyclic aromatic carbon (PAC), defined as the carbon of fused benzene rings, based on molecular markers (benzene polycarboxylic acids, BPCAs). Open biomass burning aerosols (OBBAs) of 22 rainforest plants were successively extracted with water and methanol for the analysis of water- and methanol-soluble PAC (WPAC and MPAC, respectively). PAC is an important fraction of water- and methanol-soluble organic carbon (WSOC and MSOC, respectively). WPAC/WSOC ranged from 0.03 to 0.18, and MPAC/MSOC was even higher (range: 0.16-0.80). The priority polycyclic aromatic hydrocarbons contributed less than 1% of MPAC. The mass absorption efficiency (MAE) of MSOC showed a strong linear correlation with MPAC/MSOC (r = 0.60-0.95, p < 0.01). The absorption Ångström exponent (AAE) of methanol-soluble BrC showed a strong linear correlation with the degree of aromatic condensation of MPAC, which was described by the average number of carboxylic groups of BPCA (r = -0.79, p < 0.01). This result suggested that PAC was a key fraction determining the light absorption properties (i.e., light absorptivity and wavelength dependence) of methanol-soluble BrC in OBBAs.

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Cotton fabrics were dyed with the madder and compounds of citric acid (CA) and dicarboxylic acids [tartaric acid (TTA), malic acid (MLA), succinic acid (SUA)] as cross-linking agents and sodium hypophosphite (SHP) as the catalyst. The molecular structures and crystal structures of the dyed cotton fabrics were analyzed using Fourier-transform infrared spectroscopy (FTIR) and X-ray diffractometry (XRD), respectively. The results showed that the polycarboxylic acids esterified with the hydroxyl groups in the dye and cellulose, respectively, and the reaction mainly occurred in the amorphous region of the cotton fabric. Compared with the direct dyed cotton fabric, the surface color depth (K/S) values of the CA, CA+TTA, CA+MLA, CA+SUA cross-linked dyed cotton fabrics increased by approximately 160%, 190%, 240%, 270%, respectively. The CA+SUA cross-linked dyed cotton fabric achieved the biggest K/S value due to the elimination of the negative effect by α-hydroxyl in TTA and MLA on esterification reaction, and the cross-linked dyed cotton fabrics had great levelness property. The washing and rubbing fastness of the cross-linked cotton fabrics were above four levels. The light resistance stability and the antibacterial property of the cross-linked dyed cotton fabrics was obviously improved. The sum of warp and weft wrinkle recovery angle (WRA) of the CA+SUA cross-linked dyed cotton fabric was 55° higher than that of raw cotton fabric, and its average UV transmittance for UVA was less than 5% and its UPF value was 50+, showing a great anti-wrinkle and anti-ultraviolet properties.

RESUMEN

To explore the combination of silver nanoparticles (Ag NPs) prepared in a green manner with cotton fabrics and the washing durability of the fabric after the combination. In this paper, the natural material, honeysuckle extract, was used as a reducing agent to prepare the Ag NPs' solution. The structure and size of Ag NPs were analyzed using ultraviolet-visible spectrophotometry (UV-vis), transmission electron microscopy (TEM), dynamic light scattering (DLS), X-ray powder diffraction (XRD), and Fourier transform infrared (FT-IR) spectroscopy characterization. The results showed that Ag+ was successfully reduced to Ag0 by the honeysuckle extract, the particle size was about 10.59 nm, and the potential was -42.9 mV, so it had strong electrostatic repulsion and good stability. Meanwhile, it was found that the synthesized Ag NPs were well coated by the honeysuckle extract, so they would not aggregate. Then, the cotton fabric was finished with Ag NPs' solution by the dipping method using a complex of polymaleic acid (PMA) and citric acid (CA) as a cross-linking agent to fix Ag NPs on the cotton fabric. The structures of cotton fabrics before and after finishing were characterized using FT-IR, scanning electron microscopy (SEM), XRD, X-ray photoelectron spectroscopy (XPS), and thermogravimetric (TG) analysis, and the multifunctional properties of the finished cotton fabrics were explored by measuring the antibacterial rate, the wrinkle recovery angle (WRA), and the UV protection factor (UPF) value. The results show that Ag NPs were successfully loaded onto cotton fabric, and the PMA + CA compound was successfully cross-linked to the fabric. The cross-linked Ag NPs' cotton fiber was rougher than that before cross-linking, and its TG stability improved. The PMA + CA compound fixed Ag NPs on the cotton fabric through chemical bonds, so it still had a 99% antibacterial effect against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) after 50 washings. Compared with unfinished cotton fabric, the UPF value and WRA of the cross-linked Ag NPs cotton increased by 34.09 and 98°, respectively, and its color did not change much.

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Polybenzimidazole (PBI) with a strong size-sieving ability exhibits attractive H2/CO2 separation properties for blue H2 production and CO2 capture. Herein, we report that PBI can be facilely cross-linked with polycarboxylic acids, oxalic acid (OA), and trans-aconitic acid (TaA) to improve its separation performance. The acids react with the amines on the PBI chains, decreasing free volume and increasing size-sieving ability. The acid doping increases H2/CO2 selectivity from 12 to as high as 45 at 35 °C. The acid-doped samples demonstrate stable H2/CO2 separation performance when challenged with simulated syngas containing water vapor at 150 °C, which surpasses state-of-the-art polymers and Robeson's upper bound for H2/CO2 separation.

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Scale formation is a bottleneck of most industrial and domestic water equipment, in particular, of oilfield water systems. Therefore, high-performance and environmentally-benign chemical scale inhibitors are highly needed. Phosphino-polycarboxylic acid (PPCA) is a low-in-phosphorous scale inhibitor with high inhibition efficiency, but its synthesis and performance analyses have been rarely disclosed. In this work for the first time, a PPCA copolymer is synthesized by a simple method based on free radical polymerization of acrylic acid and phosphinic acid monomers and directly employed for gypsum scale inhibition. The formation of PPCA was verified by FTIR and 31PNMR spectroscopies, and then its inhibition performance was evaluated by the complexometric determination of the Ca2+ concentration. The PPCA (2.5 ppm) showed 100% inhibition efficiency at a saturation index of 0.31 at the room temperature and without pH regulation after 24 h with practically no detectable gypsum crystallites even after two months, while the commercial ATMP showed a low inhibition efficiency of 30%. The Field Emission Scanning Microscopy (FESEM) images of the PPCA-inhibited and uninhibited samples revealed that the typical gypsum microfibers are distorted and reduced in size significantly in the inhibited sample. At a still higher saturation index of 1.47 (saturation ratio of 10), the inhibition efficiency of PPCA reduced to 16% and 24% for two dosages of 2.5 and 10 ppm which was attributed to the higher ion activity coefficients at the extremely high ionic strength, and hence, a much higher thermodynamic driving force. The rate constants for these two high supersaturation conditions and low PPCA dosages were also calculated and discussed.

RESUMEN

To convey novel properties to textile surface cotton-based fabrics were impregnated with solutions containing various chemical agents, such as butane-1,2,3,4-tetracarboxylic acid or hydrolyzed organotrialkoxysilanes (3-amino)propyltriethoxysilane), (3-glycidylpropyl)-trimethoxysilane, (3-triethoxysilylpropyl)succinic acid anhydride, octyltriethoxysilane, and Dynasylan F8815 (fluoroalkylfunctional water-borne oligosiloxane). The as-prepared cotton specimens were dried and cured at elevated temperatures. As the curing process can be performed at different temperatures, the impregnated and dried cotton samples were studied by means of time-dependent ATR-FTIR spectroscopy in an attempt to get a closer insight into the process mechanism. The results make evident that the butane-1,2,3,4-tetracarboxylic acid and (3-triethoxysilylpropyl)succinic acid anhydride reacts with the hydroxyl groups of the cellulose via a five-membered cyclic anhydride intermediate which is confirmed by vibration bands appearing at 1782 cm-1 (symmetric stretching vibration of the anhydride carbonyl group) and at 1861 cm-1 (antisymmetric stretching vibration of the anhydride carbonyl group).

RESUMEN

Six two-dimensional (2D) coordination polymers (CPs), namely, poly[{µ5-3,3-[(5-carboxylato-1,3-phenylene)bis(oxy)]dibenzoato-κ6O1:O1':O3,O3':O5:O5'}bis(N,N-dimethylformamide-κO)lanthanide(III)], [Ln(C21H11O8)(C3H7NO)2]n, with lanthanide/Ln = cerium/Ce for CP1, praseodymium/Pr for CP2, neodymium/Nd for CP3, samarium/Sm for CP4, europium/Eu for CP5 and gadolinium/Gd for CP6, have been prepared by solvothermal methods using the ligand 3,3'-[(5-carboxy-1,3-phenylene)bis(oxy)]dibenzoic acid (H3cpboda) in the presence of Ln(NO3)3. The complexes were characterized by single-crystal X-ray and powder diffraction, IR spectroscopy, elemental analysis and thermogravimetric analysis (TGA). All the structures of this family of lanthanide CPs are isomorphous with the triclinic space group P-1 and reveal that they have the same 2D network based on binuclear LnIII units, which are further extended via interlayer C-H...π interactions into a three-dimensional supramolecular structure. The carboxylate groups of the cpboda3- ligands link adjacent LnIII ions and form binuclear [Ln2(RCOO)4] secondary building units (SBUs), in which each binuclear LnIII SBU contains four carboxylate groups from different cpboda3- ligands. Moreover, with the increase of the rare-earth Ln atomic radius, the dihedral angles between the aromatic rings gradually increase. Magnetically, CP6 shows weak antiferromagnetic coupling between the GdIII ions. The solid-state luminescence properties of CP2, CP5 and CP6 were examined at ambient temperature and CP5 exhibits characteristic red emission bands derived from the Eu3+ ion (CIE 0.53, 0.31), with luminescence quantum yields of 22%. Therefore, CP5 should be regarded as a potential optical material.

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AIMS: The aim of this study was to compare the efficacy and tolerability of BP-C1 vs equal-looking placebo in metastatic breast cancer. MATERIALS AND METHODS: A randomized, double-blind, placebo-controlled multi-center study with a semicross-over design was performed. Sixteen patients received daily intramuscular injection of 0.035 mg/kg bodyweight of BP-C1 and 15 patients received equal-looking placebo for 32 days. After 32 days, the placebo patients crossed to BP-C1 with the last observation in the placebo period as baseline. The status of receptors including estrogen receptor (ER), progesterone receptor (PtR), and human EGF receptor 2 (HER2) was analyzed prior to inclusion in the study. Thoracoabdominal CT scan was blindly analyzed by the same independent radiologist in accordance with the RECIST criteria 1.1. Toxicity was assessed according to the NCI Bethesda Version 2.0 (CTC-NCI), and the quality of life (QOL) was assessed according to European Organization for the Research and Treatment of Cancer QOL-C30 and QOL-BR23. RESULTS: The sum of target lesion diameters (sum lesions) after 32 days of treatment increased by 8.9% (P=0.08) in the BP-C1 arm compared to 37.6% (P<0.001) in placebo patients. Twelve of the 15 placebo patients subsequently had BP-C1 treatment. The increase in sum lesions was 3.5% in these patients. The sum of CTC-NCI was increased 18.7% in the BP-C1 arm (P=0.38) compared to 50.9% (P=0.04) in placebo patients. Four mild/moderate adverse events (AEs) present in BP-C1. Two mild/moderate AEs and one severe AE present in placebo. The QOL benchmarks "breast cancer problems last week", "sexual interest and activity last 4 weeks", and "breast cancer-related pain and discomfort last week" were stable in the BP-C1 arm but deteriorated in placebo patients. The sum lesions increased significantly in ER+ (P=0.02) and PtR+ (P=0.03) but not in HER2+. The increase in sum lesions significantly decreased (P=0.02) with an increasing number of negative receptors. CONCLUSION: A total of 32 days of BP-C1 treatment inhibited cancer growth and was well tolerated with few and mainly mild AEs. The efficacy of BP-C1 was superior in receptor-negative patients. CLINICALTRIALSGOV IDENTIFIER: NCT03603197.

RESUMEN

Three aliphatic polycarboxylic acids (PCAs) including tartaric acid (TA), citric acid (CA) and 1,2,3,4-butanetetracarboxylic acid (BTCA) were used for the surface modification of waste cotton fiber by an industrialized pad-dry-cure process to introduce carboxyl groups, which then coordinated with Fe3+ ions to obtain three PCA modified cotton fiber Fe complexes. TA modified cotton fiber could easily react with Fe3+ ions to form its complex with high Fe content. Furthermore, TA modified cotton fiber Fe complex showed a better enhanced effect of activated Na2S2O8 to produce free oxygen radicals for the degradation of an azo dye, Reactive Red 195 than the other two complexes. Different critical Fe contents were found for three complexes to obtain the best enhanced effect.