Effect of Structure of Polycarboxylate Superplasticizer on Hydration of Cement in Early Period

2012 ◽  
Vol 487 ◽  
pp. 24-28
Author(s):  
Jian Ping Duan ◽  
Sheng Hua Lv
Keyword(s):  
Cement Paste ◽  
Setting Time ◽  
Early Period ◽  
The Other ◽  
Side Chain ◽  
Carboxyl Groups ◽  
Structure Parameters ◽  
Polycarboxylate Superplasticizer ◽  
Hydrated Product ◽  
Effect Of Structure

Effect of polycarboxylate superplasticizer (PCs) with different bond between side chain and truck chain on hydration of cement in early period was studied. The performance of PCs in concrete was investigated by setting time, TGA and SEM. PC-based superplasticizer with ester bonding between side chain and truck chain. Although they had the proximate structure parameters in density of side chain and absorption group (carboxyl groups), the setting time of cement paste was significantly different when different PCs were employed in the preparation of cement. Decomposing of this bond in alkali environment may lead to a shorter setting time. On the other hand, same difference in hydration production was observed in early period hydration of cement paste when two different PCs was incorporated, which indicated that the different bond structure in PCs affected the hydration of cement in a different manner. The result of SEM indicated that the morphological phase of hydrated product was different when PC was applied, this may be related with the different result in the TG and TGA

scholarly journals Study on adsorption, rheology and hydration behaviours of Polycarboxylate(PCE) superplasticizer synthesized by different acid to ether ratio

2021 ◽  
Vol 2133 (1) ◽  
pp. 012007
Author(s):  
Zhijun Lin ◽  
Xiaofang Zhang ◽  
Zhanhua Chen ◽  
Yue Xiao ◽  
Yunhui Fang
Keyword(s):  
Molecular Weight ◽  
Adsorption Capacity ◽  
Cement Paste ◽  
Cement Hydration ◽  
Main Chain ◽  
Chain Structure ◽  
Hydration Process ◽  
Side Chain ◽  
Structure Parameters ◽  
Polycarboxylate Superplasticizer

Abstract Polycarboxylate superplasticizer is synthesised by different acid to ether ratio, which is changing the main chain structure parameters, obtained different microstructures. The effect of different microstructure PCE superplasticizer on the fluidity of cement paste, rheological thixotropy, adsorption capacity and hydration heat are studied. The results show that dispersing performance in cement with acid to ether ratio of 3.5 is the best, the molecular weight and side chain density have rather little effect on the cement hydration process.

The Effect of Sodium Sulfate on the Dispersion of Polycarboxylate Superplasticizer

2011 ◽  
Vol 80-81 ◽  
pp. 284-287 ◽  
Author(s):  
Sheng Hua Lv ◽  
Jian Ping Duan ◽  
Rui Jun Gao
Keyword(s):  
Zeta Potential ◽  
Cement Paste ◽  
Sodium Sulfate ◽  
Carboxyl Groups ◽  
Dispersal Ability ◽  
Sulfonic Group ◽  
Polycarboxylate Superplasticizer

The effect of sodium sulfate on the dispersion of polycarboxylate superplasticizer (PC) was studied in this paper. The study of fluidity of cement paste shown that the carboxyl groups did more to improve the fluidity of cement paste than the sulfonic groups, and a quick loss of fluidity was much more likely arisen by slufonic groups in PC comparing with the carboxyl groups. The methods of zeta potential and fluidity of cement paste were applied to investigate the dispersal ability of cement particles when different PC used in the present of different concentration of sodium sulfate. The result showed that the sulfonic group was more sensitive to sodium sulfate than carboxyl groups in PC.

Binding of lead and copper(II) cations to hemicelluloses of rye bran

1986 ◽  
Vol 51 (10) ◽  
pp. 2250-2258 ◽  
Author(s):  
Rudolf Kohn ◽  
Zdena Hromádková ◽  
Anna Ebringerová
Keyword(s):  
Uronic Acid ◽  
Equilibrium Solution ◽  
Glucuronic Acid ◽  
The Other ◽  
Carboxyl Groups ◽  
Stoichiometric Ratio ◽  
Molar Ratios ◽  
Free Ions ◽  
Uronic Acid Content ◽  
The Relationship

Several fractions of acid hemicelluloses isolated from rye bran were characterized by molar ratios of saccharides (D-Xyl, L-Ara, D-Glc, D-Gal) and 4-O-methyl-D-glucuronic acid and protein content. Binding of Pb2+ and Cu2+ ions to these acid polysaccharides was considered according to function (M)b = f([M2+]f), expressing the relationship between the amount of metal (M)b bound to 1 g of the substance and the concentration of free ions [M2+]f in the equilibrium solution and according to the association degree β of these cations with carboxyl groups of uronic acid at a stoichiometric ratio of both components in the system under investigation. Acid hemicelluloses contained only a very small portion of uronic acid ((COOH) 0.05-0.18 mmol g-1); the model polysaccharide, 4-O-methyl-D-glucurono-D-xylan of beech, was substantially richer in uronic acid content ((COOH) 0.73 mmol g-1). Consequently, the amount of lead and copper bound to acid hemicelluloses is very small ((M)b 0.017-0.025 mmol g-1) at [M2+]f = 0.10 mmol l-1. On the other hand, much greater amount of cations ((M)f 0.09-0.10 mmol g-1) was bound to the glucuronoxylan. The association degree β was like with the majority of samples (β = 0.31-0.38). The amount of lead and copper(II) bound to acid hemicelluloses from rye bran is several times lower than that bound to dietary fiber isolated from vegetables (cabbage, carrot), rich in pectic substances.

Comparison of the Potency of 8-L-Arginine, 8-D-Arginine and 8-D-Homoarginine Vasopressin Analogs with Substituted Phenylalanine in Position 2

1994 ◽  
Vol 59 (6) ◽  
pp. 1439-1450 ◽  
Author(s):  
Miroslava Žertová ◽  
Jiřina Slaninová ◽  
Zdenko Procházka
Keyword(s):  
Amino Acid ◽  
Solid Phase Synthesis ◽  
Solid Phase ◽  
Basic Amino Acid ◽  
The Other ◽  
Side Chain ◽  
Inhibitory Potency ◽  
Phase Synthesis ◽  
Other Hand ◽  
Order Of Magnitude

An analysis of the uterotonic potencies of all analogs having substituted L- or D-tyrosine or -phenylalanine in position 2 and L-arginine, D-arginine or D-homoarginine in position 8 was made. The series of analogs already published was completed by the solid phase synthesis of ten new analogs having L- or D-Phe, L- or D-Phe(2-Et), L- or D-Phe(2,4,6-triMe) or D-Tyr(Me) in position 2 and either L- or D-arginine in position 8. All newly synthesized analogs were found to be uterotonic inhibitors. Deamination increases both the agonistic and antagonistic potency. In the case of phenylalanine analogs the change of configuration from L to D in position 2 enhances the uterotonic inhibition for more than 1 order of magnitude. The L to D change in position 8 enhances the inhibitory potency negligibly. Prolongation of the side chain of the D-basic amino acid in position 8 seems to decrease slightly the inhibitory potency if there is L-substituted amino acid in position 2. On the other hand there is a tendency to the increase of the inhibitory potency if there is D-substituted amino acid in position 2.

scholarly journals Effect of Calcium Nitrate on the Properties of Portland–Limestone Cement-Based Concrete Cured at Low Temperature

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1611
Author(s):  
Gintautas Skripkiūnas ◽  
Asta Kičaitė ◽  
Harald Justnes ◽  
Ina Pundienė
Keyword(s):  
Compressive Strength ◽  
Cement Paste ◽  
Setting Time ◽  
Calcium Nitrate ◽  
Curing Temperature ◽  
Hardened Concrete ◽  
Cement Pastes ◽  
Initial Setting Time ◽  
Initial Setting ◽  
Early Strength

The effect of calcium nitrate (CN) dosages from 0 to 3% (of cement mass) on the properties of fresh cement paste rheology and hardening processes and on the strength of hardened concrete with two types of limestone-blended composite cements (CEM II A-LL 42.5 R and 42.5 N) at different initial (two-day) curing temperatures (−10 °C to +20 °C) is presented. The rheology results showed that a CN dosage up to 1.5% works as a plasticizing admixture, while higher amounts demonstrate the effect of increasing viscosity. At higher CN content, the viscosity growth in normal early strength (N type) cement pastes is much slower than in high early strength (R type) cement pastes. For both cement-type pastes, shortening the initial and final setting times is more effective when using 3% at +5 °C and 0 °C. At these temperatures, the use of 3% CN reduces the initial setting time for high early strength paste by 7.4 and 5.4 times and for normal early strength cement paste by 3.5 and 3.4 times when compared to a CN-free cement paste. The most efficient use of CN is achieved at −5 °C for compressive strength enlargement; a 1% CN dosage ensures the compressive strength of samples at a −5 °C initial curing temperature, with high early strength cement exceeding 3.5 MPa but being less than the required 3.5 MPa in samples with normal early strength cement.

Study on Relationship between Structure and Properties of Polycarboxylate Superplasticizer

2012 ◽  
Vol 487 ◽  
pp. 43-47
Author(s):  
Sheng Hua Lv ◽  
Di Li ◽  
Qiang Cao
Keyword(s):  
Acrylic Acid ◽  
Zeta Potential ◽  
Ethyl Ester ◽  
Functional Groups ◽  
Cement Paste ◽  
Ethyl Acrylate ◽  
Structure And Properties ◽  
Polycarboxylate Superplasticizer ◽  
Carboxylic Groups

A polycarboxylate superplasticizer (PCs) was synthesized by copolymerization of allyl polyoxyethylene ethers (APE), acrylic acid (AA), sodium methylallyl Sulfonate (SMAS) and ethyl acrylate (EA). The effect of functional groups and branch chain on PCs properties was investigated by the test of fluidity of cement paste, retardation performance and Zeta potential of cement particles. The results showed that carboxylic groups and ethyl ester groups can improve water reducing ratio and fluidity of cement paste, and the sulfonic groups has an important contributiion to retardation performance of PCs.

Fresh State Behaviour of Cement Paste Containing Nano Kaolin

2014 ◽  
Vol 925 ◽  
pp. 28-32 ◽  
Author(s):  
Muhd Sidek Muhd Norhasri ◽  
M.S. Hamidah ◽  
A. Mohd Fadzil ◽  
A.G. Abd Halim ◽  
M.R. Zaidi
Keyword(s):  
Surface Area ◽  
Cement Paste ◽  
Setting Time ◽  
High Energy ◽  
Major Effect ◽  
Cement Replacement ◽  
High Energy Milling ◽  
Replacement Method ◽  
Fresh State ◽  
State Behaviour

The application of nanomaterials in cement by replacement method in concrete is becoming a trend in cement research. The utilisation of nanosilica, nanoalumina, titanium oxide and others are proven to enhance properties of concrete. The major effect of nanomaterials is its size in which it contributes to the packing theory due to increase in the surface area. nanokaolin which comes from kaolin, was tansformed to the nanoform by using high energy milling. The process of developing nanokaolin by using high energy milling is referred to process top to bottom approach in nanoprocessing technique. In this research, the nanokaolin will be used as an additive in cement by 7% weight of cement. Four (4) cement replacement materials catered by using metakaolin on weight basis from 0, 10%, 20% and 30% will also be adopted. To determine the fresh state, cement paste contains nanokaolin and metakaolin are tested its standard consistency and setting time. The effect of the inclusion of the nanokaolin as additive in cement paste that also contains metakaolin as cement replacement material will be investigated. It was found the inclusion of 7% nanokaolin increases the water demand of the cement paste level of metakaolin replacement. In addition to that, the setting time namely initial and final set was been delayed as compared to that of plain OPC. The nanoparticles of nanokaolin and also finer particles of metakaolin increase the surface area and refining the internal structure of cement paste which reduce the flow capabilities of cement paste containing nanokaolin and metakaolin.

Structural Studies on N-(2,4,6-Trimethylphenyl)-methyl/ chloro-acetamides, 2,4,6-(CH3)3C6H2NH-CO-CH3–yXy (X = CH3 or Cl and y = 0, 1, 2)

2006 ◽  
Vol 61 (10-11) ◽  
pp. 588-594 ◽  
Author(s):  
Basavalinganadoddy Thimme Gowda ◽  
Jozef Kožíšek ◽  
Hartmut Fuess
Keyword(s):  
Crystal Structure ◽  
Crystal Structures ◽  
Structural Data ◽  
The Other ◽  
Side Chain ◽  
Structural Studies ◽  
Asymmetric Unit ◽  
Lattice Constants ◽  
Peptide Linkage ◽  
The Mean

TMPAThe effect of substitutions in the ring and in the side chain on the crystal structure of N- (2,4,6-trimethylphenyl)-methyl/chloro-acetamides of the configuration 2,4,6-(CH3)3C6H2NH-COCH3− yXy (X = CH3 or Cl and y = 0,1, 2) has been studied by determining the crystal structures of N-(2,4,6-trimethylphenyl)-acetamide, 2,4,6-(CH3)3C6H2NH-CO-CH3 (); N-(2,4,6- trimethylphenyl)-2-methylacetamide, 2,4,6-(CH3)3C6H2NH-CO-CH2-CH3 (TMPMA); N-(2,4,6- trimethylphenyl)-2,2-dimethylacetamide, 2,4,6-(CH3)3C6H2NH-CO-CH(CH3)2 (TMPDMA) and N-(2,4,6-trimethylphenyl)-2,2-dichloroacetamide, 2,4,6-(CH3)3C6H2NH-CO-CHCl2 (TMPDCA). The crystallographic system, space group, formula units and lattice constants in Å are: TMPA: monoclinic, Pn, Z = 2, a = 8.142(3), b = 8.469(3), c = 8.223(3), β = 113.61(2)◦; TMPMA: monoclinic, P21/n, Z = 8, a = 9.103(1), b = 15.812(2), c = 16.4787(19), α = 89.974(10)◦, β = 96.951(10)◦, γ =89.967(10)◦; TMPDMA: monoclinic, P21/c, Z = 4, a =4.757(1), b= 24.644(4), c =10.785(2), β = 99.647(17)◦; TMPDCA: triclinic, P¯1, Z = 2, a = 4.652(1), b = 11.006(1), c = 12.369(1), α = 82.521(7)◦, β = 83.09(1)◦, γ = 79.84(1)◦. The results are analyzed along with the structural data of N-phenylacetamide, C6H5NH-CO-CH3; N-(2,4,6-trimethylphenyl)-2-chloroacetamide, 2,4,6-(CH3)3C6H2NH-CO-CH2Cl; N-(2,4,6-trichlorophenyl)-acetamide, 2,4,6-Cl3C6H2NH-COCH3; N-(2,4,6-trichlorophenyl)-2-chloroacetamide, 2,4,6-Cl3C6H2NH-CO-CH2Cl; N-(2,4,6-trichlorophenyl)- 2,2-dichloroacetamide, 2,4,6-Cl3C6H2NH-CO-CHCl2 and N-(2,4,6-trichlorophenyl)- 2,2,2-trichloroacetamide, 2,4,6-Cl3C6H2NH-CO-CCl3. TMPA, TMPMA and TMPDCA have one molecule each in their asymmetric units, while TMPDMA has two molecules in its asymmetric unit. Changes in the mean ring distances are smaller on substitution as the effect has to be transmitted through the peptide linkage. The comparison of the other bond parameters reveal that there are significant changes in them on substitution.

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